| Mutation - TCGA |
| Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
|---|
| ACC | 7 | 151843708 | 151843709 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-OR-A5KP-01A-11D-A30A-10 | TCGA-OR-A5KP-10A-01D-A30A-10 | g.chr7:151843708_151843709delAG | c.14006_14007delCT | c.(14005-14007)tctfs | p.S4669fs |
| ACC | 7 | 151864452 | 151864452 | + | Missense_Mutation | SNP | G | G | A | TCGA-OR-A5K4-01A-11D-A29I-10 | TCGA-OR-A5K4-10A-01D-A29L-10 | g.chr7:151864452G>A | c.9529C>T | c.(9529-9531)Cgt>Tgt | p.R3177C |
| ACC | 7 | 151878058 | 151878058 | + | Missense_Mutation | SNP | C | C | T | TCGA-OR-A5LB-01A-11D-A29I-10 | TCGA-OR-A5LB-10A-01D-A29L-10 | g.chr7:151878058C>T | c.6887G>A | c.(6886-6888)cGt>cAt | p.R2296H |
| ACC | 7 | 151879078 | 151879078 | + | Missense_Mutation | SNP | G | G | A | TCGA-OR-A5LB-01A-11D-A29I-10 | TCGA-OR-A5LB-10A-01D-A29L-10 | g.chr7:151879078G>A | c.5867C>T | c.(5866-5868)tCc>tTc | p.S1956F |
| ACC | 7 | 151879463 | 151879463 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-OR-A5JA-01A-11D-A29I-10 | TCGA-OR-A5JA-10A-01D-A29L-10 | g.chr7:151879463C>A | c.5482G>T | c.(5482-5484)Gaa>Taa | p.E1828* |
| ACC | 7 | 151932990 | 151932990 | + | Missense_Mutation | SNP | C | C | T | TCGA-OR-A5J4-01A-11D-A29I-10 | TCGA-OR-A5J4-10A-01D-A29L-10 | g.chr7:151932990C>T | c.2681G>A | c.(2680-2682)cGg>cAg | p.R894Q |
| ACC | 7 | 151947965 | 151947965 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr7:151947965C>A | c.1708G>T | c.(1708-1710)Gag>Tag | p.E570* |
| ACC | 7 | 151962269 | 151962269 | + | Silent | SNP | C | C | T | TCGA-OR-A5LP-01A-11D-A29I-10 | TCGA-OR-A5LP-10A-01D-A29L-10 | g.chr7:151962269C>T | c.1038G>A | c.(1036-1038)gtG>gtA | p.V346V |
| BLCA | 7 | 151834007 | 151834007 | + | Silent | SNP | G | G | C | TCGA-CF-A3MG-01A-11D-A20D-08 | TCGA-CF-A3MG-10A-01D-A20D-08 | g.chr7:151834007G>C | c.14646C>G | c.(14644-14646)ctC>ctG | p.L4882L |
| BLCA | 7 | 151835931 | 151835932 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-CF-A9FL-01A-11D-A38G-08 | TCGA-CF-A9FL-10A-01D-A38J-08 | g.chr7:151835931_151835932delCT | c.14592_14593delAG | c.(14590-14595)agaggafs | p.G4865fs |
| BLCA | 7 | 151841937 | 151841937 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr7:151841937G>C | c.14204C>G | c.(14203-14205)tCa>tGa | p.S4735* |
| BLCA | 7 | 151843770 | 151843770 | + | Missense_Mutation | SNP | C | C | T | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr7:151843770C>T | c.13945G>A | c.(13945-13947)Gaa>Aaa | p.E4649K |
| BLCA | 7 | 151843779 | 151843788 | + | Frame_Shift_Del | DEL | TTCTCACACA | TTCTCACACA | - | TCGA-GC-A3BM-01A-11D-A22Z-08 | TCGA-GC-A3BM-10A-01D-A22Z-08 | g.chr7:151843779_151843788delTTCTCACACA | c.13927_13936delTGTGTGAGAA | c.(13927-13938)tgtgtgagaaaafs | p.CVRK4643fs |
| BLCA | 7 | 151845284 | 151845288 | + | Frame_Shift_Del | DEL | GAAGA | GAAGA | - | TCGA-FD-A3SM-01A-11D-A22Z-08 | TCGA-FD-A3SM-10A-01D-A22Z-08 | g.chr7:151845284_151845288delGAAGA | c.13724_13728delTCTTC | c.(13723-13728)ctcttcfs | p.LF4575fs |
| BLCA | 7 | 151845346 | 151845346 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-YC-A9TC-01A-22D-A391-08 | TCGA-YC-A9TC-10A-01D-A394-08 | g.chr7:151845346delG | c.13666delC | c.(13666-13668)cacfs | p.H4556fs |
| BLCA | 7 | 151845353 | 151845353 | + | Silent | SNP | G | G | A | TCGA-FD-A5BX-01A-11D-A26M-08 | TCGA-FD-A5BX-10A-01D-A26K-08 | g.chr7:151845353G>A | c.13659C>T | c.(13657-13659)ctC>ctT | p.L4553L |
| BLCA | 7 | 151845580 | 151845580 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr7:151845580G>A | c.13432C>T | c.(13432-13434)Cga>Tga | p.R4478* |
| BLCA | 7 | 151845618 | 151845618 | + | Missense_Mutation | SNP | C | C | T | TCGA-GU-A767-01A-11D-A32B-08 | TCGA-GU-A767-10A-01D-A329-08 | g.chr7:151845618C>T | c.13394G>A | c.(13393-13395)tGt>tAt | p.C4465Y |
| BLCA | 7 | 151845784 | 151845784 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-A9T8-01A-11D-A391-08 | TCGA-XF-A9T8-10A-01D-A394-08 | g.chr7:151845784C>T | c.13228G>A | c.(13228-13230)Gat>Aat | p.D4410N |
| BLCA | 7 | 151845790 | 151845790 | + | Missense_Mutation | SNP | C | C | G | TCGA-G2-AA3B-01A-11D-A391-08 | TCGA-G2-AA3B-10A-01D-A394-08 | g.chr7:151845790C>G | c.13222G>C | c.(13222-13224)Gaa>Caa | p.E4408Q |
| BLCA | 7 | 151845834 | 151845834 | + | Missense_Mutation | SNP | T | T | C | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chr7:151845834T>C | c.13178A>G | c.(13177-13179)gAt>gGt | p.D4393G |
| BLCA | 7 | 151846037 | 151846037 | + | Silent | SNP | C | C | T | TCGA-G2-A2EJ-01A-11D-A17V-08 | TCGA-G2-A2EJ-10A-01D-A17V-08 | g.chr7:151846037C>T | c.12975G>A | c.(12973-12975)ctG>ctA | p.L4325L |
| BLCA | 7 | 151848063 | 151848063 | + | Missense_Mutation | SNP | C | C | G | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr7:151848063C>G | c.12696G>C | c.(12694-12696)gaG>gaC | p.E4232D |
| BLCA | 7 | 151849976 | 151849976 | + | Missense_Mutation | SNP | C | C | T | TCGA-GU-AATP-01A-11D-A391-08 | TCGA-GU-AATP-10A-01D-A394-08 | g.chr7:151849976C>T | c.12340G>A | c.(12340-12342)Gag>Aag | p.E4114K |
| BLCA | 7 | 151851456 | 151851456 | + | Missense_Mutation | SNP | C | C | G | TCGA-G2-A3IE-01A-11D-A20D-08 | TCGA-G2-A3IE-10A-01D-A20D-08 | g.chr7:151851456C>G | c.12035G>C | c.(12034-12036)gGg>gCg | p.G4012A |
| BLCA | 7 | 151851516 | 151851516 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-AA6X-01A-12D-A42E-08 | TCGA-DK-AA6X-10A-01D-A42H-08 | g.chr7:151851516C>T | c.11975G>A | c.(11974-11976)tGt>tAt | p.C3992Y |
| BLCA | 7 | 151853410 | 151853410 | + | Missense_Mutation | SNP | G | G | C | TCGA-2F-A9KO-01A-11D-A38G-08 | TCGA-2F-A9KO-11A-12D-A38J-08 | g.chr7:151853410G>C | c.11692C>G | c.(11692-11694)Cca>Gca | p.P3898A |
| BLCA | 7 | 151855998 | 151855998 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-C4-A0F1-01A-11D-A10S-08 | TCGA-C4-A0F1-10A-01D-A10S-08 | g.chr7:151855998C>A | c.11620G>T | c.(11620-11622)Gag>Tag | p.E3874* |
| BLCA | 7 | 151859702 | 151859702 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DK-A3WW-01A-22D-A23M-08 | TCGA-DK-A3WW-10A-01D-A23K-08 | g.chr7:151859702G>A | c.10960C>T | c.(10960-10962)Caa>Taa | p.Q3654* |
| BLCA | 7 | 151860019 | 151860019 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-4Z-AA7R-01A-11D-A391-08 | TCGA-4Z-AA7R-10A-01D-A394-08 | g.chr7:151860019delG | c.10643delC | c.(10642-10644)ccafs | p.P3548fs |
| BLCA | 7 | 151860062 | 151860062 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-C4-A0F1-01A-11D-A10S-08 | TCGA-C4-A0F1-10A-01D-A10S-08 | g.chr7:151860062G>A | c.10600C>T | c.(10600-10602)Cag>Tag | p.Q3534* |
| BLCA | 7 | 151860219 | 151860219 | + | Silent | SNP | C | C | T | TCGA-ZF-A9RN-01A-11D-A42E-08 | TCGA-ZF-A9RN-10A-01D-A42H-08 | g.chr7:151860219C>T | c.10443G>A | c.(10441-10443)caG>caA | p.Q3481Q |
| BLCA | 7 | 151860303 | 151860303 | + | Silent | SNP | G | G | A | TCGA-FD-A3SO-01A-11D-A22Z-08 | TCGA-FD-A3SO-10A-01D-A22Z-08 | g.chr7:151860303G>A | c.10359C>T | c.(10357-10359)ttC>ttT | p.F3453F |
| BLCA | 7 | 151860461 | 151860461 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-CF-A47Y-01A-11D-A23U-08 | TCGA-CF-A47Y-10A-01D-A23U-08 | g.chr7:151860461T>A | c.10201A>T | c.(10201-10203)Aag>Tag | p.K3401* |
| BLCA | 7 | 151860518 | 151860518 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SS-01A-12D-A22Z-08 | TCGA-FD-A3SS-10A-01D-A22Z-08 | g.chr7:151860518G>A | c.10144C>T | c.(10144-10146)Cgg>Tgg | p.R3382W |
| BLCA | 7 | 151864230 | 151864230 | + | Splice_Site | SNP | C | C | T | TCGA-G2-A2ES-01A-11D-A17V-08 | TCGA-G2-A2ES-11A-31D-A17V-08 | g.chr7:151864230C>T | | c.e42+1 | |
| BLCA | 7 | 151864287 | 151864287 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-YC-A8S6-01A-31D-A38G-08 | TCGA-YC-A8S6-10A-01D-A38J-08 | g.chr7:151864287C>A | c.9694G>T | c.(9694-9696)Gaa>Taa | p.E3232* |
| BLCA | 7 | 151864343 | 151864343 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A2HX-01A-12D-A18F-08 | TCGA-DK-A2HX-10A-01D-A18F-08 | g.chr7:151864343G>A | c.9638C>T | c.(9637-9639)tCa>tTa | p.S3213L |
| BLCA | 7 | 151864437 | 151864437 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-AA75-01A-11D-A391-08 | TCGA-DK-AA75-10A-01D-A394-08 | g.chr7:151864437C>G | c.9544G>C | c.(9544-9546)Gag>Cag | p.E3182Q |
| BLCA | 7 | 151868427 | 151868427 | + | Splice_Site | SNP | C | C | A | TCGA-4Z-AA80-01A-11D-A391-08 | TCGA-4Z-AA80-10A-01D-A394-08 | g.chr7:151868427C>A | c.9375G>T | c.(9373-9375)agG>agT | p.R3125S |
| BLCA | 7 | 151868429 | 151868429 | + | Splice_Site | SNP | T | T | G | TCGA-4Z-AA80-01A-11D-A391-08 | TCGA-4Z-AA80-10A-01D-A394-08 | g.chr7:151868429T>G | | c.e40-2 | |
| BLCA | 7 | 151873284 | 151873284 | + | Missense_Mutation | SNP | G | G | A | TCGA-UY-A9PF-01A-11D-A38G-08 | TCGA-UY-A9PF-10A-01D-A38J-08 | g.chr7:151873284G>A | c.9254C>T | c.(9253-9255)cCt>cTt | p.P3085L |
| BLCA | 7 | 151873559 | 151873559 | + | Silent | SNP | G | G | T | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr7:151873559G>T | c.8979C>A | c.(8977-8979)ctC>ctA | p.L2993L |
| BLCA | 7 | 151873694 | 151873694 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-4Z-AA83-01A-11D-A391-08 | TCGA-4Z-AA83-10A-01D-A394-08 | g.chr7:151873694delG | c.8844delC | c.(8842-8844)tccfs | p.S2948fs |
| BLCA | 7 | 151873749 | 151873749 | + | Missense_Mutation | SNP | G | G | A | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr7:151873749G>A | c.8789C>T | c.(8788-8790)tCa>tTa | p.S2930L |
| BLCA | 7 | 151873966 | 151873967 | + | Frame_Shift_Ins | INS | - | - | AG | TCGA-DK-A1AE-01A-11D-A13W-08 | TCGA-DK-A1AE-10A-01D-A13W-08 | g.chr7:151873966_151873967insAG | c.8571_8572insCT | c.(8569-8574)tctgctfs | p.A2858fs |
| BLCA | 7 | 151874020 | 151874020 | + | Missense_Mutation | SNP | C | C | T | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr7:151874020C>T | c.8518G>A | c.(8518-8520)Gaa>Aaa | p.E2840K |
| BLCA | 7 | 151874099 | 151874099 | + | Missense_Mutation | SNP | C | C | G | TCGA-K4-A5RH-01A-11D-A30E-08 | TCGA-K4-A5RH-10A-01D-A30H-08 | g.chr7:151874099C>G | c.8439G>C | c.(8437-8439)caG>caC | p.Q2813H |
| BLCA | 7 | 151874111 | 151874111 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-XF-AAMT-01A-11D-A42E-08 | TCGA-XF-AAMT-10A-01D-A42H-08 | g.chr7:151874111delT | c.8427delA | c.(8425-8427)aaafs | p.K2809fs |
| BLCA | 7 | 151874140 | 151874140 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr7:151874140C>A | c.8398G>T | c.(8398-8400)Gaa>Taa | p.E2800* |
| BLCA | 7 | 151874176 | 151874176 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-UY-A9PH-01A-11D-A38G-08 | TCGA-UY-A9PH-10A-01D-A38J-08 | g.chr7:151874176G>A | c.8362C>T | c.(8362-8364)Cag>Tag | p.Q2788* |
| BLCA | 7 | 151874302 | 151874302 | + | Missense_Mutation | SNP | C | C | T | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr7:151874302C>T | c.8236G>A | c.(8236-8238)Gat>Aat | p.D2746N |
| BLCA | 7 | 151875018 | 151875018 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A43P-01A-31D-A23U-08 | TCGA-FD-A43P-10A-01D-A23U-08 | g.chr7:151875018C>T | c.7520G>A | c.(7519-7521)gGa>gAa | p.G2507E |
| BLCA | 7 | 151875031 | 151875031 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-H4-A2HQ-01A-11D-A17V-08 | TCGA-H4-A2HQ-10A-01D-A17V-08 | g.chr7:151875031G>A | c.7507C>T | c.(7507-7509)Cag>Tag | p.Q2503* |
| BLCA | 7 | 151877000 | 151877000 | + | Missense_Mutation | SNP | C | C | G | TCGA-BT-A3PH-01A-11D-A21Z-08 | TCGA-BT-A3PH-10A-01D-A21Z-08 | g.chr7:151877000C>G | c.7361G>C | c.(7360-7362)aGa>aCa | p.R2454T |
| BLCA | 7 | 151877140 | 151877140 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-FD-A3SM-01A-11D-A22Z-08 | TCGA-FD-A3SM-10A-01D-A22Z-08 | g.chr7:151877140delC | c.7221delG | c.(7219-7221)gggfs | p.G2407fs |
| BLCA | 7 | 151877154 | 151877154 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr7:151877154G>A | c.7207C>T | c.(7207-7209)Cga>Tga | p.R2403* |
| BLCA | 7 | 151877847 | 151877847 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-E7-A3Y1-01A-11D-A22Z-08 | TCGA-E7-A3Y1-10A-01D-A22Z-08 | g.chr7:151877847delA | c.7098delT | c.(7096-7098)gatfs | p.D2366fs |
| BLCA | 7 | 151878184 | 151878184 | + | Missense_Mutation | SNP | G | G | A | TCGA-2F-A9KO-01A-11D-A38G-08 | TCGA-2F-A9KO-11A-12D-A38J-08 | g.chr7:151878184G>A | c.6761C>T | c.(6760-6762)gCa>gTa | p.A2254V |
| BLCA | 7 | 151878254 | 151878254 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A5BX-01A-11D-A26M-08 | TCGA-FD-A5BX-10A-01D-A26K-08 | g.chr7:151878254C>G | c.6691G>C | c.(6691-6693)Gag>Cag | p.E2231Q |
| BLCA | 7 | 151878427 | 151878427 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-E7-A519-01A-11D-A26M-08 | TCGA-E7-A519-10A-01D-A26K-08 | g.chr7:151878427delG | c.6518delC | c.(6517-6519)ccafs | p.P2173fs |
| BLCA | 7 | 151878836 | 151878836 | + | Missense_Mutation | SNP | C | C | G | TCGA-BT-A3PH-01A-11D-A21Z-08 | TCGA-BT-A3PH-10A-01D-A21Z-08 | g.chr7:151878836C>G | c.6109G>C | c.(6109-6111)Gat>Cat | p.D2037H |
| BLCA | 7 | 151879026 | 151879026 | + | Silent | SNP | C | C | T | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr7:151879026C>T | c.5919G>A | c.(5917-5919)gtG>gtA | p.V1973V |
| BLCA | 7 | 151879094 | 151879094 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-AA6L-01A-11D-A391-08 | TCGA-DK-AA6L-10A-01D-A394-08 | g.chr7:151879094C>G | c.5851G>C | c.(5851-5853)Gat>Cat | p.D1951H |
| BLCA | 7 | 151879574 | 151879574 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-2F-A9KT-01A-11D-A38G-08 | TCGA-2F-A9KT-10A-01D-A38J-08 | g.chr7:151879574G>A | c.5371C>T | c.(5371-5373)Cag>Tag | p.Q1791* |
| BLCA | 7 | 151879673 | 151879673 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3B5-01A-11D-A20D-08 | TCGA-FD-A3B5-10A-01D-A20D-08 | g.chr7:151879673G>A | c.5272C>T | c.(5272-5274)Cgt>Tgt | p.R1758C |
| BLCA | 7 | 151880090 | 151880090 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-XF-A9T8-01A-11D-A391-08 | TCGA-XF-A9T8-10A-01D-A394-08 | g.chr7:151880090G>C | c.5234C>G | c.(5233-5235)tCa>tGa | p.S1745* |
| BLCA | 7 | 151880184 | 151880184 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A3IS-01A-21D-A21A-08 | TCGA-DK-A3IS-10A-01D-A21A-08 | g.chr7:151880184C>G | c.5140G>C | c.(5140-5142)Gat>Cat | p.D1714H |
| BLCA | 7 | 151884345 | 151884345 | + | Splice_Site | SNP | A | A | G | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr7:151884345A>G | | c.e33+1 | |
| BLCA | 7 | 151884372 | 151884372 | + | Silent | SNP | G | G | A | TCGA-K4-A83P-01A-11D-A34U-08 | TCGA-K4-A83P-10A-01D-A34X-08 | g.chr7:151884372G>A | c.4983C>T | c.(4981-4983)ttC>ttT | p.F1661F |
| BLCA | 7 | 151891118 | 151891118 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CF-A47W-01A-11D-A23U-08 | TCGA-CF-A47W-10A-01D-A23U-08 | g.chr7:151891118G>A | c.4636C>T | c.(4636-4638)Cag>Tag | p.Q1546* |
| BLCA | 7 | 151891214 | 151891214 | + | Splice_Site | SNP | C | C | G | TCGA-DK-A3IS-01A-21D-A21A-08 | TCGA-DK-A3IS-10A-01D-A21A-08 | g.chr7:151891214C>G | | c.e31-1 | |
| BLCA | 7 | 151893024 | 151893024 | + | Missense_Mutation | SNP | G | G | A | TCGA-KQ-A41R-01A-21D-A34U-08 | TCGA-KQ-A41R-10G-01D-A34X-08 | g.chr7:151893024G>A | c.4346C>T | c.(4345-4347)tCa>tTa | p.S1449L |
| BLCA | 7 | 151896487 | 151896487 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr7:151896487C>T | c.4150G>A | c.(4150-4152)Gat>Aat | p.D1384N |
| BLCA | 7 | 151900066 | 151900066 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FD-A3N6-01A-11D-A21A-08 | TCGA-FD-A3N6-10A-01D-A21A-08 | g.chr7:151900066G>A | c.4045C>T | c.(4045-4047)Cga>Tga | p.R1349* |
| BLCA | 7 | 151900069 | 151900069 | + | Missense_Mutation | SNP | A | A | G | TCGA-KQ-A41N-01A-11D-A339-08 | TCGA-KQ-A41N-10D-01D-A339-08 | g.chr7:151900069A>G | c.4042T>C | c.(4042-4044)Tac>Cac | p.Y1348H |
| BLCA | 7 | 151900091 | 151900091 | + | Silent | SNP | G | G | A | TCGA-E7-A6MD-01A-41D-A34U-08 | TCGA-E7-A6MD-10B-01D-A34X-08 | g.chr7:151900091G>A | c.4020C>T | c.(4018-4020)agC>agT | p.S1340S |
| BLCA | 7 | 151902229 | 151902229 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-FD-A3SJ-01A-12D-A22Z-08 | TCGA-FD-A3SJ-10A-01D-A22Z-08 | g.chr7:151902229G>C | c.3923C>G | c.(3922-3924)tCa>tGa | p.S1308* |
| BLCA | 7 | 151904469 | 151904469 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-DK-A3WW-01A-22D-A23M-08 | TCGA-DK-A3WW-10A-01D-A23K-08 | g.chr7:151904469C>A | c.3757G>T | c.(3757-3759)Gag>Tag | p.E1253* |
| BLCA | 7 | 151917708 | 151917708 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-2F-A9KT-01A-11D-A38G-08 | TCGA-2F-A9KT-10A-01D-A38J-08 | g.chr7:151917708delC | c.3612delG | c.(3610-3612)ttgfs | p.L1204fs |
| BLCA | 7 | 151919766 | 151919766 | + | Splice_Site | SNP | A | A | G | TCGA-BT-A3PK-01A-21D-A21Z-08 | TCGA-BT-A3PK-10A-01D-A21Z-08 | g.chr7:151919766A>G | c.3325T>C | c.(3325-3327)Tgg>Cgg | p.W1109R |
| BLCA | 7 | 151921139 | 151921139 | + | Missense_Mutation | SNP | C | C | G | TCGA-2F-A9KO-01A-11D-A38G-08 | TCGA-2F-A9KO-11A-12D-A38J-08 | g.chr7:151921139C>G | c.3284G>C | c.(3283-3285)aGa>aCa | p.R1095T |
| BLCA | 7 | 151921149 | 151921149 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chr7:151921149G>A | c.3274C>T | c.(3274-3276)Cga>Tga | p.R1092* |
| BLCA | 7 | 151927069 | 151927069 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A20J-01A-11D-A14W-08 | TCGA-BT-A20J-11A-11D-A14W-08 | g.chr7:151927069C>T | c.2915G>A | c.(2914-2916)gGa>gAa | p.G972E |
| BLCA | 7 | 151927082 | 151927082 | + | Missense_Mutation | SNP | G | G | T | TCGA-DK-AA77-01A-11D-A391-08 | TCGA-DK-AA77-10A-01D-A394-08 | g.chr7:151927082G>T | c.2902C>A | c.(2902-2904)Caa>Aaa | p.Q968K |
| BLCA | 7 | 151932913 | 151932913 | + | Missense_Mutation | SNP | C | C | A | TCGA-FD-A3N6-01A-11D-A21A-08 | TCGA-FD-A3N6-10A-01D-A21A-08 | g.chr7:151932913C>A | c.2758G>T | c.(2758-2760)Gta>Tta | p.V920L |
| BLCA | 7 | 151932973 | 151932973 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-BT-A20X-01A-11D-A16O-08 | TCGA-BT-A20X-11A-12D-A16O-08 | g.chr7:151932973C>A | c.2698G>T | c.(2698-2700)Gga>Tga | p.G900* |
| BLCA | 7 | 151945062 | 151945062 | + | Silent | SNP | G | G | A | TCGA-K4-A5RJ-01A-11D-A289-08 | TCGA-K4-A5RJ-10A-01D-A289-08 | g.chr7:151945062G>A | c.2457C>T | c.(2455-2457)gtC>gtT | p.V819V |
| BLCA | 7 | 151945114 | 151945114 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A3PH-01A-11D-A21Z-08 | TCGA-BT-A3PH-10A-01D-A21Z-08 | g.chr7:151945114G>A | c.2405C>T | c.(2404-2406)tCa>tTa | p.S802L |
| BLCA | 7 | 151945127 | 151945127 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A3NA-01A-11D-A21A-08 | TCGA-FD-A3NA-10A-01D-A21A-08 | g.chr7:151945127G>C | c.2392C>G | c.(2392-2394)Cat>Gat | p.H798D |
| BLCA | 7 | 151945220 | 151945220 | + | Missense_Mutation | SNP | C | C | G | TCGA-BL-A13J-01A-11D-A10S-08 | TCGA-BL-A13J-10A-01D-A10S-08 | g.chr7:151945220C>G | c.2299G>C | c.(2299-2301)Gag>Cag | p.E767Q |
| BLCA | 7 | 151945439 | 151945439 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A3IT-01A-31D-A20D-08 | TCGA-DK-A3IT-10A-01D-A20D-08 | g.chr7:151945439G>A | c.2080C>T | c.(2080-2082)Ctt>Ttt | p.L694F |
| BLCA | 7 | 151945668 | 151945668 | + | Silent | SNP | T | T | C | TCGA-BT-A2LB-01A-11D-A18F-08 | TCGA-BT-A2LB-10A-01D-A18F-08 | g.chr7:151945668T>C | c.1851A>G | c.(1849-1851)aaA>aaG | p.K617K |
| BLCA | 7 | 151945693 | 151945693 | + | Missense_Mutation | SNP | T | T | C | TCGA-FJ-A871-01A-11D-A34U-08 | TCGA-FJ-A871-10A-01D-A34X-08 | g.chr7:151945693T>C | c.1826A>G | c.(1825-1827)cAt>cGt | p.H609R |
| BLCA | 7 | 151946985 | 151946985 | + | Missense_Mutation | SNP | C | C | G | TCGA-GU-AATO-01A-11D-A391-08 | TCGA-GU-AATO-10A-01D-A394-08 | g.chr7:151946985C>G | c.1789G>C | c.(1789-1791)Gac>Cac | p.D597H |
| BLCA | 7 | 151948040 | 151948040 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr7:151948040C>T | c.1633G>A | c.(1633-1635)Gaa>Aaa | p.E545K |
| BLCA | 7 | 151949045 | 151949045 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-GC-A3I6-01A-11D-A20D-08 | TCGA-GC-A3I6-10A-01D-A20D-08 | g.chr7:151949045C>A | c.1600G>T | c.(1600-1602)Gag>Tag | p.E534* |
| BLCA | 7 | 151949141 | 151949141 | + | Missense_Mutation | SNP | G | G | T | TCGA-DK-A6B2-01A-11D-A30E-08 | TCGA-DK-A6B2-10A-01D-A30H-08 | g.chr7:151949141G>T | c.1504C>A | c.(1504-1506)Cat>Aat | p.H502N |
| BLCA | 7 | 151949162 | 151949162 | + | Missense_Mutation | SNP | C | C | G | TCGA-BL-A13I-01A-11D-A13W-08 | TCGA-BL-A13I-11A-11D-A13W-08 | g.chr7:151949162C>G | c.1483G>C | c.(1483-1485)Gag>Cag | p.E495Q |
| BLCA | 7 | 151949177 | 151949177 | + | Splice_Site | SNP | T | T | C | TCGA-YC-A8S6-01A-31D-A38G-08 | TCGA-YC-A8S6-10A-01D-A38J-08 | g.chr7:151949177T>C | | c.e11-2 | |
| BLCA | 7 | 151949650 | 151949650 | + | Missense_Mutation | SNP | G | G | T | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chr7:151949650G>T | c.1450C>A | c.(1450-1452)Cat>Aat | p.H484N |
| BLCA | 7 | 151962147 | 151962147 | + | Missense_Mutation | SNP | T | T | A | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr7:151962147T>A | c.1160A>T | c.(1159-1161)gAg>gTg | p.E387V |
| BLCA | 7 | 151962148 | 151962148 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A43P-01A-31D-A23U-08 | TCGA-FD-A43P-10A-01D-A23U-08 | g.chr7:151962148C>T | c.1159G>A | c.(1159-1161)Gag>Aag | p.E387K |
| BLCA | 7 | 151962165 | 151962165 | + | Missense_Mutation | SNP | G | G | T | TCGA-E5-A4TZ-01A-11D-A31L-08 | TCGA-E5-A4TZ-10B-01D-A31J-08 | g.chr7:151962165G>T | c.1142C>A | c.(1141-1143)gCa>gAa | p.A381E |
| BLCA | 7 | 151962186 | 151962186 | + | Missense_Mutation | SNP | G | G | T | TCGA-C4-A0EZ-01A-21D-A10S-08 | TCGA-C4-A0EZ-10A-01D-A10S-08 | g.chr7:151962186G>T | c.1121C>A | c.(1120-1122)gCg>gAg | p.A374E |
| BLCA | 7 | 151962205 | 151962205 | + | Missense_Mutation | SNP | C | C | G | TCGA-CF-A3MF-01A-12D-A21A-08 | TCGA-CF-A3MF-10A-01D-A21A-08 | g.chr7:151962205C>G | c.1102G>C | c.(1102-1104)Gga>Cga | p.G368R |
| BLCA | 7 | 151962220 | 151962220 | + | Missense_Mutation | SNP | C | C | A | TCGA-5N-A9KI-01A-31D-A42E-08 | TCGA-5N-A9KI-10A-01D-A42H-08 | g.chr7:151962220C>A | c.1087G>T | c.(1087-1089)Ggt>Tgt | p.G363C |
| BLCA | 7 | 151962236 | 151962236 | + | Missense_Mutation | SNP | G | G | C | TCGA-E7-A5KF-01A-11D-A289-08 | TCGA-E7-A5KF-10A-01D-A289-08 | g.chr7:151962236G>C | c.1071C>G | c.(1069-1071)ttC>ttG | p.F357L |
| BLCA | 7 | 151962236 | 151962236 | + | Missense_Mutation | SNP | G | G | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr7:151962236G>T | c.1071C>A | c.(1069-1071)ttC>ttA | p.F357L |
| BLCA | 7 | 151962241 | 151962241 | + | Missense_Mutation | SNP | G | G | C | TCGA-CF-A3MI-01A-11D-A20D-08 | TCGA-CF-A3MI-10A-01D-A20D-08 | g.chr7:151962241G>C | c.1066C>G | c.(1066-1068)Cag>Gag | p.Q356E |
| BLCA | 7 | 151962241 | 151962241 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-XF-A9T5-01A-11D-A42E-08 | TCGA-XF-A9T5-10A-01D-A42H-08 | g.chr7:151962241G>A | c.1066C>T | c.(1066-1068)Cag>Tag | p.Q356* |
| BLCA | 7 | 151970902 | 151970902 | + | Missense_Mutation | SNP | C | C | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr7:151970902C>A | c.900G>T | c.(898-900)gaG>gaT | p.E300D |
| BLCA | 7 | 152008910 | 152008910 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A6TK-01A-42D-A339-08 | TCGA-FD-A6TK-10A-21D-A339-08 | g.chr7:152008910C>T | c.712G>A | c.(712-714)Gat>Aat | p.D238N |
| BLCA | 7 | 152008976 | 152008979 | + | Frame_Shift_Del | DEL | CTGT | CTGT | - | TCGA-HQ-A5ND-01A-11D-A26M-08 | TCGA-HQ-A5ND-10A-01D-A26K-08 | g.chr7:152008976_152008979delCTGT | c.643_646delACAG | c.(643-648)acagctfs | p.TA215fs |
| BLCA | 7 | 152009018 | 152009018 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-XF-A9T5-01A-11D-A42E-08 | TCGA-XF-A9T5-10A-01D-A42H-08 | g.chr7:152009018G>A | c.604C>T | c.(604-606)Cag>Tag | p.Q202* |
| BLCA | 7 | 152012391 | 152012392 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-K4-A6FZ-01A-11D-A31L-08 | TCGA-K4-A6FZ-10A-01D-A31J-08 | g.chr7:152012391_152012392insC | c.421_422insG | c.(421-423)gaafs | p.E141fs |
| BLCA | 7 | 152027735 | 152027735 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A20T-01A-11D-A14W-08 | TCGA-BT-A20T-11A-11D-A14W-08 | g.chr7:152027735C>T | c.340G>A | c.(340-342)Gag>Aag | p.E114K |
| BLCA | 7 | 152132791 | 152132791 | + | Silent | SNP | C | C | T | TCGA-HQ-A5NE-01A-12D-A289-08 | TCGA-HQ-A5NE-10A-01D-A289-08 | g.chr7:152132791C>T | c.81G>A | c.(79-81)ccG>ccA | p.P27P |
| BRCA | 7 | 151841851 | 151841852 | + | Frame_Shift_Ins | INS | - | - | CC | TCGA-D8-A1X6-01A-11D-A14K-09 | TCGA-D8-A1X6-10A-01D-A14K-09 | g.chr7:151841851_151841852insCC | c.14289_14290insGG | c.(14287-14292)cggaagfs | p.K4764fs |
| BRCA | 7 | 151843775 | 151843776 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-D8-A1JT-01A-31D-A13L-09 | TCGA-D8-A1JT-10A-01D-A13O-09 | g.chr7:151843775_151843776delTT | c.13939_13940delAA | c.(13939-13941)aagfs | p.K4647fs |
| BRCA | 7 | 151845282 | 151845283 | + | Frame_Shift_Del | DEL | GG | GG | - | TCGA-AN-A0XP-01A-11D-A117-09 | TCGA-AN-A0XP-10A-01D-A10G-09 | g.chr7:151845282_151845283delGG | c.13729_13730delCC | c.(13729-13731)cctfs | p.P4577fs |
| BRCA | 7 | 151845580 | 151845580 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr7:151845580G>A | c.13432C>T | c.(13432-13434)Cga>Tga | p.R4478* |
| BRCA | 7 | 151845739 | 151845739 | + | Missense_Mutation | SNP | C | C | A | TCGA-B6-A0RP-01A-21D-A099-09 | TCGA-B6-A0RP-10A-01D-A099-09 | g.chr7:151845739C>A | c.13273G>T | c.(13273-13275)Gat>Tat | p.D4425Y |
| BRCA | 7 | 151845841 | 151845841 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-AC-A5EH-01A-11D-A28B-09 | TCGA-AC-A5EH-10A-01D-A28E-09 | g.chr7:151845841T>A | c.13171A>T | c.(13171-13173)Aaa>Taa | p.K4391* |
| BRCA | 7 | 151845844 | 151845844 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-BH-A18N-01A-11D-A12B-09 | TCGA-BH-A18N-11A-43D-A12B-09 | g.chr7:151845844delG | c.13168delC | c.(13168-13170)cttfs | p.L4390fs |
| BRCA | 7 | 151845982 | 151845982 | + | Missense_Mutation | SNP | C | C | G | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr7:151845982C>G | c.13030G>C | c.(13030-13032)Gat>Cat | p.D4344H |
| BRCA | 7 | 151846017 | 151846017 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AC-A2QI-01A-12D-A19Y-09 | TCGA-AC-A2QI-10A-01D-A19Y-09 | g.chr7:151846017delT | c.12995delA | c.(12994-12996)aagfs | p.K4332fs |
| BRCA | 7 | 151848016 | 151848019 | + | Frame_Shift_Del | DEL | GATG | GATG | - | TCGA-A2-A3KC-01A-11D-A20S-09 | TCGA-A2-A3KC-10A-01D-A20S-09 | g.chr7:151848016_151848019delGATG | c.12740_12743delCATC | c.(12739-12744)tcatcafs | p.SS4247fs |
| BRCA | 7 | 151849846 | 151849846 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-A8-A07Z-01A-11W-A019-09 | TCGA-A8-A07Z-10A-01W-A021-09 | g.chr7:151849846delA | c.12470delT | c.(12469-12471)ttafs | p.L4157fs |
| BRCA | 7 | 151851131 | 151851132 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-A2-A0CS-01A-11D-A10Y-09 | TCGA-A2-A0CS-10A-01D-A110-09 | g.chr7:151851131_151851132insA | c.12239_12240insT | c.(12238-12240)atafs | p.I4080fs |
| BRCA | 7 | 151855984 | 151855985 | + | In_Frame_Ins | INS | - | - | TCT | TCGA-A8-A06X-01A-21W-A019-09 | TCGA-A8-A06X-10A-01W-A021-09 | g.chr7:151855984_151855985insTCT | c.11633_11634insAGA | c.(11632-11634)atg>atAGAg | p.3878_3878M>IE |
| BRCA | 7 | 151856014 | 151856014 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-C8-A12N-01A-11D-A10Y-09 | TCGA-C8-A12N-10A-01D-A110-09 | g.chr7:151856014delC | c.11604delG | c.(11602-11604)aggfs | p.R3868fs |
| BRCA | 7 | 151859396 | 151859396 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-BH-A0HQ-01A-11W-A050-09 | TCGA-BH-A0HQ-10A-01W-A055-09 | g.chr7:151859396delC | c.11266delG | c.(11266-11268)gcafs | p.A3756fs |
| BRCA | 7 | 151859457 | 151859457 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-A2-A0EN-01A-13D-A099-09 | TCGA-A2-A0EN-10A-01D-A099-09 | g.chr7:151859457delT | c.11205delA | c.(11203-11205)aaafs | p.K3735fs |
| BRCA | 7 | 151859492 | 151859492 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr7:151859492C>T | c.11170G>A | c.(11170-11172)Gag>Aag | p.E3724K |
| BRCA | 7 | 151859625 | 151859625 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-E9-A226-01A-21D-A159-09 | TCGA-E9-A226-10A-01D-A159-09 | g.chr7:151859625delT | c.11037delA | c.(11035-11037)gaafs | p.E3679fs |
| BRCA | 7 | 151859912 | 151859912 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A1ES-01A-11D-A135-09 | TCGA-BH-A1ES-11A-33D-A135-09 | g.chr7:151859912C>T | c.10750G>A | c.(10750-10752)Gga>Aga | p.G3584R |
| BRCA | 7 | 151860091 | 151860091 | + | Missense_Mutation | SNP | A | A | G | TCGA-A8-A07R-01A-21W-A050-09 | TCGA-A8-A07R-10B-01D-A047-09 | g.chr7:151860091A>G | c.10571T>C | c.(10570-10572)gTt>gCt | p.V3524A |
| BRCA | 7 | 151860481 | 151860481 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A1EY-01A-11D-A13L-09 | TCGA-BH-A1EY-11B-21D-A188-09 | g.chr7:151860481C>T | c.10181G>A | c.(10180-10182)aGt>aAt | p.S3394N |
| BRCA | 7 | 151860728 | 151860728 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AR-A24N-01A-11D-A167-09 | TCGA-AR-A24N-10A-01D-A167-09 | g.chr7:151860728G>A | c.9934C>T | c.(9934-9936)Cag>Tag | p.Q3312* |
| BRCA | 7 | 151860755 | 151860755 | + | Missense_Mutation | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr7:151860755T>G | c.9907A>C | c.(9907-9909)Acc>Ccc | p.T3303P |
| BRCA | 7 | 151860831 | 151860831 | + | Silent | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr7:151860831T>G | c.9831A>C | c.(9829-9831)ccA>ccC | p.P3277P |
| BRCA | 7 | 151860872 | 151860872 | + | Missense_Mutation | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr7:151860872C>T | c.9790G>A | c.(9790-9792)Gat>Aat | p.D3264N |
| BRCA | 7 | 151868351 | 151868351 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-C8-A3M7-01A-12D-A21Q-09 | TCGA-C8-A3M7-10A-01D-A21Q-09 | g.chr7:151868351G>A | c.9451C>T | c.(9451-9453)Cag>Tag | p.Q3151* |
| BRCA | 7 | 151868358 | 151868358 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-B6-A408-01A-12D-A243-09 | TCGA-B6-A408-10A-01D-A243-09 | g.chr7:151868358delG | c.9444delC | c.(9442-9444)gccfs | p.A3148fs |
| BRCA | 7 | 151868360 | 151868360 | + | Missense_Mutation | SNP | C | C | A | TCGA-B6-A408-01A-12D-A243-09 | TCGA-B6-A408-10A-01D-A243-09 | g.chr7:151868360C>A | c.9442G>T | c.(9442-9444)Gcc>Tcc | p.A3148S |
| BRCA | 7 | 151871273 | 151871273 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A0BW-01A-11D-A10Y-09 | TCGA-BH-A0BW-10A-01D-A110-09 | g.chr7:151871273C>T | c.9317G>A | c.(9316-9318)gGt>gAt | p.G3106D |
| BRCA | 7 | 151873885 | 151873885 | + | Missense_Mutation | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr7:151873885C>T | c.8653G>A | c.(8653-8655)Gaa>Aaa | p.E2885K |
| BRCA | 7 | 151877053 | 151877054 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-A2-A0EM-01A-11W-A050-09 | TCGA-A2-A0EM-10A-01W-A055-09 | g.chr7:151877053_151877054insG | c.7307_7308insC | c.(7306-7308)ccafs | p.P2436fs |
| BRCA | 7 | 151877802 | 151877802 | + | Silent | SNP | C | C | T | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr7:151877802C>T | c.7143G>A | c.(7141-7143)ttG>ttA | p.L2381L |
| BRCA | 7 | 151877956 | 151877957 | + | Frame_Shift_Ins | INS | - | - | AA | TCGA-AR-A0U2-01A-11D-A10G-09 | TCGA-AR-A0U2-10A-01D-A10G-09 | g.chr7:151877956_151877957insAA | c.6988_6989insTT | c.(6988-6990)tcafs | p.S2330fs |
| BRCA | 7 | 151877960 | 151877961 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-AR-A0U2-01A-11D-A10G-09 | TCGA-AR-A0U2-10A-01D-A10G-09 | g.chr7:151877960_151877961insT | c.6984_6985insA | c.(6982-6987)cctggafs | p.G2329fs |
| BRCA | 7 | 151878506 | 151878506 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-B6-A0IP-01A-11D-A045-09 | TCGA-B6-A0IP-10A-01W-A055-09 | g.chr7:151878506G>A | c.6439C>T | c.(6439-6441)Caa>Taa | p.Q2147* |
| BRCA | 7 | 151878893 | 151878894 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-BH-A0DE-01A-11D-A10Y-09 | TCGA-BH-A0DE-10A-02D-A110-09 | g.chr7:151878893_151878894insA | c.6051_6052insT | c.(6049-6054)tttcaafs | p.Q2018fs |
| BRCA | 7 | 151878971 | 151878971 | + | Missense_Mutation | SNP | C | C | G | TCGA-BH-A18P-01A-11D-A12B-09 | TCGA-BH-A18P-11A-43D-A12B-09 | g.chr7:151878971C>G | c.5974G>C | c.(5974-5976)Gaa>Caa | p.E1992Q |
| BRCA | 7 | 151879136 | 151879136 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A7-A3RF-01A-11D-A228-09 | TCGA-A7-A3RF-10A-01D-A22A-09 | g.chr7:151879136G>A | c.5809C>T | c.(5809-5811)Caa>Taa | p.Q1937* |
| BRCA | 7 | 151879296 | 151879296 | + | Silent | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr7:151879296T>G | c.5649A>C | c.(5647-5649)tcA>tcC | p.S1883S |
| BRCA | 7 | 151879377 | 151879377 | + | Silent | SNP | A | A | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr7:151879377A>G | c.5568T>C | c.(5566-5568)ccT>ccC | p.P1856P |
| BRCA | 7 | 151879436 | 151879436 | + | Missense_Mutation | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr7:151879436T>G | c.5509A>C | c.(5509-5511)Acc>Ccc | p.T1837P |
| BRCA | 7 | 151879443 | 151879443 | + | Silent | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr7:151879443T>G | c.5502A>C | c.(5500-5502)ccA>ccC | p.P1834P |
| BRCA | 7 | 151879568 | 151879568 | + | Missense_Mutation | SNP | G | G | A | TCGA-A1-A0SF-01A-11D-A142-09 | TCGA-A1-A0SF-10B-01D-A142-09 | g.chr7:151879568G>A | c.5377C>T | c.(5377-5379)Ctt>Ttt | p.L1793F |
| BRCA | 7 | 151879585 | 151879586 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr7:151879585_151879586insA | c.5359_5360insT | c.(5359-5361)caafs | p.Q1787fs |
| BRCA | 7 | 151879618 | 151879618 | + | Missense_Mutation | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr7:151879618A>C | c.5327T>G | c.(5326-5328)gTg>gGg | p.V1776G |
| BRCA | 7 | 151879634 | 151879634 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr7:151879634G>A | c.5311C>T | c.(5311-5313)Cag>Tag | p.Q1771* |
| BRCA | 7 | 151880094 | 151880094 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AO-A125-01A-11D-A10M-09 | TCGA-AO-A125-10A-01D-A10M-09 | g.chr7:151880094C>A | c.5230G>T | c.(5230-5232)Gaa>Taa | p.E1744* |
| BRCA | 7 | 151880169 | 151880169 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-LL-A50Y-01A-11D-A25Q-09 | TCGA-LL-A50Y-10A-01D-A25Q-09 | g.chr7:151880169G>A | c.5155C>T | c.(5155-5157)Cag>Tag | p.Q1719* |
| BRCA | 7 | 151880189 | 151880189 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-C8-A26Y-01A-11D-A16D-09 | TCGA-C8-A26Y-10A-01D-A16D-09 | g.chr7:151880189G>C | c.5135C>G | c.(5134-5136)tCa>tGa | p.S1712* |
| BRCA | 7 | 151882645 | 151882646 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-B6-A0WV-01A-11D-A10G-09 | TCGA-B6-A0WV-10A-01D-A10G-09 | g.chr7:151882645_151882646insA | c.5079_5080insT | c.(5077-5082)tatgtgfs | p.V1694fs |
| BRCA | 7 | 151891154 | 151891154 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EW-A1OY-01A-11D-A142-09 | TCGA-EW-A1OY-10A-01W-A187-09 | g.chr7:151891154G>A | c.4600C>T | c.(4600-4602)Cag>Tag | p.Q1534* |
| BRCA | 7 | 151891576 | 151891576 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-A8-A08P-01A-11W-A019-09 | TCGA-A8-A08P-10A-01W-A021-09 | g.chr7:151891576C>A | c.4456G>T | c.(4456-4458)Gaa>Taa | p.E1486* |
| BRCA | 7 | 151896463 | 151896463 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-OL-A5RX-01A-11D-A28B-09 | TCGA-OL-A5RX-10A-01D-A28E-09 | g.chr7:151896463G>A | c.4174C>T | c.(4174-4176)Cag>Tag | p.Q1392* |
| BRCA | 7 | 151896496 | 151896496 | + | Missense_Mutation | SNP | T | T | C | TCGA-A2-A0SV-01A-11D-A099-09 | TCGA-A2-A0SV-10A-01W-A097-09 | g.chr7:151896496T>C | c.4141A>G | c.(4141-4143)Ata>Gta | p.I1381V |
| BRCA | 7 | 151902226 | 151902226 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-OL-A66H-01A-11D-A29N-09 | TCGA-OL-A66H-10A-01D-A29N-09 | g.chr7:151902226delC | c.3926delG | c.(3925-3927)ggcfs | p.G1309fs |
| BRCA | 7 | 151904386 | 151904386 | + | Splice_Site | SNP | T | T | C | TCGA-A8-A06P-01A-11W-A019-09 | TCGA-A8-A06P-10A-01W-A021-09 | g.chr7:151904386T>C | c.3840A>G | c.(3838-3840)ccA>ccG | p.P1280P |
| BRCA | 7 | 151917645 | 151917646 | + | Frame_Shift_Del | DEL | TG | TG | - | TCGA-E2-A1LG-01A-21D-A14K-09 | TCGA-E2-A1LG-11A-42D-A14K-09 | g.chr7:151917645_151917646delTG | c.3674_3675delCA | c.(3673-3675)tcafs | p.S1225fs |
| BRCA | 7 | 151917668 | 151917668 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr7:151917668G>A | c.3652C>T | c.(3652-3654)Cag>Tag | p.Q1218* |
| BRCA | 7 | 151917808 | 151917808 | + | Missense_Mutation | SNP | G | G | C | TCGA-B6-A0I8-01A-11W-A050-09 | TCGA-B6-A0I8-10A-01W-A055-09 | g.chr7:151917808G>C | c.3512C>G | c.(3511-3513)aCt>aGt | p.T1171S |
| BRCA | 7 | 151919733 | 151919733 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AO-A0JE-01A-11W-A071-09 | TCGA-AO-A0JE-10A-01W-A071-09 | g.chr7:151919733C>A | c.3358G>T | c.(3358-3360)Gag>Tag | p.E1120* |
| BRCA | 7 | 151921673 | 151921673 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-E2-A1LG-01A-21D-A14K-09 | TCGA-E2-A1LG-11A-42D-A14K-09 | g.chr7:151921673C>T | c.3005G>A | c.(3004-3006)tGg>tAg | p.W1002* |
| BRCA | 7 | 151927054 | 151927054 | + | Missense_Mutation | SNP | C | C | T | TCGA-AR-A0U0-01A-11D-A10G-09 | TCGA-AR-A0U0-10A-01D-A10G-09 | g.chr7:151927054C>T | c.2930G>A | c.(2929-2931)tGt>tAt | p.C977Y |
| BRCA | 7 | 151932929 | 151932929 | + | Missense_Mutation | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr7:151932929A>C | c.2742T>G | c.(2740-2742)agT>agG | p.S914R |
| BRCA | 7 | 151932951 | 151932952 | + | Frame_Shift_Ins | INS | - | - | GG | TCGA-E2-A1L9-01A-11D-A13L-09 | TCGA-E2-A1L9-10A-01D-A188-09 | g.chr7:151932951_151932952insGG | c.2719_2720insCC | c.(2719-2721)cgafs | p.R907fs |
| BRCA | 7 | 151945354 | 151945354 | + | Missense_Mutation | SNP | C | C | T | TCGA-AR-A0TX-01A-11D-A099-09 | TCGA-AR-A0TX-10A-01D-A099-09 | g.chr7:151945354C>T | c.2165G>A | c.(2164-2166)gGa>gAa | p.G722E |
| BRCA | 7 | 151945451 | 151945451 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AR-A24S-01A-11D-A167-09 | TCGA-AR-A24S-10A-01D-A167-09 | g.chr7:151945451C>A | c.2068G>T | c.(2068-2070)Gaa>Taa | p.E690* |
| BRCA | 7 | 151945474 | 151945474 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-AN-A0XV-01A-11D-A10G-09 | TCGA-AN-A0XV-10A-01D-A10G-09 | g.chr7:151945474G>C | c.2045C>G | c.(2044-2046)tCa>tGa | p.S682* |
| BRCA | 7 | 151945576 | 151945577 | + | Frame_Shift_Ins | INS | - | - | AAAA | TCGA-E2-A2P5-01A-11D-A19Y-09 | TCGA-E2-A2P5-10B-01D-A19Y-09 | g.chr7:151945576_151945577insAAAA | c.1942_1943insTTTT | c.(1942-1944)gaafs | p.E648fs |
| BRCA | 7 | 151945601 | 151945601 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-B6-A0X4-01A-11D-A10G-09 | TCGA-B6-A0X4-10A-01D-A10G-09 | g.chr7:151945601C>A | c.1918G>T | c.(1918-1920)Gaa>Taa | p.E640* |
| BRCA | 7 | 151945622 | 151945622 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AO-A0JF-01A-11W-A071-09 | TCGA-AO-A0JF-10A-01W-A071-09 | g.chr7:151945622delC | c.1897delG | c.(1897-1899)gaafs | p.E633fs |
| BRCA | 7 | 151945659 | 151945660 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-A2-A0YT-01A-11D-A10G-09 | TCGA-A2-A0YT-10A-01D-A10G-09 | g.chr7:151945659_151945660insT | c.1859_1860insA | c.(1858-1860)tctfs | p.S620fs |
| BRCA | 7 | 151945694 | 151945694 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-A7-A4SD-01A-11D-A25Q-09 | TCGA-A7-A4SD-10A-01D-A25Q-09 | g.chr7:151945694delG | c.1825delC | c.(1825-1827)catfs | p.H609fs |
| BRCA | 7 | 151949160 | 151949161 | + | Frame_Shift_Ins | INS | - | - | GG | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr7:151949160_151949161insGG | c.1484_1485insCC | c.(1483-1485)gagfs | p.E495fs |
| BRCA | 7 | 151949699 | 151949699 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-OL-A66H-01A-11D-A29N-09 | TCGA-OL-A66H-10A-01D-A29N-09 | g.chr7:151949699A>T | c.1401T>A | c.(1399-1401)tgT>tgA | p.C467* |
| BRCA | 7 | 151960110 | 151960110 | + | Missense_Mutation | SNP | C | C | G | TCGA-A1-A0SI-01A-11D-A142-09 | TCGA-A1-A0SI-10B-01D-A142-09 | g.chr7:151960110C>G | c.1290G>C | c.(1288-1290)tgG>tgC | p.W430C |
| BRCA | 7 | 151960149 | 151960149 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-D8-A1JP-01A-11D-A13L-09 | TCGA-D8-A1JP-10A-01D-A13O-09 | g.chr7:151960149A>T | c.1251T>A | c.(1249-1251)tgT>tgA | p.C417* |
| BRCA | 7 | 151960160 | 151960160 | + | Missense_Mutation | SNP | G | G | A | TCGA-A8-A07E-01A-11W-A050-09 | TCGA-A8-A07E-10A-01W-A055-09 | g.chr7:151960160G>A | c.1240C>T | c.(1240-1242)Cat>Tat | p.H414Y |
| BRCA | 7 | 151962208 | 151962208 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A0HN-01A-11D-A099-09 | TCGA-BH-A0HN-10A-01D-A099-09 | g.chr7:151962208G>A | c.1099C>T | c.(1099-1101)Cat>Tat | p.H367Y |
| BRCA | 7 | 151962208 | 151962208 | + | Missense_Mutation | SNP | G | G | C | TCGA-E9-A1N8-01A-11D-A142-09 | TCGA-E9-A1N8-10A-01D-A142-09 | g.chr7:151962208G>C | c.1099C>G | c.(1099-1101)Cat>Gat | p.H367D |
| BRCA | 7 | 151962231 | 151962231 | + | Missense_Mutation | SNP | C | C | G | TCGA-C8-A3M8-01A-11D-A20S-09 | TCGA-C8-A3M8-10A-01D-A20S-09 | g.chr7:151962231C>G | c.1076G>C | c.(1075-1077)tGt>tCt | p.C359S |
| BRCA | 7 | 152007146 | 152007146 | + | Missense_Mutation | SNP | G | G | A | TCGA-A7-A5ZW-01A-12D-A29N-09 | TCGA-A7-A5ZW-10A-01D-A29N-09 | g.chr7:152007146G>A | c.754C>T | c.(754-756)Cat>Tat | p.H252Y |
| BRCA | 7 | 152009002 | 152009002 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AQ-A1H2-01A-11D-A13L-09 | TCGA-AQ-A1H2-10A-01D-A13O-09 | g.chr7:152009002delG | c.620delC | c.(619-621)tctfs | p.S207fs |
| BRCA | 7 | 152012230 | 152012230 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-E2-A1L9-01A-11D-A13L-09 | TCGA-E2-A1L9-10A-01D-A188-09 | g.chr7:152012230G>A | c.583C>T | c.(583-585)Cag>Tag | p.Q195* |
| BRCA | 7 | 152012381 | 152012381 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-A2-A0D3-01A-11D-A10Y-09 | TCGA-A2-A0D3-10A-01D-A110-09 | g.chr7:152012381delG | c.432delC | c.(430-432)tccfs | p.S144fs |
| BRCA | 7 | 152012412 | 152012412 | + | Missense_Mutation | SNP | C | C | T | TCGA-B6-A0IJ-01A-11W-A050-09 | TCGA-B6-A0IJ-10A-01W-A055-09 | g.chr7:152012412C>T | c.401G>A | c.(400-402)tGc>tAc | p.C134Y |
| BRCA | 7 | 152012425 | 152012425 | + | Splice_Site | SNP | T | T | G | TCGA-D8-A27P-01A-11D-A16D-09 | TCGA-D8-A27P-10A-01D-A16D-09 | g.chr7:152012425T>G | | c.e4-2 | |
| BRCA | 7 | 152027750 | 152027750 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A2-A259-01A-11D-A16D-09 | TCGA-A2-A259-10A-01D-A16D-09 | g.chr7:152027750G>A | c.325C>T | c.(325-327)Cag>Tag | p.Q109* |
| BRCA | 7 | 152027786 | 152027786 | + | Missense_Mutation | SNP | C | C | G | TCGA-EW-A1J5-01A-11D-A13L-09 | TCGA-EW-A1J5-10A-01D-A13O-09 | g.chr7:152027786C>G | c.289G>C | c.(289-291)Gaa>Caa | p.E97Q |
| BRCA | 7 | 152132815 | 152132815 | + | Silent | SNP | G | G | C | TCGA-AC-A5EH-01A-11D-A28B-09 | TCGA-AC-A5EH-10A-01D-A28E-09 | g.chr7:152132815G>C | c.57C>G | c.(55-57)ccC>ccG | p.P19P |
| CESC | 7 | 151836855 | 151836855 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EX-A1H6-01B-11D-A22X-09 | TCGA-EX-A1H6-10A-01D-A22X-09 | g.chr7:151836855G>A | c.14365C>T | c.(14365-14367)Cga>Tga | p.R4789* |
| CESC | 7 | 151845151 | 151845151 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-C5-A1BL-01A-11D-A13W-08 | TCGA-C5-A1BL-10A-01D-A13W-08 | g.chr7:151845151C>A | c.13861G>T | c.(13861-13863)Gaa>Taa | p.E4621* |
| CESC | 7 | 151848547 | 151848548 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-FU-A770-01A-11D-A33O-09 | TCGA-FU-A770-10A-01D-A33O-09 | g.chr7:151848547_151848548insT | c.12645_12646insA | c.(12643-12648)aaagatfs | p.D4216fs |
| CESC | 7 | 151848594 | 151848595 | + | Frame_Shift_Ins | INS | - | - | GA | TCGA-EK-A2RK-01A-11D-A18J-09 | TCGA-EK-A2RK-10A-01D-A18J-09 | g.chr7:151848594_151848595insGA | c.12598_12599insTC | c.(12598-12600)catfs | p.H4200fs |
| CESC | 7 | 151849976 | 151849976 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A7CH-01A-11D-A33O-09 | TCGA-C5-A7CH-10A-01D-A33O-09 | g.chr7:151849976C>T | c.12340G>A | c.(12340-12342)Gag>Aag | p.E4114K |
| CESC | 7 | 151856085 | 151856085 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1BJ-01A-11D-A13W-08 | TCGA-C5-A1BJ-10A-01D-A13W-08 | g.chr7:151856085C>T | c.11533G>A | c.(11533-11535)Gaa>Aaa | p.E3845K |
| CESC | 7 | 151859593 | 151859593 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr7:151859593G>C | c.11069C>G | c.(11068-11070)tCa>tGa | p.S3690* |
| CESC | 7 | 151860641 | 151860641 | + | Missense_Mutation | SNP | G | G | T | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr7:151860641G>T | c.10021C>A | c.(10021-10023)Cct>Act | p.P3341T |
| CESC | 7 | 151860728 | 151860728 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-Q1-A5R2-01A-11D-A28B-09 | TCGA-Q1-A5R2-10A-01D-A28E-09 | g.chr7:151860728G>A | c.9934C>T | c.(9934-9936)Cag>Tag | p.Q3312* |
| CESC | 7 | 151860765 | 151860765 | + | Missense_Mutation | SNP | C | C | T | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr7:151860765C>T | c.9897G>A | c.(9895-9897)atG>atA | p.M3299I |
| CESC | 7 | 151864248 | 151864248 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-C5-A3HL-01A-11D-A20U-09 | TCGA-C5-A3HL-10A-01D-A20U-09 | g.chr7:151864248G>A | c.9733C>T | c.(9733-9735)Cag>Tag | p.Q3245* |
| CESC | 7 | 151873585 | 151873585 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-C5-A2LZ-01A-11D-A20U-09 | TCGA-C5-A2LZ-10B-01D-A20U-09 | g.chr7:151873585G>A | c.8953C>T | c.(8953-8955)Cag>Tag | p.Q2985* |
| CESC | 7 | 151873963 | 151873963 | + | Missense_Mutation | SNP | G | G | A | TCGA-EK-A2RD-01A-12D-A20U-09 | TCGA-EK-A2RD-10A-01D-A20U-09 | g.chr7:151873963G>A | c.8575C>T | c.(8575-8577)Cac>Tac | p.H2859Y |
| CESC | 7 | 151874923 | 151874923 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-C5-A7UH-01A-11D-A351-09 | TCGA-C5-A7UH-10A-01D-A351-09 | g.chr7:151874923G>A | c.7615C>T | c.(7615-7617)Cag>Tag | p.Q2539* |
| CESC | 7 | 151876977 | 151876977 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-MU-A51Y-01A-11D-A26G-09 | TCGA-MU-A51Y-10A-01D-A26G-09 | g.chr7:151876977G>A | c.7384C>T | c.(7384-7386)Cag>Tag | p.Q2462* |
| CESC | 7 | 151877100 | 151877100 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-UC-A7PF-01A-11D-A351-09 | TCGA-UC-A7PF-11A-31D-A351-09 | g.chr7:151877100G>A | c.7261C>T | c.(7261-7263)Caa>Taa | p.Q2421* |
| CESC | 7 | 151877103 | 151877103 | + | Missense_Mutation | SNP | G | G | C | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr7:151877103G>C | c.7258C>G | c.(7258-7260)Ctt>Gtt | p.L2420V |
| CESC | 7 | 151877154 | 151877154 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-Q1-A6DW-01A-11D-A32I-09 | TCGA-Q1-A6DW-10B-01D-A32I-09 | g.chr7:151877154G>A | c.7207C>T | c.(7207-7209)Cga>Tga | p.R2403* |
| CESC | 7 | 151877932 | 151877932 | + | Missense_Mutation | SNP | G | G | A | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr7:151877932G>A | c.7013C>T | c.(7012-7014)tCa>tTa | p.S2338L |
| CESC | 7 | 151878287 | 151878287 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EK-A3GJ-01A-21D-A20U-09 | TCGA-EK-A3GJ-11A-11D-A20U-09 | g.chr7:151878287G>A | c.6658C>T | c.(6658-6660)Cag>Tag | p.Q2220* |
| CESC | 7 | 151878287 | 151878287 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-JX-A3Q0-01A-11D-A21Q-09 | TCGA-JX-A3Q0-10A-01D-A21Q-09 | g.chr7:151878287G>A | c.6658C>T | c.(6658-6660)Cag>Tag | p.Q2220* |
| CESC | 7 | 151878464 | 151878464 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-JX-A3Q0-01A-11D-A21Q-09 | TCGA-JX-A3Q0-10A-01D-A21Q-09 | g.chr7:151878464G>A | c.6481C>T | c.(6481-6483)Caa>Taa | p.Q2161* |
| CESC | 7 | 151878871 | 151878871 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr7:151878871G>C | c.6074C>G | c.(6073-6075)tCa>tGa | p.S2025* |
| CESC | 7 | 151879322 | 151879322 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr7:151879322G>A | c.5623C>T | c.(5623-5625)Cag>Tag | p.Q1875* |
| CESC | 7 | 151884356 | 151884356 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-EK-A3GM-01A-11D-A20U-09 | TCGA-EK-A3GM-10A-01D-A20U-09 | g.chr7:151884356C>A | c.4999G>T | c.(4999-5001)Gaa>Taa | p.E1667* |
| CESC | 7 | 151902229 | 151902229 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr7:151902229G>C | c.3923C>G | c.(3922-3924)tCa>tGa | p.S1308* |
| CESC | 7 | 151902278 | 151902278 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FU-A770-01A-11D-A33O-09 | TCGA-FU-A770-10A-01D-A33O-09 | g.chr7:151902278G>A | c.3874C>T | c.(3874-3876)Cga>Tga | p.R1292* |
| CESC | 7 | 151917668 | 151917668 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EK-A2RC-01A-11D-A18J-09 | TCGA-EK-A2RC-10A-01D-A18J-09 | g.chr7:151917668G>A | c.3652C>T | c.(3652-3654)Cag>Tag | p.Q1218* |
| CESC | 7 | 151917764 | 151917764 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DS-A0VM-01A-11D-A10S-08 | TCGA-DS-A0VM-10A-01D-A10S-08 | g.chr7:151917764G>A | c.3556C>T | c.(3556-3558)Cag>Tag | p.Q1186* |
| CESC | 7 | 151919142 | 151919142 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-C5-A2LZ-01A-11D-A20U-09 | TCGA-C5-A2LZ-10B-01D-A20U-09 | g.chr7:151919142G>C | c.3443C>G | c.(3442-3444)tCa>tGa | p.S1148* |
| CESC | 7 | 151919142 | 151919142 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr7:151919142G>C | c.3443C>G | c.(3442-3444)tCa>tGa | p.S1148* |
| CESC | 7 | 151921207 | 151921207 | + | Missense_Mutation | SNP | C | C | G | TCGA-EK-A2PG-01A-11D-A18J-09 | TCGA-EK-A2PG-10A-01D-A18J-09 | g.chr7:151921207C>G | c.3216G>C | c.(3214-3216)caG>caC | p.Q1072H |
| CESC | 7 | 151945201 | 151945201 | + | Missense_Mutation | SNP | G | G | A | TCGA-DG-A2KK-01A-11D-A17W-09 | TCGA-DG-A2KK-10A-01D-A17W-09 | g.chr7:151945201G>A | c.2318C>T | c.(2317-2319)tCa>tTa | p.S773L |
| CESC | 7 | 151945301 | 151945301 | + | Missense_Mutation | SNP | C | C | T | TCGA-IR-A3LK-01A-12D-A20U-09 | TCGA-IR-A3LK-10A-01D-A20U-09 | g.chr7:151945301C>T | c.2218G>A | c.(2218-2220)Gaa>Aaa | p.E740K |
| CESC | 7 | 151947007 | 151947007 | + | Missense_Mutation | SNP | C | C | G | TCGA-JX-A3Q0-01A-11D-A21Q-09 | TCGA-JX-A3Q0-10A-01D-A21Q-09 | g.chr7:151947007C>G | c.1767G>C | c.(1765-1767)aaG>aaC | p.K589N |
| CESC | 7 | 151962134 | 151962134 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-C5-A7CO-01A-11D-A351-09 | TCGA-C5-A7CO-10A-01D-A351-09 | g.chr7:151962134G>T | c.1173C>A | c.(1171-1173)tgC>tgA | p.C391* |
| CESC | 7 | 151970952 | 151970952 | + | Splice_Site | SNP | G | G | A | TCGA-BI-A0VS-01A-11D-A10S-08 | TCGA-BI-A0VS-10A-01D-A10S-08 | g.chr7:151970952G>A | c.850C>T | c.(850-852)Cga>Tga | p.R284* |
| CESC | 7 | 152009013 | 152009013 | + | Silent | SNP | C | C | T | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chr7:152009013C>T | c.609G>A | c.(607-609)caG>caA | p.Q203Q |
| CHOL | 7 | 151891214 | 151891214 | + | Splice_Site | SNP | C | C | G | TCGA-3X-AAVB-01A-31D-A417-09 | TCGA-3X-AAVB-10A-01D-A41A-09 | g.chr7:151891214C>G | | c.e31-1 | |
| CHOL | 7 | 151921114 | 151921114 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-W5-AA2G-01A-11D-A417-09 | TCGA-W5-AA2G-10A-01D-A41A-09 | g.chr7:151921114A>T | c.3309T>A | c.(3307-3309)tgT>tgA | p.C1103* |
| CHOL | 7 | 151921114 | 151921114 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-W5-AA2I-01A-32D-A417-09 | TCGA-W5-AA2I-10A-01D-A41A-09 | g.chr7:151921114A>T | c.3309T>A | c.(3307-3309)tgT>tgA | p.C1103* |
| CHOL | 7 | 151921114 | 151921114 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-W5-AA30-01A-31D-A417-09 | TCGA-W5-AA30-10A-01D-A41A-09 | g.chr7:151921114A>T | c.3309T>A | c.(3307-3309)tgT>tgA | p.C1103* |
| CHOL | 7 | 151921114 | 151921114 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-ZH-A8Y2-01A-11D-A417-09 | TCGA-ZH-A8Y2-10A-01D-A41A-09 | g.chr7:151921114A>T | c.3309T>A | c.(3307-3309)tgT>tgA | p.C1103* |
| CHOL | 7 | 151945305 | 151945305 | + | Missense_Mutation | SNP | G | G | C | TCGA-W5-AA2Z-01A-11D-A417-09 | TCGA-W5-AA2Z-11A-11D-A41A-09 | g.chr7:151945305G>C | c.2214C>G | c.(2212-2214)gaC>gaG | p.D738E |
| CHOL | 7 | 151962255 | 151962255 | + | Missense_Mutation | SNP | C | C | T | TCGA-W6-AA0S-01A-11D-A417-09 | TCGA-W6-AA0S-10A-01D-A41A-09 | g.chr7:151962255C>T | c.1052G>A | c.(1051-1053)gGa>gAa | p.G351E |
| COAD | 7 | 151835922 | 151835922 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CM-6167-01A-11D-1650-10 | TCGA-CM-6167-10A-01D-1650-10 | g.chr7:151835922delT | c.14602delA | c.(14602-14604)attfs | p.I4870fs |
| COAD | 7 | 151836804 | 151836804 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A6-5666-01A-01D-1650-10 | TCGA-A6-5666-10A-01D-1650-10 | g.chr7:151836804G>A | c.14416C>T | c.(14416-14418)Cga>Tga | p.R4806* |
| COAD | 7 | 151842334 | 151842334 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr7:151842334C>T | c.14078G>A | c.(14077-14079)cGa>cAa | p.R4693Q |
| COAD | 7 | 151845262 | 151845262 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-5344-01A-21D-1719-10 | TCGA-CM-5344-10A-01D-1719-10 | g.chr7:151845262G>A | c.13750C>T | c.(13750-13752)Cgg>Tgg | p.R4584W |
| COAD | 7 | 151845367 | 151845367 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr7:151845367G>A | c.13645C>T | c.(13645-13647)Cgc>Tgc | p.R4549C |
| COAD | 7 | 151845390 | 151845390 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr7:151845390C>T | c.13622G>A | c.(13621-13623)cGa>cAa | p.R4541Q |
| COAD | 7 | 151845435 | 151845435 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3869-01A-01W-0995-10 | TCGA-AA-3869-10A-01W-0995-10 | g.chr7:151845435T>C | c.13577A>G | c.(13576-13578)tAt>tGt | p.Y4526C |
| COAD | 7 | 151845451 | 151845451 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3814-01A-01W-0900-09 | TCGA-AA-3814-10A-01W-0900-09 | g.chr7:151845451C>T | c.13561G>A | c.(13561-13563)Gtc>Atc | p.V4521I |
| COAD | 7 | 151845524 | 151845524 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr7:151845524delA | c.13488delT | c.(13486-13488)tttfs | p.F4496fs |
| COAD | 7 | 151845958 | 151845959 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-A6-2671-01A-01D-1408-10 | TCGA-A6-2671-10A-01D-1408-10 | g.chr7:151845958_151845959insT | c.13053_13054insA | c.(13051-13056)aaatggfs | p.W4352fs |
| COAD | 7 | 151845972 | 151845972 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-6138-01A-11D-1771-10 | TCGA-A6-6138-10A-01D-1771-10 | g.chr7:151845972G>T | c.13040C>A | c.(13039-13041)cCg>cAg | p.P4347Q |
| COAD | 7 | 151846091 | 151846091 | + | Silent | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr7:151846091G>A | c.12921C>T | c.(12919-12921)atC>atT | p.I4307I |
| COAD | 7 | 151846091 | 151846091 | + | Silent | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr7:151846091G>A | c.12921C>T | c.(12919-12921)atC>atT | p.I4307I |
| COAD | 7 | 151846233 | 151846233 | + | Missense_Mutation | SNP | G | G | C | TCGA-DM-A28C-01A-11D-A16V-10 | TCGA-DM-A28C-10A-01D-A16V-10 | g.chr7:151846233G>C | c.12779C>G | c.(12778-12780)tCc>tGc | p.S4260C |
| COAD | 7 | 151848606 | 151848607 | + | Frame_Shift_Del | DEL | TG | TG | - | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr7:151848606_151848607delTG | c.12586_12587delCA | c.(12586-12588)cagfs | p.Q4196fs |
| COAD | 7 | 151851176 | 151851176 | + | Silent | SNP | C | C | T | TCGA-DM-A28C-01A-11D-A16V-10 | TCGA-DM-A28C-10A-01D-A16V-10 | g.chr7:151851176C>T | c.12195G>A | c.(12193-12195)gcG>gcA | p.A4065A |
| COAD | 7 | 151851208 | 151851208 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr7:151851208T>C | c.12163A>G | c.(12163-12165)Atc>Gtc | p.I4055V |
| COAD | 7 | 151851208 | 151851208 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chr7:151851208T>C | c.12163A>G | c.(12163-12165)Atc>Gtc | p.I4055V |
| COAD | 7 | 151859337 | 151859337 | + | Silent | SNP | T | T | C | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr7:151859337T>C | c.11325A>G | c.(11323-11325)gaA>gaG | p.E3775E |
| COAD | 7 | 151859337 | 151859337 | + | Silent | SNP | T | T | C | TCGA-G4-6626-01A-11D-1771-10 | TCGA-G4-6626-10A-01D-1771-10 | g.chr7:151859337T>C | c.11325A>G | c.(11323-11325)gaA>gaG | p.E3775E |
| COAD | 7 | 151859338 | 151859338 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6167-01A-11D-1650-10 | TCGA-CM-6167-10A-01D-1650-10 | g.chr7:151859338T>C | c.11324A>G | c.(11323-11325)gAa>gGa | p.E3775G |
| COAD | 7 | 151859519 | 151859519 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr7:151859519delT | c.11143delA | c.(11143-11145)acafs | p.T3715fs |
| COAD | 7 | 151859568 | 151859568 | + | Silent | SNP | C | C | T | TCGA-F4-6569-01A-11D-1771-10 | TCGA-F4-6569-10A-01D-1771-10 | g.chr7:151859568C>T | c.11094G>A | c.(11092-11094)acG>acA | p.T3698T |
| COAD | 7 | 151859569 | 151859569 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr7:151859569G>A | c.11093C>T | c.(11092-11094)aCg>aTg | p.T3698M |
| COAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-5539-01A-01D-1650-10 | TCGA-D5-5539-10A-01D-1650-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6920-01A-11D-1924-10 | TCGA-D5-6920-10A-01D-1924-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6923-01A-11D-1924-10 | TCGA-D5-6923-10A-01D-1924-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6929-01A-31D-1924-10 | TCGA-D5-6929-10A-01D-1924-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | G | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr7:151859570T>G | c.11092A>C | c.(11092-11094)Acg>Ccg | p.T3698P |
| COAD | 7 | 151859850 | 151859850 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:151859850C>A | c.10812G>T | c.(10810-10812)aaG>aaT | p.K3604N |
| COAD | 7 | 151859997 | 151859997 | + | Silent | SNP | A | A | G | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr7:151859997A>G | c.10665T>C | c.(10663-10665)ccT>ccC | p.P3555P |
| COAD | 7 | 151860278 | 151860278 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:151860278A>C | c.10384T>G | c.(10384-10386)Ttt>Gtt | p.F3462V |
| COAD | 7 | 151860293 | 151860293 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr7:151860293C>T | c.10369G>A | c.(10369-10371)Gac>Aac | p.D3457N |
| COAD | 7 | 151860621 | 151860621 | + | Silent | SNP | A | A | G | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr7:151860621A>G | c.10041T>C | c.(10039-10041)aaT>aaC | p.N3347N |
| COAD | 7 | 151864307 | 151864307 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr7:151864307T>C | c.9674A>G | c.(9673-9675)gAa>gGa | p.E3225G |
| COAD | 7 | 151864331 | 151864331 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151864331C>T | c.9650G>A | c.(9649-9651)cGt>cAt | p.R3217H |
| COAD | 7 | 151873535 | 151873535 | + | Silent | SNP | G | G | A | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr7:151873535G>A | c.9003C>T | c.(9001-9003)aaC>aaT | p.N3001N |
| COAD | 7 | 151873626 | 151873626 | + | Missense_Mutation | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:151873626G>T | c.8912C>A | c.(8911-8913)tCt>tAt | p.S2971Y |
| COAD | 7 | 151873627 | 151873627 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr7:151873627A>G | c.8911T>C | c.(8911-8913)Tct>Cct | p.S2971P |
| COAD | 7 | 151873938 | 151873939 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr7:151873938_151873939delTT | c.8599_8600delAA | c.(8599-8601)aagfs | p.K2867fs |
| COAD | 7 | 151873939 | 151873939 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr7:151873939T>C | c.8599A>G | c.(8599-8601)Aag>Gag | p.K2867E |
| COAD | 7 | 151874147 | 151874148 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr7:151874147_151874148insT | c.8390_8391insA | c.(8389-8391)aagfs | p.K2797fs |
| COAD | 7 | 151874771 | 151874771 | + | Silent | SNP | T | T | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:151874771T>C | c.7767A>G | c.(7765-7767)agA>agG | p.R2589R |
| COAD | 7 | 151876974 | 151876974 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr7:151876974G>A | c.7387C>T | c.(7387-7389)Cgt>Tgt | p.R2463C |
| COAD | 7 | 151878070 | 151878070 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr7:151878070delG | c.6875delC | c.(6874-6876)ccafs | p.P2292fs |
| COAD | 7 | 151878105 | 151878105 | + | Silent | SNP | T | T | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:151878105T>C | c.6840A>G | c.(6838-6840)ggA>ggG | p.G2280G |
| COAD | 7 | 151878529 | 151878529 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr7:151878529C>T | c.6416G>A | c.(6415-6417)cGa>cAa | p.R2139Q |
| COAD | 7 | 151878622 | 151878622 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:151878622G>T | c.6323C>A | c.(6322-6324)tCt>tAt | p.S2108Y |
| COAD | 7 | 151878642 | 151878642 | + | Silent | SNP | T | T | C | TCGA-CM-4747-01A-01D-1408-10 | TCGA-CM-4747-10A-01D-1408-10 | g.chr7:151878642T>C | c.6303A>G | c.(6301-6303)ccA>ccG | p.P2101P |
| COAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5868-01A-01D-1650-10 | TCGA-CM-5868-10A-01D-1650-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A1D7-01A-11D-A152-10 | TCGA-DM-A1D7-10A-01D-A152-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COAD | 7 | 151879228 | 151879228 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr7:151879228C>A | c.5717G>T | c.(5716-5718)cGa>cTa | p.R1906L |
| COAD | 7 | 151879229 | 151879229 | + | Silent | SNP | G | G | T | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151879229G>T | c.5716C>A | c.(5716-5718)Cga>Aga | p.R1906R |
| COAD | 7 | 151879325 | 151879325 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3846-01A-01W-0995-10 | TCGA-AA-3846-10A-01W-0995-10 | g.chr7:151879325A>C | c.5620T>G | c.(5620-5622)Tct>Gct | p.S1874A |
| COAD | 7 | 151879428 | 151879428 | + | Silent | SNP | C | C | T | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr7:151879428C>T | c.5517G>A | c.(5515-5517)acG>acA | p.T1839T |
| COAD | 7 | 151879605 | 151879605 | + | Silent | SNP | C | C | T | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr7:151879605C>T | c.5340G>A | c.(5338-5340)caG>caA | p.Q1780Q |
| COAD | 7 | 151880081 | 151880081 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr7:151880081T>G | c.5243A>C | c.(5242-5244)gAa>gCa | p.E1748A |
| COAD | 7 | 151884426 | 151884426 | + | Missense_Mutation | SNP | C | C | A | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr7:151884426C>A | c.4929G>T | c.(4927-4929)gaG>gaT | p.E1643D |
| COAD | 7 | 151884823 | 151884823 | + | Silent | SNP | T | T | C | TCGA-AA-3681-01A-01W-0900-09 | TCGA-AA-3681-10A-01W-0900-09 | g.chr7:151884823T>C | c.4770A>G | c.(4768-4770)gcA>gcG | p.A1590A |
| COAD | 7 | 151891205 | 151891205 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CM-6167-01A-11D-1650-10 | TCGA-CM-6167-10A-01D-1650-10 | g.chr7:151891205C>A | c.4549G>T | c.(4549-4551)Gga>Tga | p.G1517* |
| COAD | 7 | 151891205 | 151891205 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr7:151891205C>A | c.4549G>T | c.(4549-4551)Gga>Tga | p.G1517* |
| COAD | 7 | 151891206 | 151891206 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:151891206G>A | c.4548C>T | c.(4546-4548)ggC>ggT | p.G1516G |
| COAD | 7 | 151896440 | 151896440 | + | Missense_Mutation | SNP | C | C | T | TCGA-AU-3779-01A-01D-1719-10 | TCGA-AU-3779-10A-01D-1719-10 | g.chr7:151896440C>T | c.4197G>A | c.(4195-4197)atG>atA | p.M1399I |
| COAD | 7 | 151896508 | 151896508 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151896508T>A | c.4129A>T | c.(4129-4131)Aga>Tga | p.R1377* |
| COAD | 7 | 151904487 | 151904487 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr7:151904487T>A | c.3739A>T | c.(3739-3741)Aaa>Taa | p.K1247* |
| COAD | 7 | 151917681 | 151917681 | + | Silent | SNP | G | G | A | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr7:151917681G>A | c.3639C>T | c.(3637-3639)agC>agT | p.S1213S |
| COAD | 7 | 151921127 | 151921127 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr7:151921127A>C | c.3296T>G | c.(3295-3297)cTt>cGt | p.L1099R |
| COAD | 7 | 151921131 | 151921131 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr7:151921131C>A | c.3292G>T | c.(3292-3294)Gat>Tat | p.D1098Y |
| COAD | 7 | 151921523 | 151921523 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:151921523T>C | c.3155A>G | c.(3154-3156)aAa>aGa | p.K1052R |
| COAD | 7 | 151945103 | 151945103 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-6654-01A-21D-1835-10 | TCGA-A6-6654-10A-01D-1835-10 | g.chr7:151945103A>G | c.2416T>C | c.(2416-2418)Tcc>Ccc | p.S806P |
| COAD | 7 | 151945337 | 151945337 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:151945337C>A | c.2182G>T | c.(2182-2184)Gaa>Taa | p.E728* |
| COAD | 7 | 151945553 | 151945553 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:151945553C>T | c.1966G>A | c.(1966-1968)Gtt>Att | p.V656I |
| COAD | 7 | 151948016 | 151948016 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr7:151948016C>T | c.1657G>A | c.(1657-1659)Gat>Aat | p.D553N |
| COAD | 7 | 151949112 | 151949112 | + | Silent | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr7:151949112C>T | c.1533G>A | c.(1531-1533)gaG>gaA | p.E511E |
| COAD | 7 | 151949688 | 151949688 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr7:151949688C>A | c.1412G>T | c.(1411-1413)gGg>gTg | p.G471V |
| COAD | 7 | 151960201 | 151960201 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr7:151960201T>C | c.1199A>G | c.(1198-1200)gAt>gGt | p.D400G |
| COAD | 7 | 151960201 | 151960201 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr7:151960201T>C | c.1199A>G | c.(1198-1200)gAt>gGt | p.D400G |
| COAD | 7 | 151960201 | 151960201 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr7:151960201T>C | c.1199A>G | c.(1198-1200)gAt>gGt | p.D400G |
| COAD | 7 | 151960202 | 151960202 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-5407-01A-01D-1719-10 | TCGA-AZ-5407-10A-01D-1719-10 | g.chr7:151960202C>A | c.1198G>T | c.(1198-1200)Gat>Tat | p.D400Y |
| COAD | 7 | 151962209 | 151962209 | + | Silent | SNP | A | A | G | TCGA-CA-5796-01A-01D-1650-10 | TCGA-CA-5796-10A-01D-1650-10 | g.chr7:151962209A>G | c.1098T>C | c.(1096-1098)taT>taC | p.Y366Y |
| COAD | 7 | 151962209 | 151962209 | + | Silent | SNP | A | A | G | TCGA-CM-4747-01A-01D-1408-10 | TCGA-CM-4747-10A-01D-1408-10 | g.chr7:151962209A>G | c.1098T>C | c.(1096-1098)taT>taC | p.Y366Y |
| COAD | 7 | 151962210 | 151962210 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A1D0-01A-11D-A152-10 | TCGA-DM-A1D0-10A-01D-A152-10 | g.chr7:151962210T>C | c.1097A>G | c.(1096-1098)tAt>tGt | p.Y366C |
| COAD | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr7:151962211A>G | c.1096T>C | c.(1096-1098)Tat>Cat | p.Y366H |
| COAD | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr7:151962211A>G | c.1096T>C | c.(1096-1098)Tat>Cat | p.Y366H |
| COAD | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | T | TCGA-AZ-6603-01A-11D-1835-10 | TCGA-AZ-6603-11A-02D-1835-10 | g.chr7:151962211A>T | c.1096T>A | c.(1096-1098)Tat>Aat | p.Y366N |
| COAD | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| COAD | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| COAD | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| COAD | 7 | 151962268 | 151962268 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151962268A>G | c.1039T>C | c.(1039-1041)Tgc>Cgc | p.C347R |
| COAD | 7 | 151962268 | 151962268 | + | Missense_Mutation | SNP | A | A | G | TCGA-CK-4950-01A-01D-1719-10 | TCGA-CK-4950-10A-01D-1719-10 | g.chr7:151962268A>G | c.1039T>C | c.(1039-1041)Tgc>Cgc | p.C347R |
| COAD | 7 | 151962268 | 151962268 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr7:151962268A>G | c.1039T>C | c.(1039-1041)Tgc>Cgc | p.C347R |
| COAD | 7 | 152009030 | 152009030 | + | Splice_Site | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:152009030C>A | c.592G>T | c.(592-594)Gaa>Taa | p.E198* |
| COAD | 7 | 152012245 | 152012245 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr7:152012245G>A | c.568C>T | c.(568-570)Cga>Tga | p.R190* |
| COAD | 7 | 152027787 | 152027787 | + | Silent | SNP | T | T | C | TCGA-F4-6703-01A-11D-1835-10 | TCGA-F4-6703-10A-01D-1835-10 | g.chr7:152027787T>C | c.288A>G | c.(286-288)gcA>gcG | p.A96A |
| COAD | 7 | 152027788 | 152027788 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6310-01A-11D-1719-10 | TCGA-G4-6310-10A-01D-1720-10 | g.chr7:152027788G>A | c.287C>T | c.(286-288)gCa>gTa | p.A96V |
| COAD | 7 | 152027816 | 152027816 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AD-6899-01A-11D-1924-10 | TCGA-AD-6899-10A-01D-1924-10 | g.chr7:152027816C>A | c.259G>T | c.(259-261)Gaa>Taa | p.E87* |
| COAD | 7 | 152055685 | 152055685 | + | Silent | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr7:152055685C>T | c.237G>A | c.(235-237)acG>acA | p.T79T |
| COADREAD | 7 | 151835922 | 151835922 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CM-6167-01A-11D-1650-10 | TCGA-CM-6167-10A-01D-1650-10 | g.chr7:151835922delT | c.14602delA | c.(14602-14604)attfs | p.I4870fs |
| COADREAD | 7 | 151836804 | 151836804 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A6-5666-01A-01D-1650-10 | TCGA-A6-5666-10A-01D-1650-10 | g.chr7:151836804G>A | c.14416C>T | c.(14416-14418)Cga>Tga | p.R4806* |
| COADREAD | 7 | 151842334 | 151842334 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr7:151842334C>T | c.14078G>A | c.(14077-14079)cGa>cAa | p.R4693Q |
| COADREAD | 7 | 151845262 | 151845262 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-5344-01A-21D-1719-10 | TCGA-CM-5344-10A-01D-1719-10 | g.chr7:151845262G>A | c.13750C>T | c.(13750-13752)Cgg>Tgg | p.R4584W |
| COADREAD | 7 | 151845367 | 151845367 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr7:151845367G>A | c.13645C>T | c.(13645-13647)Cgc>Tgc | p.R4549C |
| COADREAD | 7 | 151845390 | 151845390 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr7:151845390C>T | c.13622G>A | c.(13621-13623)cGa>cAa | p.R4541Q |
| COADREAD | 7 | 151845435 | 151845435 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3869-01A-01W-0995-10 | TCGA-AA-3869-10A-01W-0995-10 | g.chr7:151845435T>C | c.13577A>G | c.(13576-13578)tAt>tGt | p.Y4526C |
| COADREAD | 7 | 151845451 | 151845451 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3814-01A-01W-0900-09 | TCGA-AA-3814-10A-01W-0900-09 | g.chr7:151845451C>T | c.13561G>A | c.(13561-13563)Gtc>Atc | p.V4521I |
| COADREAD | 7 | 151845524 | 151845524 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr7:151845524delA | c.13488delT | c.(13486-13488)tttfs | p.F4496fs |
| COADREAD | 7 | 151845958 | 151845959 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-A6-2671-01A-01D-1408-10 | TCGA-A6-2671-10A-01D-1408-10 | g.chr7:151845958_151845959insT | c.13053_13054insA | c.(13051-13056)aaatggfs | p.W4352fs |
| COADREAD | 7 | 151845972 | 151845972 | + | Missense_Mutation | SNP | G | G | T | TCGA-A6-6138-01A-11D-1771-10 | TCGA-A6-6138-10A-01D-1771-10 | g.chr7:151845972G>T | c.13040C>A | c.(13039-13041)cCg>cAg | p.P4347Q |
| COADREAD | 7 | 151845973 | 151845973 | + | Missense_Mutation | SNP | G | G | T | TCGA-EF-5830-01A-01D-1657-10 | TCGA-EF-5830-10A-01D-1657-10 | g.chr7:151845973G>T | c.13039C>A | c.(13039-13041)Ccg>Acg | p.P4347T |
| COADREAD | 7 | 151846091 | 151846091 | + | Silent | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr7:151846091G>A | c.12921C>T | c.(12919-12921)atC>atT | p.I4307I |
| COADREAD | 7 | 151846091 | 151846091 | + | Silent | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr7:151846091G>A | c.12921C>T | c.(12919-12921)atC>atT | p.I4307I |
| COADREAD | 7 | 151846233 | 151846233 | + | Missense_Mutation | SNP | G | G | C | TCGA-DM-A28C-01A-11D-A16V-10 | TCGA-DM-A28C-10A-01D-A16V-10 | g.chr7:151846233G>C | c.12779C>G | c.(12778-12780)tCc>tGc | p.S4260C |
| COADREAD | 7 | 151848606 | 151848607 | + | Frame_Shift_Del | DEL | TG | TG | - | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr7:151848606_151848607delTG | c.12586_12587delCA | c.(12586-12588)cagfs | p.Q4196fs |
| COADREAD | 7 | 151851176 | 151851176 | + | Silent | SNP | C | C | T | TCGA-DM-A28C-01A-11D-A16V-10 | TCGA-DM-A28C-10A-01D-A16V-10 | g.chr7:151851176C>T | c.12195G>A | c.(12193-12195)gcG>gcA | p.A4065A |
| COADREAD | 7 | 151851208 | 151851208 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr7:151851208T>C | c.12163A>G | c.(12163-12165)Atc>Gtc | p.I4055V |
| COADREAD | 7 | 151851208 | 151851208 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chr7:151851208T>C | c.12163A>G | c.(12163-12165)Atc>Gtc | p.I4055V |
| COADREAD | 7 | 151859337 | 151859337 | + | Silent | SNP | T | T | C | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr7:151859337T>C | c.11325A>G | c.(11323-11325)gaA>gaG | p.E3775E |
| COADREAD | 7 | 151859337 | 151859337 | + | Silent | SNP | T | T | C | TCGA-G4-6626-01A-11D-1771-10 | TCGA-G4-6626-10A-01D-1771-10 | g.chr7:151859337T>C | c.11325A>G | c.(11323-11325)gaA>gaG | p.E3775E |
| COADREAD | 7 | 151859338 | 151859338 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6167-01A-11D-1650-10 | TCGA-CM-6167-10A-01D-1650-10 | g.chr7:151859338T>C | c.11324A>G | c.(11323-11325)gAa>gGa | p.E3775G |
| COADREAD | 7 | 151859519 | 151859519 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr7:151859519delT | c.11143delA | c.(11143-11145)acafs | p.T3715fs |
| COADREAD | 7 | 151859568 | 151859568 | + | Silent | SNP | C | C | T | TCGA-F4-6569-01A-11D-1771-10 | TCGA-F4-6569-10A-01D-1771-10 | g.chr7:151859568C>T | c.11094G>A | c.(11092-11094)acG>acA | p.T3698T |
| COADREAD | 7 | 151859569 | 151859569 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr7:151859569G>A | c.11093C>T | c.(11092-11094)aCg>aTg | p.T3698M |
| COADREAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-AG-3732-01A-11D-1657-10 | TCGA-AG-3732-11A-01D-1657-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COADREAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COADREAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6608-01A-11D-1835-10 | TCGA-AZ-6608-11A-01D-1835-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COADREAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-5539-01A-01D-1650-10 | TCGA-D5-5539-10A-01D-1650-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COADREAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6920-01A-11D-1924-10 | TCGA-D5-6920-10A-01D-1924-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COADREAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6923-01A-11D-1924-10 | TCGA-D5-6923-10A-01D-1924-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COADREAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6929-01A-31D-1924-10 | TCGA-D5-6929-10A-01D-1924-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| COADREAD | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | G | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr7:151859570T>G | c.11092A>C | c.(11092-11094)Acg>Ccg | p.T3698P |
| COADREAD | 7 | 151859627 | 151859627 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A036-01A-12W-A096-10 | TCGA-AG-A036-11A-11W-A096-10 | g.chr7:151859627C>T | c.11035G>A | c.(11035-11037)Gaa>Aaa | p.E3679K |
| COADREAD | 7 | 151859850 | 151859850 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:151859850C>A | c.10812G>T | c.(10810-10812)aaG>aaT | p.K3604N |
| COADREAD | 7 | 151859997 | 151859997 | + | Silent | SNP | A | A | G | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr7:151859997A>G | c.10665T>C | c.(10663-10665)ccT>ccC | p.P3555P |
| COADREAD | 7 | 151860278 | 151860278 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:151860278A>C | c.10384T>G | c.(10384-10386)Ttt>Gtt | p.F3462V |
| COADREAD | 7 | 151860293 | 151860293 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr7:151860293C>T | c.10369G>A | c.(10369-10371)Gac>Aac | p.D3457N |
| COADREAD | 7 | 151860621 | 151860621 | + | Silent | SNP | A | A | G | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr7:151860621A>G | c.10041T>C | c.(10039-10041)aaT>aaC | p.N3347N |
| COADREAD | 7 | 151864307 | 151864307 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr7:151864307T>C | c.9674A>G | c.(9673-9675)gAa>gGa | p.E3225G |
| COADREAD | 7 | 151864331 | 151864331 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151864331C>T | c.9650G>A | c.(9649-9651)cGt>cAt | p.R3217H |
| COADREAD | 7 | 151873535 | 151873535 | + | Silent | SNP | G | G | A | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr7:151873535G>A | c.9003C>T | c.(9001-9003)aaC>aaT | p.N3001N |
| COADREAD | 7 | 151873626 | 151873626 | + | Missense_Mutation | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:151873626G>T | c.8912C>A | c.(8911-8913)tCt>tAt | p.S2971Y |
| COADREAD | 7 | 151873627 | 151873627 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr7:151873627A>G | c.8911T>C | c.(8911-8913)Tct>Cct | p.S2971P |
| COADREAD | 7 | 151873758 | 151873758 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151873758G>A | c.8780C>T | c.(8779-8781)tCt>tTt | p.S2927F |
| COADREAD | 7 | 151873938 | 151873939 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr7:151873938_151873939delTT | c.8599_8600delAA | c.(8599-8601)aagfs | p.K2867fs |
| COADREAD | 7 | 151873939 | 151873939 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr7:151873939T>C | c.8599A>G | c.(8599-8601)Aag>Gag | p.K2867E |
| COADREAD | 7 | 151874147 | 151874148 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr7:151874147_151874148insT | c.8390_8391insA | c.(8389-8391)aagfs | p.K2797fs |
| COADREAD | 7 | 151874515 | 151874515 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151874515A>C | c.8023T>G | c.(8023-8025)Tta>Gta | p.L2675V |
| COADREAD | 7 | 151874771 | 151874771 | + | Silent | SNP | T | T | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:151874771T>C | c.7767A>G | c.(7765-7767)agA>agG | p.R2589R |
| COADREAD | 7 | 151876974 | 151876974 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr7:151876974G>A | c.7387C>T | c.(7387-7389)Cgt>Tgt | p.R2463C |
| COADREAD | 7 | 151878070 | 151878070 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr7:151878070delG | c.6875delC | c.(6874-6876)ccafs | p.P2292fs |
| COADREAD | 7 | 151878105 | 151878105 | + | Silent | SNP | T | T | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr7:151878105T>C | c.6840A>G | c.(6838-6840)ggA>ggG | p.G2280G |
| COADREAD | 7 | 151878529 | 151878529 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr7:151878529C>T | c.6416G>A | c.(6415-6417)cGa>cAa | p.R2139Q |
| COADREAD | 7 | 151878622 | 151878622 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:151878622G>T | c.6323C>A | c.(6322-6324)tCt>tAt | p.S2108Y |
| COADREAD | 7 | 151878642 | 151878642 | + | Silent | SNP | T | T | C | TCGA-CM-4747-01A-01D-1408-10 | TCGA-CM-4747-10A-01D-1408-10 | g.chr7:151878642T>C | c.6303A>G | c.(6301-6303)ccA>ccG | p.P2101P |
| COADREAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COADREAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-AH-6549-01A-11D-1826-10 | TCGA-AH-6549-10A-01D-1826-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COADREAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COADREAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-5868-01A-01D-1650-10 | TCGA-CM-5868-10A-01D-1650-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COADREAD | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A1D7-01A-11D-A152-10 | TCGA-DM-A1D7-10A-01D-A152-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| COADREAD | 7 | 151879228 | 151879228 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr7:151879228C>A | c.5717G>T | c.(5716-5718)cGa>cTa | p.R1906L |
| COADREAD | 7 | 151879229 | 151879229 | + | Silent | SNP | G | G | T | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151879229G>T | c.5716C>A | c.(5716-5718)Cga>Aga | p.R1906R |
| COADREAD | 7 | 151879325 | 151879325 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3846-01A-01W-0995-10 | TCGA-AA-3846-10A-01W-0995-10 | g.chr7:151879325A>C | c.5620T>G | c.(5620-5622)Tct>Gct | p.S1874A |
| COADREAD | 7 | 151879428 | 151879428 | + | Silent | SNP | C | C | T | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr7:151879428C>T | c.5517G>A | c.(5515-5517)acG>acA | p.T1839T |
| COADREAD | 7 | 151879605 | 151879605 | + | Silent | SNP | C | C | T | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr7:151879605C>T | c.5340G>A | c.(5338-5340)caG>caA | p.Q1780Q |
| COADREAD | 7 | 151880081 | 151880081 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr7:151880081T>G | c.5243A>C | c.(5242-5244)gAa>gCa | p.E1748A |
| COADREAD | 7 | 151880121 | 151880121 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151880121G>A | c.5203C>T | c.(5203-5205)Ctt>Ttt | p.L1735F |
| COADREAD | 7 | 151884426 | 151884426 | + | Missense_Mutation | SNP | C | C | A | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr7:151884426C>A | c.4929G>T | c.(4927-4929)gaG>gaT | p.E1643D |
| COADREAD | 7 | 151884543 | 151884543 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151884543A>C | c.4812T>G | c.(4810-4812)ttT>ttG | p.F1604L |
| COADREAD | 7 | 151884823 | 151884823 | + | Silent | SNP | T | T | C | TCGA-AA-3681-01A-01W-0900-09 | TCGA-AA-3681-10A-01W-0900-09 | g.chr7:151884823T>C | c.4770A>G | c.(4768-4770)gcA>gcG | p.A1590A |
| COADREAD | 7 | 151891205 | 151891205 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CM-6167-01A-11D-1650-10 | TCGA-CM-6167-10A-01D-1650-10 | g.chr7:151891205C>A | c.4549G>T | c.(4549-4551)Gga>Tga | p.G1517* |
| COADREAD | 7 | 151891205 | 151891205 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr7:151891205C>A | c.4549G>T | c.(4549-4551)Gga>Tga | p.G1517* |
| COADREAD | 7 | 151891206 | 151891206 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:151891206G>A | c.4548C>T | c.(4546-4548)ggC>ggT | p.G1516G |
| COADREAD | 7 | 151896440 | 151896440 | + | Missense_Mutation | SNP | C | C | T | TCGA-AU-3779-01A-01D-1719-10 | TCGA-AU-3779-10A-01D-1719-10 | g.chr7:151896440C>T | c.4197G>A | c.(4195-4197)atG>atA | p.M1399I |
| COADREAD | 7 | 151896508 | 151896508 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151896508T>A | c.4129A>T | c.(4129-4131)Aga>Tga | p.R1377* |
| COADREAD | 7 | 151904487 | 151904487 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr7:151904487T>A | c.3739A>T | c.(3739-3741)Aaa>Taa | p.K1247* |
| COADREAD | 7 | 151917681 | 151917681 | + | Silent | SNP | G | G | A | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr7:151917681G>A | c.3639C>T | c.(3637-3639)agC>agT | p.S1213S |
| COADREAD | 7 | 151921127 | 151921127 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr7:151921127A>C | c.3296T>G | c.(3295-3297)cTt>cGt | p.L1099R |
| COADREAD | 7 | 151921131 | 151921131 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr7:151921131C>A | c.3292G>T | c.(3292-3294)Gat>Tat | p.D1098Y |
| COADREAD | 7 | 151921523 | 151921523 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:151921523T>C | c.3155A>G | c.(3154-3156)aAa>aGa | p.K1052R |
| COADREAD | 7 | 151945103 | 151945103 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-6654-01A-21D-1835-10 | TCGA-A6-6654-10A-01D-1835-10 | g.chr7:151945103A>G | c.2416T>C | c.(2416-2418)Tcc>Ccc | p.S806P |
| COADREAD | 7 | 151945337 | 151945337 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:151945337C>A | c.2182G>T | c.(2182-2184)Gaa>Taa | p.E728* |
| COADREAD | 7 | 151945455 | 151945455 | + | Silent | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151945455G>T | c.2064C>A | c.(2062-2064)gtC>gtA | p.V688V |
| COADREAD | 7 | 151945553 | 151945553 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr7:151945553C>T | c.1966G>A | c.(1966-1968)Gtt>Att | p.V656I |
| COADREAD | 7 | 151948016 | 151948016 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr7:151948016C>T | c.1657G>A | c.(1657-1659)Gat>Aat | p.D553N |
| COADREAD | 7 | 151949112 | 151949112 | + | Silent | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr7:151949112C>T | c.1533G>A | c.(1531-1533)gaG>gaA | p.E511E |
| COADREAD | 7 | 151949688 | 151949688 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr7:151949688C>A | c.1412G>T | c.(1411-1413)gGg>gTg | p.G471V |
| COADREAD | 7 | 151960154 | 151960155 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-DY-A1DF-01A-11D-A152-10 | TCGA-DY-A1DF-10A-01D-A152-10 | g.chr7:151960154_151960155insC | c.1245_1246insG | c.(1243-1248)acttttfs | p.F416fs |
| COADREAD | 7 | 151960201 | 151960201 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr7:151960201T>C | c.1199A>G | c.(1198-1200)gAt>gGt | p.D400G |
| COADREAD | 7 | 151960201 | 151960201 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr7:151960201T>C | c.1199A>G | c.(1198-1200)gAt>gGt | p.D400G |
| COADREAD | 7 | 151960201 | 151960201 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr7:151960201T>C | c.1199A>G | c.(1198-1200)gAt>gGt | p.D400G |
| COADREAD | 7 | 151960202 | 151960202 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-5407-01A-01D-1719-10 | TCGA-AZ-5407-10A-01D-1719-10 | g.chr7:151960202C>A | c.1198G>T | c.(1198-1200)Gat>Tat | p.D400Y |
| COADREAD | 7 | 151962209 | 151962209 | + | Silent | SNP | A | A | G | TCGA-CA-5796-01A-01D-1650-10 | TCGA-CA-5796-10A-01D-1650-10 | g.chr7:151962209A>G | c.1098T>C | c.(1096-1098)taT>taC | p.Y366Y |
| COADREAD | 7 | 151962209 | 151962209 | + | Silent | SNP | A | A | G | TCGA-CM-4747-01A-01D-1408-10 | TCGA-CM-4747-10A-01D-1408-10 | g.chr7:151962209A>G | c.1098T>C | c.(1096-1098)taT>taC | p.Y366Y |
| COADREAD | 7 | 151962210 | 151962210 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A1D0-01A-11D-A152-10 | TCGA-DM-A1D0-10A-01D-A152-10 | g.chr7:151962210T>C | c.1097A>G | c.(1096-1098)tAt>tGt | p.Y366C |
| COADREAD | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | G | TCGA-AH-6644-01A-21D-1826-10 | TCGA-AH-6644-10A-01D-1826-10 | g.chr7:151962211A>G | c.1096T>C | c.(1096-1098)Tat>Cat | p.Y366H |
| COADREAD | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr7:151962211A>G | c.1096T>C | c.(1096-1098)Tat>Cat | p.Y366H |
| COADREAD | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | G | TCGA-DC-6681-01A-11D-1826-10 | TCGA-DC-6681-10A-01D-1826-10 | g.chr7:151962211A>G | c.1096T>C | c.(1096-1098)Tat>Cat | p.Y366H |
| COADREAD | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr7:151962211A>G | c.1096T>C | c.(1096-1098)Tat>Cat | p.Y366H |
| COADREAD | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | T | TCGA-AZ-6603-01A-11D-1835-10 | TCGA-AZ-6603-11A-02D-1835-10 | g.chr7:151962211A>T | c.1096T>A | c.(1096-1098)Tat>Aat | p.Y366N |
| COADREAD | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| COADREAD | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| COADREAD | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-F5-6465-01A-11D-1733-10 | TCGA-F5-6465-10A-01D-1733-10 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| COADREAD | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| COADREAD | 7 | 151962268 | 151962268 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr7:151962268A>G | c.1039T>C | c.(1039-1041)Tgc>Cgc | p.C347R |
| COADREAD | 7 | 151962268 | 151962268 | + | Missense_Mutation | SNP | A | A | G | TCGA-CK-4950-01A-01D-1719-10 | TCGA-CK-4950-10A-01D-1719-10 | g.chr7:151962268A>G | c.1039T>C | c.(1039-1041)Tgc>Cgc | p.C347R |
| COADREAD | 7 | 151962268 | 151962268 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr7:151962268A>G | c.1039T>C | c.(1039-1041)Tgc>Cgc | p.C347R |
| COADREAD | 7 | 152009030 | 152009030 | + | Splice_Site | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr7:152009030C>A | c.592G>T | c.(592-594)Gaa>Taa | p.E198* |
| COADREAD | 7 | 152012245 | 152012245 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr7:152012245G>A | c.568C>T | c.(568-570)Cga>Tga | p.R190* |
| COADREAD | 7 | 152027787 | 152027787 | + | Silent | SNP | T | T | C | TCGA-F4-6703-01A-11D-1835-10 | TCGA-F4-6703-10A-01D-1835-10 | g.chr7:152027787T>C | c.288A>G | c.(286-288)gcA>gcG | p.A96A |
| COADREAD | 7 | 152027788 | 152027788 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6310-01A-11D-1719-10 | TCGA-G4-6310-10A-01D-1720-10 | g.chr7:152027788G>A | c.287C>T | c.(286-288)gCa>gTa | p.A96V |
| COADREAD | 7 | 152027816 | 152027816 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AD-6899-01A-11D-1924-10 | TCGA-AD-6899-10A-01D-1924-10 | g.chr7:152027816C>A | c.259G>T | c.(259-261)Gaa>Taa | p.E87* |
| COADREAD | 7 | 152055685 | 152055685 | + | Silent | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr7:152055685C>T | c.237G>A | c.(235-237)acG>acA | p.T79T |
| DLBC | 7 | 151859495 | 151859495 | + | Missense_Mutation | SNP | C | C | G | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr7:151859495C>G | c.11167G>C | c.(11167-11169)Gct>Cct | p.A3723P |
| DLBC | 7 | 151878589 | 151878589 | + | Missense_Mutation | SNP | G | G | A | TCGA-G8-6909-01A-11D-2210-10 | TCGA-G8-6909-14A-01D-2210-10 | g.chr7:151878589G>A | c.6356C>T | c.(6355-6357)cCt>cTt | p.P2119L |
| DLBC | 7 | 151896389 | 151896389 | + | Silent | SNP | C | C | T | TCGA-FF-A7CX-01A-12D-A382-10 | TCGA-FF-A7CX-10A-01D-A385-10 | g.chr7:151896389C>T | c.4248G>A | c.(4246-4248)tcG>tcA | p.S1416S |
| DLBC | 7 | 151902302 | 151902302 | + | Missense_Mutation | SNP | C | C | T | TCGA-GS-A9TW-01A-11D-A382-10 | TCGA-GS-A9TW-10A-01D-A385-10 | g.chr7:151902302C>T | c.3850G>A | c.(3850-3852)Gga>Aga | p.G1284R |
| DLBC | 7 | 151962183 | 151962183 | + | Missense_Mutation | SNP | A | A | C | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr7:151962183A>C | c.1124T>G | c.(1123-1125)gTt>gGt | p.V375G |
| DLBC | 7 | 151962289 | 151962289 | + | Missense_Mutation | SNP | C | C | T | TCGA-G8-6906-01A-11D-2210-10 | TCGA-G8-6906-14A-01D-2210-10 | g.chr7:151962289C>T | c.1018G>A | c.(1018-1020)Gaa>Aaa | p.E340K |
| DLBC | 7 | 151970811 | 151970811 | + | Missense_Mutation | SNP | T | T | C | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr7:151970811T>C | c.991A>G | c.(991-993)Att>Gtt | p.I331V |
| DLBC | 7 | 151970845 | 151970845 | + | Missense_Mutation | SNP | A | A | T | TCGA-FM-8000-01A-11D-2210-10 | TCGA-FM-8000-10A-01D-2210-10 | g.chr7:151970845A>T | c.957T>A | c.(955-957)gaT>gaA | p.D319E |
| DLBC | 7 | 151970899 | 151970899 | + | Silent | SNP | T | T | C | TCGA-G8-6326-01A-11D-2210-10 | TCGA-G8-6326-10A-01D-2210-10 | g.chr7:151970899T>C | c.903A>G | c.(901-903)aaA>aaG | p.K301K |
| ESCA | 7 | 151843811 | 151843811 | + | Missense_Mutation | SNP | T | T | A | TCGA-2H-A9GL-01A-12D-A37C-09 | TCGA-2H-A9GL-11A-11D-A37F-09 | g.chr7:151843811T>A | c.13904A>T | c.(13903-13905)gAt>gTt | p.D4635V |
| ESCA | 7 | 151848559 | 151848559 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-L5-A4OQ-01A-11D-A27G-09 | TCGA-L5-A4OQ-11A-12D-A27G-09 | g.chr7:151848559T>A | c.12634A>T | c.(12634-12636)Aaa>Taa | p.K4212* |
| ESCA | 7 | 151851097 | 151851097 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-L5-A8NG-01A-11D-A37C-09 | TCGA-L5-A8NG-11A-11D-A37F-09 | g.chr7:151851097C>A | c.12274G>T | c.(12274-12276)Gag>Tag | p.E4092* |
| ESCA | 7 | 151859283 | 151859283 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-R6-A6Y0-01B-11D-A33E-09 | TCGA-R6-A6Y0-10A-01D-A33H-09 | g.chr7:151859283delT | c.11379delA | c.(11377-11379)aaafs | p.K3793fs |
| ESCA | 7 | 151859780 | 151859780 | + | Missense_Mutation | SNP | C | C | T | TCGA-IG-A3Y9-01A-12D-A247-09 | TCGA-IG-A3Y9-10A-01D-A247-09 | g.chr7:151859780C>T | c.10882G>A | c.(10882-10884)Gat>Aat | p.D3628N |
| ESCA | 7 | 151860113 | 151860113 | + | Missense_Mutation | SNP | G | G | T | TCGA-JY-A6FH-01A-11D-A33E-09 | TCGA-JY-A6FH-10A-01D-A33H-09 | g.chr7:151860113G>T | c.10549C>A | c.(10549-10551)Cct>Act | p.P3517T |
| ESCA | 7 | 151873959 | 151873959 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-L5-A8NK-01A-21D-A37C-09 | TCGA-L5-A8NK-11A-11D-A37F-09 | g.chr7:151873959G>C | c.8579C>G | c.(8578-8580)tCa>tGa | p.S2860* |
| ESCA | 7 | 151878416 | 151878416 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-XP-A8T7-01A-11D-A36J-09 | TCGA-XP-A8T7-10A-01D-A36M-09 | g.chr7:151878416G>A | c.6529C>T | c.(6529-6531)Cag>Tag | p.Q2177* |
| ESCA | 7 | 151878492 | 151878492 | + | Silent | SNP | T | T | A | TCGA-LN-A9FP-01A-31D-A387-09 | TCGA-LN-A9FP-10A-01D-A38A-09 | g.chr7:151878492T>A | c.6453A>T | c.(6451-6453)acA>acT | p.T2151T |
| ESCA | 7 | 151878602 | 151878602 | + | Missense_Mutation | SNP | C | C | A | TCGA-VR-AA7D-01A-11D-A403-09 | TCGA-VR-AA7D-10A-01D-A403-09 | g.chr7:151878602C>A | c.6343G>T | c.(6343-6345)Gct>Tct | p.A2115S |
| ESCA | 7 | 151878713 | 151878713 | + | Missense_Mutation | SNP | T | T | C | TCGA-IG-A3QL-01A-11D-A247-09 | TCGA-IG-A3QL-10A-01D-A247-09 | g.chr7:151878713T>C | c.6232A>G | c.(6232-6234)Aca>Gca | p.T2078A |
| ESCA | 7 | 151882652 | 151882652 | + | Silent | SNP | T | T | C | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr7:151882652T>C | c.5073A>G | c.(5071-5073)gcA>gcG | p.A1691A |
| ESCA | 7 | 151884535 | 151884536 | + | Frame_Shift_Ins | INS | - | - | TT | TCGA-L5-A43C-01A-11D-A247-09 | TCGA-L5-A43C-11A-11D-A247-09 | g.chr7:151884535_151884536insTT | c.4819_4820insAA | c.(4819-4821)atgfs | p.M1607fs |
| ESCA | 7 | 151927069 | 151927069 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A4OG-01A-11D-A27G-09 | TCGA-L5-A4OG-11A-12D-A27G-09 | g.chr7:151927069C>T | c.2915G>A | c.(2914-2916)gGa>gAa | p.G972E |
| ESCA | 7 | 151935808 | 151935808 | + | Missense_Mutation | SNP | A | A | C | TCGA-2H-A9GH-01A-11D-A37C-09 | TCGA-2H-A9GH-11A-11D-A37F-09 | g.chr7:151935808A>C | c.2636T>G | c.(2635-2637)aTt>aGt | p.I879S |
| ESCA | 7 | 151947037 | 151947037 | + | Splice_Site | SNP | C | C | T | TCGA-LN-A7HZ-01A-31D-A351-09 | TCGA-LN-A7HZ-10A-01D-A351-09 | g.chr7:151947037C>T | c.1737G>A | c.(1735-1737)gcG>gcA | p.A579A |
| ESCA | 7 | 151962134 | 151962134 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-VR-A8Q7-01A-11D-A37C-09 | TCGA-VR-A8Q7-10A-01D-A37F-09 | g.chr7:151962134G>T | c.1173C>A | c.(1171-1173)tgC>tgA | p.C391* |
| ESCA | 7 | 151962168 | 151962168 | + | Missense_Mutation | SNP | C | C | A | TCGA-VR-A8Q7-01A-11D-A37C-09 | TCGA-VR-A8Q7-10A-01D-A37F-09 | g.chr7:151962168C>A | c.1139G>T | c.(1138-1140)cGt>cTt | p.R380L |
| ESCA | 7 | 151962290 | 151962290 | + | Missense_Mutation | SNP | C | C | G | TCGA-LN-A4A9-01A-11D-A28B-09 | TCGA-LN-A4A9-10A-01D-A28E-09 | g.chr7:151962290C>G | c.1017G>C | c.(1015-1017)aaG>aaC | p.K339N |
| ESCA | 7 | 152012301 | 152012301 | + | Missense_Mutation | SNP | T | T | C | TCGA-LN-A7HV-01A-21D-A351-09 | TCGA-LN-A7HV-10A-01D-A351-09 | g.chr7:152012301T>C | c.512A>G | c.(511-513)aAg>aGg | p.K171R |
| GBM | 7 | 151849845 | 151849845 | + | Silent | SNP | T | T | C | TCGA-06-0237-01A-02D-1491-08 | TCGA-06-0237-10A-01D-1491-08 | g.chr7:151849845T>C | c.12471A>G | c.(12469-12471)ttA>ttG | p.L4157L |
| GBM | 7 | 151877846 | 151877846 | + | Missense_Mutation | SNP | T | T | C | TCGA-27-1833-01A-01W-0643-08 | TCGA-27-1833-10A-01W-0644-08 | g.chr7:151877846T>C | c.7099A>G | c.(7099-7101)Aca>Gca | p.T2367A |
| GBM | 7 | 151878185 | 151878185 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr7:151878185C>T | c.6760G>A | c.(6760-6762)Gca>Aca | p.A2254T |
| GBM | 7 | 151892993 | 151892993 | + | Splice_Site | SNP | T | T | C | TCGA-06-0878-01A-01W-0424-08 | TCGA-06-0878-10A-01W-0424-08 | g.chr7:151892993T>C | c.4377A>G | c.(4375-4377)tcA>tcG | p.S1459S |
| GBM | 7 | 151904459 | 151904459 | + | Missense_Mutation | SNP | G | G | C | TCGA-28-5219-01A-01D-1486-08 | TCGA-28-5219-10A-01D-1486-08 | g.chr7:151904459G>C | c.3767C>G | c.(3766-3768)gCt>gGt | p.A1256G |
| GBM | 7 | 151921652 | 151921652 | + | Missense_Mutation | SNP | A | A | C | TCGA-76-6192-01A-11D-1696-08 | TCGA-76-6192-10A-01D-1696-08 | g.chr7:151921652A>C | c.3026T>G | c.(3025-3027)gTg>gGg | p.V1009G |
| GBM | 7 | 151927093 | 151927093 | + | Missense_Mutation | SNP | C | C | A | TCGA-06-0238-01A-02D-1492-08 | TCGA-06-0238-10A-01D-1492-08 | g.chr7:151927093C>A | c.2891G>T | c.(2890-2892)gGc>gTc | p.G964V |
| GBM | 7 | 151944990 | 151944990 | + | Silent | SNP | T | T | C | TCGA-76-4925-01A-01D-1486-08 | TCGA-76-4925-10A-01D-1486-08 | g.chr7:151944990T>C | c.2529A>G | c.(2527-2529)aaA>aaG | p.K843K |
| GBM | 7 | 151945049 | 151945049 | + | Missense_Mutation | SNP | C | C | G | TCGA-41-4097-01A-01D-1353-08 | TCGA-41-4097-10A-01D-1353-08 | g.chr7:151945049C>G | c.2470G>C | c.(2470-2472)Ggc>Cgc | p.G824R |
| GBM | 7 | 151945253 | 151945253 | + | Missense_Mutation | SNP | C | C | T | TCGA-74-6577-01A-11D-1845-08 | TCGA-74-6577-10A-01D-1845-08 | g.chr7:151945253C>T | c.2266G>A | c.(2266-2268)Gga>Aga | p.G756R |
| GBM | 7 | 151960173 | 151960173 | + | Silent | SNP | A | A | G | TCGA-06-0188-01A-01W-0254-08 | TCGA-06-0188-10B-01W-0254-08 | g.chr7:151960173A>G | c.1227T>C | c.(1225-1227)tgT>tgC | p.C409C |
| GBM | 7 | 151962124 | 151962124 | + | Splice_Site | SNP | T | T | C | TCGA-02-2470-01A-01D-1494-08 | TCGA-02-2470-10A-01D-1494-08 | g.chr7:151962124T>C | c.1183A>G | c.(1183-1185)Aaa>Gaa | p.K395E |
| GBM | 7 | 151962220 | 151962220 | + | Missense_Mutation | SNP | C | C | A | TCGA-06-0219-01A-01D-1491-08 | TCGA-06-0219-10A-01D-1491-08 | g.chr7:151962220C>A | c.1087G>T | c.(1087-1089)Ggt>Tgt | p.G363C |
| GBM | 7 | 151970848 | 151970848 | + | Missense_Mutation | SNP | C | C | A | TCGA-19-5958-01A-11D-1696-08 | TCGA-19-5958-11A-01D-1696-08 | g.chr7:151970848C>A | c.954G>T | c.(952-954)caG>caT | p.Q318H |
| GBMLGG | 7 | 151842271 | 151842271 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-5853-01A-11D-1893-08 | TCGA-DU-5853-10A-01D-1893-08 | g.chr7:151842271T>G | c.14141A>C | c.(14140-14142)aAa>aCa | p.K4714T |
| GBMLGG | 7 | 151845685 | 151845686 | + | Frame_Shift_Del | DEL | GA | GA | - | TCGA-E1-5319-01A-01D-1893-08 | TCGA-E1-5319-10A-01D-1893-08 | g.chr7:151845685_151845686delGA | c.13326_13327delTC | c.(13324-13329)actcagfs | p.Q4443fs |
| GBMLGG | 7 | 151845755 | 151845755 | + | Silent | SNP | T | T | C | TCGA-S9-A7J3-01A-21D-A34J-08 | TCGA-S9-A7J3-10A-01D-A34M-08 | g.chr7:151845755T>C | c.13257A>G | c.(13255-13257)ctA>ctG | p.L4419L |
| GBMLGG | 7 | 151848004 | 151848004 | + | Missense_Mutation | SNP | G | G | A | TCGA-S9-A7J1-01A-21D-A34J-08 | TCGA-S9-A7J1-10A-01D-A34M-08 | g.chr7:151848004G>A | c.12755C>T | c.(12754-12756)gCg>gTg | p.A4252V |
| GBMLGG | 7 | 151848014 | 151848014 | + | Missense_Mutation | SNP | T | T | C | TCGA-RY-A83Z-01A-11D-A36O-08 | TCGA-RY-A83Z-10A-01D-A367-08 | g.chr7:151848014T>C | c.12745A>G | c.(12745-12747)Act>Gct | p.T4249A |
| GBMLGG | 7 | 151849845 | 151849845 | + | Silent | SNP | T | T | C | TCGA-06-0237-01A-02D-1491-08 | TCGA-06-0237-10A-01D-1491-08 | g.chr7:151849845T>C | c.12471A>G | c.(12469-12471)ttA>ttG | p.L4157L |
| GBMLGG | 7 | 151853385 | 151853385 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151853385G>T | c.11717C>A | c.(11716-11718)cCt>cAt | p.P3906H |
| GBMLGG | 7 | 151859576 | 151859576 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-E1-A7Z2-01A-21D-A34J-08 | TCGA-E1-A7Z2-10A-01D-A34M-08 | g.chr7:151859576delG | c.11086delC | c.(11086-11088)caafs | p.Q3697fs |
| GBMLGG | 7 | 151859837 | 151859837 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151859837T>C | c.10825A>G | c.(10825-10827)Aag>Gag | p.K3609E |
| GBMLGG | 7 | 151864270 | 151864270 | + | Silent | SNP | A | A | G | TCGA-DU-A7TG-01A-21D-A34J-08 | TCGA-DU-A7TG-10A-01D-A34M-08 | g.chr7:151864270A>G | c.9711T>C | c.(9709-9711)gtT>gtC | p.V3237V |
| GBMLGG | 7 | 151873659 | 151873659 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151873659G>A | c.8879C>T | c.(8878-8880)cCg>cTg | p.P2960L |
| GBMLGG | 7 | 151873923 | 151873923 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151873923G>T | c.8615C>A | c.(8614-8616)cCt>cAt | p.P2872H |
| GBMLGG | 7 | 151877846 | 151877846 | + | Missense_Mutation | SNP | T | T | C | TCGA-27-1833-01A-01W-0643-08 | TCGA-27-1833-10A-01W-0644-08 | g.chr7:151877846T>C | c.7099A>G | c.(7099-7101)Aca>Gca | p.T2367A |
| GBMLGG | 7 | 151878079 | 151878079 | + | Missense_Mutation | SNP | C | C | T | TCGA-QH-A6X3-01A-21D-A32B-08 | TCGA-QH-A6X3-10B-01D-A329-08 | g.chr7:151878079C>T | c.6866G>A | c.(6865-6867)cGt>cAt | p.R2289H |
| GBMLGG | 7 | 151878185 | 151878185 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr7:151878185C>T | c.6760G>A | c.(6760-6762)Gca>Aca | p.A2254T |
| GBMLGG | 7 | 151878436 | 151878436 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151878436G>A | c.6509C>T | c.(6508-6510)aCt>aTt | p.T2170I |
| GBMLGG | 7 | 151892993 | 151892993 | + | Splice_Site | SNP | T | T | C | TCGA-06-0878-01A-01W-0424-08 | TCGA-06-0878-10A-01W-0424-08 | g.chr7:151892993T>C | c.4377A>G | c.(4375-4377)tcA>tcG | p.S1459S |
| GBMLGG | 7 | 151904459 | 151904459 | + | Missense_Mutation | SNP | G | G | C | TCGA-28-5219-01A-01D-1486-08 | TCGA-28-5219-10A-01D-1486-08 | g.chr7:151904459G>C | c.3767C>G | c.(3766-3768)gCt>gGt | p.A1256G |
| GBMLGG | 7 | 151917719 | 151917719 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151917719T>G | c.3601A>C | c.(3601-3603)Aaa>Caa | p.K1201Q |
| GBMLGG | 7 | 151921652 | 151921652 | + | Missense_Mutation | SNP | A | A | C | TCGA-76-6192-01A-11D-1696-08 | TCGA-76-6192-10A-01D-1696-08 | g.chr7:151921652A>C | c.3026T>G | c.(3025-3027)gTg>gGg | p.V1009G |
| GBMLGG | 7 | 151927093 | 151927093 | + | Missense_Mutation | SNP | C | C | A | TCGA-06-0238-01A-02D-1492-08 | TCGA-06-0238-10A-01D-1492-08 | g.chr7:151927093C>A | c.2891G>T | c.(2890-2892)gGc>gTc | p.G964V |
| GBMLGG | 7 | 151932981 | 151932981 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A5TS-01A-11D-A289-08 | TCGA-DU-A5TS-10A-01D-A289-08 | g.chr7:151932981C>T | c.2690G>A | c.(2689-2691)cGa>cAa | p.R897Q |
| GBMLGG | 7 | 151935819 | 151935819 | + | Silent | SNP | A | A | G | TCGA-TQ-A7RM-01A-11D-A33T-08 | TCGA-TQ-A7RM-10A-01D-A33W-08 | g.chr7:151935819A>G | c.2625T>C | c.(2623-2625)ccT>ccC | p.P875P |
| GBMLGG | 7 | 151944990 | 151944990 | + | Silent | SNP | T | T | C | TCGA-76-4925-01A-01D-1486-08 | TCGA-76-4925-10A-01D-1486-08 | g.chr7:151944990T>C | c.2529A>G | c.(2527-2529)aaA>aaG | p.K843K |
| GBMLGG | 7 | 151945049 | 151945049 | + | Missense_Mutation | SNP | C | C | G | TCGA-41-4097-01A-01D-1353-08 | TCGA-41-4097-10A-01D-1353-08 | g.chr7:151945049C>G | c.2470G>C | c.(2470-2472)Ggc>Cgc | p.G824R |
| GBMLGG | 7 | 151945083 | 151945083 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151945083C>T | c.2436G>A | c.(2434-2436)atG>atA | p.M812I |
| GBMLGG | 7 | 151945104 | 151945104 | + | Missense_Mutation | SNP | A | A | T | TCGA-CS-5397-01A-01D-1893-08 | TCGA-CS-5397-10A-03D-1893-08 | g.chr7:151945104A>T | c.2415T>A | c.(2413-2415)agT>agA | p.S805R |
| GBMLGG | 7 | 151945155 | 151945155 | + | Silent | SNP | A | A | T | TCGA-DU-A7T8-01A-21D-A34J-08 | TCGA-DU-A7T8-10A-01D-A34M-08 | g.chr7:151945155A>T | c.2364T>A | c.(2362-2364)tcT>tcA | p.S788S |
| GBMLGG | 7 | 151945175 | 151945175 | + | Missense_Mutation | SNP | A | A | G | TCGA-FG-6689-01A-11D-1893-08 | TCGA-FG-6689-10A-01D-1893-08 | g.chr7:151945175A>G | c.2344T>C | c.(2344-2346)Tct>Cct | p.S782P |
| GBMLGG | 7 | 151945253 | 151945253 | + | Missense_Mutation | SNP | C | C | T | TCGA-74-6577-01A-11D-1845-08 | TCGA-74-6577-10A-01D-1845-08 | g.chr7:151945253C>T | c.2266G>A | c.(2266-2268)Gga>Aga | p.G756R |
| GBMLGG | 7 | 151945270 | 151945270 | + | Missense_Mutation | SNP | T | T | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151945270T>A | c.2249A>T | c.(2248-2250)aAa>aTa | p.K750I |
| GBMLGG | 7 | 151945288 | 151945288 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-5852-01A-11D-1705-08 | TCGA-DU-5852-10A-01D-1705-08 | g.chr7:151945288G>T | c.2231C>A | c.(2230-2232)aCa>aAa | p.T744K |
| GBMLGG | 7 | 151960173 | 151960173 | + | Silent | SNP | A | A | G | TCGA-06-0188-01A-01W-0254-08 | TCGA-06-0188-10B-01W-0254-08 | g.chr7:151960173A>G | c.1227T>C | c.(1225-1227)tgT>tgC | p.C409C |
| GBMLGG | 7 | 151962124 | 151962124 | + | Splice_Site | SNP | T | T | C | TCGA-02-2470-01A-01D-1494-08 | TCGA-02-2470-10A-01D-1494-08 | g.chr7:151962124T>C | c.1183A>G | c.(1183-1185)Aaa>Gaa | p.K395E |
| GBMLGG | 7 | 151962220 | 151962220 | + | Missense_Mutation | SNP | C | C | A | TCGA-06-0219-01A-01D-1491-08 | TCGA-06-0219-10A-01D-1491-08 | g.chr7:151962220C>A | c.1087G>T | c.(1087-1089)Ggt>Tgt | p.G363C |
| GBMLGG | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| GBMLGG | 7 | 151962268 | 151962268 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-A6S3-01A-12D-A32B-08 | TCGA-DU-A6S3-10A-01D-A329-08 | g.chr7:151962268A>G | c.1039T>C | c.(1039-1041)Tgc>Cgc | p.C347R |
| GBMLGG | 7 | 151970801 | 151970801 | + | Missense_Mutation | SNP | G | G | T | TCGA-HT-7687-01A-11D-2253-08 | TCGA-HT-7687-10A-01D-2253-08 | g.chr7:151970801G>T | c.1001C>A | c.(1000-1002)gCt>gAt | p.A334D |
| GBMLGG | 7 | 151970848 | 151970848 | + | Missense_Mutation | SNP | C | C | A | TCGA-19-5958-01A-11D-1696-08 | TCGA-19-5958-11A-01D-1696-08 | g.chr7:151970848C>A | c.954G>T | c.(952-954)caG>caT | p.Q318H |
| GBMLGG | 7 | 152012290 | 152012290 | + | Missense_Mutation | SNP | C | C | A | TCGA-P5-A731-01A-11D-A32B-08 | TCGA-P5-A731-10A-01D-A329-08 | g.chr7:152012290C>A | c.523G>T | c.(523-525)Gac>Tac | p.D175Y |
| GBMLGG | 7 | 152012407 | 152012407 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:152012407A>G | c.406T>C | c.(406-408)Ttt>Ctt | p.F136L |
| HNSC | 7 | 151835921 | 151835921 | + | Missense_Mutation | SNP | A | A | C | TCGA-F7-A623-01A-11D-A28R-08 | TCGA-F7-A623-10A-01D-A28U-08 | g.chr7:151835921A>C | c.14603T>G | c.(14602-14604)aTt>aGt | p.I4868S |
| HNSC | 7 | 151835944 | 151835944 | + | Silent | SNP | C | C | T | TCGA-BB-A5HY-01A-11D-A28R-08 | TCGA-BB-A5HY-10A-01D-A28U-08 | g.chr7:151835944C>T | c.14580G>A | c.(14578-14580)gtG>gtA | p.V4860V |
| HNSC | 7 | 151845932 | 151845932 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CN-A63Y-01A-11D-A30E-08 | TCGA-CN-A63Y-10A-01D-A30H-08 | g.chr7:151845932C>T | c.13080G>A | c.(13078-13080)tgG>tgA | p.W4360* |
| HNSC | 7 | 151845956 | 151845956 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CV-7242-01A-11D-2012-08 | TCGA-CV-7242-10A-01D-2013-08 | g.chr7:151845956C>T | c.13056G>A | c.(13054-13056)tgG>tgA | p.W4352* |
| HNSC | 7 | 151848643 | 151848644 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-CV-A45V-01A-21D-A25D-08 | TCGA-CV-A45V-10A-01D-A25E-08 | g.chr7:151848643_151848644insA | c.12549_12550insT | c.(12547-12552)tctagtfs | p.S4184fs |
| HNSC | 7 | 151849830 | 151849830 | + | Silent | SNP | C | C | T | TCGA-P3-A5Q6-01A-11D-A28R-08 | TCGA-P3-A5Q6-10A-01D-A28U-08 | g.chr7:151849830C>T | c.12486G>A | c.(12484-12486)cgG>cgA | p.R4162R |
| HNSC | 7 | 151849901 | 151849901 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr7:151849901G>A | c.12415C>T | c.(12415-12417)Cga>Tga | p.R4139* |
| HNSC | 7 | 151849998 | 151849998 | + | Silent | SNP | G | G | A | TCGA-IQ-A61E-01A-22D-A30E-08 | TCGA-IQ-A61E-10A-01D-A30H-08 | g.chr7:151849998G>A | c.12318C>T | c.(12316-12318)caC>caT | p.H4106H |
| HNSC | 7 | 151851163 | 151851163 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-A6V1-01A-12D-A34J-08 | TCGA-CN-A6V1-10B-01D-A34M-08 | g.chr7:151851163G>A | c.12208C>T | c.(12208-12210)Cct>Tct | p.P4070S |
| HNSC | 7 | 151856002 | 151856002 | + | Silent | SNP | T | T | C | TCGA-H7-8502-01A-11D-2394-08 | TCGA-H7-8502-10A-01D-2394-08 | g.chr7:151856002T>C | c.11616A>G | c.(11614-11616)gaA>gaG | p.E3872E |
| HNSC | 7 | 151856051 | 151856051 | + | Missense_Mutation | SNP | C | C | T | TCGA-UF-A71D-01A-12D-A34J-08 | TCGA-UF-A71D-10B-01D-A34M-08 | g.chr7:151856051C>T | c.11567G>A | c.(11566-11568)aGg>aAg | p.R3856K |
| HNSC | 7 | 151859299 | 151859300 | + | Frame_Shift_Ins | INS | - | - | AAGAT | TCGA-H7-7774-01A-21D-2078-08 | TCGA-H7-7774-10A-01D-2078-08 | g.chr7:151859299_151859300insAAGAT | c.11362_11363insATCTT | c.(11362-11364)tctfs | p.S3788fs |
| HNSC | 7 | 151859737 | 151859737 | + | Missense_Mutation | SNP | G | G | C | TCGA-CV-5444-01A-02D-1512-08 | TCGA-CV-5444-11A-01D-1512-08 | g.chr7:151859737G>C | c.10925C>G | c.(10924-10926)tCt>tGt | p.S3642C |
| HNSC | 7 | 151859794 | 151859794 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-CV-5444-01A-02D-1512-08 | TCGA-CV-5444-11A-01D-1512-08 | g.chr7:151859794G>C | c.10868C>G | c.(10867-10869)tCa>tGa | p.S3623* |
| HNSC | 7 | 151860056 | 151860056 | + | Missense_Mutation | SNP | G | G | A | TCGA-UF-A7J9-01A-12D-A34J-08 | TCGA-UF-A7J9-10A-01D-A34M-08 | g.chr7:151860056G>A | c.10606C>T | c.(10606-10608)Cat>Tat | p.H3536Y |
| HNSC | 7 | 151860476 | 151860476 | + | Missense_Mutation | SNP | G | G | C | TCGA-KU-A66S-01A-21D-A30E-08 | TCGA-KU-A66S-10A-01D-A30H-08 | g.chr7:151860476G>C | c.10186C>G | c.(10186-10188)Caa>Gaa | p.Q3396E |
| HNSC | 7 | 151868382 | 151868382 | + | Silent | SNP | T | T | C | TCGA-BA-A4IF-01A-11D-A25Y-08 | TCGA-BA-A4IF-10A-01D-A25Y-08 | g.chr7:151868382T>C | c.9420A>G | c.(9418-9420)gaA>gaG | p.E3140E |
| HNSC | 7 | 151873545 | 151873545 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-RS-A6TP-01A-12D-A34J-08 | TCGA-RS-A6TP-10A-01D-A34M-08 | g.chr7:151873545G>C | c.8993C>G | c.(8992-8994)tCa>tGa | p.S2998* |
| HNSC | 7 | 151874263 | 151874263 | + | Missense_Mutation | SNP | A | A | C | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr7:151874263A>C | c.8275T>G | c.(8275-8277)Tat>Gat | p.Y2759D |
| HNSC | 7 | 151874275 | 151874275 | + | Missense_Mutation | SNP | C | C | G | TCGA-CR-6491-01A-11D-1870-08 | TCGA-CR-6491-10A-01D-1870-08 | g.chr7:151874275C>G | c.8263G>C | c.(8263-8265)Gat>Cat | p.D2755H |
| HNSC | 7 | 151874913 | 151874913 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-6023-01A-11D-1683-08 | TCGA-CN-6023-10A-01D-1683-08 | g.chr7:151874913G>A | c.7625C>T | c.(7624-7626)tCa>tTa | p.S2542L |
| HNSC | 7 | 151875040 | 151875040 | + | Missense_Mutation | SNP | C | C | T | TCGA-CR-7383-01A-11D-2129-08 | TCGA-CR-7383-10A-01D-2129-08 | g.chr7:151875040C>T | c.7498G>A | c.(7498-7500)Gtg>Atg | p.V2500M |
| HNSC | 7 | 151877135 | 151877135 | + | Missense_Mutation | SNP | T | T | C | TCGA-CR-7370-01A-11D-2129-08 | TCGA-CR-7370-10A-01D-2129-08 | g.chr7:151877135T>C | c.7226A>G | c.(7225-7227)cAg>cGg | p.Q2409R |
| HNSC | 7 | 151878682 | 151878682 | + | Missense_Mutation | SNP | T | T | C | TCGA-CN-A498-01A-11D-A24D-08 | TCGA-CN-A498-10A-01D-A24F-08 | g.chr7:151878682T>C | c.6263A>G | c.(6262-6264)aAt>aGt | p.N2088S |
| HNSC | 7 | 151879181 | 151879181 | + | Missense_Mutation | SNP | G | G | C | TCGA-CV-7416-01A-11D-2078-08 | TCGA-CV-7416-10A-01D-2078-08 | g.chr7:151879181G>C | c.5764C>G | c.(5764-5766)Cca>Gca | p.P1922A |
| HNSC | 7 | 151879195 | 151879195 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-A6K2-01A-11D-A31L-08 | TCGA-CV-A6K2-10A-01D-A31J-08 | g.chr7:151879195C>T | c.5750G>A | c.(5749-5751)aGa>aAa | p.R1917K |
| HNSC | 7 | 151879345 | 151879345 | + | Missense_Mutation | SNP | C | C | G | TCGA-CN-5360-01A-01D-1434-08 | TCGA-CN-5360-10A-01D-1434-08 | g.chr7:151879345C>G | c.5600G>C | c.(5599-5601)aGt>aCt | p.S1867T |
| HNSC | 7 | 151880197 | 151880197 | + | Silent | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr7:151880197T>C | c.5127A>G | c.(5125-5127)gtA>gtG | p.V1709V |
| HNSC | 7 | 151880230 | 151880230 | + | Missense_Mutation | SNP | T | T | A | TCGA-CN-5363-01A-01D-1434-08 | TCGA-CN-5363-10A-01D-1434-08 | g.chr7:151880230T>A | c.5094A>T | c.(5092-5094)agA>agT | p.R1698S |
| HNSC | 7 | 151884562 | 151884562 | + | Splice_Site | SNP | C | C | A | TCGA-CN-5369-01A-01D-1434-08 | TCGA-CN-5369-10A-01D-1434-08 | g.chr7:151884562C>A | | c.e33-1 | |
| HNSC | 7 | 151891214 | 151891214 | + | Splice_Site | SNP | C | C | G | TCGA-CN-6998-01A-23D-2012-08 | TCGA-CN-6998-10A-01D-2013-08 | g.chr7:151891214C>G | | c.e31-1 | |
| HNSC | 7 | 151896385 | 151896385 | + | Missense_Mutation | SNP | G | G | C | TCGA-CV-5442-01A-01D-1512-08 | TCGA-CV-5442-11A-01D-1512-08 | g.chr7:151896385G>C | c.4252C>G | c.(4252-4254)Cca>Gca | p.P1418A |
| HNSC | 7 | 151900145 | 151900145 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CN-6013-01A-11D-1683-08 | TCGA-CN-6013-10A-01D-1683-08 | g.chr7:151900145C>T | c.3966G>A | c.(3964-3966)tgG>tgA | p.W1322* |
| HNSC | 7 | 151904466 | 151904466 | + | Missense_Mutation | SNP | G | G | A | TCGA-IQ-A61H-01A-11D-A30E-08 | TCGA-IQ-A61H-10A-01D-A30H-08 | g.chr7:151904466G>A | c.3760C>T | c.(3760-3762)Cgg>Tgg | p.R1254W |
| HNSC | 7 | 151917678 | 151917678 | + | Silent | SNP | C | C | T | TCGA-CV-A465-01A-11D-A25Y-08 | TCGA-CV-A465-10A-01D-A25Y-08 | g.chr7:151917678C>T | c.3642G>A | c.(3640-3642)gtG>gtA | p.V1214V |
| HNSC | 7 | 151921619 | 151921619 | + | Missense_Mutation | SNP | C | C | A | TCGA-BA-6868-01B-12D-1912-08 | TCGA-BA-6868-10A-01D-1912-08 | g.chr7:151921619C>A | c.3059G>T | c.(3058-3060)gGa>gTa | p.G1020V |
| HNSC | 7 | 151927091 | 151927091 | + | Missense_Mutation | SNP | T | T | G | TCGA-UF-A7JA-01A-12D-A34J-08 | TCGA-UF-A7JA-10A-01D-A34M-08 | g.chr7:151927091T>G | c.2893A>C | c.(2893-2895)Agt>Cgt | p.S965R |
| HNSC | 7 | 151935847 | 151935847 | + | Missense_Mutation | SNP | C | C | T | TCGA-CQ-7072-01A-21D-A30E-08 | TCGA-CQ-7072-10A-01D-A30H-08 | g.chr7:151935847C>T | c.2597G>A | c.(2596-2598)cGg>cAg | p.R866Q |
| HNSC | 7 | 151945031 | 151945031 | + | Missense_Mutation | SNP | T | T | C | TCGA-CX-7082-01A-11D-2012-08 | TCGA-CX-7082-10A-01D-2013-08 | g.chr7:151945031T>C | c.2488A>G | c.(2488-2490)Att>Gtt | p.I830V |
| HNSC | 7 | 151945083 | 151945083 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-A63W-01A-11D-A30E-08 | TCGA-CN-A63W-10A-01D-A30H-08 | g.chr7:151945083C>T | c.2436G>A | c.(2434-2436)atG>atA | p.M812I |
| HNSC | 7 | 151945174 | 151945174 | + | Missense_Mutation | SNP | G | G | C | TCGA-BB-A5HU-01A-11D-A28R-08 | TCGA-BB-A5HU-10A-01D-A28U-08 | g.chr7:151945174G>C | c.2345C>G | c.(2344-2346)tCt>tGt | p.S782C |
| HNSC | 7 | 151945266 | 151945266 | + | Silent | SNP | A | A | G | TCGA-BB-7870-01A-11D-2229-08 | TCGA-BB-7870-10A-01D-2229-08 | g.chr7:151945266A>G | c.2253T>C | c.(2251-2253)gaT>gaC | p.D751D |
| HNSC | 7 | 151945277 | 151945277 | + | Missense_Mutation | SNP | A | A | C | TCGA-CV-5432-01A-02D-1683-08 | TCGA-CV-5432-10A-01D-1870-08 | g.chr7:151945277A>C | c.2242T>G | c.(2242-2244)Tgt>Ggt | p.C748G |
| HNSC | 7 | 151945611 | 151945611 | + | Missense_Mutation | SNP | A | A | C | TCGA-HD-7229-01A-11D-2012-08 | TCGA-HD-7229-10A-01D-2013-08 | g.chr7:151945611A>C | c.1908T>G | c.(1906-1908)caT>caG | p.H636Q |
| HNSC | 7 | 151949691 | 151949691 | + | Missense_Mutation | SNP | C | C | T | TCGA-CQ-6224-01A-11D-1912-08 | TCGA-CQ-6224-10A-01D-1912-08 | g.chr7:151949691C>T | c.1409G>A | c.(1408-1410)tGt>tAt | p.C470Y |
| HNSC | 7 | 151960216 | 151960216 | + | Splice_Site | SNP | C | C | A | TCGA-CV-A461-01A-41D-A25Y-08 | TCGA-CV-A461-10A-01D-A25Y-08 | g.chr7:151960216C>A | | c.e9-1 | |
| HNSC | 7 | 151962121 | 151962121 | + | Splice_Site | SNP | A | A | T | TCGA-UF-A71E-01A-31D-A34J-08 | TCGA-UF-A71E-10B-01D-A34M-08 | g.chr7:151962121A>T | | c.e8+1 | |
| HNSC | 7 | 151962255 | 151962255 | + | Missense_Mutation | SNP | C | C | T | TCGA-IQ-A61H-01A-11D-A30E-08 | TCGA-IQ-A61H-10A-01D-A30H-08 | g.chr7:151962255C>T | c.1052G>A | c.(1051-1053)gGa>gAa | p.G351E |
| HNSC | 7 | 151970897 | 151970897 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-5356-01A-01D-1434-08 | TCGA-CN-5356-10A-01D-1434-08 | g.chr7:151970897C>T | c.905G>A | c.(904-906)tGt>tAt | p.C302Y |
| HNSC | 7 | 152012225 | 152012228 | + | Frame_Shift_Del | DEL | TCTC | TCTC | - | TCGA-BA-A6DJ-01A-11D-A30E-08 | TCGA-BA-A6DJ-10A-01D-A30H-08 | g.chr7:152012225_152012228delTCTC | c.585_588delGAGA | c.(583-588)cagagafs | p.QR195fs |
| HNSC | 7 | 152012253 | 152012253 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-CV-6942-01A-21D-2012-08 | TCGA-CV-6942-10A-01D-2013-08 | g.chr7:152012253G>C | c.560C>G | c.(559-561)tCa>tGa | p.S187* |
| HNSC | 7 | 152055756 | 152055756 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CQ-7064-01A-11D-2394-08 | TCGA-CQ-7064-10A-01D-2394-08 | g.chr7:152055756G>A | c.166C>T | c.(166-168)Cga>Tga | p.R56* |
| KICH | 7 | 151855973 | 151855973 | + | Missense_Mutation | SNP | G | G | A | TCGA-KL-8326-01A-11D-2310-10 | TCGA-KL-8326-11A-01D-2310-10 | g.chr7:151855973G>A | c.11645C>T | c.(11644-11646)aCt>aTt | p.T3882I |
| KICH | 7 | 151917680 | 151917680 | + | Missense_Mutation | SNP | C | C | T | TCGA-KM-8442-01A-11D-2310-10 | TCGA-KM-8442-10A-01D-2311-10 | g.chr7:151917680C>T | c.3640G>A | c.(3640-3642)Gtg>Atg | p.V1214M |
| KICH | 7 | 151932923 | 151932923 | + | Silent | SNP | G | G | A | TCGA-KL-8332-01A-11D-2310-10 | TCGA-KL-8332-11A-01D-2310-10 | g.chr7:151932923G>A | c.2748C>T | c.(2746-2748)atC>atT | p.I916I |
| KICH | 7 | 151932990 | 151932990 | + | Missense_Mutation | SNP | C | C | T | TCGA-KN-8418-01A-11D-2310-10 | TCGA-KN-8418-11A-01D-2310-10 | g.chr7:151932990C>T | c.2681G>A | c.(2680-2682)cGg>cAg | p.R894Q |
| KICH | 7 | 151945291 | 151945291 | + | Missense_Mutation | SNP | G | G | A | TCGA-KO-8406-01A-11D-2310-10 | TCGA-KO-8406-11A-01D-2311-10 | g.chr7:151945291G>A | c.2228C>T | c.(2227-2229)cCt>cTt | p.P743L |
| KICH | 7 | 151945349 | 151945349 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-KM-8438-01A-11D-2310-10 | TCGA-KM-8438-10A-01D-2311-10 | g.chr7:151945349T>A | c.2170A>T | c.(2170-2172)Aag>Tag | p.K724* |
| KICH | 7 | 151962265 | 151962265 | + | Missense_Mutation | SNP | C | C | T | TCGA-KL-8333-01A-11D-2310-10 | TCGA-KL-8333-11A-01D-2310-10 | g.chr7:151962265C>T | c.1042G>A | c.(1042-1044)Gac>Aac | p.D348N |
| KICH | 7 | 151962290 | 151962290 | + | Missense_Mutation | SNP | C | C | G | TCGA-KM-8440-01A-11D-2310-10 | TCGA-KM-8440-10A-01D-2311-10 | g.chr7:151962290C>G | c.1017G>C | c.(1015-1017)aaG>aaC | p.K339N |
| KICH | 7 | 151962294 | 151962294 | + | Splice_Site | SNP | G | G | A | TCGA-KN-8432-01A-11D-2310-10 | TCGA-KN-8432-11A-01D-2311-10 | g.chr7:151962294G>A | c.1013C>T | c.(1012-1014)tCg>tTg | p.S338L |
| KICH | 7 | 152132844 | 152132845 | + | Missense_Mutation | DNP | CC | CC | TT | TCGA-KN-8424-01A-11D-2310-10 | TCGA-KN-8424-11A-01D-2310-10 | g.chr7:152132844_152132845CC>TT | c.27_28GG>AA | c.(25-30)gtGGag>gtAAag | p.E10K |
| KIPAN | 7 | 151836874 | 151836875 | + | Splice_Site | DEL | CC | CC | - | TCGA-CZ-5986-01A-11D-1669-08 | TCGA-CZ-5986-11A-01D-1669-08 | g.chr7:151836874_151836875delCC | c.14345_14346delGG | c.(14344-14346)ggg>g | p.G4782fs |
| KIPAN | 7 | 151842348 | 151842348 | + | Silent | SNP | G | G | T | TCGA-A3-3313-01A-01D-0966-08 | TCGA-A3-3313-11A-01D-0966-08 | g.chr7:151842348G>T | c.14064C>A | c.(14062-14064)acC>acA | p.T4688T |
| KIPAN | 7 | 151845739 | 151845739 | + | Missense_Mutation | SNP | C | C | A | TCGA-BQ-5893-01A-11D-1589-08 | TCGA-BQ-5893-11A-01D-1589-08 | g.chr7:151845739C>A | c.13273G>T | c.(13273-13275)Gat>Tat | p.D4425Y |
| KIPAN | 7 | 151845991 | 151845991 | + | Missense_Mutation | SNP | C | C | A | TCGA-P4-A5E7-01A-31D-A28G-10 | TCGA-P4-A5E7-11A-11D-A28G-10 | g.chr7:151845991C>A | c.13021G>T | c.(13021-13023)Ggg>Tgg | p.G4341W |
| KIPAN | 7 | 151848093 | 151848093 | + | Splice_Site | SNP | C | C | G | TCGA-CZ-4857-01A-01D-1373-10 | TCGA-CZ-4857-11A-01D-1373-10 | g.chr7:151848093C>G | | c.e51-1 | |
| KIPAN | 7 | 151851228 | 151851228 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-BP-4961-01A-01D-1462-08 | TCGA-BP-4961-11A-01D-1462-08 | g.chr7:151851228G>T | c.12143C>A | c.(12142-12144)tCa>tAa | p.S4048* |
| KIPAN | 7 | 151853289 | 151853289 | + | Splice_Site | SNP | C | C | T | TCGA-UZ-A9Q1-01A-11D-A42J-10 | TCGA-UZ-A9Q1-10A-01D-A42M-10 | g.chr7:151853289C>T | | c.e45+1 | |
| KIPAN | 7 | 151855973 | 151855973 | + | Missense_Mutation | SNP | G | G | A | TCGA-KL-8326-01A-11D-2310-10 | TCGA-KL-8326-11A-01D-2310-10 | g.chr7:151855973G>A | c.11645C>T | c.(11644-11646)aCt>aTt | p.T3882I |
| KIPAN | 7 | 151856014 | 151856014 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-GL-A9DD-01A-11D-A36X-10 | TCGA-GL-A9DD-10A-01D-A370-10 | g.chr7:151856014delC | c.11604delG | c.(11602-11604)aggfs | p.R3868fs |
| KIPAN | 7 | 151859226 | 151859226 | + | Missense_Mutation | SNP | C | C | A | TCGA-AL-A5DJ-01A-11D-A26P-10 | TCGA-AL-A5DJ-10A-01D-A26P-10 | g.chr7:151859226C>A | c.11436G>T | c.(11434-11436)gaG>gaT | p.E3812D |
| KIPAN | 7 | 151859497 | 151859497 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-B9-A5W8-01A-11D-A28G-10 | TCGA-B9-A5W8-10A-01D-A28G-10 | g.chr7:151859497delT | c.11165delA | c.(11164-11166)aagfs | p.K3722fs |
| KIPAN | 7 | 151859636 | 151859636 | + | Missense_Mutation | SNP | G | G | C | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr7:151859636G>C | c.11026C>G | c.(11026-11028)Cta>Gta | p.L3676V |
| KIPAN | 7 | 151860719 | 151860719 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-BP-4164-01A-02D-1386-10 | TCGA-BP-4164-11A-01D-1251-10 | g.chr7:151860719G>A | c.9943C>T | c.(9943-9945)Cag>Tag | p.Q3315* |
| KIPAN | 7 | 151873357 | 151873357 | + | Missense_Mutation | SNP | G | G | T | TCGA-A3-3376-01A-02D-1421-08 | TCGA-A3-3376-11A-01D-1421-08 | g.chr7:151873357G>T | c.9181C>A | c.(9181-9183)Caa>Aaa | p.Q3061K |
| KIPAN | 7 | 151873651 | 151873651 | + | Missense_Mutation | SNP | G | G | A | TCGA-B2-5633-01A-01D-1534-10 | TCGA-B2-5633-10A-01D-1535-10 | g.chr7:151873651G>A | c.8887C>T | c.(8887-8889)Cgt>Tgt | p.R2963C |
| KIPAN | 7 | 151873882 | 151873883 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-P4-A5E7-01A-31D-A28G-10 | TCGA-P4-A5E7-11A-11D-A28G-10 | g.chr7:151873882_151873883delTT | c.8655_8656delAA | c.(8653-8658)gaaactfs | p.ET2885fs |
| KIPAN | 7 | 151874116 | 151874116 | + | Missense_Mutation | SNP | C | C | T | TCGA-B9-A8YI-01A-21D-A36X-10 | TCGA-B9-A8YI-10A-01D-A370-10 | g.chr7:151874116C>T | c.8422G>A | c.(8422-8424)Gat>Aat | p.D2808N |
| KIPAN | 7 | 151874152 | 151874158 | + | Frame_Shift_Del | DEL | TTTTTGG | TTTTTGG | - | TCGA-G7-A4TM-01A-11D-A31X-10 | TCGA-G7-A4TM-10B-01D-A31X-10 | g.chr7:151874152_151874158delTTTTTGG | c.8380_8386delCCAAAAA | c.(8380-8388)ccaaaaaaafs | p.PKK2794fs |
| KIPAN | 7 | 151874432 | 151874433 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-UZ-A9PS-01A-11D-A42J-10 | TCGA-UZ-A9PS-10A-01D-A42M-10 | g.chr7:151874432_151874433delTT | c.8105_8106delAA | c.(8104-8106)aaafs | p.K2702fs |
| KIPAN | 7 | 151877112 | 151877112 | + | Missense_Mutation | SNP | G | G | T | TCGA-5P-A9KA-01A-11D-A42J-10 | TCGA-5P-A9KA-10A-01D-A42M-10 | g.chr7:151877112G>T | c.7249C>A | c.(7249-7251)Cca>Aca | p.P2417T |
| KIPAN | 7 | 151877175 | 151877175 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-B0-5099-01A-01D-1421-08 | TCGA-B0-5099-11A-01D-1421-08 | g.chr7:151877175G>A | c.7186C>T | c.(7186-7188)Cag>Tag | p.Q2396* |
| KIPAN | 7 | 151877902 | 151877902 | + | Missense_Mutation | SNP | T | T | C | TCGA-CJ-5683-01A-11D-1534-10 | TCGA-CJ-5683-11A-01D-1535-10 | g.chr7:151877902T>C | c.7043A>G | c.(7042-7044)cAg>cGg | p.Q2348R |
| KIPAN | 7 | 151878422 | 151878422 | + | Missense_Mutation | SNP | T | T | C | TCGA-V9-A7HT-01A-11D-A33Q-10 | TCGA-V9-A7HT-10A-01D-A33Q-10 | g.chr7:151878422T>C | c.6523A>G | c.(6523-6525)Agt>Ggt | p.S2175G |
| KIPAN | 7 | 151878457 | 151878457 | + | Missense_Mutation | SNP | G | G | T | TCGA-B0-4945-01A-01D-1421-08 | TCGA-B0-4945-11A-01D-1421-08 | g.chr7:151878457G>T | c.6488C>A | c.(6487-6489)cCt>cAt | p.P2163H |
| KIPAN | 7 | 151879016 | 151879016 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-B3-4104-01A-01D-1458-08 | TCGA-B3-4104-10A-01D-1458-08 | g.chr7:151879016G>A | c.5929C>T | c.(5929-5931)Caa>Taa | p.Q1977* |
| KIPAN | 7 | 151879304 | 151879304 | + | Missense_Mutation | SNP | C | C | G | TCGA-A3-3370-01A-02D-1421-08 | TCGA-A3-3370-11A-01D-1421-08 | g.chr7:151879304C>G | c.5641G>C | c.(5641-5643)Gtg>Ctg | p.V1881L |
| KIPAN | 7 | 151880116 | 151880116 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-BQ-7051-01A-12D-1961-08 | TCGA-BQ-7051-11A-02D-1961-08 | g.chr7:151880116delA | c.5208delT | c.(5206-5208)tttfs | p.F1736fs |
| KIPAN | 7 | 151882665 | 151882665 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-BP-4756-01A-01D-1366-10 | TCGA-BP-4756-11A-01D-1366-10 | g.chr7:151882665G>T | c.5060C>A | c.(5059-5061)tCa>tAa | p.S1687* |
| KIPAN | 7 | 151882674 | 151882674 | + | Missense_Mutation | SNP | T | T | G | TCGA-B9-4114-01A-01D-1252-08 | TCGA-B9-4114-10A-01D-1252-08 | g.chr7:151882674T>G | c.5051A>C | c.(5050-5052)aAa>aCa | p.K1684T |
| KIPAN | 7 | 151917680 | 151917680 | + | Missense_Mutation | SNP | C | C | T | TCGA-KM-8442-01A-11D-2310-10 | TCGA-KM-8442-10A-01D-2311-10 | g.chr7:151917680C>T | c.3640G>A | c.(3640-3642)Gtg>Atg | p.V1214M |
| KIPAN | 7 | 151917756 | 151917756 | + | Missense_Mutation | SNP | C | C | A | TCGA-A4-7997-01A-11D-2201-08 | TCGA-A4-7997-10A-01D-2201-08 | g.chr7:151917756C>A | c.3564G>T | c.(3562-3564)caG>caT | p.Q1188H |
| KIPAN | 7 | 151919089 | 151919091 | + | In_Frame_Del | DEL | GCT | GCT | - | TCGA-5P-A9KA-01A-11D-A42J-10 | TCGA-5P-A9KA-10A-01D-A42M-10 | g.chr7:151919089_151919091delGCT | c.3494_3496delAGC | c.(3493-3498)gagcta>gta | p.1165_1166EL>V |
| KIPAN | 7 | 151919708 | 151919708 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-PJ-A5Z8-01A-11D-A28G-10 | TCGA-PJ-A5Z8-10A-01D-A28G-10 | g.chr7:151919708delT | c.3383delA | c.(3382-3384)gacfs | p.D1128fs |
| KIPAN | 7 | 151921164 | 151921167 | + | Frame_Shift_Del | DEL | AGGA | AGGA | - | TCGA-B0-4810-01A-01D-1501-10 | TCGA-B0-4810-11A-02D-1501-10 | g.chr7:151921164_151921167delAGGA | c.3256_3259delTCCT | c.(3256-3261)tcctgtfs | p.SC1086fs |
| KIPAN | 7 | 151932923 | 151932923 | + | Silent | SNP | G | G | A | TCGA-KL-8332-01A-11D-2310-10 | TCGA-KL-8332-11A-01D-2310-10 | g.chr7:151932923G>A | c.2748C>T | c.(2746-2748)atC>atT | p.I916I |
| KIPAN | 7 | 151932990 | 151932990 | + | Missense_Mutation | SNP | C | C | T | TCGA-KN-8418-01A-11D-2310-10 | TCGA-KN-8418-11A-01D-2310-10 | g.chr7:151932990C>T | c.2681G>A | c.(2680-2682)cGg>cAg | p.R894Q |
| KIPAN | 7 | 151945291 | 151945291 | + | Missense_Mutation | SNP | G | G | A | TCGA-KO-8406-01A-11D-2310-10 | TCGA-KO-8406-11A-01D-2311-10 | g.chr7:151945291G>A | c.2228C>T | c.(2227-2229)cCt>cTt | p.P743L |
| KIPAN | 7 | 151945349 | 151945349 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-KM-8438-01A-11D-2310-10 | TCGA-KM-8438-10A-01D-2311-10 | g.chr7:151945349T>A | c.2170A>T | c.(2170-2172)Aag>Tag | p.K724* |
| KIPAN | 7 | 151962168 | 151962168 | + | Missense_Mutation | SNP | C | C | G | TCGA-DW-7840-01A-11D-2136-08 | TCGA-DW-7840-10A-01D-2136-08 | g.chr7:151962168C>G | c.1139G>C | c.(1138-1140)cGt>cCt | p.R380P |
| KIPAN | 7 | 151962234 | 151962234 | + | Missense_Mutation | SNP | A | A | C | TCGA-BP-4976-01A-01D-1462-08 | TCGA-BP-4976-11A-01D-1462-08 | g.chr7:151962234A>C | c.1073T>G | c.(1072-1074)tTt>tGt | p.F358C |
| KIPAN | 7 | 151962258 | 151962258 | + | Missense_Mutation | SNP | G | G | C | TCGA-CJ-5678-01A-11D-1534-10 | TCGA-CJ-5678-11A-01D-1534-10 | g.chr7:151962258G>C | c.1049C>G | c.(1048-1050)cCg>cGg | p.P350R |
| KIPAN | 7 | 151962265 | 151962265 | + | Missense_Mutation | SNP | C | C | T | TCGA-KL-8333-01A-11D-2310-10 | TCGA-KL-8333-11A-01D-2310-10 | g.chr7:151962265C>T | c.1042G>A | c.(1042-1044)Gac>Aac | p.D348N |
| KIPAN | 7 | 151962290 | 151962290 | + | Missense_Mutation | SNP | C | C | G | TCGA-KM-8440-01A-11D-2310-10 | TCGA-KM-8440-10A-01D-2311-10 | g.chr7:151962290C>G | c.1017G>C | c.(1015-1017)aaG>aaC | p.K339N |
| KIPAN | 7 | 151962294 | 151962294 | + | Splice_Site | SNP | G | G | A | TCGA-KN-8432-01A-11D-2310-10 | TCGA-KN-8432-11A-01D-2311-10 | g.chr7:151962294G>A | c.1013C>T | c.(1012-1014)tCg>tTg | p.S338L |
| KIPAN | 7 | 151970836 | 151970836 | + | Silent | SNP | G | G | A | TCGA-BP-4770-01A-01D-1501-10 | TCGA-BP-4770-11A-01D-1501-10 | g.chr7:151970836G>A | c.966C>T | c.(964-966)caC>caT | p.H322H |
| KIPAN | 7 | 152012275 | 152012275 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-B0-5097-01A-01D-1421-08 | TCGA-B0-5097-11A-01D-1421-08 | g.chr7:152012275delT | c.538delA | c.(538-540)accfs | p.T180fs |
| KIPAN | 7 | 152012386 | 152012386 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-Q2-A5QZ-01A-11D-A28G-10 | TCGA-Q2-A5QZ-10A-01D-A28G-10 | g.chr7:152012386delT | c.427delA | c.(427-429)agtfs | p.S144fs |
| KIPAN | 7 | 152132844 | 152132845 | + | Missense_Mutation | DNP | CC | CC | TT | TCGA-KN-8424-01A-11D-2310-10 | TCGA-KN-8424-11A-01D-2310-10 | g.chr7:152132844_152132845CC>TT | c.27_28GG>AA | c.(25-30)gtGGag>gtAAag | p.E10K |
| KIRC | 7 | 151836874 | 151836875 | + | Splice_Site | DEL | CC | CC | - | TCGA-CZ-5986-01A-11D-1669-08 | TCGA-CZ-5986-11A-01D-1669-08 | g.chr7:151836874_151836875delCC | c.14345_14346delGG | c.(14344-14346)ggg>g | p.G4782fs |
| KIRC | 7 | 151842348 | 151842348 | + | Silent | SNP | G | G | T | TCGA-A3-3313-01A-01D-0966-08 | TCGA-A3-3313-11A-01D-0966-08 | g.chr7:151842348G>T | c.14064C>A | c.(14062-14064)acC>acA | p.T4688T |
| KIRC | 7 | 151848093 | 151848093 | + | Splice_Site | SNP | C | C | G | TCGA-CZ-4857-01A-01D-1373-10 | TCGA-CZ-4857-11A-01D-1373-10 | g.chr7:151848093C>G | | c.e51-1 | |
| KIRC | 7 | 151851228 | 151851228 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-BP-4961-01A-01D-1462-08 | TCGA-BP-4961-11A-01D-1462-08 | g.chr7:151851228G>T | c.12143C>A | c.(12142-12144)tCa>tAa | p.S4048* |
| KIRC | 7 | 151859636 | 151859636 | + | Missense_Mutation | SNP | G | G | C | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr7:151859636G>C | c.11026C>G | c.(11026-11028)Cta>Gta | p.L3676V |
| KIRC | 7 | 151860719 | 151860719 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-BP-4164-01A-02D-1386-10 | TCGA-BP-4164-11A-01D-1251-10 | g.chr7:151860719G>A | c.9943C>T | c.(9943-9945)Cag>Tag | p.Q3315* |
| KIRC | 7 | 151873357 | 151873357 | + | Missense_Mutation | SNP | G | G | T | TCGA-A3-3376-01A-02D-1421-08 | TCGA-A3-3376-11A-01D-1421-08 | g.chr7:151873357G>T | c.9181C>A | c.(9181-9183)Caa>Aaa | p.Q3061K |
| KIRC | 7 | 151873651 | 151873651 | + | Missense_Mutation | SNP | G | G | A | TCGA-B2-5633-01A-01D-1534-10 | TCGA-B2-5633-10A-01D-1535-10 | g.chr7:151873651G>A | c.8887C>T | c.(8887-8889)Cgt>Tgt | p.R2963C |
| KIRC | 7 | 151877175 | 151877175 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-B0-5099-01A-01D-1421-08 | TCGA-B0-5099-11A-01D-1421-08 | g.chr7:151877175G>A | c.7186C>T | c.(7186-7188)Cag>Tag | p.Q2396* |
| KIRC | 7 | 151877902 | 151877902 | + | Missense_Mutation | SNP | T | T | C | TCGA-CJ-5683-01A-11D-1534-10 | TCGA-CJ-5683-11A-01D-1535-10 | g.chr7:151877902T>C | c.7043A>G | c.(7042-7044)cAg>cGg | p.Q2348R |
| KIRC | 7 | 151878457 | 151878457 | + | Missense_Mutation | SNP | G | G | T | TCGA-B0-4945-01A-01D-1421-08 | TCGA-B0-4945-11A-01D-1421-08 | g.chr7:151878457G>T | c.6488C>A | c.(6487-6489)cCt>cAt | p.P2163H |
| KIRC | 7 | 151879304 | 151879304 | + | Missense_Mutation | SNP | C | C | G | TCGA-A3-3370-01A-02D-1421-08 | TCGA-A3-3370-11A-01D-1421-08 | g.chr7:151879304C>G | c.5641G>C | c.(5641-5643)Gtg>Ctg | p.V1881L |
| KIRC | 7 | 151882665 | 151882665 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-BP-4756-01A-01D-1366-10 | TCGA-BP-4756-11A-01D-1366-10 | g.chr7:151882665G>T | c.5060C>A | c.(5059-5061)tCa>tAa | p.S1687* |
| KIRC | 7 | 151921164 | 151921167 | + | Frame_Shift_Del | DEL | AGGA | AGGA | - | TCGA-B0-4810-01A-01D-1501-10 | TCGA-B0-4810-11A-02D-1501-10 | g.chr7:151921164_151921167delAGGA | c.3256_3259delTCCT | c.(3256-3261)tcctgtfs | p.SC1086fs |
| KIRC | 7 | 151962234 | 151962234 | + | Missense_Mutation | SNP | A | A | C | TCGA-BP-4976-01A-01D-1462-08 | TCGA-BP-4976-11A-01D-1462-08 | g.chr7:151962234A>C | c.1073T>G | c.(1072-1074)tTt>tGt | p.F358C |
| KIRC | 7 | 151962258 | 151962258 | + | Missense_Mutation | SNP | G | G | C | TCGA-CJ-5678-01A-11D-1534-10 | TCGA-CJ-5678-11A-01D-1534-10 | g.chr7:151962258G>C | c.1049C>G | c.(1048-1050)cCg>cGg | p.P350R |
| KIRC | 7 | 151970836 | 151970836 | + | Silent | SNP | G | G | A | TCGA-BP-4770-01A-01D-1501-10 | TCGA-BP-4770-11A-01D-1501-10 | g.chr7:151970836G>A | c.966C>T | c.(964-966)caC>caT | p.H322H |
| KIRC | 7 | 152012275 | 152012275 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-B0-5097-01A-01D-1421-08 | TCGA-B0-5097-11A-01D-1421-08 | g.chr7:152012275delT | c.538delA | c.(538-540)accfs | p.T180fs |
| KIRP | 7 | 151845739 | 151845739 | + | Missense_Mutation | SNP | C | C | A | TCGA-BQ-5893-01A-11D-1589-08 | TCGA-BQ-5893-11A-01D-1589-08 | g.chr7:151845739C>A | c.13273G>T | c.(13273-13275)Gat>Tat | p.D4425Y |
| KIRP | 7 | 151845991 | 151845991 | + | Missense_Mutation | SNP | C | C | A | TCGA-P4-A5E7-01A-31D-A28G-10 | TCGA-P4-A5E7-11A-11D-A28G-10 | g.chr7:151845991C>A | c.13021G>T | c.(13021-13023)Ggg>Tgg | p.G4341W |
| KIRP | 7 | 151853289 | 151853289 | + | Splice_Site | SNP | C | C | T | TCGA-UZ-A9Q1-01A-11D-A42J-10 | TCGA-UZ-A9Q1-10A-01D-A42M-10 | g.chr7:151853289C>T | | c.e45+1 | |
| KIRP | 7 | 151856014 | 151856014 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-GL-A9DD-01A-11D-A36X-10 | TCGA-GL-A9DD-10A-01D-A370-10 | g.chr7:151856014delC | c.11604delG | c.(11602-11604)aggfs | p.R3868fs |
| KIRP | 7 | 151859226 | 151859226 | + | Missense_Mutation | SNP | C | C | A | TCGA-AL-A5DJ-01A-11D-A26P-10 | TCGA-AL-A5DJ-10A-01D-A26P-10 | g.chr7:151859226C>A | c.11436G>T | c.(11434-11436)gaG>gaT | p.E3812D |
| KIRP | 7 | 151859497 | 151859497 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-B9-A5W8-01A-11D-A28G-10 | TCGA-B9-A5W8-10A-01D-A28G-10 | g.chr7:151859497delT | c.11165delA | c.(11164-11166)aagfs | p.K3722fs |
| KIRP | 7 | 151873882 | 151873883 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-P4-A5E7-01A-31D-A28G-10 | TCGA-P4-A5E7-11A-11D-A28G-10 | g.chr7:151873882_151873883delTT | c.8655_8656delAA | c.(8653-8658)gaaactfs | p.ET2885fs |
| KIRP | 7 | 151874116 | 151874116 | + | Missense_Mutation | SNP | C | C | T | TCGA-B9-A8YI-01A-21D-A36X-10 | TCGA-B9-A8YI-10A-01D-A370-10 | g.chr7:151874116C>T | c.8422G>A | c.(8422-8424)Gat>Aat | p.D2808N |
| KIRP | 7 | 151874152 | 151874158 | + | Frame_Shift_Del | DEL | TTTTTGG | TTTTTGG | - | TCGA-G7-A4TM-01A-11D-A31X-10 | TCGA-G7-A4TM-10B-01D-A31X-10 | g.chr7:151874152_151874158delTTTTTGG | c.8380_8386delCCAAAAA | c.(8380-8388)ccaaaaaaafs | p.PKK2794fs |
| KIRP | 7 | 151874432 | 151874433 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-UZ-A9PS-01A-11D-A42J-10 | TCGA-UZ-A9PS-10A-01D-A42M-10 | g.chr7:151874432_151874433delTT | c.8105_8106delAA | c.(8104-8106)aaafs | p.K2702fs |
| KIRP | 7 | 151877112 | 151877112 | + | Missense_Mutation | SNP | G | G | T | TCGA-5P-A9KA-01A-11D-A42J-10 | TCGA-5P-A9KA-10A-01D-A42M-10 | g.chr7:151877112G>T | c.7249C>A | c.(7249-7251)Cca>Aca | p.P2417T |
| KIRP | 7 | 151878422 | 151878422 | + | Missense_Mutation | SNP | T | T | C | TCGA-V9-A7HT-01A-11D-A33Q-10 | TCGA-V9-A7HT-10A-01D-A33Q-10 | g.chr7:151878422T>C | c.6523A>G | c.(6523-6525)Agt>Ggt | p.S2175G |
| KIRP | 7 | 151879016 | 151879016 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-B3-4104-01A-01D-1458-08 | TCGA-B3-4104-10A-01D-1458-08 | g.chr7:151879016G>A | c.5929C>T | c.(5929-5931)Caa>Taa | p.Q1977* |
| KIRP | 7 | 151880116 | 151880116 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-BQ-7051-01A-12D-1961-08 | TCGA-BQ-7051-11A-02D-1961-08 | g.chr7:151880116delA | c.5208delT | c.(5206-5208)tttfs | p.F1736fs |
| KIRP | 7 | 151882674 | 151882674 | + | Missense_Mutation | SNP | T | T | G | TCGA-B9-4114-01A-01D-1252-08 | TCGA-B9-4114-10A-01D-1252-08 | g.chr7:151882674T>G | c.5051A>C | c.(5050-5052)aAa>aCa | p.K1684T |
| KIRP | 7 | 151917756 | 151917756 | + | Missense_Mutation | SNP | C | C | A | TCGA-A4-7997-01A-11D-2201-08 | TCGA-A4-7997-10A-01D-2201-08 | g.chr7:151917756C>A | c.3564G>T | c.(3562-3564)caG>caT | p.Q1188H |
| KIRP | 7 | 151919089 | 151919091 | + | In_Frame_Del | DEL | GCT | GCT | - | TCGA-5P-A9KA-01A-11D-A42J-10 | TCGA-5P-A9KA-10A-01D-A42M-10 | g.chr7:151919089_151919091delGCT | c.3494_3496delAGC | c.(3493-3498)gagcta>gta | p.1165_1166EL>V |
| KIRP | 7 | 151919708 | 151919708 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-PJ-A5Z8-01A-11D-A28G-10 | TCGA-PJ-A5Z8-10A-01D-A28G-10 | g.chr7:151919708delT | c.3383delA | c.(3382-3384)gacfs | p.D1128fs |
| KIRP | 7 | 151962168 | 151962168 | + | Missense_Mutation | SNP | C | C | G | TCGA-DW-7840-01A-11D-2136-08 | TCGA-DW-7840-10A-01D-2136-08 | g.chr7:151962168C>G | c.1139G>C | c.(1138-1140)cGt>cCt | p.R380P |
| KIRP | 7 | 152012386 | 152012386 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-Q2-A5QZ-01A-11D-A28G-10 | TCGA-Q2-A5QZ-10A-01D-A28G-10 | g.chr7:152012386delT | c.427delA | c.(427-429)agtfs | p.S144fs |
| LAML | 7 | 151874161 | 151874161 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AB-2940-03A-01W-0733-08 | TCGA-AB-2940-11A-01W-0732-08 | g.chr7:151874161C>A | c.8377G>T | c.(8377-8379)Gaa>Taa | p.E2793* |
| LGG | 7 | 151842271 | 151842271 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-5853-01A-11D-1893-08 | TCGA-DU-5853-10A-01D-1893-08 | g.chr7:151842271T>G | c.14141A>C | c.(14140-14142)aAa>aCa | p.K4714T |
| LGG | 7 | 151845685 | 151845686 | + | Frame_Shift_Del | DEL | GA | GA | - | TCGA-E1-5319-01A-01D-1893-08 | TCGA-E1-5319-10A-01D-1893-08 | g.chr7:151845685_151845686delGA | c.13326_13327delTC | c.(13324-13329)actcagfs | p.Q4443fs |
| LGG | 7 | 151845755 | 151845755 | + | Silent | SNP | T | T | C | TCGA-S9-A7J3-01A-21D-A34J-08 | TCGA-S9-A7J3-10A-01D-A34M-08 | g.chr7:151845755T>C | c.13257A>G | c.(13255-13257)ctA>ctG | p.L4419L |
| LGG | 7 | 151848004 | 151848004 | + | Missense_Mutation | SNP | G | G | A | TCGA-S9-A7J1-01A-21D-A34J-08 | TCGA-S9-A7J1-10A-01D-A34M-08 | g.chr7:151848004G>A | c.12755C>T | c.(12754-12756)gCg>gTg | p.A4252V |
| LGG | 7 | 151848014 | 151848014 | + | Missense_Mutation | SNP | T | T | C | TCGA-RY-A83Z-01A-11D-A36O-08 | TCGA-RY-A83Z-10A-01D-A367-08 | g.chr7:151848014T>C | c.12745A>G | c.(12745-12747)Act>Gct | p.T4249A |
| LGG | 7 | 151853385 | 151853385 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151853385G>T | c.11717C>A | c.(11716-11718)cCt>cAt | p.P3906H |
| LGG | 7 | 151859576 | 151859576 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-E1-A7Z2-01A-21D-A34J-08 | TCGA-E1-A7Z2-10A-01D-A34M-08 | g.chr7:151859576delG | c.11086delC | c.(11086-11088)caafs | p.Q3697fs |
| LGG | 7 | 151859837 | 151859837 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151859837T>C | c.10825A>G | c.(10825-10827)Aag>Gag | p.K3609E |
| LGG | 7 | 151864270 | 151864270 | + | Silent | SNP | A | A | G | TCGA-DU-A7TG-01A-21D-A34J-08 | TCGA-DU-A7TG-10A-01D-A34M-08 | g.chr7:151864270A>G | c.9711T>C | c.(9709-9711)gtT>gtC | p.V3237V |
| LGG | 7 | 151873659 | 151873659 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151873659G>A | c.8879C>T | c.(8878-8880)cCg>cTg | p.P2960L |
| LGG | 7 | 151873923 | 151873923 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151873923G>T | c.8615C>A | c.(8614-8616)cCt>cAt | p.P2872H |
| LGG | 7 | 151878079 | 151878079 | + | Missense_Mutation | SNP | C | C | T | TCGA-QH-A6X3-01A-21D-A32B-08 | TCGA-QH-A6X3-10B-01D-A329-08 | g.chr7:151878079C>T | c.6866G>A | c.(6865-6867)cGt>cAt | p.R2289H |
| LGG | 7 | 151878436 | 151878436 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151878436G>A | c.6509C>T | c.(6508-6510)aCt>aTt | p.T2170I |
| LGG | 7 | 151917719 | 151917719 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151917719T>G | c.3601A>C | c.(3601-3603)Aaa>Caa | p.K1201Q |
| LGG | 7 | 151932981 | 151932981 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A5TS-01A-11D-A289-08 | TCGA-DU-A5TS-10A-01D-A289-08 | g.chr7:151932981C>T | c.2690G>A | c.(2689-2691)cGa>cAa | p.R897Q |
| LGG | 7 | 151935819 | 151935819 | + | Silent | SNP | A | A | G | TCGA-TQ-A7RM-01A-11D-A33T-08 | TCGA-TQ-A7RM-10A-01D-A33W-08 | g.chr7:151935819A>G | c.2625T>C | c.(2623-2625)ccT>ccC | p.P875P |
| LGG | 7 | 151945083 | 151945083 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151945083C>T | c.2436G>A | c.(2434-2436)atG>atA | p.M812I |
| LGG | 7 | 151945104 | 151945104 | + | Missense_Mutation | SNP | A | A | T | TCGA-CS-5397-01A-01D-1893-08 | TCGA-CS-5397-10A-03D-1893-08 | g.chr7:151945104A>T | c.2415T>A | c.(2413-2415)agT>agA | p.S805R |
| LGG | 7 | 151945155 | 151945155 | + | Silent | SNP | A | A | T | TCGA-DU-A7T8-01A-21D-A34J-08 | TCGA-DU-A7T8-10A-01D-A34M-08 | g.chr7:151945155A>T | c.2364T>A | c.(2362-2364)tcT>tcA | p.S788S |
| LGG | 7 | 151945175 | 151945175 | + | Missense_Mutation | SNP | A | A | G | TCGA-FG-6689-01A-11D-1893-08 | TCGA-FG-6689-10A-01D-1893-08 | g.chr7:151945175A>G | c.2344T>C | c.(2344-2346)Tct>Cct | p.S782P |
| LGG | 7 | 151945270 | 151945270 | + | Missense_Mutation | SNP | T | T | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151945270T>A | c.2249A>T | c.(2248-2250)aAa>aTa | p.K750I |
| LGG | 7 | 151945288 | 151945288 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-5852-01A-11D-1705-08 | TCGA-DU-5852-10A-01D-1705-08 | g.chr7:151945288G>T | c.2231C>A | c.(2230-2232)aCa>aAa | p.T744K |
| LGG | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| LGG | 7 | 151962268 | 151962268 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-A6S3-01A-12D-A32B-08 | TCGA-DU-A6S3-10A-01D-A329-08 | g.chr7:151962268A>G | c.1039T>C | c.(1039-1041)Tgc>Cgc | p.C347R |
| LGG | 7 | 151970801 | 151970801 | + | Missense_Mutation | SNP | G | G | T | TCGA-HT-7687-01A-11D-2253-08 | TCGA-HT-7687-10A-01D-2253-08 | g.chr7:151970801G>T | c.1001C>A | c.(1000-1002)gCt>gAt | p.A334D |
| LGG | 7 | 152012290 | 152012290 | + | Missense_Mutation | SNP | C | C | A | TCGA-P5-A731-01A-11D-A32B-08 | TCGA-P5-A731-10A-01D-A329-08 | g.chr7:152012290C>A | c.523G>T | c.(523-525)Gac>Tac | p.D175Y |
| LGG | 7 | 152012407 | 152012407 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr7:152012407A>G | c.406T>C | c.(406-408)Ttt>Ctt | p.F136L |
| LIHC | 7 | 151833918 | 151833918 | + | Nonstop_Mutation | SNP | C | C | A | TCGA-BC-A10T-01A-11D-A12Z-10 | TCGA-BC-A10T-11A-11D-A12Z-10 | g.chr7:151833918C>A | c.14735G>T | c.(14734-14736)tGa>tTa | p.*4912L |
| LIHC | 7 | 151842365 | 151842365 | + | Missense_Mutation | SNP | C | C | G | TCGA-DD-AAE3-01A-11D-A40R-10 | TCGA-DD-AAE3-10A-01D-A40U-10 | g.chr7:151842365C>G | c.14047G>C | c.(14047-14049)Gca>Cca | p.A4683P |
| LIHC | 7 | 151848557 | 151848557 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chr7:151848557delT | c.12636delA | c.(12634-12636)aaafs | p.K4212fs |
| LIHC | 7 | 151849960 | 151849960 | + | Missense_Mutation | SNP | G | G | A | TCGA-DD-A73G-01A-22D-A32G-10 | TCGA-DD-A73G-10A-01D-A32G-10 | g.chr7:151849960G>A | c.12356C>T | c.(12355-12357)cCa>cTa | p.P4119L |
| LIHC | 7 | 151859254 | 151859254 | + | Missense_Mutation | SNP | T | T | C | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr7:151859254T>C | c.11408A>G | c.(11407-11409)gAc>gGc | p.D3803G |
| LIHC | 7 | 151860411 | 151860411 | + | Silent | SNP | C | C | T | TCGA-G3-A5SM-01A-12D-A28X-10 | TCGA-G3-A5SM-10A-01D-A28X-10 | g.chr7:151860411C>T | c.10251G>A | c.(10249-10251)caG>caA | p.Q3417Q |
| LIHC | 7 | 151860694 | 151860694 | + | Missense_Mutation | SNP | T | T | G | TCGA-MI-A75H-01A-11D-A32G-10 | TCGA-MI-A75H-10A-01D-A32G-10 | g.chr7:151860694T>G | c.9968A>C | c.(9967-9969)cAt>cCt | p.H3323P |
| LIHC | 7 | 151873528 | 151873528 | + | Missense_Mutation | SNP | G | G | C | TCGA-LG-A6GG-01A-11D-A30V-10 | TCGA-LG-A6GG-10A-01D-A30V-10 | g.chr7:151873528G>C | c.9010C>G | c.(9010-9012)Ctg>Gtg | p.L3004V |
| LIHC | 7 | 151873592 | 151873592 | + | Silent | SNP | A | A | C | TCGA-BC-A10Y-01A-11D-A12Z-10 | TCGA-BC-A10Y-11A-11D-A12Z-10 | g.chr7:151873592A>C | c.8946T>G | c.(8944-8946)gtT>gtG | p.V2982V |
| LIHC | 7 | 151874011 | 151874011 | + | Missense_Mutation | SNP | C | C | T | TCGA-DD-AACY-01A-11D-A40R-10 | TCGA-DD-AACY-10A-01D-A40U-10 | g.chr7:151874011C>T | c.8527G>A | c.(8527-8529)Gat>Aat | p.D2843N |
| LIHC | 7 | 151874093 | 151874093 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr7:151874093delT | c.8445delA | c.(8443-8445)aaafs | p.K2815fs |
| LIHC | 7 | 151878921 | 151878922 | + | Missense_Mutation | DNP | AG | AG | TA | TCGA-UB-A7MD-01A-12D-A34Z-10 | TCGA-UB-A7MD-10A-01D-A34Z-10 | g.chr7:151878921_151878922AG>TA | c.6023_6024CT>TA | c.(6022-6024)aCT>aTA | p.T2008I |
| LIHC | 7 | 151878935 | 151878935 | + | Missense_Mutation | SNP | T | T | A | TCGA-ED-A459-01A-11D-A25V-10 | TCGA-ED-A459-10A-01D-A25V-10 | g.chr7:151878935T>A | c.6010A>T | c.(6010-6012)Agt>Tgt | p.S2004C |
| LIHC | 7 | 151884488 | 151884488 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-BC-A10U-01A-11D-A12Z-10 | TCGA-BC-A10U-11A-11D-A12Z-10 | g.chr7:151884488C>A | c.4867G>T | c.(4867-4869)Gaa>Taa | p.E1623* |
| LIHC | 7 | 151919143 | 151919143 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-A3A1-01A-11D-A20W-10 | TCGA-DD-A3A1-11A-11D-A20W-10 | g.chr7:151919143A>G | c.3442T>C | c.(3442-3444)Tca>Cca | p.S1148P |
| LIHC | 7 | 151927092 | 151927092 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-RC-A6M6-01A-11D-A32G-10 | TCGA-RC-A6M6-10A-01D-A32G-10 | g.chr7:151927092delG | c.2892delC | c.(2890-2892)ggcfs | p.G964fs |
| LIHC | 7 | 151944994 | 151944994 | + | Missense_Mutation | SNP | G | G | T | TCGA-LG-A9QD-01A-11D-A382-10 | TCGA-LG-A9QD-10A-01D-A385-10 | g.chr7:151944994G>T | c.2525C>A | c.(2524-2526)tCc>tAc | p.S842Y |
| LIHC | 7 | 151945190 | 151945190 | + | Missense_Mutation | SNP | T | T | A | TCGA-MI-A75C-01A-11D-A32G-10 | TCGA-MI-A75C-10A-01D-A32G-10 | g.chr7:151945190T>A | c.2329A>T | c.(2329-2331)Agc>Tgc | p.S777C |
| LIHC | 7 | 151962169 | 151962169 | + | Missense_Mutation | SNP | G | G | A | TCGA-EP-A12J-01A-11D-A12Z-10 | TCGA-EP-A12J-10A-01D-A12Z-10 | g.chr7:151962169G>A | c.1138C>T | c.(1138-1140)Cgt>Tgt | p.R380C |
| LIHC | 7 | 151970850 | 151970850 | + | Missense_Mutation | SNP | G | G | T | TCGA-DD-A3A7-01A-11D-A22F-10 | TCGA-DD-A3A7-11A-11D-A22F-10 | g.chr7:151970850G>T | c.952C>A | c.(952-954)Cag>Aag | p.Q318K |
| LIHC | 7 | 151970873 | 151970873 | + | Missense_Mutation | SNP | C | C | A | TCGA-CC-A3M9-01A-11D-A20W-10 | TCGA-CC-A3M9-10A-01D-A20W-10 | g.chr7:151970873C>A | c.929G>T | c.(928-930)tGt>tTt | p.C310F |
| LIHC | 7 | 152132847 | 152132847 | + | Missense_Mutation | SNP | C | C | T | TCGA-5C-A9VH-01A-11D-A36X-10 | TCGA-5C-A9VH-10A-01D-A370-10 | g.chr7:152132847C>T | c.25G>A | c.(25-27)Gtg>Atg | p.V9M |
| LUAD | 7 | 151845739 | 151845739 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr7:151845739C>A | c.13273G>T | c.(13273-13275)Gat>Tat | p.D4425Y |
| LUAD | 7 | 151847985 | 151847985 | + | Splice_Site | SNP | C | C | A | TCGA-86-8585-01A-11D-2393-08 | TCGA-86-8585-10A-01D-2393-08 | g.chr7:151847985C>A | c.12774G>T | c.(12772-12774)aaG>aaT | p.K4258N |
| LUAD | 7 | 151849821 | 151849821 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5939-01A-11D-1625-08 | TCGA-50-5939-11A-01D-1625-08 | g.chr7:151849821C>A | c.12495G>T | c.(12493-12495)caG>caT | p.Q4165H |
| LUAD | 7 | 151849853 | 151849853 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-6972-01A-11D-1945-08 | TCGA-55-6972-11A-01D-1945-08 | g.chr7:151849853G>A | c.12463C>T | c.(12463-12465)Ccc>Tcc | p.P4155S |
| LUAD | 7 | 151850040 | 151850040 | + | Splice_Site | SNP | C | C | G | TCGA-17-Z056-01A-01W-0747-08 | TCGA-17-Z056-11A-01W-0747-08 | g.chr7:151850040C>G | | c.e49-1 | |
| LUAD | 7 | 151851382 | 151851382 | + | Missense_Mutation | SNP | T | T | G | TCGA-75-7031-01A-11D-1945-08 | TCGA-75-7031-10A-01D-1946-08 | g.chr7:151851382T>G | c.12109A>C | c.(12109-12111)Att>Ctt | p.I4037L |
| LUAD | 7 | 151856020 | 151856020 | + | Missense_Mutation | SNP | C | C | G | TCGA-53-7626-01A-12D-2063-08 | TCGA-53-7626-10A-01D-2063-08 | g.chr7:151856020C>G | c.11598G>C | c.(11596-11598)aaG>aaC | p.K3866N |
| LUAD | 7 | 151856048 | 151856048 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z025-01A-01W-0746-08 | TCGA-17-Z025-11A-01W-0746-08 | g.chr7:151856048G>A | c.11570C>T | c.(11569-11571)aCg>aTg | p.T3857M |
| LUAD | 7 | 151859569 | 151859569 | + | Missense_Mutation | SNP | G | G | A | TCGA-97-7937-01A-11D-2167-08 | TCGA-97-7937-10A-01D-2167-08 | g.chr7:151859569G>A | c.11093C>T | c.(11092-11094)aCg>aTg | p.T3698M |
| LUAD | 7 | 151859670 | 151859670 | + | Silent | SNP | G | G | A | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr7:151859670G>A | c.10992C>T | c.(10990-10992)gtC>gtT | p.V3664V |
| LUAD | 7 | 151859762 | 151859762 | + | Missense_Mutation | SNP | T | T | G | TCGA-44-8120-01A-11D-2238-08 | TCGA-44-8120-10A-01D-2238-08 | g.chr7:151859762T>G | c.10900A>C | c.(10900-10902)Act>Cct | p.T3634P |
| LUAD | 7 | 151859764 | 151859764 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-8120-01A-11D-2238-08 | TCGA-44-8120-10A-01D-2238-08 | g.chr7:151859764G>T | c.10898C>A | c.(10897-10899)cCg>cAg | p.P3633Q |
| LUAD | 7 | 151860040 | 151860040 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr7:151860040C>A | c.10622G>T | c.(10621-10623)gGg>gTg | p.G3541V |
| LUAD | 7 | 151860287 | 151860288 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr7:151860287_151860288insT | c.10374_10375insA | c.(10372-10377)ttacctfs | p.P3459fs |
| LUAD | 7 | 151860499 | 151860499 | + | Missense_Mutation | SNP | T | T | C | TCGA-44-A47G-01A-21D-A24D-08 | TCGA-44-A47G-10A-01D-A24F-08 | g.chr7:151860499T>C | c.10163A>G | c.(10162-10164)aAc>aGc | p.N3388S |
| LUAD | 7 | 151860827 | 151860827 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z021-01A-01W-0746-08 | TCGA-17-Z021-11A-01W-0746-08 | g.chr7:151860827T>C | c.9835A>G | c.(9835-9837)Acc>Gcc | p.T3279A |
| LUAD | 7 | 151864259 | 151864259 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z061-01A-01W-0747-08 | TCGA-17-Z061-11A-01W-0747-08 | g.chr7:151864259T>C | c.9722A>G | c.(9721-9723)cAa>cGa | p.Q3241R |
| LUAD | 7 | 151871221 | 151871221 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-6851-01A-11D-1945-08 | TCGA-86-6851-10A-01D-1946-08 | g.chr7:151871221C>G | c.9369G>C | c.(9367-9369)atG>atC | p.M3123I |
| LUAD | 7 | 151871326 | 151871326 | + | Splice_Site | SNP | A | A | C | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chr7:151871326A>C | c.9264T>G | c.(9262-9264)gaT>gaG | p.D3088E |
| LUAD | 7 | 151873473 | 151873473 | + | Missense_Mutation | SNP | G | G | A | TCGA-67-6217-01A-11D-1753-08 | TCGA-67-6217-10A-01D-1753-08 | g.chr7:151873473G>A | c.9065C>T | c.(9064-9066)aCc>aTc | p.T3022I |
| LUAD | 7 | 151873492 | 151873492 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr7:151873492G>A | c.9046C>T | c.(9046-9048)Caa>Taa | p.Q3016* |
| LUAD | 7 | 151874168 | 151874168 | + | Silent | SNP | T | T | C | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr7:151874168T>C | c.8370A>G | c.(8368-8370)gtA>gtG | p.V2790V |
| LUAD | 7 | 151874238 | 151874238 | + | Missense_Mutation | SNP | C | C | A | TCGA-38-4632-01A-01D-1753-08 | TCGA-38-4632-11A-01D-1753-08 | g.chr7:151874238C>A | c.8300G>T | c.(8299-8301)gGa>gTa | p.G2767V |
| LUAD | 7 | 151874411 | 151874411 | + | Silent | SNP | G | G | A | TCGA-44-7659-01A-11D-2063-08 | TCGA-44-7659-10A-01D-2063-08 | g.chr7:151874411G>A | c.8127C>T | c.(8125-8127)gtC>gtT | p.V2709V |
| LUAD | 7 | 151874497 | 151874497 | + | Missense_Mutation | SNP | G | G | C | TCGA-44-2657-01A-01D-1105-08 | TCGA-44-2657-10A-01D-1105-08 | g.chr7:151874497G>C | c.8041C>G | c.(8041-8043)Cct>Gct | p.P2681A |
| LUAD | 7 | 151874875 | 151874875 | + | Missense_Mutation | SNP | C | C | G | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr7:151874875C>G | c.7663G>C | c.(7663-7665)Ggc>Cgc | p.G2555R |
| LUAD | 7 | 151876995 | 151876995 | + | Missense_Mutation | SNP | C | C | T | TCGA-44-6777-01A-11D-1855-08 | TCGA-44-6777-10A-01D-1855-08 | g.chr7:151876995C>T | c.7366G>A | c.(7366-7368)Gct>Act | p.A2456T |
| LUAD | 7 | 151877045 | 151877045 | + | Missense_Mutation | SNP | T | T | C | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr7:151877045T>C | c.7316A>G | c.(7315-7317)tAt>tGt | p.Y2439C |
| LUAD | 7 | 151877213 | 151877213 | + | Splice_Site | SNP | T | T | G | TCGA-93-A4JQ-01A-11D-A24P-08 | TCGA-93-A4JQ-10A-01D-A24P-08 | g.chr7:151877213T>G | | c.e37-2 | |
| LUAD | 7 | 151877859 | 151877859 | + | Silent | SNP | T | T | A | TCGA-97-A4M7-01A-11D-A24P-08 | TCGA-97-A4M7-10A-01D-A24P-08 | g.chr7:151877859T>A | c.7086A>T | c.(7084-7086)tcA>tcT | p.S2362S |
| LUAD | 7 | 151878270 | 151878270 | + | Silent | SNP | T | T | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr7:151878270T>A | c.6675A>T | c.(6673-6675)ccA>ccT | p.P2225P |
| LUAD | 7 | 151878315 | 151878315 | + | Silent | SNP | T | T | C | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr7:151878315T>C | c.6630A>G | c.(6628-6630)ccA>ccG | p.P2210P |
| LUAD | 7 | 151878671 | 151878671 | + | Missense_Mutation | SNP | C | C | A | TCGA-97-7547-01A-11D-2036-08 | TCGA-97-7547-10A-01D-2036-08 | g.chr7:151878671C>A | c.6274G>T | c.(6274-6276)Gat>Tat | p.D2092Y |
| LUAD | 7 | 151878782 | 151878782 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-7978-01A-11D-2184-08 | TCGA-69-7978-10A-01D-2184-08 | g.chr7:151878782C>A | c.6163G>T | c.(6163-6165)Gat>Tat | p.D2055Y |
| LUAD | 7 | 151878797 | 151878797 | + | Missense_Mutation | SNP | G | G | A | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr7:151878797G>A | c.6148C>T | c.(6148-6150)Cct>Tct | p.P2050S |
| LUAD | 7 | 151879337 | 151879337 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-86-8056-01A-11D-2238-08 | TCGA-86-8056-10A-01D-2238-08 | g.chr7:151879337G>A | c.5608C>T | c.(5608-5610)Cag>Tag | p.Q1870* |
| LUAD | 7 | 151879370 | 151879370 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-8514-01A-11D-2393-08 | TCGA-55-8514-10A-01D-2393-08 | g.chr7:151879370G>A | c.5575C>T | c.(5575-5577)Cca>Tca | p.P1859S |
| LUAD | 7 | 151884816 | 151884816 | + | Missense_Mutation | SNP | A | A | C | TCGA-44-3396-01A-01D-1553-08 | TCGA-44-3396-10A-01D-1265-08 | g.chr7:151884816A>C | c.4777T>G | c.(4777-4779)Tct>Gct | p.S1593A |
| LUAD | 7 | 151891314 | 151891314 | + | Splice_Site | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr7:151891314C>A | c.4540G>T | c.(4540-4542)Gag>Tag | p.E1514* |
| LUAD | 7 | 151896444 | 151896445 | + | Frame_Shift_Del | DEL | TT | TT | - | TCGA-05-4434-01A-01D-1265-08 | TCGA-05-4434-10A-01D-1265-08 | g.chr7:151896444_151896445delTT | c.4192_4193delAA | c.(4192-4194)aacfs | p.N1398fs |
| LUAD | 7 | 151900020 | 151900020 | + | Splice_Site | SNP | T | T | C | TCGA-55-8514-01A-11D-2393-08 | TCGA-55-8514-10A-01D-2393-08 | g.chr7:151900020T>C | c.4091A>G | c.(4090-4092)cAa>cGa | p.Q1364R |
| LUAD | 7 | 151902280 | 151902280 | + | Missense_Mutation | SNP | C | C | A | TCGA-J2-A4AD-01A-11D-A24D-08 | TCGA-J2-A4AD-10A-01D-A24F-08 | g.chr7:151902280C>A | c.3872G>T | c.(3871-3873)aGt>aTt | p.S1291I |
| LUAD | 7 | 151902288 | 151902288 | + | Silent | SNP | C | C | A | TCGA-86-7953-01A-11D-2184-08 | TCGA-86-7953-10A-01D-2184-08 | g.chr7:151902288C>A | c.3864G>T | c.(3862-3864)cgG>cgT | p.R1288R |
| LUAD | 7 | 151904477 | 151904477 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5049-01A-01D-1625-08 | TCGA-50-5049-10A-01D-1625-08 | g.chr7:151904477G>T | c.3749C>A | c.(3748-3750)tCt>tAt | p.S1250Y |
| LUAD | 7 | 151917783 | 151917783 | + | Missense_Mutation | SNP | C | C | G | TCGA-64-1677-01A-01W-0928-08 | TCGA-64-1677-10A-01W-0928-08 | g.chr7:151917783C>G | c.3537G>C | c.(3535-3537)ttG>ttC | p.L1179F |
| LUAD | 7 | 151917800 | 151917800 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-8279-01A-11D-2284-08 | TCGA-86-8279-10A-01D-2284-08 | g.chr7:151917800G>C | c.3520C>G | c.(3520-3522)Cag>Gag | p.Q1174E |
| LUAD | 7 | 151921547 | 151921547 | + | Missense_Mutation | SNP | A | A | G | TCGA-MN-A4N5-01A-11D-A24P-08 | TCGA-MN-A4N5-10A-01D-A24P-08 | g.chr7:151921547A>G | c.3131T>C | c.(3130-3132)gTt>gCt | p.V1044A |
| LUAD | 7 | 151927017 | 151927017 | + | Silent | SNP | G | G | A | TCGA-97-A4M0-01A-11D-A24P-08 | TCGA-97-A4M0-10A-01D-A24P-08 | g.chr7:151927017G>A | c.2967C>T | c.(2965-2967)gtC>gtT | p.V989V |
| LUAD | 7 | 151927028 | 151927028 | + | Missense_Mutation | SNP | G | G | T | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr7:151927028G>T | c.2956C>A | c.(2956-2958)Cca>Aca | p.P986T |
| LUAD | 7 | 151927043 | 151927044 | + | Frame_Shift_Del | DEL | CA | CA | - | TCGA-44-5644-01A-21D-2036-08 | TCGA-44-5644-10A-01D-2036-08 | g.chr7:151927043_151927044delCA | c.2940_2941delTG | c.(2938-2943)tgtggtfs | p.CG980fs |
| LUAD | 7 | 151927076 | 151927076 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-7154-01A-11D-2036-08 | TCGA-78-7154-10A-01D-2036-08 | g.chr7:151927076C>A | c.2908G>T | c.(2908-2910)Gca>Tca | p.A970S |
| LUAD | 7 | 151927085 | 151927085 | + | Missense_Mutation | SNP | C | C | A | TCGA-38-4628-01A-01D-1265-08 | TCGA-38-4628-11A-01D-1265-08 | g.chr7:151927085C>A | c.2899G>T | c.(2899-2901)Ggc>Tgc | p.G967C |
| LUAD | 7 | 151932901 | 151932901 | + | Splice_Site | SNP | C | C | A | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr7:151932901C>A | | c.e16+1 | |
| LUAD | 7 | 151932917 | 151932917 | + | Silent | SNP | A | A | G | TCGA-95-7947-01A-11D-2184-08 | TCGA-95-7947-10A-01D-2184-08 | g.chr7:151932917A>G | c.2754T>C | c.(2752-2754)gcT>gcC | p.A918A |
| LUAD | 7 | 151932938 | 151932938 | + | Missense_Mutation | SNP | C | C | G | TCGA-86-8279-01A-11D-2284-08 | TCGA-86-8279-10A-01D-2284-08 | g.chr7:151932938C>G | c.2733G>C | c.(2731-2733)aaG>aaC | p.K911N |
| LUAD | 7 | 151932943 | 151932943 | + | Missense_Mutation | SNP | A | A | C | TCGA-69-7760-01A-11D-2167-08 | TCGA-69-7760-10A-01D-2167-08 | g.chr7:151932943A>C | c.2728T>G | c.(2728-2730)Tca>Gca | p.S910A |
| LUAD | 7 | 151932993 | 151932993 | + | Missense_Mutation | SNP | T | T | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr7:151932993T>A | c.2678A>T | c.(2677-2679)aAg>aTg | p.K893M |
| LUAD | 7 | 151933018 | 151933018 | + | Splice_Site | SNP | C | C | A | TCGA-17-Z022-01A-01W-0746-08 | TCGA-17-Z022-11A-01W-0746-08 | g.chr7:151933018C>A | c.2653G>T | c.(2653-2655)Ggc>Tgc | p.G885C |
| LUAD | 7 | 151945009 | 151945009 | + | Missense_Mutation | SNP | G | G | T | TCGA-95-7947-01A-11D-2184-08 | TCGA-95-7947-10A-01D-2184-08 | g.chr7:151945009G>T | c.2510C>A | c.(2509-2511)cCt>cAt | p.P837H |
| LUAD | 7 | 151945027 | 151945027 | + | Missense_Mutation | SNP | G | G | C | TCGA-69-A59K-01A-11D-A25L-08 | TCGA-69-A59K-10A-01D-A25L-08 | g.chr7:151945027G>C | c.2492C>G | c.(2491-2493)aCt>aGt | p.T831S |
| LUAD | 7 | 151945031 | 151945031 | + | Missense_Mutation | SNP | T | T | C | TCGA-78-8660-01A-11D-2393-08 | TCGA-78-8660-10A-01D-2393-08 | g.chr7:151945031T>C | c.2488A>G | c.(2488-2490)Att>Gtt | p.I830V |
| LUAD | 7 | 151945048 | 151945048 | + | Missense_Mutation | SNP | C | C | A | TCGA-J2-A4AD-01A-11D-A24D-08 | TCGA-J2-A4AD-10A-01D-A24F-08 | g.chr7:151945048C>A | c.2471G>T | c.(2470-2472)gGc>gTc | p.G824V |
| LUAD | 7 | 151945057 | 151945057 | + | Missense_Mutation | SNP | G | G | A | TCGA-75-5146-01A-01D-1625-08 | TCGA-75-5146-10A-01D-1625-08 | g.chr7:151945057G>A | c.2462C>T | c.(2461-2463)cCa>cTa | p.P821L |
| LUAD | 7 | 151945082 | 151945082 | + | Missense_Mutation | SNP | G | G | C | TCGA-67-3771-01A-01D-1040-01 | TCGA-67-3771-10A-01D-1040-01 | g.chr7:151945082G>C | c.2437C>G | c.(2437-2439)Cca>Gca | p.P813A |
| LUAD | 7 | 151945107 | 151945107 | + | Silent | SNP | A | A | T | TCGA-17-Z044-01A-01W-0746-08 | TCGA-17-Z044-11A-01W-0746-08 | g.chr7:151945107A>T | c.2412T>A | c.(2410-2412)ctT>ctA | p.L804L |
| LUAD | 7 | 151945112 | 151945112 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z014-01A-01W-0746-08 | TCGA-17-Z014-11A-01W-0746-08 | g.chr7:151945112C>A | c.2407G>T | c.(2407-2409)Gct>Tct | p.A803S |
| LUAD | 7 | 151945133 | 151945133 | + | Missense_Mutation | SNP | T | T | A | TCGA-53-7626-01A-12D-2063-08 | TCGA-53-7626-10A-01D-2063-08 | g.chr7:151945133T>A | c.2386A>T | c.(2386-2388)Atg>Ttg | p.M796L |
| LUAD | 7 | 151945153 | 151945153 | + | Missense_Mutation | SNP | G | G | A | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr7:151945153G>A | c.2366C>T | c.(2365-2367)tCa>tTa | p.S789L |
| LUAD | 7 | 151945156 | 151945156 | + | Missense_Mutation | SNP | G | G | A | TCGA-86-8673-01A-11D-2393-08 | TCGA-86-8673-10A-01D-2393-08 | g.chr7:151945156G>A | c.2363C>T | c.(2362-2364)tCt>tTt | p.S788F |
| LUAD | 7 | 151945162 | 151945162 | + | Missense_Mutation | SNP | G | G | T | TCGA-35-4123-01A-01D-1105-08 | TCGA-35-4123-10A-01D-1105-08 | g.chr7:151945162G>T | c.2357C>A | c.(2356-2358)aCa>aAa | p.T786K |
| LUAD | 7 | 151945170 | 151945170 | + | Silent | SNP | G | G | A | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr7:151945170G>A | c.2349C>T | c.(2347-2349)tcC>tcT | p.S783S |
| LUAD | 7 | 151945170 | 151945170 | + | Silent | SNP | G | G | C | TCGA-49-4487-01A-21D-1855-08 | TCGA-49-4487-11A-01D-1855-08 | g.chr7:151945170G>C | c.2349C>G | c.(2347-2349)tcC>tcG | p.S783S |
| LUAD | 7 | 151945183 | 151945183 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-6968-01A-11D-1945-08 | TCGA-55-6968-11A-01D-1945-08 | g.chr7:151945183G>T | c.2336C>A | c.(2335-2337)gCa>gAa | p.A779E |
| LUAD | 7 | 151945190 | 151945190 | + | Missense_Mutation | SNP | T | T | A | TCGA-49-4506-01A-01D-1265-08 | TCGA-49-4506-11A-01D-1265-08 | g.chr7:151945190T>A | c.2329A>T | c.(2329-2331)Agc>Tgc | p.S777C |
| LUAD | 7 | 151945231 | 151945231 | + | Missense_Mutation | SNP | G | G | A | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr7:151945231G>A | c.2288C>T | c.(2287-2289)tCa>tTa | p.S763L |
| LUAD | 7 | 151945260 | 151945260 | + | Silent | SNP | T | T | C | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr7:151945260T>C | c.2259A>G | c.(2257-2259)tcA>tcG | p.S753S |
| LUAD | 7 | 151945325 | 151945325 | + | Missense_Mutation | SNP | G | G | A | TCGA-50-5045-01A-01D-1625-08 | TCGA-50-5045-10A-01D-1625-08 | g.chr7:151945325G>A | c.2194C>T | c.(2194-2196)Ctt>Ttt | p.L732F |
| LUAD | 7 | 151945483 | 151945483 | + | Missense_Mutation | SNP | C | C | T | TCGA-J2-A4AD-01A-11D-A24D-08 | TCGA-J2-A4AD-10A-01D-A24F-08 | g.chr7:151945483C>T | c.2036G>A | c.(2035-2037)aGa>aAa | p.R679K |
| LUAD | 7 | 151945526 | 151945526 | + | Missense_Mutation | SNP | C | C | T | TCGA-91-6830-01A-11D-1945-08 | TCGA-91-6830-11A-01D-1945-08 | g.chr7:151945526C>T | c.1993G>A | c.(1993-1995)Gaa>Aaa | p.E665K |
| LUAD | 7 | 151945602 | 151945602 | + | Silent | SNP | G | G | A | TCGA-MP-A4T7-01A-11D-A24P-08 | TCGA-MP-A4T7-10A-01D-A24P-08 | g.chr7:151945602G>A | c.1917C>T | c.(1915-1917)ggC>ggT | p.G639G |
| LUAD | 7 | 151947003 | 151947003 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7536-01A-11D-2063-08 | TCGA-78-7536-10A-01D-2063-08 | g.chr7:151947003G>A | c.1771C>T | c.(1771-1773)Cat>Tat | p.H591Y |
| LUAD | 7 | 151960177 | 151960177 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-2657-01A-01D-1105-08 | TCGA-44-2657-10A-01D-1105-08 | g.chr7:151960177G>A | c.1223C>T | c.(1222-1224)aCg>aTg | p.T408M |
| LUAD | 7 | 151962157 | 151962157 | + | Missense_Mutation | SNP | G | G | C | TCGA-05-4249-01A-01D-1105-08 | TCGA-05-4249-10A-01D-1105-08 | g.chr7:151962157G>C | c.1150C>G | c.(1150-1152)Caa>Gaa | p.Q384E |
| LUAD | 7 | 151962157 | 151962157 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8203-01A-11D-2238-08 | TCGA-55-8203-10A-01D-2238-08 | g.chr7:151962157G>T | c.1150C>A | c.(1150-1152)Caa>Aaa | p.Q384K |
| LUAD | 7 | 151962159 | 151962159 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr7:151962159C>A | c.1148G>T | c.(1147-1149)tGg>tTg | p.W383L |
| LUAD | 7 | 151962159 | 151962159 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr7:151962159C>A | c.1148G>T | c.(1147-1149)tGg>tTg | p.W383L |
| LUAD | 7 | 151962165 | 151962165 | + | Missense_Mutation | SNP | G | G | T | TCGA-97-7938-01A-11D-2167-08 | TCGA-97-7938-10A-01D-2167-08 | g.chr7:151962165G>T | c.1142C>A | c.(1141-1143)gCa>gAa | p.A381E |
| LUAD | 7 | 151962175 | 151962175 | + | Missense_Mutation | SNP | A | A | C | TCGA-05-4384-01A-01D-1753-08 | TCGA-05-4384-10A-01D-1753-08 | g.chr7:151962175A>C | c.1132T>G | c.(1132-1134)Tta>Gta | p.L378V |
| LUAD | 7 | 151962184 | 151962184 | + | Missense_Mutation | SNP | C | C | T | TCGA-17-Z060-01A-01W-0747-08 | TCGA-17-Z060-11A-01W-0747-08 | g.chr7:151962184C>T | c.1123G>A | c.(1123-1125)Gtt>Att | p.V375I |
| LUAD | 7 | 151962209 | 151962209 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-75-7031-01A-11D-1945-08 | TCGA-75-7031-10A-01D-1946-08 | g.chr7:151962209A>C | c.1098T>G | c.(1096-1098)taT>taG | p.Y366* |
| LUAD | 7 | 151962215 | 151962215 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-7711-01A-11D-2063-08 | TCGA-86-7711-10A-01D-2063-08 | g.chr7:151962215C>A | c.1092G>T | c.(1090-1092)caG>caT | p.Q364H |
| LUAD | 7 | 151962220 | 151962220 | + | Missense_Mutation | SNP | C | C | G | TCGA-95-7947-01A-11D-2184-08 | TCGA-95-7947-10A-01D-2184-08 | g.chr7:151962220C>G | c.1087G>C | c.(1087-1089)Ggt>Cgt | p.G363R |
| LUAD | 7 | 151962236 | 151962236 | + | Missense_Mutation | SNP | G | G | T | TCGA-L9-A444-01A-21D-A24D-08 | TCGA-L9-A444-10A-01D-A24F-08 | g.chr7:151962236G>T | c.1071C>A | c.(1069-1071)ttC>ttA | p.F357L |
| LUAD | 7 | 151962241 | 151962241 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4397-01A-01D-1265-08 | TCGA-05-4397-10A-01D-1265-08 | g.chr7:151962241G>T | c.1066C>A | c.(1066-1068)Cag>Aag | p.Q356K |
| LUAD | 7 | 151962241 | 151962241 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-6594-01A-11D-1753-08 | TCGA-50-6594-11A-01D-1753-08 | g.chr7:151962241G>T | c.1066C>A | c.(1066-1068)Cag>Aag | p.Q356K |
| LUAD | 7 | 151962266 | 151962266 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-7815-01A-11D-2167-08 | TCGA-55-7815-10A-01D-2167-08 | g.chr7:151962266G>C | c.1041C>G | c.(1039-1041)tgC>tgG | p.C347W |
| LUAD | 7 | 151962287 | 151962287 | + | Missense_Mutation | SNP | T | T | A | TCGA-50-5931-01A-11D-1753-08 | TCGA-50-5931-11A-01D-1753-08 | g.chr7:151962287T>A | c.1020A>T | c.(1018-1020)gaA>gaT | p.E340D |
| LUAD | 7 | 151970792 | 151970792 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-7979-01A-11D-2184-08 | TCGA-69-7979-10A-01D-2184-08 | g.chr7:151970792C>A | c.1010G>T | c.(1009-1011)aGa>aTa | p.R337I |
| LUAD | 7 | 151970796 | 151970796 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8204-01A-11D-2238-08 | TCGA-55-8204-10A-01D-2238-08 | g.chr7:151970796C>T | c.1006G>A | c.(1006-1008)Gaa>Aaa | p.E336K |
| LUAD | 7 | 151970801 | 151970801 | + | Missense_Mutation | SNP | G | G | T | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr7:151970801G>T | c.1001C>A | c.(1000-1002)gCt>gAt | p.A334D |
| LUAD | 7 | 151970805 | 151970805 | + | Missense_Mutation | SNP | G | G | T | TCGA-99-7458-01A-11D-2036-08 | TCGA-99-7458-10A-01D-2036-08 | g.chr7:151970805G>T | c.997C>A | c.(997-999)Caa>Aaa | p.Q333K |
| LUAD | 7 | 151970819 | 151970819 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8301-01A-11D-2284-08 | TCGA-55-8301-10A-01D-2284-08 | g.chr7:151970819G>T | c.983C>A | c.(982-984)cCa>cAa | p.P328Q |
| LUAD | 7 | 151970820 | 151970820 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8301-01A-11D-2284-08 | TCGA-55-8301-10A-01D-2284-08 | g.chr7:151970820G>T | c.982C>A | c.(982-984)Cca>Aca | p.P328T |
| LUAD | 7 | 151970862 | 151970862 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-7148-01A-11D-2036-08 | TCGA-78-7148-10A-01D-2036-08 | g.chr7:151970862C>A | c.940G>T | c.(940-942)Gcc>Tcc | p.A314S |
| LUAD | 7 | 151970865 | 151970865 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8620-01A-11D-2393-08 | TCGA-55-8620-10A-01D-2393-08 | g.chr7:151970865C>T | c.937G>A | c.(937-939)Gga>Aga | p.G313R |
| LUAD | 7 | 151970866 | 151970866 | + | Silent | SNP | T | T | A | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr7:151970866T>A | c.936A>T | c.(934-936)gcA>gcT | p.A312A |
| LUAD | 7 | 151970872 | 151970872 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-17-Z042-01A-01W-0746-08 | TCGA-17-Z042-11A-01W-0746-08 | g.chr7:151970872A>T | c.930T>A | c.(928-930)tgT>tgA | p.C310* |
| LUAD | 7 | 151970887 | 151970887 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr7:151970887C>A | c.915G>T | c.(913-915)atG>atT | p.M305I |
| LUAD | 7 | 151970887 | 151970887 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr7:151970887C>A | c.915G>T | c.(913-915)atG>atT | p.M305I |
| LUAD | 7 | 151970897 | 151970897 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4397-01A-01D-1265-08 | TCGA-05-4397-10A-01D-1265-08 | g.chr7:151970897C>A | c.905G>T | c.(904-906)tGt>tTt | p.C302F |
| LUAD | 7 | 152007149 | 152007149 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5946-01A-11D-1753-08 | TCGA-50-5946-10A-01D-1753-08 | g.chr7:152007149C>A | c.751G>T | c.(751-753)Gct>Tct | p.A251S |
| LUAD | 7 | 152008931 | 152008931 | + | Missense_Mutation | SNP | C | C | G | TCGA-49-6744-01A-11D-1855-08 | TCGA-49-6744-11A-01D-1855-08 | g.chr7:152008931C>G | c.691G>C | c.(691-693)Gtt>Ctt | p.V231L |
| LUAD | 7 | 152055719 | 152055719 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z030-01A-01W-0746-08 | TCGA-17-Z030-11A-01W-0746-08 | g.chr7:152055719C>A | c.203G>T | c.(202-204)aGc>aTc | p.S68I |
| LUAD | 7 | 152055725 | 152055725 | + | Missense_Mutation | SNP | T | T | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr7:152055725T>A | c.197A>T | c.(196-198)gAg>gTg | p.E66V |
| LUSC | 7 | 151842380 | 151842380 | + | Splice_Site | SNP | G | G | T | TCGA-70-6722-01A-11D-1817-08 | TCGA-70-6722-10A-01D-1817-08 | g.chr7:151842380G>T | c.14032C>A | c.(14032-14034)Ctt>Att | p.L4678I |
| LUSC | 7 | 151851428 | 151851428 | + | Silent | SNP | C | C | A | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr7:151851428C>A | c.12063G>T | c.(12061-12063)ctG>ctT | p.L4021L |
| LUSC | 7 | 151860104 | 151860104 | + | Missense_Mutation | SNP | G | G | A | TCGA-21-5786-01A-01D-1632-08 | TCGA-21-5786-10A-01D-1632-08 | g.chr7:151860104G>A | c.10558C>T | c.(10558-10560)Cca>Tca | p.P3520S |
| LUSC | 7 | 151860306 | 151860307 | + | Missense_Mutation | DNP | GG | GG | AA | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr7:151860306_151860307GG>AA | c.10355_10356CC>TT | c.(10354-10356)cCC>cTT | p.P3452L |
| LUSC | 7 | 151871312 | 151871312 | + | Missense_Mutation | SNP | G | G | A | TCGA-43-6143-01A-11D-1817-08 | TCGA-43-6143-11A-01D-1817-08 | g.chr7:151871312G>A | c.9278C>T | c.(9277-9279)aCa>aTa | p.T3093I |
| LUSC | 7 | 151874332 | 151874332 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2781-01A-01D-1522-08 | TCGA-66-2781-11A-01D-1522-08 | g.chr7:151874332C>G | c.8206G>C | c.(8206-8208)Gat>Cat | p.D2736H |
| LUSC | 7 | 151874635 | 151874635 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-39-5036-01A-01D-1441-08 | TCGA-39-5036-11A-01D-1441-08 | g.chr7:151874635G>A | c.7903C>T | c.(7903-7905)Caa>Taa | p.Q2635* |
| LUSC | 7 | 151874731 | 151874731 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-34-5231-01A-21D-1817-08 | TCGA-34-5231-10A-01D-1817-08 | g.chr7:151874731T>A | c.7807A>T | c.(7807-7809)Aga>Tga | p.R2603* |
| LUSC | 7 | 151878026 | 151878026 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-34-5231-01A-21D-1817-08 | TCGA-34-5231-10A-01D-1817-08 | g.chr7:151878026T>A | c.6919A>T | c.(6919-6921)Aga>Tga | p.R2307* |
| LUSC | 7 | 151878701 | 151878701 | + | Missense_Mutation | SNP | T | T | C | TCGA-46-3768-01A-01D-0983-08 | TCGA-46-3768-10A-01D-0983-08 | g.chr7:151878701T>C | c.6244A>G | c.(6244-6246)Ata>Gta | p.I2082V |
| LUSC | 7 | 151878809 | 151878809 | + | Missense_Mutation | SNP | G | G | T | TCGA-39-5029-01A-01D-1441-08 | TCGA-39-5029-11A-01D-1441-08 | g.chr7:151878809G>T | c.6136C>A | c.(6136-6138)Cca>Aca | p.P2046T |
| LUSC | 7 | 151879119 | 151879119 | + | Silent | SNP | T | T | C | TCGA-34-5234-01A-01D-1632-08 | TCGA-34-5234-10A-01D-1632-08 | g.chr7:151879119T>C | c.5826A>G | c.(5824-5826)acA>acG | p.T1942T |
| LUSC | 7 | 151879142 | 151879142 | + | Missense_Mutation | SNP | G | G | A | TCGA-66-2765-01A-01D-1522-08 | TCGA-66-2765-11A-01D-1522-08 | g.chr7:151879142G>A | c.5803C>T | c.(5803-5805)Ccc>Tcc | p.P1935S |
| LUSC | 7 | 151879574 | 151879574 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-34-2600-01A-01D-1522-08 | TCGA-34-2600-11A-01D-1522-08 | g.chr7:151879574G>A | c.5371C>T | c.(5371-5373)Cag>Tag | p.Q1791* |
| LUSC | 7 | 151880070 | 151880070 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-22-5473-01A-01D-1632-08 | TCGA-22-5473-11A-11D-1632-08 | g.chr7:151880070T>A | c.5254A>T | c.(5254-5256)Aaa>Taa | p.K1752* |
| LUSC | 7 | 151880108 | 151880108 | + | Missense_Mutation | SNP | G | G | T | TCGA-85-6561-01A-11D-1817-08 | TCGA-85-6561-10A-01D-1817-08 | g.chr7:151880108G>T | c.5216C>A | c.(5215-5217)cCt>cAt | p.P1739H |
| LUSC | 7 | 151884527 | 151884527 | + | Missense_Mutation | SNP | C | C | G | TCGA-34-5239-01A-21D-1817-08 | TCGA-34-5239-10A-01D-1817-08 | g.chr7:151884527C>G | c.4828G>C | c.(4828-4830)Gat>Cat | p.D1610H |
| LUSC | 7 | 151891602 | 151891602 | + | Missense_Mutation | SNP | T | T | C | TCGA-39-5037-01A-01D-1441-08 | TCGA-39-5037-11A-01D-1441-08 | g.chr7:151891602T>C | c.4430A>G | c.(4429-4431)aAt>aGt | p.N1477S |
| LUSC | 7 | 151893021 | 151893021 | + | Missense_Mutation | SNP | T | T | C | TCGA-60-2710-01A-01D-1522-08 | TCGA-60-2710-11A-01D-1522-08 | g.chr7:151893021T>C | c.4349A>G | c.(4348-4350)gAt>gGt | p.D1450G |
| LUSC | 7 | 151921142 | 151921142 | + | Missense_Mutation | SNP | T | T | C | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr7:151921142T>C | c.3281A>G | c.(3280-3282)tAt>tGt | p.Y1094C |
| LUSC | 7 | 151932935 | 151932935 | + | Silent | SNP | C | C | T | TCGA-33-6737-01A-11D-1817-08 | TCGA-33-6737-11A-01D-1817-08 | g.chr7:151932935C>T | c.2736G>A | c.(2734-2736)ctG>ctA | p.L912L |
| LUSC | 7 | 151932996 | 151932996 | + | Missense_Mutation | SNP | C | C | A | TCGA-33-4532-01A-01D-1267-08 | TCGA-33-4532-11A-01D-1267-08 | g.chr7:151932996C>A | c.2675G>T | c.(2674-2676)gGa>gTa | p.G892V |
| LUSC | 7 | 151945252 | 151945252 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2766-01A-01D-1522-08 | TCGA-66-2766-11A-01D-1522-08 | g.chr7:151945252C>G | c.2267G>C | c.(2266-2268)gGa>gCa | p.G756A |
| LUSC | 7 | 151946970 | 151946970 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr7:151946970G>C | c.1804C>G | c.(1804-1806)Ctt>Gtt | p.L602V |
| LUSC | 7 | 151960110 | 151960110 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2778-01A-02D-1522-08 | TCGA-66-2778-11A-01D-1522-08 | g.chr7:151960110C>G | c.1290G>C | c.(1288-1290)tgG>tgC | p.W430C |
| LUSC | 7 | 151962204 | 151962204 | + | Missense_Mutation | SNP | C | C | A | TCGA-56-1622-01A-01D-1521-08 | TCGA-56-1622-11A-01D-1521-08 | g.chr7:151962204C>A | c.1103G>T | c.(1102-1104)gGa>gTa | p.G368V |
| LUSC | 7 | 151962221 | 151962221 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-66-2789-01A-01D-0983-08 | TCGA-66-2789-11A-01D-0983-08 | g.chr7:151962221A>T | c.1086T>A | c.(1084-1086)tgT>tgA | p.C362* |
| LUSC | 7 | 151962224 | 151962224 | + | Silent | SNP | A | A | T | TCGA-63-5128-01A-01D-1441-08 | TCGA-63-5128-10A-01D-1441-08 | g.chr7:151962224A>T | c.1083T>A | c.(1081-1083)acT>acA | p.T361T |
| LUSC | 7 | 151962250 | 151962250 | + | Missense_Mutation | SNP | G | G | A | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr7:151962250G>A | c.1057C>T | c.(1057-1059)Ctc>Ttc | p.L353F |
| LUSC | 7 | 151970857 | 151970857 | + | Silent | SNP | G | G | A | TCGA-60-2726-01A-01D-1522-08 | TCGA-60-2726-11A-01D-1522-08 | g.chr7:151970857G>A | c.945C>T | c.(943-945)ggC>ggT | p.G315G |
| LUSC | 7 | 151970887 | 151970887 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2773-01A-01D-1267-08 | TCGA-66-2773-11A-01D-1267-08 | g.chr7:151970887C>G | c.915G>C | c.(913-915)atG>atC | p.M305I |
| LUSC | 7 | 152007083 | 152007083 | + | Missense_Mutation | SNP | C | C | A | TCGA-60-2709-01A-21D-1817-08 | TCGA-60-2709-11A-01D-1817-08 | g.chr7:152007083C>A | c.817G>T | c.(817-819)Gtg>Ttg | p.V273L |
| LUSC | 7 | 152009027 | 152009027 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-18-3417-01A-01D-1441-08 | TCGA-18-3417-11A-01D-1441-08 | g.chr7:152009027G>A | c.595C>T | c.(595-597)Cga>Tga | p.R199* |
| LUSC | 7 | 152055756 | 152055756 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-34-5928-01A-11D-1817-08 | TCGA-34-5928-10A-01D-1817-08 | g.chr7:152055756G>A | c.166C>T | c.(166-168)Cga>Tga | p.R56* |
| OV | 7 | 151843821 | 151843821 | + | Splice_Site | SNP | C | C | G | TCGA-24-1842-01A-01W-0639-09 | TCGA-24-1842-10A-01W-0639-09 | g.chr7:151843821C>G | | c.e53-1 | |
| OV | 7 | 151846077 | 151846077 | + | Missense_Mutation | SNP | G | G | T | TCGA-29-2434-01A-01D-1526-09 | TCGA-29-2434-10A-01D-1526-09 | g.chr7:151846077G>T | c.12935C>A | c.(12934-12936)gCt>gAt | p.A4312D |
| OV | 7 | 151848574 | 151848574 | + | Missense_Mutation | SNP | C | C | G | TCGA-36-2544-01A-01D-1526-09 | TCGA-36-2544-10A-01D-1526-09 | g.chr7:151848574C>G | c.12619G>C | c.(12619-12621)Gga>Cga | p.G4207R |
| OV | 7 | 151851206 | 151851206 | + | Silent | SNP | G | G | A | TCGA-10-0935-01A-03W-0421-09 | TCGA-10-0935-11A-01W-0421-09 | g.chr7:151851206G>A | c.12165C>T | c.(12163-12165)atC>atT | p.I4055I |
| OV | 7 | 151851443 | 151851443 | + | Silent | SNP | G | G | A | TCGA-13-1404-01A-01W-0494-09 | TCGA-13-1404-10A-01W-0495-09 | g.chr7:151851443G>A | c.12048C>T | c.(12046-12048)agC>agT | p.S4016S |
| OV | 7 | 151859421 | 151859421 | + | Silent | SNP | G | G | A | TCGA-04-1369-01A-02D-1526-09 | TCGA-04-1369-11A-01D-1526-09 | g.chr7:151859421G>A | c.11241C>T | c.(11239-11241)aaC>aaT | p.N3747N |
| OV | 7 | 151860167 | 151860167 | + | Missense_Mutation | SNP | G | G | C | TCGA-13-1497-01A-01W-0549-09 | TCGA-13-1497-10A-01W-0549-09 | g.chr7:151860167G>C | c.10495C>G | c.(10495-10497)Caa>Gaa | p.Q3499E |
| OV | 7 | 151860200 | 151860200 | + | Missense_Mutation | SNP | T | T | A | TCGA-29-1691-01A-01W-0633-09 | TCGA-29-1691-10A-01W-0633-09 | g.chr7:151860200T>A | c.10462A>T | c.(10462-10464)Ata>Tta | p.I3488L |
| OV | 7 | 151860622 | 151860622 | + | Missense_Mutation | SNP | T | T | C | TCGA-13-1403-01A-01W-0494-09 | TCGA-13-1403-10A-01W-0495-09 | g.chr7:151860622T>C | c.10040A>G | c.(10039-10041)aAt>aGt | p.N3347S |
| OV | 7 | 151873627 | 151873627 | + | Missense_Mutation | SNP | A | A | C | TCGA-04-1338-01A-01W-0484-10 | TCGA-04-1338-11A-01W-0485-10 | g.chr7:151873627A>C | c.8911T>G | c.(8911-8913)Tct>Gct | p.S2971A |
| OV | 7 | 151878644 | 151878644 | + | Missense_Mutation | SNP | G | G | C | TCGA-23-1110-01A-01D-0428-08 | TCGA-23-1110-10A-01D-0428-08 | g.chr7:151878644G>C | c.6301C>G | c.(6301-6303)Cca>Gca | p.P2101A |
| OV | 7 | 151879516 | 151879516 | + | Missense_Mutation | SNP | A | A | C | TCGA-31-1953-01A-01W-0699-08 | TCGA-31-1953-10A-01W-0699-08 | g.chr7:151879516A>C | c.5429T>G | c.(5428-5430)tTg>tGg | p.L1810W |
| OV | 7 | 151904429 | 151904429 | + | Missense_Mutation | SNP | C | C | A | TCGA-29-1707-01A-01W-0633-09 | TCGA-29-1707-10A-01W-0633-09 | g.chr7:151904429C>A | c.3797G>T | c.(3796-3798)gGa>gTa | p.G1266V |
| OV | 7 | 151917707 | 151917707 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-36-2542-01A-01D-1526-09 | TCGA-36-2542-10A-01D-1526-09 | g.chr7:151917707T>A | c.3613A>T | c.(3613-3615)Aaa>Taa | p.K1205* |
| OV | 7 | 151962210 | 151962210 | + | Missense_Mutation | SNP | T | T | G | TCGA-13-0755-01A-01W-0372-09 | TCGA-13-0755-10A-01W-0372-09 | g.chr7:151962210T>G | c.1097A>C | c.(1096-1098)tAt>tCt | p.Y366S |
| PAAD | 7 | 151842259 | 151842259 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151842259T>C | c.14153A>G | c.(14152-14154)cAt>cGt | p.H4718R |
| PAAD | 7 | 151842307 | 151842307 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151842307G>A | c.14105C>T | c.(14104-14106)gCc>gTc | p.A4702V |
| PAAD | 7 | 151845337 | 151845338 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-IB-7652-01A-11D-2154-08 | TCGA-IB-7652-10A-01D-2154-08 | g.chr7:151845337_151845338insA | c.13674_13675insT | c.(13672-13677)attggtfs | p.G4559fs |
| PAAD | 7 | 151846148 | 151846148 | + | Missense_Mutation | SNP | A | A | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151846148A>C | c.12864T>G | c.(12862-12864)gaT>gaG | p.D4288E |
| PAAD | 7 | 151856009 | 151856009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-HZ-A49I-01A-12D-A26I-08 | TCGA-HZ-A49I-10A-01D-A26I-08 | g.chr7:151856009delT | c.11609delA | c.(11608-11610)aagfs | p.K3870fs |
| PAAD | 7 | 151859602 | 151859602 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151859602C>T | c.11060G>A | c.(11059-11061)aGt>aAt | p.S3687N |
| PAAD | 7 | 151860794 | 151860794 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-LB-A7SX-01A-11D-A33T-08 | TCGA-LB-A7SX-10A-01D-A33W-08 | g.chr7:151860794delG | c.9868delC | c.(9868-9870)ctafs | p.L3290fs |
| PAAD | 7 | 151877209 | 151877209 | + | Silent | SNP | C | C | A | TCGA-IB-AAUS-01A-12D-A38G-08 | TCGA-IB-AAUS-10A-01D-A38J-08 | g.chr7:151877209C>A | c.7152G>T | c.(7150-7152)cgG>cgT | p.R2384R |
| PAAD | 7 | 151878240 | 151878240 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151878240C>A | c.6705G>T | c.(6703-6705)agG>agT | p.R2235S |
| PAAD | 7 | 151878356 | 151878356 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151878356G>A | c.6589C>T | c.(6589-6591)Cag>Tag | p.Q2197* |
| PAAD | 7 | 151878579 | 151878579 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151878579T>C | c.6366A>G | c.(6364-6366)atA>atG | p.I2122M |
| PAAD | 7 | 151878668 | 151878668 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151878668G>T | c.6277C>A | c.(6277-6279)Cca>Aca | p.P2093T |
| PAAD | 7 | 151879109 | 151879109 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151879109G>T | c.5836C>A | c.(5836-5838)Cca>Aca | p.P1946T |
| PAAD | 7 | 151884809 | 151884809 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151884809G>A | c.4784C>T | c.(4783-4785)cCt>cTt | p.P1595L |
| PAAD | 7 | 151884856 | 151884856 | + | Silent | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151884856A>G | c.4737T>C | c.(4735-4737)ccT>ccC | p.P1579P |
| PAAD | 7 | 151891109 | 151891109 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151891109G>A | c.4645C>T | c.(4645-4647)Cca>Tca | p.P1549S |
| PAAD | 7 | 151917775 | 151917775 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-FB-AAQ6-01A-11D-A40W-08 | TCGA-FB-AAQ6-11A-11D-A40W-08 | g.chr7:151917775G>C | c.3545C>G | c.(3544-3546)tCa>tGa | p.S1182* |
| PAAD | 7 | 151921103 | 151921103 | + | Missense_Mutation | SNP | T | T | C | TCGA-HZ-A77O-01A-11D-A33T-08 | TCGA-HZ-A77O-10A-01D-A33W-08 | g.chr7:151921103T>C | c.3320A>G | c.(3319-3321)gAt>gGt | p.D1107G |
| PAAD | 7 | 151921114 | 151921114 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-HZ-A77P-01A-11D-A33T-08 | TCGA-HZ-A77P-10A-01D-A33W-08 | g.chr7:151921114A>T | c.3309T>A | c.(3307-3309)tgT>tgA | p.C1103* |
| PAAD | 7 | 151921149 | 151921149 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-US-A77J-01A-11D-A32N-08 | TCGA-US-A77J-11A-11D-A32N-08 | g.chr7:151921149G>A | c.3274C>T | c.(3274-3276)Cga>Tga | p.R1092* |
| PAAD | 7 | 151932919 | 151932919 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151932919C>A | c.2752G>T | c.(2752-2754)Gct>Tct | p.A918S |
| PAAD | 7 | 151933008 | 151933008 | + | Missense_Mutation | SNP | G | G | A | TCGA-FB-AAQ0-01A-31D-A40W-08 | TCGA-FB-AAQ0-11A-11D-A40W-08 | g.chr7:151933008G>A | c.2663C>T | c.(2662-2664)tCt>tTt | p.S888F |
| PAAD | 7 | 151945554 | 151945554 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151945554G>A | c.1965C>T | c.(1963-1965)gtC>gtT | p.V655V |
| PAAD | 7 | 151945602 | 151945602 | + | Silent | SNP | G | G | A | TCGA-IB-A6UG-01A-32D-A33T-08 | TCGA-IB-A6UG-10A-01D-A33W-08 | g.chr7:151945602G>A | c.1917C>T | c.(1915-1917)ggC>ggT | p.G639G |
| PAAD | 7 | 151962253 | 151962253 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151962253C>A | c.1054G>T | c.(1054-1056)Gac>Tac | p.D352Y |
| PAAD | 7 | 151970792 | 151970792 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr7:151970792C>A | c.1010G>T | c.(1009-1011)aGa>aTa | p.R337I |
| PCPG | 7 | 151864310 | 151864310 | + | Missense_Mutation | SNP | C | C | T | TCGA-S7-A7WV-01A-11D-A35I-08 | TCGA-S7-A7WV-10A-01D-A35G-08 | g.chr7:151864310C>T | c.9671G>A | c.(9670-9672)cGt>cAt | p.R3224H |
| PCPG | 7 | 151933008 | 151933008 | + | Missense_Mutation | SNP | G | G | A | TCGA-WB-A81A-01A-11D-A35I-08 | TCGA-WB-A81A-10A-01D-A35G-08 | g.chr7:151933008G>A | c.2663C>T | c.(2662-2664)tCt>tTt | p.S888F |
| PCPG | 7 | 151945602 | 151945602 | + | Silent | SNP | G | G | A | TCGA-SP-A6QD-01A-12D-A35I-08 | TCGA-SP-A6QD-10A-01D-A35G-08 | g.chr7:151945602G>A | c.1917C>T | c.(1915-1917)ggC>ggT | p.G639G |
| PCPG | 7 | 152027726 | 152027726 | + | Missense_Mutation | SNP | C | C | T | TCGA-QR-A6GT-01A-11D-A35D-08 | TCGA-QR-A6GT-10A-01D-A35B-08 | g.chr7:152027726C>T | c.349G>A | c.(349-351)Gca>Aca | p.A117T |
| PRAD | 7 | 151836271 | 151836271 | + | Splice_Site | SNP | C | C | G | TCGA-KK-A8I9-01A-11D-A364-08 | TCGA-KK-A8I9-11A-11D-A362-08 | g.chr7:151836271C>G | c.14534G>C | c.(14533-14535)aGg>aCg | p.R4845T |
| PRAD | 7 | 151836804 | 151836804 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr7:151836804G>A | c.14416C>T | c.(14416-14418)Cga>Tga | p.R4806* |
| PRAD | 7 | 151836813 | 151836813 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-J4-A83L-01A-11D-A34U-08 | TCGA-J4-A83L-10A-01D-A34X-08 | g.chr7:151836813delT | c.14407delA | c.(14407-14409)actfs | p.T4803fs |
| PRAD | 7 | 151845543 | 151845555 | + | Frame_Shift_Del | DEL | TTAATGGCGCAAG | TTAATGGCGCAAG | - | TCGA-KK-A8IL-01A-11D-A364-08 | TCGA-KK-A8IL-11A-11D-A362-08 | g.chr7:151845543_151845555delTTAATGGCGCAAG | c.13457_13469delCTTGCGCCATTAA | c.(13456-13470)acttgcgccattaaafs | p.TCAIK4486fs |
| PRAD | 7 | 151845693 | 151845693 | + | Missense_Mutation | SNP | T | T | C | TCGA-EJ-5524-01A-01D-1576-08 | TCGA-EJ-5524-10A-01D-1577-08 | g.chr7:151845693T>C | c.13319A>G | c.(13318-13320)tAt>tGt | p.Y4440C |
| PRAD | 7 | 151845693 | 151845693 | + | Missense_Mutation | SNP | T | T | C | TCGA-YL-A9WH-01A-11D-A377-08 | TCGA-YL-A9WH-10A-01D-A37A-08 | g.chr7:151845693T>C | c.13319A>G | c.(13318-13320)tAt>tGt | p.Y4440C |
| PRAD | 7 | 151845758 | 151845758 | + | Missense_Mutation | SNP | C | C | A | TCGA-CH-5752-01A-11D-1576-08 | TCGA-CH-5752-10A-01D-1576-08 | g.chr7:151845758C>A | c.13254G>T | c.(13252-13254)agG>agT | p.R4418S |
| PRAD | 7 | 151846165 | 151846165 | + | Missense_Mutation | SNP | T | T | G | TCGA-VP-AA1N-01A-31D-A41K-08 | TCGA-VP-AA1N-10A-01D-A41N-08 | g.chr7:151846165T>G | c.12847A>C | c.(12847-12849)Aac>Cac | p.N4283H |
| PRAD | 7 | 151853293 | 151853293 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CH-5752-01A-11D-1576-08 | TCGA-CH-5752-10A-01D-1576-08 | g.chr7:151853293delC | c.11809delG | c.(11809-11811)gaafs | p.E3937fs |
| PRAD | 7 | 151855999 | 151855999 | + | Silent | SNP | C | C | T | TCGA-J9-A8CL-01A-11D-A34U-08 | TCGA-J9-A8CL-10A-01D-A34X-08 | g.chr7:151855999C>T | c.11619G>A | c.(11617-11619)gaG>gaA | p.E3873E |
| PRAD | 7 | 151859486 | 151859487 | + | Frame_Shift_Ins | INS | - | - | TT | TCGA-CH-5752-01A-11D-1576-08 | TCGA-CH-5752-10A-01D-1576-08 | g.chr7:151859486_151859487insTT | c.11175_11176insAA | c.(11173-11178)acagagfs | p.E3726fs |
| PRAD | 7 | 151860195 | 151860195 | + | Silent | SNP | T | T | C | TCGA-ZG-A8QY-01A-11D-A377-08 | TCGA-ZG-A8QY-10A-01D-A37A-08 | g.chr7:151860195T>C | c.10467A>G | c.(10465-10467)caA>caG | p.Q3489Q |
| PRAD | 7 | 151860463 | 151860463 | + | Missense_Mutation | SNP | C | C | T | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr7:151860463C>T | c.10199G>A | c.(10198-10200)cGt>cAt | p.R3400H |
| PRAD | 7 | 151860707 | 151860707 | + | Missense_Mutation | SNP | C | C | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr7:151860707C>A | c.9955G>T | c.(9955-9957)Gtt>Ttt | p.V3319F |
| PRAD | 7 | 151864240 | 151864249 | + | Frame_Shift_Del | DEL | CTGTTTCTGA | CTGTTTCTGA | - | TCGA-YL-A8SR-01B-11D-A377-08 | TCGA-YL-A8SR-10A-01D-A37A-08 | g.chr7:151864240_151864249delCTGTTTCTGA | c.9732_9741delTCAGAAACAG | c.(9730-9741)gttcagaaacagfs | p.VQKQ3244fs |
| PRAD | 7 | 151873437 | 151873437 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CH-5752-01A-11D-1576-08 | TCGA-CH-5752-10A-01D-1576-08 | g.chr7:151873437delG | c.9101delC | c.(9100-9102)cctfs | p.P3034fs |
| PRAD | 7 | 151873585 | 151873585 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EJ-A7NH-01A-12D-A33T-08 | TCGA-EJ-A7NH-10A-01D-A33W-08 | g.chr7:151873585G>A | c.8953C>T | c.(8953-8955)Cag>Tag | p.Q2985* |
| PRAD | 7 | 151874059 | 151874059 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr7:151874059G>A | c.8479C>T | c.(8479-8481)Ctg>Ttg | p.L2827L |
| PRAD | 7 | 151874265 | 151874265 | + | Missense_Mutation | SNP | G | G | A | TCGA-V1-A9OX-01A-11D-A41K-08 | TCGA-V1-A9OX-10A-01D-A41N-08 | g.chr7:151874265G>A | c.8273C>T | c.(8272-8274)gCa>gTa | p.A2758V |
| PRAD | 7 | 151877140 | 151877140 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-ZG-A9KY-01A-11D-A41K-08 | TCGA-ZG-A9KY-10A-01D-A41N-08 | g.chr7:151877140delC | c.7221delG | c.(7219-7221)gggfs | p.G2407fs |
| PRAD | 7 | 151877201 | 151877201 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-KK-A8II-01A-11D-A364-08 | TCGA-KK-A8II-11A-11D-A362-08 | g.chr7:151877201A>C | c.7160T>G | c.(7159-7161)tTa>tGa | p.L2387* |
| PRAD | 7 | 151878020 | 151878020 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-KK-A8IF-01A-11D-A364-08 | TCGA-KK-A8IF-11A-11D-A362-08 | g.chr7:151878020G>A | c.6925C>T | c.(6925-6927)Cag>Tag | p.Q2309* |
| PRAD | 7 | 151878166 | 151878166 | + | Missense_Mutation | SNP | G | G | C | TCGA-HC-7817-01B-11D-A29Q-08 | TCGA-HC-7817-10A-01D-A29Q-08 | g.chr7:151878166G>C | c.6779C>G | c.(6778-6780)gCt>gGt | p.A2260G |
| PRAD | 7 | 151879016 | 151879016 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-J4-AAU2-01A-11D-A41K-08 | TCGA-J4-AAU2-10A-01D-A41N-08 | g.chr7:151879016delG | c.5929delC | c.(5929-5931)caafs | p.Q1977fs |
| PRAD | 7 | 151879308 | 151879308 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr7:151879308C>T | c.5637G>A | c.(5635-5637)ccG>ccA | p.P1879P |
| PRAD | 7 | 151879331 | 151879331 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EJ-7123-01A-11D-1961-08 | TCGA-EJ-7123-10A-01D-1961-08 | g.chr7:151879331G>A | c.5614C>T | c.(5614-5616)Cag>Tag | p.Q1872* |
| PRAD | 7 | 151884803 | 151884803 | + | Missense_Mutation | SNP | G | G | A | TCGA-VP-A875-01A-31D-A34U-08 | TCGA-VP-A875-10A-01D-A34X-08 | g.chr7:151884803G>A | c.4790C>T | c.(4789-4791)gCc>gTc | p.A1597V |
| PRAD | 7 | 151904428 | 151904429 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-G9-6373-01A-11D-1786-08 | TCGA-G9-6373-10A-01D-1786-08 | g.chr7:151904428_151904429insA | c.3797_3798insT | c.(3796-3798)ggafs | p.G1266fs |
| PRAD | 7 | 151917819 | 151917819 | + | Splice_Site | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr7:151917819G>A | c.3501C>T | c.(3499-3501)gaC>gaT | p.D1167D |
| PRAD | 7 | 151921189 | 151921189 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr7:151921189G>A | c.3234C>T | c.(3232-3234)tgC>tgT | p.C1078C |
| PRAD | 7 | 151921662 | 151921662 | + | Missense_Mutation | SNP | C | C | G | TCGA-KC-A7FD-01A-11D-A33T-08 | TCGA-KC-A7FD-10A-01D-A33W-08 | g.chr7:151921662C>G | c.3016G>C | c.(3016-3018)Gag>Cag | p.E1006Q |
| PRAD | 7 | 151932975 | 151932975 | + | Missense_Mutation | SNP | G | G | A | TCGA-YL-A9WL-01A-11D-A41K-08 | TCGA-YL-A9WL-10A-01D-A41N-08 | g.chr7:151932975G>A | c.2696C>T | c.(2695-2697)gCa>gTa | p.A899V |
| PRAD | 7 | 151932988 | 151932988 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-EJ-5519-01A-01D-1576-08 | TCGA-EJ-5519-10A-01D-1577-08 | g.chr7:151932988T>A | c.2683A>T | c.(2683-2685)Aga>Tga | p.R895* |
| PRAD | 7 | 151935890 | 151935890 | + | Missense_Mutation | SNP | T | T | C | TCGA-KK-A59X-01A-11D-A29Q-08 | TCGA-KK-A59X-11A-21D-A29Q-08 | g.chr7:151935890T>C | c.2554A>G | c.(2554-2556)Aca>Gca | p.T852A |
| PRAD | 7 | 151945083 | 151945083 | + | Missense_Mutation | SNP | C | C | T | TCGA-V1-A9OT-01A-11D-A41K-08 | TCGA-V1-A9OT-10A-01D-A41N-08 | g.chr7:151945083C>T | c.2436G>A | c.(2434-2436)atG>atA | p.M812I |
| PRAD | 7 | 151945553 | 151945553 | + | Missense_Mutation | SNP | C | C | T | TCGA-HC-A4ZV-01A-11D-A26M-08 | TCGA-HC-A4ZV-10A-01D-A26K-08 | g.chr7:151945553C>T | c.1966G>A | c.(1966-1968)Gtt>Att | p.V656I |
| PRAD | 7 | 151962178 | 151962178 | + | Missense_Mutation | SNP | G | G | T | TCGA-VN-A88L-01A-11D-A34U-08 | TCGA-VN-A88L-10A-01D-A34X-08 | g.chr7:151962178G>T | c.1129C>A | c.(1129-1131)Cca>Aca | p.P377T |
| PRAD | 7 | 151970809 | 151970809 | + | Silent | SNP | A | A | T | TCGA-HC-A6AL-01A-11D-A30E-08 | TCGA-HC-A6AL-10A-01D-A30H-08 | g.chr7:151970809A>T | c.993T>A | c.(991-993)atT>atA | p.I331I |
| PRAD | 7 | 151970814 | 151970814 | + | Missense_Mutation | SNP | G | G | T | TCGA-HI-7170-01A-11D-2114-08 | TCGA-HI-7170-10A-01D-2115-08 | g.chr7:151970814G>T | c.988C>A | c.(988-990)Cac>Aac | p.H330N |
| PRAD | 7 | 152012422 | 152012424 | + | Splice_Site | DEL | CAC | CAC | - | TCGA-HC-7233-01A-11D-2114-08 | TCGA-HC-7233-10A-01D-2115-08 | g.chr7:152012422_152012424delCAC | c.390_391delGTG | c.(388-393)aggtga>agga | p.*131del |
| READ | 7 | 151845973 | 151845973 | + | Missense_Mutation | SNP | G | G | T | TCGA-EF-5830-01A-01D-1657-10 | TCGA-EF-5830-10A-01D-1657-10 | g.chr7:151845973G>T | c.13039C>A | c.(13039-13041)Ccg>Acg | p.P4347T |
| READ | 7 | 151859570 | 151859570 | + | Missense_Mutation | SNP | T | T | C | TCGA-AG-3732-01A-11D-1657-10 | TCGA-AG-3732-11A-01D-1657-10 | g.chr7:151859570T>C | c.11092A>G | c.(11092-11094)Acg>Gcg | p.T3698A |
| READ | 7 | 151859627 | 151859627 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A036-01A-12W-A096-10 | TCGA-AG-A036-11A-11W-A096-10 | g.chr7:151859627C>T | c.11035G>A | c.(11035-11037)Gaa>Aaa | p.E3679K |
| READ | 7 | 151873758 | 151873758 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151873758G>A | c.8780C>T | c.(8779-8781)tCt>tTt | p.S2927F |
| READ | 7 | 151874515 | 151874515 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151874515A>C | c.8023T>G | c.(8023-8025)Tta>Gta | p.L2675V |
| READ | 7 | 151879124 | 151879124 | + | Missense_Mutation | SNP | T | T | C | TCGA-AH-6549-01A-11D-1826-10 | TCGA-AH-6549-10A-01D-1826-10 | g.chr7:151879124T>C | c.5821A>G | c.(5821-5823)Aca>Gca | p.T1941A |
| READ | 7 | 151880121 | 151880121 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151880121G>A | c.5203C>T | c.(5203-5205)Ctt>Ttt | p.L1735F |
| READ | 7 | 151884543 | 151884543 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151884543A>C | c.4812T>G | c.(4810-4812)ttT>ttG | p.F1604L |
| READ | 7 | 151945455 | 151945455 | + | Silent | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr7:151945455G>T | c.2064C>A | c.(2062-2064)gtC>gtA | p.V688V |
| READ | 7 | 151960154 | 151960155 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-DY-A1DF-01A-11D-A152-10 | TCGA-DY-A1DF-10A-01D-A152-10 | g.chr7:151960154_151960155insC | c.1245_1246insG | c.(1243-1248)acttttfs | p.F416fs |
| READ | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | G | TCGA-AH-6644-01A-21D-1826-10 | TCGA-AH-6644-10A-01D-1826-10 | g.chr7:151962211A>G | c.1096T>C | c.(1096-1098)Tat>Cat | p.Y366H |
| READ | 7 | 151962211 | 151962211 | + | Missense_Mutation | SNP | A | A | G | TCGA-DC-6681-01A-11D-1826-10 | TCGA-DC-6681-10A-01D-1826-10 | g.chr7:151962211A>G | c.1096T>C | c.(1096-1098)Tat>Cat | p.Y366H |
| READ | 7 | 151962266 | 151962266 | + | Silent | SNP | G | G | A | TCGA-F5-6465-01A-11D-1733-10 | TCGA-F5-6465-10A-01D-1733-10 | g.chr7:151962266G>A | c.1041C>T | c.(1039-1041)tgC>tgT | p.C347C |
| SARC | 7 | 151833996 | 151833996 | + | Missense_Mutation | SNP | T | T | G | TCGA-DX-AB3B-01A-11D-A417-09 | TCGA-DX-AB3B-10A-01D-A41A-09 | g.chr7:151833996T>G | c.14657A>C | c.(14656-14658)tAt>tCt | p.Y4886S |
| SARC | 7 | 151842337 | 151842337 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-QQ-A5VB-01A-11D-A36J-09 | TCGA-QQ-A5VB-11B-11D-A36M-09 | g.chr7:151842337delC | c.14075delG | c.(14074-14076)ggcfs | p.G4692fs |
| SARC | 7 | 151871280 | 151871280 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr7:151871280G>A | c.9310C>T | c.(9310-9312)Ctt>Ttt | p.L3104F |
| SARC | 7 | 151874147 | 151874148 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-QQ-A5VB-01A-11D-A36J-09 | TCGA-QQ-A5VB-11B-11D-A36M-09 | g.chr7:151874147_151874148insT | c.8390_8391insA | c.(8389-8391)aagfs | p.K2797fs |
| SARC | 7 | 151900117 | 151900117 | + | Missense_Mutation | SNP | C | C | T | TCGA-QQ-A5VA-01A-12D-A32I-09 | TCGA-QQ-A5VA-11A-11D-A32I-09 | g.chr7:151900117C>T | c.3994G>A | c.(3994-3996)Gat>Aat | p.D1332N |
| SARC | 7 | 151962269 | 151962269 | + | Silent | SNP | C | C | T | TCGA-DX-AB30-01A-11D-A38Z-09 | TCGA-DX-AB30-10A-01D-A38Z-09 | g.chr7:151962269C>T | c.1038G>A | c.(1036-1038)gtG>gtA | p.V346V |
| SKCM | 7 | 151835975 | 151835975 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:151835975G>A | c.14549C>T | c.(14548-14550)tCg>tTg | p.S4850L |
| SKCM | 7 | 151835979 | 151835979 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZW-06A-12D-A197-08 | TCGA-FS-A1ZW-10A-01D-A199-08 | g.chr7:151835979G>A | c.14545C>T | c.(14545-14547)Cat>Tat | p.H4849Y |
| SKCM | 7 | 151841956 | 151841956 | + | Missense_Mutation | SNP | A | A | C | TCGA-EE-A2GU-06A-11D-A196-08 | TCGA-EE-A2GU-10A-01D-A198-08 | g.chr7:151841956A>C | c.14185T>G | c.(14185-14187)Tta>Gta | p.L4729V |
| SKCM | 7 | 151845398 | 151845398 | + | Silent | SNP | G | G | A | TCGA-ER-A19W-06A-41D-A23B-08 | TCGA-ER-A19W-10A-01D-A23B-08 | g.chr7:151845398G>A | c.13614C>T | c.(13612-13614)atC>atT | p.I4538I |
| SKCM | 7 | 151845611 | 151845611 | + | Silent | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr7:151845611C>T | c.13401G>A | c.(13399-13401)aaG>aaA | p.K4467K |
| SKCM | 7 | 151845931 | 151845931 | + | Missense_Mutation | SNP | T | T | A | TCGA-FS-A4F0-06A-11D-A24R-08 | TCGA-FS-A4F0-10A-01D-A24R-08 | g.chr7:151845931T>A | c.13081A>T | c.(13081-13083)Agc>Tgc | p.S4361C |
| SKCM | 7 | 151845993 | 151845993 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A4F0-06A-11D-A24R-08 | TCGA-FS-A4F0-10A-01D-A24R-08 | g.chr7:151845993C>T | c.13019G>A | c.(13018-13020)gGt>gAt | p.G4340D |
| SKCM | 7 | 151846058 | 151846058 | + | Silent | SNP | G | G | A | TCGA-FS-A4F5-06A-11D-A25O-08 | TCGA-FS-A4F5-10B-01D-A25O-08 | g.chr7:151846058G>A | c.12954C>T | c.(12952-12954)gtC>gtT | p.V4318V |
| SKCM | 7 | 151849883 | 151849883 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr7:151849883G>A | c.12433C>T | c.(12433-12435)Cgt>Tgt | p.R4145C |
| SKCM | 7 | 151849907 | 151849907 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZE-06A-11D-A197-08 | TCGA-FS-A1ZE-10A-01D-A199-08 | g.chr7:151849907C>T | c.12409G>A | c.(12409-12411)Gag>Aag | p.E4137K |
| SKCM | 7 | 151849908 | 151849908 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZE-06A-11D-A197-08 | TCGA-FS-A1ZE-10A-01D-A199-08 | g.chr7:151849908C>T | c.12408G>A | c.(12406-12408)ttG>ttA | p.L4136L |
| SKCM | 7 | 151851144 | 151851144 | + | Missense_Mutation | SNP | C | C | G | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr7:151851144C>G | c.12227G>C | c.(12226-12228)aGa>aCa | p.R4076T |
| SKCM | 7 | 151851222 | 151851222 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A17X-06A-11D-A197-08 | TCGA-EE-A17X-10A-01D-A199-08 | g.chr7:151851222G>A | c.12149C>T | c.(12148-12150)tCa>tTa | p.S4050L |
| SKCM | 7 | 151851387 | 151851387 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr7:151851387G>A | c.12104C>T | c.(12103-12105)cCc>cTc | p.P4035L |
| SKCM | 7 | 151851430 | 151851430 | + | Silent | SNP | G | G | A | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr7:151851430G>A | c.12061C>T | c.(12061-12063)Ctg>Ttg | p.L4021L |
| SKCM | 7 | 151851483 | 151851483 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AB-06A-11D-A196-08 | TCGA-EE-A3AB-10A-01D-A198-08 | g.chr7:151851483G>A | c.12008C>T | c.(12007-12009)cCc>cTc | p.P4003L |
| SKCM | 7 | 151851484 | 151851484 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AB-06A-11D-A196-08 | TCGA-EE-A3AB-10A-01D-A198-08 | g.chr7:151851484G>A | c.12007C>T | c.(12007-12009)Ccc>Tcc | p.P4003S |
| SKCM | 7 | 151855960 | 151855960 | + | Silent | SNP | G | G | A | TCGA-D3-A5GS-06A-11D-A27K-08 | TCGA-D3-A5GS-10A-01D-A27N-08 | g.chr7:151855960G>A | c.11658C>T | c.(11656-11658)acC>acT | p.T3886T |
| SKCM | 7 | 151859299 | 151859299 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr7:151859299G>A | c.11363C>T | c.(11362-11364)tCt>tTt | p.S3788F |
| SKCM | 7 | 151859582 | 151859582 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr7:151859582G>A | c.11080C>T | c.(11080-11082)Cca>Tca | p.P3694S |
| SKCM | 7 | 151860080 | 151860080 | + | Missense_Mutation | SNP | T | T | G | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr7:151860080T>G | c.10582A>C | c.(10582-10584)Aat>Cat | p.N3528H |
| SKCM | 7 | 151860685 | 151860685 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZC-06A-11D-A197-08 | TCGA-FS-A1ZC-10A-01D-A199-08 | g.chr7:151860685G>A | c.9977C>T | c.(9976-9978)cCt>cTt | p.P3326L |
| SKCM | 7 | 151873959 | 151873959 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr7:151873959G>T | c.8579C>A | c.(8578-8580)tCa>tAa | p.S2860* |
| SKCM | 7 | 151874081 | 151874081 | + | Silent | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr7:151874081G>A | c.8457C>T | c.(8455-8457)acC>acT | p.T2819T |
| SKCM | 7 | 151874091 | 151874091 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr7:151874091G>A | c.8447C>T | c.(8446-8448)tCc>tTc | p.S2816F |
| SKCM | 7 | 151876967 | 151876967 | + | Missense_Mutation | SNP | G | G | A | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr7:151876967G>A | c.7394C>T | c.(7393-7395)cCc>cTc | p.P2465L |
| SKCM | 7 | 151877015 | 151877015 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZA-06A-11D-A197-08 | TCGA-FS-A1ZA-10A-01D-A199-08 | g.chr7:151877015G>A | c.7346C>T | c.(7345-7347)cCt>cTt | p.P2449L |
| SKCM | 7 | 151877025 | 151877025 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr7:151877025G>A | c.7336C>T | c.(7336-7338)Cct>Tct | p.P2446S |
| SKCM | 7 | 151877065 | 151877065 | + | Silent | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr7:151877065G>A | c.7296C>T | c.(7294-7296)ttC>ttT | p.F2432F |
| SKCM | 7 | 151877125 | 151877125 | + | Silent | SNP | G | G | C | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr7:151877125G>C | c.7236C>G | c.(7234-7236)ccC>ccG | p.P2412P |
| SKCM | 7 | 151878029 | 151878029 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:151878029G>A | c.6916C>T | c.(6916-6918)Cca>Tca | p.P2306S |
| SKCM | 7 | 151878118 | 151878118 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr7:151878118G>A | c.6827C>T | c.(6826-6828)cCt>cTt | p.P2276L |
| SKCM | 7 | 151878414 | 151878414 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr7:151878414C>T | c.6531G>A | c.(6529-6531)caG>caA | p.Q2177Q |
| SKCM | 7 | 151879201 | 151879201 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr7:151879201G>A | c.5744C>T | c.(5743-5745)tCc>tTc | p.S1915F |
| SKCM | 7 | 151879490 | 151879490 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr7:151879490T>A | c.5455A>T | c.(5455-5457)Atg>Ttg | p.M1819L |
| SKCM | 7 | 151880115 | 151880115 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr7:151880115T>C | c.5209A>G | c.(5209-5211)Aaa>Gaa | p.K1737E |
| SKCM | 7 | 151880143 | 151880143 | + | Silent | SNP | G | G | C | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr7:151880143G>C | c.5181C>G | c.(5179-5181)ccC>ccG | p.P1727P |
| SKCM | 7 | 151884350 | 151884350 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr7:151884350G>A | c.5005C>T | c.(5005-5007)Cct>Tct | p.P1669S |
| SKCM | 7 | 151884415 | 151884415 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr7:151884415T>C | c.4940A>G | c.(4939-4941)gAa>gGa | p.E1647G |
| SKCM | 7 | 151884809 | 151884809 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr7:151884809G>A | c.4784C>T | c.(4783-4785)cCt>cTt | p.P1595L |
| SKCM | 7 | 151891141 | 151891141 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-EE-A17Z-06A-11D-A196-08 | TCGA-EE-A17Z-10A-01D-A198-08 | g.chr7:151891141A>T | c.4613T>A | c.(4612-4614)tTg>tAg | p.L1538* |
| SKCM | 7 | 151891543 | 151891543 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:151891543C>T | c.4489G>A | c.(4489-4491)Gac>Aac | p.D1497N |
| SKCM | 7 | 151900066 | 151900066 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-D3-A1QA-06A-11D-A196-08 | TCGA-D3-A1QA-10A-01D-A198-08 | g.chr7:151900066G>A | c.4045C>T | c.(4045-4047)Cga>Tga | p.R1349* |
| SKCM | 7 | 151917674 | 151917674 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZQ-06A-11D-A197-08 | TCGA-FS-A1ZQ-10A-01D-A199-08 | g.chr7:151917674C>T | c.3646G>A | c.(3646-3648)Gtc>Atc | p.V1216I |
| SKCM | 7 | 151927040 | 151927040 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:151927040G>A | c.2944C>T | c.(2944-2946)Cag>Tag | p.Q982* |
| SKCM | 7 | 151927079 | 151927079 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr7:151927079C>T | c.2905G>A | c.(2905-2907)Gga>Aga | p.G969R |
| SKCM | 7 | 151945055 | 151945055 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr7:151945055T>C | c.2464A>G | c.(2464-2466)Aaa>Gaa | p.K822E |
| SKCM | 7 | 151945093 | 151945093 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr7:151945093C>T | c.2426G>A | c.(2425-2427)gGa>gAa | p.G809E |
| SKCM | 7 | 151945102 | 151945102 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr7:151945102G>A | c.2417C>T | c.(2416-2418)tCc>tTc | p.S806F |
| SKCM | 7 | 151945102 | 151945102 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A199-06A-11D-A197-08 | TCGA-ER-A199-10A-01D-A199-08 | g.chr7:151945102G>A | c.2417C>T | c.(2416-2418)tCc>tTc | p.S806F |
| SKCM | 7 | 151945118 | 151945118 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:151945118G>A | c.2401C>T | c.(2401-2403)Cct>Tct | p.P801S |
| SKCM | 7 | 151945143 | 151945143 | + | Silent | SNP | A | A | G | TCGA-RP-A695-06A-11D-A30X-08 | TCGA-RP-A695-10A-01D-A30X-08 | g.chr7:151945143A>G | c.2376T>C | c.(2374-2376)ccT>ccC | p.P792P |
| SKCM | 7 | 151945151 | 151945151 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3C6-06A-12D-A196-08 | TCGA-D3-A3C6-10A-01D-A198-08 | g.chr7:151945151C>T | c.2368G>A | c.(2368-2370)Gac>Aac | p.D790N |
| SKCM | 7 | 151945151 | 151945151 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr7:151945151C>T | c.2368G>A | c.(2368-2370)Gac>Aac | p.D790N |
| SKCM | 7 | 151945426 | 151945426 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:151945426G>A | c.2093C>T | c.(2092-2094)aCc>aTc | p.T698I |
| SKCM | 7 | 151960106 | 151960106 | + | Missense_Mutation | SNP | A | A | G | TCGA-DA-A1I5-06A-11D-A197-08 | TCGA-DA-A1I5-10A-01D-A199-08 | g.chr7:151960106A>G | c.1294T>C | c.(1294-1296)Tgc>Cgc | p.C432R |
| SKCM | 7 | 151962153 | 151962153 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr7:151962153C>T | c.1154G>A | c.(1153-1155)tGt>tAt | p.C385Y |
| SKCM | 7 | 151962163 | 151962163 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1Q8-06A-11D-A19A-08 | TCGA-D3-A1Q8-10A-01D-A19A-08 | g.chr7:151962163C>T | c.1144G>A | c.(1144-1146)Ggt>Agt | p.G382S |
| SKCM | 7 | 151962177 | 151962177 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr7:151962177G>A | c.1130C>T | c.(1129-1131)cCa>cTa | p.P377L |
| SKCM | 7 | 151962185 | 151962185 | + | Silent | SNP | C | C | G | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr7:151962185C>G | c.1122G>C | c.(1120-1122)gcG>gcC | p.A374A |
| SKCM | 7 | 151962193 | 151962193 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr7:151962193C>T | c.1114G>A | c.(1114-1116)Gat>Aat | p.D372N |
| SKCM | 7 | 151962193 | 151962193 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZW-06A-12D-A197-08 | TCGA-FS-A1ZW-10A-01D-A199-08 | g.chr7:151962193C>T | c.1114G>A | c.(1114-1116)Gat>Aat | p.D372N |
| SKCM | 7 | 151962239 | 151962239 | + | Silent | SNP | C | C | T | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr7:151962239C>T | c.1068G>A | c.(1066-1068)caG>caA | p.Q356Q |
| SKCM | 7 | 151970798 | 151970798 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr7:151970798G>A | c.1004C>T | c.(1003-1005)cCt>cTt | p.P335L |
| SKCM | 7 | 151970799 | 151970799 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1Z3-06A-11D-A197-08 | TCGA-FS-A1Z3-10A-01D-A199-08 | g.chr7:151970799G>A | c.1003C>T | c.(1003-1005)Cct>Tct | p.P335S |
| SKCM | 7 | 151970806 | 151970806 | + | Silent | SNP | G | G | A | TCGA-ER-A198-06A-11D-A196-08 | TCGA-ER-A198-10A-01D-A198-08 | g.chr7:151970806G>A | c.996C>T | c.(994-996)gaC>gaT | p.D332D |
| SKCM | 7 | 151970819 | 151970819 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr7:151970819G>A | c.983C>T | c.(982-984)cCa>cTa | p.P328L |
| SKCM | 7 | 151970823 | 151970823 | + | Missense_Mutation | SNP | A | A | G | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr7:151970823A>G | c.979T>C | c.(979-981)Tgt>Cgt | p.C327R |
| SKCM | 7 | 151970830 | 151970830 | + | Silent | SNP | G | G | A | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr7:151970830G>A | c.972C>T | c.(970-972)ttC>ttT | p.F324F |
| SKCM | 7 | 151970842 | 151970842 | + | Silent | SNP | G | G | A | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr7:151970842G>A | c.960C>T | c.(958-960)ttC>ttT | p.F320F |
| SKCM | 7 | 151970854 | 151970854 | + | Silent | SNP | G | G | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr7:151970854G>T | c.948C>A | c.(946-948)acC>acA | p.T316T |
| SKCM | 7 | 151970883 | 151970883 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr7:151970883G>A | c.919C>T | c.(919-921)Cat>Tat | p.H307Y |
| SKCM | 7 | 151970883 | 151970883 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr7:151970883G>A | c.919C>T | c.(919-921)Cat>Tat | p.H307Y |
| SKCM | 7 | 151970904 | 151970904 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JB-06A-11D-A21A-08 | TCGA-EE-A3JB-10A-01D-A21A-08 | g.chr7:151970904C>T | c.898G>A | c.(898-900)Gag>Aag | p.E300K |
| SKCM | 7 | 151970953 | 151970953 | + | Splice_Site | SNP | C | C | T | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr7:151970953C>T | | c.e7-1 | |
| SKCM | 7 | 152007158 | 152007158 | + | Missense_Mutation | SNP | T | T | A | TCGA-GF-A3OT-06A-23D-A23B-08 | TCGA-GF-A3OT-10A-01D-A23B-08 | g.chr7:152007158T>A | c.742A>T | c.(742-744)Act>Tct | p.T248S |
| SKCM | 7 | 152012382 | 152012382 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr7:152012382G>A | c.431C>T | c.(430-432)tCc>tTc | p.S144F |