| 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 | 6 | 82921272 | 82921272 | + | Missense_Mutation | SNP | A | A | C | TCGA-OR-A5JP-01A-11D-A29I-10 | TCGA-OR-A5JP-10A-01D-A29L-10 | g.chr6:82921272A>C | c.2309T>G | c.(2308-2310)gTg>gGg | p.V770G |
| BLCA | 6 | 82882105 | 82882105 | + | Missense_Mutation | SNP | G | G | C | TCGA-LC-A66R-01A-41D-A30E-08 | TCGA-LC-A66R-10A-01D-A30H-08 | g.chr6:82882105G>C | c.3922C>G | c.(3922-3924)Ctg>Gtg | p.L1308V |
| BLCA | 6 | 82883150 | 82883150 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9RN-01A-11D-A42E-08 | TCGA-ZF-A9RN-10A-01D-A42H-08 | g.chr6:82883150G>C | c.3731C>G | c.(3730-3732)tCt>tGt | p.S1244C |
| BLCA | 6 | 82891597 | 82891597 | + | Splice_Site | SNP | T | T | G | TCGA-G2-AA3D-01A-11D-A391-08 | TCGA-G2-AA3D-10A-01D-A394-08 | g.chr6:82891597T>G | c.3724A>C | c.(3724-3726)Aga>Cga | p.R1242R |
| BLCA | 6 | 82891615 | 82891615 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-AAN0-01A-11D-A42E-08 | TCGA-XF-AAN0-10A-01D-A42H-08 | g.chr6:82891615G>C | c.3706C>G | c.(3706-3708)Cag>Gag | p.Q1236E |
| BLCA | 6 | 82891624 | 82891624 | + | Missense_Mutation | SNP | C | C | G | TCGA-BT-A20R-01A-12D-A16O-08 | TCGA-BT-A20R-11A-11D-A16O-08 | g.chr6:82891624C>G | c.3697G>C | c.(3697-3699)Gaa>Caa | p.E1233Q |
| BLCA | 6 | 82901567 | 82901567 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-AA6M-01A-11D-A391-08 | TCGA-DK-AA6M-10A-01D-A394-08 | g.chr6:82901567C>T | c.3368G>A | c.(3367-3369)aGa>aAa | p.R1123K |
| BLCA | 6 | 82909958 | 82909958 | + | Silent | SNP | G | G | A | TCGA-KQ-A41S-01A-12D-A339-08 | TCGA-KQ-A41S-10C-01D-A339-08 | g.chr6:82909958G>A | c.2925C>T | c.(2923-2925)ttC>ttT | p.F975F |
| BLCA | 6 | 82910359 | 82910359 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1A7-01A-11D-A13W-08 | TCGA-DK-A1A7-10A-01D-A13W-08 | g.chr6:82910359C>T | c.2857G>A | c.(2857-2859)Gta>Ata | p.V953I |
| BLCA | 6 | 82924503 | 82924503 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-AAN2-01A-11D-A42E-08 | TCGA-XF-AAN2-10A-01D-A42H-08 | g.chr6:82924503C>G | c.1645G>C | c.(1645-1647)Gag>Cag | p.E549Q |
| BLCA | 6 | 82927697 | 82927697 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A3IT-01A-31D-A20D-08 | TCGA-DK-A3IT-10A-01D-A20D-08 | g.chr6:82927697C>G | c.1406G>C | c.(1405-1407)aGa>aCa | p.R469T |
| BLCA | 6 | 82933179 | 82933179 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr6:82933179G>C | c.1102C>G | c.(1102-1104)Cag>Gag | p.Q368E |
| BLCA | 6 | 82935193 | 82935193 | + | Splice_Site | SNP | C | C | T | TCGA-E5-A4TZ-01A-11D-A31L-08 | TCGA-E5-A4TZ-10B-01D-A31J-08 | g.chr6:82935193C>T | | c.e6+1 | |
| BLCA | 6 | 82936933 | 82936933 | + | Silent | SNP | T | T | G | TCGA-FD-A3N5-01A-11D-A21A-08 | TCGA-FD-A3N5-10A-01D-A21A-08 | g.chr6:82936933T>G | c.630A>C | c.(628-630)ggA>ggC | p.G210G |
| BLCA | 6 | 82941441 | 82941441 | + | Silent | SNP | G | G | A | TCGA-BT-A42E-01A-11D-A23U-08 | TCGA-BT-A42E-10A-01D-A23U-08 | g.chr6:82941441G>A | c.537C>T | c.(535-537)atC>atT | p.I179I |
| BLCA | 6 | 82950048 | 82950048 | + | Silent | SNP | G | G | A | TCGA-XF-A8HH-01A-11D-A38G-08 | TCGA-XF-A8HH-10A-01D-A38J-08 | g.chr6:82950048G>A | c.156C>T | c.(154-156)ggC>ggT | p.G52G |
| BRCA | 6 | 82906055 | 82906055 | + | Missense_Mutation | SNP | G | G | A | TCGA-C8-A275-01A-21D-A16D-09 | TCGA-C8-A275-10A-01D-A16D-09 | g.chr6:82906055G>A | c.3134C>T | c.(3133-3135)tCc>tTc | p.S1045F |
| BRCA | 6 | 82923947 | 82923947 | + | Missense_Mutation | SNP | C | C | T | TCGA-GM-A2DO-01A-11D-A19Y-09 | TCGA-GM-A2DO-10D-01D-A18P-09 | g.chr6:82923947C>T | c.2201G>A | c.(2200-2202)aGt>aAt | p.S734N |
| BRCA | 6 | 82924534 | 82924534 | + | Silent | SNP | A | A | G | TCGA-A2-A1G4-01A-11D-A13L-09 | TCGA-A2-A1G4-10A-01W-A14R-09 | g.chr6:82924534A>G | c.1614T>C | c.(1612-1614)atT>atC | p.I538I |
| BRCA | 6 | 82927697 | 82927697 | + | Missense_Mutation | SNP | C | C | G | TCGA-E2-A10C-01A-21D-A10M-09 | TCGA-E2-A10C-10A-01D-A10M-09 | g.chr6:82927697C>G | c.1406G>C | c.(1405-1407)aGa>aCa | p.R469T |
| BRCA | 6 | 82933863 | 82933863 | + | Missense_Mutation | SNP | C | C | T | TCGA-AN-A0AK-01A-21W-A019-09 | TCGA-AN-A0AK-10A-01W-A021-09 | g.chr6:82933863C>T | c.865G>A | c.(865-867)Gtt>Att | p.V289I |
| BRCA | 6 | 82936959 | 82936959 | + | Missense_Mutation | SNP | C | C | G | TCGA-GM-A5PV-01A-11D-A28B-09 | TCGA-GM-A5PV-10A-01D-A28E-09 | g.chr6:82936959C>G | c.604G>C | c.(604-606)Ggt>Cgt | p.G202R |
| BRCA | 6 | 82943948 | 82943948 | + | Missense_Mutation | SNP | C | C | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr6:82943948C>A | c.346G>T | c.(346-348)Gat>Tat | p.D116Y |
| CESC | 6 | 82906017 | 82906017 | + | Missense_Mutation | SNP | C | C | T | TCGA-IR-A3LK-01A-12D-A20U-09 | TCGA-IR-A3LK-10A-01D-A20U-09 | g.chr6:82906017C>T | c.3172G>A | c.(3172-3174)Gag>Aag | p.E1058K |
| CESC | 6 | 82912252 | 82912252 | + | Missense_Mutation | SNP | C | C | T | TCGA-MY-A5BD-01A-11D-A26G-09 | TCGA-MY-A5BD-10A-01D-A26G-09 | g.chr6:82912252C>T | c.2722G>A | c.(2722-2724)Gaa>Aaa | p.E908K |
| CESC | 6 | 82950091 | 82950091 | + | Missense_Mutation | SNP | G | G | C | TCGA-EA-A50E-01A-21D-A26G-09 | TCGA-EA-A50E-10A-01D-A26G-09 | g.chr6:82950091G>C | c.113C>G | c.(112-114)tCc>tGc | p.S38C |
| CHOL | 6 | 82920614 | 82920614 | + | Missense_Mutation | SNP | G | G | A | TCGA-YR-A95A-01A-12D-A417-09 | TCGA-YR-A95A-10A-01D-A41A-09 | g.chr6:82920614G>A | c.2426C>T | c.(2425-2427)gCa>gTa | p.A809V |
| COAD | 6 | 82881217 | 82881217 | + | Silent | SNP | A | A | G | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr6:82881217A>G | c.3987T>C | c.(3985-3987)ccT>ccC | p.P1329P |
| COAD | 6 | 82883137 | 82883137 | + | Silent | SNP | G | G | C | TCGA-AA-3655-01A-02D-1719-10 | TCGA-AA-3655-11A-01D-1719-10 | g.chr6:82883137G>C | c.3744C>G | c.(3742-3744)acC>acG | p.T1248T |
| COAD | 6 | 82891708 | 82891708 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr6:82891708G>A | c.3613C>T | c.(3613-3615)Cgg>Tgg | p.R1205W |
| COAD | 6 | 82900844 | 82900844 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr6:82900844C>A | c.3521G>T | c.(3520-3522)aGc>aTc | p.S1174I |
| COAD | 6 | 82911187 | 82911187 | + | Silent | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:82911187A>C | c.2742T>G | c.(2740-2742)gtT>gtG | p.V914V |
| COAD | 6 | 82921117 | 82921117 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr6:82921117A>C | c.2379T>G | c.(2377-2379)taT>taG | p.Y793* |
| COAD | 6 | 82921275 | 82921275 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6603-01A-11D-1835-10 | TCGA-AZ-6603-11A-02D-1835-10 | g.chr6:82921275T>C | c.2306A>G | c.(2305-2307)gAc>gGc | p.D769G |
| COAD | 6 | 82921275 | 82921275 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-6748-01A-11D-1835-10 | TCGA-CK-6748-10A-01D-1835-10 | g.chr6:82921275T>C | c.2306A>G | c.(2305-2307)gAc>gGc | p.D769G |
| COAD | 6 | 82921276 | 82921276 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6607-01A-11D-1835-10 | TCGA-AZ-6607-11A-01D-1835-10 | g.chr6:82921276C>T | c.2305G>A | c.(2305-2307)Gac>Aac | p.D769N |
| COAD | 6 | 82922424 | 82922424 | + | Splice_Site | SNP | C | C | A | TCGA-F4-6806-01A-11D-1835-10 | TCGA-F4-6806-10A-01D-1835-10 | g.chr6:82922424C>A | c.2291G>T | c.(2290-2292)tGt>tTt | p.C764F |
| COAD | 6 | 82922424 | 82922424 | + | Splice_Site | SNP | C | C | T | TCGA-F4-6459-01A-11D-1771-10 | TCGA-F4-6459-10A-01D-1771-10 | g.chr6:82922424C>T | c.2291G>A | c.(2290-2292)tGt>tAt | p.C764Y |
| COAD | 6 | 82922424 | 82922424 | + | Splice_Site | SNP | C | C | T | TCGA-G4-6321-01A-11D-1719-10 | TCGA-G4-6321-10A-01D-1720-10 | g.chr6:82922424C>T | c.2291G>A | c.(2290-2292)tGt>tAt | p.C764Y |
| COAD | 6 | 82923966 | 82923966 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:82923966C>T | c.2182G>A | c.(2182-2184)Gac>Aac | p.D728N |
| COAD | 6 | 82924181 | 82924181 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr6:82924181T>C | c.1967A>G | c.(1966-1968)aAc>aGc | p.N656S |
| COAD | 6 | 82924289 | 82924289 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr6:82924289A>G | c.1859T>C | c.(1858-1860)gTa>gCa | p.V620A |
| COAD | 6 | 82924380 | 82924381 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr6:82924380_82924381insA | c.1767_1768insT | c.(1765-1770)tttcagfs | p.Q590fs |
| COAD | 6 | 82925890 | 82925890 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr6:82925890G>A | c.1504C>T | c.(1504-1506)Cga>Tga | p.R502* |
| COAD | 6 | 82927753 | 82927753 | + | Silent | SNP | A | A | G | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr6:82927753A>G | c.1350T>C | c.(1348-1350)atT>atC | p.I450I |
| COAD | 6 | 82927805 | 82927805 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr6:82927805G>A | c.1298C>T | c.(1297-1299)gCc>gTc | p.A433V |
| COAD | 6 | 82927836 | 82927836 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr6:82927836C>T | c.1267G>A | c.(1267-1269)Gtc>Atc | p.V423I |
| COAD | 6 | 82933863 | 82933863 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3543-01A-01W-0833-10 | TCGA-AA-3543-10A-01W-0833-10 | g.chr6:82933863C>T | c.865G>A | c.(865-867)Gtt>Att | p.V289I |
| COAD | 6 | 82935240 | 82935240 | + | Missense_Mutation | SNP | T | T | A | TCGA-DM-A1D0-01A-11D-A152-10 | TCGA-DM-A1D0-10A-01D-A152-10 | g.chr6:82935240T>A | c.779A>T | c.(778-780)cAa>cTa | p.Q260L |
| COAD | 6 | 82941501 | 82941501 | + | Missense_Mutation | SNP | G | G | T | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr6:82941501G>T | c.477C>A | c.(475-477)agC>agA | p.S159R |
| COAD | 6 | 82941534 | 82941534 | + | Silent | SNP | G | G | A | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr6:82941534G>A | c.444C>T | c.(442-444)ggC>ggT | p.G148G |
| COADREAD | 6 | 82881217 | 82881217 | + | Silent | SNP | A | A | G | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr6:82881217A>G | c.3987T>C | c.(3985-3987)ccT>ccC | p.P1329P |
| COADREAD | 6 | 82883137 | 82883137 | + | Silent | SNP | G | G | C | TCGA-AA-3655-01A-02D-1719-10 | TCGA-AA-3655-11A-01D-1719-10 | g.chr6:82883137G>C | c.3744C>G | c.(3742-3744)acC>acG | p.T1248T |
| COADREAD | 6 | 82891706 | 82891706 | + | Silent | SNP | C | C | T | TCGA-AG-4001-01A-02W-1073-09 | TCGA-AG-4001-10A-01W-1073-09 | g.chr6:82891706C>T | c.3615G>A | c.(3613-3615)cgG>cgA | p.R1205R |
| COADREAD | 6 | 82891708 | 82891708 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr6:82891708G>A | c.3613C>T | c.(3613-3615)Cgg>Tgg | p.R1205W |
| COADREAD | 6 | 82900844 | 82900844 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr6:82900844C>A | c.3521G>T | c.(3520-3522)aGc>aTc | p.S1174I |
| COADREAD | 6 | 82911187 | 82911187 | + | Silent | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:82911187A>C | c.2742T>G | c.(2740-2742)gtT>gtG | p.V914V |
| COADREAD | 6 | 82921117 | 82921117 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr6:82921117A>C | c.2379T>G | c.(2377-2379)taT>taG | p.Y793* |
| COADREAD | 6 | 82921222 | 82921222 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr6:82921222G>T | c.2359C>A | c.(2359-2361)Ctt>Att | p.L787I |
| COADREAD | 6 | 82921275 | 82921275 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6603-01A-11D-1835-10 | TCGA-AZ-6603-11A-02D-1835-10 | g.chr6:82921275T>C | c.2306A>G | c.(2305-2307)gAc>gGc | p.D769G |
| COADREAD | 6 | 82921275 | 82921275 | + | Missense_Mutation | SNP | T | T | C | TCGA-CK-6748-01A-11D-1835-10 | TCGA-CK-6748-10A-01D-1835-10 | g.chr6:82921275T>C | c.2306A>G | c.(2305-2307)gAc>gGc | p.D769G |
| COADREAD | 6 | 82921276 | 82921276 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6607-01A-11D-1835-10 | TCGA-AZ-6607-11A-01D-1835-10 | g.chr6:82921276C>T | c.2305G>A | c.(2305-2307)Gac>Aac | p.D769N |
| COADREAD | 6 | 82922423 | 82922423 | + | Splice_Site | SNP | C | C | A | TCGA-CI-6621-01A-11D-1826-10 | TCGA-CI-6621-10A-01D-1826-10 | g.chr6:82922423C>A | | c.e13+1 | |
| COADREAD | 6 | 82922424 | 82922424 | + | Splice_Site | SNP | C | C | A | TCGA-F4-6806-01A-11D-1835-10 | TCGA-F4-6806-10A-01D-1835-10 | g.chr6:82922424C>A | c.2291G>T | c.(2290-2292)tGt>tTt | p.C764F |
| COADREAD | 6 | 82922424 | 82922424 | + | Splice_Site | SNP | C | C | T | TCGA-F4-6459-01A-11D-1771-10 | TCGA-F4-6459-10A-01D-1771-10 | g.chr6:82922424C>T | c.2291G>A | c.(2290-2292)tGt>tAt | p.C764Y |
| COADREAD | 6 | 82922424 | 82922424 | + | Splice_Site | SNP | C | C | T | TCGA-F5-6571-01A-12D-1826-10 | TCGA-F5-6571-10A-01D-1826-10 | g.chr6:82922424C>T | c.2291G>A | c.(2290-2292)tGt>tAt | p.C764Y |
| COADREAD | 6 | 82922424 | 82922424 | + | Splice_Site | SNP | C | C | T | TCGA-G4-6321-01A-11D-1719-10 | TCGA-G4-6321-10A-01D-1720-10 | g.chr6:82922424C>T | c.2291G>A | c.(2290-2292)tGt>tAt | p.C764Y |
| COADREAD | 6 | 82923966 | 82923966 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:82923966C>T | c.2182G>A | c.(2182-2184)Gac>Aac | p.D728N |
| COADREAD | 6 | 82924181 | 82924181 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr6:82924181T>C | c.1967A>G | c.(1966-1968)aAc>aGc | p.N656S |
| COADREAD | 6 | 82924289 | 82924289 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr6:82924289A>G | c.1859T>C | c.(1858-1860)gTa>gCa | p.V620A |
| COADREAD | 6 | 82924380 | 82924381 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr6:82924380_82924381insA | c.1767_1768insT | c.(1765-1770)tttcagfs | p.Q590fs |
| COADREAD | 6 | 82925890 | 82925890 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr6:82925890G>A | c.1504C>T | c.(1504-1506)Cga>Tga | p.R502* |
| COADREAD | 6 | 82927752 | 82927752 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr6:82927752G>T | c.1351C>A | c.(1351-1353)Cta>Ata | p.L451I |
| COADREAD | 6 | 82927753 | 82927753 | + | Silent | SNP | A | A | G | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr6:82927753A>G | c.1350T>C | c.(1348-1350)atT>atC | p.I450I |
| COADREAD | 6 | 82927805 | 82927805 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr6:82927805G>A | c.1298C>T | c.(1297-1299)gCc>gTc | p.A433V |
| COADREAD | 6 | 82927836 | 82927836 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr6:82927836C>T | c.1267G>A | c.(1267-1269)Gtc>Atc | p.V423I |
| COADREAD | 6 | 82933863 | 82933863 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3543-01A-01W-0833-10 | TCGA-AA-3543-10A-01W-0833-10 | g.chr6:82933863C>T | c.865G>A | c.(865-867)Gtt>Att | p.V289I |
| COADREAD | 6 | 82935240 | 82935240 | + | Missense_Mutation | SNP | T | T | A | TCGA-DM-A1D0-01A-11D-A152-10 | TCGA-DM-A1D0-10A-01D-A152-10 | g.chr6:82935240T>A | c.779A>T | c.(778-780)cAa>cTa | p.Q260L |
| COADREAD | 6 | 82941501 | 82941501 | + | Missense_Mutation | SNP | G | G | T | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr6:82941501G>T | c.477C>A | c.(475-477)agC>agA | p.S159R |
| COADREAD | 6 | 82941534 | 82941534 | + | Silent | SNP | G | G | A | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr6:82941534G>A | c.444C>T | c.(442-444)ggC>ggT | p.G148G |
| ESCA | 6 | 82921212 | 82921212 | + | Missense_Mutation | SNP | C | C | T | TCGA-IG-A50L-01A-11D-A27G-09 | TCGA-IG-A50L-10A-01D-A27G-09 | g.chr6:82921212C>T | c.2369G>A | c.(2368-2370)aGa>aAa | p.R790K |
| ESCA | 6 | 82924304 | 82924304 | + | Missense_Mutation | SNP | C | C | T | TCGA-Q9-A6FU-01A-11D-A31U-09 | TCGA-Q9-A6FU-10A-01D-A31U-09 | g.chr6:82924304C>T | c.1844G>A | c.(1843-1845)tGc>tAc | p.C615Y |
| ESCA | 6 | 82924380 | 82924380 | + | Missense_Mutation | SNP | G | G | C | TCGA-LN-A9FP-01A-31D-A387-09 | TCGA-LN-A9FP-10A-01D-A38A-09 | g.chr6:82924380G>C | c.1768C>G | c.(1768-1770)Cag>Gag | p.Q590E |
| ESCA | 6 | 82924426 | 82924426 | + | Silent | SNP | G | G | C | TCGA-V5-AASX-01A-11D-A387-09 | TCGA-V5-AASX-10A-01D-A38A-09 | g.chr6:82924426G>C | c.1722C>G | c.(1720-1722)ctC>ctG | p.L574L |
| ESCA | 6 | 82935221 | 82935221 | + | Silent | SNP | C | C | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr6:82935221C>A | c.798G>T | c.(796-798)ccG>ccT | p.P266P |
| ESCA | 6 | 82950160 | 82950160 | + | Missense_Mutation | SNP | A | A | G | TCGA-VR-A8ER-01A-11D-A36J-09 | TCGA-VR-A8ER-10A-01D-A36M-09 | g.chr6:82950160A>G | c.44T>C | c.(43-45)cTg>cCg | p.L15P |
| GBM | 6 | 82924063 | 82924066 | + | Frame_Shift_Del | DEL | ACTA | ACTA | - | TCGA-76-4926-01B-01D-1486-08 | TCGA-76-4926-10A-01D-1486-08 | g.chr6:82924063_82924066delACTA | c.2082_2085delTAGT | c.(2080-2085)gttagtfs | p.VS694fs |
| GBM | 6 | 82924066 | 82924066 | + | Silent | SNP | A | A | C | TCGA-27-1830-01A-01W-0643-08 | TCGA-27-1830-10A-01W-0644-08 | g.chr6:82924066A>C | c.2082T>G | c.(2080-2082)gtT>gtG | p.V694V |
| GBMLGG | 6 | 82883084 | 82883084 | + | Splice_Site | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82883084T>C | c.3797A>G | c.(3796-3798)aAt>aGt | p.N1266S |
| GBMLGG | 6 | 82883097 | 82883097 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82883097G>T | c.3784C>A | c.(3784-3786)Cta>Ata | p.L1262I |
| GBMLGG | 6 | 82912294 | 82912294 | + | Missense_Mutation | SNP | A | A | G | TCGA-FG-8191-01A-11D-2253-08 | TCGA-FG-8191-10A-01D-2253-08 | g.chr6:82912294A>G | c.2680T>C | c.(2680-2682)Tct>Cct | p.S894P |
| GBMLGG | 6 | 82912354 | 82912354 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82912354T>G | c.2620A>C | c.(2620-2622)Aag>Cag | p.K874Q |
| GBMLGG | 6 | 82924063 | 82924066 | + | Frame_Shift_Del | DEL | ACTA | ACTA | - | TCGA-76-4926-01B-01D-1486-08 | TCGA-76-4926-10A-01D-1486-08 | g.chr6:82924063_82924066delACTA | c.2082_2085delTAGT | c.(2080-2085)gttagtfs | p.VS694fs |
| GBMLGG | 6 | 82924066 | 82924066 | + | Silent | SNP | A | A | C | TCGA-27-1830-01A-01W-0643-08 | TCGA-27-1830-10A-01W-0644-08 | g.chr6:82924066A>C | c.2082T>G | c.(2080-2082)gtT>gtG | p.V694V |
| GBMLGG | 6 | 82925825 | 82925825 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82925825G>T | c.1569C>A | c.(1567-1569)aaC>aaA | p.N523K |
| GBMLGG | 6 | 82933169 | 82933169 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82933169T>C | c.1112A>G | c.(1111-1113)aAg>aGg | p.K371R |
| HNSC | 6 | 82900848 | 82900848 | + | Missense_Mutation | SNP | T | T | A | TCGA-CQ-5333-01A-01D-2394-08 | TCGA-CQ-5333-10A-01D-2394-08 | g.chr6:82900848T>A | c.3517A>T | c.(3517-3519)Aat>Tat | p.N1173Y |
| HNSC | 6 | 82910367 | 82910367 | + | Missense_Mutation | SNP | T | T | C | TCGA-BA-A6DE-01A-22D-A31L-08 | TCGA-BA-A6DE-10A-01D-A31J-08 | g.chr6:82910367T>C | c.2849A>G | c.(2848-2850)tAt>tGt | p.Y950C |
| HNSC | 6 | 82911176 | 82911176 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr6:82911176C>G | c.2753G>C | c.(2752-2754)gGt>gCt | p.G918A |
| HNSC | 6 | 82923970 | 82923970 | + | Silent | SNP | T | T | C | TCGA-CN-4741-01A-01D-1434-08 | TCGA-CN-4741-10A-01D-1434-08 | g.chr6:82923970T>C | c.2178A>G | c.(2176-2178)aaA>aaG | p.K726K |
| HNSC | 6 | 82927733 | 82927733 | + | Missense_Mutation | SNP | C | C | G | TCGA-CR-6472-01A-11D-1870-08 | TCGA-CR-6472-10A-01D-1870-08 | g.chr6:82927733C>G | c.1370G>C | c.(1369-1371)gGa>gCa | p.G457A |
| HNSC | 6 | 82935280 | 82935280 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-5442-01A-01D-1512-08 | TCGA-CV-5442-11A-01D-1512-08 | g.chr6:82935280C>T | c.739G>A | c.(739-741)Gat>Aat | p.D247N |
| HNSC | 6 | 82943951 | 82943951 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-MT-A67F-01A-11D-A30E-08 | TCGA-MT-A67F-10A-01D-A30H-08 | g.chr6:82943951G>A | c.343C>T | c.(343-345)Caa>Taa | p.Q115* |
| HNSC | 6 | 82950154 | 82950154 | + | Missense_Mutation | SNP | T | T | C | TCGA-CR-7389-01A-11D-2012-08 | TCGA-CR-7389-10A-01D-2013-08 | g.chr6:82950154T>C | c.50A>G | c.(49-51)cAt>cGt | p.H17R |
| KIPAN | 6 | 82904254 | 82904254 | + | Missense_Mutation | SNP | T | T | G | TCGA-A4-8310-01A-11D-2396-08 | TCGA-A4-8310-10A-01D-2396-08 | g.chr6:82904254T>G | c.3280A>C | c.(3280-3282)Att>Ctt | p.I1094L |
| KIPAN | 6 | 82906099 | 82906099 | + | Silent | SNP | A | A | T | TCGA-2Z-A9JQ-01A-11D-A42J-10 | TCGA-2Z-A9JQ-10A-01D-A42M-10 | g.chr6:82906099A>T | c.3090T>A | c.(3088-3090)tcT>tcA | p.S1030S |
| KIPAN | 6 | 82925803 | 82925803 | + | Missense_Mutation | SNP | G | G | A | TCGA-BP-4985-01A-01D-1462-08 | TCGA-BP-4985-11A-01D-1462-08 | g.chr6:82925803G>A | c.1591C>T | c.(1591-1593)Cct>Tct | p.P531S |
| KIPAN | 6 | 82950058 | 82950058 | + | Missense_Mutation | SNP | T | T | C | TCGA-UZ-A9PR-01A-11D-A42J-10 | TCGA-UZ-A9PR-10A-01D-A42M-10 | g.chr6:82950058T>C | c.146A>G | c.(145-147)gAt>gGt | p.D49G |
| KIPAN | 6 | 82950105 | 82950105 | + | Silent | SNP | A | A | T | TCGA-CJ-6031-01A-11D-1669-08 | TCGA-CJ-6031-11A-01D-1669-08 | g.chr6:82950105A>T | c.99T>A | c.(97-99)atT>atA | p.I33I |
| KIPAN | 6 | 82950107 | 82950107 | + | Missense_Mutation | SNP | T | T | C | TCGA-CJ-6031-01A-11D-1669-08 | TCGA-CJ-6031-11A-01D-1669-08 | g.chr6:82950107T>C | c.97A>G | c.(97-99)Att>Gtt | p.I33V |
| KIRC | 6 | 82925803 | 82925803 | + | Missense_Mutation | SNP | G | G | A | TCGA-BP-4985-01A-01D-1462-08 | TCGA-BP-4985-11A-01D-1462-08 | g.chr6:82925803G>A | c.1591C>T | c.(1591-1593)Cct>Tct | p.P531S |
| KIRC | 6 | 82950105 | 82950105 | + | Silent | SNP | A | A | T | TCGA-CJ-6031-01A-11D-1669-08 | TCGA-CJ-6031-11A-01D-1669-08 | g.chr6:82950105A>T | c.99T>A | c.(97-99)atT>atA | p.I33I |
| KIRC | 6 | 82950107 | 82950107 | + | Missense_Mutation | SNP | T | T | C | TCGA-CJ-6031-01A-11D-1669-08 | TCGA-CJ-6031-11A-01D-1669-08 | g.chr6:82950107T>C | c.97A>G | c.(97-99)Att>Gtt | p.I33V |
| KIRP | 6 | 82904254 | 82904254 | + | Missense_Mutation | SNP | T | T | G | TCGA-A4-8310-01A-11D-2396-08 | TCGA-A4-8310-10A-01D-2396-08 | g.chr6:82904254T>G | c.3280A>C | c.(3280-3282)Att>Ctt | p.I1094L |
| KIRP | 6 | 82906099 | 82906099 | + | Silent | SNP | A | A | T | TCGA-2Z-A9JQ-01A-11D-A42J-10 | TCGA-2Z-A9JQ-10A-01D-A42M-10 | g.chr6:82906099A>T | c.3090T>A | c.(3088-3090)tcT>tcA | p.S1030S |
| KIRP | 6 | 82950058 | 82950058 | + | Missense_Mutation | SNP | T | T | C | TCGA-UZ-A9PR-01A-11D-A42J-10 | TCGA-UZ-A9PR-10A-01D-A42M-10 | g.chr6:82950058T>C | c.146A>G | c.(145-147)gAt>gGt | p.D49G |
| LGG | 6 | 82883084 | 82883084 | + | Splice_Site | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82883084T>C | c.3797A>G | c.(3796-3798)aAt>aGt | p.N1266S |
| LGG | 6 | 82883097 | 82883097 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82883097G>T | c.3784C>A | c.(3784-3786)Cta>Ata | p.L1262I |
| LGG | 6 | 82912294 | 82912294 | + | Missense_Mutation | SNP | A | A | G | TCGA-FG-8191-01A-11D-2253-08 | TCGA-FG-8191-10A-01D-2253-08 | g.chr6:82912294A>G | c.2680T>C | c.(2680-2682)Tct>Cct | p.S894P |
| LGG | 6 | 82912354 | 82912354 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82912354T>G | c.2620A>C | c.(2620-2622)Aag>Cag | p.K874Q |
| LGG | 6 | 82925825 | 82925825 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82925825G>T | c.1569C>A | c.(1567-1569)aaC>aaA | p.N523K |
| LGG | 6 | 82933169 | 82933169 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:82933169T>C | c.1112A>G | c.(1111-1113)aAg>aGg | p.K371R |
| LIHC | 6 | 82891683 | 82891683 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr6:82891683delT | c.3638delA | c.(3637-3639)aagfs | p.K1213fs |
| LIHC | 6 | 82906144 | 82906144 | + | Missense_Mutation | SNP | C | C | G | TCGA-2Y-A9GU-01A-11D-A382-10 | TCGA-2Y-A9GU-10A-01D-A385-10 | g.chr6:82906144C>G | c.3045G>C | c.(3043-3045)aaG>aaC | p.K1015N |
| LIHC | 6 | 82910419 | 82910419 | + | Missense_Mutation | SNP | C | C | T | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr6:82910419C>T | c.2797G>A | c.(2797-2799)Gca>Aca | p.A933T |
| LIHC | 6 | 82912269 | 82912269 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-A73E-01A-12D-A32G-10 | TCGA-DD-A73E-10A-01D-A32G-10 | g.chr6:82912269delT | c.2705delA | c.(2704-2706)aatfs | p.N902fs |
| LIHC | 6 | 82921267 | 82921267 | + | Missense_Mutation | SNP | T | T | A | TCGA-DD-AAC8-01A-11D-A40R-10 | TCGA-DD-AAC8-10A-01D-A40U-10 | g.chr6:82921267T>A | c.2314A>T | c.(2314-2316)Atg>Ttg | p.M772L |
| LIHC | 6 | 82941527 | 82941527 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AAE8-01A-11D-A40R-10 | TCGA-DD-AAE8-10A-01D-A40U-10 | g.chr6:82941527T>C | c.451A>G | c.(451-453)Aca>Gca | p.T151A |
| LIHC | 6 | 82949918 | 82949918 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr6:82949918delA | c.286delT | c.(286-288)tatfs | p.Y96fs |
| LUAD | 6 | 82881188 | 82881188 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z030-01A-01W-0746-08 | TCGA-17-Z030-11A-01W-0746-08 | g.chr6:82881188G>A | c.4016C>T | c.(4015-4017)cCg>cTg | p.P1339L |
| LUAD | 6 | 82901516 | 82901516 | + | Missense_Mutation | SNP | T | T | A | TCGA-86-7955-01A-11D-2184-08 | TCGA-86-7955-10A-01D-2184-08 | g.chr6:82901516T>A | c.3419A>T | c.(3418-3420)aAg>aTg | p.K1140M |
| LUAD | 6 | 82906044 | 82906044 | + | Missense_Mutation | SNP | T | T | A | TCGA-91-A4BC-01A-11D-A24D-08 | TCGA-91-A4BC-10A-01D-A24F-08 | g.chr6:82906044T>A | c.3145A>T | c.(3145-3147)Aca>Tca | p.T1049S |
| LUAD | 6 | 82910357 | 82910357 | + | Silent | SNP | T | T | G | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr6:82910357T>G | c.2859A>C | c.(2857-2859)gtA>gtC | p.V953V |
| LUAD | 6 | 82910358 | 82910358 | + | Missense_Mutation | SNP | A | A | G | TCGA-86-7711-01A-11D-2063-08 | TCGA-86-7711-10A-01D-2063-08 | g.chr6:82910358A>G | c.2858T>C | c.(2857-2859)gTa>gCa | p.V953A |
| LUAD | 6 | 82911190 | 82911190 | + | Missense_Mutation | SNP | A | A | T | TCGA-17-Z025-01A-01W-0746-08 | TCGA-17-Z025-11A-01W-0746-08 | g.chr6:82911190A>T | c.2739T>A | c.(2737-2739)gaT>gaA | p.D913E |
| LUAD | 6 | 82924119 | 82924119 | + | Missense_Mutation | SNP | C | C | T | TCGA-44-A47A-01A-21D-A24D-08 | TCGA-44-A47A-10A-01D-A24F-08 | g.chr6:82924119C>T | c.2029G>A | c.(2029-2031)Gat>Aat | p.D677N |
| LUAD | 6 | 82924239 | 82924239 | + | Missense_Mutation | SNP | T | T | C | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr6:82924239T>C | c.1909A>G | c.(1909-1911)Aca>Gca | p.T637A |
| LUAD | 6 | 82924358 | 82924358 | + | Missense_Mutation | SNP | C | C | G | TCGA-91-6848-01A-11D-1945-08 | TCGA-91-6848-11A-01D-1945-08 | g.chr6:82924358C>G | c.1790G>C | c.(1789-1791)gGt>gCt | p.G597A |
| LUAD | 6 | 82927845 | 82927845 | + | Missense_Mutation | SNP | A | A | T | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr6:82927845A>T | c.1258T>A | c.(1258-1260)Tgg>Agg | p.W420R |
| LUAD | 6 | 82933844 | 82933844 | + | Missense_Mutation | SNP | T | T | G | TCGA-75-7025-01A-12D-1945-08 | TCGA-75-7025-10A-01D-1946-08 | g.chr6:82933844T>G | c.884A>C | c.(883-885)cAt>cCt | p.H295P |
| LUAD | 6 | 82936912 | 82936912 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-44-6776-01A-11D-1855-08 | TCGA-44-6776-10A-01D-1855-08 | g.chr6:82936912G>T | c.651C>A | c.(649-651)tgC>tgA | p.C217* |
| LUAD | 6 | 82950120 | 82950120 | + | Silent | SNP | C | C | A | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr6:82950120C>A | c.84G>T | c.(82-84)ggG>ggT | p.G28G |
| LUAD | 6 | 82950159 | 82950159 | + | Silent | SNP | C | C | A | TCGA-44-6144-01A-11D-1753-08 | TCGA-44-6144-10A-01D-1753-08 | g.chr6:82950159C>A | c.45G>T | c.(43-45)ctG>ctT | p.L15L |
| LUSC | 6 | 82882108 | 82882109 | + | Missense_Mutation | DNP | CC | CC | AA | TCGA-18-3410-01A-01D-0983-08 | TCGA-18-3410-11A-01D-0983-08 | g.chr6:82882108_82882109CC>AA | c.3918_3919GG>TT | c.(3916-3921)ttGGct>ttTTct | p.1306_1307LA>FS |
| LUSC | 6 | 82909856 | 82909856 | + | Splice_Site | SNP | A | A | C | TCGA-66-2734-01A-01D-0983-08 | TCGA-66-2734-11A-01D-0983-08 | g.chr6:82909856A>C | | c.e21+1 | |
| LUSC | 6 | 82909857 | 82909857 | + | Splice_Site | SNP | C | C | A | TCGA-60-2722-01A-01D-1522-08 | TCGA-60-2722-11A-01D-1522-08 | g.chr6:82909857C>A | | c.e21+1 | |
| LUSC | 6 | 82922461 | 82922461 | + | Missense_Mutation | SNP | T | T | C | TCGA-18-3410-01A-01D-0983-08 | TCGA-18-3410-11A-01D-0983-08 | g.chr6:82922461T>C | c.2254A>G | c.(2254-2256)Aac>Gac | p.N752D |
| LUSC | 6 | 82924287 | 82924287 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-37-4133-01A-01D-1352-08 | TCGA-37-4133-10A-01D-1352-08 | g.chr6:82924287C>A | c.1861G>T | c.(1861-1863)Gag>Tag | p.E621* |
| LUSC | 6 | 82950160 | 82950160 | + | Missense_Mutation | SNP | A | A | C | TCGA-46-3768-01A-01D-0983-08 | TCGA-46-3768-10A-01D-0983-08 | g.chr6:82950160A>C | c.44T>G | c.(43-45)cTg>cGg | p.L15R |
| OV | 6 | 82921274 | 82921274 | + | Missense_Mutation | SNP | G | G | C | TCGA-04-1338-01A-01W-0484-10 | TCGA-04-1338-11A-01W-0485-10 | g.chr6:82921274G>C | c.2307C>G | c.(2305-2307)gaC>gaG | p.D769E |
| OV | 6 | 82924180 | 82924180 | + | Silent | SNP | G | G | A | TCGA-25-2400-01A-01W-0799-08 | TCGA-25-2400-10A-01W-0799-08 | g.chr6:82924180G>A | c.1968C>T | c.(1966-1968)aaC>aaT | p.N656N |
| PRAD | 6 | 82922423 | 82922423 | + | Splice_Site | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr6:82922423C>T | | c.e13+1 | |
| PRAD | 6 | 82924057 | 82924057 | + | Missense_Mutation | SNP | C | C | A | TCGA-G9-7523-01A-11D-2260-08 | TCGA-G9-7523-10A-01D-2260-08 | g.chr6:82924057C>A | c.2091G>T | c.(2089-2091)agG>agT | p.R697S |
| READ | 6 | 82891706 | 82891706 | + | Silent | SNP | C | C | T | TCGA-AG-4001-01A-02W-1073-09 | TCGA-AG-4001-10A-01W-1073-09 | g.chr6:82891706C>T | c.3615G>A | c.(3613-3615)cgG>cgA | p.R1205R |
| READ | 6 | 82921222 | 82921222 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr6:82921222G>T | c.2359C>A | c.(2359-2361)Ctt>Att | p.L787I |
| READ | 6 | 82922423 | 82922423 | + | Splice_Site | SNP | C | C | A | TCGA-CI-6621-01A-11D-1826-10 | TCGA-CI-6621-10A-01D-1826-10 | g.chr6:82922423C>A | | c.e13+1 | |
| READ | 6 | 82922424 | 82922424 | + | Splice_Site | SNP | C | C | T | TCGA-F5-6571-01A-12D-1826-10 | TCGA-F5-6571-10A-01D-1826-10 | g.chr6:82922424C>T | c.2291G>A | c.(2290-2292)tGt>tAt | p.C764Y |
| READ | 6 | 82927752 | 82927752 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr6:82927752G>T | c.1351C>A | c.(1351-1353)Cta>Ata | p.L451I |
| SARC | 6 | 82911138 | 82911138 | + | Splice_Site | SNP | C | C | T | TCGA-DX-A1L2-01A-22D-A24N-09 | TCGA-DX-A1L2-10A-01D-A24N-09 | g.chr6:82911138C>T | | c.e19+1 | |
| SKCM | 6 | 82882185 | 82882185 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr6:82882185G>A | c.3842C>T | c.(3841-3843)cCa>cTa | p.P1281L |
| SKCM | 6 | 82882186 | 82882186 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr6:82882186G>A | c.3841C>T | c.(3841-3843)Cca>Tca | p.P1281S |
| SKCM | 6 | 82891638 | 82891638 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr6:82891638G>A | c.3683C>T | c.(3682-3684)tCt>tTt | p.S1228F |
| SKCM | 6 | 82891739 | 82891739 | + | Silent | SNP | A | A | T | TCGA-EE-A3JI-06A-11D-A21A-08 | TCGA-EE-A3JI-10A-01D-A21A-08 | g.chr6:82891739A>T | c.3582T>A | c.(3580-3582)tcT>tcA | p.S1194S |
| SKCM | 6 | 82924094 | 82924094 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr6:82924094A>T | c.2054T>A | c.(2053-2055)gTt>gAt | p.V685D |
| SKCM | 6 | 82924095 | 82924095 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr6:82924095C>T | c.2053G>A | c.(2053-2055)Gtt>Att | p.V685I |
| SKCM | 6 | 82924368 | 82924368 | + | Missense_Mutation | SNP | G | G | A | TCGA-FR-A3YN-06A-11D-A23B-08 | TCGA-FR-A3YN-10A-01D-A23B-08 | g.chr6:82924368G>A | c.1780C>T | c.(1780-1782)Ctt>Ttt | p.L594F |
| SKCM | 6 | 82924513 | 82924513 | + | Silent | SNP | G | G | A | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr6:82924513G>A | c.1635C>T | c.(1633-1635)tcC>tcT | p.S545S |
| SKCM | 6 | 82937003 | 82937003 | + | Missense_Mutation | SNP | A | A | T | TCGA-FS-A4FC-06A-11D-A24R-08 | TCGA-FS-A4FC-10A-01D-A24R-08 | g.chr6:82937003A>T | c.560T>A | c.(559-561)tTt>tAt | p.F187Y |