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 21 30341891 30341891 + Missense_Mutation SNP A A G TCGA-OR-A5LP-01A-11D-A29I-10 TCGA-OR-A5LP-10A-01D-A29L-10 g.chr21:30341891A>G c.1208T>C c.(1207-1209)tTa>tCa p.L403S BLCA 21 30307437 30307437 + Silent SNP G G T TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr21:30307437G>T c.4869C>A c.(4867-4869)ggC>ggA p.G1623G BLCA 21 30307608 30307608 + Silent SNP T T C TCGA-GU-A42R-01A-11D-A23M-08 TCGA-GU-A42R-10A-01D-A23K-08 g.chr21:30307608T>C c.4698A>G c.(4696-4698)tcA>tcG p.S1566S BLCA 21 30316094 30316094 + Missense_Mutation SNP T T C TCGA-FD-A3B7-01A-31D-A20D-08 TCGA-FD-A3B7-10A-01D-A20D-08 g.chr21:30316094T>C c.4115A>G c.(4114-4116)aAa>aGa p.K1372R BLCA 21 30325696 30325696 + Missense_Mutation SNP C C A TCGA-UY-A9PA-01A-11D-A38G-08 TCGA-UY-A9PA-10A-01D-A38J-08 g.chr21:30325696C>A c.3082G>T c.(3082-3084)Gca>Tca p.A1028S BLCA 21 30329183 30329183 + Missense_Mutation SNP G G C TCGA-E7-A85H-01A-11D-A34U-08 TCGA-E7-A85H-10B-01D-A34X-08 g.chr21:30329183G>C c.2980C>G c.(2980-2982)Ctt>Gtt p.L994V BLCA 21 30329695 30329695 + Missense_Mutation SNP C C T TCGA-XF-AAMY-01A-11D-A42E-08 TCGA-XF-AAMY-10A-01D-A42H-08 g.chr21:30329695C>T c.2851G>A c.(2851-2853)Gac>Aac p.D951N BLCA 21 30330766 30330766 + Missense_Mutation SNP G G A TCGA-UY-A9PD-01A-11D-A38G-08 TCGA-UY-A9PD-10A-01D-A38J-08 g.chr21:30330766G>A c.2689C>T c.(2689-2691)Cat>Tat p.H897Y BLCA 21 30331900 30331900 + Missense_Mutation SNP C C A TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr21:30331900C>A c.2473G>T c.(2473-2475)Gat>Tat p.D825Y BLCA 21 30331900 30331900 + Missense_Mutation SNP C C G TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr21:30331900C>G c.2473G>C c.(2473-2475)Gat>Cat p.D825H BLCA 21 30338207 30338207 + Missense_Mutation SNP G G A TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr21:30338207G>A c.2143C>T c.(2143-2145)Ctt>Ttt p.L715F BLCA 21 30338214 30338214 + Missense_Mutation SNP C C A TCGA-DK-A6B1-01A-12D-A30E-08 TCGA-DK-A6B1-10A-01D-A30H-08 g.chr21:30338214C>A c.2136G>T c.(2134-2136)tgG>tgT p.W712C BLCA 21 30338215 30338215 + Missense_Mutation SNP C C G TCGA-DK-A6B1-01A-12D-A30E-08 TCGA-DK-A6B1-10A-01D-A30H-08 g.chr21:30338215C>G c.2135G>C c.(2134-2136)tGg>tCg p.W712S BLCA 21 30339132 30339132 + Missense_Mutation SNP C C G TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr21:30339132C>G c.1681G>C c.(1681-1683)Gag>Cag p.E561Q BLCA 21 30339160 30339160 + Missense_Mutation SNP C C G TCGA-XF-A9SG-01A-12D-A42E-08 TCGA-XF-A9SG-10A-01D-A42H-08 g.chr21:30339160C>G c.1653G>C c.(1651-1653)gaG>gaC p.E551D BLCA 21 30339384 30339384 + Missense_Mutation SNP C C T TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr21:30339384C>T c.1429G>A c.(1429-1431)Gaa>Aaa p.E477K BLCA 21 30365150 30365150 + 5'UTR SNP G G C TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr21:30365150G>C BLCA 21 30365173 30365173 + 5'UTR SNP C C A TCGA-DK-A1AE-01A-11D-A13W-08 TCGA-DK-A1AE-10A-01D-A13W-08 g.chr21:30365173C>A BRCA 21 30316846 30316846 + Missense_Mutation SNP C C T TCGA-A2-A0ET-01A-31D-A045-09 TCGA-A2-A0ET-10A-01W-A055-09 g.chr21:30316846C>T c.3841G>A c.(3841-3843)Gcc>Acc p.A1281T BRCA 21 30331787 30331787 + Missense_Mutation SNP A A C TCGA-D8-A1XW-01A-11D-A14K-09 TCGA-D8-A1XW-10A-01D-A14K-09 g.chr21:30331787A>C c.2586T>G c.(2584-2586)caT>caG p.H862Q BRCA 21 30332984 30332984 + Silent SNP G G C TCGA-OL-A5RW-01A-11D-A28B-09 TCGA-OL-A5RW-10A-01D-A28E-09 g.chr21:30332984G>C c.2208C>G c.(2206-2208)ctC>ctG p.L736L BRCA 21 30339479 30339479 + Missense_Mutation SNP A A C TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr21:30339479A>C c.1334T>G c.(1333-1335)gTt>gGt p.V445G BRCA 21 30342948 30342948 + Silent SNP G G A TCGA-AC-A3W7-01A-11D-A228-09 TCGA-AC-A3W7-10A-01D-A22A-09 g.chr21:30342948G>A c.1101C>T c.(1099-1101)atC>atT p.I367I BRCA 21 30365115 30365115 + Silent SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr21:30365115C>T c.12G>A c.(10-12)aaG>aaA p.K4K BRCA 21 30365148 30365148 + 5'UTR SNP C C G TCGA-A2-A0CR-01A-11D-A228-09 TCGA-A2-A0CR-10A-01D-A22A-09 g.chr21:30365148C>G CESC 21 30316810 30316810 + Missense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr21:30316810G>C c.3877C>G c.(3877-3879)Ctg>Gtg p.L1293V CESC 21 30329098 30329098 + Missense_Mutation SNP T T A TCGA-EA-A3Y4-01A-51D-A243-09 TCGA-EA-A3Y4-10A-01D-A243-09 g.chr21:30329098T>A c.3065A>T c.(3064-3066)gAg>gTg p.E1022V CESC 21 30339080 30339080 + Missense_Mutation SNP G G T TCGA-C5-A0TN-01A-21D-A14W-08 TCGA-C5-A0TN-10B-01D-A14W-08 g.chr21:30339080G>T c.1733C>A c.(1732-1734)tCt>tAt p.S578Y CESC 21 30357145 30357145 + Missense_Mutation SNP C C T TCGA-UC-A7PD-01A-11D-A351-09 TCGA-UC-A7PD-11A-12D-A351-09 g.chr21:30357145C>T c.444G>A c.(442-444)atG>atA p.M148I CESC 21 30358482 30358482 + Missense_Mutation SNP C C A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr21:30358482C>A c.323G>T c.(322-324)aGa>aTa p.R108I CHOL 21 30332965 30332965 + Missense_Mutation SNP C C T TCGA-4G-AAZT-01A-11D-A417-09 TCGA-4G-AAZT-10A-01D-A41A-09 g.chr21:30332965C>T c.2227G>A c.(2227-2229)Gag>Aag p.E743K CHOL 21 30339206 30339206 + Missense_Mutation SNP T T A TCGA-ZH-A8Y5-01A-11D-A417-09 TCGA-ZH-A8Y5-10A-01D-A41A-09 g.chr21:30339206T>A c.1607A>T c.(1606-1608)aAt>aTt p.N536I COAD 21 30303489 30303489 + Silent SNP A A G TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr21:30303489A>G c.5226T>C c.(5224-5226)caT>caC p.H1742H COAD 21 30303489 30303489 + Silent SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr21:30303489A>G c.5226T>C c.(5224-5226)caT>caC p.H1742H COAD 21 30313616 30313616 + Missense_Mutation SNP C C A TCGA-AA-A00O-01A-02W-A00E-09 TCGA-AA-A00O-10A-01W-A00E-09 g.chr21:30313616C>A c.4408G>T c.(4408-4410)Gac>Tac p.D1470Y COAD 21 30318238 30318238 + Missense_Mutation SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr21:30318238A>G c.3659T>C c.(3658-3660)gTa>gCa p.V1220A COAD 21 30318545 30318545 + Silent SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr21:30318545C>T c.3552G>A c.(3550-3552)gaG>gaA p.E1184E COAD 21 30324514 30324514 + Silent SNP A A G TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr21:30324514A>G c.3312T>C c.(3310-3312)gaT>gaC p.D1104D COAD 21 30324515 30324515 + Missense_Mutation SNP T T C TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr21:30324515T>C c.3311A>G c.(3310-3312)gAt>gGt p.D1104G COAD 21 30324515 30324515 + Missense_Mutation SNP T T C TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr21:30324515T>C c.3311A>G c.(3310-3312)gAt>gGt p.D1104G COAD 21 30324515 30324515 + Missense_Mutation SNP T T C TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr21:30324515T>C c.3311A>G c.(3310-3312)gAt>gGt p.D1104G COAD 21 30324515 30324515 + Missense_Mutation SNP T T C TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr21:30324515T>C c.3311A>G c.(3310-3312)gAt>gGt p.D1104G COAD 21 30324515 30324515 + Missense_Mutation SNP T T G TCGA-AD-6965-01A-11D-1924-10 TCGA-AD-6965-10A-01D-1924-10 g.chr21:30324515T>G c.3311A>C c.(3310-3312)gAt>gCt p.D1104A COAD 21 30324516 30324516 + Missense_Mutation SNP C C T TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr21:30324516C>T c.3310G>A c.(3310-3312)Gat>Aat p.D1104N COAD 21 30325699 30325699 + Splice_Site SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr21:30325699C>A c.e17-1 COAD 21 30331792 30331792 + Frame_Shift_Del DEL T T - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr21:30331792delT c.2581delA c.(2581-2583)acafs p.T861fs COAD 21 30331798 30331798 + Nonsense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr21:30331798C>A c.2575G>T c.(2575-2577)Gaa>Taa p.E859* COAD 21 30331911 30331911 + Missense_Mutation SNP G G A TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr21:30331911G>A c.2462C>T c.(2461-2463)tCt>tTt p.S821F COAD 21 30332952 30332952 + Missense_Mutation SNP T T A TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr21:30332952T>A c.2240A>T c.(2239-2241)aAc>aTc p.N747I COAD 21 30332978 30332978 + Silent SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr21:30332978G>A c.2214C>T c.(2212-2214)ggC>ggT p.G738G COAD 21 30338724 30338724 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr21:30338724C>T c.2089G>A c.(2089-2091)Gaa>Aaa p.E697K COAD 21 30339395 30339395 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr21:30339395G>A c.1418C>T c.(1417-1419)aCg>aTg p.T473M COAD 21 30354658 30354658 + Silent SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr21:30354658A>G c.609T>C c.(607-609)ccT>ccC p.P203P COAD 21 30358519 30358519 + Missense_Mutation SNP T T C TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr21:30358519T>C c.286A>G c.(286-288)Aca>Gca p.T96A COAD 21 30358519 30358519 + Missense_Mutation SNP T T C TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr21:30358519T>C c.286A>G c.(286-288)Aca>Gca p.T96A COAD 21 30359089 30359089 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr21:30359089C>T c.209G>A c.(208-210)cGg>cAg p.R70Q COAD 21 30359137 30359137 + Missense_Mutation SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr21:30359137G>A c.161C>T c.(160-162)gCt>gTt p.A54V COADREAD 21 30303489 30303489 + Silent SNP A A G TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr21:30303489A>G c.5226T>C c.(5224-5226)caT>caC p.H1742H COADREAD 21 30303489 30303489 + Silent SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr21:30303489A>G c.5226T>C c.(5224-5226)caT>caC p.H1742H COADREAD 21 30313616 30313616 + Missense_Mutation SNP C C A TCGA-AA-A00O-01A-02W-A00E-09 TCGA-AA-A00O-10A-01W-A00E-09 g.chr21:30313616C>A c.4408G>T c.(4408-4410)Gac>Tac p.D1470Y COADREAD 21 30318238 30318238 + Missense_Mutation SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr21:30318238A>G c.3659T>C c.(3658-3660)gTa>gCa p.V1220A COADREAD 21 30318545 30318545 + Silent SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr21:30318545C>T c.3552G>A c.(3550-3552)gaG>gaA p.E1184E COADREAD 21 30324514 30324514 + Silent SNP A A G TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr21:30324514A>G c.3312T>C c.(3310-3312)gaT>gaC p.D1104D COADREAD 21 30324515 30324515 + Missense_Mutation SNP T T C TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr21:30324515T>C c.3311A>G c.(3310-3312)gAt>gGt p.D1104G COADREAD 21 30324515 30324515 + Missense_Mutation SNP T T C TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr21:30324515T>C c.3311A>G c.(3310-3312)gAt>gGt p.D1104G COADREAD 21 30324515 30324515 + Missense_Mutation SNP T T C TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr21:30324515T>C c.3311A>G c.(3310-3312)gAt>gGt p.D1104G COADREAD 21 30324515 30324515 + Missense_Mutation SNP T T C TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr21:30324515T>C c.3311A>G c.(3310-3312)gAt>gGt p.D1104G COADREAD 21 30324515 30324515 + Missense_Mutation SNP T T G TCGA-AD-6965-01A-11D-1924-10 TCGA-AD-6965-10A-01D-1924-10 g.chr21:30324515T>G c.3311A>C c.(3310-3312)gAt>gCt p.D1104A COADREAD 21 30324516 30324516 + Missense_Mutation SNP C C T TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr21:30324516C>T c.3310G>A c.(3310-3312)Gat>Aat p.D1104N COADREAD 21 30325676 30325676 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr21:30325676C>T c.3102G>A c.(3100-3102)ctG>ctA p.L1034L COADREAD 21 30325699 30325699 + Splice_Site SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr21:30325699C>A c.e17-1 COADREAD 21 30331792 30331792 + Frame_Shift_Del DEL T T - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr21:30331792delT c.2581delA c.(2581-2583)acafs p.T861fs COADREAD 21 30331798 30331798 + Nonsense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr21:30331798C>A c.2575G>T c.(2575-2577)Gaa>Taa p.E859* COADREAD 21 30331911 30331911 + Missense_Mutation SNP G G A TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr21:30331911G>A c.2462C>T c.(2461-2463)tCt>tTt p.S821F COADREAD 21 30332891 30332891 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr21:30332891G>T c.2301C>A c.(2299-2301)ttC>ttA p.F767L COADREAD 21 30332952 30332952 + Missense_Mutation SNP T T A TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr21:30332952T>A c.2240A>T c.(2239-2241)aAc>aTc p.N747I COADREAD 21 30332978 30332978 + Silent SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr21:30332978G>A c.2214C>T c.(2212-2214)ggC>ggT p.G738G COADREAD 21 30338724 30338724 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr21:30338724C>T c.2089G>A c.(2089-2091)Gaa>Aaa p.E697K COADREAD 21 30339395 30339395 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr21:30339395G>A c.1418C>T c.(1417-1419)aCg>aTg p.T473M COADREAD 21 30341850 30341850 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr21:30341850G>A c.1249C>T c.(1249-1251)Cgt>Tgt p.R417C COADREAD 21 30354658 30354658 + Silent SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr21:30354658A>G c.609T>C c.(607-609)ccT>ccC p.P203P COADREAD 21 30358519 30358519 + Missense_Mutation SNP T T C TCGA-AZ-4681-01A-01D-1408-10 TCGA-AZ-4681-10A-01D-1408-10 g.chr21:30358519T>C c.286A>G c.(286-288)Aca>Gca p.T96A COADREAD 21 30358519 30358519 + Missense_Mutation SNP T T C TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr21:30358519T>C c.286A>G c.(286-288)Aca>Gca p.T96A COADREAD 21 30358519 30358519 + Missense_Mutation SNP T T C TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr21:30358519T>C c.286A>G c.(286-288)Aca>Gca p.T96A COADREAD 21 30359089 30359089 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr21:30359089C>T c.209G>A c.(208-210)cGg>cAg p.R70Q COADREAD 21 30359137 30359137 + Missense_Mutation SNP G G A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr21:30359137G>A c.161C>T c.(160-162)gCt>gTt p.A54V DLBC 21 30365143 30365143 + 5'UTR SNP G G A TCGA-RQ-A6JB-01A-11D-A31X-10 TCGA-RQ-A6JB-10A-01D-A31X-10 g.chr21:30365143G>A ESCA 21 30338185 30338185 + Splice_Site SNP A A G TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr21:30338185A>G c.e11+1 ESCA 21 30342970 30342971 + Frame_Shift_Ins INS - - A TCGA-LN-A5U7-01A-11D-A31U-09 TCGA-LN-A5U7-10A-01D-A31U-09 g.chr21:30342970_30342971insA c.1078_1079insT c.(1078-1080)tatfs p.Y360fs ESCA 21 30357050 30357050 + Missense_Mutation SNP G G T TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr21:30357050G>T c.539C>A c.(538-540)cCt>cAt p.P180H GBM 21 30354691 30354691 + Splice_Site SNP C C T TCGA-06-0184-01A-01D-1491-08 TCGA-06-0184-10B-01D-1491-08 g.chr21:30354691C>T c.e5-1 GBM 21 30359239 30359239 + Missense_Mutation SNP C C T TCGA-32-2632-01A-01D-1495-08 TCGA-32-2632-10A-01D-1495-08 g.chr21:30359239C>T c.59G>A c.(58-60)cGa>cAa p.R20Q GBMLGG 21 30318165 30318165 + Nonsense_Mutation SNP C C T TCGA-VM-A8CA-01A-11D-A36O-08 TCGA-VM-A8CA-10A-01D-A367-08 g.chr21:30318165C>T c.3732G>A c.(3730-3732)tgG>tgA p.W1244* GBMLGG 21 30330708 30330708 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr21:30330708C>A c.2747G>T c.(2746-2748)aGt>aTt p.S916I GBMLGG 21 30338725 30338725 + Missense_Mutation SNP C C T TCGA-DU-A5TY-01A-11D-A289-08 TCGA-DU-A5TY-10A-01D-A289-08 g.chr21:30338725C>T c.2088G>A c.(2086-2088)atG>atA p.M696I GBMLGG 21 30342876 30342876 + Silent SNP A A C TCGA-DB-A64V-01A-11D-A29Q-08 TCGA-DB-A64V-10A-01D-A29Q-08 g.chr21:30342876A>C c.1173T>G c.(1171-1173)gcT>gcG p.A391A GBMLGG 21 30343646 30343646 + Missense_Mutation SNP T T C TCGA-E1-A7YS-01A-11D-A34A-08 TCGA-E1-A7YS-10A-01D-A34A-08 g.chr21:30343646T>C c.931A>G c.(931-933)Att>Gtt p.I311V GBMLGG 21 30343762 30343762 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr21:30343762C>T c.815G>A c.(814-816)cGc>cAc p.R272H GBMLGG 21 30354657 30354657 + Missense_Mutation SNP C C G TCGA-S9-A7IX-01A-12D-A34A-08 TCGA-S9-A7IX-10A-01D-A34A-08 g.chr21:30354657C>G c.610G>C c.(610-612)Gat>Cat p.D204H GBMLGG 21 30354691 30354691 + Splice_Site SNP C C T TCGA-06-0184-01A-01D-1491-08 TCGA-06-0184-10B-01D-1491-08 g.chr21:30354691C>T c.e5-1 GBMLGG 21 30359239 30359239 + Missense_Mutation SNP C C T TCGA-32-2632-01A-01D-1495-08 TCGA-32-2632-10A-01D-1495-08 g.chr21:30359239C>T c.59G>A c.(58-60)cGa>cAa p.R20Q HNSC 21 30303556 30303556 + Missense_Mutation SNP G G A TCGA-CR-6487-01A-11D-1870-08 TCGA-CR-6487-10A-01D-1870-08 g.chr21:30303556G>A c.5159C>T c.(5158-5160)tCa>tTa p.S1720L HNSC 21 30308938 30308938 + Missense_Mutation SNP C C G TCGA-IQ-A61I-01A-11D-A30E-08 TCGA-IQ-A61I-10A-01D-A30H-08 g.chr21:30308938C>G c.4564G>C c.(4564-4566)Gaa>Caa p.E1522Q HNSC 21 30308975 30308975 + Silent SNP C C T TCGA-IQ-A61I-01A-11D-A30E-08 TCGA-IQ-A61I-10A-01D-A30H-08 g.chr21:30308975C>T c.4527G>A c.(4525-4527)ttG>ttA p.L1509L HNSC 21 30309016 30309016 + Missense_Mutation SNP G G A TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr21:30309016G>A c.4486C>T c.(4486-4488)Cgg>Tgg p.R1496W HNSC 21 30315991 30315991 + Nonsense_Mutation SNP G G C TCGA-CN-4730-01A-01D-1434-08 TCGA-CN-4730-10A-01D-1434-08 g.chr21:30315991G>C c.4218C>G c.(4216-4218)taC>taG p.Y1406* HNSC 21 30318479 30318479 + Silent SNP G G A TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chr21:30318479G>A c.3618C>T c.(3616-3618)ttC>ttT p.F1206F HNSC 21 30318479 30318479 + Silent SNP G G A TCGA-CV-7252-01A-11D-2012-08 TCGA-CV-7252-10A-01D-2013-08 g.chr21:30318479G>A c.3618C>T c.(3616-3618)ttC>ttT p.F1206F HNSC 21 30339459 30339459 + Missense_Mutation SNP G G T TCGA-CN-4729-01A-01D-1434-08 TCGA-CN-4729-10A-01D-1434-08 g.chr21:30339459G>T c.1354C>A c.(1354-1356)Caa>Aaa p.Q452K HNSC 21 30339475 30339475 + Silent SNP G G C TCGA-T3-A92M-01A-31D-A391-08 TCGA-T3-A92M-10A-01D-A394-08 g.chr21:30339475G>C c.1338C>G c.(1336-1338)ctC>ctG p.L446L HNSC 21 30357237 30357237 + Missense_Mutation SNP C C T TCGA-CV-5430-01A-02D-1683-08 TCGA-CV-5430-10A-01D-1870-08 g.chr21:30357237C>T c.352G>A c.(352-354)Gac>Aac p.D118N HNSC 21 30359144 30359144 + Missense_Mutation SNP G G C TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chr21:30359144G>C c.154C>G c.(154-156)Caa>Gaa p.Q52E KICH 21 30307615 30307615 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr21:30307615G>A c.4691C>T c.(4690-4692)gCt>gTt p.A1564V KICH 21 30331996 30331996 + Missense_Mutation SNP C C T TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr21:30331996C>T c.2377G>A c.(2377-2379)Gtt>Att p.V793I KIPAN 21 30307615 30307615 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr21:30307615G>A c.4691C>T c.(4690-4692)gCt>gTt p.A1564V KIPAN 21 30331797 30331797 + Missense_Mutation SNP T T G TCGA-B0-4844-01A-01D-1361-10 TCGA-B0-4844-11A-01D-1361-10 g.chr21:30331797T>G c.2576A>C c.(2575-2577)gAa>gCa p.E859A KIPAN 21 30331996 30331996 + Missense_Mutation SNP C C T TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr21:30331996C>T c.2377G>A c.(2377-2379)Gtt>Att p.V793I KIPAN 21 30339388 30339388 + Missense_Mutation SNP T T G TCGA-IA-A83S-01A-11D-A34Z-10 TCGA-IA-A83S-11A-11D-A34Z-10 g.chr21:30339388T>G c.1425A>C c.(1423-1425)aaA>aaC p.K475N KIPAN 21 30339421 30339422 + Frame_Shift_Ins INS - - A TCGA-CZ-5465-01A-01D-1806-10 TCGA-CZ-5465-11A-01D-1501-10 g.chr21:30339421_30339422insA c.1391_1392insT c.(1390-1392)ctafs p.L464fs KIRC 21 30331797 30331797 + Missense_Mutation SNP T T G TCGA-B0-4844-01A-01D-1361-10 TCGA-B0-4844-11A-01D-1361-10 g.chr21:30331797T>G c.2576A>C c.(2575-2577)gAa>gCa p.E859A KIRC 21 30339421 30339422 + Frame_Shift_Ins INS - - A TCGA-CZ-5465-01A-01D-1806-10 TCGA-CZ-5465-11A-01D-1501-10 g.chr21:30339421_30339422insA c.1391_1392insT c.(1390-1392)ctafs p.L464fs KIRP 21 30339388 30339388 + Missense_Mutation SNP T T G TCGA-IA-A83S-01A-11D-A34Z-10 TCGA-IA-A83S-11A-11D-A34Z-10 g.chr21:30339388T>G c.1425A>C c.(1423-1425)aaA>aaC p.K475N LGG 21 30318165 30318165 + Nonsense_Mutation SNP C C T TCGA-VM-A8CA-01A-11D-A36O-08 TCGA-VM-A8CA-10A-01D-A367-08 g.chr21:30318165C>T c.3732G>A c.(3730-3732)tgG>tgA p.W1244* LGG 21 30330708 30330708 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr21:30330708C>A c.2747G>T c.(2746-2748)aGt>aTt p.S916I LGG 21 30338725 30338725 + Missense_Mutation SNP C C T TCGA-DU-A5TY-01A-11D-A289-08 TCGA-DU-A5TY-10A-01D-A289-08 g.chr21:30338725C>T c.2088G>A c.(2086-2088)atG>atA p.M696I LGG 21 30342876 30342876 + Silent SNP A A C TCGA-DB-A64V-01A-11D-A29Q-08 TCGA-DB-A64V-10A-01D-A29Q-08 g.chr21:30342876A>C c.1173T>G c.(1171-1173)gcT>gcG p.A391A LGG 21 30343646 30343646 + Missense_Mutation SNP T T C TCGA-E1-A7YS-01A-11D-A34A-08 TCGA-E1-A7YS-10A-01D-A34A-08 g.chr21:30343646T>C c.931A>G c.(931-933)Att>Gtt p.I311V LGG 21 30343762 30343762 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr21:30343762C>T c.815G>A c.(814-816)cGc>cAc p.R272H LGG 21 30354657 30354657 + Missense_Mutation SNP C C G TCGA-S9-A7IX-01A-12D-A34A-08 TCGA-S9-A7IX-10A-01D-A34A-08 g.chr21:30354657C>G c.610G>C c.(610-612)Gat>Cat p.D204H LIHC 21 30329699 30329699 + Silent SNP C C T TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chr21:30329699C>T c.2847G>A c.(2845-2847)ccG>ccA p.P949P LIHC 21 30339226 30339226 + Silent SNP C C T TCGA-BD-A3EP-01A-11D-A22F-10 TCGA-BD-A3EP-11A-12D-A22F-10 g.chr21:30339226C>T c.1587G>A c.(1585-1587)ttG>ttA p.L529L LIHC 21 30341864 30341864 + Missense_Mutation SNP A A C TCGA-DD-AACL-01A-11D-A40R-10 TCGA-DD-AACL-10A-01D-A40U-10 g.chr21:30341864A>C c.1235T>G c.(1234-1236)tTt>tGt p.F412C LIHC 21 30343736 30343736 + Missense_Mutation SNP C C A TCGA-DD-A4ND-01A-11D-A25V-10 TCGA-DD-A4ND-11A-11D-A25V-10 g.chr21:30343736C>A c.841G>T c.(841-843)Gca>Tca p.A281S LIHC 21 30354673 30354673 + Silent SNP A A G TCGA-DD-A113-01A-11D-A12Z-10 TCGA-DD-A113-10A-01D-A12Z-10 g.chr21:30354673A>G c.594T>C c.(592-594)ctT>ctC p.L198L LUAD 21 30303521 30303521 + Missense_Mutation SNP T T C TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr21:30303521T>C c.5194A>G c.(5194-5196)Aaa>Gaa p.K1732E LUAD 21 30303583 30303583 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr21:30303583C>A c.5132G>T c.(5131-5133)gGt>gTt p.G1711V LUAD 21 30304976 30304976 + Missense_Mutation SNP C C A TCGA-86-8673-01A-11D-2393-08 TCGA-86-8673-10A-01D-2393-08 g.chr21:30304976C>A c.4886G>T c.(4885-4887)cGa>cTa p.R1629L LUAD 21 30304987 30304987 + Splice_Site SNP C C A TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr21:30304987C>A c.e28-1 LUAD 21 30308959 30308959 + Missense_Mutation SNP G G C TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr21:30308959G>C c.4543C>G c.(4543-4545)Cac>Gac p.H1515D LUAD 21 30313665 30313666 + Frame_Shift_Ins INS - - A TCGA-97-7554-01A-11D-2036-08 TCGA-97-7554-10A-01D-2036-08 g.chr21:30313665_30313666insA c.4358_4359insT c.(4357-4359)ttgfs p.L1453fs LUAD 21 30315659 30315659 + Splice_Site SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr21:30315659C>A c.e24-1 LUAD 21 30316856 30316856 + Missense_Mutation SNP G G T TCGA-MP-A4TF-01A-11D-A25L-08 TCGA-MP-A4TF-10A-01D-A25L-08 g.chr21:30316856G>T c.3831C>A c.(3829-3831)agC>agA p.S1277R LUAD 21 30319883 30319883 + Silent SNP T T A TCGA-17-Z056-01A-01W-0747-08 TCGA-17-Z056-11A-01W-0747-08 g.chr21:30319883T>A c.3390A>T c.(3388-3390)ctA>ctT p.L1130L LUAD 21 30324587 30324587 + Splice_Site SNP C C A TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr21:30324587C>A c.e18-1 LUAD 21 30325585 30325585 + Missense_Mutation SNP G G A TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr21:30325585G>A c.3193C>T c.(3193-3195)Cgt>Tgt p.R1065C LUAD 21 30329087 30329087 + Missense_Mutation SNP T T A TCGA-17-Z060-01A-01W-0747-08 TCGA-17-Z060-11A-01W-0747-08 g.chr21:30329087T>A c.3076A>T c.(3076-3078)Ata>Tta p.I1026L LUAD 21 30329201 30329201 + Frame_Shift_Del DEL C C - TCGA-55-8090-01A-11D-2238-08 TCGA-55-8090-10A-01D-2238-08 g.chr21:30329201delC c.2962delG c.(2962-2964)gaafs p.E988fs LUAD 21 30342994 30342994 + Missense_Mutation SNP C C A TCGA-MP-A4TC-01A-11D-A24P-08 TCGA-MP-A4TC-10A-01D-A24P-08 g.chr21:30342994C>A c.1055G>T c.(1054-1056)gGt>gTt p.G352V LUAD 21 30342995 30342995 + Missense_Mutation SNP C C A TCGA-MP-A4TC-01A-11D-A24P-08 TCGA-MP-A4TC-10A-01D-A24P-08 g.chr21:30342995C>A c.1054G>T c.(1054-1056)Ggt>Tgt p.G352C LUAD 21 30343757 30343757 + Missense_Mutation SNP C C A TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr21:30343757C>A c.820G>T c.(820-822)Gct>Tct p.A274S LUAD 21 30353440 30353440 + Splice_Site SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr21:30353440C>A c.e6+1 LUAD 21 30357072 30357072 + Missense_Mutation SNP C C T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr21:30357072C>T c.517G>A c.(517-519)Gct>Act p.A173T LUAD 21 30359174 30359174 + Nonsense_Mutation SNP G G A TCGA-97-8174-01A-11D-2284-08 TCGA-97-8174-10A-01D-2284-08 g.chr21:30359174G>A c.124C>T c.(124-126)Cag>Tag p.Q42* LUSC 21 30302818 30302818 + Silent SNP T T C TCGA-22-5482-01A-01D-1632-08 TCGA-22-5482-11A-01D-1632-08 g.chr21:30302818T>C c.5253A>G c.(5251-5253)acA>acG p.T1751T LUSC 21 30304833 30304833 + Silent SNP G G T TCGA-46-3767-01A-01D-0983-08 TCGA-46-3767-10A-01D-0983-08 g.chr21:30304833G>T c.5029C>A c.(5029-5031)Cgg>Agg p.R1677R LUSC 21 30304965 30304965 + Silent SNP G G T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr21:30304965G>T c.4897C>A c.(4897-4899)Cga>Aga p.R1633R LUSC 21 30354687 30354687 + Silent SNP G G A TCGA-37-4135-01A-01D-1352-08 TCGA-37-4135-10A-01D-1352-08 g.chr21:30354687G>A c.580C>T c.(580-582)Ctg>Ttg p.L194L LUSC 21 30357092 30357092 + Missense_Mutation SNP G G T TCGA-66-2755-01A-01D-1522-08 TCGA-66-2755-11A-01D-1522-08 g.chr21:30357092G>T c.497C>A c.(496-498)gCa>gAa p.A166E LUSC 21 30359114 30359114 + Missense_Mutation SNP C C G TCGA-34-5928-01A-11D-1817-08 TCGA-34-5928-10A-01D-1817-08 g.chr21:30359114C>G c.184G>C c.(184-186)Gat>Cat p.D62H OV 21 30303480 30303480 + Missense_Mutation SNP G G C TCGA-13-2059-01A-01D-1526-09 TCGA-13-2059-10A-01D-1526-09 g.chr21:30303480G>C c.5235C>G c.(5233-5235)tgC>tgG p.C1745W OV 21 30303491 30303491 + Missense_Mutation SNP G G T TCGA-04-1346-01A-01W-0488-09 TCGA-04-1346-11A-01W-0489-09 g.chr21:30303491G>T c.5224C>A c.(5224-5226)Cat>Aat p.H1742N OV 21 30304906 30304906 + Silent SNP C C T TCGA-20-1686-01A-01W-0633-09 TCGA-20-1686-10A-01W-0633-09 g.chr21:30304906C>T c.4956G>A c.(4954-4956)ctG>ctA p.L1652L OV 21 30316000 30316000 + Silent SNP A A G TCGA-13-2061-01A-01D-1526-09 TCGA-13-2061-10A-01D-1526-09 g.chr21:30316000A>G c.4209T>C c.(4207-4209)caT>caC p.H1403H OV 21 30324516 30324516 + Missense_Mutation SNP C C T TCGA-57-1993-01A-01W-0699-08 TCGA-57-1993-11A-01W-0700-08 g.chr21:30324516C>T c.3310G>A c.(3310-3312)Gat>Aat p.D1104N OV 21 30331873 30331873 + Missense_Mutation SNP C C T TCGA-61-1900-01A-01W-0639-09 TCGA-61-1900-11A-01W-0640-09 g.chr21:30331873C>T c.2500G>A c.(2500-2502)Gcg>Acg p.A834T OV 21 30343693 30343693 + Missense_Mutation SNP G G C TCGA-29-1691-01A-01W-0633-09 TCGA-29-1691-10A-01W-0633-09 g.chr21:30343693G>C c.884C>G c.(883-885)tCc>tGc p.S295C OV 21 30358518 30358518 + Missense_Mutation SNP G G A TCGA-13-1497-01A-01W-0549-09 TCGA-13-1497-10A-01W-0549-09 g.chr21:30358518G>A c.287C>T c.(286-288)aCa>aTa p.T96I PAAD 21 30338786 30338786 + Missense_Mutation SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr21:30338786T>G c.2027A>C c.(2026-2028)aAg>aCg p.K676T PAAD 21 30359125 30359125 + Missense_Mutation SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr21:30359125T>G c.173A>C c.(172-174)gAc>gCc p.D58A PRAD 21 30308907 30308907 + Missense_Mutation SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr21:30308907T>C c.4595A>G c.(4594-4596)gAg>gGg p.E1532G PRAD 21 30331780 30331780 + Splice_Site SNP C C A TCGA-HC-7080-01A-11D-1961-08 TCGA-HC-7080-10A-01D-1961-08 g.chr21:30331780C>A c.2593G>T c.(2593-2595)Gat>Tat p.D865Y PRAD 21 30339290 30339290 + Missense_Mutation SNP T T G TCGA-G9-6371-01A-11D-1786-08 TCGA-G9-6371-10A-01D-1786-08 g.chr21:30339290T>G c.1523A>C c.(1522-1524)gAt>gCt p.D508A PRAD 21 30354640 30354640 + Silent SNP C C T TCGA-EJ-AB27-01A-11D-A41K-08 TCGA-EJ-AB27-10A-01D-A41N-08 g.chr21:30354640C>T c.627G>A c.(625-627)ccG>ccA p.P209P PRAD 21 30359240 30359240 + Missense_Mutation SNP G G C TCGA-ZG-A9M4-01A-11D-A41K-08 TCGA-ZG-A9M4-10A-01D-A41N-08 g.chr21:30359240G>C c.58C>G c.(58-60)Cga>Gga p.R20G READ 21 30325676 30325676 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr21:30325676C>T c.3102G>A c.(3100-3102)ctG>ctA p.L1034L READ 21 30332891 30332891 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr21:30332891G>T c.2301C>A c.(2299-2301)ttC>ttA p.F767L READ 21 30341850 30341850 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr21:30341850G>A c.1249C>T c.(1249-1251)Cgt>Tgt p.R417C READ 21 30358519 30358519 + Missense_Mutation SNP T T C TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr21:30358519T>C c.286A>G c.(286-288)Aca>Gca p.T96A SARC 21 30303544 30303544 + Missense_Mutation SNP C C T TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr21:30303544C>T c.5171G>A c.(5170-5172)gGt>gAt p.G1724D SARC 21 30316157 30316157 + Missense_Mutation SNP G G A TCGA-DX-AB2Z-01A-11D-A387-09 TCGA-DX-AB2Z-10A-01D-A38A-09 g.chr21:30316157G>A c.4052C>T c.(4051-4053)aCg>aTg p.T1351M SARC 21 30358501 30358501 + Missense_Mutation SNP C C A TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr21:30358501C>A c.304G>T c.(304-306)Gtt>Ttt p.V102F SKCM 21 30303532 30303532 + Missense_Mutation SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr21:30303532G>A c.5183C>T c.(5182-5184)tCc>tTc p.S1728F SKCM 21 30304892 30304892 + Missense_Mutation SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr21:30304892G>A c.4970C>T c.(4969-4971)cCa>cTa p.P1657L SKCM 21 30307468 30307468 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr21:30307468G>A c.4838C>T c.(4837-4839)tCt>tTt p.S1613F SKCM 21 30308901 30308901 + Missense_Mutation SNP G G T TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr21:30308901G>T c.4601C>A c.(4600-4602)cCa>cAa p.P1534Q SKCM 21 30316198 30316198 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr21:30316198G>A c.4011C>T c.(4009-4011)tcC>tcT p.S1337S SKCM 21 30316752 30316752 + Missense_Mutation SNP G G A TCGA-ER-A19G-06A-11D-A196-08 TCGA-ER-A19G-10A-01D-A198-08 g.chr21:30316752G>A c.3935C>T c.(3934-3936)tCc>tTc p.S1312F SKCM 21 30318484 30318484 + Missense_Mutation SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr21:30318484G>A c.3613C>T c.(3613-3615)Ctt>Ttt p.L1205F SKCM 21 30318520 30318520 + Missense_Mutation SNP T T C TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr21:30318520T>C c.3577A>G c.(3577-3579)Ata>Gta p.I1193V SKCM 21 30325549 30325549 + Missense_Mutation SNP A A C TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr21:30325549A>C c.3229T>G c.(3229-3231)Tta>Gta p.L1077V SKCM 21 30329142 30329142 + Missense_Mutation SNP C C T TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr21:30329142C>T c.3021G>A c.(3019-3021)atG>atA p.M1007I SKCM 21 30329731 30329731 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr21:30329731G>A c.2815C>T c.(2815-2817)Ctt>Ttt p.L939F SKCM 21 30330851 30330851 + Silent SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr21:30330851G>A c.2604C>T c.(2602-2604)atC>atT p.I868I SKCM 21 30338844 30338844 + Missense_Mutation SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr21:30338844G>A c.1969C>T c.(1969-1971)Cct>Tct p.P657S SKCM 21 30338887 30338887 + Silent SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr21:30338887G>A c.1926C>T c.(1924-1926)gtC>gtT p.V642V SKCM 21 30339281 30339281 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr21:30339281G>A c.1532C>T c.(1531-1533)tCc>tTc p.S511F SKCM 21 30339415 30339415 + Silent SNP G G A TCGA-FS-A1ZS-06A-12D-A197-08 TCGA-FS-A1ZS-10A-01D-A199-08 g.chr21:30339415G>A c.1398C>T c.(1396-1398)tcC>tcT p.S466S SKCM 21 30357190 30357190 + Silent SNP G G A TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr21:30357190G>A c.399C>T c.(397-399)atC>atT p.I133I SKCM 21 30357224 30357224 + Missense_Mutation SNP C C T TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr21:30357224C>T c.365G>A c.(364-366)cGa>cAa p.R122Q SKCM 21 30365209 30365209 + 5'Flank SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr21:30365209G>A SKCM 21 30365209 30365209 + 5'Flank SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr21:30365209G>A SKCM 21 30365209 30365209 + 5'Flank SNP G G A TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr21:30365209G>A SKCM 21 30365209 30365209 + 5'Flank SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr21:30365209G>A SKCM 21 30365209 30365209 + 5'Flank SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr21:30365209G>A SKCM 21 30365230 30365230 + 5'Flank SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr21:30365230C>T SKCM 21 30365231 30365231 + 5'Flank SNP C C T TCGA-ER-A3PL-06A-11D-A23B-08 TCGA-ER-A3PL-10A-01D-A23B-08 g.chr21:30365231C>T

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 21 30365233 30365233 single base substitution C G missense_variant G11A 32G>C ALL-US 21 30365233 30365233 single base substitution C G upstream_gene_variant BLCA-CN 21 30329105 30329105 single base substitution T A downstream_gene_variant BLCA-CN 21 30329105 30329105 single base substitution T A missense_variant N1020Y 3058A>T BLCA-CN 21 30329105 30329105 single base substitution T A missense_variant N1066Y 3196A>T BLCA-CN 21 30339475 30339475 single base substitution G C 3_prime_UTR_variant BLCA-CN 21 30339475 30339475 single base substitution G C synonymous_variant L446L 1338C>G BLCA-CN 21 30339475 30339475 single base substitution G C synonymous_variant L492L 1476C>G BLCA-CN 21 30365104 30365104 single base substitution C A missense_variant R54L 161G>T BLCA-CN 21 30365104 30365104 single base substitution C A missense_variant R8L 23G>T BLCA-US 21 30307437 30307437 single base substitution G T synonymous_variant G1623G 4869C>A BLCA-US 21 30307437 30307437 single base substitution G T synonymous_variant G1669G 5007C>A BLCA-US 21 30307608 30307608 single base substitution T C synonymous_variant S1566S 4698A>G BLCA-US 21 30307608 30307608 single base substitution T C synonymous_variant S1612S 4836A>G BLCA-US 21 30316094 30316094 single base substitution T C missense_variant K1372R 4115A>G BLCA-US 21 30316094 30316094 single base substitution T C missense_variant K1418R 4253A>G BLCA-US 21 30331900 30331900 single base substitution C A downstream_gene_variant BLCA-US 21 30331900 30331900 single base substitution C A exon_variant BLCA-US 21 30331900 30331900 single base substitution C A missense_variant D825Y 2473G>T BLCA-US 21 30331900 30331900 single base substitution C A missense_variant D871Y 2611G>T BLCA-US 21 30339132 30339132 single base substitution C G downstream_gene_variant BLCA-US 21 30339132 30339132 single base substitution C G missense_variant E561Q 1681G>C BLCA-US 21 30339132 30339132 single base substitution C G missense_variant E607Q 1819G>C BLCA-US 21 30365173 30365173 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant BLCA-US 21 30365173 30365173 single base substitution C A missense_variant R31L 92G>T BOCA-FR 21 30313773 30313773 single base substitution T A intron_variant BRCA-EU 21 30297258 30297258 single base substitution G A downstream_gene_variant BRCA-EU 21 30300924 30300924 single base substitution T G 3_prime_UTR_variant BRCA-EU 21 30302377 30302377 single base substitution C T 3_prime_UTR_variant BRCA-EU 21 30302997 30302997 single base substitution G A intron_variant BRCA-EU 21 30303920 30303920 single base substitution C G intron_variant BRCA-EU 21 30304044 30304044 single base substitution C T intron_variant BRCA-EU 21 30304311 30304311 single base substitution G T intron_variant BRCA-EU 21 30306244 30306244 single base substitution C T intron_variant BRCA-EU 21 30309023 30309023 single base substitution G C splice_region_variant BRCA-EU 21 30309540 30309540 single base substitution C T intron_variant BRCA-EU 21 30312104 30312104 single base substitution G T intron_variant BRCA-EU 21 30312880 30312880 single base substitution C G intron_variant BRCA-EU 21 30312893 30312893 deletion of <=200bp A - intron_variant BRCA-EU 21 30313454 30313454 single base substitution C G intron_variant BRCA-EU 21 30313587 30313587 single base substitution G C synonymous_variant L1479L 4437C>G BRCA-EU 21 30313587 30313587 single base substitution G C synonymous_variant L1525L 4575C>G BRCA-EU 21 30314063 30314063 single base substitution G A intron_variant BRCA-EU 21 30315149 30315149 single base substitution C T intron_variant BRCA-EU 21 30316444 30316444 single base substitution G A intron_variant BRCA-EU 21 30319338 30319338 single base substitution C G intron_variant BRCA-EU 21 30319517 30319517 single base substitution G C intron_variant BRCA-EU 21 30321145 30321145 single base substitution C G intron_variant BRCA-EU 21 30321480 30321480 single base substitution A G intron_variant BRCA-EU 21 30321884 30321884 single base substitution G T intron_variant BRCA-EU 21 30323018 30323018 single base substitution T G intron_variant BRCA-EU 21 30323062 30323062 single base substitution C A intron_variant BRCA-EU 21 30323222 30323222 deletion of <=200bp G - intron_variant BRCA-EU 21 30326787 30326787 single base substitution C G downstream_gene_variant BRCA-EU 21 30326787 30326787 single base substitution C G intron_variant BRCA-EU 21 30327555 30327555 single base substitution T C downstream_gene_variant BRCA-EU 21 30327555 30327555 single base substitution T C intron_variant BRCA-EU 21 30330411 30330411 single base substitution G C downstream_gene_variant BRCA-EU 21 30330411 30330411 single base substitution G C intron_variant BRCA-EU 21 30330746 30330746 single base substitution C T downstream_gene_variant BRCA-EU 21 30330746 30330746 single base substitution C T exon_variant BRCA-EU 21 30330746 30330746 single base substitution C T synonymous_variant L903L 2709G>A BRCA-EU 21 30330746 30330746 single base substitution C T synonymous_variant L949L 2847G>A BRCA-EU 21 30331593 30331593 single base substitution T A downstream_gene_variant BRCA-EU 21 30331593 30331593 single base substitution T A intron_variant BRCA-EU 21 30332896 30332896 single base substitution G C downstream_gene_variant BRCA-EU 21 30332896 30332896 single base substitution G C exon_variant BRCA-EU 21 30332896 30332896 single base substitution G C missense_variant H766D 2296C>G BRCA-EU 21 30332896 30332896 single base substitution G C missense_variant H812D 2434C>G BRCA-EU 21 30332896 30332896 single base substitution G C upstream_gene_variant BRCA-EU 21 30332900 30332900 single base substitution T C downstream_gene_variant BRCA-EU 21 30332900 30332900 single base substitution T C exon_variant BRCA-EU 21 30332900 30332900 single base substitution T C synonymous_variant E764E 2292A>G BRCA-EU 21 30332900 30332900 single base substitution T C synonymous_variant E810E 2430A>G BRCA-EU 21 30332900 30332900 single base substitution T C upstream_gene_variant BRCA-EU 21 30333329 30333329 single base substitution T C downstream_gene_variant BRCA-EU 21 30333329 30333329 single base substitution T C intron_variant BRCA-EU 21 30333329 30333329 single base substitution T C upstream_gene_variant BRCA-EU 21 30334065 30334065 single base substitution C A intron_variant BRCA-EU 21 30334065 30334065 single base substitution C A upstream_gene_variant BRCA-EU 21 30335499 30335499 single base substitution A C downstream_gene_variant BRCA-EU 21 30335499 30335499 single base substitution A C intron_variant BRCA-EU 21 30335499 30335499 single base substitution A C upstream_gene_variant BRCA-EU 21 30337898 30337898 single base substitution G C downstream_gene_variant BRCA-EU 21 30337898 30337898 single base substitution G C intron_variant BRCA-EU 21 30337898 30337898 single base substitution G C upstream_gene_variant BRCA-EU 21 30339266 30339266 single base substitution G T 3_prime_UTR_variant BRCA-EU 21 30339266 30339266 single base substitution G T missense_variant S516Y 1547C>A BRCA-EU 21 30339266 30339266 single base substitution G T missense_variant S562Y 1685C>A BRCA-EU 21 30339396 30339396 single base substitution T C 3_prime_UTR_variant BRCA-EU 21 30339396 30339396 single base substitution T C missense_variant T473A 1417A>G BRCA-EU 21 30339396 30339396 single base substitution T C missense_variant T519A 1555A>G BRCA-EU 21 30340300 30340300 single base substitution G A intron_variant BRCA-EU 21 30340300 30340300 single base substitution G A splice_region_variant BRCA-EU 21 30342211 30342211 single base substitution G A intron_variant BRCA-EU 21 30344797 30344797 single base substitution G C intron_variant BRCA-EU 21 30344825 30344825 single base substitution G C intron_variant BRCA-EU 21 30345166 30345166 single base substitution G A intron_variant BRCA-EU 21 30346181 30346181 single base substitution C G intron_variant BRCA-EU 21 30347810 30347810 single base substitution G T intron_variant BRCA-EU 21 30351705 30351705 single base substitution G A intron_variant BRCA-EU 21 30354248 30354248 single base substitution C A intron_variant BRCA-EU 21 30355101 30355101 single base substitution C T intron_variant BRCA-EU 21 30355621 30355621 single base substitution C A intron_variant BRCA-EU 21 30357369 30357369 deletion of <=200bp T - intron_variant BRCA-EU 21 30358856 30358856 single base substitution G A intron_variant BRCA-EU 21 30359240 30359240 single base substitution G C missense_variant R20G 58C>G BRCA-EU 21 30359240 30359240 single base substitution G C missense_variant R66G 196C>G BRCA-EU 21 30359240 30359240 single base substitution G C upstream_gene_variant BRCA-EU 21 30362098 30362098 single base substitution C T intron_variant BRCA-EU 21 30362098 30362098 single base substitution C T upstream_gene_variant BRCA-EU 21 30362181 30362181 single base substitution C G intron_variant BRCA-EU 21 30362181 30362181 single base substitution C G upstream_gene_variant BRCA-EU 21 30362349 30362349 single base substitution T C intron_variant BRCA-EU 21 30362349 30362349 single base substitution T C upstream_gene_variant BRCA-EU 21 30365049 30365049 single base substitution G A intron_variant BRCA-EU 21 30365058 30365058 single base substitution G T intron_variant BRCA-EU 21 30366200 30366200 single base substitution T A upstream_gene_variant BRCA-EU 21 30366277 30366277 single base substitution G C upstream_gene_variant BRCA-EU 21 30366333 30366333 single base substitution G A upstream_gene_variant BRCA-EU 21 30366519 30366519 single base substitution C A upstream_gene_variant BRCA-EU 21 30367069 30367069 single base substitution T C upstream_gene_variant BRCA-EU 21 30367383 30367383 single base substitution G T upstream_gene_variant BRCA-EU 21 30368118 30368118 deletion of <=200bp A - upstream_gene_variant BRCA-EU 21 30368237 30368237 single base substitution A C upstream_gene_variant BRCA-EU 21 30368339 30368340 deletion of <=200bp GA - upstream_gene_variant BRCA-FR 21 30297258 30297258 single base substitution G A downstream_gene_variant BRCA-FR 21 30312104 30312104 single base substitution G T intron_variant BRCA-FR 21 30319517 30319517 single base substitution G C intron_variant BRCA-FR 21 30325806 30325806 single base substitution C G downstream_gene_variant BRCA-FR 21 30325806 30325806 single base substitution C G intron_variant BRCA-FR 21 30344797 30344797 single base substitution G C intron_variant BRCA-FR 21 30344825 30344825 single base substitution G C intron_variant BRCA-FR 21 30345719 30345719 single base substitution G A intron_variant BRCA-FR 21 30345852 30345852 single base substitution C G intron_variant BRCA-FR 21 30346181 30346181 single base substitution C G intron_variant BRCA-FR 21 30354248 30354248 single base substitution C A intron_variant BRCA-FR 21 30355101 30355101 single base substitution C T intron_variant BRCA-FR 21 30366519 30366519 single base substitution C A upstream_gene_variant BRCA-KR 21 30308879 30308879 single base substitution G A synonymous_variant F1541F 4623C>T BRCA-KR 21 30308879 30308879 single base substitution G A synonymous_variant F1587F 4761C>T BRCA-UK 21 30359796 30359796 single base substitution G C intron_variant BRCA-UK 21 30359796 30359796 single base substitution G C upstream_gene_variant BRCA-UK 21 30362181 30362181 single base substitution C G intron_variant BRCA-UK 21 30362181 30362181 single base substitution C G upstream_gene_variant BRCA-UK 21 30364230 30364230 single base substitution C T intron_variant BRCA-US 21 30316846 30316846 single base substitution C T missense_variant A1281T 3841G>A BRCA-US 21 30316846 30316846 single base substitution C T missense_variant A1327T 3979G>A BRCA-US 21 30318544 30318544 single base substitution G T missense_variant L1185I 3553C>A BRCA-US 21 30318544 30318544 single base substitution G T missense_variant L1231I 3691C>A BRCA-US 21 30331787 30331787 single base substitution A C downstream_gene_variant BRCA-US 21 30331787 30331787 single base substitution A C exon_variant BRCA-US 21 30331787 30331787 single base substitution A C missense_variant H862Q 2586T>G BRCA-US 21 30331787 30331787 single base substitution A C missense_variant H908Q 2724T>G BRCA-US 21 30332984 30332984 single base substitution G C downstream_gene_variant BRCA-US 21 30332984 30332984 single base substitution G C exon_variant BRCA-US 21 30332984 30332984 single base substitution G C synonymous_variant L736L 2208C>G BRCA-US 21 30332984 30332984 single base substitution G C synonymous_variant L782L 2346C>G BRCA-US 21 30332984 30332984 single base substitution G C upstream_gene_variant BRCA-US 21 30339479 30339479 single base substitution A C 3_prime_UTR_variant BRCA-US 21 30339479 30339479 single base substitution A C missense_variant V445G 1334T>G BRCA-US 21 30339479 30339479 single base substitution A C missense_variant V491G 1472T>G BRCA-US 21 30365115 30365115 single base substitution C T synonymous_variant K4K 12G>A BRCA-US 21 30365115 30365115 single base substitution C T synonymous_variant K50K 150G>A BRCA-US 21 30365148 30365148 single base substitution C G 5_prime_UTR_variant BRCA-US 21 30365148 30365148 single base substitution C G missense_variant Q39H 117G>C BTCA-JP 21 30303391 30303391 single base substitution G A intron_variant BTCA-JP 21 30303392 30303392 single base substitution T G intron_variant BTCA-JP 21 30303592 30303592 single base substitution C T missense_variant R1708H 5123G>A BTCA-JP 21 30303592 30303592 single base substitution C T missense_variant R1754H 5261G>A BTCA-JP 21 30319939 30319939 deletion of <=200bp A - intron_variant BTCA-JP 21 30329069 30329069 single base substitution C A downstream_gene_variant BTCA-JP 21 30329069 30329069 single base substitution C A intron_variant BTCA-JP 21 30329265 30329265 single base substitution T G downstream_gene_variant BTCA-JP 21 30329265 30329265 single base substitution T G missense_variant L1012F 3036A>C BTCA-JP 21 30329265 30329265 single base substitution T G missense_variant L966F 2898A>C BTCA-JP 21 30330929 30330929 single base substitution G T downstream_gene_variant BTCA-JP 21 30330929 30330929 single base substitution G T intron_variant BTCA-JP 21 30331736 30331736 single base substitution G A downstream_gene_variant BTCA-JP 21 30331736 30331736 single base substitution G A exon_variant BTCA-JP 21 30331736 30331736 single base substitution G A intron_variant BTCA-JP 21 30333863 30333863 deletion of <=200bp A - intron_variant BTCA-JP 21 30333863 30333863 deletion of <=200bp A - upstream_gene_variant BTCA-JP 21 30338264 30338264 single base substitution G A downstream_gene_variant BTCA-JP 21 30338264 30338264 single base substitution G A intron_variant BTCA-JP 21 30358491 30358491 single base substitution T C exon_variant BTCA-JP 21 30358491 30358491 single base substitution T C missense_variant Y105C 314A>G BTCA-JP 21 30358491 30358491 single base substitution T C missense_variant Y151C 452A>G CESC-US 21 30316810 30316810 single base substitution G C missense_variant L1293V 3877C>G CESC-US 21 30316810 30316810 single base substitution G C missense_variant L1339V 4015C>G CESC-US 21 30329098 30329098 single base substitution T A downstream_gene_variant CESC-US 21 30329098 30329098 single base substitution T A missense_variant E1022V 3065A>T CESC-US 21 30329098 30329098 single base substitution T A missense_variant E1068V 3203A>T CESC-US 21 30339080 30339080 single base substitution G T downstream_gene_variant CESC-US 21 30339080 30339080 single base substitution G T missense_variant S578Y 1733C>A CESC-US 21 30339080 30339080 single base substitution G T missense_variant S624Y 1871C>A CESC-US 21 30339206 30339206 deletion of <=200bp T - downstream_gene_variant CESC-US 21 30339206 30339206 deletion of <=200bp T - frameshift_variant N536 CESC-US 21 30339206 30339206 deletion of <=200bp T - frameshift_variant N582 CESC-US 21 30357145 30357145 single base substitution C T exon_variant CESC-US 21 30357145 30357145 single base substitution C T missense_variant M148I 444G>A CESC-US 21 30357145 30357145 single base substitution C T missense_variant M194I 582G>A CESC-US 21 30358482 30358482 single base substitution C A exon_variant CESC-US 21 30358482 30358482 single base substitution C A missense_variant R108I 323G>T CESC-US 21 30358482 30358482 single base substitution C A missense_variant R154I 461G>T CLLE-ES 21 30332718 30332718 single base substitution A T downstream_gene_variant CLLE-ES 21 30332718 30332718 single base substitution A T intron_variant CLLE-ES 21 30332718 30332718 single base substitution A T upstream_gene_variant CLLE-ES 21 30365240 30365240 single base substitution C A missense_variant G9W 25G>T CLLE-ES 21 30365240 30365240 single base substitution C A upstream_gene_variant COAD-US 21 30325699 30325699 single base substitution C A splice_acceptor_variant COAD-US 21 30331792 30331792 deletion of <=200bp T - downstream_gene_variant COAD-US 21 30331792 30331792 deletion of <=200bp T - exon_variant COAD-US 21 30331792 30331792 deletion of <=200bp T - frameshift_variant T861 COAD-US 21 30331792 30331792 deletion of <=200bp T - frameshift_variant T907 COAD-US 21 30331798 30331798 single base substitution C A downstream_gene_variant COAD-US 21 30331798 30331798 single base substitution C A exon_variant COAD-US 21 30331798 30331798 single base substitution C A stop_gained E859* 2575G>T COAD-US 21 30331798 30331798 single base substitution C A stop_gained E905* 2713G>T COAD-US 21 30331911 30331911 single base substitution G A downstream_gene_variant COAD-US 21 30331911 30331911 single base substitution G A exon_variant COAD-US 21 30331911 30331911 single base substitution G A missense_variant S821F 2462C>T COAD-US 21 30331911 30331911 single base substitution G A missense_variant S867F 2600C>T COAD-US 21 30341891 30341891 single base substitution A G exon_variant COAD-US 21 30341891 30341891 single base substitution A G missense_variant L403S 1208T>C COAD-US 21 30341891 30341891 single base substitution A G missense_variant L449S 1346T>C COAD-US 21 30354658 30354658 single base substitution A G exon_variant COAD-US 21 30354658 30354658 single base substitution A G synonymous_variant P203P 609T>C COAD-US 21 30354658 30354658 single base substitution A G synonymous_variant P249P 747T>C COCA-CN 21 30302652 30302652 single base substitution A G 3_prime_UTR_variant COCA-CN 21 30308970 30308970 single base substitution T C missense_variant K1511R 4532A>G COCA-CN 21 30308970 30308970 single base substitution T C missense_variant K1557R 4670A>G COCA-CN 21 30319785 30319785 single base substitution C T splice_donor_variant COCA-CN 21 30331664 30331664 single base substitution A G downstream_gene_variant COCA-CN 21 30331664 30331664 single base substitution A G intron_variant COCA-CN 21 30337158 30337158 single base substitution T G downstream_gene_variant COCA-CN 21 30337158 30337158 single base substitution T G intron_variant COCA-CN 21 30337158 30337158 single base substitution T G upstream_gene_variant COCA-CN 21 30338091 30338091 single base substitution T A downstream_gene_variant COCA-CN 21 30338091 30338091 single base substitution T A intron_variant COCA-CN 21 30338091 30338091 single base substitution T A upstream_gene_variant COCA-CN 21 30338166 30338166 single base substitution A G downstream_gene_variant COCA-CN 21 30338166 30338166 single base substitution A G intron_variant COCA-CN 21 30343588 30343588 single base substitution C T splice_region_variant COCA-CN 21 30354610 30354610 single base substitution T C intron_variant COCA-CN 21 30357234 30357234 single base substitution G A exon_variant COCA-CN 21 30357234 30357234 single base substitution G A missense_variant R119C 355C>T COCA-CN 21 30357234 30357234 single base substitution G A missense_variant R165C 493C>T COCA-CN 21 30358645 30358645 single base substitution A G intron_variant COCA-CN 21 30359068 30359068 single base substitution A G exon_variant COCA-CN 21 30359068 30359068 single base substitution A G missense_variant V123A 368T>C COCA-CN 21 30359068 30359068 single base substitution A G missense_variant V77A 230T>C COCA-CN 21 30365322 30365322 single base substitution G A upstream_gene_variant EOPC-DE 21 30307775 30307775 single base substitution A G intron_variant EOPC-DE 21 30336935 30336935 single base substitution T C 3_prime_UTR_variant EOPC-DE 21 30336935 30336935 single base substitution T C downstream_gene_variant EOPC-DE 21 30336935 30336935 single base substitution T C intron_variant EOPC-DE 21 30336935 30336935 single base substitution T C upstream_gene_variant ESAD-UK 21 30298454 30298454 deletion of <=200bp A - downstream_gene_variant ESAD-UK 21 30303009 30303009 single base substitution C T intron_variant ESAD-UK 21 30305920 30305920 single base substitution C T intron_variant ESAD-UK 21 30306278 30306278 single base substitution G A intron_variant ESAD-UK 21 30306365 30306365 single base substitution G A intron_variant ESAD-UK 21 30307104 30307104 single base substitution C T intron_variant ESAD-UK 21 30307249 30307249 single base substitution G A intron_variant ESAD-UK 21 30307382 30307382 single base substitution T C intron_variant ESAD-UK 21 30310061 30310061 single base substitution C T intron_variant ESAD-UK 21 30310815 30310815 single base substitution A G intron_variant ESAD-UK 21 30313453 30313453 single base substitution C A intron_variant ESAD-UK 21 30317729 30317729 single base substitution T A intron_variant ESAD-UK 21 30325753 30325753 single base substitution A C downstream_gene_variant ESAD-UK 21 30325753 30325753 single base substitution A C intron_variant ESAD-UK 21 30327538 30327538 single base substitution G A downstream_gene_variant ESAD-UK 21 30327538 30327538 single base substitution G A intron_variant ESAD-UK 21 30330384 30330384 single base substitution T C downstream_gene_variant ESAD-UK 21 30330384 30330384 single base substitution T C intron_variant ESAD-UK 21 30330488 30330488 insertion of <=200bp - T downstream_gene_variant ESAD-UK 21 30330488 30330488 insertion of <=200bp - T intron_variant ESAD-UK 21 30331150 30331150 single base substitution A T downstream_gene_variant ESAD-UK 21 30331150 30331150 single base substitution A T intron_variant ESAD-UK 21 30333269 30333269 single base substitution C T downstream_gene_variant ESAD-UK 21 30333269 30333269 single base substitution C T intron_variant ESAD-UK 21 30333269 30333269 single base substitution C T upstream_gene_variant ESAD-UK 21 30334339 30334339 single base substitution A C downstream_gene_variant ESAD-UK 21 30334339 30334339 single base substitution A C intron_variant ESAD-UK 21 30334339 30334339 single base substitution A C upstream_gene_variant ESAD-UK 21 30338158 30338158 single base substitution A G downstream_gene_variant ESAD-UK 21 30338158 30338158 single base substitution A G intron_variant ESAD-UK 21 30343897 30343897 single base substitution T C intron_variant ESAD-UK 21 30344375 30344375 single base substitution G C intron_variant ESAD-UK 21 30346968 30346968 single base substitution A C intron_variant ESAD-UK 21 30349973 30349973 single base substitution A T intron_variant ESAD-UK 21 30351954 30351954 single base substitution T C intron_variant ESAD-UK 21 30354911 30354911 single base substitution A C intron_variant ESAD-UK 21 30359370 30359370 single base substitution T C intron_variant ESAD-UK 21 30359370 30359370 single base substitution T C upstream_gene_variant ESAD-UK 21 30359946 30359946 single base substitution G A intron_variant ESAD-UK 21 30359946 30359946 single base substitution G A upstream_gene_variant ESAD-UK 21 30362979 30362979 single base substitution G A intron_variant ESAD-UK 21 30362979 30362979 single base substitution G A upstream_gene_variant ESAD-UK 21 30364906 30364906 single base substitution T A intron_variant ESAD-UK 21 30365706 30365706 single base substitution C A upstream_gene_variant ESAD-UK 21 30368600 30368600 single base substitution C G upstream_gene_variant ESCA-CN 21 30316789 30316789 single base substitution G A missense_variant P1300S 3898C>T ESCA-CN 21 30316789 30316789 single base substitution G A missense_variant P1346S 4036C>T ESCA-CN 21 30330733 30330733 single base substitution G A downstream_gene_variant ESCA-CN 21 30330733 30330733 single base substitution G A exon_variant ESCA-CN 21 30330733 30330733 single base substitution G A stop_gained Q908* 2722C>T ESCA-CN 21 30330733 30330733 single base substitution G A stop_gained Q954* 2860C>T ESCA-CN 21 30354649 30354649 single base substitution G C exon_variant ESCA-CN 21 30354649 30354649 single base substitution G C synonymous_variant L206L 618C>G ESCA-CN 21 30354649 30354649 single base substitution G C synonymous_variant L252L 756C>G GBM-US 21 30354691 30354691 single base substitution C T splice_acceptor_variant GBM-US 21 30359239 30359239 single base substitution C T missense_variant R20Q 59G>A GBM-US 21 30359239 30359239 single base substitution C T missense_variant R66Q 197G>A GBM-US 21 30359239 30359239 single base substitution C T upstream_gene_variant KIRC-US 21 30331797 30331797 single base substitution T G downstream_gene_variant KIRC-US 21 30331797 30331797 single base substitution T G exon_variant KIRC-US 21 30331797 30331797 single base substitution T G missense_variant E859A 2576A>C KIRC-US 21 30331797 30331797 single base substitution T G missense_variant E905A 2714A>C KIRC-US 21 30339421 30339421 insertion of <=200bp - A 3_prime_UTR_variant KIRC-US 21 30339421 30339421 insertion of <=200bp - A frameshift_variant L464L? KIRC-US 21 30339421 30339421 insertion of <=200bp - A frameshift_variant L510L? LAML-CN 21 30332952 30332952 single base substitution T C downstream_gene_variant LAML-CN 21 30332952 30332952 single base substitution T C exon_variant LAML-CN 21 30332952 30332952 single base substitution T C missense_variant N747S 2240A>G LAML-CN 21 30332952 30332952 single base substitution T C missense_variant N793S 2378A>G LAML-CN 21 30332952 30332952 single base substitution T C upstream_gene_variant LAML-KR 21 30315730 30315730 single base substitution G A intron_variant LAML-KR 21 30333269 30333269 single base substitution C T downstream_gene_variant LAML-KR 21 30333269 30333269 single base substitution C T intron_variant LAML-KR 21 30333269 30333269 single base substitution C T upstream_gene_variant LGG-US 21 30338725 30338725 single base substitution C T downstream_gene_variant LGG-US 21 30338725 30338725 single base substitution C T missense_variant M696I 2088G>A LGG-US 21 30338725 30338725 single base substitution C T missense_variant M742I 2226G>A LGG-US 21 30342876 30342876 single base substitution A C splice_region_variant LICA-CN 21 30319795 30319795 single base substitution T A missense_variant S1160C 3478A>T LICA-CN 21 30319795 30319795 single base substitution T A missense_variant S1206C 3616A>T LICA-CN 21 30338738 30338738 single base substitution C G downstream_gene_variant LICA-CN 21 30338738 30338738 single base substitution C G missense_variant C692S 2075G>C LICA-CN 21 30338738 30338738 single base substitution C G missense_variant C738S 2213G>C LICA-CN 21 30339270 30339270 single base substitution C A 3_prime_UTR_variant LICA-CN 21 30339270 30339270 single base substitution C A missense_variant V515L 1543G>T LICA-CN 21 30339270 30339270 single base substitution C A missense_variant V561L 1681G>T LICA-CN 21 30339504 30339504 single base substitution G C intron_variant LICA-CN 21 30339504 30339504 single base substitution G C splice_region_variant LICA-CN 21 30354634 30354634 single base substitution T A splice_region_variant LICA-FR 21 30317678 30317678 single base substitution T G intron_variant LICA-FR 21 30325990 30325990 single base substitution T C downstream_gene_variant LICA-FR 21 30325990 30325990 single base substitution T C intron_variant LICA-FR 21 30329283 30329283 single base substitution T C downstream_gene_variant LICA-FR 21 30329283 30329283 single base substitution T C intron_variant LICA-FR 21 30338898 30338898 single base substitution G C downstream_gene_variant LICA-FR 21 30338898 30338898 single base substitution G C missense_variant Q639E 1915C>G LICA-FR 21 30338898 30338898 single base substitution G C missense_variant Q685E 2053C>G LICA-FR 21 30342918 30342918 single base substitution T C exon_variant LICA-FR 21 30342918 30342918 single base substitution T C synonymous_variant P377P 1131A>G LICA-FR 21 30342918 30342918 single base substitution T C synonymous_variant P423P 1269A>G LICA-FR 21 30346368 30346368 single base substitution T C intron_variant LICA-FR 21 30348922 30348922 deletion of <=200bp A - intron_variant LICA-FR 21 30349370 30349370 single base substitution C T intron_variant LICA-FR 21 30357168 30357168 single base substitution C T exon_variant LICA-FR 21 30357168 30357168 single base substitution C T missense_variant A141T 421G>A LICA-FR 21 30357168 30357168 single base substitution C T missense_variant A187T 559G>A LIHC-US 21 30329699 30329699 single base substitution C T downstream_gene_variant LIHC-US 21 30329699 30329699 single base substitution C T synonymous_variant P949P 2847G>A LIHC-US 21 30329699 30329699 single base substitution C T synonymous_variant P995P 2985G>A LIHC-US 21 30343736 30343736 single base substitution C A exon_variant LIHC-US 21 30343736 30343736 single base substitution C A missense_variant A281S 841G>T LIHC-US 21 30343736 30343736 single base substitution C A missense_variant A327S 979G>T LIHC-US 21 30354673 30354673 single base substitution A G exon_variant LIHC-US 21 30354673 30354673 single base substitution A G synonymous_variant L198L 594T>C LIHC-US 21 30354673 30354673 single base substitution A G synonymous_variant L244L 732T>C LINC-JP 21 30302755 30302755 single base substitution C A 3_prime_UTR_variant LINC-JP 21 30308048 30308048 single base substitution G C intron_variant LINC-JP 21 30312427 30312427 single base substitution C T intron_variant LINC-JP 21 30324417 30324417 single base substitution T C intron_variant LINC-JP 21 30325860 30325860 single base substitution G A downstream_gene_variant LINC-JP 21 30325860 30325860 single base substitution G A intron_variant LINC-JP 21 30329692 30329692 single base substitution T C downstream_gene_variant LINC-JP 21 30329692 30329692 single base substitution T C missense_variant S952G 2854A>G LINC-JP 21 30329692 30329692 single base substitution T C missense_variant S998G 2992A>G LINC-JP 21 30332007 30332007 single base substitution C T downstream_gene_variant LINC-JP 21 30332007 30332007 single base substitution C T exon_variant LINC-JP 21 30332007 30332007 single base substitution C T missense_variant G789E 2366G>A LINC-JP 21 30332007 30332007 single base substitution C T missense_variant G835E 2504G>A LINC-JP 21 30335981 30335981 single base substitution T C downstream_gene_variant LINC-JP 21 30335981 30335981 single base substitution T C intron_variant LINC-JP 21 30335981 30335981 single base substitution T C upstream_gene_variant LINC-JP 21 30338934 30338934 single base substitution T A downstream_gene_variant LINC-JP 21 30338934 30338934 single base substitution T A missense_variant S627C 1879A>T LINC-JP 21 30338934 30338934 single base substitution T A missense_variant S673C 2017A>T LINC-JP 21 30341852 30341852 single base substitution A G exon_variant LINC-JP 21 30341852 30341852 single base substitution A G missense_variant L416S 1247T>C LINC-JP 21 30341852 30341852 single base substitution A G missense_variant L462S 1385T>C LINC-JP 21 30357010 30357010 single base substitution T G splice_region_variant LINC-JP 21 30362238 30362238 single base substitution G T intron_variant LINC-JP 21 30362238 30362238 single base substitution G T upstream_gene_variant LINC-JP 21 30369269 30369269 deletion of <=200bp A - upstream_gene_variant LIRI-JP 21 30301079 30301079 single base substitution C A 3_prime_UTR_variant LIRI-JP 21 30301619 30301619 single base substitution T C 3_prime_UTR_variant LIRI-JP 21 30302578 30302578 single base substitution A C 3_prime_UTR_variant LIRI-JP 21 30302793 30302793 single base substitution G A synonymous_variant L1760L 5278C>T LIRI-JP 21 30302793 30302793 single base substitution G A synonymous_variant L1806L 5416C>T LIRI-JP 21 30303519 30303519 insertion of <=200bp - T frameshift_variant K1732K? LIRI-JP 21 30303519 30303519 insertion of <=200bp - T frameshift_variant K1778K? LIRI-JP 21 30304911 30304911 single base substitution G T missense_variant Q1651K 4951C>A LIRI-JP 21 30304911 30304911 single base substitution G T missense_variant Q1697K 5089C>A LIRI-JP 21 30304974 30304974 single base substitution C T missense_variant A1630T 4888G>A LIRI-JP 21 30304974 30304974 single base substitution C T missense_variant A1676T 5026G>A LIRI-JP 21 30306513 30306513 single base substitution T C intron_variant LIRI-JP 21 30307515 30307515 single base substitution A G synonymous_variant F1597F 4791T>C LIRI-JP 21 30307515 30307515 single base substitution A G synonymous_variant F1643F 4929T>C LIRI-JP 21 30307705 30307705 single base substitution C A intron_variant LIRI-JP 21 30309086 30309086 single base substitution T A intron_variant LIRI-JP 21 30313028 30313028 single base substitution G A intron_variant LIRI-JP 21 30314582 30314582 single base substitution C A intron_variant LIRI-JP 21 30317371 30317371 single base substitution G A intron_variant LIRI-JP 21 30320029 30320029 single base substitution T C intron_variant LIRI-JP 21 30327318 30327318 single base substitution T A downstream_gene_variant LIRI-JP 21 30327318 30327318 single base substitution T A intron_variant LIRI-JP 21 30327319 30327319 single base substitution C A downstream_gene_variant LIRI-JP 21 30327319 30327319 single base substitution C A intron_variant LIRI-JP 21 30327942 30327942 single base substitution T C downstream_gene_variant LIRI-JP 21 30327942 30327942 single base substitution T C intron_variant LIRI-JP 21 30332165 30332165 single base substitution T G downstream_gene_variant LIRI-JP 21 30332165 30332165 single base substitution T G exon_variant LIRI-JP 21 30332165 30332165 single base substitution T G intron_variant LIRI-JP 21 30333584 30333584 single base substitution T A downstream_gene_variant LIRI-JP 21 30333584 30333584 single base substitution T A intron_variant LIRI-JP 21 30333584 30333584 single base substitution T A upstream_gene_variant LIRI-JP 21 30334889 30334889 single base substitution C A downstream_gene_variant LIRI-JP 21 30334889 30334889 single base substitution C A intron_variant LIRI-JP 21 30334889 30334889 single base substitution C A upstream_gene_variant LIRI-JP 21 30335778 30335778 single base substitution T C downstream_gene_variant LIRI-JP 21 30335778 30335778 single base substitution T C intron_variant LIRI-JP 21 30335778 30335778 single base substitution T C upstream_gene_variant LIRI-JP 21 30337504 30337504 single base substitution G C downstream_gene_variant LIRI-JP 21 30337504 30337504 single base substitution G C intron_variant LIRI-JP 21 30337504 30337504 single base substitution G C upstream_gene_variant LIRI-JP 21 30338081 30338081 single base substitution A T downstream_gene_variant LIRI-JP 21 30338081 30338081 single base substitution A T intron_variant LIRI-JP 21 30338081 30338081 single base substitution A T upstream_gene_variant LIRI-JP 21 30338790 30338790 single base substitution T C downstream_gene_variant LIRI-JP 21 30338790 30338790 single base substitution T C missense_variant R675G 2023A>G LIRI-JP 21 30338790 30338790 single base substitution T C missense_variant R721G 2161A>G LIRI-JP 21 30339043 30339043 single base substitution C T downstream_gene_variant LIRI-JP 21 30339043 30339043 single base substitution C T synonymous_variant L590L 1770G>A LIRI-JP 21 30339043 30339043 single base substitution C T synonymous_variant L636L 1908G>A LIRI-JP 21 30339206 30339206 deletion of <=200bp T - downstream_gene_variant LIRI-JP 21 30339206 30339206 deletion of <=200bp T - frameshift_variant N536 LIRI-JP 21 30339206 30339206 deletion of <=200bp T - frameshift_variant N582 LIRI-JP 21 30340959 30340959 single base substitution G T intron_variant LIRI-JP 21 30344986 30344986 single base substitution A C intron_variant LIRI-JP 21 30345816 30345816 single base substitution T C intron_variant LIRI-JP 21 30346050 30346050 single base substitution G C intron_variant LIRI-JP 21 30346219 30346219 single base substitution T C intron_variant LIRI-JP 21 30347095 30347095 single base substitution T A intron_variant LIRI-JP 21 30348875 30348875 single base substitution T C intron_variant LIRI-JP 21 30356358 30356358 single base substitution T C intron_variant LIRI-JP 21 30358532 30358532 single base substitution A G exon_variant LIRI-JP 21 30358532 30358532 single base substitution A G synonymous_variant C137C 411T>C LIRI-JP 21 30358532 30358532 single base substitution A G synonymous_variant C91C 273T>C LIRI-JP 21 30359450 30359450 single base substitution C T intron_variant LIRI-JP 21 30359450 30359450 single base substitution C T upstream_gene_variant LIRI-JP 21 30359912 30359912 insertion of <=200bp - A intron_variant LIRI-JP 21 30359912 30359912 insertion of <=200bp - A upstream_gene_variant LIRI-JP 21 30363697 30363697 single base substitution T C intron_variant LIRI-JP 21 30363697 30363697 single base substitution T C upstream_gene_variant LIRI-JP 21 30367151 30367151 single base substitution G C upstream_gene_variant LIRI-JP 21 30367700 30367700 single base substitution T C upstream_gene_variant LUSC-CN 21 30302615 30302615 single base substitution T C 3_prime_UTR_variant LUSC-KR 21 30306016 30306016 single base substitution G T intron_variant LUSC-KR 21 30309851 30309851 single base substitution T C intron_variant LUSC-KR 21 30310920 30310920 single base substitution C G intron_variant LUSC-KR 21 30311795 30311795 single base substitution T C intron_variant LUSC-KR 21 30313917 30313917 single base substitution T A intron_variant LUSC-KR 21 30315265 30315265 single base substitution C T intron_variant LUSC-KR 21 30320985 30320985 single base substitution C A intron_variant LUSC-KR 21 30331935 30331935 single base substitution G A downstream_gene_variant LUSC-KR 21 30331935 30331935 single base substitution G A exon_variant LUSC-KR 21 30331935 30331935 single base substitution G A missense_variant A813V 2438C>T LUSC-KR 21 30331935 30331935 single base substitution G A missense_variant A859V 2576C>T LUSC-KR 21 30338328 30338328 single base substitution C A downstream_gene_variant LUSC-KR 21 30338328 30338328 single base substitution C A intron_variant LUSC-KR 21 30339120 30339120 single base substitution C A downstream_gene_variant LUSC-KR 21 30339120 30339120 single base substitution C A missense_variant G565C 1693G>T LUSC-KR 21 30339120 30339120 single base substitution C A missense_variant G611C 1831G>T LUSC-KR 21 30339234 30339234 single base substitution T C 3_prime_UTR_variant LUSC-KR 21 30339234 30339234 single base substitution T C missense_variant S527G 1579A>G LUSC-KR 21 30339234 30339234 single base substitution T C missense_variant S573G 1717A>G LUSC-KR 21 30342504 30342504 single base substitution A G intron_variant LUSC-KR 21 30344786 30344786 single base substitution C A intron_variant LUSC-KR 21 30354610 30354610 single base substitution T C intron_variant LUSC-KR 21 30364072 30364072 single base substitution T A intron_variant LUSC-KR 21 30364072 30364072 single base substitution T A upstream_gene_variant LUSC-KR 21 30365322 30365322 single base substitution G A upstream_gene_variant LUSC-KR 21 30366465 30366465 single base substitution G C upstream_gene_variant LUSC-KR 21 30369867 30369867 single base substitution G T upstream_gene_variant LUSC-KR 21 30369894 30369894 single base substitution G A upstream_gene_variant LUSC-US 21 30302818 30302818 single base substitution T C synonymous_variant T1751T 5253A>G LUSC-US 21 30302818 30302818 single base substitution T C synonymous_variant T1797T 5391A>G LUSC-US 21 30304833 30304833 single base substitution G T synonymous_variant R1677R 5029C>A LUSC-US 21 30304833 30304833 single base substitution G T synonymous_variant R1723R 5167C>A LUSC-US 21 30304965 30304965 single base substitution G T synonymous_variant R1633R 4897C>A LUSC-US 21 30304965 30304965 single base substitution G T synonymous_variant R1679R 5035C>A LUSC-US 21 30354687 30354687 single base substitution G A exon_variant LUSC-US 21 30354687 30354687 single base substitution G A synonymous_variant L194L 580C>T LUSC-US 21 30354687 30354687 single base substitution G A synonymous_variant L240L 718C>T LUSC-US 21 30357092 30357092 single base substitution G T exon_variant LUSC-US 21 30357092 30357092 single base substitution G T missense_variant A166E 497C>A LUSC-US 21 30357092 30357092 single base substitution G T missense_variant A212E 635C>A LUSC-US 21 30359114 30359114 single base substitution C G missense_variant D108H 322G>C LUSC-US 21 30359114 30359114 single base substitution C G missense_variant D62H 184G>C LUSC-US 21 30359114 30359114 single base substitution C G upstream_gene_variant MALY-DE 21 30303779 30303779 single base substitution A C intron_variant MALY-DE 21 30323313 30323313 single base substitution A T intron_variant MALY-DE 21 30325025 30325025 single base substitution C G intron_variant MALY-DE 21 30335619 30335619 single base substitution G A downstream_gene_variant MALY-DE 21 30335619 30335619 single base substitution G A intron_variant MALY-DE 21 30335619 30335619 single base substitution G A upstream_gene_variant MALY-DE 21 30344417 30344417 deletion of <=200bp C - intron_variant MALY-DE 21 30356661 30356662 deletion of <=200bp TA - intron_variant MALY-DE 21 30361795 30361795 single base substitution T G intron_variant MALY-DE 21 30361795 30361795 single base substitution T G upstream_gene_variant MALY-DE 21 30367438 30367438 single base substitution A T upstream_gene_variant MALY-DE 21 30368262 30368262 single base substitution A G upstream_gene_variant MELA-AU 21 30295753 30295753 single base substitution G A downstream_gene_variant MELA-AU 21 30297234 30297234 single base substitution G A downstream_gene_variant MELA-AU 21 30297492 30297492 single base substitution G A downstream_gene_variant MELA-AU 21 30297551 30297551 single base substitution G A downstream_gene_variant MELA-AU 21 30297578 30297578 single base substitution G A downstream_gene_variant MELA-AU 21 30297714 30297714 single base substitution G A downstream_gene_variant MELA-AU 21 30297738 30297738 single base substitution G A downstream_gene_variant MELA-AU 21 30297917 30297917 single base substitution C A downstream_gene_variant MELA-AU 21 30298001 30298001 single base substitution G A downstream_gene_variant MELA-AU 21 30298636 30298636 single base substitution G A downstream_gene_variant MELA-AU 21 30298834 30298834 single base substitution A G downstream_gene_variant MELA-AU 21 30298923 30298923 single base substitution G A downstream_gene_variant MELA-AU 21 30300317 30300317 single base substitution A C downstream_gene_variant MELA-AU 21 30302175 30302175 single base substitution A G 3_prime_UTR_variant MELA-AU 21 30302745 30302745 single base substitution G A 3_prime_UTR_variant MELA-AU 21 30302841 30302841 single base substitution G A intron_variant MELA-AU 21 30303096 30303096 single base substitution G A intron_variant MELA-AU 21 30303621 30303621 single base substitution T C synonymous_variant L1698L 5094A>G MELA-AU 21 30303621 30303621 single base substitution T C synonymous_variant L1744L 5232A>G MELA-AU 21 30304156 30304156 single base substitution C T intron_variant MELA-AU 21 30304675 30304675 single base substitution G A intron_variant MELA-AU 21 30305290 30305290 single base substitution G A intron_variant MELA-AU 21 30306267 30306267 single base substitution G A intron_variant MELA-AU 21 30306567 30306567 single base substitution G A intron_variant MELA-AU 21 30306615 30306615 single base substitution A G intron_variant MELA-AU 21 30306743 30306743 single base substitution G A intron_variant MELA-AU 21 30306926 30306926 single base substitution G A intron_variant MELA-AU 21 30306928 30306928 single base substitution C T intron_variant MELA-AU 21 30307699 30307699 single base substitution G A intron_variant MELA-AU 21 30307856 30307856 single base substitution G A intron_variant MELA-AU 21 30307884 30307884 single base substitution C G intron_variant MELA-AU 21 30308283 30308283 single base substitution G A intron_variant MELA-AU 21 30308373 30308373 single base substitution G C intron_variant MELA-AU 21 30308681 30308681 single base substitution A G intron_variant MELA-AU 21 30309806 30309806 single base substitution G A intron_variant MELA-AU 21 30310201 30310201 single base substitution A G intron_variant MELA-AU 21 30310448 30310448 single base substitution G A intron_variant MELA-AU 21 30310806 30310806 single base substitution A G intron_variant MELA-AU 21 30311087 30311087 single base substitution G A intron_variant MELA-AU 21 30311617 30311617 single base substitution G A intron_variant MELA-AU 21 30311857 30311857 single base substitution G A intron_variant MELA-AU 21 30312024 30312024 single base substitution G A intron_variant MELA-AU 21 30312659 30312659 single base substitution C T intron_variant MELA-AU 21 30313185 30313186 multiple base substitution (>=2bp and <=200bp) GG CA intron_variant MELA-AU 21 30315323 30315323 single base substitution C T intron_variant MELA-AU 21 30316198 30316198 single base substitution G A synonymous_variant S1337S 4011C>T MELA-AU 21 30316198 30316198 single base substitution G A synonymous_variant S1383S 4149C>T MELA-AU 21 30316240 30316240 single base substitution G A intron_variant MELA-AU 21 30316864 30316864 single base substitution A G missense_variant C1275R 3823T>C MELA-AU 21 30316864 30316864 single base substitution A G missense_variant C1321R 3961T>C MELA-AU 21 30317382 30317382 insertion of <=200bp - A intron_variant MELA-AU 21 30318186 30318186 single base substitution G A synonymous_variant S1237S 3711C>T MELA-AU 21 30318186 30318186 single base substitution G A synonymous_variant S1283S 3849C>T MELA-AU 21 30318612 30318612 single base substitution A G splice_region_variant MELA-AU 21 30318832 30318832 single base substitution G A intron_variant MELA-AU 21 30319238 30319238 single base substitution C A intron_variant MELA-AU 21 30319593 30319593 single base substitution T C intron_variant MELA-AU 21 30320223 30320223 single base substitution A G intron_variant MELA-AU 21 30321404 30321404 single base substitution T C intron_variant MELA-AU 21 30322356 30322356 single base substitution C T intron_variant MELA-AU 21 30322689 30322689 single base substitution G A intron_variant MELA-AU 21 30323898 30323898 single base substitution G A intron_variant MELA-AU 21 30323900 30323900 single base substitution G A intron_variant MELA-AU 21 30324061 30324061 single base substitution A C intron_variant MELA-AU 21 30324070 30324070 single base substitution G A intron_variant MELA-AU 21 30324778 30324778 single base substitution C A intron_variant MELA-AU 21 30324948 30324949 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 21 30325726 30325726 single base substitution G A intron_variant MELA-AU 21 30325801 30325801 single base substitution C T downstream_gene_variant MELA-AU 21 30325801 30325801 single base substitution C T intron_variant MELA-AU 21 30326608 30326609 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 21 30326608 30326609 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 21 30326647 30326647 single base substitution A G downstream_gene_variant MELA-AU 21 30326647 30326647 single base substitution A G intron_variant MELA-AU 21 30327012 30327012 single base substitution G A downstream_gene_variant MELA-AU 21 30327012 30327012 single base substitution G A intron_variant MELA-AU 21 30327116 30327116 single base substitution G A downstream_gene_variant MELA-AU 21 30327116 30327116 single base substitution G A intron_variant MELA-AU 21 30327162 30327162 single base substitution G T downstream_gene_variant MELA-AU 21 30327162 30327162 single base substitution G T intron_variant MELA-AU 21 30327247 30327247 single base substitution G T downstream_gene_variant MELA-AU 21 30327247 30327247 single base substitution G T intron_variant MELA-AU 21 30327514 30327514 single base substitution G A downstream_gene_variant MELA-AU 21 30327514 30327514 single base substitution G A intron_variant MELA-AU 21 30328001 30328001 single base substitution C T downstream_gene_variant MELA-AU 21 30328001 30328001 single base substitution C T intron_variant MELA-AU 21 30328111 30328111 single base substitution G A downstream_gene_variant MELA-AU 21 30328111 30328111 single base substitution G A intron_variant MELA-AU 21 30328718 30328718 single base substitution C A downstream_gene_variant MELA-AU 21 30328718 30328718 single base substitution C A intron_variant MELA-AU 21 30328813 30328813 single base substitution C T downstream_gene_variant MELA-AU 21 30328813 30328813 single base substitution C T intron_variant MELA-AU 21 30329897 30329897 single base substitution A T downstream_gene_variant MELA-AU 21 30329897 30329897 single base substitution A T intron_variant MELA-AU 21 30329974 30329974 single base substitution G A downstream_gene_variant MELA-AU 21 30329974 30329974 single base substitution G A intron_variant MELA-AU 21 30330950 30330950 single base substitution G A downstream_gene_variant MELA-AU 21 30330950 30330950 single base substitution G A intron_variant MELA-AU 21 30331809 30331809 single base substitution G C downstream_gene_variant MELA-AU 21 30331809 30331809 single base substitution G C exon_variant MELA-AU 21 30331809 30331809 single base substitution G C missense_variant A855G 2564C>G MELA-AU 21 30331809 30331809 single base substitution G C missense_variant A901G 2702C>G MELA-AU 21 30333825 30333825 single base substitution G A 3_prime_UTR_variant MELA-AU 21 30333825 30333825 single base substitution G A intron_variant MELA-AU 21 30333825 30333825 single base substitution G A upstream_gene_variant MELA-AU 21 30333912 30333912 single base substitution C T intron_variant MELA-AU 21 30333912 30333912 single base substitution C T upstream_gene_variant MELA-AU 21 30334262 30334263 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 21 30334262 30334263 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 21 30334262 30334263 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 21 30334959 30334959 single base substitution T C downstream_gene_variant MELA-AU 21 30334959 30334959 single base substitution T C intron_variant MELA-AU 21 30334959 30334959 single base substitution T C upstream_gene_variant MELA-AU 21 30334974 30334974 single base substitution T C downstream_gene_variant MELA-AU 21 30334974 30334974 single base substitution T C intron_variant MELA-AU 21 30334974 30334974 single base substitution T C upstream_gene_variant MELA-AU 21 30335127 30335127 single base substitution G A downstream_gene_variant MELA-AU 21 30335127 30335127 single base substitution G A intron_variant MELA-AU 21 30335127 30335127 single base substitution G A upstream_gene_variant MELA-AU 21 30335142 30335142 single base substitution G A downstream_gene_variant MELA-AU 21 30335142 30335142 single base substitution G A intron_variant MELA-AU 21 30335142 30335142 single base substitution G A upstream_gene_variant MELA-AU 21 30336317 30336317 single base substitution G A downstream_gene_variant MELA-AU 21 30336317 30336317 single base substitution G A intron_variant MELA-AU 21 30336317 30336317 single base substitution G A upstream_gene_variant MELA-AU 21 30336470 30336470 single base substitution G A downstream_gene_variant MELA-AU 21 30336470 30336470 single base substitution G A intron_variant MELA-AU 21 30336470 30336470 single base substitution G A upstream_gene_variant MELA-AU 21 30336948 30336948 single base substitution C T downstream_gene_variant MELA-AU 21 30336948 30336948 single base substitution C T intron_variant MELA-AU 21 30336948 30336948 single base substitution C T stop_retained_variant *814* 2442G>A MELA-AU 21 30336948 30336948 single base substitution C T upstream_gene_variant MELA-AU 21 30337005 30337005 single base substitution G A downstream_gene_variant MELA-AU 21 30337005 30337005 single base substitution G A intron_variant MELA-AU 21 30337005 30337005 single base substitution G A synonymous_variant A795A 2385C>T MELA-AU 21 30337005 30337005 single base substitution G A upstream_gene_variant MELA-AU 21 30337561 30337561 single base substitution G A downstream_gene_variant MELA-AU 21 30337561 30337561 single base substitution G A intron_variant MELA-AU 21 30337561 30337561 single base substitution G A upstream_gene_variant MELA-AU 21 30337941 30337941 single base substitution G A downstream_gene_variant MELA-AU 21 30337941 30337941 single base substitution G A intron_variant MELA-AU 21 30337941 30337941 single base substitution G A upstream_gene_variant MELA-AU 21 30338015 30338015 single base substitution G A downstream_gene_variant MELA-AU 21 30338015 30338015 single base substitution G A intron_variant MELA-AU 21 30338015 30338015 single base substitution G A upstream_gene_variant MELA-AU 21 30338700 30338700 single base substitution G A downstream_gene_variant MELA-AU 21 30338700 30338700 single base substitution G A synonymous_variant L705L 2113C>T MELA-AU 21 30338700 30338700 single base substitution G A synonymous_variant L751L 2251C>T MELA-AU 21 30338748 30338748 single base substitution G C downstream_gene_variant MELA-AU 21 30338748 30338748 single base substitution G C missense_variant L689V 2065C>G MELA-AU 21 30338748 30338748 single base substitution G C missense_variant L735V 2203C>G MELA-AU 21 30339489 30339489 single base substitution T A 3_prime_UTR_variant MELA-AU 21 30339489 30339489 single base substitution T A missense_variant I442F 1324A>T MELA-AU 21 30339489 30339489 single base substitution T A missense_variant I488F 1462A>T MELA-AU 21 30340315 30340315 single base substitution G A intron_variant MELA-AU 21 30340800 30340800 single base substitution C T intron_variant MELA-AU 21 30341187 30341187 single base substitution C T intron_variant MELA-AU 21 30341556 30341556 single base substitution G A intron_variant MELA-AU 21 30342179 30342179 single base substitution C T intron_variant MELA-AU 21 30342558 30342558 single base substitution T C intron_variant MELA-AU 21 30343004 30343004 single base substitution G A exon_variant MELA-AU 21 30343004 30343004 single base substitution G A missense_variant R349C 1045C>T MELA-AU 21 30343004 30343004 single base substitution G A missense_variant R395C 1183C>T MELA-AU 21 30343327 30343327 single base substitution G A intron_variant MELA-AU 21 30343449 30343449 single base substitution A T intron_variant MELA-AU 21 30344208 30344208 single base substitution G A intron_variant MELA-AU 21 30344351 30344351 single base substitution T C intron_variant MELA-AU 21 30345075 30345075 single base substitution G A intron_variant MELA-AU 21 30345218 30345218 single base substitution A G intron_variant MELA-AU 21 30346080 30346080 single base substitution G A intron_variant MELA-AU 21 30346245 30346245 single base substitution G A intron_variant MELA-AU 21 30348534 30348534 single base substitution A T intron_variant MELA-AU 21 30348731 30348731 single base substitution G A intron_variant MELA-AU 21 30349953 30349953 single base substitution G A intron_variant MELA-AU 21 30350032 30350032 single base substitution G A intron_variant MELA-AU 21 30351038 30351038 single base substitution G A intron_variant MELA-AU 21 30351103 30351103 single base substitution G A intron_variant MELA-AU 21 30351211 30351211 single base substitution G A intron_variant MELA-AU 21 30351564 30351564 single base substitution G A intron_variant MELA-AU 21 30351641 30351641 single base substitution G A intron_variant MELA-AU 21 30352131 30352131 single base substitution A T intron_variant MELA-AU 21 30352867 30352867 single base substitution A T intron_variant MELA-AU 21 30353133 30353133 single base substitution G A intron_variant MELA-AU 21 30353150 30353150 single base substitution G A intron_variant MELA-AU 21 30353411 30353411 single base substitution A G intron_variant MELA-AU 21 30354076 30354076 single base substitution G A intron_variant MELA-AU 21 30354225 30354225 single base substitution T G intron_variant MELA-AU 21 30354337 30354337 single base substitution G A intron_variant MELA-AU 21 30354819 30354819 single base substitution C T intron_variant MELA-AU 21 30354964 30354964 single base substitution G A intron_variant MELA-AU 21 30355080 30355080 single base substitution G A intron_variant MELA-AU 21 30355120 30355121 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 21 30355264 30355264 single base substitution G A intron_variant MELA-AU 21 30355753 30355753 single base substitution G A intron_variant MELA-AU 21 30356102 30356102 single base substitution G A intron_variant MELA-AU 21 30356555 30356555 single base substitution A G intron_variant MELA-AU 21 30357164 30357164 single base substitution G A exon_variant MELA-AU 21 30357164 30357164 single base substitution G A missense_variant P142L 425C>T MELA-AU 21 30357164 30357164 single base substitution G A missense_variant P188L 563C>T MELA-AU 21 30358745 30358745 single base substitution T A intron_variant MELA-AU 21 30358856 30358856 single base substitution G T intron_variant MELA-AU 21 30359025 30359025 single base substitution A C intron_variant MELA-AU 21 30359347 30359347 single base substitution G A intron_variant MELA-AU 21 30359347 30359347 single base substitution G A upstream_gene_variant MELA-AU 21 30359599 30359599 single base substitution G C intron_variant MELA-AU 21 30359599 30359599 single base substitution G C upstream_gene_variant MELA-AU 21 30359707 30359707 single base substitution G A intron_variant MELA-AU 21 30359707 30359707 single base substitution G A upstream_gene_variant MELA-AU 21 30360352 30360352 single base substitution T G intron_variant MELA-AU 21 30360352 30360352 single base substitution T G upstream_gene_variant MELA-AU 21 30360667 30360667 single base substitution A G intron_variant MELA-AU 21 30360667 30360667 single base substitution A G upstream_gene_variant MELA-AU 21 30363011 30363011 single base substitution G A intron_variant MELA-AU 21 30363011 30363011 single base substitution G A upstream_gene_variant MELA-AU 21 30363484 30363500 deletion of <=200bp AGGAGTCCTAGCTACTA - intron_variant MELA-AU 21 30363484 30363500 deletion of <=200bp AGGAGTCCTAGCTACTA - upstream_gene_variant MELA-AU 21 30363563 30363563 single base substitution G A intron_variant MELA-AU 21 30363563 30363563 single base substitution G A upstream_gene_variant MELA-AU 21 30364993 30364993 single base substitution G A intron_variant MELA-AU 21 30365209 30365209 single base substitution G A missense_variant S19F 56C>T MELA-AU 21 30365209 30365209 single base substitution G A upstream_gene_variant MELA-AU 21 30365279 30365279 single base substitution C T upstream_gene_variant MELA-AU 21 30365320 30365320 single base substitution G A upstream_gene_variant MELA-AU 21 30365348 30365348 single base substitution C T upstream_gene_variant MELA-AU 21 30365359 30365359 single base substitution C T upstream_gene_variant MELA-AU 21 30365363 30365363 single base substitution C T upstream_gene_variant MELA-AU 21 30365406 30365406 single base substitution C T upstream_gene_variant MELA-AU 21 30366301 30366301 single base substitution C T upstream_gene_variant MELA-AU 21 30366680 30366680 single base substitution G A upstream_gene_variant MELA-AU 21 30367532 30367532 single base substitution G A upstream_gene_variant MELA-AU 21 30367552 30367552 single base substitution G A upstream_gene_variant MELA-AU 21 30367776 30367776 single base substitution G A upstream_gene_variant MELA-AU 21 30367871 30367871 single base substitution C T upstream_gene_variant MELA-AU 21 30368134 30368134 single base substitution G A upstream_gene_variant MELA-AU 21 30368195 30368195 single base substitution G A upstream_gene_variant MELA-AU 21 30368377 30368377 single base substitution G A upstream_gene_variant MELA-AU 21 30368560 30368560 single base substitution G A upstream_gene_variant MELA-AU 21 30368622 30368622 single base substitution G A upstream_gene_variant MELA-AU 21 30368778 30368778 single base substitution G A upstream_gene_variant MELA-AU 21 30368779 30368779 single base substitution G A upstream_gene_variant MELA-AU 21 30370090 30370090 single base substitution C T upstream_gene_variant MELA-AU 21 30370202 30370202 single base substitution A T upstream_gene_variant MELA-AU 21 30370260 30370260 single base substitution C T upstream_gene_variant ORCA-IN 21 30307620 30307620 single base substitution G A synonymous_variant H1562H 4686C>T ORCA-IN 21 30307620 30307620 single base substitution G A synonymous_variant H1608H 4824C>T ORCA-IN 21 30339206 30339206 deletion of <=200bp T - downstream_gene_variant ORCA-IN 21 30339206 30339206 deletion of <=200bp T - frameshift_variant N536 ORCA-IN 21 30339206 30339206 deletion of <=200bp T - frameshift_variant N582 OV-AU 21 30297591 30297591 single base substitution G T downstream_gene_variant OV-AU 21 30302771 30302771 single base substitution C T stop_retained_variant *1767* 5300G>A OV-AU 21 30302771 30302771 single base substitution C T stop_retained_variant *1813* 5438G>A OV-AU 21 30306958 30306958 single base substitution T A intron_variant OV-AU 21 30310822 30310822 single base substitution T A intron_variant OV-AU 21 30318162 30318162 single base substitution G A synonymous_variant D1245D 3735C>T OV-AU 21 30318162 30318162 single base substitution G A synonymous_variant D1291D 3873C>T OV-AU 21 30326006 30326006 single base substitution A T downstream_gene_variant OV-AU 21 30326006 30326006 single base substitution A T intron_variant OV-AU 21 30326217 30326217 single base substitution G A downstream_gene_variant OV-AU 21 30326217 30326217 single base substitution G A intron_variant OV-AU 21 30328638 30328638 single base substitution C T downstream_gene_variant OV-AU 21 30328638 30328638 single base substitution C T intron_variant OV-AU 21 30329528 30329528 single base substitution A G downstream_gene_variant OV-AU 21 30329528 30329528 single base substitution A G intron_variant OV-AU 21 30332727 30332727 single base substitution A T downstream_gene_variant OV-AU 21 30332727 30332727 single base substitution A T intron_variant OV-AU 21 30332727 30332727 single base substitution A T upstream_gene_variant OV-AU 21 30333269 30333269 single base substitution C T downstream_gene_variant OV-AU 21 30333269 30333269 single base substitution C T intron_variant OV-AU 21 30333269 30333269 single base substitution C T upstream_gene_variant OV-AU 21 30339168 30339168 single base substitution T C downstream_gene_variant OV-AU 21 30339168 30339168 single base substitution T C missense_variant N549D 1645A>G OV-AU 21 30339168 30339168 single base substitution T C missense_variant N595D 1783A>G OV-AU 21 30339281 30339281 single base substitution G A 3_prime_UTR_variant OV-AU 21 30339281 30339281 single base substitution G A missense_variant S511F 1532C>T OV-AU 21 30339281 30339281 single base substitution G A missense_variant S557F 1670C>T OV-AU 21 30339285 30339285 single base substitution C G 3_prime_UTR_variant OV-AU 21 30339285 30339285 single base substitution C G missense_variant E510Q 1528G>C OV-AU 21 30339285 30339285 single base substitution C G missense_variant E556Q 1666G>C OV-AU 21 30340233 30340233 single base substitution G C 3_prime_UTR_variant OV-AU 21 30340233 30340233 single base substitution G C intron_variant OV-AU 21 30340968 30340968 single base substitution T G intron_variant OV-AU 21 30343813 30343813 single base substitution A G intron_variant OV-AU 21 30344691 30344691 single base substitution A C intron_variant OV-AU 21 30355703 30355703 single base substitution C T intron_variant OV-AU 21 30355750 30355750 single base substitution G A intron_variant OV-AU 21 30367388 30367388 single base substitution C T upstream_gene_variant OV-US 21 30303491 30303491 single base substitution G T missense_variant H1742N 5224C>A OV-US 21 30303491 30303491 single base substitution G T missense_variant H1788N 5362C>A OV-US 21 30358518 30358518 single base substitution G A exon_variant OV-US 21 30358518 30358518 single base substitution G A missense_variant T142I 425C>T OV-US 21 30358518 30358518 single base substitution G A missense_variant T96I 287C>T PACA-AU 21 30301303 30301303 single base substitution A T 3_prime_UTR_variant PACA-AU 21 30304139 30304139 single base substitution A C intron_variant PACA-AU 21 30324119 30324119 single base substitution C A intron_variant PACA-AU 21 30326577 30326577 deletion of <=200bp G - downstream_gene_variant PACA-AU 21 30326577 30326577 deletion of <=200bp G - intron_variant PACA-AU 21 30336954 30336954 single base substitution G T downstream_gene_variant PACA-AU 21 30336954 30336954 single base substitution G T intron_variant PACA-AU 21 30336954 30336954 single base substitution G T stop_gained Y812* 2436C>A PACA-AU 21 30336954 30336954 single base substitution G T upstream_gene_variant PACA-AU 21 30359036 30359036 single base substitution A T intron_variant PACA-AU 21 30359240 30359240 single base substitution G C missense_variant R20G 58C>G PACA-AU 21 30359240 30359240 single base substitution G C missense_variant R66G 196C>G PACA-AU 21 30359240 30359240 single base substitution G C upstream_gene_variant PACA-AU 21 30365988 30365988 single base substitution G A upstream_gene_variant PACA-AU 21 30368335 30368335 deletion of <=200bp G - upstream_gene_variant PACA-CA 21 30304570 30304571 deletion of <=200bp AA - intron_variant PACA-CA 21 30305184 30305184 single base substitution T C intron_variant PACA-CA 21 30313220 30313220 single base substitution G C intron_variant PACA-CA 21 30315175 30315175 single base substitution A G intron_variant PACA-CA 21 30315570 30315570 insertion of <=200bp - A intron_variant PACA-CA 21 30318667 30318667 deletion of <=200bp A - intron_variant PACA-CA 21 30323998 30323998 deletion of <=200bp A - intron_variant PACA-CA 21 30332447 30332447 single base substitution G C downstream_gene_variant PACA-CA 21 30332447 30332447 single base substitution G C intron_variant PACA-CA 21 30332447 30332447 single base substitution G C upstream_gene_variant PACA-CA 21 30334233 30334233 deletion of <=200bp T - downstream_gene_variant PACA-CA 21 30334233 30334233 deletion of <=200bp T - intron_variant PACA-CA 21 30334233 30334233 deletion of <=200bp T - upstream_gene_variant PACA-CA 21 30340210 30340210 single base substitution T G 3_prime_UTR_variant PACA-CA 21 30340210 30340210 single base substitution T G intron_variant PACA-CA 21 30341430 30341430 single base substitution C T intron_variant PACA-CA 21 30347737 30347737 single base substitution G A intron_variant PACA-CA 21 30349589 30349589 single base substitution G A intron_variant PACA-CA 21 30357234 30357234 single base substitution G A exon_variant PACA-CA 21 30357234 30357234 single base substitution G A missense_variant R119C 355C>T PACA-CA 21 30357234 30357234 single base substitution G A missense_variant R165C 493C>T PACA-CA 21 30358474 30358474 single base substitution A T exon_variant PACA-CA 21 30358474 30358474 single base substitution A T missense_variant C111S 331T>A PACA-CA 21 30358474 30358474 single base substitution A T missense_variant C157S 469T>A PACA-CA 21 30361506 30361506 single base substitution G A intron_variant PACA-CA 21 30361506 30361506 single base substitution G A upstream_gene_variant PACA-CA 21 30362398 30362398 single base substitution C T intron_variant PACA-CA 21 30362398 30362398 single base substitution C T upstream_gene_variant PACA-CA 21 30363389 30363389 single base substitution C T intron_variant PACA-CA 21 30363389 30363389 single base substitution C T upstream_gene_variant PACA-CA 21 30365221 30365221 single base substitution T C missense_variant Y15C 44A>G PACA-CA 21 30365221 30365221 single base substitution T C upstream_gene_variant PACA-CA 21 30367470 30367470 single base substitution C G upstream_gene_variant PACA-CA 21 30368908 30368908 single base substitution C T upstream_gene_variant PAEN-AU 21 30296028 30296028 single base substitution T C downstream_gene_variant PAEN-AU 21 30297166 30297166 single base substitution G A downstream_gene_variant PAEN-AU 21 30297992 30297992 single base substitution T C downstream_gene_variant PAEN-AU 21 30323466 30323466 single base substitution G T intron_variant PAEN-AU 21 30332783 30332783 single base substitution C T downstream_gene_variant PAEN-AU 21 30332783 30332783 single base substitution C T intron_variant PAEN-AU 21 30332783 30332783 single base substitution C T upstream_gene_variant PAEN-AU 21 30336806 30336806 single base substitution T G downstream_gene_variant PAEN-AU 21 30336806 30336806 single base substitution T G intron_variant PAEN-AU 21 30336806 30336806 single base substitution T G upstream_gene_variant PAEN-AU 21 30338088 30338088 single base substitution G A downstream_gene_variant PAEN-AU 21 30338088 30338088 single base substitution G A intron_variant PAEN-AU 21 30338088 30338088 single base substitution G A upstream_gene_variant PAEN-AU 21 30341014 30341014 single base substitution C T intron_variant PAEN-IT 21 30314022 30314022 single base substitution C A intron_variant PBCA-DE 21 30296985 30296985 single base substitution C A downstream_gene_variant PBCA-DE 21 30300874 30300874 insertion of <=200bp - ATAAAACTTTA 3_prime_UTR_variant PBCA-DE 21 30309231 30309231 single base substitution T A intron_variant PBCA-DE 21 30315428 30315428 single base substitution T A intron_variant PBCA-DE 21 30318781 30318781 single base substitution C A intron_variant PBCA-DE 21 30326971 30326971 single base substitution A G downstream_gene_variant PBCA-DE 21 30326971 30326971 single base substitution A G intron_variant PBCA-DE 21 30329696 30329696 single base substitution G A downstream_gene_variant PBCA-DE 21 30329696 30329696 single base substitution G A synonymous_variant N950N 2850C>T PBCA-DE 21 30329696 30329696 single base substitution G A synonymous_variant N996N 2988C>T PBCA-DE 21 30330488 30330488 insertion of <=200bp - T downstream_gene_variant PBCA-DE 21 30330488 30330488 insertion of <=200bp - T intron_variant PBCA-DE 21 30333741 30333741 insertion of <=200bp - A 3_prime_UTR_variant PBCA-DE 21 30333741 30333741 insertion of <=200bp - A intron_variant PBCA-DE 21 30333741 30333741 insertion of <=200bp - A upstream_gene_variant PBCA-DE 21 30336998 30337010 deletion of <=200bp AAACACTGGCTAG - downstream_gene_variant PBCA-DE 21 30336998 30337010 deletion of <=200bp AAACACTGGCTAG - frameshift_variant LASVC794 PBCA-DE 21 30336998 30337010 deletion of <=200bp AAACACTGGCTAG - intron_variant PBCA-DE 21 30336998 30337010 deletion of <=200bp AAACACTGGCTAG - upstream_gene_variant PBCA-DE 21 30339067 30339067 single base substitution C A downstream_gene_variant PBCA-DE 21 30339067 30339067 single base substitution C A missense_variant L582F 1746G>T PBCA-DE 21 30339067 30339067 single base substitution C A missense_variant L628F 1884G>T PBCA-DE 21 30349324 30349324 single base substitution A C intron_variant PBCA-DE 21 30367098 30367099 deletion of <=200bp AT - upstream_gene_variant PRAD-CA 21 30314656 30314656 single base substitution C T intron_variant PRAD-CA 21 30326353 30326353 single base substitution C T downstream_gene_variant PRAD-CA 21 30326353 30326353 single base substitution C T intron_variant PRAD-CA 21 30327719 30327719 single base substitution T A downstream_gene_variant PRAD-CA 21 30327719 30327719 single base substitution T A intron_variant PRAD-CA 21 30368363 30368363 single base substitution G A upstream_gene_variant PRAD-UK 21 30306001 30306001 single base substitution T C intron_variant PRAD-UK 21 30316591 30316591 single base substitution T A intron_variant PRAD-UK 21 30318072 30318072 single base substitution G A intron_variant PRAD-UK 21 30318077 30318077 deletion of <=200bp A - intron_variant PRAD-UK 21 30320948 30320948 deletion of <=200bp A - intron_variant PRAD-UK 21 30365899 30365899 single base substitution T C upstream_gene_variant PRAD-US 21 30331780 30331780 single base substitution C A downstream_gene_variant PRAD-US 21 30331780 30331780 single base substitution C A exon_variant PRAD-US 21 30331780 30331780 single base substitution C A missense_variant D865Y 2593G>T PRAD-US 21 30331780 30331780 single base substitution C A missense_variant D911Y 2731G>T PRAD-US 21 30331780 30331780 single base substitution C A splice_region_variant PRAD-US 21 30339206 30339206 deletion of <=200bp T - downstream_gene_variant PRAD-US 21 30339206 30339206 deletion of <=200bp T - frameshift_variant N536 PRAD-US 21 30339206 30339206 deletion of <=200bp T - frameshift_variant N582 PRAD-US 21 30339290 30339290 single base substitution T G 3_prime_UTR_variant PRAD-US 21 30339290 30339290 single base substitution T G missense_variant D508A 1523A>C PRAD-US 21 30339290 30339290 single base substitution T G missense_variant D554A 1661A>C READ-US 21 30324491 30324491 single base substitution C T missense_variant R1112K 3335G>A READ-US 21 30324491 30324491 single base substitution C T missense_variant R1158K 3473G>A READ-US 21 30343625 30343625 single base substitution C T exon_variant READ-US 21 30343625 30343625 single base substitution C T missense_variant E318K 952G>A READ-US 21 30343625 30343625 single base substitution C T missense_variant E364K 1090G>A READ-US 21 30343704 30343704 single base substitution T G exon_variant READ-US 21 30343704 30343704 single base substitution T G missense_variant K291N 873A>C READ-US 21 30343704 30343704 single base substitution T G missense_variant K337N 1011A>C READ-US 21 30353480 30353480 single base substitution C A exon_variant READ-US 21 30353480 30353480 single base substitution C A missense_variant Q257H 771G>T READ-US 21 30353480 30353480 single base substitution C A missense_variant Q303H 909G>T RECA-EU 21 30296967 30296967 single base substitution C A downstream_gene_variant RECA-EU 21 30323855 30323855 single base substitution T G intron_variant RECA-EU 21 30336033 30336033 single base substitution C T downstream_gene_variant RECA-EU 21 30336033 30336033 single base substitution C T intron_variant RECA-EU 21 30336033 30336033 single base substitution C T upstream_gene_variant RECA-EU 21 30343366 30343366 single base substitution A G intron_variant RECA-EU 21 30346212 30346212 single base substitution T G intron_variant RECA-EU 21 30347841 30347841 single base substitution C T intron_variant RECA-EU 21 30364010 30364010 single base substitution G T intron_variant RECA-EU 21 30364010 30364010 single base substitution G T upstream_gene_variant SKCA-BR 21 30298428 30298428 single base substitution G A downstream_gene_variant SKCA-BR 21 30307657 30307657 single base substitution G A splice_region_variant SKCA-BR 21 30310055 30310055 single base substitution G A intron_variant SKCA-BR 21 30324847 30324847 single base substitution G A intron_variant SKCA-BR 21 30333261 30333261 single base substitution A C downstream_gene_variant SKCA-BR 21 30333261 30333261 single base substitution A C intron_variant SKCA-BR 21 30333261 30333261 single base substitution A C upstream_gene_variant SKCA-BR 21 30336958 30336958 single base substitution G A downstream_gene_variant SKCA-BR 21 30336958 30336958 single base substitution G A intron_variant SKCA-BR 21 30336958 30336958 single base substitution G A missense_variant P811L 2432C>T SKCA-BR 21 30336958 30336958 single base substitution G A upstream_gene_variant SKCA-BR 21 30336959 30336959 single base substitution G A downstream_gene_variant SKCA-BR 21 30336959 30336959 single base substitution G A intron_variant SKCA-BR 21 30336959 30336959 single base substitution G A missense_variant P811S 2431C>T SKCA-BR 21 30336959 30336959 single base substitution G A upstream_gene_variant SKCA-BR 21 30337060 30337060 single base substitution A T downstream_gene_variant SKCA-BR 21 30337060 30337060 single base substitution A T intron_variant SKCA-BR 21 30337060 30337060 single base substitution A T missense_variant L777H 2330T>A SKCA-BR 21 30337060 30337060 single base substitution A T upstream_gene_variant SKCA-BR 21 30337082 30337082 single base substitution T G downstream_gene_variant SKCA-BR 21 30337082 30337082 single base substitution T G intron_variant SKCA-BR 21 30337082 30337082 single base substitution T G missense_variant T770P 2308A>C SKCA-BR 21 30337082 30337082 single base substitution T G upstream_gene_variant SKCA-BR 21 30350702 30350702 single base substitution G A intron_variant SKCA-BR 21 30354230 30354230 single base substitution C T intron_variant SKCA-BR 21 30354335 30354335 single base substitution G C intron_variant SKCA-BR 21 30355672 30355672 single base substitution C T intron_variant SKCA-BR 21 30356306 30356306 single base substitution T G intron_variant SKCA-BR 21 30358301 30358301 single base substitution C A intron_variant SKCA-BR 21 30359272 30359272 single base substitution G A intron_variant SKCA-BR 21 30359272 30359272 single base substitution G A upstream_gene_variant SKCA-BR 21 30365291 30365291 single base substitution C T upstream_gene_variant SKCA-BR 21 30366411 30366411 single base substitution G A upstream_gene_variant SKCA-BR 21 30368338 30368338 insertion of <=200bp - GA upstream_gene_variant SKCM-US 21 30303532 30303532 single base substitution G A missense_variant S1728F 5183C>T SKCM-US 21 30303532 30303532 single base substitution G A missense_variant S1774F 5321C>T SKCM-US 21 30304892 30304892 single base substitution G A missense_variant P1657L 4970C>T SKCM-US 21 30304892 30304892 single base substitution G A missense_variant P1703L 5108C>T SKCM-US 21 30307468 30307468 single base substitution G A missense_variant S1613F 4838C>T SKCM-US 21 30307468 30307468 single base substitution G A missense_variant S1659F 4976C>T SKCM-US 21 30308901 30308901 single base substitution G T missense_variant P1534Q 4601C>A SKCM-US 21 30308901 30308901 single base substitution G T missense_variant P1580Q 4739C>A SKCM-US 21 30316198 30316198 single base substitution G A synonymous_variant S1337S 4011C>T SKCM-US 21 30316198 30316198 single base substitution G A synonymous_variant S1383S 4149C>T SKCM-US 21 30316752 30316752 single base substitution G A missense_variant S1312F 3935C>T SKCM-US 21 30316752 30316752 single base substitution G A missense_variant S1358F 4073C>T SKCM-US 21 30318484 30318484 single base substitution G A missense_variant L1205F 3613C>T SKCM-US 21 30318484 30318484 single base substitution G A missense_variant L1251F 3751C>T SKCM-US 21 30318518 30318518 single base substitution T A synonymous_variant I1193I 3579A>T SKCM-US 21 30318518 30318518 single base substitution T A synonymous_variant I1239I 3717A>T SKCM-US 21 30318520 30318520 single base substitution T C missense_variant I1193V 3577A>G SKCM-US 21 30318520 30318520 single base substitution T C missense_variant I1239V 3715A>G SKCM-US 21 30325549 30325549 single base substitution A C missense_variant L1077V 3229T>G SKCM-US 21 30325549 30325549 single base substitution A C missense_variant L1123V 3367T>G SKCM-US 21 30329142 30329142 single base substitution C T downstream_gene_variant SKCM-US 21 30329142 30329142 single base substitution C T missense_variant M1007I 3021G>A SKCM-US 21 30329142 30329142 single base substitution C T missense_variant M1053I 3159G>A SKCM-US 21 30329731 30329731 single base substitution G A downstream_gene_variant SKCM-US 21 30329731 30329731 single base substitution G A missense_variant L939F 2815C>T SKCM-US 21 30329731 30329731 single base substitution G A missense_variant L985F 2953C>T SKCM-US 21 30330842 30330842 single base substitution C T downstream_gene_variant SKCM-US 21 30330842 30330842 single base substitution C T exon_variant SKCM-US 21 30330842 30330842 single base substitution C T synonymous_variant L871L 2613G>A SKCM-US 21 30330842 30330842 single base substitution C T synonymous_variant L917L 2751G>A SKCM-US 21 30330851 30330851 single base substitution G A downstream_gene_variant SKCM-US 21 30330851 30330851 single base substitution G A exon_variant SKCM-US 21 30330851 30330851 single base substitution G A synonymous_variant I868I 2604C>T SKCM-US 21 30330851 30330851 single base substitution G A synonymous_variant I914I 2742C>T SKCM-US 21 30332977 30332977 single base substitution C T downstream_gene_variant SKCM-US 21 30332977 30332977 single base substitution C T exon_variant SKCM-US 21 30332977 30332977 single base substitution C T missense_variant D739N 2215G>A SKCM-US 21 30332977 30332977 single base substitution C T missense_variant D785N 2353G>A SKCM-US 21 30332977 30332977 single base substitution C T upstream_gene_variant SKCM-US 21 30338844 30338844 single base substitution G A downstream_gene_variant SKCM-US 21 30338844 30338844 single base substitution G A missense_variant P657S 1969C>T SKCM-US 21 30338844 30338844 single base substitution G A missense_variant P703S 2107C>T SKCM-US 21 30338887 30338887 single base substitution G A downstream_gene_variant SKCM-US 21 30338887 30338887 single base substitution G A synonymous_variant V642V 1926C>T SKCM-US 21 30338887 30338887 single base substitution G A synonymous_variant V688V 2064C>T SKCM-US 21 30339281 30339281 single base substitution G A 3_prime_UTR_variant SKCM-US 21 30339281 30339281 single base substitution G A missense_variant S511F 1532C>T SKCM-US 21 30339281 30339281 single base substitution G A missense_variant S557F 1670C>T SKCM-US 21 30339415 30339415 single base substitution G A 3_prime_UTR_variant SKCM-US 21 30339415 30339415 single base substitution G A synonymous_variant S466S 1398C>T SKCM-US 21 30339415 30339415 single base substitution G A synonymous_variant S512S 1536C>T SKCM-US 21 30357190 30357190 single base substitution G A exon_variant SKCM-US 21 30357190 30357190 single base substitution G A synonymous_variant I133I 399C>T SKCM-US 21 30357190 30357190 single base substitution G A synonymous_variant I179I 537C>T SKCM-US 21 30357224 30357224 single base substitution C T exon_variant SKCM-US 21 30357224 30357224 single base substitution C T missense_variant R122Q 365G>A SKCM-US 21 30357224 30357224 single base substitution C T missense_variant R168Q 503G>A SKCM-US 21 30365209 30365209 single base substitution G A missense_variant S19F 56C>T SKCM-US 21 30365209 30365209 single base substitution G A upstream_gene_variant SKCM-US 21 30365230 30365230 single base substitution C T missense_variant G12E 35G>A SKCM-US 21 30365230 30365230 single base substitution C T upstream_gene_variant SKCM-US 21 30365231 30365231 single base substitution C T missense_variant G12R 34G>A SKCM-US 21 30365231 30365231 single base substitution C T upstream_gene_variant STAD-US 21 30302779 30302779 single base substitution C T synonymous_variant T1764T 5292G>A STAD-US 21 30302779 30302779 single base substitution C T synonymous_variant T1810T 5430G>A STAD-US 21 30309004 30309004 single base substitution A G missense_variant S1500P 4498T>C STAD-US 21 30309004 30309004 single base substitution A G missense_variant S1546P 4636T>C STAD-US 21 30316135 30316135 single base substitution T G synonymous_variant L1358L 4074A>C STAD-US 21 30316135 30316135 single base substitution T G synonymous_variant L1404L 4212A>C STAD-US 21 30316746 30316746 single base substitution C T missense_variant G1314D 3941G>A STAD-US 21 30316746 30316746 single base substitution C T missense_variant G1360D 4079G>A STAD-US 21 30324485 30324485 single base substitution T C missense_variant E1114G 3341A>G STAD-US 21 30324485 30324485 single base substitution T C missense_variant E1160G 3479A>G STAD-US 21 30325581 30325581 single base substitution A G missense_variant V1066A 3197T>C STAD-US 21 30325581 30325581 single base substitution A G missense_variant V1112A 3335T>C STAD-US 21 30329691 30329691 single base substitution C T downstream_gene_variant STAD-US 21 30329691 30329691 single base substitution C T missense_variant S952N 2855G>A STAD-US 21 30329691 30329691 single base substitution C T missense_variant S998N 2993G>A STAD-US 21 30330717 30330717 single base substitution T A downstream_gene_variant STAD-US 21 30330717 30330717 single base substitution T A missense_variant D913V 2738A>T STAD-US 21 30330717 30330717 single base substitution T A missense_variant D959V 2876A>T STAD-US 21 30338713 30338713 deletion of <=200bp T - downstream_gene_variant STAD-US 21 30338713 30338713 deletion of <=200bp T - frameshift_variant K700 STAD-US 21 30338713 30338713 deletion of <=200bp T - frameshift_variant K746 STAD-US 21 30339315 30339315 single base substitution C T 3_prime_UTR_variant STAD-US 21 30339315 30339315 single base substitution C T missense_variant A500T 1498G>A STAD-US 21 30339315 30339315 single base substitution C T missense_variant A546T 1636G>A STAD-US 21 30339484 30339484 single base substitution A G 3_prime_UTR_variant STAD-US 21 30339484 30339484 single base substitution A G synonymous_variant D443D 1329T>C STAD-US 21 30339484 30339484 single base substitution A G synonymous_variant D489D 1467T>C STAD-US 21 30341860 30341860 deletion of <=200bp A - exon_variant STAD-US 21 30341860 30341860 deletion of <=200bp A - frameshift_variant F413 STAD-US 21 30341860 30341860 deletion of <=200bp A - frameshift_variant F459 STAD-US 21 30353447 30353447 single base substitution T C exon_variant STAD-US 21 30353447 30353447 single base substitution T C synonymous_variant V268V 804A>G STAD-US 21 30353447 30353447 single base substitution T C synonymous_variant V314V 942A>G STAD-US 21 30357128 30357128 single base substitution G C exon_variant STAD-US 21 30357128 30357128 single base substitution G C missense_variant A154G 461C>G STAD-US 21 30357128 30357128 single base substitution G C missense_variant A200G 599C>G STAD-US 21 30359239 30359239 single base substitution C T missense_variant R20Q 59G>A STAD-US 21 30359239 30359239 single base substitution C T missense_variant R66Q 197G>A STAD-US 21 30359239 30359239 single base substitution C T upstream_gene_variant STAD-US 21 30365199 30365199 single base substitution G A 5_prime_UTR_variant STAD-US 21 30365199 30365199 single base substitution G A synonymous_variant A22A 66C>T THCA-SA 21 30339120 30339120 single base substitution C A downstream_gene_variant THCA-SA 21 30339120 30339120 single base substitution C A missense_variant G565C 1693G>T THCA-SA 21 30339120 30339120 single base substitution C A missense_variant G611C 1831G>T THCA-SA 21 30339234 30339234 single base substitution T C 3_prime_UTR_variant THCA-SA 21 30339234 30339234 single base substitution T C missense_variant S527G 1579A>G THCA-SA 21 30339234 30339234 single base substitution T C missense_variant S573G 1717A>G UCEC-US 21 30302787 30302787 single base substitution G A missense_variant R1762C 5284C>T UCEC-US 21 30302787 30302787 single base substitution G A missense_variant R1808C 5422C>T UCEC-US 21 30303603 30303603 single base substitution G A synonymous_variant N1704N 5112C>T UCEC-US 21 30303603 30303603 single base substitution G A synonymous_variant N1750N 5250C>T UCEC-US 21 30303645 30303645 single base substitution C T splice_acceptor_variant UCEC-US 21 30315604 30315604 single base substitution A T missense_variant D1425E 4275T>A UCEC-US 21 30315604 30315604 single base substitution A T missense_variant D1471E 4413T>A UCEC-US 21 30316192 30316192 single base substitution C A missense_variant Q1339H 4017G>T UCEC-US 21 30316192 30316192 single base substitution C A missense_variant Q1385H 4155G>T UCEC-US 21 30316797 30316797 single base substitution C T missense_variant G1297D 3890G>A UCEC-US 21 30316797 30316797 single base substitution C T missense_variant G1343D 4028G>A UCEC-US 21 30316872 30316872 single base substitution A G missense_variant L1272P 3815T>C UCEC-US 21 30316872 30316872 single base substitution A G missense_variant L1318P 3953T>C UCEC-US 21 30325604 30325604 single base substitution A G synonymous_variant N1058N 3174T>C UCEC-US 21 30325604 30325604 single base substitution A G synonymous_variant N1104N 3312T>C UCEC-US 21 30329187 30329187 single base substitution C G downstream_gene_variant UCEC-US 21 30329187 30329187 single base substitution C G missense_variant K1038N 3114G>C UCEC-US 21 30329187 30329187 single base substitution C G missense_variant K992N 2976G>C UCEC-US 21 30332842 30332842 single base substitution T G downstream_gene_variant UCEC-US 21 30332842 30332842 single base substitution T G exon_variant UCEC-US 21 30332842 30332842 single base substitution T G missense_variant N784H 2350A>C UCEC-US 21 30332842 30332842 single base substitution T G missense_variant N830H 2488A>C UCEC-US 21 30332842 30332842 single base substitution T G upstream_gene_variant UCEC-US 21 30339154 30339154 single base substitution T G downstream_gene_variant UCEC-US 21 30339154 30339154 single base substitution T G missense_variant E553D 1659A>C UCEC-US 21 30339154 30339154 single base substitution T G missense_variant E599D 1797A>C UCEC-US 21 30339387 30339387 single base substitution C A 3_prime_UTR_variant UCEC-US 21 30339387 30339387 single base substitution C A missense_variant D476Y 1426G>T UCEC-US 21 30339387 30339387 single base substitution C A missense_variant D522Y 1564G>T UCEC-US 21 30342917 30342917 single base substitution T G exon_variant UCEC-US 21 30342917 30342917 single base substitution T G missense_variant K378Q 1132A>C UCEC-US 21 30342917 30342917 single base substitution T G missense_variant K424Q 1270A>C UCEC-US 21 30353522 30353522 single base substitution C A exon_variant UCEC-US 21 30353522 30353522 single base substitution C A missense_variant E243D 729G>T UCEC-US 21 30353522 30353522 single base substitution C A missense_variant E289D 867G>T UCEC-US 21 30357117 30357117 single base substitution T C exon_variant UCEC-US 21 30357117 30357117 single base substitution T C missense_variant T158A 472A>G UCEC-US 21 30357117 30357117 single base substitution T C missense_variant T204A 610A>G UCEC-US 21 30357196 30357196 single base substitution T G exon_variant UCEC-US 21 30357196 30357196 single base substitution T G missense_variant K131N 393A>C UCEC-US 21 30357196 30357196 single base substitution T G missense_variant K177N 531A>C UCEC-US 21 30358476 30358476 single base substitution A C exon_variant UCEC-US 21 30358476 30358476 single base substitution A C missense_variant F110C 329T>G UCEC-US 21 30358476 30358476 single base substitution A C missense_variant F156C 467T>G UCEC-US 21 30359102 30359102 single base substitution G A stop_gained R112* 334C>T UCEC-US 21 30359102 30359102 single base substitution G A stop_gained R66* 196C>T UCEC-US 21 30359102 30359102 single base substitution G A upstream_gene_variant UCEC-US 21 30359208 30359208 single base substitution T A synonymous_variant G30G 90A>T UCEC-US 21 30359208 30359208 single base substitution T A synonymous_variant G76G 228A>T UCEC-US 21 30359208 30359208 single base substitution T A upstream_gene_variant UCEC-US 21 30359221 30359221 single base substitution G A missense_variant A26V 77C>T UCEC-US 21 30359221 30359221 single base substitution G A missense_variant A72V 215C>T UCEC-US 21 30359221 30359221 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PT19_1 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - 526LT COSM149214 c.2438C>T p.A813V Substitution - Missense 21:28959613-28959613 - S00838 COSM5661586 c.47C>T p.S16L Substitution - Missense 21:28986930-28986930 - CML037T COSM5802854 c.2240A>G p.N747S Substitution - Missense 21:28960630-28960630 - KM12 COSM4612790 c.1605_1607delAAA p.K535delK Deletion - In frame 21:28966884-28966886 - NPC15F COSM4996050 c.854G>A p.R285H Substitution - Missense 21:28971401-28971401 - TCGA-EB-A42Z-01 COSM3550039 c.2613G>A p.L871L Substitution - coding silent 21:28958520-28958520 - B77 COSM1751591 c.3058A>T p.N1020Y Substitution - Missense 21:28956783-28956783 - TCGA-C5-A0TN-01 COSM4856140 c.1733C>A p.S578Y Substitution - Missense 21:28966758-28966758 - A9 COSM5350650 c.5285G>T p.R1762L Substitution - Missense 21:28930464-28930464 - BD55T COSM5509576 c.2898A>C p.L966F Substitution - Missense 21:28956943-28956943 - CPCG_0042_Pr_P_F0 COSM3396393 c.3706T>G p.S1236A Substitution - Missense 21:28945869-28945869 - PD2144a COSM51909 c.1161G>A p.T387T Substitution - coding silent 21:28970566-28970566 - TCGA-GF-A6C9-06 COSM4900831 c.2815C>T p.L939F Substitution - Missense 21:28957409-28957409 - YUMOKI COSM5392754 c.4682C>T p.P1561L Substitution - Missense 21:28935302-28935302 - Pat_74_B COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - 19T COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - TCGA-FU-A3HZ-01 COSM1681904 c.323G>T p.R108I Substitution - Missense 21:28986161-28986161 - TCGA-EE-A29L-06 COSM3550034 c.4601C>A p.P1534Q Substitution - Missense 21:28936579-28936579 - TCGA-EE-A2GI-06 COSM3550038 c.3021G>A p.M1007I Substitution - Missense 21:28956820-28956820 - ESO-0015 COSM1264355 c.5169C>T p.H1723H Substitution - coding silent 21:28931224-28931224 - 93 COSM5015689 c.4799A>T p.K1600M Substitution - Missense 21:28935185-28935185 - S02400 COSM5699864 c.1349G>T p.G450V Substitution - Missense 21:28967142-28967142 - TCGA-CA-6718-01 COSM1413542 c.2575G>T p.E859* Substitution - Nonsense 21:28959476-28959476 - LS180 COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - pfg258T COSM4751968 c.241T>A p.L81I Substitution - Missense 21:28986736-28986736 - TCGA-57-1993-01 COSM72456 c.3310G>A p.D1104N Substitution - Missense 21:28952194-28952194 - 27T COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - 108482 COSM96299 c.1242A>G p.E414E Substitution - coding silent 21:28969535-28969535 - T3246 COSM4699526 c.1607_1608insA p.N536fs*3 Insertion - Frameshift 21:28966883-28966884 - ESCC-F71 COSM5048403 c.2227G>A p.E743K Substitution - Missense 21:28960643-28960643 - TCGA-IR-A3LK-01 COSM4817746 c.3877C>G p.L1293V Substitution - Missense 21:28944488-28944488 - HCT116 COSM2841680 c.1496T>C p.V499A Substitution - Missense 21:28966995-28966995 - H292 COSM1197380 c.2755G>A p.V919I Substitution - Missense 21:28957469-28957469 - TCGA-EE-A2GJ-06 COSM3550041 c.1969C>T p.P657S Substitution - Missense 21:28966522-28966522 - TCGA-DI-A0WH-01 COSM1029739 c.2259T>C p.C753C Substitution - coding silent 21:28960611-28960611 - T2938 COSM4699523 c.2895G>A p.W965* Substitution - Nonsense 21:28956946-28956946 - HT115 COSM2841634 c.3810G>A p.V1270V Substitution - coding silent 21:28944555-28944555 - TCGA-DI-A0WH-01 COSM1029740 c.2203T>C p.W735R Substitution - Missense 21:28960667-28960667 - S00022 COSM314845 c.4108G>T p.D1370Y Substitution - Missense 21:28943779-28943779 - PT42 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - TCGA-AP-A051-01 COSM1029750 c.77C>T p.A26V Substitution - Missense 21:28986900-28986900 - TCGA-EA-A3Y4-01 COSM4848053 c.3065A>T p.E1022V Substitution - Missense 21:28956776-28956776 - TCGA-AP-A054-01 COSM1029736 c.3174T>C p.N1058N Substitution - coding silent 21:28953282-28953282 - TCGA-GV-A3JZ-01 COSM1307697 c.1681G>C p.E561Q Substitution - Missense 21:28966810-28966810 - TCGA-AP-A0LM-01 COSM1029738 c.2350A>C p.N784H Substitution - Missense 21:28960520-28960520 - TCGA-HC-7080-01 COSM3783520 c.2593G>T p.D865Y Substitution - Missense 21:28959458-28959458 - TCGA-HU-A4H4-01 COSM4100992 c.4498T>C p.S1500P Substitution - Missense 21:28936682-28936682 - HCT116 COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - HCC058T COSM5805454 c.629+4A>T p.? Unknown 21:28982312-28982312 - HCC150 COSM3707994 c.1879A>T p.S627C Substitution - Missense 21:28966612-28966612 - NB-0997 COSM1287655 c.3031G>A p.A1011T Substitution - Missense 21:28956810-28956810 - TCGA-BR-7703-01 COSM4100996 c.3197T>C p.V1066A Substitution - Missense 21:28953259-28953259 - ICC013T COSM5814109 c.1543G>T p.V515L Substitution - Missense 21:28966948-28966948 - SH-0622 COSM2841630 c.3934delT p.S1312fs*13 Deletion - Frameshift 21:28944431-28944431 - B61-Tumor COSM1751593 c.23G>T p.R8L Substitution - Missense 21:28992783-28992783 - S02243 COSM5677828 c.2959A>C p.K987Q Substitution - Missense 21:28956882-28956882 - RK298_C01 COSM3701670 c.5278C>T p.L1760L Substitution - coding silent 21:28930471-28930471 - CS05 COSM4967392 c.663C>G p.F221L Substitution - Missense 21:28981266-28981266 - 234 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - T578 COSM4699522 c.3904A>C p.N1302H Substitution - Missense 21:28944461-28944461 - TCGA-A5-A0GP-01 COSM1029741 c.1659A>C p.E553D Substitution - Missense 21:28966832-28966832 - TCGA-46-3767-01 COSM725412 c.5029C>A p.R1677R Substitution - coding silent 21:28932511-28932511 - HCC2998 COSM1681904 c.323G>T p.R108I Substitution - Missense 21:28986161-28986161 - HCT-116 COSM1684633 c.1597_1598delAA p.N536fs*2 Deletion - Frameshift 21:28966893-28966894 - S00022 COSM314845 c.4108G>T p.D1370Y Substitution - Missense 21:28943779-28943779 - PT24_1 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - Gp2D COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - HT115 COSM1223925 c.3925G>T p.E1309* Substitution - Nonsense 21:28944440-28944440 - TCGA-EB-A44N-01 COSM3550036 c.3579A>T p.I1193I Substitution - coding silent 21:28946196-28946196 - TCGA-DD-A113-01 COSM4925217 c.594T>C p.L198L Substitution - coding silent 21:28982351-28982351 - TCGA-EB-A24D-01 COSM3550040 c.2215G>A p.D739N Substitution - Missense 21:28960655-28960655 - 260211 COSM3726162 c.1136T>C p.L379S Substitution - Missense 21:28970591-28970591 - TCGA-A2-A0ET-01 COSM444329 c.3841G>A p.A1281T Substitution - Missense 21:28944524-28944524 - CSCC-41-T COSM4568689 c.1140T>A p.D380E Substitution - Missense 21:28970587-28970587 - 587376 COSM1223928 c.433A>C p.K145Q Substitution - Missense 21:28984835-28984835 - Sample_1 COSM5022072 c.3763T>C p.L1255L Substitution - coding silent 21:28945812-28945812 - TCGA-EI-6917-01 COSM3423884 c.873A>C p.K291N Substitution - Missense 21:28971382-28971382 - B78-Tumor COSM1751592 c.1338C>G p.L446L Substitution - coding silent 21:28967153-28967153 - TCGA-BR-8078-01 COSM4100991 c.5292G>A p.T1764T Substitution - coding silent 21:28930457-28930457 - TCGA-AA-A00O-01 COSM298917 c.4408G>T p.D1470Y Substitution - Missense 21:28941294-28941294 - SW48 COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - TCGA-D9-A6EC-06 COSM4402975 c.2604C>T p.I868I Substitution - coding silent 21:28958529-28958529 - TCGA-BS-A0UV-01 COSM1029729 c.5112C>T p.N1704N Substitution - coding silent 21:28931281-28931281 - cSCCP7 COSM140280 c.524C>T p.P175L Substitution - Missense 21:28984744-28984744 - HCC142 COSM1615945 c.2366G>A p.G789E Substitution - Missense 21:28959685-28959685 - LS411 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - CHC892T COSM4797795 c.421G>A p.A141T Substitution - Missense 21:28984847-28984847 - TCGA-BG-A18B-01 COSM1029731 c.4275T>A p.D1425E Substitution - Missense 21:28943282-28943282 - PD7250a COSM5775237 c.4483-4C>G p.? Unknown 21:28936701-28936701 - LIM1215 COSM4295276 c.1250G>A p.R417H Substitution - Missense 21:28969527-28969527 - TCGA-04-1338-01 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - CSCC-41-T COSM4496646 c.341C>T p.S114L Substitution - Missense 21:28986143-28986143 - BCM399T COSM4955296 c.1915C>G p.Q639E Substitution - Missense 21:28966576-28966576 - TCGA-FW-A3R5-06 COSM3911988 c.4838C>T p.S1613F Substitution - Missense 21:28935146-28935146 - 2 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - S01861 COSM2841682 c.1456G>A p.V486I Substitution - Missense 21:28967035-28967035 - AOCS-057-1-2 COSM3550043 c.1532C>T p.S511F Substitution - Missense 21:28966959-28966959 - TCGA-BR-4256-01 COSM4100997 c.2855G>A p.S952N Substitution - Missense 21:28957369-28957369 - TCGA-13-2059-01 COSM1327455 c.5235C>G p.C1745W Substitution - Missense 21:28931158-28931158 - TCGA-AA-A00N-01 COSM275943 c.2089G>A p.E697K Substitution - Missense 21:28966402-28966402 - TCGA-AP-A0LM-01 COSM1029744 c.729G>T p.E243D Substitution - Missense 21:28981200-28981200 - sysucc-311T COSM5465043 c.230T>C p.V77A Substitution - Missense 21:28986747-28986747 - TCGA-BR-8687-01 COSM4100993 c.4074A>C p.L1358L Substitution - coding silent 21:28943813-28943813 - LUAD-RT-S01699 COSM378353 c.1179G>C p.L393L Substitution - coding silent 21:28969598-28969598 - YULAPE COSM1713876 c.4571C>T p.P1524L Substitution - Missense 21:28936609-28936609 - T2944 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - PD7219a COSM5775179 c.2296C>G p.H766D Substitution - Missense 21:28960574-28960574 - Pat_45_B COSM5858470 c.1384G>A p.E462K Substitution - Missense 21:28967107-28967107 - HCC128T COSM1615944 c.2854A>G p.S952G Substitution - Missense 21:28957370-28957370 - Au1 COSM5597038 c.4825C>T p.Q1609* Substitution - Nonsense 21:28935159-28935159 - TCGA-BR-4280-01 COSM4100994 c.3941G>A p.G1314D Substitution - Missense 21:28944424-28944424 - PT09_1 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - TCGA-B5-A0K2-01 COSM1029735 c.3323C>A p.P1108Q Substitution - Missense 21:28952181-28952181 - TCGA-D3-A5GO-06 COSM3550035 c.3613C>T p.L1205F Substitution - Missense 21:28946162-28946162 - Capan-1 COSM328467 c.2205G>C p.W735C Substitution - Missense 21:28960665-28960665 - TCGA-AG-A002-01 COSM261871 c.3102G>A p.L1034L Substitution - coding silent 21:28953354-28953354 - YUROC COSM2841679 c.1533C>T p.S511S Substitution - coding silent 21:28966958-28966958 - TCGA-FS-A1ZS-06 COSM3550044 c.1398C>T p.S466S Substitution - coding silent 21:28967093-28967093 - PT41 COSM5924754 c.767C>T p.S256L Substitution - Missense 21:28981162-28981162 - 91T COSM106458 c.4035C>T p.P1345P Substitution - coding silent 21:28943852-28943852 - B77-Tumor COSM1751591 c.3058A>T p.N1020Y Substitution - Missense 21:28956783-28956783 - TCGA-DD-A4ND-01 COSM4935039 c.841G>T p.A281S Substitution - Missense 21:28971414-28971414 - TCGA-BR-8678-01 COSM4101002 c.461C>G p.A154G Substitution - Missense 21:28984807-28984807 - PT32 COSM5907768 c.3611T>G p.F1204C Substitution - Missense 21:28946164-28946164 - 587316 COSM1223921 c.3194G>A p.R1065H Substitution - Missense 21:28953262-28953262 - TCGA-ER-A19G-06 COSM2841629 c.3935C>T p.S1312F Substitution - Missense 21:28944430-28944430 - S00935 COSM314846 c.1036A>T p.T346S Substitution - Missense 21:28970691-28970691 - CSCC-49-T COSM4478054 c.2068C>T p.R690W Substitution - Missense 21:28966423-28966423 - ESCC_16 COSM5625827 c.3223C>T p.Q1075* Substitution - Nonsense 21:28953233-28953233 - sysucc-867T COSM5486831 c.355C>T p.R119C Substitution - Missense 21:28984913-28984913 - HCC126T COSM5818809 c.2075G>C p.C692S Substitution - Missense 21:28966416-28966416 - CSCC-49-T COSM4523073 c.1058G>A p.R353Q Substitution - Missense 21:28970669-28970669 - T5 COSM3758819 c.1208T>C p.L403S Substitution - Missense 21:28969569-28969569 - TCGA-BS-A0UV-01 COSM1029746 c.393A>C p.K131N Substitution - Missense 21:28984875-28984875 - TCGA-B0-4842-01 COSM478466 c.1629T>A p.D543E Substitution - Missense 21:28966862-28966862 - TCGA-B5-A0JY-01 COSM1029747 c.329T>G p.F110C Substitution - Missense 21:28986155-28986155 - 587350 COSM1223923 c.3520T>C p.C1174R Substitution - Missense 21:28946255-28946255 - HX17T COSM1615947 c.576+3A>C p.? Unknown 21:28984689-28984689 - ESCC-F75 COSM5048562 c.1315A>C p.I439L Substitution - Missense 21:28967176-28967176 - RKO COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - 526LT COSM149215 c.1579A>G p.S527G Substitution - Missense 21:28966912-28966912 - Pat_15_B COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - LUAD-RT-S01840 COSM384793 c.2801G>T p.S934I Substitution - Missense 21:28957423-28957423 - CSCC-44-T COSM4568076 c.1069_1070AC>TT p.T357F Substitution - Missense 21:28970657-28970658 - GC8_T COSM149215 c.1579A>G p.S527G Substitution - Missense 21:28966912-28966912 - 24T COSM108431 c.2575G>A p.E859K Substitution - Missense 21:28959476-28959476 - 102 COSM5015690 c.2639A>G p.N880S Substitution - Missense 21:28958494-28958494 - TARGET-30-PARSBI COSM1287654 c.1489A>G p.I497V Substitution - Missense 21:28967002-28967002 - SC_9054 COSM5572358 c.4419T>C p.Y1473Y Substitution - coding silent 21:28941283-28941283 - U2940 COSM5621189 c.199A>G p.M67V Substitution - Missense 21:28986778-28986778 - T3262 COSM4699525 c.1894A>T p.M632L Substitution - Missense 21:28966597-28966597 - sysucc-880T COSM5463014 c.3487+1G>A p.? Unknown 21:28947463-28947463 - 193 COSM1741737 c.1592C>G p.S531* Substitution - Nonsense 21:28966899-28966899 - YUFIGUR COSM5413425 c.1869C>T p.S623S Substitution - coding silent 21:28966622-28966622 - TCGA-AP-A051-01 COSM1029734 c.3815T>C p.L1272P Substitution - Missense 21:28944550-28944550 - TCGA-EE-A3AA-06 COSM3550032 c.5183C>T p.S1728F Substitution - Missense 21:28931210-28931210 - TCGA-AX-A0J1-01 COSM1029733 c.3890G>A p.G1297D Substitution - Missense 21:28944475-28944475 - TCGA-F5-6814-01 COSM3423883 c.952G>A p.E318K Substitution - Missense 21:28971303-28971303 - SNUH_G72_S1 COSM4420269 c.2388C>T p.I796I Substitution - coding silent 21:28959663-28959663 - T1743 COSM4699521 c.5029C>T p.R1677W Substitution - Missense 21:28932511-28932511 - ESO-081 COSM1243571 c.2679T>C p.S893S Substitution - coding silent 21:28958454-28958454 - TCGA-22-5482-01 COSM725413 c.5253A>G p.T1751T Substitution - coding silent 21:28930496-28930496 - ccRCC-77 COSM1662652 c.1058G>T p.R353L Substitution - Missense 21:28970669-28970669 - ZZUFHECRKL-G045T COSM40786 c.3898C>T p.P1300S Substitution - Missense 21:28944467-28944467 - ESCC_143 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - TCGA-G2-A3VY-01 COSM121760 c.4869C>A p.G1623G Substitution - coding silent 21:28935115-28935115 - Gp5D COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - 587376 COSM1223927 c.1587G>T p.L529F Substitution - Missense 21:28966904-28966904 - TCGA-FD-A3B7-01 COSM1307696 c.4115A>G p.K1372R Substitution - Missense 21:28943772-28943772 - 2290929 COSM4440624 c.3210G>A p.T1070T Substitution - coding silent 21:28953246-28953246 - 587338 COSM1223922 c.4757G>A p.S1586N Substitution - Missense 21:28935227-28935227 - ICGC_MB61 COSM3764906 c.1746G>T p.L582F Substitution - Missense 21:28966745-28966745 - CHC1041T COSM3668511 c.1131A>G p.P377P Substitution - coding silent 21:28970596-28970596 - C135 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - B61 COSM1751593 c.23G>T p.R8L Substitution - Missense 21:28992783-28992783 - HN_62421 COSM125893 c.1753C>G p.L585V Substitution - Missense 21:28966738-28966738 - TCGA-AP-A059-01 COSM1029732 c.4017G>T p.Q1339H Substitution - Missense 21:28943870-28943870 - PD9575a COSM3771126 c.58C>G p.R20G Substitution - Missense 21:28986919-28986919 - TCGA-06-0184-01 COSM2150484 c.577-1G>A p.? Unknown 21:28982369-28982369 - TCGA-D1-A17Q-01 COSM1029742 c.1426G>T p.D476Y Substitution - Missense 21:28967065-28967065 - 587376 COSM1223925 c.3925G>T p.E1309* Substitution - Nonsense 21:28944440-28944440 - BCM399T COSM4955296 c.1915C>G p.Q639E Substitution - Missense 21:28966576-28966576 - HT115 COSM2841640 c.3650T>C p.V1217A Substitution - Missense 21:28945925-28945925 - TCGA-D8-A1XK-01 COSM3841688 c.1334T>G p.V445G Substitution - Missense 21:28967157-28967157 - TCGA-DU-A5TY-01 COSM3972729 c.2088G>A p.M696I Substitution - Missense 21:28966403-28966403 - HCT-116 COSM1681903 c.5230G>A p.A1744T Substitution - Missense 21:28931163-28931163 - TCGA-D1-A160-01 COSM1029745 c.472A>G p.T158A Substitution - Missense 21:28984796-28984796 - 1T COSM110003 c.1470C>T p.F490F Substitution - coding silent 21:28967021-28967021 - Sample_1 COSM5022073 c.2281G>A p.V761I Substitution - Missense 21:28960589-28960589 - 530 COSM3722438 c.4521G>A p.K1507K Substitution - coding silent 21:28936659-28936659 - LS174T COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - LOVO COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - SW1417 COSM1029748 c.196C>T p.R66* Substitution - Nonsense 21:28986781-28986781 - KPOPBR-40-T COSM5965986 c.4623C>T p.F1541F Substitution - coding silent 21:28936557-28936557 - HCA7 COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - RK199_C01 COSM3740261 c.4791T>C p.F1597F Substitution - coding silent 21:28935193-28935193 - TCGA-G9-6351-01 COSM3673171 c.3654G>T p.L1218L Substitution - coding silent 21:28945921-28945921 - TCGA-B5-A0JY-01 COSM1029728 c.5284C>T p.R1762C Substitution - Missense 21:28930465-28930465 - S01020 COSM5665151 c.1312-1G>C p.? Unknown 21:28967180-28967180 - HCC142T COSM1615945 c.2366G>A p.G789E Substitution - Missense 21:28959685-28959685 - 1T COSM106819 c.4137C>T p.L1379L Substitution - coding silent 21:28943750-28943750 - ESO-555 COSM1264358 c.2502G>A p.A834A Substitution - coding silent 21:28959549-28959549 - TCGA-AC-A3OD-01 COSM3841686 c.3553C>A p.L1185I Substitution - Missense 21:28946222-28946222 - CSCC-10-T COSM4550907 c.4998G>A p.G1666G Substitution - coding silent 21:28932542-28932542 - OSCC-GB_00470111 COSM3713379 c.4686C>T p.H1562H Substitution - coding silent 21:28935298-28935298 - Br27P COSM40786 c.3898C>T p.P1300S Substitution - Missense 21:28944467-28944467 - SNU-175 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - RK175_C01 COSM3740262 c.2023A>G p.R675G Substitution - Missense 21:28966468-28966468 - STC297 COSM5057541 c.5123G>A p.R1708H Substitution - Missense 21:28931270-28931270 - cSCCP4 COSM139207 c.469G>A p.D157N Substitution - Missense 21:28984799-28984799 - LOVO COSM2841630 c.3934delT p.S1312fs*13 Deletion - Frameshift 21:28944431-28944431 - LIM1215 COSM4295277 c.627G>A p.P209P Substitution - coding silent 21:28982318-28982318 - TCGA-HU-A4G8-01 COSM4101001 c.804A>G p.V268V Substitution - coding silent 21:28981125-28981125 - ESCC-D14 COSM5045479 c.493G>A p.A165T Substitution - Missense 21:28984775-28984775 - TCGA-EE-A29E-06 COSM3550042 c.1926C>T p.V642V Substitution - coding silent 21:28966565-28966565 - TCGA-66-2755-01 COSM725407 c.497C>A p.A166E Substitution - Missense 21:28984771-28984771 - HN_62741 COSM121760 c.4869C>A p.G1623G Substitution - coding silent 21:28935115-28935115 - TCGA-04-1346-01 COSM75320 c.5224C>A p.H1742N Substitution - Missense 21:28931169-28931169 - 587284 COSM1223924 c.4227G>A p.M1409I Substitution - Missense 21:28943330-28943330 - 12T COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - 587376 COSM1223926 c.2783T>G p.L928R Substitution - Missense 21:28957441-28957441 - 8066491 COSM3771126 c.58C>G p.R20G Substitution - Missense 21:28986919-28986919 - TCGA-HU-A4GQ-01 COSM4100998 c.2738A>T p.D913V Substitution - Missense 21:28958395-28958395 - Pat_60_B COSM5858471 c.802G>A p.V268I Substitution - Missense 21:28981127-28981127 - HCT116 COSM1681903 c.5230G>A p.A1744T Substitution - Missense 21:28931163-28931163 - Pat_45_B COSM5858472 c.124C>T p.Q42* Substitution - Nonsense 21:28986853-28986853 - T3024 COSM1264358 c.2502G>A p.A834A Substitution - coding silent 21:28959549-28959549 - RK308_C01 COSM3740263 c.273T>C p.C91C Substitution - coding silent 21:28986211-28986211 - RK071_C01 COSM1632440 c.4951C>A p.Q1651K Substitution - Missense 21:28932589-28932589 - PT42 COSM5926130 c.1153T>A p.F385I Substitution - Missense 21:28970574-28970574 - CSCC-7-T COSM4492721 c.3885C>T p.T1295T Substitution - coding silent 21:28944480-28944480 - TCGA-13-1497-01 COSM75321 c.287C>T p.T96I Substitution - Missense 21:28986197-28986197 - 3N02-VS-3T02 COSM4978512 c.1332A>C p.A444A Substitution - coding silent 21:28967159-28967159 - CSCC-10-T COSM4477701 c.2040C>T p.F680F Substitution - coding silent 21:28966451-28966451 - TCGA-34-5928-01 COSM725406 c.184G>C p.D62H Substitution - Missense 21:28986793-28986793 - HCC150T COSM3707994 c.1879A>T p.S627C Substitution - Missense 21:28966612-28966612 - C709 COSM4444027 c.3547G>T p.G1183* Substitution - Nonsense 21:28946228-28946228 - TCGA-G9-6371-01 COSM1130557 c.1523A>C p.D508A Substitution - Missense 21:28966968-28966968 - D4 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - PT14_1 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - HCT8 COSM4612565 c.331_332insT p.C111fs*6 Insertion - Frameshift 21:28986152-28986153 - HCC128 COSM1615944 c.2854A>G p.S952G Substitution - Missense 21:28957370-28957370 - HCC2998 COSM2841646 c.3421G>T p.E1141* Substitution - Nonsense 21:28947530-28947530 - TCGA-AX-A0J0-01 COSM1029743 c.1132A>C p.K378Q Substitution - Missense 21:28970595-28970595 - TCGA-29-1691-01 COSM1327451 c.884C>G p.S295C Substitution - Missense 21:28971371-28971371 - TCGA-BR-7707-01 COSM3405333 c.59G>A p.R20Q Substitution - Missense 21:28986918-28986918 - TCGA-CG-5723-01 COSM4100995 c.3341A>G p.E1114G Substitution - Missense 21:28952163-28952163 - SJACT02_D COSM4968626 c.665delA p.Y222fs*4 Deletion - Frameshift 21:28981264-28981264 - Pat_41_B COSM5858469 c.4903G>A p.V1635I Substitution - Missense 21:28932637-28932637 - HCC2998 COSM2841632 c.3927A>C p.E1309D Substitution - Missense 21:28944438-28944438 - BD232T COSM5501572 c.314A>G p.Y105C Substitution - Missense 21:28986170-28986170 - K-562 COSM1683231 c.595delA p.I199fs*1 Deletion - Frameshift 21:28982350-28982350 - TCGA-FW-A3R5-06 COSM3911989 c.4011C>T p.S1337S Substitution - coding silent 21:28943876-28943876 - AOCS-135-3-1 COSM4137207 c.1528G>C p.E510Q Substitution - Missense 21:28966963-28966963 - SNU-C2B COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - TCGA-CM-5861-01 COSM1413541 c.2581delA p.T861fs*11 Deletion - Frameshift 21:28959470-28959470 - AOCS-131-1-3 COSM4137204 c.5300G>A p.*1767* Substitution - coding silent 21:28930449-28930449 - RKO COSM2841669 c.1967delA p.N656fs*11 Deletion - Frameshift 21:28966524-28966524 - TCGA-06-0184 COSM2150484 c.577-1G>A p.? Unknown 21:28982369-28982369 - PD7219a COSM5775195 c.4437C>G p.L1479L Substitution - coding silent 21:28941265-28941265 - BN44T COSM1615946 c.1247T>C p.L416S Substitution - Missense 21:28969530-28969530 - TCGA-EE-A2GO-06 COSM3550037 c.3577A>G p.I1193V Substitution - Missense 21:28946198-28946198 - TCGA-AX-A05Z-01 COSM1029730 c.5071-1G>A p.? Unknown 21:28931323-28931323 - SNU-C4 COSM4612116 c.1606_1607delAA p.N536fs*2 Deletion - Frameshift 21:28966884-28966885 - TCGA-AM-5820-01 COSM3758819 c.1208T>C p.L403S Substitution - Missense 21:28969569-28969569 - LUAD-B02515 COSM336146 c.2871G>T p.M957I Substitution - Missense 21:28957353-28957353 - AOCS-135-8-X COSM4137207 c.1528G>C p.E510Q Substitution - Missense 21:28966963-28966963 - HCC043T COSM5811996 c.3478A>T p.S1160C Substitution - Missense 21:28947473-28947473 - T3225 COSM4699524 c.2337C>A p.S779S Substitution - coding silent 21:28960533-28960533 - Sample_1 COSM3758819 c.1208T>C p.L403S Substitution - Missense 21:28969569-28969569 - TCGA-BT-A3PK-01 COSM3799823 c.2473G>T p.D825Y Substitution - Missense 21:28959578-28959578 - TCGA-AA-A00N-01 COSM275942 c.3659T>C p.V1220A Substitution - Missense 21:28945916-28945916 - BN44 COSM1615946 c.1247T>C p.L416S Substitution - Missense 21:28969530-28969530 - 5_RESISTANT COSM1724954 c.2440G>T p.E814* Substitution - Nonsense 21:28959611-28959611 - TCGA-B0-5097-01 COSM478465 c.2198C>T p.T733I Substitution - Missense 21:28960672-28960672 - TCGA-EI-6917-01 COSM3423882 c.3335G>A p.R1112K Substitution - Missense 21:28952169-28952169 - ATL016 COSM5707541 c.1300G>A p.V434I Substitution - Missense 21:28969477-28969477 - TCGA-EE-A2MC-06 COSM3550045 c.399C>T p.I133I Substitution - coding silent 21:28984869-28984869 - B78 COSM1751592 c.1338C>G p.L446L Substitution - coding silent 21:28967153-28967153 - TCGA-BR-7851-01 COSM4101000 c.1329T>C p.D443D Substitution - coding silent 21:28967162-28967162 - C84 COSM4620107 c.1077A>G p.I359M Substitution - Missense 21:28970650-28970650 - TCGA-CA-6717-01 COSM1413540 c.3080-1G>T p.? Unknown 21:28953377-28953377 - CSCC-2-T COSM4518071 c.4996_4997GG>TT p.G1666L Substitution - Missense 21:28932543-28932544 - Region-24 COSM5749030 c.1596T>A p.S532R Substitution - Missense 21:28966895-28966895 - S00935 COSM314846 c.1036A>T p.T346S Substitution - Missense 21:28970691-28970691 - TCGA-A6-5657-01 COSM1413543 c.2462C>T p.S821F Substitution - Missense 21:28959589-28959589 - CPCG0042-F1 COSM3396393 c.3706T>G p.S1236A Substitution - Missense 21:28945869-28945869 - RK040_C01 COSM3701671 c.1770G>A p.L590L Substitution - coding silent 21:28966721-28966721 - AOCS-075-1-0 COSM4137206 c.1645A>G p.N549D Substitution - Missense 21:28966846-28966846 - ME037T COSM227949 c.1819G>A p.E607K Substitution - Missense 21:28966672-28966672 - TCGA-DB-A64V-01 COSM3972730 c.1173T>G p.A391A Substitution - coding silent 21:28970554-28970554 - 7T COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - LIM2551 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - TCGA-GF-A6C9-06 COSM4902610 c.3229T>G p.L1077V Substitution - Missense 21:28953227-28953227 - LIM2405 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - TCGA-32-2632-01 COSM3405333 c.59G>A p.R20Q Substitution - Missense 21:28986918-28986918 - BD57T COSM5057541 c.5123G>A p.R1708H Substitution - Missense 21:28931270-28931270 - PT37 COSM5921797 c.3641G>T p.S1214I Substitution - Missense 21:28945934-28945934 - sysucc-311T COSM5465042 c.4532A>G p.K1511R Substitution - Missense 21:28936648-28936648 - ESO-250 COSM1264357 c.395T>G p.L132R Substitution - Missense 21:28984873-28984873 - PT09_2 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - PT24_2 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - T97 COSM237138 c.4941A>G p.E1647E Substitution - coding silent 21:28932599-28932599 - SW1463 COSM2841685 c.1284G>T p.E428D Substitution - Missense 21:28969493-28969493 - HCC2998 COSM1681904 c.323G>T p.R108I Substitution - Missense 21:28986161-28986161 - TCGA-20-1686-01 COSM1327454 c.4956G>A p.L1652L Substitution - coding silent 21:28932584-28932584 - TCGA-13-2061-01 COSM1327453 c.4209T>C p.H1403H Substitution - coding silent 21:28943678-28943678 - LIM1215 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - TCGA-B5-A11R-01 COSM1029737 c.2976G>C p.K992N Substitution - Missense 21:28956865-28956865 - LUAD-B02515 COSM336145 c.3939A>T p.Q1313H Substitution - Missense 21:28944426-28944426 - ESCC-F3 COSM5047476 c.197G>T p.R66L Substitution - Missense 21:28986780-28986780 - TCGA-D8-A1XW-01 COSM1483892 c.2586T>G p.H862Q Substitution - Missense 21:28959465-28959465 - TCGA-EE-A2MJ-06 COSM3550043 c.1532C>T p.S511F Substitution - Missense 21:28966959-28966959 - HT115 COSM1681904 c.323G>T p.R108I Substitution - Missense 21:28986161-28986161 - GC8_T COSM149214 c.2438C>T p.A813V Substitution - Missense 21:28959613-28959613 - TCGA-BC-A3KF-01 COSM4927805 c.2847G>A p.P949P Substitution - coding silent 21:28957377-28957377 - 587220 COSM1223920 c.1608T>G p.N536K Substitution - Missense 21:28966883-28966883 - S01297 COSM5667629 c.925G>T p.D309Y Substitution - Missense 21:28971330-28971330 - ESCC-205T COSM3939473 c.618C>G p.L206L Substitution - coding silent 21:28982327-28982327 - CSCC-27-T COSM4456160 c.3448_3449CT>TA p.L1150Y Substitution - Missense 21:28947502-28947503 - C086 COSM5534109 c.2686C>T p.L896L Substitution - coding silent 21:28958447-28958447 - CRC-06T COSM5456850 c.984+5G>A p.? Unknown 21:28971266-28971266 - 9227_T COSM5042473 c.2822G>A p.G941E Substitution - Missense 21:28957402-28957402 - TCGA-EE-A3J7-06 COSM3911990 c.365G>A p.R122Q Substitution - Missense 21:28984903-28984903 - PCSI_0280_Pa_P_526 COSM4807647 c.331T>A p.C111S Substitution - Missense 21:28986153-28986153 - AOCS-149-1-7 COSM4137205 c.3735C>T p.D1245D Substitution - coding silent 21:28945840-28945840 - RK041_C01 COSM1632441 c.4888G>A p.A1630T Substitution - Missense 21:28932652-28932652 - TCGA-EI-6917-01 COSM3423885 c.771G>T p.Q257H Substitution - Missense 21:28981158-28981158 - PT21_2 COSM5902159 c.2626C>T p.L876F Substitution - Missense 21:28958507-28958507 - PD24221a COSM5787398 c.1547C>A p.S516Y Substitution - Missense 21:28966944-28966944 - CSCC-55-T COSM4489802 c.3395C>T p.P1132L Substitution - Missense 21:28947556-28947556 - CSCC-49-T COSM1713876 c.4571C>T p.P1524L Substitution - Missense 21:28936609-28936609 - HCC092T COSM5806517 c.1312-3C>G p.? Unknown 21:28967182-28967182 - TCGA-B0-4844-01 COSM3363406 c.2576A>C p.E859A Substitution - Missense 21:28959475-28959475 - ESO-122 COSM1264356 c.1074C>T p.V358V Substitution - coding silent 21:28970653-28970653 - LUAD-CHTN-3090346 COSM356958 c.3171G>A p.M1057I Substitution - Missense 21:28953285-28953285 - 47T COSM3713379 c.4686C>T p.H1562H Substitution - coding silent 21:28935298-28935298 - TCGA-EE-A2MI-06 COSM3550033 c.4970C>T p.P1657L Substitution - Missense 21:28932570-28932570 - S02292 COSM5687870 c.2847G>T p.P949P Substitution - coding silent 21:28957377-28957377 - TCGA-61-1900-01 COSM1327452 c.2500G>A p.A834T Substitution - Missense 21:28959551-28959551 - 268T COSM1727270 c.630-1G>C p.? Unknown 21:28981300-28981300 - TCGA-AC-A23H-01 COSM3841689 c.12G>A p.K4K Substitution - coding silent 21:28992794-28992794 - TCGA-F1-6874-01 COSM4100999 c.1498G>A p.A500T Substitution - Missense 21:28966993-28966993 - ACINAR28 COSM1734157 c.2100delA p.V701fs*5 Deletion - Frameshift 21:28966391-28966391 - 193 COSM1741736 c.4321C>T p.L1441F Substitution - Missense 21:28941381-28941381 - TCGA-GU-A42R-01 COSM3799822 c.4698A>G p.S1566S Substitution - coding silent 21:28935286-28935286 - TCGA-85-6561-01 COSM725409 c.4897C>A p.R1633R Substitution - coding silent 21:28932643-28932643 - TCGA-AP-A059-01 COSM1029748 c.196C>T p.R66* Substitution - Nonsense 21:28986781-28986781 - T1844 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - CHC892T COSM4797795 c.421G>A p.A141T Substitution - Missense 21:28984847-28984847 - YUKLAB COSM1713877 c.1420G>A p.E474K Substitution - Missense 21:28967071-28967071 - CCK81 COSM111380 c.1607delA p.N536fs*33 Deletion - Frameshift 21:28966884-28966884 - ESCC_BICR_041T COSM5441326 c.2722C>T p.Q908* Substitution - Nonsense 21:28958411-28958411 - QC2-32-T2 COSM3758819 c.1208T>C p.L403S Substitution - Missense 21:28969569-28969569 - TCGA-37-4135-01 COSM725408 c.580C>T p.L194L Substitution - coding silent 21:28982365-28982365 - TCGA-OL-A5RW-01 COSM3841687 c.2208C>G p.L736L Substitution - coding silent 21:28960662-28960662 - CHC1041T COSM3668511 c.1131A>G p.P377P Substitution - coding silent 21:28970596-28970596 - TCGA-AP-A059-01 COSM1029749 c.90A>T p.G30G Substitution - coding silent 21:28986887-28986887 - TCGA-AU-6004-01 COSM1413544 c.609T>C p.P203P Substitution - coding silent 21:28982336-28982336 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.288773 21q22.11 613083

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.H908Q c.2724T>G 21 30331787 BRCA A C Missense p.L178R c.533T>G 21 30357194 ESCA - A Frameshift p.S511Kfs*13 c.1529dupT 21 30339422 RCCC A G Missense p.I1690T c.5069T>C 21 30304931 CM A G Synonymous p.N1104N c.3312T>C 21 30325604 UCEC A T Missense p.D1471E c.4413T>A 21 30315604 UCEC C A Missense p.A320S c.958G>T 21 30343757 LUAD C A Missense p.D1416Y c.4246G>T 21 30316101 SCLC C A Missense p.D1516Y c.4546G>T 21 30313616 COREAD C A Missense p.D871Y c.2611G>T 21 30331900 BLCA C A Missense p.G1757V c.5270G>T 21 30303583 LUAD C A Missense p.G9W c.25G>T 21 30365240 CLL C A Missense p.L628F c.1884G>T 21 30339067 MB C A Missense p.R31L c.92G>T 21 30365173 BLCA C A Missense p.W513L c.1538G>T 21 30339413 STAD C A SpliceAcceptorSNV . c.5014-1G>T 21 30304987 LUAD CC TT Missense p.G12K c.34_35delinsAA 21 30365230 CM C G Missense p.D108H c.322G>C 21 30359114 LUSC C G Missense p.E607Q c.1819G>C 21 30339132 BLCA C G Missense p.K1038N c.3114G>C 21 30329187 UCEC C G Missense p.Q201H c.603G>C 21 30357124 STAD C T Missense p.A1057T c.3169G>A 21 30329132 NB C T Missense p.A1327T c.3979G>A 21 30316846 BRCA C T Missense p.A1676T c.5026G>A 21 30304974 HC C T Missense p.A546T c.1636G>A 21 30339315 STAD C T Missense p.D1150N c.3448G>A 21 30324516 OV C T Missense p.D164N c.490G>A 21 30357237 HNSC C T Missense p.D785N c.2353G>A 21 30332977 CM C T Missense p.E653K c.1957G>A 21 30338994 CM C T Missense p.G12E c.35G>A 21 30365230 CM C T Missense p.G1360D c.4079G>A 21 30316746 STAD C T Missense p.M1053I c.3159G>A 21 30329142 CM C T Missense p.R168Q c.503G>A 21 30357224 CM C T Missense p.R66Q c.197G>A 21 30359239 GBM C T Missense p.S998N c.2993G>A 21 30329691 STAD C T SpliceAcceptorSNV . c.715-1G>A 21 30354691 GBM C T Synonymous p.A880A c.2640G>A 21 30331871 ESCA C T Synonymous p.Q501Q c.1503G>A 21 30339448 LUAD G A 3-UTRSNV . c.5436+13C>T 21 30302760 CM G A Missense p.H1362Y c.4084C>T 21 30316741 CM G A Missense p.P1703L c.5108C>T 21 30304892 CM G A Missense p.P703S c.2107C>T 21 30338844 CM G A Missense p.S1358F c.4073C>T 21 30316752 CM G A Missense p.S1766L c.5297C>T 21 30303556 HNSC G A Missense p.S1774F c.5321C>T 21 30303532 CM G A Missense p.S19F c.56C>T 21 30365209 CM G A Missense p.S557F c.1670C>T 21 30339281 CM G A Missense p.T142I c.425C>T 21 30358518 OV G A Synonymous p.D254D c.762C>T 21 30354643 CM G A Synonymous p.F1252F c.3756C>T 21 30318479 ALL G A Synonymous p.F1252F c.3756C>T 21 30318479 HNSC G A Synonymous p.I179I c.537C>T 21 30357190 CM G A Synonymous p.L240L c.718C>T 21 30354687 LUSC G A Synonymous p.L564L c.1690C>T 21 30339261 CM G A Synonymous p.N996N c.2988C>T 21 30329696 MB G A Synonymous p.S512S c.1536C>T 21 30339415 CM G A Synonymous p.V404V c.1212C>T 21 30342975 ESCA G C Missense p.H1561D c.4681C>G 21 30308959 LUAD G C Missense p.L631V c.1891C>G 21 30339060 HNSC G C Missense p.Q98E c.292C>G 21 30359144 HNSC G C Nonsense p.Y1452* c.4356C>G 21 30315991 HNSC GG AA Missense p.P1476L c.4426_4427delinsTT 21 30315590 CM G T Missense p.A212E c.635C>A 21 30357092 LUSC G T Missense p.H1788N c.5362C>A 21 30303491 OV G T Missense p.P1580Q c.4739C>A 21 30308901 CM G T Missense p.P1607Q c.4820C>A 21 30307624 STAD G T Missense p.Q498K c.1492C>A 21 30339459 HNSC G T Nonsense p.Y268* c.804C>A 21 30353585 CM G T Synonymous p.G1669G c.5007C>A 21 30307437 HNSC G T Synonymous p.R1679R c.5035C>A 21 30304965 LUSC G T Synonymous p.R1723R c.5167C>A 21 30304833 LUSC T A Missense p.I1072L c.3214A>T 21 30329087 LUAD T A Missense p.N793I c.2378A>T 21 30332952 COREAD T A Missense p.T392S c.1174A>T 21 30343013 SCLC T A Synonymous p.L1176L c.3528A>T 21 30319883 LUAD T C Missense p.I1239V c.3715A>G 21 30318520 CM T C Missense p.I543V c.1627A>G 21 30339324 NB T C Missense p.K1418R c.4253A>G 21 30316094 BLCA T C Missense p.T204A c.610A>G 21 30357117 UCEC T C Synonymous p.T1797T c.5391A>G 21 30302818 LUSC T - Frameshift p.N582Mfs*33 c.1745delA 21 30339206 OV T - Frameshift p.N582Mfs*33 c.1745delA 21 30339206 PRAD T - Frameshift p.N582Mfs*33 c.1745delA 21 30339206 THCA T G Missense p.D554A c.1661A>C 21 30339290 PRAD T G Missense p.E599D c.1797A>C 21 30339154 UCEC T G Missense p.E905A c.2714A>C 21 30331797 RCCC T G Missense p.K8N c.24A>C 21 30365241 CM