Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 6 43020160 43020160 + Missense_Mutation SNP G G A TCGA-OR-A5K5-01A-11D-A29I-10 TCGA-OR-A5K5-10A-01D-A29L-10 g.chr6:43020160G>A c.367C>T c.(367-369)Cgg>Tgg p.R123W BLCA 6 43006171 43006171 + Missense_Mutation SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr6:43006171G>A c.4607C>T c.(4606-4608)tCg>tTg p.S1536L BLCA 6 43006203 43006203 + Silent SNP G G C TCGA-4Z-AA7W-01A-11D-A391-08 TCGA-4Z-AA7W-10A-01D-A394-08 g.chr6:43006203G>C c.4575C>G c.(4573-4575)ctC>ctG p.L1525L BLCA 6 43006375 43006375 + Missense_Mutation SNP T T C TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr6:43006375T>C c.4496A>G c.(4495-4497)aAt>aGt p.N1499S BLCA 6 43008026 43008026 + Missense_Mutation SNP C C T TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr6:43008026C>T c.4162G>A c.(4162-4164)Gaa>Aaa p.E1388K BLCA 6 43008110 43008110 + Missense_Mutation SNP C C T TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr6:43008110C>T c.4078G>A c.(4078-4080)Ggg>Agg p.G1360R BLCA 6 43008116 43008116 + Missense_Mutation SNP C C T TCGA-4Z-AA7W-01A-11D-A391-08 TCGA-4Z-AA7W-10A-01D-A394-08 g.chr6:43008116C>T c.4072G>A c.(4072-4074)Gaa>Aaa p.E1358K BLCA 6 43008119 43008119 + Missense_Mutation SNP C C G TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr6:43008119C>G c.4069G>C c.(4069-4071)Gag>Cag p.E1357Q BLCA 6 43008354 43008354 + Missense_Mutation SNP C C G TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr6:43008354C>G c.3937G>C c.(3937-3939)Gag>Cag p.E1313Q BLCA 6 43008415 43008415 + Silent SNP G G A TCGA-YC-A8S6-01A-31D-A38G-08 TCGA-YC-A8S6-10A-01D-A38J-08 g.chr6:43008415G>A c.3876C>T c.(3874-3876)atC>atT p.I1292I BLCA 6 43011253 43011253 + Silent SNP G G A TCGA-GV-A3QH-01A-11D-A21Z-08 TCGA-GV-A3QH-10A-01D-A21Z-08 g.chr6:43011253G>A c.3288C>T c.(3286-3288)ctC>ctT p.L1096L BLCA 6 43012542 43012542 + Missense_Mutation SNP C C G TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr6:43012542C>G c.3120G>C c.(3118-3120)aaG>aaC p.K1040N BLCA 6 43012596 43012596 + Silent SNP C C T TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr6:43012596C>T c.3066G>A c.(3064-3066)caG>caA p.Q1022Q BLCA 6 43012601 43012601 + Nonsense_Mutation SNP C C A TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr6:43012601C>A c.3061G>T c.(3061-3063)Gag>Tag p.E1021* BLCA 6 43012990 43012990 + Missense_Mutation SNP T T C TCGA-FT-A61P-01A-11D-A30E-08 TCGA-FT-A61P-10A-01D-A30H-08 g.chr6:43012990T>C c.3013A>G c.(3013-3015)Agg>Ggg p.R1005G BLCA 6 43013765 43013765 + Missense_Mutation SNP C C A TCGA-DK-AA6R-01A-11D-A42E-08 TCGA-DK-AA6R-10A-01D-A42H-08 g.chr6:43013765C>A c.2725G>T c.(2725-2727)Ggg>Tgg p.G909W BLCA 6 43014672 43014672 + Missense_Mutation SNP C C G TCGA-UY-A78N-01A-12D-A339-08 TCGA-UY-A78N-10A-01D-A339-08 g.chr6:43014672C>G c.2343G>C c.(2341-2343)aaG>aaC p.K781N BLCA 6 43014801 43014801 + Silent SNP C C T TCGA-UY-A78L-01A-12D-A339-08 TCGA-UY-A78L-10A-01D-A339-08 g.chr6:43014801C>T c.2214G>A c.(2212-2214)gtG>gtA p.V738V BLCA 6 43017748 43017748 + Missense_Mutation SNP C C A TCGA-FT-A61P-01A-11D-A30E-08 TCGA-FT-A61P-10A-01D-A30H-08 g.chr6:43017748C>A c.1522G>T c.(1522-1524)Gac>Tac p.D508Y BLCA 6 43019173 43019173 + Missense_Mutation SNP G G A TCGA-CF-A9FM-01A-11D-A38G-08 TCGA-CF-A9FM-10A-01D-A38J-08 g.chr6:43019173G>A c.766C>T c.(766-768)Cgg>Tgg p.R256W BLCA 6 43019388 43019388 + Missense_Mutation SNP C C T TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr6:43019388C>T c.694G>A c.(694-696)Gaa>Aaa p.E232K BLCA 6 43020305 43020305 + Silent SNP G G T TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr6:43020305G>T c.222C>A c.(220-222)atC>atA p.I74I BRCA 6 43005481 43005481 + Missense_Mutation SNP C C T TCGA-AN-A0FZ-01A-11W-A050-09 TCGA-AN-A0FZ-10A-01W-A055-09 g.chr6:43005481C>T c.5042G>A c.(5041-5043)cGg>cAg p.R1681Q BRCA 6 43005599 43005599 + Nonsense_Mutation SNP G G A TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr6:43005599G>A c.4924C>T c.(4924-4926)Cag>Tag p.Q1642* BRCA 6 43010724 43010724 + Splice_Site SNP T T G TCGA-BH-A0DZ-01A-11W-A019-09 TCGA-BH-A0DZ-10A-01W-A021-09 g.chr6:43010724T>G c.e19-2 BRCA 6 43010839 43010839 + Silent SNP G G T TCGA-A2-A3XY-01A-11D-A23C-09 TCGA-A2-A3XY-10A-01D-A23C-09 g.chr6:43010839G>T c.3435C>A c.(3433-3435)cgC>cgA p.R1145R BRCA 6 43013069 43013069 + Silent SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr6:43013069C>T c.2934G>A c.(2932-2934)cgG>cgA p.R978R BRCA 6 43013138 43013138 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr6:43013138A>C c.2865T>G c.(2863-2865)ggT>ggG p.G955G BRCA 6 43014812 43014812 + Frame_Shift_Del DEL G G - TCGA-E2-A15O-01A-11D-A10Y-09 TCGA-E2-A15O-10A-01D-A110-09 g.chr6:43014812delG c.2203delC c.(2203-2205)ctgfs p.L735fs BRCA 6 43016263 43016263 + Missense_Mutation SNP G G T TCGA-A8-A076-01A-21W-A019-09 TCGA-A8-A076-10A-01W-A021-09 g.chr6:43016263G>T c.1870C>A c.(1870-1872)Ctg>Atg p.L624M BRCA 6 43016268 43016268 + Missense_Mutation SNP T T A TCGA-BH-A0BW-01A-11D-A10Y-09 TCGA-BH-A0BW-10A-01D-A110-09 g.chr6:43016268T>A c.1865A>T c.(1864-1866)cAg>cTg p.Q622L BRCA 6 43017144 43017144 + Splice_Site SNP C C T TCGA-E2-A158-01A-11D-A12B-09 TCGA-E2-A158-11A-22D-A12B-09 g.chr6:43017144C>T c.e7+1 BRCA 6 43017793 43017793 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr6:43017793C>G c.1477G>C c.(1477-1479)Gag>Cag p.E493Q BRCA 6 43018789 43018789 + Missense_Mutation SNP G G A TCGA-A1-A0SF-01A-11D-A142-09 TCGA-A1-A0SF-10B-01D-A142-09 g.chr6:43018789G>A c.1150C>T c.(1150-1152)Cgg>Tgg p.R384W BRCA 6 43018852 43018852 + Missense_Mutation SNP A A G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr6:43018852A>G c.1087T>C c.(1087-1089)Ttc>Ctc p.F363L BRCA 6 43019030 43019030 + Silent SNP C C G TCGA-E9-A295-01A-11D-A16D-09 TCGA-E9-A295-10A-01D-A16D-09 g.chr6:43019030C>G c.909G>C c.(907-909)ctG>ctC p.L303L CESC 6 43005484 43005484 + Missense_Mutation SNP G G A TCGA-LP-A5U2-01A-11D-A28B-09 TCGA-LP-A5U2-10A-01D-A28E-09 g.chr6:43005484G>A c.5039C>T c.(5038-5040)tCc>tTc p.S1680F CESC 6 43005529 43005529 + Nonsense_Mutation SNP G G C TCGA-LP-A5U2-01A-11D-A28B-09 TCGA-LP-A5U2-10A-01D-A28E-09 g.chr6:43005529G>C c.4994C>G c.(4993-4995)tCa>tGa p.S1665* CESC 6 43006110 43006110 + Silent SNP G G A TCGA-C5-A7CO-01A-11D-A351-09 TCGA-C5-A7CO-10A-01D-A351-09 g.chr6:43006110G>A c.4668C>T c.(4666-4668)gaC>gaT p.D1556D CESC 6 43010606 43010606 + Missense_Mutation SNP G G T TCGA-DS-A5RQ-01A-11D-A28B-09 TCGA-DS-A5RQ-10A-01D-A28E-09 g.chr6:43010606G>T c.3579C>A c.(3577-3579)ttC>ttA p.F1193L CESC 6 43017742 43017742 + Missense_Mutation SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr6:43017742G>C c.1528C>G c.(1528-1530)Cag>Gag p.Q510E CESC 6 43017776 43017776 + Silent SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr6:43017776G>C c.1494C>G c.(1492-1494)ctC>ctG p.L498L CESC 6 43018878 43018878 + Nonsense_Mutation SNP G G T TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr6:43018878G>T c.1061C>A c.(1060-1062)tCa>tAa p.S354* CESC 6 43020151 43020151 + Missense_Mutation SNP C C T TCGA-JW-A5VJ-01A-11D-A28B-09 TCGA-JW-A5VJ-10A-01D-A28E-09 g.chr6:43020151C>T c.376G>A c.(376-378)Gag>Aag p.E126K CHOL 6 43007936 43007936 + Missense_Mutation SNP G G T TCGA-ZH-A8Y6-01A-11D-A417-09 TCGA-ZH-A8Y6-10A-01D-A41A-09 g.chr6:43007936G>T c.4252C>A c.(4252-4254)Ctg>Atg p.L1418M COAD 6 43005625 43005625 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr6:43005625G>A c.4898C>T c.(4897-4899)aCg>aTg p.T1633M COAD 6 43006088 43006088 + Missense_Mutation SNP G G A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr6:43006088G>A c.4690C>T c.(4690-4692)Cgg>Tgg p.R1564W COAD 6 43008690 43008690 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:43008690C>T c.3769G>A c.(3769-3771)Ggc>Agc p.G1257S COAD 6 43008716 43008716 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:43008716C>T c.3743G>A c.(3742-3744)tGc>tAc p.C1248Y COAD 6 43010677 43010677 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr6:43010677G>A c.3508C>T c.(3508-3510)Cca>Tca p.P1170S COAD 6 43011213 43011213 + Missense_Mutation SNP G G T TCGA-AA-3542-01A-02W-0831-10 TCGA-AA-3542-10A-01W-0831-10 g.chr6:43011213G>T c.3328C>A c.(3328-3330)Cct>Act p.P1110T COAD 6 43013021 43013021 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr6:43013021C>A c.2982G>T c.(2980-2982)caG>caT p.Q994H COAD 6 43013046 43013046 + Missense_Mutation SNP C C T TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr6:43013046C>T c.2957G>A c.(2956-2958)cGc>cAc p.R986H COAD 6 43013766 43013766 + Silent SNP G G A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr6:43013766G>A c.2724C>T c.(2722-2724)tgC>tgT p.C908C COAD 6 43014076 43014076 + Missense_Mutation SNP G G T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr6:43014076G>T c.2558C>A c.(2557-2559)gCc>gAc p.A853D COAD 6 43015993 43015993 + Splice_Site SNP T T C TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr6:43015993T>C c.e9-2 COAD 6 43016127 43016127 + Missense_Mutation SNP A A G TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr6:43016127A>G c.2006T>C c.(2005-2007)cTg>cCg p.L669P COAD 6 43017366 43017366 + Missense_Mutation SNP A A G TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr6:43017366A>G c.1604T>C c.(1603-1605)gTg>gCg p.V535A COAD 6 43018059 43018059 + Silent SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr6:43018059A>G c.1311T>C c.(1309-1311)atT>atC p.I437I COAD 6 43018766 43018768 + In_Frame_Del DEL CTC CTC - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr6:43018766_43018768delCTC c.1171_1173delGAG c.(1171-1173)gagdel p.E391del COAD 6 43018836 43018836 + Missense_Mutation SNP G G A TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr6:43018836G>A c.1103C>T c.(1102-1104)aCc>aTc p.T368I COAD 6 43020163 43020163 + Missense_Mutation SNP G G T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr6:43020163G>T c.364C>A c.(364-366)Ctt>Att p.L122I COADREAD 6 43005625 43005625 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr6:43005625G>A c.4898C>T c.(4897-4899)aCg>aTg p.T1633M COADREAD 6 43006088 43006088 + Missense_Mutation SNP G G A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr6:43006088G>A c.4690C>T c.(4690-4692)Cgg>Tgg p.R1564W COADREAD 6 43008690 43008690 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:43008690C>T c.3769G>A c.(3769-3771)Ggc>Agc p.G1257S COADREAD 6 43008716 43008716 + Missense_Mutation SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:43008716C>T c.3743G>A c.(3742-3744)tGc>tAc p.C1248Y COADREAD 6 43010598 43010598 + Missense_Mutation SNP G G A TCGA-AG-3583-01A-01W-0831-10 TCGA-AG-3583-10A-01W-0831-10 g.chr6:43010598G>A c.3587C>T c.(3586-3588)gCg>gTg p.A1196V COADREAD 6 43010677 43010677 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr6:43010677G>A c.3508C>T c.(3508-3510)Cca>Tca p.P1170S COADREAD 6 43011213 43011213 + Missense_Mutation SNP G G T TCGA-AA-3542-01A-02W-0831-10 TCGA-AA-3542-10A-01W-0831-10 g.chr6:43011213G>T c.3328C>A c.(3328-3330)Cct>Act p.P1110T COADREAD 6 43013021 43013021 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr6:43013021C>A c.2982G>T c.(2980-2982)caG>caT p.Q994H COADREAD 6 43013046 43013046 + Missense_Mutation SNP C C T TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr6:43013046C>T c.2957G>A c.(2956-2958)cGc>cAc p.R986H COADREAD 6 43013368 43013368 + Missense_Mutation SNP C C T TCGA-AG-3909-01A-01W-1073-09 TCGA-AG-3909-10A-01W-1073-09 g.chr6:43013368C>T c.2819G>A c.(2818-2820)cGc>cAc p.R940H COADREAD 6 43013766 43013766 + Silent SNP G G A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr6:43013766G>A c.2724C>T c.(2722-2724)tgC>tgT p.C908C COADREAD 6 43014076 43014076 + Missense_Mutation SNP G G T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr6:43014076G>T c.2558C>A c.(2557-2559)gCc>gAc p.A853D COADREAD 6 43015993 43015993 + Splice_Site SNP T T C TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr6:43015993T>C c.e9-2 COADREAD 6 43016127 43016127 + Missense_Mutation SNP A A G TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr6:43016127A>G c.2006T>C c.(2005-2007)cTg>cCg p.L669P COADREAD 6 43017366 43017366 + Missense_Mutation SNP A A G TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr6:43017366A>G c.1604T>C c.(1603-1605)gTg>gCg p.V535A COADREAD 6 43018059 43018059 + Silent SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr6:43018059A>G c.1311T>C c.(1309-1311)atT>atC p.I437I COADREAD 6 43018766 43018768 + In_Frame_Del DEL CTC CTC - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr6:43018766_43018768delCTC c.1171_1173delGAG c.(1171-1173)gagdel p.E391del COADREAD 6 43018836 43018836 + Missense_Mutation SNP G G A TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr6:43018836G>A c.1103C>T c.(1102-1104)aCc>aTc p.T368I COADREAD 6 43020163 43020163 + Missense_Mutation SNP G G T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr6:43020163G>T c.364C>A c.(364-366)Ctt>Att p.L122I DLBC 6 43006687 43006687 + Nonsense_Mutation SNP G G A TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr6:43006687G>A c.4333C>T c.(4333-4335)Cga>Tga p.R1445* DLBC 6 43007981 43007981 + Missense_Mutation SNP A A G TCGA-FF-8047-01A-11D-2210-10 TCGA-FF-8047-10A-01D-2210-10 g.chr6:43007981A>G c.4207T>C c.(4207-4209)Tca>Cca p.S1403P ESCA 6 43005594 43005594 + Silent SNP C C T TCGA-L5-A88W-01A-11D-A351-09 TCGA-L5-A88W-11A-11D-A351-09 g.chr6:43005594C>T c.4929G>A c.(4927-4929)gtG>gtA p.V1643V ESCA 6 43005697 43005697 + Missense_Mutation SNP C C T TCGA-LN-A49U-01A-31D-A27G-09 TCGA-LN-A49U-10A-01D-A27G-09 g.chr6:43005697C>T c.4826G>A c.(4825-4827)aGc>aAc p.S1609N ESCA 6 43010843 43010843 + Missense_Mutation SNP G G A TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr6:43010843G>A c.3431C>T c.(3430-3432)aCg>aTg p.T1144M ESCA 6 43013045 43013045 + Silent SNP G G T TCGA-L5-A88T-01A-11D-A351-09 TCGA-L5-A88T-11A-11D-A351-09 g.chr6:43013045G>T c.2958C>A c.(2956-2958)cgC>cgA p.R986R ESCA 6 43014654 43014654 + Silent SNP G G A TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr6:43014654G>A c.2361C>T c.(2359-2361)cgC>cgT p.R787R ESCA 6 43016152 43016152 + Silent SNP G G T TCGA-JY-A6FD-01A-11D-A33E-09 TCGA-JY-A6FD-10A-01D-A33H-09 g.chr6:43016152G>T c.1981C>A c.(1981-1983)Cgg>Agg p.R661R ESCA 6 43016265 43016265 + Missense_Mutation SNP C C T TCGA-LN-A9FR-01A-11D-A387-09 TCGA-LN-A9FR-10A-01D-A38A-09 g.chr6:43016265C>T c.1868G>A c.(1867-1869)cGt>cAt p.R623H GBMLGG 6 43006088 43006088 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:43006088G>A c.4690C>T c.(4690-4692)Cgg>Tgg p.R1564W GBMLGG 6 43010826 43010826 + Missense_Mutation SNP C C T TCGA-DU-5874-01A-11D-1705-08 TCGA-DU-5874-10A-01D-1705-08 g.chr6:43010826C>T c.3448G>A c.(3448-3450)Gtg>Atg p.V1150M GBMLGG 6 43010902 43010902 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:43010902G>A c.3372C>T c.(3370-3372)agC>agT p.S1124S GBMLGG 6 43011309 43011309 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:43011309C>T c.3232G>A c.(3232-3234)Gct>Act p.A1078T HNSC 6 43006181 43006181 + Missense_Mutation SNP C C T TCGA-CX-7085-01A-21D-2012-08 TCGA-CX-7085-10A-01D-2013-08 g.chr6:43006181C>T c.4597G>A c.(4597-4599)Gaa>Aaa p.E1533K HNSC 6 43006186 43006186 + Missense_Mutation SNP C C T TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr6:43006186C>T c.4592G>A c.(4591-4593)aGc>aAc p.S1531N HNSC 6 43006377 43006377 + Silent SNP G G C TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chr6:43006377G>C c.4494C>G c.(4492-4494)ctC>ctG p.L1498L HNSC 6 43006428 43006428 + Silent SNP C C T TCGA-CN-5374-01A-01D-1434-08 TCGA-CN-5374-10A-01D-1434-08 g.chr6:43006428C>T c.4443G>A c.(4441-4443)gcG>gcA p.A1481A HNSC 6 43007895 43007895 + Splice_Site SNP C C G TCGA-CR-7365-01A-11D-2012-08 TCGA-CR-7365-10A-01D-2013-08 g.chr6:43007895C>G c.4293G>C c.(4291-4293)aaG>aaC p.K1431N HNSC 6 43008291 43008291 + Missense_Mutation SNP C C T TCGA-CR-7365-01A-11D-2012-08 TCGA-CR-7365-10A-01D-2013-08 g.chr6:43008291C>T c.4000G>A c.(4000-4002)Gag>Aag p.E1334K HNSC 6 43011260 43011260 + Missense_Mutation SNP C C T TCGA-BA-A6DL-01A-21D-A30E-08 TCGA-BA-A6DL-10A-01D-A30H-08 g.chr6:43011260C>T c.3281G>A c.(3280-3282)cGc>cAc p.R1094H HNSC 6 43013126 43013126 + Silent SNP C C G TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr6:43013126C>G c.2877G>C c.(2875-2877)acG>acC p.T959T HNSC 6 43014265 43014265 + Silent SNP G G C TCGA-CV-A45Q-01A-11D-A24D-08 TCGA-CV-A45Q-10A-01D-A24F-08 g.chr6:43014265G>C c.2472C>G c.(2470-2472)ctC>ctG p.L824L HNSC 6 43015985 43015985 + Silent SNP C C T TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr6:43015985C>T c.2070G>A c.(2068-2070)ctG>ctA p.L690L HNSC 6 43017324 43017324 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr6:43017324T>C c.1646A>G c.(1645-1647)cAg>cGg p.Q549R HNSC 6 43018713 43018713 + Missense_Mutation SNP G G A TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr6:43018713G>A c.1226C>T c.(1225-1227)cCt>cTt p.P409L HNSC 6 43020081 43020081 + Missense_Mutation SNP C C T TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chr6:43020081C>T c.446G>A c.(445-447)aGc>aAc p.S149N KICH 6 43020113 43020113 + Silent SNP A A G TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr6:43020113A>G c.414T>C c.(412-414)ctT>ctC p.L138L KIPAN 6 43013037 43013037 + Missense_Mutation SNP T T C TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr6:43013037T>C c.2966A>G c.(2965-2967)tAc>tGc p.Y989C KIPAN 6 43017376 43017376 + Missense_Mutation SNP C C T TCGA-B0-5713-01A-11D-1669-08 TCGA-B0-5713-11A-01D-1669-08 g.chr6:43017376C>T c.1594G>A c.(1594-1596)Gaa>Aaa p.E532K KIPAN 6 43018715 43018715 + Silent SNP A A G TCGA-BP-4965-01A-01D-1462-08 TCGA-BP-4965-11A-01D-1462-08 g.chr6:43018715A>G c.1224T>C c.(1222-1224)ccT>ccC p.P408P KIPAN 6 43019452 43019452 + Missense_Mutation SNP C C G TCGA-B0-5691-01A-11D-1534-10 TCGA-B0-5691-11A-01D-1534-10 g.chr6:43019452C>G c.630G>C c.(628-630)gaG>gaC p.E210D KIPAN 6 43020004 43020004 + Missense_Mutation SNP A A C TCGA-CW-5580-01A-01D-1669-08 TCGA-CW-5580-11A-02D-1669-08 g.chr6:43020004A>C c.523T>G c.(523-525)Tat>Gat p.Y175D KIPAN 6 43020113 43020113 + Silent SNP A A G TCGA-KL-8343-01A-11D-2310-10 TCGA-KL-8343-11A-01D-2310-10 g.chr6:43020113A>G c.414T>C c.(412-414)ctT>ctC p.L138L KIPAN 6 43020188 43020188 + Missense_Mutation SNP G G C TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr6:43020188G>C c.339C>G c.(337-339)gaC>gaG p.D113E KIRC 6 43013037 43013037 + Missense_Mutation SNP T T C TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr6:43013037T>C c.2966A>G c.(2965-2967)tAc>tGc p.Y989C KIRC 6 43017376 43017376 + Missense_Mutation SNP C C T TCGA-B0-5713-01A-11D-1669-08 TCGA-B0-5713-11A-01D-1669-08 g.chr6:43017376C>T c.1594G>A c.(1594-1596)Gaa>Aaa p.E532K KIRC 6 43018715 43018715 + Silent SNP A A G TCGA-BP-4965-01A-01D-1462-08 TCGA-BP-4965-11A-01D-1462-08 g.chr6:43018715A>G c.1224T>C c.(1222-1224)ccT>ccC p.P408P KIRC 6 43019452 43019452 + Missense_Mutation SNP C C G TCGA-B0-5691-01A-11D-1534-10 TCGA-B0-5691-11A-01D-1534-10 g.chr6:43019452C>G c.630G>C c.(628-630)gaG>gaC p.E210D KIRC 6 43020004 43020004 + Missense_Mutation SNP A A C TCGA-CW-5580-01A-01D-1669-08 TCGA-CW-5580-11A-02D-1669-08 g.chr6:43020004A>C c.523T>G c.(523-525)Tat>Gat p.Y175D KIRP 6 43020188 43020188 + Missense_Mutation SNP G G C TCGA-2Z-A9JD-01A-11D-A42J-10 TCGA-2Z-A9JD-10A-01D-A42M-10 g.chr6:43020188G>C c.339C>G c.(337-339)gaC>gaG p.D113E LGG 6 43006088 43006088 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:43006088G>A c.4690C>T c.(4690-4692)Cgg>Tgg p.R1564W LGG 6 43010826 43010826 + Missense_Mutation SNP C C T TCGA-DU-5874-01A-11D-1705-08 TCGA-DU-5874-10A-01D-1705-08 g.chr6:43010826C>T c.3448G>A c.(3448-3450)Gtg>Atg p.V1150M LGG 6 43010902 43010902 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:43010902G>A c.3372C>T c.(3370-3372)agC>agT p.S1124S LGG 6 43011309 43011309 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr6:43011309C>T c.3232G>A c.(3232-3234)Gct>Act p.A1078T LIHC 6 43010877 43010877 + Silent SNP G G T TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr6:43010877G>T c.3397C>A c.(3397-3399)Cgg>Agg p.R1133R LIHC 6 43012996 43012996 + Missense_Mutation SNP C C T TCGA-DD-A114-01A-11D-A12Z-10 TCGA-DD-A114-10A-01D-A12Z-10 g.chr6:43012996C>T c.3007G>A c.(3007-3009)Gac>Aac p.D1003N LIHC 6 43017756 43017756 + Missense_Mutation SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr6:43017756T>C c.1514A>G c.(1513-1515)gAt>gGt p.D505G LUAD 6 43006189 43006189 + Missense_Mutation SNP C C T TCGA-97-8175-01A-11D-2284-08 TCGA-97-8175-10A-01D-2284-08 g.chr6:43006189C>T c.4589G>A c.(4588-4590)gGc>gAc p.G1530D LUAD 6 43007936 43007936 + Missense_Mutation SNP G G C TCGA-44-3398-01A-01D-1105-08 TCGA-44-3398-10A-01D-1105-08 g.chr6:43007936G>C c.4252C>G c.(4252-4254)Ctg>Gtg p.L1418V LUAD 6 43008794 43008794 + Missense_Mutation SNP C C T TCGA-95-8039-01A-11D-2238-08 TCGA-95-8039-10A-01D-2238-08 g.chr6:43008794C>T c.3665G>A c.(3664-3666)cGg>cAg p.R1222Q LUAD 6 43011247 43011250 + Frame_Shift_Del DEL GTGA GTGA - TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr6:43011247_43011250delGTGA c.3291_3294delTCAC c.(3289-3294)actcacfs p.TH1097fs LUAD 6 43013735 43013735 + Missense_Mutation SNP C C T TCGA-86-A456-01A-11D-A24D-08 TCGA-86-A456-10A-01D-A24F-08 g.chr6:43013735C>T c.2755G>A c.(2755-2757)Gaa>Aaa p.E919K LUAD 6 43014777 43014777 + Silent SNP C C T TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr6:43014777C>T c.2238G>A c.(2236-2238)ctG>ctA p.L746L LUAD 6 43014810 43014810 + Silent SNP C C A TCGA-55-8615-01A-11D-2393-08 TCGA-55-8615-10A-01D-2393-08 g.chr6:43014810C>A c.2205G>T c.(2203-2205)ctG>ctT p.L735L LUAD 6 43017790 43017790 + Missense_Mutation SNP A A G TCGA-05-4384-01A-01D-1753-08 TCGA-05-4384-10A-01D-1753-08 g.chr6:43017790A>G c.1480T>C c.(1480-1482)Tgg>Cgg p.W494R LUAD 6 43018826 43018826 + Missense_Mutation SNP C C G TCGA-50-6593-01A-11D-1753-08 TCGA-50-6593-11A-01D-1753-08 g.chr6:43018826C>G c.1113G>C c.(1111-1113)ttG>ttC p.L371F LUAD 6 43019057 43019057 + Silent SNP C C T TCGA-78-8655-01A-11D-2393-08 TCGA-78-8655-10A-01D-2393-08 g.chr6:43019057C>T c.882G>A c.(880-882)ctG>ctA p.L294L LUAD 6 43019062 43019062 + Missense_Mutation SNP C C G TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chr6:43019062C>G c.877G>C c.(877-879)Gag>Cag p.E293Q LUAD 6 43019092 43019092 + Missense_Mutation SNP C C T TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr6:43019092C>T c.847G>A c.(847-849)Gag>Aag p.E283K LUAD 6 43019123 43019123 + Silent SNP C C T TCGA-44-8119-01A-11D-2238-08 TCGA-44-8119-10A-01D-2238-08 g.chr6:43019123C>T c.816G>A c.(814-816)gcG>gcA p.A272A LUAD 6 43019473 43019473 + Silent SNP C C G TCGA-78-7539-01A-11D-2063-08 TCGA-78-7539-10A-01D-2063-08 g.chr6:43019473C>G c.609G>C c.(607-609)ctG>ctC p.L203L LUAD 6 43020118 43020118 + Missense_Mutation SNP G G C TCGA-44-2657-01A-01D-1105-08 TCGA-44-2657-10A-01D-1105-08 g.chr6:43020118G>C c.409C>G c.(409-411)Cta>Gta p.L137V LUAD 6 43020250 43020250 + Missense_Mutation SNP G G C TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chr6:43020250G>C c.277C>G c.(277-279)Cag>Gag p.Q93E LUAD 6 43020329 43020329 + Silent SNP C C A TCGA-99-7458-01A-11D-2036-08 TCGA-99-7458-10A-01D-2036-08 g.chr6:43020329C>A c.198G>T c.(196-198)ctG>ctT p.L66L LUSC 6 43008367 43008367 + Silent SNP C C A TCGA-46-3765-01A-01D-0983-08 TCGA-46-3765-10A-01D-0983-08 g.chr6:43008367C>A c.3924G>T c.(3922-3924)ctG>ctT p.L1308L LUSC 6 43020080 43020080 + Missense_Mutation SNP G G T TCGA-66-2757-01A-01D-1522-08 TCGA-66-2757-11A-01D-1522-08 g.chr6:43020080G>T c.447C>A c.(445-447)agC>agA p.S149R OV 6 43008015 43008015 + Silent SNP C C T TCGA-36-2537-01A-01D-1526-09 TCGA-36-2537-10A-01D-1526-09 g.chr6:43008015C>T c.4173G>A c.(4171-4173)gtG>gtA p.V1391V OV 6 43013354 43013354 + Missense_Mutation SNP T T C TCGA-13-1492-01A-01D-0472-08 TCGA-13-1492-10A-01W-0545-08 g.chr6:43013354T>C c.2833A>G c.(2833-2835)Atc>Gtc p.I945V OV 6 43017367 43017367 + Missense_Mutation SNP C C T TCGA-13-0883-01A-02W-0420-08 TCGA-13-0883-10A-01D-0399-08 g.chr6:43017367C>T c.1603G>A c.(1603-1605)Gtg>Atg p.V535M OV 6 43019995 43019995 + Missense_Mutation SNP G G A TCGA-24-1562-01A-01W-0553-09 TCGA-24-1562-10A-01W-0553-09 g.chr6:43019995G>A c.532C>T c.(532-534)Cgc>Tgc p.R178C PAAD 6 43005624 43005624 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:43005624C>T c.4899G>A c.(4897-4899)acG>acA p.T1633T PAAD 6 43006104 43006104 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:43006104C>A c.4674G>T c.(4672-4674)caG>caT p.Q1558H PAAD 6 43006154 43006154 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:43006154G>A c.4624C>T c.(4624-4626)Cgg>Tgg p.R1542W PAAD 6 43015930 43015930 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:43015930C>T c.2125G>A c.(2125-2127)Gat>Aat p.D709N PAAD 6 43016152 43016152 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:43016152G>A c.1981C>T c.(1981-1983)Cgg>Tgg p.R661W PAAD 6 43017878 43017878 + Nonsense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:43017878C>T c.1392G>A c.(1390-1392)tgG>tgA p.W464* PAAD 6 43018136 43018136 + Splice_Site SNP C C T TCGA-FB-AAPP-01A-12D-A40W-08 TCGA-FB-AAPP-11A-11D-A40W-08 g.chr6:43018136C>T c.1234G>A c.(1234-1236)Gta>Ata p.V412I PAAD 6 43020447 43020447 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:43020447C>T c.80G>A c.(79-81)cGc>cAc p.R27H PRAD 6 43010619 43010619 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:43010619G>A c.3566C>T c.(3565-3567)cCt>cTt p.P1189L PRAD 6 43012606 43012606 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:43012606C>T c.3056G>A c.(3055-3057)cGc>cAc p.R1019H PRAD 6 43017806 43017806 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:43017806G>A c.1464C>T c.(1462-1464)caC>caT p.H488H PRAD 6 43018788 43018788 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:43018788C>T c.1151G>A c.(1150-1152)cGg>cAg p.R384Q READ 6 43010598 43010598 + Missense_Mutation SNP G G A TCGA-AG-3583-01A-01W-0831-10 TCGA-AG-3583-10A-01W-0831-10 g.chr6:43010598G>A c.3587C>T c.(3586-3588)gCg>gTg p.A1196V READ 6 43013368 43013368 + Missense_Mutation SNP C C T TCGA-AG-3909-01A-01W-1073-09 TCGA-AG-3909-10A-01W-1073-09 g.chr6:43013368C>T c.2819G>A c.(2818-2820)cGc>cAc p.R940H SARC 6 43006382 43006385 + Frame_Shift_Del DEL TGTC TGTC - TCGA-IW-A3M5-01A-22D-A21Q-09 TCGA-IW-A3M5-10A-01D-A21Q-09 g.chr6:43006382_43006385delTGTC c.4486_4489delGACA c.(4486-4491)gacatgfs p.DM1496fs SARC 6 43010622 43010622 + Missense_Mutation SNP C C T TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr6:43010622C>T c.3563G>A c.(3562-3564)gGg>gAg p.G1188E SARC 6 43019973 43019973 + Missense_Mutation SNP A A G TCGA-QQ-A8VG-01A-11D-A37C-09 TCGA-QQ-A8VG-10A-01D-A37F-09 g.chr6:43019973A>G c.554T>C c.(553-555)aTa>aCa p.I185T SKCM 6 43008396 43008396 + Missense_Mutation SNP G G A TCGA-FS-A4F9-06A-11D-A24R-08 TCGA-FS-A4F9-10A-01D-A24R-08 g.chr6:43008396G>A c.3895C>T c.(3895-3897)Cgc>Tgc p.R1299C SKCM 6 43008415 43008415 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr6:43008415G>A c.3876C>T c.(3874-3876)atC>atT p.I1292I SKCM 6 43011351 43011351 + Missense_Mutation SNP G G A TCGA-EE-A3J8-06A-11D-A20D-08 TCGA-EE-A3J8-10A-01D-A20D-08 g.chr6:43011351G>A c.3190C>T c.(3190-3192)Ccc>Tcc p.P1064S SKCM 6 43013087 43013087 + Silent SNP C C A TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chr6:43013087C>A c.2916G>T c.(2914-2916)acG>acT p.T972T SKCM 6 43013404 43013404 + Missense_Mutation SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr6:43013404G>A c.2783C>T c.(2782-2784)tCt>tTt p.S928F SKCM 6 43013793 43013793 + Missense_Mutation SNP A A T TCGA-D3-A1Q7-06A-11D-A19A-08 TCGA-D3-A1Q7-10A-01D-A19A-08 g.chr6:43013793A>T c.2697T>A c.(2695-2697)agT>agA p.S899R SKCM 6 43014643 43014643 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr6:43014643G>A c.2372C>T c.(2371-2373)aCc>aTc p.T791I SKCM 6 43014734 43014734 + Nonsense_Mutation SNP T T A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr6:43014734T>A c.2281A>T c.(2281-2283)Aag>Tag p.K761* SKCM 6 43014822 43014822 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr6:43014822G>A c.2193C>T c.(2191-2193)ttC>ttT p.F731F SKCM 6 43016083 43016083 + Silent SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr6:43016083G>A c.2050C>T c.(2050-2052)Ctg>Ttg p.L684L SKCM 6 43018889 43018889 + Silent SNP G G T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr6:43018889G>T c.1050C>A c.(1048-1050)tcC>tcA p.S350S SKCM 6 43019204 43019204 + Silent SNP G G A TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr6:43019204G>A c.735C>T c.(733-735)gtC>gtT p.V245V SKCM 6 43019452 43019452 + Silent SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr6:43019452C>T c.630G>A c.(628-630)gaG>gaA p.E210E SKCM 6 43019484 43019484 + Missense_Mutation SNP G G A TCGA-ER-A19G-06A-11D-A196-08 TCGA-ER-A19G-10A-01D-A198-08 g.chr6:43019484G>A c.598C>T c.(598-600)Ctt>Ttt p.L200F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 6 43010898 43010898 single base substitution C A downstream_gene_variant BLCA-CN 6 43010898 43010898 single base substitution C A missense_variant D1126Y 3376G>T BLCA-CN 6 43010898 43010898 single base substitution C A missense_variant D1210Y 3628G>T BLCA-CN 6 43013813 43013813 single base substitution C T exon_variant BLCA-CN 6 43013813 43013813 single base substitution C T missense_variant V893M 2677G>A BLCA-CN 6 43013813 43013813 single base substitution C T missense_variant V977M 2929G>A BLCA-US 6 43006375 43006375 single base substitution T C missense_variant N1499S 4496A>G BLCA-US 6 43006375 43006375 single base substitution T C missense_variant N1583S 4748A>G BLCA-US 6 43008026 43008026 single base substitution C T missense_variant E1388K 4162G>A BLCA-US 6 43008026 43008026 single base substitution C T missense_variant E1472K 4414G>A BLCA-US 6 43008354 43008354 single base substitution C G downstream_gene_variant BLCA-US 6 43008354 43008354 single base substitution C G missense_variant E1313Q 3937G>C BLCA-US 6 43008354 43008354 single base substitution C G missense_variant E1397Q 4189G>C BLCA-US 6 43011253 43011253 single base substitution G A downstream_gene_variant BLCA-US 6 43011253 43011253 single base substitution G A synonymous_variant L1096L 3288C>T BLCA-US 6 43011253 43011253 single base substitution G A synonymous_variant L1180L 3540C>T BLCA-US 6 43012542 43012542 single base substitution C G downstream_gene_variant BLCA-US 6 43012542 43012542 single base substitution C G missense_variant K1040N 3120G>C BLCA-US 6 43012542 43012542 single base substitution C G missense_variant K1124N 3372G>C BRCA-EU 6 43000783 43000783 single base substitution G T downstream_gene_variant BRCA-EU 6 43002165 43002165 single base substitution C G downstream_gene_variant BRCA-EU 6 43004191 43004191 single base substitution C T downstream_gene_variant BRCA-EU 6 43004809 43004809 single base substitution G A downstream_gene_variant BRCA-EU 6 43005090 43005112 deletion of <=200bp CCAGATGAAAGCACTTCTGACCA - downstream_gene_variant BRCA-EU 6 43006889 43006889 single base substitution C T intron_variant BRCA-EU 6 43007107 43007107 single base substitution G C intron_variant BRCA-EU 6 43007188 43007188 single base substitution G A intron_variant BRCA-EU 6 43007427 43007427 single base substitution G C intron_variant BRCA-EU 6 43008255 43008255 single base substitution C T intron_variant BRCA-EU 6 43009023 43009023 insertion of <=200bp - A downstream_gene_variant BRCA-EU 6 43009023 43009023 insertion of <=200bp - A intron_variant BRCA-EU 6 43009065 43009065 single base substitution G C downstream_gene_variant BRCA-EU 6 43009065 43009065 single base substitution G C intron_variant BRCA-EU 6 43010491 43010491 single base substitution G C downstream_gene_variant BRCA-EU 6 43010491 43010491 single base substitution G C intron_variant BRCA-EU 6 43011312 43011312 single base substitution C G downstream_gene_variant BRCA-EU 6 43011312 43011312 single base substitution C G missense_variant E1077Q 3229G>C BRCA-EU 6 43011312 43011312 single base substitution C G missense_variant E1161Q 3481G>C BRCA-EU 6 43011449 43011449 single base substitution G C downstream_gene_variant BRCA-EU 6 43011449 43011449 single base substitution G C intron_variant BRCA-EU 6 43012177 43012177 single base substitution C A downstream_gene_variant BRCA-EU 6 43012177 43012177 single base substitution C A intron_variant BRCA-EU 6 43013128 43013128 insertion of <=200bp - T downstream_gene_variant BRCA-EU 6 43013128 43013128 insertion of <=200bp - T frameshift_variant T1043N? BRCA-EU 6 43013128 43013128 insertion of <=200bp - T frameshift_variant T959N? BRCA-EU 6 43014469 43014469 single base substitution G A intron_variant BRCA-EU 6 43015061 43015061 single base substitution G C intron_variant BRCA-EU 6 43016406 43016406 deletion of <=200bp A - intron_variant BRCA-EU 6 43016406 43016406 deletion of <=200bp A - upstream_gene_variant BRCA-EU 6 43018140 43018140 single base substitution G C splice_region_variant BRCA-EU 6 43018140 43018140 single base substitution G C upstream_gene_variant BRCA-EU 6 43019396 43019396 single base substitution G A missense_variant T229M 686C>T BRCA-EU 6 43019396 43019396 single base substitution G A missense_variant T313M 938C>T BRCA-EU 6 43019396 43019396 single base substitution G A upstream_gene_variant BRCA-EU 6 43019655 43019656 deletion of <=200bp AC - intron_variant BRCA-EU 6 43019655 43019656 deletion of <=200bp AC - upstream_gene_variant BRCA-EU 6 43021775 43021775 single base substitution A T upstream_gene_variant BRCA-EU 6 43021952 43021952 single base substitution C G upstream_gene_variant BRCA-EU 6 43021987 43021987 single base substitution G A upstream_gene_variant BRCA-EU 6 43022227 43022227 single base substitution G A upstream_gene_variant BRCA-EU 6 43022287 43022287 single base substitution A C upstream_gene_variant BRCA-EU 6 43022422 43022422 single base substitution T C upstream_gene_variant BRCA-EU 6 43022465 43022465 single base substitution C G upstream_gene_variant BRCA-EU 6 43023524 43023524 single base substitution C G upstream_gene_variant BRCA-EU 6 43024103 43024103 single base substitution C T upstream_gene_variant BRCA-EU 6 43024112 43024112 single base substitution G A upstream_gene_variant BRCA-EU 6 43024950 43024950 single base substitution G A upstream_gene_variant BRCA-EU 6 43026525 43026525 single base substitution C T upstream_gene_variant BRCA-EU 6 43026670 43026670 single base substitution C T upstream_gene_variant BRCA-FR 6 43006889 43006889 single base substitution C T intron_variant BRCA-FR 6 43007107 43007107 single base substitution G C intron_variant BRCA-FR 6 43007188 43007188 single base substitution G A intron_variant BRCA-FR 6 43007427 43007427 single base substitution G C intron_variant BRCA-FR 6 43009065 43009065 single base substitution G C downstream_gene_variant BRCA-FR 6 43009065 43009065 single base substitution G C intron_variant BRCA-FR 6 43010491 43010491 single base substitution G C downstream_gene_variant BRCA-FR 6 43010491 43010491 single base substitution G C intron_variant BRCA-FR 6 43011449 43011449 single base substitution G C downstream_gene_variant BRCA-FR 6 43011449 43011449 single base substitution G C intron_variant BRCA-FR 6 43012511 43012511 single base substitution C G downstream_gene_variant BRCA-FR 6 43012511 43012511 single base substitution C G missense_variant V1051L 3151G>C BRCA-FR 6 43012511 43012511 single base substitution C G missense_variant V1135L 3403G>C BRCA-FR 6 43014469 43014469 single base substitution G A intron_variant BRCA-UK 6 43005398 43005398 single base substitution C G 3_prime_UTR_variant BRCA-UK 6 43016093 43016093 single base substitution C A missense_variant R680S 2040G>T BRCA-UK 6 43016093 43016093 single base substitution C A missense_variant R764S 2292G>T BRCA-UK 6 43016093 43016093 single base substitution C A upstream_gene_variant BRCA-US 6 43005481 43005481 single base substitution C T missense_variant R1681Q 5042G>A BRCA-US 6 43005481 43005481 single base substitution C T missense_variant R1765Q 5294G>A BRCA-US 6 43005599 43005599 single base substitution G A stop_gained Q1642* 4924C>T BRCA-US 6 43005599 43005599 single base substitution G A stop_gained Q1726* 5176C>T BRCA-US 6 43010724 43010724 single base substitution T G downstream_gene_variant BRCA-US 6 43010724 43010724 single base substitution T G splice_acceptor_variant BRCA-US 6 43010839 43010839 single base substitution G T downstream_gene_variant BRCA-US 6 43010839 43010839 single base substitution G T synonymous_variant R1145R 3435C>A BRCA-US 6 43010839 43010839 single base substitution G T synonymous_variant R1229R 3687C>A BRCA-US 6 43013069 43013069 single base substitution C T downstream_gene_variant BRCA-US 6 43013069 43013069 single base substitution C T synonymous_variant R1062R 3186G>A BRCA-US 6 43013069 43013069 single base substitution C T synonymous_variant R978R 2934G>A BRCA-US 6 43013138 43013138 single base substitution A C downstream_gene_variant BRCA-US 6 43013138 43013138 single base substitution A C splice_region_variant BRCA-US 6 43014812 43014812 deletion of <=200bp G - exon_variant BRCA-US 6 43014812 43014812 deletion of <=200bp G - frameshift_variant L735 BRCA-US 6 43014812 43014812 deletion of <=200bp G - frameshift_variant L819 BRCA-US 6 43016263 43016263 single base substitution G T missense_variant L624M 1870C>A BRCA-US 6 43016263 43016263 single base substitution G T missense_variant L708M 2122C>A BRCA-US 6 43016263 43016263 single base substitution G T upstream_gene_variant BRCA-US 6 43016268 43016268 single base substitution T A missense_variant Q622L 1865A>T BRCA-US 6 43016268 43016268 single base substitution T A missense_variant Q706L 2117A>T BRCA-US 6 43016268 43016268 single base substitution T A upstream_gene_variant BRCA-US 6 43017144 43017144 single base substitution C T splice_donor_variant BRCA-US 6 43017144 43017144 single base substitution C T upstream_gene_variant BRCA-US 6 43017793 43017793 single base substitution C G missense_variant E493Q 1477G>C BRCA-US 6 43017793 43017793 single base substitution C G missense_variant E577Q 1729G>C BRCA-US 6 43017793 43017793 single base substitution C G upstream_gene_variant BRCA-US 6 43018789 43018789 single base substitution G A missense_variant R384W 1150C>T BRCA-US 6 43018789 43018789 single base substitution G A missense_variant R468W 1402C>T BRCA-US 6 43018789 43018789 single base substitution G A upstream_gene_variant BRCA-US 6 43018852 43018852 single base substitution A G missense_variant F363L 1087T>C BRCA-US 6 43018852 43018852 single base substitution A G missense_variant F447L 1339T>C BRCA-US 6 43018852 43018852 single base substitution A G upstream_gene_variant BRCA-US 6 43019030 43019030 single base substitution C G synonymous_variant L303L 909G>C BRCA-US 6 43019030 43019030 single base substitution C G synonymous_variant L387L 1161G>C BRCA-US 6 43019030 43019030 single base substitution C G upstream_gene_variant BRCA-US 6 43022095 43022095 single base substitution C T upstream_gene_variant BRCA-US 6 43022206 43022206 single base substitution C A upstream_gene_variant BRCA-US 6 43023887 43023887 single base substitution A C upstream_gene_variant BRCA-US 6 43025966 43025966 single base substitution C T upstream_gene_variant BTCA-JP 6 43005396 43005396 single base substitution C A 3_prime_UTR_variant BTCA-JP 6 43012738 43012738 single base substitution G A downstream_gene_variant BTCA-JP 6 43012738 43012738 single base substitution G A intron_variant BTCA-JP 6 43019925 43019925 single base substitution T G intron_variant BTCA-JP 6 43019925 43019925 single base substitution T G missense_variant E253A 758A>C BTCA-JP 6 43019925 43019925 single base substitution T G upstream_gene_variant BTCA-JP 6 43020170 43020170 single base substitution C G missense_variant Q119H 357G>C BTCA-JP 6 43020170 43020170 single base substitution C G missense_variant Q171H 513G>C BTCA-JP 6 43020170 43020170 single base substitution C G upstream_gene_variant BTCA-JP 6 43020254 43020254 single base substitution G T synonymous_variant P143P 429C>A BTCA-JP 6 43020254 43020254 single base substitution G T synonymous_variant P91P 273C>A BTCA-JP 6 43020254 43020254 single base substitution G T upstream_gene_variant BTCA-JP 6 43020287 43020287 single base substitution C G missense_variant K132N 396G>C BTCA-JP 6 43020287 43020287 single base substitution C G missense_variant K80N 240G>C BTCA-JP 6 43020287 43020287 single base substitution C G upstream_gene_variant BTCA-JP 6 43022193 43022193 single base substitution C T upstream_gene_variant BTCA-JP 6 43023600 43023600 single base substitution A T upstream_gene_variant CESC-US 6 43005484 43005484 single base substitution G A missense_variant S1680F 5039C>T CESC-US 6 43005484 43005484 single base substitution G A missense_variant S1764F 5291C>T CESC-US 6 43005529 43005529 single base substitution G C stop_gained S1665* 4994C>G CESC-US 6 43005529 43005529 single base substitution G C stop_gained S1749* 5246C>G CESC-US 6 43006110 43006110 single base substitution G A synonymous_variant D1556D 4668C>T CESC-US 6 43006110 43006110 single base substitution G A synonymous_variant D1640D 4920C>T CESC-US 6 43010606 43010606 single base substitution G T downstream_gene_variant CESC-US 6 43010606 43010606 single base substitution G T missense_variant F1193L 3579C>A CESC-US 6 43010606 43010606 single base substitution G T missense_variant F1277L 3831C>A CESC-US 6 43017742 43017742 single base substitution G C missense_variant Q510E 1528C>G CESC-US 6 43017742 43017742 single base substitution G C missense_variant Q594E 1780C>G CESC-US 6 43017742 43017742 single base substitution G C upstream_gene_variant CESC-US 6 43017776 43017776 single base substitution G C synonymous_variant L498L 1494C>G CESC-US 6 43017776 43017776 single base substitution G C synonymous_variant L582L 1746C>G CESC-US 6 43017776 43017776 single base substitution G C upstream_gene_variant CESC-US 6 43018878 43018878 single base substitution G T stop_gained S354* 1061C>A CESC-US 6 43018878 43018878 single base substitution G T stop_gained S438* 1313C>A CESC-US 6 43018878 43018878 single base substitution G T upstream_gene_variant CESC-US 6 43020151 43020151 single base substitution C T missense_variant E126K 376G>A CESC-US 6 43020151 43020151 single base substitution C T missense_variant E178K 532G>A CESC-US 6 43020151 43020151 single base substitution C T upstream_gene_variant COAD-US 6 43005625 43005625 single base substitution G A missense_variant T1633M 4898C>T COAD-US 6 43005625 43005625 single base substitution G A missense_variant T1717M 5150C>T COAD-US 6 43008690 43008690 single base substitution C T downstream_gene_variant COAD-US 6 43008690 43008690 single base substitution C T missense_variant G1257S 3769G>A COAD-US 6 43008690 43008690 single base substitution C T missense_variant G1341S 4021G>A COAD-US 6 43008716 43008716 single base substitution C T downstream_gene_variant COAD-US 6 43008716 43008716 single base substitution C T missense_variant C1248Y 3743G>A COAD-US 6 43008716 43008716 single base substitution C T missense_variant C1332Y 3995G>A COAD-US 6 43010677 43010677 single base substitution G A downstream_gene_variant COAD-US 6 43010677 43010677 single base substitution G A missense_variant P1170S 3508C>T COAD-US 6 43010677 43010677 single base substitution G A missense_variant P1254S 3760C>T COAD-US 6 43013046 43013046 single base substitution C T downstream_gene_variant COAD-US 6 43013046 43013046 single base substitution C T missense_variant R1070H 3209G>A COAD-US 6 43013046 43013046 single base substitution C T missense_variant R986H 2957G>A COAD-US 6 43015993 43015993 single base substitution T C splice_acceptor_variant COAD-US 6 43015993 43015993 single base substitution T C upstream_gene_variant COAD-US 6 43018766 43018768 deletion of <=200bp CTC - inframe_deletion E391 COAD-US 6 43018766 43018768 deletion of <=200bp CTC - inframe_deletion E475 COAD-US 6 43018766 43018768 deletion of <=200bp CTC - upstream_gene_variant COAD-US 6 43018836 43018836 single base substitution G A missense_variant T368I 1103C>T COAD-US 6 43018836 43018836 single base substitution G A missense_variant T452I 1355C>T COAD-US 6 43018836 43018836 single base substitution G A upstream_gene_variant COAD-US 6 43020163 43020163 single base substitution G T missense_variant L122I 364C>A COAD-US 6 43020163 43020163 single base substitution G T missense_variant L174I 520C>A COAD-US 6 43020163 43020163 single base substitution G T upstream_gene_variant COAD-US 6 43022057 43022057 deletion of <=200bp G - upstream_gene_variant COAD-US 6 43022100 43022100 single base substitution C T upstream_gene_variant COAD-US 6 43023336 43023336 single base substitution G A upstream_gene_variant COAD-US 6 43025881 43025881 single base substitution A C upstream_gene_variant COCA-CN 6 43006616 43006616 single base substitution C T synonymous_variant V1468V 4404G>A COCA-CN 6 43006616 43006616 single base substitution C T synonymous_variant V1552V 4656G>A COCA-CN 6 43010715 43010715 single base substitution T C downstream_gene_variant COCA-CN 6 43010715 43010715 single base substitution T C missense_variant N1157S 3470A>G COCA-CN 6 43010715 43010715 single base substitution T C missense_variant N1241S 3722A>G COCA-CN 6 43013185 43013185 single base substitution A G downstream_gene_variant COCA-CN 6 43013185 43013185 single base substitution A G intron_variant COCA-CN 6 43013868 43013868 single base substitution C T intron_variant COCA-CN 6 43013871 43013871 single base substitution G T intron_variant COCA-CN 6 43017868 43017868 single base substitution T C missense_variant T468A 1402A>G COCA-CN 6 43017868 43017868 single base substitution T C missense_variant T552A 1654A>G COCA-CN 6 43017868 43017868 single base substitution T C upstream_gene_variant COCA-CN 6 43020439 43020439 single base substitution C T missense_variant V30M 88G>A COCA-CN 6 43020439 43020439 single base substitution C T missense_variant V82M 244G>A COCA-CN 6 43020439 43020439 single base substitution C T upstream_gene_variant COCA-CN 6 43021943 43021943 single base substitution C T upstream_gene_variant COCA-CN 6 43023123 43023123 single base substitution C T upstream_gene_variant COCA-CN 6 43023736 43023736 single base substitution C T upstream_gene_variant ESAD-UK 6 43002771 43002771 single base substitution G A downstream_gene_variant ESAD-UK 6 43003934 43003935 deletion of <=200bp AG - downstream_gene_variant ESAD-UK 6 43004097 43004097 single base substitution A G downstream_gene_variant ESAD-UK 6 43004324 43004324 single base substitution C T downstream_gene_variant ESAD-UK 6 43007599 43007599 single base substitution C T intron_variant ESAD-UK 6 43010068 43010068 deletion of <=200bp T - downstream_gene_variant ESAD-UK 6 43010068 43010068 deletion of <=200bp T - intron_variant ESAD-UK 6 43013292 43013292 single base substitution A G downstream_gene_variant ESAD-UK 6 43013292 43013292 single base substitution A G intron_variant ESAD-UK 6 43013784 43013784 single base substitution C T exon_variant ESAD-UK 6 43013784 43013784 single base substitution C T synonymous_variant P902P 2706G>A ESAD-UK 6 43013784 43013784 single base substitution C T synonymous_variant P986P 2958G>A ESAD-UK 6 43015474 43015474 single base substitution T C intron_variant ESAD-UK 6 43019852 43019852 single base substitution G C intron_variant ESAD-UK 6 43019852 43019852 single base substitution G C missense_variant I277M 831C>G ESAD-UK 6 43019852 43019852 single base substitution G C upstream_gene_variant ESAD-UK 6 43019979 43019979 single base substitution C T missense_variant R183Q 548G>A ESAD-UK 6 43019979 43019979 single base substitution C T missense_variant R235Q 704G>A ESAD-UK 6 43019979 43019979 single base substitution C T upstream_gene_variant ESAD-UK 6 43022457 43022457 single base substitution C A upstream_gene_variant ESAD-UK 6 43023409 43023409 single base substitution G C upstream_gene_variant ESCA-CN 6 43014142 43014142 single base substitution G A exon_variant ESCA-CN 6 43014142 43014142 single base substitution G A missense_variant S831F 2492C>T ESCA-CN 6 43014142 43014142 single base substitution G A missense_variant S915F 2744C>T ESCA-CN 6 43019100 43019100 single base substitution G C missense_variant S280C 839C>G ESCA-CN 6 43019100 43019100 single base substitution G C missense_variant S364C 1091C>G ESCA-CN 6 43019100 43019100 single base substitution G C upstream_gene_variant ESCA-CN 6 43021977 43021977 deletion of <=200bp G - upstream_gene_variant GACA-CN 6 43010674 43010674 single base substitution G C downstream_gene_variant GACA-CN 6 43010674 43010674 single base substitution G C missense_variant R1171G 3511C>G GACA-CN 6 43010674 43010674 single base substitution G C missense_variant R1255G 3763C>G KIRC-US 6 43013037 43013037 single base substitution T C downstream_gene_variant KIRC-US 6 43013037 43013037 single base substitution T C missense_variant Y1073C 3218A>G KIRC-US 6 43013037 43013037 single base substitution T C missense_variant Y989C 2966A>G KIRC-US 6 43017376 43017376 single base substitution C T missense_variant E532K 1594G>A KIRC-US 6 43017376 43017376 single base substitution C T missense_variant E616K 1846G>A KIRC-US 6 43017376 43017376 single base substitution C T upstream_gene_variant KIRC-US 6 43019452 43019452 single base substitution C G missense_variant E210D 630G>C KIRC-US 6 43019452 43019452 single base substitution C G missense_variant E294D 882G>C KIRC-US 6 43019452 43019452 single base substitution C G upstream_gene_variant KIRC-US 6 43020004 43020004 single base substitution A C missense_variant Y175D 523T>G KIRC-US 6 43020004 43020004 single base substitution A C missense_variant Y227D 679T>G KIRC-US 6 43020004 43020004 single base substitution A C upstream_gene_variant KIRC-US 6 43024130 43024130 single base substitution T G upstream_gene_variant KIRP-US 6 43008726 43008726 single base substitution G A downstream_gene_variant KIRP-US 6 43008726 43008726 single base substitution G A synonymous_variant L1245L 3733C>T KIRP-US 6 43008726 43008726 single base substitution G A synonymous_variant L1329L 3985C>T KIRP-US 6 43023646 43023646 single base substitution A C upstream_gene_variant KIRP-US 6 43023807 43023820 deletion of <=200bp GCCATCTCTCACCT - upstream_gene_variant LAML-KR 6 43008298 43008298 single base substitution C T synonymous_variant L1331L 3993G>A LAML-KR 6 43008298 43008298 single base substitution C T synonymous_variant L1415L 4245G>A LAML-KR 6 43012704 43012704 single base substitution A C downstream_gene_variant LAML-KR 6 43012704 43012704 single base substitution A C intron_variant LAML-KR 6 43023371 43023371 single base substitution T C upstream_gene_variant LGG-US 6 43010826 43010826 single base substitution C T downstream_gene_variant LGG-US 6 43010826 43010826 single base substitution C T missense_variant V1150M 3448G>A LGG-US 6 43010826 43010826 single base substitution C T missense_variant V1234M 3700G>A LGG-US 6 43023893 43023893 single base substitution C T upstream_gene_variant LICA-CN 6 43018134 43018134 single base substitution T C splice_region_variant LICA-CN 6 43018134 43018134 single base substitution T C upstream_gene_variant LICA-FR 6 43013768 43013768 single base substitution A C exon_variant LICA-FR 6 43013768 43013768 single base substitution A C missense_variant C908G 2722T>G LICA-FR 6 43013768 43013768 single base substitution A C missense_variant C992G 2974T>G LICA-FR 6 43015955 43015955 single base substitution C T synonymous_variant L700L 2100G>A LICA-FR 6 43015955 43015955 single base substitution C T synonymous_variant L784L 2352G>A LICA-FR 6 43015955 43015955 single base substitution C T upstream_gene_variant LICA-FR 6 43018145 43018145 single base substitution T C intron_variant LICA-FR 6 43018145 43018145 single base substitution T C upstream_gene_variant LICA-FR 6 43018288 43018307 deletion of <=200bp ACACACACACACACACACAC - intron_variant LICA-FR 6 43018288 43018307 deletion of <=200bp ACACACACACACACACACAC - upstream_gene_variant LICA-FR 6 43025950 43025950 single base substitution G A upstream_gene_variant LIHC-US 6 43005507 43005507 single base substitution G A synonymous_variant T1672T 5016C>T LIHC-US 6 43005507 43005507 single base substitution G A synonymous_variant T1756T 5268C>T LIHC-US 6 43012996 43012996 single base substitution C T downstream_gene_variant LIHC-US 6 43012996 43012996 single base substitution C T missense_variant D1003N 3007G>A LIHC-US 6 43012996 43012996 single base substitution C T missense_variant D1087N 3259G>A LIHC-US 6 43016296 43016296 single base substitution G T missense_variant P613T 1837C>A LIHC-US 6 43016296 43016296 single base substitution G T missense_variant P697T 2089C>A LIHC-US 6 43016296 43016296 single base substitution G T upstream_gene_variant LIHC-US 6 43023661 43023661 single base substitution C T upstream_gene_variant LINC-JP 6 43011310 43011310 single base substitution T A downstream_gene_variant LINC-JP 6 43011310 43011310 single base substitution T A missense_variant E1077D 3231A>T LINC-JP 6 43011310 43011310 single base substitution T A missense_variant E1161D 3483A>T LINC-JP 6 43013995 43013995 single base substitution A C exon_variant LINC-JP 6 43013995 43013995 single base substitution A C missense_variant M880R 2639T>G LINC-JP 6 43013995 43013995 single base substitution A C missense_variant M964R 2891T>G LINC-JP 6 43019617 43019617 single base substitution T C intron_variant LINC-JP 6 43019617 43019617 single base substitution T C upstream_gene_variant LINC-JP 6 43021911 43021911 insertion of <=200bp - A upstream_gene_variant LIRI-JP 6 43003641 43003641 single base substitution A G downstream_gene_variant LIRI-JP 6 43003668 43003668 single base substitution T G downstream_gene_variant LIRI-JP 6 43004054 43004054 single base substitution T C downstream_gene_variant LIRI-JP 6 43005145 43005145 single base substitution T C downstream_gene_variant LIRI-JP 6 43005821 43005821 single base substitution C T intron_variant LIRI-JP 6 43006102 43006102 single base substitution T G missense_variant N1559T 4676A>C LIRI-JP 6 43006102 43006102 single base substitution T G missense_variant N1643T 4928A>C LIRI-JP 6 43006436 43006436 single base substitution G A splice_region_variant LIRI-JP 6 43007324 43007324 single base substitution A G intron_variant LIRI-JP 6 43008395 43008395 single base substitution C T downstream_gene_variant LIRI-JP 6 43008395 43008395 single base substitution C T missense_variant R1299H 3896G>A LIRI-JP 6 43008395 43008395 single base substitution C T missense_variant R1383H 4148G>A LIRI-JP 6 43008472 43008472 single base substitution C T downstream_gene_variant LIRI-JP 6 43008472 43008472 single base substitution C T synonymous_variant A1273A 3819G>A LIRI-JP 6 43008472 43008472 single base substitution C T synonymous_variant A1357A 4071G>A LIRI-JP 6 43008801 43008801 single base substitution A G downstream_gene_variant LIRI-JP 6 43008801 43008801 single base substitution A G missense_variant F1220L 3658T>C LIRI-JP 6 43008801 43008801 single base substitution A G missense_variant F1304L 3910T>C LIRI-JP 6 43011033 43011033 deletion of <=200bp G - downstream_gene_variant LIRI-JP 6 43011033 43011033 deletion of <=200bp G - intron_variant LIRI-JP 6 43012768 43012768 single base substitution A G downstream_gene_variant LIRI-JP 6 43012768 43012768 single base substitution A G intron_variant LIRI-JP 6 43014205 43014205 single base substitution A T intron_variant LIRI-JP 6 43016209 43016209 single base substitution G A missense_variant L642F 1924C>T LIRI-JP 6 43016209 43016209 single base substitution G A missense_variant L726F 2176C>T LIRI-JP 6 43016209 43016209 single base substitution G A upstream_gene_variant LIRI-JP 6 43017638 43017638 single base substitution C A intron_variant LIRI-JP 6 43017638 43017638 single base substitution C A upstream_gene_variant LIRI-JP 6 43017870 43017870 single base substitution A G missense_variant M467T 1400T>C LIRI-JP 6 43017870 43017870 single base substitution A G missense_variant M551T 1652T>C LIRI-JP 6 43017870 43017870 single base substitution A G upstream_gene_variant LIRI-JP 6 43023926 43023926 single base substitution T C upstream_gene_variant LIRI-JP 6 43024654 43024654 single base substitution G A upstream_gene_variant LIRI-JP 6 43024890 43024890 single base substitution T C upstream_gene_variant LIRI-JP 6 43025675 43025675 single base substitution G A upstream_gene_variant LIRI-JP 6 43026583 43026583 single base substitution T C upstream_gene_variant LUSC-KR 6 43005037 43005037 single base substitution C G downstream_gene_variant LUSC-KR 6 43025681 43025681 single base substitution A G upstream_gene_variant LUSC-US 6 43008367 43008367 single base substitution C A downstream_gene_variant LUSC-US 6 43008367 43008367 single base substitution C A synonymous_variant L1308L 3924G>T LUSC-US 6 43008367 43008367 single base substitution C A synonymous_variant L1392L 4176G>T LUSC-US 6 43020080 43020080 single base substitution G T missense_variant S149R 447C>A LUSC-US 6 43020080 43020080 single base substitution G T missense_variant S201R 603C>A LUSC-US 6 43020080 43020080 single base substitution G T upstream_gene_variant MALY-DE 6 43013445 43013445 single base substitution C T intron_variant MALY-DE 6 43021628 43021628 single base substitution C T 5_prime_UTR_variant MALY-DE 6 43021628 43021628 single base substitution C T upstream_gene_variant MELA-AU 6 43000575 43000575 single base substitution G A downstream_gene_variant MELA-AU 6 43000705 43000705 single base substitution C T downstream_gene_variant MELA-AU 6 43001601 43001601 single base substitution G A downstream_gene_variant MELA-AU 6 43001772 43001772 single base substitution C T downstream_gene_variant MELA-AU 6 43001840 43001840 single base substitution C T downstream_gene_variant MELA-AU 6 43003539 43003539 single base substitution C T downstream_gene_variant MELA-AU 6 43003626 43003626 single base substitution C T downstream_gene_variant MELA-AU 6 43003846 43003846 single base substitution G A downstream_gene_variant MELA-AU 6 43004708 43004708 single base substitution G A downstream_gene_variant MELA-AU 6 43005288 43005288 single base substitution C T downstream_gene_variant MELA-AU 6 43008501 43008502 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 6 43008501 43008502 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 6 43008857 43008857 single base substitution G C downstream_gene_variant MELA-AU 6 43008857 43008857 single base substitution G C intron_variant MELA-AU 6 43009360 43009360 single base substitution A G downstream_gene_variant MELA-AU 6 43009360 43009360 single base substitution A G intron_variant MELA-AU 6 43009675 43009675 single base substitution G A downstream_gene_variant MELA-AU 6 43009675 43009675 single base substitution G A intron_variant MELA-AU 6 43010533 43010533 single base substitution G A downstream_gene_variant MELA-AU 6 43010533 43010533 single base substitution G A splice_region_variant MELA-AU 6 43012188 43012188 single base substitution G A downstream_gene_variant MELA-AU 6 43012188 43012188 single base substitution G A intron_variant MELA-AU 6 43012406 43012406 single base substitution G A downstream_gene_variant MELA-AU 6 43012406 43012406 single base substitution G A intron_variant MELA-AU 6 43012729 43012729 single base substitution G A downstream_gene_variant MELA-AU 6 43012729 43012729 single base substitution G A intron_variant MELA-AU 6 43013315 43013315 single base substitution C T downstream_gene_variant MELA-AU 6 43013315 43013315 single base substitution C T intron_variant MELA-AU 6 43014374 43014374 single base substitution G A intron_variant MELA-AU 6 43014409 43014409 single base substitution G A intron_variant MELA-AU 6 43014635 43014635 single base substitution G A exon_variant MELA-AU 6 43014635 43014635 single base substitution G A synonymous_variant L794L 2380C>T MELA-AU 6 43014635 43014635 single base substitution G A synonymous_variant L878L 2632C>T MELA-AU 6 43015644 43015644 single base substitution G A intron_variant MELA-AU 6 43016001 43016001 single base substitution G A intron_variant MELA-AU 6 43016001 43016001 single base substitution G A upstream_gene_variant MELA-AU 6 43016083 43016083 single base substitution G A synonymous_variant L684L 2050C>T MELA-AU 6 43016083 43016083 single base substitution G A synonymous_variant L768L 2302C>T MELA-AU 6 43016083 43016083 single base substitution G A upstream_gene_variant MELA-AU 6 43016929 43016929 single base substitution A G intron_variant MELA-AU 6 43016929 43016929 single base substitution A G upstream_gene_variant MELA-AU 6 43017457 43017457 single base substitution G A intron_variant MELA-AU 6 43017457 43017457 single base substitution G A upstream_gene_variant MELA-AU 6 43017924 43017924 single base substitution G A intron_variant MELA-AU 6 43017924 43017924 single base substitution G A upstream_gene_variant MELA-AU 6 43018080 43018080 single base substitution G T synonymous_variant I430I 1290C>A MELA-AU 6 43018080 43018080 single base substitution G T synonymous_variant I514I 1542C>A MELA-AU 6 43018080 43018080 single base substitution G T upstream_gene_variant MELA-AU 6 43018465 43018465 single base substitution G A intron_variant MELA-AU 6 43018465 43018465 single base substitution G A upstream_gene_variant MELA-AU 6 43018738 43018738 single base substitution G A missense_variant R401W 1201C>T MELA-AU 6 43018738 43018738 single base substitution G A missense_variant R485W 1453C>T MELA-AU 6 43018738 43018738 single base substitution G A upstream_gene_variant MELA-AU 6 43019177 43019177 single base substitution C A synonymous_variant V254V 762G>T MELA-AU 6 43019177 43019177 single base substitution C A synonymous_variant V338V 1014G>T MELA-AU 6 43019177 43019177 single base substitution C A upstream_gene_variant MELA-AU 6 43019213 43019213 single base substitution G A splice_region_variant MELA-AU 6 43019213 43019213 single base substitution G A upstream_gene_variant MELA-AU 6 43019626 43019626 single base substitution A C intron_variant MELA-AU 6 43019626 43019626 single base substitution A C upstream_gene_variant MELA-AU 6 43019679 43019679 single base substitution G A intron_variant MELA-AU 6 43019679 43019679 single base substitution G A upstream_gene_variant MELA-AU 6 43020180 43020180 single base substitution G A missense_variant S116F 347C>T MELA-AU 6 43020180 43020180 single base substitution G A missense_variant S168F 503C>T MELA-AU 6 43020180 43020180 single base substitution G A upstream_gene_variant MELA-AU 6 43020646 43020646 single base substitution G C intron_variant MELA-AU 6 43020646 43020646 single base substitution G C upstream_gene_variant MELA-AU 6 43021219 43021220 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 6 43021700 43021700 single base substitution T C upstream_gene_variant MELA-AU 6 43022893 43022893 single base substitution G A upstream_gene_variant MELA-AU 6 43023420 43023420 single base substitution G A upstream_gene_variant MELA-AU 6 43023693 43023693 single base substitution G A upstream_gene_variant MELA-AU 6 43024108 43024108 single base substitution G A upstream_gene_variant MELA-AU 6 43024431 43024431 single base substitution G A upstream_gene_variant MELA-AU 6 43024682 43024682 single base substitution A T upstream_gene_variant MELA-AU 6 43024916 43024916 single base substitution G A upstream_gene_variant MELA-AU 6 43024982 43024982 single base substitution G A upstream_gene_variant MELA-AU 6 43025052 43025052 single base substitution G T upstream_gene_variant MELA-AU 6 43025080 43025080 single base substitution G A upstream_gene_variant MELA-AU 6 43026015 43026015 single base substitution G A upstream_gene_variant ORCA-IN 6 43007602 43007602 single base substitution G A intron_variant ORCA-IN 6 43011351 43011351 single base substitution G T downstream_gene_variant ORCA-IN 6 43011351 43011351 single base substitution G T missense_variant P1064T 3190C>A ORCA-IN 6 43011351 43011351 single base substitution G T missense_variant P1148T 3442C>A ORCA-IN 6 43018037 43018037 single base substitution C T missense_variant E445K 1333G>A ORCA-IN 6 43018037 43018037 single base substitution C T missense_variant E529K 1585G>A ORCA-IN 6 43018037 43018037 single base substitution C T upstream_gene_variant OV-AU 6 43004461 43004461 single base substitution G A downstream_gene_variant OV-AU 6 43010883 43010883 single base substitution C A downstream_gene_variant OV-AU 6 43010883 43010883 single base substitution C A missense_variant A1131S 3391G>T OV-AU 6 43010883 43010883 single base substitution C A missense_variant A1215S 3643G>T OV-AU 6 43018957 43018957 single base substitution C T missense_variant G328S 982G>A OV-AU 6 43018957 43018957 single base substitution C T missense_variant G412S 1234G>A OV-AU 6 43018957 43018957 single base substitution C T upstream_gene_variant OV-AU 6 43019429 43019429 single base substitution C T missense_variant R218H 653G>A OV-AU 6 43019429 43019429 single base substitution C T missense_variant R302H 905G>A OV-AU 6 43019429 43019429 single base substitution C T upstream_gene_variant OV-AU 6 43025418 43025418 single base substitution T C upstream_gene_variant OV-AU 6 43026239 43026239 single base substitution C A upstream_gene_variant OV-US 6 43019995 43019995 single base substitution G A missense_variant R178C 532C>T OV-US 6 43019995 43019995 single base substitution G A missense_variant R230C 688C>T OV-US 6 43019995 43019995 single base substitution G A upstream_gene_variant PACA-AU 6 43004056 43004059 deletion of <=200bp ATTT - downstream_gene_variant PACA-AU 6 43010597 43010597 single base substitution C T downstream_gene_variant PACA-AU 6 43010597 43010597 single base substitution C T synonymous_variant A1196A 3588G>A PACA-AU 6 43010597 43010597 single base substitution C T synonymous_variant A1280A 3840G>A PACA-AU 6 43011620 43011620 deletion of <=200bp A - downstream_gene_variant PACA-AU 6 43011620 43011620 deletion of <=200bp A - intron_variant PACA-AU 6 43012918 43012918 single base substitution C T downstream_gene_variant PACA-AU 6 43012918 43012918 single base substitution C T intron_variant PACA-AU 6 43016667 43016667 single base substitution C G intron_variant PACA-AU 6 43016667 43016667 single base substitution C G upstream_gene_variant PACA-AU 6 43023142 43023142 single base substitution T C upstream_gene_variant PACA-CA 6 43004070 43004070 single base substitution T A downstream_gene_variant PACA-CA 6 43005952 43005952 single base substitution G T intron_variant PACA-CA 6 43008642 43008642 single base substitution T C downstream_gene_variant PACA-CA 6 43008642 43008642 single base substitution T C intron_variant PACA-CA 6 43010253 43010253 single base substitution A C downstream_gene_variant PACA-CA 6 43010253 43010253 single base substitution A C intron_variant PACA-CA 6 43011458 43011458 single base substitution A T downstream_gene_variant PACA-CA 6 43011458 43011458 single base substitution A T intron_variant PACA-CA 6 43013195 43013195 single base substitution G T downstream_gene_variant PACA-CA 6 43013195 43013195 single base substitution G T intron_variant PACA-CA 6 43013680 43013680 single base substitution T A intron_variant PACA-CA 6 43014979 43014979 single base substitution G A intron_variant PACA-CA 6 43018788 43018788 single base substitution C T missense_variant R384Q 1151G>A PACA-CA 6 43018788 43018788 single base substitution C T missense_variant R468Q 1403G>A PACA-CA 6 43018788 43018788 single base substitution C T upstream_gene_variant PACA-CA 6 43020781 43020781 single base substitution G A intron_variant PACA-CA 6 43020781 43020781 single base substitution G A upstream_gene_variant PACA-CA 6 43021572 43021572 single base substitution C T missense_variant E9K 25G>A PACA-CA 6 43021572 43021572 single base substitution C T upstream_gene_variant PACA-CA 6 43021573 43021573 single base substitution C T synonymous_variant A8A 24G>A PACA-CA 6 43021573 43021573 single base substitution C T upstream_gene_variant PACA-CA 6 43022191 43022191 single base substitution C G upstream_gene_variant PACA-CA 6 43022320 43022320 single base substitution A G upstream_gene_variant PAEN-AU 6 43023301 43023301 single base substitution G A upstream_gene_variant PAEN-IT 6 43022497 43022497 single base substitution G C upstream_gene_variant PBCA-DE 6 43012857 43012857 single base substitution G A downstream_gene_variant PBCA-DE 6 43012857 43012857 single base substitution G A intron_variant PBCA-DE 6 43013606 43013606 single base substitution A G intron_variant PBCA-DE 6 43026477 43026477 single base substitution C T upstream_gene_variant PRAD-UK 6 43014049 43014049 single base substitution T G exon_variant PRAD-UK 6 43014049 43014049 single base substitution T G missense_variant K862T 2585A>C PRAD-UK 6 43014049 43014049 single base substitution T G missense_variant K946T 2837A>C PRAD-UK 6 43018238 43018253 deletion of <=200bp CCAGGTTTTAGAAAAA - intron_variant PRAD-UK 6 43018238 43018253 deletion of <=200bp CCAGGTTTTAGAAAAA - upstream_gene_variant PRAD-US 6 43023654 43023654 single base substitution G A upstream_gene_variant PRAD-US 6 43024050 43024050 single base substitution G T upstream_gene_variant READ-US 6 43006429 43006429 single base substitution G A missense_variant A1481V 4442C>T READ-US 6 43006429 43006429 single base substitution G A missense_variant A1565V 4694C>T READ-US 6 43017358 43017358 single base substitution C A stop_gained E538* 1612G>T READ-US 6 43017358 43017358 single base substitution C A stop_gained E622* 1864G>T READ-US 6 43017358 43017358 single base substitution C A upstream_gene_variant RECA-CN 6 43010858 43010858 single base substitution A G downstream_gene_variant RECA-CN 6 43010858 43010858 single base substitution A G missense_variant I1139T 3416T>C RECA-CN 6 43010858 43010858 single base substitution A G missense_variant I1223T 3668T>C RECA-EU 6 43005522 43005522 single base substitution G A synonymous_variant P1667P 5001C>T RECA-EU 6 43005522 43005522 single base substitution G A synonymous_variant P1751P 5253C>T RECA-EU 6 43006864 43006864 single base substitution G C intron_variant RECA-EU 6 43009696 43009696 single base substitution C T downstream_gene_variant RECA-EU 6 43009696 43009696 single base substitution C T intron_variant SKCA-BR 6 43006918 43006918 single base substitution G A intron_variant SKCA-BR 6 43008404 43008404 single base substitution A G downstream_gene_variant SKCA-BR 6 43008404 43008404 single base substitution A G missense_variant F1296S 3887T>C SKCA-BR 6 43008404 43008404 single base substitution A G missense_variant F1380S 4139T>C SKCA-BR 6 43009741 43009745 deletion of <=200bp CAAAA - downstream_gene_variant SKCA-BR 6 43009741 43009745 deletion of <=200bp CAAAA - intron_variant SKCA-BR 6 43017969 43017969 single base substitution G A intron_variant SKCA-BR 6 43017969 43017969 single base substitution G A upstream_gene_variant SKCM-US 6 43008396 43008396 single base substitution G A downstream_gene_variant SKCM-US 6 43008396 43008396 single base substitution G A missense_variant R1299C 3895C>T SKCM-US 6 43008396 43008396 single base substitution G A missense_variant R1383C 4147C>T SKCM-US 6 43008415 43008415 single base substitution G A downstream_gene_variant SKCM-US 6 43008415 43008415 single base substitution G A synonymous_variant I1292I 3876C>T SKCM-US 6 43008415 43008415 single base substitution G A synonymous_variant I1376I 4128C>T SKCM-US 6 43011351 43011351 single base substitution G A downstream_gene_variant SKCM-US 6 43011351 43011351 single base substitution G A missense_variant P1064S 3190C>T SKCM-US 6 43011351 43011351 single base substitution G A missense_variant P1148S 3442C>T SKCM-US 6 43013087 43013087 single base substitution C A downstream_gene_variant SKCM-US 6 43013087 43013087 single base substitution C A synonymous_variant T1056T 3168G>T SKCM-US 6 43013087 43013087 single base substitution C A synonymous_variant T972T 2916G>T SKCM-US 6 43013404 43013404 single base substitution G A exon_variant SKCM-US 6 43013404 43013404 single base substitution G A missense_variant S1012F 3035C>T SKCM-US 6 43013404 43013404 single base substitution G A missense_variant S928F 2783C>T SKCM-US 6 43013793 43013793 single base substitution A T exon_variant SKCM-US 6 43013793 43013793 single base substitution A T missense_variant S899R 2697T>A SKCM-US 6 43013793 43013793 single base substitution A T missense_variant S983R 2949T>A SKCM-US 6 43014252 43014252 single base substitution G A exon_variant SKCM-US 6 43014252 43014252 single base substitution G A stop_gained Q829* 2485C>T SKCM-US 6 43014252 43014252 single base substitution G A stop_gained Q913* 2737C>T SKCM-US 6 43014643 43014643 single base substitution G A exon_variant SKCM-US 6 43014643 43014643 single base substitution G A missense_variant T791I 2372C>T SKCM-US 6 43014643 43014643 single base substitution G A missense_variant T875I 2624C>T SKCM-US 6 43014734 43014734 single base substitution T A exon_variant SKCM-US 6 43014734 43014734 single base substitution T A stop_gained K761* 2281A>T SKCM-US 6 43014734 43014734 single base substitution T A stop_gained K845* 2533A>T SKCM-US 6 43016083 43016083 single base substitution G A synonymous_variant L684L 2050C>T SKCM-US 6 43016083 43016083 single base substitution G A synonymous_variant L768L 2302C>T SKCM-US 6 43016083 43016083 single base substitution G A upstream_gene_variant SKCM-US 6 43018889 43018889 single base substitution G T synonymous_variant S350S 1050C>A SKCM-US 6 43018889 43018889 single base substitution G T synonymous_variant S434S 1302C>A SKCM-US 6 43018889 43018889 single base substitution G T upstream_gene_variant SKCM-US 6 43019204 43019204 single base substitution G A splice_region_variant SKCM-US 6 43019204 43019204 single base substitution G A upstream_gene_variant SKCM-US 6 43019452 43019452 single base substitution C T synonymous_variant E210E 630G>A SKCM-US 6 43019452 43019452 single base substitution C T synonymous_variant E294E 882G>A SKCM-US 6 43019452 43019452 single base substitution C T upstream_gene_variant SKCM-US 6 43019484 43019484 single base substitution G A missense_variant L200F 598C>T SKCM-US 6 43019484 43019484 single base substitution G A missense_variant L284F 850C>T SKCM-US 6 43019484 43019484 single base substitution G A upstream_gene_variant SKCM-US 6 43023662 43023662 single base substitution G A upstream_gene_variant SKCM-US 6 43023883 43023883 single base substitution G A upstream_gene_variant SKCM-US 6 43024063 43024063 single base substitution A C upstream_gene_variant SKCM-US 6 43024176 43024176 single base substitution G A upstream_gene_variant SKCM-US 6 43025923 43025923 single base substitution G A upstream_gene_variant STAD-US 6 43008318 43008318 single base substitution G A stop_gained Q1325* 3973C>T STAD-US 6 43008318 43008318 single base substitution G A stop_gained Q1409* 4225C>T STAD-US 6 43008323 43008323 single base substitution A C missense_variant L1323R 3968T>G STAD-US 6 43008323 43008323 single base substitution A C missense_variant L1407R 4220T>G STAD-US 6 43010580 43010580 single base substitution G A downstream_gene_variant STAD-US 6 43010580 43010580 single base substitution G A missense_variant A1202V 3605C>T STAD-US 6 43010580 43010580 single base substitution G A missense_variant A1286V 3857C>T STAD-US 6 43010695 43010695 single base substitution G A downstream_gene_variant STAD-US 6 43010695 43010695 single base substitution G A missense_variant R1164W 3490C>T STAD-US 6 43010695 43010695 single base substitution G A missense_variant R1248W 3742C>T STAD-US 6 43010844 43010844 single base substitution T C downstream_gene_variant STAD-US 6 43010844 43010844 single base substitution T C missense_variant T1144A 3430A>G STAD-US 6 43010844 43010844 single base substitution T C missense_variant T1228A 3682A>G STAD-US 6 43013029 43013029 single base substitution G A downstream_gene_variant STAD-US 6 43013029 43013029 single base substitution G A missense_variant R1076W 3226C>T STAD-US 6 43013029 43013029 single base substitution G A missense_variant R992W 2974C>T STAD-US 6 43013124 43013124 single base substitution C T downstream_gene_variant STAD-US 6 43013124 43013124 single base substitution C T missense_variant R1044H 3131G>A STAD-US 6 43013124 43013124 single base substitution C T missense_variant R960H 2879G>A STAD-US 6 43013343 43013343 single base substitution G A exon_variant STAD-US 6 43013343 43013343 single base substitution G A synonymous_variant R1032R 3096C>T STAD-US 6 43013343 43013343 single base substitution G A synonymous_variant R948R 2844C>T STAD-US 6 43013345 43013345 single base substitution G A exon_variant STAD-US 6 43013345 43013345 single base substitution G A missense_variant R1032C 3094C>T STAD-US 6 43013345 43013345 single base substitution G A missense_variant R948C 2842C>T STAD-US 6 43013989 43013989 single base substitution C T exon_variant STAD-US 6 43013989 43013989 single base substitution C T missense_variant R882Q 2645G>A STAD-US 6 43013989 43013989 single base substitution C T missense_variant R966Q 2897G>A STAD-US 6 43017368 43017368 single base substitution G A synonymous_variant A534A 1602C>T STAD-US 6 43017368 43017368 single base substitution G A synonymous_variant A618A 1854C>T STAD-US 6 43017368 43017368 single base substitution G A upstream_gene_variant STAD-US 6 43017887 43017887 single base substitution G A synonymous_variant A461A 1383C>T STAD-US 6 43017887 43017887 single base substitution G A synonymous_variant A545A 1635C>T STAD-US 6 43017887 43017887 single base substitution G A upstream_gene_variant STAD-US 6 43018130 43018130 deletion of <=200bp A - frameshift_variant W414 STAD-US 6 43018130 43018130 deletion of <=200bp A - frameshift_variant W498 STAD-US 6 43018130 43018130 deletion of <=200bp A - upstream_gene_variant STAD-US 6 43018788 43018788 single base substitution C T missense_variant R384Q 1151G>A STAD-US 6 43018788 43018788 single base substitution C T missense_variant R468Q 1403G>A STAD-US 6 43018788 43018788 single base substitution C T upstream_gene_variant STAD-US 6 43019075 43019075 single base substitution C A missense_variant E288D 864G>T STAD-US 6 43019075 43019075 single base substitution C A missense_variant E372D 1116G>T STAD-US 6 43019075 43019075 single base substitution C A upstream_gene_variant STAD-US 6 43019974 43019974 single base substitution T G missense_variant I185L 553A>C STAD-US 6 43019974 43019974 single base substitution T G missense_variant I237L 709A>C STAD-US 6 43019974 43019974 single base substitution T G upstream_gene_variant STAD-US 6 43019980 43019980 single base substitution G A missense_variant R183W 547C>T STAD-US 6 43019980 43019980 single base substitution G A missense_variant R235W 703C>T STAD-US 6 43019980 43019980 single base substitution G A upstream_gene_variant STAD-US 6 43020028 43020028 single base substitution T C missense_variant M167V 499A>G STAD-US 6 43020028 43020028 single base substitution T C missense_variant M219V 655A>G STAD-US 6 43020028 43020028 single base substitution T C upstream_gene_variant STAD-US 6 43020085 43020085 single base substitution C T missense_variant A148T 442G>A STAD-US 6 43020085 43020085 single base substitution C T missense_variant A200T 598G>A STAD-US 6 43020085 43020085 single base substitution C T upstream_gene_variant STAD-US 6 43020092 43020092 single base substitution G A synonymous_variant S145S 435C>T STAD-US 6 43020092 43020092 single base substitution G A synonymous_variant S197S 591C>T STAD-US 6 43020092 43020092 single base substitution G A upstream_gene_variant STAD-US 6 43020260 43020260 single base substitution G A synonymous_variant I141I 423C>T STAD-US 6 43020260 43020260 single base substitution G A synonymous_variant I89I 267C>T STAD-US 6 43020260 43020260 single base substitution G A upstream_gene_variant STAD-US 6 43020464 43020464 single base substitution A G synonymous_variant Y21Y 63T>C STAD-US 6 43020464 43020464 single base substitution A G synonymous_variant Y73Y 219T>C STAD-US 6 43020464 43020464 single base substitution A G upstream_gene_variant STAD-US 6 43020479 43020479 single base substitution G A synonymous_variant P16P 48C>T STAD-US 6 43020479 43020479 single base substitution G A synonymous_variant P68P 204C>T STAD-US 6 43020479 43020479 single base substitution G A upstream_gene_variant STAD-US 6 43020511 43020511 single base substitution G A missense_variant R58C 172C>T STAD-US 6 43020511 43020511 single base substitution G A missense_variant R6C 16C>T STAD-US 6 43020511 43020511 single base substitution G A upstream_gene_variant STAD-US 6 43022057 43022057 deletion of <=200bp G - upstream_gene_variant STAD-US 6 43022174 43022174 single base substitution A G upstream_gene_variant STAD-US 6 43023356 43023356 single base substitution C A upstream_gene_variant STAD-US 6 43023644 43023644 single base substitution G A upstream_gene_variant STAD-US 6 43023745 43023745 single base substitution A G upstream_gene_variant STAD-US 6 43023827 43023827 single base substitution C T upstream_gene_variant STAD-US 6 43024071 43024071 single base substitution A C upstream_gene_variant STAD-US 6 43025842 43025842 single base substitution G A upstream_gene_variant UCEC-US 6 43006702 43006702 single base substitution G A stop_gained R1440* 4318C>T UCEC-US 6 43006702 43006702 single base substitution G A stop_gained R1524* 4570C>T UCEC-US 6 43008397 43008397 single base substitution G A downstream_gene_variant UCEC-US 6 43008397 43008397 single base substitution G A synonymous_variant N1298N 3894C>T UCEC-US 6 43008397 43008397 single base substitution G A synonymous_variant N1382N 4146C>T UCEC-US 6 43008685 43008685 single base substitution C A downstream_gene_variant UCEC-US 6 43008685 43008685 single base substitution C A missense_variant L1258F 3774G>T UCEC-US 6 43008685 43008685 single base substitution C A missense_variant L1342F 4026G>T UCEC-US 6 43010621 43010621 single base substitution C T downstream_gene_variant UCEC-US 6 43010621 43010621 single base substitution C T synonymous_variant G1188G 3564G>A UCEC-US 6 43010621 43010621 single base substitution C T synonymous_variant G1272G 3816G>A UCEC-US 6 43011323 43011323 single base substitution A G downstream_gene_variant UCEC-US 6 43011323 43011323 single base substitution A G missense_variant L1073P 3218T>C UCEC-US 6 43011323 43011323 single base substitution A G missense_variant L1157P 3470T>C UCEC-US 6 43013126 43013126 single base substitution C T downstream_gene_variant UCEC-US 6 43013126 43013126 single base substitution C T synonymous_variant T1043T 3129G>A UCEC-US 6 43013126 43013126 single base substitution C T synonymous_variant T959T 2877G>A UCEC-US 6 43013336 43013336 single base substitution G A exon_variant UCEC-US 6 43013336 43013336 single base substitution G A missense_variant R1035C 3103C>T UCEC-US 6 43013336 43013336 single base substitution G A missense_variant R951C 2851C>T UCEC-US 6 43013766 43013766 single base substitution G A exon_variant UCEC-US 6 43013766 43013766 single base substitution G A synonymous_variant C908C 2724C>T UCEC-US 6 43013766 43013766 single base substitution G A synonymous_variant C992C 2976C>T UCEC-US 6 43014049 43014049 single base substitution T A exon_variant UCEC-US 6 43014049 43014049 single base substitution T A missense_variant K862M 2585A>T UCEC-US 6 43014049 43014049 single base substitution T A missense_variant K946M 2837A>T UCEC-US 6 43014723 43014723 single base substitution T C exon_variant UCEC-US 6 43014723 43014723 single base substitution T C synonymous_variant G764G 2292A>G UCEC-US 6 43014723 43014723 single base substitution T C synonymous_variant G848G 2544A>G UCEC-US 6 43014744 43014744 single base substitution C A exon_variant UCEC-US 6 43014744 43014744 single base substitution C A missense_variant K757N 2271G>T UCEC-US 6 43014744 43014744 single base substitution C A missense_variant K841N 2523G>T UCEC-US 6 43015922 43015922 single base substitution G A synonymous_variant C711C 2133C>T UCEC-US 6 43015922 43015922 single base substitution G A synonymous_variant C795C 2385C>T UCEC-US 6 43015922 43015922 single base substitution G A upstream_gene_variant UCEC-US 6 43016230 43016230 single base substitution G T missense_variant L635I 1903C>A UCEC-US 6 43016230 43016230 single base substitution G T missense_variant L719I 2155C>A UCEC-US 6 43016230 43016230 single base substitution G T upstream_gene_variant UCEC-US 6 43017156 43017156 single base substitution G A missense_variant A605V 1814C>T UCEC-US 6 43017156 43017156 single base substitution G A missense_variant A689V 2066C>T UCEC-US 6 43017156 43017156 single base substitution G A upstream_gene_variant UCEC-US 6 43017310 43017310 single base substitution T C missense_variant S554G 1660A>G UCEC-US 6 43017310 43017310 single base substitution T C missense_variant S638G 1912A>G UCEC-US 6 43017310 43017310 single base substitution T C upstream_gene_variant UCEC-US 6 43017322 43017322 single base substitution G A stop_gained R550* 1648C>T UCEC-US 6 43017322 43017322 single base substitution G A stop_gained R634* 1900C>T UCEC-US 6 43017322 43017322 single base substitution G A upstream_gene_variant UCEC-US 6 43017716 43017716 single base substitution C A missense_variant E518D 1554G>T UCEC-US 6 43017716 43017716 single base substitution C A missense_variant E602D 1806G>T UCEC-US 6 43017716 43017716 single base substitution C A upstream_gene_variant UCEC-US 6 43017747 43017747 single base substitution T G missense_variant D508A 1523A>C UCEC-US 6 43017747 43017747 single base substitution T G missense_variant D592A 1775A>C UCEC-US 6 43017747 43017747 single base substitution T G upstream_gene_variant UCEC-US 6 43018738 43018738 single base substitution G A missense_variant R401W 1201C>T UCEC-US 6 43018738 43018738 single base substitution G A missense_variant R485W 1453C>T UCEC-US 6 43018738 43018738 single base substitution G A upstream_gene_variant UCEC-US 6 43018803 43018803 single base substitution G A missense_variant P379L 1136C>T UCEC-US 6 43018803 43018803 single base substitution G A missense_variant P463L 1388C>T UCEC-US 6 43018803 43018803 single base substitution G A upstream_gene_variant UCEC-US 6 43018850 43018850 single base substitution G A synonymous_variant F363F 1089C>T UCEC-US 6 43018850 43018850 single base substitution G A synonymous_variant F447F 1341C>T UCEC-US 6 43018850 43018850 single base substitution G A upstream_gene_variant UCEC-US 6 43018860 43018860 single base substitution C T missense_variant R360H 1079G>A UCEC-US 6 43018860 43018860 single base substitution C T missense_variant R444H 1331G>A UCEC-US 6 43018860 43018860 single base substitution C T upstream_gene_variant UCEC-US 6 43018867 43018867 single base substitution G A missense_variant R358C 1072C>T UCEC-US 6 43018867 43018867 single base substitution G A missense_variant R442C 1324C>T UCEC-US 6 43018867 43018867 single base substitution G A upstream_gene_variant UCEC-US 6 43019016 43019016 single base substitution A G missense_variant V308A 923T>C UCEC-US 6 43019016 43019016 single base substitution A G missense_variant V392A 1175T>C UCEC-US 6 43019016 43019016 single base substitution A G upstream_gene_variant UCEC-US 6 43019173 43019173 single base substitution G A missense_variant R256W 766C>T UCEC-US 6 43019173 43019173 single base substitution G A missense_variant R340W 1018C>T UCEC-US 6 43019173 43019173 single base substitution G A upstream_gene_variant UCEC-US 6 43019484 43019484 single base substitution G T missense_variant L200I 598C>A UCEC-US 6 43019484 43019484 single base substitution G T missense_variant L284I 850C>A UCEC-US 6 43019484 43019484 single base substitution G T upstream_gene_variant UCEC-US 6 43020138 43020138 single base substitution C T missense_variant G130D 389G>A UCEC-US 6 43020138 43020138 single base substitution C T missense_variant G182D 545G>A UCEC-US 6 43020138 43020138 single base substitution C T upstream_gene_variant UCEC-US 6 43020440 43020440 single base substitution G A synonymous_variant R29R 87C>T UCEC-US 6 43020440 43020440 single base substitution G A synonymous_variant R81R 243C>T UCEC-US 6 43020440 43020440 single base substitution G A upstream_gene_variant UCEC-US 6 43022075 43022075 single base substitution C A upstream_gene_variant UCEC-US 6 43022145 43022145 single base substitution C T upstream_gene_variant UCEC-US 6 43023356 43023356 single base substitution C A upstream_gene_variant UCEC-US 6 43023660 43023660 single base substitution C A upstream_gene_variant UCEC-US 6 43023675 43023675 single base substitution T G upstream_gene_variant UCEC-US 6 43023723 43023723 single base substitution C T upstream_gene_variant UCEC-US 6 43023737 43023737 single base substitution G A upstream_gene_variant UCEC-US 6 43024149 43024149 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 TCGA-BR-6452-01 COSM3874194 c.63T>C p.Y21Y Substitution - coding silent 6:43052726-43052726 - GB19 COSM1743124 c.1361T>G p.V454G Substitution - Missense 6:43050271-43050271 - TCGA-AP-A059-01 COSM1079434 c.598C>A p.L200I Substitution - Missense 6:43051746-43051746 - TCGA-B5-A0JY-01 COSM1079427 c.1201C>T p.R401W Substitution - Missense 6:43051000-43051000 - TCGA-ER-A19G-06 COSM3921809 c.598C>T p.L200F Substitution - Missense 6:43051746-43051746 - TCGA-AP-A056-01 COSM1079410 c.3564G>A p.G1188G Substitution - coding silent 6:43042883-43042883 - ESO-1872 COSM1249462 c.3839T>C p.V1280A Substitution - Missense 6:43040714-43040714 - TCGA-AY-6197-01 COSM1444626 c.364C>A p.L122I Substitution - Missense 6:43052425-43052425 - TCGA-AP-A059-01 COSM1079420 c.1814C>T p.A605V Substitution - Missense 6:43049418-43049418 - LP6005690-DNA_C01 COSM4409313 c.548G>A p.R183Q Substitution - Missense 6:43052241-43052241 - YUWIA COSM5405357 c.3167C>T p.S1056F Substitution - Missense 6:43044757-43044757 - PTC-14C COSM4161208 c.1212C>T p.N404N Substitution - coding silent 6:43050989-43050989 - 5 COSM5732245 c.1600G>T p.A534S Substitution - Missense 6:43049632-43049632 - ME009T COSM223088 c.2523G>A p.W841* Substitution - Nonsense 6:43046373-43046373 - CHC923T COSM4801417 c.2100G>A p.L700L Substitution - coding silent 6:43048217-43048217 - 587238 COSM1202693 c.4345A>G p.T1449A Substitution - Missense 6:43038937-43038937 - 401 COSM1079410 c.3564G>A p.G1188G Substitution - coding silent 6:43042883-43042883 - TCGA-BS-A0UV-01 COSM1079423 c.1554G>T p.E518D Substitution - Missense 6:43049978-43049978 - TCGA-BH-A0DZ-01 COSM451492 c.3463-2A>C p.? Unknown 6:43042986-43042986 - TCGA-AP-A0LM-01 COSM1079429 c.1089C>T p.F363F Substitution - coding silent 6:43051112-43051112 - S01366 COSM310418 c.2701A>G p.M901V Substitution - Missense 6:43046051-43046051 - 8047575 COSM3394207 c.3588G>A p.A1196A Substitution - coding silent 6:43042859-43042859 - TCGA-AP-A051-01 COSM1079436 c.87C>T p.R29R Substitution - coding silent 6:43052702-43052702 - TCGA-BR-8382-01 COSM3874191 c.499A>G p.M167V Substitution - Missense 6:43052290-43052290 - TCGA-AA-3542-01 COSM291984 c.3328C>A p.P1110T Substitution - Missense 6:43043475-43043475 - TCGA-E2-A158-01 COSM451498 c.1825+1G>A p.? Unknown 6:43049406-43049406 - CSCC-55-T COSM4488734 c.3123C>A p.T1041T Substitution - coding silent 6:43044801-43044801 - LUAD-F00121 COSM365857 c.436G>A p.A146T Substitution - Missense 6:43052353-43052353 - TCGA-AX-A05Z-01 COSM1079431 c.1072C>T p.R358C Substitution - Missense 6:43051129-43051129 - AOCS-064-3-3 COSM4153416 c.982G>A p.G328S Substitution - Missense 6:43051219-43051219 - RK194_C01 COSM1634807 c.4441-6C>T p.? Unknown 6:43038698-43038698 - TCGA-BR-8363-01 COSM3874186 c.1602C>T p.A534A Substitution - coding silent 6:43049630-43049630 - TCGA-AD-5900-01 COSM1444622 c.2064-2A>G p.? Unknown 6:43048255-43048255 - AOCS-064-1-6 COSM4153416 c.982G>A p.G328S Substitution - Missense 6:43051219-43051219 - K338 COSM249298 c.733-2_735delAGGTC p.? Unknown 6:43051466-43051470 - 5202_PT COSM5756869 c.1397C>T p.P466L Substitution - Missense 6:43050135-43050135 - TCGA-CG-5728-01 COSM3874187 c.1383C>T p.A461A Substitution - coding silent 6:43050149-43050149 - TCGA-AZ-6601-01 COSM1444620 c.3508C>T p.P1170S Substitution - Missense 6:43042939-43042939 - PA167 COSM1162562 c.4429A>T p.N1477Y Substitution - Missense 6:43038853-43038853 - SNUH_G16_S1 COSM3684317 c.2803C>T p.L935L Substitution - coding silent 6:43045646-43045646 - 2492729 COSM5726550 c.701C>T p.P234L Substitution - Missense 6:43051643-43051643 - T3202 COSM4675609 c.2916G>A p.T972T Substitution - coding silent 6:43045349-43045349 - TCGA-G3-A25T-01 COSM4941739 c.1837C>A p.P613T Substitution - Missense 6:43048558-43048558 - TCGA-AX-A0J1-01 COSM1079414 c.2851C>T p.R951C Substitution - Missense 6:43045598-43045598 - ESCC_122 COSM5640792 c.1055G>T p.R352M Substitution - Missense 6:43051146-43051146 - TCGA-F5-6814-01 COSM3430684 c.1612G>T p.E538* Substitution - Nonsense 6:43049620-43049620 - HT115 COSM3079702 c.17G>A p.R6H Substitution - Missense 6:43052772-43052772 - TCGA-BR-8284-01 COSM3874185 c.2645G>A p.R882Q Substitution - Missense 6:43046251-43046251 - TCGA-46-3765-01 COSM742919 c.3924G>T p.L1308L Substitution - coding silent 6:43040629-43040629 - BD183T COSM5508057 c.240G>C p.K80N Substitution - Missense 6:43052549-43052549 - RK308_C01 COSM3745248 c.3896G>A p.R1299H Substitution - Missense 6:43040657-43040657 - TCGA-A8-A0A6-01 COSM3830564 c.2865T>G p.G955G Substitution - coding silent 6:43045400-43045400 - TCGA-AX-A0J1-01 COSM1079432 c.923T>C p.V308A Substitution - Missense 6:43051278-43051278 - TCGA-AP-A059-01 COSM1079430 c.1079G>A p.R360H Substitution - Missense 6:43051122-43051122 - TCGA-D1-A103-01 COSM1079413 c.2877G>A p.T959T Substitution - coding silent 6:43045388-43045388 - TCGA-A6-2672-01 COSM291005 c.2006T>C p.L669P Substitution - Missense 6:43048389-43048389 - RK233_C01 COSM4778530 c.1924C>T p.L642F Substitution - Missense 6:43048471-43048471 - RK210_C01 COSM3745250 c.3658T>C p.F1220L Substitution - Missense 6:43041063-43041063 - TCGA-B5-A0JY-01 COSM1079435 c.389G>A p.G130D Substitution - Missense 6:43052400-43052400 - B86-Tumor COSM1754815 c.3376G>T p.D1126Y Substitution - Missense 6:43043160-43043160 - TCGA-D3-A2JF-06 COSM3627466 c.735C>T p.V245V Substitution - coding silent 6:43051466-43051466 - 0076_CRUK_PC_0076_T1_DNA COSM5422733 c.2585A>C p.K862T Substitution - Missense 6:43046311-43046311 - TCGA-DA-A1HV-06 COSM3627461 c.2783C>T p.S928F Substitution - Missense 6:43045666-43045666 - TCGA-D3-A1Q7-06 COSM3627462 c.2697T>A p.S899R Substitution - Missense 6:43046055-43046055 - RK308_C01 COSM3745249 c.3819G>A p.A1273A Substitution - coding silent 6:43040734-43040734 - K127 COSM249494 c.4802G>A p.C1601Y Substitution - Missense 6:43037983-43037983 - TCGA-AC-A23H-01 COSM3830565 c.1477G>C p.E493Q Substitution - Missense 6:43050055-43050055 - CN-AML-NR-08-Dx COSM5425417 c.3993G>A p.L1331L Substitution - coding silent 6:43040560-43040560 - TCGA-HU-A4H3-01 COSM3079693 c.442G>A p.A148T Substitution - Missense 6:43052347-43052347 - 587336 COSM1202691 c.2878C>T p.R960C Substitution - Missense 6:43045387-43045387 - CSCC-49-T COSM4475341 c.1728C>T p.N576N Substitution - coding silent 6:43049504-43049504 - WA25 COSM239486 c.3512G>A p.R1171H Substitution - Missense 6:43042935-43042935 - YUKAT COSM5405359 c.2902G>A p.G968S Substitution - Missense 6:43045363-43045363 - SJRHB047 COSM3737209 c.78_79insCGCCAG p.R29_V30insQR Insertion - In frame 6:43052710-43052711 - TCGA-DD-A114-01 COSM4925420 c.3007G>A p.D1003N Substitution - Missense 6:43045258-43045258 - PTC-28C COSM4161207 c.2259C>T p.D753D Substitution - coding silent 6:43047018-43047018 - ESOCB11T COSM1173230 c.1981C>T p.R661W Substitution - Missense 6:43048414-43048414 - TCGA-D7-8579-01 COSM3874189 c.553A>C p.I185L Substitution - Missense 6:43052236-43052236 - TCGA-13-0883-01 COSM70346 c.1603G>A p.V535M Substitution - Missense 6:43049629-43049629 - TCGA-UB-A7MA-01 COSM4910044 c.5016C>T p.T1672T Substitution - coding silent 6:43037769-43037769 - ESO-887 COSM1249464 c.544G>A p.G182S Substitution - Missense 6:43052245-43052245 - TCGA-EE-A20C-06 COSM3627464 c.2050C>T p.L684L Substitution - coding silent 6:43048345-43048345 - TCGA-D7-8579-01 COSM3874193 c.267C>T p.I89I Substitution - coding silent 6:43052522-43052522 - AOCS-139-1-5 COSM4153417 c.653G>A p.R218H Substitution - Missense 6:43051691-43051691 - TCGA-HU-A4GQ-01 COSM3874184 c.2842C>T p.R948C Substitution - Missense 6:43045607-43045607 - T24 COSM5425417 c.3993G>A p.L1331L Substitution - coding silent 6:43040560-43040560 - PD4954a COSM5778295 c.1234-4C>G p.? Unknown 6:43050402-43050402 - HCC87 COSM1621677 c.2639T>G p.M880R Substitution - Missense 6:43046257-43046257 - CSCC-5-T COSM4462054 c.978C>T p.S326S Substitution - coding silent 6:43051223-43051223 - TCGA-BR-8059-01 COSM3874181 c.2974C>T p.R992W Substitution - Missense 6:43045291-43045291 - CHC059T COSM4803115 c.2722T>G p.C908G Substitution - Missense 6:43046030-43046030 - TCGA-HC-7080-01 COSM3674711 c.4375G>T p.G1459W Substitution - Missense 6:43038907-43038907 - TCGA-LP-A5U2-01 COSM4833921 c.5039C>T p.S1680F Substitution - Missense 6:43037746-43037746 - PT37 COSM5918893 c.3856G>A p.G1286R Substitution - Missense 6:43040697-43040697 - BD124T COSM5492076 c.273C>A p.P91P Substitution - coding silent 6:43052516-43052516 - TCGA-C5-A7CO-01 COSM4856288 c.4668C>T p.D1556D Substitution - coding silent 6:43038372-43038372 - Gp5D COSM3079640 c.2810A>G p.N937S Substitution - Missense 6:43045639-43045639 - TCGA-B5-A0JV-01 COSM1079417 c.2271G>T p.K757N Substitution - Missense 6:43047006-43047006 - K48-Tumor COSM249271 c.3416T>C p.I1139T Substitution - Missense 6:43043120-43043120 - SC_9047 COSM5553581 c.1407A>C p.E469D Substitution - Missense 6:43050125-43050125 - ME001T COSM221722 c.1714G>T p.A572S Substitution - Missense 6:43049518-43049518 - TCGA-BR-8361-01 COSM3874178 c.3968T>G p.L1323R Substitution - Missense 6:43040585-43040585 - MT-198-T2 COSM5651358 c.786G>T p.S262S Substitution - coding silent 6:43051415-43051415 - TCGA-B0-5691-01 COSM484090 c.630G>C p.E210D Substitution - Missense 6:43051714-43051714 - PCSI_0083_Pa_X COSM3381600 c.1151G>A p.R384Q Substitution - Missense 6:43051050-43051050 - TCGA-CD-A4MG-01 COSM3874183 c.2844C>T p.R948R Substitution - coding silent 6:43045605-43045605 - TCGA-CD-A4MG-01 COSM3874180 c.3430A>G p.T1144A Substitution - Missense 6:43043106-43043106 - TCGA-HU-A4G8-01 COSM3874182 c.2879G>A p.R960H Substitution - Missense 6:43045386-43045386 - TCGA-H4-A2HQ-01 COSM1312224 c.4496A>G p.N1499S Substitution - Missense 6:43038637-43038637 - C608 COSM4443049 c.1205A>C p.Q402P Substitution - Missense 6:43050996-43050996 - CSCC-44-T COSM596623 c.877G>C p.E293Q Substitution - Missense 6:43051324-43051324 - PD3996a COSM160284 c.2040G>T p.R680S Substitution - Missense 6:43048355-43048355 - CHC923T COSM4801417 c.2100G>A p.L700L Substitution - coding silent 6:43048217-43048217 - T3262 COSM4675613 c.1257C>T p.R419R Substitution - coding silent 6:43050375-43050375 - ESCC_54 COSM5631573 c.3951G>C p.Q1317H Substitution - Missense 6:43040602-43040602 - 401 COSM4429687 c.3565C>A p.P1189T Substitution - Missense 6:43042882-43042882 - TCGA-A8-A076-01 COSM451496 c.1870C>A p.L624M Substitution - Missense 6:43048525-43048525 - T96 COSM3079700 c.122G>A p.R41H Substitution - Missense 6:43052667-43052667 - TCGA-EB-A5UL-06 COSM3921806 c.2916G>T p.T972T Substitution - coding silent 6:43045349-43045349 - PD9702a COSM5772671 c.3229G>C p.E1077Q Substitution - Missense 6:43043574-43043574 - CN-AML-08-T COSM5425417 c.3993G>A p.L1331L Substitution - coding silent 6:43040560-43040560 - SNUH_G26_S1 COSM4004046 c.339C>T p.D113D Substitution - coding silent 6:43052450-43052450 - TCGA-AA-3663-01 COSM1444619 c.3743G>A p.C1248Y Substitution - Missense 6:43040978-43040978 - TCGA-A1-A0SF-01 COSM1487772 c.1150C>T p.R384W Substitution - Missense 6:43051051-43051051 - TCGA-AA-3663-01 COSM1444618 c.3769G>A p.G1257S Substitution - Missense 6:43040952-43040952 - TCGA-AP-A051-01 COSM1079408 c.3894C>T p.N1298N Substitution - coding silent 6:43040659-43040659 - TCGA-AP-A056-01 COSM188584 c.2724C>T p.C908C Substitution - coding silent 6:43046028-43046028 - C658 COSM3928473 c.3448G>A p.V1150M Substitution - Missense 6:43043088-43043088 - CSB1 COSM5026545 c.4902G>A p.L1634L Substitution - coding silent 6:43037883-43037883 - TCGA-HU-A4GX-01 COSM3874177 c.3973C>T p.Q1325* Substitution - Nonsense 6:43040580-43040580 - S01366 COSM310418 c.2701A>G p.M901V Substitution - Missense 6:43046051-43046051 - SC_9083 COSM5553763 c.72G>A p.E24E Substitution - coding silent 6:43052717-43052717 - TCGA-E9-A295-01 COSM1487774 c.909G>C p.L303L Substitution - coding silent 6:43051292-43051292 - TCGA-BS-A0UF-01 COSM1079424 c.1523A>C p.D508A Substitution - Missense 6:43050009-43050009 - MO_1410 COSM4856288 c.4668C>T p.D1556D Substitution - coding silent 6:43038372-43038372 - 2293756 COSM4606847 c.1868G>A p.R623H Substitution - Missense 6:43048527-43048527 - SNU-C2B COSM3079621 c.3943C>T p.Q1315* Substitution - Nonsense 6:43040610-43040610 - CCK81 COSM3079680 c.958C>T p.P320S Substitution - Missense 6:43051243-43051243 - TCGA-AP-A0LM-01 COSM1079422 c.1648C>T p.R550* Substitution - Nonsense 6:43049584-43049584 - Pat_41_B COSM5870691 c.748C>T p.L250F Substitution - Missense 6:43051453-43051453 - TCGA-BS-A0UJ-01 COSM1079411 c.3218T>C p.L1073P Substitution - Missense 6:43043585-43043585 - TCGA-BK-A0C9-01 COSM1079426 c.1415C>T p.A472V Substitution - Missense 6:43050117-43050117 - ESO-0590 COSM1249459 c.2604C>T p.N868N Substitution - coding silent 6:43046292-43046292 - 5202_CLM COSM5756869 c.1397C>T p.P466L Substitution - Missense 6:43050135-43050135 - Pat_41_B COSM5870687 c.2410C>T p.Q804* Substitution - Nonsense 6:43046589-43046589 - MCF7 COSM484089 c.1594G>A p.E532K Substitution - Missense 6:43049638-43049638 - MOLT-4 COSM1079426 c.1415C>T p.A472V Substitution - Missense 6:43050117-43050117 - TCGA-B5-A11H-01 COSM1079428 c.1136C>T p.P379L Substitution - Missense 6:43051065-43051065 - BRC32 COSM5026547 c.402T>C p.P134P Substitution - coding silent 6:43052387-43052387 - TCGA-CD-A4MI-01 COSM3381600 c.1151G>A p.R384Q Substitution - Missense 6:43051050-43051050 - LUAD-D02185 COSM338819 c.4881C>T p.H1627H Substitution - coding silent 6:43037904-43037904 - HCC10T COSM131368 c.2368A>T p.I790F Substitution - Missense 6:43046909-43046909 - RK245_C01 COSM4945116 c.4676A>C p.N1559T Substitution - Missense 6:43038364-43038364 - WA51 COSM239487 c.718A>G p.I240V Substitution - Missense 6:43051626-43051626 - YUDEDE COSM1697245 c.1339C>T p.Q447* Substitution - Nonsense 6:43050293-43050293 - TCGA-BG-A0VZ-01 COSM1079421 c.1660A>G p.S554G Substitution - Missense 6:43049572-43049572 - SC_9104 COSM5572381 c.4645T>C p.Y1549H Substitution - Missense 6:43038395-43038395 - PD2152a COSM28458 c.1430T>A p.L477Q Substitution - Missense 6:43050102-43050102 - TCGA-BT-A20J-01 COSM421305 c.3937G>C p.E1313Q Substitution - Missense 6:43040616-43040616 - 1N26-VS-1T26 COSM4973545 c.3553G>A p.E1185K Substitution - Missense 6:43042894-43042894 - ESO-173 COSM1249461 c.3665G>A p.R1222Q Substitution - Missense 6:43041056-43041056 - TCGA-AC-A23H-01 COSM3830563 c.2934G>A p.R978R Substitution - coding silent 6:43045331-43045331 - 326_CLM COSM5756871 c.1034C>T p.A345V Substitution - Missense 6:43051167-43051167 - T578 COSM4675619 c.711C>T p.F237F Substitution - coding silent 6:43051633-43051633 - TCGA-CG-4306-01 COSM3874190 c.547C>T p.R183W Substitution - Missense 6:43052242-43052242 - TCGA-13-1492-01 COSM70345 c.2833A>G p.I945V Substitution - Missense 6:43045616-43045616 - C10 COSM4616635 c.4446C>A p.V1482V Substitution - coding silent 6:43038687-43038687 - TCGA-FS-A4F9-06 COSM3627459 c.3895C>T p.R1299C Substitution - Missense 6:43040658-43040658 - ESO-081 COSM1243191 c.1423T>C p.Y475H Substitution - Missense 6:43050109-43050109 - 587234 COSM1202692 c.3056G>A p.R1019H Substitution - Missense 6:43044868-43044868 - TCGA-A5-A0VQ-01 COSM1079418 c.2133C>T p.C711C Substitution - coding silent 6:43048184-43048184 - ATL058 COSM5710140 c.887T>A p.F296Y Substitution - Missense 6:43051314-43051314 - TCGA-LP-A5U2-01 COSM4833903 c.4994C>G p.S1665* Substitution - Nonsense 6:43037791-43037791 - TCGA-CM-6676-01 COSM1444621 c.2957G>A p.R986H Substitution - Missense 6:43045308-43045308 - PCSI_0083_Pa_P_526 COSM3381600 c.1151G>A p.R384Q Substitution - Missense 6:43051050-43051050 - CSCC-54-T COSM4544610 c.3351G>A p.R1117R Substitution - coding silent 6:43043452-43043452 - HCT15 COSM3079686 c.786G>A p.S262S Substitution - coding silent 6:43051415-43051415 - ESO-805 COSM1249463 c.2885G>A p.R962Q Substitution - Missense 6:43045380-43045380 - T3091 COSM4675611 c.2201G>A p.R734H Substitution - Missense 6:43047076-43047076 - 9113_T COSM5040942 c.4454A>G p.E1485G Substitution - Missense 6:43038679-43038679 - 2492730 COSM5728509 c.1639C>T p.L547L Substitution - coding silent 6:43049593-43049593 - 90482 COSM329289 c.45G>A p.G15G Substitution - coding silent 6:43052744-43052744 - AOCS-094-1-1 COSM4153415 c.3391G>T p.A1131S Substitution - Missense 6:43043145-43043145 - LUAD-S01409 COSM346854 c.1113G>T p.L371F Substitution - Missense 6:43051088-43051088 - PT49 COSM5935104 c.4030C>T p.L1344F Substitution - Missense 6:43040420-43040420 - 326_PT COSM5756871 c.1034C>T p.A345V Substitution - Missense 6:43051167-43051167 - TCGA-GV-A3QH-01 COSM1312226 c.3288C>T p.L1096L Substitution - coding silent 6:43043515-43043515 - TCGA-C8-A26Y-01 COSM3830561 c.4924C>T p.Q1642* Substitution - Nonsense 6:43037861-43037861 - 50 COSM5014602 c.400C>G p.P134A Substitution - Missense 6:43052389-43052389 - TCGA-D1-A163-01 COSM1079425 c.1520C>A p.P507H Substitution - Missense 6:43050012-43050012 - TCGA-E2-A15O-01 COSM451494 c.2203delC p.L735fs*1 Deletion - Frameshift 6:43047074-43047074 - CRC-19T COSM5482061 c.88G>A p.V30M Substitution - Missense 6:43052701-43052701 - TCGA-D9-A6EC-06 COSM4401483 c.2281A>T p.K761* Substitution - Nonsense 6:43046996-43046996 - UM-SCC-17B COSM4598227 c.3930_3937delCTCTAAGG p.S1311fs*65 Deletion - Frameshift 6:43040616-43040623 - TCGA-BR-8361-01 COSM3874179 c.3490C>T p.R1164W Substitution - Missense 6:43042957-43042957 - TCGA-EE-A2GC-06 COSM3921808 c.630G>A p.E210E Substitution - coding silent 6:43051714-43051714 - DLD1 COSM3079686 c.786G>A p.S262S Substitution - coding silent 6:43051415-43051415 - LC_C18 COSM1187038 c.2487G>C p.Q829H Substitution - Missense 6:43046512-43046512 - ATL059 COSM3079634 c.3275G>A p.R1092Q Substitution - Missense 6:43043528-43043528 - TCGA-HU-A4H4-01 COSM3874195 c.48C>T p.P16P Substitution - coding silent 6:43052741-43052741 - TCGA-AP-A056-01 COSM1079433 c.766C>T p.R256W Substitution - Missense 6:43051435-43051435 - TCGA-EE-A2MJ-06 COSM3627465 c.1050C>A p.S350S Substitution - coding silent 6:43051151-43051151 - TCGA-JW-A5VJ-01 COSM4818582 c.376G>A p.E126K Substitution - Missense 6:43052413-43052413 - PTC-14C COSM4161205 c.4492C>A p.L1498I Substitution - Missense 6:43038641-43038641 - OSCC-GB_01360111 COSM5955566 c.1333G>A p.E445K Substitution - Missense 6:43050299-43050299 - ESCC-158T COSM3941762 c.839C>G p.S280C Substitution - Missense 6:43051362-43051362 - TCGA-EE-A3JD-06 COSM4395110 c.3876C>T p.I1292I Substitution - coding silent 6:43040677-43040677 - JVM-2 COSM1739302 c.771T>G p.Y257* Substitution - Nonsense 6:43051430-43051430 - B86 COSM1754815 c.3376G>T p.D1126Y Substitution - Missense 6:43043160-43043160 - TCGA-CW-6093-01 COSM484088 c.2966A>G p.Y989C Substitution - Missense 6:43045299-43045299 - Gp2D COSM4611839 c.3193_3194insC p.L1065fs*43 Insertion - Frameshift 6:43043609-43043610 - PTC-28C COSM4161206 c.3096C>T p.D1032D Substitution - coding silent 6:43044828-43044828 - PTC-28C COSM4161209 c.1202G>A p.R401Q Substitution - Missense 6:43050999-43050999 - TCGA-A2-A3XY-01 COSM3830562 c.3435C>A p.R1145R Substitution - coding silent 6:43043101-43043101 - U2940 COSM5620609 c.4999C>T p.P1667S Substitution - Missense 6:43037786-43037786 - SNUH_G10_S1 COSM4004046 c.339C>T p.D113D Substitution - coding silent 6:43052450-43052450 - TCGA-AA-3492-01 COSM1444624 c.1171_1173delGAG p.E391delE Deletion - In frame 6:43051028-43051030 - LUAD-E00897 COSM364701 c.1759G>A p.E587K Substitution - Missense 6:43049473-43049473 - NCI-H716 COSM4647029 c.4356C>G p.G1452G Substitution - coding silent 6:43038926-43038926 - PCSI_0083_Pa_P COSM3381600 c.1151G>A p.R384Q Substitution - Missense 6:43051050-43051050 - TCGA-BR-7851-01 COSM3874192 c.435C>T p.S145S Substitution - coding silent 6:43052354-43052354 - T2197 COSM4675605 c.4643C>T p.T1548M Substitution - Missense 6:43038397-43038397 - HCT8 COSM4635407 c.1923C>A p.A641A Substitution - coding silent 6:43048472-43048472 - SW48 COSM3079644 c.2610C>T p.S870S Substitution - coding silent 6:43046286-43046286 - 3N46-VS-3T46 COSM4982552 c.3362G>A p.R1121K Substitution - Missense 6:43043174-43043174 - YUKAT COSM5405361 c.1078C>T p.R360C Substitution - Missense 6:43051123-43051123 - B23-Tumor COSM1754816 c.2677G>A p.V893M Substitution - Missense 6:43046075-43046075 - TCGA-AG-3909-01 COSM258825 c.2819G>A p.R940H Substitution - Missense 6:43045630-43045630 - TCGA-EE-A2GR-06 COSM3627463 c.2372C>T p.T791I Substitution - Missense 6:43046905-43046905 - MOLT-4 COSM221722 c.1714G>T p.A572S Substitution - Missense 6:43049518-43049518 - TCGA-HU-A4GN-01 COSM3874188 c.864G>T p.E288D Substitution - Missense 6:43051337-43051337 - CSCC-32-T COSM4491062 c.3486C>T p.S1162S Substitution - coding silent 6:43042961-43042961 - Au4 COSM5603318 c.347C>T p.S116F Substitution - Missense 6:43052442-43052442 - ACINAR03 COSM1734552 c.4861G>A p.V1621I Substitution - Missense 6:43037924-43037924 - YUMOBER COSM5405363 c.793G>A p.D265N Substitution - Missense 6:43051408-43051408 - TCGA-66-2757-01 COSM742918 c.447C>A p.S149R Substitution - Missense 6:43052342-43052342 - PD5950a COSM5802551 c.2874_2875insA p.T959fs*55 Insertion - Frameshift 6:43045390-43045391 - HCC87T COSM1621677 c.2639T>G p.M880R Substitution - Missense 6:43046257-43046257 - B23 COSM1754816 c.2677G>A p.V893M Substitution - Missense 6:43046075-43046075 - TCGA-24-1562-01 COSM74295 c.532C>T p.R178C Substitution - Missense 6:43052257-43052257 - ESO-1060 COSM1249460 c.4902G>C p.L1634L Substitution - coding silent 6:43037883-43037883 - TCGA-B0-5713-01 COSM484089 c.1594G>A p.E532K Substitution - Missense 6:43049638-43049638 - Pat_76_A COSM5870693 c.586C>T p.R196W Substitution - Missense 6:43051758-43051758 - T3658 COSM4675621 c.427G>A p.V143M Substitution - Missense 6:43052362-43052362 - TCGA-BP-4965-01 COSM1496401 c.1224T>C p.P408P Substitution - coding silent 6:43050977-43050977 - TCGA-GD-A3OP-01 COSM1312227 c.3120G>C p.K1040N Substitution - Missense 6:43044804-43044804 - TCGA-AN-A0FZ-01 COSM451490 c.5042G>A p.R1681Q Substitution - Missense 6:43037743-43037743 - ESCC_BICR_048T COSM5432392 c.2492C>T p.S831F Substitution - Missense 6:43046404-43046404 - RK308_C01 COSM3745251 c.1400T>C p.M467T Substitution - Missense 6:43050132-43050132 - HCC075T COSM5821997 c.1236A>G p.V412V Substitution - coding silent 6:43050396-43050396 - KYSE-450 COSM3079611 c.4431C>T p.N1477N Substitution - coding silent 6:43038851-43038851 - TCGA-F5-6814-01 COSM3430683 c.4442C>T p.A1481V Substitution - Missense 6:43038691-43038691 - TCGA-CG-5723-01 COSM1672422 c.3605C>T p.A1202V Substitution - Missense 6:43042842-43042842 - SNU-283 COSM3079660 c.1781C>T p.A594V Substitution - Missense 6:43049451-43049451 - T3021 COSM4675617 c.716G>A p.G239D Substitution - Missense 6:43051628-43051628 - TCGA-D8-A1XK-01 COSM3830566 c.1087T>C p.F363L Substitution - Missense 6:43051114-43051114 - cSCCP6 COSM143641 c.3665_3666GG>AA p.R1222Q Substitution - Missense 6:43041055-43041056 - LUAD-QJN9L COSM342733 c.4818G>C p.L1606F Substitution - Missense 6:43037967-43037967 - TCGA-BS-A0U8-01 COSM1079415 c.2585A>T p.K862M Substitution - Missense 6:43046311-43046311 - BD183T COSM5508055 c.357G>C p.Q119H Substitution - Missense 6:43052432-43052432 - TCGA-AP-A0LT-01 COSM1079409 c.3774G>T p.L1258F Substitution - Missense 6:43040947-43040947 - TCGA-HE-7130-01 COSM3994982 c.3733C>T p.L1245L Substitution - coding silent 6:43040988-43040988 - TCGA-BS-A0TA-01 COSM1079412 c.2915C>T p.T972M Substitution - Missense 6:43045350-43045350 - 19M COSM5405361 c.1078C>T p.R360C Substitution - Missense 6:43051123-43051123 - C0062T COSM4155231 c.5001C>T p.P1667P Substitution - coding silent 6:43037784-43037784 - SC_9100 COSM5569141 c.3395C>T p.T1132I Substitution - Missense 6:43043141-43043141 - SNUH_G76_S1 COSM3684317 c.2803C>T p.L935L Substitution - coding silent 6:43045646-43045646 - Pat_16_B COSM5870685 c.3329delC p.P1110fs*31 Deletion - Frameshift 6:43043474-43043474 - SNU-175 COSM3079629 c.3491G>A p.R1164Q Substitution - Missense 6:43042956-43042956 - YUOMEGA COSM5405355 c.3276G>A p.R1092R Substitution - coding silent 6:43043527-43043527 - Pat_66_A COSM5870695 c.340G>A p.V114M Substitution - Missense 6:43052449-43052449 - TCGA-DU-5874-01 COSM3928473 c.3448G>A p.V1150M Substitution - Missense 6:43043088-43043088 - TCGA-36-2537-01 COSM1329677 c.4173G>A p.V1391V Substitution - coding silent 6:43040277-43040277 - TCGA-E5-A2PC-01 COSM1312225 c.4162G>A p.E1388K Substitution - Missense 6:43040288-43040288 - TCGA-BS-A0UJ-01 COSM1079416 c.2292A>G p.G764G Substitution - coding silent 6:43046985-43046985 - TCGA-CW-5580-01 COSM484091 c.523T>G p.Y175D Substitution - Missense 6:43052266-43052266 - T368 COSM4675607 c.4253T>C p.L1418P Substitution - Missense 6:43040197-43040197 - TCGA-BR-6566-01 COSM3874196 c.16C>T p.R6C Substitution - Missense 6:43052773-43052773 - LUAD-E00934 COSM403428 c.3350G>T p.R1117L Substitution - Missense 6:43043453-43043453 - TCGA-D1-A17Q-01 COSM1079407 c.4318C>T p.R1440* Substitution - Nonsense 6:43038964-43038964 - T3182 COSM4675615 c.1120C>T p.R374W Substitution - Missense 6:43051081-43051081 - K48 COSM249271 c.3416T>C p.I1139T Substitution - Missense 6:43043120-43043120 - OSCC-GB_00560111 COSM4883764 c.3190C>A p.P1064T Substitution - Missense 6:43043613-43043613 - MEL-Ma-Mel-55 COSM1167732 c.5075delA p.Q1692fs*>7 Deletion - Frameshift 6:43037710-43037710 - GC1_T COSM150090 c.3511C>G p.R1171G Substitution - Missense 6:43042936-43042936 - TCGA-G4-6293-01 COSM1444625 c.1103C>T p.T368I Substitution - Missense 6:43051098-43051098 - PT18_1 COSM5899260 c.1768C>T p.L590F Substitution - Missense 6:43049464-43049464 - CHC059T COSM4803115 c.2722T>G p.C908G Substitution - Missense 6:43046030-43046030 - TCGA-BH-A0BW-01 COSM451497 c.1865A>T p.Q622L Substitution - Missense 6:43048530-43048530 - LS411 COSM3079614 c.4282T>C p.F1428L Substitution - Missense 6:43040168-43040168 - HCC108T COSM1621676 c.3231A>T p.E1077D Substitution - Missense 6:43043572-43043572 - TCGA-EE-A3J8-06 COSM3627460 c.3190C>T p.P1064S Substitution - Missense 6:43043613-43043613 - NB-1942 COSM1284364 c.804C>T p.N268N Substitution - coding silent 6:43051397-43051397 - TCGA-AP-A056-01 COSM1079419 c.1903C>A p.L635I Substitution - Missense 6:43048492-43048492 - TCGA-BF-A3DM-01 COSM3921807 c.2485C>T p.Q829* Substitution - Nonsense 6:43046514-43046514 - TCGA-AZ-6601-01 COSM1444616 c.4898C>T p.T1633M Substitution - Missense 6:43037887-43037887 - H1155 COSM1196151 c.4160C>T p.P1387L Substitution - Missense 6:43040290-43040290 - Pat_44_A COSM5870689 c.1223C>T p.P408L Substitution - Missense 6:43050978-43050978 - TC71 COSM3079659 c.1782G>A p.A594A Substitution - coding silent 6:43049450-43049450 - MOLT-4 COSM1672422 c.3605C>T p.A1202V Substitution - Missense 6:43042842-43042842 - HCC108 COSM1621676 c.3231A>T p.E1077D Substitution - Missense 6:43043572-43043572 - STC263 COSM5061802 c.3272C>T p.S1091L Substitution - Missense 6:43043531-43043531 - DN111A7 COSM5962031 c.3151G>C p.V1051L Substitution - Missense 6:43044773-43044773 - SC_9081 COSM5569427 c.461C>T p.T154I Substitution - Missense 6:43052328-43052328 - 18195 COSM1312225 c.4162G>A p.E1388K Substitution - Missense 6:43040288-43040288 - CSCC-17-T COSM4488673 c.3112C>T p.L1038L Substitution - coding silent 6:43044812-43044812 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.520136 6p21.1 609577

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.Y227D c.679T>G 6 43020004 RCCC A G Missense p.V1364A c.4091T>C 6 43008452 ESCA A G Missense p.W578R c.1732T>C 6 43017790 LUAD A G Synonymous p.P186P c.558T>C 6 43020125 BRCA A T Missense p.S983R c.2949T>A 6 43013793 CM C A Missense p.G1543W c.4627G>T 6 43006645 PRAD C A Missense p.G606W c.1816G>T 6 43017706 CM C A Missense p.K841N c.2523G>T 6 43014744 UCEC C A Missense p.L1342F c.4026G>T 6 43008685 UCEC C A Missense p.R1178L c.3533G>T 6 43011260 LUAD C A Missense p.R764S c.2292G>T 6 43016093 BRCA C A Synonymous p.L1392L c.4176G>T 6 43008367 LUSC C G IntronicSNV . c.3607+5G>C 6 43011181 CM C G Missense p.E1397Q c.4189G>C 6 43008354 BLCA C G Missense p.E294D c.882G>C 6 43019452 RCCC C G Missense p.E377Q c.1129G>C 6 43019062 LUAD C G Missense p.K1124N c.3372G>C 6 43012542 BLCA C G Missense p.K1515N c.4545G>C 6 43007895 HNSC C G Missense p.L455F c.1365G>C 6 43018826 LUAD C G Synonymous p.L1718L c.5154G>C 6 43005621 ESCA C G Synonymous p.L387L c.1161G>C 6 43019030 BRCA C G Synonymous p.T1043T c.3129G>C 6 43013126 HNSC C T Missense p.E1418K c.4252G>A 6 43008291 HNSC C T Missense p.E1472K c.4414G>A 6 43008026 BLCA C T Missense p.E1617K c.4849G>A 6 43006181 HNSC C T Missense p.E367K c.1099G>A 6 43019092 LUAD C T Missense p.E616K c.1846G>A 6 43017376 RCCC C T Missense p.G234S c.700G>A 6 43019983 ESCA C T Missense p.G879E c.2636G>A 6 43014631 BRCA C T Missense p.R1024H c.3071G>A 6 43013368 COREAD C T Missense p.R1046Q c.3137G>A 6 43013118 ESCA C T Missense p.R1765Q c.5294G>A 6 43005481 BRCA C T Missense p.S201N c.602G>A 6 43020081 HNSC C T Missense p.V1060M c.3178G>A 6 43013077 CM C T Missense p.V1234M c.3700G>A 6 43010826 LGG C T Missense p.V619M c.1855G>A 6 43017367 OV C T Nonsense p.W925* c.2775G>A 6 43014111 CM C T SpliceDonorSNV . c.2077+1G>A 6 43017144 BRCA C T Synonymous p.A1565A c.4695G>A 6 43006428 HNSC C T Synonymous p.E294E c.882G>A 6 43019452 CM C T Synonymous p.L1718L c.5154G>A 6 43005621 BRCA C T Synonymous p.L830L c.2490G>A 6 43014777 LUAD C T Synonymous p.V989V c.2967G>A 6 43013775 CM G A Missense p.A1280V c.3839C>T 6 43010598 COREAD G A Missense p.L284F c.850C>T 6 43019484 CM G A Missense p.P1148S c.3442C>T 6 43011351 CM G A Missense p.P463L c.1388C>T 6 43018803 UCEC G A Missense p.R230C c.688C>T 6 43019995 OV G A Missense p.R235W c.703C>T 6 43019980 STAD G A Missense p.R468W c.1402C>T 6 43018789 BRCA G A Missense p.S1012F c.3035C>T 6 43013404 CM G A Missense p.T875I c.2624C>T 6 43014643 CM G A Nonsense p.Q913* c.2737C>T 6 43014252 CM G A Synonymous p.A545A c.1635C>T 6 43017887 STAD G A Synonymous p.C795C c.2385C>T 6 43015922 UCEC G A Synonymous p.L1180L c.3540C>T 6 43011253 BLCA G A Synonymous p.L768L c.2302C>T 6 43016083 CM G A Synonymous p.N352N c.1056C>T 6 43019135 NB G A Synonymous p.N952N c.2856C>T 6 43014030 ESCA G A Synonymous p.V329V c.987C>T 6 43019204 CM G C Missense p.L1502V c.4504C>G 6 43007936 LUAD G C Missense p.L189V c.565C>G 6 43020118 LUAD G C Missense p.Q145E c.433C>G 6 43020250 LUAD GCTCACATCTGCCAGCTGA - Frameshift p.L419Gfs*127 c.1251_1269delTCAGCTGGCAGATGTGAGC 6 43018922 BRCA G - Frameshift p.L819*fs*1 c.2455delC 6 43014812 BRCA GGTGCAGG - Frameshift p.F815Lfs*47 c.2445_2452delCCTGCACC 6 43014815 BRCA G - IntronicDeletion . c.3608-114delA 6 43011032 HC G T Missense p.L708M c.2122C>A 6 43016263 BRCA G T Missense p.P1194T c.3580C>A 6 43011213 COREAD G T Missense p.S201R c.603C>A 6 43020080 LUSC G T Synonymous p.S434S c.1302C>A 6 43018889 CM T A Missense p.K946M c.2837A>T 6 43014049 UCEC T A Missense p.Q706L c.2117A>T 6 43016268 BRCA T C Missense p.I1029V c.3085A>G 6 43013354 OV T C Missense p.M985V c.2953A>G 6 43013789 SCLC T C Missense p.N1583S c.4748A>G 6 43006375 BLCA T C Missense p.S638G c.1912A>G 6 43017310 UCEC T C Missense p.Y1073C c.3218A>G 6 43013037 RCCC T - Frameshift p.Q1776Rfs*104 c.5327delA 6 43005448 CM