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 11 113679796 113679796 + Missense_Mutation SNP G G C TCGA-OR-A5L2-01A-11D-A30A-10 TCGA-OR-A5L2-10A-01D-A30A-10 g.chr11:113679796G>C c.2153C>G c.(2152-2154)tCt>tGt p.S718C BLCA 11 113672370 113672370 + Missense_Mutation SNP C C T TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chr11:113672370C>T c.2893G>A c.(2893-2895)Gaa>Aaa p.E965K BLCA 11 113674600 113674600 + Splice_Site SNP C C G TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr11:113674600C>G c.e22-1 BLCA 11 113674600 113674600 + Splice_Site SNP C C G TCGA-DK-AA74-01A-11D-A391-08 TCGA-DK-AA74-10A-01D-A394-08 g.chr11:113674600C>G c.e22-1 BLCA 11 113679872 113679872 + Nonsense_Mutation SNP C C A TCGA-UY-A78M-01A-21D-A34U-08 TCGA-UY-A78M-10A-01D-A34X-08 g.chr11:113679872C>A c.2077G>T c.(2077-2079)Gag>Tag p.E693* BLCA 11 113679918 113679918 + Silent SNP G G C TCGA-DK-AA6T-01A-11D-A391-08 TCGA-DK-AA6T-10A-01D-A394-08 g.chr11:113679918G>C c.2031C>G c.(2029-2031)ctC>ctG p.L677L BLCA 11 113683113 113683113 + Silent SNP G G A TCGA-DK-A3IQ-01A-31D-A20D-08 TCGA-DK-A3IQ-10A-01D-A20D-08 g.chr11:113683113G>A c.1857C>T c.(1855-1857)atC>atT p.I619I BLCA 11 113683118 113683118 + Missense_Mutation SNP C C T TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr11:113683118C>T c.1852G>A c.(1852-1854)Gac>Aac p.D618N BLCA 11 113686082 113686082 + Nonsense_Mutation SNP G G A TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr11:113686082G>A c.1486C>T c.(1486-1488)Cag>Tag p.Q496* BLCA 11 113694349 113694350 + Frame_Shift_Del DEL TT TT - TCGA-GV-A3QI-01A-11D-A21Z-08 TCGA-GV-A3QI-10A-01D-A21Z-08 g.chr11:113694349_113694350delTT c.1260_1261delAA c.(1258-1263)aaaattfs p.KI420fs BLCA 11 113694378 113694378 + Missense_Mutation SNP C C A TCGA-FD-A6TF-01A-52D-A32B-08 TCGA-FD-A6TF-10A-21D-A329-08 g.chr11:113694378C>A c.1232G>T c.(1231-1233)tGt>tTt p.C411F BLCA 11 113694393 113694393 + Missense_Mutation SNP C C T TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr11:113694393C>T c.1217G>A c.(1216-1218)cGa>cAa p.R406Q BLCA 11 113697974 113697974 + Nonsense_Mutation SNP G G A TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr11:113697974G>A c.1168C>T c.(1168-1170)Cag>Tag p.Q390* BLCA 11 113711320 113711320 + Splice_Site SNP C C T TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr11:113711320C>T c.534G>A c.(532-534)caG>caA p.Q178Q BLCA 11 113711387 113711387 + Missense_Mutation SNP C C G TCGA-ZF-A9R4-01A-11D-A38G-08 TCGA-ZF-A9R4-10A-01D-A38J-08 g.chr11:113711387C>G c.467G>C c.(466-468)aGa>aCa p.R156T BLCA 11 113712400 113712400 + Frame_Shift_Del DEL C C - TCGA-4Z-AA7O-01A-31D-A391-08 TCGA-4Z-AA7O-10A-01D-A394-08 g.chr11:113712400delC c.359delG c.(358-360)ggafs p.G120fs BRCA 11 113700047 113700047 + Nonsense_Mutation SNP C C A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:113700047C>A c.931G>T c.(931-933)Gag>Tag p.E311* BRCA 11 113702712 113702712 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:113702712C>G c.763G>C c.(763-765)Gat>Cat p.D255H BRCA 11 113704158 113704158 + Missense_Mutation SNP G G A TCGA-AR-A2LE-01A-11D-A17W-09 TCGA-AR-A2LE-10A-01D-A17W-09 g.chr11:113704158G>A c.743C>T c.(742-744)tCa>tTa p.S248L BRCA 11 113704197 113704197 + Missense_Mutation SNP G G A TCGA-E9-A244-01A-11D-A167-09 TCGA-E9-A244-10A-01D-A167-09 g.chr11:113704197G>A c.704C>T c.(703-705)cCg>cTg p.P235L BRCA 11 113723334 113723334 + Nonsense_Mutation SNP G G A TCGA-BH-A0HP-01A-12D-A099-09 TCGA-BH-A0HP-10A-01D-A099-09 g.chr11:113723334G>A c.157C>T c.(157-159)Cag>Tag p.Q53* CESC 11 113674600 113674600 + Splice_Site SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr11:113674600C>G c.e22-1 CESC 11 113685932 113685932 + Nonsense_Mutation SNP G G A TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr11:113685932G>A c.1636C>T c.(1636-1638)Cag>Tag p.Q546* CESC 11 113698046 113698046 + Missense_Mutation SNP C C T TCGA-DS-A0VM-01A-11D-A10S-08 TCGA-DS-A0VM-10A-01D-A10S-08 g.chr11:113698046C>T c.1096G>A c.(1096-1098)Gaa>Aaa p.E366K CESC 11 113711322 113711322 + Nonsense_Mutation SNP G G A TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr11:113711322G>A c.532C>T c.(532-534)Cag>Tag p.Q178* CHOL 11 113674003 113674003 + Splice_Site SNP C C A TCGA-W5-AA2U-01A-11D-A417-09 TCGA-W5-AA2U-10A-01D-A41A-09 g.chr11:113674003C>A c.2739G>T c.(2737-2739)aaG>aaT p.K913N CHOL 11 113683165 113683165 + Missense_Mutation SNP C C A TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr11:113683165C>A c.1805G>T c.(1804-1806)tGg>tTg p.W602L COAD 11 113670046 113670046 + Silent SNP T T C TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr11:113670046T>C c.3150A>G c.(3148-3150)cgA>cgG p.R1050R COAD 11 113670047 113670047 + Missense_Mutation SNP C C T TCGA-AA-3692-01A-01W-0900-09 TCGA-AA-3692-10A-01W-0900-09 g.chr11:113670047C>T c.3149G>A c.(3148-3150)cGa>cAa p.R1050Q COAD 11 113670047 113670047 + Missense_Mutation SNP C C T TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr11:113670047C>T c.3149G>A c.(3148-3150)cGa>cAa p.R1050Q COAD 11 113670058 113670058 + Silent SNP A A G TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr11:113670058A>G c.3138T>C c.(3136-3138)ccT>ccC p.P1046P COAD 11 113672326 113672326 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:113672326C>A c.2937G>T c.(2935-2937)atG>atT p.M979I COAD 11 113672349 113672349 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:113672349C>T c.2914G>A c.(2914-2916)Gta>Ata p.V972I COAD 11 113673918 113673918 + Nonsense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:113673918C>A c.2824G>T c.(2824-2826)Gaa>Taa p.E942* COAD 11 113673924 113673924 + Frame_Shift_Del DEL C C - TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr11:113673924delC c.2818delG c.(2818-2820)gtcfs p.V940fs COAD 11 113674518 113674518 + Splice_Site SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:113674518A>G c.e22+1 COAD 11 113677252 113677252 + Nonsense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:113677252G>A c.2359C>T c.(2359-2361)Cag>Tag p.Q787* COAD 11 113677254 113677254 + Missense_Mutation SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr11:113677254C>T c.2357G>A c.(2356-2358)cGt>cAt p.R786H COAD 11 113679897 113679897 + Silent SNP A A G TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr11:113679897A>G c.2052T>C c.(2050-2052)gaT>gaC p.D684D COAD 11 113679898 113679898 + Missense_Mutation SNP T T C TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr11:113679898T>C c.2051A>G c.(2050-2052)gAt>gGt p.D684G COAD 11 113683037 113683037 + Missense_Mutation SNP G G C TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr11:113683037G>C c.1933C>G c.(1933-1935)Ctg>Gtg p.L645V COAD 11 113683045 113683045 + Missense_Mutation SNP G G A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr11:113683045G>A c.1925C>T c.(1924-1926)gCt>gTt p.A642V COAD 11 113684607 113684607 + Splice_Site SNP C C A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:113684607C>A c.1743G>T c.(1741-1743)caG>caT p.Q581H COAD 11 113688554 113688554 + Missense_Mutation SNP A A G TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:113688554A>G c.1289T>C c.(1288-1290)gTg>gCg p.V430A COAD 11 113697985 113697985 + Missense_Mutation SNP A A G TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr11:113697985A>G c.1157T>C c.(1156-1158)cTg>cCg p.L386P COAD 11 113698036 113698036 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:113698036C>A c.1106G>T c.(1105-1107)aGa>aTa p.R369I COAD 11 113700048 113700048 + Missense_Mutation SNP A A C TCGA-AA-3693-01A-01W-0900-09 TCGA-AA-3693-10A-01W-0900-09 g.chr11:113700048A>C c.930T>G c.(928-930)aaT>aaG p.N310K COAD 11 113700063 113700063 + Frame_Shift_Del DEL T T - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:113700063delT c.915delA c.(913-915)aaafs p.K305fs COAD 11 113701594 113701594 + Missense_Mutation SNP C C T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr11:113701594C>T c.905G>A c.(904-906)cGt>cAt p.R302H COAD 11 113701639 113701639 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:113701639G>A c.860C>T c.(859-861)cCa>cTa p.P287L COAD 11 113701644 113701644 + Silent SNP T T C TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr11:113701644T>C c.855A>G c.(853-855)gaA>gaG p.E285E COAD 11 113704162 113704162 + Nonsense_Mutation SNP G G A TCGA-D5-6922-01A-11D-1924-10 TCGA-D5-6922-10A-01D-1924-10 g.chr11:113704162G>A c.739C>T c.(739-741)Cga>Tga p.R247* COAD 11 113704203 113704203 + Missense_Mutation SNP A A C TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr11:113704203A>C c.698T>G c.(697-699)gTa>gGa p.V233G COAD 11 113704982 113704982 + Nonsense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:113704982G>A c.610C>T c.(610-612)Cga>Tga p.R204* COAD 11 113711469 113711469 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:113711469C>T c.385G>A c.(385-387)Gca>Aca p.A129T COAD 11 113723235 113723235 + Nonsense_Mutation SNP C C A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr11:113723235C>A c.256G>T c.(256-258)Gaa>Taa p.E86* COAD 11 113723244 113723244 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:113723244C>T c.247G>A c.(247-249)Gcc>Acc p.A83T COADREAD 11 113670046 113670046 + Silent SNP T T C TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr11:113670046T>C c.3150A>G c.(3148-3150)cgA>cgG p.R1050R COADREAD 11 113670047 113670047 + Missense_Mutation SNP C C T TCGA-AA-3692-01A-01W-0900-09 TCGA-AA-3692-10A-01W-0900-09 g.chr11:113670047C>T c.3149G>A c.(3148-3150)cGa>cAa p.R1050Q COADREAD 11 113670047 113670047 + Missense_Mutation SNP C C T TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr11:113670047C>T c.3149G>A c.(3148-3150)cGa>cAa p.R1050Q COADREAD 11 113670058 113670058 + Silent SNP A A G TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr11:113670058A>G c.3138T>C c.(3136-3138)ccT>ccC p.P1046P COADREAD 11 113670059 113670059 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:113670059G>T c.3137C>A c.(3136-3138)cCt>cAt p.P1046H COADREAD 11 113670059 113670059 + Missense_Mutation SNP G G T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr11:113670059G>T c.3137C>A c.(3136-3138)cCt>cAt p.P1046H COADREAD 11 113672326 113672326 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:113672326C>A c.2937G>T c.(2935-2937)atG>atT p.M979I COADREAD 11 113672349 113672349 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr11:113672349C>T c.2914G>A c.(2914-2916)Gta>Ata p.V972I COADREAD 11 113673918 113673918 + Nonsense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:113673918C>A c.2824G>T c.(2824-2826)Gaa>Taa p.E942* COADREAD 11 113673924 113673924 + Frame_Shift_Del DEL C C - TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr11:113673924delC c.2818delG c.(2818-2820)gtcfs p.V940fs COADREAD 11 113674518 113674518 + Splice_Site SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:113674518A>G c.e22+1 COADREAD 11 113674554 113674554 + Missense_Mutation SNP G G A TCGA-AF-2692-01A-01W-0831-10 TCGA-AF-2692-10A-01W-0831-10 g.chr11:113674554G>A c.2704C>T c.(2704-2706)Ctc>Ttc p.L902F COADREAD 11 113677252 113677252 + Nonsense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:113677252G>A c.2359C>T c.(2359-2361)Cag>Tag p.Q787* COADREAD 11 113677254 113677254 + Missense_Mutation SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr11:113677254C>T c.2357G>A c.(2356-2358)cGt>cAt p.R786H COADREAD 11 113679081 113679081 + Missense_Mutation SNP T T C TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr11:113679081T>C c.2243A>G c.(2242-2244)cAg>cGg p.Q748R COADREAD 11 113679897 113679897 + Silent SNP A A G TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr11:113679897A>G c.2052T>C c.(2050-2052)gaT>gaC p.D684D COADREAD 11 113679898 113679898 + Missense_Mutation SNP T T C TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr11:113679898T>C c.2051A>G c.(2050-2052)gAt>gGt p.D684G COADREAD 11 113683037 113683037 + Missense_Mutation SNP G G C TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr11:113683037G>C c.1933C>G c.(1933-1935)Ctg>Gtg p.L645V COADREAD 11 113683045 113683045 + Missense_Mutation SNP G G A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr11:113683045G>A c.1925C>T c.(1924-1926)gCt>gTt p.A642V COADREAD 11 113684607 113684607 + Splice_Site SNP C C A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:113684607C>A c.1743G>T c.(1741-1743)caG>caT p.Q581H COADREAD 11 113688554 113688554 + Missense_Mutation SNP A A G TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:113688554A>G c.1289T>C c.(1288-1290)gTg>gCg p.V430A COADREAD 11 113697985 113697985 + Missense_Mutation SNP A A G TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr11:113697985A>G c.1157T>C c.(1156-1158)cTg>cCg p.L386P COADREAD 11 113698036 113698036 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:113698036C>A c.1106G>T c.(1105-1107)aGa>aTa p.R369I COADREAD 11 113700048 113700048 + Missense_Mutation SNP A A C TCGA-AA-3693-01A-01W-0900-09 TCGA-AA-3693-10A-01W-0900-09 g.chr11:113700048A>C c.930T>G c.(928-930)aaT>aaG p.N310K COADREAD 11 113700063 113700063 + Frame_Shift_Del DEL T T - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr11:113700063delT c.915delA c.(913-915)aaafs p.K305fs COADREAD 11 113701594 113701594 + Missense_Mutation SNP C C T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr11:113701594C>T c.905G>A c.(904-906)cGt>cAt p.R302H COADREAD 11 113701632 113701632 + Silent SNP C C T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr11:113701632C>T c.867G>A c.(865-867)gtG>gtA p.V289V COADREAD 11 113701639 113701639 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:113701639G>A c.860C>T c.(859-861)cCa>cTa p.P287L COADREAD 11 113701644 113701644 + Silent SNP T T C TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr11:113701644T>C c.855A>G c.(853-855)gaA>gaG p.E285E COADREAD 11 113704162 113704162 + Nonsense_Mutation SNP G G A TCGA-D5-6922-01A-11D-1924-10 TCGA-D5-6922-10A-01D-1924-10 g.chr11:113704162G>A c.739C>T c.(739-741)Cga>Tga p.R247* COADREAD 11 113704203 113704203 + Missense_Mutation SNP A A C TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr11:113704203A>C c.698T>G c.(697-699)gTa>gGa p.V233G COADREAD 11 113704982 113704982 + Missense_Mutation SNP G G C TCGA-DY-A1DC-01A-31D-A152-10 TCGA-DY-A1DC-10A-01D-A152-10 g.chr11:113704982G>C c.610C>G c.(610-612)Cga>Gga p.R204G COADREAD 11 113704982 113704982 + Nonsense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:113704982G>A c.610C>T c.(610-612)Cga>Tga p.R204* COADREAD 11 113711469 113711469 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:113711469C>T c.385G>A c.(385-387)Gca>Aca p.A129T COADREAD 11 113723235 113723235 + Nonsense_Mutation SNP C C A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr11:113723235C>A c.256G>T c.(256-258)Gaa>Taa p.E86* COADREAD 11 113723244 113723244 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:113723244C>T c.247G>A c.(247-249)Gcc>Acc p.A83T ESCA 11 113672343 113672343 + Missense_Mutation SNP C C T TCGA-LN-A49M-01A-21D-A27G-09 TCGA-LN-A49M-10A-01D-A27G-09 g.chr11:113672343C>T c.2920G>A c.(2920-2922)Gag>Aag p.E974K ESCA 11 113683093 113683093 + Missense_Mutation SNP C C G TCGA-R6-A6L6-01B-11D-A33E-09 TCGA-R6-A6L6-10A-01D-A33H-09 g.chr11:113683093C>G c.1877G>C c.(1876-1878)tGg>tCg p.W626S ESCA 11 113698017 113698017 + Silent SNP G G A TCGA-L5-A43C-01A-11D-A247-09 TCGA-L5-A43C-11A-11D-A247-09 g.chr11:113698017G>A c.1125C>T c.(1123-1125)tcC>tcT p.S375S ESCA 11 113700044 113700044 + Missense_Mutation SNP T T C TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr11:113700044T>C c.934A>G c.(934-936)Acc>Gcc p.T312A GBM 11 113672259 113672259 + Missense_Mutation SNP C C T TCGA-28-2509-01A-01D-1494-08 TCGA-28-2509-10A-01D-1494-08 g.chr11:113672259C>T c.3004G>A c.(3004-3006)Gcc>Acc p.A1002T GBM 11 113677209 113677209 + Splice_Site SNP A A G TCGA-06-0209-01A-01D-1491-08 TCGA-06-0209-10A-01D-1491-08 g.chr11:113677209A>G c.e19+1 GBM 11 113688486 113688486 + Missense_Mutation SNP T T C TCGA-27-1832-01A-01W-0643-08 TCGA-27-1832-10A-01W-0644-08 g.chr11:113688486T>C c.1357A>G c.(1357-1359)Agt>Ggt p.S453G GBMLGG 11 113672259 113672259 + Missense_Mutation SNP C C T TCGA-28-2509-01A-01D-1494-08 TCGA-28-2509-10A-01D-1494-08 g.chr11:113672259C>T c.3004G>A c.(3004-3006)Gcc>Acc p.A1002T GBMLGG 11 113673879 113673879 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:113673879C>A c.e23+1 GBMLGG 11 113673911 113673911 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:113673911A>G c.2831T>C c.(2830-2832)gTg>gCg p.V944A GBMLGG 11 113677209 113677209 + Splice_Site SNP A A G TCGA-06-0209-01A-01D-1491-08 TCGA-06-0209-10A-01D-1491-08 g.chr11:113677209A>G c.e19+1 GBMLGG 11 113683095 113683095 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:113683095G>T c.1875C>A c.(1873-1875)tcC>tcA p.S625S GBMLGG 11 113688486 113688486 + Missense_Mutation SNP T T C TCGA-27-1832-01A-01W-0643-08 TCGA-27-1832-10A-01W-0644-08 g.chr11:113688486T>C c.1357A>G c.(1357-1359)Agt>Ggt p.S453G GBMLGG 11 113698033 113698033 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:113698033A>G c.1109T>C c.(1108-1110)tTt>tCt p.F370S GBMLGG 11 113704275 113704276 + Frame_Shift_Del DEL TT TT - TCGA-P5-A77X-01A-11D-A32B-08 TCGA-P5-A77X-10A-01D-A329-08 g.chr11:113704275_113704276delTT c.625_626delAA c.(625-627)aagfs p.K209fs HNSC 11 113670017 113670017 + Missense_Mutation SNP C C A TCGA-CQ-5331-01A-02D-1870-08 TCGA-CQ-5331-10A-01D-1870-08 g.chr11:113670017C>A c.3179G>T c.(3178-3180)cGa>cTa p.R1060L HNSC 11 113670032 113670032 + Missense_Mutation SNP T T C TCGA-IQ-A6SG-01A-12D-A34J-08 TCGA-IQ-A6SG-10A-01D-A34M-08 g.chr11:113670032T>C c.3164A>G c.(3163-3165)tAt>tGt p.Y1055C HNSC 11 113673937 113673937 + Silent SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:113673937C>T c.2805G>A c.(2803-2805)ggG>ggA p.G935G HNSC 11 113679958 113679958 + Nonsense_Mutation SNP G G C TCGA-D6-A4ZB-01A-11D-A25D-08 TCGA-D6-A4ZB-10A-01D-A25E-08 g.chr11:113679958G>C c.1991C>G c.(1990-1992)tCa>tGa p.S664* HNSC 11 113683157 113683157 + Missense_Mutation SNP T T A TCGA-T3-A92N-01A-11D-A391-08 TCGA-T3-A92N-10A-01D-A394-08 g.chr11:113683157T>A c.1813A>T c.(1813-1815)Atc>Ttc p.I605F HNSC 11 113683178 113683178 + Missense_Mutation SNP C C A TCGA-CV-7248-01A-11D-2012-08 TCGA-CV-7248-10A-01D-2013-08 g.chr11:113683178C>A c.1792G>T c.(1792-1794)Gct>Tct p.A598S HNSC 11 113683212 113683212 + Silent SNP C C T TCGA-CN-A6V3-01A-12D-A34J-08 TCGA-CN-A6V3-10A-01D-A34M-08 g.chr11:113683212C>T c.1758G>A c.(1756-1758)ttG>ttA p.L586L HNSC 11 113684607 113684607 + Splice_Site SNP C C T TCGA-H7-A6C4-01A-11D-A30E-08 TCGA-H7-A6C4-10A-01D-A30H-08 g.chr11:113684607C>T c.1743G>A c.(1741-1743)caG>caA p.Q581Q HNSC 11 113701592 113701592 + Missense_Mutation SNP C C T TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr11:113701592C>T c.907G>A c.(907-909)Gaa>Aaa p.E303K HNSC 11 113711342 113711342 + Missense_Mutation SNP C C T TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr11:113711342C>T c.512G>A c.(511-513)tGt>tAt p.C171Y HNSC 11 113711431 113711431 + Silent SNP G G A TCGA-CV-5439-01A-01D-1683-08 TCGA-CV-5439-11B-01D-1683-08 g.chr11:113711431G>A c.423C>T c.(421-423)cgC>cgT p.R141R HNSC 11 113712437 113712437 + Silent SNP A A G TCGA-CQ-6225-01A-11D-1912-08 TCGA-CQ-6225-10A-01D-1912-08 g.chr11:113712437A>G c.322T>C c.(322-324)Ttg>Ctg p.L108L KICH 11 113685956 113685956 + Missense_Mutation SNP T T C TCGA-KN-8424-01A-11D-2310-10 TCGA-KN-8424-11A-01D-2310-10 g.chr11:113685956T>C c.1612A>G c.(1612-1614)Ata>Gta p.I538V KIPAN 11 113679118 113679119 + Frame_Shift_Ins INS - - TG TCGA-BQ-5878-01A-11D-1589-08 TCGA-BQ-5878-11A-01D-1589-08 g.chr11:113679118_113679119insTG c.2205_2206insCA c.(2203-2208)tcgtctfs p.S736fs KIPAN 11 113683009 113683009 + Missense_Mutation SNP T T A TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr11:113683009T>A c.1961A>T c.(1960-1962)tAc>tTc p.Y654F KIPAN 11 113684670 113684670 + Missense_Mutation SNP C C A TCGA-B0-4693-01A-01D-1361-10 TCGA-B0-4693-11A-01D-1361-10 g.chr11:113684670C>A c.1680G>T c.(1678-1680)aaG>aaT p.K560N KIPAN 11 113685956 113685956 + Missense_Mutation SNP T T C TCGA-KN-8424-01A-11D-2310-10 TCGA-KN-8424-11A-01D-2310-10 g.chr11:113685956T>C c.1612A>G c.(1612-1614)Ata>Gta p.I538V KIPAN 11 113694390 113694391 + Frame_Shift_Del DEL TT TT - TCGA-B8-5551-01A-01D-1534-10 TCGA-B8-5551-10A-01D-1535-10 g.chr11:113694390_113694391delTT c.1219_1220delAA c.(1219-1221)aatfs p.N407fs KIPAN 11 113701632 113701632 + Silent SNP C C A TCGA-AK-3458-01A-01D-1501-10 TCGA-AK-3458-10A-01D-1501-10 g.chr11:113701632C>A c.867G>T c.(865-867)gtG>gtT p.V289V KIPAN 11 113705056 113705056 + Splice_Site SNP G G C TCGA-A4-7732-01A-11D-2136-08 TCGA-A4-7732-10A-01D-2136-08 g.chr11:113705056G>C c.536C>G c.(535-537)tCt>tGt p.S179C KIRC 11 113684670 113684670 + Missense_Mutation SNP C C A TCGA-B0-4693-01A-01D-1361-10 TCGA-B0-4693-11A-01D-1361-10 g.chr11:113684670C>A c.1680G>T c.(1678-1680)aaG>aaT p.K560N KIRC 11 113694390 113694391 + Frame_Shift_Del DEL TT TT - TCGA-B8-5551-01A-01D-1534-10 TCGA-B8-5551-10A-01D-1535-10 g.chr11:113694390_113694391delTT c.1219_1220delAA c.(1219-1221)aatfs p.N407fs KIRC 11 113701632 113701632 + Silent SNP C C A TCGA-AK-3458-01A-01D-1501-10 TCGA-AK-3458-10A-01D-1501-10 g.chr11:113701632C>A c.867G>T c.(865-867)gtG>gtT p.V289V KIRP 11 113679118 113679119 + Frame_Shift_Ins INS - - TG TCGA-BQ-5878-01A-11D-1589-08 TCGA-BQ-5878-11A-01D-1589-08 g.chr11:113679118_113679119insTG c.2205_2206insCA c.(2203-2208)tcgtctfs p.S736fs KIRP 11 113683009 113683009 + Missense_Mutation SNP T T A TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr11:113683009T>A c.1961A>T c.(1960-1962)tAc>tTc p.Y654F KIRP 11 113705056 113705056 + Splice_Site SNP G G C TCGA-A4-7732-01A-11D-2136-08 TCGA-A4-7732-10A-01D-2136-08 g.chr11:113705056G>C c.536C>G c.(535-537)tCt>tGt p.S179C LGG 11 113673879 113673879 + Splice_Site SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:113673879C>A c.e23+1 LGG 11 113673911 113673911 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:113673911A>G c.2831T>C c.(2830-2832)gTg>gCg p.V944A LGG 11 113683095 113683095 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:113683095G>T c.1875C>A c.(1873-1875)tcC>tcA p.S625S LGG 11 113698033 113698033 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:113698033A>G c.1109T>C c.(1108-1110)tTt>tCt p.F370S LGG 11 113704275 113704276 + Frame_Shift_Del DEL TT TT - TCGA-P5-A77X-01A-11D-A32B-08 TCGA-P5-A77X-10A-01D-A329-08 g.chr11:113704275_113704276delTT c.625_626delAA c.(625-627)aagfs p.K209fs LIHC 11 113683133 113683133 + Missense_Mutation SNP A A T TCGA-DD-AAEI-01A-11D-A40R-10 TCGA-DD-AAEI-10A-01D-A40U-10 g.chr11:113683133A>T c.1837T>A c.(1837-1839)Tgg>Agg p.W613R LIHC 11 113683141 113683141 + Missense_Mutation SNP C C T TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr11:113683141C>T c.1829G>A c.(1828-1830)cGa>cAa p.R610Q LIHC 11 113694377 113694377 + Silent SNP A A G TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr11:113694377A>G c.1233T>C c.(1231-1233)tgT>tgC p.C411C LIHC 11 113704215 113704215 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr11:113704215delT c.686delA c.(685-687)aatfs p.N229fs LUAD 11 113670056 113670056 + Missense_Mutation SNP G G T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr11:113670056G>T c.3140C>A c.(3139-3141)cCa>cAa p.P1047Q LUAD 11 113670093 113670093 + Missense_Mutation SNP C C A TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr11:113670093C>A c.3103G>T c.(3103-3105)Gat>Tat p.D1035Y LUAD 11 113672268 113672268 + Missense_Mutation SNP C C A TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr11:113672268C>A c.2995G>T c.(2995-2997)Gat>Tat p.D999Y LUAD 11 113673937 113673937 + Silent SNP C C A TCGA-78-7536-01A-11D-2063-08 TCGA-78-7536-10A-01D-2063-08 g.chr11:113673937C>A c.2805G>T c.(2803-2805)ggG>ggT p.G935G LUAD 11 113673938 113673938 + Missense_Mutation SNP C C A TCGA-78-7536-01A-11D-2063-08 TCGA-78-7536-10A-01D-2063-08 g.chr11:113673938C>A c.2804G>T c.(2803-2805)gGg>gTg p.G935V LUAD 11 113675615 113675615 + Missense_Mutation SNP C C A TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr11:113675615C>A c.2554G>T c.(2554-2556)Gat>Tat p.D852Y LUAD 11 113675622 113675622 + Silent SNP C C T TCGA-55-6987-01A-11D-1945-08 TCGA-55-6987-11A-01D-1945-08 g.chr11:113675622C>T c.2547G>A c.(2545-2547)caG>caA p.Q849Q LUAD 11 113675628 113675628 + Silent SNP C C A TCGA-49-6742-01A-11D-1855-08 TCGA-49-6742-11A-01D-1855-08 g.chr11:113675628C>A c.2541G>T c.(2539-2541)ctG>ctT p.L847L LUAD 11 113677221 113677221 + Missense_Mutation SNP C C A TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr11:113677221C>A c.2390G>T c.(2389-2391)gGg>gTg p.G797V LUAD 11 113679033 113679033 + Missense_Mutation SNP G G A TCGA-55-7283-01A-11D-2036-08 TCGA-55-7283-10A-01D-2036-08 g.chr11:113679033G>A c.2291C>T c.(2290-2292)gCg>gTg p.A764V LUAD 11 113679905 113679905 + Nonsense_Mutation SNP G G A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr11:113679905G>A c.2044C>T c.(2044-2046)Cag>Tag p.Q682* LUAD 11 113683174 113683174 + Missense_Mutation SNP C C A TCGA-55-6969-01A-11D-1945-08 TCGA-55-6969-11A-01D-1945-08 g.chr11:113683174C>A c.1796G>T c.(1795-1797)gGa>gTa p.G599V LUAD 11 113683217 113683217 + Missense_Mutation SNP G G A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr11:113683217G>A c.1753C>T c.(1753-1755)Cgc>Tgc p.R585C LUAD 11 113688419 113688419 + Nonsense_Mutation SNP G G T TCGA-62-8395-01A-11D-2323-08 TCGA-62-8395-10A-01D-2323-08 g.chr11:113688419G>T c.1424C>A c.(1423-1425)tCa>tAa p.S475* LUAD 11 113699991 113699991 + Nonsense_Mutation SNP A A T TCGA-44-4112-01A-01D-1105-08 TCGA-44-4112-10A-01D-1458-08 g.chr11:113699991A>T c.987T>A c.(985-987)tgT>tgA p.C329* LUAD 11 113700007 113700007 + Missense_Mutation SNP C C T TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chr11:113700007C>T c.971G>A c.(970-972)cGc>cAc p.R324H LUAD 11 113702712 113702712 + Missense_Mutation SNP C C T TCGA-05-5420-01A-01D-1625-08 TCGA-05-5420-11A-01D-1625-08 g.chr11:113702712C>T c.763G>A c.(763-765)Gat>Aat p.D255N LUAD 11 113704163 113704163 + Missense_Mutation SNP G G C TCGA-55-8299-01A-11D-2284-08 TCGA-55-8299-10B-01D-2323-08 g.chr11:113704163G>C c.738C>G c.(736-738)ttC>ttG p.F246L LUAD 11 113705003 113705003 + Nonsense_Mutation SNP G G A TCGA-55-8205-01A-11D-2238-08 TCGA-55-8205-10A-01D-2238-08 g.chr11:113705003G>A c.589C>T c.(589-591)Caa>Taa p.Q197* LUAD 11 113711322 113711322 + Nonsense_Mutation SNP G G A TCGA-05-4396-01A-21D-1855-08 TCGA-05-4396-10A-01D-1855-08 g.chr11:113711322G>A c.532C>T c.(532-534)Cag>Tag p.Q178* LUAD 11 113712397 113712397 + Missense_Mutation SNP C C A TCGA-55-6985-01A-11D-1945-08 TCGA-55-6985-11A-01D-1945-08 g.chr11:113712397C>A c.362G>T c.(361-363)aGa>aTa p.R121I LUSC 11 113675696 113675696 + Missense_Mutation SNP G G A TCGA-60-2719-01A-01D-1522-08 TCGA-60-2719-11A-01D-1522-08 g.chr11:113675696G>A c.2473C>T c.(2473-2475)Ctt>Ttt p.L825F LUSC 11 113679872 113679872 + Missense_Mutation SNP C C G TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr11:113679872C>G c.2077G>C c.(2077-2079)Gag>Cag p.E693Q LUSC 11 113679924 113679924 + Silent SNP C C A TCGA-60-2724-01A-01D-1522-08 TCGA-60-2724-11A-01D-1522-08 g.chr11:113679924C>A c.2025G>T c.(2023-2025)gtG>gtT p.V675V LUSC 11 113688476 113688476 + Missense_Mutation SNP G G A TCGA-66-2777-01A-01D-1267-08 TCGA-66-2777-11A-01D-1267-08 g.chr11:113688476G>A c.1367C>T c.(1366-1368)cCt>cTt p.P456L LUSC 11 113704153 113704153 + Nonsense_Mutation SNP C C A TCGA-18-3419-01A-01D-0983-08 TCGA-18-3419-11A-01D-0983-08 g.chr11:113704153C>A c.748G>T c.(748-750)Gag>Tag p.E250* OV 11 113674595 113674595 + Nonsense_Mutation SNP C C T TCGA-04-1651-01A-01W-0639-09 TCGA-04-1651-11A-01W-0639-09 g.chr11:113674595C>T c.2663G>A c.(2662-2664)tGg>tAg p.W888* OV 11 113694327 113694327 + Splice_Site SNP C C G TCGA-29-1761-01A-01W-0633-09 TCGA-29-1761-10A-01W-0633-09 g.chr11:113694327C>G c.1283G>C c.(1282-1284)aGg>aCg p.R428T OV 11 113701646 113701646 + Nonsense_Mutation SNP C C A TCGA-36-1578-01A-01W-0615-10 TCGA-36-1578-10A-01W-0615-10 g.chr11:113701646C>A c.853G>T c.(853-855)Gaa>Taa p.E285* PAAD 11 113679043 113679043 + Missense_Mutation SNP C C T TCGA-2L-AAQM-01A-11D-A397-08 TCGA-2L-AAQM-11A-11D-A39A-08 g.chr11:113679043C>T c.2281G>A c.(2281-2283)Ggt>Agt p.G761S PAAD 11 113683039 113683039 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:113683039C>T c.1931G>A c.(1930-1932)tGt>tAt p.C644Y PAAD 11 113683095 113683095 + Silent SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:113683095G>T c.1875C>A c.(1873-1875)tcC>tcA p.S625S PAAD 11 113688414 113688414 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:113688414G>A c.1429C>T c.(1429-1431)Cac>Tac p.H477Y PAAD 11 113702669 113702669 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:113702669T>C c.806A>G c.(805-807)gAc>gGc p.D269G PAAD 11 113711433 113711433 + Missense_Mutation SNP G G A TCGA-FB-AAPP-01A-12D-A40W-08 TCGA-FB-AAPP-11A-11D-A40W-08 g.chr11:113711433G>A c.421C>T c.(421-423)Cgc>Tgc p.R141C PCPG 11 113699965 113699965 + Missense_Mutation SNP T T C TCGA-W2-A7HD-01A-11D-A35I-08 TCGA-W2-A7HD-10D-01D-A35G-08 g.chr11:113699965T>C c.1013A>G c.(1012-1014)gAt>gGt p.D338G PRAD 11 113675464 113675464 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:113675464G>A c.2589C>T c.(2587-2589)agC>agT p.S863S PRAD 11 113675698 113675698 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:113675698C>T c.2471G>A c.(2470-2472)cGa>cAa p.R824Q PRAD 11 113683078 113683079 + In_Frame_Ins INS - - GAA TCGA-J4-8200-01A-11D-A29Q-08 TCGA-J4-8200-10A-01D-A29Q-08 g.chr11:113683078_113683079insGAA c.1891_1892insTTC c.(1891-1893)aga>aTTCga p.630_631insI PRAD 11 113683227 113683227 + Splice_Site SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:113683227C>T c.e16-1 PRAD 11 113704168 113704168 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:113704168C>T c.733G>A c.(733-735)Gca>Aca p.A245T PRAD 11 113704218 113704218 + Nonsense_Mutation SNP G G C TCGA-EJ-5518-01A-01D-1576-08 TCGA-EJ-5518-10A-01D-1577-08 g.chr11:113704218G>C c.683C>G c.(682-684)tCa>tGa p.S228* PRAD 11 113711419 113711419 + Nonsense_Mutation SNP C C T TCGA-J4-AAU2-01A-11D-A41K-08 TCGA-J4-AAU2-10A-01D-A41N-08 g.chr11:113711419C>T c.435G>A c.(433-435)tgG>tgA p.W145* READ 11 113670059 113670059 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:113670059G>T c.3137C>A c.(3136-3138)cCt>cAt p.P1046H READ 11 113670059 113670059 + Missense_Mutation SNP G G T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr11:113670059G>T c.3137C>A c.(3136-3138)cCt>cAt p.P1046H READ 11 113674554 113674554 + Missense_Mutation SNP G G A TCGA-AF-2692-01A-01W-0831-10 TCGA-AF-2692-10A-01W-0831-10 g.chr11:113674554G>A c.2704C>T c.(2704-2706)Ctc>Ttc p.L902F READ 11 113679081 113679081 + Missense_Mutation SNP T T C TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr11:113679081T>C c.2243A>G c.(2242-2244)cAg>cGg p.Q748R READ 11 113701632 113701632 + Silent SNP C C T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr11:113701632C>T c.867G>A c.(865-867)gtG>gtA p.V289V READ 11 113704982 113704982 + Missense_Mutation SNP G G C TCGA-DY-A1DC-01A-31D-A152-10 TCGA-DY-A1DC-10A-01D-A152-10 g.chr11:113704982G>C c.610C>G c.(610-612)Cga>Gga p.R204G SARC 11 113711441 113711441 + Missense_Mutation SNP T T G TCGA-DX-A7EL-01A-12D-A36J-09 TCGA-DX-A7EL-10A-01D-A36M-09 g.chr11:113711441T>G c.413A>C c.(412-414)aAg>aCg p.K138T SKCM 11 113672276 113672276 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr11:113672276G>A c.2987C>T c.(2986-2988)tCc>tTc p.S996F SKCM 11 113672311 113672311 + Silent SNP G G A TCGA-EE-A183-06A-11D-A196-08 TCGA-EE-A183-10A-01D-A198-08 g.chr11:113672311G>A c.2952C>T c.(2950-2952)atC>atT p.I984I SKCM 11 113673885 113673885 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr11:113673885G>A c.2857C>T c.(2857-2859)Ctt>Ttt p.L953F SKCM 11 113673928 113673928 + Silent SNP C C T TCGA-EE-A29H-06A-12D-A197-08 TCGA-EE-A29H-10A-01D-A199-08 g.chr11:113673928C>T c.2814G>A c.(2812-2814)cgG>cgA p.R938R SKCM 11 113673986 113673986 + Missense_Mutation SNP G G A TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr11:113673986G>A c.2756C>T c.(2755-2757)tCc>tTc p.S919F SKCM 11 113675607 113675607 + Missense_Mutation SNP A A T TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr11:113675607A>T c.2562T>A c.(2560-2562)aaT>aaA p.N854K SKCM 11 113675655 113675655 + Silent SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr11:113675655G>A c.2514C>T c.(2512-2514)ccC>ccT p.P838P SKCM 11 113675656 113675656 + Missense_Mutation SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr11:113675656G>A c.2513C>T c.(2512-2514)cCc>cTc p.P838L SKCM 11 113677220 113677220 + Silent SNP C C T TCGA-DA-A1HW-06A-11D-A19A-08 TCGA-DA-A1HW-10A-01D-A19A-08 g.chr11:113677220C>T c.2391G>A c.(2389-2391)ggG>ggA p.G797G SKCM 11 113679831 113679831 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:113679831C>T c.2118G>A c.(2116-2118)atG>atA p.M706I SKCM 11 113679953 113679953 + Nonsense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:113679953G>A c.1996C>T c.(1996-1998)Caa>Taa p.Q666* SKCM 11 113694393 113694393 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:113694393C>T c.1217G>A c.(1216-1218)cGa>cAa p.R406Q SKCM 11 113698048 113698048 + Missense_Mutation SNP A A G TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr11:113698048A>G c.1094T>C c.(1093-1095)tTt>tCt p.F365S SKCM 11 113699951 113699951 + Missense_Mutation SNP G G A TCGA-FW-A5DY-06A-11D-A30X-08 TCGA-FW-A5DY-11A-12D-A30X-08 g.chr11:113699951G>A c.1027C>T c.(1027-1029)Ccc>Tcc p.P343S SKCM 11 113700008 113700008 + Missense_Mutation SNP G G A TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr11:113700008G>A c.970C>T c.(970-972)Cgc>Tgc p.R324C SKCM 11 113700029 113700029 + Missense_Mutation SNP G G A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr11:113700029G>A c.949C>T c.(949-951)Cct>Tct p.P317S SKCM 11 113700029 113700029 + Missense_Mutation SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr11:113700029G>A c.949C>T c.(949-951)Cct>Tct p.P317S SKCM 11 113701610 113701610 + Silent SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr11:113701610G>A c.889C>T c.(889-891)Ctg>Ttg p.L297L SKCM 11 113705054 113705054 + Missense_Mutation SNP G G A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr11:113705054G>A c.538C>T c.(538-540)Ctc>Ttc p.L180F SKCM 11 113712389 113712389 + Missense_Mutation SNP T T C TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:113712389T>C c.370A>G c.(370-372)Aac>Gac p.N124D

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 11 113698036 113698036 single base substitution C G 3_prime_UTR_variant BLCA-CN 11 113698036 113698036 single base substitution C G downstream_gene_variant BLCA-CN 11 113698036 113698036 single base substitution C G missense_variant R133T 398G>C BLCA-CN 11 113698036 113698036 single base substitution C G missense_variant R244T 731G>C BLCA-CN 11 113698036 113698036 single base substitution C G missense_variant R369T 1106G>C BLCA-CN 11 113698036 113698036 single base substitution C G missense_variant R77T 230G>C BLCA-CN 11 113704218 113704218 single base substitution G C 3_prime_UTR_variant BLCA-CN 11 113704218 113704218 single base substitution G C exon_variant BLCA-CN 11 113704218 113704218 single base substitution G C stop_gained S103* 308C>G BLCA-CN 11 113704218 113704218 single base substitution G C stop_gained S127* 380C>G BLCA-CN 11 113704218 113704218 single base substitution G C stop_gained S228* 683C>G BLCA-CN 11 113704218 113704218 single base substitution G C upstream_gene_variant BLCA-US 11 113672370 113672370 single base substitution C T 3_prime_UTR_variant BLCA-US 11 113672370 113672370 single base substitution C T downstream_gene_variant BLCA-US 11 113672370 113672370 single base substitution C T exon_variant BLCA-US 11 113672370 113672370 single base substitution C T missense_variant E641K 1921G>A BLCA-US 11 113672370 113672370 single base substitution C T missense_variant E808K 2422G>A BLCA-US 11 113672370 113672370 single base substitution C T missense_variant E933K 2797G>A BLCA-US 11 113672370 113672370 single base substitution C T missense_variant E965K 2893G>A BLCA-US 11 113683113 113683113 single base substitution G A 3_prime_UTR_variant BLCA-US 11 113683113 113683113 single base substitution G A downstream_gene_variant BLCA-US 11 113683113 113683113 single base substitution G A synonymous_variant I323I 969C>T BLCA-US 11 113683113 113683113 single base substitution G A synonymous_variant I327I 981C>T BLCA-US 11 113683113 113683113 single base substitution G A synonymous_variant I494I 1482C>T BLCA-US 11 113683113 113683113 single base substitution G A synonymous_variant I619I 1857C>T BLCA-US 11 113683113 113683113 single base substitution G A upstream_gene_variant BLCA-US 11 113694349 113694350 deletion of <=200bp TT - 3_prime_UTR_variant BLCA-US 11 113694349 113694350 deletion of <=200bp TT - frameshift_variant KI128 BLCA-US 11 113694349 113694350 deletion of <=200bp TT - frameshift_variant KI184 BLCA-US 11 113694349 113694350 deletion of <=200bp TT - frameshift_variant KI295 BLCA-US 11 113694349 113694350 deletion of <=200bp TT - frameshift_variant KI420 BLCA-US 11 113694393 113694393 single base substitution C T 3_prime_UTR_variant BLCA-US 11 113694393 113694393 single base substitution C T missense_variant R114Q 341G>A BLCA-US 11 113694393 113694393 single base substitution C T missense_variant R170Q 509G>A BLCA-US 11 113694393 113694393 single base substitution C T missense_variant R281Q 842G>A BLCA-US 11 113694393 113694393 single base substitution C T missense_variant R406Q 1217G>A BLCA-US 11 113697974 113697974 single base substitution G A 3_prime_UTR_variant BLCA-US 11 113697974 113697974 single base substitution G A downstream_gene_variant BLCA-US 11 113697974 113697974 single base substitution G A stop_gained Q154* 460C>T BLCA-US 11 113697974 113697974 single base substitution G A stop_gained Q265* 793C>T BLCA-US 11 113697974 113697974 single base substitution G A stop_gained Q390* 1168C>T BLCA-US 11 113697974 113697974 single base substitution G A stop_gained Q98* 292C>T BRCA-EU 11 113663616 113663616 single base substitution G T downstream_gene_variant BRCA-EU 11 113664288 113664288 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 113664387 113664387 deletion of <=200bp C - downstream_gene_variant BRCA-EU 11 113665383 113665383 single base substitution G A downstream_gene_variant BRCA-EU 11 113667964 113667964 single base substitution C T downstream_gene_variant BRCA-EU 11 113668505 113668505 single base substitution G A downstream_gene_variant BRCA-EU 11 113671533 113671533 single base substitution G T downstream_gene_variant BRCA-EU 11 113671533 113671533 single base substitution G T intron_variant BRCA-EU 11 113672931 113672931 single base substitution C T downstream_gene_variant BRCA-EU 11 113672931 113672931 single base substitution C T intron_variant BRCA-EU 11 113672931 113672931 single base substitution C T upstream_gene_variant BRCA-EU 11 113672936 113672936 single base substitution T C downstream_gene_variant BRCA-EU 11 113672936 113672936 single base substitution T C intron_variant BRCA-EU 11 113672936 113672936 single base substitution T C upstream_gene_variant BRCA-EU 11 113673075 113673075 single base substitution G C downstream_gene_variant BRCA-EU 11 113673075 113673075 single base substitution G C intron_variant BRCA-EU 11 113673075 113673075 single base substitution G C upstream_gene_variant BRCA-EU 11 113673130 113673130 single base substitution C T downstream_gene_variant BRCA-EU 11 113673130 113673130 single base substitution C T intron_variant BRCA-EU 11 113673130 113673130 single base substitution C T upstream_gene_variant BRCA-EU 11 113673943 113673943 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 113673943 113673943 single base substitution C T downstream_gene_variant BRCA-EU 11 113673943 113673943 single base substitution C T missense_variant M609I 1827G>A BRCA-EU 11 113673943 113673943 single base substitution C T missense_variant M776I 2328G>A BRCA-EU 11 113673943 113673943 single base substitution C T missense_variant M901I 2703G>A BRCA-EU 11 113673943 113673943 single base substitution C T missense_variant M933I 2799G>A BRCA-EU 11 113673943 113673943 single base substitution C T upstream_gene_variant BRCA-EU 11 113675713 113675713 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 113675713 113675713 single base substitution G A missense_variant S173F 518C>T BRCA-EU 11 113675713 113675713 single base substitution G A missense_variant S495F 1484C>T BRCA-EU 11 113675713 113675713 single base substitution G A missense_variant S662F 1985C>T BRCA-EU 11 113675713 113675713 single base substitution G A missense_variant S787F 2360C>T BRCA-EU 11 113675713 113675713 single base substitution G A missense_variant S819F 2456C>T BRCA-EU 11 113675713 113675713 single base substitution G A upstream_gene_variant BRCA-EU 11 113675875 113675875 insertion of <=200bp - A intron_variant BRCA-EU 11 113675875 113675875 insertion of <=200bp - A upstream_gene_variant BRCA-EU 11 113676620 113676620 single base substitution A C intron_variant BRCA-EU 11 113676620 113676620 single base substitution A C upstream_gene_variant BRCA-EU 11 113677388 113677388 single base substitution G C intron_variant BRCA-EU 11 113677388 113677388 single base substitution G C upstream_gene_variant BRCA-EU 11 113677534 113677534 single base substitution C T intron_variant BRCA-EU 11 113678339 113678339 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 113678339 113678339 deletion of <=200bp A - intron_variant BRCA-EU 11 113678890 113678890 insertion of <=200bp - A downstream_gene_variant BRCA-EU 11 113678890 113678890 insertion of <=200bp - A intron_variant BRCA-EU 11 113679465 113679465 single base substitution G T downstream_gene_variant BRCA-EU 11 113679465 113679465 single base substitution G T intron_variant BRCA-EU 11 113679674 113679674 single base substitution T C downstream_gene_variant BRCA-EU 11 113679674 113679674 single base substitution T C intron_variant BRCA-EU 11 113679948 113679948 single base substitution C A 3_prime_UTR_variant BRCA-EU 11 113679948 113679948 single base substitution C A downstream_gene_variant BRCA-EU 11 113679948 113679948 single base substitution C A missense_variant M375I 1125G>T BRCA-EU 11 113679948 113679948 single base substitution C A missense_variant M542I 1626G>T BRCA-EU 11 113679948 113679948 single base substitution C A missense_variant M667I 2001G>T BRCA-EU 11 113679948 113679948 single base substitution C A upstream_gene_variant BRCA-EU 11 113680454 113680454 single base substitution G C downstream_gene_variant BRCA-EU 11 113680454 113680454 single base substitution G C intron_variant BRCA-EU 11 113680454 113680454 single base substitution G C upstream_gene_variant BRCA-EU 11 113683141 113683141 single base substitution C G downstream_gene_variant BRCA-EU 11 113683141 113683141 single base substitution C G missense_variant R314P 941G>C BRCA-EU 11 113683141 113683141 single base substitution C G missense_variant R318P 953G>C BRCA-EU 11 113683141 113683141 single base substitution C G missense_variant R485P 1454G>C BRCA-EU 11 113683141 113683141 single base substitution C G missense_variant R610P 1829G>C BRCA-EU 11 113683141 113683141 single base substitution C G splice_region_variant BRCA-EU 11 113683141 113683141 single base substitution C G upstream_gene_variant BRCA-EU 11 113683904 113683904 single base substitution G A downstream_gene_variant BRCA-EU 11 113683904 113683904 single base substitution G A intron_variant BRCA-EU 11 113683904 113683904 single base substitution G A upstream_gene_variant BRCA-EU 11 113685479 113685479 single base substitution C G downstream_gene_variant BRCA-EU 11 113685479 113685479 single base substitution C G intron_variant BRCA-EU 11 113685953 113685953 single base substitution T G downstream_gene_variant BRCA-EU 11 113685953 113685953 single base substitution T G intron_variant BRCA-EU 11 113685953 113685953 single base substitution T G missense_variant N243H 727A>C BRCA-EU 11 113685953 113685953 single base substitution T G missense_variant N247H 739A>C BRCA-EU 11 113685953 113685953 single base substitution T G missense_variant N414H 1240A>C BRCA-EU 11 113685953 113685953 single base substitution T G missense_variant N539H 1615A>C BRCA-EU 11 113686329 113686329 single base substitution G C downstream_gene_variant BRCA-EU 11 113686329 113686329 single base substitution G C intron_variant BRCA-EU 11 113686507 113686507 single base substitution G C downstream_gene_variant BRCA-EU 11 113686507 113686507 single base substitution G C intron_variant BRCA-EU 11 113687827 113687827 single base substitution C G downstream_gene_variant BRCA-EU 11 113687827 113687827 single base substitution C G intron_variant BRCA-EU 11 113689605 113689605 single base substitution A C intron_variant BRCA-EU 11 113690768 113690768 single base substitution T C intron_variant BRCA-EU 11 113693152 113693152 single base substitution C T intron_variant BRCA-EU 11 113693520 113693520 single base substitution T G intron_variant BRCA-EU 11 113695517 113695517 single base substitution G C downstream_gene_variant BRCA-EU 11 113695517 113695517 single base substitution G C intron_variant BRCA-EU 11 113697385 113697385 single base substitution T C downstream_gene_variant BRCA-EU 11 113697385 113697385 single base substitution T C intron_variant BRCA-EU 11 113697779 113697779 single base substitution G C downstream_gene_variant BRCA-EU 11 113697779 113697779 single base substitution G C intron_variant BRCA-EU 11 113698128 113698128 single base substitution G C downstream_gene_variant BRCA-EU 11 113698128 113698128 single base substitution G C intron_variant BRCA-EU 11 113698197 113698197 single base substitution C G downstream_gene_variant BRCA-EU 11 113698197 113698197 single base substitution C G intron_variant BRCA-EU 11 113701791 113701791 single base substitution C G intron_variant BRCA-EU 11 113701791 113701791 single base substitution C G upstream_gene_variant BRCA-EU 11 113702209 113702209 single base substitution C T intron_variant BRCA-EU 11 113702209 113702209 single base substitution C T upstream_gene_variant BRCA-EU 11 113704968 113704968 single base substitution T A intron_variant BRCA-EU 11 113704968 113704968 single base substitution T A splice_region_variant BRCA-EU 11 113704968 113704968 single base substitution T A upstream_gene_variant BRCA-EU 11 113705230 113705230 single base substitution C G intron_variant BRCA-EU 11 113705230 113705230 single base substitution C G upstream_gene_variant BRCA-EU 11 113705632 113705632 single base substitution A T intron_variant BRCA-EU 11 113705632 113705632 single base substitution A T upstream_gene_variant BRCA-EU 11 113707771 113707771 single base substitution C T intron_variant BRCA-EU 11 113707771 113707771 single base substitution C T upstream_gene_variant BRCA-EU 11 113708216 113708216 single base substitution T G intron_variant BRCA-EU 11 113708216 113708216 single base substitution T G upstream_gene_variant BRCA-EU 11 113708409 113708409 insertion of <=200bp - GAAAAAAAAAAAGACTAGACACTACTTCAACTCTAATTTGCAGTTATCATTTCTTCCTCTTCCCTTCCCATTACTCTCC intron_variant BRCA-EU 11 113708409 113708409 insertion of <=200bp - GAAAAAAAAAAAGACTAGACACTACTTCAACTCTAATTTGCAGTTATCATTTCTTCCTCTTCCCTTCCCATTACTCTCC upstream_gene_variant BRCA-EU 11 113708428 113708428 single base substitution C T intron_variant BRCA-EU 11 113708428 113708428 single base substitution C T upstream_gene_variant BRCA-EU 11 113708664 113708664 single base substitution C G intron_variant BRCA-EU 11 113708664 113708664 single base substitution C G upstream_gene_variant BRCA-EU 11 113708934 113708934 deletion of <=200bp G - intron_variant BRCA-EU 11 113708934 113708934 deletion of <=200bp G - upstream_gene_variant BRCA-EU 11 113709499 113709511 deletion of <=200bp AGTAAACCATGAG - intron_variant BRCA-EU 11 113711223 113711223 single base substitution C G intron_variant BRCA-EU 11 113711286 113711286 single base substitution C G intron_variant BRCA-EU 11 113711313 113711313 single base substitution A G splice_region_variant BRCA-EU 11 113713515 113713515 single base substitution G A intron_variant BRCA-EU 11 113713791 113713791 insertion of <=200bp - A intron_variant BRCA-EU 11 113714884 113714884 single base substitution C G intron_variant BRCA-EU 11 113715814 113715814 single base substitution C A intron_variant BRCA-EU 11 113717543 113717543 single base substitution C G intron_variant BRCA-EU 11 113718365 113718365 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 113718365 113718365 deletion of <=200bp A - intron_variant BRCA-EU 11 113718999 113718999 single base substitution C T downstream_gene_variant BRCA-EU 11 113718999 113718999 single base substitution C T intron_variant BRCA-EU 11 113721381 113721381 single base substitution G T downstream_gene_variant BRCA-EU 11 113721381 113721381 single base substitution G T intron_variant BRCA-EU 11 113724285 113724285 single base substitution C T intron_variant BRCA-EU 11 113725552 113725552 single base substitution G A intron_variant BRCA-EU 11 113725767 113725767 single base substitution C T intron_variant BRCA-EU 11 113726125 113726125 single base substitution G C intron_variant BRCA-EU 11 113727806 113727806 single base substitution G C intron_variant BRCA-EU 11 113728998 113728998 single base substitution C A intron_variant BRCA-EU 11 113729240 113729240 single base substitution C G intron_variant BRCA-EU 11 113729488 113729488 single base substitution C A intron_variant BRCA-EU 11 113729747 113729747 single base substitution T C intron_variant BRCA-EU 11 113730659 113730659 single base substitution A G intron_variant BRCA-EU 11 113732489 113732489 single base substitution T C intron_variant BRCA-EU 11 113732653 113732653 single base substitution G A intron_variant BRCA-EU 11 113735258 113735258 single base substitution G C intron_variant BRCA-EU 11 113737477 113737477 single base substitution T G intron_variant BRCA-EU 11 113737657 113737657 single base substitution A G intron_variant BRCA-EU 11 113737819 113737819 single base substitution G C intron_variant BRCA-EU 11 113739744 113739744 single base substitution C T intron_variant BRCA-EU 11 113742030 113742030 single base substitution G C intron_variant BRCA-EU 11 113742217 113742217 single base substitution T G intron_variant BRCA-EU 11 113745886 113745886 single base substitution C T intron_variant BRCA-EU 11 113746350 113746350 single base substitution G C upstream_gene_variant BRCA-EU 11 113748253 113748253 single base substitution G A upstream_gene_variant BRCA-EU 11 113749533 113749533 single base substitution C T upstream_gene_variant BRCA-EU 11 113749534 113749534 single base substitution A G upstream_gene_variant BRCA-EU 11 113750132 113750132 single base substitution G C upstream_gene_variant BRCA-EU 11 113750394 113750394 single base substitution A C upstream_gene_variant BRCA-FR 11 113673943 113673943 single base substitution C T 3_prime_UTR_variant BRCA-FR 11 113673943 113673943 single base substitution C T downstream_gene_variant BRCA-FR 11 113673943 113673943 single base substitution C T missense_variant M609I 1827G>A BRCA-FR 11 113673943 113673943 single base substitution C T missense_variant M776I 2328G>A BRCA-FR 11 113673943 113673943 single base substitution C T missense_variant M901I 2703G>A BRCA-FR 11 113673943 113673943 single base substitution C T missense_variant M933I 2799G>A BRCA-FR 11 113673943 113673943 single base substitution C T upstream_gene_variant BRCA-FR 11 113677388 113677388 single base substitution G C intron_variant BRCA-FR 11 113677388 113677388 single base substitution G C upstream_gene_variant BRCA-FR 11 113683904 113683904 single base substitution G A downstream_gene_variant BRCA-FR 11 113683904 113683904 single base substitution G A intron_variant BRCA-FR 11 113683904 113683904 single base substitution G A upstream_gene_variant BRCA-FR 11 113687827 113687827 single base substitution C G downstream_gene_variant BRCA-FR 11 113687827 113687827 single base substitution C G intron_variant BRCA-FR 11 113698197 113698197 single base substitution C G downstream_gene_variant BRCA-FR 11 113698197 113698197 single base substitution C G intron_variant BRCA-FR 11 113726125 113726125 single base substitution G C intron_variant BRCA-FR 11 113742030 113742030 single base substitution G C intron_variant BRCA-UK 11 113677534 113677534 single base substitution C T intron_variant BRCA-UK 11 113686507 113686507 single base substitution G C downstream_gene_variant BRCA-UK 11 113686507 113686507 single base substitution G C intron_variant BRCA-UK 11 113718365 113718365 deletion of <=200bp A - downstream_gene_variant BRCA-UK 11 113718365 113718365 deletion of <=200bp A - intron_variant BRCA-UK 11 113725036 113725036 single base substitution G A exon_variant BRCA-UK 11 113725036 113725036 single base substitution G A intron_variant BRCA-UK 11 113725036 113725036 single base substitution G A stop_gained Q24* 70C>T BRCA-UK 11 113725036 113725036 single base substitution G A stop_gained Q27* 79C>T BRCA-UK 11 113739403 113739403 single base substitution G A intron_variant BRCA-UK 11 113750394 113750394 single base substitution A C upstream_gene_variant BRCA-US 11 113700047 113700047 single base substitution C A 3_prime_UTR_variant BRCA-US 11 113700047 113700047 single base substitution C A downstream_gene_variant BRCA-US 11 113700047 113700047 single base substitution C A exon_variant BRCA-US 11 113700047 113700047 single base substitution C A stop_gained E186* 556G>T BRCA-US 11 113700047 113700047 single base substitution C A stop_gained E19* 55G>T BRCA-US 11 113700047 113700047 single base substitution C A stop_gained E210* 628G>T BRCA-US 11 113700047 113700047 single base substitution C A stop_gained E311* 931G>T BRCA-US 11 113700047 113700047 single base substitution C A stop_gained E75* 223G>T BRCA-US 11 113702712 113702712 single base substitution C G intron_variant BRCA-US 11 113702712 113702712 single base substitution C G missense_variant D130H 388G>C BRCA-US 11 113702712 113702712 single base substitution C G missense_variant D154H 460G>C BRCA-US 11 113702712 113702712 single base substitution C G missense_variant D19H 55G>C BRCA-US 11 113702712 113702712 single base substitution C G missense_variant D255H 763G>C BRCA-US 11 113702712 113702712 single base substitution C G splice_acceptor_variant BRCA-US 11 113702712 113702712 single base substitution C G upstream_gene_variant BRCA-US 11 113704158 113704158 single base substitution G A 3_prime_UTR_variant BRCA-US 11 113704158 113704158 single base substitution G A exon_variant BRCA-US 11 113704158 113704158 single base substitution G A missense_variant S123L 368C>T BRCA-US 11 113704158 113704158 single base substitution G A missense_variant S12L 35C>T BRCA-US 11 113704158 113704158 single base substitution G A missense_variant S147L 440C>T BRCA-US 11 113704158 113704158 single base substitution G A missense_variant S248L 743C>T BRCA-US 11 113704158 113704158 single base substitution G A upstream_gene_variant BRCA-US 11 113704197 113704197 single base substitution G A 3_prime_UTR_variant BRCA-US 11 113704197 113704197 single base substitution G A exon_variant BRCA-US 11 113704197 113704197 single base substitution G A missense_variant P110L 329C>T BRCA-US 11 113704197 113704197 single base substitution G A missense_variant P134L 401C>T BRCA-US 11 113704197 113704197 single base substitution G A missense_variant P235L 704C>T BRCA-US 11 113704197 113704197 single base substitution G A upstream_gene_variant BRCA-US 11 113723334 113723334 single base substitution G A downstream_gene_variant BRCA-US 11 113723334 113723334 single base substitution G A exon_variant BRCA-US 11 113723334 113723334 single base substitution G A intron_variant BRCA-US 11 113723334 113723334 single base substitution G A stop_gained Q50* 148C>T BRCA-US 11 113723334 113723334 single base substitution G A stop_gained Q53* 157C>T BTCA-JP 11 113674364 113674364 single base substitution T C downstream_gene_variant BTCA-JP 11 113674364 113674364 single base substitution T C intron_variant BTCA-JP 11 113674364 113674364 single base substitution T C upstream_gene_variant BTCA-JP 11 113675680 113675680 single base substitution A C 3_prime_UTR_variant BTCA-JP 11 113675680 113675680 single base substitution A C missense_variant V184G 551T>G BTCA-JP 11 113675680 113675680 single base substitution A C missense_variant V506G 1517T>G BTCA-JP 11 113675680 113675680 single base substitution A C missense_variant V673G 2018T>G BTCA-JP 11 113675680 113675680 single base substitution A C missense_variant V798G 2393T>G BTCA-JP 11 113675680 113675680 single base substitution A C missense_variant V830G 2489T>G BTCA-JP 11 113675680 113675680 single base substitution A C upstream_gene_variant BTCA-JP 11 113704257 113704257 single base substitution A T 3_prime_UTR_variant BTCA-JP 11 113704257 113704257 single base substitution A T exon_variant BTCA-JP 11 113704257 113704257 single base substitution A T missense_variant M114K 341T>A BTCA-JP 11 113704257 113704257 single base substitution A T missense_variant M215K 644T>A BTCA-JP 11 113704257 113704257 single base substitution A T missense_variant M90K 269T>A BTCA-JP 11 113704257 113704257 single base substitution A T upstream_gene_variant BTCA-JP 11 113712421 113712421 single base substitution G A 5_prime_UTR_variant BTCA-JP 11 113712421 113712421 single base substitution G A exon_variant BTCA-JP 11 113712421 113712421 single base substitution G A missense_variant S113F 338C>T BTCA-JP 11 113712421 113712421 single base substitution G A missense_variant S41F 122C>T CESC-US 11 113674600 113674600 single base substitution C G downstream_gene_variant CESC-US 11 113674600 113674600 single base substitution C G splice_acceptor_variant CESC-US 11 113674600 113674600 single base substitution C G upstream_gene_variant CESC-US 11 113685932 113685932 single base substitution G A downstream_gene_variant CESC-US 11 113685932 113685932 single base substitution G A intron_variant CESC-US 11 113685932 113685932 single base substitution G A stop_gained Q250* 748C>T CESC-US 11 113685932 113685932 single base substitution G A stop_gained Q254* 760C>T CESC-US 11 113685932 113685932 single base substitution G A stop_gained Q421* 1261C>T CESC-US 11 113685932 113685932 single base substitution G A stop_gained Q546* 1636C>T CESC-US 11 113698046 113698046 single base substitution C T 3_prime_UTR_variant CESC-US 11 113698046 113698046 single base substitution C T downstream_gene_variant CESC-US 11 113698046 113698046 single base substitution C T missense_variant E130K 388G>A CESC-US 11 113698046 113698046 single base substitution C T missense_variant E241K 721G>A CESC-US 11 113698046 113698046 single base substitution C T missense_variant E366K 1096G>A CESC-US 11 113698046 113698046 single base substitution C T missense_variant E74K 220G>A CESC-US 11 113711322 113711322 single base substitution G A splice_region_variant CESC-US 11 113711322 113711322 single base substitution G A stop_gained Q106* 316C>T CESC-US 11 113711322 113711322 single base substitution G A stop_gained Q178* 532C>T CESC-US 11 113711322 113711322 single base substitution G A stop_gained Q53* 157C>T CLLE-ES 11 113675739 113675739 single base substitution A T 3_prime_UTR_variant CLLE-ES 11 113675739 113675739 single base substitution A T stop_gained Y164* 492T>A CLLE-ES 11 113675739 113675739 single base substitution A T stop_gained Y486* 1458T>A CLLE-ES 11 113675739 113675739 single base substitution A T stop_gained Y653* 1959T>A CLLE-ES 11 113675739 113675739 single base substitution A T stop_gained Y778* 2334T>A CLLE-ES 11 113675739 113675739 single base substitution A T stop_gained Y810* 2430T>A CLLE-ES 11 113675739 113675739 single base substitution A T upstream_gene_variant CLLE-ES 11 113678408 113678408 single base substitution T C downstream_gene_variant CLLE-ES 11 113678408 113678408 single base substitution T C intron_variant CLLE-ES 11 113684043 113684051 deletion of <=200bp ACAGAAGCC - downstream_gene_variant CLLE-ES 11 113684043 113684051 deletion of <=200bp ACAGAAGCC - intron_variant CLLE-ES 11 113684043 113684051 deletion of <=200bp ACAGAAGCC - upstream_gene_variant CLLE-ES 11 113711317 113711317 single base substitution T A splice_region_variant CLLE-ES 11 113711359 113711359 single base substitution T A exon_variant CLLE-ES 11 113711359 113711359 single base substitution T A missense_variant K165N 495A>T CLLE-ES 11 113711359 113711359 single base substitution T A missense_variant K40N 120A>T CLLE-ES 11 113711359 113711359 single base substitution T A missense_variant K93N 279A>T CLLE-ES 11 113721310 113721310 single base substitution C T downstream_gene_variant CLLE-ES 11 113721310 113721310 single base substitution C T intron_variant CLLE-ES 11 113733853 113733853 single base substitution T C intron_variant COAD-US 11 113673918 113673918 single base substitution C A 3_prime_UTR_variant COAD-US 11 113673918 113673918 single base substitution C A downstream_gene_variant COAD-US 11 113673918 113673918 single base substitution C A stop_gained E618* 1852G>T COAD-US 11 113673918 113673918 single base substitution C A stop_gained E785* 2353G>T COAD-US 11 113673918 113673918 single base substitution C A stop_gained E910* 2728G>T COAD-US 11 113673918 113673918 single base substitution C A stop_gained E942* 2824G>T COAD-US 11 113673918 113673918 single base substitution C A upstream_gene_variant COAD-US 11 113677252 113677252 single base substitution G A intron_variant COAD-US 11 113677252 113677252 single base substitution G A stop_gained Q141* 421C>T COAD-US 11 113677252 113677252 single base substitution G A stop_gained Q787* 2359C>T COAD-US 11 113677252 113677252 single base substitution G A upstream_gene_variant COAD-US 11 113677254 113677254 single base substitution C T intron_variant COAD-US 11 113677254 113677254 single base substitution C T missense_variant R140H 419G>A COAD-US 11 113677254 113677254 single base substitution C T missense_variant R786H 2357G>A COAD-US 11 113677254 113677254 single base substitution C T upstream_gene_variant COAD-US 11 113684607 113684607 single base substitution C A downstream_gene_variant COAD-US 11 113684607 113684607 single base substitution C A intron_variant COAD-US 11 113684607 113684607 single base substitution C A missense_variant Q285H 855G>T COAD-US 11 113684607 113684607 single base substitution C A missense_variant Q289H 867G>T COAD-US 11 113684607 113684607 single base substitution C A missense_variant Q456H 1368G>T COAD-US 11 113684607 113684607 single base substitution C A missense_variant Q581H 1743G>T COAD-US 11 113684607 113684607 single base substitution C A upstream_gene_variant COAD-US 11 113688554 113688554 single base substitution A G 3_prime_UTR_variant COAD-US 11 113688554 113688554 single base substitution A G intron_variant COAD-US 11 113688554 113688554 single base substitution A G missense_variant V138A 413T>C COAD-US 11 113688554 113688554 single base substitution A G missense_variant V305A 914T>C COAD-US 11 113688554 113688554 single base substitution A G missense_variant V430A 1289T>C COAD-US 11 113700063 113700063 deletion of <=200bp T - 3_prime_UTR_variant COAD-US 11 113700063 113700063 deletion of <=200bp T - downstream_gene_variant COAD-US 11 113700063 113700063 deletion of <=200bp T - exon_variant COAD-US 11 113700063 113700063 deletion of <=200bp T - frameshift_variant K13 COAD-US 11 113700063 113700063 deletion of <=200bp T - frameshift_variant K180 COAD-US 11 113700063 113700063 deletion of <=200bp T - frameshift_variant K204 COAD-US 11 113700063 113700063 deletion of <=200bp T - frameshift_variant K305 COAD-US 11 113700063 113700063 deletion of <=200bp T - frameshift_variant K69 COAD-US 11 113701594 113701594 single base substitution C T 3_prime_UTR_variant COAD-US 11 113701594 113701594 single base substitution C T downstream_gene_variant COAD-US 11 113701594 113701594 single base substitution C T exon_variant COAD-US 11 113701594 113701594 single base substitution C T missense_variant R177H 530G>A COAD-US 11 113701594 113701594 single base substitution C T missense_variant R201H 602G>A COAD-US 11 113701594 113701594 single base substitution C T missense_variant R302H 905G>A COAD-US 11 113701594 113701594 single base substitution C T missense_variant R66H 197G>A COAD-US 11 113701594 113701594 single base substitution C T upstream_gene_variant COAD-US 11 113704162 113704162 single base substitution G A 3_prime_UTR_variant COAD-US 11 113704162 113704162 single base substitution G A exon_variant COAD-US 11 113704162 113704162 single base substitution G A stop_gained R11* 31C>T COAD-US 11 113704162 113704162 single base substitution G A stop_gained R122* 364C>T COAD-US 11 113704162 113704162 single base substitution G A stop_gained R146* 436C>T COAD-US 11 113704162 113704162 single base substitution G A stop_gained R247* 739C>T COAD-US 11 113704162 113704162 single base substitution G A upstream_gene_variant COAD-US 11 113704982 113704982 single base substitution G A 3_prime_UTR_variant COAD-US 11 113704982 113704982 single base substitution G A exon_variant COAD-US 11 113704982 113704982 single base substitution G A intron_variant COAD-US 11 113704982 113704982 single base substitution G A stop_gained R204* 610C>T COAD-US 11 113704982 113704982 single base substitution G A stop_gained R79* 235C>T COAD-US 11 113704982 113704982 single base substitution G A upstream_gene_variant COAD-US 11 113711469 113711469 single base substitution C T exon_variant COAD-US 11 113711469 113711469 single base substitution C T missense_variant A129T 385G>A COAD-US 11 113711469 113711469 single base substitution C T missense_variant A4T 10G>A COAD-US 11 113711469 113711469 single base substitution C T missense_variant A57T 169G>A COAD-US 11 113723235 113723235 single base substitution C A downstream_gene_variant COAD-US 11 113723235 113723235 single base substitution C A exon_variant COAD-US 11 113723235 113723235 single base substitution C A intron_variant COAD-US 11 113723235 113723235 single base substitution C A stop_gained E86* 256G>T COCA-CN 11 113665579 113665579 single base substitution G A downstream_gene_variant COCA-CN 11 113670259 113670259 single base substitution T C intron_variant COCA-CN 11 113672257 113672257 single base substitution G A 3_prime_UTR_variant COCA-CN 11 113672257 113672257 single base substitution G A downstream_gene_variant COCA-CN 11 113672257 113672257 single base substitution G A exon_variant COCA-CN 11 113672257 113672257 single base substitution G A synonymous_variant A1002A 3006C>T COCA-CN 11 113672257 113672257 single base substitution G A synonymous_variant A678A 2034C>T COCA-CN 11 113672257 113672257 single base substitution G A synonymous_variant A845A 2535C>T COCA-CN 11 113672257 113672257 single base substitution G A synonymous_variant A970A 2910C>T COCA-CN 11 113674516 113674516 single base substitution A C downstream_gene_variant COCA-CN 11 113674516 113674516 single base substitution A C splice_region_variant COCA-CN 11 113674516 113674516 single base substitution A C upstream_gene_variant COCA-CN 11 113675647 113675647 single base substitution A G 3_prime_UTR_variant COCA-CN 11 113675647 113675647 single base substitution A G downstream_gene_variant COCA-CN 11 113675647 113675647 single base substitution A G missense_variant V517A 1550T>C COCA-CN 11 113675647 113675647 single base substitution A G missense_variant V684A 2051T>C COCA-CN 11 113675647 113675647 single base substitution A G missense_variant V809A 2426T>C COCA-CN 11 113675647 113675647 single base substitution A G missense_variant V841A 2522T>C COCA-CN 11 113675647 113675647 single base substitution A G upstream_gene_variant COCA-CN 11 113679154 113679154 single base substitution A G 3_prime_UTR_variant COCA-CN 11 113679154 113679154 single base substitution A G downstream_gene_variant COCA-CN 11 113679154 113679154 single base substitution A G missense_variant S40P 118T>C COCA-CN 11 113679154 113679154 single base substitution A G missense_variant S432P 1294T>C COCA-CN 11 113679154 113679154 single base substitution A G missense_variant S599P 1795T>C COCA-CN 11 113679154 113679154 single base substitution A G missense_variant S724P 2170T>C COCA-CN 11 113699530 113699530 single base substitution A C downstream_gene_variant COCA-CN 11 113699530 113699530 single base substitution A C intron_variant COCA-CN 11 113699740 113699740 single base substitution T G downstream_gene_variant COCA-CN 11 113699740 113699740 single base substitution T G intron_variant COCA-CN 11 113699997 113699997 single base substitution G A 3_prime_UTR_variant COCA-CN 11 113699997 113699997 single base substitution G A downstream_gene_variant COCA-CN 11 113699997 113699997 single base substitution G A exon_variant COCA-CN 11 113699997 113699997 single base substitution G A synonymous_variant D202D 606C>T COCA-CN 11 113699997 113699997 single base substitution G A synonymous_variant D226D 678C>T COCA-CN 11 113699997 113699997 single base substitution G A synonymous_variant D327D 981C>T COCA-CN 11 113699997 113699997 single base substitution G A synonymous_variant D35D 105C>T COCA-CN 11 113699997 113699997 single base substitution G A synonymous_variant D91D 273C>T COCA-CN 11 113704139 113704139 single base substitution T C intron_variant COCA-CN 11 113704139 113704139 single base substitution T C splice_region_variant COCA-CN 11 113704139 113704139 single base substitution T C upstream_gene_variant COCA-CN 11 113711302 113711302 single base substitution C A intron_variant COCA-CN 11 113711314 113711314 single base substitution T A splice_region_variant COCA-CN 11 113711374 113711374 single base substitution C T exon_variant COCA-CN 11 113711374 113711374 single base substitution C T stop_gained W160* 480G>A COCA-CN 11 113711374 113711374 single base substitution C T stop_gained W35* 105G>A COCA-CN 11 113711374 113711374 single base substitution C T stop_gained W88* 264G>A COCA-CN 11 113720727 113720727 single base substitution C T downstream_gene_variant COCA-CN 11 113720727 113720727 single base substitution C T intron_variant COCA-CN 11 113721792 113721792 single base substitution C T downstream_gene_variant COCA-CN 11 113721792 113721792 single base substitution C T intron_variant COCA-CN 11 113724964 113724964 single base substitution A C intron_variant COCA-CN 11 113735136 113735136 single base substitution G A intron_variant COCA-CN 11 113745174 113745174 single base substitution G T intron_variant COCA-CN 11 113745211 113745211 single base substitution G T intron_variant EOPC-DE 11 113715958 113715958 single base substitution C G intron_variant EOPC-DE 11 113725280 113725280 single base substitution C T intron_variant EOPC-DE 11 113746430 113746430 single base substitution C T upstream_gene_variant ESAD-UK 11 113664288 113664288 deletion of <=200bp A - downstream_gene_variant ESAD-UK 11 113664999 113664999 single base substitution C T downstream_gene_variant ESAD-UK 11 113665326 113665326 single base substitution T C downstream_gene_variant ESAD-UK 11 113665941 113665941 single base substitution C T downstream_gene_variant ESAD-UK 11 113667361 113667361 single base substitution G A downstream_gene_variant ESAD-UK 11 113668642 113668642 insertion of <=200bp - T 3_prime_UTR_variant ESAD-UK 11 113668642 113668642 insertion of <=200bp - T downstream_gene_variant ESAD-UK 11 113670232 113670232 single base substitution G A intron_variant ESAD-UK 11 113673184 113673184 single base substitution G A downstream_gene_variant ESAD-UK 11 113673184 113673184 single base substitution G A intron_variant ESAD-UK 11 113673184 113673184 single base substitution G A upstream_gene_variant ESAD-UK 11 113674208 113674208 single base substitution C T downstream_gene_variant ESAD-UK 11 113674208 113674208 single base substitution C T intron_variant ESAD-UK 11 113674208 113674208 single base substitution C T upstream_gene_variant ESAD-UK 11 113676873 113676873 single base substitution C G intron_variant ESAD-UK 11 113676873 113676873 single base substitution C G upstream_gene_variant ESAD-UK 11 113677734 113677734 single base substitution A T intron_variant ESAD-UK 11 113680169 113680169 insertion of <=200bp - T downstream_gene_variant ESAD-UK 11 113680169 113680169 insertion of <=200bp - T intron_variant ESAD-UK 11 113680169 113680169 insertion of <=200bp - T upstream_gene_variant ESAD-UK 11 113682118 113682118 single base substitution C T downstream_gene_variant ESAD-UK 11 113682118 113682118 single base substitution C T intron_variant ESAD-UK 11 113682118 113682118 single base substitution C T upstream_gene_variant ESAD-UK 11 113685325 113685325 single base substitution G T downstream_gene_variant ESAD-UK 11 113685325 113685325 single base substitution G T intron_variant ESAD-UK 11 113689298 113689298 single base substitution C T intron_variant ESAD-UK 11 113691174 113691174 single base substitution A C intron_variant ESAD-UK 11 113691584 113691584 single base substitution C T intron_variant ESAD-UK 11 113692220 113692220 single base substitution G A intron_variant ESAD-UK 11 113695241 113695241 single base substitution A T downstream_gene_variant ESAD-UK 11 113695241 113695241 single base substitution A T intron_variant ESAD-UK 11 113697835 113697835 single base substitution G T downstream_gene_variant ESAD-UK 11 113697835 113697835 single base substitution G T intron_variant ESAD-UK 11 113702210 113702210 single base substitution G A intron_variant ESAD-UK 11 113702210 113702210 single base substitution G A upstream_gene_variant ESAD-UK 11 113703964 113703964 single base substitution C G intron_variant ESAD-UK 11 113703964 113703964 single base substitution C G upstream_gene_variant ESAD-UK 11 113705256 113705256 single base substitution A G intron_variant ESAD-UK 11 113705256 113705256 single base substitution A G upstream_gene_variant ESAD-UK 11 113706227 113706227 single base substitution C T intron_variant ESAD-UK 11 113706227 113706227 single base substitution C T upstream_gene_variant ESAD-UK 11 113707118 113707118 single base substitution C T intron_variant ESAD-UK 11 113707118 113707118 single base substitution C T upstream_gene_variant ESAD-UK 11 113707555 113707555 single base substitution C T intron_variant ESAD-UK 11 113707555 113707555 single base substitution C T upstream_gene_variant ESAD-UK 11 113709840 113709840 single base substitution C T intron_variant ESAD-UK 11 113710162 113710162 single base substitution C T intron_variant ESAD-UK 11 113715114 113715119 deletion of <=200bp CGAGAT - intron_variant ESAD-UK 11 113721721 113721721 single base substitution G A downstream_gene_variant ESAD-UK 11 113721721 113721721 single base substitution G A intron_variant ESAD-UK 11 113722371 113722371 single base substitution A C downstream_gene_variant ESAD-UK 11 113722371 113722371 single base substitution A C intron_variant ESAD-UK 11 113722561 113722561 single base substitution T G downstream_gene_variant ESAD-UK 11 113722561 113722561 single base substitution T G intron_variant ESAD-UK 11 113726947 113726947 single base substitution C G intron_variant ESAD-UK 11 113728615 113728615 single base substitution C G intron_variant ESAD-UK 11 113729390 113729390 single base substitution G A intron_variant ESAD-UK 11 113730813 113730813 single base substitution C T intron_variant ESAD-UK 11 113732251 113732251 deletion of <=200bp A - intron_variant ESAD-UK 11 113734242 113734242 single base substitution C T intron_variant ESAD-UK 11 113738374 113738374 single base substitution C A intron_variant ESAD-UK 11 113739205 113739205 single base substitution C G intron_variant ESAD-UK 11 113739212 113739212 single base substitution C T intron_variant ESAD-UK 11 113739671 113739671 single base substitution G A intron_variant ESAD-UK 11 113741873 113741873 single base substitution T C intron_variant ESAD-UK 11 113742045 113742045 single base substitution G A intron_variant ESAD-UK 11 113742974 113742974 single base substitution C T intron_variant ESAD-UK 11 113744514 113744514 single base substitution G A intron_variant ESAD-UK 11 113747510 113747510 deletion of <=200bp T - upstream_gene_variant ESAD-UK 11 113748930 113748930 single base substitution C A upstream_gene_variant ESCA-CN 11 113688405 113688405 single base substitution C T 3_prime_UTR_variant ESCA-CN 11 113688405 113688405 single base substitution C T downstream_gene_variant ESCA-CN 11 113688405 113688405 single base substitution C T intron_variant ESCA-CN 11 113688405 113688405 single base substitution C T missense_variant V188I 562G>A ESCA-CN 11 113688405 113688405 single base substitution C T missense_variant V355I 1063G>A ESCA-CN 11 113688405 113688405 single base substitution C T missense_variant V480I 1438G>A GBM-US 11 113672259 113672259 single base substitution C T 3_prime_UTR_variant GBM-US 11 113672259 113672259 single base substitution C T downstream_gene_variant GBM-US 11 113672259 113672259 single base substitution C T exon_variant GBM-US 11 113672259 113672259 single base substitution C T missense_variant A1002T 3004G>A GBM-US 11 113672259 113672259 single base substitution C T missense_variant A678T 2032G>A GBM-US 11 113672259 113672259 single base substitution C T missense_variant A845T 2533G>A GBM-US 11 113672259 113672259 single base substitution C T missense_variant A970T 2908G>A GBM-US 11 113677209 113677209 single base substitution A G intron_variant GBM-US 11 113677209 113677209 single base substitution A G splice_donor_variant GBM-US 11 113677209 113677209 single base substitution A G upstream_gene_variant GBM-US 11 113688486 113688486 single base substitution T C 3_prime_UTR_variant GBM-US 11 113688486 113688486 single base substitution T C downstream_gene_variant GBM-US 11 113688486 113688486 single base substitution T C intron_variant GBM-US 11 113688486 113688486 single base substitution T C missense_variant S161G 481A>G GBM-US 11 113688486 113688486 single base substitution T C missense_variant S328G 982A>G GBM-US 11 113688486 113688486 single base substitution T C missense_variant S453G 1357A>G KIRC-US 11 113684670 113684670 single base substitution C A downstream_gene_variant KIRC-US 11 113684670 113684670 single base substitution C A intron_variant KIRC-US 11 113684670 113684670 single base substitution C A missense_variant K264N 792G>T KIRC-US 11 113684670 113684670 single base substitution C A missense_variant K268N 804G>T KIRC-US 11 113684670 113684670 single base substitution C A missense_variant K435N 1305G>T KIRC-US 11 113684670 113684670 single base substitution C A missense_variant K560N 1680G>T KIRC-US 11 113684670 113684670 single base substitution C A upstream_gene_variant KIRC-US 11 113694390 113694391 deletion of <=200bp TT - 3_prime_UTR_variant KIRC-US 11 113694390 113694391 deletion of <=200bp TT - frameshift_variant N115 KIRC-US 11 113694390 113694391 deletion of <=200bp TT - frameshift_variant N171 KIRC-US 11 113694390 113694391 deletion of <=200bp TT - frameshift_variant N282 KIRC-US 11 113694390 113694391 deletion of <=200bp TT - frameshift_variant N407 KIRC-US 11 113701632 113701632 single base substitution C A 3_prime_UTR_variant KIRC-US 11 113701632 113701632 single base substitution C A exon_variant KIRC-US 11 113701632 113701632 single base substitution C A synonymous_variant V164V 492G>T KIRC-US 11 113701632 113701632 single base substitution C A synonymous_variant V188V 564G>T KIRC-US 11 113701632 113701632 single base substitution C A synonymous_variant V289V 867G>T KIRC-US 11 113701632 113701632 single base substitution C A synonymous_variant V53V 159G>T KIRC-US 11 113701632 113701632 single base substitution C A upstream_gene_variant KIRP-US 11 113679118 113679118 insertion of <=200bp - TG 3_prime_UTR_variant KIRP-US 11 113679118 113679118 insertion of <=200bp - TG downstream_gene_variant KIRP-US 11 113679118 113679118 insertion of <=200bp - TG frameshift_variant S444S? KIRP-US 11 113679118 113679118 insertion of <=200bp - TG frameshift_variant S52S? KIRP-US 11 113679118 113679118 insertion of <=200bp - TG frameshift_variant S611S? KIRP-US 11 113679118 113679118 insertion of <=200bp - TG frameshift_variant S736S? KIRP-US 11 113679909 113679909 single base substitution G T 3_prime_UTR_variant KIRP-US 11 113679909 113679909 single base substitution G T downstream_gene_variant KIRP-US 11 113679909 113679909 single base substitution G T stop_gained Y388* 1164C>A KIRP-US 11 113679909 113679909 single base substitution G T stop_gained Y555* 1665C>A KIRP-US 11 113679909 113679909 single base substitution G T stop_gained Y680* 2040C>A KIRP-US 11 113679909 113679909 single base substitution G T upstream_gene_variant KIRP-US 11 113705056 113705056 single base substitution G C intron_variant KIRP-US 11 113705056 113705056 single base substitution G C missense_variant S179C 536C>G KIRP-US 11 113705056 113705056 single base substitution G C missense_variant S54C 161C>G KIRP-US 11 113705056 113705056 single base substitution G C splice_region_variant KIRP-US 11 113705056 113705056 single base substitution G C upstream_gene_variant LAML-CN 11 113688566 113688566 single base substitution G A intron_variant LAML-CN 11 113688566 113688566 single base substitution G A splice_region_variant LAML-KR 11 113665238 113665238 single base substitution C A downstream_gene_variant LAML-KR 11 113714414 113714414 single base substitution T A intron_variant LAML-KR 11 113731716 113731716 single base substitution G T intron_variant LICA-CN 11 113673983 113673983 single base substitution T A 3_prime_UTR_variant LICA-CN 11 113673983 113673983 single base substitution T A downstream_gene_variant LICA-CN 11 113673983 113673983 single base substitution T A missense_variant Y596F 1787A>T LICA-CN 11 113673983 113673983 single base substitution T A missense_variant Y763F 2288A>T LICA-CN 11 113673983 113673983 single base substitution T A missense_variant Y888F 2663A>T LICA-CN 11 113673983 113673983 single base substitution T A missense_variant Y920F 2759A>T LICA-CN 11 113673983 113673983 single base substitution T A upstream_gene_variant LICA-CN 11 113683193 113683193 single base substitution C A downstream_gene_variant LICA-CN 11 113683193 113683193 single base substitution C A intron_variant LICA-CN 11 113683193 113683193 single base substitution C A stop_gained E297* 889G>T LICA-CN 11 113683193 113683193 single base substitution C A stop_gained E301* 901G>T LICA-CN 11 113683193 113683193 single base substitution C A stop_gained E468* 1402G>T LICA-CN 11 113683193 113683193 single base substitution C A stop_gained E593* 1777G>T LICA-CN 11 113683193 113683193 single base substitution C A upstream_gene_variant LICA-FR 11 113664093 113664093 single base substitution C A downstream_gene_variant LICA-FR 11 113677282 113677282 single base substitution C A intron_variant LICA-FR 11 113677282 113677282 single base substitution C A missense_variant G131W 391G>T LICA-FR 11 113677282 113677282 single base substitution C A missense_variant G777W 2329G>T LICA-FR 11 113677282 113677282 single base substitution C A upstream_gene_variant LICA-FR 11 113679936 113679950 deletion of <=200bp TTCCACTTCTGACAT - 3_prime_UTR_variant LICA-FR 11 113679936 113679950 deletion of <=200bp TTCCACTTCTGACAT - downstream_gene_variant LICA-FR 11 113679936 113679950 deletion of <=200bp TTCCACTTCTGACAT - inframe_deletion MSEVE375 LICA-FR 11 113679936 113679950 deletion of <=200bp TTCCACTTCTGACAT - inframe_deletion MSEVE542 LICA-FR 11 113679936 113679950 deletion of <=200bp TTCCACTTCTGACAT - inframe_deletion MSEVE667 LICA-FR 11 113679936 113679950 deletion of <=200bp TTCCACTTCTGACAT - upstream_gene_variant LICA-FR 11 113694507 113694507 single base substitution T A intron_variant LICA-FR 11 113711338 113711338 single base substitution C T exon_variant LICA-FR 11 113711338 113711338 single base substitution C T stop_gained W100* 300G>A LICA-FR 11 113711338 113711338 single base substitution C T stop_gained W172* 516G>A LICA-FR 11 113711338 113711338 single base substitution C T stop_gained W47* 141G>A LICA-FR 11 113732843 113732843 single base substitution C T intron_variant LIHC-US 11 113699932 113699932 single base substitution T C 3_prime_UTR_variant LIHC-US 11 113699932 113699932 single base substitution T C downstream_gene_variant LIHC-US 11 113699932 113699932 single base substitution T C exon_variant LIHC-US 11 113699932 113699932 single base substitution T C missense_variant K113R 338A>G LIHC-US 11 113699932 113699932 single base substitution T C missense_variant K224R 671A>G LIHC-US 11 113699932 113699932 single base substitution T C missense_variant K349R 1046A>G LIHC-US 11 113699932 113699932 single base substitution T C missense_variant K57R 170A>G LINC-JP 11 113670042 113670042 single base substitution T C 3_prime_UTR_variant LINC-JP 11 113670042 113670042 single base substitution T C exon_variant LINC-JP 11 113670042 113670042 single base substitution T C missense_variant N1020D 3058A>G LINC-JP 11 113670042 113670042 single base substitution T C missense_variant N1052D 3154A>G LINC-JP 11 113670042 113670042 single base substitution T C missense_variant N728D 2182A>G LINC-JP 11 113670042 113670042 single base substitution T C missense_variant N895D 2683A>G LINC-JP 11 113672324 113672324 single base substitution T G 3_prime_UTR_variant LINC-JP 11 113672324 113672324 single base substitution T G downstream_gene_variant LINC-JP 11 113672324 113672324 single base substitution T G exon_variant LINC-JP 11 113672324 113672324 single base substitution T G missense_variant N656T 1967A>C LINC-JP 11 113672324 113672324 single base substitution T G missense_variant N823T 2468A>C LINC-JP 11 113672324 113672324 single base substitution T G missense_variant N948T 2843A>C LINC-JP 11 113672324 113672324 single base substitution T G missense_variant N980T 2939A>C LINC-JP 11 113674390 113674390 single base substitution G C downstream_gene_variant LINC-JP 11 113674390 113674390 single base substitution G C intron_variant LINC-JP 11 113674390 113674390 single base substitution G C upstream_gene_variant LINC-JP 11 113675382 113675382 single base substitution G T downstream_gene_variant LINC-JP 11 113675382 113675382 single base substitution G T intron_variant LINC-JP 11 113675382 113675382 single base substitution G T upstream_gene_variant LINC-JP 11 113675577 113675577 single base substitution A T downstream_gene_variant LINC-JP 11 113675577 113675577 single base substitution A T intron_variant LINC-JP 11 113675577 113675577 single base substitution A T upstream_gene_variant LINC-JP 11 113683120 113683120 single base substitution T C 3_prime_UTR_variant LINC-JP 11 113683120 113683120 single base substitution T C downstream_gene_variant LINC-JP 11 113683120 113683120 single base substitution T C missense_variant N321S 962A>G LINC-JP 11 113683120 113683120 single base substitution T C missense_variant N325S 974A>G LINC-JP 11 113683120 113683120 single base substitution T C missense_variant N492S 1475A>G LINC-JP 11 113683120 113683120 single base substitution T C missense_variant N617S 1850A>G LINC-JP 11 113683120 113683120 single base substitution T C upstream_gene_variant LINC-JP 11 113684611 113684611 single base substitution C T downstream_gene_variant LINC-JP 11 113684611 113684611 single base substitution C T intron_variant LINC-JP 11 113684611 113684611 single base substitution C T missense_variant R284H 851G>A LINC-JP 11 113684611 113684611 single base substitution C T missense_variant R288H 863G>A LINC-JP 11 113684611 113684611 single base substitution C T missense_variant R455H 1364G>A LINC-JP 11 113684611 113684611 single base substitution C T missense_variant R580H 1739G>A LINC-JP 11 113684611 113684611 single base substitution C T upstream_gene_variant LINC-JP 11 113687740 113687740 insertion of <=200bp - A downstream_gene_variant LINC-JP 11 113687740 113687740 insertion of <=200bp - A intron_variant LINC-JP 11 113688437 113688437 single base substitution A G 3_prime_UTR_variant LINC-JP 11 113688437 113688437 single base substitution A G downstream_gene_variant LINC-JP 11 113688437 113688437 single base substitution A G intron_variant LINC-JP 11 113688437 113688437 single base substitution A G missense_variant M177T 530T>C LINC-JP 11 113688437 113688437 single base substitution A G missense_variant M344T 1031T>C LINC-JP 11 113688437 113688437 single base substitution A G missense_variant M469T 1406T>C LINC-JP 11 113688493 113688493 single base substitution T C 3_prime_UTR_variant LINC-JP 11 113688493 113688493 single base substitution T C downstream_gene_variant LINC-JP 11 113688493 113688493 single base substitution T C intron_variant LINC-JP 11 113688493 113688493 single base substitution T C synonymous_variant E158E 474A>G LINC-JP 11 113688493 113688493 single base substitution T C synonymous_variant E325E 975A>G LINC-JP 11 113688493 113688493 single base substitution T C synonymous_variant E450E 1350A>G LINC-JP 11 113697657 113697657 single base substitution C A downstream_gene_variant LINC-JP 11 113697657 113697657 single base substitution C A intron_variant LINC-JP 11 113698096 113698096 single base substitution T C downstream_gene_variant LINC-JP 11 113698096 113698096 single base substitution T C intron_variant LINC-JP 11 113698824 113698824 insertion of <=200bp - A downstream_gene_variant LINC-JP 11 113698824 113698824 insertion of <=200bp - A intron_variant LINC-JP 11 113712421 113712421 single base substitution G A 5_prime_UTR_variant LINC-JP 11 113712421 113712421 single base substitution G A exon_variant LINC-JP 11 113712421 113712421 single base substitution G A missense_variant S113F 338C>T LINC-JP 11 113712421 113712421 single base substitution G A missense_variant S41F 122C>T LINC-JP 11 113730733 113730733 single base substitution A C intron_variant LINC-JP 11 113739143 113739143 single base substitution A G intron_variant LINC-JP 11 113747809 113747809 single base substitution A G upstream_gene_variant LINC-JP 11 113750907 113750907 single base substitution T C upstream_gene_variant LIRI-JP 11 113665975 113665975 single base substitution G A downstream_gene_variant LIRI-JP 11 113667289 113667289 single base substitution G C downstream_gene_variant LIRI-JP 11 113669103 113669103 single base substitution C T 3_prime_UTR_variant LIRI-JP 11 113669103 113669103 single base substitution C T downstream_gene_variant LIRI-JP 11 113670089 113670089 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 113670089 113670089 single base substitution G A exon_variant LIRI-JP 11 113670089 113670089 single base substitution G A missense_variant P1004L 3011C>T LIRI-JP 11 113670089 113670089 single base substitution G A missense_variant P1036L 3107C>T LIRI-JP 11 113670089 113670089 single base substitution G A missense_variant P712L 2135C>T LIRI-JP 11 113670089 113670089 single base substitution G A missense_variant P879L 2636C>T LIRI-JP 11 113673450 113673450 single base substitution C A downstream_gene_variant LIRI-JP 11 113673450 113673450 single base substitution C A intron_variant LIRI-JP 11 113673450 113673450 single base substitution C A upstream_gene_variant LIRI-JP 11 113674315 113674315 single base substitution C A downstream_gene_variant LIRI-JP 11 113674315 113674315 single base substitution C A intron_variant LIRI-JP 11 113674315 113674315 single base substitution C A upstream_gene_variant LIRI-JP 11 113674370 113674370 single base substitution G A downstream_gene_variant LIRI-JP 11 113674370 113674370 single base substitution G A intron_variant LIRI-JP 11 113674370 113674370 single base substitution G A upstream_gene_variant LIRI-JP 11 113676903 113676903 single base substitution C T intron_variant LIRI-JP 11 113676903 113676903 single base substitution C T upstream_gene_variant LIRI-JP 11 113680310 113680310 single base substitution T C downstream_gene_variant LIRI-JP 11 113680310 113680310 single base substitution T C intron_variant LIRI-JP 11 113680310 113680310 single base substitution T C upstream_gene_variant LIRI-JP 11 113681296 113681296 single base substitution T C downstream_gene_variant LIRI-JP 11 113681296 113681296 single base substitution T C intron_variant LIRI-JP 11 113681296 113681296 single base substitution T C upstream_gene_variant LIRI-JP 11 113683618 113683618 single base substitution T A downstream_gene_variant LIRI-JP 11 113683618 113683618 single base substitution T A intron_variant LIRI-JP 11 113683618 113683618 single base substitution T A upstream_gene_variant LIRI-JP 11 113684040 113684040 single base substitution C G downstream_gene_variant LIRI-JP 11 113684040 113684040 single base substitution C G intron_variant LIRI-JP 11 113684040 113684040 single base substitution C G upstream_gene_variant LIRI-JP 11 113687129 113687129 single base substitution G C downstream_gene_variant LIRI-JP 11 113687129 113687129 single base substitution G C intron_variant LIRI-JP 11 113690790 113690790 single base substitution T C intron_variant LIRI-JP 11 113691701 113691701 single base substitution T C intron_variant LIRI-JP 11 113694630 113694630 single base substitution T C intron_variant LIRI-JP 11 113694811 113694811 single base substitution C T intron_variant LIRI-JP 11 113696873 113696873 single base substitution T A downstream_gene_variant LIRI-JP 11 113696873 113696873 single base substitution T A intron_variant LIRI-JP 11 113698129 113698129 single base substitution G A downstream_gene_variant LIRI-JP 11 113698129 113698129 single base substitution G A intron_variant LIRI-JP 11 113700242 113700242 single base substitution T G downstream_gene_variant LIRI-JP 11 113700242 113700242 single base substitution T G intron_variant LIRI-JP 11 113700242 113700242 single base substitution T G upstream_gene_variant LIRI-JP 11 113702121 113702121 single base substitution A C intron_variant LIRI-JP 11 113702121 113702121 single base substitution A C upstream_gene_variant LIRI-JP 11 113703715 113703715 single base substitution G A intron_variant LIRI-JP 11 113703715 113703715 single base substitution G A upstream_gene_variant LIRI-JP 11 113704049 113704049 single base substitution G C intron_variant LIRI-JP 11 113704049 113704049 single base substitution G C upstream_gene_variant LIRI-JP 11 113706839 113706839 single base substitution A C intron_variant LIRI-JP 11 113706839 113706839 single base substitution A C upstream_gene_variant LIRI-JP 11 113708399 113708399 single base substitution A C intron_variant LIRI-JP 11 113708399 113708399 single base substitution A C upstream_gene_variant LIRI-JP 11 113708817 113708817 single base substitution C G intron_variant LIRI-JP 11 113708817 113708817 single base substitution C G upstream_gene_variant LIRI-JP 11 113710998 113710998 single base substitution C A intron_variant LIRI-JP 11 113711029 113711029 single base substitution T C intron_variant LIRI-JP 11 113712408 113712408 single base substitution T A 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 11 113712408 113712408 single base substitution T A exon_variant LIRI-JP 11 113712408 113712408 single base substitution T A missense_variant Q117H 351A>T LIRI-JP 11 113712408 113712408 single base substitution T A missense_variant Q45H 135A>T LIRI-JP 11 113713046 113713046 single base substitution G A intron_variant LIRI-JP 11 113713691 113713691 single base substitution G A intron_variant LIRI-JP 11 113714580 113714580 single base substitution G C intron_variant LIRI-JP 11 113716598 113716598 single base substitution A G intron_variant LIRI-JP 11 113717529 113717529 single base substitution C T intron_variant LIRI-JP 11 113725050 113725050 single base substitution T G exon_variant LIRI-JP 11 113725050 113725050 single base substitution T G intron_variant LIRI-JP 11 113725050 113725050 single base substitution T G missense_variant Q19P 56A>C LIRI-JP 11 113725050 113725050 single base substitution T G missense_variant Q22P 65A>C LIRI-JP 11 113725860 113725860 single base substitution A T intron_variant LIRI-JP 11 113726485 113726485 single base substitution C T intron_variant LIRI-JP 11 113727884 113727884 single base substitution T C intron_variant LIRI-JP 11 113730214 113730214 deletion of <=200bp T - intron_variant LIRI-JP 11 113731409 113731409 single base substitution C T intron_variant LIRI-JP 11 113733523 113733523 single base substitution T C intron_variant LIRI-JP 11 113735623 113735623 single base substitution G C intron_variant LIRI-JP 11 113737622 113737622 single base substitution G A intron_variant LIRI-JP 11 113737650 113737650 single base substitution T A intron_variant LIRI-JP 11 113737656 113737656 single base substitution T C intron_variant LIRI-JP 11 113738036 113738036 single base substitution T C intron_variant LIRI-JP 11 113739411 113739411 single base substitution G C intron_variant LIRI-JP 11 113740518 113740518 single base substitution G T intron_variant LIRI-JP 11 113743335 113743335 single base substitution T C intron_variant LIRI-JP 11 113744519 113744524 deletion of <=200bp TTTCGT - intron_variant LIRI-JP 11 113744536 113744541 deletion of <=200bp GGACCT - intron_variant LIRI-JP 11 113747779 113747779 single base substitution G A upstream_gene_variant LIRI-JP 11 113751033 113751033 single base substitution G A upstream_gene_variant LUSC-KR 11 113679865 113679865 single base substitution C T 3_prime_UTR_variant LUSC-KR 11 113679865 113679865 single base substitution C T downstream_gene_variant LUSC-KR 11 113679865 113679865 single base substitution C T stop_gained W11* 32G>A LUSC-KR 11 113679865 113679865 single base substitution C T stop_gained W403* 1208G>A LUSC-KR 11 113679865 113679865 single base substitution C T stop_gained W570* 1709G>A LUSC-KR 11 113679865 113679865 single base substitution C T stop_gained W695* 2084G>A LUSC-KR 11 113680099 113680099 single base substitution T A downstream_gene_variant LUSC-KR 11 113680099 113680099 single base substitution T A intron_variant LUSC-KR 11 113680099 113680099 single base substitution T A upstream_gene_variant LUSC-KR 11 113681555 113681555 single base substitution C G downstream_gene_variant LUSC-KR 11 113681555 113681555 single base substitution C G intron_variant LUSC-KR 11 113681555 113681555 single base substitution C G upstream_gene_variant LUSC-KR 11 113684547 113684547 single base substitution G A 3_prime_UTR_variant LUSC-KR 11 113684547 113684547 single base substitution G A downstream_gene_variant LUSC-KR 11 113684547 113684547 single base substitution G A intron_variant LUSC-KR 11 113684547 113684547 single base substitution G A upstream_gene_variant LUSC-KR 11 113684765 113684765 single base substitution T A downstream_gene_variant LUSC-KR 11 113684765 113684765 single base substitution T A intron_variant LUSC-KR 11 113684765 113684765 single base substitution T A upstream_gene_variant LUSC-KR 11 113686757 113686757 single base substitution T C downstream_gene_variant LUSC-KR 11 113686757 113686757 single base substitution T C intron_variant LUSC-KR 11 113690055 113690055 single base substitution G A intron_variant LUSC-KR 11 113692496 113692496 single base substitution C G intron_variant LUSC-KR 11 113693784 113693784 single base substitution C A intron_variant LUSC-KR 11 113695816 113695816 single base substitution G C downstream_gene_variant LUSC-KR 11 113695816 113695816 single base substitution G C intron_variant LUSC-KR 11 113697020 113697020 single base substitution G A downstream_gene_variant LUSC-KR 11 113697020 113697020 single base substitution G A intron_variant LUSC-KR 11 113697280 113697280 single base substitution C T downstream_gene_variant LUSC-KR 11 113697280 113697280 single base substitution C T intron_variant LUSC-KR 11 113702209 113702209 single base substitution C G intron_variant LUSC-KR 11 113702209 113702209 single base substitution C G upstream_gene_variant LUSC-KR 11 113706886 113706886 single base substitution C T intron_variant LUSC-KR 11 113706886 113706886 single base substitution C T upstream_gene_variant LUSC-KR 11 113708610 113708610 single base substitution C G intron_variant LUSC-KR 11 113708610 113708610 single base substitution C G upstream_gene_variant LUSC-KR 11 113708801 113708801 single base substitution T A intron_variant LUSC-KR 11 113708801 113708801 single base substitution T A upstream_gene_variant LUSC-KR 11 113708893 113708893 single base substitution C A intron_variant LUSC-KR 11 113708893 113708893 single base substitution C A upstream_gene_variant LUSC-KR 11 113710692 113710692 single base substitution C T intron_variant LUSC-KR 11 113710693 113710693 single base substitution G A intron_variant LUSC-KR 11 113712437 113712437 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 11 113712437 113712437 single base substitution A T exon_variant LUSC-KR 11 113712437 113712437 single base substitution A T missense_variant L108M 322T>A LUSC-KR 11 113712437 113712437 single base substitution A T missense_variant L36M 106T>A LUSC-KR 11 113714527 113714527 single base substitution T C intron_variant LUSC-KR 11 113716910 113716910 single base substitution T A intron_variant LUSC-KR 11 113717223 113717223 single base substitution C G intron_variant LUSC-KR 11 113721215 113721215 single base substitution G C downstream_gene_variant LUSC-KR 11 113721215 113721215 single base substitution G C intron_variant LUSC-KR 11 113723345 113723345 single base substitution C A exon_variant LUSC-KR 11 113723345 113723345 single base substitution C A intron_variant LUSC-KR 11 113723345 113723345 single base substitution C A missense_variant G46V 137G>T LUSC-KR 11 113723345 113723345 single base substitution C A missense_variant G49V 146G>T LUSC-KR 11 113723346 113723346 single base substitution C A exon_variant LUSC-KR 11 113723346 113723346 single base substitution C A intron_variant LUSC-KR 11 113723346 113723346 single base substitution C A missense_variant G46C 136G>T LUSC-KR 11 113723346 113723346 single base substitution C A missense_variant G49C 145G>T LUSC-KR 11 113724265 113724265 single base substitution C T intron_variant LUSC-KR 11 113726609 113726609 single base substitution G A intron_variant LUSC-KR 11 113732581 113732581 single base substitution C A intron_variant LUSC-KR 11 113746439 113746439 single base substitution A T upstream_gene_variant LUSC-KR 11 113748214 113748214 single base substitution G A upstream_gene_variant LUSC-US 11 113675696 113675696 single base substitution G A 3_prime_UTR_variant LUSC-US 11 113675696 113675696 single base substitution G A missense_variant L179F 535C>T LUSC-US 11 113675696 113675696 single base substitution G A missense_variant L501F 1501C>T LUSC-US 11 113675696 113675696 single base substitution G A missense_variant L668F 2002C>T LUSC-US 11 113675696 113675696 single base substitution G A missense_variant L793F 2377C>T LUSC-US 11 113675696 113675696 single base substitution G A missense_variant L825F 2473C>T LUSC-US 11 113675696 113675696 single base substitution G A upstream_gene_variant LUSC-US 11 113679872 113679872 single base substitution C G 3_prime_UTR_variant LUSC-US 11 113679872 113679872 single base substitution C G downstream_gene_variant LUSC-US 11 113679872 113679872 single base substitution C G missense_variant E401Q 1201G>C LUSC-US 11 113679872 113679872 single base substitution C G missense_variant E568Q 1702G>C LUSC-US 11 113679872 113679872 single base substitution C G missense_variant E693Q 2077G>C LUSC-US 11 113679872 113679872 single base substitution C G missense_variant E9Q 25G>C LUSC-US 11 113679924 113679924 single base substitution C A 3_prime_UTR_variant LUSC-US 11 113679924 113679924 single base substitution C A downstream_gene_variant LUSC-US 11 113679924 113679924 single base substitution C A synonymous_variant V383V 1149G>T LUSC-US 11 113679924 113679924 single base substitution C A synonymous_variant V550V 1650G>T LUSC-US 11 113679924 113679924 single base substitution C A synonymous_variant V675V 2025G>T LUSC-US 11 113679924 113679924 single base substitution C A upstream_gene_variant LUSC-US 11 113688476 113688476 single base substitution G A 3_prime_UTR_variant LUSC-US 11 113688476 113688476 single base substitution G A downstream_gene_variant LUSC-US 11 113688476 113688476 single base substitution G A intron_variant LUSC-US 11 113688476 113688476 single base substitution G A missense_variant P164L 491C>T LUSC-US 11 113688476 113688476 single base substitution G A missense_variant P331L 992C>T LUSC-US 11 113688476 113688476 single base substitution G A missense_variant P456L 1367C>T LUSC-US 11 113704153 113704153 single base substitution C A 3_prime_UTR_variant LUSC-US 11 113704153 113704153 single base substitution C A exon_variant LUSC-US 11 113704153 113704153 single base substitution C A stop_gained E125* 373G>T LUSC-US 11 113704153 113704153 single base substitution C A stop_gained E14* 40G>T LUSC-US 11 113704153 113704153 single base substitution C A stop_gained E149* 445G>T LUSC-US 11 113704153 113704153 single base substitution C A stop_gained E250* 748G>T LUSC-US 11 113704153 113704153 single base substitution C A upstream_gene_variant MALY-DE 11 113665275 113665275 single base substitution A G downstream_gene_variant MALY-DE 11 113668194 113668194 single base substitution G A downstream_gene_variant MALY-DE 11 113668810 113668814 deletion of <=200bp TTTTG - 3_prime_UTR_variant MALY-DE 11 113668810 113668814 deletion of <=200bp TTTTG - downstream_gene_variant MALY-DE 11 113671913 113671913 single base substitution G T downstream_gene_variant MALY-DE 11 113671913 113671913 single base substitution G T intron_variant MALY-DE 11 113672121 113672121 single base substitution T G downstream_gene_variant MALY-DE 11 113672121 113672121 single base substitution T G intron_variant MALY-DE 11 113677211 113677211 single base substitution C T intron_variant MALY-DE 11 113677211 113677211 single base substitution C T splice_region_variant MALY-DE 11 113677211 113677211 single base substitution C T upstream_gene_variant MALY-DE 11 113697286 113697286 deletion of <=200bp C - downstream_gene_variant MALY-DE 11 113697286 113697286 deletion of <=200bp C - intron_variant MALY-DE 11 113705293 113705293 single base substitution A C intron_variant MALY-DE 11 113705293 113705293 single base substitution A C upstream_gene_variant MALY-DE 11 113706930 113706930 single base substitution C A intron_variant MALY-DE 11 113706930 113706930 single base substitution C A upstream_gene_variant MALY-DE 11 113712345 113712345 single base substitution A T intron_variant MALY-DE 11 113727617 113727617 single base substitution C A intron_variant MALY-DE 11 113733375 113733375 insertion of <=200bp - AACATCTC intron_variant MALY-DE 11 113734305 113734305 single base substitution T C intron_variant MALY-DE 11 113739231 113739231 single base substitution A G intron_variant MALY-DE 11 113746705 113746705 single base substitution A G upstream_gene_variant MELA-AU 11 113663957 113663957 single base substitution G A downstream_gene_variant MELA-AU 11 113664681 113664681 single base substitution G A downstream_gene_variant MELA-AU 11 113664828 113664828 single base substitution G A downstream_gene_variant MELA-AU 11 113665027 113665027 single base substitution G T downstream_gene_variant MELA-AU 11 113665725 113665725 single base substitution C T downstream_gene_variant MELA-AU 11 113666037 113666037 single base substitution G A downstream_gene_variant MELA-AU 11 113666145 113666145 single base substitution G A downstream_gene_variant MELA-AU 11 113666300 113666300 single base substitution G T downstream_gene_variant MELA-AU 11 113666910 113666910 single base substitution A T downstream_gene_variant MELA-AU 11 113666965 113666965 single base substitution G A downstream_gene_variant MELA-AU 11 113667203 113667204 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 113667891 113667891 single base substitution G A downstream_gene_variant MELA-AU 11 113667943 113667943 single base substitution G A downstream_gene_variant MELA-AU 11 113668737 113668737 single base substitution A G 3_prime_UTR_variant MELA-AU 11 113668737 113668737 single base substitution A G downstream_gene_variant MELA-AU 11 113669124 113669124 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113669124 113669124 single base substitution G A downstream_gene_variant MELA-AU 11 113669902 113669902 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113669902 113669902 single base substitution G A exon_variant MELA-AU 11 113670048 113670048 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113670048 113670048 single base substitution G A exon_variant MELA-AU 11 113670048 113670048 single base substitution G A stop_gained R1018* 3052C>T MELA-AU 11 113670048 113670048 single base substitution G A stop_gained R1050* 3148C>T MELA-AU 11 113670048 113670048 single base substitution G A stop_gained R726* 2176C>T MELA-AU 11 113670048 113670048 single base substitution G A stop_gained R893* 2677C>T MELA-AU 11 113671936 113671936 single base substitution C T downstream_gene_variant MELA-AU 11 113671936 113671936 single base substitution C T intron_variant MELA-AU 11 113672276 113672276 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113672276 113672276 single base substitution G A downstream_gene_variant MELA-AU 11 113672276 113672276 single base substitution G A exon_variant MELA-AU 11 113672276 113672276 single base substitution G A missense_variant S672F 2015C>T MELA-AU 11 113672276 113672276 single base substitution G A missense_variant S839F 2516C>T MELA-AU 11 113672276 113672276 single base substitution G A missense_variant S964F 2891C>T MELA-AU 11 113672276 113672276 single base substitution G A missense_variant S996F 2987C>T MELA-AU 11 113672428 113672428 single base substitution G A downstream_gene_variant MELA-AU 11 113672428 113672428 single base substitution G A intron_variant MELA-AU 11 113672428 113672428 single base substitution G A upstream_gene_variant MELA-AU 11 113672773 113672773 single base substitution C T downstream_gene_variant MELA-AU 11 113672773 113672773 single base substitution C T intron_variant MELA-AU 11 113672773 113672773 single base substitution C T upstream_gene_variant MELA-AU 11 113673588 113673588 single base substitution A G downstream_gene_variant MELA-AU 11 113673588 113673588 single base substitution A G intron_variant MELA-AU 11 113673588 113673588 single base substitution A G upstream_gene_variant MELA-AU 11 113673597 113673597 single base substitution G A downstream_gene_variant MELA-AU 11 113673597 113673597 single base substitution G A intron_variant MELA-AU 11 113673597 113673597 single base substitution G A upstream_gene_variant MELA-AU 11 113673638 113673638 single base substitution G A downstream_gene_variant MELA-AU 11 113673638 113673638 single base substitution G A intron_variant MELA-AU 11 113673638 113673638 single base substitution G A upstream_gene_variant MELA-AU 11 113673651 113673651 single base substitution G A downstream_gene_variant MELA-AU 11 113673651 113673651 single base substitution G A intron_variant MELA-AU 11 113673651 113673651 single base substitution G A upstream_gene_variant MELA-AU 11 113673692 113673693 multiple base substitution (>=2bp and <=200bp) AG TA downstream_gene_variant MELA-AU 11 113673692 113673693 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU 11 113673692 113673693 multiple base substitution (>=2bp and <=200bp) AG TA upstream_gene_variant MELA-AU 11 113673711 113673711 single base substitution A T downstream_gene_variant MELA-AU 11 113673711 113673711 single base substitution A T intron_variant MELA-AU 11 113673711 113673711 single base substitution A T upstream_gene_variant MELA-AU 11 113673930 113673931 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 11 113673930 113673931 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 113673930 113673931 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant RR613RW MELA-AU 11 113673930 113673931 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant RR780RW MELA-AU 11 113673930 113673931 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant RR905RW MELA-AU 11 113673930 113673931 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant RR937RW MELA-AU 11 113673930 113673931 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 113673985 113673985 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113673985 113673985 single base substitution G A downstream_gene_variant MELA-AU 11 113673985 113673985 single base substitution G A synonymous_variant S595S 1785C>T MELA-AU 11 113673985 113673985 single base substitution G A synonymous_variant S762S 2286C>T MELA-AU 11 113673985 113673985 single base substitution G A synonymous_variant S887S 2661C>T MELA-AU 11 113673985 113673985 single base substitution G A synonymous_variant S919S 2757C>T MELA-AU 11 113673985 113673985 single base substitution G A upstream_gene_variant MELA-AU 11 113674108 113674108 single base substitution G A downstream_gene_variant MELA-AU 11 113674108 113674108 single base substitution G A intron_variant MELA-AU 11 113674108 113674108 single base substitution G A upstream_gene_variant MELA-AU 11 113674525 113674525 single base substitution T G 3_prime_UTR_variant MELA-AU 11 113674525 113674525 single base substitution T G downstream_gene_variant MELA-AU 11 113674525 113674525 single base substitution T G missense_variant K587N 1761A>C MELA-AU 11 113674525 113674525 single base substitution T G missense_variant K754N 2262A>C MELA-AU 11 113674525 113674525 single base substitution T G missense_variant K879N 2637A>C MELA-AU 11 113674525 113674525 single base substitution T G missense_variant K911N 2733A>C MELA-AU 11 113674525 113674525 single base substitution T G upstream_gene_variant MELA-AU 11 113674562 113674562 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113674562 113674562 single base substitution G A downstream_gene_variant MELA-AU 11 113674562 113674562 single base substitution G A missense_variant S575F 1724C>T MELA-AU 11 113674562 113674562 single base substitution G A missense_variant S742F 2225C>T MELA-AU 11 113674562 113674562 single base substitution G A missense_variant S867F 2600C>T MELA-AU 11 113674562 113674562 single base substitution G A missense_variant S899F 2696C>T MELA-AU 11 113674562 113674562 single base substitution G A upstream_gene_variant MELA-AU 11 113674953 113674953 single base substitution G A downstream_gene_variant MELA-AU 11 113674953 113674953 single base substitution G A intron_variant MELA-AU 11 113674953 113674953 single base substitution G A upstream_gene_variant MELA-AU 11 113675172 113675172 single base substitution G A downstream_gene_variant MELA-AU 11 113675172 113675172 single base substitution G A intron_variant MELA-AU 11 113675172 113675172 single base substitution G A upstream_gene_variant MELA-AU 11 113675269 113675269 single base substitution G A downstream_gene_variant MELA-AU 11 113675269 113675269 single base substitution G A intron_variant MELA-AU 11 113675269 113675269 single base substitution G A upstream_gene_variant MELA-AU 11 113676112 113676112 single base substitution G A intron_variant MELA-AU 11 113676112 113676112 single base substitution G A upstream_gene_variant MELA-AU 11 113676608 113676608 single base substitution A C intron_variant MELA-AU 11 113676608 113676608 single base substitution A C upstream_gene_variant MELA-AU 11 113676649 113676649 single base substitution G A intron_variant MELA-AU 11 113676649 113676649 single base substitution G A upstream_gene_variant MELA-AU 11 113676844 113676844 single base substitution G A intron_variant MELA-AU 11 113676844 113676844 single base substitution G A upstream_gene_variant MELA-AU 11 113677706 113677706 single base substitution G A intron_variant MELA-AU 11 113678382 113678382 single base substitution C T downstream_gene_variant MELA-AU 11 113678382 113678382 single base substitution C T intron_variant MELA-AU 11 113678387 113678387 single base substitution A G downstream_gene_variant MELA-AU 11 113678387 113678387 single base substitution A G intron_variant MELA-AU 11 113678398 113678398 single base substitution G A downstream_gene_variant MELA-AU 11 113678398 113678398 single base substitution G A intron_variant MELA-AU 11 113679808 113679808 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113679808 113679808 single base substitution G A downstream_gene_variant MELA-AU 11 113679808 113679808 single base substitution G A missense_variant S30L 89C>T MELA-AU 11 113679808 113679808 single base substitution G A missense_variant S422L 1265C>T MELA-AU 11 113679808 113679808 single base substitution G A missense_variant S589L 1766C>T MELA-AU 11 113679808 113679808 single base substitution G A missense_variant S714L 2141C>T MELA-AU 11 113680049 113680049 single base substitution G C downstream_gene_variant MELA-AU 11 113680049 113680049 single base substitution G C intron_variant MELA-AU 11 113680049 113680049 single base substitution G C upstream_gene_variant MELA-AU 11 113680200 113680200 single base substitution T G downstream_gene_variant MELA-AU 11 113680200 113680200 single base substitution T G intron_variant MELA-AU 11 113680200 113680200 single base substitution T G upstream_gene_variant MELA-AU 11 113680792 113680792 single base substitution G A downstream_gene_variant MELA-AU 11 113680792 113680792 single base substitution G A intron_variant MELA-AU 11 113680792 113680792 single base substitution G A upstream_gene_variant MELA-AU 11 113681390 113681390 single base substitution G A downstream_gene_variant MELA-AU 11 113681390 113681390 single base substitution G A intron_variant MELA-AU 11 113681390 113681390 single base substitution G A upstream_gene_variant MELA-AU 11 113681587 113681587 single base substitution G A downstream_gene_variant MELA-AU 11 113681587 113681587 single base substitution G A intron_variant MELA-AU 11 113681587 113681587 single base substitution G A upstream_gene_variant MELA-AU 11 113682424 113682424 single base substitution G A downstream_gene_variant MELA-AU 11 113682424 113682424 single base substitution G A intron_variant MELA-AU 11 113682424 113682424 single base substitution G A upstream_gene_variant MELA-AU 11 113683223 113683223 single base substitution G A downstream_gene_variant MELA-AU 11 113683223 113683223 single base substitution G A intron_variant MELA-AU 11 113683223 113683223 single base substitution G A missense_variant P287S 859C>T MELA-AU 11 113683223 113683223 single base substitution G A missense_variant P291S 871C>T MELA-AU 11 113683223 113683223 single base substitution G A missense_variant P458S 1372C>T MELA-AU 11 113683223 113683223 single base substitution G A missense_variant P583S 1747C>T MELA-AU 11 113683223 113683223 single base substitution G A upstream_gene_variant MELA-AU 11 113683725 113683725 single base substitution T C downstream_gene_variant MELA-AU 11 113683725 113683725 single base substitution T C intron_variant MELA-AU 11 113683725 113683725 single base substitution T C upstream_gene_variant MELA-AU 11 113683886 113683886 single base substitution T A downstream_gene_variant MELA-AU 11 113683886 113683886 single base substitution T A intron_variant MELA-AU 11 113683886 113683886 single base substitution T A upstream_gene_variant MELA-AU 11 113684081 113684081 single base substitution G A downstream_gene_variant MELA-AU 11 113684081 113684081 single base substitution G A intron_variant MELA-AU 11 113684081 113684081 single base substitution G A upstream_gene_variant MELA-AU 11 113684234 113684234 single base substitution G A downstream_gene_variant MELA-AU 11 113684234 113684234 single base substitution G A intron_variant MELA-AU 11 113684234 113684234 single base substitution G A upstream_gene_variant MELA-AU 11 113684432 113684432 single base substitution A G downstream_gene_variant MELA-AU 11 113684432 113684432 single base substitution A G intron_variant MELA-AU 11 113684432 113684432 single base substitution A G upstream_gene_variant MELA-AU 11 113684691 113684691 single base substitution G A downstream_gene_variant MELA-AU 11 113684691 113684691 single base substitution G A intron_variant MELA-AU 11 113684691 113684691 single base substitution G A upstream_gene_variant MELA-AU 11 113684949 113684949 single base substitution G A downstream_gene_variant MELA-AU 11 113684949 113684949 single base substitution G A intron_variant MELA-AU 11 113685112 113685112 single base substitution G A downstream_gene_variant MELA-AU 11 113685112 113685112 single base substitution G A intron_variant MELA-AU 11 113685783 113685783 single base substitution G A downstream_gene_variant MELA-AU 11 113685783 113685783 single base substitution G A intron_variant MELA-AU 11 113685935 113685935 single base substitution G A downstream_gene_variant MELA-AU 11 113685935 113685935 single base substitution G A intron_variant MELA-AU 11 113685935 113685935 single base substitution G A missense_variant L249F 745C>T MELA-AU 11 113685935 113685935 single base substitution G A missense_variant L253F 757C>T MELA-AU 11 113685935 113685935 single base substitution G A missense_variant L420F 1258C>T MELA-AU 11 113685935 113685935 single base substitution G A missense_variant L545F 1633C>T MELA-AU 11 113686133 113686133 single base substitution G A downstream_gene_variant MELA-AU 11 113686133 113686133 single base substitution G A intron_variant MELA-AU 11 113686193 113686193 single base substitution G A downstream_gene_variant MELA-AU 11 113686193 113686193 single base substitution G A intron_variant MELA-AU 11 113686581 113686581 single base substitution G A downstream_gene_variant MELA-AU 11 113686581 113686581 single base substitution G A intron_variant MELA-AU 11 113687058 113687058 single base substitution G A downstream_gene_variant MELA-AU 11 113687058 113687058 single base substitution G A intron_variant MELA-AU 11 113687576 113687576 single base substitution C T downstream_gene_variant MELA-AU 11 113687576 113687576 single base substitution C T intron_variant MELA-AU 11 113688001 113688001 single base substitution G A downstream_gene_variant MELA-AU 11 113688001 113688001 single base substitution G A intron_variant MELA-AU 11 113688885 113688886 multiple base substitution (>=2bp and <=200bp) TT AA intron_variant MELA-AU 11 113688906 113688906 single base substitution C T intron_variant MELA-AU 11 113689340 113689340 single base substitution G A intron_variant MELA-AU 11 113689512 113689512 single base substitution G A intron_variant MELA-AU 11 113689673 113689673 single base substitution A G intron_variant MELA-AU 11 113690410 113690410 single base substitution G A intron_variant MELA-AU 11 113690666 113690666 single base substitution C T intron_variant MELA-AU 11 113690732 113690732 single base substitution T C intron_variant MELA-AU 11 113691116 113691116 single base substitution G A intron_variant MELA-AU 11 113691902 113691902 single base substitution C T intron_variant MELA-AU 11 113692334 113692334 single base substitution G A intron_variant MELA-AU 11 113692623 113692623 single base substitution G A intron_variant MELA-AU 11 113692671 113692672 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 113693158 113693158 single base substitution G A intron_variant MELA-AU 11 113693254 113693254 single base substitution T C intron_variant MELA-AU 11 113693271 113693271 single base substitution G A intron_variant MELA-AU 11 113694009 113694009 single base substitution C T intron_variant MELA-AU 11 113694637 113694637 single base substitution C G intron_variant MELA-AU 11 113694913 113694913 single base substitution A T intron_variant MELA-AU 11 113695144 113695144 single base substitution A G downstream_gene_variant MELA-AU 11 113695144 113695144 single base substitution A G intron_variant MELA-AU 11 113695276 113695277 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 113695276 113695277 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 113695579 113695579 single base substitution G A downstream_gene_variant MELA-AU 11 113695579 113695579 single base substitution G A intron_variant MELA-AU 11 113695641 113695641 single base substitution G A downstream_gene_variant MELA-AU 11 113695641 113695641 single base substitution G A intron_variant MELA-AU 11 113696322 113696322 single base substitution T A downstream_gene_variant MELA-AU 11 113696322 113696322 single base substitution T A intron_variant MELA-AU 11 113696362 113696362 single base substitution G A downstream_gene_variant MELA-AU 11 113696362 113696362 single base substitution G A intron_variant MELA-AU 11 113697568 113697568 single base substitution G A downstream_gene_variant MELA-AU 11 113697568 113697568 single base substitution G A intron_variant MELA-AU 11 113697793 113697793 single base substitution G A downstream_gene_variant MELA-AU 11 113697793 113697793 single base substitution G A intron_variant MELA-AU 11 113697809 113697809 single base substitution G A downstream_gene_variant MELA-AU 11 113697809 113697809 single base substitution G A intron_variant MELA-AU 11 113698172 113698172 single base substitution C T downstream_gene_variant MELA-AU 11 113698172 113698172 single base substitution C T intron_variant MELA-AU 11 113698243 113698243 single base substitution G A downstream_gene_variant MELA-AU 11 113698243 113698243 single base substitution G A intron_variant MELA-AU 11 113698244 113698244 single base substitution G A downstream_gene_variant MELA-AU 11 113698244 113698244 single base substitution G A intron_variant MELA-AU 11 113698356 113698356 single base substitution A G downstream_gene_variant MELA-AU 11 113698356 113698356 single base substitution A G intron_variant MELA-AU 11 113698713 113698713 single base substitution T C downstream_gene_variant MELA-AU 11 113698713 113698713 single base substitution T C intron_variant MELA-AU 11 113699113 113699113 single base substitution C T downstream_gene_variant MELA-AU 11 113699113 113699113 single base substitution C T intron_variant MELA-AU 11 113699951 113699951 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113699951 113699951 single base substitution G A downstream_gene_variant MELA-AU 11 113699951 113699951 single base substitution G A exon_variant MELA-AU 11 113699951 113699951 single base substitution G A missense_variant P107S 319C>T MELA-AU 11 113699951 113699951 single base substitution G A missense_variant P218S 652C>T MELA-AU 11 113699951 113699951 single base substitution G A missense_variant P242S 724C>T MELA-AU 11 113699951 113699951 single base substitution G A missense_variant P343S 1027C>T MELA-AU 11 113699951 113699951 single base substitution G A missense_variant P51S 151C>T MELA-AU 11 113700062 113700062 single base substitution G A 3_prime_UTR_variant MELA-AU 11 113700062 113700062 single base substitution G A downstream_gene_variant MELA-AU 11 113700062 113700062 single base substitution G A exon_variant MELA-AU 11 113700062 113700062 single base substitution G A missense_variant P14S 40C>T MELA-AU 11 113700062 113700062 single base substitution G A missense_variant P181S 541C>T MELA-AU 11 113700062 113700062 single base substitution G A missense_variant P205S 613C>T MELA-AU 11 113700062 113700062 single base substitution G A missense_variant P306S 916C>T MELA-AU 11 113700062 113700062 single base substitution G A missense_variant P70S 208C>T MELA-AU 11 113701208 113701208 single base substitution G A downstream_gene_variant MELA-AU 11 113701208 113701208 single base substitution G A intron_variant MELA-AU 11 113701208 113701208 single base substitution G A upstream_gene_variant MELA-AU 11 113702293 113702293 single base substitution G A intron_variant MELA-AU 11 113702293 113702293 single base substitution G A upstream_gene_variant MELA-AU 11 113704484 113704484 single base substitution A C intron_variant MELA-AU 11 113704484 113704484 single base substitution A C upstream_gene_variant MELA-AU 11 113704601 113704601 single base substitution G A intron_variant MELA-AU 11 113704601 113704601 single base substitution G A upstream_gene_variant MELA-AU 11 113705202 113705202 single base substitution G A intron_variant MELA-AU 11 113705202 113705202 single base substitution G A upstream_gene_variant MELA-AU 11 113705354 113705354 single base substitution G A intron_variant MELA-AU 11 113705354 113705354 single base substitution G A upstream_gene_variant MELA-AU 11 113705584 113705584 single base substitution G A intron_variant MELA-AU 11 113705584 113705584 single base substitution G A upstream_gene_variant MELA-AU 11 113705624 113705624 single base substitution C G intron_variant MELA-AU 11 113705624 113705624 single base substitution C G upstream_gene_variant MELA-AU 11 113705941 113705941 single base substitution A G 3_prime_UTR_variant MELA-AU 11 113705941 113705941 single base substitution A G intron_variant MELA-AU 11 113705941 113705941 single base substitution A G upstream_gene_variant MELA-AU 11 113706222 113706222 single base substitution G A intron_variant MELA-AU 11 113706222 113706222 single base substitution G A upstream_gene_variant MELA-AU 11 113706798 113706798 single base substitution C T intron_variant MELA-AU 11 113706798 113706798 single base substitution C T upstream_gene_variant MELA-AU 11 113707639 113707639 single base substitution A G intron_variant MELA-AU 11 113707639 113707639 single base substitution A G upstream_gene_variant MELA-AU 11 113708000 113708000 single base substitution G A intron_variant MELA-AU 11 113708000 113708000 single base substitution G A upstream_gene_variant MELA-AU 11 113708209 113708209 single base substitution G A intron_variant MELA-AU 11 113708209 113708209 single base substitution G A upstream_gene_variant MELA-AU 11 113709649 113709649 single base substitution C T intron_variant MELA-AU 11 113710038 113710038 single base substitution G A intron_variant MELA-AU 11 113710119 113710119 single base substitution C T intron_variant MELA-AU 11 113710223 113710223 single base substitution C T intron_variant MELA-AU 11 113710738 113710738 single base substitution G A intron_variant MELA-AU 11 113711584 113711584 single base substitution A G intron_variant MELA-AU 11 113711812 113711812 single base substitution G A intron_variant MELA-AU 11 113711974 113711974 single base substitution A G intron_variant MELA-AU 11 113712271 113712271 single base substitution A G intron_variant MELA-AU 11 113713344 113713344 single base substitution G A intron_variant MELA-AU 11 113714213 113714213 single base substitution G A intron_variant MELA-AU 11 113714268 113714268 single base substitution C T intron_variant MELA-AU 11 113714494 113714494 single base substitution G A intron_variant MELA-AU 11 113714873 113714873 single base substitution G A intron_variant MELA-AU 11 113714961 113714961 single base substitution G A intron_variant MELA-AU 11 113715429 113715429 single base substitution A G intron_variant MELA-AU 11 113715669 113715669 single base substitution A C intron_variant MELA-AU 11 113715737 113715737 single base substitution G A intron_variant MELA-AU 11 113716129 113716129 single base substitution A G intron_variant MELA-AU 11 113716189 113716189 single base substitution A T intron_variant MELA-AU 11 113716397 113716397 single base substitution A G intron_variant MELA-AU 11 113716567 113716567 single base substitution G A intron_variant MELA-AU 11 113716850 113716850 single base substitution G A intron_variant MELA-AU 11 113717433 113717433 single base substitution C T intron_variant MELA-AU 11 113717920 113717920 single base substitution G A intron_variant MELA-AU 11 113718499 113718499 single base substitution A T downstream_gene_variant MELA-AU 11 113718499 113718499 single base substitution A T intron_variant MELA-AU 11 113718607 113718607 single base substitution G A downstream_gene_variant MELA-AU 11 113718607 113718607 single base substitution G A intron_variant MELA-AU 11 113718842 113718842 single base substitution G A downstream_gene_variant MELA-AU 11 113718842 113718842 single base substitution G A intron_variant MELA-AU 11 113718964 113718964 single base substitution G A downstream_gene_variant MELA-AU 11 113718964 113718964 single base substitution G A intron_variant MELA-AU 11 113719218 113719218 single base substitution G A downstream_gene_variant MELA-AU 11 113719218 113719218 single base substitution G A intron_variant MELA-AU 11 113719708 113719708 single base substitution A C downstream_gene_variant MELA-AU 11 113719708 113719708 single base substitution A C intron_variant MELA-AU 11 113720279 113720279 single base substitution C T downstream_gene_variant MELA-AU 11 113720279 113720279 single base substitution C T intron_variant MELA-AU 11 113720487 113720487 single base substitution G T downstream_gene_variant MELA-AU 11 113720487 113720487 single base substitution G T intron_variant MELA-AU 11 113720510 113720510 single base substitution C T downstream_gene_variant MELA-AU 11 113720510 113720510 single base substitution C T intron_variant MELA-AU 11 113720595 113720595 single base substitution G A downstream_gene_variant MELA-AU 11 113720595 113720595 single base substitution G A intron_variant MELA-AU 11 113720683 113720683 single base substitution A G downstream_gene_variant MELA-AU 11 113720683 113720683 single base substitution A G intron_variant MELA-AU 11 113720975 113720975 single base substitution G A downstream_gene_variant MELA-AU 11 113720975 113720975 single base substitution G A intron_variant MELA-AU 11 113721430 113721430 single base substitution T A downstream_gene_variant MELA-AU 11 113721430 113721430 single base substitution T A intron_variant MELA-AU 11 113722103 113722103 single base substitution G A downstream_gene_variant MELA-AU 11 113722103 113722103 single base substitution G A intron_variant MELA-AU 11 113722331 113722331 single base substitution A G downstream_gene_variant MELA-AU 11 113722331 113722331 single base substitution A G intron_variant MELA-AU 11 113722368 113722368 single base substitution A T downstream_gene_variant MELA-AU 11 113722368 113722368 single base substitution A T intron_variant MELA-AU 11 113723424 113723424 single base substitution A C intron_variant MELA-AU 11 113724994 113724994 single base substitution G A exon_variant MELA-AU 11 113724994 113724994 single base substitution G A intron_variant MELA-AU 11 113724994 113724994 single base substitution G A missense_variant H38Y 112C>T MELA-AU 11 113724994 113724994 single base substitution G A missense_variant H41Y 121C>T MELA-AU 11 113725628 113725628 single base substitution A T intron_variant MELA-AU 11 113725981 113725981 single base substitution A G intron_variant MELA-AU 11 113726789 113726789 single base substitution G A intron_variant MELA-AU 11 113727022 113727022 single base substitution G A intron_variant MELA-AU 11 113727328 113727328 single base substitution G A intron_variant MELA-AU 11 113727629 113727629 single base substitution A C intron_variant MELA-AU 11 113727840 113727840 single base substitution G A intron_variant MELA-AU 11 113728012 113728012 single base substitution C T intron_variant MELA-AU 11 113728464 113728464 single base substitution C T intron_variant MELA-AU 11 113728589 113728589 single base substitution C T intron_variant MELA-AU 11 113729066 113729066 single base substitution A G intron_variant MELA-AU 11 113729121 113729121 single base substitution C T intron_variant MELA-AU 11 113729627 113729627 single base substitution G A intron_variant MELA-AU 11 113729675 113729676 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 113729704 113729704 single base substitution T A intron_variant MELA-AU 11 113730569 113730569 single base substitution G C intron_variant MELA-AU 11 113730707 113730707 single base substitution A T intron_variant MELA-AU 11 113730715 113730715 single base substitution G A intron_variant MELA-AU 11 113731160 113731160 single base substitution G A intron_variant MELA-AU 11 113731920 113731920 single base substitution G A intron_variant MELA-AU 11 113731924 113731924 single base substitution G A intron_variant MELA-AU 11 113732042 113732042 single base substitution G A intron_variant MELA-AU 11 113732259 113732259 single base substitution G A intron_variant MELA-AU 11 113732354 113732354 single base substitution G A intron_variant MELA-AU 11 113732819 113732819 single base substitution A G intron_variant MELA-AU 11 113732860 113732860 single base substitution G A intron_variant MELA-AU 11 113733186 113733186 single base substitution C T intron_variant MELA-AU 11 113733974 113733974 single base substitution G A intron_variant MELA-AU 11 113734379 113734379 single base substitution A G intron_variant MELA-AU 11 113735116 113735116 single base substitution G A intron_variant MELA-AU 11 113735693 113735693 single base substitution G A intron_variant MELA-AU 11 113735942 113735942 single base substitution G A intron_variant MELA-AU 11 113737336 113737336 single base substitution G A intron_variant MELA-AU 11 113738052 113738052 single base substitution G A intron_variant MELA-AU 11 113738223 113738223 single base substitution C T intron_variant MELA-AU 11 113739143 113739143 single base substitution A G intron_variant MELA-AU 11 113739360 113739360 single base substitution G A intron_variant MELA-AU 11 113740667 113740667 single base substitution C T intron_variant MELA-AU 11 113741369 113741369 single base substitution G A intron_variant MELA-AU 11 113742493 113742493 single base substitution C T intron_variant MELA-AU 11 113743318 113743318 single base substitution A T intron_variant MELA-AU 11 113744777 113744777 single base substitution C T intron_variant MELA-AU 11 113745133 113745133 single base substitution G A intron_variant MELA-AU 11 113745134 113745134 single base substitution G A intron_variant MELA-AU 11 113748919 113748919 single base substitution G T upstream_gene_variant MELA-AU 11 113749027 113749027 single base substitution G A upstream_gene_variant MELA-AU 11 113749507 113749507 single base substitution A T upstream_gene_variant MELA-AU 11 113749913 113749913 single base substitution G A upstream_gene_variant MELA-AU 11 113749957 113749957 single base substitution C T upstream_gene_variant MELA-AU 11 113750002 113750003 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 113750122 113750123 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 113750278 113750278 single base substitution C T upstream_gene_variant MELA-AU 11 113750301 113750301 single base substitution G A upstream_gene_variant MELA-AU 11 113750621 113750621 single base substitution G A upstream_gene_variant MELA-AU 11 113750668 113750668 single base substitution C T upstream_gene_variant MELA-AU 11 113750718 113750718 single base substitution C T upstream_gene_variant MELA-AU 11 113750731 113750731 single base substitution G A upstream_gene_variant MELA-AU 11 113751010 113751010 single base substitution T A upstream_gene_variant MELA-AU 11 113751036 113751036 single base substitution G A upstream_gene_variant ORCA-IN 11 113689108 113689108 single base substitution C T intron_variant ORCA-IN 11 113708308 113708308 single base substitution C G intron_variant ORCA-IN 11 113708308 113708308 single base substitution C G upstream_gene_variant ORCA-IN 11 113750882 113750882 single base substitution C T upstream_gene_variant OV-AU 11 113678296 113678296 single base substitution C T downstream_gene_variant OV-AU 11 113678296 113678296 single base substitution C T intron_variant OV-AU 11 113686540 113686540 single base substitution C A downstream_gene_variant OV-AU 11 113686540 113686540 single base substitution C A intron_variant OV-AU 11 113688771 113688771 single base substitution G C intron_variant OV-AU 11 113693078 113693078 single base substitution G A intron_variant OV-AU 11 113698192 113698192 single base substitution A G downstream_gene_variant OV-AU 11 113698192 113698192 single base substitution A G intron_variant OV-AU 11 113699775 113699775 single base substitution C G downstream_gene_variant OV-AU 11 113699775 113699775 single base substitution C G intron_variant OV-AU 11 113713907 113713907 single base substitution T C intron_variant OV-AU 11 113720298 113720298 single base substitution A G downstream_gene_variant OV-AU 11 113720298 113720298 single base substitution A G intron_variant OV-AU 11 113720818 113720818 single base substitution C G downstream_gene_variant OV-AU 11 113720818 113720818 single base substitution C G intron_variant OV-AU 11 113731006 113731006 single base substitution C G intron_variant OV-AU 11 113741193 113741193 single base substitution G A intron_variant PACA-AU 11 113664415 113664415 single base substitution G T downstream_gene_variant PACA-AU 11 113668958 113668958 single base substitution G A 3_prime_UTR_variant PACA-AU 11 113668958 113668958 single base substitution G A downstream_gene_variant PACA-AU 11 113684558 113684558 single base substitution C G 3_prime_UTR_variant PACA-AU 11 113684558 113684558 single base substitution C G downstream_gene_variant PACA-AU 11 113684558 113684558 single base substitution C G intron_variant PACA-AU 11 113684558 113684558 single base substitution C G upstream_gene_variant PACA-AU 11 113687258 113687258 deletion of <=200bp A - downstream_gene_variant PACA-AU 11 113687258 113687258 deletion of <=200bp A - intron_variant PACA-AU 11 113687439 113687439 single base substitution T C downstream_gene_variant PACA-AU 11 113687439 113687439 single base substitution T C intron_variant PACA-AU 11 113687731 113687731 insertion of <=200bp - T downstream_gene_variant PACA-AU 11 113687731 113687731 insertion of <=200bp - T intron_variant PACA-AU 11 113688312 113688312 single base substitution G T downstream_gene_variant PACA-AU 11 113688312 113688312 single base substitution G T intron_variant PACA-AU 11 113691733 113691733 single base substitution C T intron_variant PACA-AU 11 113699707 113699707 single base substitution C G downstream_gene_variant PACA-AU 11 113699707 113699707 single base substitution C G intron_variant PACA-AU 11 113711364 113711364 single base substitution G A exon_variant PACA-AU 11 113711364 113711364 single base substitution G A synonymous_variant L164L 490C>T PACA-AU 11 113711364 113711364 single base substitution G A synonymous_variant L39L 115C>T PACA-AU 11 113711364 113711364 single base substitution G A synonymous_variant L92L 274C>T PACA-AU 11 113714423 113714423 single base substitution A T intron_variant PACA-AU 11 113725730 113725730 single base substitution C T intron_variant PACA-AU 11 113729487 113729487 single base substitution A C intron_variant PACA-AU 11 113736216 113736216 single base substitution G A intron_variant PACA-AU 11 113737017 113737017 single base substitution G A intron_variant PACA-AU 11 113738510 113738510 insertion of <=200bp - AAGGAAAG intron_variant PACA-AU 11 113742304 113742304 single base substitution A C intron_variant PACA-AU 11 113742934 113742934 single base substitution T A intron_variant PACA-AU 11 113743314 113743314 single base substitution A G intron_variant PACA-AU 11 113747388 113747388 single base substitution G T upstream_gene_variant PACA-AU 11 113750747 113750747 single base substitution A C upstream_gene_variant PACA-CA 11 113663820 113663820 single base substitution C T downstream_gene_variant PACA-CA 11 113672064 113672064 single base substitution G C downstream_gene_variant PACA-CA 11 113672064 113672064 single base substitution G C intron_variant PACA-CA 11 113672573 113672573 single base substitution T C downstream_gene_variant PACA-CA 11 113672573 113672573 single base substitution T C intron_variant PACA-CA 11 113672573 113672573 single base substitution T C upstream_gene_variant PACA-CA 11 113675677 113675677 single base substitution T C 3_prime_UTR_variant PACA-CA 11 113675677 113675677 single base substitution T C missense_variant Y185C 554A>G PACA-CA 11 113675677 113675677 single base substitution T C missense_variant Y507C 1520A>G PACA-CA 11 113675677 113675677 single base substitution T C missense_variant Y674C 2021A>G PACA-CA 11 113675677 113675677 single base substitution T C missense_variant Y799C 2396A>G PACA-CA 11 113675677 113675677 single base substitution T C missense_variant Y831C 2492A>G PACA-CA 11 113675677 113675677 single base substitution T C upstream_gene_variant PACA-CA 11 113676175 113676175 single base substitution G T intron_variant PACA-CA 11 113676175 113676175 single base substitution G T upstream_gene_variant PACA-CA 11 113676719 113676719 single base substitution T C intron_variant PACA-CA 11 113676719 113676719 single base substitution T C upstream_gene_variant PACA-CA 11 113678054 113678054 single base substitution C G downstream_gene_variant PACA-CA 11 113678054 113678054 single base substitution C G intron_variant PACA-CA 11 113679890 113679890 single base substitution G A 3_prime_UTR_variant PACA-CA 11 113679890 113679890 single base substitution G A downstream_gene_variant PACA-CA 11 113679890 113679890 single base substitution G A missense_variant R395W 1183C>T PACA-CA 11 113679890 113679890 single base substitution G A missense_variant R3W 7C>T PACA-CA 11 113679890 113679890 single base substitution G A missense_variant R562W 1684C>T PACA-CA 11 113679890 113679890 single base substitution G A missense_variant R687W 2059C>T PACA-CA 11 113681997 113681997 single base substitution G C downstream_gene_variant PACA-CA 11 113681997 113681997 single base substitution G C intron_variant PACA-CA 11 113681997 113681997 single base substitution G C upstream_gene_variant PACA-CA 11 113682367 113682367 single base substitution G A downstream_gene_variant PACA-CA 11 113682367 113682367 single base substitution G A intron_variant PACA-CA 11 113682367 113682367 single base substitution G A upstream_gene_variant PACA-CA 11 113684876 113684876 single base substitution G A downstream_gene_variant PACA-CA 11 113684876 113684876 single base substitution G A intron_variant PACA-CA 11 113684876 113684876 single base substitution G A upstream_gene_variant PACA-CA 11 113689810 113689810 single base substitution G A intron_variant PACA-CA 11 113691306 113691306 single base substitution G T intron_variant PACA-CA 11 113691591 113691591 single base substitution T C intron_variant PACA-CA 11 113692457 113692457 single base substitution C T intron_variant PACA-CA 11 113696579 113696579 single base substitution A C downstream_gene_variant PACA-CA 11 113696579 113696579 single base substitution A C intron_variant PACA-CA 11 113697700 113697700 single base substitution C T downstream_gene_variant PACA-CA 11 113697700 113697700 single base substitution C T intron_variant PACA-CA 11 113700851 113700851 single base substitution G A downstream_gene_variant PACA-CA 11 113700851 113700851 single base substitution G A intron_variant PACA-CA 11 113700851 113700851 single base substitution G A upstream_gene_variant PACA-CA 11 113702934 113702934 single base substitution C T intron_variant PACA-CA 11 113702934 113702934 single base substitution C T upstream_gene_variant PACA-CA 11 113702935 113702935 single base substitution G A intron_variant PACA-CA 11 113702935 113702935 single base substitution G A upstream_gene_variant PACA-CA 11 113709683 113709683 single base substitution G A intron_variant PACA-CA 11 113711400 113711400 single base substitution T C exon_variant PACA-CA 11 113711400 113711400 single base substitution T C missense_variant N152D 454A>G PACA-CA 11 113711400 113711400 single base substitution T C missense_variant N27D 79A>G PACA-CA 11 113711400 113711400 single base substitution T C missense_variant N80D 238A>G PACA-CA 11 113712445 113712445 single base substitution G A 5_prime_UTR_variant PACA-CA 11 113712445 113712445 single base substitution G A exon_variant PACA-CA 11 113712445 113712445 single base substitution G A missense_variant A105V 314C>T PACA-CA 11 113712445 113712445 single base substitution G A missense_variant A33V 98C>T PACA-CA 11 113714142 113714142 single base substitution C T intron_variant PACA-CA 11 113715586 113715586 single base substitution A T intron_variant PACA-CA 11 113718597 113718597 single base substitution C G downstream_gene_variant PACA-CA 11 113718597 113718597 single base substitution C G intron_variant PACA-CA 11 113720862 113720862 single base substitution C T downstream_gene_variant PACA-CA 11 113720862 113720862 single base substitution C T intron_variant PACA-CA 11 113720893 113720893 insertion of <=200bp - AAA downstream_gene_variant PACA-CA 11 113720893 113720893 insertion of <=200bp - AAA intron_variant PACA-CA 11 113723803 113723803 single base substitution T A intron_variant PACA-CA 11 113723922 113723922 single base substitution A C intron_variant PACA-CA 11 113725512 113725512 single base substitution C G intron_variant PACA-CA 11 113726362 113726362 single base substitution G A intron_variant PACA-CA 11 113726487 113726487 single base substitution G C intron_variant PACA-CA 11 113728169 113728169 insertion of <=200bp - T intron_variant PACA-CA 11 113728373 113728373 single base substitution T A intron_variant PACA-CA 11 113731247 113731247 single base substitution A C intron_variant PACA-CA 11 113732153 113732153 single base substitution A G intron_variant PACA-CA 11 113732251 113732251 deletion of <=200bp A - intron_variant PACA-CA 11 113732839 113732839 single base substitution C T intron_variant PACA-CA 11 113733947 113733947 single base substitution A G intron_variant PACA-CA 11 113738230 113738230 single base substitution C A intron_variant PACA-CA 11 113739503 113739503 single base substitution G A intron_variant PACA-CA 11 113743692 113743692 single base substitution C A intron_variant PACA-CA 11 113747181 113747181 single base substitution C T upstream_gene_variant PACA-CA 11 113747834 113747834 single base substitution C T upstream_gene_variant PACA-CA 11 113748546 113748549 deletion of <=200bp CAAT - upstream_gene_variant PACA-CA 11 113749704 113749704 single base substitution C T upstream_gene_variant PAEN-AU 11 113685446 113685446 deletion of <=200bp T - downstream_gene_variant PAEN-AU 11 113685446 113685446 deletion of <=200bp T - intron_variant PAEN-AU 11 113731498 113731498 single base substitution A C intron_variant PAEN-AU 11 113750687 113750687 single base substitution A T upstream_gene_variant PAEN-IT 11 113745656 113745656 single base substitution G C intron_variant PAEN-IT 11 113745918 113745918 single base substitution G A intron_variant PBCA-DE 11 113664288 113664288 insertion of <=200bp - A downstream_gene_variant PBCA-DE 11 113670092 113670092 single base substitution T A 3_prime_UTR_variant PBCA-DE 11 113670092 113670092 single base substitution T A exon_variant PBCA-DE 11 113670092 113670092 single base substitution T A missense_variant D1003V 3008A>T PBCA-DE 11 113670092 113670092 single base substitution T A missense_variant D1035V 3104A>T PBCA-DE 11 113670092 113670092 single base substitution T A missense_variant D711V 2132A>T PBCA-DE 11 113670092 113670092 single base substitution T A missense_variant D878V 2633A>T PBCA-DE 11 113674958 113674958 single base substitution G A downstream_gene_variant PBCA-DE 11 113674958 113674958 single base substitution G A intron_variant PBCA-DE 11 113674958 113674958 single base substitution G A upstream_gene_variant PBCA-DE 11 113674959 113674959 single base substitution G T downstream_gene_variant PBCA-DE 11 113674959 113674959 single base substitution G T intron_variant PBCA-DE 11 113674959 113674959 single base substitution G T upstream_gene_variant PBCA-DE 11 113706888 113706888 single base substitution G T intron_variant PBCA-DE 11 113706888 113706888 single base substitution G T upstream_gene_variant PBCA-DE 11 113710287 113710287 single base substitution C G intron_variant PBCA-DE 11 113719751 113719751 deletion of <=200bp C - downstream_gene_variant PBCA-DE 11 113719751 113719751 deletion of <=200bp C - intron_variant PBCA-DE 11 113723814 113723814 single base substitution C T intron_variant PBCA-DE 11 113725080 113725080 single base substitution C A intron_variant PBCA-DE 11 113747054 113747054 single base substitution T C upstream_gene_variant PRAD-CA 11 113689510 113689510 single base substitution G A intron_variant PRAD-CA 11 113702891 113702891 single base substitution G A intron_variant PRAD-CA 11 113702891 113702891 single base substitution G A upstream_gene_variant PRAD-CA 11 113720036 113720036 single base substitution G T downstream_gene_variant PRAD-CA 11 113720036 113720036 single base substitution G T intron_variant PRAD-CA 11 113727385 113727385 single base substitution T C intron_variant PRAD-CA 11 113728064 113728064 single base substitution G A intron_variant PRAD-CA 11 113729298 113729298 single base substitution G C intron_variant PRAD-CA 11 113729877 113729877 single base substitution G A intron_variant PRAD-CA 11 113747055 113747055 single base substitution C T upstream_gene_variant PRAD-UK 11 113668319 113668319 single base substitution G C downstream_gene_variant PRAD-UK 11 113685738 113685738 single base substitution C T downstream_gene_variant PRAD-UK 11 113685738 113685738 single base substitution C T intron_variant PRAD-UK 11 113744818 113744818 single base substitution G A intron_variant PRAD-US 11 113683078 113683078 insertion of <=200bp - GAA 3_prime_UTR_variant PRAD-US 11 113683078 113683078 insertion of <=200bp - GAA disruptive_inframe_insertion R335SS PRAD-US 11 113683078 113683078 insertion of <=200bp - GAA disruptive_inframe_insertion R339SS PRAD-US 11 113683078 113683078 insertion of <=200bp - GAA disruptive_inframe_insertion R506SS PRAD-US 11 113683078 113683078 insertion of <=200bp - GAA disruptive_inframe_insertion R631SS PRAD-US 11 113683078 113683078 insertion of <=200bp - GAA downstream_gene_variant PRAD-US 11 113683078 113683078 insertion of <=200bp - GAA upstream_gene_variant PRAD-US 11 113704218 113704218 single base substitution G C 3_prime_UTR_variant PRAD-US 11 113704218 113704218 single base substitution G C exon_variant PRAD-US 11 113704218 113704218 single base substitution G C stop_gained S103* 308C>G PRAD-US 11 113704218 113704218 single base substitution G C stop_gained S127* 380C>G PRAD-US 11 113704218 113704218 single base substitution G C stop_gained S228* 683C>G PRAD-US 11 113704218 113704218 single base substitution G C upstream_gene_variant READ-US 11 113672258 113672258 single base substitution G A 3_prime_UTR_variant READ-US 11 113672258 113672258 single base substitution G A downstream_gene_variant READ-US 11 113672258 113672258 single base substitution G A exon_variant READ-US 11 113672258 113672258 single base substitution G A missense_variant A1002V 3005C>T READ-US 11 113672258 113672258 single base substitution G A missense_variant A678V 2033C>T READ-US 11 113672258 113672258 single base substitution G A missense_variant A845V 2534C>T READ-US 11 113672258 113672258 single base substitution G A missense_variant A970V 2909C>T READ-US 11 113704161 113704161 single base substitution C T 3_prime_UTR_variant READ-US 11 113704161 113704161 single base substitution C T exon_variant READ-US 11 113704161 113704161 single base substitution C T missense_variant R11Q 32G>A READ-US 11 113704161 113704161 single base substitution C T missense_variant R122Q 365G>A READ-US 11 113704161 113704161 single base substitution C T missense_variant R146Q 437G>A READ-US 11 113704161 113704161 single base substitution C T missense_variant R247Q 740G>A READ-US 11 113704161 113704161 single base substitution C T upstream_gene_variant READ-US 11 113704982 113704982 single base substitution G A 3_prime_UTR_variant READ-US 11 113704982 113704982 single base substitution G A exon_variant READ-US 11 113704982 113704982 single base substitution G A intron_variant READ-US 11 113704982 113704982 single base substitution G A stop_gained R204* 610C>T READ-US 11 113704982 113704982 single base substitution G A stop_gained R79* 235C>T READ-US 11 113704982 113704982 single base substitution G A upstream_gene_variant READ-US 11 113704982 113704982 single base substitution G C 3_prime_UTR_variant READ-US 11 113704982 113704982 single base substitution G C exon_variant READ-US 11 113704982 113704982 single base substitution G C intron_variant READ-US 11 113704982 113704982 single base substitution G C missense_variant R204G 610C>G READ-US 11 113704982 113704982 single base substitution G C missense_variant R79G 235C>G READ-US 11 113704982 113704982 single base substitution G C upstream_gene_variant READ-US 11 113705033 113705033 single base substitution G A 3_prime_UTR_variant READ-US 11 113705033 113705033 single base substitution G A exon_variant READ-US 11 113705033 113705033 single base substitution G A intron_variant READ-US 11 113705033 113705033 single base substitution G A stop_gained R187* 559C>T READ-US 11 113705033 113705033 single base substitution G A stop_gained R62* 184C>T READ-US 11 113705033 113705033 single base substitution G A upstream_gene_variant READ-US 11 113711350 113711350 single base substitution G A exon_variant READ-US 11 113711350 113711350 single base substitution G A synonymous_variant G168G 504C>T READ-US 11 113711350 113711350 single base substitution G A synonymous_variant G43G 129C>T READ-US 11 113711350 113711350 single base substitution G A synonymous_variant G96G 288C>T RECA-EU 11 113665187 113665187 single base substitution C A downstream_gene_variant RECA-EU 11 113670928 113670928 single base substitution C T downstream_gene_variant RECA-EU 11 113670928 113670928 single base substitution C T intron_variant RECA-EU 11 113679445 113679445 single base substitution A G downstream_gene_variant RECA-EU 11 113679445 113679445 single base substitution A G intron_variant RECA-EU 11 113684663 113684663 single base substitution T C downstream_gene_variant RECA-EU 11 113684663 113684663 single base substitution T C intron_variant RECA-EU 11 113684663 113684663 single base substitution T C missense_variant I267V 799A>G RECA-EU 11 113684663 113684663 single base substitution T C missense_variant I271V 811A>G RECA-EU 11 113684663 113684663 single base substitution T C missense_variant I438V 1312A>G RECA-EU 11 113684663 113684663 single base substitution T C missense_variant I563V 1687A>G RECA-EU 11 113684663 113684663 single base substitution T C upstream_gene_variant RECA-EU 11 113710730 113710730 single base substitution G A intron_variant RECA-EU 11 113717134 113717134 single base substitution C A intron_variant RECA-EU 11 113732140 113732140 single base substitution C T intron_variant RECA-EU 11 113736702 113736702 single base substitution A C intron_variant RECA-EU 11 113745969 113745969 single base substitution G T intron_variant RECA-EU 11 113746858 113746858 single base substitution T A upstream_gene_variant RECA-EU 11 113747045 113747045 single base substitution T G upstream_gene_variant RECA-EU 11 113750686 113750686 single base substitution A T upstream_gene_variant SKCA-BR 11 113666308 113666308 single base substitution C T downstream_gene_variant SKCA-BR 11 113671563 113671563 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 11 113671563 113671563 insertion of <=200bp - AT intron_variant SKCA-BR 11 113672203 113672203 single base substitution A T downstream_gene_variant SKCA-BR 11 113672203 113672203 single base substitution A T splice_donor_variant SKCA-BR 11 113676875 113676875 single base substitution G A intron_variant SKCA-BR 11 113676875 113676875 single base substitution G A upstream_gene_variant SKCA-BR 11 113678775 113678775 single base substitution A C downstream_gene_variant SKCA-BR 11 113678775 113678775 single base substitution A C intron_variant SKCA-BR 11 113678775 113678775 single base substitution A C missense_variant D112E 336T>G SKCA-BR 11 113680410 113680410 single base substitution G A downstream_gene_variant SKCA-BR 11 113680410 113680410 single base substitution G A intron_variant SKCA-BR 11 113680410 113680410 single base substitution G A upstream_gene_variant SKCA-BR 11 113680756 113680757 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 11 113680756 113680757 deletion of <=200bp CA - intron_variant SKCA-BR 11 113680756 113680757 deletion of <=200bp CA - upstream_gene_variant SKCA-BR 11 113682931 113682931 single base substitution A C downstream_gene_variant SKCA-BR 11 113682931 113682931 single base substitution A C intron_variant SKCA-BR 11 113682931 113682931 single base substitution A C upstream_gene_variant SKCA-BR 11 113685152 113685152 single base substitution G A downstream_gene_variant SKCA-BR 11 113685152 113685152 single base substitution G A intron_variant SKCA-BR 11 113685608 113685609 deletion of <=200bp TA - downstream_gene_variant SKCA-BR 11 113685608 113685609 deletion of <=200bp TA - intron_variant SKCA-BR 11 113685784 113685784 single base substitution A G downstream_gene_variant SKCA-BR 11 113685784 113685784 single base substitution A G intron_variant SKCA-BR 11 113687751 113687751 single base substitution A G downstream_gene_variant SKCA-BR 11 113687751 113687751 single base substitution A G intron_variant SKCA-BR 11 113688244 113688244 single base substitution C A downstream_gene_variant SKCA-BR 11 113688244 113688244 single base substitution C A intron_variant SKCA-BR 11 113695653 113695653 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 11 113695653 113695653 insertion of <=200bp - TA intron_variant SKCA-BR 11 113695673 113695673 single base substitution G A downstream_gene_variant SKCA-BR 11 113695673 113695673 single base substitution G A intron_variant SKCA-BR 11 113696164 113696164 single base substitution G A downstream_gene_variant SKCA-BR 11 113696164 113696164 single base substitution G A intron_variant SKCA-BR 11 113697250 113697250 single base substitution A C downstream_gene_variant SKCA-BR 11 113697250 113697250 single base substitution A C intron_variant SKCA-BR 11 113700546 113700548 deletion of <=200bp CAA - downstream_gene_variant SKCA-BR 11 113700546 113700548 deletion of <=200bp CAA - intron_variant SKCA-BR 11 113700546 113700548 deletion of <=200bp CAA - upstream_gene_variant SKCA-BR 11 113712773 113712773 single base substitution G A intron_variant SKCA-BR 11 113716949 113716949 single base substitution G A intron_variant SKCA-BR 11 113718461 113718461 single base substitution G A downstream_gene_variant SKCA-BR 11 113718461 113718461 single base substitution G A intron_variant SKCA-BR 11 113720813 113720813 single base substitution G A downstream_gene_variant SKCA-BR 11 113720813 113720813 single base substitution G A intron_variant SKCA-BR 11 113724023 113724023 single base substitution C G intron_variant SKCA-BR 11 113725010 113725010 single base substitution C T exon_variant SKCA-BR 11 113725010 113725010 single base substitution C T intron_variant SKCA-BR 11 113725010 113725010 single base substitution C T synonymous_variant Q32Q 96G>A SKCA-BR 11 113725010 113725010 single base substitution C T synonymous_variant Q35Q 105G>A SKCA-BR 11 113725139 113725139 single base substitution C T intron_variant SKCA-BR 11 113725934 113725934 single base substitution G A intron_variant SKCA-BR 11 113728793 113728793 single base substitution G A intron_variant SKCA-BR 11 113735494 113735494 single base substitution A G intron_variant SKCA-BR 11 113736963 113736963 single base substitution G A intron_variant SKCA-BR 11 113739979 113739979 single base substitution A C intron_variant SKCA-BR 11 113741983 113741983 single base substitution G A intron_variant SKCA-BR 11 113747233 113747233 single base substitution C T upstream_gene_variant SKCA-BR 11 113750823 113750823 single base substitution G A upstream_gene_variant SKCM-US 11 113672276 113672276 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113672276 113672276 single base substitution G A downstream_gene_variant SKCM-US 11 113672276 113672276 single base substitution G A exon_variant SKCM-US 11 113672276 113672276 single base substitution G A missense_variant S672F 2015C>T SKCM-US 11 113672276 113672276 single base substitution G A missense_variant S839F 2516C>T SKCM-US 11 113672276 113672276 single base substitution G A missense_variant S964F 2891C>T SKCM-US 11 113672276 113672276 single base substitution G A missense_variant S996F 2987C>T SKCM-US 11 113672311 113672311 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113672311 113672311 single base substitution G A downstream_gene_variant SKCM-US 11 113672311 113672311 single base substitution G A exon_variant SKCM-US 11 113672311 113672311 single base substitution G A synonymous_variant I660I 1980C>T SKCM-US 11 113672311 113672311 single base substitution G A synonymous_variant I827I 2481C>T SKCM-US 11 113672311 113672311 single base substitution G A synonymous_variant I952I 2856C>T SKCM-US 11 113672311 113672311 single base substitution G A synonymous_variant I984I 2952C>T SKCM-US 11 113673885 113673885 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113673885 113673885 single base substitution G A downstream_gene_variant SKCM-US 11 113673885 113673885 single base substitution G A missense_variant L629F 1885C>T SKCM-US 11 113673885 113673885 single base substitution G A missense_variant L796F 2386C>T SKCM-US 11 113673885 113673885 single base substitution G A missense_variant L921F 2761C>T SKCM-US 11 113673885 113673885 single base substitution G A missense_variant L953F 2857C>T SKCM-US 11 113673885 113673885 single base substitution G A upstream_gene_variant SKCM-US 11 113673914 113673914 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113673914 113673914 single base substitution G A downstream_gene_variant SKCM-US 11 113673914 113673914 single base substitution G A missense_variant S619F 1856C>T SKCM-US 11 113673914 113673914 single base substitution G A missense_variant S786F 2357C>T SKCM-US 11 113673914 113673914 single base substitution G A missense_variant S911F 2732C>T SKCM-US 11 113673914 113673914 single base substitution G A missense_variant S943F 2828C>T SKCM-US 11 113673914 113673914 single base substitution G A upstream_gene_variant SKCM-US 11 113673923 113673923 insertion of <=200bp - C 3_prime_UTR_variant SKCM-US 11 113673923 113673923 insertion of <=200bp - C downstream_gene_variant SKCM-US 11 113673923 113673923 insertion of <=200bp - C frameshift_variant V616V? SKCM-US 11 113673923 113673923 insertion of <=200bp - C frameshift_variant V783V? SKCM-US 11 113673923 113673923 insertion of <=200bp - C frameshift_variant V908V? SKCM-US 11 113673923 113673923 insertion of <=200bp - C frameshift_variant V940V? SKCM-US 11 113673923 113673923 insertion of <=200bp - C upstream_gene_variant SKCM-US 11 113673928 113673928 single base substitution C T 3_prime_UTR_variant SKCM-US 11 113673928 113673928 single base substitution C T downstream_gene_variant SKCM-US 11 113673928 113673928 single base substitution C T synonymous_variant R614R 1842G>A SKCM-US 11 113673928 113673928 single base substitution C T synonymous_variant R781R 2343G>A SKCM-US 11 113673928 113673928 single base substitution C T synonymous_variant R906R 2718G>A SKCM-US 11 113673928 113673928 single base substitution C T synonymous_variant R938R 2814G>A SKCM-US 11 113673928 113673928 single base substitution C T upstream_gene_variant SKCM-US 11 113673986 113673986 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113673986 113673986 single base substitution G A downstream_gene_variant SKCM-US 11 113673986 113673986 single base substitution G A missense_variant S595F 1784C>T SKCM-US 11 113673986 113673986 single base substitution G A missense_variant S762F 2285C>T SKCM-US 11 113673986 113673986 single base substitution G A missense_variant S887F 2660C>T SKCM-US 11 113673986 113673986 single base substitution G A missense_variant S919F 2756C>T SKCM-US 11 113673986 113673986 single base substitution G A upstream_gene_variant SKCM-US 11 113675607 113675607 single base substitution A T 3_prime_UTR_variant SKCM-US 11 113675607 113675607 single base substitution A T downstream_gene_variant SKCM-US 11 113675607 113675607 single base substitution A T missense_variant N530K 1590T>A SKCM-US 11 113675607 113675607 single base substitution A T missense_variant N697K 2091T>A SKCM-US 11 113675607 113675607 single base substitution A T missense_variant N822K 2466T>A SKCM-US 11 113675607 113675607 single base substitution A T missense_variant N854K 2562T>A SKCM-US 11 113675607 113675607 single base substitution A T upstream_gene_variant SKCM-US 11 113677220 113677220 single base substitution C T intron_variant SKCM-US 11 113677220 113677220 single base substitution C T synonymous_variant G151G 453G>A SKCM-US 11 113677220 113677220 single base substitution C T synonymous_variant G797G 2391G>A SKCM-US 11 113677220 113677220 single base substitution C T upstream_gene_variant SKCM-US 11 113679831 113679831 single base substitution C T 3_prime_UTR_variant SKCM-US 11 113679831 113679831 single base substitution C T downstream_gene_variant SKCM-US 11 113679831 113679831 single base substitution C T missense_variant M22I 66G>A SKCM-US 11 113679831 113679831 single base substitution C T missense_variant M414I 1242G>A SKCM-US 11 113679831 113679831 single base substitution C T missense_variant M581I 1743G>A SKCM-US 11 113679831 113679831 single base substitution C T missense_variant M706I 2118G>A SKCM-US 11 113679953 113679953 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113679953 113679953 single base substitution G A downstream_gene_variant SKCM-US 11 113679953 113679953 single base substitution G A stop_gained Q374* 1120C>T SKCM-US 11 113679953 113679953 single base substitution G A stop_gained Q541* 1621C>T SKCM-US 11 113679953 113679953 single base substitution G A stop_gained Q666* 1996C>T SKCM-US 11 113679953 113679953 single base substitution G A upstream_gene_variant SKCM-US 11 113694393 113694393 single base substitution C T 3_prime_UTR_variant SKCM-US 11 113694393 113694393 single base substitution C T missense_variant R114Q 341G>A SKCM-US 11 113694393 113694393 single base substitution C T missense_variant R170Q 509G>A SKCM-US 11 113694393 113694393 single base substitution C T missense_variant R281Q 842G>A SKCM-US 11 113694393 113694393 single base substitution C T missense_variant R406Q 1217G>A SKCM-US 11 113697977 113697977 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113697977 113697977 single base substitution G A downstream_gene_variant SKCM-US 11 113697977 113697977 single base substitution G A missense_variant P153S 457C>T SKCM-US 11 113697977 113697977 single base substitution G A missense_variant P264S 790C>T SKCM-US 11 113697977 113697977 single base substitution G A missense_variant P389S 1165C>T SKCM-US 11 113697977 113697977 single base substitution G A missense_variant P97S 289C>T SKCM-US 11 113698048 113698048 single base substitution A G 3_prime_UTR_variant SKCM-US 11 113698048 113698048 single base substitution A G downstream_gene_variant SKCM-US 11 113698048 113698048 single base substitution A G missense_variant F129S 386T>C SKCM-US 11 113698048 113698048 single base substitution A G missense_variant F240S 719T>C SKCM-US 11 113698048 113698048 single base substitution A G missense_variant F365S 1094T>C SKCM-US 11 113698048 113698048 single base substitution A G missense_variant F73S 218T>C SKCM-US 11 113699951 113699951 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113699951 113699951 single base substitution G A downstream_gene_variant SKCM-US 11 113699951 113699951 single base substitution G A exon_variant SKCM-US 11 113699951 113699951 single base substitution G A missense_variant P107S 319C>T SKCM-US 11 113699951 113699951 single base substitution G A missense_variant P218S 652C>T SKCM-US 11 113699951 113699951 single base substitution G A missense_variant P242S 724C>T SKCM-US 11 113699951 113699951 single base substitution G A missense_variant P343S 1027C>T SKCM-US 11 113699951 113699951 single base substitution G A missense_variant P51S 151C>T SKCM-US 11 113700008 113700008 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113700008 113700008 single base substitution G A downstream_gene_variant SKCM-US 11 113700008 113700008 single base substitution G A exon_variant SKCM-US 11 113700008 113700008 single base substitution G A missense_variant R199C 595C>T SKCM-US 11 113700008 113700008 single base substitution G A missense_variant R223C 667C>T SKCM-US 11 113700008 113700008 single base substitution G A missense_variant R324C 970C>T SKCM-US 11 113700008 113700008 single base substitution G A missense_variant R32C 94C>T SKCM-US 11 113700008 113700008 single base substitution G A missense_variant R88C 262C>T SKCM-US 11 113700029 113700029 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113700029 113700029 single base substitution G A downstream_gene_variant SKCM-US 11 113700029 113700029 single base substitution G A exon_variant SKCM-US 11 113700029 113700029 single base substitution G A missense_variant P192S 574C>T SKCM-US 11 113700029 113700029 single base substitution G A missense_variant P216S 646C>T SKCM-US 11 113700029 113700029 single base substitution G A missense_variant P25S 73C>T SKCM-US 11 113700029 113700029 single base substitution G A missense_variant P317S 949C>T SKCM-US 11 113700029 113700029 single base substitution G A missense_variant P81S 241C>T SKCM-US 11 113701610 113701610 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113701610 113701610 single base substitution G A exon_variant SKCM-US 11 113701610 113701610 single base substitution G A synonymous_variant L172L 514C>T SKCM-US 11 113701610 113701610 single base substitution G A synonymous_variant L196L 586C>T SKCM-US 11 113701610 113701610 single base substitution G A synonymous_variant L297L 889C>T SKCM-US 11 113701610 113701610 single base substitution G A synonymous_variant L61L 181C>T SKCM-US 11 113701610 113701610 single base substitution G A upstream_gene_variant SKCM-US 11 113705054 113705054 single base substitution G A 3_prime_UTR_variant SKCM-US 11 113705054 113705054 single base substitution G A exon_variant SKCM-US 11 113705054 113705054 single base substitution G A intron_variant SKCM-US 11 113705054 113705054 single base substitution G A missense_variant L180F 538C>T SKCM-US 11 113705054 113705054 single base substitution G A missense_variant L55F 163C>T SKCM-US 11 113705054 113705054 single base substitution G A upstream_gene_variant SKCM-US 11 113712389 113712389 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 11 113712389 113712389 single base substitution T C exon_variant SKCM-US 11 113712389 113712389 single base substitution T C missense_variant N124D 370A>G SKCM-US 11 113712389 113712389 single base substitution T C missense_variant N52D 154A>G STAD-US 11 113670038 113670038 single base substitution G T 3_prime_UTR_variant STAD-US 11 113670038 113670038 single base substitution G T exon_variant STAD-US 11 113670038 113670038 single base substitution G T missense_variant S1021Y 3062C>A STAD-US 11 113670038 113670038 single base substitution G T missense_variant S1053Y 3158C>A STAD-US 11 113670038 113670038 single base substitution G T missense_variant S729Y 2186C>A STAD-US 11 113670038 113670038 single base substitution G T missense_variant S896Y 2687C>A STAD-US 11 113672318 113672318 single base substitution A G 3_prime_UTR_variant STAD-US 11 113672318 113672318 single base substitution A G downstream_gene_variant STAD-US 11 113672318 113672318 single base substitution A G exon_variant STAD-US 11 113672318 113672318 single base substitution A G missense_variant L658P 1973T>C STAD-US 11 113672318 113672318 single base substitution A G missense_variant L825P 2474T>C STAD-US 11 113672318 113672318 single base substitution A G missense_variant L950P 2849T>C STAD-US 11 113672318 113672318 single base substitution A G missense_variant L982P 2945T>C STAD-US 11 113673924 113673924 deletion of <=200bp C - 3_prime_UTR_variant STAD-US 11 113673924 113673924 deletion of <=200bp C - downstream_gene_variant STAD-US 11 113673924 113673924 deletion of <=200bp C - frameshift_variant V616 STAD-US 11 113673924 113673924 deletion of <=200bp C - frameshift_variant V783 STAD-US 11 113673924 113673924 deletion of <=200bp C - frameshift_variant V908 STAD-US 11 113673924 113673924 deletion of <=200bp C - frameshift_variant V940 STAD-US 11 113673924 113673924 deletion of <=200bp C - upstream_gene_variant STAD-US 11 113674571 113674571 single base substitution C T 3_prime_UTR_variant STAD-US 11 113674571 113674571 single base substitution C T downstream_gene_variant STAD-US 11 113674571 113674571 single base substitution C T missense_variant R572Q 1715G>A STAD-US 11 113674571 113674571 single base substitution C T missense_variant R739Q 2216G>A STAD-US 11 113674571 113674571 single base substitution C T missense_variant R864Q 2591G>A STAD-US 11 113674571 113674571 single base substitution C T missense_variant R896Q 2687G>A STAD-US 11 113674571 113674571 single base substitution C T upstream_gene_variant STAD-US 11 113679043 113679043 single base substitution C T 3_prime_UTR_variant STAD-US 11 113679043 113679043 single base substitution C T downstream_gene_variant STAD-US 11 113679043 113679043 single base substitution C T missense_variant G469S 1405G>A STAD-US 11 113679043 113679043 single base substitution C T missense_variant G636S 1906G>A STAD-US 11 113679043 113679043 single base substitution C T missense_variant G761S 2281G>A STAD-US 11 113679043 113679043 single base substitution C T missense_variant G77S 229G>A STAD-US 11 113684655 113684655 single base substitution A G downstream_gene_variant STAD-US 11 113684655 113684655 single base substitution A G intron_variant STAD-US 11 113684655 113684655 single base substitution A G synonymous_variant S269S 807T>C STAD-US 11 113684655 113684655 single base substitution A G synonymous_variant S273S 819T>C STAD-US 11 113684655 113684655 single base substitution A G synonymous_variant S440S 1320T>C STAD-US 11 113684655 113684655 single base substitution A G synonymous_variant S565S 1695T>C STAD-US 11 113684655 113684655 single base substitution A G upstream_gene_variant STAD-US 11 113685907 113685907 single base substitution T C downstream_gene_variant STAD-US 11 113685907 113685907 single base substitution T C intron_variant STAD-US 11 113685907 113685907 single base substitution T C missense_variant Q258R 773A>G STAD-US 11 113685907 113685907 single base substitution T C missense_variant Q262R 785A>G STAD-US 11 113685907 113685907 single base substitution T C missense_variant Q429R 1286A>G STAD-US 11 113685907 113685907 single base substitution T C missense_variant Q554R 1661A>G STAD-US 11 113694409 113694409 single base substitution T A 3_prime_UTR_variant STAD-US 11 113694409 113694409 single base substitution T A missense_variant S109C 325A>T STAD-US 11 113694409 113694409 single base substitution T A missense_variant S165C 493A>T STAD-US 11 113694409 113694409 single base substitution T A missense_variant S276C 826A>T STAD-US 11 113694409 113694409 single base substitution T A missense_variant S401C 1201A>T STAD-US 11 113698007 113698007 single base substitution G C 3_prime_UTR_variant STAD-US 11 113698007 113698007 single base substitution G C downstream_gene_variant STAD-US 11 113698007 113698007 single base substitution G C missense_variant P143A 427C>G STAD-US 11 113698007 113698007 single base substitution G C missense_variant P254A 760C>G STAD-US 11 113698007 113698007 single base substitution G C missense_variant P379A 1135C>G STAD-US 11 113698007 113698007 single base substitution G C missense_variant P87A 259C>G STAD-US 11 113699980 113699980 single base substitution G A 3_prime_UTR_variant STAD-US 11 113699980 113699980 single base substitution G A downstream_gene_variant STAD-US 11 113699980 113699980 single base substitution G A exon_variant STAD-US 11 113699980 113699980 single base substitution G A missense_variant A208V 623C>T STAD-US 11 113699980 113699980 single base substitution G A missense_variant A232V 695C>T STAD-US 11 113699980 113699980 single base substitution G A missense_variant A333V 998C>T STAD-US 11 113699980 113699980 single base substitution G A missense_variant A41V 122C>T STAD-US 11 113699980 113699980 single base substitution G A missense_variant A97V 290C>T STAD-US 11 113700038 113700038 single base substitution C T 3_prime_UTR_variant STAD-US 11 113700038 113700038 single base substitution C T downstream_gene_variant STAD-US 11 113700038 113700038 single base substitution C T exon_variant STAD-US 11 113700038 113700038 single base substitution C T missense_variant G189S 565G>A STAD-US 11 113700038 113700038 single base substitution C T missense_variant G213S 637G>A STAD-US 11 113700038 113700038 single base substitution C T missense_variant G22S 64G>A STAD-US 11 113700038 113700038 single base substitution C T missense_variant G314S 940G>A STAD-US 11 113700038 113700038 single base substitution C T missense_variant G78S 232G>A STAD-US 11 113700069 113700069 single base substitution T C downstream_gene_variant STAD-US 11 113700069 113700069 single base substitution T C splice_acceptor_variant STAD-US 11 113700069 113700069 single base substitution T C synonymous_variant L11L 33A>G STAD-US 11 113704196 113704196 single base substitution C T 3_prime_UTR_variant STAD-US 11 113704196 113704196 single base substitution C T exon_variant STAD-US 11 113704196 113704196 single base substitution C T synonymous_variant P110P 330G>A STAD-US 11 113704196 113704196 single base substitution C T synonymous_variant P134P 402G>A STAD-US 11 113704196 113704196 single base substitution C T synonymous_variant P235P 705G>A STAD-US 11 113704196 113704196 single base substitution C T upstream_gene_variant STAD-US 11 113704197 113704197 single base substitution G A 3_prime_UTR_variant STAD-US 11 113704197 113704197 single base substitution G A exon_variant STAD-US 11 113704197 113704197 single base substitution G A missense_variant P110L 329C>T STAD-US 11 113704197 113704197 single base substitution G A missense_variant P134L 401C>T STAD-US 11 113704197 113704197 single base substitution G A missense_variant P235L 704C>T STAD-US 11 113704197 113704197 single base substitution G A upstream_gene_variant STAD-US 11 113704991 113704991 single base substitution C A 3_prime_UTR_variant STAD-US 11 113704991 113704991 single base substitution C A exon_variant STAD-US 11 113704991 113704991 single base substitution C A intron_variant STAD-US 11 113704991 113704991 single base substitution C A stop_gained E201* 601G>T STAD-US 11 113704991 113704991 single base substitution C A stop_gained E76* 226G>T STAD-US 11 113704991 113704991 single base substitution C A upstream_gene_variant STAD-US 11 113711447 113711447 single base substitution C T exon_variant STAD-US 11 113711447 113711447 single base substitution C T missense_variant R11H 32G>A STAD-US 11 113711447 113711447 single base substitution C T missense_variant R136H 407G>A STAD-US 11 113711447 113711447 single base substitution C T missense_variant R64H 191G>A THCA-US 11 113705033 113705033 single base substitution G A 3_prime_UTR_variant THCA-US 11 113705033 113705033 single base substitution G A exon_variant THCA-US 11 113705033 113705033 single base substitution G A intron_variant THCA-US 11 113705033 113705033 single base substitution G A stop_gained R187* 559C>T THCA-US 11 113705033 113705033 single base substitution G A stop_gained R62* 184C>T THCA-US 11 113705033 113705033 single base substitution G A upstream_gene_variant UCEC-US 11 113672230 113672230 single base substitution G T 3_prime_UTR_variant UCEC-US 11 113672230 113672230 single base substitution G T downstream_gene_variant UCEC-US 11 113672230 113672230 single base substitution G T exon_variant UCEC-US 11 113672230 113672230 single base substitution G T stop_gained C1011* 3033C>A UCEC-US 11 113672230 113672230 single base substitution G T stop_gained C687* 2061C>A UCEC-US 11 113672230 113672230 single base substitution G T stop_gained C854* 2562C>A UCEC-US 11 113672230 113672230 single base substitution G T stop_gained C979* 2937C>A UCEC-US 11 113672387 113672387 single base substitution T C 3_prime_UTR_variant UCEC-US 11 113672387 113672387 single base substitution T C downstream_gene_variant UCEC-US 11 113672387 113672387 single base substitution T C exon_variant UCEC-US 11 113672387 113672387 single base substitution T C missense_variant K635R 1904A>G UCEC-US 11 113672387 113672387 single base substitution T C missense_variant K802R 2405A>G UCEC-US 11 113672387 113672387 single base substitution T C missense_variant K927R 2780A>G UCEC-US 11 113672387 113672387 single base substitution T C missense_variant K959R 2876A>G UCEC-US 11 113673913 113673913 single base substitution G A 3_prime_UTR_variant UCEC-US 11 113673913 113673913 single base substitution G A downstream_gene_variant UCEC-US 11 113673913 113673913 single base substitution G A synonymous_variant S619S 1857C>T UCEC-US 11 113673913 113673913 single base substitution G A synonymous_variant S786S 2358C>T UCEC-US 11 113673913 113673913 single base substitution G A synonymous_variant S911S 2733C>T UCEC-US 11 113673913 113673913 single base substitution G A synonymous_variant S943S 2829C>T UCEC-US 11 113673913 113673913 single base substitution G A upstream_gene_variant UCEC-US 11 113674585 113674585 single base substitution A C 3_prime_UTR_variant UCEC-US 11 113674585 113674585 single base substitution A C downstream_gene_variant UCEC-US 11 113674585 113674585 single base substitution A C missense_variant D567E 1701T>G UCEC-US 11 113674585 113674585 single base substitution A C missense_variant D734E 2202T>G UCEC-US 11 113674585 113674585 single base substitution A C missense_variant D859E 2577T>G UCEC-US 11 113674585 113674585 single base substitution A C missense_variant D891E 2673T>G UCEC-US 11 113674585 113674585 single base substitution A C upstream_gene_variant UCEC-US 11 113675639 113675639 single base substitution G A 3_prime_UTR_variant UCEC-US 11 113675639 113675639 single base substitution G A downstream_gene_variant UCEC-US 11 113675639 113675639 single base substitution G A stop_gained R520* 1558C>T UCEC-US 11 113675639 113675639 single base substitution G A stop_gained R687* 2059C>T UCEC-US 11 113675639 113675639 single base substitution G A stop_gained R812* 2434C>T UCEC-US 11 113675639 113675639 single base substitution G A stop_gained R844* 2530C>T UCEC-US 11 113675639 113675639 single base substitution G A upstream_gene_variant UCEC-US 11 113675754 113675754 single base substitution T A 3_prime_UTR_variant UCEC-US 11 113675754 113675754 single base substitution T A missense_variant E159D 477A>T UCEC-US 11 113675754 113675754 single base substitution T A missense_variant E481D 1443A>T UCEC-US 11 113675754 113675754 single base substitution T A missense_variant E648D 1944A>T UCEC-US 11 113675754 113675754 single base substitution T A missense_variant E773D 2319A>T UCEC-US 11 113675754 113675754 single base substitution T A missense_variant E805D 2415A>T UCEC-US 11 113675754 113675754 single base substitution T A upstream_gene_variant UCEC-US 11 113683225 113683225 single base substitution A G downstream_gene_variant UCEC-US 11 113683225 113683225 single base substitution A G intron_variant UCEC-US 11 113683225 113683225 single base substitution A G missense_variant V286A 857T>C UCEC-US 11 113683225 113683225 single base substitution A G missense_variant V290A 869T>C UCEC-US 11 113683225 113683225 single base substitution A G missense_variant V457A 1370T>C UCEC-US 11 113683225 113683225 single base substitution A G missense_variant V582A 1745T>C UCEC-US 11 113683225 113683225 single base substitution A G upstream_gene_variant UCEC-US 11 113684625 113684625 single base substitution G A downstream_gene_variant UCEC-US 11 113684625 113684625 single base substitution G A intron_variant UCEC-US 11 113684625 113684625 single base substitution G A synonymous_variant C279C 837C>T UCEC-US 11 113684625 113684625 single base substitution G A synonymous_variant C283C 849C>T UCEC-US 11 113684625 113684625 single base substitution G A synonymous_variant C450C 1350C>T UCEC-US 11 113684625 113684625 single base substitution G A synonymous_variant C575C 1725C>T UCEC-US 11 113684625 113684625 single base substitution G A upstream_gene_variant UCEC-US 11 113701595 113701595 single base substitution G A 3_prime_UTR_variant UCEC-US 11 113701595 113701595 single base substitution G A downstream_gene_variant UCEC-US 11 113701595 113701595 single base substitution G A exon_variant UCEC-US 11 113701595 113701595 single base substitution G A missense_variant R177C 529C>T UCEC-US 11 113701595 113701595 single base substitution G A missense_variant R201C 601C>T UCEC-US 11 113701595 113701595 single base substitution G A missense_variant R302C 904C>T UCEC-US 11 113701595 113701595 single base substitution G A missense_variant R66C 196C>T UCEC-US 11 113701595 113701595 single base substitution G A upstream_gene_variant UCEC-US 11 113704272 113704272 single base substitution C A 3_prime_UTR_variant UCEC-US 11 113704272 113704272 single base substitution C A exon_variant UCEC-US 11 113704272 113704272 single base substitution C A missense_variant R109I 326G>T UCEC-US 11 113704272 113704272 single base substitution C A missense_variant R210I 629G>T UCEC-US 11 113704272 113704272 single base substitution C A missense_variant R85I 254G>T UCEC-US 11 113704272 113704272 single base substitution C A upstream_gene_variant UCEC-US 11 113704982 113704982 single base substitution G A 3_prime_UTR_variant UCEC-US 11 113704982 113704982 single base substitution G A exon_variant UCEC-US 11 113704982 113704982 single base substitution G A intron_variant UCEC-US 11 113704982 113704982 single base substitution G A stop_gained R204* 610C>T UCEC-US 11 113704982 113704982 single base substitution G A stop_gained R79* 235C>T UCEC-US 11 113704982 113704982 single base substitution G A upstream_gene_variant UCEC-US 11 113705058 113705058 single base substitution C T intron_variant UCEC-US 11 113705058 113705058 single base substitution C T splice_acceptor_variant UCEC-US 11 113705058 113705058 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-BR-6566-01 COSM923242 c.705G>A p.P235P Substitution - coding silent 11:113833474-113833474 - Pat_08_A COSM923241 c.904C>T p.R302C Substitution - Missense 11:113830873-113830873 - TCGA-D1-A103-01 COSM923240 c.1725C>T p.C575C Substitution - coding silent 11:113813903-113813903 - TCGA-BC-A10Q-01 COSM4927674 c.1046A>G p.K349R Substitution - Missense 11:113829210-113829210 - TCGA-BR-6706-01 COSM4017948 c.2687G>A p.R896Q Substitution - Missense 11:113803849-113803849 - PCSI_0083_Pa_X COSM1316756 c.454A>G p.N152D Substitution - Missense 11:113840678-113840678 - TCGA-28-2509-01 COSM2103496 c.3004G>A p.A1002T Substitution - Missense 11:113801537-113801537 - S02328 COSM5691762 c.2171C>T p.S724L Substitution - Missense 11:113808431-113808431 - ESO-114 COSM1270070 c.911G>A p.G304E Substitution - Missense 11:113829345-113829345 - 587342 COSM1232013 c.1744-1G>T p.? Unknown 11:113812505-113812505 - LPJ119 COSM1316756 c.454A>G p.N152D Substitution - Missense 11:113840678-113840678 - PT42 COSM5925648 c.1082C>T p.P361L Substitution - Missense 11:113827338-113827338 - U87 COSM5211122 c.2818_2819insG p.V940fs*26 Insertion - Frameshift 11:113803201-113803202 - 1431232 COSM51319 c.2050G>A p.D684N Substitution - Missense 11:113809177-113809177 - S02322 COSM5691140 c.58-1G>A p.? Unknown 11:113854336-113854336 - NCI-H727 COSM2103534 c.1829G>A p.R610Q Substitution - Missense 11:113812419-113812419 - CSCC-52-T COSM4485623 c.2953C>T p.P985S Substitution - Missense 11:113801588-113801588 - sysucc-1972T COSM5480318 c.2522T>C p.V841A Substitution - Missense 11:113804925-113804925 - 587376 COSM1232015 c.695T>G p.F232C Substitution - Missense 11:113833484-113833484 - 6115123 COSM5547697 c.2694_2695delGT p.S899fs*66 Deletion - Frameshift 11:113803841-113803842 - HT115 COSM2103525 c.2240C>T p.A747V Substitution - Missense 11:113808362-113808362 - 8030245 COSM1159348 c.490C>T p.L164L Substitution - coding silent 11:113840642-113840642 - PD2218a COSM25718 c.3136C>T p.P1046S Substitution - Missense 11:113799338-113799338 - J83_T COSM3979123 c.145G>T p.G49C Substitution - Missense 11:113852624-113852624 - H1672 COSM316402 c.142A>T p.N48Y Substitution - Missense 11:113852627-113852627 - TCGA-B5-A11G-01 COSM923238 c.2415A>T p.E805D Substitution - Missense 11:113805032-113805032 - TCGA-EE-A2MI-06 COSM3443583 c.949C>T p.P317S Substitution - Missense 11:113829307-113829307 - CMPC11-3104 COSM5095406 c.227C>G p.S76C Substitution - Missense 11:113852542-113852542 - TCGA-DJ-A1QL-01 COSM136033 c.559C>T p.R187* Substitution - Nonsense 11:113834311-113834311 - ccRCC-3 COSM1666002 c.759+2T>C p.? Unknown 11:113833418-113833418 - ACINAR03 COSM1732886 c.2818delG p.V940fs*5 Deletion - Frameshift 11:113803202-113803202 - GCT51 COSM5749840 c.1744-22_1746del25 p.? Unknown 11:113812502-113812526 - TCGA-HU-A4GQ-01 COSM242196 c.2281G>A p.G761S Substitution - Missense 11:113808321-113808321 - CSCC-37-T COSM4551041 c.516G>A p.W172* Substitution - Nonsense 11:113840616-113840616 - HCC107 COSM1604125 c.1739G>A p.R580H Substitution - Missense 11:113813889-113813889 - TCGA-CG-5721-01 COSM4017947 c.2945T>C p.L982P Substitution - Missense 11:113801596-113801596 - 1604875 COSM141356 c.2879C>A p.A960E Substitution - Missense 11:113801662-113801662 - TCGA-EE-A29H-06 COSM3443575 c.2814G>A p.R938R Substitution - coding silent 11:113803206-113803206 - TCGA-BR-6458-01 COSM4017952 c.1135C>G p.P379A Substitution - Missense 11:113827285-113827285 - TCGA-06-0209-01 COSM3397419 c.2400+2T>C p.? Unknown 11:113806487-113806487 - PT37 COSM5920309 c.2954C>T p.P985L Substitution - Missense 11:113801587-113801587 - T3090 COSM923240 c.1725C>T p.C575C Substitution - coding silent 11:113813903-113813903 - SNU-175 COSM2103520 c.2321C>G p.A774G Substitution - Missense 11:113806568-113806568 - TCGA-60-2724-01 COSM686310 c.2025G>T p.V675V Substitution - coding silent 11:113809202-113809202 - 587254 COSM1232012 c.3178C>T p.R1060* Substitution - Nonsense 11:113799296-113799296 - TCGA-FW-A5DY-06 COSM3443581 c.1027C>T p.P343S Substitution - Missense 11:113829229-113829229 - HX4T COSM1604122 c.3154A>G p.N1052D Substitution - Missense 11:113799320-113799320 - TCGA-60-2719-01 COSM686312 c.2473C>T p.L825F Substitution - Missense 11:113804974-113804974 - TCGA-CG-5721-01 COSM4017949 c.1695T>C p.S565S Substitution - coding silent 11:113813933-113813933 - HCC60 COSM1604127 c.1350A>G p.E450E Substitution - coding silent 11:113817771-113817771 - cSCCP1 COSM136033 c.559C>T p.R187* Substitution - Nonsense 11:113834311-113834311 - T2940 COSM4739743 c.760-1G>A p.? Unknown 11:113831994-113831994 - CCC5 COSM3666096 c.338C>T p.S113F Substitution - Missense 11:113841699-113841699 - PCSI_0083_Pa_X COSM3375650 c.2059C>T p.R687W Substitution - Missense 11:113809168-113809168 - TCGA-A4-7732-01 COSM3985942 c.536C>G p.S179C Substitution - Missense 11:113834334-113834334 - TCGA-EJ-5518-01 COSM1127904 c.683C>G p.S228* Substitution - Nonsense 11:113833496-113833496 - BD5T COSM3666096 c.338C>T p.S113F Substitution - Missense 11:113841699-113841699 - CCC5T COSM3666096 c.338C>T p.S113F Substitution - Missense 11:113841699-113841699 - STC252 COSM5050535 c.2811C>T p.R937R Substitution - coding silent 11:113803209-113803209 - B66-Tumor COSM1746040 c.1106G>C p.R369T Substitution - Missense 11:113827314-113827314 - TCGA-FS-A4FC-06 COSM3443576 c.2756C>T p.S919F Substitution - Missense 11:113803264-113803264 - YUDEXA COSM1704564 c.500T>C p.V167A Substitution - Missense 11:113840632-113840632 - 2334192 COSM316402 c.142A>T p.N48Y Substitution - Missense 11:113852627-113852627 - PT48 COSM5932925 c.340C>T p.P114S Substitution - Missense 11:113841697-113841697 - TCGA-DA-A1HY-06 COSM3443584 c.889C>T p.L297L Substitution - coding silent 11:113830888-113830888 - TCGA-BR-8680-01 COSM4017946 c.3158C>A p.S1053Y Substitution - Missense 11:113799316-113799316 - HT115 COSM2103505 c.2686C>T p.R896* Substitution - Nonsense 11:113803850-113803850 - TCGA-BR-7851-01 COSM1475052 c.704C>T p.P235L Substitution - Missense 11:113833475-113833475 - TCGA-B0-5693-01 COSM466342 c.1886T>G p.V629G Substitution - Missense 11:113812362-113812362 - TCGA-66-2777-01 COSM686309 c.1367C>T p.P456L Substitution - Missense 11:113817754-113817754 - TCGA-AZ-4315-01 COSM1351399 c.385G>A p.A129T Substitution - Missense 11:113840747-113840747 - Gp5D COSM2103506 c.2662T>C p.W888R Substitution - Missense 11:113803874-113803874 - TCGA-AX-A0J1-01 COSM923244 c.610C>T p.R204* Substitution - Nonsense 11:113834260-113834260 - TCGA-FW-A3R5-06 COSM3868459 c.2118G>A p.M706I Substitution - Missense 11:113809109-113809109 - S02277 COSM5683007 c.585G>A p.L195L Substitution - coding silent 11:113834285-113834285 - PCSI_0083_Pa_P COSM3375650 c.2059C>T p.R687W Substitution - Missense 11:113809168-113809168 - sysucc-274T COSM5475467 c.981C>T p.D327D Substitution - coding silent 11:113829275-113829275 - S2_post COSM5575076 c.1104_1105insTC p.R369fs*48 Insertion - Frameshift 11:113827315-113827316 - TCGA-F1-A448-01 COSM4017957 c.407G>A p.R136H Substitution - Missense 11:113840725-113840725 - TCGA-29-1761-01 COSM1321903 c.1283G>C p.R428T Substitution - Missense 11:113823605-113823605 - LAU165 COSM235548 c.1125C>T p.S375S Substitution - coding silent 11:113827295-113827295 - PD4120a COSM165436 c.79C>T p.Q27* Substitution - Nonsense 11:113854314-113854314 - TCGA-F5-6814-01 COSM136033 c.559C>T p.R187* Substitution - Nonsense 11:113834311-113834311 - BN36T COSM1604124 c.1850A>G p.N617S Substitution - Missense 11:113812398-113812398 - JEKO-1 COSM1739782 c.251A>G p.N84S Substitution - Missense 11:113852518-113852518 - TCGA-E9-A244-01 COSM1475052 c.704C>T p.P235L Substitution - Missense 11:113833475-113833475 - ccRCC-9 COSM1664915 c.2722C>G p.L908V Substitution - Missense 11:113803814-113803814 - DU-145 COSM1676444 c.941G>A p.G314D Substitution - Missense 11:113829315-113829315 - TCGA-36-1578-01 COSM79431 c.853G>T p.E285* Substitution - Nonsense 11:113830924-113830924 - TCGA-GF-A3OT-06 COSM3443577 c.2562T>A p.N854K Substitution - Missense 11:113804885-113804885 - TCGA-A6-5661-01 COSM1351392 c.1743G>T p.Q581H Substitution - Missense 11:113813885-113813885 - TCGA-EE-A2MD-06 COSM3443573 c.2987C>T p.S996F Substitution - Missense 11:113801554-113801554 - T2269 COSM4739742 c.1412T>G p.L471* Substitution - Nonsense 11:113817709-113817709 - SC_9030 COSM5574128 c.834-2_834-1insC p.? Unknown 11:113830944-113830945 - 392 COSM3724110 c.3087T>C p.F1029F Substitution - coding silent 11:113799387-113799387 - TCGA-BS-A0UV-01 COSM923241 c.904C>T p.R302C Substitution - Missense 11:113830873-113830873 - TCGA-BR-6452-01 COSM4017955 c.911-2A>G p.? Unknown 11:113829347-113829347 - CSCC-35-T COSM4449565 c.2659-1G>A p.? Unknown 11:113803878-113803878 - CHEWS008 COSM4574055 c.1467A>C p.T489T Substitution - coding silent 11:113815379-113815379 - HCC107T COSM1604125 c.1739G>A p.R580H Substitution - Missense 11:113813889-113813889 - B66 COSM1746040 c.1106G>C p.R369T Substitution - Missense 11:113827314-113827314 - 1056-01-02TD COSM5416727 c.2430T>A p.Y810* Substitution - Nonsense 11:113805017-113805017 - SC_9034 COSM5551217 c.1383T>A p.C461* Substitution - Nonsense 11:113817738-113817738 - H358 COSM1194100 c.3133G>A p.E1045K Substitution - Missense 11:113799341-113799341 - CHC097T COSM5347280 c.1999_2013del15 p.M667_E671delMSEVE Deletion - In frame 11:113809214-113809228 - TCGA-GV-A3JX-01 COSM138845 c.2893G>A p.E965K Substitution - Missense 11:113801648-113801648 - PAPNNX COSM5004838 c.2465A>T p.D822V Substitution - Missense 11:113804982-113804982 - TCGA-FS-A1ZA-06 COSM3443580 c.1094T>C p.F365S Substitution - Missense 11:113827326-113827326 - PT46 COSM3443576 c.2756C>T p.S919F Substitution - Missense 11:113803264-113803264 - TCGA-D3-A2JF-06 COSM3443582 c.970C>T p.R324C Substitution - Missense 11:113829286-113829286 - pfg127T COSM4760303 c.1591C>T p.R531* Substitution - Nonsense 11:113815255-113815255 - Pat_40_A COSM5837822 c.751G>T p.E251* Substitution - Nonsense 11:113833428-113833428 - TCGA-27-1832-01 COSM3397420 c.1357A>G p.S453G Substitution - Missense 11:113817764-113817764 - TCGA-D1-A17Q-01 COSM923239 c.1745T>C p.V582A Substitution - Missense 11:113812503-113812503 - Mx22 COSM50875 c.3148C>T p.R1050* Substitution - Nonsense 11:113799326-113799326 - BN50 COSM1604127 c.1350A>G p.E450E Substitution - coding silent 11:113817771-113817771 - CSCC-47-T COSM4541920 c.3095G>A p.R1032K Substitution - Missense 11:113799379-113799379 - 2492723 COSM2103523 c.2282G>A p.G761D Substitution - Missense 11:113808320-113808320 - HN_62854 COSM130113 c.1111G>C p.E371Q Substitution - Missense 11:113827309-113827309 - B80-5-Tumor COSM1127904 c.683C>G p.S228* Substitution - Nonsense 11:113833496-113833496 - HCC61T COSM1604123 c.2939A>C p.N980T Substitution - Missense 11:113801602-113801602 - TCGA-AR-A2LE-01 COSM3808382 c.743C>T p.S248L Substitution - Missense 11:113833436-113833436 - TCGA-EI-6917-01 COSM3415552 c.740G>A p.R247Q Substitution - Missense 11:113833439-113833439 - TCGA-C5-A1BQ-01 COSM540923 c.532C>T p.Q178* Substitution - Nonsense 11:113840600-113840600 - 199-06-01TD COSM5418051 c.534+3A>T p.? Unknown 11:113840595-113840595 - TCGA-D3-A3ML-06 COSM3443583 c.949C>T p.P317S Substitution - Missense 11:113829307-113829307 - J73_T COSM3979121 c.322T>A p.L108M Substitution - Missense 11:113841715-113841715 - HCC2998 COSM248240 c.1753C>T p.R585C Substitution - Missense 11:113812495-113812495 - HCC2998 COSM1351385 c.2824G>T p.E942* Substitution - Nonsense 11:113803196-113803196 - LUAD-B02477 COSM335786 c.1672+1G>T p.? Unknown 11:113815173-113815173 - TCGA-GV-A3JZ-01 COSM1297665 c.1217G>A p.R406Q Substitution - Missense 11:113823671-113823671 - TCGA-DY-A1DC-01 COSM1561083 c.610C>G p.R204G Substitution - Missense 11:113834260-113834260 - HCC147T COSM5811540 c.1777G>T p.E593* Substitution - Nonsense 11:113812471-113812471 - T90 COSM242196 c.2281G>A p.G761S Substitution - Missense 11:113808321-113808321 - ICGC_0056 COSM1159348 c.490C>T p.L164L Substitution - coding silent 11:113840642-113840642 - MT-439-T2 COSM5651581 c.770G>A p.S257N Substitution - Missense 11:113831983-113831983 - RK195_C01 COSM3738864 c.65A>C p.Q22P Substitution - Missense 11:113854328-113854328 - TCGA-EI-6882-01 COSM3415553 c.504C>T p.G168G Substitution - coding silent 11:113840628-113840628 - sysucc-1163T COSM5458175 c.3006C>T p.A1002A Substitution - coding silent 11:113801535-113801535 - TCGA-EE-A3J7-06 COSM3868461 c.538C>T p.L180F Substitution - Missense 11:113834332-113834332 - TCGA-AA-3510-01 COSM923244 c.610C>T p.R204* Substitution - Nonsense 11:113834260-113834260 - PT31 COSM5906916 c.2110C>T p.P704S Substitution - Missense 11:113809117-113809117 - CSCC-47-T COSM4482435 c.2605C>T p.Q869* Substitution - Nonsense 11:113804726-113804726 - SWE-35 COSM1179709 c.571C>T p.L191F Substitution - Missense 11:113834299-113834299 - ME009T COSM223499 c.622-1G>A p.? Unknown 11:113833558-113833558 - 587376 COSM1232014 c.2714G>A p.G905D Substitution - Missense 11:113803822-113803822 - 2492721 COSM2103523 c.2282G>A p.G761D Substitution - Missense 11:113808320-113808320 - Pat_40_B COSM5837822 c.751G>T p.E251* Substitution - Nonsense 11:113833428-113833428 - RK072_C01 COSM1627794 c.3107C>T p.P1036L Substitution - Missense 11:113799367-113799367 - CSCC-31-T COSM4569667 c.1926T>C p.A642A Substitution - coding silent 11:113812322-113812322 - TCGA-FW-A3R5-06 COSM3868460 c.1996C>T p.Q666* Substitution - Nonsense 11:113809231-113809231 - NCI-H23 COSM138845 c.2893G>A p.E965K Substitution - Missense 11:113801648-113801648 - 594-01-1TD COSM5419469 c.495A>T p.K165N Substitution - Missense 11:113840637-113840637 - Pat_08_B COSM923241 c.904C>T p.R302C Substitution - Missense 11:113830873-113830873 - 403 COSM4429878 c.1530C>G p.P510P Substitution - coding silent 11:113815316-113815316 - sysucc-880T COSM5461914 c.534+6A>T p.? Unknown 11:113840592-113840592 - TCGA-D1-A101-01 COSM923245 c.535-1G>A p.? Unknown 11:113834336-113834336 - TCGA-D1-A103-01 COSM923234 c.2876A>G p.K959R Substitution - Missense 11:113801665-113801665 - BN36 COSM1604124 c.1850A>G p.N617S Substitution - Missense 11:113812398-113812398 - MO_1012 COSM5573785 c.2878_2879insA p.A960fs*6 Insertion - Frameshift 11:113801662-113801663 - WA51 COSM242198 c.484G>T p.V162F Substitution - Missense 11:113840648-113840648 - PCSI_0083_Pa_P_526 COSM3375650 c.2059C>T p.R687W Substitution - Missense 11:113809168-113809168 - PCSI_0083_Pa_P_526 COSM1316756 c.454A>G p.N152D Substitution - Missense 11:113840678-113840678 - LS411 COSM2103536 c.1790A>G p.N597S Substitution - Missense 11:113812458-113812458 - PT52 COSM5940214 c.2485C>T p.L829F Substitution - Missense 11:113804962-113804962 - ccRCC-60 COSM1664914 c.2974A>C p.N992H Substitution - Missense 11:113801567-113801567 - TCGA-18-3419-01 COSM686308 c.748G>T p.E250* Substitution - Nonsense 11:113833431-113833431 - EGC8 COSM5050536 c.2488G>T p.V830F Substitution - Missense 11:113804959-113804959 - T3152 COSM4739741 c.2254A>G p.N752D Substitution - Missense 11:113808348-113808348 - MedB-1 COSM5622117 c.986G>A p.C329Y Substitution - Missense 11:113829270-113829270 - YUKAT COSM5371684 c.1160A>G p.E387G Substitution - Missense 11:113827260-113827260 - TCGA-EE-A3JD-06 COSM4394421 c.2857C>T p.L953F Substitution - Missense 11:113803163-113803163 - LUAD-F00121 COSM365640 c.1861G>T p.V621F Substitution - Missense 11:113812387-113812387 - SC_9094 COSM5547843 c.2842_2843delTA p.Y948fs*17 Deletion - Frameshift 11:113803177-113803178 - TCGA-AP-A059-01 COSM923233 c.3033C>A p.C1011* Substitution - Nonsense 11:113801508-113801508 - sysucc-918T COSM5453424 c.2170T>C p.S724P Substitution - Missense 11:113808432-113808432 - LC_C5 COSM1188390 c.2513C>T p.P838L Substitution - Missense 11:113804934-113804934 - PT46 COSM5929353 c.2194C>T p.R732C Substitution - Missense 11:113808408-113808408 - TCGA-IR-A3LK-01 COSM4817933 c.2659-1G>C p.? Unknown 11:113803878-113803878 - 2521259 COSM5890664 c.1464-6C>T p.? Unknown 11:113815388-113815388 - YUQUEST COSM3868458 c.2828C>T p.S943F Substitution - Missense 11:113803192-113803192 - TCGA-B5-A0JY-01 COSM923243 c.629G>T p.R210I Substitution - Missense 11:113833550-113833550 - TCGA-CG-5721-01 COSM4017951 c.1201A>T p.S401C Substitution - Missense 11:113823687-113823687 - PD7215a COSM5788937 c.1615A>C p.N539H Substitution - Missense 11:113815231-113815231 - CSCC-29-T COSM4473800 c.1874C>T p.S625F Substitution - Missense 11:113812374-113812374 - GCT60 COSM25718 c.3136C>T p.P1046S Substitution - Missense 11:113799338-113799338 - TCGA-AY-6197-01 COSM1351387 c.2359C>T p.Q787* Substitution - Nonsense 11:113806530-113806530 - TCGA-EI-6917-01 COSM923244 c.610C>T p.R204* Substitution - Nonsense 11:113834260-113834260 - TCGA-A3-3346-01 COSM1492391 c.1805G>A p.W602* Substitution - Nonsense 11:113812443-113812443 - YUKAT COSM3443576 c.2756C>T p.S919F Substitution - Missense 11:113803264-113803264 - CHC2099T COSM4793302 c.2329G>T p.G777W Substitution - Missense 11:113806560-113806560 - TCGA-CD-A4MG-01 COSM4017948 c.2687G>A p.R896Q Substitution - Missense 11:113803849-113803849 - TCGA-EI-6917-01 COSM3415551 c.3005C>T p.A1002V Substitution - Missense 11:113801536-113801536 - TCGA-BF-A3DM-01 COSM3868458 c.2828C>T p.S943F Substitution - Missense 11:113803192-113803192 - TCGA-04-1651-01 COSM1321904 c.2663G>A p.W888* Substitution - Nonsense 11:113803873-113803873 - 105243 COSM95446 c.1342G>T p.V448F Substitution - Missense 11:113817779-113817779 - TCGA-DS-A0VM-01 COSM458725 c.1096G>A p.E366K Substitution - Missense 11:113827324-113827324 - TCGA-DK-A3IQ-01 COSM1297664 c.1857C>T p.I619I Substitution - coding silent 11:113812391-113812391 - SJHGG010324 COSM4970029 c.1332G>A p.M444I Substitution - Missense 11:113817789-113817789 - H23 COSM138845 c.2893G>A p.E965K Substitution - Missense 11:113801648-113801648 - T3021 COSM4739744 c.428A>G p.E143G Substitution - Missense 11:113840704-113840704 - HCC147T COSM5811481 c.2759A>T p.Y920F Substitution - Missense 11:113803261-113803261 - 112467 COSM95445 c.2483T>A p.V828D Substitution - Missense 11:113804964-113804964 - ESCC_73 COSM5634474 c.3124G>A p.V1042I Substitution - Missense 11:113799350-113799350 - TCGA-66-2759-01 COSM686311 c.2077G>C p.E693Q Substitution - Missense 11:113809150-113809150 - WA56 COSM242197 c.1052G>T p.G351V Substitution - Missense 11:113829204-113829204 - sysucc-783T COSM5483513 c.759+3A>G p.? Unknown 11:113833417-113833417 - EGC8 COSM5050534 c.2846G>A p.R949Q Substitution - Missense 11:113803174-113803174 - TCGA-D1-A17Q-01 COSM923241 c.904C>T p.R302C Substitution - Missense 11:113830873-113830873 - 2492722 COSM2103523 c.2282G>A p.G761D Substitution - Missense 11:113808320-113808320 - 18 COSM5211122 c.2818_2819insG p.V940fs*26 Insertion - Frameshift 11:113803201-113803202 - B80-5 COSM1127904 c.683C>G p.S228* Substitution - Nonsense 11:113833496-113833496 - PD4985a COSM5791333 c.2001G>T p.M667I Substitution - Missense 11:113809226-113809226 - HCC2998 COSM1351385 c.2824G>T p.E942* Substitution - Nonsense 11:113803196-113803196 - cSCCP4 COSM138845 c.2893G>A p.E965K Substitution - Missense 11:113801648-113801648 - TCGA-AA-A00N-01 COSM278036 c.1106G>T p.R369I Substitution - Missense 11:113827314-113827314 - CML021T COSM5189616 c.1284-7C>T p.? Unknown 11:113817844-113817844 - 541 COSM5612454 c.2297T>C p.L766P Substitution - Missense 11:113808305-113808305 - J83_T COSM3979122 c.146G>T p.G49V Substitution - Missense 11:113852623-113852623 - TCGA-AP-A051-01 COSM923237 c.2530C>T p.R844* Substitution - Nonsense 11:113804917-113804917 - YUKLAB COSM1704563 c.1120C>T p.Q374* Substitution - Nonsense 11:113827300-113827300 - TCGA-AX-A0J0-01 COSM923235 c.2829C>T p.S943S Substitution - coding silent 11:113803191-113803191 - GCT59 COSM5749916 c.1775A>T p.H592L Substitution - Missense 11:113812473-113812473 - PT36 COSM5916138 c.2407C>T p.H803Y Substitution - Missense 11:113805040-113805040 - CSCC-19-T COSM923241 c.904C>T p.R302C Substitution - Missense 11:113830873-113830873 - ESCC-128T COSM3935321 c.1438G>A p.V480I Substitution - Missense 11:113817683-113817683 - TCGA-AP-A0LE-01 COSM923242 c.705G>A p.P235P Substitution - coding silent 11:113833474-113833474 - 1342576 COSM51319 c.2050G>A p.D684N Substitution - Missense 11:113809177-113809177 - TCGA-BQ-5893-01 COSM3985941 c.2040C>A p.Y680* Substitution - Nonsense 11:113809187-113809187 - TCGA-BR-8081-01 COSM4017953 c.998C>T p.A333V Substitution - Missense 11:113829258-113829258 - TCGA-IR-A3LA-01 COSM4845892 c.1636C>T p.Q546* Substitution - Nonsense 11:113815210-113815210 - CHC892T COSM4551041 c.516G>A p.W172* Substitution - Nonsense 11:113840616-113840616 - C91 COSM4444324 c.341C>T p.P114L Substitution - Missense 11:113841696-113841696 - BN50T COSM1604127 c.1350A>G p.E450E Substitution - coding silent 11:113817771-113817771 - CHEWS004 COSM4574056 c.929A>G p.N310S Substitution - Missense 11:113829327-113829327 - TCGA-D1-A17Q-01 COSM923243 c.629G>T p.R210I Substitution - Missense 11:113833550-113833550 - TCGA-BH-A0HP-01 COSM3808383 c.157C>T p.Q53* Substitution - Nonsense 11:113852612-113852612 - GCT05 COSM5749159 c.618delT p.H206fs*19 Deletion - Frameshift 11:113834252-113834252 - GCT42 COSM5749798 c.814C>T p.Q272* Substitution - Nonsense 11:113831939-113831939 - TCGA-AA-3693-01 COSM268358 c.930T>G p.N310K Substitution - Missense 11:113829326-113829326 - T3498 COSM2103579 c.497delA p.N166fs*59 Deletion - Frameshift 11:113840635-113840635 - TCGA-BR-6452-01 COSM4017954 c.940G>A p.G314S Substitution - Missense 11:113829316-113829316 - Gp2D COSM2103506 c.2662T>C p.W888R Substitution - Missense 11:113803874-113803874 - RMS10_ COSM4985994 c.820G>A p.A274T Substitution - Missense 11:113831933-113831933 - 2492720 COSM2103523 c.2282G>A p.G761D Substitution - Missense 11:113808320-113808320 - TCGA-AK-3458-01 COSM466343 c.867G>T p.V289V Substitution - coding silent 11:113830910-113830910 - TCGA-D5-6533-01 COSM1351400 c.256G>T p.E86* Substitution - Nonsense 11:113852513-113852513 - TCGA-D7-A4YT-01 COSM4017956 c.601G>T p.E201* Substitution - Nonsense 11:113834269-113834269 - TCGA-A6-6780-01 COSM1351388 c.2357G>A p.R786H Substitution - Missense 11:113806532-113806532 - 01-P131 COSM4574054 c.2019A>T p.L673L Substitution - coding silent 11:113809208-113809208 - Gp2D COSM4626745 c.2912C>A p.S971Y Substitution - Missense 11:113801629-113801629 - QC2-19-T2 COSM5652709 c.963C>T p.N321N Substitution - coding silent 11:113829293-113829293 - HCC60T COSM1604127 c.1350A>G p.E450E Substitution - coding silent 11:113817771-113817771 - Gp2D COSM4626746 c.982G>A p.E328K Substitution - Missense 11:113829274-113829274 - TCGA-EE-A2MS-06 COSM3443585 c.370A>G p.N124D Substitution - Missense 11:113841667-113841667 - TCGA-EB-A5SE-01 COSM3443579 c.1165C>T p.P389S Substitution - Missense 11:113827255-113827255 - SA077 COSM213383 c.2047G>T p.E683* Substitution - Nonsense 11:113809180-113809180 - TCGA-AA-3692-01 COSM293278 c.3149G>A p.R1050Q Substitution - Missense 11:113799325-113799325 - TCGA-B0-4693-01 COSM3773576 c.1680G>T p.K560N Substitution - Missense 11:113813948-113813948 - TCGA-DA-A1HW-06 COSM3443578 c.2391G>A p.G797G Substitution - coding silent 11:113806498-113806498 - CHC2099T COSM4793302 c.2329G>T p.G777W Substitution - Missense 11:113806560-113806560 - S00936 COSM316403 c.3082G>T p.E1028* Substitution - Nonsense 11:113799392-113799392 - LC_S3 COSM1188391 c.686A>G p.N229S Substitution - Missense 11:113833493-113833493 - TCGA-G4-6299-01 COSM1351396 c.905G>A p.R302H Substitution - Missense 11:113830872-113830872 - HCC18T COSM1604126 c.1406T>C p.M469T Substitution - Missense 11:113817715-113817715 - Pat_41_B COSM3443581 c.1027C>T p.P343S Substitution - Missense 11:113829229-113829229 - SW48 COSM2103543 c.1609G>A p.E537K Substitution - Missense 11:113815237-113815237 - TCGA-D5-6922-01 COSM1351398 c.739C>T p.R247* Substitution - Nonsense 11:113833440-113833440 - TCGA-AC-A23H-01 COSM3808380 c.931G>T p.E311* Substitution - Nonsense 11:113829325-113829325 - PT48 COSM4444324 c.341C>T p.P114L Substitution - Missense 11:113841696-113841696 - TCGA-BS-A0UF-01 COSM923236 c.2673T>G p.D891E Substitution - Missense 11:113803863-113803863 - HCC18 COSM1604126 c.1406T>C p.M469T Substitution - Missense 11:113817715-113817715 - TCGA-BT-A0YX-01 COSM415338 c.1168C>T p.Q390* Substitution - Nonsense 11:113827252-113827252 - TCGA-AP-A059-01 COSM923237 c.2530C>T p.R844* Substitution - Nonsense 11:113804917-113804917 - TCGA-FW-A3R5-06 COSM1297665 c.1217G>A p.R406Q Substitution - Missense 11:113823671-113823671 - CSCC-29-T COSM4570679 c.305T>C p.L102P Substitution - Missense 11:113841732-113841732 - TCGA-AA-3510-01 COSM1351393 c.1289T>C p.V430A Substitution - Missense 11:113817832-113817832 - 49M COSM1506912 c.362G>T p.R121I Substitution - Missense 11:113841675-113841675 - PR-00-1165 COSM248240 c.1753C>T p.R585C Substitution - Missense 11:113812495-113812495 - TCGA-EE-A183-06 COSM3443574 c.2952C>T p.I984I Substitution - coding silent 11:113801589-113801589 - TCGA-BR-4361-01 COSM4017950 c.1661A>G p.Q554R Substitution - Missense 11:113815185-113815185 - TCGA-AA-A010-01 COSM286390 c.860C>T p.P287L Substitution - Missense 11:113830917-113830917 - BD10T COSM5514544 c.2489T>G p.V830G Substitution - Missense 11:113804958-113804958 - GC_297_T-GC_297_N COSM4772713 c.883A>C p.T295P Substitution - Missense 11:113830894-113830894 - HCC2998 COSM248240 c.1753C>T p.R585C Substitution - Missense 11:113812495-113812495 - LUAD-B00416 COSM330788 c.136-1G>T p.? Unknown 11:113852634-113852634 - SW48 COSM2103557 c.1061G>A p.R354H Substitution - Missense 11:113827359-113827359 - C0026T COSM4165648 c.1687A>G p.I563V Substitution - Missense 11:113813941-113813941 - 61 COSM5739463 c.175A>G p.T59A Substitution - Missense 11:113852594-113852594 - PD11372a COSM5767146 c.621+3A>T p.? Unknown 11:113834246-113834246 - CHC892T COSM4551041 c.516G>A p.W172* Substitution - Nonsense 11:113840616-113840616 - T1 COSM5617665 c.169C>G p.L57V Substitution - Missense 11:113852600-113852600 - HCC61 COSM1604123 c.2939A>C p.N980T Substitution - Missense 11:113801602-113801602 - TCGA-AC-A23H-01 COSM3808381 c.763G>C p.D255H Substitution - Missense 11:113831990-113831990 - TCGA-AY-6197-01 COSM1351395 c.915delA p.K305fs*16 Deletion - Frameshift 11:113829341-113829341 - TCGA-AA-3510-01 COSM1351385 c.2824G>T p.E942* Substitution - Nonsense 11:113803196-113803196 - CRC-03T COSM5451117 c.480G>A p.W160* Substitution - Nonsense 11:113840652-113840652 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.503891 11q23 610748

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AATT - IntronicDeletion . c.1973-224_1973-221delAATT 11 113680197 ESCA A C Missense p.N310K c.930T>G 11 113700048 COREAD A G Missense p.F365S c.1094T>C 11 113698048 CM A G SpliceDonorSNV . c.2400+2T>C 11 113677209 GBM A G Synonymous p.L108L c.322T>C 11 113712437 HNSC - A IntronicInsertion . c.833+217dupT 11 113702425 CM A T Nonsense p.C329* c.987T>A 11 113699991 LUAD A T Nonsense p.Y293* c.879T>A 11 113701620 CM C A Missense p.A598S c.1792G>T 11 113683178 HNSC C A Missense p.D852Y c.2554G>T 11 113675615 LUAD C A Missense p.G797V c.2390G>T 11 113677221 LUAD C A Missense p.K560N c.1680G>T 11 113684670 RCCC C A Missense p.R1060L c.3179G>T 11 113670017 HNSC C A Nonsense p.E1028* c.3082G>T 11 113670114 SCLC C A Nonsense p.E250* c.748G>T 11 113704153 LUSC C A Nonsense p.E285* c.853G>T 11 113701646 OV C A Nonsense p.E683* c.2047G>T 11 113679902 BRCA C A Synonymous p.L847L c.2541G>T 11 113675628 LUAD C A Synonymous p.P442P c.1326G>T 11 113688517 STAD C A Synonymous p.V289V c.867G>T 11 113701632 RCCC C A Synonymous p.V675V c.2025G>T 11 113679924 LUSC - C Frameshift p.V940Gfs*26 c.2818dupG 11 113673924 CM C - Frameshift p.V940Sfs*5 c.2818delG 11 113673924 STAD C G Missense p.E371Q c.1111G>C 11 113698031 HNSC C G Missense p.E693Q c.2077G>C 11 113679872 LUSC C T IntronicSNV . c.57+8236G>A 11 113737931 PIA C T Missense p.A1002T c.3004G>A 11 113672259 GBM C T Missense p.D255N c.763G>A 11 113702712 LUAD C T Missense p.E965K c.2893G>A 11 113672370 BLCA C T Missense p.G304E c.911G>A 11 113700067 ESCA C T Missense p.R1050Q c.3149G>A 11 113670047 COREAD C T Missense p.R324H c.971G>A 11 113700007 LUAD C T Missense p.R406Q c.1217G>A 11 113694393 BLCA C T Missense p.R896Q c.2687G>A 11 113674571 STAD C T SpliceAcceptorSNV . c.535-1G>A 11 113705058 UCEC C T Synonymous p.G797G c.2391G>A 11 113677220 CM C T Synonymous p.R938R c.2814G>A 11 113673928 CM - GAA InFrameInsertion p.E630_R631insF c.1890_1891insTTC 11 113683079 PRAD G A IntronicSNV . c.1283+2143C>T 11 113692184 CM G A IntronicSNV . c.1283+2292C>T 11 113692035 CM G A Missense p.L180F c.538C>T 11 113705054 CM G A Missense p.L825F c.2473C>T 11 113675696 LUSC G A Missense p.L902F c.2704C>T 11 113674554 COREAD G A Missense p.L953F c.2857C>T 11 113673885 CM G A Missense p.P235L c.704C>T 11 113704197 BRCA G A Missense p.P317S c.949C>T 11 113700029 CM G A Missense p.P456L c.1367C>T 11 113688476 LUSC G A Missense p.R324C c.970C>T 11 113700008 CM G A Missense p.R585C c.1753C>T 11 113683217 LUAD G A Missense p.S633F c.1898C>T 11 113683072 CM G A Missense p.S943F c.2828C>T 11 113673914 CM G A Missense p.S996F c.2987C>T 11 113672276 CM G A Nonsense p.Q27* c.79C>T 11 113725036 BRCA G A Nonsense p.Q390* c.1168C>T 11 113697974 BLCA G A Nonsense p.Q682* c.2044C>T 11 113679905 LUAD G A Nonsense p.R187* c.559C>T 11 113705033 THCA G A Nonsense p.R824* c.2470C>T 11 113675699 BRCA G A Synonymous p.I619I c.1857C>T 11 113683113 BLCA G A Synonymous p.I984I c.2952C>T 11 113672311 CM G A Synonymous p.L164L c.490C>T 11 113711364 PAAD G A Synonymous p.L297L c.889C>T 11 113701610 CM G A Synonymous p.R141R c.423C>T 11 113711431 HNSC G C Missense p.P379A c.1135C>G 11 113698007 STAD G C Nonsense p.S228* c.683C>G 11 113704218 PRAD GG TT Missense p.P661K c.1981_1982delinsAA 11 113679967 CM T A Missense p.E805D c.2415A>T 11 113675754 UCEC T A Missense p.N48Y c.142A>T 11 113723349 SCLC T C Missense p.N124D c.370A>G 11 113712389 CM T C Missense p.S453G c.1357A>G 11 113688486 GBM TT - Frameshift p.K420Nfs*30 c.1260_1261delAA 11 113694349 BLCA TT - Frameshift p.N407*fs*1 c.1219_1220delAA 11 113694390 RCCC