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 9 37516027 37516027 + Missense_Mutation SNP C C T TCGA-OR-A5K4-01A-11D-A29I-10 TCGA-OR-A5K4-10A-01D-A29L-10 g.chr9:37516027C>T c.2570G>A c.(2569-2571)cGt>cAt p.R857H BLCA 9 37515909 37515909 + Missense_Mutation SNP G G C TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr9:37515909G>C c.2688C>G c.(2686-2688)ttC>ttG p.F896L BLCA 9 37529146 37529146 + Silent SNP G G A TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr9:37529146G>A c.1681C>T c.(1681-1683)Ctg>Ttg p.L561L BLCA 9 37529147 37529147 + Silent SNP G G A TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr9:37529147G>A c.1680C>T c.(1678-1680)atC>atT p.I560I BLCA 9 37537106 37537106 + Splice_Site SNP C C A TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr9:37537106C>A c.e3+1 BLCA 9 37537289 37537289 + Missense_Mutation SNP C C G TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr9:37537289C>G c.1237G>C c.(1237-1239)Gag>Cag p.E413Q BLCA 9 37537511 37537511 + Missense_Mutation SNP C C G TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr9:37537511C>G c.1015G>C c.(1015-1017)Gag>Cag p.E339Q BRCA 9 37521593 37521593 + Missense_Mutation SNP C C G TCGA-D8-A1JL-01A-11D-A13L-09 TCGA-D8-A1JL-10A-01D-A188-09 g.chr9:37521593C>G c.2173G>C c.(2173-2175)Gag>Cag p.E725Q BRCA 9 37537587 37537587 + Silent SNP G G A TCGA-E2-A15M-01A-11D-A12B-09 TCGA-E2-A15M-11A-22D-A12B-09 g.chr9:37537587G>A c.939C>T c.(937-939)atC>atT p.I313I CESC 9 37537857 37537857 + Silent SNP C C T TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr9:37537857C>T c.669G>A c.(667-669)gtG>gtA p.V223V CHOL 9 37537628 37537628 + Silent SNP G G T TCGA-W5-AA2W-01A-11D-A417-09 TCGA-W5-AA2W-10A-01D-A41A-09 g.chr9:37537628G>T c.898C>A c.(898-900)Cgg>Agg p.R300R COAD 9 37516059 37516059 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr9:37516059C>T c.2538G>A c.(2536-2538)tcG>tcA p.S846S COAD 9 37516069 37516069 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr9:37516069C>T c.2528G>A c.(2527-2529)cGg>cAg p.R843Q COAD 9 37516074 37516074 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:37516074C>A c.2523G>T c.(2521-2523)aaG>aaT p.K841N COAD 9 37518143 37518143 + Silent SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr9:37518143C>T c.2493G>A c.(2491-2493)ctG>ctA p.L831L COAD 9 37518163 37518163 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr9:37518163G>A c.2473C>T c.(2473-2475)Cgg>Tgg p.R825W COAD 9 37518244 37518244 + Missense_Mutation SNP C C A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr9:37518244C>A c.2392G>T c.(2392-2394)Ggt>Tgt p.G798C COAD 9 37518347 37518347 + Silent SNP G G T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr9:37518347G>T c.2289C>A c.(2287-2289)gcC>gcA p.A763A COAD 9 37521617 37521617 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr9:37521617G>A c.2149C>T c.(2149-2151)Cgg>Tgg p.R717W COAD 9 37521630 37521630 + Silent SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr9:37521630G>A c.2136C>T c.(2134-2136)gaC>gaT p.D712D COAD 9 37521757 37521757 + Missense_Mutation SNP A A T TCGA-AA-A02Y-01A-43W-A096-10 TCGA-AA-A02Y-10A-01W-A096-10 g.chr9:37521757A>T c.2009T>A c.(2008-2010)cTg>cAg p.L670Q COAD 9 37521773 37521773 + Missense_Mutation SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr9:37521773C>T c.1993G>A c.(1993-1995)Gtc>Atc p.V665I COAD 9 37522822 37522822 + Splice_Site SNP C C T TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr9:37522822C>T c.1930G>A c.(1930-1932)Gct>Act p.A644T COAD 9 37522871 37522871 + Silent SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:37522871C>A c.1881G>T c.(1879-1881)gtG>gtT p.V627V COAD 9 37522875 37522875 + Missense_Mutation SNP C C A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr9:37522875C>A c.1877G>T c.(1876-1878)gGt>gTt p.G626V COAD 9 37525117 37525117 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:37525117C>T c.1759G>A c.(1759-1761)Ggc>Agc p.G587S COAD 9 37532021 37532021 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr9:37532021C>T c.1454G>A c.(1453-1455)cGa>cAa p.R485Q COAD 9 37537509 37537509 + Missense_Mutation SNP C C A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr9:37537509C>A c.1017G>T c.(1015-1017)gaG>gaT p.E339D COAD 9 37537792 37537792 + Frame_Shift_Del DEL T T - TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr9:37537792delT c.734delA c.(733-735)aacfs p.N245fs COAD 9 37537815 37537815 + Silent SNP G G A TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr9:37537815G>A c.711C>T c.(709-711)aaC>aaT p.N237N COAD 9 37537870 37537870 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr9:37537870C>T c.656G>A c.(655-657)gGt>gAt p.G219D COAD 9 37541446 37541446 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:37541446C>T c.320G>A c.(319-321)cGa>cAa p.R107Q COADREAD 9 37516059 37516059 + Silent SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr9:37516059C>T c.2538G>A c.(2536-2538)tcG>tcA p.S846S COADREAD 9 37516069 37516069 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr9:37516069C>T c.2528G>A c.(2527-2529)cGg>cAg p.R843Q COADREAD 9 37516074 37516074 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:37516074C>A c.2523G>T c.(2521-2523)aaG>aaT p.K841N COADREAD 9 37518143 37518143 + Silent SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr9:37518143C>T c.2493G>A c.(2491-2493)ctG>ctA p.L831L COADREAD 9 37518163 37518163 + Missense_Mutation SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr9:37518163G>A c.2473C>T c.(2473-2475)Cgg>Tgg p.R825W COADREAD 9 37518244 37518244 + Missense_Mutation SNP C C A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr9:37518244C>A c.2392G>T c.(2392-2394)Ggt>Tgt p.G798C COADREAD 9 37518347 37518347 + Silent SNP G G T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr9:37518347G>T c.2289C>A c.(2287-2289)gcC>gcA p.A763A COADREAD 9 37521617 37521617 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr9:37521617G>A c.2149C>T c.(2149-2151)Cgg>Tgg p.R717W COADREAD 9 37521630 37521630 + Silent SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr9:37521630G>A c.2136C>T c.(2134-2136)gaC>gaT p.D712D COADREAD 9 37521757 37521757 + Missense_Mutation SNP A A T TCGA-AA-A02Y-01A-43W-A096-10 TCGA-AA-A02Y-10A-01W-A096-10 g.chr9:37521757A>T c.2009T>A c.(2008-2010)cTg>cAg p.L670Q COADREAD 9 37521773 37521773 + Missense_Mutation SNP C C T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr9:37521773C>T c.1993G>A c.(1993-1995)Gtc>Atc p.V665I COADREAD 9 37522822 37522822 + Splice_Site SNP C C T TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr9:37522822C>T c.1930G>A c.(1930-1932)Gct>Act p.A644T COADREAD 9 37522871 37522871 + Silent SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:37522871C>A c.1881G>T c.(1879-1881)gtG>gtT p.V627V COADREAD 9 37522875 37522875 + Missense_Mutation SNP C C A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr9:37522875C>A c.1877G>T c.(1876-1878)gGt>gTt p.G626V COADREAD 9 37525117 37525117 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:37525117C>T c.1759G>A c.(1759-1761)Ggc>Agc p.G587S COADREAD 9 37532021 37532021 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr9:37532021C>T c.1454G>A c.(1453-1455)cGa>cAa p.R485Q COADREAD 9 37537509 37537509 + Missense_Mutation SNP C C A TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr9:37537509C>A c.1017G>T c.(1015-1017)gaG>gaT p.E339D COADREAD 9 37537792 37537792 + Frame_Shift_Del DEL T T - TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr9:37537792delT c.734delA c.(733-735)aacfs p.N245fs COADREAD 9 37537815 37537815 + Silent SNP G G A TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr9:37537815G>A c.711C>T c.(709-711)aaC>aaT p.N237N COADREAD 9 37537831 37537831 + Missense_Mutation SNP T T C TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr9:37537831T>C c.695A>G c.(694-696)cAt>cGt p.H232R COADREAD 9 37537870 37537870 + Missense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr9:37537870C>T c.656G>A c.(655-657)gGt>gAt p.G219D COADREAD 9 37541446 37541446 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:37541446C>T c.320G>A c.(319-321)cGa>cAa p.R107Q DLBC 9 37537892 37537892 + Missense_Mutation SNP G G T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr9:37537892G>T c.634C>A c.(634-636)Cac>Aac p.H212N ESCA 9 37515946 37515946 + Missense_Mutation SNP C C T TCGA-2H-A9GK-01A-11D-A37C-09 TCGA-2H-A9GK-11A-11D-A37F-09 g.chr9:37515946C>T c.2651G>A c.(2650-2652)cGa>cAa p.R884Q ESCA 9 37516074 37516074 + Missense_Mutation SNP C C G TCGA-2H-A9GK-01A-11D-A37C-09 TCGA-2H-A9GK-11A-11D-A37F-09 g.chr9:37516074C>G c.2523G>C c.(2521-2523)aaG>aaC p.K841N ESCA 9 37518154 37518154 + Missense_Mutation SNP C C T TCGA-L7-A56G-01A-21D-A27G-09 TCGA-L7-A56G-10A-01D-A27G-09 g.chr9:37518154C>T c.2482G>A c.(2482-2484)Ggg>Agg p.G828R ESCA 9 37537267 37537267 + Missense_Mutation SNP G G A TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr9:37537267G>A c.1259C>T c.(1258-1260)gCc>gTc p.A420V ESCA 9 37541505 37541505 + Missense_Mutation SNP C C G TCGA-JY-A6FH-01A-11D-A33E-09 TCGA-JY-A6FH-10A-01D-A33H-09 g.chr9:37541505C>G c.261G>C c.(259-261)aaG>aaC p.K87N ESCA 9 37541711 37541711 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr9:37541711G>A c.55C>T c.(55-57)Cac>Tac p.H19Y GBM 9 37515999 37515999 + Silent SNP G G T TCGA-76-6286-01A-11D-1845-08 TCGA-76-6286-10A-01D-1845-08 g.chr9:37515999G>T c.2598C>A c.(2596-2598)atC>atA p.I866I GBM 9 37522884 37522884 + Missense_Mutation SNP T T C TCGA-06-5417-01A-01D-1486-08 TCGA-06-5417-10A-01D-1486-08 g.chr9:37522884T>C c.1868A>G c.(1867-1869)tAt>tGt p.Y623C GBMLGG 9 37512652 37512652 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:37512652G>T c.2763C>A c.(2761-2763)ccC>ccA p.P921P GBMLGG 9 37515999 37515999 + Silent SNP G G T TCGA-76-6286-01A-11D-1845-08 TCGA-76-6286-10A-01D-1845-08 g.chr9:37515999G>T c.2598C>A c.(2596-2598)atC>atA p.I866I GBMLGG 9 37518375 37518375 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:37518375G>A c.2261C>T c.(2260-2262)gCg>gTg p.A754V GBMLGG 9 37522884 37522884 + Missense_Mutation SNP T T C TCGA-06-5417-01A-01D-1486-08 TCGA-06-5417-10A-01D-1486-08 g.chr9:37522884T>C c.1868A>G c.(1867-1869)tAt>tGt p.Y623C HNSC 9 37512610 37512610 + Silent SNP C C T TCGA-CR-6484-01A-11D-1870-08 TCGA-CR-6484-10A-01D-1870-08 g.chr9:37512610C>T c.2805G>A c.(2803-2805)acG>acA p.T935T HNSC 9 37512661 37512661 + Silent SNP G G C TCGA-CN-6013-01A-11D-1683-08 TCGA-CN-6013-10A-01D-1683-08 g.chr9:37512661G>C c.2754C>G c.(2752-2754)ctC>ctG p.L918L HNSC 9 37518252 37518252 + Missense_Mutation SNP C C T TCGA-HD-8635-01A-11D-2394-08 TCGA-HD-8635-10A-01D-2394-08 g.chr9:37518252C>T c.2384G>A c.(2383-2385)cGg>cAg p.R795Q HNSC 9 37518327 37518327 + Missense_Mutation SNP C C T TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chr9:37518327C>T c.2309G>A c.(2308-2310)cGa>cAa p.R770Q HNSC 9 37518331 37518331 + Missense_Mutation SNP T T A TCGA-CR-7399-01A-11D-2012-08 TCGA-CR-7399-10A-01D-2013-08 g.chr9:37518331T>A c.2305A>T c.(2305-2307)Acc>Tcc p.T769S HNSC 9 37521758 37521758 + Silent SNP G G A TCGA-CV-7178-01A-21D-2012-08 TCGA-CV-7178-10A-01D-2013-08 g.chr9:37521758G>A c.2008C>T c.(2008-2010)Ctg>Ttg p.L670L HNSC 9 37531943 37531943 + Missense_Mutation SNP C C G TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr9:37531943C>G c.1532G>C c.(1531-1533)gGt>gCt p.G511A HNSC 9 37531963 37531963 + Missense_Mutation SNP A A C TCGA-CR-5248-01A-01D-2012-08 TCGA-CR-5248-10A-01D-2013-08 g.chr9:37531963A>C c.1512T>G c.(1510-1512)atT>atG p.I504M HNSC 9 37537656 37537656 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr9:37537656G>A c.870C>T c.(868-870)gaC>gaT p.D290D HNSC 9 37537796 37537796 + Missense_Mutation SNP C C G TCGA-CV-7424-01A-11D-2078-08 TCGA-CV-7424-10A-01D-2078-08 g.chr9:37537796C>G c.730G>C c.(730-732)Gaa>Caa p.E244Q KIPAN 9 37537307 37537307 + Missense_Mutation SNP G G T TCGA-BQ-5882-01A-11D-1589-08 TCGA-BQ-5882-11A-01D-1589-08 g.chr9:37537307G>T c.1219C>A c.(1219-1221)Ctg>Atg p.L407M KIPAN 9 37537374 37537374 + Silent SNP T T A TCGA-BP-4354-01A-02D-1366-10 TCGA-BP-4354-11A-01D-1366-10 g.chr9:37537374T>A c.1152A>T c.(1150-1152)gtA>gtT p.V384V KIRC 9 37537374 37537374 + Silent SNP T T A TCGA-BP-4354-01A-02D-1366-10 TCGA-BP-4354-11A-01D-1366-10 g.chr9:37537374T>A c.1152A>T c.(1150-1152)gtA>gtT p.V384V KIRP 9 37537307 37537307 + Missense_Mutation SNP G G T TCGA-BQ-5882-01A-11D-1589-08 TCGA-BQ-5882-11A-01D-1589-08 g.chr9:37537307G>T c.1219C>A c.(1219-1221)Ctg>Atg p.L407M LGG 9 37512652 37512652 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:37512652G>T c.2763C>A c.(2761-2763)ccC>ccA p.P921P LGG 9 37518375 37518375 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:37518375G>A c.2261C>T c.(2260-2262)gCg>gTg p.A754V LIHC 9 37525102 37525102 + Missense_Mutation SNP T T A TCGA-G3-AAV4-01A-11D-A382-10 TCGA-G3-AAV4-10A-01D-A385-10 g.chr9:37525102T>A c.1774A>T c.(1774-1776)Aca>Tca p.T592S LIHC 9 37525156 37525156 + Missense_Mutation SNP A A G TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr9:37525156A>G c.1720T>C c.(1720-1722)Ttc>Ctc p.F574L LIHC 9 37541364 37541364 + Silent SNP A A G TCGA-DD-AAEG-01A-11D-A38X-10 TCGA-DD-AAEG-10A-01D-A38X-10 g.chr9:37541364A>G c.402T>C c.(400-402)atT>atC p.I134I LIHC 9 37541574 37541574 + Silent SNP T T C TCGA-CC-A7IK-01A-12D-A33Q-10 TCGA-CC-A7IK-10A-01D-A33Q-10 g.chr9:37541574T>C c.192A>G c.(190-192)ccA>ccG p.P64P LUAD 9 37516041 37516041 + Silent SNP G G A TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr9:37516041G>A c.2556C>T c.(2554-2556)atC>atT p.I852I LUAD 9 37516063 37516063 + Missense_Mutation SNP T T A TCGA-35-4123-01A-01D-1105-08 TCGA-35-4123-10A-01D-1105-08 g.chr9:37516063T>A c.2534A>T c.(2533-2535)cAc>cTc p.H845L LUAD 9 37537272 37537272 + Silent SNP C C T TCGA-64-5774-01A-01D-1625-08 TCGA-64-5774-10A-01D-1625-08 g.chr9:37537272C>T c.1254G>A c.(1252-1254)aaG>aaA p.K418K LUAD 9 37537899 37537899 + Missense_Mutation SNP C C G TCGA-86-8056-01A-11D-2238-08 TCGA-86-8056-10A-01D-2238-08 g.chr9:37537899C>G c.627G>C c.(625-627)gaG>gaC p.E209D LUAD 9 37541372 37541372 + Missense_Mutation SNP C C G TCGA-05-4433-01A-22D-1855-08 TCGA-05-4433-10A-01D-1855-08 g.chr9:37541372C>G c.394G>C c.(394-396)Gac>Cac p.D132H LUAD 9 37541466 37541466 + Silent SNP T T C TCGA-55-6971-01A-11D-1945-08 TCGA-55-6971-11A-01D-1945-08 g.chr9:37541466T>C c.300A>G c.(298-300)ctA>ctG p.L100L LUSC 9 37516034 37516034 + Missense_Mutation SNP G G A TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr9:37516034G>A c.2563C>T c.(2563-2565)Cgg>Tgg p.R855W LUSC 9 37537356 37537356 + Silent SNP C C T TCGA-21-5786-01A-01D-1632-08 TCGA-21-5786-10A-01D-1632-08 g.chr9:37537356C>T c.1170G>A c.(1168-1170)ctG>ctA p.L390L LUSC 9 37541208 37541208 + Silent SNP T T A TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr9:37541208T>A c.558A>T c.(556-558)ccA>ccT p.P186P LUSC 9 37541752 37541752 + Missense_Mutation SNP C C A TCGA-22-4595-01A-01D-1267-08 TCGA-22-4595-11A-01D-1267-08 g.chr9:37541752C>A c.14G>T c.(13-15)gGc>gTc p.G5V PAAD 9 37518160 37518160 + Missense_Mutation SNP C C T TCGA-US-A776-01A-13D-A33T-08 TCGA-US-A776-11A-11D-A33W-08 g.chr9:37518160C>T c.2476G>A c.(2476-2478)Ggc>Agc p.G826S PAAD 9 37537233 37537233 + Silent SNP G G C TCGA-HZ-A8P1-01A-11D-A377-08 TCGA-HZ-A8P1-10A-01D-A37A-08 g.chr9:37537233G>C c.1293C>G c.(1291-1293)ctC>ctG p.L431L PAAD 9 37537896 37537896 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:37537896G>A c.630C>T c.(628-630)aaC>aaT p.N210N PCPG 9 37518298 37518298 + Missense_Mutation SNP G G A TCGA-TT-A6YN-01A-12D-A35I-08 TCGA-TT-A6YN-10A-01D-A35G-08 g.chr9:37518298G>A c.2338C>T c.(2338-2340)Cgg>Tgg p.R780W PRAD 9 37516001 37516001 + Missense_Mutation SNP T T C TCGA-EJ-5515-01A-01D-1576-08 TCGA-EJ-5515-10A-01D-1577-08 g.chr9:37516001T>C c.2596A>G c.(2596-2598)Atc>Gtc p.I866V PRAD 9 37541447 37541447 + Nonsense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:37541447G>A c.319C>T c.(319-321)Cga>Tga p.R107* READ 9 37537831 37537831 + Missense_Mutation SNP T T C TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr9:37537831T>C c.695A>G c.(694-696)cAt>cGt p.H232R SARC 9 37537587 37537587 + Silent SNP G G A TCGA-QQ-A5VD-01A-21D-A32I-09 TCGA-QQ-A5VD-10A-01D-A32I-09 g.chr9:37537587G>A c.939C>T c.(937-939)atC>atT p.I313I SKCM 9 37512591 37512591 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr9:37512591C>T c.2824G>A c.(2824-2826)Gaa>Aaa p.E942K SKCM 9 37515909 37515909 + Silent SNP G G A TCGA-EE-A185-06A-11D-A196-08 TCGA-EE-A185-10A-01D-A198-08 g.chr9:37515909G>A c.2688C>T c.(2686-2688)ttC>ttT p.F896F SKCM 9 37515999 37515999 + Silent SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr9:37515999G>A c.2598C>T c.(2596-2598)atC>atT p.I866I SKCM 9 37518344 37518344 + Silent SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr9:37518344C>T c.2292G>A c.(2290-2292)caG>caA p.Q764Q SKCM 9 37521630 37521630 + Missense_Mutation SNP G G C TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr9:37521630G>C c.2136C>G c.(2134-2136)gaC>gaG p.D712E SKCM 9 37521635 37521635 + Missense_Mutation SNP C C T TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr9:37521635C>T c.2131G>A c.(2131-2133)Gag>Aag p.E711K SKCM 9 37521655 37521655 + Missense_Mutation SNP C C A TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr9:37521655C>A c.2111G>T c.(2110-2112)tGg>tTg p.W704L SKCM 9 37521707 37521707 + Nonsense_Mutation SNP G G A TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chr9:37521707G>A c.2059C>T c.(2059-2061)Cga>Tga p.R687* SKCM 9 37522954 37522954 + Nonsense_Mutation SNP G G A TCGA-EE-A29R-06A-11D-A197-08 TCGA-EE-A29R-10A-01D-A199-08 g.chr9:37522954G>A c.1798C>T c.(1798-1800)Cag>Tag p.Q600* SKCM 9 37537208 37537208 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr9:37537208C>T c.1318G>A c.(1318-1320)Ggg>Agg p.G440R SKCM 9 37537215 37537215 + Silent SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr9:37537215G>A c.1311C>T c.(1309-1311)ttC>ttT p.F437F SKCM 9 37537249 37537249 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr9:37537249G>A c.1277C>T c.(1276-1278)tCc>tTc p.S426F SKCM 9 37537332 37537332 + Silent SNP G G A TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr9:37537332G>A c.1194C>T c.(1192-1194)tcC>tcT p.S398S SKCM 9 37541212 37541212 + Missense_Mutation SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr9:37541212G>A c.554C>T c.(553-555)aCg>aTg p.T185M SKCM 9 37541213 37541213 + Missense_Mutation SNP T T A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr9:37541213T>A c.553A>T c.(553-555)Acg>Tcg p.T185S SKCM 9 37541368 37541368 + Missense_Mutation SNP C C T TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chr9:37541368C>T c.398G>A c.(397-399)cGa>cAa p.R133Q

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 9 37521616 37521616 single base substitution C T 3_prime_UTR_variant AML-US 9 37521616 37521616 single base substitution C T downstream_gene_variant AML-US 9 37521616 37521616 single base substitution C T missense_variant R242Q 725G>A AML-US 9 37521616 37521616 single base substitution C T missense_variant R717Q 2150G>A BLCA-US 9 37537289 37537289 single base substitution C G downstream_gene_variant BLCA-US 9 37537289 37537289 single base substitution C G exon_variant BLCA-US 9 37537289 37537289 single base substitution C G intron_variant BLCA-US 9 37537289 37537289 single base substitution C G missense_variant E413Q 1237G>C BLCA-US 9 37537289 37537289 single base substitution C G upstream_gene_variant BRCA-EU 9 37506447 37506447 single base substitution G A downstream_gene_variant BRCA-EU 9 37506739 37506739 single base substitution C G downstream_gene_variant BRCA-EU 9 37507040 37507040 single base substitution C G downstream_gene_variant BRCA-EU 9 37507828 37507828 single base substitution G A downstream_gene_variant BRCA-EU 9 37507867 37507867 single base substitution G T downstream_gene_variant BRCA-EU 9 37508034 37508034 single base substitution C T downstream_gene_variant BRCA-EU 9 37508150 37508150 single base substitution G A downstream_gene_variant BRCA-EU 9 37510053 37510053 single base substitution G A downstream_gene_variant BRCA-EU 9 37510122 37510122 single base substitution C T downstream_gene_variant BRCA-EU 9 37510689 37510689 single base substitution C T downstream_gene_variant BRCA-EU 9 37510998 37510998 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 37510998 37510998 single base substitution G A downstream_gene_variant BRCA-EU 9 37511144 37511144 single base substitution A G 3_prime_UTR_variant BRCA-EU 9 37511144 37511144 single base substitution A G downstream_gene_variant BRCA-EU 9 37511554 37511554 single base substitution G C 3_prime_UTR_variant BRCA-EU 9 37511554 37511554 single base substitution G C downstream_gene_variant BRCA-EU 9 37511812 37511812 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 37511812 37511812 single base substitution C T downstream_gene_variant BRCA-EU 9 37512568 37512568 single base substitution G A downstream_gene_variant BRCA-EU 9 37512568 37512568 single base substitution G A synonymous_variant R474R 1422C>T BRCA-EU 9 37512568 37512568 single base substitution G A synonymous_variant R949R 2847C>T BRCA-EU 9 37513410 37513411 deletion of <=200bp TG - downstream_gene_variant BRCA-EU 9 37513410 37513411 deletion of <=200bp TG - intron_variant BRCA-EU 9 37513556 37513556 deletion of <=200bp T - downstream_gene_variant BRCA-EU 9 37513556 37513556 deletion of <=200bp T - intron_variant BRCA-EU 9 37513712 37513712 single base substitution G A downstream_gene_variant BRCA-EU 9 37513712 37513712 single base substitution G A intron_variant BRCA-EU 9 37514978 37514978 single base substitution G A downstream_gene_variant BRCA-EU 9 37514978 37514978 single base substitution G A intron_variant BRCA-EU 9 37515240 37515240 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 37515240 37515240 single base substitution G A intron_variant BRCA-EU 9 37515809 37515809 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 37515809 37515809 single base substitution C T intron_variant BRCA-EU 9 37517578 37517578 single base substitution G A downstream_gene_variant BRCA-EU 9 37517578 37517578 single base substitution G A intron_variant BRCA-EU 9 37520019 37520019 single base substitution T C downstream_gene_variant BRCA-EU 9 37520019 37520019 single base substitution T C intron_variant BRCA-EU 9 37520926 37520929 deletion of <=200bp AAAT - downstream_gene_variant BRCA-EU 9 37520926 37520929 deletion of <=200bp AAAT - intron_variant BRCA-EU 9 37522229 37522229 single base substitution C T downstream_gene_variant BRCA-EU 9 37522229 37522229 single base substitution C T intron_variant BRCA-EU 9 37523979 37523979 single base substitution C A intron_variant BRCA-EU 9 37524758 37524758 single base substitution C T intron_variant BRCA-EU 9 37525365 37525365 single base substitution C T intron_variant BRCA-EU 9 37525365 37525365 single base substitution C T upstream_gene_variant BRCA-EU 9 37526150 37526150 single base substitution C T intron_variant BRCA-EU 9 37526150 37526150 single base substitution C T upstream_gene_variant BRCA-EU 9 37528247 37528247 single base substitution T A intron_variant BRCA-EU 9 37528247 37528247 single base substitution T A upstream_gene_variant BRCA-EU 9 37528733 37528733 single base substitution T C intron_variant BRCA-EU 9 37528733 37528733 single base substitution T C upstream_gene_variant BRCA-EU 9 37529559 37529559 single base substitution A C intron_variant BRCA-EU 9 37529559 37529559 single base substitution A C upstream_gene_variant BRCA-EU 9 37530378 37530378 single base substitution G A intron_variant BRCA-EU 9 37531697 37531697 single base substitution C T intron_variant BRCA-EU 9 37532238 37532238 single base substitution C T intron_variant BRCA-EU 9 37532927 37532927 single base substitution G C intron_variant BRCA-EU 9 37533784 37533784 single base substitution G A intron_variant BRCA-EU 9 37533796 37533796 single base substitution G A intron_variant BRCA-EU 9 37533906 37533906 insertion of <=200bp - A intron_variant BRCA-EU 9 37535177 37535177 single base substitution C G intron_variant BRCA-EU 9 37535279 37535279 single base substitution G C intron_variant BRCA-EU 9 37535711 37535711 single base substitution T C intron_variant BRCA-EU 9 37537695 37537695 single base substitution G C downstream_gene_variant BRCA-EU 9 37537695 37537695 single base substitution G C exon_variant BRCA-EU 9 37537695 37537695 single base substitution G C intron_variant BRCA-EU 9 37537695 37537695 single base substitution G C missense_variant I277M 831C>G BRCA-EU 9 37537695 37537695 single base substitution G C upstream_gene_variant BRCA-EU 9 37538769 37538769 single base substitution C G downstream_gene_variant BRCA-EU 9 37538769 37538769 single base substitution C G intron_variant BRCA-EU 9 37538769 37538769 single base substitution C G upstream_gene_variant BRCA-EU 9 37539139 37539139 single base substitution C G downstream_gene_variant BRCA-EU 9 37539139 37539139 single base substitution C G intron_variant BRCA-EU 9 37539139 37539139 single base substitution C G upstream_gene_variant BRCA-EU 9 37539474 37539474 single base substitution C T downstream_gene_variant BRCA-EU 9 37539474 37539474 single base substitution C T intron_variant BRCA-EU 9 37539474 37539474 single base substitution C T upstream_gene_variant BRCA-EU 9 37539981 37539981 single base substitution C T downstream_gene_variant BRCA-EU 9 37539981 37539981 single base substitution C T intron_variant BRCA-EU 9 37539981 37539981 single base substitution C T upstream_gene_variant BRCA-EU 9 37541073 37541073 single base substitution T C downstream_gene_variant BRCA-EU 9 37541073 37541073 single base substitution T C intron_variant BRCA-EU 9 37542151 37542151 single base substitution C T intron_variant BRCA-EU 9 37542732 37542732 single base substitution A G intron_variant BRCA-EU 9 37544192 37544192 single base substitution G A intron_variant BRCA-EU 9 37546082 37546082 single base substitution T G intron_variant BRCA-EU 9 37546835 37546835 single base substitution G A intron_variant BRCA-EU 9 37549341 37549341 single base substitution C G intron_variant BRCA-EU 9 37550585 37550585 single base substitution C G intron_variant BRCA-EU 9 37551446 37551446 deletion of <=200bp C - intron_variant BRCA-EU 9 37552086 37552086 single base substitution G C intron_variant BRCA-EU 9 37553315 37553315 single base substitution C T intron_variant BRCA-EU 9 37554526 37554526 single base substitution C T intron_variant BRCA-EU 9 37554736 37554736 single base substitution G C intron_variant BRCA-EU 9 37554820 37554820 single base substitution A T intron_variant BRCA-EU 9 37555038 37555038 single base substitution A G intron_variant BRCA-EU 9 37556000 37556000 single base substitution G A intron_variant BRCA-EU 9 37556038 37556038 single base substitution C A intron_variant BRCA-EU 9 37556174 37556174 single base substitution T C intron_variant BRCA-EU 9 37556183 37556183 single base substitution C G intron_variant BRCA-EU 9 37556285 37556285 single base substitution C G intron_variant BRCA-EU 9 37556657 37556657 single base substitution C T intron_variant BRCA-EU 9 37557968 37557968 single base substitution C G intron_variant BRCA-EU 9 37559332 37559332 single base substitution C T intron_variant BRCA-EU 9 37559338 37559338 single base substitution C G intron_variant BRCA-EU 9 37559834 37559834 single base substitution G A intron_variant BRCA-EU 9 37560055 37560055 single base substitution C A intron_variant BRCA-EU 9 37560404 37560404 single base substitution C T intron_variant BRCA-EU 9 37562027 37562027 single base substitution G A intron_variant BRCA-EU 9 37562520 37562520 single base substitution C T intron_variant BRCA-EU 9 37562896 37562896 single base substitution C T intron_variant BRCA-EU 9 37563622 37563622 single base substitution G A intron_variant BRCA-EU 9 37563917 37563917 single base substitution T A intron_variant BRCA-EU 9 37563968 37563968 single base substitution C T intron_variant BRCA-EU 9 37563978 37563978 single base substitution C G intron_variant BRCA-EU 9 37564049 37564049 single base substitution C G intron_variant BRCA-EU 9 37565143 37565143 single base substitution C G intron_variant BRCA-EU 9 37566184 37566184 single base substitution C G intron_variant BRCA-EU 9 37566206 37566206 single base substitution C T intron_variant BRCA-EU 9 37568438 37568438 single base substitution G A intron_variant BRCA-EU 9 37568894 37568894 deletion of <=200bp A - intron_variant BRCA-EU 9 37569148 37569148 single base substitution T G intron_variant BRCA-EU 9 37569336 37569336 single base substitution T C intron_variant BRCA-EU 9 37571855 37571855 single base substitution G C intron_variant BRCA-EU 9 37572371 37572371 single base substitution C T intron_variant BRCA-EU 9 37572569 37572569 single base substitution T C intron_variant BRCA-EU 9 37573507 37573507 single base substitution C A intron_variant BRCA-EU 9 37574515 37574515 single base substitution G C intron_variant BRCA-EU 9 37574777 37574779 deletion of <=200bp ATT - intron_variant BRCA-EU 9 37575705 37575705 deletion of <=200bp A - intron_variant BRCA-EU 9 37575927 37575927 single base substitution T C intron_variant BRCA-EU 9 37576238 37576238 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 9 37576238 37576238 single base substitution G A intron_variant BRCA-EU 9 37576521 37576521 single base substitution G C intron_variant BRCA-EU 9 37576521 37576521 single base substitution G C upstream_gene_variant BRCA-EU 9 37576757 37576757 single base substitution G A intron_variant BRCA-EU 9 37576757 37576757 single base substitution G A upstream_gene_variant BRCA-EU 9 37578217 37578217 single base substitution G T intron_variant BRCA-EU 9 37578217 37578217 single base substitution G T upstream_gene_variant BRCA-EU 9 37581056 37581056 single base substitution T C intron_variant BRCA-EU 9 37581056 37581056 single base substitution T C upstream_gene_variant BRCA-EU 9 37582296 37582296 single base substitution C T intron_variant BRCA-EU 9 37585024 37585024 single base substitution G C intron_variant BRCA-EU 9 37585727 37585727 single base substitution C G intron_variant BRCA-EU 9 37586389 37586389 single base substitution A G intron_variant BRCA-EU 9 37586707 37586707 single base substitution A G intron_variant BRCA-EU 9 37586929 37586931 deletion of <=200bp ATG - intron_variant BRCA-EU 9 37587093 37587093 single base substitution T G intron_variant BRCA-EU 9 37587523 37587523 single base substitution C G intron_variant BRCA-EU 9 37587969 37587969 single base substitution G T intron_variant BRCA-EU 9 37587978 37587978 single base substitution C T intron_variant BRCA-EU 9 37588098 37588098 single base substitution G T intron_variant BRCA-EU 9 37588512 37588512 single base substitution G C intron_variant BRCA-EU 9 37589102 37589102 single base substitution C T upstream_gene_variant BRCA-EU 9 37589512 37589512 single base substitution G C upstream_gene_variant BRCA-EU 9 37590812 37590812 single base substitution C G upstream_gene_variant BRCA-EU 9 37591247 37591247 deletion of <=200bp A - upstream_gene_variant BRCA-EU 9 37591491 37591491 single base substitution C T upstream_gene_variant BRCA-EU 9 37591496 37591496 single base substitution T G upstream_gene_variant BRCA-EU 9 37591868 37591868 single base substitution A G upstream_gene_variant BRCA-EU 9 37592443 37592443 single base substitution C G upstream_gene_variant BRCA-EU 9 37592606 37592606 single base substitution T C upstream_gene_variant BRCA-EU 9 37593404 37593404 single base substitution A T upstream_gene_variant BRCA-FR 9 37507828 37507828 single base substitution G A downstream_gene_variant BRCA-FR 9 37515809 37515809 single base substitution C T 3_prime_UTR_variant BRCA-FR 9 37515809 37515809 single base substitution C T intron_variant BRCA-FR 9 37515971 37515971 single base substitution T A 3_prime_UTR_variant BRCA-FR 9 37515971 37515971 single base substitution T A missense_variant I401F 1201A>T BRCA-FR 9 37515971 37515971 single base substitution T A missense_variant I876F 2626A>T BRCA-FR 9 37515972 37515972 single base substitution G T 3_prime_UTR_variant BRCA-FR 9 37515972 37515972 single base substitution G T synonymous_variant T400T 1200C>A BRCA-FR 9 37515972 37515972 single base substitution G T synonymous_variant T875T 2625C>A BRCA-FR 9 37525365 37525365 single base substitution C T intron_variant BRCA-FR 9 37525365 37525365 single base substitution C T upstream_gene_variant BRCA-FR 9 37535177 37535177 single base substitution C G intron_variant BRCA-FR 9 37537695 37537695 single base substitution G C downstream_gene_variant BRCA-FR 9 37537695 37537695 single base substitution G C exon_variant BRCA-FR 9 37537695 37537695 single base substitution G C intron_variant BRCA-FR 9 37537695 37537695 single base substitution G C missense_variant I277M 831C>G BRCA-FR 9 37537695 37537695 single base substitution G C upstream_gene_variant BRCA-FR 9 37547224 37547224 single base substitution T C intron_variant BRCA-FR 9 37556285 37556285 single base substitution C G intron_variant BRCA-FR 9 37569148 37569148 single base substitution T G intron_variant BRCA-FR 9 37572371 37572371 single base substitution C T intron_variant BRCA-FR 9 37581805 37581805 single base substitution G T intron_variant BRCA-FR 9 37590162 37590162 single base substitution G A upstream_gene_variant BRCA-UK 9 37507867 37507867 single base substitution G T downstream_gene_variant BRCA-UK 9 37513384 37513384 single base substitution A C downstream_gene_variant BRCA-UK 9 37513384 37513384 single base substitution A C intron_variant BRCA-UK 9 37532927 37532927 single base substitution G C intron_variant BRCA-UK 9 37554820 37554820 single base substitution A T intron_variant BRCA-UK 9 37557344 37557351 deletion of <=200bp CTTTACCC - intron_variant BRCA-UK 9 37565756 37565756 single base substitution G C intron_variant BRCA-UK 9 37571855 37571855 single base substitution G C intron_variant BRCA-UK 9 37577467 37577467 single base substitution A C intron_variant BRCA-UK 9 37577467 37577467 single base substitution A C upstream_gene_variant BRCA-UK 9 37587093 37587093 single base substitution T G intron_variant BRCA-UK 9 37587969 37587969 single base substitution G T intron_variant BRCA-UK 9 37591496 37591496 single base substitution T G upstream_gene_variant BRCA-UK 9 37593404 37593404 single base substitution A T upstream_gene_variant BRCA-US 9 37521593 37521593 single base substitution C G 3_prime_UTR_variant BRCA-US 9 37521593 37521593 single base substitution C G downstream_gene_variant BRCA-US 9 37521593 37521593 single base substitution C G missense_variant E250Q 748G>C BRCA-US 9 37521593 37521593 single base substitution C G missense_variant E725Q 2173G>C BRCA-US 9 37537587 37537587 single base substitution G A downstream_gene_variant BRCA-US 9 37537587 37537587 single base substitution G A exon_variant BRCA-US 9 37537587 37537587 single base substitution G A intron_variant BRCA-US 9 37537587 37537587 single base substitution G A synonymous_variant I313I 939C>T BRCA-US 9 37537587 37537587 single base substitution G A upstream_gene_variant BTCA-JP 9 37518097 37518097 single base substitution G A downstream_gene_variant BTCA-JP 9 37518097 37518097 single base substitution G A intron_variant BTCA-JP 9 37537963 37537963 single base substitution C T downstream_gene_variant BTCA-JP 9 37537963 37537963 single base substitution C T intron_variant BTCA-JP 9 37537963 37537963 single base substitution C T upstream_gene_variant CESC-US 9 37537857 37537857 single base substitution C T downstream_gene_variant CESC-US 9 37537857 37537857 single base substitution C T exon_variant CESC-US 9 37537857 37537857 single base substitution C T intron_variant CESC-US 9 37537857 37537857 single base substitution C T synonymous_variant V223V 669G>A CESC-US 9 37537857 37537857 single base substitution C T upstream_gene_variant CLLE-ES 9 37520522 37520522 single base substitution T C downstream_gene_variant CLLE-ES 9 37520522 37520522 single base substitution T C intron_variant CLLE-ES 9 37577319 37577319 single base substitution T A intron_variant CLLE-ES 9 37577319 37577319 single base substitution T A upstream_gene_variant COAD-US 9 37518163 37518163 single base substitution G A 3_prime_UTR_variant COAD-US 9 37518163 37518163 single base substitution G A downstream_gene_variant COAD-US 9 37518163 37518163 single base substitution G A missense_variant R350W 1048C>T COAD-US 9 37518163 37518163 single base substitution G A missense_variant R825W 2473C>T COAD-US 9 37518244 37518244 single base substitution C A 3_prime_UTR_variant COAD-US 9 37518244 37518244 single base substitution C A downstream_gene_variant COAD-US 9 37518244 37518244 single base substitution C A missense_variant G323C 967G>T COAD-US 9 37518244 37518244 single base substitution C A missense_variant G798C 2392G>T COAD-US 9 37518347 37518347 single base substitution G T 3_prime_UTR_variant COAD-US 9 37518347 37518347 single base substitution G T downstream_gene_variant COAD-US 9 37518347 37518347 single base substitution G T synonymous_variant A288A 864C>A COAD-US 9 37518347 37518347 single base substitution G T synonymous_variant A763A 2289C>A COAD-US 9 37518375 37518375 single base substitution G A 3_prime_UTR_variant COAD-US 9 37518375 37518375 single base substitution G A downstream_gene_variant COAD-US 9 37518375 37518375 single base substitution G A missense_variant A279V 836C>T COAD-US 9 37518375 37518375 single base substitution G A missense_variant A754V 2261C>T COAD-US 9 37521617 37521617 single base substitution G A 3_prime_UTR_variant COAD-US 9 37521617 37521617 single base substitution G A downstream_gene_variant COAD-US 9 37521617 37521617 single base substitution G A missense_variant R242W 724C>T COAD-US 9 37521617 37521617 single base substitution G A missense_variant R717W 2149C>T COAD-US 9 37521630 37521630 single base substitution G A 3_prime_UTR_variant COAD-US 9 37521630 37521630 single base substitution G A downstream_gene_variant COAD-US 9 37521630 37521630 single base substitution G A synonymous_variant D237D 711C>T COAD-US 9 37521630 37521630 single base substitution G A synonymous_variant D712D 2136C>T COAD-US 9 37522871 37522871 single base substitution C A 3_prime_UTR_variant COAD-US 9 37522871 37522871 single base substitution C A exon_variant COAD-US 9 37522871 37522871 single base substitution C A synonymous_variant V152V 456G>T COAD-US 9 37522871 37522871 single base substitution C A synonymous_variant V627V 1881G>T COAD-US 9 37522875 37522875 single base substitution C A 3_prime_UTR_variant COAD-US 9 37522875 37522875 single base substitution C A exon_variant COAD-US 9 37522875 37522875 single base substitution C A missense_variant G151V 452G>T COAD-US 9 37522875 37522875 single base substitution C A missense_variant G626V 1877G>T COAD-US 9 37532021 37532021 single base substitution C T exon_variant COAD-US 9 37532021 37532021 single base substitution C T missense_variant R10Q 29G>A COAD-US 9 37532021 37532021 single base substitution C T missense_variant R485Q 1454G>A COAD-US 9 37537557 37537557 single base substitution G A downstream_gene_variant COAD-US 9 37537557 37537557 single base substitution G A exon_variant COAD-US 9 37537557 37537557 single base substitution G A intron_variant COAD-US 9 37537557 37537557 single base substitution G A synonymous_variant A323A 969C>T COAD-US 9 37537557 37537557 single base substitution G A upstream_gene_variant COAD-US 9 37541290 37541290 single base substitution C T downstream_gene_variant COAD-US 9 37541290 37541290 single base substitution C T exon_variant COAD-US 9 37541290 37541290 single base substitution C T intron_variant COAD-US 9 37541290 37541290 single base substitution C T missense_variant G159E 476G>A COAD-US 9 37541446 37541446 single base substitution C T downstream_gene_variant COAD-US 9 37541446 37541446 single base substitution C T exon_variant COAD-US 9 37541446 37541446 single base substitution C T intron_variant COAD-US 9 37541446 37541446 single base substitution C T missense_variant R107Q 320G>A COAD-US 9 37592452 37592452 single base substitution G A upstream_gene_variant COCA-CN 9 37513743 37513743 single base substitution T C downstream_gene_variant COCA-CN 9 37513743 37513743 single base substitution T C intron_variant COCA-CN 9 37518252 37518252 single base substitution C T 3_prime_UTR_variant COCA-CN 9 37518252 37518252 single base substitution C T downstream_gene_variant COCA-CN 9 37518252 37518252 single base substitution C T missense_variant R320Q 959G>A COCA-CN 9 37518252 37518252 single base substitution C T missense_variant R795Q 2384G>A COCA-CN 9 37518441 37518441 single base substitution G A downstream_gene_variant COCA-CN 9 37518441 37518441 single base substitution G A splice_region_variant COCA-CN 9 37537196 37537196 single base substitution C T downstream_gene_variant COCA-CN 9 37537196 37537196 single base substitution C T exon_variant COCA-CN 9 37537196 37537196 single base substitution C T intron_variant COCA-CN 9 37537196 37537196 single base substitution C T missense_variant V444I 1330G>A COCA-CN 9 37537196 37537196 single base substitution C T upstream_gene_variant COCA-CN 9 37537437 37537437 single base substitution C T downstream_gene_variant COCA-CN 9 37537437 37537437 single base substitution C T exon_variant COCA-CN 9 37537437 37537437 single base substitution C T intron_variant COCA-CN 9 37537437 37537437 single base substitution C T synonymous_variant E363E 1089G>A COCA-CN 9 37537437 37537437 single base substitution C T upstream_gene_variant COCA-CN 9 37537965 37537965 single base substitution G A downstream_gene_variant COCA-CN 9 37537965 37537965 single base substitution G A intron_variant COCA-CN 9 37537965 37537965 single base substitution G A upstream_gene_variant COCA-CN 9 37541368 37541368 single base substitution C T downstream_gene_variant COCA-CN 9 37541368 37541368 single base substitution C T exon_variant COCA-CN 9 37541368 37541368 single base substitution C T intron_variant COCA-CN 9 37541368 37541368 single base substitution C T missense_variant R133Q 398G>A COCA-CN 9 37541488 37541488 single base substitution T G downstream_gene_variant COCA-CN 9 37541488 37541488 single base substitution T G exon_variant COCA-CN 9 37541488 37541488 single base substitution T G intron_variant COCA-CN 9 37541488 37541488 single base substitution T G missense_variant E93A 278A>C COCA-CN 9 37550158 37550158 single base substitution C T intron_variant COCA-CN 9 37566456 37566456 single base substitution G A intron_variant COCA-CN 9 37569410 37569410 single base substitution T A intron_variant COCA-CN 9 37592327 37592327 single base substitution C T upstream_gene_variant EOPC-DE 9 37513112 37513112 single base substitution G C downstream_gene_variant EOPC-DE 9 37513112 37513112 single base substitution G C intron_variant EOPC-DE 9 37556832 37556832 single base substitution G A intron_variant EOPC-DE 9 37579917 37579917 single base substitution C T intron_variant EOPC-DE 9 37579917 37579917 single base substitution C T upstream_gene_variant ESAD-UK 9 37506235 37506235 single base substitution C T downstream_gene_variant ESAD-UK 9 37512260 37512260 single base substitution A C 3_prime_UTR_variant ESAD-UK 9 37512260 37512260 single base substitution A C downstream_gene_variant ESAD-UK 9 37512435 37512435 single base substitution C T 3_prime_UTR_variant ESAD-UK 9 37512435 37512435 single base substitution C T downstream_gene_variant ESAD-UK 9 37512710 37512710 single base substitution G A downstream_gene_variant ESAD-UK 9 37512710 37512710 single base substitution G A missense_variant T427M 1280C>T ESAD-UK 9 37512710 37512710 single base substitution G A missense_variant T902M 2705C>T ESAD-UK 9 37513733 37513733 single base substitution C T downstream_gene_variant ESAD-UK 9 37513733 37513733 single base substitution C T intron_variant ESAD-UK 9 37514654 37514654 single base substitution G A downstream_gene_variant ESAD-UK 9 37514654 37514654 single base substitution G A intron_variant ESAD-UK 9 37518527 37518527 single base substitution G A downstream_gene_variant ESAD-UK 9 37518527 37518527 single base substitution G A intron_variant ESAD-UK 9 37520055 37520055 single base substitution C A downstream_gene_variant ESAD-UK 9 37520055 37520055 single base substitution C A intron_variant ESAD-UK 9 37523234 37523234 single base substitution G C intron_variant ESAD-UK 9 37523380 37523380 single base substitution C T intron_variant ESAD-UK 9 37527429 37527429 single base substitution C T intron_variant ESAD-UK 9 37527429 37527429 single base substitution C T upstream_gene_variant ESAD-UK 9 37528184 37528184 single base substitution G A intron_variant ESAD-UK 9 37528184 37528184 single base substitution G A upstream_gene_variant ESAD-UK 9 37530078 37530078 single base substitution T C intron_variant ESAD-UK 9 37530078 37530078 single base substitution T C upstream_gene_variant ESAD-UK 9 37531334 37531334 single base substitution C T intron_variant ESAD-UK 9 37531742 37531742 single base substitution C T intron_variant ESAD-UK 9 37536381 37536381 single base substitution T G intron_variant ESAD-UK 9 37536381 37536381 single base substitution T G upstream_gene_variant ESAD-UK 9 37537578 37537578 single base substitution G T downstream_gene_variant ESAD-UK 9 37537578 37537578 single base substitution G T exon_variant ESAD-UK 9 37537578 37537578 single base substitution G T intron_variant ESAD-UK 9 37537578 37537578 single base substitution G T missense_variant S316R 948C>A ESAD-UK 9 37537578 37537578 single base substitution G T upstream_gene_variant ESAD-UK 9 37539689 37539689 single base substitution G C downstream_gene_variant ESAD-UK 9 37539689 37539689 single base substitution G C intron_variant ESAD-UK 9 37539689 37539689 single base substitution G C upstream_gene_variant ESAD-UK 9 37540874 37540874 single base substitution C T downstream_gene_variant ESAD-UK 9 37540874 37540874 single base substitution C T intron_variant ESAD-UK 9 37540874 37540874 single base substitution C T upstream_gene_variant ESAD-UK 9 37542348 37542348 single base substitution T G intron_variant ESAD-UK 9 37542548 37542548 single base substitution G A intron_variant ESAD-UK 9 37544641 37544641 single base substitution G A intron_variant ESAD-UK 9 37547563 37547563 single base substitution G A intron_variant ESAD-UK 9 37547788 37547788 single base substitution A G intron_variant ESAD-UK 9 37549461 37549461 single base substitution C T intron_variant ESAD-UK 9 37551735 37551735 single base substitution T G intron_variant ESAD-UK 9 37552356 37552356 single base substitution G A intron_variant ESAD-UK 9 37552489 37552489 single base substitution G C intron_variant ESAD-UK 9 37555698 37555698 insertion of <=200bp - T intron_variant ESAD-UK 9 37556119 37556119 insertion of <=200bp - A intron_variant ESAD-UK 9 37558006 37558006 single base substitution C T intron_variant ESAD-UK 9 37558955 37558955 single base substitution G A intron_variant ESAD-UK 9 37559287 37559287 single base substitution T C intron_variant ESAD-UK 9 37561903 37561903 single base substitution C T intron_variant ESAD-UK 9 37566820 37566820 single base substitution G A intron_variant ESAD-UK 9 37569035 37569035 single base substitution A C intron_variant ESAD-UK 9 37569817 37569817 single base substitution G C intron_variant ESAD-UK 9 37570623 37570623 deletion of <=200bp A - intron_variant ESAD-UK 9 37570948 37570948 single base substitution G A intron_variant ESAD-UK 9 37574338 37574338 single base substitution C T intron_variant ESAD-UK 9 37577641 37577641 single base substitution A G intron_variant ESAD-UK 9 37577641 37577641 single base substitution A G upstream_gene_variant ESAD-UK 9 37581348 37581348 single base substitution T G intron_variant ESAD-UK 9 37581359 37581359 single base substitution T C intron_variant ESAD-UK 9 37585073 37585073 single base substitution A C intron_variant ESAD-UK 9 37586692 37586695 deletion of <=200bp ATAA - intron_variant ESAD-UK 9 37589913 37589925 deletion of <=200bp GAAAAAAATCCAT - upstream_gene_variant ESCA-CN 9 37537892 37537892 single base substitution G T downstream_gene_variant ESCA-CN 9 37537892 37537892 single base substitution G T exon_variant ESCA-CN 9 37537892 37537892 single base substitution G T intron_variant ESCA-CN 9 37537892 37537892 single base substitution G T missense_variant H212N 634C>A ESCA-CN 9 37537892 37537892 single base substitution G T upstream_gene_variant GBM-US 9 37515999 37515999 single base substitution G T 3_prime_UTR_variant GBM-US 9 37515999 37515999 single base substitution G T synonymous_variant I391I 1173C>A GBM-US 9 37515999 37515999 single base substitution G T synonymous_variant I866I 2598C>A GBM-US 9 37522884 37522884 single base substitution T C 3_prime_UTR_variant GBM-US 9 37522884 37522884 single base substitution T C exon_variant GBM-US 9 37522884 37522884 single base substitution T C missense_variant Y148C 443A>G GBM-US 9 37522884 37522884 single base substitution T C missense_variant Y623C 1868A>G KIRC-US 9 37537374 37537374 single base substitution T A downstream_gene_variant KIRC-US 9 37537374 37537374 single base substitution T A exon_variant KIRC-US 9 37537374 37537374 single base substitution T A intron_variant KIRC-US 9 37537374 37537374 single base substitution T A synonymous_variant V384V 1152A>T KIRC-US 9 37537374 37537374 single base substitution T A upstream_gene_variant KIRP-US 9 37537307 37537307 single base substitution G T downstream_gene_variant KIRP-US 9 37537307 37537307 single base substitution G T exon_variant KIRP-US 9 37537307 37537307 single base substitution G T intron_variant KIRP-US 9 37537307 37537307 single base substitution G T missense_variant L407M 1219C>A KIRP-US 9 37537307 37537307 single base substitution G T upstream_gene_variant LAML-KR 9 37512734 37512734 single base substitution G A downstream_gene_variant LAML-KR 9 37512734 37512734 single base substitution G A intron_variant LAML-KR 9 37515711 37515711 single base substitution T C 3_prime_UTR_variant LAML-KR 9 37515711 37515711 single base substitution T C intron_variant LAML-KR 9 37533638 37533638 single base substitution C T intron_variant LICA-FR 9 37512582 37512582 single base substitution A G downstream_gene_variant LICA-FR 9 37512582 37512582 single base substitution A G missense_variant Y470H 1408T>C LICA-FR 9 37512582 37512582 single base substitution A G missense_variant Y945H 2833T>C LICA-FR 9 37531435 37531435 single base substitution C T intron_variant LICA-FR 9 37541628 37541628 single base substitution C T exon_variant LICA-FR 9 37541628 37541628 single base substitution C T intron_variant LICA-FR 9 37541628 37541628 single base substitution C T synonymous_variant R46R 138G>A LICA-FR 9 37541699 37541699 single base substitution G C exon_variant LICA-FR 9 37541699 37541699 single base substitution G C intron_variant LICA-FR 9 37541699 37541699 single base substitution G C missense_variant L23V 67C>G LICA-FR 9 37567308 37567308 insertion of <=200bp - T intron_variant LICA-FR 9 37582881 37582881 single base substitution A G intron_variant LIHC-US 9 37518350 37518350 single base substitution C T 3_prime_UTR_variant LIHC-US 9 37518350 37518350 single base substitution C T downstream_gene_variant LIHC-US 9 37518350 37518350 single base substitution C T synonymous_variant V287V 861G>A LIHC-US 9 37518350 37518350 single base substitution C T synonymous_variant V762V 2286G>A LIHC-US 9 37541574 37541574 single base substitution T C exon_variant LIHC-US 9 37541574 37541574 single base substitution T C intron_variant LIHC-US 9 37541574 37541574 single base substitution T C synonymous_variant P64P 192A>G LINC-JP 9 37509373 37509373 single base substitution T G downstream_gene_variant LINC-JP 9 37512633 37512633 single base substitution G A downstream_gene_variant LINC-JP 9 37512633 37512633 single base substitution G A stop_gained Q453* 1357C>T LINC-JP 9 37512633 37512633 single base substitution G A stop_gained Q928* 2782C>T LINC-JP 9 37518341 37518341 single base substitution G A 3_prime_UTR_variant LINC-JP 9 37518341 37518341 single base substitution G A downstream_gene_variant LINC-JP 9 37518341 37518341 single base substitution G A synonymous_variant S290S 870C>T LINC-JP 9 37518341 37518341 single base substitution G A synonymous_variant S765S 2295C>T LINC-JP 9 37518465 37518465 single base substitution G T downstream_gene_variant LINC-JP 9 37518465 37518465 single base substitution G T intron_variant LINC-JP 9 37521502 37521502 single base substitution G A downstream_gene_variant LINC-JP 9 37521502 37521502 single base substitution G A intron_variant LINC-JP 9 37521871 37521871 single base substitution A G downstream_gene_variant LINC-JP 9 37521871 37521871 single base substitution A G exon_variant LINC-JP 9 37521871 37521871 single base substitution A G intron_variant LINC-JP 9 37529158 37529158 single base substitution C T exon_variant LINC-JP 9 37529158 37529158 single base substitution C T missense_variant G557S 1669G>A LINC-JP 9 37529158 37529158 single base substitution C T missense_variant G82S 244G>A LINC-JP 9 37529158 37529158 single base substitution C T upstream_gene_variant LINC-JP 9 37535118 37535118 single base substitution G A intron_variant LINC-JP 9 37581095 37581095 single base substitution C G intron_variant LINC-JP 9 37581095 37581095 single base substitution C G upstream_gene_variant LINC-JP 9 37588525 37588525 single base substitution T C intron_variant LIRI-JP 9 37508101 37508101 single base substitution A C downstream_gene_variant LIRI-JP 9 37508105 37508105 single base substitution A G downstream_gene_variant LIRI-JP 9 37509273 37509273 single base substitution A G downstream_gene_variant LIRI-JP 9 37509412 37509412 single base substitution A G downstream_gene_variant LIRI-JP 9 37510380 37510380 single base substitution T A downstream_gene_variant LIRI-JP 9 37510383 37510383 single base substitution T A downstream_gene_variant LIRI-JP 9 37512436 37512436 single base substitution C A 3_prime_UTR_variant LIRI-JP 9 37512436 37512436 single base substitution C A downstream_gene_variant LIRI-JP 9 37515575 37515575 single base substitution T C 3_prime_UTR_variant LIRI-JP 9 37515575 37515575 single base substitution T C intron_variant LIRI-JP 9 37519186 37519186 single base substitution G A downstream_gene_variant LIRI-JP 9 37519186 37519186 single base substitution G A intron_variant LIRI-JP 9 37523899 37523899 single base substitution A G intron_variant LIRI-JP 9 37530587 37530587 single base substitution C T intron_variant LIRI-JP 9 37533087 37533087 single base substitution T C intron_variant LIRI-JP 9 37533972 37533972 single base substitution G C intron_variant LIRI-JP 9 37534527 37534527 single base substitution T A intron_variant LIRI-JP 9 37535400 37535400 single base substitution C T intron_variant LIRI-JP 9 37537147 37537147 single base substitution C T downstream_gene_variant LIRI-JP 9 37537147 37537147 single base substitution C T exon_variant LIRI-JP 9 37537147 37537147 single base substitution C T intron_variant LIRI-JP 9 37537147 37537147 single base substitution C T missense_variant R460Q 1379G>A LIRI-JP 9 37537147 37537147 single base substitution C T upstream_gene_variant LIRI-JP 9 37542121 37542121 single base substitution C T intron_variant LIRI-JP 9 37544354 37544354 single base substitution T C intron_variant LIRI-JP 9 37548923 37548923 single base substitution T C intron_variant LIRI-JP 9 37549020 37549020 single base substitution T C intron_variant LIRI-JP 9 37550032 37550032 single base substitution C T intron_variant LIRI-JP 9 37551200 37551200 single base substitution C A intron_variant LIRI-JP 9 37553280 37553280 single base substitution C T intron_variant LIRI-JP 9 37554579 37554579 single base substitution G A intron_variant LIRI-JP 9 37565239 37565239 single base substitution C T intron_variant LIRI-JP 9 37569589 37569589 single base substitution C A intron_variant LIRI-JP 9 37569615 37569615 single base substitution A G intron_variant LIRI-JP 9 37572472 37572472 single base substitution T C intron_variant LIRI-JP 9 37572597 37572597 single base substitution T C intron_variant LIRI-JP 9 37572967 37572967 single base substitution G T intron_variant LIRI-JP 9 37575467 37575467 single base substitution G A intron_variant LIRI-JP 9 37577465 37577465 single base substitution A C intron_variant LIRI-JP 9 37577465 37577465 single base substitution A C upstream_gene_variant LIRI-JP 9 37577492 37577492 single base substitution A G intron_variant LIRI-JP 9 37577492 37577492 single base substitution A G upstream_gene_variant LIRI-JP 9 37579415 37579415 single base substitution T C intron_variant LIRI-JP 9 37579415 37579415 single base substitution T C upstream_gene_variant LIRI-JP 9 37579576 37579576 single base substitution G A intron_variant LIRI-JP 9 37579576 37579576 single base substitution G A upstream_gene_variant LIRI-JP 9 37584236 37584236 single base substitution C A intron_variant LIRI-JP 9 37591209 37591209 single base substitution T C upstream_gene_variant LIRI-JP 9 37592783 37592783 single base substitution A C upstream_gene_variant LIRI-JP 9 37593404 37593404 single base substitution A T upstream_gene_variant LUSC-KR 9 37506701 37506701 single base substitution C A downstream_gene_variant LUSC-KR 9 37509264 37509264 single base substitution C G downstream_gene_variant LUSC-KR 9 37514090 37514090 single base substitution C G downstream_gene_variant LUSC-KR 9 37514090 37514090 single base substitution C G intron_variant LUSC-KR 9 37518817 37518817 single base substitution C G downstream_gene_variant LUSC-KR 9 37518817 37518817 single base substitution C G intron_variant LUSC-KR 9 37526397 37526397 single base substitution A G intron_variant LUSC-KR 9 37526397 37526397 single base substitution A G upstream_gene_variant LUSC-KR 9 37529857 37529857 single base substitution G T intron_variant LUSC-KR 9 37529857 37529857 single base substitution G T upstream_gene_variant LUSC-KR 9 37530484 37530484 single base substitution A G intron_variant LUSC-KR 9 37533327 37533327 single base substitution G A intron_variant LUSC-KR 9 37533469 37533469 single base substitution G A intron_variant LUSC-KR 9 37535650 37535650 single base substitution C A intron_variant LUSC-KR 9 37541033 37541033 single base substitution C T downstream_gene_variant LUSC-KR 9 37541033 37541033 single base substitution C T intron_variant LUSC-KR 9 37541033 37541033 single base substitution C T upstream_gene_variant LUSC-KR 9 37541309 37541309 single base substitution C G downstream_gene_variant LUSC-KR 9 37541309 37541309 single base substitution C G exon_variant LUSC-KR 9 37541309 37541309 single base substitution C G intron_variant LUSC-KR 9 37541309 37541309 single base substitution C G missense_variant V153L 457G>C LUSC-KR 9 37541519 37541519 single base substitution T G downstream_gene_variant LUSC-KR 9 37541519 37541519 single base substitution T G exon_variant LUSC-KR 9 37541519 37541519 single base substitution T G intron_variant LUSC-KR 9 37541519 37541519 single base substitution T G missense_variant K83Q 247A>C LUSC-KR 9 37543922 37543922 single base substitution T C intron_variant LUSC-KR 9 37547421 37547421 single base substitution T C intron_variant LUSC-KR 9 37548639 37548639 single base substitution C G intron_variant LUSC-KR 9 37560919 37560919 single base substitution C A intron_variant LUSC-KR 9 37561946 37561946 single base substitution G C intron_variant LUSC-KR 9 37564827 37564827 single base substitution T C intron_variant LUSC-KR 9 37566083 37566083 single base substitution C A intron_variant LUSC-KR 9 37568864 37568864 single base substitution A G intron_variant LUSC-KR 9 37571538 37571538 single base substitution T A intron_variant LUSC-KR 9 37572504 37572504 single base substitution C G intron_variant LUSC-KR 9 37573180 37573180 single base substitution G C intron_variant LUSC-KR 9 37573519 37573519 single base substitution T C intron_variant LUSC-KR 9 37574104 37574104 single base substitution A G intron_variant LUSC-KR 9 37579880 37579880 single base substitution G T intron_variant LUSC-KR 9 37579880 37579880 single base substitution G T upstream_gene_variant LUSC-KR 9 37587242 37587242 single base substitution C T intron_variant LUSC-KR 9 37592792 37592792 single base substitution G C upstream_gene_variant LUSC-KR 9 37593529 37593529 single base substitution G T upstream_gene_variant LUSC-US 9 37516034 37516034 single base substitution G A 3_prime_UTR_variant LUSC-US 9 37516034 37516034 single base substitution G A missense_variant R380W 1138C>T LUSC-US 9 37516034 37516034 single base substitution G A missense_variant R855W 2563C>T LUSC-US 9 37537356 37537356 single base substitution C T downstream_gene_variant LUSC-US 9 37537356 37537356 single base substitution C T exon_variant LUSC-US 9 37537356 37537356 single base substitution C T intron_variant LUSC-US 9 37537356 37537356 single base substitution C T synonymous_variant L390L 1170G>A LUSC-US 9 37537356 37537356 single base substitution C T upstream_gene_variant LUSC-US 9 37541208 37541208 single base substitution T A downstream_gene_variant LUSC-US 9 37541208 37541208 single base substitution T A exon_variant LUSC-US 9 37541208 37541208 single base substitution T A intron_variant LUSC-US 9 37541208 37541208 single base substitution T A synonymous_variant P186P 558A>T LUSC-US 9 37541752 37541752 single base substitution C A exon_variant LUSC-US 9 37541752 37541752 single base substitution C A intron_variant LUSC-US 9 37541752 37541752 single base substitution C A missense_variant G5V 14G>T MALY-DE 9 37508717 37508717 single base substitution G A downstream_gene_variant MALY-DE 9 37511995 37511995 single base substitution C T 3_prime_UTR_variant MALY-DE 9 37511995 37511995 single base substitution C T downstream_gene_variant MALY-DE 9 37513555 37513555 single base substitution G T downstream_gene_variant MALY-DE 9 37513555 37513555 single base substitution G T intron_variant MALY-DE 9 37526006 37526007 deletion of <=200bp TG - intron_variant MALY-DE 9 37526006 37526007 deletion of <=200bp TG - upstream_gene_variant MALY-DE 9 37536022 37536022 single base substitution T C exon_variant MALY-DE 9 37536022 37536022 single base substitution T C intron_variant MALY-DE 9 37537132 37537132 single base substitution G A downstream_gene_variant MALY-DE 9 37537132 37537132 single base substitution G A exon_variant MALY-DE 9 37537132 37537132 single base substitution G A intron_variant MALY-DE 9 37537132 37537132 single base substitution G A missense_variant A465V 1394C>T MALY-DE 9 37537132 37537132 single base substitution G A upstream_gene_variant MALY-DE 9 37538566 37538566 single base substitution G A downstream_gene_variant MALY-DE 9 37538566 37538566 single base substitution G A intron_variant MALY-DE 9 37538566 37538566 single base substitution G A upstream_gene_variant MALY-DE 9 37570623 37570623 single base substitution A G intron_variant MALY-DE 9 37571089 37571089 single base substitution A G intron_variant MALY-DE 9 37572745 37572745 single base substitution C A intron_variant MALY-DE 9 37575711 37575711 single base substitution C A intron_variant MALY-DE 9 37576292 37576292 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MALY-DE 9 37576292 37576292 single base substitution G A intron_variant MALY-DE 9 37576292 37576292 single base substitution G A upstream_gene_variant MALY-DE 9 37576322 37576322 single base substitution C T 5_prime_UTR_variant MALY-DE 9 37576322 37576322 single base substitution C T intron_variant MALY-DE 9 37576322 37576322 single base substitution C T upstream_gene_variant MALY-DE 9 37576462 37576462 single base substitution G A intron_variant MALY-DE 9 37576462 37576462 single base substitution G A upstream_gene_variant MALY-DE 9 37581169 37581169 single base substitution C T intron_variant MALY-DE 9 37581169 37581169 single base substitution C T upstream_gene_variant MALY-DE 9 37590409 37590409 single base substitution G T upstream_gene_variant MALY-DE 9 37591856 37591856 single base substitution T G upstream_gene_variant MALY-DE 9 37592455 37592455 single base substitution G T upstream_gene_variant MALY-DE 9 37593084 37593084 single base substitution T C upstream_gene_variant MELA-AU 9 37507465 37507465 single base substitution G A downstream_gene_variant MELA-AU 9 37507727 37507727 single base substitution G A downstream_gene_variant MELA-AU 9 37509937 37509937 single base substitution A C downstream_gene_variant MELA-AU 9 37511746 37511746 single base substitution G A 3_prime_UTR_variant MELA-AU 9 37511746 37511746 single base substitution G A downstream_gene_variant MELA-AU 9 37512114 37512114 single base substitution G A 3_prime_UTR_variant MELA-AU 9 37512114 37512114 single base substitution G A downstream_gene_variant MELA-AU 9 37513631 37513631 single base substitution G A downstream_gene_variant MELA-AU 9 37513631 37513631 single base substitution G A intron_variant MELA-AU 9 37514372 37514372 single base substitution G A downstream_gene_variant MELA-AU 9 37514372 37514372 single base substitution G A intron_variant MELA-AU 9 37514377 37514377 single base substitution G A downstream_gene_variant MELA-AU 9 37514377 37514377 single base substitution G A intron_variant MELA-AU 9 37515066 37515066 single base substitution G A 3_prime_UTR_variant MELA-AU 9 37515066 37515066 single base substitution G A intron_variant MELA-AU 9 37515454 37515454 single base substitution G A 3_prime_UTR_variant MELA-AU 9 37515454 37515454 single base substitution G A intron_variant MELA-AU 9 37515778 37515778 single base substitution G T 3_prime_UTR_variant MELA-AU 9 37515778 37515778 single base substitution G T intron_variant MELA-AU 9 37515909 37515909 single base substitution G A 3_prime_UTR_variant MELA-AU 9 37515909 37515909 single base substitution G A synonymous_variant F421F 1263C>T MELA-AU 9 37515909 37515909 single base substitution G A synonymous_variant F896F 2688C>T MELA-AU 9 37516910 37516910 single base substitution A C downstream_gene_variant MELA-AU 9 37516910 37516910 single base substitution A C intron_variant MELA-AU 9 37517518 37517518 single base substitution G A downstream_gene_variant MELA-AU 9 37517518 37517518 single base substitution G A intron_variant MELA-AU 9 37517948 37517949 multiple base substitution (>=2bp and <=200bp) CC GT downstream_gene_variant MELA-AU 9 37517948 37517949 multiple base substitution (>=2bp and <=200bp) CC GT intron_variant MELA-AU 9 37517978 37517978 single base substitution C T downstream_gene_variant MELA-AU 9 37517978 37517978 single base substitution C T intron_variant MELA-AU 9 37518536 37518536 single base substitution G A downstream_gene_variant MELA-AU 9 37518536 37518536 single base substitution G A intron_variant MELA-AU 9 37519005 37519005 single base substitution C T downstream_gene_variant MELA-AU 9 37519005 37519005 single base substitution C T intron_variant MELA-AU 9 37519218 37519218 single base substitution C T downstream_gene_variant MELA-AU 9 37519218 37519218 single base substitution C T intron_variant MELA-AU 9 37519263 37519263 single base substitution G A downstream_gene_variant MELA-AU 9 37519263 37519263 single base substitution G A intron_variant MELA-AU 9 37519336 37519336 single base substitution G A downstream_gene_variant MELA-AU 9 37519336 37519336 single base substitution G A intron_variant MELA-AU 9 37519715 37519715 single base substitution A G downstream_gene_variant MELA-AU 9 37519715 37519715 single base substitution A G intron_variant MELA-AU 9 37520913 37520913 single base substitution G A downstream_gene_variant MELA-AU 9 37520913 37520913 single base substitution G A intron_variant MELA-AU 9 37521013 37521013 single base substitution T C downstream_gene_variant MELA-AU 9 37521013 37521013 single base substitution T C intron_variant MELA-AU 9 37522550 37522550 single base substitution C T intron_variant MELA-AU 9 37522594 37522594 single base substitution G A intron_variant MELA-AU 9 37522625 37522625 single base substitution G A intron_variant MELA-AU 9 37523140 37523140 single base substitution G A intron_variant MELA-AU 9 37523547 37523547 single base substitution C T intron_variant MELA-AU 9 37523685 37523685 single base substitution G A intron_variant MELA-AU 9 37523726 37523726 single base substitution C T intron_variant MELA-AU 9 37524556 37524556 single base substitution G A intron_variant MELA-AU 9 37524790 37524790 single base substitution C T intron_variant MELA-AU 9 37525088 37525088 single base substitution C T intron_variant MELA-AU 9 37526823 37526823 single base substitution T C intron_variant MELA-AU 9 37526823 37526823 single base substitution T C upstream_gene_variant MELA-AU 9 37527010 37527010 single base substitution G A intron_variant MELA-AU 9 37527010 37527010 single base substitution G A upstream_gene_variant MELA-AU 9 37527097 37527097 single base substitution C T intron_variant MELA-AU 9 37527097 37527097 single base substitution C T upstream_gene_variant MELA-AU 9 37527143 37527143 single base substitution G A intron_variant MELA-AU 9 37527143 37527143 single base substitution G A upstream_gene_variant MELA-AU 9 37527454 37527454 single base substitution A C intron_variant MELA-AU 9 37527454 37527454 single base substitution A C upstream_gene_variant MELA-AU 9 37527958 37527958 single base substitution G A intron_variant MELA-AU 9 37527958 37527958 single base substitution G A upstream_gene_variant MELA-AU 9 37528029 37528029 single base substitution A T intron_variant MELA-AU 9 37528029 37528029 single base substitution A T upstream_gene_variant MELA-AU 9 37529064 37529064 single base substitution G A intron_variant MELA-AU 9 37529064 37529064 single base substitution G A upstream_gene_variant MELA-AU 9 37529130 37529130 single base substitution G A exon_variant MELA-AU 9 37529130 37529130 single base substitution G A missense_variant P566L 1697C>T MELA-AU 9 37529130 37529130 single base substitution G A missense_variant P91L 272C>T MELA-AU 9 37529130 37529130 single base substitution G A upstream_gene_variant MELA-AU 9 37529449 37529449 single base substitution G A intron_variant MELA-AU 9 37529449 37529449 single base substitution G A upstream_gene_variant MELA-AU 9 37529681 37529681 single base substitution G A intron_variant MELA-AU 9 37529681 37529681 single base substitution G A upstream_gene_variant MELA-AU 9 37529697 37529697 single base substitution G A intron_variant MELA-AU 9 37529697 37529697 single base substitution G A upstream_gene_variant MELA-AU 9 37529863 37529863 single base substitution G A intron_variant MELA-AU 9 37529863 37529863 single base substitution G A upstream_gene_variant MELA-AU 9 37530006 37530006 single base substitution G A intron_variant MELA-AU 9 37530006 37530006 single base substitution G A upstream_gene_variant MELA-AU 9 37530261 37530261 single base substitution C T intron_variant MELA-AU 9 37530309 37530309 single base substitution G A intron_variant MELA-AU 9 37530379 37530379 single base substitution G A intron_variant MELA-AU 9 37530592 37530592 single base substitution G A intron_variant MELA-AU 9 37530897 37530897 single base substitution C T intron_variant MELA-AU 9 37531476 37531476 single base substitution G A intron_variant MELA-AU 9 37533732 37533732 single base substitution G A intron_variant MELA-AU 9 37534308 37534308 single base substitution G A intron_variant MELA-AU 9 37534362 37534362 single base substitution G A intron_variant MELA-AU 9 37534668 37534668 single base substitution G A intron_variant MELA-AU 9 37534739 37534739 single base substitution G A intron_variant MELA-AU 9 37534999 37534999 single base substitution G A intron_variant MELA-AU 9 37535352 37535352 single base substitution A T intron_variant MELA-AU 9 37535953 37535953 single base substitution C T intron_variant MELA-AU 9 37536470 37536470 single base substitution A T intron_variant MELA-AU 9 37536470 37536470 single base substitution A T upstream_gene_variant MELA-AU 9 37536807 37536807 single base substitution G A downstream_gene_variant MELA-AU 9 37536807 37536807 single base substitution G A intron_variant MELA-AU 9 37536807 37536807 single base substitution G A upstream_gene_variant MELA-AU 9 37537050 37537050 single base substitution A C downstream_gene_variant MELA-AU 9 37537050 37537050 single base substitution A C intron_variant MELA-AU 9 37537050 37537050 single base substitution A C upstream_gene_variant MELA-AU 9 37537146 37537146 single base substitution C T downstream_gene_variant MELA-AU 9 37537146 37537146 single base substitution C T exon_variant MELA-AU 9 37537146 37537146 single base substitution C T intron_variant MELA-AU 9 37537146 37537146 single base substitution C T synonymous_variant R460R 1380G>A MELA-AU 9 37537146 37537146 single base substitution C T upstream_gene_variant MELA-AU 9 37537191 37537191 single base substitution G A downstream_gene_variant MELA-AU 9 37537191 37537191 single base substitution G A exon_variant MELA-AU 9 37537191 37537191 single base substitution G A intron_variant MELA-AU 9 37537191 37537191 single base substitution G A synonymous_variant F445F 1335C>T MELA-AU 9 37537191 37537191 single base substitution G A upstream_gene_variant MELA-AU 9 37537378 37537378 single base substitution G A downstream_gene_variant MELA-AU 9 37537378 37537378 single base substitution G A exon_variant MELA-AU 9 37537378 37537378 single base substitution G A intron_variant MELA-AU 9 37537378 37537378 single base substitution G A missense_variant P383L 1148C>T MELA-AU 9 37537378 37537378 single base substitution G A upstream_gene_variant MELA-AU 9 37537684 37537684 single base substitution G A downstream_gene_variant MELA-AU 9 37537684 37537684 single base substitution G A exon_variant MELA-AU 9 37537684 37537684 single base substitution G A intron_variant MELA-AU 9 37537684 37537684 single base substitution G A missense_variant P281L 842C>T MELA-AU 9 37537684 37537684 single base substitution G A upstream_gene_variant MELA-AU 9 37538176 37538176 single base substitution G A downstream_gene_variant MELA-AU 9 37538176 37538176 single base substitution G A intron_variant MELA-AU 9 37538176 37538176 single base substitution G A upstream_gene_variant MELA-AU 9 37538261 37538261 single base substitution G A downstream_gene_variant MELA-AU 9 37538261 37538261 single base substitution G A intron_variant MELA-AU 9 37538261 37538261 single base substitution G A upstream_gene_variant MELA-AU 9 37538263 37538263 single base substitution A G downstream_gene_variant MELA-AU 9 37538263 37538263 single base substitution A G intron_variant MELA-AU 9 37538263 37538263 single base substitution A G upstream_gene_variant MELA-AU 9 37539050 37539051 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 37539050 37539051 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 37539050 37539051 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 37539125 37539125 single base substitution C T downstream_gene_variant MELA-AU 9 37539125 37539125 single base substitution C T intron_variant MELA-AU 9 37539125 37539125 single base substitution C T upstream_gene_variant MELA-AU 9 37539148 37539148 single base substitution A G downstream_gene_variant MELA-AU 9 37539148 37539148 single base substitution A G intron_variant MELA-AU 9 37539148 37539148 single base substitution A G upstream_gene_variant MELA-AU 9 37539320 37539320 single base substitution G A downstream_gene_variant MELA-AU 9 37539320 37539320 single base substitution G A intron_variant MELA-AU 9 37539320 37539320 single base substitution G A upstream_gene_variant MELA-AU 9 37540288 37540288 single base substitution G A downstream_gene_variant MELA-AU 9 37540288 37540288 single base substitution G A intron_variant MELA-AU 9 37540288 37540288 single base substitution G A upstream_gene_variant MELA-AU 9 37540512 37540512 single base substitution T C downstream_gene_variant MELA-AU 9 37540512 37540512 single base substitution T C intron_variant MELA-AU 9 37540512 37540512 single base substitution T C upstream_gene_variant MELA-AU 9 37540733 37540733 single base substitution C T downstream_gene_variant MELA-AU 9 37540733 37540733 single base substitution C T intron_variant MELA-AU 9 37540733 37540733 single base substitution C T upstream_gene_variant MELA-AU 9 37540928 37540928 single base substitution G A downstream_gene_variant MELA-AU 9 37540928 37540928 single base substitution G A intron_variant MELA-AU 9 37540928 37540928 single base substitution G A upstream_gene_variant MELA-AU 9 37541189 37541189 single base substitution T A downstream_gene_variant MELA-AU 9 37541189 37541189 single base substitution T A exon_variant MELA-AU 9 37541189 37541189 single base substitution T A intron_variant MELA-AU 9 37541189 37541189 single base substitution T A missense_variant M193L 577A>T MELA-AU 9 37541981 37541981 single base substitution C T intron_variant MELA-AU 9 37542403 37542403 single base substitution A G intron_variant MELA-AU 9 37542955 37542955 single base substitution G A intron_variant MELA-AU 9 37543419 37543419 single base substitution G A intron_variant MELA-AU 9 37544310 37544310 single base substitution A G intron_variant MELA-AU 9 37544578 37544578 single base substitution G A intron_variant MELA-AU 9 37545062 37545062 single base substitution G C intron_variant MELA-AU 9 37546174 37546174 single base substitution G A intron_variant MELA-AU 9 37548033 37548033 single base substitution G A intron_variant MELA-AU 9 37548203 37548203 single base substitution G A intron_variant MELA-AU 9 37548730 37548730 single base substitution G A intron_variant MELA-AU 9 37549178 37549178 single base substitution G A intron_variant MELA-AU 9 37549458 37549458 single base substitution C T intron_variant MELA-AU 9 37549936 37549936 single base substitution G A intron_variant MELA-AU 9 37550271 37550271 single base substitution C T intron_variant MELA-AU 9 37552107 37552107 deletion of <=200bp C - intron_variant MELA-AU 9 37552973 37552973 single base substitution G A intron_variant MELA-AU 9 37553387 37553387 single base substitution G A intron_variant MELA-AU 9 37553513 37553513 single base substitution T G intron_variant MELA-AU 9 37554094 37554094 single base substitution A T intron_variant MELA-AU 9 37554900 37554900 single base substitution C T intron_variant MELA-AU 9 37555988 37555988 single base substitution G A intron_variant MELA-AU 9 37556010 37556010 single base substitution G A intron_variant MELA-AU 9 37556118 37556118 single base substitution C T intron_variant MELA-AU 9 37556810 37556810 single base substitution G A intron_variant MELA-AU 9 37557379 37557379 single base substitution C T intron_variant MELA-AU 9 37557597 37557597 single base substitution C T intron_variant MELA-AU 9 37557875 37557875 single base substitution A C intron_variant MELA-AU 9 37558641 37558641 single base substitution G A intron_variant MELA-AU 9 37558736 37558736 single base substitution C T intron_variant MELA-AU 9 37559011 37559011 single base substitution G A intron_variant MELA-AU 9 37559625 37559625 single base substitution C A intron_variant MELA-AU 9 37560620 37560620 single base substitution G T intron_variant MELA-AU 9 37560956 37560956 single base substitution G C intron_variant MELA-AU 9 37561046 37561046 single base substitution G A intron_variant MELA-AU 9 37561642 37561642 single base substitution A T intron_variant MELA-AU 9 37562489 37562489 single base substitution G A intron_variant MELA-AU 9 37563762 37563762 single base substitution G A intron_variant MELA-AU 9 37563846 37563846 single base substitution G T intron_variant MELA-AU 9 37564676 37564676 single base substitution G A intron_variant MELA-AU 9 37565262 37565262 single base substitution G A intron_variant MELA-AU 9 37565853 37565853 single base substitution G A intron_variant MELA-AU 9 37567243 37567243 single base substitution G A intron_variant MELA-AU 9 37567979 37567979 single base substitution C T intron_variant MELA-AU 9 37567995 37567995 single base substitution G A intron_variant MELA-AU 9 37569116 37569116 single base substitution G A intron_variant MELA-AU 9 37569479 37569479 single base substitution G A intron_variant MELA-AU 9 37569490 37569490 single base substitution A C intron_variant MELA-AU 9 37569950 37569950 single base substitution G A intron_variant MELA-AU 9 37570329 37570329 single base substitution G A intron_variant MELA-AU 9 37570622 37570622 single base substitution G A intron_variant MELA-AU 9 37570975 37570975 single base substitution G A intron_variant MELA-AU 9 37571905 37571905 single base substitution G A intron_variant MELA-AU 9 37572165 37572165 single base substitution G A intron_variant MELA-AU 9 37572895 37572895 single base substitution T A intron_variant MELA-AU 9 37573010 37573010 single base substitution C T intron_variant MELA-AU 9 37573443 37573443 single base substitution G A intron_variant MELA-AU 9 37573625 37573625 single base substitution A G intron_variant MELA-AU 9 37574541 37574541 single base substitution G A intron_variant MELA-AU 9 37574541 37574541 single base substitution G C intron_variant MELA-AU 9 37576034 37576034 single base substitution C T intron_variant MELA-AU 9 37576841 37576841 single base substitution A C intron_variant MELA-AU 9 37576841 37576841 single base substitution A C upstream_gene_variant MELA-AU 9 37578371 37578371 single base substitution G A intron_variant MELA-AU 9 37578371 37578371 single base substitution G A upstream_gene_variant MELA-AU 9 37578667 37578667 single base substitution G A intron_variant MELA-AU 9 37578667 37578667 single base substitution G A upstream_gene_variant MELA-AU 9 37579689 37579689 single base substitution C T intron_variant MELA-AU 9 37579689 37579689 single base substitution C T upstream_gene_variant MELA-AU 9 37580420 37580420 single base substitution C T intron_variant MELA-AU 9 37580420 37580420 single base substitution C T upstream_gene_variant MELA-AU 9 37580883 37580884 deletion of <=200bp CT - intron_variant MELA-AU 9 37580883 37580884 deletion of <=200bp CT - upstream_gene_variant MELA-AU 9 37581711 37581711 single base substitution G A intron_variant MELA-AU 9 37582259 37582259 single base substitution T C intron_variant MELA-AU 9 37582380 37582380 single base substitution A G intron_variant MELA-AU 9 37584769 37584769 single base substitution C T intron_variant MELA-AU 9 37584937 37584937 single base substitution G A intron_variant MELA-AU 9 37588004 37588004 single base substitution G A intron_variant MELA-AU 9 37589269 37589269 single base substitution G A upstream_gene_variant MELA-AU 9 37589939 37589939 single base substitution G A upstream_gene_variant MELA-AU 9 37591006 37591006 single base substitution G A upstream_gene_variant MELA-AU 9 37591402 37591402 single base substitution G A upstream_gene_variant MELA-AU 9 37592280 37592280 single base substitution A G upstream_gene_variant MELA-AU 9 37592449 37592450 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 37592702 37592703 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 37592966 37592966 single base substitution C T upstream_gene_variant MELA-AU 9 37592969 37592969 single base substitution C T upstream_gene_variant MELA-AU 9 37593167 37593168 multiple base substitution (>=2bp and <=200bp) AA GG upstream_gene_variant MELA-AU 9 37593723 37593723 single base substitution G A upstream_gene_variant MELA-AU 9 37593729 37593729 single base substitution C T upstream_gene_variant ORCA-IN 9 37509123 37509123 single base substitution G T downstream_gene_variant ORCA-IN 9 37521655 37521655 single base substitution C A 3_prime_UTR_variant ORCA-IN 9 37521655 37521655 single base substitution C A downstream_gene_variant ORCA-IN 9 37521655 37521655 single base substitution C A missense_variant W229L 686G>T ORCA-IN 9 37521655 37521655 single base substitution C A missense_variant W704L 2111G>T ORCA-IN 9 37527139 37527139 single base substitution C T intron_variant ORCA-IN 9 37527139 37527139 single base substitution C T upstream_gene_variant ORCA-IN 9 37537842 37537842 single base substitution G C downstream_gene_variant ORCA-IN 9 37537842 37537842 single base substitution G C exon_variant ORCA-IN 9 37537842 37537842 single base substitution G C intron_variant ORCA-IN 9 37537842 37537842 single base substitution G C missense_variant F228L 684C>G ORCA-IN 9 37537842 37537842 single base substitution G C upstream_gene_variant ORCA-IN 9 37538583 37538583 single base substitution T C downstream_gene_variant ORCA-IN 9 37538583 37538583 single base substitution T C intron_variant ORCA-IN 9 37538583 37538583 single base substitution T C upstream_gene_variant ORCA-IN 9 37547326 37547326 single base substitution C T intron_variant ORCA-IN 9 37566748 37566748 single base substitution C T intron_variant ORCA-IN 9 37584549 37584549 single base substitution G A intron_variant ORCA-IN 9 37586020 37586020 single base substitution C G intron_variant ORCA-IN 9 37587694 37587694 single base substitution T C intron_variant ORCA-IN 9 37588008 37588008 single base substitution G C intron_variant OV-AU 9 37508011 37508011 single base substitution T A downstream_gene_variant OV-AU 9 37512937 37512937 single base substitution C T downstream_gene_variant OV-AU 9 37512937 37512937 single base substitution C T intron_variant OV-AU 9 37514287 37514287 single base substitution T G downstream_gene_variant OV-AU 9 37514287 37514287 single base substitution T G intron_variant OV-AU 9 37517256 37517256 single base substitution G A downstream_gene_variant OV-AU 9 37517256 37517256 single base substitution G A intron_variant OV-AU 9 37518174 37518174 single base substitution A T 3_prime_UTR_variant OV-AU 9 37518174 37518174 single base substitution A T downstream_gene_variant OV-AU 9 37518174 37518174 single base substitution A T missense_variant I346N 1037T>A OV-AU 9 37518174 37518174 single base substitution A T missense_variant I821N 2462T>A OV-AU 9 37525691 37525691 single base substitution C T intron_variant OV-AU 9 37525691 37525691 single base substitution C T upstream_gene_variant OV-AU 9 37535167 37535167 single base substitution C G intron_variant OV-AU 9 37535325 37535325 single base substitution C G intron_variant OV-AU 9 37535459 37535459 single base substitution C A intron_variant OV-AU 9 37536508 37536508 single base substitution G C intron_variant OV-AU 9 37536508 37536508 single base substitution G C upstream_gene_variant OV-AU 9 37536856 37536856 single base substitution C A downstream_gene_variant OV-AU 9 37536856 37536856 single base substitution C A intron_variant OV-AU 9 37536856 37536856 single base substitution C A upstream_gene_variant OV-AU 9 37537858 37537858 single base substitution A G downstream_gene_variant OV-AU 9 37537858 37537858 single base substitution A G exon_variant OV-AU 9 37537858 37537858 single base substitution A G intron_variant OV-AU 9 37537858 37537858 single base substitution A G missense_variant V223A 668T>C OV-AU 9 37537858 37537858 single base substitution A G upstream_gene_variant OV-AU 9 37538443 37538443 single base substitution G A downstream_gene_variant OV-AU 9 37538443 37538443 single base substitution G A intron_variant OV-AU 9 37538443 37538443 single base substitution G A upstream_gene_variant OV-AU 9 37548070 37548070 single base substitution G T intron_variant OV-AU 9 37552028 37552028 single base substitution A G intron_variant OV-AU 9 37555156 37555156 single base substitution T G intron_variant OV-AU 9 37563020 37563020 single base substitution T C intron_variant OV-AU 9 37565349 37565349 single base substitution C A intron_variant OV-AU 9 37574298 37574298 single base substitution G C intron_variant OV-AU 9 37578232 37578232 single base substitution A G intron_variant OV-AU 9 37578232 37578232 single base substitution A G upstream_gene_variant OV-AU 9 37582610 37582610 single base substitution G T intron_variant OV-AU 9 37586149 37586149 single base substitution C G intron_variant OV-AU 9 37589446 37589446 single base substitution G C upstream_gene_variant OV-AU 9 37593119 37593119 single base substitution A C upstream_gene_variant PACA-AU 9 37506515 37506515 single base substitution T A downstream_gene_variant PACA-AU 9 37509103 37509103 single base substitution G A downstream_gene_variant PACA-AU 9 37512167 37512167 single base substitution T C 3_prime_UTR_variant PACA-AU 9 37512167 37512167 single base substitution T C downstream_gene_variant PACA-AU 9 37512770 37512770 single base substitution G A downstream_gene_variant PACA-AU 9 37512770 37512770 single base substitution G A intron_variant PACA-AU 9 37516055 37516055 deletion of <=200bp G - 3_prime_UTR_variant PACA-AU 9 37516055 37516055 deletion of <=200bp G - frameshift_variant R373 PACA-AU 9 37516055 37516055 deletion of <=200bp G - frameshift_variant R848 PACA-AU 9 37519997 37519997 single base substitution A T downstream_gene_variant PACA-AU 9 37519997 37519997 single base substitution A T intron_variant PACA-AU 9 37527880 37527880 single base substitution T A intron_variant PACA-AU 9 37527880 37527880 single base substitution T A upstream_gene_variant PACA-AU 9 37533882 37533882 single base substitution A C intron_variant PACA-AU 9 37537196 37537196 single base substitution C T downstream_gene_variant PACA-AU 9 37537196 37537196 single base substitution C T exon_variant PACA-AU 9 37537196 37537196 single base substitution C T intron_variant PACA-AU 9 37537196 37537196 single base substitution C T missense_variant V444I 1330G>A PACA-AU 9 37537196 37537196 single base substitution C T upstream_gene_variant PACA-AU 9 37539634 37539634 single base substitution T A downstream_gene_variant PACA-AU 9 37539634 37539634 single base substitution T A intron_variant PACA-AU 9 37539634 37539634 single base substitution T A upstream_gene_variant PACA-AU 9 37540527 37540527 single base substitution C T downstream_gene_variant PACA-AU 9 37540527 37540527 single base substitution C T intron_variant PACA-AU 9 37540527 37540527 single base substitution C T upstream_gene_variant PACA-AU 9 37541481 37541481 single base substitution G A downstream_gene_variant PACA-AU 9 37541481 37541481 single base substitution G A exon_variant PACA-AU 9 37541481 37541481 single base substitution G A intron_variant PACA-AU 9 37541481 37541481 single base substitution G A synonymous_variant S95S 285C>T PACA-AU 9 37547633 37547633 single base substitution A G intron_variant PACA-AU 9 37557354 37557354 single base substitution T A intron_variant PACA-AU 9 37557640 37557640 single base substitution T A intron_variant PACA-AU 9 37559232 37559232 single base substitution G A intron_variant PACA-AU 9 37560698 37560698 single base substitution G A intron_variant PACA-AU 9 37562897 37562898 deletion of <=200bp AA - intron_variant PACA-AU 9 37568017 37568017 single base substitution C A intron_variant PACA-AU 9 37570372 37570372 single base substitution C A intron_variant PACA-AU 9 37587572 37587572 single base substitution C T intron_variant PACA-CA 9 37509429 37509429 single base substitution C T downstream_gene_variant PACA-CA 9 37513209 37513209 single base substitution C T downstream_gene_variant PACA-CA 9 37513209 37513209 single base substitution C T intron_variant PACA-CA 9 37513733 37513733 single base substitution C T downstream_gene_variant PACA-CA 9 37513733 37513733 single base substitution C T intron_variant PACA-CA 9 37523207 37523207 single base substitution G A intron_variant PACA-CA 9 37526615 37526615 single base substitution A G intron_variant PACA-CA 9 37526615 37526615 single base substitution A G upstream_gene_variant PACA-CA 9 37532901 37532901 single base substitution G A intron_variant PACA-CA 9 37533988 37533988 single base substitution G T intron_variant PACA-CA 9 37537404 37537404 single base substitution T C downstream_gene_variant PACA-CA 9 37537404 37537404 single base substitution T C exon_variant PACA-CA 9 37537404 37537404 single base substitution T C intron_variant PACA-CA 9 37537404 37537404 single base substitution T C synonymous_variant L374L 1122A>G PACA-CA 9 37537404 37537404 single base substitution T C upstream_gene_variant PACA-CA 9 37539347 37539347 single base substitution G A downstream_gene_variant PACA-CA 9 37539347 37539347 single base substitution G A intron_variant PACA-CA 9 37539347 37539347 single base substitution G A upstream_gene_variant PACA-CA 9 37541636 37541636 single base substitution G A exon_variant PACA-CA 9 37541636 37541636 single base substitution G A intron_variant PACA-CA 9 37541636 37541636 single base substitution G A missense_variant R44C 130C>T PACA-CA 9 37549219 37549219 single base substitution T C intron_variant PACA-CA 9 37555705 37555705 single base substitution T A intron_variant PACA-CA 9 37558942 37558942 single base substitution C T intron_variant PACA-CA 9 37560628 37560628 insertion of <=200bp - TTTTA intron_variant PACA-CA 9 37565014 37565014 single base substitution C G intron_variant PACA-CA 9 37572589 37572589 single base substitution T C intron_variant PACA-CA 9 37580379 37580379 single base substitution T G intron_variant PACA-CA 9 37580379 37580379 single base substitution T G upstream_gene_variant PACA-CA 9 37586007 37586007 single base substitution C T intron_variant PACA-CA 9 37587350 37587350 single base substitution T C intron_variant PACA-CA 9 37589550 37589550 deletion of <=200bp A - upstream_gene_variant PACA-CA 9 37590409 37590409 single base substitution G A upstream_gene_variant PACA-CA 9 37591435 37591435 single base substitution C T upstream_gene_variant PACA-CA 9 37591924 37591924 insertion of <=200bp - T upstream_gene_variant PACA-CA 9 37592966 37592966 single base substitution C T upstream_gene_variant PAEN-AU 9 37553049 37553049 single base substitution A T intron_variant PAEN-AU 9 37574005 37574005 single base substitution C T intron_variant PAEN-IT 9 37551266 37551266 single base substitution G A intron_variant PAEN-IT 9 37562538 37562538 single base substitution C T intron_variant PAEN-IT 9 37579383 37579383 single base substitution T A intron_variant PAEN-IT 9 37579383 37579383 single base substitution T A upstream_gene_variant PAEN-IT 9 37583872 37583872 single base substitution C G intron_variant PBCA-DE 9 37513575 37513586 deletion of <=200bp TATTTTTTAATA - downstream_gene_variant PBCA-DE 9 37513575 37513586 deletion of <=200bp TATTTTTTAATA - intron_variant PBCA-DE 9 37522384 37522384 single base substitution G T exon_variant PBCA-DE 9 37522384 37522384 single base substitution G T intron_variant PBCA-DE 9 37525095 37525095 single base substitution G A intron_variant PBCA-DE 9 37525095 37525095 single base substitution G A splice_region_variant PBCA-DE 9 37553772 37553772 single base substitution C T intron_variant PBCA-DE 9 37555253 37555253 single base substitution T C intron_variant PBCA-DE 9 37570381 37570381 single base substitution C T intron_variant PBCA-DE 9 37570623 37570623 insertion of <=200bp - A intron_variant PBCA-DE 9 37573831 37573831 single base substitution A G intron_variant PBCA-DE 9 37585083 37585083 single base substitution T G intron_variant PBCA-DE 9 37585359 37585359 single base substitution C T intron_variant PBCA-DE 9 37588586 37588586 single base substitution C G intron_variant PRAD-CA 9 37521323 37521323 single base substitution G A downstream_gene_variant PRAD-CA 9 37521323 37521323 single base substitution G A intron_variant PRAD-CA 9 37528047 37528047 single base substitution T A intron_variant PRAD-CA 9 37528047 37528047 single base substitution T A upstream_gene_variant PRAD-CA 9 37532984 37532984 single base substitution C A intron_variant PRAD-CA 9 37562028 37562028 single base substitution G A intron_variant PRAD-CA 9 37575009 37575009 single base substitution C T intron_variant PRAD-CA 9 37577911 37577911 single base substitution G A intron_variant PRAD-CA 9 37577911 37577911 single base substitution G A upstream_gene_variant PRAD-UK 9 37514770 37514770 single base substitution G A downstream_gene_variant PRAD-UK 9 37514770 37514770 single base substitution G A intron_variant PRAD-UK 9 37536642 37536642 single base substitution T G downstream_gene_variant PRAD-UK 9 37536642 37536642 single base substitution T G intron_variant PRAD-UK 9 37536642 37536642 single base substitution T G upstream_gene_variant PRAD-UK 9 37537133 37537133 single base substitution C A downstream_gene_variant PRAD-UK 9 37537133 37537133 single base substitution C A exon_variant PRAD-UK 9 37537133 37537133 single base substitution C A intron_variant PRAD-UK 9 37537133 37537133 single base substitution C A missense_variant A465S 1393G>T PRAD-UK 9 37537133 37537133 single base substitution C A upstream_gene_variant PRAD-UK 9 37549773 37549773 single base substitution C A intron_variant PRAD-UK 9 37563632 37563632 single base substitution T A intron_variant PRAD-UK 9 37590234 37590234 insertion of <=200bp - A upstream_gene_variant PRAD-UK 9 37590240 37590240 insertion of <=200bp - A upstream_gene_variant PRAD-US 9 37516001 37516001 single base substitution T C 3_prime_UTR_variant PRAD-US 9 37516001 37516001 single base substitution T C missense_variant I391V 1171A>G PRAD-US 9 37516001 37516001 single base substitution T C missense_variant I866V 2596A>G READ-US 9 37522975 37522975 single base substitution C A splice_acceptor_variant RECA-EU 9 37508157 37508157 single base substitution G C downstream_gene_variant RECA-EU 9 37519811 37519811 single base substitution C G downstream_gene_variant RECA-EU 9 37519811 37519811 single base substitution C G intron_variant RECA-EU 9 37520522 37520522 single base substitution T C downstream_gene_variant RECA-EU 9 37520522 37520522 single base substitution T C intron_variant RECA-EU 9 37529581 37529581 single base substitution C T intron_variant RECA-EU 9 37529581 37529581 single base substitution C T upstream_gene_variant RECA-EU 9 37533324 37533324 single base substitution C T intron_variant RECA-EU 9 37535694 37535694 single base substitution C A intron_variant RECA-EU 9 37543017 37543017 single base substitution G C intron_variant RECA-EU 9 37549446 37549446 single base substitution T A intron_variant RECA-EU 9 37558952 37558952 single base substitution C T intron_variant RECA-EU 9 37567072 37567072 single base substitution G T intron_variant RECA-EU 9 37581513 37581513 single base substitution T A intron_variant RECA-EU 9 37582814 37582814 single base substitution G A intron_variant RECA-EU 9 37589590 37589590 single base substitution T C upstream_gene_variant RECA-EU 9 37590404 37590404 single base substitution A G upstream_gene_variant SKCA-BR 9 37505925 37505925 single base substitution T A downstream_gene_variant SKCA-BR 9 37512001 37512001 single base substitution C T 3_prime_UTR_variant SKCA-BR 9 37512001 37512001 single base substitution C T downstream_gene_variant SKCA-BR 9 37515591 37515591 single base substitution G A 3_prime_UTR_variant SKCA-BR 9 37515591 37515591 single base substitution G A intron_variant SKCA-BR 9 37517709 37517709 single base substitution G A downstream_gene_variant SKCA-BR 9 37517709 37517709 single base substitution G A intron_variant SKCA-BR 9 37517939 37517939 single base substitution C T downstream_gene_variant SKCA-BR 9 37517939 37517939 single base substitution C T intron_variant SKCA-BR 9 37517954 37517955 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 9 37517954 37517955 deletion of <=200bp CT - intron_variant SKCA-BR 9 37521554 37521554 single base substitution G A downstream_gene_variant SKCA-BR 9 37521554 37521554 single base substitution G A intron_variant SKCA-BR 9 37522672 37522672 single base substitution G A intron_variant SKCA-BR 9 37526819 37526819 single base substitution T C intron_variant SKCA-BR 9 37526819 37526819 single base substitution T C upstream_gene_variant SKCA-BR 9 37527765 37527765 single base substitution A G intron_variant SKCA-BR 9 37527765 37527765 single base substitution A G upstream_gene_variant SKCA-BR 9 37528609 37528609 single base substitution C T intron_variant SKCA-BR 9 37528609 37528609 single base substitution C T upstream_gene_variant SKCA-BR 9 37532691 37532691 single base substitution C T intron_variant SKCA-BR 9 37533197 37533197 single base substitution G A intron_variant SKCA-BR 9 37535514 37535514 single base substitution A T intron_variant SKCA-BR 9 37536086 37536086 single base substitution G C intron_variant SKCA-BR 9 37536086 37536086 single base substitution G C upstream_gene_variant SKCA-BR 9 37537349 37537349 single base substitution G A downstream_gene_variant SKCA-BR 9 37537349 37537349 single base substitution G A exon_variant SKCA-BR 9 37537349 37537349 single base substitution G A intron_variant SKCA-BR 9 37537349 37537349 single base substitution G A missense_variant P393S 1177C>T SKCA-BR 9 37537349 37537349 single base substitution G A upstream_gene_variant SKCA-BR 9 37538291 37538291 single base substitution G A downstream_gene_variant SKCA-BR 9 37538291 37538291 single base substitution G A intron_variant SKCA-BR 9 37538291 37538291 single base substitution G A upstream_gene_variant SKCA-BR 9 37538292 37538292 single base substitution T A downstream_gene_variant SKCA-BR 9 37538292 37538292 single base substitution T A intron_variant SKCA-BR 9 37538292 37538292 single base substitution T A upstream_gene_variant SKCA-BR 9 37538385 37538385 single base substitution G A downstream_gene_variant SKCA-BR 9 37538385 37538385 single base substitution G A intron_variant SKCA-BR 9 37538385 37538385 single base substitution G A upstream_gene_variant SKCA-BR 9 37538705 37538706 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 9 37538705 37538706 deletion of <=200bp CA - intron_variant SKCA-BR 9 37538705 37538706 deletion of <=200bp CA - upstream_gene_variant SKCA-BR 9 37540117 37540117 single base substitution G A downstream_gene_variant SKCA-BR 9 37540117 37540117 single base substitution G A intron_variant SKCA-BR 9 37540117 37540117 single base substitution G A upstream_gene_variant SKCA-BR 9 37541238 37541238 single base substitution G A downstream_gene_variant SKCA-BR 9 37541238 37541238 single base substitution G A exon_variant SKCA-BR 9 37541238 37541238 single base substitution G A intron_variant SKCA-BR 9 37541238 37541238 single base substitution G A synonymous_variant T176T 528C>T SKCA-BR 9 37541594 37541594 single base substitution G A exon_variant SKCA-BR 9 37541594 37541594 single base substitution G A intron_variant SKCA-BR 9 37541594 37541594 single base substitution G A missense_variant P58S 172C>T SKCA-BR 9 37544195 37544195 single base substitution G A intron_variant SKCA-BR 9 37544974 37544974 single base substitution G A intron_variant SKCA-BR 9 37545763 37545763 single base substitution T C intron_variant SKCA-BR 9 37546357 37546357 single base substitution G A intron_variant SKCA-BR 9 37554508 37554508 single base substitution A G intron_variant SKCA-BR 9 37556676 37556676 single base substitution G A intron_variant SKCA-BR 9 37557001 37557001 single base substitution T C intron_variant SKCA-BR 9 37558888 37558888 single base substitution A G intron_variant SKCA-BR 9 37562390 37562390 single base substitution G A intron_variant SKCA-BR 9 37564213 37564213 single base substitution C T intron_variant SKCA-BR 9 37565604 37565604 single base substitution G A intron_variant SKCA-BR 9 37566454 37566455 deletion of <=200bp CG - intron_variant SKCA-BR 9 37566456 37566456 single base substitution G A intron_variant SKCA-BR 9 37566456 37566457 deletion of <=200bp GA - intron_variant SKCA-BR 9 37567770 37567770 single base substitution G A intron_variant SKCA-BR 9 37572751 37572751 single base substitution G A intron_variant SKCA-BR 9 37577115 37577115 single base substitution C T intron_variant SKCA-BR 9 37577115 37577115 single base substitution C T upstream_gene_variant SKCA-BR 9 37578814 37578814 insertion of <=200bp - CA intron_variant SKCA-BR 9 37578814 37578814 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 9 37582969 37582969 insertion of <=200bp - AG intron_variant SKCA-BR 9 37583453 37583453 single base substitution C G intron_variant SKCA-BR 9 37584301 37584301 single base substitution C T intron_variant SKCA-BR 9 37585270 37585270 single base substitution G A intron_variant SKCA-BR 9 37589323 37589323 single base substitution G A upstream_gene_variant SKCA-BR 9 37592609 37592609 single base substitution C T upstream_gene_variant SKCA-BR 9 37592812 37592812 single base substitution C T upstream_gene_variant SKCA-BR 9 37592821 37592821 single base substitution C T upstream_gene_variant SKCA-BR 9 37592939 37592939 insertion of <=200bp - AAAT upstream_gene_variant SKCM-US 9 37512591 37512591 single base substitution C T downstream_gene_variant SKCM-US 9 37512591 37512591 single base substitution C T missense_variant E467K 1399G>A SKCM-US 9 37512591 37512591 single base substitution C T missense_variant E942K 2824G>A SKCM-US 9 37515909 37515909 single base substitution G A 3_prime_UTR_variant SKCM-US 9 37515909 37515909 single base substitution G A synonymous_variant F421F 1263C>T SKCM-US 9 37515909 37515909 single base substitution G A synonymous_variant F896F 2688C>T SKCM-US 9 37515999 37515999 single base substitution G A 3_prime_UTR_variant SKCM-US 9 37515999 37515999 single base substitution G A synonymous_variant I391I 1173C>T SKCM-US 9 37515999 37515999 single base substitution G A synonymous_variant I866I 2598C>T SKCM-US 9 37518344 37518344 single base substitution C T 3_prime_UTR_variant SKCM-US 9 37518344 37518344 single base substitution C T downstream_gene_variant SKCM-US 9 37518344 37518344 single base substitution C T synonymous_variant Q289Q 867G>A SKCM-US 9 37518344 37518344 single base substitution C T synonymous_variant Q764Q 2292G>A SKCM-US 9 37521630 37521630 single base substitution G C 3_prime_UTR_variant SKCM-US 9 37521630 37521630 single base substitution G C downstream_gene_variant SKCM-US 9 37521630 37521630 single base substitution G C missense_variant D237E 711C>G SKCM-US 9 37521630 37521630 single base substitution G C missense_variant D712E 2136C>G SKCM-US 9 37521635 37521635 single base substitution C T 3_prime_UTR_variant SKCM-US 9 37521635 37521635 single base substitution C T downstream_gene_variant SKCM-US 9 37521635 37521635 single base substitution C T missense_variant E236K 706G>A SKCM-US 9 37521635 37521635 single base substitution C T missense_variant E711K 2131G>A SKCM-US 9 37521655 37521655 single base substitution C A 3_prime_UTR_variant SKCM-US 9 37521655 37521655 single base substitution C A downstream_gene_variant SKCM-US 9 37521655 37521655 single base substitution C A missense_variant W229L 686G>T SKCM-US 9 37521655 37521655 single base substitution C A missense_variant W704L 2111G>T SKCM-US 9 37521707 37521707 single base substitution G A 3_prime_UTR_variant SKCM-US 9 37521707 37521707 single base substitution G A downstream_gene_variant SKCM-US 9 37521707 37521707 single base substitution G A stop_gained R212* 634C>T SKCM-US 9 37521707 37521707 single base substitution G A stop_gained R687* 2059C>T SKCM-US 9 37522954 37522954 single base substitution G A 3_prime_UTR_variant SKCM-US 9 37522954 37522954 single base substitution G A exon_variant SKCM-US 9 37522954 37522954 single base substitution G A stop_gained Q125* 373C>T SKCM-US 9 37522954 37522954 single base substitution G A stop_gained Q600* 1798C>T SKCM-US 9 37537208 37537208 single base substitution C T downstream_gene_variant SKCM-US 9 37537208 37537208 single base substitution C T exon_variant SKCM-US 9 37537208 37537208 single base substitution C T intron_variant SKCM-US 9 37537208 37537208 single base substitution C T missense_variant G440R 1318G>A SKCM-US 9 37537208 37537208 single base substitution C T upstream_gene_variant SKCM-US 9 37537215 37537215 single base substitution G A downstream_gene_variant SKCM-US 9 37537215 37537215 single base substitution G A exon_variant SKCM-US 9 37537215 37537215 single base substitution G A intron_variant SKCM-US 9 37537215 37537215 single base substitution G A synonymous_variant F437F 1311C>T SKCM-US 9 37537215 37537215 single base substitution G A upstream_gene_variant SKCM-US 9 37537249 37537249 single base substitution G A downstream_gene_variant SKCM-US 9 37537249 37537249 single base substitution G A exon_variant SKCM-US 9 37537249 37537249 single base substitution G A intron_variant SKCM-US 9 37537249 37537249 single base substitution G A missense_variant S426F 1277C>T SKCM-US 9 37537249 37537249 single base substitution G A upstream_gene_variant SKCM-US 9 37537332 37537332 single base substitution G A downstream_gene_variant SKCM-US 9 37537332 37537332 single base substitution G A exon_variant SKCM-US 9 37537332 37537332 single base substitution G A intron_variant SKCM-US 9 37537332 37537332 single base substitution G A synonymous_variant S398S 1194C>T SKCM-US 9 37537332 37537332 single base substitution G A upstream_gene_variant SKCM-US 9 37541368 37541368 single base substitution C T downstream_gene_variant SKCM-US 9 37541368 37541368 single base substitution C T exon_variant SKCM-US 9 37541368 37541368 single base substitution C T intron_variant SKCM-US 9 37541368 37541368 single base substitution C T missense_variant R133Q 398G>A SKCM-US 9 37541670 37541670 single base substitution G A exon_variant SKCM-US 9 37541670 37541670 single base substitution G A intron_variant SKCM-US 9 37541670 37541670 single base substitution G A synonymous_variant A32A 96C>T SKCM-US 9 37541745 37541745 single base substitution G A exon_variant SKCM-US 9 37541745 37541745 single base substitution G A intron_variant SKCM-US 9 37541745 37541745 single base substitution G A synonymous_variant P7P 21C>T STAD-US 9 37516037 37516037 single base substitution C T 3_prime_UTR_variant STAD-US 9 37516037 37516037 single base substitution C T missense_variant V379M 1135G>A STAD-US 9 37516037 37516037 single base substitution C T missense_variant V854M 2560G>A STAD-US 9 37516069 37516069 single base substitution C T 3_prime_UTR_variant STAD-US 9 37516069 37516069 single base substitution C T missense_variant R368Q 1103G>A STAD-US 9 37516069 37516069 single base substitution C T missense_variant R843Q 2528G>A STAD-US 9 37518122 37518122 single base substitution T C downstream_gene_variant STAD-US 9 37518122 37518122 single base substitution T C splice_region_variant STAD-US 9 37521626 37521626 single base substitution G T 3_prime_UTR_variant STAD-US 9 37521626 37521626 single base substitution G T downstream_gene_variant STAD-US 9 37521626 37521626 single base substitution G T missense_variant P239T 715C>A STAD-US 9 37521626 37521626 single base substitution G T missense_variant P714T 2140C>A STAD-US 9 37521665 37521665 single base substitution C T 3_prime_UTR_variant STAD-US 9 37521665 37521665 single base substitution C T downstream_gene_variant STAD-US 9 37521665 37521665 single base substitution C T missense_variant A226T 676G>A STAD-US 9 37521665 37521665 single base substitution C T missense_variant A701T 2101G>A STAD-US 9 37521836 37521836 single base substitution C T downstream_gene_variant STAD-US 9 37521836 37521836 single base substitution C T exon_variant STAD-US 9 37521836 37521836 single base substitution C T splice_acceptor_variant STAD-US 9 37532017 37532017 single base substitution C T exon_variant STAD-US 9 37532017 37532017 single base substitution C T synonymous_variant A11A 33G>A STAD-US 9 37532017 37532017 single base substitution C T synonymous_variant A486A 1458G>A STAD-US 9 37537214 37537214 single base substitution G A downstream_gene_variant STAD-US 9 37537214 37537214 single base substitution G A exon_variant STAD-US 9 37537214 37537214 single base substitution G A intron_variant STAD-US 9 37537214 37537214 single base substitution G A missense_variant R438W 1312C>T STAD-US 9 37537214 37537214 single base substitution G A upstream_gene_variant STAD-US 9 37541398 37541398 single base substitution C T downstream_gene_variant STAD-US 9 37541398 37541398 single base substitution C T exon_variant STAD-US 9 37541398 37541398 single base substitution C T intron_variant STAD-US 9 37541398 37541398 single base substitution C T missense_variant S123N 368G>A STAD-US 9 37541449 37541449 single base substitution T C downstream_gene_variant STAD-US 9 37541449 37541449 single base substitution T C exon_variant STAD-US 9 37541449 37541449 single base substitution T C intron_variant STAD-US 9 37541449 37541449 single base substitution T C missense_variant E106G 317A>G STAD-US 9 37541762 37541762 single base substitution C T exon_variant STAD-US 9 37541762 37541762 single base substitution C T intron_variant STAD-US 9 37541762 37541762 single base substitution C T missense_variant E2K 4G>A THCA-US 9 37537802 37537802 single base substitution C T downstream_gene_variant THCA-US 9 37537802 37537802 single base substitution C T exon_variant THCA-US 9 37537802 37537802 single base substitution C T intron_variant THCA-US 9 37537802 37537802 single base substitution C T missense_variant V242I 724G>A THCA-US 9 37537802 37537802 single base substitution C T upstream_gene_variant UCEC-US 9 37512665 37512665 single base substitution G T downstream_gene_variant UCEC-US 9 37512665 37512665 single base substitution G T missense_variant S442Y 1325C>A UCEC-US 9 37512665 37512665 single base substitution G T missense_variant S917Y 2750C>A UCEC-US 9 37515996 37515996 single base substitution G T 3_prime_UTR_variant UCEC-US 9 37515996 37515996 single base substitution G T synonymous_variant I392I 1176C>A UCEC-US 9 37515996 37515996 single base substitution G T synonymous_variant I867I 2601C>A UCEC-US 9 37515999 37515999 single base substitution G T 3_prime_UTR_variant UCEC-US 9 37515999 37515999 single base substitution G T synonymous_variant I391I 1173C>A UCEC-US 9 37515999 37515999 single base substitution G T synonymous_variant I866I 2598C>A UCEC-US 9 37516027 37516027 single base substitution C T 3_prime_UTR_variant UCEC-US 9 37516027 37516027 single base substitution C T missense_variant R382H 1145G>A UCEC-US 9 37516027 37516027 single base substitution C T missense_variant R857H 2570G>A UCEC-US 9 37521677 37521677 single base substitution C T 3_prime_UTR_variant UCEC-US 9 37521677 37521677 single base substitution C T downstream_gene_variant UCEC-US 9 37521677 37521677 single base substitution C T missense_variant E222K 664G>A UCEC-US 9 37521677 37521677 single base substitution C T missense_variant E697K 2089G>A UCEC-US 9 37522823 37522823 single base substitution G A splice_region_variant UCEC-US 9 37525146 37525146 single base substitution C T exon_variant UCEC-US 9 37525146 37525146 single base substitution C T intron_variant UCEC-US 9 37525146 37525146 single base substitution C T missense_variant R102H 305G>A UCEC-US 9 37525146 37525146 single base substitution C T missense_variant R577H 1730G>A UCEC-US 9 37537126 37537126 single base substitution C T downstream_gene_variant UCEC-US 9 37537126 37537126 single base substitution C T exon_variant UCEC-US 9 37537126 37537126 single base substitution C T intron_variant UCEC-US 9 37537126 37537126 single base substitution C T missense_variant R467Q 1400G>A UCEC-US 9 37537126 37537126 single base substitution C T upstream_gene_variant UCEC-US 9 37537191 37537191 single base substitution G A downstream_gene_variant UCEC-US 9 37537191 37537191 single base substitution G A exon_variant UCEC-US 9 37537191 37537191 single base substitution G A intron_variant UCEC-US 9 37537191 37537191 single base substitution G A synonymous_variant F445F 1335C>T UCEC-US 9 37537191 37537191 single base substitution G A upstream_gene_variant UCEC-US 9 37537197 37537197 single base substitution G A downstream_gene_variant UCEC-US 9 37537197 37537197 single base substitution G A exon_variant UCEC-US 9 37537197 37537197 single base substitution G A intron_variant UCEC-US 9 37537197 37537197 single base substitution G A synonymous_variant G443G 1329C>T UCEC-US 9 37537197 37537197 single base substitution G A upstream_gene_variant UCEC-US 9 37537228 37537228 single base substitution C T downstream_gene_variant UCEC-US 9 37537228 37537228 single base substitution C T exon_variant UCEC-US 9 37537228 37537228 single base substitution C T intron_variant UCEC-US 9 37537228 37537228 single base substitution C T missense_variant R433H 1298G>A UCEC-US 9 37537228 37537228 single base substitution C T upstream_gene_variant UCEC-US 9 37537464 37537464 single base substitution G A downstream_gene_variant UCEC-US 9 37537464 37537464 single base substitution G A exon_variant UCEC-US 9 37537464 37537464 single base substitution G A intron_variant UCEC-US 9 37537464 37537464 single base substitution G A synonymous_variant S354S 1062C>T UCEC-US 9 37537464 37537464 single base substitution G A upstream_gene_variant UCEC-US 9 37541343 37541343 single base substitution G A downstream_gene_variant UCEC-US 9 37541343 37541343 single base substitution G A exon_variant UCEC-US 9 37541343 37541343 single base substitution G A intron_variant UCEC-US 9 37541343 37541343 single base substitution G A synonymous_variant Y141Y 423C>T UCEC-US 9 37541743 37541743 single base substitution A G exon_variant UCEC-US 9 37541743 37541743 single base substitution A G intron_variant UCEC-US 9 37541743 37541743 single base substitution A G missense_variant L8S 23T>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CSCC-35-T COSM4464639 c.1343C>T p.S448F Substitution - Missense 9:37537186-37537186 - STC246 COSM5063979 c.1144C>T p.R382C Substitution - Missense 9:37537385-37537385 - TCGA-D3-A2JO-06 COSM3657396 c.398G>A p.R133Q Substitution - Missense 9:37541371-37541371 - CHC1211T COSM4954999 c.138G>A p.R46R Substitution - coding silent 9:37541631-37541631 - TCGA-AD-6889-01 COSM1462416 c.2473C>T p.R825W Substitution - Missense 9:37518166-37518166 - TCGA-AA-3672-01 COSM266527 c.656G>A p.G219D Substitution - Missense 9:37537873-37537873 - TCGA-B5-A11E-01 COSM1109006 c.1400G>A p.R467Q Substitution - Missense 9:37537129-37537129 - HCC68 COSM1624995 c.2800C>T p.Q934* Substitution - Nonsense 9:37512636-37512636 - OSCC-GB_00730111 COSM4889036 c.684C>G p.F228L Substitution - Missense 9:37537845-37537845 - TCGA-D1-A103-01 COSM1109001 c.2588G>A p.R863H Substitution - Missense 9:37516030-37516030 - 86793 COSM94281 c.1829G>T p.G610V Substitution - Missense 9:37522926-37522926 - 2334196 COSM320377 c.2624A>T p.Q875L Substitution - Missense 9:37515994-37515994 - 86319 COSM94283 c.116G>A p.S39N Substitution - Missense 9:37541653-37541653 - LC_C28 COSM1187723 c.2588G>T p.R863L Substitution - Missense 9:37516030-37516030 - Gp5D COSM2775726 c.347G>A p.R116H Substitution - Missense 9:37541422-37541422 - 631076 COSM325329 c.483G>T p.L161F Substitution - Missense 9:37541286-37541286 - LUAD-NYU284 COSM373377 c.1607T>C p.V536A Substitution - Missense 9:37529223-37529223 - TCGA-AD-6964-01 COSM1462421 c.1877G>T p.G626V Substitution - Missense 9:37522878-37522878 - PT35 COSM5912910 c.1612C>T p.L538F Substitution - Missense 9:37529218-37529218 - TCGA-CC-5260-01 COSM4937496 c.2286G>A p.V762V Substitution - coding silent 9:37518353-37518353 - TCGA-EE-A185-06 COSM3657387 c.2706C>T p.F902F Substitution - coding silent 9:37515912-37515912 - TCGA-BQ-5882-01 COSM3996556 c.1219C>A p.L407M Substitution - Missense 9:37537310-37537310 - TCGA-BR-8078-01 COSM186953 c.2546G>A p.R849Q Substitution - Missense 9:37516072-37516072 - YUPAER COSM5411083 c.212G>A p.W71* Substitution - Nonsense 9:37541557-37541557 - T1154 COSM4683908 c.2729G>A p.R910H Substitution - Missense 9:37512707-37512707 - TCGA-BP-5201-01 COSM1497055 c.2474G>A p.R825Q Substitution - Missense 9:37518165-37518165 - AOCS-137-1-X COSM4152301 c.2462T>A p.I821N Substitution - Missense 9:37518177-37518177 - TCGA-AA-A02W-01 COSM300961 c.711C>T p.N237N Substitution - coding silent 9:37537818-37537818 - TCGA-IR-A3LA-01 COSM4845002 c.669G>A p.V223V Substitution - coding silent 9:37537860-37537860 - T3603 COSM4683910 c.2458G>A p.D820N Substitution - Missense 9:37518181-37518181 - SNU-C2B COSM2775724 c.382G>A p.A128T Substitution - Missense 9:37541387-37541387 - CSCC-10-T COSM2775708 c.1318G>A p.G440R Substitution - Missense 9:37537211-37537211 - SW48 COSM1109011 c.423C>T p.Y141Y Substitution - coding silent 9:37541346-37541346 - SNU_09_S1 COSM4420034 c.1279G>A p.V427M Substitution - Missense 9:37537250-37537250 - BD165T COSM5506280 c.2532+7C>T p.? Unknown 9:37518100-37518100 - TCGA-AA-A010-01 COSM281087 c.2541G>T p.K847N Substitution - Missense 9:37516077-37516077 - TCGA-AX-A0J0-01 COSM1109014 c.23T>C p.L8S Substitution - Missense 9:37541746-37541746 - PTC-14C COSM4163861 c.918A>C p.P306P Substitution - coding silent 9:37537611-37537611 - HCC169T COSM3664359 c.2295C>T p.S765S Substitution - coding silent 9:37518344-37518344 - TCGA-BR-8487-01 COSM2775695 c.2101G>A p.A701T Substitution - Missense 9:37521668-37521668 - T3145 COSM4463146 c.1278C>T p.S426S Substitution - coding silent 9:37537251-37537251 - TCGA-B5-A11Y-01 COSM1109010 c.1062C>T p.S354S Substitution - coding silent 9:37537467-37537467 - CSCC-11-T COSM4513041 c.924C>T p.T308T Substitution - coding silent 9:37537605-37537605 - TCGA-AZ-4315-01 COSM1462424 c.320G>A p.R107Q Substitution - Missense 9:37541449-37541449 - P09-2497 COSM244467 c.2136C>T p.D712D Substitution - coding silent 9:37521633-37521633 - J73_T COSM3952718 c.457G>C p.V153L Substitution - Missense 9:37541312-37541312 - TCGA-D1-A103-01 COSM1109003 c.1929C>T p.Y643Y Substitution - coding silent 9:37522826-37522826 - 49M COSM5590954 c.345C>T p.G115G Substitution - coding silent 9:37541424-37541424 - TCGA-BR-6452-01 COSM3907378 c.1931-1G>A p.? Unknown 9:37521839-37521839 - CHC433T COSM3763931 c.969C>T p.A323A Substitution - coding silent 9:37537560-37537560 - TCGA-AZ-6601-01 COSM244467 c.2136C>T p.D712D Substitution - coding silent 9:37521633-37521633 - T3064 COSM4683913 c.34C>T p.R12C Substitution - Missense 9:37541735-37541735 - Pat_58_B COSM5876249 c.2137G>A p.D713N Substitution - Missense 9:37521632-37521632 - 18 COSM5745041 c.547G>A p.V183I Substitution - Missense 9:37541222-37541222 - RK308_C01 COSM3746004 c.1379G>A p.R460Q Substitution - Missense 9:37537150-37537150 - TCGA-BR-8380-01 COSM3907377 c.2140C>A p.P714T Substitution - Missense 9:37521629-37521629 - TCGA-G4-6320-01 COSM3699689 c.476G>A p.G159E Substitution - Missense 9:37541293-37541293 - TCGA-22-4595-01 COSM753427 c.14G>T p.G5V Substitution - Missense 9:37541755-37541755 - TCGA-AP-A051-01 COSM1109008 c.1329C>T p.G443G Substitution - coding silent 9:37537200-37537200 - CHC2200T COSM4952961 c.67C>G p.L23V Substitution - Missense 9:37541702-37541702 - Pat_28_B COSM5876251 c.1021G>A p.G341S Substitution - Missense 9:37537508-37537508 - 0076_CRUK_PC_0076_T1_DNA COSM5422746 c.1393G>T p.A465S Substitution - Missense 9:37537136-37537136 - HCC68T COSM1624995 c.2800C>T p.Q934* Substitution - Nonsense 9:37512636-37512636 - sysucc-882T COSM5447857 c.278A>C p.E93A Substitution - Missense 9:37541491-37541491 - PCSI_0465_Pa_P_526 COSM4964551 c.130C>T p.R44C Substitution - Missense 9:37541639-37541639 - CHC1211T COSM4954999 c.138G>A p.R46R Substitution - coding silent 9:37541631-37541631 - T3225 COSM4683912 c.1543C>T p.R515W Substitution - Missense 9:37531935-37531935 - C086 COSM5531102 c.1835C>T p.P612L Substitution - Missense 9:37522920-37522920 - TCGA-FS-A1ZZ-06 COSM3657393 c.1311C>T p.F437F Substitution - coding silent 9:37537218-37537218 - PT33 COSM5908914 c.1834C>T p.P612S Substitution - Missense 9:37522921-37522921 - TCGA-AP-A059-01 COSM1109007 c.1335C>T p.F445F Substitution - coding silent 9:37537194-37537194 - TCGA-EJ-5515-01 COSM1472300 c.2614A>G p.I872V Substitution - Missense 9:37516004-37516004 - HN_62493 COSM123117 c.2170G>A p.V724I Substitution - Missense 9:37521599-37521599 - 19M COSM5578561 c.2057C>T p.P686L Substitution - Missense 9:37521712-37521712 - TCGA-AP-A0LM-01 COSM1109007 c.1335C>T p.F445F Substitution - coding silent 9:37537194-37537194 - 112281 COSM94280 c.2191C>T p.H731Y Substitution - Missense 9:37521578-37521578 - QC2-03-T2 COSM5651753 c.883C>G p.L295V Substitution - Missense 9:37537646-37537646 - LXFL529 COSM1197170 c.1766G>A p.G589D Substitution - Missense 9:37525113-37525113 - 86503 COSM94282 c.1159G>T p.G387C Substitution - Missense 9:37537370-37537370 - TCGA-EE-A184-06 COSM3657390 c.2111G>T p.W704L Substitution - Missense 9:37521658-37521658 - 587234 COSM1206791 c.2723C>T p.T908M Substitution - Missense 9:37512713-37512713 - HX26T COSM3664360 c.1669G>A p.G557S Substitution - Missense 9:37529161-37529161 - TCGA-D3-A5GO-06 COSM3657389 c.2131G>A p.E711K Substitution - Missense 9:37521638-37521638 - CRC-02T COSM5455786 c.1089G>A p.E363E Substitution - coding silent 9:37537440-37537440 - TCGA-39-5031-01 COSM753428 c.558A>T p.P186P Substitution - coding silent 9:37541211-37541211 - TCGA-AD-6889-01 COSM1462418 c.2289C>A p.A763A Substitution - coding silent 9:37518350-37518350 - ESO-859 COSM1238872 c.679A>G p.T227A Substitution - Missense 9:37537850-37537850 - TCGA-BS-A0UF-01 COSM1108998 c.2768C>A p.S923Y Substitution - Missense 9:37512668-37512668 - CSCC-31-T COSM4463146 c.1278C>T p.S426S Substitution - coding silent 9:37537251-37537251 - I2L-P7-Tumor-Organoid COSM5359542 c.1410T>C p.H470H Substitution - coding silent 9:37537119-37537119 - TCGA-CU-A3YL-01 COSM3780014 c.1237G>C p.E413Q Substitution - Missense 9:37537292-37537292 - TCGA-D1-A17H-01 COSM1109012 c.230A>G p.Q77R Substitution - Missense 9:37541539-37541539 - XHDG32 COSM4769363 c.2116A>T p.T706S Substitution - Missense 9:37521653-37521653 - 8035125 COSM3395817 c.285C>T p.S95S Substitution - coding silent 9:37541484-37541484 - TCGA-CG-4306-01 COSM3907381 c.368G>A p.S123N Substitution - Missense 9:37541401-37541401 - LUAD-S00488 COSM395394 c.1054G>T p.D352Y Substitution - Missense 9:37537475-37537475 - TCGA-EL-A3N2-01 COSM3375245 c.724G>A p.V242I Substitution - Missense 9:37537805-37537805 - TCGA-D1-A103-01 COSM1109009 c.1298G>A p.R433H Substitution - Missense 9:37537231-37537231 - TCGA-EE-A3AG-06 COSM3657388 c.2136C>G p.D712E Substitution - Missense 9:37521633-37521633 - TCGA-D9-A6EC-06 COSM4402775 c.2842G>A p.E948K Substitution - Missense 9:37512594-37512594 - CSCC-46-T COSM4537754 c.2458G>C p.D820H Substitution - Missense 9:37518181-37518181 - ESCC_BICR_054T COSM5444350 c.634C>A p.H212N Substitution - Missense 9:37537895-37537895 - ESO-859 COSM1238873 c.2259C>T p.H753H Substitution - coding silent 9:37518380-37518380 - TCGA-BR-4201-01 COSM3907380 c.1312C>T p.R438W Substitution - Missense 9:37537217-37537217 - HCT8 COSM2775691 c.2380C>T p.L794F Substitution - Missense 9:37518259-37518259 - 8034048 COSM3395816 c.1330G>A p.V444I Substitution - Missense 9:37537199-37537199 - CHC2200T COSM4952961 c.67C>G p.L23V Substitution - Missense 9:37541702-37541702 - AOCS-094-1-1 COSM4152302 c.668T>C p.V223A Substitution - Missense 9:37537861-37537861 - TP_2009 COSM5561954 c.717C>A p.P239P Substitution - coding silent 9:37537812-37537812 - C086 COSM5531101 c.413C>T p.P138L Substitution - Missense 9:37541356-37541356 - HCC169 COSM3664359 c.2295C>T p.S765S Substitution - coding silent 9:37518344-37518344 - TCGA-76-6286-01 COSM1109000 c.2616C>A p.I872I Substitution - coding silent 9:37516002-37516002 - EGC15 COSM5063978 c.1485C>T p.G495G Substitution - coding silent 9:37531993-37531993 - TCGA-BR-8589-01 COSM3907376 c.2514A>G p.K838K Substitution - coding silent 9:37518125-37518125 - TCGA-D1-A16X-01 COSM1109011 c.423C>T p.Y141Y Substitution - coding silent 9:37541346-37541346 - TCGA-EE-A3AE-06 COSM2775708 c.1318G>A p.G440R Substitution - Missense 9:37537211-37537211 - 86319 COSM95882 c.1662G>A p.K554K Substitution - coding silent 9:37529168-37529168 - TCGA-E2-A15M-01 COSM455956 c.939C>T p.I313I Substitution - coding silent 9:37537590-37537590 - PCSI_0090_Pa_P COSM3382531 c.1122A>G p.L374L Substitution - coding silent 9:37537407-37537407 - TCGA-ER-A194-01 COSM3657398 c.21C>T p.P7P Substitution - coding silent 9:37541748-37541748 - LUAD-B02077 COSM356280 c.1099G>T p.E367* Substitution - Nonsense 9:37537430-37537430 - TCGA-33-4532-01 COSM753430 c.2581C>T p.R861W Substitution - Missense 9:37516037-37516037 - TARGET-20-PARENB-09A-02D COSM5487190 c.2150G>A p.R717Q Substitution - Missense 9:37521619-37521619 - TCGA-06-5417-01 COSM3413653 c.1868A>G p.Y623C Substitution - Missense 9:37522887-37522887 - OSCC-GB_00460111 COSM3657390 c.2111G>T p.W704L Substitution - Missense 9:37521658-37521658 - DLD1 COSM2775691 c.2380C>T p.L794F Substitution - Missense 9:37518259-37518259 - Pat_06_B COSM5876250 c.1297C>T p.R433C Substitution - Missense 9:37537232-37537232 - STC252 COSM5063980 c.159C>T p.T53T Substitution - coding silent 9:37541610-37541610 - TCGA-GF-A6C9-06 COSM4900947 c.2292G>A p.Q764Q Substitution - coding silent 9:37518347-37518347 - TCGA-D1-A17Q-01 COSM1108998 c.2768C>A p.S923Y Substitution - Missense 9:37512668-37512668 - T276 COSM1497055 c.2474G>A p.R825Q Substitution - Missense 9:37518165-37518165 - TCGA-AP-A0LD-01 COSM1109013 c.33G>A p.W11* Substitution - Nonsense 9:37541736-37541736 - TCGA-F5-6814-01 COSM3433139 c.1778-1G>T p.? Unknown 9:37522978-37522978 - DN14011 COSM5962302 c.2643C>A p.T881T Substitution - coding silent 9:37515975-37515975 - TCGA-CG-5728-01 COSM3907379 c.1458G>A p.A486A Substitution - coding silent 9:37532020-37532020 - TCGA-FI-A2EX-01 COSM1109004 c.1790G>A p.R597H Substitution - Missense 9:37522965-37522965 - TCGA-EE-A29R-06 COSM3657392 c.1798C>T p.Q600* Substitution - Nonsense 9:37522957-37522957 - PT08_2 COSM5893361 c.881C>T p.S294F Substitution - Missense 9:37537648-37537648 - TCGA-DA-A1IC-06 COSM3657395 c.1194C>T p.S398S Substitution - coding silent 9:37537335-37537335 - TCGA-GN-A266-06 COSM2775685 c.2616C>T p.I872I Substitution - coding silent 9:37516002-37516002 - TCGA-CC-A7IK-01 COSM4924979 c.192A>G p.P64P Substitution - coding silent 9:37541577-37541577 - TCGA-CK-5913-01 COSM1462417 c.2392G>T p.G798C Substitution - Missense 9:37518247-37518247 - S48_post COSM5574628 c.1681C>A p.L561M Substitution - Missense 9:37529149-37529149 - TCGA-D8-A1JL-01 COSM1490025 c.2173G>C p.E725Q Substitution - Missense 9:37521596-37521596 - TCGA-AP-A0LM-01 COSM1109000 c.2616C>A p.I872I Substitution - coding silent 9:37516002-37516002 - 46T COSM3657390 c.2111G>T p.W704L Substitution - Missense 9:37521658-37521658 - 18D COSM1235227 c.1520A>G p.N507S Substitution - Missense 9:37531958-37531958 - T3255 COSM3395816 c.1330G>A p.V444I Substitution - Missense 9:37537199-37537199 - PT13 COSM5896002 c.2297G>A p.S766N Substitution - Missense 9:37518342-37518342 - CHC609T COSM4950611 c.2851T>C p.Y951H Substitution - Missense 9:37512585-37512585 - TCGA-CM-6171-01 COSM1462419 c.2149C>T p.R717W Substitution - Missense 9:37521620-37521620 - MO_1012 COSM4964551 c.130C>T p.R44C Substitution - Missense 9:37541639-37541639 - TCGA-BS-A0UV-01 COSM1108999 c.2619C>A p.I873I Substitution - coding silent 9:37515999-37515999 - TCGA-AX-A060-01 COSM1109002 c.2089G>A p.E697K Substitution - Missense 9:37521680-37521680 - AOCS-094-6-X COSM4152302 c.668T>C p.V223A Substitution - Missense 9:37537861-37537861 - T2269 COSM4683909 c.2550C>T p.I850I Substitution - coding silent 9:37516068-37516068 - TCGA-AA-A02Y-01 COSM301037 c.2009T>A p.L670Q Substitution - Missense 9:37521760-37521760 - pfg057T COSM4753023 c.1465A>G p.I489V Substitution - Missense 9:37532013-37532013 - TCGA-CD-A4MG-01 COSM3907375 c.2578G>A p.V860M Substitution - Missense 9:37516040-37516040 - ESCC_5 COSM5623304 c.1038G>T p.R346S Substitution - Missense 9:37537491-37537491 - Pat_58_A COSM5876249 c.2137G>A p.D713N Substitution - Missense 9:37521632-37521632 - KM12 COSM1462416 c.2473C>T p.R825W Substitution - Missense 9:37518166-37518166 - C32 COSM4619347 c.2681T>C p.M894T Substitution - Missense 9:37515937-37515937 - TCGA-G4-6628-01 COSM1462420 c.1881G>T p.V627V Substitution - coding silent 9:37522874-37522874 - CRC-10T COSM5457734 c.2384G>A p.R795Q Substitution - Missense 9:37518255-37518255 - TCGA-G4-6320-01 COSM3699688 c.2261C>T p.A754V Substitution - Missense 9:37518378-37518378 - PT08_1 COSM5893361 c.881C>T p.S294F Substitution - Missense 9:37537648-37537648 - SJHGG003_A COSM4968845 c.323G>A p.R108H Substitution - Missense 9:37541446-37541446 - C91 COSM4445200 c.2363C>T p.A788V Substitution - Missense 9:37518276-37518276 - CSCC-20-T COSM4459919 c.1146C>T p.R382R Substitution - coding silent 9:37537383-37537383 - TCGA-GN-A26A-06 COSM3657391 c.2059C>T p.R687* Substitution - Nonsense 9:37521710-37521710 - Pat_53_B COSM5876248 c.2714+2T>G p.? Unknown 9:37515902-37515902 - TCGA-EE-A2GC-06 COSM3657394 c.1277C>T p.S426F Substitution - Missense 9:37537252-37537252 - PCSI_0090_Pa_X COSM3382531 c.1122A>G p.L374L Substitution - coding silent 9:37537407-37537407 - TCGA-AM-5820-01 COSM3763931 c.969C>T p.A323A Substitution - coding silent 9:37537560-37537560 - TCGA-A6-5661-01 COSM1462422 c.1454G>A p.R485Q Substitution - Missense 9:37532024-37532024 - TCGA-21-5786-01 COSM753429 c.1170G>A p.L390L Substitution - coding silent 9:37537359-37537359 - TCGA-EB-A1NK-01 COSM3657397 c.96C>T p.A32A Substitution - coding silent 9:37541673-37541673 - S02294 COSM5688947 c.1160G>T p.G387V Substitution - Missense 9:37537369-37537369 - TCGA-BS-A0UV-01 COSM1109011 c.423C>T p.Y141Y Substitution - coding silent 9:37541346-37541346 - ICGC_MB66 COSM3765457 c.1777+4C>T p.? Unknown 9:37525098-37525098 - T28 COSM3763931 c.969C>T p.A323A Substitution - coding silent 9:37537560-37537560 - 2334192 COSM320376 c.1451G>C p.C484S Substitution - Missense 9:37532027-37532027 - ESO-0009 COSM1252247 c.2112G>A p.W704* Substitution - Nonsense 9:37521657-37521657 - J33_T COSM4139374 c.247A>C p.K83Q Substitution - Missense 9:37541522-37541522 - CHC609T COSM4950611 c.2851T>C p.Y951H Substitution - Missense 9:37512585-37512585 - MO_1179 COSM5561895 c.653C>T p.P218L Substitution - Missense 9:37537876-37537876 - HCT15 COSM2775691 c.2380C>T p.L794F Substitution - Missense 9:37518259-37518259 - TCGA-CG-5721-01 COSM3907382 c.317A>G p.E106G Substitution - Missense 9:37541452-37541452 - 220 COSM4425287 c.2174A>T p.E725V Substitution - Missense 9:37521595-37521595 - T3724 COSM4683911 c.1550delA p.K517fs*52 Deletion - Frameshift 9:37531928-37531928 - DN14011 COSM5962344 c.2644A>T p.I882F Substitution - Missense 9:37515974-37515974 - SNU-C2B COSM2775714 c.899G>A p.R300Q Substitution - Missense 9:37537630-37537630 - TCGA-BP-4354-01 COSM3367719 c.1152A>T p.V384V Substitution - coding silent 9:37537377-37537377 - TCGA-D1-A101-01 COSM1109005 c.1730G>A p.R577H Substitution - Missense 9:37525149-37525149 - 260211 COSM325329 c.483G>T p.L161F Substitution - Missense 9:37541286-37541286 - TCGA-CG-4469-01 COSM3907383 c.4G>A p.E2K Substitution - Missense 9:37541765-37541765 - AOCS-137-3-7 COSM4152301 c.2462T>A p.I821N Substitution - Missense 9:37518177-37518177 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.709527 9p13.2 609092

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.I504M c.1512T>G 9 37531963 HNSC A T Missense p.L670Q c.2009T>A 9 37521757 COREAD C A 3-UTRSNV . c.2868+111G>T 9 37512436 HC C A Missense p.G5V c.14G>T 9 37541752 LUSC C A Missense p.L161F c.483G>T 9 37541283 SCLC C A Missense p.W704L c.2111G>T 9 37521655 CM C G Missense p.C484S c.1451G>C 9 37532024 SCLC C G Missense p.D132H c.394G>C 9 37541372 LUAD C G Missense p.E244Q c.730G>C 9 37537796 HNSC C G Missense p.E725Q c.2173G>C 9 37521593 BRCA C T Missense p.E2K c.4G>A 9 37541762 STAD C T Missense p.E697K c.2089G>A 9 37521677 UCEC C T Missense p.G440R c.1318G>A 9 37537208 CM C T Missense p.R133Q c.398G>A 9 37541368 CM C T Missense p.R577H c.1730G>A 9 37525146 UCEC C T Missense p.R770Q c.2309G>A 9 37518327 HNSC C T Missense p.S123N c.368G>A 9 37541398 STAD C T Missense p.V242I c.724G>A 9 37537802 THCA C T Missense p.V724I c.2170G>A 9 37521596 HNSC C T Nonsense p.W704* c.2112G>A 9 37521654 ESCA C T Synonymous p.A486A c.1458G>A 9 37532017 STAD C T Synonymous p.K418K c.1254G>A 9 37537272 LUAD C T Synonymous p.L390L c.1170G>A 9 37537356 LUSC C T Synonymous p.T935T c.2805G>A 9 37512610 HNSC G A Missense p.R438W c.1312C>T 9 37537214 STAD G A Missense p.R855W c.2563C>T 9 37516034 LUSC G A Missense p.S426F c.1277C>T 9 37537249 CM G A Nonsense p.Q600* c.1798C>T 9 37522954 CM G A Nonsense p.R687* c.2059C>T 9 37521707 CM G A Synonymous p.A32A c.96C>T 9 37541670 CM G A Synonymous p.F137F c.411C>T 9 37541355 CM G A Synonymous p.F437F c.1311C>T 9 37537215 CM G A Synonymous p.F896F c.2688C>T 9 37515909 CM G A Synonymous p.I313I c.939C>T 9 37537587 BRCA G A Synonymous p.L670L c.2008C>T 9 37521758 HNSC G A Synonymous p.N237N c.711C>T 9 37537815 COREAD G A Synonymous p.P7P c.21C>T 9 37541745 CM G A Synonymous p.S354S c.1062C>T 9 37537464 UCEC G A Synonymous p.S398S c.1194C>T 9 37537332 CM G A Synonymous p.S518S c.1554C>T 9 37531921 CM G C Missense p.D712E c.2136C>G 9 37521630 CM G C Synonymous p.L918L c.2754C>G 9 37512661 HNSC GT AA Missense p.T185L c.553_554delinsTT 9 37541212 CM G T Synonymous p.I866I c.2598C>A 9 37515999 GBM T A Missense p.H845L c.2534A>T 9 37516063 LUAD T A Missense p.Q869L c.2606A>T 9 37515991 SCLC T A Missense p.T769S c.2305A>T 9 37518331 HNSC T A Synonymous p.P186P c.558A>T 9 37541208 LUSC T C Missense p.I866V c.2596A>G 9 37516001 PRAD T C Missense p.T227A c.679A>G 9 37537847 ESCA T C Missense p.Y623C c.1868A>G 9 37522884 GBM T G Missense p.S947R c.2839A>C 9 37512576 BRCA