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 BLCA 1 154987446 154987446 + Missense_Mutation SNP G G C TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr1:154987446G>C c.310G>C c.(310-312)Gaa>Caa p.E104Q BLCA 1 154987500 154987500 + Missense_Mutation SNP C C T TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr1:154987500C>T c.364C>T c.(364-366)Ctc>Ttc p.L122F BLCA 1 154988052 154988052 + Missense_Mutation SNP G G A TCGA-GD-A76B-01A-11D-A32B-08 TCGA-GD-A76B-10A-01D-A329-08 g.chr1:154988052G>A c.916G>A c.(916-918)Gat>Aat p.D306N BLCA 1 154988052 154988052 + Missense_Mutation SNP G G C TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr1:154988052G>C c.916G>C c.(916-918)Gat>Cat p.D306H BLCA 1 154988172 154988172 + Nonsense_Mutation SNP C C T TCGA-UY-A9PF-01A-11D-A38G-08 TCGA-UY-A9PF-10A-01D-A38J-08 g.chr1:154988172C>T c.1036C>T c.(1036-1038)Cag>Tag p.Q346* BLCA 1 154988201 154988201 + Frame_Shift_Del DEL C C - TCGA-4Z-AA89-01A-11D-A391-08 TCGA-4Z-AA89-10A-01D-A394-08 g.chr1:154988201delC c.1065delC c.(1063-1065)atcfs p.I355fs BLCA 1 154988247 154988247 + Missense_Mutation SNP G G A TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr1:154988247G>A c.1111G>A c.(1111-1113)Gag>Aag p.E371K BLCA 1 154988705 154988705 + Missense_Mutation SNP G G C TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr1:154988705G>C c.1164G>C c.(1162-1164)aaG>aaC p.K388N BLCA 1 154988705 154988705 + Missense_Mutation SNP G G T TCGA-FD-A3B7-01A-31D-A20D-08 TCGA-FD-A3B7-10A-01D-A20D-08 g.chr1:154988705G>T c.1164G>T c.(1162-1164)aaG>aaT p.K388N BLCA 1 154988705 154988705 + Missense_Mutation SNP G G T TCGA-KQ-A41N-01A-11D-A339-08 TCGA-KQ-A41N-10D-01D-A339-08 g.chr1:154988705G>T c.1164G>T c.(1162-1164)aaG>aaT p.K388N BLCA 1 154988787 154988787 + Missense_Mutation SNP G G A TCGA-GV-A40E-01A-12D-A23M-08 TCGA-GV-A40E-10A-01D-A23K-08 g.chr1:154988787G>A c.1246G>A c.(1246-1248)Gac>Aac p.D416N BLCA 1 154988787 154988787 + Missense_Mutation SNP G G C TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr1:154988787G>C c.1246G>C c.(1246-1248)Gac>Cac p.D416H BLCA 1 154988999 154988999 + Silent SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr1:154988999C>T c.1458C>T c.(1456-1458)ctC>ctT p.L486L BRCA 1 154987144 154987144 + Missense_Mutation SNP G G A TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr1:154987144G>A c.8G>A c.(7-9)aGc>aAc p.S3N BRCA 1 154987160 154987160 + Silent SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr1:154987160G>C c.24G>C c.(22-24)ctG>ctC p.L8L BRCA 1 154988894 154988894 + Silent SNP C C A TCGA-A7-A4SF-01A-11D-A25Q-09 TCGA-A7-A4SF-10A-01D-A25Q-09 g.chr1:154988894C>A c.1353C>A c.(1351-1353)ggC>ggA p.G451G CESC 1 154987929 154987929 + Missense_Mutation SNP G G A TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr1:154987929G>A c.793G>A c.(793-795)Gag>Aag p.E265K COAD 1 154987308 154987308 + Missense_Mutation SNP T T C TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr1:154987308T>C c.172T>C c.(172-174)Tac>Cac p.Y58H COAD 1 154987403 154987403 + Nonsense_Mutation SNP T T A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr1:154987403T>A c.267T>A c.(265-267)tgT>tgA p.C89* COAD 1 154987865 154987865 + Silent SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr1:154987865C>T c.729C>T c.(727-729)ggC>ggT p.G243G COAD 1 154987872 154987872 + Frame_Shift_Del DEL G G - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr1:154987872delG c.736delG c.(736-738)gggfs p.G247fs COAD 1 154987965 154987967 + In_Frame_Del DEL GAA GAA - TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr1:154987965_154987967delGAA c.829_831delGAA c.(829-831)gaadel p.E281del COAD 1 154988002 154988002 + Missense_Mutation SNP G G T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr1:154988002G>T c.866G>T c.(865-867)gGg>gTg p.G289V COAD 1 154988154 154988154 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr1:154988154C>T c.1018C>T c.(1018-1020)Cgc>Tgc p.R340C COAD 1 154988273 154988273 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr1:154988273C>T c.1137C>T c.(1135-1137)tgC>tgT p.C379C COAD 1 154988698 154988700 + In_Frame_Del DEL ACG ACG - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr1:154988698_154988700delACG c.1157_1159delACG c.(1156-1161)aacgac>aac p.D387del COADREAD 1 154987308 154987308 + Missense_Mutation SNP T T C TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr1:154987308T>C c.172T>C c.(172-174)Tac>Cac p.Y58H COADREAD 1 154987403 154987403 + Nonsense_Mutation SNP T T A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr1:154987403T>A c.267T>A c.(265-267)tgT>tgA p.C89* COADREAD 1 154987865 154987865 + Silent SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr1:154987865C>T c.729C>T c.(727-729)ggC>ggT p.G243G COADREAD 1 154987872 154987872 + Frame_Shift_Del DEL G G - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr1:154987872delG c.736delG c.(736-738)gggfs p.G247fs COADREAD 1 154987965 154987967 + In_Frame_Del DEL GAA GAA - TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr1:154987965_154987967delGAA c.829_831delGAA c.(829-831)gaadel p.E281del COADREAD 1 154988002 154988002 + Missense_Mutation SNP G G T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr1:154988002G>T c.866G>T c.(865-867)gGg>gTg p.G289V COADREAD 1 154988154 154988154 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr1:154988154C>T c.1018C>T c.(1018-1020)Cgc>Tgc p.R340C COADREAD 1 154988273 154988273 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr1:154988273C>T c.1137C>T c.(1135-1137)tgC>tgT p.C379C COADREAD 1 154988698 154988700 + In_Frame_Del DEL ACG ACG - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr1:154988698_154988700delACG c.1157_1159delACG c.(1156-1161)aacgac>aac p.D387del DLBC 1 154987363 154987363 + Missense_Mutation SNP G G T TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr1:154987363G>T c.227G>T c.(226-228)gGt>gTt p.G76V ESCA 1 154987149 154987149 + Missense_Mutation SNP G G A TCGA-V5-AASX-01A-11D-A387-09 TCGA-V5-AASX-10A-01D-A38A-09 g.chr1:154987149G>A c.13G>A c.(13-15)Gag>Aag p.E5K ESCA 1 154987266 154987266 + Missense_Mutation SNP G G C TCGA-Z6-AAPN-01A-11D-A403-09 TCGA-Z6-AAPN-10A-01D-A403-09 g.chr1:154987266G>C c.130G>C c.(130-132)Gaa>Caa p.E44Q ESCA 1 154987372 154987372 + Missense_Mutation SNP C C T TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr1:154987372C>T c.236C>T c.(235-237)aCg>aTg p.T79M ESCA 1 154987712 154987712 + Silent SNP G G T TCGA-2H-A9GI-01A-11D-A37C-09 TCGA-2H-A9GI-11A-11D-A37F-09 g.chr1:154987712G>T c.576G>T c.(574-576)ccG>ccT p.P192P ESCA 1 154987852 154987852 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr1:154987852C>T c.716C>T c.(715-717)gCg>gTg p.A239V ESCA 1 154987921 154987921 + Missense_Mutation SNP C C T TCGA-V5-AASW-01A-11D-A403-09 TCGA-V5-AASW-10A-01D-A403-09 g.chr1:154987921C>T c.785C>T c.(784-786)tCc>tTc p.S262F ESCA 1 154988714 154988714 + Frame_Shift_Del DEL C C - TCGA-2H-A9GJ-01A-11D-A37C-09 TCGA-2H-A9GJ-11A-11D-A37F-09 g.chr1:154988714delC c.1173delC c.(1171-1173)atcfs p.I391fs GBM 1 154987218 154987218 + Missense_Mutation SNP C C T TCGA-74-6578-01A-11D-1845-08 TCGA-74-6578-10A-01D-1845-08 g.chr1:154987218C>T c.82C>T c.(82-84)Cgc>Tgc p.R28C GBMLGG 1 154987218 154987218 + Missense_Mutation SNP C C T TCGA-74-6578-01A-11D-1845-08 TCGA-74-6578-10A-01D-1845-08 g.chr1:154987218C>T c.82C>T c.(82-84)Cgc>Tgc p.R28C GBMLGG 1 154988695 154988695 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:154988695G>T c.e4-1 GBMLGG 1 154988753 154988753 + Silent SNP C C T TCGA-HT-7602-01A-21D-2086-08 TCGA-HT-7602-10A-01D-2086-08 g.chr1:154988753C>T c.1212C>T c.(1210-1212)tgC>tgT p.C404C HNSC 1 154987239 154987239 + Missense_Mutation SNP G G A TCGA-UF-A7JV-01A-11D-A34J-08 TCGA-UF-A7JV-10A-01D-A34M-08 g.chr1:154987239G>A c.103G>A c.(103-105)Gac>Aac p.D35N HNSC 1 154987574 154987574 + Silent SNP A A C TCGA-BA-6871-01A-11D-1870-08 TCGA-BA-6871-10A-01D-1870-08 g.chr1:154987574A>C c.438A>C c.(436-438)ctA>ctC p.L146L HNSC 1 154987971 154987971 + Missense_Mutation SNP G G A TCGA-CR-7385-01A-11D-2012-08 TCGA-CR-7385-10A-01D-2013-08 g.chr1:154987971G>A c.835G>A c.(835-837)Gaa>Aaa p.E279K HNSC 1 154988249 154988249 + Missense_Mutation SNP G G C TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr1:154988249G>C c.1113G>C c.(1111-1113)gaG>gaC p.E371D KIPAN 1 154987232 154987232 + Missense_Mutation SNP C C G TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr1:154987232C>G c.96C>G c.(94-96)caC>caG p.H32Q KIPAN 1 154987953 154987953 + Missense_Mutation SNP T T A TCGA-UZ-A9PP-01A-11D-A42J-10 TCGA-UZ-A9PP-10A-01D-A42M-10 g.chr1:154987953T>A c.817T>A c.(817-819)Tat>Aat p.Y273N KIRP 1 154987232 154987232 + Missense_Mutation SNP C C G TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr1:154987232C>G c.96C>G c.(94-96)caC>caG p.H32Q KIRP 1 154987953 154987953 + Missense_Mutation SNP T T A TCGA-UZ-A9PP-01A-11D-A42J-10 TCGA-UZ-A9PP-10A-01D-A42M-10 g.chr1:154987953T>A c.817T>A c.(817-819)Tat>Aat p.Y273N LAML 1 154987446 154987446 + Missense_Mutation SNP G G A TCGA-AB-2910-03A-01W-0745-08 TCGA-AB-2910-11A-01W-0745-08 g.chr1:154987446G>A c.310G>A c.(310-312)Gaa>Aaa p.E104K LGG 1 154988695 154988695 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr1:154988695G>T c.e4-1 LGG 1 154988753 154988753 + Silent SNP C C T TCGA-HT-7602-01A-21D-2086-08 TCGA-HT-7602-10A-01D-2086-08 g.chr1:154988753C>T c.1212C>T c.(1210-1212)tgC>tgT p.C404C LIHC 1 154987493 154987493 + Silent SNP A A G TCGA-DD-AAVY-01A-11D-A40R-10 TCGA-DD-AAVY-10A-01D-A40U-10 g.chr1:154987493A>G c.357A>G c.(355-357)ccA>ccG p.P119P LIHC 1 154988092 154988092 + Missense_Mutation SNP G G A TCGA-DD-A115-01A-11D-A12Z-10 TCGA-DD-A115-10A-01D-A12Z-10 g.chr1:154988092G>A c.956G>A c.(955-957)aGc>aAc p.S319N LIHC 1 154988092 154988092 + Missense_Mutation SNP G G A TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr1:154988092G>A c.956G>A c.(955-957)aGc>aAc p.S319N LUAD 1 154987712 154987712 + Silent SNP G G T TCGA-49-4486-01A-01D-1265-08 TCGA-49-4486-11A-01D-1265-08 g.chr1:154987712G>T c.576G>T c.(574-576)ccG>ccT p.P192P LUAD 1 154987854 154987854 + Missense_Mutation SNP G G T TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr1:154987854G>T c.718G>T c.(718-720)Ggc>Tgc p.G240C LUAD 1 154987882 154987882 + Missense_Mutation SNP G G A TCGA-44-6775-01A-11D-1855-08 TCGA-44-6775-10A-01D-1855-08 g.chr1:154987882G>A c.746G>A c.(745-747)gGg>gAg p.G249E LUAD 1 154987926 154987926 + Missense_Mutation SNP C C T TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr1:154987926C>T c.790C>T c.(790-792)Cct>Tct p.P264S LUAD 1 154988082 154988082 + Missense_Mutation SNP G G T TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr1:154988082G>T c.946G>T c.(946-948)Gcc>Tcc p.A316S LUAD 1 154988244 154988244 + Missense_Mutation SNP G G C TCGA-53-A4EZ-01A-12D-A24P-08 TCGA-53-A4EZ-10A-01D-A24P-08 g.chr1:154988244G>C c.1108G>C c.(1108-1110)Ggc>Cgc p.G370R LUAD 1 154988740 154988740 + Missense_Mutation SNP G G T TCGA-86-7701-01A-11D-2167-08 TCGA-86-7701-10A-01D-2167-08 g.chr1:154988740G>T c.1199G>T c.(1198-1200)cGc>cTc p.R400L LUAD 1 154988870 154988870 + Silent SNP C C T TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr1:154988870C>T c.1329C>T c.(1327-1329)gaC>gaT p.D443D LUAD 1 154988888 154988888 + Silent SNP C C G TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chr1:154988888C>G c.1347C>G c.(1345-1347)ctC>ctG p.L449L LUAD 1 154989004 154989004 + Missense_Mutation SNP A A G TCGA-91-6835-01A-11D-1855-08 TCGA-91-6835-11A-01D-1855-08 g.chr1:154989004A>G c.1463A>G c.(1462-1464)aAt>aGt p.N488S LUAD 1 154989067 154989067 + Missense_Mutation SNP G G T TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chr1:154989067G>T c.1526G>T c.(1525-1527)gGg>gTg p.G509V LUSC 1 154987802 154987802 + Missense_Mutation SNP G G T TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr1:154987802G>T c.666G>T c.(664-666)gaG>gaT p.E222D LUSC 1 154987962 154987962 + Missense_Mutation SNP G G C TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr1:154987962G>C c.826G>C c.(826-828)Gag>Cag p.E276Q LUSC 1 154988739 154988739 + Missense_Mutation SNP C C T TCGA-51-4079-01A-01D-1458-08 TCGA-51-4079-11A-01D-1458-08 g.chr1:154988739C>T c.1198C>T c.(1198-1200)Cgc>Tgc p.R400C LUSC 1 154988918 154988918 + Silent SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr1:154988918C>T c.1377C>T c.(1375-1377)acC>acT p.T459T OV 1 154987672 154987672 + Missense_Mutation SNP A A G TCGA-61-1740-01A-01W-0639-09 TCGA-61-1740-11A-01W-0639-09 g.chr1:154987672A>G c.536A>G c.(535-537)gAc>gGc p.D179G PAAD 1 154988148 154988148 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr1:154988148C>T c.1012C>T c.(1012-1014)Cgc>Tgc p.R338C PRAD 1 154987273 154987273 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr1:154987273G>A c.137G>A c.(136-138)cGc>cAc p.R46H PRAD 1 154988264 154988264 + Silent SNP C C T TCGA-ZG-A8QY-01A-11D-A377-08 TCGA-ZG-A8QY-10A-01D-A37A-08 g.chr1:154988264C>T c.1128C>T c.(1126-1128)tgC>tgT p.C376C PRAD 1 154988869 154988869 + Missense_Mutation SNP A A G TCGA-HC-A8D1-01A-11D-A364-08 TCGA-HC-A8D1-10A-01D-A362-08 g.chr1:154988869A>G c.1328A>G c.(1327-1329)gAc>gGc p.D443G SKCM 1 154987313 154987313 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr1:154987313C>T c.177C>T c.(175-177)ttC>ttT p.F59F SKCM 1 154987342 154987342 + Missense_Mutation SNP G G A TCGA-EE-A29N-06A-12D-A197-08 TCGA-EE-A29N-10A-01D-A199-08 g.chr1:154987342G>A c.206G>A c.(205-207)gGa>gAa p.G69E SKCM 1 154987431 154987431 + Missense_Mutation SNP C C A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr1:154987431C>A c.295C>A c.(295-297)Cta>Ata p.L99I SKCM 1 154987619 154987619 + Missense_Mutation SNP G G C TCGA-EE-A20H-06A-11D-A197-08 TCGA-EE-A20H-10A-01D-A199-08 g.chr1:154987619G>C c.483G>C c.(481-483)caG>caC p.Q161H SKCM 1 154987719 154987719 + Missense_Mutation SNP C C T TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr1:154987719C>T c.583C>T c.(583-585)Cgg>Tgg p.R195W SKCM 1 154987748 154987748 + Silent SNP C C T TCGA-EE-A2MK-06A-11D-A196-08 TCGA-EE-A2MK-10A-01D-A198-08 g.chr1:154987748C>T c.612C>T c.(610-612)ccC>ccT p.P204P SKCM 1 154987922 154987922 + Silent SNP C C T TCGA-DA-A1IA-06A-11D-A196-08 TCGA-DA-A1IA-10A-01D-A198-08 g.chr1:154987922C>T c.786C>T c.(784-786)tcC>tcT p.S262S SKCM 1 154987923 154987923 + Missense_Mutation SNP C C T TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr1:154987923C>T c.787C>T c.(787-789)Cct>Tct p.P263S SKCM 1 154987938 154987938 + Nonsense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr1:154987938C>T c.802C>T c.(802-804)Cag>Tag p.Q268* SKCM 1 154988032 154988032 + Missense_Mutation SNP C C T TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr1:154988032C>T c.896C>T c.(895-897)tCc>tTc p.S299F SKCM 1 154988033 154988033 + Silent SNP C C T TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr1:154988033C>T c.897C>T c.(895-897)tcC>tcT p.S299S SKCM 1 154988095 154988095 + Missense_Mutation SNP C C A TCGA-D3-A1QB-06A-11D-A19A-08 TCGA-D3-A1QB-10A-01D-A19A-08 g.chr1:154988095C>A c.959C>A c.(958-960)tCc>tAc p.S320Y SKCM 1 154988817 154988817 + Missense_Mutation SNP G G C TCGA-EE-A2GT-06A-12D-A197-08 TCGA-EE-A2GT-10A-01D-A199-08 g.chr1:154988817G>C c.1276G>C c.(1276-1278)Ggg>Cgg p.G426R

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 1 154987446 154987446 single base substitution G C downstream_gene_variant BLCA-US 1 154987446 154987446 single base substitution G C exon_variant BLCA-US 1 154987446 154987446 single base substitution G C missense_variant E104Q 310G>C BLCA-US 1 154987446 154987446 single base substitution G C missense_variant E138Q 412G>C BLCA-US 1 154987500 154987500 single base substitution C T downstream_gene_variant BLCA-US 1 154987500 154987500 single base substitution C T exon_variant BLCA-US 1 154987500 154987500 single base substitution C T missense_variant L122F 364C>T BLCA-US 1 154987500 154987500 single base substitution C T missense_variant L156F 466C>T BLCA-US 1 154988052 154988052 single base substitution G C downstream_gene_variant BLCA-US 1 154988052 154988052 single base substitution G C missense_variant D306H 916G>C BLCA-US 1 154988052 154988052 single base substitution G C missense_variant D340H 1018G>C BLCA-US 1 154988705 154988705 single base substitution G T downstream_gene_variant BLCA-US 1 154988705 154988705 single base substitution G T missense_variant K388N 1164G>T BLCA-US 1 154988705 154988705 single base substitution G T missense_variant K422N 1266G>T BLCA-US 1 154988787 154988787 single base substitution G A downstream_gene_variant BLCA-US 1 154988787 154988787 single base substitution G A missense_variant D416N 1246G>A BLCA-US 1 154988787 154988787 single base substitution G A missense_variant D450N 1348G>A BLCA-US 1 154988999 154988999 single base substitution C T downstream_gene_variant BLCA-US 1 154988999 154988999 single base substitution C T synonymous_variant L486L 1458C>T BLCA-US 1 154988999 154988999 single base substitution C T synonymous_variant L520L 1560C>T BLCA-US 1 154995858 154995858 single base substitution C A downstream_gene_variant BLCA-US 1 154995910 154995910 single base substitution G A downstream_gene_variant BRCA-EU 1 154971609 154971609 single base substitution C A upstream_gene_variant BRCA-EU 1 154971712 154971712 single base substitution G T upstream_gene_variant BRCA-EU 1 154971714 154971714 single base substitution A T upstream_gene_variant BRCA-EU 1 154971842 154971842 single base substitution G T upstream_gene_variant BRCA-EU 1 154972417 154972417 single base substitution C A upstream_gene_variant BRCA-EU 1 154972819 154972819 single base substitution G C upstream_gene_variant BRCA-EU 1 154973363 154973363 single base substitution G T upstream_gene_variant BRCA-EU 1 154973740 154973740 single base substitution C G upstream_gene_variant BRCA-EU 1 154974316 154974316 single base substitution C T upstream_gene_variant BRCA-EU 1 154975576 154975576 single base substitution G A intron_variant BRCA-EU 1 154977568 154977579 deletion of <=200bp CCTAGTGCCTGC - intron_variant BRCA-EU 1 154977781 154977781 single base substitution G C intron_variant BRCA-EU 1 154978110 154978110 single base substitution G A intron_variant BRCA-EU 1 154978289 154978289 single base substitution C G intron_variant BRCA-EU 1 154980180 154980180 single base substitution C G intron_variant BRCA-EU 1 154980663 154980664 deletion of <=200bp CT - intron_variant BRCA-EU 1 154980890 154980890 single base substitution G C intron_variant BRCA-EU 1 154981352 154981352 single base substitution G C intron_variant BRCA-EU 1 154982465 154982465 single base substitution G C intron_variant BRCA-EU 1 154982465 154982465 single base substitution G C upstream_gene_variant BRCA-EU 1 154982595 154982595 single base substitution G A intron_variant BRCA-EU 1 154982595 154982595 single base substitution G A upstream_gene_variant BRCA-EU 1 154982613 154982613 single base substitution C T intron_variant BRCA-EU 1 154982613 154982613 single base substitution C T upstream_gene_variant BRCA-EU 1 154983634 154983634 single base substitution G T intron_variant BRCA-EU 1 154983634 154983634 single base substitution G T upstream_gene_variant BRCA-EU 1 154983964 154983964 single base substitution C T intron_variant BRCA-EU 1 154983964 154983964 single base substitution C T upstream_gene_variant BRCA-EU 1 154984036 154984036 single base substitution G T intron_variant BRCA-EU 1 154984036 154984036 single base substitution G T upstream_gene_variant BRCA-EU 1 154986467 154986467 single base substitution C T intron_variant BRCA-EU 1 154986467 154986467 single base substitution C T upstream_gene_variant BRCA-EU 1 154986871 154986871 single base substitution G A intron_variant BRCA-EU 1 154986871 154986871 single base substitution G A upstream_gene_variant BRCA-EU 1 154986950 154986950 single base substitution G T 5_prime_UTR_variant BRCA-EU 1 154986950 154986950 single base substitution G T intron_variant BRCA-EU 1 154987237 154987237 single base substitution G A downstream_gene_variant BRCA-EU 1 154987237 154987237 single base substitution G A exon_variant BRCA-EU 1 154987237 154987237 single base substitution G A missense_variant C34Y 101G>A BRCA-EU 1 154987237 154987237 single base substitution G A missense_variant C68Y 203G>A BRCA-EU 1 154987575 154987575 single base substitution G C downstream_gene_variant BRCA-EU 1 154987575 154987575 single base substitution G C exon_variant BRCA-EU 1 154987575 154987575 single base substitution G C missense_variant E147Q 439G>C BRCA-EU 1 154987575 154987575 single base substitution G C missense_variant E181Q 541G>C BRCA-EU 1 154988106 154988106 single base substitution G C downstream_gene_variant BRCA-EU 1 154988106 154988106 single base substitution G C missense_variant D324H 970G>C BRCA-EU 1 154988106 154988106 single base substitution G C missense_variant D358H 1072G>C BRCA-EU 1 154988743 154988743 single base substitution C T downstream_gene_variant BRCA-EU 1 154988743 154988743 single base substitution C T missense_variant P401L 1202C>T BRCA-EU 1 154988743 154988743 single base substitution C T missense_variant P435L 1304C>T BRCA-EU 1 154988937 154988937 single base substitution G A downstream_gene_variant BRCA-EU 1 154988937 154988937 single base substitution G A missense_variant D466N 1396G>A BRCA-EU 1 154988937 154988937 single base substitution G A missense_variant D500N 1498G>A BRCA-EU 1 154989039 154989039 single base substitution C T downstream_gene_variant BRCA-EU 1 154989039 154989039 single base substitution C T stop_gained R500* 1498C>T BRCA-EU 1 154989039 154989039 single base substitution C T stop_gained R534* 1600C>T BRCA-EU 1 154989108 154989108 single base substitution G C downstream_gene_variant BRCA-EU 1 154989108 154989108 single base substitution G C missense_variant E523Q 1567G>C BRCA-EU 1 154989108 154989108 single base substitution G C missense_variant E557Q 1669G>C BRCA-EU 1 154989485 154989485 single base substitution C T 3_prime_UTR_variant BRCA-EU 1 154989485 154989485 single base substitution C T downstream_gene_variant BRCA-EU 1 154990283 154990283 single base substitution G T 3_prime_UTR_variant BRCA-EU 1 154990283 154990283 single base substitution G T downstream_gene_variant BRCA-EU 1 154990914 154990914 deletion of <=200bp C - 3_prime_UTR_variant BRCA-EU 1 154990914 154990914 deletion of <=200bp C - downstream_gene_variant BRCA-EU 1 154991296 154991296 single base substitution C T downstream_gene_variant BRCA-EU 1 154992665 154992665 single base substitution A G downstream_gene_variant BRCA-EU 1 154993778 154993778 single base substitution A T downstream_gene_variant BRCA-EU 1 154994070 154994070 single base substitution G C downstream_gene_variant BRCA-EU 1 154995746 154995746 single base substitution C A downstream_gene_variant BRCA-FR 1 154973591 154973591 single base substitution G C upstream_gene_variant BRCA-FR 1 154981352 154981352 single base substitution G C intron_variant BRCA-FR 1 154982595 154982595 single base substitution G A intron_variant BRCA-FR 1 154982595 154982595 single base substitution G A upstream_gene_variant BRCA-FR 1 154988401 154988401 single base substitution G T downstream_gene_variant BRCA-FR 1 154988401 154988401 single base substitution G T intron_variant BRCA-FR 1 154989108 154989108 single base substitution G C downstream_gene_variant BRCA-FR 1 154989108 154989108 single base substitution G C missense_variant E523Q 1567G>C BRCA-FR 1 154989108 154989108 single base substitution G C missense_variant E557Q 1669G>C BRCA-FR 1 154995746 154995746 single base substitution C A downstream_gene_variant BRCA-US 1 154987144 154987144 single base substitution G A exon_variant BRCA-US 1 154987144 154987144 single base substitution G A missense_variant S37N 110G>A BRCA-US 1 154987144 154987144 single base substitution G A missense_variant S3N 8G>A BRCA-US 1 154987160 154987160 single base substitution G C exon_variant BRCA-US 1 154987160 154987160 single base substitution G C synonymous_variant L42L 126G>C BRCA-US 1 154987160 154987160 single base substitution G C synonymous_variant L8L 24G>C BRCA-US 1 154988894 154988894 single base substitution C A downstream_gene_variant BRCA-US 1 154988894 154988894 single base substitution C A synonymous_variant G451G 1353C>A BRCA-US 1 154988894 154988894 single base substitution C A synonymous_variant G485G 1455C>A BRCA-US 1 154991032 154991032 single base substitution T G downstream_gene_variant BRCA-US 1 154991036 154991036 single base substitution T G downstream_gene_variant BRCA-US 1 154991075 154991075 single base substitution G C downstream_gene_variant BRCA-US 1 154995617 154995617 single base substitution G A downstream_gene_variant BTCA-JP 1 154983287 154983287 deletion of <=200bp G - intron_variant BTCA-JP 1 154983287 154983287 deletion of <=200bp G - upstream_gene_variant BTCA-JP 1 154987589 154987589 single base substitution G A downstream_gene_variant BTCA-JP 1 154987589 154987589 single base substitution G A exon_variant BTCA-JP 1 154987589 154987589 single base substitution G A synonymous_variant P151P 453G>A BTCA-JP 1 154987589 154987589 single base substitution G A synonymous_variant P185P 555G>A BTCA-JP 1 154988131 154988131 single base substitution G T downstream_gene_variant BTCA-JP 1 154988131 154988131 single base substitution G T missense_variant S332I 995G>T BTCA-JP 1 154988131 154988131 single base substitution G T missense_variant S366I 1097G>T CESC-US 1 154975263 154975263 single base substitution G A exon_variant CESC-US 1 154975263 154975263 single base substitution G A intron_variant CESC-US 1 154975263 154975263 single base substitution G A upstream_gene_variant CESC-US 1 154987929 154987929 single base substitution G A downstream_gene_variant CESC-US 1 154987929 154987929 single base substitution G A missense_variant E265K 793G>A CESC-US 1 154987929 154987929 single base substitution G A missense_variant E299K 895G>A CLLE-ES 1 154976943 154976943 single base substitution T C intron_variant COAD-US 1 154987403 154987403 single base substitution T A downstream_gene_variant COAD-US 1 154987403 154987403 single base substitution T A exon_variant COAD-US 1 154987403 154987403 single base substitution T A stop_gained C123* 369T>A COAD-US 1 154987403 154987403 single base substitution T A stop_gained C89* 267T>A COAD-US 1 154987872 154987872 deletion of <=200bp G - downstream_gene_variant COAD-US 1 154987872 154987872 deletion of <=200bp G - frameshift_variant G246 COAD-US 1 154987872 154987872 deletion of <=200bp G - frameshift_variant G280 COAD-US 1 154987959 154987959 single base substitution G A downstream_gene_variant COAD-US 1 154987959 154987959 single base substitution G A missense_variant G275S 823G>A COAD-US 1 154987959 154987959 single base substitution G A missense_variant G309S 925G>A COAD-US 1 154988002 154988002 single base substitution G T downstream_gene_variant COAD-US 1 154988002 154988002 single base substitution G T missense_variant G289V 866G>T COAD-US 1 154988002 154988002 single base substitution G T missense_variant G323V 968G>T COAD-US 1 154988154 154988154 single base substitution C T downstream_gene_variant COAD-US 1 154988154 154988154 single base substitution C T missense_variant R340C 1018C>T COAD-US 1 154988154 154988154 single base substitution C T missense_variant R374C 1120C>T COAD-US 1 154988273 154988273 single base substitution C T downstream_gene_variant COAD-US 1 154988273 154988273 single base substitution C T synonymous_variant C379C 1137C>T COAD-US 1 154988273 154988273 single base substitution C T synonymous_variant C413C 1239C>T COAD-US 1 154988698 154988700 deletion of <=200bp ACG - downstream_gene_variant COAD-US 1 154988698 154988700 deletion of <=200bp ACG - splice_region_variant COAD-US 1 154995714 154995716 deletion of <=200bp CCT - downstream_gene_variant COCA-CN 1 154983401 154983401 single base substitution A G exon_variant COCA-CN 1 154983401 154983401 single base substitution A G intron_variant COCA-CN 1 154983401 154983401 single base substitution A G synonymous_variant L2L 6A>G COCA-CN 1 154983401 154983401 single base substitution A G upstream_gene_variant COCA-CN 1 154987757 154987757 single base substitution T G downstream_gene_variant COCA-CN 1 154987757 154987757 single base substitution T G exon_variant COCA-CN 1 154987757 154987757 single base substitution T G synonymous_variant A207A 621T>G COCA-CN 1 154987757 154987757 single base substitution T G synonymous_variant A241A 723T>G COCA-CN 1 154988223 154988223 single base substitution C T downstream_gene_variant COCA-CN 1 154988223 154988223 single base substitution C T missense_variant R363C 1087C>T COCA-CN 1 154988223 154988223 single base substitution C T missense_variant R397C 1189C>T COCA-CN 1 154988705 154988705 single base substitution G C downstream_gene_variant COCA-CN 1 154988705 154988705 single base substitution G C missense_variant K388N 1164G>C COCA-CN 1 154988705 154988705 single base substitution G C missense_variant K422N 1266G>C EOPC-DE 1 154976447 154976447 single base substitution T C intron_variant EOPC-DE 1 154983397 154983397 single base substitution T C exon_variant EOPC-DE 1 154983397 154983397 single base substitution T C intron_variant EOPC-DE 1 154983397 154983397 single base substitution T C start_lost M1T 2T>C EOPC-DE 1 154983397 154983397 single base substitution T C upstream_gene_variant EOPC-DE 1 154985276 154985276 single base substitution A C intron_variant EOPC-DE 1 154985276 154985276 single base substitution A C upstream_gene_variant ESAD-UK 1 154970361 154970361 single base substitution C G upstream_gene_variant ESAD-UK 1 154970820 154970820 single base substitution C A upstream_gene_variant ESAD-UK 1 154971592 154971593 deletion of <=200bp AG - upstream_gene_variant ESAD-UK 1 154973247 154973247 single base substitution T A upstream_gene_variant ESAD-UK 1 154973740 154973740 single base substitution C G upstream_gene_variant ESAD-UK 1 154975874 154975874 single base substitution C T intron_variant ESAD-UK 1 154977417 154977417 single base substitution C G intron_variant ESAD-UK 1 154978229 154978229 single base substitution G T intron_variant ESAD-UK 1 154978289 154978289 single base substitution C T intron_variant ESAD-UK 1 154980039 154980039 single base substitution C A intron_variant ESAD-UK 1 154980246 154980246 single base substitution C G intron_variant ESAD-UK 1 154980929 154980929 single base substitution C G intron_variant ESAD-UK 1 154981487 154981487 single base substitution G A intron_variant ESAD-UK 1 154983539 154983539 single base substitution C T intron_variant ESAD-UK 1 154983539 154983539 single base substitution C T upstream_gene_variant ESAD-UK 1 154986851 154986851 single base substitution A G intron_variant ESAD-UK 1 154986851 154986851 single base substitution A G upstream_gene_variant ESAD-UK 1 154986867 154986867 single base substitution G A intron_variant ESAD-UK 1 154986867 154986867 single base substitution G A upstream_gene_variant ESAD-UK 1 154989970 154989970 single base substitution C T 3_prime_UTR_variant ESAD-UK 1 154989970 154989970 single base substitution C T downstream_gene_variant ESAD-UK 1 154990017 154990017 single base substitution G C 3_prime_UTR_variant ESAD-UK 1 154990017 154990017 single base substitution G C downstream_gene_variant ESAD-UK 1 154990914 154990914 deletion of <=200bp C - 3_prime_UTR_variant ESAD-UK 1 154990914 154990914 deletion of <=200bp C - downstream_gene_variant ESAD-UK 1 154991781 154991781 single base substitution A G downstream_gene_variant ESAD-UK 1 154992721 154992724 deletion of <=200bp CTCT - downstream_gene_variant ESAD-UK 1 154992881 154992882 deletion of <=200bp TG - downstream_gene_variant ESAD-UK 1 154993448 154993448 single base substitution G A downstream_gene_variant GBM-US 1 154987218 154987218 single base substitution C T downstream_gene_variant GBM-US 1 154987218 154987218 single base substitution C T exon_variant GBM-US 1 154987218 154987218 single base substitution C T missense_variant R28C 82C>T GBM-US 1 154987218 154987218 single base substitution C T missense_variant R62C 184C>T KIRC-US 1 154995893 154995893 single base substitution G A downstream_gene_variant KIRP-US 1 154987232 154987232 single base substitution C G downstream_gene_variant KIRP-US 1 154987232 154987232 single base substitution C G exon_variant KIRP-US 1 154987232 154987232 single base substitution C G missense_variant H32Q 96C>G KIRP-US 1 154987232 154987232 single base substitution C G missense_variant H66Q 198C>G LAML-KR 1 154995396 154995396 single base substitution C T downstream_gene_variant LICA-FR 1 154975944 154975944 single base substitution A G intron_variant LICA-FR 1 154991223 154991223 single base substitution C G downstream_gene_variant LICA-FR 1 154993914 154993914 single base substitution C T downstream_gene_variant LIHC-US 1 154987976 154987976 single base substitution G A downstream_gene_variant LIHC-US 1 154987976 154987976 single base substitution G A synonymous_variant E280E 840G>A LIHC-US 1 154987976 154987976 single base substitution G A synonymous_variant E314E 942G>A LIHC-US 1 154988092 154988092 single base substitution G A downstream_gene_variant LIHC-US 1 154988092 154988092 single base substitution G A missense_variant S319N 956G>A LIHC-US 1 154988092 154988092 single base substitution G A missense_variant S353N 1058G>A LINC-JP 1 154975843 154975843 single base substitution C A intron_variant LINC-JP 1 154981267 154981267 single base substitution A G intron_variant LINC-JP 1 154983200 154983200 single base substitution C G intron_variant LINC-JP 1 154983200 154983200 single base substitution C G upstream_gene_variant LINC-JP 1 154985284 154985284 single base substitution A C intron_variant LINC-JP 1 154985284 154985284 single base substitution A C upstream_gene_variant LINC-JP 1 154988830 154988830 single base substitution A G downstream_gene_variant LINC-JP 1 154988830 154988830 single base substitution A G missense_variant Y430C 1289A>G LINC-JP 1 154988830 154988830 single base substitution A G missense_variant Y464C 1391A>G LINC-JP 1 154991245 154991245 single base substitution G T downstream_gene_variant LINC-JP 1 154991295 154991295 single base substitution C T downstream_gene_variant LINC-JP 1 154992435 154992435 single base substitution T A downstream_gene_variant LIRI-JP 1 154974090 154974090 single base substitution G A upstream_gene_variant LIRI-JP 1 154991160 154991160 single base substitution T A downstream_gene_variant LIRI-JP 1 154993206 154993206 single base substitution C T downstream_gene_variant LIRI-JP 1 154994706 154994710 deletion of <=200bp AAGTT - downstream_gene_variant LUSC-KR 1 154985747 154985747 single base substitution A G intron_variant LUSC-KR 1 154985747 154985747 single base substitution A G upstream_gene_variant LUSC-KR 1 154987970 154987970 single base substitution A C downstream_gene_variant LUSC-KR 1 154987970 154987970 single base substitution A C missense_variant E278D 834A>C LUSC-KR 1 154987970 154987970 single base substitution A C missense_variant E312D 936A>C LUSC-US 1 154987802 154987802 single base substitution G T downstream_gene_variant LUSC-US 1 154987802 154987802 single base substitution G T missense_variant E222D 666G>T LUSC-US 1 154987802 154987802 single base substitution G T missense_variant E256D 768G>T LUSC-US 1 154987962 154987962 single base substitution G C downstream_gene_variant LUSC-US 1 154987962 154987962 single base substitution G C missense_variant E276Q 826G>C LUSC-US 1 154987962 154987962 single base substitution G C missense_variant E310Q 928G>C LUSC-US 1 154988739 154988739 single base substitution C T downstream_gene_variant LUSC-US 1 154988739 154988739 single base substitution C T missense_variant R400C 1198C>T LUSC-US 1 154988739 154988739 single base substitution C T missense_variant R434C 1300C>T LUSC-US 1 154988918 154988918 single base substitution C T downstream_gene_variant LUSC-US 1 154988918 154988918 single base substitution C T synonymous_variant T459T 1377C>T LUSC-US 1 154988918 154988918 single base substitution C T synonymous_variant T493T 1479C>T MALY-DE 1 154975739 154975739 single base substitution C T intron_variant MALY-DE 1 154980850 154980850 single base substitution G T intron_variant MALY-DE 1 154989823 154989823 single base substitution T C 3_prime_UTR_variant MALY-DE 1 154989823 154989823 single base substitution T C downstream_gene_variant MELA-AU 1 154970133 154970133 single base substitution G A upstream_gene_variant MELA-AU 1 154970176 154970176 single base substitution G A upstream_gene_variant MELA-AU 1 154970218 154970218 single base substitution C T upstream_gene_variant MELA-AU 1 154970694 154970694 single base substitution C T upstream_gene_variant MELA-AU 1 154970857 154970857 single base substitution G A upstream_gene_variant MELA-AU 1 154971308 154971308 single base substitution C T upstream_gene_variant MELA-AU 1 154971720 154971720 single base substitution C T upstream_gene_variant MELA-AU 1 154971796 154971796 single base substitution T C upstream_gene_variant MELA-AU 1 154973607 154973607 single base substitution G A upstream_gene_variant MELA-AU 1 154974503 154974503 single base substitution G A upstream_gene_variant MELA-AU 1 154974548 154974548 single base substitution G A upstream_gene_variant MELA-AU 1 154974640 154974640 single base substitution C T upstream_gene_variant MELA-AU 1 154975897 154975897 single base substitution G T intron_variant MELA-AU 1 154976794 154976795 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 1 154976907 154976910 deletion of <=200bp GTAT - intron_variant MELA-AU 1 154977706 154977706 single base substitution C T intron_variant MELA-AU 1 154978404 154978404 single base substitution C A intron_variant MELA-AU 1 154979076 154979076 single base substitution C T intron_variant MELA-AU 1 154979128 154979128 single base substitution C T intron_variant MELA-AU 1 154979200 154979200 single base substitution C T intron_variant MELA-AU 1 154979287 154979287 single base substitution C T intron_variant MELA-AU 1 154980356 154980356 single base substitution C T intron_variant MELA-AU 1 154980428 154980428 single base substitution C T intron_variant MELA-AU 1 154980598 154980598 single base substitution C T intron_variant MELA-AU 1 154980608 154980608 single base substitution C T intron_variant MELA-AU 1 154980679 154980679 single base substitution C T intron_variant MELA-AU 1 154981036 154981036 single base substitution C T intron_variant MELA-AU 1 154981127 154981127 single base substitution C A intron_variant MELA-AU 1 154981138 154981138 single base substitution C T intron_variant MELA-AU 1 154981334 154981334 single base substitution C T intron_variant MELA-AU 1 154981499 154981499 single base substitution C T intron_variant MELA-AU 1 154982024 154982024 single base substitution C T intron_variant MELA-AU 1 154982024 154982024 single base substitution C T upstream_gene_variant MELA-AU 1 154982647 154982647 single base substitution C T intron_variant MELA-AU 1 154982647 154982647 single base substitution C T upstream_gene_variant MELA-AU 1 154983456 154983456 single base substitution C T exon_variant MELA-AU 1 154983456 154983456 single base substitution C T intron_variant MELA-AU 1 154983456 154983456 single base substitution C T missense_variant P21S 61C>T MELA-AU 1 154983456 154983456 single base substitution C T upstream_gene_variant MELA-AU 1 154983935 154983935 single base substitution C T intron_variant MELA-AU 1 154983935 154983935 single base substitution C T upstream_gene_variant MELA-AU 1 154984079 154984079 single base substitution C T intron_variant MELA-AU 1 154984079 154984079 single base substitution C T upstream_gene_variant MELA-AU 1 154984917 154984917 single base substitution C T intron_variant MELA-AU 1 154984917 154984917 single base substitution C T upstream_gene_variant MELA-AU 1 154985053 154985053 single base substitution C T intron_variant MELA-AU 1 154985053 154985053 single base substitution C T upstream_gene_variant MELA-AU 1 154985268 154985268 single base substitution C T intron_variant MELA-AU 1 154985268 154985268 single base substitution C T upstream_gene_variant MELA-AU 1 154985350 154985350 single base substitution G A intron_variant MELA-AU 1 154985350 154985350 single base substitution G A upstream_gene_variant MELA-AU 1 154986946 154986946 single base substitution C T 5_prime_UTR_variant MELA-AU 1 154986946 154986946 single base substitution C T intron_variant MELA-AU 1 154987748 154987748 single base substitution C T downstream_gene_variant MELA-AU 1 154987748 154987748 single base substitution C T exon_variant MELA-AU 1 154987748 154987748 single base substitution C T synonymous_variant P204P 612C>T MELA-AU 1 154987748 154987748 single base substitution C T synonymous_variant P238P 714C>T MELA-AU 1 154987938 154987938 single base substitution C T downstream_gene_variant MELA-AU 1 154987938 154987938 single base substitution C T stop_gained Q268* 802C>T MELA-AU 1 154987938 154987938 single base substitution C T stop_gained Q302* 904C>T MELA-AU 1 154988706 154988706 single base substitution C T downstream_gene_variant MELA-AU 1 154988706 154988706 single base substitution C T synonymous_variant L389L 1165C>T MELA-AU 1 154988706 154988706 single base substitution C T synonymous_variant L423L 1267C>T MELA-AU 1 154989534 154989534 single base substitution C T 3_prime_UTR_variant MELA-AU 1 154989534 154989534 single base substitution C T downstream_gene_variant MELA-AU 1 154989596 154989596 single base substitution C T 3_prime_UTR_variant MELA-AU 1 154989596 154989596 single base substitution C T downstream_gene_variant MELA-AU 1 154989716 154989716 single base substitution G A 3_prime_UTR_variant MELA-AU 1 154989716 154989716 single base substitution G A downstream_gene_variant MELA-AU 1 154989725 154989725 single base substitution G A 3_prime_UTR_variant MELA-AU 1 154989725 154989725 single base substitution G A downstream_gene_variant MELA-AU 1 154989777 154989777 single base substitution G A 3_prime_UTR_variant MELA-AU 1 154989777 154989777 single base substitution G A downstream_gene_variant MELA-AU 1 154989894 154989894 single base substitution C T 3_prime_UTR_variant MELA-AU 1 154989894 154989894 single base substitution C T downstream_gene_variant MELA-AU 1 154990493 154990494 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 1 154990493 154990494 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 1 154990868 154990868 single base substitution C T 3_prime_UTR_variant MELA-AU 1 154990868 154990868 single base substitution C T downstream_gene_variant MELA-AU 1 154990922 154990922 single base substitution C T 3_prime_UTR_variant MELA-AU 1 154990922 154990922 single base substitution C T downstream_gene_variant MELA-AU 1 154990948 154990948 single base substitution C T 3_prime_UTR_variant MELA-AU 1 154990948 154990948 single base substitution C T downstream_gene_variant MELA-AU 1 154991219 154991219 single base substitution T C downstream_gene_variant MELA-AU 1 154991971 154991971 single base substitution G A downstream_gene_variant MELA-AU 1 154992190 154992190 single base substitution C T downstream_gene_variant MELA-AU 1 154992517 154992517 single base substitution G A downstream_gene_variant MELA-AU 1 154992915 154992915 single base substitution G A downstream_gene_variant MELA-AU 1 154993947 154993947 single base substitution T C downstream_gene_variant MELA-AU 1 154994802 154994802 single base substitution C T downstream_gene_variant MELA-AU 1 154994864 154994864 single base substitution C T downstream_gene_variant MELA-AU 1 154994947 154994947 single base substitution C T downstream_gene_variant MELA-AU 1 154994948 154994948 single base substitution C T downstream_gene_variant MELA-AU 1 154995426 154995427 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 1 154995445 154995445 single base substitution C T downstream_gene_variant MELA-AU 1 154995715 154995715 single base substitution C T downstream_gene_variant MELA-AU 1 154995872 154995872 single base substitution G A downstream_gene_variant MELA-AU 1 154995910 154995910 single base substitution G A downstream_gene_variant ORCA-IN 1 154987137 154987137 single base substitution A C exon_variant ORCA-IN 1 154987137 154987137 single base substitution A C initiator_codon_variant M1L 1A>C ORCA-IN 1 154987137 154987137 single base substitution A C missense_variant M35L 103A>C ORCA-IN 1 154988149 154988149 single base substitution G T downstream_gene_variant ORCA-IN 1 154988149 154988149 single base substitution G T missense_variant R338L 1013G>T ORCA-IN 1 154988149 154988149 single base substitution G T missense_variant R372L 1115G>T OV-AU 1 154972376 154972376 single base substitution T A upstream_gene_variant OV-AU 1 154974259 154974259 single base substitution C G upstream_gene_variant OV-AU 1 154974535 154974535 single base substitution A G upstream_gene_variant OV-AU 1 154974615 154974615 single base substitution G C upstream_gene_variant OV-AU 1 154982804 154982804 single base substitution C T 5_prime_UTR_variant OV-AU 1 154982804 154982804 single base substitution C T exon_variant OV-AU 1 154982804 154982804 single base substitution C T intron_variant OV-AU 1 154982804 154982804 single base substitution C T upstream_gene_variant PACA-AU 1 154970762 154970762 single base substitution A G upstream_gene_variant PACA-AU 1 154971324 154971324 single base substitution A T upstream_gene_variant PACA-AU 1 154972694 154972694 deletion of <=200bp G - upstream_gene_variant PACA-AU 1 154978076 154978076 single base substitution C A intron_variant PACA-AU 1 154989777 154989777 single base substitution G A 3_prime_UTR_variant PACA-AU 1 154989777 154989777 single base substitution G A downstream_gene_variant PACA-AU 1 154992516 154992516 single base substitution G T downstream_gene_variant PACA-AU 1 154992897 154992922 deletion of <=200bp GTGCAGTGGCACGATCTCGGCTCACT - downstream_gene_variant PACA-CA 1 154971927 154971927 single base substitution C T upstream_gene_variant PACA-CA 1 154973703 154973703 single base substitution G A upstream_gene_variant PACA-CA 1 154974271 154974271 single base substitution C T upstream_gene_variant PACA-CA 1 154979262 154979262 single base substitution C A intron_variant PACA-CA 1 154982457 154982457 deletion of <=200bp A - intron_variant PACA-CA 1 154982457 154982457 deletion of <=200bp A - upstream_gene_variant PACA-CA 1 154982460 154982460 insertion of <=200bp - TC intron_variant PACA-CA 1 154982460 154982460 insertion of <=200bp - TC upstream_gene_variant PACA-CA 1 154982462 154982462 insertion of <=200bp - C intron_variant PACA-CA 1 154982462 154982462 insertion of <=200bp - C upstream_gene_variant PACA-CA 1 154984305 154984305 single base substitution C G intron_variant PACA-CA 1 154984305 154984305 single base substitution C G upstream_gene_variant PACA-CA 1 154984418 154984418 single base substitution G C intron_variant PACA-CA 1 154984418 154984418 single base substitution G C upstream_gene_variant PACA-CA 1 154984643 154984643 single base substitution T C intron_variant PACA-CA 1 154984643 154984643 single base substitution T C upstream_gene_variant PACA-CA 1 154988937 154988937 single base substitution G A downstream_gene_variant PACA-CA 1 154988937 154988937 single base substitution G A missense_variant D466N 1396G>A PACA-CA 1 154988937 154988937 single base substitution G A missense_variant D500N 1498G>A PACA-CA 1 154989576 154989576 single base substitution G C 3_prime_UTR_variant PACA-CA 1 154989576 154989576 single base substitution G C downstream_gene_variant PACA-CA 1 154989881 154989881 single base substitution C G 3_prime_UTR_variant PACA-CA 1 154989881 154989881 single base substitution C G downstream_gene_variant PACA-CA 1 154990063 154990063 single base substitution C T 3_prime_UTR_variant PACA-CA 1 154990063 154990063 single base substitution C T downstream_gene_variant PACA-CA 1 154990566 154990566 single base substitution T G 3_prime_UTR_variant PACA-CA 1 154990566 154990566 single base substitution T G downstream_gene_variant PACA-CA 1 154994618 154994618 single base substitution C T downstream_gene_variant PBCA-DE 1 154975191 154975191 single base substitution T G intron_variant PBCA-DE 1 154975191 154975191 single base substitution T G upstream_gene_variant PBCA-DE 1 154989915 154989915 single base substitution T G 3_prime_UTR_variant PBCA-DE 1 154989915 154989915 single base substitution T G downstream_gene_variant PBCA-DE 1 154993465 154993465 single base substitution A T downstream_gene_variant PBCA-DE 1 154994750 154994750 single base substitution T C downstream_gene_variant PBCA-DE 1 154995601 154995601 single base substitution G A downstream_gene_variant PRAD-UK 1 154975591 154975591 insertion of <=200bp - T intron_variant PRAD-UK 1 154975913 154975913 single base substitution A T intron_variant PRAD-UK 1 154987099 154987099 single base substitution G A 5_prime_UTR_variant PRAD-UK 1 154987099 154987099 single base substitution G A intron_variant PRAD-UK 1 154992781 154992781 single base substitution T A downstream_gene_variant RECA-EU 1 154977255 154977255 single base substitution G A intron_variant RECA-EU 1 154985920 154985920 single base substitution G A intron_variant RECA-EU 1 154985920 154985920 single base substitution G A upstream_gene_variant SKCA-BR 1 154972651 154972651 single base substitution C G upstream_gene_variant SKCA-BR 1 154972982 154972982 single base substitution G A upstream_gene_variant SKCA-BR 1 154977669 154977669 single base substitution T G intron_variant SKCA-BR 1 154978031 154978031 single base substitution G A intron_variant SKCA-BR 1 154978886 154978886 single base substitution C T intron_variant SKCA-BR 1 154978887 154978887 single base substitution C T intron_variant SKCA-BR 1 154979362 154979362 single base substitution C T intron_variant SKCA-BR 1 154980434 154980434 single base substitution T G intron_variant SKCA-BR 1 154981657 154981657 single base substitution C G intron_variant SKCA-BR 1 154982112 154982112 single base substitution C T intron_variant SKCA-BR 1 154982112 154982112 single base substitution C T upstream_gene_variant SKCA-BR 1 154982113 154982113 single base substitution C T intron_variant SKCA-BR 1 154982113 154982113 single base substitution C T upstream_gene_variant SKCA-BR 1 154983785 154983785 single base substitution T G intron_variant SKCA-BR 1 154983785 154983785 single base substitution T G upstream_gene_variant SKCA-BR 1 154984743 154984743 single base substitution T G intron_variant SKCA-BR 1 154984743 154984743 single base substitution T G upstream_gene_variant SKCA-BR 1 154984752 154984752 single base substitution A G intron_variant SKCA-BR 1 154984752 154984752 single base substitution A G upstream_gene_variant SKCA-BR 1 154988668 154988668 single base substitution C T downstream_gene_variant SKCA-BR 1 154988668 154988668 single base substitution C T intron_variant SKCA-BR 1 154988957 154988957 single base substitution A G downstream_gene_variant SKCA-BR 1 154988957 154988957 single base substitution A G synonymous_variant P472P 1416A>G SKCA-BR 1 154988957 154988957 single base substitution A G synonymous_variant P506P 1518A>G SKCA-BR 1 154989502 154989502 single base substitution A G 3_prime_UTR_variant SKCA-BR 1 154989502 154989502 single base substitution A G downstream_gene_variant SKCA-BR 1 154991058 154991058 single base substitution G T downstream_gene_variant SKCA-BR 1 154993243 154993243 single base substitution G A downstream_gene_variant SKCA-BR 1 154995636 154995636 single base substitution C T downstream_gene_variant SKCM-US 1 154987313 154987313 single base substitution C T downstream_gene_variant SKCM-US 1 154987313 154987313 single base substitution C T exon_variant SKCM-US 1 154987313 154987313 single base substitution C T synonymous_variant F59F 177C>T SKCM-US 1 154987313 154987313 single base substitution C T synonymous_variant F93F 279C>T SKCM-US 1 154987342 154987342 single base substitution G A downstream_gene_variant SKCM-US 1 154987342 154987342 single base substitution G A exon_variant SKCM-US 1 154987342 154987342 single base substitution G A missense_variant G103E 308G>A SKCM-US 1 154987342 154987342 single base substitution G A missense_variant G69E 206G>A SKCM-US 1 154987431 154987431 single base substitution C A downstream_gene_variant SKCM-US 1 154987431 154987431 single base substitution C A exon_variant SKCM-US 1 154987431 154987431 single base substitution C A missense_variant L133I 397C>A SKCM-US 1 154987431 154987431 single base substitution C A missense_variant L99I 295C>A SKCM-US 1 154987619 154987619 single base substitution G C downstream_gene_variant SKCM-US 1 154987619 154987619 single base substitution G C exon_variant SKCM-US 1 154987619 154987619 single base substitution G C missense_variant Q161H 483G>C SKCM-US 1 154987619 154987619 single base substitution G C missense_variant Q195H 585G>C SKCM-US 1 154987719 154987719 single base substitution C T downstream_gene_variant SKCM-US 1 154987719 154987719 single base substitution C T exon_variant SKCM-US 1 154987719 154987719 single base substitution C T missense_variant R195W 583C>T SKCM-US 1 154987719 154987719 single base substitution C T missense_variant R229W 685C>T SKCM-US 1 154987748 154987748 single base substitution C T downstream_gene_variant SKCM-US 1 154987748 154987748 single base substitution C T exon_variant SKCM-US 1 154987748 154987748 single base substitution C T synonymous_variant P204P 612C>T SKCM-US 1 154987748 154987748 single base substitution C T synonymous_variant P238P 714C>T SKCM-US 1 154987922 154987922 single base substitution C T downstream_gene_variant SKCM-US 1 154987922 154987922 single base substitution C T synonymous_variant S262S 786C>T SKCM-US 1 154987922 154987922 single base substitution C T synonymous_variant S296S 888C>T SKCM-US 1 154987923 154987923 single base substitution C T downstream_gene_variant SKCM-US 1 154987923 154987923 single base substitution C T missense_variant P263S 787C>T SKCM-US 1 154987923 154987923 single base substitution C T missense_variant P297S 889C>T SKCM-US 1 154987938 154987938 single base substitution C T downstream_gene_variant SKCM-US 1 154987938 154987938 single base substitution C T stop_gained Q268* 802C>T SKCM-US 1 154987938 154987938 single base substitution C T stop_gained Q302* 904C>T SKCM-US 1 154988095 154988095 single base substitution C A downstream_gene_variant SKCM-US 1 154988095 154988095 single base substitution C A missense_variant S320Y 959C>A SKCM-US 1 154988095 154988095 single base substitution C A missense_variant S354Y 1061C>A SKCM-US 1 154988817 154988817 single base substitution G C downstream_gene_variant SKCM-US 1 154988817 154988817 single base substitution G C missense_variant G426R 1276G>C SKCM-US 1 154988817 154988817 single base substitution G C missense_variant G460R 1378G>C SKCM-US 1 154988846 154988846 single base substitution C T downstream_gene_variant SKCM-US 1 154988846 154988846 single base substitution C T synonymous_variant C435C 1305C>T SKCM-US 1 154988846 154988846 single base substitution C T synonymous_variant C469C 1407C>T SKCM-US 1 154988852 154988852 single base substitution G A downstream_gene_variant SKCM-US 1 154988852 154988852 single base substitution G A synonymous_variant K437K 1311G>A SKCM-US 1 154988852 154988852 single base substitution G A synonymous_variant K471K 1413G>A SKCM-US 1 154995717 154995717 single base substitution C T downstream_gene_variant STAD-US 1 154987252 154987252 single base substitution G A downstream_gene_variant STAD-US 1 154987252 154987252 single base substitution G A exon_variant STAD-US 1 154987252 154987252 single base substitution G A missense_variant R39Q 116G>A STAD-US 1 154987252 154987252 single base substitution G A missense_variant R73Q 218G>A STAD-US 1 154987334 154987334 single base substitution C T downstream_gene_variant STAD-US 1 154987334 154987334 single base substitution C T exon_variant STAD-US 1 154987334 154987334 single base substitution C T synonymous_variant G100G 300C>T STAD-US 1 154987334 154987334 single base substitution C T synonymous_variant G66G 198C>T STAD-US 1 154987740 154987740 single base substitution C T downstream_gene_variant STAD-US 1 154987740 154987740 single base substitution C T exon_variant STAD-US 1 154987740 154987740 single base substitution C T missense_variant R202C 604C>T STAD-US 1 154987740 154987740 single base substitution C T missense_variant R236C 706C>T STAD-US 1 154987838 154987838 single base substitution G T downstream_gene_variant STAD-US 1 154987838 154987838 single base substitution G T missense_variant E234D 702G>T STAD-US 1 154987838 154987838 single base substitution G T missense_variant E268D 804G>T STAD-US 1 154987844 154987844 single base substitution G T downstream_gene_variant STAD-US 1 154987844 154987844 single base substitution G T missense_variant E236D 708G>T STAD-US 1 154987844 154987844 single base substitution G T missense_variant E270D 810G>T STAD-US 1 154988174 154988174 single base substitution G A downstream_gene_variant STAD-US 1 154988174 154988174 single base substitution G A synonymous_variant Q346Q 1038G>A STAD-US 1 154988174 154988174 single base substitution G A synonymous_variant Q380Q 1140G>A STAD-US 1 154988858 154988858 single base substitution C T downstream_gene_variant STAD-US 1 154988858 154988858 single base substitution C T synonymous_variant F439F 1317C>T STAD-US 1 154988858 154988858 single base substitution C T synonymous_variant F473F 1419C>T UCEC-US 1 154987219 154987219 single base substitution G A downstream_gene_variant UCEC-US 1 154987219 154987219 single base substitution G A exon_variant UCEC-US 1 154987219 154987219 single base substitution G A missense_variant R28H 83G>A UCEC-US 1 154987219 154987219 single base substitution G A missense_variant R62H 185G>A UCEC-US 1 154987270 154987270 single base substitution A G downstream_gene_variant UCEC-US 1 154987270 154987270 single base substitution A G exon_variant UCEC-US 1 154987270 154987270 single base substitution A G missense_variant Y45C 134A>G UCEC-US 1 154987270 154987270 single base substitution A G missense_variant Y79C 236A>G UCEC-US 1 154987340 154987340 single base substitution C T downstream_gene_variant UCEC-US 1 154987340 154987340 single base substitution C T exon_variant UCEC-US 1 154987340 154987340 single base substitution C T synonymous_variant G102G 306C>T UCEC-US 1 154987340 154987340 single base substitution C T synonymous_variant G68G 204C>T UCEC-US 1 154987431 154987431 single base substitution C T downstream_gene_variant UCEC-US 1 154987431 154987431 single base substitution C T exon_variant UCEC-US 1 154987431 154987431 single base substitution C T synonymous_variant L133L 397C>T UCEC-US 1 154987431 154987431 single base substitution C T synonymous_variant L99L 295C>T UCEC-US 1 154987481 154987481 single base substitution C T downstream_gene_variant UCEC-US 1 154987481 154987481 single base substitution C T exon_variant UCEC-US 1 154987481 154987481 single base substitution C T synonymous_variant S115S 345C>T UCEC-US 1 154987481 154987481 single base substitution C T synonymous_variant S149S 447C>T UCEC-US 1 154987528 154987528 single base substitution C T downstream_gene_variant UCEC-US 1 154987528 154987528 single base substitution C T exon_variant UCEC-US 1 154987528 154987528 single base substitution C T missense_variant P131L 392C>T UCEC-US 1 154987528 154987528 single base substitution C T missense_variant P165L 494C>T UCEC-US 1 154987592 154987592 single base substitution C T downstream_gene_variant UCEC-US 1 154987592 154987592 single base substitution C T exon_variant UCEC-US 1 154987592 154987592 single base substitution C T synonymous_variant D152D 456C>T UCEC-US 1 154987592 154987592 single base substitution C T synonymous_variant D186D 558C>T UCEC-US 1 154988027 154988027 single base substitution G A downstream_gene_variant UCEC-US 1 154988027 154988027 single base substitution G A synonymous_variant P297P 891G>A UCEC-US 1 154988027 154988027 single base substitution G A synonymous_variant P331P 993G>A UCEC-US 1 154988066 154988066 single base substitution C T downstream_gene_variant UCEC-US 1 154988066 154988066 single base substitution C T synonymous_variant I310I 930C>T UCEC-US 1 154988066 154988066 single base substitution C T synonymous_variant I344I 1032C>T UCEC-US 1 154988209 154988235 deletion of <=200bp CAGGCAAACTGCCTCGCCACATGAGGA - disruptive_inframe_deletion AGKLPRHMRT358A UCEC-US 1 154988209 154988235 deletion of <=200bp CAGGCAAACTGCCTCGCCACATGAGGA - disruptive_inframe_deletion AGKLPRHMRT392A UCEC-US 1 154988209 154988235 deletion of <=200bp CAGGCAAACTGCCTCGCCACATGAGGA - downstream_gene_variant UCEC-US 1 154988224 154988224 single base substitution G A downstream_gene_variant UCEC-US 1 154988224 154988224 single base substitution G A missense_variant R363H 1088G>A UCEC-US 1 154988224 154988224 single base substitution G A missense_variant R397H 1190G>A UCEC-US 1 154988235 154988235 single base substitution A G downstream_gene_variant UCEC-US 1 154988235 154988235 single base substitution A G missense_variant T367A 1099A>G UCEC-US 1 154988235 154988235 single base substitution A G missense_variant T401A 1201A>G UCEC-US 1 154988264 154988264 single base substitution C T downstream_gene_variant UCEC-US 1 154988264 154988264 single base substitution C T synonymous_variant C376C 1128C>T UCEC-US 1 154988264 154988264 single base substitution C T synonymous_variant C410C 1230C>T UCEC-US 1 154988280 154988280 single base substitution C T downstream_gene_variant UCEC-US 1 154988280 154988280 single base substitution C T stop_gained R382* 1144C>T UCEC-US 1 154988280 154988280 single base substitution C T stop_gained R416* 1246C>T UCEC-US 1 154988705 154988705 single base substitution G T downstream_gene_variant UCEC-US 1 154988705 154988705 single base substitution G T missense_variant K388N 1164G>T UCEC-US 1 154988705 154988705 single base substitution G T missense_variant K422N 1266G>T UCEC-US 1 154988976 154988976 single base substitution G A downstream_gene_variant UCEC-US 1 154988976 154988976 single base substitution G A missense_variant A479T 1435G>A UCEC-US 1 154988976 154988976 single base substitution G A missense_variant A513T 1537G>A UCEC-US 1 154991221 154991223 deletion of <=200bp CTC - downstream_gene_variant UCEC-US 1 154995639 154995639 single base substitution C A downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PD8830a COSM3376004 c.1396G>A p.D466N Substitution - Missense 1:155016461-155016461 + TCGA-G4-6322-01 COSM3689031 c.823G>A p.G275S Substitution - Missense 1:155015483-155015483 + PD11386a COSM5786441 c.1600C>T p.R534* Substitution - Nonsense 1:155016563-155016563 + LS180 COSM2209660 c.393G>A p.P131P Substitution - coding silent 1:155015053-155015053 + TCGA-AC-A23H-01 COSM3802062 c.24G>C p.L8L Substitution - coding silent 1:155014684-155014684 + TCGA-GD-A3OP-01 COSM1295154 c.364C>T p.L122F Substitution - Missense 1:155015024-155015024 + PD22355a COSM5793659 c.203G>A p.C68Y Substitution - Missense 1:155014761-155014761 + SNUH_G20_S1 COSM3677405 c.699T>C p.Y233Y Substitution - coding silent 1:155015359-155015359 + TCGA-D3-A1QB-06 COSM3474807 c.959C>A p.S320Y Substitution - Missense 1:155015619-155015619 + SWE-32 COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + TCGA-HF-7132-01 COSM4022904 c.708G>T p.E236D Substitution - Missense 1:155015368-155015368 + LC_S11 COSM1185608 c.1415C>T p.P472L Substitution - Missense 1:155016480-155016480 + LUAD-YINHD COSM349786 c.1296C>A p.C432* Substitution - Nonsense 1:155016361-155016361 + Pat_63_A COSM5843839 c.248G>A p.G83E Substitution - Missense 1:155014908-155014908 + Gp2D COSM2209681 c.1180C>T p.R394W Substitution - Missense 1:155016245-155016245 + Pat_32_A COSM2209665 c.599G>A p.R200H Substitution - Missense 1:155015259-155015259 + T45458580 COSM5715375 c.121G>A p.D41N Substitution - Missense 1:155014679-155014679 + 2521260 COSM4545125 c.268G>A p.E90K Substitution - Missense 1:155014928-155014928 + SW48 COSM2209662 c.411C>T p.C137C Substitution - coding silent 1:155015071-155015071 + TCGA-F1-A448-01 COSM4022906 c.1317C>T p.F439F Substitution - coding silent 1:155016382-155016382 + KM12 COSM4638822 c.1482C>T p.F494F Substitution - coding silent 1:155016547-155016547 + NOKSI COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + TCGA-G4-6322-01 COSM5827511 c.925G>A p.G309S Substitution - Missense 1:155015483-155015483 + sysucc-1972T COSM5480326 c.1164G>C p.K388N Substitution - Missense 1:155016229-155016229 + TCGA-D8-A27G-01 COSM3802061 c.8G>A p.S3N Substitution - Missense 1:155014668-155014668 + TCGA-B5-A11E-01 COSM896723 c.1435G>A p.A479T Substitution - Missense 1:155016500-155016500 + TCGA-AZ-6601-01 COSM5142076 c.549G>T p.Q183H Substitution - Missense 1:155015209-155015209 + 721LT COSM4382675 c.1388G>A p.R463H Substitution - Missense 1:155016453-155016453 + TCGA-BR-8360-01 COSM4022905 c.1038G>A p.Q346Q Substitution - coding silent 1:155015698-155015698 + TCGA-AA-3663-01 COSM5827509 c.369T>A p.C123* Substitution - Nonsense 1:155014927-155014927 + TCGA-B5-A11H-01 COSM896719 c.1088G>A p.R363H Substitution - Missense 1:155015748-155015748 + CLL097 COSM1289992 c.1307A>G p.H436R Substitution - Missense 1:155016372-155016372 + Pat_63_A COSM5843840 c.350G>A p.G117E Substitution - Missense 1:155014908-155014908 + GCT27 COSM5749293 c.1516G>A p.A506T Substitution - Missense 1:155016581-155016581 + T3174 COSM4742215 c.341G>A p.S114N Substitution - Missense 1:155015001-155015001 + TCGA-AP-A056-01 COSM896711 c.204C>T p.G68G Substitution - coding silent 1:155014864-155014864 + LOVO COSM2209683 c.1214C>T p.P405L Substitution - Missense 1:155016279-155016279 + T24 COSM5619081 c.492C>T p.I164I Substitution - coding silent 1:155015050-155015050 + GCT27 COSM5749294 c.1618G>A p.A540T Substitution - Missense 1:155016581-155016581 + LUAD-B00416 COSM390972 c.1343delA p.H448fs*51 Deletion - Frameshift 1:155016408-155016408 + OSCC-GB_00440111 COSM3711156 c.1013G>T p.R338L Substitution - Missense 1:155015673-155015673 + TCGA-23-1032-01 COSM115877 c.463G>A p.D155N Substitution - Missense 1:155015123-155015123 + TCGA-74-6578-01 COSM3399792 c.82C>T p.R28C Substitution - Missense 1:155014742-155014742 + sysucc-311T COSM5477635 c.6A>G p.L2L Substitution - coding silent 1:155010925-155010925 + TCGA-CH-5748-01 COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + LC_C28 COSM1185607 c.211G>T p.V71F Substitution - Missense 1:155014871-155014871 + TCGA-AC-A23H-01 COSM5832295 c.126G>C p.L42L Substitution - coding silent 1:155014684-155014684 + TCGA-FS-A1ZW-06 COSM3474802 c.583C>T p.R195W Substitution - Missense 1:155015243-155015243 + J30_T COSM3976186 c.834A>C p.E278D Substitution - Missense 1:155015494-155015494 + TCGA-AA-3492-01 COSM1334518 c.1137C>T p.C379C Substitution - coding silent 1:155015797-155015797 + TCGA-A6-2686-01 COSM5083286 c.223delG p.G76fs*19 Deletion - Frameshift 1:155014883-155014883 + TCGA-BR-8382-01 COSM4022901 c.198C>T p.G66G Substitution - coding silent 1:155014858-155014858 + TCGA-BG-A0VZ-01 COSM463080 c.1164G>T p.K388N Substitution - Missense 1:155016229-155016229 + Pat_32_A COSM5843841 c.701G>A p.R234H Substitution - Missense 1:155015259-155015259 + UM-SCC-2 COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + BD136T COSM5507525 c.555G>A p.P185P Substitution - coding silent 1:155015113-155015113 + TCGA-D1-A17Q-01 COSM896722 c.1144C>T p.R382* Substitution - Nonsense 1:155015804-155015804 + HCT8 COSM4633338 c.881G>A p.G294D Substitution - Missense 1:155015541-155015541 + TCGA-DK-A2I4-01 COSM3788764 c.916G>C p.D306H Substitution - Missense 1:155015576-155015576 + 587332 COSM1233172 c.848T>C p.V283A Substitution - Missense 1:155015508-155015508 + TCGA-BF-A1Q0-01 COSM3474809 c.1305C>T p.C435C Substitution - coding silent 1:155016370-155016370 + OSCC-GB_00890111 COSM4887544 c.1A>C p.M1L Substitution - Missense 1:155014661-155014661 + T24 COSM424019 c.390C>T p.I130I Substitution - coding silent 1:155015050-155015050 + LUAD-RT-S01702 COSM392140 c.829_831delGAA p.E277delE Deletion - In frame 1:155015489-155015491 + TCGA-G4-6588-01 COSM1334515 c.736delG p.G247fs*68 Deletion - Frameshift 1:155015396-155015396 + TCGA-EJ-5522-01 COSM1127364 c.1407C>A p.P469P Substitution - coding silent 1:155016472-155016472 + CAL33 COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + ESCC_143 COSM5643903 c.823G>T p.G275C Substitution - Missense 1:155015483-155015483 + P56 COSM328995 c.338C>T p.T113I Substitution - Missense 1:155014998-155014998 + HCC137T COSM1600897 c.1289A>G p.Y430C Substitution - Missense 1:155016354-155016354 + TCGA-DK-A1AC-01 COSM1295155 c.1458C>T p.L486L Substitution - coding silent 1:155016523-155016523 + TCGA-AA-3516-01 COSM291655 c.729C>T p.G243G Substitution - coding silent 1:155015389-155015389 + EOPC-139_tumor_01 COSM5950288 c.2T>C p.M1T Substitution - Missense 1:155010921-155010921 + TCGA-EE-A2A0-06 COSM3474805 c.787C>T p.P263S Substitution - Missense 1:155015447-155015447 + HCA7 COSM896714 c.392C>T p.P131L Substitution - Missense 1:155015052-155015052 + PCSI_0037_Pa_X COSM3376004 c.1396G>A p.D466N Substitution - Missense 1:155016461-155016461 + TCGA-FD-A3B7-01 COSM463080 c.1164G>T p.K388N Substitution - Missense 1:155016229-155016229 + TCGA-B5-A11G-01 COSM896710 c.134A>G p.Y45C Substitution - Missense 1:155014794-155014794 + SCC-9 COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + T3724 COSM4742218 c.1247A>G p.D416G Substitution - Missense 1:155016312-155016312 + LUAD-S01357 COSM386130 c.1167G>C p.L389L Substitution - coding silent 1:155016232-155016232 + T3064 COSM4742214 c.258C>T p.A86A Substitution - coding silent 1:155014918-155014918 + TCGA-AA-3492-01 COSM5827513 c.1120C>T p.R374C Substitution - Missense 1:155015678-155015678 + TCGA-DD-A1EK-01 COSM2209672 c.840G>A p.E280E Substitution - coding silent 1:155015500-155015500 + TCGA-EE-A2GT-06 COSM3474808 c.1276G>C p.G426R Substitution - Missense 1:155016341-155016341 + TCGA-EE-A2MK-06 COSM3474803 c.612C>T p.P204P Substitution - coding silent 1:155015272-155015272 + T23 COSM424019 c.390C>T p.I130I Substitution - coding silent 1:155015050-155015050 + TCGA-AA-3492-01 COSM1334517 c.1018C>T p.R340C Substitution - Missense 1:155015678-155015678 + TCGA-AX-A0J1-01 COSM896721 c.1128C>T p.C376C Substitution - coding silent 1:155015788-155015788 + TCGA-GV-A40E-01 COSM3788765 c.1246G>A p.D416N Substitution - Missense 1:155016311-155016311 + TCGA-18-3409-01 COSM675820 c.1377C>T p.T459T Substitution - coding silent 1:155016442-155016442 + SCC-25 COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + 2521260 COSM5891317 c.370G>A p.E124K Substitution - Missense 1:155014928-155014928 + T3444 COSM4742219 c.1324G>T p.E442* Substitution - Nonsense 1:155016389-155016389 + TCGA-51-4079-01 COSM675821 c.1198C>T p.R400C Substitution - Missense 1:155016263-155016263 + TCGA-DD-A115-01 COSM4919667 c.956G>A p.S319N Substitution - Missense 1:155015616-155015616 + TCGA-AB-2910-03 COSM1317662 c.310G>A p.E104K Substitution - Missense 1:155014970-155014970 + QC2-35-T2 COSM5655060 c.1049C>A p.A350D Substitution - Missense 1:155015607-155015607 + TCGA-AX-A0J1-01 COSM896716 c.891G>A p.P297P Substitution - coding silent 1:155015551-155015551 + TCGA-AA-3710-01 COSM5103986 c.1528delC p.P511fs*>29 Deletion - Frameshift 1:155016593-155016593 + TCGA-BG-A0MT-01 COSM896718 c.1073_1099del27 p.G359_T367delGKLPRHMRT Deletion - In frame 1:155015733-155015759 + CSCC-44-T COSM4545125 c.268G>A p.E90K Substitution - Missense 1:155014928-155014928 + BD165T COSM5506627 c.1097G>T p.S366I Substitution - Missense 1:155015655-155015655 + LOVO COSM2209652 c.41C>T p.P14L Substitution - Missense 1:155014701-155014701 + TCGA-CM-4743-01 COSM5156084 c.478C>T p.R160C Substitution - Missense 1:155015138-155015138 + BD165T COSM5506626 c.995G>T p.S332I Substitution - Missense 1:155015655-155015655 + T2197 COSM4742213 c.199G>A p.G67S Substitution - Missense 1:155014859-155014859 + TCGA-DA-A1IA-06 COSM3474804 c.786C>T p.S262S Substitution - coding silent 1:155015446-155015446 + ME050T COSM230461 c.3_4GG>AT p.M1>? Complex 1:155014663-155014664 + LS174T COSM2209660 c.393G>A p.P131P Substitution - coding silent 1:155015053-155015053 + TCGA-AX-A06H-01 COSM896709 c.83G>A p.R28H Substitution - Missense 1:155014743-155014743 + T263 COSM4742216 c.453G>A p.P151P Substitution - coding silent 1:155015113-155015113 + Gp5D COSM2209681 c.1180C>T p.R394W Substitution - Missense 1:155016245-155016245 + T155 COSM1176466 c.1087C>T p.R363C Substitution - Missense 1:155015747-155015747 + PT23_1 COSM673519 c.115C>T p.R39W Substitution - Missense 1:155014775-155014775 + TCGA-AD-6889-01 COSM5827512 c.968G>T p.G323V Substitution - Missense 1:155015526-155015526 + LUAD-YINHD COSM349785 c.6G>A p.G2G Substitution - coding silent 1:155014666-155014666 + BD136T COSM4742216 c.453G>A p.P151P Substitution - coding silent 1:155015113-155015113 + TCGA-AA-3492-01 COSM5827514 c.1239C>T p.C413C Substitution - coding silent 1:155015797-155015797 + TCGA-AP-A051-01 COSM896715 c.456C>T p.D152D Substitution - coding silent 1:155015116-155015116 + ME029T COSM226462 c.593C>T p.A198V Substitution - Missense 1:155015253-155015253 + U2940 COSM5622209 c.475G>A p.A159T Substitution - Missense 1:155015135-155015135 + QC2-35-T2 COSM5655059 c.947C>A p.A316D Substitution - Missense 1:155015607-155015607 + ESCC_143 COSM5643904 c.925G>T p.G309C Substitution - Missense 1:155015483-155015483 + PT23_1 COSM5902528 c.217C>T p.R73W Substitution - Missense 1:155014775-155014775 + TCGA-D1-A177-01 COSM896714 c.392C>T p.P131L Substitution - Missense 1:155015052-155015052 + TCGA-A7-A4SF-01 COSM5832296 c.1455C>A p.G485G Substitution - coding silent 1:155016418-155016418 + 2334202 COSM324362 c.517G>A p.G173R Substitution - Missense 1:155015177-155015177 + TCGA-61-1740-01 COSM1319920 c.536A>G p.D179G Substitution - Missense 1:155015196-155015196 + TCGA-EE-A20H-06 COSM3474801 c.483G>C p.Q161H Substitution - Missense 1:155015143-155015143 + TCGA-EE-A3J7-06 COSM3862892 c.295C>A p.L99I Substitution - Missense 1:155014955-155014955 + ML_73_T_01 COSM5033578 c.1416A>G p.P472P Substitution - coding silent 1:155016481-155016481 + WSU-HN8 COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + HCT116 COSM4631991 c.872C>T p.A291V Substitution - Missense 1:155015532-155015532 + T45458580 COSM5715374 c.19G>A p.D7N Substitution - Missense 1:155014679-155014679 + TCGA-CJ-6031-01 COSM463080 c.1164G>T p.K388N Substitution - Missense 1:155016229-155016229 + PR-04-3113 COSM248417 c.1532C>T p.P511L Substitution - Missense 1:155016597-155016597 + TCGA-EE-A20C-06 COSM3474806 c.802C>T p.Q268* Substitution - Nonsense 1:155015462-155015462 + TCGA-AX-A060-01 COSM896712 c.295C>T p.L99L Substitution - coding silent 1:155014955-155014955 + PD8830a COSM5775538 c.1498G>A p.D500N Substitution - Missense 1:155016461-155016461 + TCGA-D8-A27G-01 COSM5832294 c.110G>A p.S37N Substitution - Missense 1:155014668-155014668 + BK0043 COSM4187356 c.1511A>T p.Q504L Substitution - Missense 1:155016576-155016576 + TCGA-F4-6856-01 COSM1334519 c.1157_1159delACG p.D387delD Deletion - In frame 1:155016222-155016224 + S02290 COSM5686327 c.1425T>C p.S475S Substitution - coding silent 1:155016490-155016490 + TCGA-66-2782-01 COSM675822 c.826G>C p.E276Q Substitution - Missense 1:155015486-155015486 + PD11386a COSM2209689 c.1498C>T p.R500* Substitution - Nonsense 1:155016563-155016563 + TCGA-BR-4362-01 COSM4022900 c.116G>A p.R39Q Substitution - Missense 1:155014776-155014776 + T2583 COSM4742217 c.647C>A p.A216E Substitution - Missense 1:155015307-155015307 + T222 COSM896716 c.891G>A p.P297P Substitution - coding silent 1:155015551-155015551 + TCGA-AA-3680-01 COSM293042 c.172T>C p.Y58H Substitution - Missense 1:155014832-155014832 + TCGA-IR-A3LA-01 COSM4844382 c.793G>A p.E265K Substitution - Missense 1:155015453-155015453 + TCGA-EE-A29N-06 COSM3474800 c.206G>A p.G69E Substitution - Missense 1:155014866-155014866 + TCGA-BG-A0MT-01 COSM896720 c.1099A>G p.T367A Substitution - Missense 1:155015759-155015759 + TCGA-BR-4201-01 COSM4022906 c.1317C>T p.F439F Substitution - coding silent 1:155016382-155016382 + STC252 COSM5052606 c.1385G>A p.R462H Substitution - Missense 1:155016450-155016450 + HCA7 COSM4629754 c.1116G>A p.K372K Substitution - coding silent 1:155015776-155015776 + PD22355a COSM5793658 c.101G>A p.C34Y Substitution - Missense 1:155014761-155014761 + CSCC-55-T COSM4564518 c.1138_1139GG>AT p.G380I Substitution - Missense 1:155015798-155015799 + M022 COSM1127365 c.980C>A p.A327E Substitution - Missense 1:155015640-155015640 + TCGA-FW-A3R5-06 COSM3862891 c.177C>T p.F59F Substitution - coding silent 1:155014837-155014837 + CSCC-27-T COSM4468797 c.1461C>T p.S487S Substitution - coding silent 1:155016526-155016526 + TCGA-F4-6856-01 COSM5827515 c.1259_1261delACG p.D421delD Deletion - In frame 1:155016222-155016224 + FM474T COSM673519 c.115C>T p.R39W Substitution - Missense 1:155014775-155014775 + CSCC-27-T COSM4468405 c.1439C>T p.S480F Substitution - Missense 1:155016504-155016504 + TCGA-66-2756-01 COSM675823 c.666G>T p.E222D Substitution - Missense 1:155015326-155015326 + TCGA-CG-5728-01 COSM4022903 c.702G>T p.E234D Substitution - Missense 1:155015362-155015362 + cSCCP1 COSM143426 c.1589_1590CC>TT p.P530L Substitution - Missense 1:155016654-155016655 + TCGA-AA-3663-01 COSM1334514 c.267T>A p.C89* Substitution - Nonsense 1:155014927-155014927 + TCGA-NH-A5IV-01 COSM5181901 c.1401A>G p.A467A Substitution - coding silent 1:155016466-155016466 + ESO-187 COSM1270737 c.1567G>A p.E523K Substitution - Missense 1:155016632-155016632 + TCGA-AP-A051-01 COSM896713 c.345C>T p.S115S Substitution - coding silent 1:155015005-155015005 + TCGA-DK-A2I4-01 COSM3788763 c.310G>C p.E104Q Substitution - Missense 1:155014970-155014970 + TCGA-G4-6588-01 COSM5827510 c.838delG p.G281fs*68 Deletion - Frameshift 1:155015396-155015396 + TCGA-P4-A5EB-01 COSM3984284 c.96C>G p.H32Q Substitution - Missense 1:155014756-155014756 + 44T COSM3711156 c.1013G>T p.R338L Substitution - Missense 1:155015673-155015673 + TCGA-EB-A551-01 COSM3474810 c.1311G>A p.K437K Substitution - coding silent 1:155016376-155016376 + HCC137 COSM1600897 c.1289A>G p.Y430C Substitution - Missense 1:155016354-155016354 + sysucc-311T COSM5477636 c.621T>G p.A207A Substitution - coding silent 1:155015281-155015281 + TCGA-AX-A0J0-01 COSM896717 c.930C>T p.I310I Substitution - coding silent 1:155015590-155015590 + ESO-D76 COSM1270738 c.1554T>C p.P518P Substitution - coding silent 1:155016619-155016619 + CSCC-29-T COSM4513915 c.853C>T p.P285S Substitution - Missense 1:155015513-155015513 + T3498 COSM4022906 c.1317C>T p.F439F Substitution - coding silent 1:155016382-155016382 + T23 COSM5619081 c.492C>T p.I164I Substitution - coding silent 1:155015050-155015050 + LOVO COSM2209660 c.393G>A p.P131P Substitution - coding silent 1:155015053-155015053 + S02290 COSM5686328 c.1527T>C p.S509S Substitution - coding silent 1:155016490-155016490 + TCGA-CK-6747-01 COSM392140 c.829_831delGAA p.E277delE Deletion - In frame 1:155015489-155015491 + TCGA-AD-6889-01 COSM1334516 c.866G>T p.G289V Substitution - Missense 1:155015526-155015526 + SN12C COSM1668018 c.164G>T p.C55F Substitution - Missense 1:155014824-155014824 + TCGA-BR-7851-01 COSM4022901 c.198C>T p.G66G Substitution - coding silent 1:155014858-155014858 + U2940 COSM5622210 c.577G>A p.A193T Substitution - Missense 1:155015135-155015135 + 477 COSM4438609 c.130G>A p.E44K Substitution - Missense 1:155014790-155014790 + ESO-0015 COSM1270736 c.1344C>T p.H448H Substitution - coding silent 1:155016409-155016409 + CHC197T COSM424019 c.390C>T p.I130I Substitution - coding silent 1:155015050-155015050 + TCGA-A7-A4SF-01 COSM3802063 c.1353C>A p.G451G Substitution - coding silent 1:155016418-155016418 + TCGA-B7-5816-01 COSM4022902 c.604C>T p.R202C Substitution - Missense 1:155015264-155015264 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.729267;Hs.729269;Hs.729271;Hs.729275;Hs.729279 1q21.3 607646

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Synonymous p.L146L c.438A>C 1 154987574 HNSC A G Missense p.H436R c.1307A>G 1 154988848 CLL A G Missense p.N488S c.1463A>G 1 154989004 LUAD A G Missense p.T367A c.1099A>G 1 154988235 UCEC A G Missense p.Y45C c.134A>G 1 154987270 UCEC CAGGCAAACTGCCTCGCCACATGAGGA - InFrameDeletion p.G359_T367delGKLPRHMRT c.1074_1100delAGGCAAACTGCCTCGCCACATGAGGAC 1 154988209 UCEC C A Missense p.L99I c.295C>A 1 154987431 CM C A Missense p.R202S c.604C>A 1 154987740 LUAD C A Missense p.S320Y c.959C>A 1 154988095 CM C A Synonymous p.P469P c.1407C>A 1 154988948 PRAD C A Synonymous p.R382R c.1144C>A 1 154988280 STAD CC TT Missense p.S299F c.896_897delinsTT 1 154988032 CM C G Missense p.P401R c.1202C>G 1 154988743 LUAD C G Synonymous p.L449L c.1347C>G 1 154988888 LUAD C T 3-UTRSNV . c.1617+1778C>T 1 154990936 CM C T Missense p.L122F c.364C>T 1 154987500 BLCA C T Missense p.P131L c.392C>T 1 154987528 UCEC C T Missense p.P263S c.787C>T 1 154987923 CM C T Missense p.P264S c.790C>T 1 154987926 LUAD C T Missense p.R195W c.583C>T 1 154987719 CM C T Missense p.R202C c.604C>T 1 154987740 STAD C T Missense p.R28C c.82C>T 1 154987218 GBM C T Missense p.R400C c.1198C>T 1 154988739 LUSC C T Missense p.R463C c.1387C>T 1 154988928 STAD C T Nonsense p.Q268* c.802C>T 1 154987938 CM C T Synonymous p.C435C c.1305C>T 1 154988846 CM C T Synonymous p.F439F c.1317C>T 1 154988858 STAD C T Synonymous p.H448H c.1344C>T 1 154988885 ESCA C T Synonymous p.L99L c.295C>T 1 154987431 UCEC C T Synonymous p.P204P c.612C>T 1 154987748 CM C T Synonymous p.S262S c.786C>T 1 154987922 CM G A Missense p.D155N c.463G>A 1 154987599 OV G A Missense p.E104K c.310G>A 1 154987446 AML G A Missense p.E279K c.835G>A 1 154987971 HNSC G A Missense p.E523K c.1567G>A 1 154989108 ESCA G A Missense p.G173R c.517G>A 1 154987653 SCLC G A Missense p.G249E c.746G>A 1 154987882 LUAD G A Missense p.G69E c.206G>A 1 154987342 CM G A Missense p.R28H c.83G>A 1 154987219 UCEC G A Missense p.R363H c.1088G>A 1 154988224 UCEC G A Synonymous p.K437K c.1311G>A 1 154988852 CM G C Missense p.D306H c.916G>C 1 154988052 BLCA G C Missense p.E104Q c.310G>C 1 154987446 BLCA G C Missense p.E276Q c.826G>C 1 154987962 LUSC G C Missense p.E371D c.1113G>C 1 154988249 HNSC G C Missense p.G426R c.1276G>C 1 154988817 CM G C Missense p.Q161H c.483G>C 1 154987619 CM GG AT MultiAAMissense p.M1_G2delinsIW c.3_4delinsAT 1 154987139 CM GT - Frameshift p.C89*fs*1 c.267_268delTG 1 154987396 HNSC G T IntronicSNV . c.1-11957G>T 1 154975180 CLL G T Missense p.E222D c.666G>T 1 154987802 LUSC G T Missense p.E234D c.702G>T 1 154987838 STAD G T Missense p.G240C c.718G>T 1 154987854 LUAD G T Missense p.K388N c.1164G>T 1 154988705 BLCA G T Missense p.K388N c.1164G>T 1 154988705 UCEC G T Synonymous p.P151P c.453G>T 1 154987589 LUAD G T Synonymous p.P192P c.576G>T 1 154987712 LUAD T C Missense p.Y58H c.172T>C 1 154987308 COREAD T C Synonymous p.P518P c.1554T>C 1 154989095 ESCA