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 23 132160659 132160659 + Silent SNP A A G TCGA-K4-A6FZ-01A-11D-A31L-08 TCGA-K4-A6FZ-10A-01D-A31J-08 g.chrX:132160659A>G c.1590T>C c.(1588-1590)tgT>tgC p.C530C BLCA 23 132160985 132160985 + Missense_Mutation SNP C C T TCGA-DK-A2HX-01A-12D-A18F-08 TCGA-DK-A2HX-10A-01D-A18F-08 g.chrX:132160985C>T c.1264G>A c.(1264-1266)Gct>Act p.A422T BLCA 23 132161288 132161288 + Missense_Mutation SNP C C T TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chrX:132161288C>T c.961G>A c.(961-963)Gat>Aat p.D321N BLCA 23 132161616 132161616 + Silent SNP C C T TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chrX:132161616C>T c.633G>A c.(631-633)tcG>tcA p.S211S BLCA 23 132161712 132161712 + Silent SNP C C T TCGA-BT-A20T-01A-11D-A14W-08 TCGA-BT-A20T-11A-11D-A14W-08 g.chrX:132161712C>T c.537G>A c.(535-537)aaG>aaA p.K179K BLCA 23 132161945 132161945 + Missense_Mutation SNP G G A TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chrX:132161945G>A c.304C>T c.(304-306)Cat>Tat p.H102Y BLCA 23 132162129 132162129 + Silent SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chrX:132162129C>T c.120G>A c.(118-120)ctG>ctA p.L40L BRCA 23 132159686 132159686 + Missense_Mutation SNP A A G TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chrX:132159686A>G c.2563T>C c.(2563-2565)Ttc>Ctc p.F855L BRCA 23 132160197 132160197 + Silent SNP G G T TCGA-EW-A1PB-01A-11D-A142-09 TCGA-EW-A1PB-10A-01D-A142-09 g.chrX:132160197G>T c.2052C>A c.(2050-2052)ctC>ctA p.L684L BRCA 23 132160788 132160788 + Frame_Shift_Del DEL A A - TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chrX:132160788delA c.1461delT c.(1459-1461)tttfs p.F487fs BRCA 23 132161352 132161352 + Missense_Mutation SNP A A T TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chrX:132161352A>T c.897T>A c.(895-897)aaT>aaA p.N299K BRCA 23 132161376 132161376 + Silent SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:132161376C>T c.873G>A c.(871-873)gaG>gaA p.E291E BRCA 23 132161848 132161848 + Missense_Mutation SNP T T G TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:132161848T>G c.401A>C c.(400-402)aAa>aCa p.K134T CESC 23 132159590 132159590 + Missense_Mutation SNP C C T TCGA-Q1-A5R2-01A-11D-A28B-09 TCGA-Q1-A5R2-10A-01D-A28E-09 g.chrX:132159590C>T c.2659G>A c.(2659-2661)Gag>Aag p.E887K CESC 23 132159901 132159901 + Missense_Mutation SNP G G C TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chrX:132159901G>C c.2348C>G c.(2347-2349)tCt>tGt p.S783C CESC 23 132159937 132159937 + Missense_Mutation SNP T T G TCGA-Q1-A6DT-01A-11D-A32I-09 TCGA-Q1-A6DT-10A-01D-A32I-09 g.chrX:132159937T>G c.2312A>C c.(2311-2313)aAc>aCc p.N771T CESC 23 132161099 132161099 + Missense_Mutation SNP G G A TCGA-FU-A23K-01A-11D-A16O-08 TCGA-FU-A23K-10A-01D-A16O-08 g.chrX:132161099G>A c.1150C>T c.(1150-1152)Cat>Tat p.H384Y CESC 23 132161143 132161143 + Nonsense_Mutation SNP G G T TCGA-C5-A1BN-01B-11D-A14W-08 TCGA-C5-A1BN-10A-01D-A14W-08 g.chrX:132161143G>T c.1106C>A c.(1105-1107)tCa>tAa p.S369* CESC 23 132161383 132161383 + Missense_Mutation SNP A A G TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chrX:132161383A>G c.866T>C c.(865-867)tTt>tCt p.F289S CESC 23 132161543 132161543 + Nonsense_Mutation SNP C C A TCGA-EK-A3GJ-01A-21D-A20U-09 TCGA-EK-A3GJ-11A-11D-A20U-09 g.chrX:132161543C>A c.706G>T c.(706-708)Gaa>Taa p.E236* COAD 23 132159625 132159625 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chrX:132159625C>T c.2624G>A c.(2623-2625)cGt>cAt p.R875H COAD 23 132159667 132159667 + Missense_Mutation SNP C C T TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chrX:132159667C>T c.2582G>A c.(2581-2583)cGg>cAg p.R861Q COAD 23 132159667 132159667 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:132159667C>T c.2582G>A c.(2581-2583)cGg>cAg p.R861Q COAD 23 132160053 132160053 + Silent SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chrX:132160053G>A c.2196C>T c.(2194-2196)ttC>ttT p.F732F COAD 23 132160273 132160273 + Missense_Mutation SNP G G A TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chrX:132160273G>A c.1976C>T c.(1975-1977)aCg>aTg p.T659M COAD 23 132160291 132160291 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chrX:132160291G>A c.1958C>T c.(1957-1959)cCg>cTg p.P653L COAD 23 132160412 132160413 + Frame_Shift_Ins INS - - T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chrX:132160412_132160413insT c.1836_1837insA c.(1834-1839)aaaggcfs p.G613fs COAD 23 132160413 132160413 + Frame_Shift_Del DEL T T - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chrX:132160413delT c.1836delA c.(1834-1836)aaafs p.K612fs COAD 23 132160413 132160413 + Frame_Shift_Del DEL T T - TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chrX:132160413delT c.1836delA c.(1834-1836)aaafs p.K612fs COAD 23 132160413 132160413 + Frame_Shift_Del DEL T T - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:132160413delT c.1836delA c.(1834-1836)aaafs p.K612fs COAD 23 132160413 132160414 + Frame_Shift_Del DEL TT TT - TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chrX:132160413_132160414delTT c.1835_1836delAA c.(1834-1836)aaafs p.K612fs COAD 23 132160553 132160553 + Nonsense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:132160553C>A c.1696G>T c.(1696-1698)Gaa>Taa p.E566* COAD 23 132160787 132160788 + Frame_Shift_Ins INS - - A TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chrX:132160787_132160788insA c.1461_1462insT c.(1459-1464)tttggafs p.G488fs COAD 23 132160788 132160788 + Frame_Shift_Del DEL A A - TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:132160788delA c.1461delT c.(1459-1461)tttfs p.F487fs COAD 23 132160804 132160804 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:132160804G>A c.1445C>T c.(1444-1446)aCt>aTt p.T482I COAD 23 132160837 132160837 + Missense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chrX:132160837C>A c.1412G>T c.(1411-1413)aGa>aTa p.R471I COAD 23 132161009 132161009 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:132161009C>A c.1240G>T c.(1240-1242)Gat>Tat p.D414Y COAD 23 132161063 132161063 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:132161063C>A c.1186G>T c.(1186-1188)Gat>Tat p.D396Y COAD 23 132161158 132161158 + Missense_Mutation SNP A A T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chrX:132161158A>T c.1091T>A c.(1090-1092)cTt>cAt p.L364H COAD 23 132161204 132161205 + Frame_Shift_Ins INS - - A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chrX:132161204_132161205insA c.1044_1045insT c.(1042-1047)tttaaafs p.K349fs COAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COAD 23 132161522 132161522 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:132161522C>T c.727G>A c.(727-729)Gcc>Acc p.A243T COAD 23 132161863 132161863 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:132161863T>G c.386A>C c.(385-387)aAa>aCa p.K129T COADREAD 23 132159625 132159625 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chrX:132159625C>T c.2624G>A c.(2623-2625)cGt>cAt p.R875H COADREAD 23 132159667 132159667 + Missense_Mutation SNP C C T TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chrX:132159667C>T c.2582G>A c.(2581-2583)cGg>cAg p.R861Q COADREAD 23 132159667 132159667 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:132159667C>T c.2582G>A c.(2581-2583)cGg>cAg p.R861Q COADREAD 23 132159678 132159678 + Silent SNP G G A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:132159678G>A c.2571C>T c.(2569-2571)taC>taT p.Y857Y COADREAD 23 132160053 132160053 + Silent SNP G G A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chrX:132160053G>A c.2196C>T c.(2194-2196)ttC>ttT p.F732F COADREAD 23 132160273 132160273 + Missense_Mutation SNP G G A TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chrX:132160273G>A c.1976C>T c.(1975-1977)aCg>aTg p.T659M COADREAD 23 132160291 132160291 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chrX:132160291G>A c.1958C>T c.(1957-1959)cCg>cTg p.P653L COADREAD 23 132160412 132160413 + Frame_Shift_Ins INS - - T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chrX:132160412_132160413insT c.1836_1837insA c.(1834-1839)aaaggcfs p.G613fs COADREAD 23 132160413 132160413 + Frame_Shift_Del DEL T T - TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chrX:132160413delT c.1836delA c.(1834-1836)aaafs p.K612fs COADREAD 23 132160413 132160413 + Frame_Shift_Del DEL T T - TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chrX:132160413delT c.1836delA c.(1834-1836)aaafs p.K612fs COADREAD 23 132160413 132160413 + Frame_Shift_Del DEL T T - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:132160413delT c.1836delA c.(1834-1836)aaafs p.K612fs COADREAD 23 132160413 132160414 + Frame_Shift_Del DEL TT TT - TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chrX:132160413_132160414delTT c.1835_1836delAA c.(1834-1836)aaafs p.K612fs COADREAD 23 132160488 132160488 + Silent SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:132160488T>G c.1761A>C c.(1759-1761)tcA>tcC p.S587S COADREAD 23 132160553 132160553 + Nonsense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:132160553C>A c.1696G>T c.(1696-1698)Gaa>Taa p.E566* COADREAD 23 132160787 132160788 + Frame_Shift_Ins INS - - A TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chrX:132160787_132160788insA c.1461_1462insT c.(1459-1464)tttggafs p.G488fs COADREAD 23 132160788 132160788 + Frame_Shift_Del DEL A A - TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:132160788delA c.1461delT c.(1459-1461)tttfs p.F487fs COADREAD 23 132160804 132160804 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:132160804G>A c.1445C>T c.(1444-1446)aCt>aTt p.T482I COADREAD 23 132160837 132160837 + Missense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chrX:132160837C>A c.1412G>T c.(1411-1413)aGa>aTa p.R471I COADREAD 23 132161009 132161009 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chrX:132161009C>A c.1240G>T c.(1240-1242)Gat>Tat p.D414Y COADREAD 23 132161063 132161063 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:132161063C>A c.1186G>T c.(1186-1188)Gat>Tat p.D396Y COADREAD 23 132161158 132161158 + Missense_Mutation SNP A A T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chrX:132161158A>T c.1091T>A c.(1090-1092)cTt>cAt p.L364H COADREAD 23 132161204 132161205 + Frame_Shift_Ins INS - - A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chrX:132161204_132161205insA c.1044_1045insT c.(1042-1047)tttaaafs p.K349fs COADREAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COADREAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COADREAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COADREAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COADREAD 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs COADREAD 23 132161522 132161522 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:132161522C>T c.727G>A c.(727-729)Gcc>Acc p.A243T COADREAD 23 132161838 132161838 + Missense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:132161838C>A c.411G>T c.(409-411)gaG>gaT p.E137D COADREAD 23 132161863 132161863 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:132161863T>G c.386A>C c.(385-387)aAa>aCa p.K129T DLBC 23 132161159 132161159 + Missense_Mutation SNP G G A TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chrX:132161159G>A c.1090C>T c.(1090-1092)Ctt>Ttt p.L364F ESCA 23 132160963 132160963 + Missense_Mutation SNP C C A TCGA-L5-A8NF-01A-11D-A37C-09 TCGA-L5-A8NF-11A-11D-A37F-09 g.chrX:132160963C>A c.1286G>T c.(1285-1287)gGg>gTg p.G429V ESCA 23 132161204 132161205 + Frame_Shift_Ins INS - - A TCGA-L5-A4OX-01A-21D-A28B-09 TCGA-L5-A4OX-11A-13D-A28E-09 g.chrX:132161204_132161205insA c.1044_1045insT c.(1042-1047)tttaaafs p.K349fs ESCA 23 132161455 132161455 + Missense_Mutation SNP A A G TCGA-L5-A4OE-01A-11D-A27G-09 TCGA-L5-A4OE-11A-11D-A27G-09 g.chrX:132161455A>G c.794T>C c.(793-795)gTa>gCa p.V265A GBM 23 132160788 132160788 + Frame_Shift_Del DEL A A - TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chrX:132160788delA c.1461delT c.(1459-1461)tttfs p.F487fs GBM 23 132161219 132161219 + Missense_Mutation SNP G G A TCGA-76-6286-01A-11D-1845-08 TCGA-76-6286-10A-01D-1845-08 g.chrX:132161219G>A c.1030C>T c.(1030-1032)Cgg>Tgg p.R344W GBM 23 132161937 132161937 + Silent SNP G G A TCGA-41-3393-01A-01D-1353-08 TCGA-41-3393-10A-01D-1353-08 g.chrX:132161937G>A c.312C>T c.(310-312)aaC>aaT p.N104N GBMLGG 23 132159579 132159579 + Silent SNP T T C TCGA-DB-A64W-01A-11D-A29Q-08 TCGA-DB-A64W-10A-01D-A29Q-08 g.chrX:132159579T>C c.2670A>G c.(2668-2670)gaA>gaG p.E890E GBMLGG 23 132160182 132160182 + Silent SNP A A G TCGA-P5-A780-01A-12D-A32B-08 TCGA-P5-A780-10A-01D-A329-08 g.chrX:132160182A>G c.2067T>C c.(2065-2067)ttT>ttC p.F689F GBMLGG 23 132160495 132160495 + Missense_Mutation SNP C C G TCGA-VM-A8CB-01A-11D-A36O-08 TCGA-VM-A8CB-10A-01D-A367-08 g.chrX:132160495C>G c.1754G>C c.(1753-1755)aGt>aCt p.S585T GBMLGG 23 132160551 132160551 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:132160551T>C c.1698A>G c.(1696-1698)gaA>gaG p.E566E GBMLGG 23 132160726 132160726 + Missense_Mutation SNP T T C TCGA-DH-A66G-01A-21D-A31L-08 TCGA-DH-A66G-10A-01D-A31J-08 g.chrX:132160726T>C c.1523A>G c.(1522-1524)cAc>cGc p.H508R GBMLGG 23 132160788 132160788 + Frame_Shift_Del DEL A A - TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chrX:132160788delA c.1461delT c.(1459-1461)tttfs p.F487fs GBMLGG 23 132161017 132161017 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:132161017A>G c.1232T>C c.(1231-1233)tTt>tCt p.F411S GBMLGG 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs GBMLGG 23 132161219 132161219 + Missense_Mutation SNP G G A TCGA-76-6286-01A-11D-1845-08 TCGA-76-6286-10A-01D-1845-08 g.chrX:132161219G>A c.1030C>T c.(1030-1032)Cgg>Tgg p.R344W GBMLGG 23 132161316 132161316 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:132161316C>A c.933G>T c.(931-933)caG>caT p.Q311H GBMLGG 23 132161937 132161937 + Silent SNP G G A TCGA-41-3393-01A-01D-1353-08 TCGA-41-3393-10A-01D-1353-08 g.chrX:132161937G>A c.312C>T c.(310-312)aaC>aaT p.N104N GBMLGG 23 132162098 132162098 + Missense_Mutation SNP G G A TCGA-QH-A6CV-01A-11D-A31L-08 TCGA-QH-A6CV-10A-01D-A31J-08 g.chrX:132162098G>A c.151C>T c.(151-153)Cgg>Tgg p.R51W HNSC 23 132159533 132159533 + Missense_Mutation SNP C C A TCGA-CN-4742-01A-02D-1512-08 TCGA-CN-4742-10A-01D-1512-08 g.chrX:132159533C>A c.2716G>T c.(2716-2718)Gta>Tta p.V906L HNSC 23 132159687 132159687 + Missense_Mutation SNP C C A TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chrX:132159687C>A c.2562G>T c.(2560-2562)tgG>tgT p.W854C HNSC 23 132159731 132159731 + Missense_Mutation SNP C C A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chrX:132159731C>A c.2518G>T c.(2518-2520)Ggc>Tgc p.G840C HNSC 23 132161099 132161099 + Missense_Mutation SNP G G C TCGA-CN-6998-01A-23D-2012-08 TCGA-CN-6998-10A-01D-2013-08 g.chrX:132161099G>C c.1150C>G c.(1150-1152)Cat>Gat p.H384D HNSC 23 132161248 132161248 + Missense_Mutation SNP G G T TCGA-CN-6988-01A-11D-1912-08 TCGA-CN-6988-10A-01D-1912-08 g.chrX:132161248G>T c.1001C>A c.(1000-1002)cCc>cAc p.P334H HNSC 23 132162111 132162111 + Frame_Shift_Del DEL T T - TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chrX:132162111delT c.138delA c.(136-138)aaafs p.K46fs HNSC 23 132162179 132162179 + Missense_Mutation SNP C C G TCGA-CN-5360-01A-01D-1434-08 TCGA-CN-5360-10A-01D-1434-08 g.chrX:132162179C>G c.70G>C c.(70-72)Gaa>Caa p.E24Q KICH 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-KO-8404-01A-11D-2310-10 TCGA-KO-8404-11A-01D-2311-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs KIPAN 23 132160221 132160221 + Silent SNP A A C TCGA-BQ-5879-01A-11D-1589-08 TCGA-BQ-5879-11A-01D-1589-08 g.chrX:132160221A>C c.2028T>G c.(2026-2028)ccT>ccG p.P676P KIPAN 23 132160271 132160271 + Missense_Mutation SNP A A G TCGA-B0-5099-01A-01D-1421-08 TCGA-B0-5099-11A-01D-1421-08 g.chrX:132160271A>G c.1978T>C c.(1978-1980)Tat>Cat p.Y660H KIPAN 23 132161106 132161106 + Silent SNP G G A TCGA-CJ-4873-01A-01D-1373-10 TCGA-CJ-4873-11A-01D-1373-10 g.chrX:132161106G>A c.1143C>T c.(1141-1143)aaC>aaT p.N381N KIPAN 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-KO-8404-01A-11D-2310-10 TCGA-KO-8404-11A-01D-2311-10 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs KIRC 23 132160271 132160271 + Missense_Mutation SNP A A G TCGA-B0-5099-01A-01D-1421-08 TCGA-B0-5099-11A-01D-1421-08 g.chrX:132160271A>G c.1978T>C c.(1978-1980)Tat>Cat p.Y660H KIRC 23 132161106 132161106 + Silent SNP G G A TCGA-CJ-4873-01A-01D-1373-10 TCGA-CJ-4873-11A-01D-1373-10 g.chrX:132161106G>A c.1143C>T c.(1141-1143)aaC>aaT p.N381N KIRP 23 132160221 132160221 + Silent SNP A A C TCGA-BQ-5879-01A-11D-1589-08 TCGA-BQ-5879-11A-01D-1589-08 g.chrX:132160221A>C c.2028T>G c.(2026-2028)ccT>ccG p.P676P LGG 23 132159579 132159579 + Silent SNP T T C TCGA-DB-A64W-01A-11D-A29Q-08 TCGA-DB-A64W-10A-01D-A29Q-08 g.chrX:132159579T>C c.2670A>G c.(2668-2670)gaA>gaG p.E890E LGG 23 132160182 132160182 + Silent SNP A A G TCGA-P5-A780-01A-12D-A32B-08 TCGA-P5-A780-10A-01D-A329-08 g.chrX:132160182A>G c.2067T>C c.(2065-2067)ttT>ttC p.F689F LGG 23 132160495 132160495 + Missense_Mutation SNP C C G TCGA-VM-A8CB-01A-11D-A36O-08 TCGA-VM-A8CB-10A-01D-A367-08 g.chrX:132160495C>G c.1754G>C c.(1753-1755)aGt>aCt p.S585T LGG 23 132160551 132160551 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:132160551T>C c.1698A>G c.(1696-1698)gaA>gaG p.E566E LGG 23 132160726 132160726 + Missense_Mutation SNP T T C TCGA-DH-A66G-01A-21D-A31L-08 TCGA-DH-A66G-10A-01D-A31J-08 g.chrX:132160726T>C c.1523A>G c.(1522-1524)cAc>cGc p.H508R LGG 23 132161017 132161017 + Missense_Mutation SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:132161017A>G c.1232T>C c.(1231-1233)tTt>tCt p.F411S LGG 23 132161205 132161205 + Frame_Shift_Del DEL A A - TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chrX:132161205delA c.1044delT c.(1042-1044)tttfs p.F348fs LGG 23 132161316 132161316 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:132161316C>A c.933G>T c.(931-933)caG>caT p.Q311H LGG 23 132162098 132162098 + Missense_Mutation SNP G G A TCGA-QH-A6CV-01A-11D-A31L-08 TCGA-QH-A6CV-10A-01D-A31J-08 g.chrX:132162098G>A c.151C>T c.(151-153)Cgg>Tgg p.R51W LIHC 23 132159790 132159790 + Missense_Mutation SNP C C A TCGA-CC-A5UE-01A-11D-A28X-10 TCGA-CC-A5UE-10A-01D-A28X-10 g.chrX:132159790C>A c.2459G>T c.(2458-2460)gGa>gTa p.G820V LIHC 23 132160217 132160217 + Missense_Mutation SNP T T A TCGA-WX-AA44-01A-11D-A38X-10 TCGA-WX-AA44-10A-01D-A38X-10 g.chrX:132160217T>A c.2032A>T c.(2032-2034)Agc>Tgc p.S678C LIHC 23 132161219 132161219 + Missense_Mutation SNP G G A TCGA-DD-A73B-01A-12D-A32G-10 TCGA-DD-A73B-10A-01D-A32G-10 g.chrX:132161219G>A c.1030C>T c.(1030-1032)Cgg>Tgg p.R344W LIHC 23 132161579 132161579 + Silent SNP A A G TCGA-DD-AACI-01A-11D-A40R-10 TCGA-DD-AACI-10A-01D-A40U-10 g.chrX:132161579A>G c.670T>C c.(670-672)Tta>Cta p.L224L LUAD 23 132159518 132159518 + Missense_Mutation SNP G G T TCGA-NJ-A55R-01A-11D-A25L-08 TCGA-NJ-A55R-10A-01D-A25L-08 g.chrX:132159518G>T c.2731C>A c.(2731-2733)Cag>Aag p.Q911K LUAD 23 132159638 132159638 + Missense_Mutation SNP G G T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chrX:132159638G>T c.2611C>A c.(2611-2613)Cag>Aag p.Q871K LUAD 23 132159646 132159646 + Missense_Mutation SNP G G C TCGA-NJ-A55O-01A-11D-A25L-08 TCGA-NJ-A55O-10A-01D-A25L-08 g.chrX:132159646G>C c.2603C>G c.(2602-2604)gCc>gGc p.A868G LUAD 23 132159788 132159788 + Missense_Mutation SNP C C T TCGA-80-5607-01A-31D-1945-08 TCGA-80-5607-10A-01D-1946-08 g.chrX:132159788C>T c.2461G>A c.(2461-2463)Gat>Aat p.D821N LUAD 23 132159958 132159958 + Missense_Mutation SNP C C A TCGA-38-4626-01A-01D-1553-08 TCGA-38-4626-11A-01D-1553-08 g.chrX:132159958C>A c.2291G>T c.(2290-2292)gGc>gTc p.G764V LUAD 23 132160099 132160099 + Missense_Mutation SNP G G T TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chrX:132160099G>T c.2150C>A c.(2149-2151)aCt>aAt p.T717N LUAD 23 132160157 132160157 + Nonsense_Mutation SNP G G A TCGA-55-6987-01A-11D-1945-08 TCGA-55-6987-11A-01D-1945-08 g.chrX:132160157G>A c.2092C>T c.(2092-2094)Cga>Tga p.R698* LUAD 23 132160165 132160165 + Missense_Mutation SNP T T C TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chrX:132160165T>C c.2084A>G c.(2083-2085)aAt>aGt p.N695S LUAD 23 132160222 132160222 + Missense_Mutation SNP G G T TCGA-78-7542-01A-21D-2063-08 TCGA-78-7542-11A-01D-2063-08 g.chrX:132160222G>T c.2027C>A c.(2026-2028)cCt>cAt p.P676H LUAD 23 132160223 132160223 + Missense_Mutation SNP G G T TCGA-78-7542-01A-21D-2063-08 TCGA-78-7542-11A-01D-2063-08 g.chrX:132160223G>T c.2026C>A c.(2026-2028)Cct>Act p.P676T LUAD 23 132160483 132160483 + Missense_Mutation SNP G G T TCGA-55-6968-01A-11D-1945-08 TCGA-55-6968-11A-01D-1945-08 g.chrX:132160483G>T c.1766C>A c.(1765-1767)cCt>cAt p.P589H LUAD 23 132160639 132160639 + Missense_Mutation SNP T T A TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chrX:132160639T>A c.1610A>T c.(1609-1611)cAg>cTg p.Q537L LUAD 23 132160640 132160640 + Missense_Mutation SNP G G T TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chrX:132160640G>T c.1609C>A c.(1609-1611)Cag>Aag p.Q537K LUAD 23 132160953 132160953 + Nonsense_Mutation SNP G G T TCGA-44-6774-01A-21D-1855-08 TCGA-44-6774-10A-01D-1855-08 g.chrX:132160953G>T c.1296C>A c.(1294-1296)tgC>tgA p.C432* LUAD 23 132160973 132160973 + Missense_Mutation SNP C C G TCGA-55-7574-01A-11D-2036-08 TCGA-55-7574-10A-01D-2036-08 g.chrX:132160973C>G c.1276G>C c.(1276-1278)Gac>Cac p.D426H LUAD 23 132160979 132160979 + Missense_Mutation SNP C C A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chrX:132160979C>A c.1270G>T c.(1270-1272)Gat>Tat p.D424Y LUAD 23 132161025 132161025 + Missense_Mutation SNP T T A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chrX:132161025T>A c.1224A>T c.(1222-1224)aaA>aaT p.K408N LUAD 23 132161214 132161214 + Silent SNP T T G TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chrX:132161214T>G c.1035A>C c.(1033-1035)ctA>ctC p.L345L LUAD 23 132161322 132161322 + Silent SNP C C T TCGA-55-8511-01A-11D-2393-08 TCGA-55-8511-10A-01D-2393-08 g.chrX:132161322C>T c.927G>A c.(925-927)gtG>gtA p.V309V LUAD 23 132161441 132161441 + Missense_Mutation SNP G G C TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chrX:132161441G>C c.808C>G c.(808-810)Caa>Gaa p.Q270E LUAD 23 132161641 132161641 + Missense_Mutation SNP T T C TCGA-50-5068-01A-01D-1625-08 TCGA-50-5068-10A-01D-1625-08 g.chrX:132161641T>C c.608A>G c.(607-609)tAc>tGc p.Y203C LUAD 23 132161731 132161731 + Nonsense_Mutation SNP G G C TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chrX:132161731G>C c.518C>G c.(517-519)tCa>tGa p.S173* LUAD 23 132161911 132161911 + Missense_Mutation SNP C C A TCGA-95-7562-01A-11D-2238-08 TCGA-95-7562-10B-01D-2238-08 g.chrX:132161911C>A c.338G>T c.(337-339)gGt>gTt p.G113V LUAD 23 132161952 132161952 + Missense_Mutation SNP G G T TCGA-78-7159-01A-11D-2036-08 TCGA-78-7159-10A-01D-2036-08 g.chrX:132161952G>T c.297C>A c.(295-297)gaC>gaA p.D99E LUAD 23 132162134 132162134 + Missense_Mutation SNP C C A TCGA-05-4405-01A-21D-1855-08 TCGA-05-4405-10A-01D-1855-08 g.chrX:132162134C>A c.115G>T c.(115-117)Gtg>Ttg p.V39L LUSC 23 132159856 132159856 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chrX:132159856C>T c.2393G>A c.(2392-2394)aGa>aAa p.R798K LUSC 23 132160305 132160305 + Missense_Mutation SNP G G C TCGA-39-5036-01A-01D-1441-08 TCGA-39-5036-11A-01D-1441-08 g.chrX:132160305G>C c.1944C>G c.(1942-1944)ttC>ttG p.F648L LUSC 23 132161178 132161178 + Silent SNP C C T TCGA-39-5039-01A-01D-1441-08 TCGA-39-5039-11A-01D-1441-08 g.chrX:132161178C>T c.1071G>A c.(1069-1071)aaG>aaA p.K357K LUSC 23 132161299 132161299 + Missense_Mutation SNP G G T TCGA-39-5028-01A-01D-1441-08 TCGA-39-5028-11A-01D-1441-08 g.chrX:132161299G>T c.950C>A c.(949-951)cCa>cAa p.P317Q LUSC 23 132162097 132162097 + Missense_Mutation SNP C C A TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chrX:132162097C>A c.152G>T c.(151-153)cGg>cTg p.R51L OV 23 132162152 132162152 + Nonsense_Mutation SNP T T A TCGA-36-2539-01A-01D-1526-09 TCGA-36-2539-10A-01D-1526-09 g.chrX:132162152T>A c.97A>T c.(97-99)Aag>Tag p.K33* PAAD 23 132159668 132159668 + Missense_Mutation SNP G G A TCGA-3A-A9IH-01A-12D-A397-08 TCGA-3A-A9IH-10A-01D-A39A-08 g.chrX:132159668G>A c.2581C>T c.(2581-2583)Cgg>Tgg p.R861W PAAD 23 132160788 132160788 + Frame_Shift_Del DEL A A - TCGA-IB-A5SS-01A-11D-A32N-08 TCGA-IB-A5SS-10A-01D-A32N-08 g.chrX:132160788delA c.1461delT c.(1459-1461)tttfs p.F487fs PRAD 23 132159947 132159947 + Missense_Mutation SNP G G T TCGA-KK-A6DY-01A-12D-A30X-08 TCGA-KK-A6DY-11A-11D-A30X-08 g.chrX:132159947G>T c.2302C>A c.(2302-2304)Cac>Aac p.H768N PRAD 23 132160413 132160413 + Frame_Shift_Del DEL T T - TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chrX:132160413delT c.1836delA c.(1834-1836)aaafs p.K612fs READ 23 132159678 132159678 + Silent SNP G G A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:132159678G>A c.2571C>T c.(2569-2571)taC>taT p.Y857Y READ 23 132160488 132160488 + Silent SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:132160488T>G c.1761A>C c.(1759-1761)tcA>tcC p.S587S READ 23 132161838 132161838 + Missense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:132161838C>A c.411G>T c.(409-411)gaG>gaT p.E137D SARC 23 132160344 132160344 + Silent SNP T T A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chrX:132160344T>A c.1905A>T c.(1903-1905)ccA>ccT p.P635P SARC 23 132161247 132161247 + Silent SNP G G A TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chrX:132161247G>A c.1002C>T c.(1000-1002)ccC>ccT p.P334P SKCM 23 132159790 132159790 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chrX:132159790C>T c.2459G>A c.(2458-2460)gGa>gAa p.G820E SKCM 23 132159888 132159888 + Silent SNP G G A TCGA-EE-A2GD-06A-11D-A196-08 TCGA-EE-A2GD-10A-01D-A198-08 g.chrX:132159888G>A c.2361C>T c.(2359-2361)tcC>tcT p.S787S SKCM 23 132159894 132159894 + Silent SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chrX:132159894C>T c.2355G>A c.(2353-2355)agG>agA p.R785R SKCM 23 132160053 132160053 + Silent SNP G G A TCGA-D3-A3MU-06A-11D-A21A-08 TCGA-D3-A3MU-10A-01D-A21A-08 g.chrX:132160053G>A c.2196C>T c.(2194-2196)ttC>ttT p.F732F SKCM 23 132160103 132160103 + Missense_Mutation SNP G G A TCGA-FR-A44A-06A-11D-A24R-08 TCGA-FR-A44A-10A-01D-A24R-08 g.chrX:132160103G>A c.2146C>T c.(2146-2148)Cct>Tct p.P716S SKCM 23 132160128 132160128 + Missense_Mutation SNP A A C TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chrX:132160128A>C c.2121T>G c.(2119-2121)ttT>ttG p.F707L SKCM 23 132160170 132160170 + Silent SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chrX:132160170G>A c.2079C>T c.(2077-2079)ccC>ccT p.P693P SKCM 23 132160265 132160265 + Missense_Mutation SNP C C T TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chrX:132160265C>T c.1984G>A c.(1984-1986)Gaa>Aaa p.E662K SKCM 23 132160351 132160351 + Missense_Mutation SNP G G A TCGA-D3-A3C3-06A-12D-A19A-08 TCGA-D3-A3C3-10A-01D-A19A-08 g.chrX:132160351G>A c.1898C>T c.(1897-1899)tCt>tTt p.S633F SKCM 23 132160351 132160351 + Missense_Mutation SNP G G A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chrX:132160351G>A c.1898C>T c.(1897-1899)tCt>tTt p.S633F SKCM 23 132160463 132160463 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:132160463C>T c.1786G>A c.(1786-1788)Gat>Aat p.D596N SKCM 23 132160489 132160489 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chrX:132160489G>A c.1760C>T c.(1759-1761)tCa>tTa p.S587L SKCM 23 132160519 132160519 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:132160519C>T c.1730G>A c.(1729-1731)cGa>cAa p.R577Q SKCM 23 132160520 132160520 + Nonsense_Mutation SNP G G A TCGA-EE-A2GD-06A-11D-A196-08 TCGA-EE-A2GD-10A-01D-A198-08 g.chrX:132160520G>A c.1729C>T c.(1729-1731)Cga>Tga p.R577* SKCM 23 132160571 132160571 + Missense_Mutation SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chrX:132160571G>A c.1678C>T c.(1678-1680)Ccc>Tcc p.P560S SKCM 23 132160571 132160571 + Missense_Mutation SNP G G A TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chrX:132160571G>A c.1678C>T c.(1678-1680)Ccc>Tcc p.P560S SKCM 23 132160819 132160819 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chrX:132160819G>A c.1430C>T c.(1429-1431)tCa>tTa p.S477L SKCM 23 132161000 132161000 + Missense_Mutation SNP G G A TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chrX:132161000G>A c.1249C>T c.(1249-1251)Cct>Tct p.P417S SKCM 23 132161158 132161158 + Missense_Mutation SNP A A G TCGA-EE-A2GL-06A-11D-A196-08 TCGA-EE-A2GL-10A-01D-A198-08 g.chrX:132161158A>G c.1091T>C c.(1090-1092)cTt>cCt p.L364P SKCM 23 132161249 132161249 + Missense_Mutation SNP G G A TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chrX:132161249G>A c.1000C>T c.(1000-1002)Ccc>Tcc p.P334S SKCM 23 132161263 132161263 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chrX:132161263G>A c.986C>T c.(985-987)cCa>cTa p.P329L SKCM 23 132161510 132161510 + Missense_Mutation SNP G G A TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chrX:132161510G>A c.739C>T c.(739-741)Cct>Tct p.P247S SKCM 23 132161550 132161550 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chrX:132161550C>T c.699G>A c.(697-699)ttG>ttA p.L233L SKCM 23 132161573 132161573 + Missense_Mutation SNP C C T TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chrX:132161573C>T c.676G>A c.(676-678)Gag>Aag p.E226K SKCM 23 132161645 132161645 + Missense_Mutation SNP C C G TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chrX:132161645C>G c.604G>C c.(604-606)Gaa>Caa p.E202Q SKCM 23 132161665 132161665 + Missense_Mutation SNP A A G TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chrX:132161665A>G c.584T>C c.(583-585)tTg>tCg p.L195S SKCM 23 132161704 132161704 + Missense_Mutation SNP C C T TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chrX:132161704C>T c.545G>A c.(544-546)aGa>aAa p.R182K SKCM 23 132161740 132161740 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chrX:132161740C>T c.509G>A c.(508-510)gGa>gAa p.G170E SKCM 23 132161741 132161741 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chrX:132161741C>T c.508G>A c.(508-510)Gga>Aga p.G170R SKCM 23 132161796 132161796 + Silent SNP C C T TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chrX:132161796C>T c.453G>A c.(451-453)ggG>ggA p.G151G SKCM 23 132161803 132161803 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chrX:132161803C>T c.446G>A c.(445-447)gGa>gAa p.G149E SKCM 23 132161857 132161857 + Missense_Mutation SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chrX:132161857G>A c.392C>T c.(391-393)tCa>tTa p.S131L SKCM 23 132161988 132161988 + Silent SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chrX:132161988G>A c.261C>T c.(259-261)tcC>tcT p.S87S SKCM 23 132161995 132161995 + Missense_Mutation SNP C C T TCGA-EE-A2A1-06A-11D-A197-08 TCGA-EE-A2A1-10A-01D-A199-08 g.chrX:132161995C>T c.254G>A c.(253-255)gGa>gAa p.G85E SKCM 23 132162061 132162061 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chrX:132162061G>A c.188C>T c.(187-189)tCc>tTc p.S63F SKCM 23 132162210 132162210 + Silent SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chrX:132162210C>T c.39G>A c.(37-39)ggG>ggA p.G13G SKCM 23 132162218 132162218 + Nonsense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chrX:132162218G>A c.31C>T c.(31-33)Caa>Taa p.Q11* SKCM 23 132162238 132162238 + Missense_Mutation SNP A A C TCGA-EE-A29P-06A-11D-A197-08 TCGA-EE-A29P-10A-01D-A199-08 g.chrX:132162238A>C c.11T>G c.(10-12)cTa>cGa p.L4R

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN X 132159590 132159590 single base substitution C T missense_variant E887K 2659G>A BLCA-US X 132160985 132160985 single base substitution C T missense_variant A422T 1264G>A BLCA-US X 132161712 132161712 single base substitution C T synonymous_variant K179K 537G>A BLCA-US X 132162129 132162129 single base substitution C T synonymous_variant L40L 120G>A BLCA-US X 132162154 132162154 single base substitution C A missense_variant R32I 95G>T BOCA-FR X 132207819 132207819 single base substitution C T intron_variant BRCA-EU X 132153749 132153749 single base substitution A C downstream_gene_variant BRCA-EU X 132154440 132154440 single base substitution C A downstream_gene_variant BRCA-EU X 132154924 132154924 single base substitution A G downstream_gene_variant BRCA-EU X 132156020 132156020 single base substitution C T downstream_gene_variant BRCA-EU X 132157159 132157159 single base substitution C A downstream_gene_variant BRCA-EU X 132157647 132157647 single base substitution A G downstream_gene_variant BRCA-EU X 132157963 132157963 single base substitution C A downstream_gene_variant BRCA-EU X 132159132 132159132 single base substitution C T 3_prime_UTR_variant BRCA-EU X 132160741 132160741 single base substitution G A missense_variant T503I 1508C>T BRCA-EU X 132160811 132160811 single base substitution G T missense_variant Q480K 1438C>A BRCA-EU X 132161205 132161205 single base substitution A T missense_variant F348L 1044T>A BRCA-EU X 132161219 132161219 single base substitution G A missense_variant R344W 1030C>T BRCA-EU X 132161273 132161273 single base substitution G A stop_gained Q326* 976C>T BRCA-EU X 132161303 132161303 single base substitution T C missense_variant I316V 946A>G BRCA-EU X 132162154 132162154 single base substitution C G missense_variant R32T 95G>C BRCA-EU X 132163374 132163374 single base substitution G A intron_variant BRCA-EU X 132163374 132163374 single base substitution G A upstream_gene_variant BRCA-EU X 132163516 132163516 single base substitution A T intron_variant BRCA-EU X 132163516 132163516 single base substitution A T upstream_gene_variant BRCA-EU X 132164162 132164162 single base substitution G A intron_variant BRCA-EU X 132164162 132164162 single base substitution G A upstream_gene_variant BRCA-EU X 132164368 132164368 deletion of <=200bp A - intron_variant BRCA-EU X 132164368 132164368 deletion of <=200bp A - upstream_gene_variant BRCA-EU X 132164766 132164766 single base substitution A T intron_variant BRCA-EU X 132164766 132164766 single base substitution A T upstream_gene_variant BRCA-EU X 132165366 132165366 single base substitution T C intron_variant BRCA-EU X 132165366 132165366 single base substitution T C upstream_gene_variant BRCA-EU X 132168706 132168706 single base substitution C A intron_variant BRCA-EU X 132168746 132168746 single base substitution G A intron_variant BRCA-EU X 132169466 132169466 single base substitution G A intron_variant BRCA-EU X 132169708 132169708 single base substitution C T intron_variant BRCA-EU X 132169850 132169850 single base substitution G C intron_variant BRCA-EU X 132169915 132169915 single base substitution G C intron_variant BRCA-EU X 132171631 132171631 single base substitution T C intron_variant BRCA-EU X 132172457 132172457 single base substitution G T intron_variant BRCA-EU X 132172909 132172909 single base substitution T C intron_variant BRCA-EU X 132173245 132173245 single base substitution G T intron_variant BRCA-EU X 132173695 132173695 single base substitution G C intron_variant BRCA-EU X 132175059 132175059 single base substitution C T downstream_gene_variant BRCA-EU X 132175059 132175059 single base substitution C T intron_variant BRCA-EU X 132176194 132176194 single base substitution G T downstream_gene_variant BRCA-EU X 132176194 132176194 single base substitution G T intron_variant BRCA-EU X 132177688 132177688 single base substitution C A downstream_gene_variant BRCA-EU X 132177688 132177688 single base substitution C A intron_variant BRCA-EU X 132177911 132177911 deletion of <=200bp A - downstream_gene_variant BRCA-EU X 132177911 132177911 deletion of <=200bp A - intron_variant BRCA-EU X 132178305 132178305 single base substitution C T downstream_gene_variant BRCA-EU X 132178305 132178305 single base substitution C T intron_variant BRCA-EU X 132178662 132178662 single base substitution C A downstream_gene_variant BRCA-EU X 132178662 132178662 single base substitution C A intron_variant BRCA-EU X 132179595 132179595 single base substitution C T downstream_gene_variant BRCA-EU X 132179595 132179595 single base substitution C T intron_variant BRCA-EU X 132180214 132180214 single base substitution A G intron_variant BRCA-EU X 132180444 132180444 single base substitution G C intron_variant BRCA-EU X 132180582 132180582 single base substitution C T intron_variant BRCA-EU X 132180778 132180778 single base substitution T G intron_variant BRCA-EU X 132181391 132181391 single base substitution T C intron_variant BRCA-EU X 132181468 132181468 single base substitution C T intron_variant BRCA-EU X 132181881 132181881 single base substitution C T intron_variant BRCA-EU X 132182064 132182064 single base substitution C A intron_variant BRCA-EU X 132183202 132183202 single base substitution G A intron_variant BRCA-EU X 132183566 132183566 single base substitution T A intron_variant BRCA-EU X 132183812 132183812 single base substitution G C intron_variant BRCA-EU X 132183984 132183984 single base substitution A C intron_variant BRCA-EU X 132184102 132184102 single base substitution C T intron_variant BRCA-EU X 132184190 132184190 single base substitution G C intron_variant BRCA-EU X 132184627 132184627 insertion of <=200bp - T intron_variant BRCA-EU X 132184635 132184635 single base substitution T A intron_variant BRCA-EU X 132184636 132184636 single base substitution A T intron_variant BRCA-EU X 132186111 132186111 single base substitution G C intron_variant BRCA-EU X 132187136 132187136 single base substitution C A intron_variant BRCA-EU X 132187443 132187443 single base substitution G T intron_variant BRCA-EU X 132187704 132187704 single base substitution T C intron_variant BRCA-EU X 132188038 132188038 single base substitution C A intron_variant BRCA-EU X 132189184 132189184 deletion of <=200bp A - intron_variant BRCA-EU X 132190158 132190158 single base substitution A T intron_variant BRCA-EU X 132190500 132190500 single base substitution T A intron_variant BRCA-EU X 132191025 132191025 single base substitution C T intron_variant BRCA-EU X 132191602 132191602 single base substitution G A intron_variant BRCA-EU X 132192424 132192424 single base substitution A G intron_variant BRCA-EU X 132192458 132192458 single base substitution G A intron_variant BRCA-EU X 132192925 132192925 single base substitution T A intron_variant BRCA-EU X 132193026 132193026 single base substitution G C intron_variant BRCA-EU X 132193296 132193296 single base substitution T C intron_variant BRCA-EU X 132195637 132195637 single base substitution C G intron_variant BRCA-EU X 132196876 132196876 single base substitution G C intron_variant BRCA-EU X 132197155 132197155 single base substitution C G intron_variant BRCA-EU X 132197203 132197203 single base substitution G A intron_variant BRCA-EU X 132197632 132197632 single base substitution C T intron_variant BRCA-EU X 132197696 132197696 single base substitution C A intron_variant BRCA-EU X 132197855 132197855 single base substitution T G intron_variant BRCA-EU X 132198085 132198085 deletion of <=200bp A - intron_variant BRCA-EU X 132198446 132198446 single base substitution G C intron_variant BRCA-EU X 132198520 132198520 single base substitution C G intron_variant BRCA-EU X 132198765 132198765 single base substitution G A intron_variant BRCA-EU X 132199332 132199332 single base substitution G C intron_variant BRCA-EU X 132199523 132199523 single base substitution G A intron_variant BRCA-EU X 132201066 132201066 single base substitution A T intron_variant BRCA-EU X 132202303 132202303 single base substitution G A intron_variant BRCA-EU X 132203297 132203297 single base substitution A C intron_variant BRCA-EU X 132203667 132203667 single base substitution A G intron_variant BRCA-EU X 132203802 132203802 single base substitution T A intron_variant BRCA-EU X 132204717 132204717 single base substitution C T intron_variant BRCA-EU X 132205575 132205575 single base substitution A T intron_variant BRCA-EU X 132209743 132209743 single base substitution T G intron_variant BRCA-EU X 132209821 132209821 single base substitution C T intron_variant BRCA-EU X 132210321 132210321 single base substitution C G intron_variant BRCA-EU X 132210542 132210542 single base substitution C G intron_variant BRCA-EU X 132210900 132210900 single base substitution C T intron_variant BRCA-EU X 132211366 132211366 single base substitution A G intron_variant BRCA-EU X 132211526 132211526 single base substitution G C intron_variant BRCA-EU X 132212304 132212304 single base substitution T A intron_variant BRCA-EU X 132212464 132212464 single base substitution G C intron_variant BRCA-EU X 132213201 132213201 single base substitution G A intron_variant BRCA-EU X 132213409 132213409 single base substitution T G intron_variant BRCA-EU X 132213455 132213455 single base substitution A G intron_variant BRCA-EU X 132213696 132213696 single base substitution C T intron_variant BRCA-EU X 132214071 132214071 single base substitution A C intron_variant BRCA-EU X 132214696 132214696 single base substitution C T intron_variant BRCA-EU X 132216103 132216103 single base substitution G T intron_variant BRCA-EU X 132216832 132216832 single base substitution T C intron_variant BRCA-EU X 132217357 132217357 single base substitution T C intron_variant BRCA-EU X 132217523 132217523 single base substitution G A intron_variant BRCA-EU X 132218314 132218314 single base substitution C A intron_variant BRCA-EU X 132218314 132218314 single base substitution C A upstream_gene_variant BRCA-EU X 132218725 132218725 single base substitution G T intron_variant BRCA-EU X 132218725 132218725 single base substitution G T upstream_gene_variant BRCA-EU X 132218802 132218802 single base substitution C T intron_variant BRCA-EU X 132218802 132218802 single base substitution C T upstream_gene_variant BRCA-EU X 132218815 132218815 single base substitution G T intron_variant BRCA-EU X 132218815 132218815 single base substitution G T upstream_gene_variant BRCA-EU X 132219263 132219263 single base substitution C G intron_variant BRCA-EU X 132219263 132219263 single base substitution C G upstream_gene_variant BRCA-EU X 132219735 132219735 single base substitution A T intron_variant BRCA-EU X 132219735 132219735 single base substitution A T upstream_gene_variant BRCA-EU X 132220045 132220045 single base substitution T A intron_variant BRCA-EU X 132220045 132220045 single base substitution T A upstream_gene_variant BRCA-EU X 132221097 132221097 single base substitution C T intron_variant BRCA-EU X 132221097 132221097 single base substitution C T upstream_gene_variant BRCA-EU X 132222064 132222064 single base substitution T C intron_variant BRCA-EU X 132222064 132222064 single base substitution T C upstream_gene_variant BRCA-EU X 132223734 132223734 single base substitution G C intron_variant BRCA-EU X 132224026 132224026 single base substitution T C intron_variant BRCA-EU X 132224776 132224776 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU X 132224776 132224776 single base substitution G C exon_variant BRCA-EU X 132226409 132226409 single base substitution C A intron_variant BRCA-EU X 132226409 132226409 single base substitution C T intron_variant BRCA-EU X 132228753 132228753 single base substitution T C intron_variant BRCA-EU X 132229649 132229649 single base substitution G C intron_variant BRCA-EU X 132229962 132229962 single base substitution G C intron_variant BRCA-EU X 132230923 132230923 deletion of <=200bp A - intron_variant BRCA-EU X 132230961 132230961 single base substitution A T intron_variant BRCA-EU X 132233439 132233439 single base substitution C T upstream_gene_variant BRCA-EU X 132234320 132234320 single base substitution T A upstream_gene_variant BRCA-EU X 132235267 132235267 deletion of <=200bp A - upstream_gene_variant BRCA-EU X 132235699 132235699 single base substitution A G upstream_gene_variant BRCA-FR X 132156020 132156020 single base substitution C T downstream_gene_variant BRCA-FR X 132160811 132160811 single base substitution G T missense_variant Q480K 1438C>A BRCA-FR X 132161273 132161273 single base substitution G A stop_gained Q326* 976C>T BRCA-FR X 132180214 132180214 single base substitution A G intron_variant BRCA-FR X 132181881 132181881 single base substitution C T intron_variant BRCA-FR X 132184635 132184635 single base substitution T A intron_variant BRCA-FR X 132186111 132186111 single base substitution G C intron_variant BRCA-FR X 132188396 132188396 single base substitution C G intron_variant BRCA-FR X 132197641 132197641 single base substitution C T intron_variant BRCA-FR X 132197696 132197696 single base substitution C A intron_variant BRCA-FR X 132211366 132211366 single base substitution A G intron_variant BRCA-FR X 132211526 132211526 single base substitution G C intron_variant BRCA-FR X 132213208 132213208 single base substitution C A intron_variant BRCA-FR X 132218314 132218314 single base substitution C A intron_variant BRCA-FR X 132218314 132218314 single base substitution C A upstream_gene_variant BRCA-FR X 132220159 132220159 single base substitution T C intron_variant BRCA-FR X 132220159 132220159 single base substitution T C upstream_gene_variant BRCA-FR X 132234092 132234092 single base substitution C T upstream_gene_variant BRCA-UK X 132160304 132160304 single base substitution T C missense_variant I649V 1945A>G BRCA-UK X 132160915 132160915 single base substitution G T missense_variant S445Y 1334C>A BRCA-UK X 132166869 132166869 single base substitution G A intron_variant BRCA-UK X 132166869 132166869 single base substitution G A upstream_gene_variant BRCA-UK X 132184635 132184635 single base substitution T A intron_variant BRCA-UK X 132232486 132232486 single base substitution G T upstream_gene_variant BRCA-US X 132159686 132159686 single base substitution A G missense_variant F855L 2563T>C BRCA-US X 132160197 132160197 single base substitution G T synonymous_variant L684L 2052C>A BRCA-US X 132160788 132160788 deletion of <=200bp A - frameshift_variant F487 BRCA-US X 132161352 132161352 single base substitution A T missense_variant N299K 897T>A BRCA-US X 132161376 132161376 single base substitution C T synonymous_variant E291E 873G>A BRCA-US X 132161848 132161848 single base substitution T G missense_variant K134T 401A>C BRCA-US X 132162002 132162002 single base substitution T A missense_variant I83F 247A>T BTCA-JP X 132159748 132159748 single base substitution C T missense_variant G834E 2501G>A BTCA-JP X 132159774 132159774 single base substitution C T synonymous_variant R825R 2475G>A BTCA-JP X 132159985 132159985 single base substitution G A missense_variant A755V 2264C>T BTCA-JP X 132160119 132160119 single base substitution A G synonymous_variant F710F 2130T>C BTCA-JP X 132160686 132160686 single base substitution G C synonymous_variant L521L 1563C>G BTCA-JP X 132161205 132161205 deletion of <=200bp A - frameshift_variant F348 BTCA-JP X 132161205 132161205 insertion of <=200bp - A frameshift_variant F348F? BTCA-JP X 132161233 132161233 single base substitution G C missense_variant T339S 1016C>G CESC-US X 132159590 132159590 single base substitution C T missense_variant E887K 2659G>A CESC-US X 132159901 132159901 single base substitution G C missense_variant S783C 2348C>G CESC-US X 132159937 132159937 single base substitution T G missense_variant N771T 2312A>C CESC-US X 132161099 132161099 single base substitution G A missense_variant H384Y 1150C>T CESC-US X 132161143 132161143 single base substitution G T stop_gained S369* 1106C>A CESC-US X 132161383 132161383 single base substitution A G missense_variant F289S 866T>C CESC-US X 132161543 132161543 single base substitution C A stop_gained E236* 706G>T CLLE-ES X 132155783 132155783 single base substitution G A downstream_gene_variant CLLE-ES X 132159066 132159066 single base substitution A C 3_prime_UTR_variant CLLE-ES X 132168333 132168333 single base substitution A G intron_variant CLLE-ES X 132193842 132193842 single base substitution C G intron_variant CLLE-ES X 132197068 132197068 single base substitution T C intron_variant CLLE-ES X 132215742 132215742 single base substitution A C intron_variant CLLE-ES X 132225119 132225119 single base substitution C T intron_variant CLLE-ES X 132228439 132228439 single base substitution T C intron_variant COAD-US X 132159625 132159625 single base substitution C T missense_variant R875H 2624G>A COAD-US X 132159632 132159632 single base substitution C A missense_variant D873Y 2617G>T COAD-US X 132160273 132160273 single base substitution G A missense_variant T659M 1976C>T COAD-US X 132160291 132160291 single base substitution G A missense_variant P653L 1958C>T COAD-US X 132160553 132160553 single base substitution C A stop_gained E566* 1696G>T COAD-US X 132160787 132160787 insertion of <=200bp - A frameshift_variant G488V? COAD-US X 132160788 132160788 deletion of <=200bp A - frameshift_variant F487 COAD-US X 132160804 132160804 single base substitution G A missense_variant T482I 1445C>T COAD-US X 132160837 132160837 single base substitution C A missense_variant R471I 1412G>T COAD-US X 132161009 132161009 single base substitution C A missense_variant D414Y 1240G>T COAD-US X 132161204 132161204 insertion of <=200bp - A frameshift_variant K349I? COAD-US X 132161673 132161673 single base substitution C T synonymous_variant E192E 576G>A COCA-CN X 132159805 132159805 single base substitution C A missense_variant R815I 2444G>T COCA-CN X 132159925 132159925 single base substitution G T missense_variant P775H 2324C>A COCA-CN X 132160085 132160085 single base substitution C T missense_variant E722K 2164G>A COCA-CN X 132160132 132160132 single base substitution T G missense_variant K706T 2117A>C COCA-CN X 132160157 132160157 single base substitution G A stop_gained R698* 2092C>T COCA-CN X 132160313 132160313 single base substitution G A stop_gained R646* 1936C>T COCA-CN X 132160428 132160428 single base substitution C A missense_variant E607D 1821G>T COCA-CN X 132160837 132160837 single base substitution C A missense_variant R471I 1412G>T COCA-CN X 132161704 132161704 single base substitution C A missense_variant R182I 545G>T COCA-CN X 132165469 132165469 single base substitution C T intron_variant COCA-CN X 132165469 132165469 single base substitution C T upstream_gene_variant EOPC-DE X 132209925 132209925 single base substitution T G intron_variant ESCA-CN X 132160412 132160412 insertion of <=200bp - T frameshift_variant G613E? ESCA-CN X 132160656 132160656 single base substitution T G synonymous_variant A531A 1593A>C ESCA-CN X 132161143 132161143 single base substitution G A missense_variant S369L 1106C>T GBM-US X 132160788 132160788 deletion of <=200bp A - frameshift_variant F487 GBM-US X 132161219 132161219 single base substitution G A missense_variant R344W 1030C>T GBM-US X 132161937 132161937 single base substitution G A synonymous_variant N104N 312C>T KIRC-US X 132160053 132160053 single base substitution G C missense_variant F732L 2196C>G KIRC-US X 132160271 132160271 single base substitution A G missense_variant Y660H 1978T>C KIRC-US X 132161106 132161106 single base substitution G A synonymous_variant N381N 1143C>T KIRC-US X 132161721 132161721 single base substitution C A missense_variant Q176H 528G>T KIRP-US X 132160221 132160221 single base substitution A C synonymous_variant P676P 2028T>G LAML-KR X 132161216 132161216 single base substitution G A synonymous_variant L345L 1033C>T LAML-KR X 132190376 132190376 single base substitution C T intron_variant LAML-KR X 132222987 132222987 single base substitution C T intron_variant LAML-KR X 132227574 132227574 single base substitution T C intron_variant LAML-KR X 132232550 132232550 single base substitution G A upstream_gene_variant LGG-US X 132159579 132159579 single base substitution T C synonymous_variant E890E 2670A>G LGG-US X 132161205 132161205 deletion of <=200bp A - frameshift_variant F348 LICA-CN X 132160763 132160763 single base substitution A T missense_variant C496S 1486T>A LICA-CN X 132161976 132161976 single base substitution A T synonymous_variant A91A 273T>A LICA-FR X 132169765 132169765 single base substitution C T intron_variant LICA-FR X 132180169 132180169 single base substitution T G intron_variant LICA-FR X 132184026 132184026 single base substitution G T intron_variant LICA-FR X 132192501 132192501 single base substitution C G intron_variant LICA-FR X 132196645 132196645 single base substitution T A intron_variant LICA-FR X 132214110 132214110 single base substitution A C intron_variant LICA-FR X 132218541 132218543 deletion of <=200bp TTT - intron_variant LICA-FR X 132218541 132218543 deletion of <=200bp TTT - upstream_gene_variant LICA-FR X 132221006 132221006 single base substitution C A intron_variant LICA-FR X 132221006 132221006 single base substitution C A upstream_gene_variant LICA-FR X 132224274 132224274 single base substitution A G intron_variant LICA-FR X 132229087 132229087 single base substitution C T intron_variant LIHC-US X 132159790 132159790 single base substitution C A missense_variant G820V 2459G>T LIHC-US X 132161219 132161219 single base substitution G A missense_variant R344W 1030C>T LINC-JP X 132155132 132155132 single base substitution T A downstream_gene_variant LINC-JP X 132158307 132158307 deletion of <=200bp A - downstream_gene_variant LINC-JP X 132160394 132160394 single base substitution C A missense_variant G619W 1855G>T LINC-JP X 132161158 132161158 single base substitution A G missense_variant L364P 1091T>C LINC-JP X 132161777 132161777 single base substitution T A missense_variant M158L 472A>T LINC-JP X 132162200 132162200 single base substitution T G missense_variant T17P 49A>C LINC-JP X 132164368 132164368 deletion of <=200bp A - intron_variant LINC-JP X 132164368 132164368 deletion of <=200bp A - upstream_gene_variant LINC-JP X 132206753 132206753 single base substitution C G intron_variant LINC-JP X 132213092 132213092 single base substitution T A intron_variant LINC-JP X 132222418 132222418 single base substitution G C intron_variant LINC-JP X 132222418 132222418 single base substitution G C upstream_gene_variant LINC-JP X 132227262 132227262 single base substitution C A intron_variant LINC-JP X 132232173 132232173 single base substitution T A upstream_gene_variant LIRI-JP X 132154420 132154420 single base substitution T A downstream_gene_variant LIRI-JP X 132158959 132158959 single base substitution A G 3_prime_UTR_variant LIRI-JP X 132158959 132158959 single base substitution A G downstream_gene_variant LIRI-JP X 132160606 132160606 single base substitution G T missense_variant S548Y 1643C>A LIRI-JP X 132161205 132161205 deletion of <=200bp A - frameshift_variant F348 LIRI-JP X 132161426 132161426 single base substitution C A missense_variant G275C 823G>T LIRI-JP X 132162603 132162603 single base substitution T C intron_variant LIRI-JP X 132162603 132162603 single base substitution T C upstream_gene_variant LIRI-JP X 132164436 132164436 single base substitution T G intron_variant LIRI-JP X 132164436 132164436 single base substitution T G upstream_gene_variant LIRI-JP X 132164828 132164828 single base substitution A G intron_variant LIRI-JP X 132164828 132164828 single base substitution A G upstream_gene_variant LIRI-JP X 132164942 132164942 single base substitution C G intron_variant LIRI-JP X 132164942 132164942 single base substitution C G upstream_gene_variant LIRI-JP X 132165037 132165037 single base substitution A G intron_variant LIRI-JP X 132165037 132165037 single base substitution A G upstream_gene_variant LIRI-JP X 132165179 132165179 single base substitution C A intron_variant LIRI-JP X 132165179 132165179 single base substitution C A upstream_gene_variant LIRI-JP X 132165180 132165180 single base substitution C A intron_variant LIRI-JP X 132165180 132165180 single base substitution C A upstream_gene_variant LIRI-JP X 132165413 132165413 single base substitution C T intron_variant LIRI-JP X 132165413 132165413 single base substitution C T upstream_gene_variant LIRI-JP X 132168429 132168429 single base substitution A G intron_variant LIRI-JP X 132169998 132169998 single base substitution G A intron_variant LIRI-JP X 132170328 132170328 single base substitution T C intron_variant LIRI-JP X 132172295 132172295 single base substitution T A intron_variant LIRI-JP X 132173092 132173092 single base substitution T C intron_variant LIRI-JP X 132173785 132173785 single base substitution T A intron_variant LIRI-JP X 132175366 132175366 single base substitution T C downstream_gene_variant LIRI-JP X 132175366 132175366 single base substitution T C intron_variant LIRI-JP X 132175447 132175447 single base substitution G A downstream_gene_variant LIRI-JP X 132175447 132175447 single base substitution G A intron_variant LIRI-JP X 132175974 132175974 single base substitution G A downstream_gene_variant LIRI-JP X 132175974 132175974 single base substitution G A intron_variant LIRI-JP X 132176658 132176658 single base substitution G A downstream_gene_variant LIRI-JP X 132176658 132176658 single base substitution G A intron_variant LIRI-JP X 132177791 132177791 single base substitution C G downstream_gene_variant LIRI-JP X 132177791 132177791 single base substitution C G intron_variant LIRI-JP X 132177926 132177926 single base substitution A G downstream_gene_variant LIRI-JP X 132177926 132177926 single base substitution A G intron_variant LIRI-JP X 132181292 132181292 single base substitution A G intron_variant LIRI-JP X 132181447 132181447 single base substitution G A intron_variant LIRI-JP X 132184928 132184928 single base substitution G A intron_variant LIRI-JP X 132185540 132185540 single base substitution G A intron_variant LIRI-JP X 132187798 132187798 single base substitution A G intron_variant LIRI-JP X 132188000 132188000 single base substitution G T intron_variant LIRI-JP X 132188001 132188001 single base substitution G T intron_variant LIRI-JP X 132192338 132192338 single base substitution G A intron_variant LIRI-JP X 132193827 132193827 single base substitution T C intron_variant LIRI-JP X 132193999 132193999 single base substitution G T intron_variant LIRI-JP X 132194197 132194197 single base substitution A T intron_variant LIRI-JP X 132194198 132194198 single base substitution G T intron_variant LIRI-JP X 132194249 132194249 single base substitution C G intron_variant LIRI-JP X 132198305 132198305 single base substitution G A intron_variant LIRI-JP X 132198969 132198969 single base substitution T C intron_variant LIRI-JP X 132199428 132199428 single base substitution C T intron_variant LIRI-JP X 132202931 132202931 single base substitution A C intron_variant LIRI-JP X 132205012 132205012 single base substitution A T intron_variant LIRI-JP X 132206316 132206316 single base substitution C A intron_variant LIRI-JP X 132207801 132207801 single base substitution C A intron_variant LIRI-JP X 132209109 132209109 single base substitution C T intron_variant LIRI-JP X 132209397 132209397 single base substitution C T intron_variant LIRI-JP X 132210349 132210349 single base substitution A G intron_variant LIRI-JP X 132212535 132212535 single base substitution G T intron_variant LIRI-JP X 132217431 132217431 single base substitution T G intron_variant LIRI-JP X 132217687 132217687 single base substitution T C intron_variant LIRI-JP X 132218372 132218372 single base substitution G A intron_variant LIRI-JP X 132218372 132218372 single base substitution G A upstream_gene_variant LIRI-JP X 132218627 132218627 single base substitution T C intron_variant LIRI-JP X 132218627 132218627 single base substitution T C upstream_gene_variant LIRI-JP X 132218889 132218889 single base substitution C T intron_variant LIRI-JP X 132218889 132218889 single base substitution C T upstream_gene_variant LIRI-JP X 132218933 132218933 single base substitution C T intron_variant LIRI-JP X 132218933 132218933 single base substitution C T upstream_gene_variant LIRI-JP X 132218937 132218937 single base substitution T A intron_variant LIRI-JP X 132218937 132218937 single base substitution T A upstream_gene_variant LIRI-JP X 132222094 132222094 single base substitution G C intron_variant LIRI-JP X 132222094 132222094 single base substitution G C upstream_gene_variant LIRI-JP X 132222505 132222505 single base substitution T A intron_variant LIRI-JP X 132222505 132222505 single base substitution T A upstream_gene_variant LIRI-JP X 132222737 132222737 single base substitution C A intron_variant LIRI-JP X 132222737 132222737 single base substitution C A upstream_gene_variant LIRI-JP X 132223395 132223395 single base substitution G A intron_variant LIRI-JP X 132223577 132223577 single base substitution C A intron_variant LIRI-JP X 132224705 132224705 single base substitution T A intron_variant LIRI-JP X 132225891 132225891 single base substitution A G intron_variant LIRI-JP X 132226579 132226579 single base substitution T A intron_variant LIRI-JP X 132228900 132228900 single base substitution A G intron_variant LIRI-JP X 132230684 132230684 single base substitution A G intron_variant LIRI-JP X 132230934 132230934 single base substitution A G intron_variant LIRI-JP X 132231291 132231291 single base substitution C A upstream_gene_variant LIRI-JP X 132231293 132231293 single base substitution T A upstream_gene_variant LIRI-JP X 132233231 132233231 single base substitution A G upstream_gene_variant LIRI-JP X 132234665 132234665 single base substitution T G upstream_gene_variant LIRI-JP X 132234857 132234857 single base substitution A G upstream_gene_variant LUSC-KR X 132158601 132158601 single base substitution T A downstream_gene_variant LUSC-KR X 132166315 132166315 single base substitution A T intron_variant LUSC-KR X 132166315 132166315 single base substitution A T upstream_gene_variant LUSC-KR X 132174991 132174991 single base substitution C T downstream_gene_variant LUSC-KR X 132174991 132174991 single base substitution C T intron_variant LUSC-KR X 132186447 132186447 single base substitution C T intron_variant LUSC-KR X 132195783 132195783 single base substitution C A intron_variant LUSC-KR X 132197592 132197592 single base substitution G A intron_variant LUSC-KR X 132200754 132200754 single base substitution G C intron_variant LUSC-KR X 132206462 132206462 single base substitution A T intron_variant LUSC-KR X 132207559 132207559 single base substitution C A intron_variant LUSC-KR X 132208698 132208698 single base substitution T A intron_variant LUSC-KR X 132208813 132208813 single base substitution G A intron_variant LUSC-KR X 132212278 132212278 single base substitution A G intron_variant LUSC-KR X 132215082 132215082 single base substitution T A intron_variant LUSC-KR X 132220156 132220156 single base substitution G C intron_variant LUSC-KR X 132220156 132220156 single base substitution G C upstream_gene_variant LUSC-KR X 132229924 132229924 single base substitution C A intron_variant LUSC-KR X 132232821 132232821 single base substitution C A upstream_gene_variant LUSC-KR X 132232973 132232973 single base substitution G T upstream_gene_variant LUSC-US X 132159856 132159856 single base substitution C T missense_variant R798K 2393G>A LUSC-US X 132160305 132160305 single base substitution G C missense_variant F648L 1944C>G LUSC-US X 132161178 132161178 single base substitution C T synonymous_variant K357K 1071G>A LUSC-US X 132161299 132161299 single base substitution G T missense_variant P317Q 950C>A LUSC-US X 132162097 132162097 single base substitution C A missense_variant R51L 152G>T MALY-DE X 132153717 132153717 single base substitution T C downstream_gene_variant MALY-DE X 132156512 132156513 deletion of <=200bp AC - downstream_gene_variant MALY-DE X 132157267 132157267 single base substitution C A downstream_gene_variant MALY-DE X 132160634 132160634 single base substitution C A missense_variant V539F 1615G>T MALY-DE X 132162064 132162064 single base substitution T G missense_variant K62T 185A>C MALY-DE X 132162879 132162879 deletion of <=200bp G - intron_variant MALY-DE X 132162879 132162879 deletion of <=200bp G - upstream_gene_variant MALY-DE X 132168199 132168199 single base substitution G A intron_variant MALY-DE X 132168333 132168333 single base substitution A C intron_variant MALY-DE X 132168817 132168817 single base substitution G C intron_variant MALY-DE X 132175256 132175256 single base substitution C A downstream_gene_variant MALY-DE X 132175256 132175256 single base substitution C A intron_variant MALY-DE X 132178435 132178435 single base substitution C T downstream_gene_variant MALY-DE X 132178435 132178435 single base substitution C T intron_variant MALY-DE X 132180661 132180662 deletion of <=200bp GA - intron_variant MALY-DE X 132180661 132180664 deletion of <=200bp GAGA - intron_variant MALY-DE X 132181110 132181110 single base substitution A G intron_variant MALY-DE X 132182841 132182841 single base substitution T C intron_variant MALY-DE X 132183324 132183324 single base substitution C G intron_variant MALY-DE X 132184228 132184228 single base substitution T C intron_variant MALY-DE X 132184635 132184635 single base substitution T A intron_variant MALY-DE X 132186366 132186366 single base substitution A C intron_variant MALY-DE X 132186382 132186382 single base substitution T C intron_variant MALY-DE X 132187566 132187566 single base substitution A T intron_variant MALY-DE X 132194759 132194759 single base substitution A G intron_variant MALY-DE X 132196386 132196386 single base substitution A C intron_variant MALY-DE X 132196643 132196643 single base substitution A G intron_variant MALY-DE X 132199263 132199263 single base substitution A C intron_variant MALY-DE X 132199780 132199780 single base substitution A G intron_variant MALY-DE X 132202408 132202408 single base substitution G T intron_variant MALY-DE X 132204129 132204129 single base substitution C A intron_variant MALY-DE X 132213830 132213830 single base substitution G A intron_variant MALY-DE X 132214630 132214630 single base substitution G T intron_variant MALY-DE X 132217957 132217957 single base substitution C G intron_variant MALY-DE X 132217957 132217957 single base substitution C G upstream_gene_variant MALY-DE X 132218274 132218274 single base substitution T C intron_variant MALY-DE X 132218274 132218274 single base substitution T C upstream_gene_variant MALY-DE X 132218471 132218471 single base substitution C T intron_variant MALY-DE X 132218471 132218471 single base substitution C T upstream_gene_variant MALY-DE X 132220192 132220192 single base substitution C T intron_variant MALY-DE X 132220192 132220192 single base substitution C T upstream_gene_variant MALY-DE X 132222058 132222058 single base substitution G A intron_variant MALY-DE X 132222058 132222058 single base substitution G A upstream_gene_variant MALY-DE X 132222935 132222935 single base substitution T G intron_variant MALY-DE X 132223154 132223154 deletion of <=200bp T - intron_variant MALY-DE X 132225762 132225762 single base substitution C A intron_variant MALY-DE X 132226348 132226348 single base substitution T C intron_variant MALY-DE X 132226466 132226466 single base substitution G A intron_variant MALY-DE X 132227515 132227515 single base substitution C T intron_variant MALY-DE X 132229759 132229759 single base substitution G A intron_variant MALY-DE X 132230257 132230257 single base substitution C T intron_variant MALY-DE X 132230777 132230777 single base substitution G A intron_variant MALY-DE X 132233114 132233114 single base substitution G T upstream_gene_variant MALY-DE X 132235267 132235267 deletion of <=200bp A - upstream_gene_variant MELA-AU X 132153769 132153769 single base substitution G A downstream_gene_variant MELA-AU X 132153790 132153790 single base substitution G A downstream_gene_variant MELA-AU X 132154568 132154568 single base substitution G A downstream_gene_variant MELA-AU X 132154643 132154643 single base substitution G A downstream_gene_variant MELA-AU X 132154721 132154721 single base substitution G A downstream_gene_variant MELA-AU X 132154796 132154797 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU X 132154984 132154984 single base substitution C T downstream_gene_variant MELA-AU X 132155098 132155098 single base substitution G A downstream_gene_variant MELA-AU X 132155105 132155105 single base substitution C A downstream_gene_variant MELA-AU X 132155221 132155221 single base substitution G T downstream_gene_variant MELA-AU X 132155370 132155370 single base substitution G A downstream_gene_variant MELA-AU X 132155685 132155685 single base substitution G A downstream_gene_variant MELA-AU X 132155762 132155762 single base substitution C T downstream_gene_variant MELA-AU X 132155884 132155884 single base substitution G A downstream_gene_variant MELA-AU X 132156204 132156204 single base substitution C T downstream_gene_variant MELA-AU X 132156222 132156222 single base substitution G A downstream_gene_variant MELA-AU X 132156271 132156271 single base substitution C T downstream_gene_variant MELA-AU X 132156624 132156624 single base substitution C T downstream_gene_variant MELA-AU X 132156889 132156889 single base substitution G A downstream_gene_variant MELA-AU X 132157119 132157119 single base substitution C T downstream_gene_variant MELA-AU X 132157315 132157315 single base substitution G A downstream_gene_variant MELA-AU X 132157332 132157332 single base substitution C T downstream_gene_variant MELA-AU X 132157592 132157592 single base substitution C T downstream_gene_variant MELA-AU X 132157687 132157687 single base substitution C T downstream_gene_variant MELA-AU X 132157700 132157700 single base substitution C T downstream_gene_variant MELA-AU X 132157784 132157784 single base substitution C T downstream_gene_variant MELA-AU X 132158212 132158212 single base substitution A G downstream_gene_variant MELA-AU X 132158318 132158318 single base substitution A T downstream_gene_variant MELA-AU X 132158465 132158465 single base substitution G A downstream_gene_variant MELA-AU X 132158493 132158493 single base substitution G A downstream_gene_variant MELA-AU X 132158716 132158716 single base substitution G A 3_prime_UTR_variant MELA-AU X 132158716 132158716 single base substitution G A downstream_gene_variant MELA-AU X 132158982 132158982 single base substitution G A 3_prime_UTR_variant MELA-AU X 132158982 132158982 single base substitution G A downstream_gene_variant MELA-AU X 132159041 132159041 single base substitution C T 3_prime_UTR_variant MELA-AU X 132159041 132159041 single base substitution C T downstream_gene_variant MELA-AU X 132159155 132159155 single base substitution G A 3_prime_UTR_variant MELA-AU X 132159205 132159205 single base substitution G A 3_prime_UTR_variant MELA-AU X 132159292 132159292 single base substitution G A 3_prime_UTR_variant MELA-AU X 132159293 132159293 single base substitution G A 3_prime_UTR_variant MELA-AU X 132159377 132159377 single base substitution C T 3_prime_UTR_variant MELA-AU X 132159438 132159438 single base substitution C T 3_prime_UTR_variant MELA-AU X 132159747 132159747 single base substitution C T synonymous_variant G834G 2502G>A MELA-AU X 132159790 132159790 single base substitution C T missense_variant G820E 2459G>A MELA-AU X 132159889 132159889 single base substitution G A missense_variant S787F 2360C>T MELA-AU X 132159894 132159894 single base substitution C T synonymous_variant R785R 2355G>A MELA-AU X 132160156 132160156 single base substitution C T missense_variant R698Q 2093G>A MELA-AU X 132160265 132160265 single base substitution C T missense_variant E662K 1984G>A MELA-AU X 132160291 132160292 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P653L 1957CC>TT MELA-AU X 132160321 132160321 single base substitution G A missense_variant S643L 1928C>T MELA-AU X 132160323 132160323 single base substitution G T stop_gained Y642* 1926C>A MELA-AU X 132160770 132160770 single base substitution C T synonymous_variant E493E 1479G>A MELA-AU X 132160844 132160844 single base substitution G A missense_variant P469S 1405C>T MELA-AU X 132161000 132161000 single base substitution G A missense_variant P417S 1249C>T MELA-AU X 132161012 132161012 single base substitution C T missense_variant E413K 1237G>A MELA-AU X 132161105 132161105 single base substitution C T missense_variant D382N 1144G>A MELA-AU X 132161186 132161186 single base substitution C T missense_variant E355K 1063G>A MELA-AU X 132161498 132161498 single base substitution C T missense_variant D251N 751G>A MELA-AU X 132161560 132161560 single base substitution T A missense_variant N230I 689A>T MELA-AU X 132161596 132161596 single base substitution C T missense_variant R218Q 653G>A MELA-AU X 132161617 132161617 single base substitution G A missense_variant S211L 632C>T MELA-AU X 132161821 132161821 single base substitution G A missense_variant S143F 428C>T MELA-AU X 132161857 132161857 single base substitution G A missense_variant S131L 392C>T MELA-AU X 132161873 132161873 single base substitution C T missense_variant E126K 376G>A MELA-AU X 132162158 132162158 single base substitution C T missense_variant E31K 91G>A MELA-AU X 132162190 132162190 single base substitution G A missense_variant S20F 59C>T MELA-AU X 132162359 132162359 single base substitution T C intron_variant MELA-AU X 132162359 132162359 single base substitution T C upstream_gene_variant MELA-AU X 132162444 132162444 single base substitution G A intron_variant MELA-AU X 132162444 132162444 single base substitution G A upstream_gene_variant MELA-AU X 132162530 132162530 single base substitution G A intron_variant MELA-AU X 132162530 132162530 single base substitution G A upstream_gene_variant MELA-AU X 132162628 132162628 single base substitution C T intron_variant MELA-AU X 132162628 132162628 single base substitution C T upstream_gene_variant MELA-AU X 132162632 132162632 single base substitution C T intron_variant MELA-AU X 132162632 132162632 single base substitution C T upstream_gene_variant MELA-AU X 132162840 132162840 single base substitution C T intron_variant MELA-AU X 132162840 132162840 single base substitution C T upstream_gene_variant MELA-AU X 132162855 132162855 single base substitution G A intron_variant MELA-AU X 132162855 132162855 single base substitution G A upstream_gene_variant MELA-AU X 132163199 132163199 single base substitution C T intron_variant MELA-AU X 132163199 132163199 single base substitution C T upstream_gene_variant MELA-AU X 132163238 132163238 single base substitution C T intron_variant MELA-AU X 132163238 132163238 single base substitution C T upstream_gene_variant MELA-AU X 132163436 132163436 single base substitution G A intron_variant MELA-AU X 132163436 132163436 single base substitution G A upstream_gene_variant MELA-AU X 132163506 132163506 single base substitution C T intron_variant MELA-AU X 132163506 132163506 single base substitution C T upstream_gene_variant MELA-AU X 132163567 132163567 single base substitution A T intron_variant MELA-AU X 132163567 132163567 single base substitution A T upstream_gene_variant MELA-AU X 132163731 132163731 single base substitution C T intron_variant MELA-AU X 132163731 132163731 single base substitution C T upstream_gene_variant MELA-AU X 132164212 132164212 single base substitution C T intron_variant MELA-AU X 132164212 132164212 single base substitution C T upstream_gene_variant MELA-AU X 132164537 132164537 single base substitution G A intron_variant MELA-AU X 132164537 132164537 single base substitution G A upstream_gene_variant MELA-AU X 132164725 132164725 single base substitution G A intron_variant MELA-AU X 132164725 132164725 single base substitution G A upstream_gene_variant MELA-AU X 132164765 132164765 single base substitution G A intron_variant MELA-AU X 132164765 132164765 single base substitution G A upstream_gene_variant MELA-AU X 132164785 132164785 single base substitution C G intron_variant MELA-AU X 132164785 132164785 single base substitution C G upstream_gene_variant MELA-AU X 132165042 132165042 single base substitution C T intron_variant MELA-AU X 132165042 132165042 single base substitution C T upstream_gene_variant MELA-AU X 132165180 132165180 single base substitution C T intron_variant MELA-AU X 132165180 132165180 single base substitution C T upstream_gene_variant MELA-AU X 132165761 132165761 single base substitution G A intron_variant MELA-AU X 132165761 132165761 single base substitution G A upstream_gene_variant MELA-AU X 132165789 132165789 single base substitution G A intron_variant MELA-AU X 132165789 132165789 single base substitution G A upstream_gene_variant MELA-AU X 132165964 132165964 single base substitution C A intron_variant MELA-AU X 132165964 132165964 single base substitution C A upstream_gene_variant MELA-AU X 132166149 132166150 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 132166149 132166150 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU X 132166303 132166303 single base substitution G A intron_variant MELA-AU X 132166303 132166303 single base substitution G A upstream_gene_variant MELA-AU X 132167298 132167298 single base substitution C T intron_variant MELA-AU X 132167298 132167298 single base substitution C T upstream_gene_variant MELA-AU X 132167500 132167500 single base substitution G A intron_variant MELA-AU X 132167620 132167620 single base substitution C T intron_variant MELA-AU X 132167641 132167641 single base substitution C T intron_variant MELA-AU X 132167685 132167685 single base substitution G A intron_variant MELA-AU X 132167799 132167799 single base substitution G A intron_variant MELA-AU X 132167870 132167870 single base substitution C T intron_variant MELA-AU X 132167940 132167940 single base substitution T G intron_variant MELA-AU X 132167974 132167974 single base substitution A G intron_variant MELA-AU X 132168024 132168024 single base substitution C T intron_variant MELA-AU X 132168339 132168339 single base substitution C T intron_variant MELA-AU X 132168360 132168360 single base substitution G A intron_variant MELA-AU X 132169308 132169308 single base substitution A C intron_variant MELA-AU X 132169400 132169400 single base substitution C T intron_variant MELA-AU X 132170042 132170042 single base substitution G A intron_variant MELA-AU X 132170113 132170113 single base substitution C T intron_variant MELA-AU X 132170381 132170381 single base substitution G T intron_variant MELA-AU X 132170391 132170391 single base substitution C T intron_variant MELA-AU X 132170518 132170518 single base substitution C T intron_variant MELA-AU X 132170526 132170526 single base substitution G A intron_variant MELA-AU X 132171169 132171169 single base substitution G A intron_variant MELA-AU X 132171348 132171348 single base substitution A G intron_variant MELA-AU X 132171406 132171406 single base substitution C T intron_variant MELA-AU X 132171462 132171462 single base substitution C T intron_variant MELA-AU X 132171723 132171723 single base substitution T C intron_variant MELA-AU X 132171813 132171813 single base substitution G A intron_variant MELA-AU X 132171879 132171879 single base substitution A C intron_variant MELA-AU X 132171934 132171934 single base substitution C T intron_variant MELA-AU X 132172084 132172084 single base substitution G A intron_variant MELA-AU X 132172163 132172163 single base substitution C T intron_variant MELA-AU X 132172538 132172538 single base substitution G A intron_variant MELA-AU X 132172735 132172735 single base substitution C T intron_variant MELA-AU X 132173006 132173006 single base substitution A G intron_variant MELA-AU X 132173187 132173187 single base substitution C T intron_variant MELA-AU X 132173415 132173415 single base substitution G A intron_variant MELA-AU X 132173478 132173478 single base substitution C T intron_variant MELA-AU X 132173520 132173520 single base substitution C T intron_variant MELA-AU X 132173627 132173654 deletion of <=200bp AGAATATGTGCTTTGTGGTGCTGAAAGG - intron_variant MELA-AU X 132173682 132173682 single base substitution G A intron_variant MELA-AU X 132173771 132173771 single base substitution C T intron_variant MELA-AU X 132173928 132173928 single base substitution G A intron_variant MELA-AU X 132173958 132173958 single base substitution C A intron_variant MELA-AU X 132174098 132174098 single base substitution C T intron_variant MELA-AU X 132174253 132174253 single base substitution C T intron_variant MELA-AU X 132174366 132174366 single base substitution C T intron_variant MELA-AU X 132174391 132174391 single base substitution G A intron_variant MELA-AU X 132174427 132174427 single base substitution C T intron_variant MELA-AU X 132174498 132174498 single base substitution G A intron_variant MELA-AU X 132174546 132174547 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 132174658 132174658 single base substitution C T intron_variant MELA-AU X 132174708 132174708 single base substitution C T intron_variant MELA-AU X 132174802 132174802 single base substitution C T intron_variant MELA-AU X 132174882 132174882 single base substitution C T intron_variant MELA-AU X 132175040 132175040 single base substitution G A downstream_gene_variant MELA-AU X 132175040 132175040 single base substitution G A intron_variant MELA-AU X 132175162 132175162 single base substitution A G downstream_gene_variant MELA-AU X 132175162 132175162 single base substitution A G intron_variant MELA-AU X 132175478 132175478 single base substitution C T downstream_gene_variant MELA-AU X 132175478 132175478 single base substitution C T intron_variant MELA-AU X 132175670 132175670 single base substitution G A downstream_gene_variant MELA-AU X 132175670 132175670 single base substitution G A intron_variant MELA-AU X 132175840 132175840 single base substitution G A downstream_gene_variant MELA-AU X 132175840 132175840 single base substitution G A intron_variant MELA-AU X 132175914 132175914 single base substitution C T downstream_gene_variant MELA-AU X 132175914 132175914 single base substitution C T intron_variant MELA-AU X 132176019 132176019 single base substitution C T downstream_gene_variant MELA-AU X 132176019 132176019 single base substitution C T intron_variant MELA-AU X 132176297 132176297 single base substitution C T downstream_gene_variant MELA-AU X 132176297 132176297 single base substitution C T intron_variant MELA-AU X 132176891 132176891 single base substitution G A downstream_gene_variant MELA-AU X 132176891 132176891 single base substitution G A intron_variant MELA-AU X 132177214 132177214 single base substitution T C downstream_gene_variant MELA-AU X 132177214 132177214 single base substitution T C intron_variant MELA-AU X 132177255 132177255 single base substitution C T downstream_gene_variant MELA-AU X 132177255 132177255 single base substitution C T intron_variant MELA-AU X 132177270 132177270 single base substitution A G downstream_gene_variant MELA-AU X 132177270 132177270 single base substitution A G intron_variant MELA-AU X 132177426 132177426 single base substitution C T downstream_gene_variant MELA-AU X 132177426 132177426 single base substitution C T intron_variant MELA-AU X 132177693 132177693 single base substitution G A downstream_gene_variant MELA-AU X 132177693 132177693 single base substitution G A intron_variant MELA-AU X 132177740 132177740 single base substitution C T downstream_gene_variant MELA-AU X 132177740 132177740 single base substitution C T intron_variant MELA-AU X 132177771 132177771 single base substitution G A downstream_gene_variant MELA-AU X 132177771 132177771 single base substitution G A intron_variant MELA-AU X 132177794 132177794 single base substitution G A downstream_gene_variant MELA-AU X 132177794 132177794 single base substitution G A intron_variant MELA-AU X 132177878 132177878 single base substitution C T downstream_gene_variant MELA-AU X 132177878 132177878 single base substitution C T intron_variant MELA-AU X 132178251 132178251 single base substitution C T downstream_gene_variant MELA-AU X 132178251 132178251 single base substitution C T intron_variant MELA-AU X 132178402 132178402 single base substitution G A downstream_gene_variant MELA-AU X 132178402 132178402 single base substitution G A intron_variant MELA-AU X 132178618 132178618 single base substitution C T downstream_gene_variant MELA-AU X 132178618 132178618 single base substitution C T intron_variant MELA-AU X 132178651 132178651 single base substitution C T downstream_gene_variant MELA-AU X 132178651 132178651 single base substitution C T intron_variant MELA-AU X 132178883 132178883 single base substitution G A downstream_gene_variant MELA-AU X 132178883 132178883 single base substitution G A intron_variant MELA-AU X 132179381 132179381 single base substitution G A downstream_gene_variant MELA-AU X 132179381 132179381 single base substitution G A intron_variant MELA-AU X 132179578 132179578 single base substitution C T downstream_gene_variant MELA-AU X 132179578 132179578 single base substitution C T intron_variant MELA-AU X 132179581 132179581 single base substitution C T downstream_gene_variant MELA-AU X 132179581 132179581 single base substitution C T intron_variant MELA-AU X 132179840 132179840 single base substitution G A downstream_gene_variant MELA-AU X 132179840 132179840 single base substitution G A intron_variant MELA-AU X 132179982 132179982 single base substitution G A intron_variant MELA-AU X 132180211 132180211 single base substitution G A intron_variant MELA-AU X 132180566 132180566 single base substitution G A intron_variant MELA-AU X 132180570 132180570 single base substitution A T intron_variant MELA-AU X 132180623 132180623 single base substitution C T intron_variant MELA-AU X 132180822 132180822 single base substitution G A intron_variant MELA-AU X 132181113 132181113 single base substitution C T intron_variant MELA-AU X 132181127 132181127 single base substitution C T intron_variant MELA-AU X 132181666 132181666 single base substitution C T intron_variant MELA-AU X 132181890 132181890 single base substitution C T intron_variant MELA-AU X 132181898 132181898 single base substitution C T intron_variant MELA-AU X 132181968 132181968 single base substitution C T intron_variant MELA-AU X 132182119 132182119 single base substitution G A intron_variant MELA-AU X 132182153 132182153 single base substitution C T intron_variant MELA-AU X 132182353 132182353 single base substitution G A intron_variant MELA-AU X 132182465 132182465 single base substitution G A intron_variant MELA-AU X 132183008 132183008 single base substitution G A intron_variant MELA-AU X 132183086 132183086 single base substitution C T intron_variant MELA-AU X 132183097 132183097 single base substitution C T intron_variant MELA-AU X 132183264 132183264 single base substitution G A intron_variant MELA-AU X 132183470 132183470 single base substitution C T intron_variant MELA-AU X 132183471 132183471 single base substitution C T intron_variant MELA-AU X 132183597 132183597 single base substitution G A intron_variant MELA-AU X 132184421 132184421 single base substitution A C intron_variant MELA-AU X 132184425 132184425 single base substitution G A intron_variant MELA-AU X 132184944 132184944 single base substitution T A intron_variant MELA-AU X 132185295 132185295 single base substitution C T intron_variant MELA-AU X 132185323 132185323 single base substitution G A intron_variant MELA-AU X 132185324 132185324 single base substitution G A intron_variant MELA-AU X 132185910 132185910 single base substitution C T intron_variant MELA-AU X 132185945 132185945 single base substitution A T intron_variant MELA-AU X 132186023 132186023 single base substitution T A intron_variant MELA-AU X 132186051 132186051 single base substitution G A intron_variant MELA-AU X 132186097 132186097 single base substitution G A intron_variant MELA-AU X 132186113 132186113 single base substitution A T intron_variant MELA-AU X 132186123 132186123 single base substitution C T intron_variant MELA-AU X 132186153 132186153 single base substitution G A intron_variant MELA-AU X 132186186 132186186 single base substitution G A intron_variant MELA-AU X 132186422 132186422 single base substitution C T intron_variant MELA-AU X 132186657 132186657 single base substitution G A intron_variant MELA-AU X 132186895 132186895 single base substitution G A intron_variant MELA-AU X 132186952 132186952 single base substitution C T intron_variant MELA-AU X 132187584 132187584 single base substitution A G intron_variant MELA-AU X 132187752 132187752 single base substitution G A intron_variant MELA-AU X 132188256 132188256 single base substitution A T intron_variant MELA-AU X 132188556 132188556 single base substitution C T intron_variant MELA-AU X 132188965 132188965 single base substitution G A intron_variant MELA-AU X 132189183 132189183 single base substitution G A intron_variant MELA-AU X 132189211 132189212 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 132189556 132189556 single base substitution G A intron_variant MELA-AU X 132189638 132189638 single base substitution A T intron_variant MELA-AU X 132189783 132189783 single base substitution C T intron_variant MELA-AU X 132189975 132189975 single base substitution G C intron_variant MELA-AU X 132190014 132190014 single base substitution G T intron_variant MELA-AU X 132190057 132190057 single base substitution G A intron_variant MELA-AU X 132190104 132190104 single base substitution C T intron_variant MELA-AU X 132190827 132190827 single base substitution C T intron_variant MELA-AU X 132191140 132191140 single base substitution G A intron_variant MELA-AU X 132191612 132191612 single base substitution C A intron_variant MELA-AU X 132191679 132191679 single base substitution C T intron_variant MELA-AU X 132192647 132192647 single base substitution C T intron_variant MELA-AU X 132192932 132192932 single base substitution C T intron_variant MELA-AU X 132192966 132192966 single base substitution C T intron_variant MELA-AU X 132193062 132193062 single base substitution G A intron_variant MELA-AU X 132193320 132193320 single base substitution G A intron_variant MELA-AU X 132193847 132193847 single base substitution C T intron_variant MELA-AU X 132194927 132194927 single base substitution C T intron_variant MELA-AU X 132195284 132195284 single base substitution A T intron_variant MELA-AU X 132195639 132195639 single base substitution C T intron_variant MELA-AU X 132195732 132195732 single base substitution G T intron_variant MELA-AU X 132195739 132195739 single base substitution C T intron_variant MELA-AU X 132195755 132195755 single base substitution G A intron_variant MELA-AU X 132195883 132195883 single base substitution G A intron_variant MELA-AU X 132195985 132195986 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 132196106 132196106 single base substitution G A intron_variant MELA-AU X 132196148 132196148 single base substitution C T intron_variant MELA-AU X 132196162 132196162 single base substitution G A intron_variant MELA-AU X 132196172 132196172 single base substitution G A intron_variant MELA-AU X 132196276 132196276 single base substitution G A intron_variant MELA-AU X 132196305 132196305 single base substitution G A intron_variant MELA-AU X 132196306 132196306 single base substitution G A intron_variant MELA-AU X 132196320 132196320 single base substitution G A intron_variant MELA-AU X 132196321 132196321 single base substitution G A intron_variant MELA-AU X 132196396 132196396 single base substitution C T intron_variant MELA-AU X 132196696 132196696 single base substitution G A intron_variant MELA-AU X 132196801 132196801 single base substitution G A intron_variant MELA-AU X 132196938 132196938 single base substitution G A intron_variant MELA-AU X 132196993 132196993 single base substitution G A intron_variant MELA-AU X 132197197 132197198 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 132197298 132197298 single base substitution G A intron_variant MELA-AU X 132197359 132197359 single base substitution C T intron_variant MELA-AU X 132197470 132197470 single base substitution T C intron_variant MELA-AU X 132197625 132197625 single base substitution T A intron_variant MELA-AU X 132197641 132197641 single base substitution C T intron_variant MELA-AU X 132198544 132198544 single base substitution C T intron_variant MELA-AU X 132198592 132198592 single base substitution A G intron_variant MELA-AU X 132198675 132198675 single base substitution G A intron_variant MELA-AU X 132198999 132198999 single base substitution G A intron_variant MELA-AU X 132199040 132199040 single base substitution C T intron_variant MELA-AU X 132199157 132199157 single base substitution G A intron_variant MELA-AU X 132199219 132199219 single base substitution C A intron_variant MELA-AU X 132199220 132199220 single base substitution C T intron_variant MELA-AU X 132199245 132199245 single base substitution G A intron_variant MELA-AU X 132199262 132199262 single base substitution T C intron_variant MELA-AU X 132199350 132199350 single base substitution C T intron_variant MELA-AU X 132199380 132199380 single base substitution G A intron_variant MELA-AU X 132199388 132199388 single base substitution C T intron_variant MELA-AU X 132199391 132199391 single base substitution C T intron_variant MELA-AU X 132200026 132200026 single base substitution C T intron_variant MELA-AU X 132200042 132200042 single base substitution A T intron_variant MELA-AU X 132200056 132200056 single base substitution C T intron_variant MELA-AU X 132200059 132200059 single base substitution A T intron_variant MELA-AU X 132200207 132200207 single base substitution A G intron_variant MELA-AU X 132200279 132200279 single base substitution C T intron_variant MELA-AU X 132200356 132200356 single base substitution C T intron_variant MELA-AU X 132200642 132200642 single base substitution C G intron_variant MELA-AU X 132200800 132200800 single base substitution T G intron_variant MELA-AU X 132200802 132200802 single base substitution G A intron_variant MELA-AU X 132200855 132200855 single base substitution G A intron_variant MELA-AU X 132200964 132200964 single base substitution C T intron_variant MELA-AU X 132201283 132201283 single base substitution G A intron_variant MELA-AU X 132201376 132201376 single base substitution C T intron_variant MELA-AU X 132201427 132201427 single base substitution C T intron_variant MELA-AU X 132201497 132201497 single base substitution C T intron_variant MELA-AU X 132201580 132201580 single base substitution G A intron_variant MELA-AU X 132201772 132201772 single base substitution G A intron_variant MELA-AU X 132201969 132201969 single base substitution G A intron_variant MELA-AU X 132202554 132202554 single base substitution C T intron_variant MELA-AU X 132202627 132202627 single base substitution C T intron_variant MELA-AU X 132202779 132202779 single base substitution G A intron_variant MELA-AU X 132202901 132202901 single base substitution C T intron_variant MELA-AU X 132202992 132202992 single base substitution C T intron_variant MELA-AU X 132203011 132203011 single base substitution G A intron_variant MELA-AU X 132203280 132203281 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 132203956 132203956 single base substitution C T intron_variant MELA-AU X 132204449 132204449 single base substitution C T intron_variant MELA-AU X 132204585 132204585 single base substitution C T intron_variant MELA-AU X 132204793 132204793 single base substitution G A intron_variant MELA-AU X 132204928 132204928 single base substitution C T intron_variant MELA-AU X 132204961 132204961 single base substitution G A intron_variant MELA-AU X 132205627 132205627 single base substitution G A intron_variant MELA-AU X 132205887 132205887 single base substitution C T intron_variant MELA-AU X 132205930 132205930 single base substitution G A intron_variant MELA-AU X 132206036 132206036 single base substitution C T intron_variant MELA-AU X 132206077 132206077 single base substitution C T intron_variant MELA-AU X 132206443 132206443 single base substitution C T intron_variant MELA-AU X 132206507 132206507 single base substitution A C intron_variant MELA-AU X 132207028 132207028 single base substitution C T intron_variant MELA-AU X 132207301 132207301 single base substitution C T intron_variant MELA-AU X 132207616 132207616 single base substitution G A intron_variant MELA-AU X 132207720 132207720 single base substitution G A intron_variant MELA-AU X 132207735 132207735 single base substitution G A intron_variant MELA-AU X 132207929 132207929 single base substitution C T intron_variant MELA-AU X 132207953 132207953 single base substitution G A intron_variant MELA-AU X 132208055 132208055 single base substitution C T intron_variant MELA-AU X 132208185 132208185 single base substitution G A intron_variant MELA-AU X 132208190 132208190 single base substitution G A intron_variant MELA-AU X 132208259 132208259 single base substitution A G intron_variant MELA-AU X 132208659 132208659 single base substitution C T intron_variant MELA-AU X 132208729 132208729 single base substitution G A intron_variant MELA-AU X 132208854 132208854 single base substitution G A intron_variant MELA-AU X 132209273 132209273 single base substitution C T intron_variant MELA-AU X 132209375 132209375 single base substitution C T intron_variant MELA-AU X 132209881 132209881 single base substitution G A intron_variant MELA-AU X 132210030 132210030 single base substitution A G intron_variant MELA-AU X 132210072 132210072 single base substitution G A intron_variant MELA-AU X 132210088 132210088 single base substitution G A intron_variant MELA-AU X 132210146 132210146 single base substitution C T intron_variant MELA-AU X 132210175 132210175 single base substitution G A intron_variant MELA-AU X 132210289 132210289 single base substitution G A intron_variant MELA-AU X 132210326 132210326 single base substitution G A intron_variant MELA-AU X 132210550 132210550 single base substitution G A intron_variant MELA-AU X 132210599 132210599 single base substitution G A intron_variant MELA-AU X 132210817 132210817 single base substitution C T intron_variant MELA-AU X 132210988 132210988 single base substitution C T intron_variant MELA-AU X 132211120 132211120 single base substitution G A intron_variant MELA-AU X 132211760 132211760 single base substitution G A intron_variant MELA-AU X 132211807 132211807 single base substitution C T intron_variant MELA-AU X 132211856 132211856 single base substitution C T intron_variant MELA-AU X 132212036 132212036 single base substitution C T intron_variant MELA-AU X 132212095 132212095 single base substitution G A intron_variant MELA-AU X 132212199 132212199 single base substitution C T intron_variant MELA-AU X 132212408 132212408 single base substitution G A intron_variant MELA-AU X 132212603 132212603 single base substitution G C intron_variant MELA-AU X 132212877 132212877 single base substitution G A intron_variant MELA-AU X 132212905 132212905 single base substitution G A intron_variant MELA-AU X 132212993 132212993 single base substitution C T intron_variant MELA-AU X 132213217 132213217 single base substitution C T intron_variant MELA-AU X 132213307 132213307 single base substitution G A intron_variant MELA-AU X 132213414 132213414 single base substitution G A intron_variant MELA-AU X 132213782 132213782 single base substitution G A intron_variant MELA-AU X 132213820 132213820 single base substitution G A intron_variant MELA-AU X 132214251 132214251 single base substitution C T intron_variant MELA-AU X 132214387 132214387 single base substitution C T intron_variant MELA-AU X 132214433 132214433 single base substitution G A intron_variant MELA-AU X 132214711 132214711 single base substitution C T intron_variant MELA-AU X 132214986 132214986 single base substitution G A intron_variant MELA-AU X 132215189 132215189 single base substitution T C intron_variant MELA-AU X 132215222 132215222 single base substitution C A intron_variant MELA-AU X 132215292 132215292 single base substitution G A intron_variant MELA-AU X 132215300 132215300 single base substitution G A intron_variant MELA-AU X 132215389 132215389 single base substitution A C intron_variant MELA-AU X 132215391 132215391 single base substitution C G intron_variant MELA-AU X 132215460 132215460 single base substitution G A intron_variant MELA-AU X 132215487 132215487 single base substitution G A intron_variant MELA-AU X 132215641 132215641 single base substitution G A intron_variant MELA-AU X 132215883 132215883 single base substitution G A intron_variant MELA-AU X 132215885 132215885 single base substitution A T intron_variant MELA-AU X 132216343 132216343 single base substitution C T intron_variant MELA-AU X 132216363 132216363 single base substitution A G intron_variant MELA-AU X 132216669 132216669 single base substitution T C intron_variant MELA-AU X 132216674 132216674 single base substitution C T intron_variant MELA-AU X 132216987 132216987 single base substitution G A intron_variant MELA-AU X 132217103 132217103 single base substitution G A intron_variant MELA-AU X 132217390 132217390 single base substitution G A intron_variant MELA-AU X 132217484 132217484 single base substitution G A intron_variant MELA-AU X 132217662 132217662 single base substitution C T intron_variant MELA-AU X 132217744 132217744 single base substitution G A 5_prime_UTR_variant MELA-AU X 132217744 132217744 single base substitution G A exon_variant MELA-AU X 132217928 132217928 single base substitution C T intron_variant MELA-AU X 132217928 132217928 single base substitution C T upstream_gene_variant MELA-AU X 132217984 132217984 single base substitution G A intron_variant MELA-AU X 132217984 132217984 single base substitution G A upstream_gene_variant MELA-AU X 132218227 132218227 single base substitution A T intron_variant MELA-AU X 132218227 132218227 single base substitution A T upstream_gene_variant MELA-AU X 132218662 132218662 single base substitution C T intron_variant MELA-AU X 132218662 132218662 single base substitution C T upstream_gene_variant MELA-AU X 132218977 132218977 single base substitution G A intron_variant MELA-AU X 132218977 132218977 single base substitution G A upstream_gene_variant MELA-AU X 132218980 132218980 single base substitution G A intron_variant MELA-AU X 132218980 132218980 single base substitution G A upstream_gene_variant MELA-AU X 132219066 132219066 single base substitution C T intron_variant MELA-AU X 132219066 132219066 single base substitution C T upstream_gene_variant MELA-AU X 132219290 132219290 single base substitution C T intron_variant MELA-AU X 132219290 132219290 single base substitution C T upstream_gene_variant MELA-AU X 132219685 132219685 single base substitution G A intron_variant MELA-AU X 132219685 132219685 single base substitution G A upstream_gene_variant MELA-AU X 132219891 132219891 single base substitution G A intron_variant MELA-AU X 132219891 132219891 single base substitution G A upstream_gene_variant MELA-AU X 132219919 132219919 single base substitution G A intron_variant MELA-AU X 132219919 132219919 single base substitution G A upstream_gene_variant MELA-AU X 132220305 132220305 single base substitution G A intron_variant MELA-AU X 132220305 132220305 single base substitution G A upstream_gene_variant MELA-AU X 132220698 132220698 single base substitution G A intron_variant MELA-AU X 132220698 132220698 single base substitution G A upstream_gene_variant MELA-AU X 132220805 132220805 single base substitution C T intron_variant MELA-AU X 132220805 132220805 single base substitution C T upstream_gene_variant MELA-AU X 132221022 132221022 single base substitution C T intron_variant MELA-AU X 132221022 132221022 single base substitution C T upstream_gene_variant MELA-AU X 132221649 132221649 single base substitution C T intron_variant MELA-AU X 132221649 132221649 single base substitution C T upstream_gene_variant MELA-AU X 132221774 132221774 single base substitution A T intron_variant MELA-AU X 132221774 132221774 single base substitution A T upstream_gene_variant MELA-AU X 132221995 132221995 single base substitution C T intron_variant MELA-AU X 132221995 132221995 single base substitution C T upstream_gene_variant MELA-AU X 132222542 132222542 single base substitution C T intron_variant MELA-AU X 132222542 132222542 single base substitution C T upstream_gene_variant MELA-AU X 132222680 132222680 single base substitution C T intron_variant MELA-AU X 132222680 132222680 single base substitution C T upstream_gene_variant MELA-AU X 132222949 132222949 single base substitution C T intron_variant MELA-AU X 132223151 132223151 single base substitution G A intron_variant MELA-AU X 132223798 132223798 single base substitution G A intron_variant MELA-AU X 132224344 132224344 single base substitution G A intron_variant MELA-AU X 132224449 132224449 single base substitution G A intron_variant MELA-AU X 132224602 132224602 single base substitution G A intron_variant MELA-AU X 132224888 132224888 single base substitution C T intron_variant MELA-AU X 132224943 132224943 single base substitution G A intron_variant MELA-AU X 132225263 132225263 single base substitution G A intron_variant MELA-AU X 132225362 132225362 single base substitution C T intron_variant MELA-AU X 132225364 132225364 single base substitution G A intron_variant MELA-AU X 132225415 132225415 single base substitution C T 5_prime_UTR_variant MELA-AU X 132225415 132225415 single base substitution C T exon_variant MELA-AU X 132225451 132225451 single base substitution C T 5_prime_UTR_variant MELA-AU X 132225451 132225451 single base substitution C T exon_variant MELA-AU X 132225643 132225643 single base substitution G A intron_variant MELA-AU X 132225743 132225743 single base substitution G A intron_variant MELA-AU X 132225803 132225803 single base substitution C T intron_variant MELA-AU X 132225881 132225881 single base substitution C T intron_variant MELA-AU X 132225890 132225890 single base substitution C T intron_variant MELA-AU X 132225929 132225929 single base substitution C T intron_variant MELA-AU X 132226132 132226132 single base substitution G A intron_variant MELA-AU X 132226494 132226494 single base substitution G A intron_variant MELA-AU X 132226791 132226791 single base substitution T C intron_variant MELA-AU X 132226952 132226952 single base substitution G T intron_variant MELA-AU X 132226993 132226993 single base substitution A G intron_variant MELA-AU X 132227458 132227458 single base substitution G A intron_variant MELA-AU X 132227480 132227480 single base substitution G A intron_variant MELA-AU X 132227502 132227502 single base substitution G A intron_variant MELA-AU X 132227524 132227524 single base substitution G A intron_variant MELA-AU X 132228047 132228047 single base substitution C T intron_variant MELA-AU X 132228128 132228128 single base substitution C T intron_variant MELA-AU X 132228224 132228224 single base substitution G A intron_variant MELA-AU X 132228471 132228471 single base substitution G A intron_variant MELA-AU X 132228542 132228542 single base substitution C T intron_variant MELA-AU X 132228711 132228711 single base substitution C T intron_variant MELA-AU X 132228939 132228939 single base substitution T C intron_variant MELA-AU X 132229005 132229005 single base substitution C T intron_variant MELA-AU X 132229048 132229048 single base substitution G A intron_variant MELA-AU X 132229212 132229212 single base substitution C T intron_variant MELA-AU X 132229335 132229335 single base substitution C T intron_variant MELA-AU X 132229373 132229373 single base substitution A G intron_variant MELA-AU X 132229565 132229565 single base substitution T A intron_variant MELA-AU X 132229567 132229567 single base substitution C T intron_variant MELA-AU X 132229713 132229713 single base substitution C T intron_variant MELA-AU X 132229791 132229791 single base substitution G A intron_variant MELA-AU X 132229938 132229938 single base substitution G A intron_variant MELA-AU X 132229944 132229944 single base substitution C T intron_variant MELA-AU X 132230312 132230312 single base substitution C T intron_variant MELA-AU X 132230458 132230458 single base substitution T A intron_variant MELA-AU X 132230546 132230546 single base substitution C T intron_variant MELA-AU X 132230821 132230821 single base substitution G A intron_variant MELA-AU X 132230917 132230917 single base substitution C T intron_variant MELA-AU X 132230946 132230946 single base substitution G A intron_variant MELA-AU X 132231301 132231301 single base substitution G A upstream_gene_variant MELA-AU X 132231361 132231361 single base substitution G A upstream_gene_variant MELA-AU X 132231561 132231561 single base substitution G A upstream_gene_variant MELA-AU X 132231811 132231811 single base substitution G A upstream_gene_variant MELA-AU X 132231818 132231818 single base substitution C T upstream_gene_variant MELA-AU X 132231891 132231891 single base substitution G A upstream_gene_variant MELA-AU X 132231921 132231921 single base substitution C T upstream_gene_variant MELA-AU X 132231987 132231987 single base substitution C T upstream_gene_variant MELA-AU X 132232001 132232002 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU X 132232081 132232081 single base substitution C T upstream_gene_variant MELA-AU X 132232681 132232681 single base substitution C T upstream_gene_variant MELA-AU X 132232694 132232694 single base substitution G A upstream_gene_variant MELA-AU X 132233307 132233307 single base substitution C G upstream_gene_variant MELA-AU X 132233336 132233337 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU X 132233356 132233356 single base substitution G A upstream_gene_variant MELA-AU X 132233385 132233385 single base substitution G A upstream_gene_variant MELA-AU X 132234034 132234034 single base substitution C T upstream_gene_variant MELA-AU X 132234205 132234205 single base substitution G A upstream_gene_variant MELA-AU X 132234232 132234232 single base substitution C T upstream_gene_variant MELA-AU X 132234723 132234723 single base substitution G A upstream_gene_variant MELA-AU X 132234756 132234756 single base substitution C T upstream_gene_variant MELA-AU X 132235793 132235793 single base substitution T A upstream_gene_variant MELA-AU X 132236018 132236018 single base substitution C T upstream_gene_variant MELA-AU X 132236035 132236035 single base substitution C T upstream_gene_variant MELA-AU X 132236062 132236062 single base substitution G A upstream_gene_variant MELA-AU X 132236089 132236089 single base substitution G A upstream_gene_variant ORCA-IN X 132159625 132159625 single base substitution C T missense_variant R875H 2624G>A ORCA-IN X 132164074 132164074 single base substitution T G intron_variant ORCA-IN X 132164074 132164074 single base substitution T G upstream_gene_variant ORCA-IN X 132204473 132204473 single base substitution C T intron_variant OV-AU X 132153832 132153832 single base substitution T G downstream_gene_variant OV-AU X 132154610 132154610 single base substitution C T downstream_gene_variant OV-AU X 132156625 132156625 single base substitution G C downstream_gene_variant OV-AU X 132159151 132159151 single base substitution G A 3_prime_UTR_variant OV-AU X 132159972 132159972 single base substitution G C missense_variant S759R 2277C>G OV-AU X 132164724 132164724 single base substitution A G intron_variant OV-AU X 132164724 132164724 single base substitution A G upstream_gene_variant OV-AU X 132167379 132167379 single base substitution T A intron_variant OV-AU X 132169879 132169879 single base substitution G A intron_variant OV-AU X 132173255 132173255 single base substitution C A intron_variant OV-AU X 132174732 132174732 single base substitution A G intron_variant OV-AU X 132179640 132179640 single base substitution C T downstream_gene_variant OV-AU X 132179640 132179640 single base substitution C T intron_variant OV-AU X 132182921 132182921 single base substitution C T intron_variant OV-AU X 132183699 132183699 single base substitution A T intron_variant OV-AU X 132187294 132187294 single base substitution G C intron_variant OV-AU X 132187730 132187730 single base substitution C T intron_variant OV-AU X 132196061 132196061 single base substitution G A intron_variant OV-AU X 132197330 132197330 single base substitution A T intron_variant OV-AU X 132199226 132199226 single base substitution T C intron_variant OV-AU X 132199499 132199499 single base substitution A T intron_variant OV-AU X 132204249 132204249 single base substitution C A intron_variant OV-AU X 132205246 132205246 single base substitution A T intron_variant OV-AU X 132207054 132207054 single base substitution A C intron_variant OV-AU X 132209886 132209886 single base substitution C T intron_variant OV-AU X 132219906 132219906 single base substitution G A intron_variant OV-AU X 132219906 132219906 single base substitution G A upstream_gene_variant OV-AU X 132225380 132225380 single base substitution C T splice_donor_variant OV-AU X 132228449 132228449 single base substitution T C intron_variant OV-AU X 132228643 132228643 single base substitution T G intron_variant OV-AU X 132228962 132228962 single base substitution A C intron_variant OV-AU X 132229842 132229842 single base substitution G A intron_variant OV-AU X 132231853 132231853 single base substitution C G upstream_gene_variant PACA-AU X 132153991 132153991 single base substitution C T downstream_gene_variant PACA-AU X 132154396 132154396 single base substitution A G downstream_gene_variant PACA-AU X 132154642 132154642 single base substitution G A downstream_gene_variant PACA-AU X 132160638 132160638 single base substitution C G missense_variant Q537H 1611G>C PACA-AU X 132161044 132161044 single base substitution T A missense_variant N402I 1205A>T PACA-AU X 132165438 132165438 single base substitution C T intron_variant PACA-AU X 132165438 132165438 single base substitution C T upstream_gene_variant PACA-AU X 132168571 132168571 single base substitution A C intron_variant PACA-AU X 132172946 132172946 single base substitution C A intron_variant PACA-AU X 132173915 132173915 single base substitution C A intron_variant PACA-AU X 132178734 132178734 single base substitution G A downstream_gene_variant PACA-AU X 132178734 132178734 single base substitution G A intron_variant PACA-AU X 132202371 132202371 single base substitution A T intron_variant PACA-AU X 132204703 132204703 single base substitution C T intron_variant PACA-AU X 132220016 132220016 single base substitution T G intron_variant PACA-AU X 132220016 132220016 single base substitution T G upstream_gene_variant PACA-AU X 132220062 132220062 single base substitution G A intron_variant PACA-AU X 132220062 132220062 single base substitution G A upstream_gene_variant PACA-AU X 132224945 132224945 single base substitution G T intron_variant PACA-CA X 132155227 132155227 single base substitution T C downstream_gene_variant PACA-CA X 132155910 132155910 single base substitution C T downstream_gene_variant PACA-CA X 132156481 132156481 single base substitution A G downstream_gene_variant PACA-CA X 132158556 132158556 single base substitution T A downstream_gene_variant PACA-CA X 132165123 132165123 insertion of <=200bp - T intron_variant PACA-CA X 132165123 132165123 insertion of <=200bp - T upstream_gene_variant PACA-CA X 132165145 132165145 single base substitution A T intron_variant PACA-CA X 132165145 132165145 single base substitution A T upstream_gene_variant PACA-CA X 132166226 132166226 single base substitution C A intron_variant PACA-CA X 132166226 132166226 single base substitution C A upstream_gene_variant PACA-CA X 132166511 132166511 single base substitution A C intron_variant PACA-CA X 132166511 132166511 single base substitution A C upstream_gene_variant PACA-CA X 132167323 132167323 single base substitution G A intron_variant PACA-CA X 132168365 132168365 single base substitution A T intron_variant PACA-CA X 132169138 132169138 deletion of <=200bp A - intron_variant PACA-CA X 132172172 132172172 single base substitution A G intron_variant PACA-CA X 132172537 132172537 single base substitution C T intron_variant PACA-CA X 132172574 132172574 single base substitution G A intron_variant PACA-CA X 132173634 132173634 single base substitution G A intron_variant PACA-CA X 132181505 132181505 single base substitution G A intron_variant PACA-CA X 132183689 132183689 single base substitution A G intron_variant PACA-CA X 132184634 132184634 single base substitution T A intron_variant PACA-CA X 132189274 132189274 single base substitution A C intron_variant PACA-CA X 132190226 132190226 single base substitution A T intron_variant PACA-CA X 132190333 132190333 single base substitution C T intron_variant PACA-CA X 132190382 132190382 single base substitution C T intron_variant PACA-CA X 132190587 132190587 single base substitution T C intron_variant PACA-CA X 132191487 132191487 insertion of <=200bp - T intron_variant PACA-CA X 132193796 132193796 single base substitution G A intron_variant PACA-CA X 132195434 132195434 single base substitution C T intron_variant PACA-CA X 132196820 132196820 single base substitution T C intron_variant PACA-CA X 132197921 132197921 single base substitution T A intron_variant PACA-CA X 132200656 132200656 single base substitution T C intron_variant PACA-CA X 132205024 132205024 single base substitution C T intron_variant PACA-CA X 132205284 132205284 single base substitution G C intron_variant PACA-CA X 132206209 132206209 single base substitution A G intron_variant PACA-CA X 132211444 132211444 single base substitution T A intron_variant PACA-CA X 132215150 132215150 single base substitution T A intron_variant PACA-CA X 132223240 132223240 single base substitution C A intron_variant PACA-CA X 132229444 132229444 single base substitution T A intron_variant PACA-CA X 132231520 132231520 single base substitution T C upstream_gene_variant PAEN-AU X 132170821 132170821 single base substitution T A intron_variant PAEN-AU X 132200897 132200897 single base substitution C G intron_variant PAEN-AU X 132228082 132228082 single base substitution T A intron_variant PAEN-IT X 132192773 132192773 single base substitution A G intron_variant PBCA-DE X 132156512 132156513 deletion of <=200bp AC - downstream_gene_variant PBCA-DE X 132165683 132165683 single base substitution C A intron_variant PBCA-DE X 132165683 132165683 single base substitution C A upstream_gene_variant PBCA-DE X 132176640 132176640 single base substitution G A downstream_gene_variant PBCA-DE X 132176640 132176640 single base substitution G A intron_variant PBCA-DE X 132177979 132177979 insertion of <=200bp - A downstream_gene_variant PBCA-DE X 132177979 132177979 insertion of <=200bp - A intron_variant PBCA-DE X 132182776 132182776 single base substitution G A intron_variant PBCA-DE X 132184635 132184635 single base substitution T A intron_variant PBCA-DE X 132185194 132185194 single base substitution C A intron_variant PBCA-DE X 132188014 132188014 single base substitution A T intron_variant PBCA-DE X 132188431 132188431 single base substitution T C intron_variant PBCA-DE X 132190006 132190006 single base substitution A T intron_variant PBCA-DE X 132190752 132190752 single base substitution T C intron_variant PBCA-DE X 132191991 132191991 single base substitution C T intron_variant PBCA-DE X 132192999 132192999 single base substitution A G intron_variant PBCA-DE X 132196274 132196274 single base substitution G C intron_variant PBCA-DE X 132203276 132203276 single base substitution A G intron_variant PBCA-DE X 132205565 132205565 deletion of <=200bp A - intron_variant PBCA-DE X 132206217 132206217 single base substitution T C intron_variant PBCA-DE X 132211740 132211740 single base substitution G A intron_variant PBCA-DE X 132215364 132215364 deletion of <=200bp C - intron_variant PBCA-DE X 132219867 132219867 deletion of <=200bp A - intron_variant PBCA-DE X 132219867 132219867 deletion of <=200bp A - upstream_gene_variant PBCA-DE X 132228515 132228515 single base substitution C T intron_variant PBCA-DE X 132229059 132229059 single base substitution G A intron_variant PBCA-DE X 132230001 132230001 single base substitution G T intron_variant PRAD-CA X 132174258 132174258 single base substitution T C intron_variant PRAD-CA X 132200387 132200387 single base substitution A G intron_variant PRAD-CA X 132224082 132224082 single base substitution T A intron_variant PRAD-CA X 132225355 132225355 single base substitution T G intron_variant PRAD-CA X 132231555 132231555 single base substitution G A upstream_gene_variant PRAD-UK X 132158510 132158510 single base substitution C A downstream_gene_variant PRAD-UK X 132158821 132158821 single base substitution A C 3_prime_UTR_variant PRAD-UK X 132158821 132158821 single base substitution A C downstream_gene_variant PRAD-UK X 132173105 132173105 single base substitution G T intron_variant PRAD-UK X 132174073 132174073 deletion of <=200bp T - intron_variant PRAD-UK X 132180718 132180718 single base substitution G T intron_variant PRAD-UK X 132180719 132180719 single base substitution C T intron_variant PRAD-UK X 132209385 132209385 single base substitution G A intron_variant PRAD-UK X 132210716 132210716 single base substitution G T intron_variant PRAD-UK X 132222662 132222662 single base substitution A G intron_variant PRAD-UK X 132222662 132222662 single base substitution A G upstream_gene_variant PRAD-UK X 132235080 132235080 single base substitution G C upstream_gene_variant PRAD-US X 132159947 132159947 single base substitution G T missense_variant H768N 2302C>A PRAD-US X 132160413 132160413 deletion of <=200bp T - frameshift_variant K612 RECA-EU X 132162379 132162379 single base substitution T A intron_variant RECA-EU X 132162379 132162379 single base substitution T A upstream_gene_variant RECA-EU X 132163650 132163650 single base substitution C G intron_variant RECA-EU X 132163650 132163650 single base substitution C G upstream_gene_variant RECA-EU X 132171564 132171564 single base substitution A T intron_variant RECA-EU X 132180907 132180907 single base substitution T A intron_variant RECA-EU X 132181656 132181656 single base substitution A T intron_variant RECA-EU X 132196646 132196646 single base substitution A G intron_variant RECA-EU X 132196647 132196647 single base substitution G A intron_variant RECA-EU X 132196649 132196649 single base substitution G T intron_variant RECA-EU X 132199301 132199301 single base substitution A C intron_variant RECA-EU X 132200697 132200697 single base substitution T A intron_variant RECA-EU X 132210161 132210161 single base substitution T A intron_variant RECA-EU X 132216893 132216893 single base substitution G T intron_variant RECA-EU X 132224573 132224573 single base substitution G T intron_variant RECA-EU X 132228586 132228586 single base substitution G A intron_variant RECA-EU X 132232631 132232631 single base substitution A T upstream_gene_variant RECA-EU X 132233010 132233010 single base substitution A T upstream_gene_variant RECA-EU X 132233011 132233011 single base substitution C A upstream_gene_variant RECA-EU X 132233728 132233728 single base substitution A T upstream_gene_variant SKCA-BR X 132154568 132154568 single base substitution G A downstream_gene_variant SKCA-BR X 132155740 132155740 single base substitution C T downstream_gene_variant SKCA-BR X 132156415 132156415 single base substitution C T downstream_gene_variant SKCA-BR X 132156915 132156915 single base substitution G A downstream_gene_variant SKCA-BR X 132157724 132157724 single base substitution G C downstream_gene_variant SKCA-BR X 132158610 132158610 single base substitution G A downstream_gene_variant SKCA-BR X 132159042 132159042 single base substitution C T 3_prime_UTR_variant SKCA-BR X 132159042 132159042 single base substitution C T downstream_gene_variant SKCA-BR X 132159774 132159774 single base substitution C T synonymous_variant R825R 2475G>A SKCA-BR X 132161857 132161857 single base substitution G A missense_variant S131L 392C>T SKCA-BR X 132162212 132162212 single base substitution C A missense_variant G13W 37G>T SKCA-BR X 132163374 132163374 single base substitution G A intron_variant SKCA-BR X 132163374 132163374 single base substitution G A upstream_gene_variant SKCA-BR X 132163650 132163650 single base substitution C T intron_variant SKCA-BR X 132163650 132163650 single base substitution C T upstream_gene_variant SKCA-BR X 132165691 132165691 single base substitution C T intron_variant SKCA-BR X 132165691 132165691 single base substitution C T upstream_gene_variant SKCA-BR X 132167133 132167133 single base substitution G A intron_variant SKCA-BR X 132167133 132167133 single base substitution G A upstream_gene_variant SKCA-BR X 132167799 132167799 single base substitution G A intron_variant SKCA-BR X 132167801 132167801 single base substitution T A intron_variant SKCA-BR X 132167871 132167871 single base substitution G A intron_variant SKCA-BR X 132169628 132169628 single base substitution C T intron_variant SKCA-BR X 132170196 132170196 insertion of <=200bp - GT intron_variant SKCA-BR X 132170589 132170589 single base substitution C T intron_variant SKCA-BR X 132170590 132170590 single base substitution T A intron_variant SKCA-BR X 132173201 132173201 single base substitution C T intron_variant SKCA-BR X 132173492 132173492 single base substitution T C intron_variant SKCA-BR X 132173928 132173928 single base substitution G A intron_variant SKCA-BR X 132175914 132175914 single base substitution C T downstream_gene_variant SKCA-BR X 132175914 132175914 single base substitution C T intron_variant SKCA-BR X 132176500 132176500 single base substitution C T downstream_gene_variant SKCA-BR X 132176500 132176500 single base substitution C T intron_variant SKCA-BR X 132176980 132176980 single base substitution G A downstream_gene_variant SKCA-BR X 132176980 132176980 single base substitution G A intron_variant SKCA-BR X 132177363 132177363 single base substitution C T downstream_gene_variant SKCA-BR X 132177363 132177363 single base substitution C T intron_variant SKCA-BR X 132177437 132177437 single base substitution C T downstream_gene_variant SKCA-BR X 132177437 132177437 single base substitution C T intron_variant SKCA-BR X 132177898 132177898 single base substitution G A downstream_gene_variant SKCA-BR X 132177898 132177898 single base substitution G A intron_variant SKCA-BR X 132179738 132179738 single base substitution G A downstream_gene_variant SKCA-BR X 132179738 132179738 single base substitution G A intron_variant SKCA-BR X 132181402 132181402 single base substitution G C intron_variant SKCA-BR X 132183641 132183641 single base substitution G A intron_variant SKCA-BR X 132185130 132185130 single base substitution T C intron_variant SKCA-BR X 132185456 132185456 single base substitution C T intron_variant SKCA-BR X 132186111 132186111 single base substitution G A intron_variant SKCA-BR X 132187583 132187583 single base substitution G A intron_variant SKCA-BR X 132187725 132187725 single base substitution C T intron_variant SKCA-BR X 132187926 132187926 single base substitution C T intron_variant SKCA-BR X 132190730 132190730 single base substitution T G intron_variant SKCA-BR X 132192237 132192237 single base substitution A T intron_variant SKCA-BR X 132193761 132193761 single base substitution G A intron_variant SKCA-BR X 132194057 132194057 single base substitution C T intron_variant SKCA-BR X 132194187 132194187 single base substitution C T intron_variant SKCA-BR X 132195147 132195147 single base substitution C T intron_variant SKCA-BR X 132195440 132195440 single base substitution C T intron_variant SKCA-BR X 132195885 132195885 single base substitution G A intron_variant SKCA-BR X 132195985 132195985 single base substitution C T intron_variant SKCA-BR X 132196455 132196455 single base substitution C T intron_variant SKCA-BR X 132196850 132196859 deletion of <=200bp CTCCACATGA - intron_variant SKCA-BR X 132196992 132196992 single base substitution G A intron_variant SKCA-BR X 132197149 132197149 single base substitution G A intron_variant SKCA-BR X 132198733 132198733 single base substitution C T intron_variant SKCA-BR X 132199157 132199157 single base substitution G A intron_variant SKCA-BR X 132199219 132199219 single base substitution C T intron_variant SKCA-BR X 132199652 132199652 single base substitution C A intron_variant SKCA-BR X 132200202 132200202 single base substitution G A intron_variant SKCA-BR X 132200948 132200948 single base substitution C T intron_variant SKCA-BR X 132201610 132201610 single base substitution G A intron_variant SKCA-BR X 132202643 132202643 single base substitution G A intron_variant SKCA-BR X 132202869 132202869 single base substitution T C intron_variant SKCA-BR X 132203800 132203800 single base substitution C T intron_variant SKCA-BR X 132204077 132204077 single base substitution G A intron_variant SKCA-BR X 132205332 132205332 single base substitution G A intron_variant SKCA-BR X 132205526 132205526 single base substitution A G intron_variant SKCA-BR X 132205564 132205565 deletion of <=200bp TA - intron_variant SKCA-BR X 132206071 132206071 single base substitution G A intron_variant SKCA-BR X 132208282 132208282 single base substitution C T intron_variant SKCA-BR X 132208441 132208441 single base substitution G A intron_variant SKCA-BR X 132208594 132208594 single base substitution C A intron_variant SKCA-BR X 132208670 132208670 single base substitution C T intron_variant SKCA-BR X 132209136 132209136 single base substitution C T intron_variant SKCA-BR X 132210605 132210605 single base substitution G A intron_variant SKCA-BR X 132210797 132210797 single base substitution G A intron_variant SKCA-BR X 132212961 132212961 single base substitution G A intron_variant SKCA-BR X 132214140 132214140 single base substitution G A intron_variant SKCA-BR X 132218390 132218390 single base substitution A G intron_variant SKCA-BR X 132218390 132218390 single base substitution A G upstream_gene_variant SKCA-BR X 132218540 132218541 deletion of <=200bp CT - intron_variant SKCA-BR X 132218540 132218541 deletion of <=200bp CT - upstream_gene_variant SKCA-BR X 132221596 132221596 single base substitution G A intron_variant SKCA-BR X 132221596 132221596 single base substitution G A upstream_gene_variant SKCA-BR X 132223818 132223818 single base substitution G A intron_variant SKCA-BR X 132225615 132225615 single base substitution G T intron_variant SKCA-BR X 132226524 132226524 single base substitution G A intron_variant SKCA-BR X 132227303 132227303 single base substitution G A intron_variant SKCA-BR X 132227458 132227458 single base substitution G A intron_variant SKCA-BR X 132228678 132228678 single base substitution T A intron_variant SKCA-BR X 132229906 132229906 single base substitution G A intron_variant SKCA-BR X 132231135 132231135 single base substitution T G 5_prime_UTR_variant SKCA-BR X 132231135 132231135 single base substitution T G exon_variant SKCA-BR X 132231266 132231266 single base substitution C T upstream_gene_variant SKCA-BR X 132232033 132232033 single base substitution G A upstream_gene_variant SKCA-BR X 132233473 132233473 single base substitution G A upstream_gene_variant SKCA-BR X 132234957 132234957 single base substitution C T upstream_gene_variant SKCA-BR X 132235119 132235119 single base substitution T A upstream_gene_variant SKCA-BR X 132235276 132235276 single base substitution C T upstream_gene_variant SKCM-US X 132159790 132159790 single base substitution C T missense_variant G820E 2459G>A SKCM-US X 132159888 132159888 single base substitution G A synonymous_variant S787S 2361C>T SKCM-US X 132159894 132159894 single base substitution C T synonymous_variant R785R 2355G>A SKCM-US X 132160034 132160034 single base substitution T G missense_variant T739P 2215A>C SKCM-US X 132160053 132160053 single base substitution G A synonymous_variant F732F 2196C>T SKCM-US X 132160102 132160102 single base substitution G A missense_variant P716L 2147C>T SKCM-US X 132160103 132160103 single base substitution G A missense_variant P716S 2146C>T SKCM-US X 132160128 132160128 single base substitution A C missense_variant F707L 2121T>G SKCM-US X 132160163 132160163 single base substitution G A missense_variant P696S 2086C>T SKCM-US X 132160170 132160170 single base substitution G A synonymous_variant P693P 2079C>T SKCM-US X 132160255 132160255 single base substitution G A missense_variant S665L 1994C>T SKCM-US X 132160265 132160265 single base substitution C T missense_variant E662K 1984G>A SKCM-US X 132160351 132160351 single base substitution G A missense_variant S633F 1898C>T SKCM-US X 132160463 132160463 single base substitution C T missense_variant D596N 1786G>A SKCM-US X 132160489 132160489 single base substitution G A missense_variant S587L 1760C>T SKCM-US X 132160519 132160519 single base substitution C T missense_variant R577Q 1730G>A SKCM-US X 132160520 132160520 single base substitution G A stop_gained R577* 1729C>T SKCM-US X 132160569 132160569 single base substitution G A synonymous_variant P560P 1680C>T SKCM-US X 132160571 132160571 single base substitution G A missense_variant P560S 1678C>T SKCM-US X 132160819 132160819 single base substitution G A missense_variant S477L 1430C>T SKCM-US X 132161000 132161000 single base substitution G A missense_variant P417S 1249C>T SKCM-US X 132161123 132161123 single base substitution G A missense_variant H376Y 1126C>T SKCM-US X 132161158 132161158 single base substitution A G missense_variant L364P 1091T>C SKCM-US X 132161249 132161249 single base substitution G A missense_variant P334S 1000C>T SKCM-US X 132161263 132161263 single base substitution G A missense_variant P329L 986C>T SKCM-US X 132161510 132161510 single base substitution G A missense_variant P247S 739C>T SKCM-US X 132161550 132161550 single base substitution C T synonymous_variant L233L 699G>A SKCM-US X 132161573 132161573 single base substitution C T missense_variant E226K 676G>A SKCM-US X 132161645 132161645 single base substitution C G missense_variant E202Q 604G>C SKCM-US X 132161665 132161665 single base substitution A G missense_variant L195S 584T>C SKCM-US X 132161704 132161704 single base substitution C T missense_variant R182K 545G>A SKCM-US X 132161796 132161796 single base substitution C T synonymous_variant G151G 453G>A SKCM-US X 132161803 132161803 single base substitution C T missense_variant G149E 446G>A SKCM-US X 132161857 132161857 single base substitution G A missense_variant S131L 392C>T SKCM-US X 132161988 132161988 single base substitution G A synonymous_variant S87S 261C>T SKCM-US X 132161995 132161995 single base substitution C T missense_variant G85E 254G>A SKCM-US X 132162061 132162061 single base substitution G A missense_variant S63F 188C>T SKCM-US X 132162210 132162210 single base substitution C T synonymous_variant G13G 39G>A SKCM-US X 132162218 132162218 single base substitution G A stop_gained Q11* 31C>T SKCM-US X 132162238 132162238 single base substitution A C missense_variant L4R 11T>G STAD-US X 132159805 132159805 single base substitution C A missense_variant R815I 2444G>T STAD-US X 132160099 132160099 single base substitution G A missense_variant T717I 2150C>T STAD-US X 132160305 132160305 single base substitution G T missense_variant F648L 1944C>A STAD-US X 132160633 132160633 single base substitution A C missense_variant V539G 1616T>G STAD-US X 132160682 132160682 single base substitution G A missense_variant R523C 1567C>T STAD-US X 132160701 132160701 single base substitution G A synonymous_variant I516I 1548C>T STAD-US X 132160788 132160788 insertion of <=200bp - A frameshift_variant F487F? STAD-US X 132160803 132160803 single base substitution A G synonymous_variant T482T 1446T>C STAD-US X 132160981 132160981 single base substitution T G missense_variant D423A 1268A>C STAD-US X 132161101 132161101 single base substitution G A missense_variant A383V 1148C>T STAD-US X 132161102 132161102 single base substitution C T missense_variant A383T 1147G>A STAD-US X 132161217 132161217 single base substitution C T synonymous_variant R344R 1032G>A STAD-US X 132161318 132161318 single base substitution G C missense_variant Q311E 931C>G STAD-US X 132161368 132161368 single base substitution C T missense_variant C294Y 881G>A STAD-US X 132161820 132161820 single base substitution A C synonymous_variant S143S 429T>G STAD-US X 132162027 132162027 single base substitution A C synonymous_variant T74T 222T>G UCEC-US X 132159590 132159590 single base substitution C A stop_gained E887* 2659G>T UCEC-US X 132159805 132159805 single base substitution C A missense_variant R815I 2444G>T UCEC-US X 132159906 132159906 single base substitution C T synonymous_variant Q781Q 2343G>A UCEC-US X 132160042 132160042 single base substitution G T missense_variant S736Y 2207C>A UCEC-US X 132160082 132160082 single base substitution C A missense_variant D723Y 2167G>T UCEC-US X 132160340 132160340 single base substitution C A stop_gained E637* 1909G>T UCEC-US X 132160507 132160507 single base substitution G T missense_variant S581Y 1742C>A UCEC-US X 132160573 132160573 single base substitution A G missense_variant L559P 1676T>C UCEC-US X 132160874 132160874 single base substitution C A stop_gained E459* 1375G>T UCEC-US X 132160874 132160874 single base substitution C T missense_variant E459K 1375G>A UCEC-US X 132161036 132161036 single base substitution A G missense_variant W405R 1213T>C UCEC-US X 132161331 132161331 single base substitution C A missense_variant M306I 918G>T UCEC-US X 132161431 132161431 single base substitution C A missense_variant S273I 818G>T UCEC-US X 132161573 132161573 single base substitution C A stop_gained E226* 676G>T UCEC-US X 132161660 132161660 single base substitution C A stop_gained E197* 589G>T UCEC-US X 132161704 132161704 single base substitution C A missense_variant R182I 545G>T UCEC-US X 132161834 132161834 single base substitution A G missense_variant S139P 415T>C UCEC-US X 132161981 132161981 single base substitution C A missense_variant D90Y 268G>T UCEC-US X 132162116 132162116 single base substitution C A stop_gained G45* 133G>T UCEC-US X 132162147 132162147 single base substitution C T synonymous_variant K34K 102G>A UCEC-US X 132162229 132162229 single base substitution C T missense_variant R7H 20G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand pfg008T COSM1643955 c.1837_1838insA p.G613fs*6 Insertion - Frameshift 23:133026383-133026384 - TCGA-AX-A0J0-01 COSM1115348 c.2444G>T p.R815I Substitution - Missense 23:133025777-133025777 - TCGA-BT-A20T-01 COSM422228 c.537G>A p.K179K Substitution - coding silent 23:133027684-133027684 - CSCC-5-T COSM3558018 c.2146C>T p.P716S Substitution - Missense 23:133026075-133026075 - LUAD-F00257 COSM366935 c.571A>C p.N191H Substitution - Missense 23:133027650-133027650 - 1_RESISTANT COSM1720945 c.2018G>A p.G673E Substitution - Missense 23:133026203-133026203 - TCGA-D8-A1XK-01 COSM1465695 c.1461delT p.F487fs*40 Deletion - Frameshift 23:133026760-133026760 - Pat_40_A COSM4934003 c.2459G>T p.G820V Substitution - Missense 23:133025762-133025762 - TCGA-EE-A29E-06 COSM3558039 c.188C>T p.S63F Substitution - Missense 23:133028033-133028033 - TCGA-FS-A1ZW-06 COSM3558032 c.676G>A p.E226K Substitution - Missense 23:133027545-133027545 - TCGA-B0-5099-01 COSM487974 c.1978T>C p.Y660H Substitution - Missense 23:133026243-133026243 - OSCC-GB_00140111 COSM1465689 c.2624G>A p.R875H Substitution - Missense 23:133025597-133025597 - ESCC_BICR_051T COSM5444141 c.1106C>T p.S369L Substitution - Missense 23:133027115-133027115 - TCGA-AP-A056-01 COSM1115352 c.2167G>T p.D723Y Substitution - Missense 23:133026054-133026054 - 1960590 COSM53533 c.1091T>C p.L364P Substitution - Missense 23:133027130-133027130 - B82-Tumor COSM254999 c.2659G>A p.E887K Substitution - Missense 23:133025562-133025562 - TCGA-A6-6781-01 COSM1465689 c.2624G>A p.R875H Substitution - Missense 23:133025597-133025597 - HCC66 COSM1625523 c.49A>C p.T17P Substitution - Missense 23:133028172-133028172 - CN-AML-NR-08-Dx COSM2726497 c.1033C>T p.L345L Substitution - coding silent 23:133027188-133027188 - HCC063T COSM5812893 c.1486T>A p.C496S Substitution - Missense 23:133026735-133026735 - TCGA-59-2354-01 COSM120128 c.1919C>G p.S640C Substitution - Missense 23:133026302-133026302 - CSCC-32-T COSM4563247 c.964G>A p.D322N Substitution - Missense 23:133027257-133027257 - EC109 COSM5049370 c.946A>G p.I316V Substitution - Missense 23:133027275-133027275 - TCGA-FR-A44A-06 COSM3558018 c.2146C>T p.P716S Substitution - Missense 23:133026075-133026075 - TCGA-ER-A2NC-06 COSM3558029 c.1000C>T p.P334S Substitution - Missense 23:133027221-133027221 - CSCC-31-T COSM4506231 c.713C>T p.S238L Substitution - Missense 23:133027508-133027508 - TCGA-FW-A3R5-06 COSM3913385 c.1730G>A p.R577Q Substitution - Missense 23:133026491-133026491 - Pat_40_A COSM5877103 c.2461G>T p.D821Y Substitution - Missense 23:133025760-133025760 - TCGA-B5-A11E-01 COSM1115360 c.818G>T p.S273I Substitution - Missense 23:133027403-133027403 - SNUH_G10_S1 COSM3681569 c.1423C>T p.H475Y Substitution - Missense 23:133026798-133026798 - LB996-RCC COSM24334 c.1612delG p.E538fs*8 Deletion - Frameshift 23:133026609-133026609 - HCC66T COSM1625523 c.49A>C p.T17P Substitution - Missense 23:133028172-133028172 - TCGA-AZ-4315-01 COSM1465696 c.1445C>T p.T482I Substitution - Missense 23:133026776-133026776 - TCGA-BS-A0TC-01 COSM1115365 c.268G>T p.D90Y Substitution - Missense 23:133027953-133027953 - HCC19T COSM3708441 c.472A>T p.M158L Substitution - Missense 23:133027749-133027749 - TCGA-AA-A010-01 COSM286389 c.1186G>T p.D396Y Substitution - Missense 23:133027035-133027035 - LAU618 COSM233728 c.1549C>T p.L517F Substitution - Missense 23:133026672-133026672 - SNU-C4 COSM4654533 c.1380G>A p.L460L Substitution - coding silent 23:133026841-133026841 - HCC2998 COSM1465697 c.1412G>T p.R471I Substitution - Missense 23:133026809-133026809 - TCGA-AS-3778-01 COSM1465690 c.1976C>T p.T659M Substitution - Missense 23:133026245-133026245 - 389 COSM204162 c.727G>A p.A243T Substitution - Missense 23:133027494-133027494 - TCGA-39-5028-01 COSM755318 c.950C>A p.P317Q Substitution - Missense 23:133027271-133027271 - Pat_40_B COSM4934003 c.2459G>T p.G820V Substitution - Missense 23:133025762-133025762 - TCGA-AZ-4315-01 COSM1465694 c.1696G>T p.E566* Substitution - Nonsense 23:133026525-133026525 - TCGA-AG-3892-01 COSM258332 c.2571C>T p.Y857Y Substitution - coding silent 23:133025650-133025650 - TCGA-BS-A0TC-01 COSM1115359 c.918G>T p.M306I Substitution - Missense 23:133027303-133027303 - T96 COSM1465700 c.1044_1045insT p.K349fs*1 Insertion - Frameshift 23:133027176-133027177 - TCGA-AG-A01W-01 COSM1465692 c.1836_1837insA p.G613fs*6 Insertion - Frameshift 23:133026384-133026385 - SJBALL264_D COSM4399387 c.2086C>T p.P696S Substitution - Missense 23:133026135-133026135 - Pat_40_B COSM5877103 c.2461G>T p.D821Y Substitution - Missense 23:133025760-133025760 - TCGA-GN-A26A-06 COSM2726507 c.739C>T p.P247S Substitution - Missense 23:133027482-133027482 - 3N09-VS-3T09 COSM3558020 c.2079C>T p.P693P Substitution - coding silent 23:133026142-133026142 - 49M COSM5593899 c.1072G>A p.E358K Substitution - Missense 23:133027149-133027149 - HX5T COSM53533 c.1091T>C p.L364P Substitution - Missense 23:133027130-133027130 - 2521252 COSM5889441 c.1412G>A p.R471K Substitution - Missense 23:133026809-133026809 - CCK81 COSM204161 c.1044delT p.F348fs*7 Deletion - Frameshift 23:133027177-133027177 - TCGA-DC-6160-01 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - B82 COSM254999 c.2659G>A p.E887K Substitution - Missense 23:133025562-133025562 - TCGA-EE-A29M-06 COSM135949 c.446G>A p.G149E Substitution - Missense 23:133027775-133027775 - BD25T COSM5509047 c.1016C>G p.T339S Substitution - Missense 23:133027205-133027205 - HCC2998 COSM1682891 c.2237G>T p.R746I Substitution - Missense 23:133025984-133025984 - 8016571 COSM1169184 c.1454T>C p.L485P Substitution - Missense 23:133026767-133026767 - SNUH_G10_S1 COSM3681570 c.494T>C p.L165S Substitution - Missense 23:133027727-133027727 - SJLGG012_D COSM1716246 c.600T>G p.S200S Substitution - coding silent 23:133027621-133027621 - BD124T COSM5490931 c.1043_1044insT p.K349fs*1 Insertion - Frameshift 23:133027177-133027178 - TCGA-DA-A1HV-06 COSM3558020 c.2079C>T p.P693P Substitution - coding silent 23:133026142-133026142 - T3724 COSM1465692 c.1836_1837insA p.G613fs*6 Insertion - Frameshift 23:133026384-133026385 - TCGA-AS-3778-01 COSM1497160 c.1375G>C p.E459Q Substitution - Missense 23:133026846-133026846 - TCGA-AP-A0L8-01 COSM1115355 c.1676T>C p.L559P Substitution - Missense 23:133026545-133026545 - TCGA-AM-5821-01 COSM3759362 c.576G>A p.E192E Substitution - coding silent 23:133027645-133027645 - HCT15 COSM2726484 c.1838G>A p.G613D Substitution - Missense 23:133026383-133026383 - LUAD-F00365 COSM367589 c.1406C>T p.P469L Substitution - Missense 23:133026815-133026815 - P162 COSM755317 c.152G>T p.R51L Substitution - Missense 23:133028069-133028069 - YUZINO COSM1715563 c.1228G>A p.E410K Substitution - Missense 23:133026993-133026993 - 2492712 COSM5607192 c.902G>A p.G301E Substitution - Missense 23:133027319-133027319 - TCGA-AA-3663-01 COSM1465700 c.1044_1045insT p.K349fs*1 Insertion - Frameshift 23:133027176-133027177 - DLD1 COSM2726484 c.1838G>A p.G613D Substitution - Missense 23:133026383-133026383 - 71M COSM5596138 c.1027G>A p.A343T Substitution - Missense 23:133027194-133027194 - TCGA-EE-A3AC-06 COSM3558023 c.1898C>T p.S633F Substitution - Missense 23:133026323-133026323 - LS180 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - 14T COSM1465689 c.2624G>A p.R875H Substitution - Missense 23:133025597-133025597 - T55 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - T2269 COSM3558025 c.1729C>T p.R577* Substitution - Nonsense 23:133026492-133026492 - TCGA-A8-A0A6-01 COSM3843604 c.897T>A p.N299K Substitution - Missense 23:133027324-133027324 - pfg017T COSM1465695 c.1461delT p.F487fs*40 Deletion - Frameshift 23:133026760-133026760 - TCGA-B5-A11E-01 COSM1115364 c.415T>C p.S139P Substitution - Missense 23:133027806-133027806 - P56 COSM328994 c.2572G>A p.D858N Substitution - Missense 23:133025649-133025649 - TCGA-GF-A6C9-06 COSM4901870 c.1430C>T p.S477L Substitution - Missense 23:133026791-133026791 - CSCC-27-T COSM4537552 c.2434G>A p.E812K Substitution - Missense 23:133025787-133025787 - TCGA-D5-6932-01 COSM1465690 c.1976C>T p.T659M Substitution - Missense 23:133026245-133026245 - TCGA-DB-A64W-01 COSM3973258 c.2670A>G p.E890E Substitution - coding silent 23:133025551-133025551 - PT19_2 COSM5900440 c.1357C>A p.Q453K Substitution - Missense 23:133026864-133026864 - TCGA-BS-A0UV-01 COSM1115358 c.1213T>C p.W405R Substitution - Missense 23:133027008-133027008 - PT35 COSM5914523 c.2299G>A p.G767R Substitution - Missense 23:133025922-133025922 - TCGA-EE-A2GO-06 COSM3558033 c.604G>C p.E202Q Substitution - Missense 23:133027617-133027617 - TCGA-DA-A1HV-06 COSM3558027 c.1678C>T p.P560S Substitution - Missense 23:133026543-133026543 - 8044630 COSM4389503 c.1205A>T p.N402I Substitution - Missense 23:133027016-133027016 - TCGA-41-3393-01 COSM3405977 c.312C>T p.N104N Substitution - coding silent 23:133027909-133027909 - Pat_76_A COSM3558027 c.1678C>T p.P560S Substitution - Missense 23:133026543-133026543 - TCGA-BR-8487-01 COSM4106731 c.1032G>A p.R344R Substitution - coding silent 23:133027189-133027189 - TCGA-CG-5728-01 COSM4106733 c.881G>A p.C294Y Substitution - Missense 23:133027340-133027340 - Pat_70_B COSM1465695 c.1461delT p.F487fs*40 Deletion - Frameshift 23:133026760-133026760 - TCGA-GF-A6C8-06 COSM3913386 c.584T>C p.L195S Substitution - Missense 23:133027637-133027637 - P123 COSM1735930 c.536_538delAGA p.K179delK Deletion - In frame 23:133027683-133027685 - PD13752a COSM1664913 c.1030C>T p.R344W Substitution - Missense 23:133027191-133027191 - TCGA-A6-6653-01 COSM1465691 c.1958C>T p.P653L Substitution - Missense 23:133026263-133026263 - 49M COSM5593898 c.2533G>A p.D845N Substitution - Missense 23:133025688-133025688 - 2011-2259:2012-1326-T COSM4604735 c.2142C>G p.I714M Substitution - Missense 23:133026079-133026079 - cSCCP1 COSM135949 c.446G>A p.G149E Substitution - Missense 23:133027775-133027775 - LN229 COSM5713012 c.1877A>G p.Q626R Substitution - Missense 23:133026344-133026344 - SNUH_G16_S1 COSM3681570 c.494T>C p.L165S Substitution - Missense 23:133027727-133027727 - 86502 COSM95442 c.2712G>T p.K904N Substitution - Missense 23:133025509-133025509 - T3724 COSM4739736 c.1917A>G p.E639E Substitution - coding silent 23:133026304-133026304 - TCGA-BR-6706-01 COSM4106724 c.1616T>G p.V539G Substitution - Missense 23:133026605-133026605 - HCC078T COSM5806114 c.273T>A p.A91A Substitution - coding silent 23:133027948-133027948 - SNUH_G16_S1 COSM3681569 c.1423C>T p.H475Y Substitution - Missense 23:133026798-133026798 - S00941 COSM4879287 c.2302C>A p.H768N Substitution - Missense 23:133025919-133025919 - HCC19 COSM3708441 c.472A>T p.M158L Substitution - Missense 23:133027749-133027749 - pfg181T COSM4761453 c.622G>A p.A208T Substitution - Missense 23:133027599-133027599 - TCGA-BR-8589-01 COSM4106727 c.1446T>C p.T482T Substitution - coding silent 23:133026775-133026775 - pfg057T COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - I2L-P19Ta-Tumor-Organoid COSM5367005 c.2696C>T p.A899V Substitution - Missense 23:133025525-133025525 - YUVAIL COSM328994 c.2572G>A p.D858N Substitution - Missense 23:133025649-133025649 - TCGA-BR-6452-01 COSM4106723 c.1944C>A p.F648L Substitution - Missense 23:133026277-133026277 - I2L-P19Ta-Tumor-Biopsy COSM5367005 c.2696C>T p.A899V Substitution - Missense 23:133025525-133025525 - 61 COSM5742427 c.1726A>T p.I576F Substitution - Missense 23:133026495-133026495 - 61 COSM40905 c.1461_1462insT p.G488fs*6 Insertion - Frameshift 23:133026759-133026760 - LAU50_2 COSM233729 c.2620A>G p.R874G Substitution - Missense 23:133025601-133025601 - T368 COSM204161 c.1044delT p.F348fs*7 Deletion - Frameshift 23:133027177-133027177 - TCGA-EE-A2MC-06 COSM3558022 c.1984G>A p.E662K Substitution - Missense 23:133026237-133026237 - TCGA-D3-A3C3-06 COSM3558023 c.1898C>T p.S633F Substitution - Missense 23:133026323-133026323 - ATL052 COSM5711488 c.1996delC p.L666fs*37 Deletion - Frameshift 23:133026225-133026225 - PT48 COSM5927983 c.151C>T p.R51W Substitution - Missense 23:133028070-133028070 - TCGA-EE-A29P-06 COSM3558041 c.11T>G p.L4R Substitution - Missense 23:133028210-133028210 - ATL047 COSM3558024 c.1760C>T p.S587L Substitution - Missense 23:133026461-133026461 - TCGA-AA-A00E-01 COSM298296 c.1835_1836delAA p.K612fs*6 Deletion - Frameshift 23:133026385-133026386 - CSCC-55-T COSM4528160 c.1516G>A p.G506R Substitution - Missense 23:133026705-133026705 - TCGA-Q1-A6DT-01 COSM4850798 c.2312A>C p.N771T Substitution - Missense 23:133025909-133025909 - HX20T COSM3708440 c.1855G>T p.G619W Substitution - Missense 23:133026366-133026366 - PT37 COSM5921963 c.509G>A p.G170E Substitution - Missense 23:133027712-133027712 - TCGA-EE-A2A1-06 COSM3558038 c.254G>A p.G85E Substitution - Missense 23:133027967-133027967 - ESO-887 COSM755318 c.950C>A p.P317Q Substitution - Missense 23:133027271-133027271 - TCGA-B5-A0JY-01 COSM1115367 c.102G>A p.K34K Substitution - coding silent 23:133028119-133028119 - C086 COSM5541479 c.837G>A p.W279* Substitution - Nonsense 23:133027384-133027384 - B82 COSM254999 c.2659G>A p.E887K Substitution - Missense 23:133025562-133025562 - PD24325a COSM5781290 c.1044T>A p.F348L Substitution - Missense 23:133027177-133027177 - ESO-081 COSM258332 c.2571C>T p.Y857Y Substitution - coding silent 23:133025650-133025650 - ATL030 COSM1115365 c.268G>T p.D90Y Substitution - Missense 23:133027953-133027953 - C086 COSM5541481 c.720C>T p.I240I Substitution - coding silent 23:133027501-133027501 - TCGA-BR-6565-01 COSM4106734 c.429T>G p.S143S Substitution - coding silent 23:133027792-133027792 - S00501 COSM316401 c.783A>T p.K261N Substitution - Missense 23:133027438-133027438 - HCC2998 COSM1682891 c.2237G>T p.R746I Substitution - Missense 23:133025984-133025984 - LOVO COSM2726498 c.1019T>C p.M340T Substitution - Missense 23:133027202-133027202 - HCA7 COSM1465700 c.1044_1045insT p.K349fs*1 Insertion - Frameshift 23:133027176-133027177 - TCGA-76-6286-01 COSM1664913 c.1030C>T p.R344W Substitution - Missense 23:133027191-133027191 - C13 COSM5037446 c.2117A>C p.K706T Substitution - Missense 23:133026104-133026104 - KYSE50 COSM2726517 c.269A>C p.D90A Substitution - Missense 23:133027952-133027952 - TCGA-AA-3510-01 COSM1465697 c.1412G>T p.R471I Substitution - Missense 23:133026809-133026809 - 2492711 COSM5607192 c.902G>A p.G301E Substitution - Missense 23:133027319-133027319 - 1N35-VS-1T35 COSM4974866 c.313G>A p.E105K Substitution - Missense 23:133027908-133027908 - TCGA-18-3409-01 COSM755321 c.2393G>A p.R798K Substitution - Missense 23:133025828-133025828 - CSCC-37-T COSM1664912 c.1249C>T p.P417S Substitution - Missense 23:133026972-133026972 - S00501 COSM316401 c.783A>T p.K261N Substitution - Missense 23:133027438-133027438 - B17 COSM255067 c.1831_1841del11 p.K611fs*4 Deletion - Frameshift 23:133026380-133026390 - TCGA-G4-6297-01 COSM3694337 c.2617G>T p.D873Y Substitution - Missense 23:133025604-133025604 - TCGA-AK-3450-01 COSM3363814 c.2196C>G p.F732L Substitution - Missense 23:133026025-133026025 - TCGA-BS-A0UF-01 COSM1115361 c.676G>T p.E226* Substitution - Nonsense 23:133027545-133027545 - TCGA-EE-A29D-06 COSM3558031 c.699G>A p.L233L Substitution - coding silent 23:133027522-133027522 - TCGA-EE-A2GM-06 COSM3558035 c.453G>A p.G151G Substitution - coding silent 23:133027768-133027768 - TCGA-AG-3892-01 COSM258333 c.1761A>C p.S587S Substitution - coding silent 23:133026460-133026460 - RK232_C01 COSM4944873 c.1643C>A p.S548Y Substitution - Missense 23:133026578-133026578 - TCGA-B5-A0JY-01 COSM1115356 c.1375G>A p.E459K Substitution - Missense 23:133026846-133026846 - TCGA-AP-A0LM-01 COSM1115354 c.1742C>A p.S581Y Substitution - Missense 23:133026479-133026479 - LUAD-CHTN-MAD06-00678 COSM361081 c.1083C>A p.L361L Substitution - coding silent 23:133027138-133027138 - BD236T COSM204161 c.1044delT p.F348fs*7 Deletion - Frameshift 23:133027177-133027177 - T3152 COSM1465695 c.1461delT p.F487fs*40 Deletion - Frameshift 23:133026760-133026760 - TCGA-FU-A23K-01 COSM462318 c.1150C>T p.H384Y Substitution - Missense 23:133027071-133027071 - C086 COSM5541478 c.2068C>T p.Q690* Substitution - Nonsense 23:133026153-133026153 - 234 COSM3730583 c.1692T>C p.D564D Substitution - coding silent 23:133026529-133026529 - TCGA-B7-5818-01 COSM4106728 c.1268A>C p.D423A Substitution - Missense 23:133026953-133026953 - TCGA-RP-A695-06 COSM3558027 c.1678C>T p.P560S Substitution - Missense 23:133026543-133026543 - 587220 COSM1232010 c.365C>T p.T122I Substitution - Missense 23:133027856-133027856 - TCGA-BS-A0UF-01 COSM1115363 c.545G>T p.R182I Substitution - Missense 23:133027676-133027676 - TCGA-EE-A2GL-06 COSM53533 c.1091T>C p.L364P Substitution - Missense 23:133027130-133027130 - TCGA-D1-A15Z-01 COSM1115368 c.20G>A p.R7H Substitution - Missense 23:133028201-133028201 - TCGA-Q1-A5R2-01 COSM254999 c.2659G>A p.E887K Substitution - Missense 23:133025562-133025562 - YUPAER COSM5412029 c.679T>C p.L227L Substitution - coding silent 23:133027542-133027542 - LUAD-CHTN-MAD06-00668 COSM360657 c.50C>A p.T17N Substitution - Missense 23:133028171-133028171 - PTC-14C COSM204162 c.727G>A p.A243T Substitution - Missense 23:133027494-133027494 - TCGA-EE-A3AC-06 COSM3558034 c.545G>A p.R182K Substitution - Missense 23:133027676-133027676 - C086 COSM5541482 c.2469C>T p.T823T Substitution - coding silent 23:133025752-133025752 - sysucc-1370T COSM4604737 c.2164G>A p.E722K Substitution - Missense 23:133026057-133026057 - TCGA-IR-A3LH-01 COSM4832809 c.2348C>G p.S783C Substitution - Missense 23:133025873-133025873 - S02093 COSM5673319 c.59C>G p.S20C Substitution - Missense 23:133028162-133028162 - PD9702a COSM5792975 c.95G>C p.R32T Substitution - Missense 23:133028126-133028126 - LAU50_1 COSM233729 c.2620A>G p.R874G Substitution - Missense 23:133025601-133025601 - PD4315a COSM5049370 c.946A>G p.I316V Substitution - Missense 23:133027275-133027275 - CCK81 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - ME100L COSM231491 c.2596C>T p.Q866* Substitution - Nonsense 23:133025625-133025625 - TCGA-CJ-4873-01 COSM3363815 c.1143C>T p.N381N Substitution - coding silent 23:133027078-133027078 - TCGA-EE-A29M-06 COSM3558024 c.1760C>T p.S587L Substitution - Missense 23:133026461-133026461 - TCGA-B5-A11N-01 COSM1115362 c.589G>T p.E197* Substitution - Nonsense 23:133027632-133027632 - TCGA-IH-A3EA-01 COSM2726469 c.2215A>C p.T739P Substitution - Missense 23:133026006-133026006 - PTC-14C COSM4156591 c.1575C>A p.S525R Substitution - Missense 23:133026646-133026646 - TCGA-39-5036-01 COSM755320 c.1944C>G p.F648L Substitution - Missense 23:133026277-133026277 - TCGA-F4-6703-01 COSM1465695 c.1461delT p.F487fs*40 Deletion - Frameshift 23:133026760-133026760 - ccRCC-64 COSM1664912 c.1249C>T p.P417S Substitution - Missense 23:133026972-133026972 - I2L-P7-Tumor-Organoid COSM5367364 c.1433C>G p.S478C Substitution - Missense 23:133026788-133026788 - TCGA-AN-A046-01 COSM3843606 c.401A>C p.K134T Substitution - Missense 23:133027820-133027820 - HN_62995 COSM130111 c.2716G>T p.V906L Substitution - Missense 23:133025505-133025505 - TCGA-BS-A0UV-01 COSM1115350 c.2343G>A p.Q781Q Substitution - coding silent 23:133025878-133025878 - ESCC_BICR_008T COSM1465692 c.1836_1837insA p.G613fs*6 Insertion - Frameshift 23:133026384-133026385 - 1N03-VS-1T03 COSM4972691 c.635G>T p.R212M Substitution - Missense 23:133027586-133027586 - SJLGG012 COSM1716246 c.600T>G p.S200S Substitution - coding silent 23:133027621-133027621 - TCGA-DD-A73B-01 COSM1664913 c.1030C>T p.R344W Substitution - Missense 23:133027191-133027191 - CN-AML-08-T COSM2726497 c.1033C>T p.L345L Substitution - coding silent 23:133027188-133027188 - TCGA-EE-A20C-06 COSM3558036 c.392C>T p.S131L Substitution - Missense 23:133027829-133027829 - T276 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - pfg008T COSM1643955 c.1837_1838insA p.G613fs*6 Insertion - Frameshift 23:133026383-133026384 - TCGA-AN-A046-01 COSM3843605 c.873G>A p.E291E Substitution - coding silent 23:133027348-133027348 - TCGA-EQ-8122-01 COSM4106730 c.1147G>A p.A383T Substitution - Missense 23:133027074-133027074 - TCGA-66-2795-01 COSM755317 c.152G>T p.R51L Substitution - Missense 23:133028069-133028069 - BD112T COSM5490916 c.2475G>A p.R825R Substitution - coding silent 23:133025746-133025746 - T3091 COSM4739740 c.118C>T p.L40L Substitution - coding silent 23:133028103-133028103 - Pat_76_B COSM3558027 c.1678C>T p.P560S Substitution - Missense 23:133026543-133026543 - T3094 COSM4739739 c.327T>C p.P109P Substitution - coding silent 23:133027894-133027894 - TCGA-D7-6520-01 COSM4106732 c.931C>G p.Q311E Substitution - Missense 23:133027290-133027290 - TCGA-C5-A1BN-01 COSM4837245 c.1106C>A p.S369* Substitution - Nonsense 23:133027115-133027115 - TCGA-BF-A1PZ-01 COSM4399387 c.2086C>T p.P696S Substitution - Missense 23:133026135-133026135 - ESCC-191T COSM3939791 c.1593A>C p.A531A Substitution - coding silent 23:133026628-133026628 - Br27P COSM40905 c.1461_1462insT p.G488fs*6 Insertion - Frameshift 23:133026759-133026760 - 2293767 COSM4607181 c.2177T>G p.I726S Substitution - Missense 23:133026044-133026044 - PT45 COSM5927983 c.151C>T p.R51W Substitution - Missense 23:133028070-133028070 - YUSIV COSM5412028 c.1031G>A p.R344Q Substitution - Missense 23:133027190-133027190 - WA33 COSM242194 c.1340C>T p.A447V Substitution - Missense 23:133026881-133026881 - TCGA-EE-A2MJ-06 COSM3558040 c.39G>A p.G13G Substitution - coding silent 23:133028182-133028182 - LAU63 COSM235547 c.1401C>T p.N467N Substitution - coding silent 23:133026820-133026820 - TCGA-AH-6644-01 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - AOCS-155-3-5 COSM4137683 c.2277C>G p.S759R Substitution - Missense 23:133025944-133025944 - PD4109a COSM165435 c.1334C>A p.S445Y Substitution - Missense 23:133026887-133026887 - TCGA-DK-A3IQ-01 COSM1315223 c.95G>T p.R32I Substitution - Missense 23:133028126-133028126 - TCGA-EB-A3Y6-01 COSM3558028 c.1126C>T p.H376Y Substitution - Missense 23:133027095-133027095 - TCGA-BQ-5879-01 COSM3992356 c.2028T>G p.P676P Substitution - coding silent 23:133026193-133026193 - TCGA-A7-A13E-01 COSM3843607 c.247A>T p.I83F Substitution - Missense 23:133027974-133027974 - TCGA-BS-A0UF-01 COSM1115348 c.2444G>T p.R815I Substitution - Missense 23:133025777-133025777 - LB996-RCC COSM24334 c.1612delG p.E538fs*8 Deletion - Frameshift 23:133026609-133026609 - tumor_4191799 COSM3357382 c.1615G>T p.V539F Substitution - Missense 23:133026606-133026606 - TCGA-BR-6452-01 COSM4106729 c.1148C>T p.A383V Substitution - Missense 23:133027073-133027073 - TCGA-D8-A1XQ-01 COSM3843603 c.2563T>C p.F855L Substitution - Missense 23:133025658-133025658 - TCGA-CD-5801-01 COSM4106735 c.222T>G p.T74T Substitution - coding silent 23:133027999-133027999 - 40M COSM5586977 c.1819G>A p.E607K Substitution - Missense 23:133026402-133026402 - HCC2998 COSM1115348 c.2444G>T p.R815I Substitution - Missense 23:133025777-133025777 - TCGA-BS-A0UF-01 COSM1115351 c.2207C>A p.S736Y Substitution - Missense 23:133026014-133026014 - LS174T COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - TCGA-EE-A3AE-06 COSM3558037 c.261C>T p.S87S Substitution - coding silent 23:133027960-133027960 - 2011-2299:2012-1334-T COSM4604737 c.2164G>A p.E722K Substitution - Missense 23:133026057-133026057 - sysucc-882T COSM5447880 c.2324C>A p.P775H Substitution - Missense 23:133025897-133025897 - TCGA-EW-A1PB-01 COSM1490502 c.2052C>A p.L684L Substitution - coding silent 23:133026169-133026169 - TCGA-AG-3892-01 COSM258334 c.411G>T p.E137D Substitution - Missense 23:133027810-133027810 - EGC15 COSM5064387 c.629G>A p.C210Y Substitution - Missense 23:133027592-133027592 - TCGA-BR-6452-01 COSM4106722 c.2150C>T p.T717I Substitution - Missense 23:133026071-133026071 - ME009T COSM224141 c.1402C>T p.L468F Substitution - Missense 23:133026819-133026819 - 1_PRE-TREATMENT COSM1720945 c.2018G>A p.G673E Substitution - Missense 23:133026203-133026203 - 101692 COSM95444 c.532A>C p.K178Q Substitution - Missense 23:133027689-133027689 - TCGA-EE-A2GC-06 COSM3558030 c.986C>T p.P329L Substitution - Missense 23:133027235-133027235 - TCGA-BR-8680-01 COSM1115348 c.2444G>T p.R815I Substitution - Missense 23:133025777-133025777 - TCGA-DK-A2HX-01 COSM1315221 c.1264G>A p.A422T Substitution - Missense 23:133026957-133026957 - CSCC-31-T COSM4457657 c.1053C>T p.T351T Substitution - coding silent 23:133027168-133027168 - TCGA-D1-A16Y-01 COSM1115353 c.1909G>T p.E637* Substitution - Nonsense 23:133026312-133026312 - TCGA-A5-A0G9-01 COSM1115349 c.2440A>G p.K814E Substitution - Missense 23:133025781-133025781 - TCGA-39-5039-01 COSM755319 c.1071G>A p.K357K Substitution - coding silent 23:133027150-133027150 - TCGA-D3-A3MU-06 COSM204160 c.2196C>T p.F732F Substitution - coding silent 23:133026025-133026025 - TCGA-FW-A3R5-06 COSM3913384 c.1786G>A p.D596N Substitution - Missense 23:133026435-133026435 - CSCC-29-T COSM4482818 c.2643C>T p.F881F Substitution - coding silent 23:133025578-133025578 - TCGA-BR-7715-01 COSM4106725 c.1567C>T p.R523C Substitution - Missense 23:133026654-133026654 - TCGA-EK-A3GJ-01 COSM4852367 c.706G>T p.E236* Substitution - Nonsense 23:133027515-133027515 - TCGA-GN-A263-01 COSM3558021 c.1994C>T p.S665L Substitution - Missense 23:133026227-133026227 - TCGA-EB-A44P-01 COSM3558026 c.1680C>T p.P560P Substitution - coding silent 23:133026541-133026541 - TCGA-DK-A1AC-01 COSM1315222 c.120G>A p.L40L Substitution - coding silent 23:133028101-133028101 - PT20_2 COSM1715564 c.838G>A p.D280N Substitution - Missense 23:133027383-133027383 - TCGA-D1-A17Q-01 COSM1115366 c.133G>T p.G45* Substitution - Nonsense 23:133028088-133028088 - PA028 COSM1162268 c.1996C>T p.L666F Substitution - Missense 23:133026225-133026225 - ESCC-D2 COSM5045828 c.554C>T p.S185L Substitution - Missense 23:133027667-133027667 - 585276 COSM324215 c.636G>C p.R212S Substitution - Missense 23:133027585-133027585 - TCGA-A3-3346-01 COSM487975 c.528G>T p.Q176H Substitution - Missense 23:133027693-133027693 - PD3983a COSM165434 c.1945A>G p.I649V Substitution - Missense 23:133026276-133026276 - 1115157 COSM5552157 c.1174G>C p.D392H Substitution - Missense 23:133027047-133027047 - TCGA-EB-A3XB-01 COSM3558017 c.2147C>T p.P716L Substitution - Missense 23:133026074-133026074 - TCGA-FU-A3HZ-01 COSM4840302 c.866T>C p.F289S Substitution - Missense 23:133027355-133027355 - 587350 COSM1232011 c.1379T>C p.L460P Substitution - Missense 23:133026842-133026842 - Pat_66_A COSM5877104 c.1606G>A p.D536N Substitution - Missense 23:133026615-133026615 - KM12 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - Br27P COSM40905 c.1461_1462insT p.G488fs*6 Insertion - Frameshift 23:133026759-133026760 - 2492714 COSM5607192 c.902G>A p.G301E Substitution - Missense 23:133027319-133027319 - TCGA-GF-A6C9-06 COSM4900738 c.31C>T p.Q11* Substitution - Nonsense 23:133028190-133028190 - 585208 COSM326833 c.921T>G p.N307K Substitution - Missense 23:133027300-133027300 - TCGA-B5-A11E-01 COSM1115357 c.1375G>T p.E459* Substitution - Nonsense 23:133026846-133026846 - TCGA-AF-3911-01 COSM1465695 c.1461delT p.F487fs*40 Deletion - Frameshift 23:133026760-133026760 - TCGA-GN-A262-06 COSM1664912 c.1249C>T p.P417S Substitution - Missense 23:133026972-133026972 - TCGA-GN-A266-06 COSM3558016 c.2355G>A p.R785R Substitution - coding silent 23:133025866-133025866 - TCGA-EE-A3AA-06 COSM3558014 c.2459G>A p.G820E Substitution - Missense 23:133025762-133025762 - T207 COSM4739738 c.507C>A p.C169* Substitution - Nonsense 23:133027714-133027714 - TCGA-F4-6806-01 COSM40905 c.1461_1462insT p.G488fs*6 Insertion - Frameshift 23:133026759-133026760 - ccRCC-26 COSM1664913 c.1030C>T p.R344W Substitution - Missense 23:133027191-133027191 - PD18259a COSM5800533 c.1508C>T p.T503I Substitution - Missense 23:133026713-133026713 - TCGA-EE-A2GD-06 COSM3558015 c.2361C>T p.S787S Substitution - coding silent 23:133025860-133025860 - T3724 COSM4739737 c.1872G>A p.Q624Q Substitution - coding silent 23:133026349-133026349 - HCC2998 COSM2726510 c.632C>T p.S211L Substitution - Missense 23:133027589-133027589 - TCGA-BR-6566-01 COSM4106726 c.1548C>T p.I516I Substitution - coding silent 23:133026673-133026673 - HN_62469 COSM130112 c.2202A>C p.K734N Substitution - Missense 23:133026019-133026019 - WA57 COSM242195 c.1236delG p.E413fs*28 Deletion - Frameshift 23:133026985-133026985 - TCGA-CC-A5UE-01 COSM4934003 c.2459G>T p.G820V Substitution - Missense 23:133025762-133025762 - T2944 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - 610184AML COSM1963619 c.243G>T p.L81F Substitution - Missense 23:133027978-133027978 - BRC48 COSM5029021 c.511G>C p.E171Q Substitution - Missense 23:133027710-133027710 - BD212T COSM5501473 c.2264C>T p.A755V Substitution - Missense 23:133025957-133025957 - TCGA-EE-A2GD-06 COSM3558025 c.1729C>T p.R577* Substitution - Nonsense 23:133026492-133026492 - YUZINO COSM1715564 c.838G>A p.D280N Substitution - Missense 23:133027383-133027383 - C086 COSM5541480 c.2712G>A p.K904K Substitution - coding silent 23:133025509-133025509 - ESCC_45 COSM3843607 c.247A>T p.I83F Substitution - Missense 23:133027974-133027974 - Au8 COSM5607192 c.902G>A p.G301E Substitution - Missense 23:133027319-133027319 - ESO-021 COSM1270069 c.2535T>A p.D845E Substitution - Missense 23:133025686-133025686 - CLL120 COSM1292936 c.178G>T p.V60F Substitution - Missense 23:133028043-133028043 - TCGA-KK-A6DY-01 COSM4879287 c.2302C>A p.H768N Substitution - Missense 23:133025919-133025919 - T3021 COSM1465693 c.1836delA p.G613fs*26 Deletion - Frameshift 23:133026385-133026385 - HN_63021 COSM128449 c.921T>C p.N307N Substitution - coding silent 23:133027300-133027300 - 2492713 COSM5607192 c.902G>A p.G301E Substitution - Missense 23:133027319-133027319 - PD4109a COSM165435 c.1334C>A p.S445Y Substitution - Missense 23:133026887-133026887 - TCGA-D1-A17Q-01 COSM1115347 c.2659G>T p.E887* Substitution - Nonsense 23:133025562-133025562 - TCGA-CA-6717-01 COSM1465698 c.1240G>T p.D414Y Substitution - Missense 23:133026981-133026981 - 100912 COSM95443 c.1813G>T p.D605Y Substitution - Missense 23:133026408-133026408 - TCGA-BF-A3DM-01 COSM3558040 c.39G>A p.G13G Substitution - coding silent 23:133028182-133028182 - TCGA-D3-A51J-06 COSM3558019 c.2121T>G p.F707L Substitution - Missense 23:133026100-133026100 - 8044594 COSM3390426 c.1611G>C p.Q537H Substitution - Missense 23:133026610-133026610 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.333137 Xq26.2 300309 Hs.731246;Hs.731248;Hs.731249 Xq26.2 300309

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.L4R c.11T>G X 132162238 CM A C Missense p.N307K c.921T>G X 132161328 SCLC A C Missense p.V539G c.1616T>G X 132160633 STAD A C Synonymous p.S143S c.429T>G X 132161820 STAD A C Synonymous p.T74T c.222T>G X 132162027 STAD A - Frameshift p.F487Lfs*40 c.1461delT X 132160788 GBM A - Frameshift p.F487Lfs*40 c.1461delT X 132160788 STAD A - Frameshift p.F487Lfs*40 c.1461delT X 132160788 THCA A G Missense p.L364P c.1091T>C X 132161158 CM A G Missense p.L559P c.1676T>C X 132160573 UCEC A G Missense p.Y660H c.1978T>C X 132160271 RCCC A G Synonymous p.N307N c.921T>C X 132161328 HNSC A T Missense p.D845E c.2535T>A X 132159714 ESCA C A Missense p.D424Y c.1270G>T X 132160979 LUAD C A Missense p.D90Y c.268G>T X 132161981 UCEC C A Missense p.G764V c.2291G>T X 132159958 LUAD C A Missense p.M306I c.918G>T X 132161331 UCEC C A Missense p.Q176H c.528G>T X 132161721 RCCC C A Missense p.R32I c.95G>T X 132162154 BLCA C A Missense p.R51L c.152G>T X 132162097 LUSC C A Missense p.V39L c.115G>T X 132162134 LUAD C A Missense p.V60F c.178G>T X 132162071 CLL C A Missense p.V906L c.2716G>T X 132159533 HNSC C A Nonsense p.E637* c.1909G>T X 132160340 UCEC CC TT Missense p.G170K c.508_509delinsAA X 132161740 CM C G IntronicSNV . c.1-31594G>C X 132193842 CLL C G Missense p.E171Q c.511G>C X 132161738 BRCA C G Missense p.E202Q c.604G>C X 132161645 CM C G Missense p.E24Q c.70G>C X 132162179 HNSC C G Missense p.G115A c.344G>C X 132161905 MM C G Missense p.R212S c.636G>C X 132161613 SCLC C G Missense p.S150T c.449G>C X 132161800 CM C T 3-UTRSNV . c.2739+98G>A X 132159412 CM C T 5-UTRSNV . c.1-60G>A X 132162308 CM C T Missense p.A422T c.1264G>A X 132160985 BLCA C T Missense p.C294Y c.881G>A X 132161368 STAD C T Missense p.E226K c.676G>A X 132161573 CM C T Missense p.E662K c.1984G>A X 132160265 CM C T Missense p.G149E c.446G>A X 132161803 CM C T Missense p.G820E c.2459G>A X 132159790 CM C T Missense p.G85E c.254G>A X 132161995 CM C T Missense p.R182K c.545G>A X 132161704 CM C T Missense p.R7H c.20G>A X 132162229 UCEC C T Synonymous p.E850E c.2550G>A X 132159699 CM C T Synonymous p.G13G c.39G>A X 132162210 CM C T Synonymous p.G151G c.453G>A X 132161796 CM C T Synonymous p.K179K c.537G>A X 132161712 BLCA C T Synonymous p.K357K c.1071G>A X 132161178 LUSC C T Synonymous p.K762K c.2286G>A X 132159963 CM C T Synonymous p.L460L c.1380G>A X 132160869 CM G A Missense p.L468F c.1402C>T X 132160847 CM G A Missense p.P247S c.739C>T X 132161510 CM G A Missense p.P329L c.986C>T X 132161263 CM G A Missense p.P334S c.1000C>T X 132161249 CM G A Missense p.P417S c.1249C>T X 132161000 CM G A Missense p.P560S c.1678C>T X 132160571 CM G A Missense p.P696S c.2086C>T X 132160163 CM G A Missense p.R344W c.1030C>T X 132161219 GBM G A Missense p.S131L c.392C>T X 132161857 CM G A Missense p.S211L c.632C>T X 132161617 CM G A Missense p.S587L c.1760C>T X 132160489 CM G A Missense p.S633F c.1898C>T X 132160351 CM G A Missense p.S665L c.1994C>T X 132160255 CM G A Missense p.S787F c.2360C>T X 132159889 CM G A Nonsense p.Q866* c.2596C>T X 132159653 CM G A Nonsense p.R577* c.1729C>T X 132160520 CM G A Synonymous p.F732F c.2196C>T X 132160053 CM G A Synonymous p.I240I c.720C>T X 132161529 CM G A Synonymous p.N381N c.1143C>T X 132161106 RCCC G A Synonymous p.P693P c.2079C>T X 132160170 CM G A Synonymous p.S787S c.2361C>T X 132159888 CM G A Synonymous p.S87S c.261C>T X 132161988 CM G C Missense p.F648L c.1944C>G X 132160305 LUSC G C Missense p.F732L c.2196C>G X 132160053 RCCC G C Missense p.H384D c.1150C>G X 132161099 HNSC G C Missense p.Q270E c.808C>G X 132161441 LUAD G C Missense p.Q311E c.931C>G X 132161318 STAD G C Missense p.S640C c.1919C>G X 132160330 OV G C Nonsense p.S173* c.518C>G X 132161731 LUAD G T Missense p.H768N c.2302C>A X 132159947 PRAD G T Missense p.P317Q c.950C>A X 132161299 ESCA G T Missense p.P317Q c.950C>A X 132161299 LUSC G T Missense p.P334H c.1001C>A X 132161248 HNSC G T Missense p.S445Y c.1334C>A X 132160915 BRCA G T Missense p.T717N c.2150C>A X 132160099 LUAD G T Nonsense p.C432* c.1296C>A X 132160953 LUAD G T Synonymous p.L684L c.2052C>A X 132160197 BRCA T A Missense p.K261N c.783A>T X 132161466 SCLC T A Missense p.T49S c.145A>T X 132162104 CM T C Missense p.I649V c.1945A>G X 132160304 BRCA T C Missense p.Y203C c.608A>G X 132161641 LUAD T C Missense p.Y47C c.140A>G X 132162109 COREAD - T Frameshift p.G488Wfs*6 c.1461dupT X 132160789 GBM - T Frameshift p.G613Rfs*6 c.1836dupA X 132160414 STAD T G Missense p.K734N c.2202A>C X 132160047 HNSC T G Missense p.T739P c.2215A>C X 132160034 CM