Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 10 102265847 102265847 + Missense_Mutation SNP A A C TCGA-OR-A5LK-01A-11D-A29I-10 TCGA-OR-A5LK-10A-01D-A29L-10 g.chr10:102265847A>C c.994T>G c.(994-996)Tct>Gct p.S332A BLCA 10 102248677 102248677 + Nonsense_Mutation SNP G G A TCGA-GU-AATP-01A-11D-A391-08 TCGA-GU-AATP-10A-01D-A394-08 g.chr10:102248677G>A c.3226C>T c.(3226-3228)Cag>Tag p.Q1076* BLCA 10 102249108 102249108 + Missense_Mutation SNP C C T TCGA-G2-A2EF-01A-12D-A18F-08 TCGA-G2-A2EF-10A-01D-A18F-08 g.chr10:102249108C>T c.3072G>A c.(3070-3072)atG>atA p.M1024I BLCA 10 102256137 102256137 + Missense_Mutation SNP C C T TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chr10:102256137C>T c.2188G>A c.(2188-2190)Ggt>Agt p.G730S BLCA 10 102256971 102256971 + Missense_Mutation SNP T T C TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr10:102256971T>C c.2057A>G c.(2056-2058)tAt>tGt p.Y686C BLCA 10 102257038 102257038 + Splice_Site SNP C C T TCGA-G2-AA3C-01A-21D-A391-08 TCGA-G2-AA3C-10A-01D-A394-08 g.chr10:102257038C>T c.e17-1 BLCA 10 102262099 102262099 + Missense_Mutation SNP A A G TCGA-FD-A3SL-01A-21D-A22Z-08 TCGA-FD-A3SL-10A-01D-A22Z-08 g.chr10:102262099A>G c.1322T>C c.(1321-1323)tTg>tCg p.L441S BLCA 10 102265222 102265222 + Missense_Mutation SNP G G C TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr10:102265222G>C c.1075C>G c.(1075-1077)Ctc>Gtc p.L359V BLCA 10 102265906 102265906 + Missense_Mutation SNP C C A TCGA-BT-A20X-01A-11D-A16O-08 TCGA-BT-A20X-11A-12D-A16O-08 g.chr10:102265906C>A c.935G>T c.(934-936)tGc>tTc p.C312F BLCA 10 102265919 102265919 + Missense_Mutation SNP C C G TCGA-CF-A1HS-01A-11D-A13W-08 TCGA-CF-A1HS-10A-01D-A13W-08 g.chr10:102265919C>G c.922G>C c.(922-924)Gat>Cat p.D308H BLCA 10 102266078 102266078 + Splice_Site SNP C C G TCGA-FD-A6TH-01A-11D-A32B-08 TCGA-FD-A6TH-10A-01D-A329-08 g.chr10:102266078C>G c.882G>C c.(880-882)gaG>gaC p.E294D BLCA 10 102267742 102267742 + Missense_Mutation SNP G G C TCGA-DK-A3IN-01A-11D-A20D-08 TCGA-DK-A3IN-10A-01D-A20D-08 g.chr10:102267742G>C c.562C>G c.(562-564)Cac>Gac p.H188D BLCA 10 102269090 102269090 + Missense_Mutation SNP C C G TCGA-ZF-A9RG-01A-21D-A42E-08 TCGA-ZF-A9RG-10A-01D-A42H-08 g.chr10:102269090C>G c.382G>C c.(382-384)Gac>Cac p.D128H BRCA 10 102247412 102247412 + Silent SNP C C T TCGA-AO-A0J5-01A-11W-A050-09 TCGA-AO-A0J5-10A-01W-A055-09 g.chr10:102247412C>T c.3501G>A c.(3499-3501)ctG>ctA p.L1167L BRCA 10 102250466 102250466 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr10:102250466G>A c.2647C>T c.(2647-2649)Cct>Tct p.P883S BRCA 10 102250551 102250551 + Missense_Mutation SNP C C A TCGA-A8-A09C-01A-11W-A019-09 TCGA-A8-A09C-10A-01W-A021-09 g.chr10:102250551C>A c.2562G>T c.(2560-2562)caG>caT p.Q854H BRCA 10 102255183 102255183 + Missense_Mutation SNP C C G TCGA-AO-A12D-01A-11D-A10Y-09 TCGA-AO-A12D-10A-01D-A110-09 g.chr10:102255183C>G c.2431G>C c.(2431-2433)Gag>Cag p.E811Q BRCA 10 102258465 102258465 + Missense_Mutation SNP T T C TCGA-A8-A09C-01A-11W-A019-09 TCGA-A8-A09C-10A-01W-A021-09 g.chr10:102258465T>C c.1681A>G c.(1681-1683)Aaa>Gaa p.K561E BRCA 10 102265865 102265865 + Missense_Mutation SNP C C A TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr10:102265865C>A c.976G>T c.(976-978)Ggc>Tgc p.G326C BRCA 10 102266117 102266117 + Silent SNP C C T TCGA-BH-A1EY-01A-11D-A13L-09 TCGA-BH-A1EY-11B-21D-A188-09 g.chr10:102266117C>T c.843G>A c.(841-843)aaG>aaA p.K281K BRCA 10 102267700 102267700 + Nonsense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr10:102267700C>A c.604G>T c.(604-606)Gaa>Taa p.E202* CESC 10 102247514 102247514 + Silent SNP G G T TCGA-JW-A69B-01A-11D-A32I-09 TCGA-JW-A69B-10A-01D-A32I-09 g.chr10:102247514G>T c.3399C>A c.(3397-3399)gcC>gcA p.A1133A CESC 10 102247537 102247537 + Missense_Mutation SNP C C T TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr10:102247537C>T c.3376G>A c.(3376-3378)Gtg>Atg p.V1126M COAD 10 102247408 102247408 + Missense_Mutation SNP C C A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr10:102247408C>A c.3505G>T c.(3505-3507)Gct>Tct p.A1169S COAD 10 102247788 102247788 + Missense_Mutation SNP C C A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr10:102247788C>A c.3356G>T c.(3355-3357)gGg>gTg p.G1119V COAD 10 102256018 102256018 + Silent SNP A A C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:102256018A>C c.2307T>G c.(2305-2307)gcT>gcG p.A769A COAD 10 102256971 102256971 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr10:102256971T>C c.2057A>G c.(2056-2058)tAt>tGt p.Y686C COAD 10 102258466 102258466 + Silent SNP T T A TCGA-D5-6924-01A-11D-1924-10 TCGA-D5-6924-10A-01D-1924-10 g.chr10:102258466T>A c.1680A>T c.(1678-1680)acA>acT p.T560T COAD 10 102258917 102258917 + Splice_Site SNP C C G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:102258917C>G c.1584G>C c.(1582-1584)caG>caC p.Q528H COAD 10 102265243 102265243 + Missense_Mutation SNP A A G TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr10:102265243A>G c.1054T>C c.(1054-1056)Tcc>Ccc p.S352P COAD 10 102265847 102265847 + Missense_Mutation SNP A A C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:102265847A>C c.994T>G c.(994-996)Tct>Gct p.S332A COAD 10 102265865 102265865 + Missense_Mutation SNP C C T TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr10:102265865C>T c.976G>A c.(976-978)Ggc>Agc p.G326S COAD 10 102267231 102267231 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr10:102267231C>T c.733G>A c.(733-735)Gac>Aac p.D245N COADREAD 10 102247408 102247408 + Missense_Mutation SNP C C A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr10:102247408C>A c.3505G>T c.(3505-3507)Gct>Tct p.A1169S COADREAD 10 102247788 102247788 + Missense_Mutation SNP C C A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr10:102247788C>A c.3356G>T c.(3355-3357)gGg>gTg p.G1119V COADREAD 10 102256018 102256018 + Silent SNP A A C TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:102256018A>C c.2307T>G c.(2305-2307)gcT>gcG p.A769A COADREAD 10 102256971 102256971 + Missense_Mutation SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr10:102256971T>C c.2057A>G c.(2056-2058)tAt>tGt p.Y686C COADREAD 10 102258466 102258466 + Silent SNP T T A TCGA-D5-6924-01A-11D-1924-10 TCGA-D5-6924-10A-01D-1924-10 g.chr10:102258466T>A c.1680A>T c.(1678-1680)acA>acT p.T560T COADREAD 10 102258917 102258917 + Splice_Site SNP C C G TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:102258917C>G c.1584G>C c.(1582-1584)caG>caC p.Q528H COADREAD 10 102262142 102262142 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:102262142C>A c.1279G>T c.(1279-1281)Gaa>Taa p.E427* COADREAD 10 102265243 102265243 + Missense_Mutation SNP A A G TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr10:102265243A>G c.1054T>C c.(1054-1056)Tcc>Ccc p.S352P COADREAD 10 102265847 102265847 + Missense_Mutation SNP A A C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:102265847A>C c.994T>G c.(994-996)Tct>Gct p.S332A COADREAD 10 102265865 102265865 + Missense_Mutation SNP C C T TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr10:102265865C>T c.976G>A c.(976-978)Ggc>Agc p.G326S COADREAD 10 102267231 102267231 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr10:102267231C>T c.733G>A c.(733-735)Gac>Aac p.D245N COADREAD 10 102269148 102269148 + Silent SNP C C T TCGA-AG-3609-01A-02W-0833-10 TCGA-AG-3609-10A-01W-0833-10 g.chr10:102269148C>T c.324G>A c.(322-324)tcG>tcA p.S108S DLBC 10 102262227 102262227 + Silent SNP C C G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr10:102262227C>G c.1194G>C c.(1192-1194)ctG>ctC p.L398L ESCA 10 102248621 102248621 + Silent SNP A A G TCGA-2H-A9GI-01A-11D-A37C-09 TCGA-2H-A9GI-11A-11D-A37F-09 g.chr10:102248621A>G c.3282T>C c.(3280-3282)acT>acC p.T1094T ESCA 10 102249885 102249885 + Missense_Mutation SNP G G A TCGA-L5-A8NV-01A-11D-A37C-09 TCGA-L5-A8NV-11A-11D-A37F-09 g.chr10:102249885G>A c.2845C>T c.(2845-2847)Cgc>Tgc p.R949C ESCA 10 102250010 102250010 + Missense_Mutation SNP G G A TCGA-2H-A9GO-01A-11D-A37C-09 TCGA-2H-A9GO-11A-11D-A37F-09 g.chr10:102250010G>A c.2720C>T c.(2719-2721)aCa>aTa p.T907I ESCA 10 102255158 102255158 + Missense_Mutation SNP G G T TCGA-L5-A4OT-01A-11D-A28B-09 TCGA-L5-A4OT-11A-11D-A28E-09 g.chr10:102255158G>T c.2456C>A c.(2455-2457)tCc>tAc p.S819Y ESCA 10 102256019 102256019 + Missense_Mutation SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr10:102256019G>A c.2306C>T c.(2305-2307)gCt>gTt p.A769V GBMLGG 10 102258994 102258994 + Missense_Mutation SNP C C G TCGA-E1-A7YS-01A-11D-A34A-08 TCGA-E1-A7YS-10A-01D-A34A-08 g.chr10:102258994C>G c.1507G>C c.(1507-1509)Gac>Cac p.D503H GBMLGG 10 102265250 102265250 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:102265250G>T c.1047C>A c.(1045-1047)atC>atA p.I349I HNSC 10 102247522 102247522 + Missense_Mutation SNP C C T TCGA-CN-6022-01A-21D-1683-08 TCGA-CN-6022-10A-01D-1683-08 g.chr10:102247522C>T c.3391G>A c.(3391-3393)Gag>Aag p.E1131K HNSC 10 102247816 102247816 + Nonsense_Mutation SNP C C A TCGA-CV-7253-01A-11D-2012-08 TCGA-CV-7253-10A-01D-2013-08 g.chr10:102247816C>A c.3328G>T c.(3328-3330)Gag>Tag p.E1110* HNSC 10 102249138 102249138 + Missense_Mutation SNP C C T TCGA-CV-7089-01A-11D-2012-08 TCGA-CV-7089-10A-01D-2013-08 g.chr10:102249138C>T c.3042G>A c.(3040-3042)atG>atA p.M1014I HNSC 10 102249149 102249149 + Missense_Mutation SNP C C T TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr10:102249149C>T c.3031G>A c.(3031-3033)Gag>Aag p.E1011K HNSC 10 102249490 102249490 + Silent SNP T T A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr10:102249490T>A c.2994A>T c.(2992-2994)ccA>ccT p.P998P HNSC 10 102256959 102256959 + Missense_Mutation SNP C C A TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr10:102256959C>A c.2069G>T c.(2068-2070)gGg>gTg p.G690V HNSC 10 102267289 102267289 + Silent SNP T T A TCGA-CV-7254-01A-11D-2012-08 TCGA-CV-7254-10A-01D-2013-08 g.chr10:102267289T>A c.675A>T c.(673-675)atA>atT p.I225I KIPAN 10 102249094 102249094 + Missense_Mutation SNP T T A TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr10:102249094T>A c.3086A>T c.(3085-3087)gAg>gTg p.E1029V KIPAN 10 102255181 102255181 + Missense_Mutation SNP C C G TCGA-B9-4117-01A-01D-1252-08 TCGA-B9-4117-10A-01D-1252-08 g.chr10:102255181C>G c.2433G>C c.(2431-2433)gaG>gaC p.E811D KIPAN 10 102265129 102265129 + Missense_Mutation SNP C C A TCGA-2Z-A9JL-01A-11D-A42J-10 TCGA-2Z-A9JL-10A-01D-A42M-10 g.chr10:102265129C>A c.1168G>T c.(1168-1170)Gtt>Ttt p.V390F KIRC 10 102249094 102249094 + Missense_Mutation SNP T T A TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr10:102249094T>A c.3086A>T c.(3085-3087)gAg>gTg p.E1029V KIRP 10 102255181 102255181 + Missense_Mutation SNP C C G TCGA-B9-4117-01A-01D-1252-08 TCGA-B9-4117-10A-01D-1252-08 g.chr10:102255181C>G c.2433G>C c.(2431-2433)gaG>gaC p.E811D KIRP 10 102265129 102265129 + Missense_Mutation SNP C C A TCGA-2Z-A9JL-01A-11D-A42J-10 TCGA-2Z-A9JL-10A-01D-A42M-10 g.chr10:102265129C>A c.1168G>T c.(1168-1170)Gtt>Ttt p.V390F LGG 10 102258994 102258994 + Missense_Mutation SNP C C G TCGA-E1-A7YS-01A-11D-A34A-08 TCGA-E1-A7YS-10A-01D-A34A-08 g.chr10:102258994C>G c.1507G>C c.(1507-1509)Gac>Cac p.D503H LGG 10 102265250 102265250 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:102265250G>T c.1047C>A c.(1045-1047)atC>atA p.I349I LIHC 10 102249484 102249484 + Frame_Shift_Del DEL G G - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr10:102249484delG c.3000delC c.(2998-3000)cccfs p.P1000fs LIHC 10 102250575 102250575 + Silent SNP T T A TCGA-DD-AACT-01A-11D-A40R-10 TCGA-DD-AACT-10A-01D-A40U-10 g.chr10:102250575T>A c.2538A>T c.(2536-2538)gcA>gcT p.A846A LIHC 10 102256018 102256018 + Silent SNP A A G TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chr10:102256018A>G c.2307T>C c.(2305-2307)gcT>gcC p.A769A LIHC 10 102256096 102256096 + Missense_Mutation SNP C C A TCGA-G3-AAV6-01A-21D-A36X-10 TCGA-G3-AAV6-10A-01D-A370-10 g.chr10:102256096C>A c.2229G>T c.(2227-2229)agG>agT p.R743S LIHC 10 102265220 102265221 + Frame_Shift_Ins INS - - A TCGA-DD-A4NO-01A-11D-A28X-10 TCGA-DD-A4NO-10A-01D-A28X-10 g.chr10:102265220_102265221insA c.1076_1077insT c.(1075-1077)ctcfs p.L359fs LIHC 10 102267799 102267799 + Missense_Mutation SNP C C T TCGA-CC-A7IE-01A-21D-A382-10 TCGA-CC-A7IE-10A-01D-A385-10 g.chr10:102267799C>T c.505G>A c.(505-507)Gag>Aag p.E169K LIHC 10 102269083 102269083 + Missense_Mutation SNP T T C TCGA-RC-A6M4-01A-11D-A32G-10 TCGA-RC-A6M4-10A-01D-A32G-10 g.chr10:102269083T>C c.389A>G c.(388-390)aAt>aGt p.N130S LIHC 10 102275905 102275905 + Missense_Mutation SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr10:102275905T>C c.151A>G c.(151-153)Agg>Ggg p.R51G LUAD 10 102249088 102249088 + Missense_Mutation SNP T T A TCGA-50-5933-01A-11D-1753-08 TCGA-50-5933-11A-01D-1753-08 g.chr10:102249088T>A c.3092A>T c.(3091-3093)cAa>cTa p.Q1031L LUAD 10 102249904 102249904 + Silent SNP C C G TCGA-38-4626-01A-01D-1553-08 TCGA-38-4626-11A-01D-1553-08 g.chr10:102249904C>G c.2826G>C c.(2824-2826)ctG>ctC p.L942L LUAD 10 102250470 102250470 + Silent SNP T T C TCGA-MP-A4T4-01A-11D-A25L-08 TCGA-MP-A4T4-10A-01D-A25L-08 g.chr10:102250470T>C c.2643A>G c.(2641-2643)gtA>gtG p.V881V LUAD 10 102255201 102255201 + Missense_Mutation SNP C C A TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr10:102255201C>A c.2413G>T c.(2413-2415)Gct>Tct p.A805S LUAD 10 102256062 102256062 + Missense_Mutation SNP C C A TCGA-55-6985-01A-11D-1945-08 TCGA-55-6985-11A-01D-1945-08 g.chr10:102256062C>A c.2263G>T c.(2263-2265)Ggc>Tgc p.G755C LUAD 10 102256138 102256138 + Silent SNP C C G TCGA-55-6543-01A-11D-1753-08 TCGA-55-6543-10A-01D-1753-08 g.chr10:102256138C>G c.2187G>C c.(2185-2187)cgG>cgC p.R729R LUAD 10 102256170 102256170 + Missense_Mutation SNP T T C TCGA-49-6767-01A-11D-1855-08 TCGA-49-6767-11A-01D-1855-08 g.chr10:102256170T>C c.2155A>G c.(2155-2157)Atg>Gtg p.M719V LUAD 10 102256930 102256930 + Missense_Mutation SNP C C A TCGA-55-5899-01A-11D-1625-08 TCGA-55-5899-10A-01D-1625-08 g.chr10:102256930C>A c.2098G>T c.(2098-2100)Gca>Tca p.A700S LUAD 10 102256931 102256931 + Missense_Mutation SNP C C A TCGA-55-5899-01A-11D-1625-08 TCGA-55-5899-10A-01D-1625-08 g.chr10:102256931C>A c.2097G>T c.(2095-2097)tgG>tgT p.W699C LUAD 10 102258531 102258531 + Missense_Mutation SNP C C A TCGA-86-7954-01A-11D-2184-08 TCGA-86-7954-10A-01D-2184-08 g.chr10:102258531C>A c.1615G>T c.(1615-1617)Gct>Tct p.A539S LUAD 10 102269195 102269195 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr10:102269195C>A c.277G>T c.(277-279)Gac>Tac p.D93Y LUSC 10 102256950 102256950 + Missense_Mutation SNP T T C TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr10:102256950T>C c.2078A>G c.(2077-2079)gAg>gGg p.E693G LUSC 10 102257543 102257543 + Missense_Mutation SNP G G T TCGA-34-5236-01A-21D-1817-08 TCGA-34-5236-10A-01D-1817-08 g.chr10:102257543G>T c.1871C>A c.(1870-1872)gCc>gAc p.A624D LUSC 10 102262016 102262016 + Missense_Mutation SNP G G T TCGA-18-3421-01A-01D-0983-08 TCGA-18-3421-11A-01D-0983-08 g.chr10:102262016G>T c.1405C>A c.(1405-1407)Ctg>Atg p.L469M OV 10 102255224 102255224 + Missense_Mutation SNP G G C TCGA-59-2351-01A-01W-0799-08 TCGA-59-2351-10A-01W-0800-08 g.chr10:102255224G>C c.2390C>G c.(2389-2391)cCc>cGc p.P797R PAAD 10 102265204 102265204 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:102265204G>A c.1093C>T c.(1093-1095)Cca>Tca p.P365S PAAD 10 102267770 102267770 + Silent SNP C C T TCGA-3A-A9IB-01A-21D-A397-08 TCGA-3A-A9IB-10A-01D-A39A-08 g.chr10:102267770C>T c.534G>A c.(532-534)cgG>cgA p.R178R PRAD 10 102248628 102248628 + Missense_Mutation SNP G G T TCGA-HC-7742-01A-11D-2114-08 TCGA-HC-7742-10A-01D-2115-08 g.chr10:102248628G>T c.3275C>A c.(3274-3276)tCt>tAt p.S1092Y PRAD 10 102257878 102257878 + Missense_Mutation SNP C C A TCGA-J4-A83N-01A-11D-A34U-08 TCGA-J4-A83N-10A-01D-A34X-08 g.chr10:102257878C>A c.1771G>T c.(1771-1773)Gat>Tat p.D591Y READ 10 102262142 102262142 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:102262142C>A c.1279G>T c.(1279-1281)Gaa>Taa p.E427* READ 10 102269148 102269148 + Silent SNP C C T TCGA-AG-3609-01A-02W-0833-10 TCGA-AG-3609-10A-01W-0833-10 g.chr10:102269148C>T c.324G>A c.(322-324)tcG>tcA p.S108S SARC 10 102258919 102258919 + Missense_Mutation SNP G G C TCGA-3B-A9I1-01A-11D-A38Z-09 TCGA-3B-A9I1-10A-01D-A38Z-09 g.chr10:102258919G>C c.1582C>G c.(1582-1584)Cag>Gag p.Q528E SARC 10 102275970 102275970 + Missense_Mutation SNP G G A TCGA-QQ-A8VG-01A-11D-A37C-09 TCGA-QQ-A8VG-10A-01D-A37F-09 g.chr10:102275970G>A c.86C>T c.(85-87)tCt>tTt p.S29F SKCM 10 102248687 102248687 + Silent SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr10:102248687G>A c.3216C>T c.(3214-3216)ccC>ccT p.P1072P SKCM 10 102249076 102249076 + Missense_Mutation SNP G G A TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr10:102249076G>A c.3104C>T c.(3103-3105)cCc>cTc p.P1035L SKCM 10 102249077 102249077 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:102249077G>A c.3103C>T c.(3103-3105)Ccc>Tcc p.P1035S SKCM 10 102249077 102249077 + Missense_Mutation SNP G G A TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr10:102249077G>A c.3103C>T c.(3103-3105)Ccc>Tcc p.P1035S SKCM 10 102249812 102249812 + Missense_Mutation SNP G G A TCGA-ER-A19S-06A-11D-A196-08 TCGA-ER-A19S-10A-01D-A198-08 g.chr10:102249812G>A c.2918C>T c.(2917-2919)cCa>cTa p.P973L SKCM 10 102249834 102249834 + Missense_Mutation SNP G G A TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr10:102249834G>A c.2896C>T c.(2896-2898)Ctt>Ttt p.L966F SKCM 10 102249852 102249852 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr10:102249852T>G c.2878A>C c.(2878-2880)Agc>Cgc p.S960R SKCM 10 102249868 102249868 + Silent SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr10:102249868G>A c.2862C>T c.(2860-2862)acC>acT p.T954T SKCM 10 102249886 102249886 + Silent SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr10:102249886G>A c.2844C>T c.(2842-2844)ggC>ggT p.G948G SKCM 10 102249894 102249894 + Missense_Mutation SNP C C T TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr10:102249894C>T c.2836G>A c.(2836-2838)Ggt>Agt p.G946S SKCM 10 102250017 102250017 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr10:102250017G>A c.2713C>T c.(2713-2715)Cct>Tct p.P905S SKCM 10 102250508 102250508 + Missense_Mutation SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr10:102250508G>A c.2605C>T c.(2605-2607)Ccc>Tcc p.P869S SKCM 10 102250605 102250605 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:102250605G>A c.2508C>T c.(2506-2508)acC>acT p.T836T SKCM 10 102255225 102255225 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr10:102255225G>A c.2389C>T c.(2389-2391)Ccc>Tcc p.P797S SKCM 10 102256030 102256030 + Silent SNP G G C TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr10:102256030G>C c.2295C>G c.(2293-2295)ccC>ccG p.P765P SKCM 10 102256031 102256031 + Missense_Mutation SNP G G A TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr10:102256031G>A c.2294C>T c.(2293-2295)cCc>cTc p.P765L SKCM 10 102256891 102256891 + Splice_Site SNP C C T TCGA-FR-A3YO-06A-11D-A23B-08 TCGA-FR-A3YO-10A-01D-A23B-08 g.chr10:102256891C>T c.e17+1 SKCM 10 102257436 102257436 + Missense_Mutation SNP G G A TCGA-EE-A29R-06A-11D-A197-08 TCGA-EE-A29R-10A-01D-A199-08 g.chr10:102257436G>A c.1978C>T c.(1978-1980)Ccc>Tcc p.P660S SKCM 10 102257790 102257790 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr10:102257790G>A c.1859C>T c.(1858-1860)tCc>tTc p.S620F SKCM 10 102257867 102257867 + Silent SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr10:102257867G>A c.1782C>T c.(1780-1782)atC>atT p.I594I SKCM 10 102262131 102262131 + Silent SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr10:102262131G>A c.1290C>T c.(1288-1290)ttC>ttT p.F430F SKCM 10 102262191 102262191 + Silent SNP C C T TCGA-EE-A2MU-06A-21D-A196-08 TCGA-EE-A2MU-10A-01D-A198-08 g.chr10:102262191C>T c.1230G>A c.(1228-1230)ctG>ctA p.L410L SKCM 10 102265162 102265162 + Nonsense_Mutation SNP T T A TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr10:102265162T>A c.1135A>T c.(1135-1137)Aaa>Taa p.K379* SKCM 10 102266174 102266174 + Silent SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr10:102266174C>T c.786G>A c.(784-786)ggG>ggA p.G262G SKCM 10 102267248 102267248 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr10:102267248G>A c.716C>T c.(715-717)cCc>cTc p.P239L SKCM 10 102269264 102269264 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:102269264G>A c.208C>T c.(208-210)Cac>Tac p.H70Y

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 10 102249108 102249108 single base substitution C T 3_prime_UTR_variant BLCA-US 10 102249108 102249108 single base substitution C T exon_variant BLCA-US 10 102249108 102249108 single base substitution C T intron_variant BLCA-US 10 102249108 102249108 single base substitution C T missense_variant M1024I 3072G>A BLCA-US 10 102256971 102256971 single base substitution T C 3_prime_UTR_variant BLCA-US 10 102256971 102256971 single base substitution T C downstream_gene_variant BLCA-US 10 102256971 102256971 single base substitution T C exon_variant BLCA-US 10 102256971 102256971 single base substitution T C intron_variant BLCA-US 10 102256971 102256971 single base substitution T C missense_variant Y686C 2057A>G BLCA-US 10 102262099 102262099 single base substitution A G 3_prime_UTR_variant BLCA-US 10 102262099 102262099 single base substitution A G downstream_gene_variant BLCA-US 10 102262099 102262099 single base substitution A G exon_variant BLCA-US 10 102262099 102262099 single base substitution A G missense_variant L441S 1322T>C BLCA-US 10 102262099 102262099 single base substitution A G upstream_gene_variant BLCA-US 10 102265919 102265919 single base substitution C G 3_prime_UTR_variant BLCA-US 10 102265919 102265919 single base substitution C G downstream_gene_variant BLCA-US 10 102265919 102265919 single base substitution C G exon_variant BLCA-US 10 102265919 102265919 single base substitution C G missense_variant D151H 451G>C BLCA-US 10 102265919 102265919 single base substitution C G missense_variant D308H 922G>C BLCA-US 10 102265919 102265919 single base substitution C G missense_variant D311H 931G>C BLCA-US 10 102267742 102267742 single base substitution G C 3_prime_UTR_variant BLCA-US 10 102267742 102267742 single base substitution G C exon_variant BLCA-US 10 102267742 102267742 single base substitution G C missense_variant H188D 562C>G BLCA-US 10 102267742 102267742 single base substitution G C missense_variant H191D 571C>G BLCA-US 10 102267742 102267742 single base substitution G C missense_variant H31D 91C>G BLCA-US 10 102267742 102267742 single base substitution G C upstream_gene_variant BOCA-FR 10 102264749 102264749 single base substitution C T downstream_gene_variant BOCA-FR 10 102264749 102264749 single base substitution C T intron_variant BOCA-FR 10 102283577 102283577 single base substitution A G intron_variant BOCA-FR 10 102283577 102283577 single base substitution A G upstream_gene_variant BRCA-EU 10 102241655 102241655 single base substitution C G downstream_gene_variant BRCA-EU 10 102244139 102244139 single base substitution C T downstream_gene_variant BRCA-EU 10 102245120 102245120 single base substitution C G downstream_gene_variant BRCA-EU 10 102247839 102247839 single base substitution A G 3_prime_UTR_variant BRCA-EU 10 102247839 102247839 single base substitution A G exon_variant BRCA-EU 10 102247839 102247839 single base substitution A G missense_variant L1102P 3305T>C BRCA-EU 10 102247886 102247886 single base substitution G A intron_variant BRCA-EU 10 102248573 102248573 single base substitution G T intron_variant BRCA-EU 10 102252680 102252680 single base substitution C T downstream_gene_variant BRCA-EU 10 102252680 102252680 single base substitution C T intron_variant BRCA-EU 10 102252680 102252680 single base substitution C T upstream_gene_variant BRCA-EU 10 102252738 102252738 single base substitution C T downstream_gene_variant BRCA-EU 10 102252738 102252738 single base substitution C T intron_variant BRCA-EU 10 102252738 102252738 single base substitution C T upstream_gene_variant BRCA-EU 10 102253976 102253976 single base substitution C G downstream_gene_variant BRCA-EU 10 102253976 102253976 single base substitution C G intron_variant BRCA-EU 10 102253976 102253976 single base substitution C G upstream_gene_variant BRCA-EU 10 102255756 102255756 single base substitution G A downstream_gene_variant BRCA-EU 10 102255756 102255756 single base substitution G A intron_variant BRCA-EU 10 102256265 102256265 single base substitution G C downstream_gene_variant BRCA-EU 10 102256265 102256265 single base substitution G C intron_variant BRCA-EU 10 102261303 102261303 single base substitution C G downstream_gene_variant BRCA-EU 10 102261303 102261303 single base substitution C G intron_variant BRCA-EU 10 102261303 102261303 single base substitution C G upstream_gene_variant BRCA-EU 10 102264337 102264337 single base substitution G C downstream_gene_variant BRCA-EU 10 102264337 102264337 single base substitution G C intron_variant BRCA-EU 10 102264895 102264895 single base substitution G C downstream_gene_variant BRCA-EU 10 102264895 102264895 single base substitution G C intron_variant BRCA-EU 10 102265159 102265159 single base substitution G T 3_prime_UTR_variant BRCA-EU 10 102265159 102265159 single base substitution G T downstream_gene_variant BRCA-EU 10 102265159 102265159 single base substitution G T exon_variant BRCA-EU 10 102265159 102265159 single base substitution G T missense_variant P380T 1138C>A BRCA-EU 10 102266421 102266421 single base substitution C G intron_variant BRCA-EU 10 102266421 102266421 single base substitution C G upstream_gene_variant BRCA-EU 10 102266851 102266851 single base substitution G A intron_variant BRCA-EU 10 102266851 102266851 single base substitution G A upstream_gene_variant BRCA-EU 10 102267230 102267230 single base substitution T A 3_prime_UTR_variant BRCA-EU 10 102267230 102267230 single base substitution T A exon_variant BRCA-EU 10 102267230 102267230 single base substitution T A intron_variant BRCA-EU 10 102267230 102267230 single base substitution T A missense_variant D245V 734A>T BRCA-EU 10 102267230 102267230 single base substitution T A missense_variant D248V 743A>T BRCA-EU 10 102267230 102267230 single base substitution T A missense_variant D88V 263A>T BRCA-EU 10 102267230 102267230 single base substitution T A upstream_gene_variant BRCA-EU 10 102267256 102267256 single base substitution A T 3_prime_UTR_variant BRCA-EU 10 102267256 102267256 single base substitution A T exon_variant BRCA-EU 10 102267256 102267256 single base substitution A T intron_variant BRCA-EU 10 102267256 102267256 single base substitution A T missense_variant D236E 708T>A BRCA-EU 10 102267256 102267256 single base substitution A T missense_variant D239E 717T>A BRCA-EU 10 102267256 102267256 single base substitution A T missense_variant D79E 237T>A BRCA-EU 10 102267256 102267256 single base substitution A T upstream_gene_variant BRCA-EU 10 102268740 102268740 single base substitution T C intron_variant BRCA-EU 10 102268740 102268740 single base substitution T C upstream_gene_variant BRCA-EU 10 102273235 102273235 deletion of <=200bp T - intron_variant BRCA-EU 10 102273235 102273235 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 102274158 102274158 single base substitution T A intron_variant BRCA-EU 10 102274639 102274639 single base substitution G A intron_variant BRCA-EU 10 102275050 102275050 single base substitution A T intron_variant BRCA-EU 10 102276249 102276249 deletion of <=200bp A - intron_variant BRCA-EU 10 102276751 102276751 single base substitution C T 5_prime_UTR_variant BRCA-EU 10 102276751 102276751 single base substitution C T intron_variant BRCA-EU 10 102279691 102279691 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 10 102279691 102279691 single base substitution G A intron_variant BRCA-EU 10 102279691 102279691 single base substitution G A upstream_gene_variant BRCA-EU 10 102282236 102282236 single base substitution G A intron_variant BRCA-EU 10 102282236 102282236 single base substitution G A upstream_gene_variant BRCA-EU 10 102282528 102282528 single base substitution C T intron_variant BRCA-EU 10 102282528 102282528 single base substitution C T upstream_gene_variant BRCA-EU 10 102282564 102282564 deletion of <=200bp T - intron_variant BRCA-EU 10 102282564 102282564 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 102283056 102283056 insertion of <=200bp - T intron_variant BRCA-EU 10 102283056 102283056 insertion of <=200bp - T upstream_gene_variant BRCA-EU 10 102283616 102283616 single base substitution C T intron_variant BRCA-EU 10 102283616 102283616 single base substitution C T upstream_gene_variant BRCA-EU 10 102284020 102284038 deletion of <=200bp AATGAGACGATGCATCCAT - intron_variant BRCA-EU 10 102284020 102284038 deletion of <=200bp AATGAGACGATGCATCCAT - upstream_gene_variant BRCA-EU 10 102286565 102286565 single base substitution C T intron_variant BRCA-EU 10 102287455 102287455 single base substitution G T intron_variant BRCA-EU 10 102288978 102288978 single base substitution C A intron_variant BRCA-EU 10 102289588 102289588 single base substitution C A 5_prime_UTR_variant BRCA-EU 10 102289797 102289797 single base substitution G A upstream_gene_variant BRCA-EU 10 102290921 102290921 single base substitution G C upstream_gene_variant BRCA-EU 10 102293204 102293204 single base substitution C T upstream_gene_variant BRCA-FR 10 102244139 102244139 single base substitution C T downstream_gene_variant BRCA-FR 10 102245120 102245120 single base substitution C G downstream_gene_variant BRCA-FR 10 102252738 102252738 single base substitution C T downstream_gene_variant BRCA-FR 10 102252738 102252738 single base substitution C T intron_variant BRCA-FR 10 102252738 102252738 single base substitution C T upstream_gene_variant BRCA-FR 10 102268546 102268546 single base substitution C T exon_variant BRCA-FR 10 102268546 102268546 single base substitution C T intron_variant BRCA-FR 10 102268546 102268546 single base substitution C T upstream_gene_variant BRCA-FR 10 102274158 102274158 single base substitution T A intron_variant BRCA-FR 10 102274639 102274639 single base substitution G A intron_variant BRCA-FR 10 102275999 102275999 single base substitution T C intron_variant BRCA-FR 10 102289588 102289588 single base substitution C A 5_prime_UTR_variant BRCA-FR 10 102292343 102292343 single base substitution A G upstream_gene_variant BRCA-UK 10 102265951 102265951 single base substitution T A 3_prime_UTR_variant BRCA-UK 10 102265951 102265951 single base substitution T A downstream_gene_variant BRCA-UK 10 102265951 102265951 single base substitution T A exon_variant BRCA-UK 10 102265951 102265951 single base substitution T A missense_variant Y140F 419A>T BRCA-UK 10 102265951 102265951 single base substitution T A missense_variant Y297F 890A>T BRCA-UK 10 102265951 102265951 single base substitution T A missense_variant Y300F 899A>T BRCA-US 10 102242188 102242188 single base substitution C G downstream_gene_variant BRCA-US 10 102247412 102247412 single base substitution C T 3_prime_UTR_variant BRCA-US 10 102247412 102247412 single base substitution C T exon_variant BRCA-US 10 102247412 102247412 single base substitution C T synonymous_variant L1167L 3501G>A BRCA-US 10 102250466 102250466 single base substitution G A 3_prime_UTR_variant BRCA-US 10 102250466 102250466 single base substitution G A downstream_gene_variant BRCA-US 10 102250466 102250466 single base substitution G A missense_variant P883S 2647C>T BRCA-US 10 102250466 102250466 single base substitution G A upstream_gene_variant BRCA-US 10 102250551 102250551 single base substitution C A 3_prime_UTR_variant BRCA-US 10 102250551 102250551 single base substitution C A downstream_gene_variant BRCA-US 10 102250551 102250551 single base substitution C A missense_variant Q854H 2562G>T BRCA-US 10 102250551 102250551 single base substitution C A upstream_gene_variant BRCA-US 10 102255183 102255183 single base substitution C G 3_prime_UTR_variant BRCA-US 10 102255183 102255183 single base substitution C G downstream_gene_variant BRCA-US 10 102255183 102255183 single base substitution C G exon_variant BRCA-US 10 102255183 102255183 single base substitution C G missense_variant E811Q 2431G>C BRCA-US 10 102255183 102255183 single base substitution C G upstream_gene_variant BRCA-US 10 102258465 102258465 single base substitution T C 3_prime_UTR_variant BRCA-US 10 102258465 102258465 single base substitution T C downstream_gene_variant BRCA-US 10 102258465 102258465 single base substitution T C exon_variant BRCA-US 10 102258465 102258465 single base substitution T C intron_variant BRCA-US 10 102258465 102258465 single base substitution T C missense_variant K561E 1681A>G BRCA-US 10 102258465 102258465 single base substitution T C upstream_gene_variant BRCA-US 10 102265865 102265865 single base substitution C A 3_prime_UTR_variant BRCA-US 10 102265865 102265865 single base substitution C A downstream_gene_variant BRCA-US 10 102265865 102265865 single base substitution C A exon_variant BRCA-US 10 102265865 102265865 single base substitution C A missense_variant G169C 505G>T BRCA-US 10 102265865 102265865 single base substitution C A missense_variant G326C 976G>T BRCA-US 10 102265865 102265865 single base substitution C A missense_variant G329C 985G>T BRCA-US 10 102266117 102266117 single base substitution C T 3_prime_UTR_variant BRCA-US 10 102266117 102266117 single base substitution C T exon_variant BRCA-US 10 102266117 102266117 single base substitution C T synonymous_variant K124K 372G>A BRCA-US 10 102266117 102266117 single base substitution C T synonymous_variant K281K 843G>A BRCA-US 10 102266117 102266117 single base substitution C T synonymous_variant K284K 852G>A BRCA-US 10 102267700 102267700 single base substitution C A 3_prime_UTR_variant BRCA-US 10 102267700 102267700 single base substitution C A exon_variant BRCA-US 10 102267700 102267700 single base substitution C A stop_gained E202* 604G>T BRCA-US 10 102267700 102267700 single base substitution C A stop_gained E205* 613G>T BRCA-US 10 102267700 102267700 single base substitution C A stop_gained E45* 133G>T BRCA-US 10 102267700 102267700 single base substitution C A upstream_gene_variant BRCA-US 10 102286175 102286175 single base substitution T G intron_variant BTCA-JP 10 102248685 102248685 deletion of <=200bp G - 3_prime_UTR_variant BTCA-JP 10 102248685 102248685 deletion of <=200bp G - exon_variant BTCA-JP 10 102248685 102248685 deletion of <=200bp G - frameshift_variant P1073 BTCA-JP 10 102248821 102248821 single base substitution C T exon_variant BTCA-JP 10 102248821 102248821 single base substitution C T intron_variant BTCA-JP 10 102257346 102257346 single base substitution C T downstream_gene_variant BTCA-JP 10 102257346 102257346 single base substitution C T exon_variant BTCA-JP 10 102257346 102257346 single base substitution C T intron_variant BTCA-JP 10 102259143 102259143 single base substitution A G downstream_gene_variant BTCA-JP 10 102259143 102259143 single base substitution A G intron_variant BTCA-JP 10 102259143 102259143 single base substitution A G upstream_gene_variant BTCA-JP 10 102266074 102266074 single base substitution C A downstream_gene_variant BTCA-JP 10 102266074 102266074 single base substitution C A intron_variant BTCA-JP 10 102266074 102266074 single base substitution C A splice_region_variant BTCA-JP 10 102267307 102267307 single base substitution C A 3_prime_UTR_variant BTCA-JP 10 102267307 102267307 single base substitution C A exon_variant BTCA-JP 10 102267307 102267307 single base substitution C A intron_variant BTCA-JP 10 102267307 102267307 single base substitution C A synonymous_variant L219L 657G>T BTCA-JP 10 102267307 102267307 single base substitution C A synonymous_variant L222L 666G>T BTCA-JP 10 102267307 102267307 single base substitution C A synonymous_variant L62L 186G>T BTCA-JP 10 102267307 102267307 single base substitution C A upstream_gene_variant BTCA-JP 10 102268212 102268212 single base substitution A G intron_variant BTCA-JP 10 102268212 102268212 single base substitution A G splice_region_variant BTCA-JP 10 102268212 102268212 single base substitution A G upstream_gene_variant BTCA-JP 10 102269285 102269285 single base substitution C A intron_variant BTCA-JP 10 102269285 102269285 single base substitution C A upstream_gene_variant CESC-US 10 102241723 102241723 single base substitution C T downstream_gene_variant CESC-US 10 102242219 102242219 single base substitution C G downstream_gene_variant CESC-US 10 102247514 102247514 single base substitution G T 3_prime_UTR_variant CESC-US 10 102247514 102247514 single base substitution G T exon_variant CESC-US 10 102247514 102247514 single base substitution G T synonymous_variant A1133A 3399C>A CESC-US 10 102247537 102247537 single base substitution C T 3_prime_UTR_variant CESC-US 10 102247537 102247537 single base substitution C T exon_variant CESC-US 10 102247537 102247537 single base substitution C T missense_variant V1126M 3376G>A COAD-US 10 102242169 102242169 single base substitution G A downstream_gene_variant COAD-US 10 102242180 102242180 single base substitution G A downstream_gene_variant COAD-US 10 102247788 102247788 single base substitution C A 3_prime_UTR_variant COAD-US 10 102247788 102247788 single base substitution C A exon_variant COAD-US 10 102247788 102247788 single base substitution C A missense_variant G1119V 3356G>T COAD-US 10 102256971 102256971 single base substitution T C 3_prime_UTR_variant COAD-US 10 102256971 102256971 single base substitution T C downstream_gene_variant COAD-US 10 102256971 102256971 single base substitution T C exon_variant COAD-US 10 102256971 102256971 single base substitution T C intron_variant COAD-US 10 102256971 102256971 single base substitution T C missense_variant Y686C 2057A>G COAD-US 10 102258466 102258466 single base substitution T A 3_prime_UTR_variant COAD-US 10 102258466 102258466 single base substitution T A downstream_gene_variant COAD-US 10 102258466 102258466 single base substitution T A exon_variant COAD-US 10 102258466 102258466 single base substitution T A intron_variant COAD-US 10 102258466 102258466 single base substitution T A synonymous_variant T560T 1680A>T COAD-US 10 102258466 102258466 single base substitution T A upstream_gene_variant COAD-US 10 102265865 102265865 single base substitution C T 3_prime_UTR_variant COAD-US 10 102265865 102265865 single base substitution C T downstream_gene_variant COAD-US 10 102265865 102265865 single base substitution C T exon_variant COAD-US 10 102265865 102265865 single base substitution C T missense_variant G169S 505G>A COAD-US 10 102265865 102265865 single base substitution C T missense_variant G326S 976G>A COAD-US 10 102265865 102265865 single base substitution C T missense_variant G329S 985G>A COAD-US 10 102267231 102267231 single base substitution C T 3_prime_UTR_variant COAD-US 10 102267231 102267231 single base substitution C T exon_variant COAD-US 10 102267231 102267231 single base substitution C T intron_variant COAD-US 10 102267231 102267231 single base substitution C T missense_variant D245N 733G>A COAD-US 10 102267231 102267231 single base substitution C T missense_variant D248N 742G>A COAD-US 10 102267231 102267231 single base substitution C T missense_variant D88N 262G>A COAD-US 10 102267231 102267231 single base substitution C T upstream_gene_variant COAD-US 10 102283664 102283664 single base substitution T G intron_variant COAD-US 10 102283664 102283664 single base substitution T G upstream_gene_variant COAD-US 10 102289192 102289192 insertion of <=200bp - GGC 5_prime_UTR_variant COAD-US 10 102289578 102289578 single base substitution C T 5_prime_UTR_variant COCA-CN 10 102241902 102241902 single base substitution T G downstream_gene_variant COCA-CN 10 102241983 102241983 single base substitution C T downstream_gene_variant COCA-CN 10 102242103 102242103 single base substitution C T downstream_gene_variant COCA-CN 10 102259034 102259034 single base substitution G A downstream_gene_variant COCA-CN 10 102259034 102259034 single base substitution G A intron_variant COCA-CN 10 102259034 102259034 single base substitution G A upstream_gene_variant COCA-CN 10 102259080 102259080 single base substitution T G downstream_gene_variant COCA-CN 10 102259080 102259080 single base substitution T G intron_variant COCA-CN 10 102259080 102259080 single base substitution T G upstream_gene_variant COCA-CN 10 102259305 102259305 single base substitution G A 3_prime_UTR_variant COCA-CN 10 102259305 102259305 single base substitution G A downstream_gene_variant COCA-CN 10 102259305 102259305 single base substitution G A exon_variant COCA-CN 10 102259305 102259305 single base substitution G A synonymous_variant Y487Y 1461C>T COCA-CN 10 102259305 102259305 single base substitution G A upstream_gene_variant COCA-CN 10 102266055 102266055 single base substitution T C downstream_gene_variant COCA-CN 10 102266055 102266055 single base substitution T C intron_variant COCA-CN 10 102267162 102267162 single base substitution G A intron_variant COCA-CN 10 102267162 102267162 single base substitution G A upstream_gene_variant COCA-CN 10 102267200 102267200 single base substitution A G 3_prime_UTR_variant COCA-CN 10 102267200 102267200 single base substitution A G exon_variant COCA-CN 10 102267200 102267200 single base substitution A G intron_variant COCA-CN 10 102267200 102267200 single base substitution A G missense_variant V255A 764T>C COCA-CN 10 102267200 102267200 single base substitution A G missense_variant V258A 773T>C COCA-CN 10 102267200 102267200 single base substitution A G missense_variant V98A 293T>C COCA-CN 10 102267200 102267200 single base substitution A G upstream_gene_variant COCA-CN 10 102268323 102268323 single base substitution C G exon_variant COCA-CN 10 102268323 102268323 single base substitution C G intron_variant COCA-CN 10 102268323 102268323 single base substitution C G upstream_gene_variant COCA-CN 10 102276066 102276066 single base substitution G T intron_variant COCA-CN 10 102276872 102276872 single base substitution A C intron_variant COCA-CN 10 102276872 102276872 single base substitution A C upstream_gene_variant COCA-CN 10 102286623 102286623 single base substitution T G intron_variant EOPC-DE 10 102268166 102268166 single base substitution G A intron_variant EOPC-DE 10 102268166 102268166 single base substitution G A upstream_gene_variant ESAD-UK 10 102241578 102241578 deletion of <=200bp C - downstream_gene_variant ESAD-UK 10 102241856 102241856 single base substitution C G downstream_gene_variant ESAD-UK 10 102246041 102246041 single base substitution C T downstream_gene_variant ESAD-UK 10 102246337 102246337 single base substitution G C downstream_gene_variant ESAD-UK 10 102247645 102247645 single base substitution C T exon_variant ESAD-UK 10 102247645 102247645 single base substitution C T intron_variant ESAD-UK 10 102249429 102249429 single base substitution C T exon_variant ESAD-UK 10 102249429 102249429 single base substitution C T intron_variant ESAD-UK 10 102251234 102251234 single base substitution T G downstream_gene_variant ESAD-UK 10 102251234 102251234 single base substitution T G intron_variant ESAD-UK 10 102251234 102251234 single base substitution T G upstream_gene_variant ESAD-UK 10 102253787 102253787 deletion of <=200bp A - downstream_gene_variant ESAD-UK 10 102253787 102253787 deletion of <=200bp A - intron_variant ESAD-UK 10 102253787 102253787 deletion of <=200bp A - upstream_gene_variant ESAD-UK 10 102255761 102255761 single base substitution G T downstream_gene_variant ESAD-UK 10 102255761 102255761 single base substitution G T intron_variant ESAD-UK 10 102256088 102256088 single base substitution T A 3_prime_UTR_variant ESAD-UK 10 102256088 102256088 single base substitution T A downstream_gene_variant ESAD-UK 10 102256088 102256088 single base substitution T A exon_variant ESAD-UK 10 102256088 102256088 single base substitution T A missense_variant Q746L 2237A>T ESAD-UK 10 102256901 102256901 single base substitution C T 3_prime_UTR_variant ESAD-UK 10 102256901 102256901 single base substitution C T downstream_gene_variant ESAD-UK 10 102256901 102256901 single base substitution C T exon_variant ESAD-UK 10 102256901 102256901 single base substitution C T intron_variant ESAD-UK 10 102256901 102256901 single base substitution C T missense_variant M709I 2127G>A ESAD-UK 10 102257093 102257093 single base substitution C T downstream_gene_variant ESAD-UK 10 102257093 102257093 single base substitution C T intron_variant ESAD-UK 10 102258654 102258654 single base substitution C T downstream_gene_variant ESAD-UK 10 102258654 102258654 single base substitution C T intron_variant ESAD-UK 10 102258654 102258654 single base substitution C T upstream_gene_variant ESAD-UK 10 102258673 102258673 single base substitution A C downstream_gene_variant ESAD-UK 10 102258673 102258673 single base substitution A C intron_variant ESAD-UK 10 102258673 102258673 single base substitution A C upstream_gene_variant ESAD-UK 10 102264252 102264252 single base substitution T A downstream_gene_variant ESAD-UK 10 102264252 102264252 single base substitution T A intron_variant ESAD-UK 10 102264252 102264252 single base substitution T A upstream_gene_variant ESAD-UK 10 102264312 102264312 single base substitution G A downstream_gene_variant ESAD-UK 10 102264312 102264312 single base substitution G A intron_variant ESAD-UK 10 102264312 102264312 single base substitution G A upstream_gene_variant ESAD-UK 10 102265157 102265157 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 102265157 102265157 single base substitution G A downstream_gene_variant ESAD-UK 10 102265157 102265157 single base substitution G A exon_variant ESAD-UK 10 102265157 102265157 single base substitution G A synonymous_variant P380P 1140C>T ESAD-UK 10 102267165 102267165 single base substitution G A intron_variant ESAD-UK 10 102267165 102267165 single base substitution G A upstream_gene_variant ESAD-UK 10 102268025 102268025 single base substitution T G intron_variant ESAD-UK 10 102268025 102268025 single base substitution T G upstream_gene_variant ESAD-UK 10 102270729 102270729 single base substitution T C intron_variant ESAD-UK 10 102270729 102270729 single base substitution T C upstream_gene_variant ESAD-UK 10 102271369 102271369 single base substitution T A intron_variant ESAD-UK 10 102271369 102271369 single base substitution T A upstream_gene_variant ESAD-UK 10 102271657 102271657 single base substitution C A intron_variant ESAD-UK 10 102271657 102271657 single base substitution C A upstream_gene_variant ESAD-UK 10 102273974 102273974 single base substitution A G intron_variant ESAD-UK 10 102274997 102274997 single base substitution C T intron_variant ESAD-UK 10 102277243 102277243 single base substitution C T intron_variant ESAD-UK 10 102277243 102277243 single base substitution C T upstream_gene_variant ESAD-UK 10 102277482 102277482 single base substitution G C intron_variant ESAD-UK 10 102277482 102277482 single base substitution G C upstream_gene_variant ESAD-UK 10 102277612 102277612 single base substitution C G intron_variant ESAD-UK 10 102277612 102277612 single base substitution C G upstream_gene_variant ESAD-UK 10 102277927 102277927 single base substitution T C intron_variant ESAD-UK 10 102277927 102277927 single base substitution T C upstream_gene_variant ESAD-UK 10 102277949 102277949 single base substitution G A intron_variant ESAD-UK 10 102277949 102277949 single base substitution G A upstream_gene_variant ESAD-UK 10 102279605 102279605 single base substitution G A 5_prime_UTR_variant ESAD-UK 10 102279605 102279605 single base substitution G A intron_variant ESAD-UK 10 102279605 102279605 single base substitution G A upstream_gene_variant ESAD-UK 10 102280707 102280707 single base substitution T A intron_variant ESAD-UK 10 102280707 102280707 single base substitution T A upstream_gene_variant ESAD-UK 10 102281654 102281654 single base substitution C G intron_variant ESAD-UK 10 102281654 102281654 single base substitution C G upstream_gene_variant ESAD-UK 10 102283840 102283840 single base substitution C T intron_variant ESAD-UK 10 102283840 102283840 single base substitution C T upstream_gene_variant ESAD-UK 10 102287740 102287740 single base substitution C T intron_variant ESAD-UK 10 102289670 102289670 single base substitution G C upstream_gene_variant ESAD-UK 10 102290752 102290752 single base substitution C T upstream_gene_variant ESAD-UK 10 102292670 102292670 single base substitution G A upstream_gene_variant ESAD-UK 10 102292880 102292880 single base substitution C T upstream_gene_variant ESAD-UK 10 102293112 102293112 single base substitution A G upstream_gene_variant ESAD-UK 10 102293810 102293810 single base substitution G A upstream_gene_variant ESAD-UK 10 102293831 102293831 single base substitution G A upstream_gene_variant ESCA-CN 10 102241743 102241743 single base substitution G A downstream_gene_variant ESCA-CN 10 102248666 102248666 single base substitution C T 3_prime_UTR_variant ESCA-CN 10 102248666 102248666 single base substitution C T exon_variant ESCA-CN 10 102248666 102248666 single base substitution C T synonymous_variant K1079K 3237G>A KIRC-US 10 102249094 102249094 single base substitution T A 3_prime_UTR_variant KIRC-US 10 102249094 102249094 single base substitution T A exon_variant KIRC-US 10 102249094 102249094 single base substitution T A intron_variant KIRC-US 10 102249094 102249094 single base substitution T A missense_variant E1029V 3086A>T LAML-KR 10 102266235 102266235 single base substitution G T intron_variant LAML-KR 10 102266235 102266235 single base substitution G T upstream_gene_variant LICA-FR 10 102241787 102241787 single base substitution G T downstream_gene_variant LICA-FR 10 102242247 102242247 single base substitution C A downstream_gene_variant LICA-FR 10 102250009 102250009 single base substitution T A 3_prime_UTR_variant LICA-FR 10 102250009 102250009 single base substitution T A downstream_gene_variant LICA-FR 10 102250009 102250009 single base substitution T A exon_variant LICA-FR 10 102250009 102250009 single base substitution T A intron_variant LICA-FR 10 102250009 102250009 single base substitution T A synonymous_variant T907T 2721A>T LICA-FR 10 102250009 102250009 single base substitution T A upstream_gene_variant LICA-FR 10 102265955 102265955 single base substitution C T 3_prime_UTR_variant LICA-FR 10 102265955 102265955 single base substitution C T downstream_gene_variant LICA-FR 10 102265955 102265955 single base substitution C T exon_variant LICA-FR 10 102265955 102265955 single base substitution C T missense_variant V139I 415G>A LICA-FR 10 102265955 102265955 single base substitution C T missense_variant V296I 886G>A LICA-FR 10 102265955 102265955 single base substitution C T missense_variant V299I 895G>A LICA-FR 10 102282596 102282596 insertion of <=200bp - T intron_variant LICA-FR 10 102282596 102282596 insertion of <=200bp - T upstream_gene_variant LICA-FR 10 102288814 102288814 single base substitution G A intron_variant LIHC-US 10 102250534 102250534 single base substitution T C 3_prime_UTR_variant LIHC-US 10 102250534 102250534 single base substitution T C downstream_gene_variant LIHC-US 10 102250534 102250534 single base substitution T C missense_variant N860S 2579A>G LIHC-US 10 102250534 102250534 single base substitution T C upstream_gene_variant LIHC-US 10 102265220 102265220 insertion of <=200bp - A 3_prime_UTR_variant LIHC-US 10 102265220 102265220 insertion of <=200bp - A downstream_gene_variant LIHC-US 10 102265220 102265220 insertion of <=200bp - A exon_variant LIHC-US 10 102265220 102265220 insertion of <=200bp - A frameshift_variant L359L? LIHC-US 10 102275905 102275905 single base substitution T C 5_prime_UTR_variant LIHC-US 10 102275905 102275905 single base substitution T C exon_variant LIHC-US 10 102275905 102275905 single base substitution T C missense_variant R51G 151A>G LINC-JP 10 102242536 102242536 single base substitution G A downstream_gene_variant LINC-JP 10 102247724 102247724 single base substitution T C exon_variant LINC-JP 10 102247724 102247724 single base substitution T C intron_variant LINC-JP 10 102247875 102247875 single base substitution T A intron_variant LINC-JP 10 102262127 102262127 single base substitution T G 3_prime_UTR_variant LINC-JP 10 102262127 102262127 single base substitution T G downstream_gene_variant LINC-JP 10 102262127 102262127 single base substitution T G exon_variant LINC-JP 10 102262127 102262127 single base substitution T G missense_variant M432L 1294A>C LINC-JP 10 102262127 102262127 single base substitution T G upstream_gene_variant LINC-JP 10 102265282 102265282 single base substitution C T 3_prime_UTR_variant LINC-JP 10 102265282 102265282 single base substitution C T downstream_gene_variant LINC-JP 10 102265282 102265282 single base substitution C T exon_variant LINC-JP 10 102265282 102265282 single base substitution C T intron_variant LINC-JP 10 102274581 102274581 single base substitution C A intron_variant LINC-JP 10 102277801 102277801 single base substitution C A intron_variant LINC-JP 10 102277801 102277801 single base substitution C A upstream_gene_variant LINC-JP 10 102282564 102282564 deletion of <=200bp T - intron_variant LINC-JP 10 102282564 102282564 deletion of <=200bp T - upstream_gene_variant LINC-JP 10 102286754 102286754 single base substitution A T 5_prime_UTR_variant LINC-JP 10 102289674 102289674 single base substitution C T upstream_gene_variant LIRI-JP 10 102243322 102243322 single base substitution C T downstream_gene_variant LIRI-JP 10 102245987 102245987 deletion of <=200bp A - downstream_gene_variant LIRI-JP 10 102247426 102247426 single base substitution A G 3_prime_UTR_variant LIRI-JP 10 102247426 102247426 single base substitution A G exon_variant LIRI-JP 10 102247426 102247426 single base substitution A G missense_variant F1163L 3487T>C LIRI-JP 10 102249367 102249367 insertion of <=200bp - T exon_variant LIRI-JP 10 102249367 102249367 insertion of <=200bp - T intron_variant LIRI-JP 10 102251248 102251248 single base substitution C A downstream_gene_variant LIRI-JP 10 102251248 102251248 single base substitution C A intron_variant LIRI-JP 10 102251248 102251248 single base substitution C A upstream_gene_variant LIRI-JP 10 102251249 102251249 single base substitution C A downstream_gene_variant LIRI-JP 10 102251249 102251249 single base substitution C A intron_variant LIRI-JP 10 102251249 102251249 single base substitution C A upstream_gene_variant LIRI-JP 10 102254482 102254482 single base substitution C A downstream_gene_variant LIRI-JP 10 102254482 102254482 single base substitution C A intron_variant LIRI-JP 10 102254482 102254482 single base substitution C A upstream_gene_variant LIRI-JP 10 102256874 102256874 single base substitution C T downstream_gene_variant LIRI-JP 10 102256874 102256874 single base substitution C T intron_variant LIRI-JP 10 102259769 102259769 single base substitution T C downstream_gene_variant LIRI-JP 10 102259769 102259769 single base substitution T C intron_variant LIRI-JP 10 102259769 102259769 single base substitution T C upstream_gene_variant LIRI-JP 10 102260415 102260415 single base substitution T C downstream_gene_variant LIRI-JP 10 102260415 102260415 single base substitution T C intron_variant LIRI-JP 10 102260415 102260415 single base substitution T C upstream_gene_variant LIRI-JP 10 102261200 102261200 single base substitution T C downstream_gene_variant LIRI-JP 10 102261200 102261200 single base substitution T C intron_variant LIRI-JP 10 102261200 102261200 single base substitution T C upstream_gene_variant LIRI-JP 10 102264856 102264856 single base substitution C T downstream_gene_variant LIRI-JP 10 102264856 102264856 single base substitution C T intron_variant LIRI-JP 10 102265550 102265550 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 102265550 102265550 single base substitution T C downstream_gene_variant LIRI-JP 10 102265550 102265550 single base substitution T C exon_variant LIRI-JP 10 102265550 102265550 single base substitution T C intron_variant LIRI-JP 10 102268641 102268641 single base substitution T G intron_variant LIRI-JP 10 102268641 102268641 single base substitution T G upstream_gene_variant LIRI-JP 10 102272559 102272559 single base substitution T A intron_variant LIRI-JP 10 102272559 102272559 single base substitution T A upstream_gene_variant LIRI-JP 10 102273084 102273084 single base substitution C G intron_variant LIRI-JP 10 102273084 102273084 single base substitution C G upstream_gene_variant LIRI-JP 10 102276940 102276940 single base substitution C A intron_variant LIRI-JP 10 102276940 102276940 single base substitution C A upstream_gene_variant LIRI-JP 10 102277202 102277202 single base substitution C A intron_variant LIRI-JP 10 102277202 102277202 single base substitution C A upstream_gene_variant LIRI-JP 10 102277820 102277820 single base substitution T C intron_variant LIRI-JP 10 102277820 102277820 single base substitution T C upstream_gene_variant LIRI-JP 10 102282435 102282435 single base substitution T C intron_variant LIRI-JP 10 102282435 102282435 single base substitution T C upstream_gene_variant LIRI-JP 10 102283275 102283275 single base substitution A G intron_variant LIRI-JP 10 102283275 102283275 single base substitution A G upstream_gene_variant LIRI-JP 10 102285275 102285275 single base substitution C A intron_variant LIRI-JP 10 102285336 102285336 single base substitution C T intron_variant LIRI-JP 10 102287055 102287055 single base substitution T C intron_variant LIRI-JP 10 102289779 102289779 single base substitution G A upstream_gene_variant LIRI-JP 10 102290792 102290792 single base substitution T C upstream_gene_variant LIRI-JP 10 102294555 102294555 single base substitution G A upstream_gene_variant LUSC-KR 10 102242030 102242030 single base substitution G T downstream_gene_variant LUSC-KR 10 102242332 102242332 single base substitution G T downstream_gene_variant LUSC-KR 10 102246512 102246512 single base substitution C T 3_prime_UTR_variant LUSC-KR 10 102246512 102246512 single base substitution C T downstream_gene_variant LUSC-KR 10 102246512 102246512 single base substitution C T exon_variant LUSC-KR 10 102256875 102256875 single base substitution C A downstream_gene_variant LUSC-KR 10 102256875 102256875 single base substitution C A intron_variant LUSC-KR 10 102257354 102257354 single base substitution T C downstream_gene_variant LUSC-KR 10 102257354 102257354 single base substitution T C exon_variant LUSC-KR 10 102257354 102257354 single base substitution T C intron_variant LUSC-KR 10 102260426 102260426 single base substitution C A downstream_gene_variant LUSC-KR 10 102260426 102260426 single base substitution C A intron_variant LUSC-KR 10 102260426 102260426 single base substitution C A upstream_gene_variant LUSC-KR 10 102262794 102262794 single base substitution C A downstream_gene_variant LUSC-KR 10 102262794 102262794 single base substitution C A intron_variant LUSC-KR 10 102262794 102262794 single base substitution C A upstream_gene_variant LUSC-KR 10 102273380 102273380 single base substitution C A intron_variant LUSC-KR 10 102273380 102273380 single base substitution C A upstream_gene_variant LUSC-KR 10 102281024 102281024 single base substitution C G intron_variant LUSC-KR 10 102281024 102281024 single base substitution C G upstream_gene_variant LUSC-KR 10 102281823 102281823 single base substitution C A intron_variant LUSC-KR 10 102281823 102281823 single base substitution C A upstream_gene_variant LUSC-KR 10 102282904 102282904 single base substitution C A intron_variant LUSC-KR 10 102282904 102282904 single base substitution C A upstream_gene_variant LUSC-KR 10 102292276 102292276 single base substitution G C upstream_gene_variant LUSC-KR 10 102292838 102292838 single base substitution C T upstream_gene_variant LUSC-US 10 102256950 102256950 single base substitution T C 3_prime_UTR_variant LUSC-US 10 102256950 102256950 single base substitution T C downstream_gene_variant LUSC-US 10 102256950 102256950 single base substitution T C exon_variant LUSC-US 10 102256950 102256950 single base substitution T C intron_variant LUSC-US 10 102256950 102256950 single base substitution T C missense_variant E693G 2078A>G LUSC-US 10 102257543 102257543 single base substitution G T 3_prime_UTR_variant LUSC-US 10 102257543 102257543 single base substitution G T downstream_gene_variant LUSC-US 10 102257543 102257543 single base substitution G T exon_variant LUSC-US 10 102257543 102257543 single base substitution G T missense_variant A624D 1871C>A LUSC-US 10 102262016 102262016 single base substitution G T 3_prime_UTR_variant LUSC-US 10 102262016 102262016 single base substitution G T downstream_gene_variant LUSC-US 10 102262016 102262016 single base substitution G T exon_variant LUSC-US 10 102262016 102262016 single base substitution G T missense_variant L469M 1405C>A LUSC-US 10 102262016 102262016 single base substitution G T upstream_gene_variant LUSC-US 10 102286181 102286181 single base substitution T A intron_variant LUSC-US 10 102289241 102289241 single base substitution C A 5_prime_UTR_variant MALY-DE 10 102242607 102242607 single base substitution T C downstream_gene_variant MALY-DE 10 102244403 102244403 single base substitution C T downstream_gene_variant MALY-DE 10 102249757 102249757 single base substitution A C downstream_gene_variant MALY-DE 10 102249757 102249757 single base substitution A C exon_variant MALY-DE 10 102249757 102249757 single base substitution A C intron_variant MALY-DE 10 102249757 102249757 single base substitution A C splice_region_variant MALY-DE 10 102256580 102256580 single base substitution T G downstream_gene_variant MALY-DE 10 102256580 102256580 single base substitution T G intron_variant MALY-DE 10 102256586 102256586 single base substitution T C downstream_gene_variant MALY-DE 10 102256586 102256586 single base substitution T C intron_variant MALY-DE 10 102256762 102256762 single base substitution T C downstream_gene_variant MALY-DE 10 102256762 102256762 single base substitution T C intron_variant MALY-DE 10 102263598 102263598 single base substitution G T downstream_gene_variant MALY-DE 10 102263598 102263598 single base substitution G T intron_variant MALY-DE 10 102263598 102263598 single base substitution G T upstream_gene_variant MALY-DE 10 102267082 102267082 single base substitution G A intron_variant MALY-DE 10 102267082 102267082 single base substitution G A upstream_gene_variant MALY-DE 10 102269282 102269282 single base substitution G A intron_variant MALY-DE 10 102269282 102269282 single base substitution G A upstream_gene_variant MALY-DE 10 102270561 102270561 single base substitution C T intron_variant MALY-DE 10 102270561 102270561 single base substitution C T upstream_gene_variant MALY-DE 10 102277137 102277137 single base substitution T G intron_variant MALY-DE 10 102277137 102277137 single base substitution T G upstream_gene_variant MELA-AU 10 102242085 102242085 single base substitution A C downstream_gene_variant MELA-AU 10 102242580 102242580 insertion of <=200bp - C downstream_gene_variant MELA-AU 10 102242594 102242594 insertion of <=200bp - T downstream_gene_variant MELA-AU 10 102243677 102243677 single base substitution A T downstream_gene_variant MELA-AU 10 102245059 102245060 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 102245085 102245085 single base substitution C T downstream_gene_variant MELA-AU 10 102245129 102245129 single base substitution G A downstream_gene_variant MELA-AU 10 102245344 102245344 single base substitution G A downstream_gene_variant MELA-AU 10 102245489 102245489 single base substitution G A downstream_gene_variant MELA-AU 10 102245509 102245509 single base substitution A G downstream_gene_variant MELA-AU 10 102245925 102245925 single base substitution G A downstream_gene_variant MELA-AU 10 102246167 102246167 single base substitution G A downstream_gene_variant MELA-AU 10 102246168 102246168 single base substitution G A downstream_gene_variant MELA-AU 10 102246912 102246912 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102246912 102246912 single base substitution G A exon_variant MELA-AU 10 102247127 102247127 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102247127 102247127 single base substitution G A exon_variant MELA-AU 10 102247183 102247183 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102247183 102247183 single base substitution G A exon_variant MELA-AU 10 102247265 102247265 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102247265 102247265 single base substitution G A exon_variant MELA-AU 10 102247324 102247324 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102247324 102247324 single base substitution G A exon_variant MELA-AU 10 102247371 102247371 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102247371 102247371 single base substitution G A exon_variant MELA-AU 10 102247415 102247415 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102247415 102247415 single base substitution G A exon_variant MELA-AU 10 102247415 102247415 single base substitution G A synonymous_variant I1166I 3498C>T MELA-AU 10 102247514 102247514 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102247514 102247514 single base substitution G A exon_variant MELA-AU 10 102247514 102247514 single base substitution G A synonymous_variant A1133A 3399C>T MELA-AU 10 102247612 102247612 single base substitution G A exon_variant MELA-AU 10 102247612 102247612 single base substitution G A intron_variant MELA-AU 10 102247705 102247705 single base substitution G A exon_variant MELA-AU 10 102247705 102247705 single base substitution G A intron_variant MELA-AU 10 102247758 102247758 single base substitution G A exon_variant MELA-AU 10 102247758 102247758 single base substitution G A intron_variant MELA-AU 10 102248075 102248075 single base substitution G A intron_variant MELA-AU 10 102248335 102248335 single base substitution G A intron_variant MELA-AU 10 102248986 102248986 single base substitution G A exon_variant MELA-AU 10 102248986 102248986 single base substitution G A intron_variant MELA-AU 10 102249032 102249032 single base substitution C T 3_prime_UTR_variant MELA-AU 10 102249032 102249032 single base substitution C T exon_variant MELA-AU 10 102249032 102249032 single base substitution C T intron_variant MELA-AU 10 102249032 102249032 single base substitution C T missense_variant V1050I 3148G>A MELA-AU 10 102249035 102249035 single base substitution C T 3_prime_UTR_variant MELA-AU 10 102249035 102249035 single base substitution C T exon_variant MELA-AU 10 102249035 102249035 single base substitution C T intron_variant MELA-AU 10 102249035 102249035 single base substitution C T missense_variant G1049R 3145G>A MELA-AU 10 102249076 102249076 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102249076 102249076 single base substitution G A exon_variant MELA-AU 10 102249076 102249076 single base substitution G A intron_variant MELA-AU 10 102249076 102249076 single base substitution G A missense_variant P1035L 3104C>T MELA-AU 10 102249200 102249200 single base substitution C A exon_variant MELA-AU 10 102249200 102249200 single base substitution C A intron_variant MELA-AU 10 102249305 102249305 single base substitution G A exon_variant MELA-AU 10 102249305 102249305 single base substitution G A intron_variant MELA-AU 10 102249400 102249400 single base substitution G A exon_variant MELA-AU 10 102249400 102249400 single base substitution G A intron_variant MELA-AU 10 102249590 102249590 single base substitution G A exon_variant MELA-AU 10 102249590 102249590 single base substitution G A intron_variant MELA-AU 10 102249742 102249742 single base substitution G A downstream_gene_variant MELA-AU 10 102249742 102249742 single base substitution G A exon_variant MELA-AU 10 102249742 102249742 single base substitution G A intron_variant MELA-AU 10 102249889 102249889 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102249889 102249889 single base substitution G A downstream_gene_variant MELA-AU 10 102249889 102249889 single base substitution G A exon_variant MELA-AU 10 102249889 102249889 single base substitution G A intron_variant MELA-AU 10 102249889 102249889 single base substitution G A synonymous_variant P947P 2841C>T MELA-AU 10 102249890 102249890 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102249890 102249890 single base substitution G A downstream_gene_variant MELA-AU 10 102249890 102249890 single base substitution G A exon_variant MELA-AU 10 102249890 102249890 single base substitution G A intron_variant MELA-AU 10 102249890 102249890 single base substitution G A missense_variant P947L 2840C>T MELA-AU 10 102250250 102250250 single base substitution C T downstream_gene_variant MELA-AU 10 102250250 102250250 single base substitution C T exon_variant MELA-AU 10 102250250 102250250 single base substitution C T intron_variant MELA-AU 10 102250250 102250250 single base substitution C T upstream_gene_variant MELA-AU 10 102250716 102250716 single base substitution G A downstream_gene_variant MELA-AU 10 102250716 102250716 single base substitution G A intron_variant MELA-AU 10 102250716 102250716 single base substitution G A upstream_gene_variant MELA-AU 10 102250877 102250877 single base substitution G A downstream_gene_variant MELA-AU 10 102250877 102250877 single base substitution G A intron_variant MELA-AU 10 102250877 102250877 single base substitution G A upstream_gene_variant MELA-AU 10 102251192 102251192 single base substitution G A downstream_gene_variant MELA-AU 10 102251192 102251192 single base substitution G A intron_variant MELA-AU 10 102251192 102251192 single base substitution G A upstream_gene_variant MELA-AU 10 102251451 102251451 single base substitution G A downstream_gene_variant MELA-AU 10 102251451 102251451 single base substitution G A intron_variant MELA-AU 10 102251451 102251451 single base substitution G A upstream_gene_variant MELA-AU 10 102251715 102251715 single base substitution G C downstream_gene_variant MELA-AU 10 102251715 102251715 single base substitution G C intron_variant MELA-AU 10 102251715 102251715 single base substitution G C upstream_gene_variant MELA-AU 10 102251835 102251835 single base substitution G A downstream_gene_variant MELA-AU 10 102251835 102251835 single base substitution G A intron_variant MELA-AU 10 102251835 102251835 single base substitution G A upstream_gene_variant MELA-AU 10 102252550 102252550 single base substitution G A downstream_gene_variant MELA-AU 10 102252550 102252550 single base substitution G A intron_variant MELA-AU 10 102252550 102252550 single base substitution G A upstream_gene_variant MELA-AU 10 102252699 102252699 single base substitution C T downstream_gene_variant MELA-AU 10 102252699 102252699 single base substitution C T intron_variant MELA-AU 10 102252699 102252699 single base substitution C T upstream_gene_variant MELA-AU 10 102253051 102253051 single base substitution A G downstream_gene_variant MELA-AU 10 102253051 102253051 single base substitution A G intron_variant MELA-AU 10 102253051 102253051 single base substitution A G upstream_gene_variant MELA-AU 10 102253234 102253234 single base substitution A G downstream_gene_variant MELA-AU 10 102253234 102253234 single base substitution A G intron_variant MELA-AU 10 102253234 102253234 single base substitution A G upstream_gene_variant MELA-AU 10 102253738 102253738 single base substitution G A downstream_gene_variant MELA-AU 10 102253738 102253738 single base substitution G A intron_variant MELA-AU 10 102253738 102253738 single base substitution G A upstream_gene_variant MELA-AU 10 102253760 102253760 single base substitution G A downstream_gene_variant MELA-AU 10 102253760 102253760 single base substitution G A intron_variant MELA-AU 10 102253760 102253760 single base substitution G A upstream_gene_variant MELA-AU 10 102253776 102253776 single base substitution G A downstream_gene_variant MELA-AU 10 102253776 102253776 single base substitution G A intron_variant MELA-AU 10 102253776 102253776 single base substitution G A upstream_gene_variant MELA-AU 10 102253786 102253786 single base substitution G A downstream_gene_variant MELA-AU 10 102253786 102253786 single base substitution G A intron_variant MELA-AU 10 102253786 102253786 single base substitution G A upstream_gene_variant MELA-AU 10 102253987 102253987 single base substitution A G downstream_gene_variant MELA-AU 10 102253987 102253987 single base substitution A G intron_variant MELA-AU 10 102253987 102253987 single base substitution A G upstream_gene_variant MELA-AU 10 102254619 102254619 single base substitution C T downstream_gene_variant MELA-AU 10 102254619 102254619 single base substitution C T exon_variant MELA-AU 10 102254619 102254619 single base substitution C T intron_variant MELA-AU 10 102254619 102254619 single base substitution C T upstream_gene_variant MELA-AU 10 102255224 102255224 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102255224 102255224 single base substitution G A downstream_gene_variant MELA-AU 10 102255224 102255224 single base substitution G A exon_variant MELA-AU 10 102255224 102255224 single base substitution G A missense_variant P797L 2390C>T MELA-AU 10 102255224 102255224 single base substitution G A upstream_gene_variant MELA-AU 10 102256074 102256074 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102256074 102256074 single base substitution G A downstream_gene_variant MELA-AU 10 102256074 102256074 single base substitution G A exon_variant MELA-AU 10 102256074 102256074 single base substitution G A synonymous_variant L751L 2251C>T MELA-AU 10 102256114 102256114 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102256114 102256114 single base substitution G A downstream_gene_variant MELA-AU 10 102256114 102256114 single base substitution G A exon_variant MELA-AU 10 102256114 102256114 single base substitution G A synonymous_variant G737G 2211C>T MELA-AU 10 102256221 102256221 single base substitution C T downstream_gene_variant MELA-AU 10 102256221 102256221 single base substitution C T intron_variant MELA-AU 10 102256355 102256355 single base substitution G A downstream_gene_variant MELA-AU 10 102256355 102256355 single base substitution G A intron_variant MELA-AU 10 102256508 102256508 single base substitution C T downstream_gene_variant MELA-AU 10 102256508 102256508 single base substitution C T intron_variant MELA-AU 10 102256736 102256736 single base substitution G A downstream_gene_variant MELA-AU 10 102256736 102256736 single base substitution G A intron_variant MELA-AU 10 102256756 102256756 single base substitution G A downstream_gene_variant MELA-AU 10 102256756 102256756 single base substitution G A intron_variant MELA-AU 10 102257243 102257243 single base substitution C T downstream_gene_variant MELA-AU 10 102257243 102257243 single base substitution C T intron_variant MELA-AU 10 102257436 102257436 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102257436 102257436 single base substitution G A downstream_gene_variant MELA-AU 10 102257436 102257436 single base substitution G A exon_variant MELA-AU 10 102257436 102257436 single base substitution G A missense_variant P660S 1978C>T MELA-AU 10 102257775 102257775 single base substitution T A downstream_gene_variant MELA-AU 10 102257775 102257775 single base substitution T A intron_variant MELA-AU 10 102258030 102258030 single base substitution G A downstream_gene_variant MELA-AU 10 102258030 102258030 single base substitution G A exon_variant MELA-AU 10 102258030 102258030 single base substitution G A intron_variant MELA-AU 10 102258030 102258030 single base substitution G A upstream_gene_variant MELA-AU 10 102258349 102258349 single base substitution C G downstream_gene_variant MELA-AU 10 102258349 102258349 single base substitution C G intron_variant MELA-AU 10 102258349 102258349 single base substitution C G upstream_gene_variant MELA-AU 10 102258422 102258422 single base substitution C T downstream_gene_variant MELA-AU 10 102258422 102258422 single base substitution C T intron_variant MELA-AU 10 102258422 102258422 single base substitution C T upstream_gene_variant MELA-AU 10 102258850 102258850 single base substitution G A downstream_gene_variant MELA-AU 10 102258850 102258850 single base substitution G A intron_variant MELA-AU 10 102258850 102258850 single base substitution G A upstream_gene_variant MELA-AU 10 102259034 102259034 single base substitution G A downstream_gene_variant MELA-AU 10 102259034 102259034 single base substitution G A intron_variant MELA-AU 10 102259034 102259034 single base substitution G A upstream_gene_variant MELA-AU 10 102259262 102259262 single base substitution G A downstream_gene_variant MELA-AU 10 102259262 102259262 single base substitution G A exon_variant MELA-AU 10 102259262 102259262 single base substitution G A intron_variant MELA-AU 10 102259262 102259262 single base substitution G A upstream_gene_variant MELA-AU 10 102259597 102259597 single base substitution C T downstream_gene_variant MELA-AU 10 102259597 102259597 single base substitution C T intron_variant MELA-AU 10 102259597 102259597 single base substitution C T upstream_gene_variant MELA-AU 10 102260469 102260469 single base substitution G A downstream_gene_variant MELA-AU 10 102260469 102260469 single base substitution G A intron_variant MELA-AU 10 102260469 102260469 single base substitution G A upstream_gene_variant MELA-AU 10 102260605 102260605 single base substitution C T downstream_gene_variant MELA-AU 10 102260605 102260605 single base substitution C T intron_variant MELA-AU 10 102260605 102260605 single base substitution C T upstream_gene_variant MELA-AU 10 102260633 102260633 single base substitution G A downstream_gene_variant MELA-AU 10 102260633 102260633 single base substitution G A intron_variant MELA-AU 10 102260633 102260633 single base substitution G A upstream_gene_variant MELA-AU 10 102260833 102260833 single base substitution A C downstream_gene_variant MELA-AU 10 102260833 102260833 single base substitution A C intron_variant MELA-AU 10 102260833 102260833 single base substitution A C upstream_gene_variant MELA-AU 10 102260889 102260889 single base substitution C T downstream_gene_variant MELA-AU 10 102260889 102260889 single base substitution C T intron_variant MELA-AU 10 102260889 102260889 single base substitution C T upstream_gene_variant MELA-AU 10 102262016 102262016 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102262016 102262016 single base substitution G A downstream_gene_variant MELA-AU 10 102262016 102262016 single base substitution G A exon_variant MELA-AU 10 102262016 102262016 single base substitution G A synonymous_variant L469L 1405C>T MELA-AU 10 102262016 102262016 single base substitution G A upstream_gene_variant MELA-AU 10 102262364 102262364 single base substitution G A downstream_gene_variant MELA-AU 10 102262364 102262364 single base substitution G A intron_variant MELA-AU 10 102262364 102262364 single base substitution G A upstream_gene_variant MELA-AU 10 102262443 102262443 single base substitution G A downstream_gene_variant MELA-AU 10 102262443 102262443 single base substitution G A intron_variant MELA-AU 10 102262443 102262443 single base substitution G A upstream_gene_variant MELA-AU 10 102262716 102262716 single base substitution C T downstream_gene_variant MELA-AU 10 102262716 102262716 single base substitution C T intron_variant MELA-AU 10 102262716 102262716 single base substitution C T upstream_gene_variant MELA-AU 10 102262831 102262831 single base substitution G A downstream_gene_variant MELA-AU 10 102262831 102262831 single base substitution G A intron_variant MELA-AU 10 102262831 102262831 single base substitution G A upstream_gene_variant MELA-AU 10 102263160 102263160 single base substitution G A downstream_gene_variant MELA-AU 10 102263160 102263160 single base substitution G A intron_variant MELA-AU 10 102263160 102263160 single base substitution G A upstream_gene_variant MELA-AU 10 102263325 102263325 single base substitution G A downstream_gene_variant MELA-AU 10 102263325 102263325 single base substitution G A intron_variant MELA-AU 10 102263325 102263325 single base substitution G A upstream_gene_variant MELA-AU 10 102263837 102263837 single base substitution T G downstream_gene_variant MELA-AU 10 102263837 102263837 single base substitution T G intron_variant MELA-AU 10 102263837 102263837 single base substitution T G upstream_gene_variant MELA-AU 10 102264357 102264357 single base substitution G A downstream_gene_variant MELA-AU 10 102264357 102264357 single base substitution G A intron_variant MELA-AU 10 102264578 102264578 single base substitution G A downstream_gene_variant MELA-AU 10 102264578 102264578 single base substitution G A intron_variant MELA-AU 10 102264740 102264740 single base substitution C T downstream_gene_variant MELA-AU 10 102264740 102264740 single base substitution C T intron_variant MELA-AU 10 102264839 102264839 single base substitution G A downstream_gene_variant MELA-AU 10 102264839 102264839 single base substitution G A intron_variant MELA-AU 10 102265489 102265489 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102265489 102265489 single base substitution G A downstream_gene_variant MELA-AU 10 102265489 102265489 single base substitution G A exon_variant MELA-AU 10 102265489 102265489 single base substitution G A intron_variant MELA-AU 10 102266016 102266016 single base substitution C T downstream_gene_variant MELA-AU 10 102266016 102266016 single base substitution C T intron_variant MELA-AU 10 102266564 102266564 single base substitution G A intron_variant MELA-AU 10 102266564 102266564 single base substitution G A upstream_gene_variant MELA-AU 10 102267215 102267215 single base substitution G A 3_prime_UTR_variant MELA-AU 10 102267215 102267215 single base substitution G A exon_variant MELA-AU 10 102267215 102267215 single base substitution G A intron_variant MELA-AU 10 102267215 102267215 single base substitution G A missense_variant S250F 749C>T MELA-AU 10 102267215 102267215 single base substitution G A missense_variant S253F 758C>T MELA-AU 10 102267215 102267215 single base substitution G A missense_variant S93F 278C>T MELA-AU 10 102267215 102267215 single base substitution G A upstream_gene_variant MELA-AU 10 102268005 102268005 single base substitution G A intron_variant MELA-AU 10 102268005 102268005 single base substitution G A upstream_gene_variant MELA-AU 10 102268540 102268540 single base substitution T C exon_variant MELA-AU 10 102268540 102268540 single base substitution T C intron_variant MELA-AU 10 102268540 102268540 single base substitution T C upstream_gene_variant MELA-AU 10 102268750 102268750 single base substitution G A intron_variant MELA-AU 10 102268750 102268750 single base substitution G A upstream_gene_variant MELA-AU 10 102268977 102268977 single base substitution G A intron_variant MELA-AU 10 102268977 102268977 single base substitution G A upstream_gene_variant MELA-AU 10 102268979 102268979 single base substitution G A intron_variant MELA-AU 10 102268979 102268979 single base substitution G A upstream_gene_variant MELA-AU 10 102269586 102269586 single base substitution A C intron_variant MELA-AU 10 102269586 102269586 single base substitution A C upstream_gene_variant MELA-AU 10 102269710 102269710 single base substitution C T intron_variant MELA-AU 10 102269710 102269710 single base substitution C T upstream_gene_variant MELA-AU 10 102269804 102269804 single base substitution G A intron_variant MELA-AU 10 102269804 102269804 single base substitution G A upstream_gene_variant MELA-AU 10 102271209 102271209 insertion of <=200bp - A intron_variant MELA-AU 10 102271209 102271209 insertion of <=200bp - A upstream_gene_variant MELA-AU 10 102271299 102271299 single base substitution G A intron_variant MELA-AU 10 102271299 102271299 single base substitution G A upstream_gene_variant MELA-AU 10 102271604 102271604 single base substitution G A intron_variant MELA-AU 10 102271604 102271604 single base substitution G A upstream_gene_variant MELA-AU 10 102271743 102271743 single base substitution A G intron_variant MELA-AU 10 102271743 102271743 single base substitution A G upstream_gene_variant MELA-AU 10 102271813 102271813 single base substitution G A intron_variant MELA-AU 10 102271813 102271813 single base substitution G A upstream_gene_variant MELA-AU 10 102272281 102272282 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 102272281 102272282 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 102272381 102272381 single base substitution G A intron_variant MELA-AU 10 102272381 102272381 single base substitution G A upstream_gene_variant MELA-AU 10 102272509 102272509 single base substitution G A intron_variant MELA-AU 10 102272509 102272509 single base substitution G A upstream_gene_variant MELA-AU 10 102272567 102272567 single base substitution G A intron_variant MELA-AU 10 102272567 102272567 single base substitution G A upstream_gene_variant MELA-AU 10 102273646 102273646 single base substitution A T intron_variant MELA-AU 10 102273735 102273735 single base substitution A T intron_variant MELA-AU 10 102273837 102273837 single base substitution G A intron_variant MELA-AU 10 102274552 102274552 single base substitution A G intron_variant MELA-AU 10 102274657 102274657 single base substitution G A intron_variant MELA-AU 10 102274955 102274955 single base substitution G C intron_variant MELA-AU 10 102275028 102275028 single base substitution G A intron_variant MELA-AU 10 102275104 102275104 single base substitution A C intron_variant MELA-AU 10 102275139 102275139 single base substitution G A intron_variant MELA-AU 10 102276332 102276332 single base substitution G A intron_variant MELA-AU 10 102276393 102276393 single base substitution G A intron_variant MELA-AU 10 102277060 102277060 single base substitution G A intron_variant MELA-AU 10 102277060 102277060 single base substitution G A upstream_gene_variant MELA-AU 10 102278259 102278259 single base substitution G T intron_variant MELA-AU 10 102278259 102278259 single base substitution G T upstream_gene_variant MELA-AU 10 102278530 102278530 single base substitution G A intron_variant MELA-AU 10 102278530 102278530 single base substitution G A upstream_gene_variant MELA-AU 10 102280064 102280064 single base substitution G A intron_variant MELA-AU 10 102280064 102280064 single base substitution G A upstream_gene_variant MELA-AU 10 102282889 102282889 single base substitution T C intron_variant MELA-AU 10 102282889 102282889 single base substitution T C upstream_gene_variant MELA-AU 10 102283130 102283130 single base substitution C T intron_variant MELA-AU 10 102283130 102283130 single base substitution C T upstream_gene_variant MELA-AU 10 102283274 102283274 single base substitution G A intron_variant MELA-AU 10 102283274 102283274 single base substitution G A upstream_gene_variant MELA-AU 10 102283482 102283482 single base substitution G A intron_variant MELA-AU 10 102283482 102283482 single base substitution G A upstream_gene_variant MELA-AU 10 102283642 102283642 single base substitution G A intron_variant MELA-AU 10 102283642 102283642 single base substitution G A upstream_gene_variant MELA-AU 10 102287947 102287947 single base substitution A C intron_variant MELA-AU 10 102288560 102288560 single base substitution A C intron_variant MELA-AU 10 102288585 102288585 single base substitution G A intron_variant MELA-AU 10 102288774 102288774 single base substitution C T intron_variant MELA-AU 10 102291170 102291170 single base substitution T A upstream_gene_variant MELA-AU 10 102291237 102291237 single base substitution A C upstream_gene_variant MELA-AU 10 102292181 102292181 single base substitution C T upstream_gene_variant MELA-AU 10 102292811 102292811 single base substitution C T upstream_gene_variant MELA-AU 10 102292858 102292858 single base substitution G A upstream_gene_variant MELA-AU 10 102293016 102293016 single base substitution G A upstream_gene_variant MELA-AU 10 102293217 102293217 single base substitution C T upstream_gene_variant MELA-AU 10 102293499 102293499 single base substitution C T upstream_gene_variant MELA-AU 10 102293742 102293742 single base substitution C T upstream_gene_variant MELA-AU 10 102294235 102294235 single base substitution A G upstream_gene_variant ORCA-IN 10 102245317 102245317 single base substitution C T downstream_gene_variant ORCA-IN 10 102255789 102255789 single base substitution C A downstream_gene_variant ORCA-IN 10 102255789 102255789 single base substitution C A intron_variant ORCA-IN 10 102267323 102267323 single base substitution A G intron_variant ORCA-IN 10 102267323 102267323 single base substitution A G missense_variant M214T 641T>C ORCA-IN 10 102267323 102267323 single base substitution A G missense_variant M217T 650T>C ORCA-IN 10 102267323 102267323 single base substitution A G missense_variant M57T 170T>C ORCA-IN 10 102267323 102267323 single base substitution A G splice_region_variant ORCA-IN 10 102267323 102267323 single base substitution A G upstream_gene_variant ORCA-IN 10 102269202 102269202 single base substitution G A exon_variant ORCA-IN 10 102269202 102269202 single base substitution G A intron_variant ORCA-IN 10 102269202 102269202 single base substitution G A synonymous_variant G90G 270C>T ORCA-IN 10 102269202 102269202 single base substitution G A upstream_gene_variant ORCA-IN 10 102269245 102269245 single base substitution C A exon_variant ORCA-IN 10 102269245 102269245 single base substitution C A intron_variant ORCA-IN 10 102269245 102269245 single base substitution C A missense_variant S76I 227G>T ORCA-IN 10 102269245 102269245 single base substitution C A upstream_gene_variant OV-AU 10 102249348 102249348 single base substitution G C exon_variant OV-AU 10 102249348 102249348 single base substitution G C intron_variant OV-AU 10 102253380 102253380 single base substitution C G downstream_gene_variant OV-AU 10 102253380 102253380 single base substitution C G intron_variant OV-AU 10 102253380 102253380 single base substitution C G upstream_gene_variant OV-AU 10 102269124 102269124 single base substitution C G exon_variant OV-AU 10 102269124 102269124 single base substitution C G intron_variant OV-AU 10 102269124 102269124 single base substitution C G missense_variant Q116H 348G>C OV-AU 10 102269124 102269124 single base substitution C G upstream_gene_variant OV-AU 10 102270740 102270740 single base substitution C A intron_variant OV-AU 10 102270740 102270740 single base substitution C A upstream_gene_variant OV-AU 10 102273708 102273708 single base substitution G A intron_variant OV-AU 10 102273983 102273983 single base substitution C A intron_variant OV-AU 10 102274232 102274232 single base substitution C G intron_variant OV-AU 10 102274236 102274236 single base substitution G C intron_variant OV-AU 10 102283815 102283815 single base substitution G C intron_variant OV-AU 10 102283815 102283815 single base substitution G C upstream_gene_variant OV-AU 10 102293465 102293465 single base substitution C T upstream_gene_variant PACA-AU 10 102242045 102242045 single base substitution G A downstream_gene_variant PACA-AU 10 102245389 102245389 single base substitution T C downstream_gene_variant PACA-AU 10 102245753 102245753 single base substitution G A downstream_gene_variant PACA-AU 10 102252176 102252176 single base substitution C T downstream_gene_variant PACA-AU 10 102252176 102252176 single base substitution C T intron_variant PACA-AU 10 102252176 102252176 single base substitution C T upstream_gene_variant PACA-AU 10 102252656 102252656 single base substitution A T downstream_gene_variant PACA-AU 10 102252656 102252656 single base substitution A T intron_variant PACA-AU 10 102252656 102252656 single base substitution A T upstream_gene_variant PACA-AU 10 102256781 102256783 deletion of <=200bp GTG - downstream_gene_variant PACA-AU 10 102256781 102256783 deletion of <=200bp GTG - intron_variant PACA-AU 10 102258392 102258392 single base substitution T A downstream_gene_variant PACA-AU 10 102258392 102258392 single base substitution T A intron_variant PACA-AU 10 102258392 102258392 single base substitution T A upstream_gene_variant PACA-AU 10 102275230 102275230 single base substitution G A intron_variant PACA-AU 10 102276289 102276289 single base substitution C T intron_variant PACA-AU 10 102287139 102287139 single base substitution C T intron_variant PACA-CA 10 102244039 102244039 single base substitution T G downstream_gene_variant PACA-CA 10 102246712 102246712 single base substitution G A 3_prime_UTR_variant PACA-CA 10 102246712 102246712 single base substitution G A exon_variant PACA-CA 10 102250350 102250350 single base substitution C T downstream_gene_variant PACA-CA 10 102250350 102250350 single base substitution C T intron_variant PACA-CA 10 102250350 102250350 single base substitution C T upstream_gene_variant PACA-CA 10 102251049 102251049 single base substitution C G downstream_gene_variant PACA-CA 10 102251049 102251049 single base substitution C G intron_variant PACA-CA 10 102251049 102251049 single base substitution C G upstream_gene_variant PACA-CA 10 102251714 102251714 single base substitution C T downstream_gene_variant PACA-CA 10 102251714 102251714 single base substitution C T intron_variant PACA-CA 10 102251714 102251714 single base substitution C T upstream_gene_variant PACA-CA 10 102251916 102251916 single base substitution T C downstream_gene_variant PACA-CA 10 102251916 102251916 single base substitution T C intron_variant PACA-CA 10 102251916 102251916 single base substitution T C upstream_gene_variant PACA-CA 10 102252004 102252004 single base substitution A C downstream_gene_variant PACA-CA 10 102252004 102252004 single base substitution A C intron_variant PACA-CA 10 102252004 102252004 single base substitution A C upstream_gene_variant PACA-CA 10 102252582 102252582 single base substitution C G downstream_gene_variant PACA-CA 10 102252582 102252582 single base substitution C G intron_variant PACA-CA 10 102252582 102252582 single base substitution C G upstream_gene_variant PACA-CA 10 102252680 102252680 single base substitution C T downstream_gene_variant PACA-CA 10 102252680 102252680 single base substitution C T intron_variant PACA-CA 10 102252680 102252680 single base substitution C T upstream_gene_variant PACA-CA 10 102252987 102252987 single base substitution G A downstream_gene_variant PACA-CA 10 102252987 102252987 single base substitution G A intron_variant PACA-CA 10 102252987 102252987 single base substitution G A upstream_gene_variant PACA-CA 10 102254453 102254453 single base substitution G A downstream_gene_variant PACA-CA 10 102254453 102254453 single base substitution G A intron_variant PACA-CA 10 102254453 102254453 single base substitution G A upstream_gene_variant PACA-CA 10 102259594 102259594 single base substitution T G downstream_gene_variant PACA-CA 10 102259594 102259594 single base substitution T G intron_variant PACA-CA 10 102259594 102259594 single base substitution T G upstream_gene_variant PACA-CA 10 102262172 102262172 single base substitution G A 3_prime_UTR_variant PACA-CA 10 102262172 102262172 single base substitution G A downstream_gene_variant PACA-CA 10 102262172 102262172 single base substitution G A exon_variant PACA-CA 10 102262172 102262172 single base substitution G A missense_variant R417C 1249C>T PACA-CA 10 102262172 102262172 single base substitution G A upstream_gene_variant PACA-CA 10 102263060 102263060 single base substitution C A downstream_gene_variant PACA-CA 10 102263060 102263060 single base substitution C A intron_variant PACA-CA 10 102263060 102263060 single base substitution C A upstream_gene_variant PACA-CA 10 102264592 102264592 single base substitution C T downstream_gene_variant PACA-CA 10 102264592 102264592 single base substitution C T intron_variant PACA-CA 10 102264916 102264916 single base substitution A T downstream_gene_variant PACA-CA 10 102264916 102264916 single base substitution A T intron_variant PACA-CA 10 102265159 102265159 insertion of <=200bp - T 3_prime_UTR_variant PACA-CA 10 102265159 102265159 insertion of <=200bp - T downstream_gene_variant PACA-CA 10 102265159 102265159 insertion of <=200bp - T exon_variant PACA-CA 10 102265159 102265159 insertion of <=200bp - T frameshift_variant P380H? PACA-CA 10 102266720 102266720 insertion of <=200bp - A intron_variant PACA-CA 10 102266720 102266720 insertion of <=200bp - A upstream_gene_variant PACA-CA 10 102285180 102285180 insertion of <=200bp - T intron_variant PACA-CA 10 102292701 102292701 single base substitution T C upstream_gene_variant PAEN-IT 10 102279913 102279913 single base substitution C T intron_variant PAEN-IT 10 102279913 102279913 single base substitution C T upstream_gene_variant PBCA-DE 10 102250028 102250028 single base substitution G A 3_prime_UTR_variant PBCA-DE 10 102250028 102250028 single base substitution G A downstream_gene_variant PBCA-DE 10 102250028 102250028 single base substitution G A exon_variant PBCA-DE 10 102250028 102250028 single base substitution G A intron_variant PBCA-DE 10 102250028 102250028 single base substitution G A missense_variant P901L 2702C>T PBCA-DE 10 102250028 102250028 single base substitution G A upstream_gene_variant PBCA-DE 10 102262276 102262276 single base substitution C A downstream_gene_variant PBCA-DE 10 102262276 102262276 single base substitution C A intron_variant PBCA-DE 10 102262276 102262276 single base substitution C A upstream_gene_variant PBCA-DE 10 102265057 102265058 deletion of <=200bp AC - downstream_gene_variant PBCA-DE 10 102265057 102265058 deletion of <=200bp AC - intron_variant PBCA-DE 10 102279265 102279265 single base substitution C A intron_variant PBCA-DE 10 102279265 102279265 single base substitution C A upstream_gene_variant PBCA-DE 10 102282605 102282605 insertion of <=200bp - T intron_variant PBCA-DE 10 102282605 102282605 insertion of <=200bp - T upstream_gene_variant PRAD-CA 10 102284590 102284590 single base substitution G T intron_variant PRAD-CA 10 102284590 102284590 single base substitution G T upstream_gene_variant PRAD-CA 10 102293087 102293087 single base substitution G C upstream_gene_variant PRAD-US 10 102248628 102248628 single base substitution G T 3_prime_UTR_variant PRAD-US 10 102248628 102248628 single base substitution G T exon_variant PRAD-US 10 102248628 102248628 single base substitution G T missense_variant S1092Y 3275C>A READ-US 10 102267224 102267224 single base substitution C T 3_prime_UTR_variant READ-US 10 102267224 102267224 single base substitution C T exon_variant READ-US 10 102267224 102267224 single base substitution C T intron_variant READ-US 10 102267224 102267224 single base substitution C T missense_variant R247H 740G>A READ-US 10 102267224 102267224 single base substitution C T missense_variant R250H 749G>A READ-US 10 102267224 102267224 single base substitution C T missense_variant R90H 269G>A READ-US 10 102267224 102267224 single base substitution C T upstream_gene_variant READ-US 10 102289180 102289180 single base substitution T G 5_prime_UTR_premature_start_codon_gain_variant RECA-EU 10 102242027 102242027 single base substitution G T downstream_gene_variant RECA-EU 10 102250534 102250534 single base substitution T G 3_prime_UTR_variant RECA-EU 10 102250534 102250534 single base substitution T G downstream_gene_variant RECA-EU 10 102250534 102250534 single base substitution T G missense_variant N860T 2579A>C RECA-EU 10 102250534 102250534 single base substitution T G upstream_gene_variant RECA-EU 10 102257642 102257642 single base substitution T A downstream_gene_variant RECA-EU 10 102257642 102257642 single base substitution T A intron_variant RECA-EU 10 102257648 102257648 single base substitution C T downstream_gene_variant RECA-EU 10 102257648 102257648 single base substitution C T intron_variant RECA-EU 10 102264450 102264450 single base substitution G T downstream_gene_variant RECA-EU 10 102264450 102264450 single base substitution G T intron_variant RECA-EU 10 102287999 102287999 single base substitution G A intron_variant RECA-EU 10 102289183 102289183 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 10 102243387 102243387 single base substitution T G downstream_gene_variant SKCA-BR 10 102249228 102249228 single base substitution A G exon_variant SKCA-BR 10 102249228 102249228 single base substitution A G intron_variant SKCA-BR 10 102253129 102253129 insertion of <=200bp - CAAAAAA downstream_gene_variant SKCA-BR 10 102253129 102253129 insertion of <=200bp - CAAAAAA intron_variant SKCA-BR 10 102253129 102253129 insertion of <=200bp - CAAAAAA upstream_gene_variant SKCA-BR 10 102253737 102253737 single base substitution G A downstream_gene_variant SKCA-BR 10 102253737 102253737 single base substitution G A intron_variant SKCA-BR 10 102253737 102253737 single base substitution G A upstream_gene_variant SKCA-BR 10 102253785 102253785 single base substitution G A downstream_gene_variant SKCA-BR 10 102253785 102253785 single base substitution G A intron_variant SKCA-BR 10 102253785 102253785 single base substitution G A upstream_gene_variant SKCA-BR 10 102256941 102256941 single base substitution A C 3_prime_UTR_variant SKCA-BR 10 102256941 102256941 single base substitution A C downstream_gene_variant SKCA-BR 10 102256941 102256941 single base substitution A C exon_variant SKCA-BR 10 102256941 102256941 single base substitution A C intron_variant SKCA-BR 10 102256941 102256941 single base substitution A C missense_variant V696G 2087T>G SKCA-BR 10 102259323 102259323 single base substitution G A 3_prime_UTR_variant SKCA-BR 10 102259323 102259323 single base substitution G A downstream_gene_variant SKCA-BR 10 102259323 102259323 single base substitution G A exon_variant SKCA-BR 10 102259323 102259323 single base substitution G A synonymous_variant F481F 1443C>T SKCA-BR 10 102259323 102259323 single base substitution G A upstream_gene_variant SKCA-BR 10 102260456 102260456 single base substitution T C downstream_gene_variant SKCA-BR 10 102260456 102260456 single base substitution T C intron_variant SKCA-BR 10 102260456 102260456 single base substitution T C upstream_gene_variant SKCA-BR 10 102269194 102269194 single base substitution T C exon_variant SKCA-BR 10 102269194 102269194 single base substitution T C intron_variant SKCA-BR 10 102269194 102269194 single base substitution T C missense_variant D93G 278A>G SKCA-BR 10 102269194 102269194 single base substitution T C upstream_gene_variant SKCA-BR 10 102274986 102274986 single base substitution T G intron_variant SKCA-BR 10 102277255 102277255 single base substitution A G intron_variant SKCA-BR 10 102277255 102277255 single base substitution A G upstream_gene_variant SKCA-BR 10 102277455 102277455 single base substitution G A intron_variant SKCA-BR 10 102277455 102277455 single base substitution G A upstream_gene_variant SKCA-BR 10 102280495 102280495 insertion of <=200bp - CA intron_variant SKCA-BR 10 102280495 102280495 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 10 102287657 102287657 single base substitution A C intron_variant SKCA-BR 10 102287663 102287663 single base substitution A C intron_variant SKCA-BR 10 102289733 102289733 single base substitution T G upstream_gene_variant SKCA-BR 10 102291579 102291579 single base substitution G A upstream_gene_variant SKCA-BR 10 102291761 102291761 single base substitution T C upstream_gene_variant SKCA-BR 10 102294570 102294570 single base substitution C A upstream_gene_variant SKCM-US 10 102241672 102241672 single base substitution G A downstream_gene_variant SKCM-US 10 102242085 102242085 single base substitution A C downstream_gene_variant SKCM-US 10 102242541 102242541 single base substitution G A downstream_gene_variant SKCM-US 10 102248687 102248687 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102248687 102248687 single base substitution G A exon_variant SKCM-US 10 102248687 102248687 single base substitution G A synonymous_variant P1072P 3216C>T SKCM-US 10 102249077 102249077 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102249077 102249077 single base substitution G A exon_variant SKCM-US 10 102249077 102249077 single base substitution G A intron_variant SKCM-US 10 102249077 102249077 single base substitution G A missense_variant P1035S 3103C>T SKCM-US 10 102249812 102249812 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102249812 102249812 single base substitution G A downstream_gene_variant SKCM-US 10 102249812 102249812 single base substitution G A exon_variant SKCM-US 10 102249812 102249812 single base substitution G A intron_variant SKCM-US 10 102249812 102249812 single base substitution G A missense_variant P973L 2918C>T SKCM-US 10 102249852 102249852 single base substitution T G 3_prime_UTR_variant SKCM-US 10 102249852 102249852 single base substitution T G downstream_gene_variant SKCM-US 10 102249852 102249852 single base substitution T G exon_variant SKCM-US 10 102249852 102249852 single base substitution T G intron_variant SKCM-US 10 102249852 102249852 single base substitution T G missense_variant S960R 2878A>C SKCM-US 10 102249868 102249868 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102249868 102249868 single base substitution G A downstream_gene_variant SKCM-US 10 102249868 102249868 single base substitution G A exon_variant SKCM-US 10 102249868 102249868 single base substitution G A intron_variant SKCM-US 10 102249868 102249868 single base substitution G A synonymous_variant T954T 2862C>T SKCM-US 10 102249886 102249886 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102249886 102249886 single base substitution G A downstream_gene_variant SKCM-US 10 102249886 102249886 single base substitution G A exon_variant SKCM-US 10 102249886 102249886 single base substitution G A intron_variant SKCM-US 10 102249886 102249886 single base substitution G A synonymous_variant G948G 2844C>T SKCM-US 10 102249894 102249894 single base substitution C T 3_prime_UTR_variant SKCM-US 10 102249894 102249894 single base substitution C T downstream_gene_variant SKCM-US 10 102249894 102249894 single base substitution C T exon_variant SKCM-US 10 102249894 102249894 single base substitution C T intron_variant SKCM-US 10 102249894 102249894 single base substitution C T missense_variant G946S 2836G>A SKCM-US 10 102250017 102250017 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102250017 102250017 single base substitution G A downstream_gene_variant SKCM-US 10 102250017 102250017 single base substitution G A exon_variant SKCM-US 10 102250017 102250017 single base substitution G A intron_variant SKCM-US 10 102250017 102250017 single base substitution G A missense_variant P905S 2713C>T SKCM-US 10 102250017 102250017 single base substitution G A upstream_gene_variant SKCM-US 10 102250018 102250018 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102250018 102250018 single base substitution G A downstream_gene_variant SKCM-US 10 102250018 102250018 single base substitution G A exon_variant SKCM-US 10 102250018 102250018 single base substitution G A intron_variant SKCM-US 10 102250018 102250018 single base substitution G A synonymous_variant F904F 2712C>T SKCM-US 10 102250018 102250018 single base substitution G A upstream_gene_variant SKCM-US 10 102250508 102250508 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102250508 102250508 single base substitution G A downstream_gene_variant SKCM-US 10 102250508 102250508 single base substitution G A missense_variant P869S 2605C>T SKCM-US 10 102250508 102250508 single base substitution G A upstream_gene_variant SKCM-US 10 102250605 102250605 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102250605 102250605 single base substitution G A downstream_gene_variant SKCM-US 10 102250605 102250605 single base substitution G A synonymous_variant T836T 2508C>T SKCM-US 10 102250605 102250605 single base substitution G A upstream_gene_variant SKCM-US 10 102255225 102255225 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102255225 102255225 single base substitution G A downstream_gene_variant SKCM-US 10 102255225 102255225 single base substitution G A exon_variant SKCM-US 10 102255225 102255225 single base substitution G A missense_variant P797S 2389C>T SKCM-US 10 102255225 102255225 single base substitution G A upstream_gene_variant SKCM-US 10 102256030 102256030 single base substitution G C 3_prime_UTR_variant SKCM-US 10 102256030 102256030 single base substitution G C downstream_gene_variant SKCM-US 10 102256030 102256030 single base substitution G C exon_variant SKCM-US 10 102256030 102256030 single base substitution G C synonymous_variant P765P 2295C>G SKCM-US 10 102256031 102256031 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102256031 102256031 single base substitution G A downstream_gene_variant SKCM-US 10 102256031 102256031 single base substitution G A exon_variant SKCM-US 10 102256031 102256031 single base substitution G A missense_variant P765L 2294C>T SKCM-US 10 102256891 102256891 single base substitution C T downstream_gene_variant SKCM-US 10 102256891 102256891 single base substitution C T intron_variant SKCM-US 10 102256891 102256891 single base substitution C T splice_donor_variant SKCM-US 10 102257436 102257436 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102257436 102257436 single base substitution G A downstream_gene_variant SKCM-US 10 102257436 102257436 single base substitution G A exon_variant SKCM-US 10 102257436 102257436 single base substitution G A missense_variant P660S 1978C>T SKCM-US 10 102257790 102257790 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102257790 102257790 single base substitution G A downstream_gene_variant SKCM-US 10 102257790 102257790 single base substitution G A exon_variant SKCM-US 10 102257790 102257790 single base substitution G A missense_variant S620F 1859C>T SKCM-US 10 102257867 102257867 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102257867 102257867 single base substitution G A downstream_gene_variant SKCM-US 10 102257867 102257867 single base substitution G A exon_variant SKCM-US 10 102257867 102257867 single base substitution G A synonymous_variant I594I 1782C>T SKCM-US 10 102262131 102262131 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102262131 102262131 single base substitution G A downstream_gene_variant SKCM-US 10 102262131 102262131 single base substitution G A exon_variant SKCM-US 10 102262131 102262131 single base substitution G A synonymous_variant F430F 1290C>T SKCM-US 10 102262131 102262131 single base substitution G A upstream_gene_variant SKCM-US 10 102262191 102262191 single base substitution C T 3_prime_UTR_variant SKCM-US 10 102262191 102262191 single base substitution C T downstream_gene_variant SKCM-US 10 102262191 102262191 single base substitution C T exon_variant SKCM-US 10 102262191 102262191 single base substitution C T synonymous_variant L410L 1230G>A SKCM-US 10 102262191 102262191 single base substitution C T upstream_gene_variant SKCM-US 10 102265162 102265162 single base substitution T A 3_prime_UTR_variant SKCM-US 10 102265162 102265162 single base substitution T A downstream_gene_variant SKCM-US 10 102265162 102265162 single base substitution T A exon_variant SKCM-US 10 102265162 102265162 single base substitution T A stop_gained K379* 1135A>T SKCM-US 10 102267248 102267248 single base substitution G A 3_prime_UTR_variant SKCM-US 10 102267248 102267248 single base substitution G A exon_variant SKCM-US 10 102267248 102267248 single base substitution G A intron_variant SKCM-US 10 102267248 102267248 single base substitution G A missense_variant P239L 716C>T SKCM-US 10 102267248 102267248 single base substitution G A missense_variant P242L 725C>T SKCM-US 10 102267248 102267248 single base substitution G A missense_variant P82L 245C>T SKCM-US 10 102267248 102267248 single base substitution G A upstream_gene_variant SKCM-US 10 102269264 102269264 single base substitution G A exon_variant SKCM-US 10 102269264 102269264 single base substitution G A intron_variant SKCM-US 10 102269264 102269264 single base substitution G A missense_variant H70Y 208C>T SKCM-US 10 102269264 102269264 single base substitution G A upstream_gene_variant STAD-US 10 102242433 102242433 single base substitution G A downstream_gene_variant STAD-US 10 102247505 102247505 single base substitution C A 3_prime_UTR_variant STAD-US 10 102247505 102247505 single base substitution C A exon_variant STAD-US 10 102247505 102247505 single base substitution C A synonymous_variant V1136V 3408G>T STAD-US 10 102248625 102248625 single base substitution G A 3_prime_UTR_variant STAD-US 10 102248625 102248625 single base substitution G A exon_variant STAD-US 10 102248625 102248625 single base substitution G A missense_variant A1093V 3278C>T STAD-US 10 102249885 102249885 single base substitution G A 3_prime_UTR_variant STAD-US 10 102249885 102249885 single base substitution G A downstream_gene_variant STAD-US 10 102249885 102249885 single base substitution G A exon_variant STAD-US 10 102249885 102249885 single base substitution G A intron_variant STAD-US 10 102249885 102249885 single base substitution G A missense_variant R949C 2845C>T STAD-US 10 102255254 102255254 single base substitution G A 3_prime_UTR_variant STAD-US 10 102255254 102255254 single base substitution G A downstream_gene_variant STAD-US 10 102255254 102255254 single base substitution G A exon_variant STAD-US 10 102255254 102255254 single base substitution G A missense_variant A787V 2360C>T STAD-US 10 102255254 102255254 single base substitution G A upstream_gene_variant STAD-US 10 102255279 102255279 single base substitution G A 3_prime_UTR_variant STAD-US 10 102255279 102255279 single base substitution G A downstream_gene_variant STAD-US 10 102255279 102255279 single base substitution G A exon_variant STAD-US 10 102255279 102255279 single base substitution G A missense_variant R779W 2335C>T STAD-US 10 102255279 102255279 single base substitution G A upstream_gene_variant STAD-US 10 102256140 102256140 single base substitution G A 3_prime_UTR_variant STAD-US 10 102256140 102256140 single base substitution G A downstream_gene_variant STAD-US 10 102256140 102256140 single base substitution G A exon_variant STAD-US 10 102256140 102256140 single base substitution G A missense_variant R729W 2185C>T STAD-US 10 102257433 102257433 single base substitution C T 3_prime_UTR_variant STAD-US 10 102257433 102257433 single base substitution C T downstream_gene_variant STAD-US 10 102257433 102257433 single base substitution C T exon_variant STAD-US 10 102257433 102257433 single base substitution C T missense_variant E661K 1981G>A STAD-US 10 102257863 102257863 single base substitution C A 3_prime_UTR_variant STAD-US 10 102257863 102257863 single base substitution C A downstream_gene_variant STAD-US 10 102257863 102257863 single base substitution C A exon_variant STAD-US 10 102257863 102257863 single base substitution C A missense_variant A596S 1786G>T STAD-US 10 102265160 102265160 deletion of <=200bp T - 3_prime_UTR_variant STAD-US 10 102265160 102265160 deletion of <=200bp T - downstream_gene_variant STAD-US 10 102265160 102265160 deletion of <=200bp T - exon_variant STAD-US 10 102265160 102265160 deletion of <=200bp T - frameshift_variant K379 STAD-US 10 102265255 102265255 deletion of <=200bp G - 3_prime_UTR_variant STAD-US 10 102265255 102265255 deletion of <=200bp G - downstream_gene_variant STAD-US 10 102265255 102265255 deletion of <=200bp G - exon_variant STAD-US 10 102265255 102265255 deletion of <=200bp G - splice_region_variant STAD-US 10 102265860 102265860 single base substitution C A 3_prime_UTR_variant STAD-US 10 102265860 102265860 single base substitution C A downstream_gene_variant STAD-US 10 102265860 102265860 single base substitution C A exon_variant STAD-US 10 102265860 102265860 single base substitution C A missense_variant W170C 510G>T STAD-US 10 102265860 102265860 single base substitution C A missense_variant W327C 981G>T STAD-US 10 102265860 102265860 single base substitution C A missense_variant W330C 990G>T STAD-US 10 102265915 102265915 single base substitution A G 3_prime_UTR_variant STAD-US 10 102265915 102265915 single base substitution A G downstream_gene_variant STAD-US 10 102265915 102265915 single base substitution A G exon_variant STAD-US 10 102265915 102265915 single base substitution A G missense_variant V152A 455T>C STAD-US 10 102265915 102265915 single base substitution A G missense_variant V309A 926T>C STAD-US 10 102265915 102265915 single base substitution A G missense_variant V312A 935T>C STAD-US 10 102265959 102265959 single base substitution C A downstream_gene_variant STAD-US 10 102265959 102265959 single base substitution C A splice_acceptor_variant STAD-US 10 102267696 102267696 single base substitution G T 3_prime_UTR_variant STAD-US 10 102267696 102267696 single base substitution G T exon_variant STAD-US 10 102267696 102267696 single base substitution G T missense_variant P203H 608C>A STAD-US 10 102267696 102267696 single base substitution G T missense_variant P206H 617C>A STAD-US 10 102267696 102267696 single base substitution G T missense_variant P46H 137C>A STAD-US 10 102267696 102267696 single base substitution G T upstream_gene_variant STAD-US 10 102267705 102267705 single base substitution T A 3_prime_UTR_variant STAD-US 10 102267705 102267705 single base substitution T A exon_variant STAD-US 10 102267705 102267705 single base substitution T A missense_variant K200M 599A>T STAD-US 10 102267705 102267705 single base substitution T A missense_variant K203M 608A>T STAD-US 10 102267705 102267705 single base substitution T A missense_variant K43M 128A>T STAD-US 10 102267705 102267705 single base substitution T A upstream_gene_variant STAD-US 10 102289218 102289218 single base substitution G T 5_prime_UTR_variant THCA-US 10 102267770 102267770 single base substitution C T 3_prime_UTR_variant THCA-US 10 102267770 102267770 single base substitution C T exon_variant THCA-US 10 102267770 102267770 single base substitution C T synonymous_variant R178R 534G>A THCA-US 10 102267770 102267770 single base substitution C T synonymous_variant R181R 543G>A THCA-US 10 102267770 102267770 single base substitution C T synonymous_variant R21R 63G>A THCA-US 10 102267770 102267770 single base substitution C T upstream_gene_variant UCEC-US 10 102241669 102241669 single base substitution G T downstream_gene_variant UCEC-US 10 102241717 102241717 single base substitution G A downstream_gene_variant UCEC-US 10 102248652 102248652 single base substitution G A 3_prime_UTR_variant UCEC-US 10 102248652 102248652 single base substitution G A exon_variant UCEC-US 10 102248652 102248652 single base substitution G A missense_variant A1084V 3251C>T UCEC-US 10 102248661 102248661 single base substitution C G 3_prime_UTR_variant UCEC-US 10 102248661 102248661 single base substitution C G exon_variant UCEC-US 10 102248661 102248661 single base substitution C G missense_variant S1081T 3242G>C UCEC-US 10 102249071 102249071 single base substitution G T 3_prime_UTR_variant UCEC-US 10 102249071 102249071 single base substitution G T exon_variant UCEC-US 10 102249071 102249071 single base substitution G T intron_variant UCEC-US 10 102249071 102249071 single base substitution G T missense_variant Q1037K 3109C>A UCEC-US 10 102249808 102249808 single base substitution G A 3_prime_UTR_variant UCEC-US 10 102249808 102249808 single base substitution G A downstream_gene_variant UCEC-US 10 102249808 102249808 single base substitution G A exon_variant UCEC-US 10 102249808 102249808 single base substitution G A intron_variant UCEC-US 10 102249808 102249808 single base substitution G A synonymous_variant C974C 2922C>T UCEC-US 10 102249969 102249969 single base substitution C A 3_prime_UTR_variant UCEC-US 10 102249969 102249969 single base substitution C A downstream_gene_variant UCEC-US 10 102249969 102249969 single base substitution C A exon_variant UCEC-US 10 102249969 102249969 single base substitution C A intron_variant UCEC-US 10 102249969 102249969 single base substitution C A missense_variant G921C 2761G>T UCEC-US 10 102249969 102249969 single base substitution C A upstream_gene_variant UCEC-US 10 102249984 102249984 single base substitution G A 3_prime_UTR_variant UCEC-US 10 102249984 102249984 single base substitution G A downstream_gene_variant UCEC-US 10 102249984 102249984 single base substitution G A exon_variant UCEC-US 10 102249984 102249984 single base substitution G A intron_variant UCEC-US 10 102249984 102249984 single base substitution G A missense_variant P916S 2746C>T UCEC-US 10 102249984 102249984 single base substitution G A upstream_gene_variant UCEC-US 10 102250561 102250561 single base substitution C T 3_prime_UTR_variant UCEC-US 10 102250561 102250561 single base substitution C T downstream_gene_variant UCEC-US 10 102250561 102250561 single base substitution C T missense_variant S851N 2552G>A UCEC-US 10 102250561 102250561 single base substitution C T upstream_gene_variant UCEC-US 10 102256985 102256985 single base substitution T A 3_prime_UTR_variant UCEC-US 10 102256985 102256985 single base substitution T A downstream_gene_variant UCEC-US 10 102256985 102256985 single base substitution T A exon_variant UCEC-US 10 102256985 102256985 single base substitution T A intron_variant UCEC-US 10 102256985 102256985 single base substitution T A missense_variant E681D 2043A>T UCEC-US 10 102257899 102257899 single base substitution G A 3_prime_UTR_variant UCEC-US 10 102257899 102257899 single base substitution G A downstream_gene_variant UCEC-US 10 102257899 102257899 single base substitution G A exon_variant UCEC-US 10 102257899 102257899 single base substitution G A synonymous_variant L584L 1750C>T UCEC-US 10 102257953 102257953 single base substitution G A 3_prime_UTR_variant UCEC-US 10 102257953 102257953 single base substitution G A downstream_gene_variant UCEC-US 10 102257953 102257953 single base substitution G A exon_variant UCEC-US 10 102257953 102257953 single base substitution G A missense_variant L566F 1696C>T UCEC-US 10 102262028 102262028 single base substitution G T 3_prime_UTR_variant UCEC-US 10 102262028 102262028 single base substitution G T downstream_gene_variant UCEC-US 10 102262028 102262028 single base substitution G T exon_variant UCEC-US 10 102262028 102262028 single base substitution G T missense_variant L465M 1393C>A UCEC-US 10 102262028 102262028 single base substitution G T upstream_gene_variant UCEC-US 10 102265892 102265892 single base substitution A G 3_prime_UTR_variant UCEC-US 10 102265892 102265892 single base substitution A G downstream_gene_variant UCEC-US 10 102265892 102265892 single base substitution A G exon_variant UCEC-US 10 102265892 102265892 single base substitution A G missense_variant S160P 478T>C UCEC-US 10 102265892 102265892 single base substitution A G missense_variant S317P 949T>C UCEC-US 10 102265892 102265892 single base substitution A G missense_variant S320P 958T>C UCEC-US 10 102267211 102267211 single base substitution C T 3_prime_UTR_variant UCEC-US 10 102267211 102267211 single base substitution C T exon_variant UCEC-US 10 102267211 102267211 single base substitution C T intron_variant UCEC-US 10 102267211 102267211 single base substitution C T synonymous_variant S251S 753G>A UCEC-US 10 102267211 102267211 single base substitution C T synonymous_variant S254S 762G>A UCEC-US 10 102267211 102267211 single base substitution C T synonymous_variant S94S 282G>A UCEC-US 10 102267211 102267211 single base substitution C T upstream_gene_variant UCEC-US 10 102267212 102267212 single base substitution G A 3_prime_UTR_variant UCEC-US 10 102267212 102267212 single base substitution G A exon_variant UCEC-US 10 102267212 102267212 single base substitution G A intron_variant UCEC-US 10 102267212 102267212 single base substitution G A missense_variant S251L 752C>T UCEC-US 10 102267212 102267212 single base substitution G A missense_variant S254L 761C>T UCEC-US 10 102267212 102267212 single base substitution G A missense_variant S94L 281C>T UCEC-US 10 102267212 102267212 single base substitution G A upstream_gene_variant UCEC-US 10 102269110 102269110 single base substitution G A exon_variant UCEC-US 10 102269110 102269110 single base substitution G A intron_variant UCEC-US 10 102269110 102269110 single base substitution G A missense_variant T121M 362C>T UCEC-US 10 102269110 102269110 single base substitution G A upstream_gene_variant UCEC-US 10 102269199 102269199 single base substitution G A exon_variant UCEC-US 10 102269199 102269199 single base substitution G A intron_variant UCEC-US 10 102269199 102269199 single base substitution G A synonymous_variant G91G 273C>T UCEC-US 10 102269199 102269199 single base substitution G A upstream_gene_variant UCEC-US 10 102269201 102269201 single base substitution C T exon_variant UCEC-US 10 102269201 102269201 single base substitution C T intron_variant UCEC-US 10 102269201 102269201 single base substitution C T missense_variant G91S 271G>A UCEC-US 10 102269201 102269201 single base substitution C T upstream_gene_variant UCEC-US 10 102269202 102269202 single base substitution G A exon_variant UCEC-US 10 102269202 102269202 single base substitution G A intron_variant UCEC-US 10 102269202 102269202 single base substitution G A synonymous_variant G90G 270C>T UCEC-US 10 102269202 102269202 single base substitution G A upstream_gene_variant UCEC-US 10 102283617 102283617 single base substitution G A intron_variant UCEC-US 10 102283617 102283617 single base substitution G A upstream_gene_variant UCEC-US 10 102286732 102286732 single base substitution C T splice_region_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-CJ-4923-01 COSM465174 c.1709C>A p.A570D Substitution - Missense 10:100498183-100498183 - STC252 COSM5049830 c.941G>A p.R314Q Substitution - Missense 10:100506143-100506143 - PT48 COSM5932680 c.1660C>T p.P554S Substitution - Missense 10:100498729-100498729 - TCGA-G2-A2EF-01 COSM1296851 c.3072G>A p.M1024I Substitution - Missense 10:100489351-100489351 - TCGA-DJ-A2QC-01 COSM3367856 c.534G>A p.R178R Substitution - coding silent 10:100508013-100508013 - PT38 COSM3433560 c.1859C>T p.S620F Substitution - Missense 10:100498033-100498033 - pfg017T COSM1638417 c.1045-3delC p.? Unknown 10:100505498-100505498 - SNUH_G47_S1 COSM3997734 c.3387C>G p.L1129L Substitution - coding silent 10:100487769-100487769 - RK079_C01 COSM1627280 c.3487T>C p.F1163L Substitution - Missense 10:100487669-100487669 - PD4200a COSM164241 c.890A>T p.Y297F Substitution - Missense 10:100506194-100506194 - YURIF COSM1702908 c.2855C>T p.S952F Substitution - Missense 10:100490118-100490118 - KM12 COSM2058011 c.1023G>A p.Q341Q Substitution - coding silent 10:100506061-100506061 - CSCC-56-T COSM4485921 c.2992C>T p.P998S Substitution - Missense 10:100489735-100489735 - TCGA-FW-A3R5-06 COSM3866346 c.208C>T p.H70Y Substitution - Missense 10:100509507-100509507 - TCGA-EK-A2R8-01 COSM2057965 c.3376G>A p.V1126M Substitution - Missense 10:100487780-100487780 - BD239T COSM5497190 c.657G>T p.L219L Substitution - coding silent 10:100507550-100507550 - 19 COSM5747168 c.308C>T p.T103I Substitution - Missense 10:100509407-100509407 - 2492726 COSM5725433 c.3096G>A p.G1032G Substitution - coding silent 10:100489327-100489327 - PT46 COSM2057993 c.2272G>A p.A758T Substitution - Missense 10:100496296-100496296 - TCGA-EE-A2GR-06 COSM3433555 c.2389C>T p.P797S Substitution - Missense 10:100495468-100495468 - TCGA-BT-A2LB-01 COSM1345314 c.2057A>G p.Y686C Substitution - Missense 10:100497214-100497214 - CRC-03T COSM5451053 c.1461C>T p.Y487Y Substitution - coding silent 10:100499548-100499548 - TCGA-CF-A1HS-01 COSM415203 c.922G>C p.D308H Substitution - Missense 10:100506162-100506162 - TCGA-AN-A046-01 COSM3806279 c.2647C>T p.P883S Substitution - Missense 10:100490709-100490709 - TCGA-IN-7806-01 COSM4011037 c.981G>T p.W327C Substitution - Missense 10:100506103-100506103 - PD9606a COSM5772571 c.3305T>C p.L1102P Substitution - Missense 10:100488082-100488082 - TCGA-D1-A103-01 COSM913934 c.2552G>A p.S851N Substitution - Missense 10:100490804-100490804 - CHC892T COSM4796230 c.886G>A p.V296I Substitution - Missense 10:100506198-100506198 - YUKLAB COSM1702911 c.2110C>T p.Q704* Substitution - Nonsense 10:100497161-100497161 - 2492720 COSM5721572 c.1049C>T p.S350F Substitution - Missense 10:100505491-100505491 - SNUH_G76_S1 COSM426929 c.3505G>T p.A1169S Substitution - Missense 10:100487651-100487651 - CSCC-44-T COSM4474811 c.1943C>T p.A648V Substitution - Missense 10:100497714-100497714 - T3049 COSM2057963 c.3400C>T p.R1134* Substitution - Nonsense 10:100487756-100487756 - PD7188a COSM3769679 c.917G>A p.C306Y Substitution - Missense 10:100506167-100506167 - CSCC-16-T COSM4471651 c.1732C>T p.P578S Substitution - Missense 10:100498160-100498160 - TCGA-A8-A09C-01 COSM426934 c.1681A>G p.K561E Substitution - Missense 10:100498708-100498708 - PCSI_0083_Pa_P COSM3375368 c.1249C>T p.R417C Substitution - Missense 10:100502415-100502415 - TCGA-CG-5733-01 COSM4011030 c.3408G>T p.V1136V Substitution - coding silent 10:100487748-100487748 - CSCC-17-T COSM2057980 c.2696C>T p.P899L Substitution - Missense 10:100490277-100490277 - NCI-H747 COSM2058022 c.402C>A p.G134G Substitution - coding silent 10:100509100-100509100 - TCGA-D9-A1JW-06 COSM3433550 c.2844C>T p.G948G Substitution - coding silent 10:100490129-100490129 - YULAN COSM1702907 c.2969C>T p.P990L Substitution - Missense 10:100489758-100489758 - SNU-C4 COSM4651730 c.1761G>T p.E587D Substitution - Missense 10:100498131-100498131 - PTC-10C COSM4144286 c.266T>C p.V89A Substitution - Missense 10:100509449-100509449 - TCGA-CC-A3MC-01 COSM4919540 c.2579A>G p.N860S Substitution - Missense 10:100490777-100490777 - MedB-1 COSM5621790 c.530A>G p.N177S Substitution - Missense 10:100508017-100508017 - 2492721 COSM5721573 c.431C>T p.S144F Substitution - Missense 10:100509071-100509071 - PT52 COSM5932679 c.1661C>T p.P554L Substitution - Missense 10:100498728-100498728 - TCGA-EI-6882-01 COSM3414618 c.740G>A p.R247H Substitution - Missense 10:100507467-100507467 - TCGA-D1-A16N-01 COSM913939 c.1166G>T p.G389V Substitution - Missense 10:100505374-100505374 - 2492725 COSM5725433 c.3096G>A p.G1032G Substitution - coding silent 10:100489327-100489327 - LUAD-B01811 COSM333726 c.952G>T p.V318L Substitution - Missense 10:100506132-100506132 - TCGA-FW-A3R5-06 COSM3866344 c.2508C>T p.T836T Substitution - coding silent 10:100490848-100490848 - TCGA-D1-A101-01 COSM913941 c.753G>A p.S251S Substitution - coding silent 10:100507454-100507454 - TCGA-EE-A2MU-06 COSM3433563 c.1230G>A p.L410L Substitution - coding silent 10:100502434-100502434 - CSCC-44-T COSM4488718 c.3370C>G p.H1124D Substitution - Missense 10:100487786-100487786 - S00050 COSM318005 c.2218A>G p.T740A Substitution - Missense 10:100496350-100496350 - pfg043T COSM4759544 c.1670T>A p.I557N Substitution - Missense 10:100498719-100498719 - TCGA-DI-A0WH-01 COSM913946 c.270C>T p.G90G Substitution - coding silent 10:100509445-100509445 - SWE-4A COSM1179475 c.3134A>T p.H1045L Substitution - Missense 10:100489289-100489289 - YUNEKI COSM5369930 c.1857C>T p.I619I Substitution - coding silent 10:100498035-100498035 - YUJUBE COSM5369929 c.3370C>T p.H1124Y Substitution - Missense 10:100487786-100487786 - SA225 COSM212565 c.2867C>G p.A956G Substitution - Missense 10:100490106-100490106 - 2521243 COSM3433559 c.1978C>T p.P660S Substitution - Missense 10:100497679-100497679 - TCGA-FD-A3SL-01 COSM3790400 c.1322T>C p.L441S Substitution - Missense 10:100502342-100502342 - OSCC-GB_00900111 COSM4884078 c.227G>T p.S76I Substitution - Missense 10:100509488-100509488 - PT37 COSM5919984 c.2136+7C>T p.? Unknown 10:100497128-100497128 - TCGA-18-3421-01 COSM682496 c.1405C>A p.L469M Substitution - Missense 10:100502259-100502259 - TCGA-BK-A0C9-01 COSM913928 c.3251C>T p.A1084V Substitution - Missense 10:100488895-100488895 - PT27 COSM5905824 c.783-8C>T p.? Unknown 10:100506428-100506428 - YULETA COSM3433556 c.2295C>G p.P765P Substitution - coding silent 10:100496273-100496273 - TCGA-AG-3609-01 COSM288139 c.324G>A p.S108S Substitution - coding silent 10:100509391-100509391 - 3 COSM4166635 c.1517T>C p.L506P Substitution - Missense 10:100499227-100499227 - CSCC-17-T COSM4451797 c.1414A>C p.T472P Substitution - Missense 10:100499595-100499595 - TCGA-GN-A266-06 COSM3433560 c.1859C>T p.S620F Substitution - Missense 10:100498033-100498033 - CSCC-31-T COSM4564238 c.1077_1078CC>TT p.P360S Substitution - Missense 10:100505462-100505463 - OSCC-GB_00980111 COSM913946 c.270C>T p.G90G Substitution - coding silent 10:100509445-100509445 - S00501 COSM315050 c.2087T>G p.V696G Substitution - Missense 10:100497184-100497184 - 2492721 COSM5721575 c.157C>A p.P53T Substitution - Missense 10:100516142-100516142 - CHC892T COSM4796230 c.886G>A p.V296I Substitution - Missense 10:100506198-100506198 - ESO-177 COSM426931 c.3401G>A p.R1134Q Substitution - Missense 10:100487755-100487755 - SNUH_G76_S1 COSM4417597 c.1026T>C p.H342H Substitution - coding silent 10:100506058-100506058 - HCC101T COSM1602864 c.1294A>C p.M432L Substitution - Missense 10:100502370-100502370 - LP6005690-DNA_C01 COSM4409273 c.2237A>T p.Q746L Substitution - Missense 10:100496331-100496331 - 2492723 COSM5721572 c.1049C>T p.S350F Substitution - Missense 10:100505491-100505491 - TCGA-33-4566-01 COSM682498 c.2078A>G p.E693G Substitution - Missense 10:100497193-100497193 - 587336 COSM1225091 c.1024C>T p.H342Y Substitution - Missense 10:100506060-100506060 - TCGA-HU-A4GN-01 COSM4011040 c.608C>A p.P203H Substitution - Missense 10:100507939-100507939 - 2492722 COSM5721573 c.431C>T p.S144F Substitution - Missense 10:100509071-100509071 - TCGA-HU-8602-01 COSM4011032 c.2360C>T p.A787V Substitution - Missense 10:100495497-100495497 - TCGA-AP-A056-01 COSM913940 c.949T>C p.S317P Substitution - Missense 10:100506135-100506135 - BD72T COSM5512691 c.882+4G>T p.? Unknown 10:100506317-100506317 - TCGA-BR-8589-01 COSM4011041 c.599A>T p.K200M Substitution - Missense 10:100507948-100507948 - 2293776 COSM4607452 c.3437C>A p.A1146E Substitution - Missense 10:100487719-100487719 - TP_2064 COSM5570457 c.2783C>T p.T928I Substitution - Missense 10:100490190-100490190 - sysucc-311T COSM5477060 c.764T>C p.V255A Substitution - Missense 10:100507443-100507443 - PD4986a COSM2058009 c.1138C>A p.P380T Substitution - Missense 10:100505402-100505402 - TCGA-DA-A1I1-06 COSM3433556 c.2295C>G p.P765P Substitution - coding silent 10:100496273-100496273 - TCGA-AO-A12D-01 COSM426933 c.2431G>C p.E811Q Substitution - Missense 10:100495426-100495426 - 19 COSM5747170 c.256G>A p.G86R Substitution - Missense 10:100509459-100509459 - TCGA-DK-A3IN-01 COSM3790401 c.562C>G p.H188D Substitution - Missense 10:100507985-100507985 - TCGA-FR-A3YN-06 COSM3433557 c.2294C>T p.P765L Substitution - Missense 10:100496274-100496274 - TCGA-A8-A09C-01 COSM426932 c.2562G>T p.Q854H Substitution - Missense 10:100490794-100490794 - 4_PRE-TREATMENT COSM1724276 c.715C>T p.P239S Substitution - Missense 10:100507492-100507492 - S01297 COSM5667343 c.2265C>T p.G755G Substitution - coding silent 10:100496303-100496303 - S02382 COSM5697703 c.2767A>G p.M923V Substitution - Missense 10:100490206-100490206 - CSCC-56-T COSM1702910 c.2456C>T p.S819F Substitution - Missense 10:100495401-100495401 - TCGA-HU-A4G8-01 COSM4011035 c.1981G>A p.E661K Substitution - Missense 10:100497676-100497676 - TCGA-AK-3427-01 COSM465174 c.1709C>A p.A570D Substitution - Missense 10:100498183-100498183 - TCGA-AD-6895-01 COSM1345320 c.733G>A p.D245N Substitution - Missense 10:100507474-100507474 - C086 COSM5538718 c.2482C>T p.P828S Substitution - Missense 10:100490874-100490874 - TCGA-D1-A163-01 COSM913930 c.3109C>A p.Q1037K Substitution - Missense 10:100489314-100489314 - 2492723 COSM5721573 c.431C>T p.S144F Substitution - Missense 10:100509071-100509071 - LUAD-NYU284 COSM372624 c.381C>T p.L127L Substitution - coding silent 10:100509334-100509334 - C086 COSM5538719 c.2997C>T p.A999A Substitution - coding silent 10:100489730-100489730 - TCGA-D5-6924-01 COSM1345315 c.1680A>T p.T560T Substitution - coding silent 10:100498709-100498709 - PD22360a COSM5792976 c.708T>A p.D236E Substitution - Missense 10:100507499-100507499 - 12586 COSM5613125 c.1988G>C p.C663S Substitution - Missense 10:100497669-100497669 - 2492724 COSM5725433 c.3096G>A p.G1032G Substitution - coding silent 10:100489327-100489327 - S02255 COSM5680362 c.2536G>T p.A846S Substitution - Missense 10:100490820-100490820 - C086 COSM5538717 c.3151C>T p.P1051S Substitution - Missense 10:100489272-100489272 - TCGA-EE-A2MJ-06 COSM3433561 c.1782C>T p.I594I Substitution - coding silent 10:100498110-100498110 - D12 COSM5006863 c.278A>G p.D93G Substitution - Missense 10:100509437-100509437 - T368 COSM4724588 c.1330G>T p.G444* Substitution - Nonsense 10:100502334-100502334 - PTC-28C COSM4144286 c.266T>C p.V89A Substitution - Missense 10:100509449-100509449 - T3446 COSM4724590 c.113G>A p.S38N Substitution - Missense 10:100516186-100516186 - 587284 COSM1225092 c.3455C>T p.A1152V Substitution - Missense 10:100487701-100487701 - 98 COSM5012222 c.1000A>C p.M334L Substitution - Missense 10:100506084-100506084 - 2492723 COSM5721575 c.157C>A p.P53T Substitution - Missense 10:100516142-100516142 - T3267 COSM4724589 c.391C>T p.P131S Substitution - Missense 10:100509324-100509324 - TCGA-D3-A5GO-06 COSM3433562 c.1290C>T p.F430F Substitution - coding silent 10:100502374-100502374 - TCGA-BP-5182-01 COSM465172 c.3086A>T p.E1029V Substitution - Missense 10:100489337-100489337 - PT48 COSM5932679 c.1661C>T p.P554L Substitution - Missense 10:100498728-100498728 - 2492722 COSM5721572 c.1049C>T p.S350F Substitution - Missense 10:100505491-100505491 - C0075T COSM4165367 c.2579A>C p.N860T Substitution - Missense 10:100490777-100490777 - TCGA-JW-A69B-01 COSM4829526 c.3399C>A p.A1133A Substitution - coding silent 10:100487757-100487757 - Gp5D COSM2057988 c.2384delC p.P795fs*67 Deletion - Frameshift 10:100495473-100495473 - LP6005409-DNA_A01 COSM5952020 c.1140C>T p.P380P Substitution - coding silent 10:100505400-100505400 - H1155 COSM1195804 c.2720C>T p.T907I Substitution - Missense 10:100490253-100490253 - TCGA-EE-A3J7-06 COSM3866345 c.1135A>T p.K379* Substitution - Nonsense 10:100505405-100505405 - OSCC-GB_00520111 COSM3709741 c.641T>C p.M214T Substitution - Missense 10:100507566-100507566 - TCGA-AO-A0J5-01 COSM426930 c.3501G>A p.L1167L Substitution - coding silent 10:100487655-100487655 - pfg220T COSM2058009 c.1138C>A p.P380T Substitution - Missense 10:100505402-100505402 - TCGA-D1-A17H-01 COSM913933 c.2746C>T p.P916S Substitution - Missense 10:100490227-100490227 - PCSI_0083_Pa_X COSM3375368 c.1249C>T p.R417C Substitution - Missense 10:100502415-100502415 - 52T COSM3709741 c.641T>C p.M214T Substitution - Missense 10:100507566-100507566 - T1154 COSM4724586 c.3389A>G p.H1130R Substitution - Missense 10:100487767-100487767 - BRC18 COSM5027283 c.3199G>C p.E1067Q Substitution - Missense 10:100488947-100488947 - ESO-075 COSM1265144 c.840T>G p.A280A Substitution - coding silent 10:100506363-100506363 - TCGA-D9-A6EC-06 COSM4405394 c.2878A>C p.S960R Substitution - Missense 10:100490095-100490095 - 2492722 COSM5721575 c.157C>A p.P53T Substitution - Missense 10:100516142-100516142 - TCGA-HC-7742-01 COSM3670415 c.3275C>A p.S1092Y Substitution - Missense 10:100488871-100488871 - TCGA-CG-5721-01 COSM4011031 c.2845C>T p.R949C Substitution - Missense 10:100490128-100490128 - T3064 COSM4724587 c.2702C>T p.P901L Substitution - Missense 10:100490271-100490271 - ESCC_8 COSM315050 c.2087T>G p.V696G Substitution - Missense 10:100497184-100497184 - YURAY COSM4724587 c.2702C>T p.P901L Substitution - Missense 10:100490271-100490271 - TCGA-D3-A2JH-06 COSM3433551 c.2836G>A p.G946S Substitution - Missense 10:100490137-100490137 - SNUH_G76_S1 COSM4144286 c.266T>C p.V89A Substitution - Missense 10:100509449-100509449 - 3N26-VS-3T26 COSM4980073 c.1311G>T p.L437L Substitution - coding silent 10:100502353-100502353 - H2009 COSM1193958 c.3415G>C p.G1139R Substitution - Missense 10:100487741-100487741 - ESCC_BICR_064T COSM5437037 c.3237G>A p.K1079K Substitution - coding silent 10:100488909-100488909 - TCGA-AD-5900-01 COSM1345313 c.3356G>T p.G1119V Substitution - Missense 10:100488031-100488031 - TCGA-BT-A20X-01 COSM1296852 c.935G>T p.C312F Substitution - Missense 10:100506149-100506149 - CSCC-10-T COSM4537281 c.23G>A p.R8Q Substitution - Missense 10:100516930-100516930 - HCT15 COSM2057983 c.2640G>T p.G880G Substitution - coding silent 10:100490716-100490716 - C547 COSM913943 c.362C>T p.T121M Substitution - Missense 10:100509353-100509353 - TCGA-AX-A05Z-01 COSM913944 c.273C>T p.G91G Substitution - coding silent 10:100509442-100509442 - TCGA-BH-A1EY-01 COSM1474300 c.843G>A p.K281K Substitution - coding silent 10:100506360-100506360 - TCGA-D5-5538-01 COSM1345319 c.976G>A p.G326S Substitution - Missense 10:100506108-100506108 - SNUH_G76_S1 COSM4419768 c.387G>C p.L129F Substitution - Missense 10:100509328-100509328 - 06-P036 COSM4573295 c.896T>A p.L299Q Substitution - Missense 10:100506188-100506188 - Gp2D COSM2057988 c.2384delC p.P795fs*67 Deletion - Frameshift 10:100495473-100495473 - ESCC_57 COSM315050 c.2087T>G p.V696G Substitution - Missense 10:100497184-100497184 - CHC2115T COSM4793371 c.2721A>T p.T907T Substitution - coding silent 10:100490252-100490252 - HCC101 COSM1602864 c.1294A>C p.M432L Substitution - Missense 10:100502370-100502370 - S00938 COSM5663188 c.2966-3T>C p.? Unknown 10:100489764-100489764 - TCGA-AX-A060-01 COSM913932 c.2761G>T p.G921C Substitution - Missense 10:100490212-100490212 - 2492721 COSM5721572 c.1049C>T p.S350F Substitution - Missense 10:100505491-100505491 - TCGA-AP-A059-01 COSM913936 c.1750C>T p.L584L Substitution - coding silent 10:100498142-100498142 - TCGA-AP-A059-01 COSM913943 c.362C>T p.T121M Substitution - Missense 10:100509353-100509353 - TCGA-EE-A29R-06 COSM3433559 c.1978C>T p.P660S Substitution - Missense 10:100497679-100497679 - TCGA-D1-A16X-01 COSM913942 c.752C>T p.S251L Substitution - Missense 10:100507455-100507455 - TCGA-FR-A3YO-06 COSM3433558 c.2136+1G>A p.? Unknown 10:100497134-100497134 - CCK81 COSM2057971 c.3116delC p.P1039fs*5 Deletion - Frameshift 10:100489307-100489307 - TCGA-D9-A6EC-06 COSM4401102 c.3216C>T p.P1072P Substitution - coding silent 10:100488930-100488930 - SNUH_G76_S1 COSM1345318 c.994T>G p.S332A Substitution - Missense 10:100506090-100506090 - TCGA-EE-A29E-06 COSM3433549 c.2862C>T p.T954T Substitution - coding silent 10:100490111-100490111 - 2492720 COSM5721573 c.431C>T p.S144F Substitution - Missense 10:100509071-100509071 - TCGA-B5-A11E-01 COSM913937 c.1696C>T p.L566F Substitution - Missense 10:100498196-100498196 - TCGA-BR-8078-01 COSM4011034 c.2185C>T p.R729W Substitution - Missense 10:100496383-100496383 - TCGA-EE-A2GI-06 COSM3433552 c.2713C>T p.P905S Substitution - Missense 10:100490260-100490260 - SNUH_G76_S1 COSM4419114 c.1114C>T p.P372S Substitution - Missense 10:100505426-100505426 - TCGA-D1-A16F-01 COSM913935 c.2043A>T p.E681D Substitution - Missense 10:100497228-100497228 - PD4975a COSM5799956 c.734A>T p.D245V Substitution - Missense 10:100507473-100507473 - TCGA-HU-A4GQ-01 COSM4011039 c.883-1G>T p.? Unknown 10:100506202-100506202 - PT37 COSM5919983 c.2831C>T p.P944L Substitution - Missense 10:100490142-100490142 - TCGA-34-5236-01 COSM682497 c.1871C>A p.A624D Substitution - Missense 10:100497786-100497786 - TCGA-BG-A0MG-01 COSM913945 c.271G>A p.G91S Substitution - Missense 10:100509444-100509444 - YURED COSM1702910 c.2456C>T p.S819F Substitution - Missense 10:100495401-100495401 - 522_T COSM3978026 c.2076G>T p.V692V Substitution - coding silent 10:100497195-100497195 - TCGA-AP-A051-01 COSM913929 c.3242G>C p.S1081T Substitution - Missense 10:100488904-100488904 - TCGA-ER-A19S-06 COSM3433548 c.2918C>T p.P973L Substitution - Missense 10:100490055-100490055 - TCGA-D1-A16Y-01 COSM913931 c.2922C>T p.C974C Substitution - coding silent 10:100490051-100490051 - Gp2D COSM4611682 c.3117delT p.V1040fs*4 Deletion - Frameshift 10:100489306-100489306 - YUDEXA COSM1702909 c.2738C>T p.S913F Substitution - Missense 10:100490235-100490235 - LP6005334-DNA_C03 COSM4408035 c.2127G>A p.M709I Substitution - Missense 10:100497144-100497144 - 2492720 COSM5721575 c.157C>A p.P53T Substitution - Missense 10:100516142-100516142 - TCGA-AN-A046-01 COSM3806281 c.604G>T p.E202* Substitution - Nonsense 10:100507943-100507943 - CSCC-31-T COSM3433553 c.2712C>T p.F904F Substitution - coding silent 10:100490261-100490261 - 4_RESISTANT COSM1724276 c.715C>T p.P239S Substitution - Missense 10:100507492-100507492 - TCGA-HU-A4GU-01 COSM4011033 c.2335C>T p.R779W Substitution - Missense 10:100495522-100495522 - TCGA-EB-A431-01 COSM3433553 c.2712C>T p.F904F Substitution - coding silent 10:100490261-100490261 - TCGA-CM-6171-01 COSM1345314 c.2057A>G p.Y686C Substitution - Missense 10:100497214-100497214 - PCSI_0083_Pa_P_526 COSM3375368 c.1249C>T p.R417C Substitution - Missense 10:100502415-100502415 - YURAY COSM5369931 c.1328C>T p.S443L Substitution - Missense 10:100502336-100502336 - YUKLAB COSM1702912 c.2106C>G p.C702W Substitution - Missense 10:100497165-100497165 - CSCC-55-T COSM4483752 c.2731C>T p.P911S Substitution - Missense 10:100490242-100490242 - AOCS-091-3-0 COSM3952758 c.348G>C p.Q116H Substitution - Missense 10:100509367-100509367 - TCGA-59-2351-01 COSM72579 c.2390C>G p.P797R Substitution - Missense 10:100495467-100495467 - CHC2115T COSM4793371 c.2721A>T p.T907T Substitution - coding silent 10:100490252-100490252 - TCGA-EE-A2GJ-06 COSM3433554 c.2605C>T p.P869S Substitution - Missense 10:100490751-100490751 - TCGA-HU-A4H8-01 COSM2057967 c.3278C>T p.A1093V Substitution - Missense 10:100488868-100488868 - TCGA-EE-A2GC-06 COSM3433564 c.716C>T p.P239L Substitution - Missense 10:100507491-100507491 - TCGA-HU-A4H3-01 COSM4011038 c.926T>C p.V309A Substitution - Missense 10:100506158-100506158 - ESO-187 COSM1265145 c.1935G>T p.E645D Substitution - Missense 10:100497722-100497722 - TCGA-AN-A0AK-01 COSM3806280 c.976G>T p.G326C Substitution - Missense 10:100506108-100506108 - SC_9008 COSM5564119 c.3263G>A p.R1088H Substitution - Missense 10:100488883-100488883 - TCGA-DD-A39Y-01 COSM4934472 c.151A>G p.R51G Substitution - Missense 10:100516148-100516148 - TCGA-D7-8579-01 COSM4011036 c.1786G>T p.A596S Substitution - Missense 10:100498106-100498106 - TCGA-EE-A2MR-06 COSM3433547 c.3103C>T p.P1035S Substitution - Missense 10:100489320-100489320 - CLN3 COSM5024625 c.1789C>T p.Q597* Substitution - Nonsense 10:100498103-100498103 - TCGA-B5-A11E-01 COSM913938 c.1393C>A p.L465M Substitution - Missense 10:100502271-100502271 - C086 COSM3433553 c.2712C>T p.F904F Substitution - coding silent 10:100490261-100490261 - 1N31-VS-1T31 COSM4974239 c.171G>A p.L57L Substitution - coding silent 10:100516128-100516128 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.18889 10q24.31 610258

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.2472+12T>G 10 102255130 CM A C Missense p.V696G c.2087T>G 10 102256941 SCLC A C Synonymous p.A280A c.840T>G 10 102266120 ESCA A G Missense p.F1163L c.3487T>C 10 102247426 HC C A Missense p.A805S c.2413G>T 10 102255201 LUAD C A Missense p.C312F c.935G>T 10 102265906 BLCA C A Missense p.E645D c.1935G>T 10 102257479 ESCA C A Missense p.G690V c.2069G>T 10 102256959 HNSC C A Missense p.G921C c.2761G>T 10 102249969 UCEC C A Missense p.Q854H c.2562G>T 10 102250551 BRCA C A Missense p.R314L c.941G>T 10 102265900 LUAD C A Nonsense p.E1110* c.3328G>T 10 102247816 HNSC C A Synonymous p.T121T c.363G>T 10 102269109 LUAD C A Synonymous p.V1136V c.3408G>T 10 102247505 STAD CC AA MultiAAMissense p.W699_A700delinsCS c.2097_2098delinsTT 10 102256930 LUAD CC TT IntronicBlockSubstitution . c.1045-107_1045-106delinsAA 10 102265358 CM C G Missense p.C663S c.1988G>C 10 102257426 NSCLC C G Missense p.D308H c.922G>C 10 102265919 BLCA C G Missense p.E1067Q c.3199G>C 10 102248704 BRCA C G Missense p.E811Q c.2431G>C 10 102255183 BRCA C G Synonymous p.L942L c.2826G>C 10 102249904 LUAD C G Synonymous p.R729R c.2187G>C 10 102256138 LUAD C T Missense p.E1131K c.3391G>A 10 102247522 HNSC C T Missense p.G946S c.2836G>A 10 102249894 CM C T Missense p.M1014I c.3042G>A 10 102249138 HNSC C T Missense p.M1024I c.3072G>A 10 102249108 BLCA C T Missense p.R1134Q c.3401G>A 10 102247512 BRCA C T Synonymous p.K281K c.843G>A 10 102266117 BRCA C T Synonymous p.L1102L c.3306G>A 10 102247838 BRCA C T Synonymous p.L1167L c.3501G>A 10 102247412 BRCA C T Synonymous p.L410L c.1230G>A 10 102262191 CM C T Synonymous p.R178R c.534G>A 10 102267770 THCA C T Synonymous p.S108S c.324G>A 10 102269148 COREAD C T Synonymous p.S251S c.753G>A 10 102267211 UCEC G A IntronicSNV . c.1045-135C>T 10 102265387 CM G A IntronicSNV . c.1045-8C>T 10 102265260 CM G A IntronicSNV . c.1045-8C>T 10 102265260 STAD G A IntronicSNV . c.1485+82C>T 10 102259199 CM G A IntronicSNV . c.3172-19C>T 10 102248750 CM G A Missense p.P239L c.716C>T 10 102267248 CM G A Missense p.P660S c.1978C>T 10 102257436 CM G A Missense p.P797S c.2389C>T 10 102255225 CM G A Missense p.P869S c.2605C>T 10 102250508 CM G A Missense p.P905S c.2713C>T 10 102250017 CM G A Missense p.P916S c.2746C>T 10 102249984 UCEC G A Missense p.P947L c.2840C>T 10 102249890 CM G A Missense p.P973L c.2918C>T 10 102249812 CM G A Missense p.S108L c.323C>T 10 102269149 BRCA G A Missense p.S391L c.1172C>T 10 102265125 CM G A Synonymous p.C974C c.2922C>T 10 102249808 UCEC G A Synonymous p.F798F c.2394C>T 10 102255220 CM G A Synonymous p.G90G c.270C>T 10 102269202 UCEC G A Synonymous p.G948G c.2844C>T 10 102249886 CM G A Synonymous p.I594I c.1782C>T 10 102257867 CM G A Synonymous p.L55L c.163C>T 10 102275893 CM G C Missense p.A956G c.2867C>G 10 102249863 BRCA G C Missense p.H188D c.562C>G 10 102267742 BLCA G C Missense p.P797R c.2390C>G 10 102255224 OV G C Synonymous p.P1035P c.3105C>G 10 102249075 LUAD G C Synonymous p.P765P c.2295C>G 10 102256030 CM GG AA Missense p.P1035F c.3103_3104delinsTT 10 102249076 CM G - IntronicDeletion . c.1045-3delC 10 102265255 STAD G T Missense p.A624D c.1871C>A 10 102257543 LUSC G T Missense p.L469M c.1405C>A 10 102262016 LUSC G T Missense p.P998Q c.2993C>A 10 102249491 LUAD G T Missense p.Q1037K c.3109C>A 10 102249071 UCEC G T Missense p.S1092Y c.3275C>A 10 102248628 PRAD G T Missense p.T472N c.1415C>A 10 102259351 CM T A IntronicSNV . c.1045-101A>T 10 102265353 RCCC T A Missense p.E1029V c.3086A>T 10 102249094 RCCC T A Missense p.E681D c.2043A>T 10 102256985 UCEC T A Missense p.Q1031L c.3092A>T 10 102249088 LUAD T A Missense p.Y297F c.890A>T 10 102265951 BRCA T A Nonsense p.K379* c.1135A>T 10 102265162 CM T A Synonymous p.I225I c.675A>T 10 102267289 HNSC T C Missense p.K561E c.1681A>G 10 102258465 BRCA T C Missense p.M719V c.2155A>G 10 102256170 LUAD T C Missense p.T740A c.2218A>G 10 102256107 SCLC T C Missense p.Y686C c.2057A>G 10 102256971 BLCA T C Synonymous p.Q460Q c.1380A>G 10 102262041 CM T G Missense p.M1164L c.3490A>C 10 102247423 STAD