Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 9 125645584 125645584 + Missense_Mutation SNP C C A TCGA-OR-A5JB-01A-11D-A29I-10 TCGA-OR-A5JB-10A-01D-A29L-10 g.chr9:125645584C>A c.658G>T c.(658-660)Gta>Tta p.V220L BLCA 9 125613386 125613386 + Missense_Mutation SNP C C G TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr9:125613386C>G c.3354G>C c.(3352-3354)caG>caC p.Q1118H BLCA 9 125617570 125617570 + Nonsense_Mutation SNP G G C TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr9:125617570G>C c.2708C>G c.(2707-2709)tCa>tGa p.S903* BLCA 9 125621070 125621070 + Missense_Mutation SNP C C G TCGA-CF-A9FF-01A-11D-A38G-08 TCGA-CF-A9FF-10A-01D-A38J-08 g.chr9:125621070C>G c.2161G>C c.(2161-2163)Gat>Cat p.D721H BLCA 9 125621301 125621301 + Nonsense_Mutation SNP C C A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr9:125621301C>A c.1930G>T c.(1930-1932)Gag>Tag p.E644* BLCA 9 125621378 125621378 + Missense_Mutation SNP T T A TCGA-PQ-A6FI-01A-11D-A31L-08 TCGA-PQ-A6FI-10A-01D-A31J-08 g.chr9:125621378T>A c.1853A>T c.(1852-1854)tAc>tTc p.Y618F BLCA 9 125642878 125642878 + Missense_Mutation SNP C C G TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr9:125642878C>G c.955G>C c.(955-957)Gat>Cat p.D319H BLCA 9 125643058 125643058 + Nonsense_Mutation SNP C C A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr9:125643058C>A c.775G>T c.(775-777)Gaa>Taa p.E259* BRCA 9 125616341 125616341 + Nonsense_Mutation SNP G G A TCGA-AN-A0XW-01A-11D-A10G-09 TCGA-AN-A0XW-10A-01D-A10G-09 g.chr9:125616341G>A c.3007C>T c.(3007-3009)Cag>Tag p.Q1003* BRCA 9 125618153 125618153 + Nonsense_Mutation SNP G G C TCGA-A8-A094-01A-11W-A019-09 TCGA-A8-A094-10A-01W-A021-09 g.chr9:125618153G>C c.2459C>G c.(2458-2460)tCa>tGa p.S820* BRCA 9 125621108 125621108 + Missense_Mutation SNP C C T TCGA-EW-A1OV-01A-11D-A142-09 TCGA-EW-A1OV-10A-01D-A142-09 g.chr9:125621108C>T c.2123G>A c.(2122-2124)cGa>cAa p.R708Q BRCA 9 125621114 125621114 + Missense_Mutation SNP T T C TCGA-D8-A140-01A-11D-A10Y-09 TCGA-D8-A140-10A-01D-A110-09 g.chr9:125621114T>C c.2117A>G c.(2116-2118)tAc>tGc p.Y706C BRCA 9 125622277 125622277 + Missense_Mutation SNP G G C TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr9:125622277G>C c.1768C>G c.(1768-1770)Cct>Gct p.P590A BRCA 9 125642124 125642124 + Silent SNP C C T TCGA-BH-A0W7-01A-11D-A10Y-09 TCGA-BH-A0W7-10A-01D-A110-09 g.chr9:125642124C>T c.1122G>A c.(1120-1122)ctG>ctA p.L374L BRCA 9 125652667 125652667 + Silent SNP C C T TCGA-E9-A1RH-01A-21D-A167-09 TCGA-E9-A1RH-10A-01D-A167-09 g.chr9:125652667C>T c.507G>A c.(505-507)caG>caA p.Q169Q BRCA 9 125659702 125659702 + Silent SNP G G A TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr9:125659702G>A c.87C>T c.(85-87)atC>atT p.I29I CESC 9 125613673 125613673 + Missense_Mutation SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr9:125613673C>G c.3160G>C c.(3160-3162)Gat>Cat p.D1054H CESC 9 125616293 125616293 + Missense_Mutation SNP C C A TCGA-JW-A852-01A-11D-A351-09 TCGA-JW-A852-10A-01D-A351-09 g.chr9:125616293C>A c.3055G>T c.(3055-3057)Gat>Tat p.D1019Y CESC 9 125617541 125617541 + Missense_Mutation SNP G G A TCGA-EA-A50E-01A-21D-A26G-09 TCGA-EA-A50E-10A-01D-A26G-09 g.chr9:125617541G>A c.2737C>T c.(2737-2739)Cgt>Tgt p.R913C CESC 9 125621235 125621235 + Nonsense_Mutation SNP G G A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr9:125621235G>A c.1996C>T c.(1996-1998)Cga>Tga p.R666* CESC 9 125639816 125639816 + Missense_Mutation SNP C C G TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr9:125639816C>G c.1259G>C c.(1258-1260)cGa>cCa p.R420P CESC 9 125645647 125645647 + Missense_Mutation SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr9:125645647C>G c.595G>C c.(595-597)Gag>Cag p.E199Q CHOL 9 125613429 125613429 + Missense_Mutation SNP G G T TCGA-W5-AA2X-01A-11D-A417-09 TCGA-W5-AA2X-10A-01D-A41A-09 g.chr9:125613429G>T c.3311C>A c.(3310-3312)cCa>cAa p.P1104Q COAD 9 125611951 125611951 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:125611951G>A c.3531C>T c.(3529-3531)aaC>aaT p.N1177N COAD 9 125612009 125612011 + In_Frame_Del DEL GTG GTG - TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chr9:125612009_125612011delGTG c.3471_3473delCAC c.(3469-3474)accaca>aca p.1157_1158TT>T COAD 9 125612077 125612077 + Silent SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:125612077C>T c.3405G>A c.(3403-3405)ccG>ccA p.P1135P COAD 9 125612088 125612088 + Frame_Shift_Del DEL T T - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr9:125612088delT c.3394delA c.(3394-3396)acafs p.T1132fs COAD 9 125616176 125616176 + Intron SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr9:125616176C>T COAD 9 125616529 125616529 + Missense_Mutation SNP T T C TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr9:125616529T>C c.2917A>G c.(2917-2919)Act>Gct p.T973A COAD 9 125621109 125621109 + Nonsense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:125621109G>A c.2122C>T c.(2122-2124)Cga>Tga p.R708* COAD 9 125622278 125622278 + Silent SNP A A G TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr9:125622278A>G c.1767T>C c.(1765-1767)taT>taC p.Y589Y COAD 9 125622279 125622279 + Missense_Mutation SNP T T C TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr9:125622279T>C c.1766A>G c.(1765-1767)tAt>tGt p.Y589C COAD 9 125622280 125622280 + Missense_Mutation SNP A A G TCGA-CK-6748-01A-11D-1835-10 TCGA-CK-6748-10A-01D-1835-10 g.chr9:125622280A>G c.1765T>C c.(1765-1767)Tat>Cat p.Y589H COAD 9 125622280 125622280 + Missense_Mutation SNP A A G TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr9:125622280A>G c.1765T>C c.(1765-1767)Tat>Cat p.Y589H COAD 9 125622280 125622280 + Missense_Mutation SNP A A T TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr9:125622280A>T c.1765T>A c.(1765-1767)Tat>Aat p.Y589N COAD 9 125655207 125655207 + Frame_Shift_Del DEL T T - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr9:125655207delT c.330delA c.(328-330)aaafs p.K110fs COADREAD 9 125611951 125611951 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:125611951G>A c.3531C>T c.(3529-3531)aaC>aaT p.N1177N COADREAD 9 125612009 125612011 + In_Frame_Del DEL GTG GTG - TCGA-F4-6806-01A-11D-1835-10 TCGA-F4-6806-10A-01D-1835-10 g.chr9:125612009_125612011delGTG c.3471_3473delCAC c.(3469-3474)accaca>aca p.1157_1158TT>T COADREAD 9 125612077 125612077 + Silent SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr9:125612077C>T c.3405G>A c.(3403-3405)ccG>ccA p.P1135P COADREAD 9 125612088 125612088 + Frame_Shift_Del DEL T T - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr9:125612088delT c.3394delA c.(3394-3396)acafs p.T1132fs COADREAD 9 125616176 125616176 + Intron SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr9:125616176C>T COADREAD 9 125616529 125616529 + Missense_Mutation SNP T T C TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr9:125616529T>C c.2917A>G c.(2917-2919)Act>Gct p.T973A COADREAD 9 125621109 125621109 + Nonsense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:125621109G>A c.2122C>T c.(2122-2124)Cga>Tga p.R708* COADREAD 9 125622278 125622278 + Silent SNP A A G TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr9:125622278A>G c.1767T>C c.(1765-1767)taT>taC p.Y589Y COADREAD 9 125622278 125622278 + Silent SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr9:125622278A>G c.1767T>C c.(1765-1767)taT>taC p.Y589Y COADREAD 9 125622279 125622279 + Missense_Mutation SNP T T C TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr9:125622279T>C c.1766A>G c.(1765-1767)tAt>tGt p.Y589C COADREAD 9 125622280 125622280 + Missense_Mutation SNP A A G TCGA-CK-6748-01A-11D-1835-10 TCGA-CK-6748-10A-01D-1835-10 g.chr9:125622280A>G c.1765T>C c.(1765-1767)Tat>Cat p.Y589H COADREAD 9 125622280 125622280 + Missense_Mutation SNP A A G TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr9:125622280A>G c.1765T>C c.(1765-1767)Tat>Cat p.Y589H COADREAD 9 125622280 125622280 + Missense_Mutation SNP A A T TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr9:125622280A>T c.1765T>A c.(1765-1767)Tat>Aat p.Y589N COADREAD 9 125655189 125655189 + Splice_Site SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:125655189T>G c.348A>C c.(346-348)aaA>aaC p.K116N COADREAD 9 125655207 125655207 + Frame_Shift_Del DEL T T - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr9:125655207delT c.330delA c.(328-330)aaafs p.K110fs COADREAD 9 125659649 125659649 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:125659649C>T c.140G>A c.(139-141)cGa>cAa p.R47Q DLBC 9 125639808 125639808 + Missense_Mutation SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr9:125639808C>T c.1267G>A c.(1267-1269)Ggg>Agg p.G423R ESCA 9 125621075 125621075 + Missense_Mutation SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr9:125621075G>T c.2156C>A c.(2155-2157)cCa>cAa p.P719Q ESCA 9 125621243 125621243 + Missense_Mutation SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr9:125621243G>T c.1988C>A c.(1987-1989)cCt>cAt p.P663H ESCA 9 125639797 125639797 + Silent SNP T T C TCGA-LN-A4A6-01A-11D-A27G-09 TCGA-LN-A4A6-10A-01D-A27G-09 g.chr9:125639797T>C c.1278A>G c.(1276-1278)ccA>ccG p.P426P ESCA 9 125652614 125652614 + Missense_Mutation SNP C C A TCGA-V5-AASX-01A-11D-A387-09 TCGA-V5-AASX-10A-01D-A38A-09 g.chr9:125652614C>A c.560G>T c.(559-561)cGa>cTa p.R187L ESCA 9 125652626 125652626 + Missense_Mutation SNP G G T TCGA-IG-A4P3-01A-11D-A27G-09 TCGA-IG-A4P3-10A-01D-A27G-09 g.chr9:125652626G>T c.548C>A c.(547-549)gCt>gAt p.A183D ESCA 9 125659575 125659575 + Missense_Mutation SNP G G T TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr9:125659575G>T c.214C>A c.(214-216)Cag>Aag p.Q72K ESCA 9 125659702 125659702 + Silent SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr9:125659702G>T c.87C>A c.(85-87)atC>atA p.I29I GBM 9 125617558 125617558 + Missense_Mutation SNP G G A TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr9:125617558G>A c.2720C>T c.(2719-2721)gCg>gTg p.A907V GBMLGG 9 125617558 125617558 + Missense_Mutation SNP G G A TCGA-06-5858-01A-01D-1696-08 TCGA-06-5858-10A-01D-1696-08 g.chr9:125617558G>A c.2720C>T c.(2719-2721)gCg>gTg p.A907V GBMLGG 9 125618095 125618095 + Nonsense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:125618095C>T c.2517G>A c.(2515-2517)tgG>tgA p.W839* GBMLGG 9 125639774 125639774 + Missense_Mutation SNP G G A TCGA-RY-A83Z-01A-11D-A36O-08 TCGA-RY-A83Z-10A-01D-A367-08 g.chr9:125639774G>A c.1301C>T c.(1300-1302)gCc>gTc p.A434V GBMLGG 9 125652610 125652610 + Silent SNP T T A TCGA-S9-A89Z-01A-11D-A36O-08 TCGA-S9-A89Z-10A-01D-A367-08 g.chr9:125652610T>A c.564A>T c.(562-564)ggA>ggT p.G188G HNSC 9 125618102 125618102 + Missense_Mutation SNP G G A TCGA-BA-A4IF-01A-11D-A25Y-08 TCGA-BA-A4IF-10A-01D-A25Y-08 g.chr9:125618102G>A c.2510C>T c.(2509-2511)tCt>tTt p.S837F HNSC 9 125618118 125618118 + Missense_Mutation SNP G G A TCGA-BA-A4IF-01A-11D-A25Y-08 TCGA-BA-A4IF-10A-01D-A25Y-08 g.chr9:125618118G>A c.2494C>T c.(2494-2496)Cat>Tat p.H832Y HNSC 9 125618124 125618124 + Missense_Mutation SNP C C T TCGA-BA-6870-01A-11D-1870-08 TCGA-BA-6870-10A-01D-1870-08 g.chr9:125618124C>T c.2488G>A c.(2488-2490)Gaa>Aaa p.E830K HNSC 9 125621230 125621230 + Missense_Mutation SNP C C T TCGA-BA-6870-01A-11D-1870-08 TCGA-BA-6870-10A-01D-1870-08 g.chr9:125621230C>T c.2001G>A c.(1999-2001)atG>atA p.M667I HNSC 9 125622334 125622334 + Missense_Mutation SNP C C G TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr9:125622334C>G c.1711G>C c.(1711-1713)Gag>Cag p.E571Q HNSC 9 125627747 125627747 + Silent SNP C C T TCGA-D6-8569-01A-11D-2394-08 TCGA-D6-8569-10A-01D-2394-08 g.chr9:125627747C>T c.1515G>A c.(1513-1515)caG>caA p.Q505Q HNSC 9 125642045 125642045 + Missense_Mutation SNP C C G TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr9:125642045C>G c.1201G>C c.(1201-1203)Gag>Cag p.E401Q HNSC 9 125642364 125642364 + Missense_Mutation SNP A A G TCGA-BB-A6UO-01A-12D-A34J-08 TCGA-BB-A6UO-10A-01D-A34M-08 g.chr9:125642364A>G c.1001T>C c.(1000-1002)tTg>tCg p.L334S HNSC 9 125643074 125643074 + Splice_Site SNP C C A TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr9:125643074C>A c.e5-1 KICH 9 125616244 125616244 + Missense_Mutation SNP A A G TCGA-KL-8344-01A-11D-2310-10 TCGA-KL-8344-11A-01D-2310-10 g.chr9:125616244A>G c.3104T>C c.(3103-3105)cTa>cCa p.L1035P KICH 9 125620200 125620200 + Splice_Site SNP A A G TCGA-KN-8423-01A-11D-2310-10 TCGA-KN-8423-11A-01D-2310-10 g.chr9:125620200A>G c.e12+1 KICH 9 125639808 125639808 + Missense_Mutation SNP C C T TCGA-KN-8430-01A-11D-2310-10 TCGA-KN-8430-11A-01D-2311-10 g.chr9:125639808C>T c.1267G>A c.(1267-1269)Ggg>Agg p.G423R KIPAN 9 125612011 125612011 + Silent SNP G G C TCGA-4A-A93W-01A-11D-A36X-10 TCGA-4A-A93W-10A-01D-A370-10 g.chr9:125612011G>C c.3471C>G c.(3469-3471)acC>acG p.T1157T KIPAN 9 125612089 125612089 + Missense_Mutation SNP T T G TCGA-A4-A7UZ-01A-12D-A34Z-10 TCGA-A4-A7UZ-10A-01D-A34Z-10 g.chr9:125612089T>G c.3393A>C c.(3391-3393)aaA>aaC p.K1131N KIPAN 9 125616244 125616244 + Missense_Mutation SNP A A G TCGA-KL-8344-01A-11D-2310-10 TCGA-KL-8344-11A-01D-2310-10 g.chr9:125616244A>G c.3104T>C c.(3103-3105)cTa>cCa p.L1035P KIPAN 9 125620200 125620200 + Splice_Site SNP A A G TCGA-KN-8423-01A-11D-2310-10 TCGA-KN-8423-11A-01D-2310-10 g.chr9:125620200A>G c.e12+1 KIPAN 9 125621286 125621286 + Missense_Mutation SNP G G T TCGA-CJ-4874-01A-01D-1373-10 TCGA-CJ-4874-11A-01D-1373-10 g.chr9:125621286G>T c.1945C>A c.(1945-1947)Cct>Act p.P649T KIPAN 9 125639776 125639776 + Frame_Shift_Del DEL A A - TCGA-CZ-5459-01A-01D-1501-10 TCGA-CZ-5459-11A-01D-1501-10 g.chr9:125639776delA c.1299delT c.(1297-1299)tttfs p.F433fs KIPAN 9 125639808 125639808 + Missense_Mutation SNP C C T TCGA-KN-8430-01A-11D-2310-10 TCGA-KN-8430-11A-01D-2311-10 g.chr9:125639808C>T c.1267G>A c.(1267-1269)Ggg>Agg p.G423R KIRC 9 125621286 125621286 + Missense_Mutation SNP G G T TCGA-CJ-4874-01A-01D-1373-10 TCGA-CJ-4874-11A-01D-1373-10 g.chr9:125621286G>T c.1945C>A c.(1945-1947)Cct>Act p.P649T KIRC 9 125639776 125639776 + Frame_Shift_Del DEL A A - TCGA-CZ-5459-01A-01D-1501-10 TCGA-CZ-5459-11A-01D-1501-10 g.chr9:125639776delA c.1299delT c.(1297-1299)tttfs p.F433fs KIRP 9 125612011 125612011 + Silent SNP G G C TCGA-4A-A93W-01A-11D-A36X-10 TCGA-4A-A93W-10A-01D-A370-10 g.chr9:125612011G>C c.3471C>G c.(3469-3471)acC>acG p.T1157T KIRP 9 125612089 125612089 + Missense_Mutation SNP T T G TCGA-A4-A7UZ-01A-12D-A34Z-10 TCGA-A4-A7UZ-10A-01D-A34Z-10 g.chr9:125612089T>G c.3393A>C c.(3391-3393)aaA>aaC p.K1131N LGG 9 125618095 125618095 + Nonsense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:125618095C>T c.2517G>A c.(2515-2517)tgG>tgA p.W839* LGG 9 125639774 125639774 + Missense_Mutation SNP G G A TCGA-RY-A83Z-01A-11D-A36O-08 TCGA-RY-A83Z-10A-01D-A367-08 g.chr9:125639774G>A c.1301C>T c.(1300-1302)gCc>gTc p.A434V LGG 9 125652610 125652610 + Silent SNP T T A TCGA-S9-A89Z-01A-11D-A36O-08 TCGA-S9-A89Z-10A-01D-A367-08 g.chr9:125652610T>A c.564A>T c.(562-564)ggA>ggT p.G188G LIHC 9 125613389 125613389 + Silent SNP T T C TCGA-CC-A3MB-01A-11D-A20W-10 TCGA-CC-A3MB-10A-01D-A20W-10 g.chr9:125613389T>C c.3351A>G c.(3349-3351)aaA>aaG p.K1117K LIHC 9 125642094 125642094 + Silent SNP T T C TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr9:125642094T>C c.1152A>G c.(1150-1152)gtA>gtG p.V384V LIHC 9 125652757 125652757 + Frame_Shift_Del DEL G G - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr9:125652757delG c.417delC c.(415-417)aacfs p.N139fs LUAD 9 125613379 125613379 + Missense_Mutation SNP C C G TCGA-78-7160-01A-11D-2036-08 TCGA-78-7160-10A-01D-2036-08 g.chr9:125613379C>G c.3361G>C c.(3361-3363)Ggt>Cgt p.G1121R LUAD 9 125613429 125613429 + Missense_Mutation SNP G G A TCGA-55-7725-01A-11D-2167-08 TCGA-55-7725-10A-01D-2167-08 g.chr9:125613429G>A c.3311C>T c.(3310-3312)cCa>cTa p.P1104L LUAD 9 125613500 125613500 + Missense_Mutation SNP C C A TCGA-05-4244-01A-01D-1105-08 TCGA-05-4244-10A-01D-1105-08 g.chr9:125613500C>A c.3240G>T c.(3238-3240)ttG>ttT p.L1080F LUAD 9 125617600 125617600 + Missense_Mutation SNP A A C TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr9:125617600A>C c.2678T>G c.(2677-2679)aTa>aGa p.I893R LUAD 9 125617621 125617621 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr9:125617621C>A c.2657G>T c.(2656-2658)aGg>aTg p.R886M LUAD 9 125618088 125618088 + Missense_Mutation SNP C C A TCGA-80-5608-01A-31D-1945-08 TCGA-80-5608-10A-01D-1946-08 g.chr9:125618088C>A c.2524G>T c.(2524-2526)Ggc>Tgc p.G842C LUAD 9 125620205 125620205 + Silent SNP C C A TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr9:125620205C>A c.2451G>T c.(2449-2451)gcG>gcT p.A817A LUAD 9 125620998 125620998 + Missense_Mutation SNP C C A TCGA-17-Z018-01A-01W-0746-08 TCGA-17-Z018-11A-01W-0746-08 g.chr9:125620998C>A c.2233G>T c.(2233-2235)Gtg>Ttg p.V745L LUAD 9 125621032 125621032 + Silent SNP C C A TCGA-91-6836-01A-21D-1855-08 TCGA-91-6836-11A-01D-1855-08 g.chr9:125621032C>A c.2199G>T c.(2197-2199)cgG>cgT p.R733R LUAD 9 125621297 125621297 + Missense_Mutation SNP G G A TCGA-86-8076-01A-31D-2238-08 TCGA-86-8076-10A-01D-2238-08 g.chr9:125621297G>A c.1934C>T c.(1933-1935)tCc>tTc p.S645F LUAD 9 125621313 125621313 + Missense_Mutation SNP T T A TCGA-J2-8194-01A-11D-2238-08 TCGA-J2-8194-10A-01D-2238-08 g.chr9:125621313T>A c.1918A>T c.(1918-1920)Aat>Tat p.N640Y LUAD 9 125621336 125621336 + Missense_Mutation SNP C C A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr9:125621336C>A c.1895G>T c.(1894-1896)tGt>tTt p.C632F LUAD 9 125622316 125622316 + Missense_Mutation SNP G G T TCGA-95-7944-01A-11D-2184-08 TCGA-95-7944-10A-01D-2184-08 g.chr9:125622316G>T c.1729C>A c.(1729-1731)Caa>Aaa p.Q577K LUAD 9 125627701 125627701 + Missense_Mutation SNP C C A TCGA-91-A4BC-01A-11D-A24D-08 TCGA-91-A4BC-10A-01D-A24F-08 g.chr9:125627701C>A c.1561G>T c.(1561-1563)Gtg>Ttg p.V521L LUAD 9 125642152 125642152 + Splice_Site SNP T T G TCGA-55-6982-01A-11D-1945-08 TCGA-55-6982-11A-01D-1945-08 g.chr9:125642152T>G c.1094A>C c.(1093-1095)gAc>gCc p.D365A LUAD 9 125642884 125642884 + Missense_Mutation SNP T T C TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr9:125642884T>C c.949A>G c.(949-951)Atc>Gtc p.I317V LUAD 9 125643034 125643034 + Nonsense_Mutation SNP T T A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr9:125643034T>A c.799A>T c.(799-801)Aag>Tag p.K267* LUAD 9 125659558 125659558 + Splice_Site SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr9:125659558C>A c.231G>T c.(229-231)caG>caT p.Q77H LUAD 9 125659558 125659558 + Splice_Site SNP C C G TCGA-91-A4BC-01A-11D-A24D-08 TCGA-91-A4BC-10A-01D-A24F-08 g.chr9:125659558C>G c.231G>C c.(229-231)caG>caC p.Q77H LUSC 9 125613661 125613661 + Nonsense_Mutation SNP C C A TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr9:125613661C>A c.3172G>T c.(3172-3174)Gag>Tag p.E1058* LUSC 9 125655289 125655289 + Missense_Mutation SNP G G A TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr9:125655289G>A c.248C>T c.(247-249)tCa>tTa p.S83L OV 9 125622280 125622280 + Missense_Mutation SNP A A G TCGA-13-0903-01A-01W-0421-09 TCGA-13-0903-10A-01W-0421-09 g.chr9:125622280A>G c.1765T>C c.(1765-1767)Tat>Cat p.Y589H OV 9 125642404 125642404 + Splice_Site SNP G G A TCGA-24-1845-01A-01W-0639-09 TCGA-24-1845-10A-01W-0639-09 g.chr9:125642404G>A c.961C>T c.(961-963)Cta>Tta p.L321L PAAD 9 125627791 125627791 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:125627791G>A c.1471C>T c.(1471-1473)Cca>Tca p.P491S PAAD 9 125652725 125652725 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:125652725C>A c.449G>T c.(448-450)aGa>aTa p.R150I PAAD 9 125659639 125659639 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:125659639A>G c.150T>C c.(148-150)tgT>tgC p.C50C PAAD 9 125659725 125659725 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:125659725C>T c.64G>A c.(64-66)Gat>Aat p.D22N PRAD 9 125613481 125613481 + Missense_Mutation SNP T T C TCGA-EJ-5515-01A-01D-1576-08 TCGA-EJ-5515-10A-01D-1577-08 g.chr9:125613481T>C c.3259A>G c.(3259-3261)Agt>Ggt p.S1087G PRAD 9 125621135 125621135 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:125621135C>T c.2096G>A c.(2095-2097)cGc>cAc p.R699H READ 9 125622278 125622278 + Silent SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr9:125622278A>G c.1767T>C c.(1765-1767)taT>taC p.Y589Y READ 9 125655189 125655189 + Splice_Site SNP T T G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:125655189T>G c.348A>C c.(346-348)aaA>aaC p.K116N READ 9 125659649 125659649 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:125659649C>T c.140G>A c.(139-141)cGa>cAa p.R47Q SARC 9 125627715 125627715 + Missense_Mutation SNP C C A TCGA-3B-A9HU-01A-11D-A38Z-09 TCGA-3B-A9HU-10A-01D-A38Z-09 g.chr9:125627715C>A c.1547G>T c.(1546-1548)aGa>aTa p.R516I SKCM 9 125616864 125616864 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr9:125616864G>A c.2846C>T c.(2845-2847)tCa>tTa p.S949L SKCM 9 125617595 125617595 + Missense_Mutation SNP G G A TCGA-EE-A2GB-06A-11D-A197-08 TCGA-EE-A2GB-10A-01D-A199-08 g.chr9:125617595G>A c.2683C>T c.(2683-2685)Ccc>Tcc p.P895S SKCM 9 125617595 125617595 + Missense_Mutation SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr9:125617595G>A c.2683C>T c.(2683-2685)Ccc>Tcc p.P895S SKCM 9 125617604 125617604 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr9:125617604G>A c.2674C>T c.(2674-2676)Cca>Tca p.P892S SKCM 9 125620264 125620264 + Missense_Mutation SNP G G A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr9:125620264G>A c.2392C>T c.(2392-2394)Cct>Tct p.P798S SKCM 9 125620300 125620300 + Missense_Mutation SNP G G A TCGA-ER-A42K-06A-11D-A24R-08 TCGA-ER-A42K-10A-01D-A24R-08 g.chr9:125620300G>A c.2356C>T c.(2356-2358)Cac>Tac p.H786Y SKCM 9 125621031 125621031 + Missense_Mutation SNP C C T TCGA-EE-A3AD-06A-11D-A196-08 TCGA-EE-A3AD-10A-01D-A198-08 g.chr9:125621031C>T c.2200G>A c.(2200-2202)Gaa>Aaa p.E734K SKCM 9 125621201 125621201 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr9:125621201G>A c.2030C>T c.(2029-2031)cCg>cTg p.P677L SKCM 9 125622214 125622214 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:125622214G>A c.1831C>T c.(1831-1833)Cca>Tca p.P611S SKCM 9 125622240 125622240 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr9:125622240G>A c.1805C>T c.(1804-1806)cCa>cTa p.P602L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 9 125612039 125612039 single base substitution A G 3_prime_UTR_variant BLCA-CN 9 125612039 125612039 single base substitution A G downstream_gene_variant BLCA-CN 9 125612039 125612039 single base substitution A G missense_variant I1148T 3443T>C BLCA-CN 9 125627728 125627728 single base substitution C T 3_prime_UTR_variant BLCA-CN 9 125627728 125627728 single base substitution C T downstream_gene_variant BLCA-CN 9 125627728 125627728 single base substitution C T missense_variant D512N 1534G>A BLCA-US 9 125613386 125613386 single base substitution C G 3_prime_UTR_variant BLCA-US 9 125613386 125613386 single base substitution C G downstream_gene_variant BLCA-US 9 125613386 125613386 single base substitution C G exon_variant BLCA-US 9 125613386 125613386 single base substitution C G missense_variant Q1118H 3354G>C BLCA-US 9 125613386 125613386 single base substitution C G missense_variant Q176H 528G>C BLCA-US 9 125621301 125621301 single base substitution C A 3_prime_UTR_variant BLCA-US 9 125621301 125621301 single base substitution C A stop_gained E644* 1930G>T BLCA-US 9 125621301 125621301 single base substitution C A upstream_gene_variant BLCA-US 9 125642878 125642878 single base substitution C G exon_variant BLCA-US 9 125642878 125642878 single base substitution C G missense_variant D319H 955G>C BRCA-EU 9 125602486 125602486 single base substitution A G downstream_gene_variant BRCA-EU 9 125602669 125602669 single base substitution G A downstream_gene_variant BRCA-EU 9 125603619 125603619 single base substitution C T downstream_gene_variant BRCA-EU 9 125603917 125603917 single base substitution T C downstream_gene_variant BRCA-EU 9 125605014 125605014 single base substitution C G downstream_gene_variant BRCA-EU 9 125606650 125606650 single base substitution T C downstream_gene_variant BRCA-EU 9 125607282 125607282 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 125607282 125607282 single base substitution G A downstream_gene_variant BRCA-EU 9 125607366 125607366 single base substitution C G 3_prime_UTR_variant BRCA-EU 9 125607366 125607366 single base substitution C G downstream_gene_variant BRCA-EU 9 125607481 125607481 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 125607481 125607481 single base substitution C T downstream_gene_variant BRCA-EU 9 125607821 125607821 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU 9 125607821 125607821 insertion of <=200bp - A downstream_gene_variant BRCA-EU 9 125608281 125608281 single base substitution A G 3_prime_UTR_variant BRCA-EU 9 125608281 125608281 single base substitution A G downstream_gene_variant BRCA-EU 9 125610400 125610400 single base substitution T C 3_prime_UTR_variant BRCA-EU 9 125610400 125610400 single base substitution T C downstream_gene_variant BRCA-EU 9 125611253 125611253 single base substitution A C 3_prime_UTR_variant BRCA-EU 9 125611253 125611253 single base substitution A C downstream_gene_variant BRCA-EU 9 125611809 125611809 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU 9 125611809 125611809 insertion of <=200bp - A downstream_gene_variant BRCA-EU 9 125612963 125612963 single base substitution G A downstream_gene_variant BRCA-EU 9 125612963 125612963 single base substitution G A intron_variant BRCA-EU 9 125614310 125614310 single base substitution C T downstream_gene_variant BRCA-EU 9 125614310 125614310 single base substitution C T intron_variant BRCA-EU 9 125614310 125614310 single base substitution C T upstream_gene_variant BRCA-EU 9 125616655 125616655 single base substitution C T intron_variant BRCA-EU 9 125616655 125616655 single base substitution C T upstream_gene_variant BRCA-EU 9 125616982 125616982 single base substitution T C intron_variant BRCA-EU 9 125616982 125616982 single base substitution T C upstream_gene_variant BRCA-EU 9 125618851 125618851 single base substitution G C intron_variant BRCA-EU 9 125618851 125618851 single base substitution G C upstream_gene_variant BRCA-EU 9 125619370 125619370 deletion of <=200bp G - intron_variant BRCA-EU 9 125619370 125619370 deletion of <=200bp G - upstream_gene_variant BRCA-EU 9 125619759 125619759 single base substitution G C intron_variant BRCA-EU 9 125619759 125619759 single base substitution G C upstream_gene_variant BRCA-EU 9 125619978 125619978 single base substitution A G intron_variant BRCA-EU 9 125619978 125619978 single base substitution A G upstream_gene_variant BRCA-EU 9 125620205 125620205 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 125620205 125620205 single base substitution C T synonymous_variant A817A 2451G>A BRCA-EU 9 125620205 125620205 single base substitution C T upstream_gene_variant BRCA-EU 9 125620400 125620400 insertion of <=200bp - A intron_variant BRCA-EU 9 125620400 125620400 insertion of <=200bp - A upstream_gene_variant BRCA-EU 9 125621067 125621067 single base substitution C G 3_prime_UTR_variant BRCA-EU 9 125621067 125621067 single base substitution C G missense_variant V722L 2164G>C BRCA-EU 9 125621067 125621067 single base substitution C G upstream_gene_variant BRCA-EU 9 125621154 125621154 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 125621154 125621154 single base substitution G A missense_variant P693S 2077C>T BRCA-EU 9 125621154 125621154 single base substitution G A upstream_gene_variant BRCA-EU 9 125622110 125622110 single base substitution A T intron_variant BRCA-EU 9 125622110 125622110 single base substitution A T upstream_gene_variant BRCA-EU 9 125622164 125622164 insertion of <=200bp - T intron_variant BRCA-EU 9 125622164 125622164 insertion of <=200bp - T upstream_gene_variant BRCA-EU 9 125622256 125622256 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 125622256 125622256 single base substitution G A stop_gained Q597* 1789C>T BRCA-EU 9 125622256 125622256 single base substitution G A upstream_gene_variant BRCA-EU 9 125624480 125624480 single base substitution T G downstream_gene_variant BRCA-EU 9 125624480 125624480 single base substitution T G intron_variant BRCA-EU 9 125630456 125630456 single base substitution C A intron_variant BRCA-EU 9 125630570 125630570 single base substitution G A intron_variant BRCA-EU 9 125631107 125631107 single base substitution T A downstream_gene_variant BRCA-EU 9 125631107 125631107 single base substitution T A intron_variant BRCA-EU 9 125634416 125634416 single base substitution G C downstream_gene_variant BRCA-EU 9 125634416 125634416 single base substitution G C intron_variant BRCA-EU 9 125634593 125634593 single base substitution T A downstream_gene_variant BRCA-EU 9 125634593 125634593 single base substitution T A intron_variant BRCA-EU 9 125636121 125636121 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 125636121 125636121 single base substitution G A intron_variant BRCA-EU 9 125637351 125637351 single base substitution G C 3_prime_UTR_variant BRCA-EU 9 125637351 125637351 single base substitution G C intron_variant BRCA-EU 9 125638432 125638432 single base substitution G C intron_variant BRCA-EU 9 125643254 125643254 single base substitution T A intron_variant BRCA-EU 9 125645692 125645692 single base substitution A T intron_variant BRCA-EU 9 125645929 125645929 single base substitution A T intron_variant BRCA-EU 9 125647371 125647371 single base substitution G C intron_variant BRCA-EU 9 125647752 125647752 single base substitution G A downstream_gene_variant BRCA-EU 9 125647752 125647752 single base substitution G A intron_variant BRCA-EU 9 125648106 125648106 single base substitution C T downstream_gene_variant BRCA-EU 9 125648106 125648106 single base substitution C T intron_variant BRCA-EU 9 125648123 125648123 single base substitution C T downstream_gene_variant BRCA-EU 9 125648123 125648123 single base substitution C T intron_variant BRCA-EU 9 125649598 125649598 single base substitution G A downstream_gene_variant BRCA-EU 9 125649598 125649598 single base substitution G A intron_variant BRCA-EU 9 125650339 125650339 single base substitution T A downstream_gene_variant BRCA-EU 9 125650339 125650339 single base substitution T A intron_variant BRCA-EU 9 125651154 125651154 single base substitution T C downstream_gene_variant BRCA-EU 9 125651154 125651154 single base substitution T C intron_variant BRCA-EU 9 125652322 125652322 single base substitution G C downstream_gene_variant BRCA-EU 9 125652322 125652322 single base substitution G C intron_variant BRCA-EU 9 125652725 125652725 single base substitution C G exon_variant BRCA-EU 9 125652725 125652725 single base substitution C G missense_variant R150T 449G>C BRCA-EU 9 125652811 125652811 single base substitution C G exon_variant BRCA-EU 9 125652811 125652811 single base substitution C G missense_variant L121F 363G>C BRCA-EU 9 125654244 125654244 single base substitution C A intron_variant BRCA-EU 9 125654888 125654888 single base substitution C T intron_variant BRCA-EU 9 125658274 125658274 deletion of <=200bp C - intron_variant BRCA-EU 9 125658622 125658622 deletion of <=200bp A - intron_variant BRCA-EU 9 125658644 125658644 deletion of <=200bp A - intron_variant BRCA-EU 9 125659148 125659148 deletion of <=200bp A - intron_variant BRCA-EU 9 125660523 125660523 single base substitution A C intron_variant BRCA-EU 9 125660523 125660523 single base substitution A C upstream_gene_variant BRCA-EU 9 125660630 125660630 single base substitution G A intron_variant BRCA-EU 9 125660630 125660630 single base substitution G A upstream_gene_variant BRCA-EU 9 125661262 125661262 single base substitution G T intron_variant BRCA-EU 9 125661262 125661262 single base substitution G T upstream_gene_variant BRCA-EU 9 125661303 125661303 single base substitution A C intron_variant BRCA-EU 9 125661303 125661303 single base substitution A C upstream_gene_variant BRCA-EU 9 125661696 125661696 single base substitution G C intron_variant BRCA-EU 9 125661696 125661696 single base substitution G C upstream_gene_variant BRCA-EU 9 125665039 125665039 single base substitution G A intron_variant BRCA-EU 9 125665039 125665039 single base substitution G A upstream_gene_variant BRCA-EU 9 125665113 125665113 single base substitution G C intron_variant BRCA-EU 9 125665113 125665113 single base substitution G C upstream_gene_variant BRCA-EU 9 125665236 125665236 single base substitution T C intron_variant BRCA-EU 9 125665236 125665236 single base substitution T C upstream_gene_variant BRCA-EU 9 125666295 125666295 single base substitution G A intron_variant BRCA-EU 9 125667551 125667551 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 9 125667551 125667551 single base substitution G A exon_variant BRCA-EU 9 125667551 125667551 single base substitution G A upstream_gene_variant BRCA-EU 9 125667790 125667790 single base substitution G C upstream_gene_variant BRCA-EU 9 125667874 125667874 single base substitution T A upstream_gene_variant BRCA-EU 9 125668042 125668042 single base substitution G C upstream_gene_variant BRCA-EU 9 125668788 125668788 insertion of <=200bp - G upstream_gene_variant BRCA-EU 9 125668867 125668867 single base substitution C T upstream_gene_variant BRCA-EU 9 125669456 125669456 single base substitution T C upstream_gene_variant BRCA-EU 9 125671794 125671794 single base substitution C G upstream_gene_variant BRCA-FR 9 125607366 125607366 single base substitution C G 3_prime_UTR_variant BRCA-FR 9 125607366 125607366 single base substitution C G downstream_gene_variant BRCA-FR 9 125612467 125612467 single base substitution T G downstream_gene_variant BRCA-FR 9 125612467 125612467 single base substitution T G intron_variant BRCA-FR 9 125623311 125623311 single base substitution T C downstream_gene_variant BRCA-FR 9 125623311 125623311 single base substitution T C intron_variant BRCA-FR 9 125634416 125634416 single base substitution G C downstream_gene_variant BRCA-FR 9 125634416 125634416 single base substitution G C intron_variant BRCA-FR 9 125637351 125637351 single base substitution G C 3_prime_UTR_variant BRCA-FR 9 125637351 125637351 single base substitution G C intron_variant BRCA-FR 9 125650339 125650339 single base substitution T A downstream_gene_variant BRCA-FR 9 125650339 125650339 single base substitution T A intron_variant BRCA-FR 9 125652322 125652322 single base substitution G C downstream_gene_variant BRCA-FR 9 125652322 125652322 single base substitution G C intron_variant BRCA-FR 9 125660630 125660630 single base substitution G A intron_variant BRCA-FR 9 125660630 125660630 single base substitution G A upstream_gene_variant BRCA-FR 9 125667551 125667551 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-FR 9 125667551 125667551 single base substitution G A exon_variant BRCA-FR 9 125667551 125667551 single base substitution G A upstream_gene_variant BRCA-UK 9 125637622 125637622 single base substitution G A intron_variant BRCA-UK 9 125637622 125637622 single base substitution G A missense_variant H451Y 1351C>T BRCA-UK 9 125639842 125639842 single base substitution G C exon_variant BRCA-UK 9 125639842 125639842 single base substitution G C stop_gained Y411* 1233C>G BRCA-UK 9 125648123 125648123 single base substitution C T downstream_gene_variant BRCA-UK 9 125648123 125648123 single base substitution C T intron_variant BRCA-UK 9 125668042 125668042 single base substitution G C upstream_gene_variant BRCA-US 9 125616341 125616341 single base substitution G A 3_prime_UTR_variant BRCA-US 9 125616341 125616341 single base substitution G A stop_gained Q1003* 3007C>T BRCA-US 9 125616341 125616341 single base substitution G A stop_gained Q61* 181C>T BRCA-US 9 125616341 125616341 single base substitution G A upstream_gene_variant BRCA-US 9 125618153 125618153 single base substitution G C 3_prime_UTR_variant BRCA-US 9 125618153 125618153 single base substitution G C stop_gained S820* 2459C>G BRCA-US 9 125618153 125618153 single base substitution G C upstream_gene_variant BRCA-US 9 125621108 125621108 single base substitution C T 3_prime_UTR_variant BRCA-US 9 125621108 125621108 single base substitution C T missense_variant R708Q 2123G>A BRCA-US 9 125621108 125621108 single base substitution C T upstream_gene_variant BRCA-US 9 125621114 125621114 single base substitution T C 3_prime_UTR_variant BRCA-US 9 125621114 125621114 single base substitution T C missense_variant Y706C 2117A>G BRCA-US 9 125621114 125621114 single base substitution T C upstream_gene_variant BRCA-US 9 125622277 125622277 single base substitution G C 3_prime_UTR_variant BRCA-US 9 125622277 125622277 single base substitution G C missense_variant P590A 1768C>G BRCA-US 9 125622277 125622277 single base substitution G C upstream_gene_variant BRCA-US 9 125642124 125642124 single base substitution C T exon_variant BRCA-US 9 125642124 125642124 single base substitution C T synonymous_variant L374L 1122G>A BRCA-US 9 125652667 125652667 single base substitution C T exon_variant BRCA-US 9 125652667 125652667 single base substitution C T synonymous_variant Q169Q 507G>A BRCA-US 9 125659702 125659702 single base substitution G A exon_variant BRCA-US 9 125659702 125659702 single base substitution G A intron_variant BRCA-US 9 125659702 125659702 single base substitution G A synonymous_variant I29I 87C>T BTCA-JP 9 125616301 125616301 single base substitution T A 3_prime_UTR_variant BTCA-JP 9 125616301 125616301 single base substitution T A missense_variant N1016I 3047A>T BTCA-JP 9 125616301 125616301 single base substitution T A missense_variant N74I 221A>T BTCA-JP 9 125616301 125616301 single base substitution T A upstream_gene_variant BTCA-JP 9 125616690 125616690 single base substitution T G intron_variant BTCA-JP 9 125616690 125616690 single base substitution T G upstream_gene_variant BTCA-JP 9 125618164 125618164 deletion of <=200bp A - splice_region_variant BTCA-JP 9 125618164 125618164 deletion of <=200bp A - upstream_gene_variant BTCA-JP 9 125621200 125621200 single base substitution C T 3_prime_UTR_variant BTCA-JP 9 125621200 125621200 single base substitution C T synonymous_variant P677P 2031G>A BTCA-JP 9 125621200 125621200 single base substitution C T upstream_gene_variant BTCA-JP 9 125622357 125622357 single base substitution G T 3_prime_UTR_variant BTCA-JP 9 125622357 125622357 single base substitution G T missense_variant A563D 1688C>A BTCA-JP 9 125622357 125622357 single base substitution G T upstream_gene_variant BTCA-JP 9 125639817 125639817 single base substitution G A exon_variant BTCA-JP 9 125639817 125639817 single base substitution G A stop_gained R420* 1258C>T BTCA-JP 9 125642183 125642183 deletion of <=200bp G - intron_variant CESC-US 9 125613673 125613673 single base substitution C G 3_prime_UTR_variant CESC-US 9 125613673 125613673 single base substitution C G downstream_gene_variant CESC-US 9 125613673 125613673 single base substitution C G exon_variant CESC-US 9 125613673 125613673 single base substitution C G missense_variant D1054H 3160G>C CESC-US 9 125613673 125613673 single base substitution C G missense_variant D112H 334G>C CESC-US 9 125616293 125616293 single base substitution C A 3_prime_UTR_variant CESC-US 9 125616293 125616293 single base substitution C A missense_variant D1019Y 3055G>T CESC-US 9 125616293 125616293 single base substitution C A missense_variant D77Y 229G>T CESC-US 9 125616293 125616293 single base substitution C A upstream_gene_variant CESC-US 9 125617541 125617541 single base substitution G A 3_prime_UTR_variant CESC-US 9 125617541 125617541 single base substitution G A missense_variant R48C 142C>T CESC-US 9 125617541 125617541 single base substitution G A missense_variant R913C 2737C>T CESC-US 9 125617541 125617541 single base substitution G A upstream_gene_variant CESC-US 9 125621235 125621235 single base substitution G A 3_prime_UTR_variant CESC-US 9 125621235 125621235 single base substitution G A stop_gained R666* 1996C>T CESC-US 9 125621235 125621235 single base substitution G A upstream_gene_variant CESC-US 9 125639816 125639816 single base substitution C G exon_variant CESC-US 9 125639816 125639816 single base substitution C G missense_variant R420P 1259G>C CESC-US 9 125642499 125642499 single base substitution C G intron_variant CESC-US 9 125645647 125645647 single base substitution C G exon_variant CESC-US 9 125645647 125645647 single base substitution C G missense_variant E199Q 595G>C CESC-US 9 125667492 125667492 single base substitution G A 5_prime_UTR_variant CESC-US 9 125667492 125667492 single base substitution G A exon_variant CLLE-ES 9 125620480 125620480 single base substitution A C intron_variant CLLE-ES 9 125620480 125620480 single base substitution A C upstream_gene_variant CLLE-ES 9 125648291 125648291 single base substitution C T downstream_gene_variant CLLE-ES 9 125648291 125648291 single base substitution C T intron_variant CLLE-ES 9 125668650 125668650 single base substitution A T upstream_gene_variant COAD-US 9 125611951 125611951 single base substitution G A 3_prime_UTR_variant COAD-US 9 125611951 125611951 single base substitution G A downstream_gene_variant COAD-US 9 125611951 125611951 single base substitution G A synonymous_variant N1177N 3531C>T COAD-US 9 125612009 125612011 deletion of <=200bp GTG - 3_prime_UTR_variant COAD-US 9 125612009 125612011 deletion of <=200bp GTG - disruptive_inframe_deletion TT1157T COAD-US 9 125612009 125612011 deletion of <=200bp GTG - downstream_gene_variant COAD-US 9 125612077 125612077 single base substitution C T 3_prime_UTR_variant COAD-US 9 125612077 125612077 single base substitution C T downstream_gene_variant COAD-US 9 125612077 125612077 single base substitution C T missense_variant R187Q 560G>A COAD-US 9 125612077 125612077 single base substitution C T synonymous_variant P1135P 3405G>A COAD-US 9 125612088 125612088 deletion of <=200bp T - 3_prime_UTR_variant COAD-US 9 125612088 125612088 deletion of <=200bp T - downstream_gene_variant COAD-US 9 125612088 125612088 deletion of <=200bp T - exon_variant COAD-US 9 125612088 125612088 deletion of <=200bp T - frameshift_variant K183 COAD-US 9 125612088 125612088 deletion of <=200bp T - frameshift_variant T1132 COAD-US 9 125616176 125616176 single base substitution C T 3_prime_UTR_variant COAD-US 9 125616176 125616176 single base substitution C T intron_variant COAD-US 9 125616176 125616176 single base substitution C T missense_variant A1058T 3172G>A COAD-US 9 125616176 125616176 single base substitution C T upstream_gene_variant COAD-US 9 125616529 125616529 single base substitution T C 3_prime_UTR_variant COAD-US 9 125616529 125616529 single base substitution T C missense_variant T31A 91A>G COAD-US 9 125616529 125616529 single base substitution T C missense_variant T973A 2917A>G COAD-US 9 125616529 125616529 single base substitution T C synonymous_variant L96L 288A>G COAD-US 9 125616529 125616529 single base substitution T C upstream_gene_variant COAD-US 9 125652757 125652757 single base substitution G A exon_variant COAD-US 9 125652757 125652757 single base substitution G A synonymous_variant N139N 417C>T COAD-US 9 125655207 125655207 deletion of <=200bp T - exon_variant COAD-US 9 125655207 125655207 deletion of <=200bp T - frameshift_variant K110 COAD-US 9 125655207 125655207 deletion of <=200bp T - intron_variant COCA-CN 9 125613212 125613212 single base substitution T A downstream_gene_variant COCA-CN 9 125613212 125613212 single base substitution T A intron_variant COCA-CN 9 125616361 125616361 single base substitution T C 3_prime_UTR_variant COCA-CN 9 125616361 125616361 single base substitution T C missense_variant K54R 161A>G COCA-CN 9 125616361 125616361 single base substitution T C missense_variant K996R 2987A>G COCA-CN 9 125616361 125616361 single base substitution T C upstream_gene_variant COCA-CN 9 125617468 125617468 single base substitution A G 3_prime_UTR_variant COCA-CN 9 125617468 125617468 single base substitution A G missense_variant V72A 215T>C COCA-CN 9 125617468 125617468 single base substitution A G missense_variant V937A 2810T>C COCA-CN 9 125617468 125617468 single base substitution A G upstream_gene_variant COCA-CN 9 125618155 125618155 single base substitution G T missense_variant F819L 2457C>A COCA-CN 9 125618155 125618155 single base substitution G T splice_region_variant COCA-CN 9 125618155 125618155 single base substitution G T upstream_gene_variant COCA-CN 9 125618200 125618200 single base substitution A G intron_variant COCA-CN 9 125618200 125618200 single base substitution A G upstream_gene_variant COCA-CN 9 125620188 125620188 single base substitution A C intron_variant COCA-CN 9 125620188 125620188 single base substitution A C upstream_gene_variant COCA-CN 9 125626005 125626005 single base substitution G T downstream_gene_variant COCA-CN 9 125626005 125626005 single base substitution G T intron_variant COCA-CN 9 125626637 125626637 single base substitution A T downstream_gene_variant COCA-CN 9 125626637 125626637 single base substitution A T intron_variant COCA-CN 9 125626639 125626639 single base substitution T A downstream_gene_variant COCA-CN 9 125626639 125626639 single base substitution T A intron_variant COCA-CN 9 125631146 125631146 single base substitution G A downstream_gene_variant COCA-CN 9 125631146 125631146 single base substitution G A intron_variant COCA-CN 9 125631201 125631201 single base substitution G T downstream_gene_variant COCA-CN 9 125631201 125631201 single base substitution G T intron_variant COCA-CN 9 125635004 125635004 single base substitution C T downstream_gene_variant COCA-CN 9 125635004 125635004 single base substitution C T intron_variant COCA-CN 9 125639796 125639796 single base substitution G A exon_variant COCA-CN 9 125639796 125639796 single base substitution G A stop_gained R427* 1279C>T COCA-CN 9 125645500 125645500 single base substitution G A exon_variant COCA-CN 9 125645500 125645500 single base substitution G A stop_gained R248* 742C>T COCA-CN 9 125649149 125649149 single base substitution T C downstream_gene_variant COCA-CN 9 125649149 125649149 single base substitution T C intron_variant COCA-CN 9 125655141 125655141 single base substitution T C intron_variant COCA-CN 9 125655272 125655272 single base substitution G A exon_variant COCA-CN 9 125655272 125655272 single base substitution G A intron_variant COCA-CN 9 125655272 125655272 single base substitution G A synonymous_variant L89L 265C>T COCA-CN 9 125657099 125657099 single base substitution C T intron_variant COCA-CN 9 125657984 125657984 single base substitution G C intron_variant COCA-CN 9 125659584 125659584 single base substitution C T exon_variant COCA-CN 9 125659584 125659584 single base substitution C T intron_variant COCA-CN 9 125659584 125659584 single base substitution C T missense_variant A69T 205G>A COCA-CN 9 125661370 125661370 single base substitution T G intron_variant COCA-CN 9 125661370 125661370 single base substitution T G upstream_gene_variant COCA-CN 9 125670945 125670945 single base substitution A C upstream_gene_variant ESAD-UK 9 125602696 125602696 single base substitution T C downstream_gene_variant ESAD-UK 9 125604413 125604413 single base substitution G A downstream_gene_variant ESAD-UK 9 125605264 125605264 single base substitution C G downstream_gene_variant ESAD-UK 9 125605265 125605265 single base substitution T G downstream_gene_variant ESAD-UK 9 125606752 125606753 deletion of <=200bp CT - downstream_gene_variant ESAD-UK 9 125607149 125607149 single base substitution T C 3_prime_UTR_variant ESAD-UK 9 125607149 125607149 single base substitution T C downstream_gene_variant ESAD-UK 9 125608621 125608621 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 9 125608621 125608621 deletion of <=200bp T - downstream_gene_variant ESAD-UK 9 125609691 125609691 single base substitution C T 3_prime_UTR_variant ESAD-UK 9 125609691 125609691 single base substitution C T downstream_gene_variant ESAD-UK 9 125611713 125611713 single base substitution A C 3_prime_UTR_variant ESAD-UK 9 125611713 125611713 single base substitution A C downstream_gene_variant ESAD-UK 9 125612292 125612292 single base substitution G A downstream_gene_variant ESAD-UK 9 125612292 125612292 single base substitution G A intron_variant ESAD-UK 9 125616200 125616200 single base substitution A C 3_prime_UTR_variant ESAD-UK 9 125616200 125616200 single base substitution A C intron_variant ESAD-UK 9 125616200 125616200 single base substitution A C missense_variant L1050V 3148T>G ESAD-UK 9 125616200 125616200 single base substitution A C upstream_gene_variant ESAD-UK 9 125619604 125619604 single base substitution T C intron_variant ESAD-UK 9 125619604 125619604 single base substitution T C upstream_gene_variant ESAD-UK 9 125621847 125621847 insertion of <=200bp - T intron_variant ESAD-UK 9 125621847 125621847 insertion of <=200bp - T upstream_gene_variant ESAD-UK 9 125624173 125624173 single base substitution A T downstream_gene_variant ESAD-UK 9 125624173 125624173 single base substitution A T intron_variant ESAD-UK 9 125625368 125625368 single base substitution G A downstream_gene_variant ESAD-UK 9 125625368 125625368 single base substitution G A intron_variant ESAD-UK 9 125627025 125627025 single base substitution G C downstream_gene_variant ESAD-UK 9 125627025 125627025 single base substitution G C intron_variant ESAD-UK 9 125627352 125627352 deletion of <=200bp G - downstream_gene_variant ESAD-UK 9 125627352 125627352 deletion of <=200bp G - intron_variant ESAD-UK 9 125627571 125627571 single base substitution C T downstream_gene_variant ESAD-UK 9 125627571 125627571 single base substitution C T intron_variant ESAD-UK 9 125628244 125628244 single base substitution G T intron_variant ESAD-UK 9 125628382 125628382 single base substitution T A intron_variant ESAD-UK 9 125631021 125631024 deletion of <=200bp AAAT - intron_variant ESAD-UK 9 125632621 125632621 single base substitution T C downstream_gene_variant ESAD-UK 9 125632621 125632621 single base substitution T C intron_variant ESAD-UK 9 125634966 125634966 single base substitution C T downstream_gene_variant ESAD-UK 9 125634966 125634966 single base substitution C T intron_variant ESAD-UK 9 125635287 125635287 single base substitution T C downstream_gene_variant ESAD-UK 9 125635287 125635287 single base substitution T C intron_variant ESAD-UK 9 125637484 125637484 deletion of <=200bp A - frameshift_variant S497 ESAD-UK 9 125637484 125637484 deletion of <=200bp A - intron_variant ESAD-UK 9 125641694 125641694 single base substitution A T intron_variant ESAD-UK 9 125645605 125645605 single base substitution C A exon_variant ESAD-UK 9 125645605 125645605 single base substitution C A missense_variant A213S 637G>T ESAD-UK 9 125645953 125645953 deletion of <=200bp A - intron_variant ESAD-UK 9 125646098 125646098 deletion of <=200bp A - intron_variant ESAD-UK 9 125648800 125648800 single base substitution C T downstream_gene_variant ESAD-UK 9 125648800 125648800 single base substitution C T intron_variant ESAD-UK 9 125650418 125650418 single base substitution A C downstream_gene_variant ESAD-UK 9 125650418 125650418 single base substitution A C intron_variant ESAD-UK 9 125650627 125650627 single base substitution T C downstream_gene_variant ESAD-UK 9 125650627 125650627 single base substitution T C intron_variant ESAD-UK 9 125651616 125651616 single base substitution T C downstream_gene_variant ESAD-UK 9 125651616 125651616 single base substitution T C intron_variant ESAD-UK 9 125654156 125654156 single base substitution C T intron_variant ESAD-UK 9 125655026 125655026 single base substitution C T intron_variant ESAD-UK 9 125655234 125655234 single base substitution G A exon_variant ESAD-UK 9 125655234 125655234 single base substitution G A intron_variant ESAD-UK 9 125655234 125655234 single base substitution G A synonymous_variant C101C 303C>T ESAD-UK 9 125656399 125656399 single base substitution G A intron_variant ESAD-UK 9 125658622 125658622 deletion of <=200bp A - intron_variant ESAD-UK 9 125661866 125661866 single base substitution C T intron_variant ESAD-UK 9 125661866 125661866 single base substitution C T upstream_gene_variant ESAD-UK 9 125665332 125665332 single base substitution C T intron_variant ESAD-UK 9 125665332 125665332 single base substitution C T upstream_gene_variant ESAD-UK 9 125665637 125665637 deletion of <=200bp T - intron_variant ESAD-UK 9 125666664 125666664 single base substitution T A intron_variant ESAD-UK 9 125668703 125668703 single base substitution G A upstream_gene_variant ESAD-UK 9 125668829 125668829 insertion of <=200bp - A upstream_gene_variant ESAD-UK 9 125670311 125670311 single base substitution A C upstream_gene_variant ESAD-UK 9 125670770 125670770 single base substitution C G upstream_gene_variant ESCA-CN 9 125617737 125617737 single base substitution T C intron_variant ESCA-CN 9 125617737 125617737 single base substitution T C upstream_gene_variant GACA-CN 9 125618017 125618017 single base substitution C T 3_prime_UTR_variant GACA-CN 9 125618017 125618017 single base substitution C T synonymous_variant V865V 2595G>A GACA-CN 9 125618017 125618017 single base substitution C T upstream_gene_variant GBM-US 9 125617558 125617558 single base substitution G A 3_prime_UTR_variant GBM-US 9 125617558 125617558 single base substitution G A missense_variant A42V 125C>T GBM-US 9 125617558 125617558 single base substitution G A missense_variant A907V 2720C>T GBM-US 9 125617558 125617558 single base substitution G A upstream_gene_variant KIRC-US 9 125621286 125621286 single base substitution G T 3_prime_UTR_variant KIRC-US 9 125621286 125621286 single base substitution G T missense_variant P649T 1945C>A KIRC-US 9 125621286 125621286 single base substitution G T upstream_gene_variant KIRC-US 9 125639776 125639776 deletion of <=200bp A - exon_variant KIRC-US 9 125639776 125639776 deletion of <=200bp A - frameshift_variant F433 LAML-KR 9 125615161 125615161 single base substitution G A downstream_gene_variant LAML-KR 9 125615161 125615161 single base substitution G A intron_variant LAML-KR 9 125615161 125615161 single base substitution G A upstream_gene_variant LAML-KR 9 125629540 125629540 single base substitution G A intron_variant LICA-CN 9 125617489 125617489 single base substitution C A 3_prime_UTR_variant LICA-CN 9 125617489 125617489 single base substitution C A missense_variant S65I 194G>T LICA-CN 9 125617489 125617489 single base substitution C A missense_variant S930I 2789G>T LICA-CN 9 125617489 125617489 single base substitution C A upstream_gene_variant LICA-CN 9 125642062 125642062 single base substitution T C exon_variant LICA-CN 9 125642062 125642062 single base substitution T C missense_variant Y395C 1184A>G LICA-FR 9 125604714 125604714 single base substitution A T downstream_gene_variant LICA-FR 9 125612060 125612060 single base substitution C T 3_prime_UTR_variant LICA-FR 9 125612060 125612060 single base substitution C T downstream_gene_variant LICA-FR 9 125612060 125612060 single base substitution C T missense_variant S1141N 3422G>A LICA-FR 9 125613729 125613729 single base substitution T G downstream_gene_variant LICA-FR 9 125613729 125613729 single base substitution T G exon_variant LICA-FR 9 125613729 125613729 single base substitution T G intron_variant LICA-FR 9 125621361 125621361 single base substitution T C 3_prime_UTR_variant LICA-FR 9 125621361 125621361 single base substitution T C missense_variant T624A 1870A>G LICA-FR 9 125621361 125621361 single base substitution T C upstream_gene_variant LICA-FR 9 125622685 125622687 deletion of <=200bp TTT - intron_variant LICA-FR 9 125622685 125622687 deletion of <=200bp TTT - upstream_gene_variant LICA-FR 9 125625171 125625171 deletion of <=200bp A - downstream_gene_variant LICA-FR 9 125625171 125625171 deletion of <=200bp A - intron_variant LICA-FR 9 125628351 125628351 single base substitution G C intron_variant LICA-FR 9 125629539 125629539 single base substitution C G intron_variant LICA-FR 9 125632684 125632684 single base substitution C A downstream_gene_variant LICA-FR 9 125632684 125632684 single base substitution C A intron_variant LICA-FR 9 125633786 125633786 deletion of <=200bp G - downstream_gene_variant LICA-FR 9 125633786 125633786 deletion of <=200bp G - intron_variant LICA-FR 9 125642819 125642819 single base substitution T C intron_variant LICA-FR 9 125642965 125642965 single base substitution C A exon_variant LICA-FR 9 125642965 125642965 single base substitution C A stop_gained E290* 868G>T LICA-FR 9 125642966 125642966 single base substitution C A exon_variant LICA-FR 9 125642966 125642966 single base substitution C A missense_variant M289I 867G>T LIHC-US 9 125613389 125613389 single base substitution T C 3_prime_UTR_variant LIHC-US 9 125613389 125613389 single base substitution T C downstream_gene_variant LIHC-US 9 125613389 125613389 single base substitution T C exon_variant LIHC-US 9 125613389 125613389 single base substitution T C synonymous_variant K1117K 3351A>G LIHC-US 9 125613389 125613389 single base substitution T C synonymous_variant K175K 525A>G LINC-JP 9 125611830 125611830 single base substitution A C 3_prime_UTR_variant LINC-JP 9 125611830 125611830 single base substitution A C downstream_gene_variant LINC-JP 9 125617485 125617485 single base substitution C T 3_prime_UTR_variant LINC-JP 9 125617485 125617485 single base substitution C T synonymous_variant A66A 198G>A LINC-JP 9 125617485 125617485 single base substitution C T synonymous_variant A931A 2793G>A LINC-JP 9 125617485 125617485 single base substitution C T upstream_gene_variant LINC-JP 9 125617724 125617724 deletion of <=200bp C - intron_variant LINC-JP 9 125617724 125617724 deletion of <=200bp C - upstream_gene_variant LINC-JP 9 125620472 125620472 insertion of <=200bp - A intron_variant LINC-JP 9 125620472 125620472 insertion of <=200bp - A upstream_gene_variant LINC-JP 9 125625509 125625509 single base substitution T C downstream_gene_variant LINC-JP 9 125625509 125625509 single base substitution T C intron_variant LINC-JP 9 125637347 125637347 single base substitution A T 3_prime_UTR_variant LINC-JP 9 125637347 125637347 single base substitution A T intron_variant LINC-JP 9 125643528 125643528 single base substitution G A intron_variant LINC-JP 9 125651265 125651265 single base substitution A C downstream_gene_variant LINC-JP 9 125651265 125651265 single base substitution A C intron_variant LINC-JP 9 125655323 125655323 single base substitution A G intron_variant LINC-JP 9 125661461 125661461 single base substitution A C intron_variant LINC-JP 9 125661461 125661461 single base substitution A C upstream_gene_variant LINC-JP 9 125662511 125662511 single base substitution T C intron_variant LINC-JP 9 125662511 125662511 single base substitution T C upstream_gene_variant LIRI-JP 9 125604028 125604028 single base substitution G A downstream_gene_variant LIRI-JP 9 125605897 125605897 single base substitution C G downstream_gene_variant LIRI-JP 9 125606006 125606006 single base substitution C G downstream_gene_variant LIRI-JP 9 125606308 125606308 single base substitution T C downstream_gene_variant LIRI-JP 9 125606823 125606823 single base substitution T C downstream_gene_variant LIRI-JP 9 125608137 125608137 single base substitution C A 3_prime_UTR_variant LIRI-JP 9 125608137 125608137 single base substitution C A downstream_gene_variant LIRI-JP 9 125608138 125608138 single base substitution C A 3_prime_UTR_variant LIRI-JP 9 125608138 125608138 single base substitution C A downstream_gene_variant LIRI-JP 9 125608529 125608529 single base substitution C A 3_prime_UTR_variant LIRI-JP 9 125608529 125608529 single base substitution C A downstream_gene_variant LIRI-JP 9 125609990 125609993 deletion of <=200bp AAAT - 3_prime_UTR_variant LIRI-JP 9 125609990 125609993 deletion of <=200bp AAAT - downstream_gene_variant LIRI-JP 9 125617354 125617354 single base substitution T C intron_variant LIRI-JP 9 125617354 125617354 single base substitution T C upstream_gene_variant LIRI-JP 9 125620698 125620698 single base substitution T C intron_variant LIRI-JP 9 125620698 125620698 single base substitution T C upstream_gene_variant LIRI-JP 9 125620762 125620762 single base substitution C T intron_variant LIRI-JP 9 125620762 125620762 single base substitution C T upstream_gene_variant LIRI-JP 9 125622252 125622252 single base substitution T C 3_prime_UTR_variant LIRI-JP 9 125622252 125622252 single base substitution T C missense_variant Y598C 1793A>G LIRI-JP 9 125622252 125622252 single base substitution T C upstream_gene_variant LIRI-JP 9 125622606 125622606 single base substitution C T intron_variant LIRI-JP 9 125622606 125622606 single base substitution C T upstream_gene_variant LIRI-JP 9 125623084 125623084 single base substitution T C downstream_gene_variant LIRI-JP 9 125623084 125623084 single base substitution T C intron_variant LIRI-JP 9 125628526 125628526 single base substitution T C intron_variant LIRI-JP 9 125633072 125633072 single base substitution T C downstream_gene_variant LIRI-JP 9 125633072 125633072 single base substitution T C intron_variant LIRI-JP 9 125635284 125635284 single base substitution T C downstream_gene_variant LIRI-JP 9 125635284 125635284 single base substitution T C intron_variant LIRI-JP 9 125636057 125636057 single base substitution T C downstream_gene_variant LIRI-JP 9 125636057 125636057 single base substitution T C intron_variant LIRI-JP 9 125638400 125638400 single base substitution T C intron_variant LIRI-JP 9 125641616 125641616 single base substitution T G intron_variant LIRI-JP 9 125641626 125641626 single base substitution T G intron_variant LIRI-JP 9 125641825 125641825 single base substitution T C intron_variant LIRI-JP 9 125641993 125641993 single base substitution T C intron_variant LIRI-JP 9 125643986 125643986 single base substitution T C intron_variant LIRI-JP 9 125644186 125644186 single base substitution G A intron_variant LIRI-JP 9 125644369 125644369 single base substitution T C intron_variant LIRI-JP 9 125645193 125645193 single base substitution T G intron_variant LIRI-JP 9 125645683 125645683 single base substitution T C intron_variant LIRI-JP 9 125647123 125647123 single base substitution T C intron_variant LIRI-JP 9 125649440 125649440 single base substitution G C downstream_gene_variant LIRI-JP 9 125649440 125649440 single base substitution G C intron_variant LIRI-JP 9 125650277 125650277 single base substitution G A downstream_gene_variant LIRI-JP 9 125650277 125650277 single base substitution G A intron_variant LIRI-JP 9 125650951 125650951 single base substitution G A downstream_gene_variant LIRI-JP 9 125650951 125650951 single base substitution G A intron_variant LIRI-JP 9 125652197 125652197 single base substitution G C downstream_gene_variant LIRI-JP 9 125652197 125652197 single base substitution G C intron_variant LIRI-JP 9 125652369 125652369 single base substitution A C downstream_gene_variant LIRI-JP 9 125652369 125652369 single base substitution A C intron_variant LIRI-JP 9 125652549 125652549 single base substitution C T exon_variant LIRI-JP 9 125652549 125652549 single base substitution C T intron_variant LIRI-JP 9 125652549 125652549 single base substitution C T missense_variant G209S 625G>A LIRI-JP 9 125654002 125654002 single base substitution T A intron_variant LIRI-JP 9 125655262 125655262 single base substitution T A exon_variant LIRI-JP 9 125655262 125655262 single base substitution T A intron_variant LIRI-JP 9 125655262 125655262 single base substitution T A missense_variant N92I 275A>T LIRI-JP 9 125656148 125656148 single base substitution T A intron_variant LIRI-JP 9 125658374 125658374 single base substitution C A intron_variant LIRI-JP 9 125659162 125659162 single base substitution G T intron_variant LIRI-JP 9 125663406 125663406 single base substitution T C intron_variant LIRI-JP 9 125663406 125663406 single base substitution T C upstream_gene_variant LIRI-JP 9 125663522 125663522 single base substitution A G intron_variant LIRI-JP 9 125663522 125663522 single base substitution A G upstream_gene_variant LIRI-JP 9 125665367 125665367 single base substitution G T intron_variant LIRI-JP 9 125665367 125665367 single base substitution G T upstream_gene_variant LIRI-JP 9 125666048 125666048 single base substitution A C intron_variant LIRI-JP 9 125666123 125666123 single base substitution A G intron_variant LIRI-JP 9 125667217 125667217 single base substitution G A intron_variant LIRI-JP 9 125667546 125667546 single base substitution G T 5_prime_UTR_variant LIRI-JP 9 125667546 125667546 single base substitution G T exon_variant LIRI-JP 9 125667546 125667546 single base substitution G T upstream_gene_variant LIRI-JP 9 125668906 125668906 single base substitution C A upstream_gene_variant LIRI-JP 9 125669045 125669045 single base substitution G A upstream_gene_variant LIRI-JP 9 125669051 125669051 single base substitution G A upstream_gene_variant LIRI-JP 9 125669705 125669705 single base substitution G A upstream_gene_variant LIRI-JP 9 125670711 125670711 single base substitution A G upstream_gene_variant LIRI-JP 9 125671797 125671797 single base substitution A C upstream_gene_variant LIRI-JP 9 125672058 125672058 single base substitution T C upstream_gene_variant LIRI-JP 9 125672485 125672485 single base substitution T C upstream_gene_variant LUSC-KR 9 125603741 125603741 single base substitution C T downstream_gene_variant LUSC-KR 9 125614293 125614293 single base substitution C G downstream_gene_variant LUSC-KR 9 125614293 125614293 single base substitution C G intron_variant LUSC-KR 9 125614293 125614293 single base substitution C G upstream_gene_variant LUSC-KR 9 125614585 125614585 single base substitution G A downstream_gene_variant LUSC-KR 9 125614585 125614585 single base substitution G A intron_variant LUSC-KR 9 125614585 125614585 single base substitution G A upstream_gene_variant LUSC-KR 9 125614595 125614595 single base substitution A G downstream_gene_variant LUSC-KR 9 125614595 125614595 single base substitution A G intron_variant LUSC-KR 9 125614595 125614595 single base substitution A G upstream_gene_variant LUSC-KR 9 125614783 125614783 single base substitution T C downstream_gene_variant LUSC-KR 9 125614783 125614783 single base substitution T C intron_variant LUSC-KR 9 125614783 125614783 single base substitution T C upstream_gene_variant LUSC-KR 9 125614798 125614798 single base substitution T C downstream_gene_variant LUSC-KR 9 125614798 125614798 single base substitution T C intron_variant LUSC-KR 9 125614798 125614798 single base substitution T C upstream_gene_variant LUSC-KR 9 125615071 125615071 single base substitution A G downstream_gene_variant LUSC-KR 9 125615071 125615071 single base substitution A G intron_variant LUSC-KR 9 125615071 125615071 single base substitution A G upstream_gene_variant LUSC-KR 9 125615161 125615161 single base substitution G A downstream_gene_variant LUSC-KR 9 125615161 125615161 single base substitution G A intron_variant LUSC-KR 9 125615161 125615161 single base substitution G A upstream_gene_variant LUSC-KR 9 125622643 125622643 single base substitution C T intron_variant LUSC-KR 9 125622643 125622643 single base substitution C T upstream_gene_variant LUSC-KR 9 125624813 125624813 single base substitution C G downstream_gene_variant LUSC-KR 9 125624813 125624813 single base substitution C G intron_variant LUSC-KR 9 125626637 125626637 single base substitution A G downstream_gene_variant LUSC-KR 9 125626637 125626637 single base substitution A G intron_variant LUSC-KR 9 125629331 125629331 single base substitution G A intron_variant LUSC-KR 9 125629671 125629671 single base substitution C T intron_variant LUSC-KR 9 125629901 125629901 single base substitution C A intron_variant LUSC-KR 9 125630411 125630411 single base substitution C T intron_variant LUSC-KR 9 125633836 125633836 single base substitution T A downstream_gene_variant LUSC-KR 9 125633836 125633836 single base substitution T A intron_variant LUSC-KR 9 125640694 125640694 single base substitution C A intron_variant LUSC-KR 9 125641331 125641331 single base substitution T A intron_variant LUSC-KR 9 125657833 125657833 single base substitution C A intron_variant LUSC-KR 9 125658629 125658629 single base substitution A T intron_variant LUSC-KR 9 125660331 125660331 single base substitution C G 5_prime_UTR_variant LUSC-KR 9 125660331 125660331 single base substitution C G intron_variant LUSC-KR 9 125660331 125660331 single base substitution C G upstream_gene_variant LUSC-KR 9 125663442 125663442 single base substitution T A intron_variant LUSC-KR 9 125663442 125663442 single base substitution T A upstream_gene_variant LUSC-KR 9 125666802 125666802 single base substitution G T intron_variant LUSC-KR 9 125667270 125667270 single base substitution C G intron_variant LUSC-KR 9 125667557 125667557 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 9 125667557 125667557 single base substitution C A exon_variant LUSC-KR 9 125667557 125667557 single base substitution C A upstream_gene_variant LUSC-KR 9 125667678 125667678 single base substitution G A upstream_gene_variant LUSC-KR 9 125667977 125667977 single base substitution G C upstream_gene_variant LUSC-KR 9 125669001 125669001 single base substitution A C upstream_gene_variant LUSC-US 9 125613661 125613661 single base substitution C A 3_prime_UTR_variant LUSC-US 9 125613661 125613661 single base substitution C A downstream_gene_variant LUSC-US 9 125613661 125613661 single base substitution C A exon_variant LUSC-US 9 125613661 125613661 single base substitution C A stop_gained E1058* 3172G>T LUSC-US 9 125613661 125613661 single base substitution C A stop_gained E116* 346G>T LUSC-US 9 125655289 125655289 single base substitution G A exon_variant LUSC-US 9 125655289 125655289 single base substitution G A intron_variant LUSC-US 9 125655289 125655289 single base substitution G A missense_variant S83L 248C>T MALY-DE 9 125605783 125605783 single base substitution T A downstream_gene_variant MALY-DE 9 125611809 125611809 deletion of <=200bp A - 3_prime_UTR_variant MALY-DE 9 125611809 125611809 deletion of <=200bp A - downstream_gene_variant MALY-DE 9 125619311 125619311 deletion of <=200bp T - intron_variant MALY-DE 9 125619311 125619311 deletion of <=200bp T - upstream_gene_variant MALY-DE 9 125619444 125619444 single base substitution T A intron_variant MALY-DE 9 125619444 125619444 single base substitution T A upstream_gene_variant MALY-DE 9 125631021 125631021 insertion of <=200bp - AAAT intron_variant MALY-DE 9 125631833 125631833 single base substitution T A downstream_gene_variant MALY-DE 9 125631833 125631833 single base substitution T A intron_variant MALY-DE 9 125633829 125633829 single base substitution C T downstream_gene_variant MALY-DE 9 125633829 125633829 single base substitution C T intron_variant MALY-DE 9 125640787 125640787 single base substitution G T intron_variant MALY-DE 9 125649178 125649178 single base substitution G T downstream_gene_variant MALY-DE 9 125649178 125649178 single base substitution G T intron_variant MALY-DE 9 125653474 125653474 deletion of <=200bp G - intron_variant MALY-DE 9 125656122 125656122 single base substitution G C intron_variant MALY-DE 9 125658033 125658033 single base substitution C G intron_variant MALY-DE 9 125660756 125660756 single base substitution T A intron_variant MALY-DE 9 125660756 125660756 single base substitution T A upstream_gene_variant MALY-DE 9 125664959 125664959 single base substitution C T intron_variant MALY-DE 9 125664959 125664959 single base substitution C T upstream_gene_variant MALY-DE 9 125671185 125671185 single base substitution C G upstream_gene_variant MELA-AU 9 125602157 125602157 single base substitution C T downstream_gene_variant MELA-AU 9 125602282 125602282 single base substitution C T downstream_gene_variant MELA-AU 9 125603105 125603105 single base substitution C T downstream_gene_variant MELA-AU 9 125603628 125603628 single base substitution G A downstream_gene_variant MELA-AU 9 125604413 125604413 single base substitution G A downstream_gene_variant MELA-AU 9 125604618 125604618 single base substitution G A downstream_gene_variant MELA-AU 9 125606018 125606018 single base substitution G A downstream_gene_variant MELA-AU 9 125606518 125606518 single base substitution A G downstream_gene_variant MELA-AU 9 125607122 125607122 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125607122 125607122 single base substitution G A downstream_gene_variant MELA-AU 9 125607123 125607123 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125607123 125607123 single base substitution G A downstream_gene_variant MELA-AU 9 125607139 125607139 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125607139 125607139 single base substitution G A downstream_gene_variant MELA-AU 9 125607337 125607337 single base substitution A T 3_prime_UTR_variant MELA-AU 9 125607337 125607337 single base substitution A T downstream_gene_variant MELA-AU 9 125607339 125607339 single base substitution C T 3_prime_UTR_variant MELA-AU 9 125607339 125607339 single base substitution C T downstream_gene_variant MELA-AU 9 125607360 125607360 single base substitution A T 3_prime_UTR_variant MELA-AU 9 125607360 125607360 single base substitution A T downstream_gene_variant MELA-AU 9 125607438 125607438 single base substitution C T 3_prime_UTR_variant MELA-AU 9 125607438 125607438 single base substitution C T downstream_gene_variant MELA-AU 9 125607857 125607857 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125607857 125607857 single base substitution G A downstream_gene_variant MELA-AU 9 125610577 125610577 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125610577 125610577 single base substitution G A downstream_gene_variant MELA-AU 9 125611751 125611751 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125611751 125611751 single base substitution G A downstream_gene_variant MELA-AU 9 125611777 125611777 single base substitution G T 3_prime_UTR_variant MELA-AU 9 125611777 125611777 single base substitution G T downstream_gene_variant MELA-AU 9 125613231 125613231 single base substitution C T downstream_gene_variant MELA-AU 9 125613231 125613231 single base substitution C T intron_variant MELA-AU 9 125613988 125613988 single base substitution G A downstream_gene_variant MELA-AU 9 125613988 125613988 single base substitution G A intron_variant MELA-AU 9 125613988 125613988 single base substitution G A upstream_gene_variant MELA-AU 9 125614801 125614802 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 125614801 125614802 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 125614801 125614802 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 125614950 125614950 single base substitution G A downstream_gene_variant MELA-AU 9 125614950 125614950 single base substitution G A intron_variant MELA-AU 9 125614950 125614950 single base substitution G A upstream_gene_variant MELA-AU 9 125615745 125615745 single base substitution G A downstream_gene_variant MELA-AU 9 125615745 125615745 single base substitution G A intron_variant MELA-AU 9 125615745 125615745 single base substitution G A upstream_gene_variant MELA-AU 9 125615825 125615825 single base substitution G A downstream_gene_variant MELA-AU 9 125615825 125615825 single base substitution G A intron_variant MELA-AU 9 125615825 125615825 single base substitution G A upstream_gene_variant MELA-AU 9 125616008 125616009 multiple base substitution (>=2bp and <=200bp) AG TA downstream_gene_variant MELA-AU 9 125616008 125616009 multiple base substitution (>=2bp and <=200bp) AG TA intron_variant MELA-AU 9 125616008 125616009 multiple base substitution (>=2bp and <=200bp) AG TA upstream_gene_variant MELA-AU 9 125617595 125617595 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125617595 125617595 single base substitution G A missense_variant P30S 88C>T MELA-AU 9 125617595 125617595 single base substitution G A missense_variant P895S 2683C>T MELA-AU 9 125617595 125617595 single base substitution G A upstream_gene_variant MELA-AU 9 125617706 125617706 single base substitution G A intron_variant MELA-AU 9 125617706 125617706 single base substitution G A upstream_gene_variant MELA-AU 9 125619363 125619363 single base substitution G A intron_variant MELA-AU 9 125619363 125619363 single base substitution G A upstream_gene_variant MELA-AU 9 125619827 125619827 single base substitution G A intron_variant MELA-AU 9 125619827 125619827 single base substitution G A upstream_gene_variant MELA-AU 9 125619828 125619828 single base substitution G A intron_variant MELA-AU 9 125619828 125619828 single base substitution G A upstream_gene_variant MELA-AU 9 125619984 125619984 single base substitution G A intron_variant MELA-AU 9 125619984 125619984 single base substitution G A upstream_gene_variant MELA-AU 9 125620264 125620264 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125620264 125620264 single base substitution G A missense_variant P798S 2392C>T MELA-AU 9 125620264 125620264 single base substitution G A upstream_gene_variant MELA-AU 9 125620518 125620518 single base substitution T C intron_variant MELA-AU 9 125620518 125620518 single base substitution T C upstream_gene_variant MELA-AU 9 125621004 125621004 single base substitution A G 3_prime_UTR_variant MELA-AU 9 125621004 125621004 single base substitution A G missense_variant Y743H 2227T>C MELA-AU 9 125621004 125621004 single base substitution A G upstream_gene_variant MELA-AU 9 125621246 125621246 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125621246 125621246 single base substitution G A missense_variant S662F 1985C>T MELA-AU 9 125621246 125621246 single base substitution G A upstream_gene_variant MELA-AU 9 125621278 125621278 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125621278 125621278 single base substitution G A synonymous_variant S651S 1953C>T MELA-AU 9 125621278 125621278 single base substitution G A upstream_gene_variant MELA-AU 9 125622197 125622197 single base substitution T G splice_region_variant MELA-AU 9 125622197 125622197 single base substitution T G upstream_gene_variant MELA-AU 9 125622240 125622240 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125622240 125622240 single base substitution G A missense_variant P602L 1805C>T MELA-AU 9 125622240 125622240 single base substitution G A upstream_gene_variant MELA-AU 9 125622247 125622247 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125622247 125622247 single base substitution G A stop_gained Q600* 1798C>T MELA-AU 9 125622247 125622247 single base substitution G A upstream_gene_variant MELA-AU 9 125622954 125622954 single base substitution A G downstream_gene_variant MELA-AU 9 125622954 125622954 single base substitution A G intron_variant MELA-AU 9 125622954 125622954 single base substitution A G upstream_gene_variant MELA-AU 9 125623535 125623535 single base substitution C G downstream_gene_variant MELA-AU 9 125623535 125623535 single base substitution C G intron_variant MELA-AU 9 125623536 125623536 single base substitution G A downstream_gene_variant MELA-AU 9 125623536 125623536 single base substitution G A intron_variant MELA-AU 9 125624234 125624234 single base substitution G A downstream_gene_variant MELA-AU 9 125624234 125624234 single base substitution G A intron_variant MELA-AU 9 125625021 125625021 single base substitution A T downstream_gene_variant MELA-AU 9 125625021 125625021 single base substitution A T intron_variant MELA-AU 9 125625158 125625158 single base substitution G A downstream_gene_variant MELA-AU 9 125625158 125625158 single base substitution G A intron_variant MELA-AU 9 125625224 125625224 single base substitution G A downstream_gene_variant MELA-AU 9 125625224 125625224 single base substitution G A intron_variant MELA-AU 9 125627125 125627125 single base substitution G A downstream_gene_variant MELA-AU 9 125627125 125627125 single base substitution G A intron_variant MELA-AU 9 125627128 125627128 single base substitution C T downstream_gene_variant MELA-AU 9 125627128 125627128 single base substitution C T intron_variant MELA-AU 9 125628212 125628212 single base substitution G T intron_variant MELA-AU 9 125631024 125631024 single base substitution T C intron_variant MELA-AU 9 125631250 125631250 single base substitution G A downstream_gene_variant MELA-AU 9 125631250 125631250 single base substitution G A intron_variant MELA-AU 9 125631507 125631507 single base substitution G A downstream_gene_variant MELA-AU 9 125631507 125631507 single base substitution G A intron_variant MELA-AU 9 125632118 125632118 single base substitution G A downstream_gene_variant MELA-AU 9 125632118 125632118 single base substitution G A intron_variant MELA-AU 9 125632482 125632482 single base substitution C T downstream_gene_variant MELA-AU 9 125632482 125632482 single base substitution C T intron_variant MELA-AU 9 125633624 125633624 single base substitution T C downstream_gene_variant MELA-AU 9 125633624 125633624 single base substitution T C intron_variant MELA-AU 9 125633855 125633855 single base substitution G A downstream_gene_variant MELA-AU 9 125633855 125633855 single base substitution G A intron_variant MELA-AU 9 125635811 125635811 single base substitution A G downstream_gene_variant MELA-AU 9 125635811 125635811 single base substitution A G intron_variant MELA-AU 9 125636666 125636666 single base substitution G A 3_prime_UTR_variant MELA-AU 9 125636666 125636666 single base substitution G A intron_variant MELA-AU 9 125637643 125637643 single base substitution T A intron_variant MELA-AU 9 125637643 125637643 single base substitution T A missense_variant N444Y 1330A>T MELA-AU 9 125637975 125637975 single base substitution G A intron_variant MELA-AU 9 125638160 125638160 single base substitution G A intron_variant MELA-AU 9 125638443 125638443 single base substitution G A intron_variant MELA-AU 9 125638721 125638721 single base substitution A G intron_variant MELA-AU 9 125640207 125640207 single base substitution G C intron_variant MELA-AU 9 125640776 125640776 single base substitution C T intron_variant MELA-AU 9 125641098 125641098 single base substitution G A intron_variant MELA-AU 9 125643954 125643954 single base substitution G A intron_variant MELA-AU 9 125643962 125643962 single base substitution G A intron_variant MELA-AU 9 125646082 125646082 single base substitution G A intron_variant MELA-AU 9 125646498 125646498 single base substitution G A intron_variant MELA-AU 9 125648585 125648585 single base substitution T A downstream_gene_variant MELA-AU 9 125648585 125648585 single base substitution T A intron_variant MELA-AU 9 125648624 125648624 single base substitution G A downstream_gene_variant MELA-AU 9 125648624 125648624 single base substitution G A intron_variant MELA-AU 9 125648786 125648786 single base substitution G A downstream_gene_variant MELA-AU 9 125648786 125648786 single base substitution G A intron_variant MELA-AU 9 125649948 125649948 single base substitution C G downstream_gene_variant MELA-AU 9 125649948 125649948 single base substitution C G intron_variant MELA-AU 9 125650115 125650115 single base substitution G A downstream_gene_variant MELA-AU 9 125650115 125650115 single base substitution G A intron_variant MELA-AU 9 125652243 125652243 single base substitution G A downstream_gene_variant MELA-AU 9 125652243 125652243 single base substitution G A intron_variant MELA-AU 9 125652317 125652317 single base substitution G A downstream_gene_variant MELA-AU 9 125652317 125652317 single base substitution G A intron_variant MELA-AU 9 125653143 125653143 single base substitution G A intron_variant MELA-AU 9 125653144 125653144 single base substitution C T intron_variant MELA-AU 9 125654509 125654509 single base substitution G A intron_variant MELA-AU 9 125654638 125654638 single base substitution C T intron_variant MELA-AU 9 125655083 125655083 deletion of <=200bp G - intron_variant MELA-AU 9 125656392 125656392 single base substitution G A intron_variant MELA-AU 9 125656532 125656532 single base substitution C T intron_variant MELA-AU 9 125658233 125658233 single base substitution A T intron_variant MELA-AU 9 125658244 125658244 single base substitution G A intron_variant MELA-AU 9 125658247 125658247 single base substitution T G intron_variant MELA-AU 9 125659418 125659418 single base substitution G A intron_variant MELA-AU 9 125661086 125661086 single base substitution G A intron_variant MELA-AU 9 125661086 125661086 single base substitution G A upstream_gene_variant MELA-AU 9 125661553 125661553 single base substitution G A intron_variant MELA-AU 9 125661553 125661553 single base substitution G A upstream_gene_variant MELA-AU 9 125661658 125661658 single base substitution C T intron_variant MELA-AU 9 125661658 125661658 single base substitution C T upstream_gene_variant MELA-AU 9 125662082 125662082 single base substitution A C intron_variant MELA-AU 9 125662082 125662082 single base substitution A C upstream_gene_variant MELA-AU 9 125662591 125662591 single base substitution A C intron_variant MELA-AU 9 125662591 125662591 single base substitution A C upstream_gene_variant MELA-AU 9 125662704 125662704 single base substitution G A intron_variant MELA-AU 9 125662704 125662704 single base substitution G A upstream_gene_variant MELA-AU 9 125663065 125663065 single base substitution C T intron_variant MELA-AU 9 125663065 125663065 single base substitution C T upstream_gene_variant MELA-AU 9 125664136 125664136 single base substitution G A intron_variant MELA-AU 9 125664136 125664136 single base substitution G A upstream_gene_variant MELA-AU 9 125664896 125664896 single base substitution G A intron_variant MELA-AU 9 125664896 125664896 single base substitution G A upstream_gene_variant MELA-AU 9 125666604 125666604 single base substitution C T intron_variant MELA-AU 9 125666907 125666907 single base substitution G A intron_variant MELA-AU 9 125667615 125667615 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 9 125667615 125667615 single base substitution C G upstream_gene_variant MELA-AU 9 125667694 125667695 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 125667813 125667813 single base substitution T G upstream_gene_variant MELA-AU 9 125668023 125668023 single base substitution C T upstream_gene_variant MELA-AU 9 125668281 125668281 single base substitution A T upstream_gene_variant MELA-AU 9 125669059 125669059 single base substitution C T upstream_gene_variant MELA-AU 9 125669433 125669433 single base substitution G A upstream_gene_variant MELA-AU 9 125669854 125669854 single base substitution C G upstream_gene_variant MELA-AU 9 125670109 125670109 single base substitution C T upstream_gene_variant MELA-AU 9 125670213 125670213 single base substitution T C upstream_gene_variant MELA-AU 9 125670425 125670425 single base substitution G A upstream_gene_variant MELA-AU 9 125670520 125670520 single base substitution A G upstream_gene_variant MELA-AU 9 125670644 125670644 single base substitution G A upstream_gene_variant MELA-AU 9 125671309 125671309 single base substitution T A upstream_gene_variant MELA-AU 9 125671602 125671602 single base substitution G A upstream_gene_variant MELA-AU 9 125672470 125672470 single base substitution G A upstream_gene_variant MELA-AU 9 125672620 125672620 single base substitution A C upstream_gene_variant ORCA-IN 9 125651414 125651414 single base substitution C T downstream_gene_variant ORCA-IN 9 125651414 125651414 single base substitution C T intron_variant ORCA-IN 9 125655234 125655234 single base substitution G A exon_variant ORCA-IN 9 125655234 125655234 single base substitution G A intron_variant ORCA-IN 9 125655234 125655234 single base substitution G A synonymous_variant C101C 303C>T OV-AU 9 125603312 125603312 single base substitution C T downstream_gene_variant OV-AU 9 125603790 125603790 single base substitution G A downstream_gene_variant OV-AU 9 125609185 125609185 single base substitution C G 3_prime_UTR_variant OV-AU 9 125609185 125609185 single base substitution C G downstream_gene_variant OV-AU 9 125622298 125622298 single base substitution G C 3_prime_UTR_variant OV-AU 9 125622298 125622298 single base substitution G C missense_variant L583V 1747C>G OV-AU 9 125622298 125622298 single base substitution G C upstream_gene_variant OV-AU 9 125622448 125622448 single base substitution A T intron_variant OV-AU 9 125622448 125622448 single base substitution A T upstream_gene_variant OV-AU 9 125622449 125622449 single base substitution C T intron_variant OV-AU 9 125622449 125622449 single base substitution C T upstream_gene_variant OV-AU 9 125631446 125631446 single base substitution A C downstream_gene_variant OV-AU 9 125631446 125631446 single base substitution A C intron_variant OV-AU 9 125641799 125641799 single base substitution G T intron_variant OV-AU 9 125646775 125646775 single base substitution G A intron_variant OV-AU 9 125647217 125647217 single base substitution G A intron_variant OV-AU 9 125671169 125671169 single base substitution T C upstream_gene_variant OV-US 9 125622280 125622280 single base substitution A G 3_prime_UTR_variant OV-US 9 125622280 125622280 single base substitution A G missense_variant Y589H 1765T>C OV-US 9 125622280 125622280 single base substitution A G upstream_gene_variant PACA-AU 9 125604299 125604299 single base substitution A C downstream_gene_variant PACA-AU 9 125604302 125604302 single base substitution A C downstream_gene_variant PACA-AU 9 125610295 125610295 single base substitution A C 3_prime_UTR_variant PACA-AU 9 125610295 125610295 single base substitution A C downstream_gene_variant PACA-AU 9 125613482 125613482 single base substitution G A 3_prime_UTR_variant PACA-AU 9 125613482 125613482 single base substitution G A downstream_gene_variant PACA-AU 9 125613482 125613482 single base substitution G A exon_variant PACA-AU 9 125613482 125613482 single base substitution G A synonymous_variant I1086I 3258C>T PACA-AU 9 125613482 125613482 single base substitution G A synonymous_variant I144I 432C>T PACA-AU 9 125615953 125615953 single base substitution C T downstream_gene_variant PACA-AU 9 125615953 125615953 single base substitution C T intron_variant PACA-AU 9 125615953 125615953 single base substitution C T upstream_gene_variant PACA-AU 9 125616688 125616688 single base substitution A G intron_variant PACA-AU 9 125616688 125616688 single base substitution A G upstream_gene_variant PACA-AU 9 125624198 125624198 single base substitution C A downstream_gene_variant PACA-AU 9 125624198 125624198 single base substitution C A intron_variant PACA-AU 9 125627250 125627250 single base substitution A G downstream_gene_variant PACA-AU 9 125627250 125627250 single base substitution A G intron_variant PACA-AU 9 125633221 125633221 single base substitution A G downstream_gene_variant PACA-AU 9 125633221 125633221 single base substitution A G intron_variant PACA-AU 9 125659894 125659894 single base substitution T C 5_prime_UTR_variant PACA-AU 9 125659894 125659894 single base substitution T C intron_variant PACA-AU 9 125659894 125659894 single base substitution T C upstream_gene_variant PACA-AU 9 125660896 125660896 single base substitution C G intron_variant PACA-AU 9 125660896 125660896 single base substitution C G upstream_gene_variant PACA-AU 9 125667517 125667517 single base substitution C T 5_prime_UTR_variant PACA-AU 9 125667517 125667517 single base substitution C T exon_variant PACA-AU 9 125667517 125667517 single base substitution C T upstream_gene_variant PACA-AU 9 125667683 125667683 single base substitution A T upstream_gene_variant PACA-CA 9 125602067 125602067 single base substitution C G downstream_gene_variant PACA-CA 9 125605680 125605680 single base substitution C T downstream_gene_variant PACA-CA 9 125611389 125611390 deletion of <=200bp TT - 3_prime_UTR_variant PACA-CA 9 125611389 125611390 deletion of <=200bp TT - downstream_gene_variant PACA-CA 9 125617485 125617485 single base substitution C T 3_prime_UTR_variant PACA-CA 9 125617485 125617485 single base substitution C T synonymous_variant A66A 198G>A PACA-CA 9 125617485 125617485 single base substitution C T synonymous_variant A931A 2793G>A PACA-CA 9 125617485 125617485 single base substitution C T upstream_gene_variant PACA-CA 9 125618322 125618322 single base substitution T G intron_variant PACA-CA 9 125618322 125618322 single base substitution T G upstream_gene_variant PACA-CA 9 125619031 125619031 single base substitution T C intron_variant PACA-CA 9 125619031 125619031 single base substitution T C upstream_gene_variant PACA-CA 9 125632650 125632650 single base substitution T C downstream_gene_variant PACA-CA 9 125632650 125632650 single base substitution T C intron_variant PACA-CA 9 125636368 125636368 single base substitution G C 3_prime_UTR_variant PACA-CA 9 125636368 125636368 single base substitution G C intron_variant PACA-CA 9 125642699 125642699 single base substitution C T intron_variant PACA-CA 9 125646016 125646016 single base substitution G A intron_variant PACA-CA 9 125646097 125646097 insertion of <=200bp - A intron_variant PACA-CA 9 125649903 125649903 single base substitution T C downstream_gene_variant PACA-CA 9 125649903 125649903 single base substitution T C intron_variant PACA-CA 9 125657107 125657107 single base substitution C T intron_variant PACA-CA 9 125657401 125657401 single base substitution T G intron_variant PACA-CA 9 125657897 125657897 single base substitution T C intron_variant PACA-CA 9 125658055 125658055 single base substitution G A intron_variant PACA-CA 9 125659556 125659556 single base substitution A G intron_variant PACA-CA 9 125659556 125659556 single base substitution A G splice_donor_variant PACA-CA 9 125659626 125659626 single base substitution T C exon_variant PACA-CA 9 125659626 125659626 single base substitution T C intron_variant PACA-CA 9 125659626 125659626 single base substitution T C missense_variant T55A 163A>G PACA-CA 9 125660047 125660047 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 9 125660047 125660047 single base substitution C A intron_variant PACA-CA 9 125660047 125660047 single base substitution C A upstream_gene_variant PACA-CA 9 125661420 125661420 single base substitution C A intron_variant PACA-CA 9 125661420 125661420 single base substitution C A upstream_gene_variant PACA-CA 9 125666435 125666435 insertion of <=200bp - A intron_variant PACA-CA 9 125670020 125670020 single base substitution G A upstream_gene_variant PAEN-AU 9 125606965 125606965 single base substitution T C 3_prime_UTR_variant PAEN-AU 9 125606965 125606965 single base substitution T C downstream_gene_variant PAEN-AU 9 125640895 125640895 single base substitution T C intron_variant PAEN-AU 9 125649713 125649713 single base substitution T C downstream_gene_variant PAEN-AU 9 125649713 125649713 single base substitution T C intron_variant PAEN-IT 9 125670294 125670294 single base substitution T C upstream_gene_variant PBCA-DE 9 125603645 125603645 single base substitution T C downstream_gene_variant PBCA-DE 9 125614701 125614701 insertion of <=200bp - CCA downstream_gene_variant PBCA-DE 9 125614701 125614701 insertion of <=200bp - CCA intron_variant PBCA-DE 9 125614701 125614701 insertion of <=200bp - CCA upstream_gene_variant PBCA-DE 9 125631056 125631056 single base substitution G T intron_variant PBCA-DE 9 125635517 125635517 single base substitution C G downstream_gene_variant PBCA-DE 9 125635517 125635517 single base substitution C G intron_variant PBCA-DE 9 125643736 125643736 deletion of <=200bp C - intron_variant PBCA-DE 9 125655145 125655145 insertion of <=200bp - C intron_variant PRAD-CA 9 125604921 125604921 single base substitution A G downstream_gene_variant PRAD-CA 9 125614172 125614172 single base substitution G A downstream_gene_variant PRAD-CA 9 125614172 125614172 single base substitution G A intron_variant PRAD-CA 9 125614172 125614172 single base substitution G A upstream_gene_variant PRAD-CA 9 125614428 125614428 single base substitution G T downstream_gene_variant PRAD-CA 9 125614428 125614428 single base substitution G T intron_variant PRAD-CA 9 125614428 125614428 single base substitution G T upstream_gene_variant PRAD-CA 9 125619941 125619941 single base substitution C A intron_variant PRAD-CA 9 125619941 125619941 single base substitution C A upstream_gene_variant PRAD-CA 9 125636653 125636653 single base substitution A G 3_prime_UTR_variant PRAD-CA 9 125636653 125636653 single base substitution A G intron_variant PRAD-UK 9 125608940 125608940 single base substitution A C 3_prime_UTR_variant PRAD-UK 9 125608940 125608940 single base substitution A C downstream_gene_variant PRAD-UK 9 125609306 125609306 single base substitution G C 3_prime_UTR_variant PRAD-UK 9 125609306 125609306 single base substitution G C downstream_gene_variant PRAD-UK 9 125628920 125628920 single base substitution G A intron_variant PRAD-UK 9 125637643 125637643 single base substitution T C intron_variant PRAD-UK 9 125637643 125637643 single base substitution T C missense_variant N444D 1330A>G PRAD-UK 9 125660306 125660306 single base substitution T G 5_prime_UTR_variant PRAD-UK 9 125660306 125660306 single base substitution T G intron_variant PRAD-UK 9 125660306 125660306 single base substitution T G upstream_gene_variant PRAD-UK 9 125661342 125661342 single base substitution C T intron_variant PRAD-UK 9 125661342 125661342 single base substitution C T upstream_gene_variant PRAD-UK 9 125667346 125667346 single base substitution C A intron_variant PRAD-US 9 125613481 125613481 single base substitution T C 3_prime_UTR_variant PRAD-US 9 125613481 125613481 single base substitution T C downstream_gene_variant PRAD-US 9 125613481 125613481 single base substitution T C exon_variant PRAD-US 9 125613481 125613481 single base substitution T C missense_variant S1087G 3259A>G PRAD-US 9 125613481 125613481 single base substitution T C missense_variant S145G 433A>G RECA-EU 9 125607654 125607654 single base substitution T C 3_prime_UTR_variant RECA-EU 9 125607654 125607654 single base substitution T C downstream_gene_variant RECA-EU 9 125616889 125616889 single base substitution C A 3_prime_UTR_variant RECA-EU 9 125616889 125616889 single base substitution C A intron_variant RECA-EU 9 125616889 125616889 single base substitution C A missense_variant V941F 2821G>T RECA-EU 9 125616889 125616889 single base substitution C A upstream_gene_variant RECA-EU 9 125623154 125623154 single base substitution A C downstream_gene_variant RECA-EU 9 125623154 125623154 single base substitution A C intron_variant SKCA-BR 9 125604290 125604290 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 9 125611976 125611976 single base substitution G A 3_prime_UTR_variant SKCA-BR 9 125611976 125611976 single base substitution G A downstream_gene_variant SKCA-BR 9 125611976 125611976 single base substitution G A missense_variant T1169I 3506C>T SKCA-BR 9 125612019 125612019 single base substitution G A 3_prime_UTR_variant SKCA-BR 9 125612019 125612019 single base substitution G A downstream_gene_variant SKCA-BR 9 125612019 125612019 single base substitution G A missense_variant P1155S 3463C>T SKCA-BR 9 125612714 125612714 insertion of <=200bp - TATAGATAGATAGATAGATAG downstream_gene_variant SKCA-BR 9 125612714 125612714 insertion of <=200bp - TATAGATAGATAGATAGATAG intron_variant SKCA-BR 9 125614684 125614684 single base substitution T G downstream_gene_variant SKCA-BR 9 125614684 125614684 single base substitution T G intron_variant SKCA-BR 9 125614684 125614684 single base substitution T G upstream_gene_variant SKCA-BR 9 125614808 125614808 single base substitution A G downstream_gene_variant SKCA-BR 9 125614808 125614808 single base substitution A G intron_variant SKCA-BR 9 125614808 125614808 single base substitution A G upstream_gene_variant SKCA-BR 9 125629725 125629725 single base substitution A G intron_variant SKCA-BR 9 125629731 125629731 single base substitution G A intron_variant SKCA-BR 9 125629788 125629827 deletion of <=200bp GCCTCTGCCCGGCCGCCTATCGTCTGGGACGTGAGGAGCC - intron_variant SKCA-BR 9 125630610 125630610 single base substitution C G intron_variant SKCA-BR 9 125631224 125631224 single base substitution A G downstream_gene_variant SKCA-BR 9 125631224 125631224 single base substitution A G intron_variant SKCA-BR 9 125632688 125632688 single base substitution C A downstream_gene_variant SKCA-BR 9 125632688 125632688 single base substitution C A intron_variant SKCA-BR 9 125632689 125632692 deletion of <=200bp AAAC - downstream_gene_variant SKCA-BR 9 125632689 125632692 deletion of <=200bp AAAC - intron_variant SKCA-BR 9 125632692 125632692 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 9 125632692 125632692 insertion of <=200bp - CA intron_variant SKCA-BR 9 125633927 125633927 single base substitution T G downstream_gene_variant SKCA-BR 9 125633927 125633927 single base substitution T G intron_variant SKCA-BR 9 125640285 125640285 single base substitution A T intron_variant SKCA-BR 9 125643896 125643896 single base substitution A G intron_variant SKCA-BR 9 125646341 125646341 single base substitution A G intron_variant SKCA-BR 9 125646392 125646392 single base substitution T G intron_variant SKCA-BR 9 125646396 125646396 single base substitution A C intron_variant SKCA-BR 9 125647055 125647055 single base substitution C A intron_variant SKCA-BR 9 125650020 125650021 deletion of <=200bp CT - downstream_gene_variant SKCA-BR 9 125650020 125650021 deletion of <=200bp CT - intron_variant SKCA-BR 9 125652757 125652757 single base substitution G A exon_variant SKCA-BR 9 125652757 125652757 single base substitution G A synonymous_variant N139N 417C>T SKCA-BR 9 125659057 125659057 single base substitution C A intron_variant SKCA-BR 9 125660120 125660120 single base substitution A G 5_prime_UTR_variant SKCA-BR 9 125660120 125660120 single base substitution A G intron_variant SKCA-BR 9 125660120 125660120 single base substitution A G upstream_gene_variant SKCA-BR 9 125660224 125660224 single base substitution T A 5_prime_UTR_variant SKCA-BR 9 125660224 125660224 single base substitution T A intron_variant SKCA-BR 9 125660224 125660224 single base substitution T A upstream_gene_variant SKCA-BR 9 125661368 125661368 insertion of <=200bp - TG intron_variant SKCA-BR 9 125661368 125661368 insertion of <=200bp - TG upstream_gene_variant SKCA-BR 9 125661370 125661370 single base substitution T G intron_variant SKCA-BR 9 125661370 125661370 single base substitution T G upstream_gene_variant SKCA-BR 9 125663805 125663805 single base substitution A C intron_variant SKCA-BR 9 125663805 125663805 single base substitution A C upstream_gene_variant SKCA-BR 9 125663865 125663866 deletion of <=200bp CT - intron_variant SKCA-BR 9 125663865 125663866 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 9 125666014 125666014 single base substitution G T intron_variant SKCA-BR 9 125667359 125667359 single base substitution C G intron_variant SKCA-BR 9 125667496 125667496 single base substitution T G 5_prime_UTR_variant SKCA-BR 9 125667496 125667496 single base substitution T G exon_variant SKCA-BR 9 125667496 125667496 single base substitution T G upstream_gene_variant SKCM-US 9 125616864 125616864 single base substitution G A 3_prime_UTR_variant SKCM-US 9 125616864 125616864 single base substitution G A missense_variant S7L 20C>T SKCM-US 9 125616864 125616864 single base substitution G A missense_variant S949L 2846C>T SKCM-US 9 125616864 125616864 single base substitution G A splice_region_variant SKCM-US 9 125616864 125616864 single base substitution G A upstream_gene_variant SKCM-US 9 125617595 125617595 single base substitution G A 3_prime_UTR_variant SKCM-US 9 125617595 125617595 single base substitution G A missense_variant P30S 88C>T SKCM-US 9 125617595 125617595 single base substitution G A missense_variant P895S 2683C>T SKCM-US 9 125617595 125617595 single base substitution G A upstream_gene_variant SKCM-US 9 125617604 125617604 single base substitution G A 3_prime_UTR_variant SKCM-US 9 125617604 125617604 single base substitution G A missense_variant P27S 79C>T SKCM-US 9 125617604 125617604 single base substitution G A missense_variant P892S 2674C>T SKCM-US 9 125617604 125617604 single base substitution G A upstream_gene_variant SKCM-US 9 125620264 125620264 single base substitution G A 3_prime_UTR_variant SKCM-US 9 125620264 125620264 single base substitution G A missense_variant P798S 2392C>T SKCM-US 9 125620264 125620264 single base substitution G A upstream_gene_variant SKCM-US 9 125620300 125620300 single base substitution G A 3_prime_UTR_variant SKCM-US 9 125620300 125620300 single base substitution G A missense_variant H786Y 2356C>T SKCM-US 9 125620300 125620300 single base substitution G A upstream_gene_variant SKCM-US 9 125621031 125621031 single base substitution C T 3_prime_UTR_variant SKCM-US 9 125621031 125621031 single base substitution C T missense_variant E734K 2200G>A SKCM-US 9 125621031 125621031 single base substitution C T upstream_gene_variant SKCM-US 9 125621201 125621201 single base substitution G A 3_prime_UTR_variant SKCM-US 9 125621201 125621201 single base substitution G A missense_variant P677L 2030C>T SKCM-US 9 125621201 125621201 single base substitution G A upstream_gene_variant SKCM-US 9 125622214 125622214 single base substitution G A 3_prime_UTR_variant SKCM-US 9 125622214 125622214 single base substitution G A missense_variant P611S 1831C>T SKCM-US 9 125622214 125622214 single base substitution G A upstream_gene_variant SKCM-US 9 125622240 125622240 single base substitution G A 3_prime_UTR_variant SKCM-US 9 125622240 125622240 single base substitution G A missense_variant P602L 1805C>T SKCM-US 9 125622240 125622240 single base substitution G A upstream_gene_variant STAD-US 9 125617540 125617540 single base substitution C T 3_prime_UTR_variant STAD-US 9 125617540 125617540 single base substitution C T missense_variant R48H 143G>A STAD-US 9 125617540 125617540 single base substitution C T missense_variant R913H 2738G>A STAD-US 9 125617540 125617540 single base substitution C T upstream_gene_variant STAD-US 9 125617543 125617543 single base substitution G A 3_prime_UTR_variant STAD-US 9 125617543 125617543 single base substitution G A missense_variant S47F 140C>T STAD-US 9 125617543 125617543 single base substitution G A missense_variant S912F 2735C>T STAD-US 9 125617543 125617543 single base substitution G A upstream_gene_variant STAD-US 9 125618021 125618021 single base substitution G A 3_prime_UTR_variant STAD-US 9 125618021 125618021 single base substitution G A missense_variant A864V 2591C>T STAD-US 9 125618021 125618021 single base substitution G A upstream_gene_variant STAD-US 9 125621307 125621307 single base substitution C T 3_prime_UTR_variant STAD-US 9 125621307 125621307 single base substitution C T missense_variant V642I 1924G>A STAD-US 9 125621307 125621307 single base substitution C T upstream_gene_variant STAD-US 9 125627678 125627678 single base substitution G A 3_prime_UTR_variant STAD-US 9 125627678 125627678 single base substitution G A downstream_gene_variant STAD-US 9 125627678 125627678 single base substitution G A synonymous_variant G528G 1584C>T STAD-US 9 125627905 125627905 single base substitution T C missense_variant T453A 1357A>G STAD-US 9 125627905 125627905 single base substitution T C splice_region_variant STAD-US 9 125643021 125643021 single base substitution C T exon_variant STAD-US 9 125643021 125643021 single base substitution C T missense_variant R271Q 812G>A STAD-US 9 125659721 125659721 single base substitution T G exon_variant STAD-US 9 125659721 125659721 single base substitution T G intron_variant STAD-US 9 125659721 125659721 single base substitution T G missense_variant E23A 68A>C THCA-US 9 125639844 125639844 single base substitution A G exon_variant THCA-US 9 125639844 125639844 single base substitution A G missense_variant Y411H 1231T>C UCEC-US 9 125611951 125611951 single base substitution G A 3_prime_UTR_variant UCEC-US 9 125611951 125611951 single base substitution G A downstream_gene_variant UCEC-US 9 125611951 125611951 single base substitution G A synonymous_variant N1177N 3531C>T UCEC-US 9 125612042 125612042 single base substitution G T 3_prime_UTR_variant UCEC-US 9 125612042 125612042 single base substitution G T downstream_gene_variant UCEC-US 9 125612042 125612042 single base substitution G T missense_variant S1147Y 3440C>A UCEC-US 9 125612056 125612056 single base substitution C T 3_prime_UTR_variant UCEC-US 9 125612056 125612056 single base substitution C T downstream_gene_variant UCEC-US 9 125612056 125612056 single base substitution C T synonymous_variant Q1142Q 3426G>A UCEC-US 9 125612078 125612078 single base substitution G A 3_prime_UTR_variant UCEC-US 9 125612078 125612078 single base substitution G A downstream_gene_variant UCEC-US 9 125612078 125612078 single base substitution G A exon_variant UCEC-US 9 125612078 125612078 single base substitution G A missense_variant P1135L 3404C>T UCEC-US 9 125612078 125612078 single base substitution G A missense_variant R187W 559C>T UCEC-US 9 125613437 125613437 single base substitution A G 3_prime_UTR_variant UCEC-US 9 125613437 125613437 single base substitution A G downstream_gene_variant UCEC-US 9 125613437 125613437 single base substitution A G exon_variant UCEC-US 9 125613437 125613437 single base substitution A G synonymous_variant N1101N 3303T>C UCEC-US 9 125613437 125613437 single base substitution A G synonymous_variant N159N 477T>C UCEC-US 9 125613503 125613503 single base substitution G T 3_prime_UTR_variant UCEC-US 9 125613503 125613503 single base substitution G T downstream_gene_variant UCEC-US 9 125613503 125613503 single base substitution G T exon_variant UCEC-US 9 125613503 125613503 single base substitution G T synonymous_variant I1079I 3237C>A UCEC-US 9 125613503 125613503 single base substitution G T synonymous_variant I137I 411C>A UCEC-US 9 125620210 125620210 single base substitution G A 3_prime_UTR_variant UCEC-US 9 125620210 125620210 single base substitution G A missense_variant R816C 2446C>T UCEC-US 9 125620210 125620210 single base substitution G A upstream_gene_variant UCEC-US 9 125621000 125621000 single base substitution G A 3_prime_UTR_variant UCEC-US 9 125621000 125621000 single base substitution G A missense_variant S744L 2231C>T UCEC-US 9 125621000 125621000 single base substitution G A upstream_gene_variant UCEC-US 9 125621111 125621111 single base substitution T C 3_prime_UTR_variant UCEC-US 9 125621111 125621111 single base substitution T C missense_variant Q707R 2120A>G UCEC-US 9 125621111 125621111 single base substitution T C upstream_gene_variant UCEC-US 9 125621156 125621156 single base substitution G A 3_prime_UTR_variant UCEC-US 9 125621156 125621156 single base substitution G A missense_variant A692V 2075C>T UCEC-US 9 125621156 125621156 single base substitution G A upstream_gene_variant UCEC-US 9 125621180 125621180 single base substitution G T 3_prime_UTR_variant UCEC-US 9 125621180 125621180 single base substitution G T missense_variant P684H 2051C>A UCEC-US 9 125621180 125621180 single base substitution G T upstream_gene_variant UCEC-US 9 125621235 125621235 single base substitution G A 3_prime_UTR_variant UCEC-US 9 125621235 125621235 single base substitution G A stop_gained R666* 1996C>T UCEC-US 9 125621235 125621235 single base substitution G A upstream_gene_variant UCEC-US 9 125621331 125621331 single base substitution G T 3_prime_UTR_variant UCEC-US 9 125621331 125621331 single base substitution G T missense_variant P634T 1900C>A UCEC-US 9 125621331 125621331 single base substitution G T upstream_gene_variant UCEC-US 9 125621359 125621359 single base substitution C T 3_prime_UTR_variant UCEC-US 9 125621359 125621359 single base substitution C T synonymous_variant T624T 1872G>A UCEC-US 9 125621359 125621359 single base substitution C T upstream_gene_variant UCEC-US 9 125627702 125627702 single base substitution G A 3_prime_UTR_variant UCEC-US 9 125627702 125627702 single base substitution G A downstream_gene_variant UCEC-US 9 125627702 125627702 single base substitution G A synonymous_variant T520T 1560C>T UCEC-US 9 125642036 125642036 single base substitution G A splice_region_variant UCEC-US 9 125642036 125642036 single base substitution G A stop_gained Q404* 1210C>T UCEC-US 9 125643050 125643051 deletion of <=200bp AG - exon_variant UCEC-US 9 125643050 125643051 deletion of <=200bp AG - frameshift_variant S261 UCEC-US 9 125652724 125652724 single base substitution T C exon_variant UCEC-US 9 125652724 125652724 single base substitution T C synonymous_variant R150R 450A>G UCEC-US 9 125659637 125659637 single base substitution G T exon_variant UCEC-US 9 125659637 125659637 single base substitution G T intron_variant UCEC-US 9 125659637 125659637 single base substitution G T missense_variant P51H 152C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T3021 COSM4720852 c.2215T>C p.L739L Substitution - coding silent 9:122858737-122858737 - TCGA-D1-A103-01 COSM1104917 c.3426G>A p.Q1142Q Substitution - coding silent 9:122849777-122849777 - TCGA-D3-A5GU-06 COSM3654100 c.2846C>T p.S949L Substitution - Missense 9:122854585-122854585 - 543 COSM5612528 c.1430T>C p.I477T Substitution - Missense 9:122865553-122865553 - TCGA-D1-A15Z-01 COSM1104921 c.3197C>A p.T1066N Substitution - Missense 9:122851357-122851357 - 215 COSM1735869 c.232-4delT p.? Unknown 9:122893030-122893030 - TCGA-AG-A002-01 COSM263287 c.348A>C p.K116N Substitution - Missense 9:122892910-122892910 - YUROC COSM5410362 c.628G>A p.D210N Substitution - Missense 9:122883335-122883335 - YUKAT COSM5410359 c.857A>T p.H286L Substitution - Missense 9:122880697-122880697 - TCGA-66-2787-01 COSM752767 c.3172G>T p.E1058* Substitution - Nonsense 9:122851382-122851382 - P158 COSM1735869 c.232-4delT p.? Unknown 9:122893030-122893030 - CADO-ES1 COSM3323830 c.2165T>C p.V722A Substitution - Missense 9:122858787-122858787 - PR-09-5245 COSM246991 c.1212G>A p.Q404Q Substitution - coding silent 9:122879755-122879755 - TCGA-B5-A0K9-01 COSM1104925 c.2075C>T p.A692V Substitution - Missense 9:122858877-122858877 - 2171663 COSM1735869 c.232-4delT p.? Unknown 9:122893030-122893030 - Pat_24_B COSM5875507 c.547G>A p.A183T Substitution - Missense 9:122890348-122890348 - 86797 COSM95163 c.945G>T p.Q315H Substitution - Missense 9:122880609-122880609 - pfg011T COSM1643728 c.275A>G p.N92S Substitution - Missense 9:122892983-122892983 - CHC301T COSM251108 c.1870A>G p.T624A Substitution - Missense 9:122859082-122859082 - TCGA-D3-A3ML-06 COSM3654104 c.2392C>T p.P798S Substitution - Missense 9:122857985-122857985 - CCK81 COSM3323947 c.548C>T p.A183V Substitution - Missense 9:122890347-122890347 - HCC2998 COSM1674807 c.134T>G p.L45R Substitution - Missense 9:122897376-122897376 - 6115233 COSM5551879 c.64G>C p.D22H Substitution - Missense 9:122897446-122897446 - TCGA-E9-A1RH-01 COSM1489658 c.507G>A p.Q169Q Substitution - coding silent 9:122890388-122890388 - TCGA-CM-6674-01 COSM1459895 c.2917A>G p.T973A Substitution - Missense 9:122854250-122854250 - SC_9072 COSM5550853 c.3417C>G p.C1139W Substitution - Missense 9:122849786-122849786 - T2963 COSM4720851 c.3125G>A p.S1042N Substitution - Missense 9:122851429-122851429 - SJMB024 COSM255713 c.1241G>A p.S414N Substitution - Missense 9:122877555-122877555 - TCGA-AP-A0LM-01 COSM1104923 c.2231C>T p.S744L Substitution - Missense 9:122858721-122858721 - CHEWS032 COSM4588445 c.295A>G p.K99E Substitution - Missense 9:122892963-122892963 - LUAD-S00488 COSM360554 c.2853G>A p.W951* Substitution - Nonsense 9:122854578-122854578 - 8033510 COSM3395557 c.3258C>T p.I1086I Substitution - coding silent 9:122851203-122851203 - 19 COSM5747061 c.2354A>G p.Y785C Substitution - Missense 9:122858023-122858023 - TCGA-FU-A3HZ-01 COSM1104927 c.1996C>T p.R666* Substitution - Nonsense 9:122858956-122858956 - TCGA-F1-6177-01 COSM3903856 c.2738G>A p.R913H Substitution - Missense 9:122855261-122855261 - SC_9072 COSM5569021 c.2996C>T p.S999L Substitution - Missense 9:122854073-122854073 - C0083T COSM4138828 c.2821G>T p.V941F Substitution - Missense 9:122854610-122854610 - TCGA-DK-A2I4-01 COSM3779611 c.955G>C p.D319H Substitution - Missense 9:122880599-122880599 - TCGA-13-0903-01 COSM76197 c.1765T>C p.Y589H Substitution - Missense 9:122860001-122860001 - P125 COSM1735809 c.232-4_232-3insT p.? Unknown 9:122893029-122893030 - H23 COSM1196365 c.1069C>T p.L357F Substitution - Missense 9:122880017-122880017 - PT22_1 COSM1104922 c.2446C>T p.R816C Substitution - Missense 9:122857931-122857931 - HCC127T COSM3664069 c.2793G>A p.A931A Substitution - coding silent 9:122855206-122855206 - TCGA-EE-A2MR-06 COSM3654108 c.2030C>T p.P677L Substitution - Missense 9:122858922-122858922 - TCGA-CC-A3MB-01 COSM4933673 c.3351A>G p.K1117K Substitution - coding silent 9:122851110-122851110 - 513 COSM3723333 c.2917A>T p.T973S Substitution - Missense 9:122854250-122854250 - LUAD-NYU284 COSM373394 c.1723G>T p.V575L Substitution - Missense 9:122860043-122860043 - LS180 COSM3323920 c.1127delA p.N376fs*4 Deletion - Frameshift 9:122879840-122879840 - DLD1 COSM1674803 c.583G>T p.A195S Substitution - Missense 9:122890312-122890312 - CSCC-56-T COSM4447024 c.1635-3C>T p.? Unknown 9:122860134-122860134 - HN_00313 COSM125803 c.323A>G p.Y108C Substitution - Missense 9:122892935-122892935 - TCGA-BR-7851-01 COSM3903862 c.1924G>A p.V642I Substitution - Missense 9:122859028-122859028 - ESCC_125 COSM5641189 c.134T>C p.L45P Substitution - Missense 9:122897376-122897376 - pfg144T COSM4761059 c.3031A>T p.M1011L Substitution - Missense 9:122854038-122854038 - TCGA-EE-A3AD-06 COSM3654106 c.2200G>A p.E734K Substitution - Missense 9:122858752-122858752 - HT55 COSM3323974 c.59A>T p.E20V Substitution - Missense 9:122897451-122897451 - TCGA-BG-A18B-01 COSM1104932 c.1550C>A p.A517D Substitution - Missense 9:122865433-122865433 - TCGA-06-5858-01 COSM3413320 c.2720C>T p.A907V Substitution - Missense 9:122855279-122855279 - B52-Tumor COSM1755915 c.3443T>C p.I1148T Substitution - Missense 9:122849760-122849760 - TCGA-EE-A3JD-06 COSM4394517 c.2674C>T p.P892S Substitution - Missense 9:122855325-122855325 - CRC-34T COSM1223438 c.205G>A p.A69T Substitution - Missense 9:122897305-122897305 - TCGA-EE-A2MD-06 COSM3654110 c.1805C>T p.P602L Substitution - Missense 9:122859961-122859961 - sysucc-311T COSM5467586 c.2810T>C p.V937A Substitution - Missense 9:122855189-122855189 - Gp5D COSM1104927 c.1996C>T p.R666* Substitution - Nonsense 9:122858956-122858956 - HCT15 COSM1674803 c.583G>T p.A195S Substitution - Missense 9:122890312-122890312 - sysucc-1247T COSM5764577 c.265C>T p.L89L Substitution - coding silent 9:122892993-122892993 - TCGA-B5-A11Y-01 COSM1104915 c.3531C>T p.N1177N Substitution - coding silent 9:122849672-122849672 - LUAD-S01302 COSM396330 c.562G>A p.G188R Substitution - Missense 9:122890333-122890333 - TCGA-AP-A0LM-01 COSM1104922 c.2446C>T p.R816C Substitution - Missense 9:122857931-122857931 - D11 COSM3323917 c.1140T>C p.A380A Substitution - coding silent 9:122879827-122879827 - PCSI_0083_Pa_P_526 COSM3788165 c.163A>G p.T55A Substitution - Missense 9:122897347-122897347 - LUAD-NYU1021 COSM368231 c.3430C>T p.L1144F Substitution - Missense 9:122849773-122849773 - TCGA-A6-6653-01 COSM1104915 c.3531C>T p.N1177N Substitution - coding silent 9:122849672-122849672 - T3048 COSM4720854 c.1623T>G p.S541S Substitution - coding silent 9:122865360-122865360 - TCGA-FW-A3R5-06 COSM3926141 c.1831C>T p.P611S Substitution - Missense 9:122859935-122859935 - TCGA-AP-A051-01 COSM1104927 c.1996C>T p.R666* Substitution - Nonsense 9:122858956-122858956 - TCGA-AX-A0J0-01 COSM1104937 c.450A>G p.R150R Substitution - coding silent 9:122890445-122890445 - PCSI_0083_Pa_P_526 COSM3788162 c.231+2T>C p.? Unknown 9:122897277-122897277 - CSCC-38-T COSM4475726 c.2011C>T p.P671S Substitution - Missense 9:122858941-122858941 - B52 COSM1755915 c.3443T>C p.I1148T Substitution - Missense 9:122849760-122849760 - 347 COSM3323862 c.1923C>T p.N641N Substitution - coding silent 9:122859029-122859029 - CHC301T COSM251108 c.1870A>G p.T624A Substitution - Missense 9:122859082-122859082 - ATL023 COSM5711138 c.2204G>T p.R735I Substitution - Missense 9:122858748-122858748 - TCGA-IR-A3LK-01 COSM4818100 c.595G>C p.E199Q Substitution - Missense 9:122883368-122883368 - PT55 COSM1735869 c.232-4delT p.? Unknown 9:122893030-122893030 - TCGA-IR-A3LA-01 COSM4845046 c.1259G>C p.R420P Substitution - Missense 9:122877537-122877537 - TCGA-D8-A140-01 COSM455313 c.2117A>G p.Y706C Substitution - Missense 9:122858835-122858835 - TCGA-BH-A0W7-01 COSM455315 c.1122G>A p.L374L Substitution - coding silent 9:122879845-122879845 - CHC892T COSM4794486 c.3422G>A p.S1141N Substitution - Missense 9:122849781-122849781 - TCGA-A8-A094-01 COSM455312 c.2459C>G p.S820* Substitution - Nonsense 9:122855874-122855874 - TCGA-HU-A4GT-01 COSM3903866 c.1357A>G p.T453A Substitution - Missense 9:122865626-122865626 - TCGA-AG-3891-01 COSM5069294 c.2742A>C p.T914T Substitution - coding silent 9:122855257-122855257 - PT45 COSM5927559 c.1635-4C>T p.? Unknown 9:122860135-122860135 - HCT8 COSM1674803 c.583G>T p.A195S Substitution - Missense 9:122890312-122890312 - 3N63-VS-3T63 COSM4984614 c.1468G>A p.V490I Substitution - Missense 9:122865515-122865515 - TCGA-22-5473-01 COSM752763 c.248C>T p.S83L Substitution - Missense 9:122893010-122893010 - 46T COSM3716205 c.303C>T p.C101C Substitution - coding silent 9:122892955-122892955 - 234 COSM3730687 c.232-7_232-4delTTTT p.? Unknown 9:122893030-122893033 - TCGA-EA-A50E-01 COSM4822208 c.2737C>T p.R913C Substitution - Missense 9:122855262-122855262 - CSB25 COSM5027135 c.1480A>G p.N494D Substitution - Missense 9:122865503-122865503 - TCGA-EW-A1OV-01 COSM1489657 c.2123G>A p.R708Q Substitution - Missense 9:122858829-122858829 - TCGA-AF-3914-01 COSM5065748 c.3170T>A p.I1057N Substitution - Missense 9:122851384-122851384 - 2521243 COSM5886639 c.350-7C>T p.? Unknown 9:122890552-122890552 - SH-0829 COSM5017946 c.1591G>T p.G531C Substitution - Missense 9:122865392-122865392 - LUAD-CHTN-MAD06-00668 COSM360554 c.2853G>A p.W951* Substitution - Nonsense 9:122854578-122854578 - 786-0 COSM1674800 c.2371C>T p.P791S Substitution - Missense 9:122858006-122858006 - pfg122T COSM4761063 c.1326-1G>T p.? Unknown 9:122865658-122865658 - RKO COSM4649278 c.1681A>G p.T561A Substitution - Missense 9:122860085-122860085 - PR-01-1934 COSM242615 c.1396A>G p.N466D Substitution - Missense 9:122865587-122865587 - HCT-15 COSM1674803 c.583G>T p.A195S Substitution - Missense 9:122890312-122890312 - P122 COSM1735809 c.232-4_232-3insT p.? Unknown 9:122893029-122893030 - PD5950a COSM5785431 c.2077C>T p.P693S Substitution - Missense 9:122858875-122858875 - TCGA-AG-A002-01 COSM263289 c.140G>A p.R47Q Substitution - Missense 9:122897370-122897370 - LUAD-NYU689 COSM375986 c.433G>A p.E145K Substitution - Missense 9:122890462-122890462 - TCGA-HU-A4GQ-01 COSM3903864 c.1584C>T p.G528G Substitution - coding silent 9:122865399-122865399 - TCGA-AX-A05Z-01 COSM1104924 c.2120A>G p.Q707R Substitution - Missense 9:122858832-122858832 - SC_9018 COSM5569061 c.3197C>T p.T1066I Substitution - Missense 9:122851357-122851357 - YUKAT COSM5410357 c.1661C>T p.P554L Substitution - Missense 9:122860105-122860105 - TCGA-D1-A103-01 COSM1104920 c.3237C>A p.I1079I Substitution - coding silent 9:122851224-122851224 - 01-P1216 COSM4588443 c.1871C>T p.T624M Substitution - Missense 9:122859081-122859081 - TCGA-AX-A0J0-01 COSM1104923 c.2231C>T p.S744L Substitution - Missense 9:122858721-122858721 - Gp5D COSM3323761 c.3315A>G p.V1105V Substitution - coding silent 9:122851146-122851146 - RK015_C COSM1636013 c.275A>T p.N92I Substitution - Missense 9:122892983-122892983 - HCC2998 COSM263289 c.140G>A p.R47Q Substitution - Missense 9:122897370-122897370 - TCGA-AN-A0XW-01 COSM455311 c.3007C>T p.Q1003* Substitution - Nonsense 9:122854062-122854062 - TCGA-F4-6806-01 COSM1459891 c.3471_3473delCAC p.T1158delT Deletion - In frame 9:122849730-122849732 - 225 COSM1735869 c.232-4delT p.? Unknown 9:122893030-122893030 - HCC2998 COSM1674807 c.134T>G p.L45R Substitution - Missense 9:122897376-122897376 - BD72T COSM5512605 c.2455-7delT p.? Unknown 9:122855885-122855885 - SC_9008 COSM5574110 c.2455-6_2455-5insT p.? Unknown 9:122855883-122855884 - TCGA-EJ-5515-01 COSM1132602 c.3259A>G p.S1087G Substitution - Missense 9:122851202-122851202 - BD124T COSM3323911 c.1258C>T p.R420* Substitution - Nonsense 9:122877538-122877538 - PT50 COSM5937400 c.2675C>T p.P892L Substitution - Missense 9:122855324-122855324 - TCGA-24-1845-01 COSM1330742 c.961C>T p.L321L Substitution - coding silent 9:122880125-122880125 - TCGA-HU-A4GN-01 COSM3903860 c.2591C>T p.A864V Substitution - Missense 9:122855742-122855742 - T16 COSM5345700 c.960+9A>T p.? Unknown 9:122880585-122880585 - PD11358a COSM5786237 c.1789C>T p.Q597* Substitution - Nonsense 9:122859977-122859977 - AOCS-141-8-0 COSM4152037 c.1747C>G p.L583V Substitution - Missense 9:122860019-122860019 - QC2-32-T2 COSM5654135 c.560G>T p.R187L Substitution - Missense 9:122890335-122890335 - 2521259 COSM5890451 c.470C>T p.S157F Substitution - Missense 9:122890425-122890425 - C086 COSM5538079 c.1208C>T p.P403L Substitution - Missense 9:122879759-122879759 - 3N33-VS-3T33 COSM1459892 c.3405G>A p.P1135P Substitution - coding silent 9:122849798-122849798 - TCGA-EE-A2GB-06 COSM3654102 c.2683C>T p.P895S Substitution - Missense 9:122855316-122855316 - TCGA-DK-A2I4-01 COSM3779609 c.1930G>T p.E644* Substitution - Nonsense 9:122859022-122859022 - pfg181T COSM4761061 c.1966G>A p.D656N Substitution - Missense 9:122858986-122858986 - T3090 COSM4720858 c.1561delG p.V521fs*1 Deletion - Frameshift 9:122865422-122865422 - LS180 COSM3323838 c.2095C>T p.R699C Substitution - Missense 9:122858857-122858857 - 2171670 COSM1735809 c.232-4_232-3insT p.? Unknown 9:122893029-122893030 - PT45 COSM4447024 c.1635-3C>T p.? Unknown 9:122860134-122860134 - PT20_2 COSM5900758 c.905C>T p.S302F Substitution - Missense 9:122880649-122880649 - PD4137a COSM163970 c.1233C>G p.Y411* Substitution - Nonsense 9:122877563-122877563 - CHC314T COSM4957122 c.867G>T p.M289I Substitution - Missense 9:122880687-122880687 - CHEWS031 COSM4588441 c.2688T>C p.F896F Substitution - coding silent 9:122855311-122855311 - TCGA-E2-A10C-01 COSM455314 c.1768C>G p.P590A Substitution - Missense 9:122859998-122859998 - TCGA-B5-A11E-01 COSM1104939 c.152C>A p.P51H Substitution - Missense 9:122897358-122897358 - TCGA-D1-A17L-01 COSM1104933 c.1210C>T p.Q404* Substitution - Nonsense 9:122879757-122879757 - TCGA-BR-6452-01 COSM3903858 c.2735C>T p.S912F Substitution - Missense 9:122855264-122855264 - TCGA-BS-A0UA-01 COSM1104935 c.782_783delCT p.S261fs*13 Deletion - Frameshift 9:122880771-122880772 - GC7_T COSM3748977 c.2595G>A p.V865V Substitution - coding silent 9:122855738-122855738 - LS174T COSM3323920 c.1127delA p.N376fs*4 Deletion - Frameshift 9:122879840-122879840 - TCGA-JW-A852-01 COSM4823709 c.3055G>T p.D1019Y Substitution - Missense 9:122854014-122854014 - HCC061T COSM5805680 c.2789G>T p.S930I Substitution - Missense 9:122855210-122855210 - TCGA-CM-4743-01 COSM1459893 c.3394delA p.T1132fs*5 Deletion - Frameshift 9:122849809-122849809 - B86-Tumor COSM1755916 c.1534G>A p.D512N Substitution - Missense 9:122865449-122865449 - PD5932a COSM5778551 c.2164G>C p.V722L Substitution - Missense 9:122858788-122858788 - NCI-H23 COSM1196365 c.1069C>T p.L357F Substitution - Missense 9:122880017-122880017 - Gp2D COSM4628822 c.1558A>G p.T520A Substitution - Missense 9:122865425-122865425 - HCC003T COSM5819554 c.1184A>G p.Y395C Substitution - Missense 9:122879783-122879783 - NPC3D COSM4997006 c.742C>T p.R248* Substitution - Nonsense 9:122883221-122883221 - T3024 COSM4720850 c.3511G>C p.V1171L Substitution - Missense 9:122849692-122849692 - ccRCC-40 COSM1663872 c.806A>G p.E269G Substitution - Missense 9:122880748-122880748 - PCSI_0083_Pa_X COSM3788165 c.163A>G p.T55A Substitution - Missense 9:122897347-122897347 - TCGA-IR-A3LK-01 COSM4817271 c.3160G>C p.D1054H Substitution - Missense 9:122851394-122851394 - TCGA-D8-A27G-01 COSM3847581 c.87C>T p.I29I Substitution - coding silent 9:122897423-122897423 - TCGA-AP-A0LM-01 COSM1104928 c.1900C>A p.P634T Substitution - Missense 9:122859052-122859052 - TCGA-A6-6653-01 COSM1459892 c.3405G>A p.P1135P Substitution - coding silent 9:122849798-122849798 - PAPNNX COSM3903856 c.2738G>A p.R913H Substitution - Missense 9:122855261-122855261 - Sample_1 COSM5021631 c.232G>A p.V78I Substitution - Missense 9:122893026-122893026 - BD220T COSM5495610 c.3047A>T p.N1016I Substitution - Missense 9:122854022-122854022 - BD236T COSM5518905 c.2031G>A p.P677P Substitution - coding silent 9:122858921-122858921 - TCGA-AA-A010-01 COSM299462 c.2601+9T>G p.? Unknown 9:122855723-122855723 - TCGA-EE-A3AE-06 COSM3654102 c.2683C>T p.P895S Substitution - Missense 9:122855316-122855316 - OSCC-GB_00460111 COSM3716205 c.303C>T p.C101C Substitution - coding silent 9:122892955-122892955 - TCGA-B5-A11E-01 COSM1104931 c.1560C>T p.T520T Substitution - coding silent 9:122865423-122865423 - T613 COSM4720856 c.1588A>G p.N530D Substitution - Missense 9:122865395-122865395 - CHC314T COSM4950304 c.868G>T p.E290* Substitution - Nonsense 9:122880686-122880686 - Single_Sample COSM3323917 c.1140T>C p.A380A Substitution - coding silent 9:122879827-122879827 - TCGA-D1-A103-01 COSM1104915 c.3531C>T p.N1177N Substitution - coding silent 9:122849672-122849672 - CHC314T COSM4957122 c.867G>T p.M289I Substitution - Missense 9:122880687-122880687 - Pat_45_B COSM5875505 c.2956G>A p.D986N Substitution - Missense 9:122854211-122854211 - TCGA-B7-5816-01 COSM3903871 c.68A>C p.E23A Substitution - Missense 9:122897442-122897442 - CHC892T COSM4794486 c.3422G>A p.S1141N Substitution - Missense 9:122849781-122849781 - PT25 COSM1735869 c.232-4delT p.? Unknown 9:122893030-122893030 - M029 COSM1739540 c.1420G>A p.G474R Substitution - Missense 9:122865563-122865563 - T3306 COSM4720860 c.880C>T p.R294C Substitution - Missense 9:122880674-122880674 - sysucc-834T COSM5486700 c.1279C>T p.R427* Substitution - Nonsense 9:122877517-122877517 - TCGA-CJ-4874-01 COSM3367542 c.1945C>A p.P649T Substitution - Missense 9:122859007-122859007 - TCGA-AP-A0LM-01 COSM1104926 c.2051C>A p.P684H Substitution - Missense 9:122858901-122858901 - 169 COSM3728930 c.232-6_232-4delTTT p.? Unknown 9:122893030-122893032 - P84 COSM1735809 c.232-4_232-3insT p.? Unknown 9:122893029-122893030 - HCC127 COSM3664069 c.2793G>A p.A931A Substitution - coding silent 9:122855206-122855206 - TCGA-B5-A11E-01 COSM1104916 c.3440C>A p.S1147Y Substitution - Missense 9:122849763-122849763 - 409 COSM4430802 c.628G>C p.D210H Substitution - Missense 9:122883335-122883335 - RK015_C01 COSM1636013 c.275A>T p.N92I Substitution - Missense 9:122892983-122892983 - TCGA-ER-A42K-06 COSM4894997 c.2356C>T p.H786Y Substitution - Missense 9:122858021-122858021 - 587342 COSM1223438 c.205G>A p.A69T Substitution - Missense 9:122897305-122897305 - TCGA-EM-A22I-01 COSM3375065 c.1231T>C p.Y411H Substitution - Missense 9:122877565-122877565 - 113274 COSM96178 c.1170C>T p.D390D Substitution - coding silent 9:122879797-122879797 - TCGA-B5-A0JY-01 COSM1104918 c.3404C>T p.P1135L Substitution - Missense 9:122849799-122849799 - TCGA-BS-A0UM-01 COSM1104919 c.3303T>C p.N1101N Substitution - coding silent 9:122851158-122851158 - ME009T COSM223368 c.1825G>A p.E609K Substitution - Missense 9:122859941-122859941 - TCGA-CG-5726-01 COSM3903868 c.812G>A p.R271Q Substitution - Missense 9:122880742-122880742 - HCC2998 COSM263289 c.140G>A p.R47Q Substitution - Missense 9:122897370-122897370 - 112503 COSM95162 c.1421G>A p.G474E Substitution - Missense 9:122865562-122865562 - S00339 COSM5657412 c.3011_3035del25 p.R1004fs*15 Deletion - Frameshift 9:122854034-122854058 - TCGA-D1-A103-01 COSM1104929 c.1872G>A p.T624T Substitution - coding silent 9:122859080-122859080 - LS174T COSM3323838 c.2095C>T p.R699C Substitution - Missense 9:122858857-122858857 - Gp2D COSM1104927 c.1996C>T p.R666* Substitution - Nonsense 9:122858956-122858956 - 9-RS COSM1731869 c.2455-4C>G p.? Unknown 9:122855882-122855882 - TCGA-GC-A3RC-01 COSM3779608 c.3354G>C p.Q1118H Substitution - Missense 9:122851107-122851107 - 2171661 COSM1735869 c.232-4delT p.? Unknown 9:122893030-122893030 - Au4 COSM5604673 c.2227T>C p.Y743H Substitution - Missense 9:122858725-122858725 - 2521249 COSM5888060 c.2684C>T p.P895L Substitution - Missense 9:122855315-122855315 - LOVO COSM3323800 c.2450C>T p.A817V Substitution - Missense 9:122857927-122857927 - CHC314T COSM4950304 c.868G>T p.E290* Substitution - Nonsense 9:122880686-122880686 - TCGA-DI-A0WH-01 COSM1104930 c.1758A>G p.V586V Substitution - coding silent 9:122860008-122860008 - TCGA-G4-6586-01 COSM1459899 c.330delA p.K110fs*3 Deletion - Frameshift 9:122892928-122892928 - ccRCC-32 COSM1663869 c.856C>T p.H286Y Substitution - Missense 9:122880698-122880698 - BK0057 COSM4188232 c.2471G>A p.S824N Substitution - Missense 9:122855862-122855862 - 587336 COSM1223437 c.2096G>A p.R699H Substitution - Missense 9:122858856-122858856 - B86 COSM1755916 c.1534G>A p.D512N Substitution - Missense 9:122865449-122865449 - TCGA-AM-5821-01 COSM3763611 c.417C>T p.N139N Substitution - coding silent 9:122890478-122890478 - PT19_2 COSM5900164 c.1987C>T p.P663S Substitution - Missense 9:122858965-122858965 - SJMB024 COSM255713 c.1241G>A p.S414N Substitution - Missense 9:122877555-122877555 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.533491;Hs.533499 9q34

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.F433Lfs*13 c.1299delT 9 125639776 RCCC AG - Frameshift p.S261Ffs*13 c.782_783delCT 9 125643050 UCEC A G IntronicSNV . c.1325+2266T>C 9 125637484 MM A G IntronicSNV . c.583+2189T>C 9 125650402 PIA A G Missense p.Y411H c.1231T>C 9 125639844 THCA A G Missense p.Y589H c.1765T>C 9 125622280 OV A G Synonymous p.N1101N c.3303T>C 9 125613437 UCEC C A 3-UTRSNV . c.3573+3380G>T 9 125608529 HC C A Missense p.L1080F c.3240G>T 9 125613500 LUAD C A Missense p.R886M c.2657G>T 9 125617621 LUAD C A Missense p.V745L c.2233G>T 9 125620998 LUAD C A Nonsense p.E1058* c.3172G>T 9 125613661 LUSC C A Nonsense p.E259* c.775G>T 9 125643058 BLCA C A Nonsense p.E644* c.1930G>T 9 125621301 BLCA C A Synonymous p.R733R c.2199G>T 9 125621032 LUAD C G Missense p.D319H c.955G>C 9 125642878 BLCA C G Missense p.E441Q c.1321G>C 9 125639754 BRCA C G Missense p.Q1041H c.3123G>C 9 125613710 LUAD C T IntronicSNV . c.3118-27G>A 9 125613742 CM C T IntronicSNV . c.583+42G>A 9 125652549 HC C T IntronicSNV . c.961-89G>A 9 125642493 PRAD C T Missense p.E609K c.1825G>A 9 125622220 CM C T Missense p.E734K c.2200G>A 9 125621031 CM C T Missense p.E830K c.2488G>A 9 125618124 HNSC C T Missense p.M667I c.2001G>A 9 125621230 HNSC C T Missense p.R271Q c.812G>A 9 125643021 STAD C T Missense p.R708Q c.2123G>A 9 125621108 BRCA C T Missense p.R913H c.2738G>A 9 125617540 STAD C T Synonymous p.L374L c.1122G>A 9 125642124 BRCA C T Synonymous p.Q169Q c.507G>A 9 125652667 BRCA G A IntronicSNV . c.1325+2128C>T 9 125637622 BRCA G A IntronicSNV . c.3118-51C>T 9 125613766 CM G A Missense p.A692V c.2075C>T 9 125621156 UCEC G A Missense p.P602L c.1805C>T 9 125622240 CM G A Missense p.P798S c.2392C>T 9 125620264 CM G A Missense p.P892S c.2674C>T 9 125617604 CM G A Missense p.P895S c.2683C>T 9 125617595 CM G A Missense p.S662F c.1985C>T 9 125621246 CM G A Missense p.S83L c.248C>T 9 125655289 LUSC G A Nonsense p.Q1003* c.3007C>T 9 125616341 BRCA G A Nonsense p.Q404* c.1210C>T 9 125642036 UCEC G A Synonymous p.N1177N c.3531C>T 9 125611951 UCEC G A Synonymous p.T402T c.1206C>T 9 125642040 CM G C Nonsense p.S820* c.2459C>G 9 125618153 BRCA G C Nonsense p.Y411* c.1233C>G 9 125639842 BRCA G C Synonymous p.V793V c.2379C>G 9 125620277 MM G T Missense p.P649T c.1945C>A 9 125621286 RCCC T A Missense p.N92I c.275A>T 9 125655262 HC T C Missense p.I317V c.949A>G 9 125642884 LUAD T C Missense p.N494D c.1480A>G 9 125627782 BRCA T C Missense p.N92S c.275A>G 9 125655262 STAD T C Missense p.S1087G c.3259A>G 9 125613481 PRAD T C Missense p.Y108C c.323A>G 9 125655214 HNSC T C Missense p.Y706C c.2117A>G 9 125621114 BRCA TCTCCCTCTCCCCATGG - IntronicDeletion . c.3118-51_3118-35delCCATGGGGAGAGGGAGA 9 125613750 ESCA T G Missense p.E23A c.68A>C 9 125659721 STAD