Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 10 69682876 69682876 + Missense_Mutation SNP G G A TCGA-GC-A6I3-01A-11D-A31L-08 TCGA-GC-A6I3-10A-01D-A31J-08 g.chr10:69682876G>A c.2986C>T c.(2986-2988)Cgc>Tgc p.R996C BLCA 10 69699371 69699371 + Missense_Mutation SNP C C G TCGA-FD-A62P-01A-32D-A30E-08 TCGA-FD-A62P-10A-01D-A30H-08 g.chr10:69699371C>G c.2569G>C c.(2569-2571)Gag>Cag p.E857Q BLCA 10 69716710 69716710 + Missense_Mutation SNP G G C TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr10:69716710G>C c.1974C>G c.(1972-1974)atC>atG p.I658M BLCA 10 69748513 69748513 + Frame_Shift_Del DEL C C - TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr10:69748513delC c.1713delG c.(1711-1713)ttgfs p.L571fs BLCA 10 69750954 69750954 + Missense_Mutation SNP T T G TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr10:69750954T>G c.1274A>C c.(1273-1275)gAg>gCg p.E425A BLCA 10 69773880 69773881 + Frame_Shift_Ins INS - - T TCGA-G2-AA3C-01A-21D-A391-08 TCGA-G2-AA3C-10A-01D-A394-08 g.chr10:69773880_69773881insT c.971_972insA c.(970-972)aatfs p.N324fs BLCA 10 69785433 69785433 + Splice_Site SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr10:69785433C>A c.778G>T c.(778-780)Gaa>Taa p.E260* BLCA 10 69804185 69804185 + Nonsense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr10:69804185G>C c.362C>G c.(361-363)tCa>tGa p.S121* BLCA 10 69804295 69804295 + Missense_Mutation SNP T T G TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr10:69804295T>G c.252A>C c.(250-252)caA>caC p.Q84H BRCA 10 69684843 69684843 + Splice_Site SNP C C A TCGA-AO-A0JB-01A-11W-A071-09 TCGA-AO-A0JB-10A-01W-A071-09 g.chr10:69684843C>A c.2964G>T c.(2962-2964)ctG>ctT p.L988L BRCA 10 69692462 69692462 + Silent SNP C C T TCGA-AO-A12E-01A-11D-A10M-09 TCGA-AO-A12E-10A-01D-A10M-09 g.chr10:69692462C>T c.2754G>A c.(2752-2754)gcG>gcA p.A918A BRCA 10 69695914 69695917 + Frame_Shift_Del DEL TTTG TTTG - TCGA-E9-A1N8-01A-11D-A142-09 TCGA-E9-A1N8-10A-01D-A142-09 g.chr10:69695914_69695917delTTTG c.2671_2674delCAAA c.(2671-2676)caaaatfs p.QN891fs BRCA 10 69700784 69700784 + Missense_Mutation SNP G G A TCGA-BH-A0HF-01A-11W-A071-09 TCGA-BH-A0HF-10A-01W-A071-09 g.chr10:69700784G>A c.2440C>T c.(2440-2442)Ctc>Ttc p.L814F BRCA 10 69714455 69714455 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:69714455A>C c.2258T>G c.(2257-2259)gTg>gGg p.V753G BRCA 10 69773908 69773908 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr10:69773908C>T c.944G>A c.(943-945)cGa>cAa p.R315Q BRCA 10 69785428 69785428 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:69785428A>C c.783T>G c.(781-783)ggT>ggG p.G261G BRCA 10 69793826 69793829 + Frame_Shift_Del DEL TGCA TGCA - TCGA-A8-A08R-01A-11W-A050-09 TCGA-A8-A08R-10A-01W-A055-09 g.chr10:69793826_69793829delTGCA c.578_581delTGCA c.(577-582)atgcaafs p.MQ193fs BRCA 10 69832821 69832821 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:69832821A>C c.45T>G c.(43-45)ggT>ggG p.G15G BRCA 10 69832857 69832857 + Nonsense_Mutation SNP G G T TCGA-A8-A07C-01A-11D-A045-09 TCGA-A8-A07C-10A-01W-A055-09 g.chr10:69832857G>T c.9C>A c.(7-9)tgC>tgA p.C3* CESC 10 69682816 69682816 + Nonsense_Mutation SNP C C A TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chr10:69682816C>A c.3046G>T c.(3046-3048)Gag>Tag p.E1016* CESC 10 69726539 69726539 + Silent SNP C C T TCGA-DS-A0VK-01A-21D-A10S-08 TCGA-DS-A0VK-10A-01D-A10S-08 g.chr10:69726539C>T c.1827G>A c.(1825-1827)caG>caA p.Q609Q CESC 10 69748552 69748552 + Missense_Mutation SNP C C A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr10:69748552C>A c.1674G>T c.(1672-1674)aaG>aaT p.K558N CHOL 10 69750950 69750950 + Missense_Mutation SNP T T C TCGA-W5-AA34-01A-11D-A417-09 TCGA-W5-AA34-10A-01D-A41A-09 g.chr10:69750950T>C c.1278A>G c.(1276-1278)atA>atG p.I426M CHOL 10 69785435 69785435 + Splice_Site SNP T T A TCGA-W6-AA0S-01A-11D-A417-09 TCGA-W6-AA0S-10A-01D-A41A-09 g.chr10:69785435T>A c.e8-2 COAD 10 69682746 69682746 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr10:69682746G>T c.3116C>A c.(3115-3117)aCt>aAt p.T1039N COAD 10 69692354 69692354 + Splice_Site SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:69692354C>T c.2862G>A c.(2860-2862)aaG>aaA p.K954K COAD 10 69699377 69699377 + Missense_Mutation SNP C C A TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr10:69699377C>A c.2563G>T c.(2563-2565)Gac>Tac p.D855Y COAD 10 69700825 69700825 + Missense_Mutation SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:69700825A>G c.2399T>C c.(2398-2400)gTt>gCt p.V800A COAD 10 69714393 69714393 + Missense_Mutation SNP T T C TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr10:69714393T>C c.2320A>G c.(2320-2322)Agg>Ggg p.R774G COAD 10 69714420 69714420 + Missense_Mutation SNP A A T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr10:69714420A>T c.2293T>A c.(2293-2295)Tta>Ata p.L765I COAD 10 69726553 69726553 + Missense_Mutation SNP C C T TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr10:69726553C>T c.1813G>A c.(1813-1815)Gag>Aag p.E605K COAD 10 69750115 69750115 + Missense_Mutation SNP T T C TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr10:69750115T>C c.1486A>G c.(1486-1488)Agc>Ggc p.S496G COAD 10 69750905 69750906 + Frame_Shift_Ins INS - - A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr10:69750905_69750906insA c.1322_1323insT c.(1321-1323)ttafs p.L441fs COAD 10 69750919 69750919 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:69750919T>G c.1309A>C c.(1309-1311)Aat>Cat p.N437H COAD 10 69773912 69773912 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:69773912C>A c.940G>T c.(940-942)Gga>Tga p.G314* COAD 10 69793760 69793760 + Missense_Mutation SNP C C T TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr10:69793760C>T c.647G>A c.(646-648)cGc>cAc p.R216H COAD 10 69832742 69832742 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:69832742C>T c.124G>A c.(124-126)Gga>Aga p.G42R COADREAD 10 69682746 69682746 + Missense_Mutation SNP G G T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr10:69682746G>T c.3116C>A c.(3115-3117)aCt>aAt p.T1039N COADREAD 10 69692354 69692354 + Splice_Site SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:69692354C>T c.2862G>A c.(2860-2862)aaG>aaA p.K954K COADREAD 10 69695911 69695911 + Splice_Site SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:69695911G>A c.2677C>T c.(2677-2679)Cgg>Tgg p.R893W COADREAD 10 69699377 69699377 + Missense_Mutation SNP C C A TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr10:69699377C>A c.2563G>T c.(2563-2565)Gac>Tac p.D855Y COADREAD 10 69700825 69700825 + Missense_Mutation SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:69700825A>G c.2399T>C c.(2398-2400)gTt>gCt p.V800A COADREAD 10 69714393 69714393 + Missense_Mutation SNP T T C TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr10:69714393T>C c.2320A>G c.(2320-2322)Agg>Ggg p.R774G COADREAD 10 69714420 69714420 + Missense_Mutation SNP A A T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr10:69714420A>T c.2293T>A c.(2293-2295)Tta>Ata p.L765I COADREAD 10 69726553 69726553 + Missense_Mutation SNP C C T TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr10:69726553C>T c.1813G>A c.(1813-1815)Gag>Aag p.E605K COADREAD 10 69750115 69750115 + Missense_Mutation SNP T T C TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr10:69750115T>C c.1486A>G c.(1486-1488)Agc>Ggc p.S496G COADREAD 10 69750905 69750906 + Frame_Shift_Ins INS - - A TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr10:69750905_69750906insA c.1322_1323insT c.(1321-1323)ttafs p.L441fs COADREAD 10 69750919 69750919 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:69750919T>G c.1309A>C c.(1309-1311)Aat>Cat p.N437H COADREAD 10 69773912 69773912 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:69773912C>A c.940G>T c.(940-942)Gga>Tga p.G314* COADREAD 10 69793760 69793760 + Missense_Mutation SNP C C T TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr10:69793760C>T c.647G>A c.(646-648)cGc>cAc p.R216H COADREAD 10 69832742 69832742 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:69832742C>T c.124G>A c.(124-126)Gga>Aga p.G42R DLBC 10 69695935 69695935 + Missense_Mutation SNP C C G TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr10:69695935C>G c.2653G>C c.(2653-2655)Gac>Cac p.D885H DLBC 10 69695973 69695973 + Missense_Mutation SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr10:69695973C>T c.2615G>A c.(2614-2616)gGt>gAt p.G872D DLBC 10 69695974 69695974 + Missense_Mutation SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr10:69695974C>T c.2614G>A c.(2614-2616)Ggt>Agt p.G872S ESCA 10 69751986 69751986 + Missense_Mutation SNP G G C TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr10:69751986G>C c.1241C>G c.(1240-1242)cCt>cGt p.P414R ESCA 10 69804297 69804297 + Missense_Mutation SNP G G T TCGA-2H-A9GO-01A-11D-A37C-09 TCGA-2H-A9GO-11A-11D-A37F-09 g.chr10:69804297G>T c.250C>A c.(250-252)Caa>Aaa p.Q84K GBMLGG 10 69682740 69682740 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:69682740C>T c.3122G>A c.(3121-3123)cGc>cAc p.R1041H GBMLGG 10 69714744 69714744 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:69714744G>A c.2193C>T c.(2191-2193)aaC>aaT p.N731N GBMLGG 10 69750132 69750132 + Missense_Mutation SNP A A C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:69750132A>C c.1469T>G c.(1468-1470)cTt>cGt p.L490R GBMLGG 10 69804316 69804316 + Missense_Mutation SNP C C G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:69804316C>G c.231G>C c.(229-231)caG>caC p.Q77H HNSC 10 69684939 69684939 + Silent SNP T T C TCGA-UF-A71E-01A-31D-A34J-08 TCGA-UF-A71E-10B-01D-A34M-08 g.chr10:69684939T>C c.2868A>G c.(2866-2868)acA>acG p.T956T HNSC 10 69695987 69695987 + Silent SNP T T A TCGA-CN-4739-01A-02D-1512-08 TCGA-CN-4739-10A-01D-1512-08 g.chr10:69695987T>A c.2601A>T c.(2599-2601)acA>acT p.T867T HNSC 10 69699408 69699408 + Silent SNP G G A TCGA-CR-7368-01A-11D-2129-08 TCGA-CR-7368-10A-01D-2129-08 g.chr10:69699408G>A c.2532C>T c.(2530-2532)agC>agT p.S844S HNSC 10 69748547 69748547 + Missense_Mutation SNP A A G TCGA-CV-5966-01A-11D-1683-08 TCGA-CV-5966-11A-01D-1683-08 g.chr10:69748547A>G c.1679T>C c.(1678-1680)gTa>gCa p.V560A KIPAN 10 69714847 69714847 + Missense_Mutation SNP A A G TCGA-B9-5155-01A-01D-1589-08 TCGA-B9-5155-10A-01D-1589-08 g.chr10:69714847A>G c.2090T>C c.(2089-2091)cTt>cCt p.L697P KIPAN 10 69749982 69749982 + Missense_Mutation SNP G G A TCGA-2Z-A9JK-01A-11D-A42J-10 TCGA-2Z-A9JK-10A-01D-A42M-10 g.chr10:69749982G>A c.1619C>T c.(1618-1620)cCa>cTa p.P540L KIPAN 10 69797906 69797908 + In_Frame_Del DEL TCT TCT - TCGA-B8-4153-01B-11D-1669-08 TCGA-B8-4153-11A-01D-1669-08 g.chr10:69797906_69797908delTCT c.405_407delAGA c.(403-408)tcagat>tct p.D136del KIPAN 10 69804160 69804160 + Splice_Site SNP C C T TCGA-G7-A8LB-01A-11D-A35Z-10 TCGA-G7-A8LB-10A-01D-A35Z-10 g.chr10:69804160C>T c.e4+1 KIRC 10 69797906 69797908 + In_Frame_Del DEL TCT TCT - TCGA-B8-4153-01B-11D-1669-08 TCGA-B8-4153-11A-01D-1669-08 g.chr10:69797906_69797908delTCT c.405_407delAGA c.(403-408)tcagat>tct p.D136del KIRP 10 69714847 69714847 + Missense_Mutation SNP A A G TCGA-B9-5155-01A-01D-1589-08 TCGA-B9-5155-10A-01D-1589-08 g.chr10:69714847A>G c.2090T>C c.(2089-2091)cTt>cCt p.L697P KIRP 10 69749982 69749982 + Missense_Mutation SNP G G A TCGA-2Z-A9JK-01A-11D-A42J-10 TCGA-2Z-A9JK-10A-01D-A42M-10 g.chr10:69749982G>A c.1619C>T c.(1618-1620)cCa>cTa p.P540L KIRP 10 69804160 69804160 + Splice_Site SNP C C T TCGA-G7-A8LB-01A-11D-A35Z-10 TCGA-G7-A8LB-10A-01D-A35Z-10 g.chr10:69804160C>T c.e4+1 LGG 10 69682740 69682740 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:69682740C>T c.3122G>A c.(3121-3123)cGc>cAc p.R1041H LGG 10 69714744 69714744 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:69714744G>A c.2193C>T c.(2191-2193)aaC>aaT p.N731N LGG 10 69750132 69750132 + Missense_Mutation SNP A A C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:69750132A>C c.1469T>G c.(1468-1470)cTt>cGt p.L490R LGG 10 69804316 69804316 + Missense_Mutation SNP C C G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:69804316C>G c.231G>C c.(229-231)caG>caC p.Q77H LIHC 10 69726472 69726472 + Missense_Mutation SNP T T C TCGA-G3-A25W-01A-11D-A16V-10 TCGA-G3-A25W-11A-12D-A16V-10 g.chr10:69726472T>C c.1894A>G c.(1894-1896)Atc>Gtc p.I632V LIHC 10 69748547 69748547 + Missense_Mutation SNP A A G TCGA-DD-AACC-01A-11D-A40R-10 TCGA-DD-AACC-10A-01D-A40U-10 g.chr10:69748547A>G c.1679T>C c.(1678-1680)gTa>gCa p.V560A LIHC 10 69750905 69750906 + Frame_Shift_Ins INS - - A TCGA-DD-AAVP-01A-11D-A40R-10 TCGA-DD-AAVP-10A-01D-A40U-10 g.chr10:69750905_69750906insA c.1322_1323insT c.(1321-1323)ttafs p.L441fs LIHC 10 69785411 69785412 + Missense_Mutation DNP CC CC AA TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr10:69785411_69785412CC>AA c.799_800GG>TT c.(799-801)GGa>TTa p.G267L LIHC 10 69797855 69797855 + Missense_Mutation SNP G G C TCGA-FV-A3I0-01A-11D-A22F-10 TCGA-FV-A3I0-11A-11D-A22F-10 g.chr10:69797855G>C c.458C>G c.(457-459)tCt>tGt p.S153C LUAD 10 69684945 69684945 + Splice_Site SNP C C G TCGA-73-7499-01A-11D-2184-08 TCGA-73-7499-10A-01D-2184-08 g.chr10:69684945C>G c.e25-1 LUAD 10 69699384 69699384 + Silent SNP T T C TCGA-50-8459-01A-11D-2323-08 TCGA-50-8459-10A-01D-2323-08 g.chr10:69699384T>C c.2556A>G c.(2554-2556)ccA>ccG p.P852P LUAD 10 69700696 69700696 + Splice_Site SNP C C A TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr10:69700696C>A c.2528G>T c.(2527-2529)aGa>aTa p.R843I LUAD 10 69700789 69700789 + Missense_Mutation SNP A A T TCGA-99-7458-01A-11D-2036-08 TCGA-99-7458-10A-01D-2036-08 g.chr10:69700789A>T c.2435T>A c.(2434-2436)gTg>gAg p.V812E LUAD 10 69714383 69714383 + Missense_Mutation SNP T T A TCGA-44-6777-01A-11D-1855-08 TCGA-44-6777-10A-01D-1855-08 g.chr10:69714383T>A c.2330A>T c.(2329-2331)gAa>gTa p.E777V LUAD 10 69714447 69714447 + Missense_Mutation SNP C C T TCGA-17-Z062-01A-01W-0747-08 TCGA-17-Z062-11A-01W-0747-08 g.chr10:69714447C>T c.2266G>A c.(2266-2268)Gaa>Aaa p.E756K LUAD 10 69714793 69714793 + Missense_Mutation SNP C C G TCGA-55-8205-01A-11D-2238-08 TCGA-55-8205-10A-01D-2238-08 g.chr10:69714793C>G c.2144G>C c.(2143-2145)aGa>aCa p.R715T LUAD 10 69716678 69716678 + Missense_Mutation SNP G G T TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chr10:69716678G>T c.2006C>A c.(2005-2007)gCa>gAa p.A669E LUAD 10 69726544 69726544 + Nonsense_Mutation SNP C C A TCGA-50-5946-01A-11D-1753-08 TCGA-50-5946-10A-01D-1753-08 g.chr10:69726544C>A c.1822G>T c.(1822-1824)Gga>Tga p.G608* LUAD 10 69749992 69749992 + Missense_Mutation SNP C C G TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr10:69749992C>G c.1609G>C c.(1609-1611)Gaa>Caa p.E537Q LUAD 10 69751983 69751983 + Missense_Mutation SNP G G A TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr10:69751983G>A c.1244C>T c.(1243-1245)tCt>tTt p.S415F LUAD 10 69752385 69752385 + Missense_Mutation SNP A A T TCGA-MP-A4T4-01A-11D-A25L-08 TCGA-MP-A4T4-10A-01D-A25L-08 g.chr10:69752385A>T c.1124T>A c.(1123-1125)tTt>tAt p.F375Y LUAD 10 69785392 69785392 + Missense_Mutation SNP C C A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr10:69785392C>A c.819G>T c.(817-819)caG>caT p.Q273H LUAD 10 69793920 69793920 + Nonsense_Mutation SNP G G A TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr10:69793920G>A c.487C>T c.(487-489)Cag>Tag p.Q163* LUAD 10 69793923 69793923 + Nonsense_Mutation SNP C C A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr10:69793923C>A c.484G>T c.(484-486)Gga>Tga p.G162* LUAD 10 69832647 69832647 + Missense_Mutation SNP C C G TCGA-95-7948-01A-11D-2184-08 TCGA-95-7948-10A-01D-2184-08 g.chr10:69832647C>G c.219G>C c.(217-219)aaG>aaC p.K73N LUSC 10 69700823 69700823 + Missense_Mutation SNP T T A TCGA-18-3419-01A-01D-0983-08 TCGA-18-3419-11A-01D-0983-08 g.chr10:69700823T>A c.2401A>T c.(2401-2403)Atc>Ttc p.I801F LUSC 10 69804216 69804216 + Missense_Mutation SNP C C G TCGA-18-3416-01A-01D-0983-08 TCGA-18-3416-11A-01D-0983-08 g.chr10:69804216C>G c.331G>C c.(331-333)Gat>Cat p.D111H OV 10 69692499 69692499 + Missense_Mutation SNP T T C TCGA-23-2078-01A-01W-0722-08 TCGA-23-2078-10A-01W-0722-08 g.chr10:69692499T>C c.2717A>G c.(2716-2718)aAt>aGt p.N906S PRAD 10 69748522 69748522 + Silent SNP T T G TCGA-YL-A8SQ-01B-11D-A377-08 TCGA-YL-A8SQ-10A-01D-A37A-08 g.chr10:69748522T>G c.1704A>C c.(1702-1704)gtA>gtC p.V568V PRAD 10 69750903 69750903 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:69750903G>A c.1325C>T c.(1324-1326)gCt>gTt p.A442V READ 10 69695911 69695911 + Splice_Site SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:69695911G>A c.2677C>T c.(2677-2679)Cgg>Tgg p.R893W SARC 10 69832684 69832684 + Missense_Mutation SNP T T C TCGA-FX-A3TO-01A-11D-A228-09 TCGA-FX-A3TO-10A-01D-A22A-09 g.chr10:69832684T>C c.182A>G c.(181-183)aAt>aGt p.N61S SARC 10 69832687 69832687 + Missense_Mutation SNP C C T TCGA-IE-A4EI-01A-11D-A24N-09 TCGA-IE-A4EI-10A-01D-A24N-09 g.chr10:69832687C>T c.179G>A c.(178-180)tGt>tAt p.C60Y SKCM 10 69684878 69684878 + Missense_Mutation SNP G G A TCGA-EE-A29B-06A-11D-A197-08 TCGA-EE-A29B-10A-01D-A199-08 g.chr10:69684878G>A c.2929C>T c.(2929-2931)Cac>Tac p.H977Y SKCM 10 69726449 69726449 + Silent SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr10:69726449G>A c.1917C>T c.(1915-1917)gcC>gcT p.A639A SKCM 10 69750152 69750152 + Silent SNP T T G TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr10:69750152T>G c.1449A>C c.(1447-1449)gcA>gcC p.A483A SKCM 10 69751987 69751987 + Missense_Mutation SNP G G A TCGA-EE-A2MU-06A-21D-A196-08 TCGA-EE-A2MU-10A-01D-A198-08 g.chr10:69751987G>A c.1240C>T c.(1240-1242)Cct>Tct p.P414S SKCM 10 69752044 69752044 + Missense_Mutation SNP G G A TCGA-DA-A1I5-06A-11D-A197-08 TCGA-DA-A1I5-10A-01D-A199-08 g.chr10:69752044G>A c.1183C>T c.(1183-1185)Ccg>Tcg p.P395S SKCM 10 69785421 69785421 + Missense_Mutation SNP A A G TCGA-D3-A3CE-06A-11D-A19A-08 TCGA-D3-A3CE-10A-01D-A19A-08 g.chr10:69785421A>G c.790T>C c.(790-792)Ttt>Ctt p.F264L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 10 69748513 69748513 deletion of <=200bp C - 3_prime_UTR_variant BLCA-US 10 69748513 69748513 deletion of <=200bp C - exon_variant BLCA-US 10 69748513 69748513 deletion of <=200bp C - frameshift_variant L461 BLCA-US 10 69748513 69748513 deletion of <=200bp C - frameshift_variant L571 BOCA-FR 10 69725586 69725586 single base substitution C T exon_variant BOCA-FR 10 69725586 69725586 single base substitution C T intron_variant BRCA-EU 10 69678385 69678385 single base substitution T A downstream_gene_variant BRCA-EU 10 69679021 69679021 single base substitution A G downstream_gene_variant BRCA-EU 10 69681066 69681066 single base substitution C T downstream_gene_variant BRCA-EU 10 69684794 69684794 single base substitution A G intron_variant BRCA-EU 10 69686115 69686115 single base substitution T C intron_variant BRCA-EU 10 69686187 69686187 insertion of <=200bp - C intron_variant BRCA-EU 10 69687708 69687708 single base substitution C T intron_variant BRCA-EU 10 69688096 69688096 single base substitution C G intron_variant BRCA-EU 10 69691108 69691108 single base substitution G A intron_variant BRCA-EU 10 69691175 69691175 single base substitution C T intron_variant BRCA-EU 10 69692603 69692603 single base substitution C T intron_variant BRCA-EU 10 69693160 69693160 deletion of <=200bp A - intron_variant BRCA-EU 10 69693367 69693367 deletion of <=200bp T - intron_variant BRCA-EU 10 69694429 69694429 single base substitution T C intron_variant BRCA-EU 10 69694996 69694996 single base substitution G A intron_variant BRCA-EU 10 69695244 69695244 single base substitution G A intron_variant BRCA-EU 10 69696640 69696640 single base substitution T C intron_variant BRCA-EU 10 69696692 69696692 single base substitution G A intron_variant BRCA-EU 10 69697118 69697118 insertion of <=200bp - A intron_variant BRCA-EU 10 69698205 69698205 single base substitution A G intron_variant BRCA-EU 10 69698974 69698974 single base substitution T C intron_variant BRCA-EU 10 69701131 69701131 single base substitution A G intron_variant BRCA-EU 10 69701226 69701226 single base substitution G C intron_variant BRCA-EU 10 69703312 69703312 single base substitution G A intron_variant BRCA-EU 10 69703378 69703378 single base substitution T A intron_variant BRCA-EU 10 69704115 69704115 single base substitution T C intron_variant BRCA-EU 10 69704279 69704279 single base substitution T A intron_variant BRCA-EU 10 69704639 69704639 single base substitution G C intron_variant BRCA-EU 10 69706938 69706938 single base substitution C T intron_variant BRCA-EU 10 69708359 69708359 single base substitution G C intron_variant BRCA-EU 10 69709191 69709191 single base substitution G C downstream_gene_variant BRCA-EU 10 69709191 69709191 single base substitution G C intron_variant BRCA-EU 10 69709406 69709406 single base substitution G A downstream_gene_variant BRCA-EU 10 69709406 69709406 single base substitution G A intron_variant BRCA-EU 10 69709805 69709805 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 69709805 69709805 deletion of <=200bp A - intron_variant BRCA-EU 10 69711675 69711675 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 69711675 69711675 deletion of <=200bp A - intron_variant BRCA-EU 10 69717484 69717484 single base substitution C A intron_variant BRCA-EU 10 69717484 69717484 single base substitution C A upstream_gene_variant BRCA-EU 10 69717570 69717570 insertion of <=200bp - T intron_variant BRCA-EU 10 69717570 69717570 insertion of <=200bp - T upstream_gene_variant BRCA-EU 10 69718131 69718131 single base substitution T A intron_variant BRCA-EU 10 69718131 69718131 single base substitution T A upstream_gene_variant BRCA-EU 10 69718331 69718331 single base substitution G A intron_variant BRCA-EU 10 69718331 69718331 single base substitution G A upstream_gene_variant BRCA-EU 10 69718944 69718944 single base substitution T A intron_variant BRCA-EU 10 69718944 69718944 single base substitution T A upstream_gene_variant BRCA-EU 10 69719554 69719554 single base substitution G A downstream_gene_variant BRCA-EU 10 69719554 69719554 single base substitution G A intron_variant BRCA-EU 10 69719554 69719554 single base substitution G A upstream_gene_variant BRCA-EU 10 69719742 69719742 single base substitution G C downstream_gene_variant BRCA-EU 10 69719742 69719742 single base substitution G C intron_variant BRCA-EU 10 69719742 69719742 single base substitution G C upstream_gene_variant BRCA-EU 10 69720356 69720356 single base substitution G A downstream_gene_variant BRCA-EU 10 69720356 69720356 single base substitution G A intron_variant BRCA-EU 10 69720356 69720356 single base substitution G A upstream_gene_variant BRCA-EU 10 69721140 69721140 single base substitution C G downstream_gene_variant BRCA-EU 10 69721140 69721140 single base substitution C G intron_variant BRCA-EU 10 69721140 69721140 single base substitution C G upstream_gene_variant BRCA-EU 10 69722820 69722820 single base substitution G A downstream_gene_variant BRCA-EU 10 69722820 69722820 single base substitution G A intron_variant BRCA-EU 10 69722828 69722828 single base substitution G A downstream_gene_variant BRCA-EU 10 69722828 69722828 single base substitution G A intron_variant BRCA-EU 10 69722843 69722843 single base substitution G C downstream_gene_variant BRCA-EU 10 69722843 69722843 single base substitution G C intron_variant BRCA-EU 10 69722899 69722899 single base substitution G A downstream_gene_variant BRCA-EU 10 69722899 69722899 single base substitution G A intron_variant BRCA-EU 10 69723023 69723023 single base substitution G C downstream_gene_variant BRCA-EU 10 69723023 69723023 single base substitution G C intron_variant BRCA-EU 10 69723162 69723162 single base substitution C T downstream_gene_variant BRCA-EU 10 69723162 69723162 single base substitution C T intron_variant BRCA-EU 10 69723310 69723310 single base substitution T C downstream_gene_variant BRCA-EU 10 69723310 69723310 single base substitution T C intron_variant BRCA-EU 10 69723334 69723334 single base substitution G C downstream_gene_variant BRCA-EU 10 69723334 69723334 single base substitution G C intron_variant BRCA-EU 10 69724089 69724101 deletion of <=200bp CTCCTAGTTTTCC - downstream_gene_variant BRCA-EU 10 69724089 69724101 deletion of <=200bp CTCCTAGTTTTCC - intron_variant BRCA-EU 10 69728523 69728523 single base substitution G T intron_variant BRCA-EU 10 69729224 69729224 insertion of <=200bp - G intron_variant BRCA-EU 10 69732534 69732534 single base substitution C G intron_variant BRCA-EU 10 69733105 69733105 single base substitution G C intron_variant BRCA-EU 10 69733369 69733369 single base substitution G C intron_variant BRCA-EU 10 69734344 69734344 single base substitution G C intron_variant BRCA-EU 10 69734515 69734515 single base substitution G A intron_variant BRCA-EU 10 69734940 69734940 single base substitution C T intron_variant BRCA-EU 10 69734947 69734947 single base substitution T A intron_variant BRCA-EU 10 69737846 69737846 single base substitution A C intron_variant BRCA-EU 10 69737982 69737982 single base substitution G C intron_variant BRCA-EU 10 69737997 69737997 single base substitution C T intron_variant BRCA-EU 10 69738381 69738381 single base substitution T C intron_variant BRCA-EU 10 69738409 69738409 single base substitution A T intron_variant BRCA-EU 10 69740829 69740829 single base substitution G C intron_variant BRCA-EU 10 69742753 69742753 single base substitution C T intron_variant BRCA-EU 10 69745910 69745910 single base substitution G A intron_variant BRCA-EU 10 69745955 69745955 single base substitution T C intron_variant BRCA-EU 10 69747951 69747951 single base substitution C T intron_variant BRCA-EU 10 69748665 69748665 deletion of <=200bp T - intron_variant BRCA-EU 10 69748863 69748863 deletion of <=200bp A - intron_variant BRCA-EU 10 69749187 69749187 single base substitution C G intron_variant BRCA-EU 10 69751663 69751663 deletion of <=200bp T - intron_variant BRCA-EU 10 69751663 69751663 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 69751893 69751893 single base substitution A T intron_variant BRCA-EU 10 69751893 69751893 single base substitution A T upstream_gene_variant BRCA-EU 10 69752753 69752753 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU 10 69752753 69752753 insertion of <=200bp - A intron_variant BRCA-EU 10 69752753 69752753 insertion of <=200bp - A upstream_gene_variant BRCA-EU 10 69753154 69753154 single base substitution T C 3_prime_UTR_variant BRCA-EU 10 69753154 69753154 single base substitution T C intron_variant BRCA-EU 10 69753154 69753154 single base substitution T C upstream_gene_variant BRCA-EU 10 69753725 69753725 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 69753725 69753725 single base substitution C T intron_variant BRCA-EU 10 69753725 69753725 single base substitution C T upstream_gene_variant BRCA-EU 10 69754179 69754179 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 10 69754179 69754179 deletion of <=200bp T - intron_variant BRCA-EU 10 69754179 69754179 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 69755313 69755313 single base substitution C G intron_variant BRCA-EU 10 69756694 69756694 single base substitution G T intron_variant BRCA-EU 10 69757672 69757672 single base substitution G C intron_variant BRCA-EU 10 69759861 69759861 single base substitution C T intron_variant BRCA-EU 10 69760535 69760535 single base substitution C A intron_variant BRCA-EU 10 69761914 69761914 single base substitution G T intron_variant BRCA-EU 10 69764452 69764452 single base substitution T A intron_variant BRCA-EU 10 69764679 69764679 single base substitution G A intron_variant BRCA-EU 10 69765501 69765501 single base substitution C T intron_variant BRCA-EU 10 69766325 69766325 single base substitution G C intron_variant BRCA-EU 10 69768391 69768391 single base substitution G C intron_variant BRCA-EU 10 69769676 69769676 single base substitution G T intron_variant BRCA-EU 10 69770140 69770140 single base substitution G T intron_variant BRCA-EU 10 69770341 69770341 single base substitution C G intron_variant BRCA-EU 10 69770357 69770357 single base substitution C T intron_variant BRCA-EU 10 69772194 69772194 single base substitution G C intron_variant BRCA-EU 10 69772272 69772272 single base substitution G C intron_variant BRCA-EU 10 69773753 69773753 single base substitution G C intron_variant BRCA-EU 10 69773789 69773789 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 69773789 69773789 single base substitution C T exon_variant BRCA-EU 10 69773789 69773789 single base substitution C T missense_variant D245N 733G>A BRCA-EU 10 69773789 69773789 single base substitution C T missense_variant D355N 1063G>A BRCA-EU 10 69773956 69773956 single base substitution G A intron_variant BRCA-EU 10 69775189 69775189 single base substitution C T intron_variant BRCA-EU 10 69776129 69776129 single base substitution G A intron_variant BRCA-EU 10 69776203 69776203 single base substitution G A intron_variant BRCA-EU 10 69777928 69777928 single base substitution A T intron_variant BRCA-EU 10 69778135 69778135 single base substitution G C intron_variant BRCA-EU 10 69778560 69778560 single base substitution G C intron_variant BRCA-EU 10 69778835 69778835 single base substitution C G intron_variant BRCA-EU 10 69778981 69778981 single base substitution G A intron_variant BRCA-EU 10 69779417 69779417 single base substitution G A intron_variant BRCA-EU 10 69779531 69779531 single base substitution T C intron_variant BRCA-EU 10 69780380 69780380 single base substitution G C intron_variant BRCA-EU 10 69780684 69780684 deletion of <=200bp A - intron_variant BRCA-EU 10 69781042 69781042 single base substitution G A intron_variant BRCA-EU 10 69782317 69782317 single base substitution G C intron_variant BRCA-EU 10 69786200 69786200 deletion of <=200bp A - intron_variant BRCA-EU 10 69787983 69787983 single base substitution A G downstream_gene_variant BRCA-EU 10 69787983 69787983 single base substitution A G intron_variant BRCA-EU 10 69791517 69791517 deletion of <=200bp C - downstream_gene_variant BRCA-EU 10 69791517 69791517 deletion of <=200bp C - intron_variant BRCA-EU 10 69791518 69791518 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 69791518 69791518 deletion of <=200bp T - intron_variant BRCA-EU 10 69791518 69791518 insertion of <=200bp - T downstream_gene_variant BRCA-EU 10 69791518 69791518 insertion of <=200bp - T intron_variant BRCA-EU 10 69791597 69791597 single base substitution G A downstream_gene_variant BRCA-EU 10 69791597 69791597 single base substitution G A intron_variant BRCA-EU 10 69791949 69791949 single base substitution T A downstream_gene_variant BRCA-EU 10 69791949 69791949 single base substitution T A intron_variant BRCA-EU 10 69792236 69792236 single base substitution C G downstream_gene_variant BRCA-EU 10 69792236 69792236 single base substitution C G intron_variant BRCA-EU 10 69793864 69793864 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 69793864 69793864 single base substitution C T exon_variant BRCA-EU 10 69793864 69793864 single base substitution C T synonymous_variant P181P 543G>A BRCA-EU 10 69793864 69793864 single base substitution C T synonymous_variant P205P 615G>A BRCA-EU 10 69793864 69793864 single base substitution C T synonymous_variant P71P 213G>A BRCA-EU 10 69794133 69794133 single base substitution G C intron_variant BRCA-EU 10 69794813 69794813 single base substitution T G intron_variant BRCA-EU 10 69795763 69795763 single base substitution T C intron_variant BRCA-EU 10 69796188 69796188 single base substitution G A intron_variant BRCA-EU 10 69797336 69797336 single base substitution G A intron_variant BRCA-EU 10 69797403 69797403 single base substitution C G intron_variant BRCA-EU 10 69798245 69798245 single base substitution G A intron_variant BRCA-EU 10 69798245 69798245 single base substitution G A upstream_gene_variant BRCA-EU 10 69798478 69798478 deletion of <=200bp T - intron_variant BRCA-EU 10 69798478 69798478 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 69798822 69798822 single base substitution G A intron_variant BRCA-EU 10 69798822 69798822 single base substitution G A upstream_gene_variant BRCA-EU 10 69798974 69798974 single base substitution G A intron_variant BRCA-EU 10 69798974 69798974 single base substitution G A upstream_gene_variant BRCA-EU 10 69799307 69799307 single base substitution T A 5_prime_UTR_variant BRCA-EU 10 69799307 69799307 single base substitution T A intron_variant BRCA-EU 10 69799307 69799307 single base substitution T A upstream_gene_variant BRCA-EU 10 69799608 69799608 deletion of <=200bp A - 5_prime_UTR_variant BRCA-EU 10 69799608 69799608 deletion of <=200bp A - intron_variant BRCA-EU 10 69799608 69799608 deletion of <=200bp A - upstream_gene_variant BRCA-EU 10 69800467 69800467 single base substitution G T intron_variant BRCA-EU 10 69800467 69800467 single base substitution G T upstream_gene_variant BRCA-EU 10 69800602 69800602 single base substitution C T intron_variant BRCA-EU 10 69800602 69800602 single base substitution C T upstream_gene_variant BRCA-EU 10 69803923 69803923 deletion of <=200bp T - intron_variant BRCA-EU 10 69803923 69803923 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 69804059 69804059 single base substitution G T intron_variant BRCA-EU 10 69804059 69804059 single base substitution G T upstream_gene_variant BRCA-EU 10 69804829 69804829 single base substitution G C intron_variant BRCA-EU 10 69806616 69806616 single base substitution G C intron_variant BRCA-EU 10 69809005 69809005 single base substitution T C intron_variant BRCA-EU 10 69809514 69809514 single base substitution A T intron_variant BRCA-EU 10 69809680 69809680 single base substitution A G intron_variant BRCA-EU 10 69811310 69811310 single base substitution G C intron_variant BRCA-EU 10 69811759 69811759 deletion of <=200bp A - intron_variant BRCA-EU 10 69813678 69813678 single base substitution A C intron_variant BRCA-EU 10 69814865 69814865 single base substitution G C intron_variant BRCA-EU 10 69817091 69817091 single base substitution G C intron_variant BRCA-EU 10 69817899 69817899 single base substitution C G intron_variant BRCA-EU 10 69818410 69818410 single base substitution A T intron_variant BRCA-EU 10 69823687 69823687 single base substitution A G downstream_gene_variant BRCA-EU 10 69823687 69823687 single base substitution A G intron_variant BRCA-EU 10 69823920 69823920 single base substitution C G downstream_gene_variant BRCA-EU 10 69823920 69823920 single base substitution C G intron_variant BRCA-EU 10 69824333 69824333 single base substitution A G downstream_gene_variant BRCA-EU 10 69824333 69824333 single base substitution A G intron_variant BRCA-EU 10 69826191 69826191 single base substitution C T downstream_gene_variant BRCA-EU 10 69826191 69826191 single base substitution C T intron_variant BRCA-EU 10 69827725 69827725 single base substitution G C 3_prime_UTR_variant BRCA-EU 10 69827725 69827725 single base substitution G C intron_variant BRCA-EU 10 69828374 69828374 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 69828374 69828374 single base substitution G A downstream_gene_variant BRCA-EU 10 69828374 69828374 single base substitution G A intron_variant BRCA-EU 10 69828732 69828732 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU 10 69828732 69828732 insertion of <=200bp - A downstream_gene_variant BRCA-EU 10 69828732 69828732 insertion of <=200bp - A intron_variant BRCA-EU 10 69830319 69830319 single base substitution C T downstream_gene_variant BRCA-EU 10 69830319 69830319 single base substitution C T intron_variant BRCA-EU 10 69830319 69830319 single base substitution C T synonymous_variant A88A 264G>A BRCA-EU 10 69830956 69830956 single base substitution G C downstream_gene_variant BRCA-EU 10 69830956 69830956 single base substitution G C intron_variant BRCA-EU 10 69831351 69831351 single base substitution G C downstream_gene_variant BRCA-EU 10 69831351 69831351 single base substitution G C intron_variant BRCA-EU 10 69831474 69831474 single base substitution G C downstream_gene_variant BRCA-EU 10 69831474 69831474 single base substitution G C intron_variant BRCA-EU 10 69832227 69832227 single base substitution G C downstream_gene_variant BRCA-EU 10 69832227 69832227 single base substitution G C intron_variant BRCA-EU 10 69832391 69832391 single base substitution G A downstream_gene_variant BRCA-EU 10 69832391 69832391 single base substitution G A intron_variant BRCA-EU 10 69832946 69832946 single base substitution G C intron_variant BRCA-EU 10 69832946 69832946 single base substitution G C splice_region_variant BRCA-EU 10 69832946 69832946 single base substitution G C upstream_gene_variant BRCA-EU 10 69834060 69834060 single base substitution C G intron_variant BRCA-EU 10 69834060 69834060 single base substitution C G upstream_gene_variant BRCA-EU 10 69835494 69835494 single base substitution A C upstream_gene_variant BRCA-EU 10 69835702 69835702 single base substitution G T upstream_gene_variant BRCA-EU 10 69837531 69837531 single base substitution A G upstream_gene_variant BRCA-EU 10 69838424 69838424 single base substitution G C upstream_gene_variant BRCA-EU 10 69839183 69839183 single base substitution C A upstream_gene_variant BRCA-EU 10 69839484 69839484 single base substitution G A upstream_gene_variant BRCA-FR 10 69690513 69690513 single base substitution C T intron_variant BRCA-FR 10 69690705 69690705 single base substitution G A intron_variant BRCA-FR 10 69691693 69691693 single base substitution A G intron_variant BRCA-FR 10 69706938 69706938 single base substitution C T intron_variant BRCA-FR 10 69709028 69709028 single base substitution G C downstream_gene_variant BRCA-FR 10 69709028 69709028 single base substitution G C intron_variant BRCA-FR 10 69709406 69709406 single base substitution G A downstream_gene_variant BRCA-FR 10 69709406 69709406 single base substitution G A intron_variant BRCA-FR 10 69719042 69719042 single base substitution T C intron_variant BRCA-FR 10 69719042 69719042 single base substitution T C upstream_gene_variant BRCA-FR 10 69719742 69719742 single base substitution G C downstream_gene_variant BRCA-FR 10 69719742 69719742 single base substitution G C intron_variant BRCA-FR 10 69719742 69719742 single base substitution G C upstream_gene_variant BRCA-FR 10 69719855 69719855 single base substitution C T downstream_gene_variant BRCA-FR 10 69719855 69719855 single base substitution C T intron_variant BRCA-FR 10 69719855 69719855 single base substitution C T upstream_gene_variant BRCA-FR 10 69725943 69725943 single base substitution C T exon_variant BRCA-FR 10 69725943 69725943 single base substitution C T intron_variant BRCA-FR 10 69737108 69737108 single base substitution G C intron_variant BRCA-FR 10 69745910 69745910 single base substitution G A intron_variant BRCA-FR 10 69747136 69747136 single base substitution A G intron_variant BRCA-FR 10 69749187 69749187 single base substitution C G intron_variant BRCA-FR 10 69756694 69756694 single base substitution G T intron_variant BRCA-FR 10 69768391 69768391 single base substitution G C intron_variant BRCA-FR 10 69773789 69773789 single base substitution C T 3_prime_UTR_variant BRCA-FR 10 69773789 69773789 single base substitution C T exon_variant BRCA-FR 10 69773789 69773789 single base substitution C T missense_variant D245N 733G>A BRCA-FR 10 69773789 69773789 single base substitution C T missense_variant D355N 1063G>A BRCA-FR 10 69779531 69779531 single base substitution T C intron_variant BRCA-FR 10 69791597 69791597 single base substitution G A downstream_gene_variant BRCA-FR 10 69791597 69791597 single base substitution G A intron_variant BRCA-FR 10 69794133 69794133 single base substitution G C intron_variant BRCA-FR 10 69798245 69798245 single base substitution G A intron_variant BRCA-FR 10 69798245 69798245 single base substitution G A upstream_gene_variant BRCA-FR 10 69804059 69804059 single base substitution G T intron_variant BRCA-FR 10 69804059 69804059 single base substitution G T upstream_gene_variant BRCA-FR 10 69812969 69812969 single base substitution C A intron_variant BRCA-FR 10 69817899 69817899 single base substitution C G intron_variant BRCA-FR 10 69827611 69827611 single base substitution G A 3_prime_UTR_variant BRCA-FR 10 69827611 69827611 single base substitution G A intron_variant BRCA-FR 10 69827725 69827725 single base substitution G C 3_prime_UTR_variant BRCA-FR 10 69827725 69827725 single base substitution G C intron_variant BRCA-FR 10 69830956 69830956 single base substitution G C downstream_gene_variant BRCA-FR 10 69830956 69830956 single base substitution G C intron_variant BRCA-FR 10 69835702 69835702 single base substitution G T upstream_gene_variant BRCA-UK 10 69688002 69688002 single base substitution G A intron_variant BRCA-UK 10 69699881 69699881 single base substitution C T intron_variant BRCA-UK 10 69703378 69703378 single base substitution T A intron_variant BRCA-UK 10 69706612 69706612 single base substitution C G intron_variant BRCA-UK 10 69721140 69721140 single base substitution C G downstream_gene_variant BRCA-UK 10 69721140 69721140 single base substitution C G intron_variant BRCA-UK 10 69721140 69721140 single base substitution C G upstream_gene_variant BRCA-UK 10 69734089 69734089 single base substitution G A intron_variant BRCA-UK 10 69765708 69765708 single base substitution C T intron_variant BRCA-UK 10 69781928 69781928 single base substitution G A intron_variant BRCA-UK 10 69809730 69809730 single base substitution G A intron_variant BRCA-UK 10 69817091 69817091 single base substitution G C intron_variant BRCA-UK 10 69832582 69832582 single base substitution C G downstream_gene_variant BRCA-UK 10 69832582 69832582 single base substitution C G intron_variant BRCA-US 10 69684843 69684843 single base substitution C A splice_region_variant BRCA-US 10 69692462 69692462 single base substitution C T 3_prime_UTR_variant BRCA-US 10 69692462 69692462 single base substitution C T synonymous_variant A808A 2424G>A BRCA-US 10 69692462 69692462 single base substitution C T synonymous_variant A840A 2520G>A BRCA-US 10 69692462 69692462 single base substitution C T synonymous_variant A910A 2730G>A BRCA-US 10 69692462 69692462 single base substitution C T synonymous_variant A918A 2754G>A BRCA-US 10 69695914 69695917 deletion of <=200bp TTTG - 3_prime_UTR_variant BRCA-US 10 69695914 69695917 deletion of <=200bp TTTG - frameshift_variant QN781 BRCA-US 10 69695914 69695917 deletion of <=200bp TTTG - frameshift_variant QN813 BRCA-US 10 69695914 69695917 deletion of <=200bp TTTG - frameshift_variant QN883 BRCA-US 10 69695914 69695917 deletion of <=200bp TTTG - frameshift_variant QN891 BRCA-US 10 69700784 69700784 single base substitution G A 3_prime_UTR_variant BRCA-US 10 69700784 69700784 single base substitution G A intron_variant BRCA-US 10 69700784 69700784 single base substitution G A missense_variant L704F 2110C>T BRCA-US 10 69700784 69700784 single base substitution G A missense_variant L806F 2416C>T BRCA-US 10 69700784 69700784 single base substitution G A missense_variant L814F 2440C>T BRCA-US 10 69714455 69714455 single base substitution A C 3_prime_UTR_variant BRCA-US 10 69714455 69714455 single base substitution A C exon_variant BRCA-US 10 69714455 69714455 single base substitution A C missense_variant V643G 1928T>G BRCA-US 10 69714455 69714455 single base substitution A C missense_variant V745G 2234T>G BRCA-US 10 69714455 69714455 single base substitution A C missense_variant V753G 2258T>G BRCA-US 10 69773908 69773908 single base substitution C T 3_prime_UTR_variant BRCA-US 10 69773908 69773908 single base substitution C T exon_variant BRCA-US 10 69773908 69773908 single base substitution C T missense_variant R205Q 614G>A BRCA-US 10 69773908 69773908 single base substitution C T missense_variant R315Q 944G>A BRCA-US 10 69785428 69785428 single base substitution A C 3_prime_UTR_variant BRCA-US 10 69785428 69785428 single base substitution A C exon_variant BRCA-US 10 69785428 69785428 single base substitution A C synonymous_variant G151G 453T>G BRCA-US 10 69785428 69785428 single base substitution A C synonymous_variant G261G 783T>G BRCA-US 10 69793826 69793829 deletion of <=200bp TGCA - 3_prime_UTR_variant BRCA-US 10 69793826 69793829 deletion of <=200bp TGCA - exon_variant BRCA-US 10 69793826 69793829 deletion of <=200bp TGCA - frameshift_variant MQ193 BRCA-US 10 69793826 69793829 deletion of <=200bp TGCA - frameshift_variant MQ217 BRCA-US 10 69793826 69793829 deletion of <=200bp TGCA - frameshift_variant MQ83 BRCA-US 10 69832821 69832821 single base substitution A C downstream_gene_variant BRCA-US 10 69832821 69832821 single base substitution A C exon_variant BRCA-US 10 69832821 69832821 single base substitution A C synonymous_variant G15G 45T>G BRCA-US 10 69832857 69832857 single base substitution G T downstream_gene_variant BRCA-US 10 69832857 69832857 single base substitution G T exon_variant BRCA-US 10 69832857 69832857 single base substitution G T stop_gained C3* 9C>A BRCA-US 10 69832857 69832857 single base substitution G T upstream_gene_variant BRCA-US 10 69834957 69834957 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 10 69834957 69834957 single base substitution G A exon_variant BRCA-US 10 69834957 69834957 single base substitution G A upstream_gene_variant BTCA-JP 10 69685111 69685111 single base substitution G T intron_variant BTCA-JP 10 69714747 69714747 single base substitution C A 3_prime_UTR_variant BTCA-JP 10 69714747 69714747 single base substitution C A exon_variant BTCA-JP 10 69714747 69714747 single base substitution C A missense_variant K620N 1860G>T BTCA-JP 10 69714747 69714747 single base substitution C A missense_variant K722N 2166G>T BTCA-JP 10 69714747 69714747 single base substitution C A missense_variant K730N 2190G>T BTCA-JP 10 69716603 69716603 deletion of <=200bp A - exon_variant BTCA-JP 10 69716603 69716603 deletion of <=200bp A - intron_variant BTCA-JP 10 69832551 69832551 single base substitution T C downstream_gene_variant BTCA-JP 10 69832551 69832551 single base substitution T C intron_variant CESC-US 10 69682816 69682816 single base substitution C A 3_prime_UTR_variant CESC-US 10 69682816 69682816 single base substitution C A stop_gained E1008* 3022G>T CESC-US 10 69682816 69682816 single base substitution C A stop_gained E1016* 3046G>T CESC-US 10 69682816 69682816 single base substitution C A stop_gained E906* 2716G>T CESC-US 10 69682816 69682816 single base substitution C A stop_gained E938* 2812G>T CESC-US 10 69716602 69716602 insertion of <=200bp - A exon_variant CESC-US 10 69716602 69716602 insertion of <=200bp - A intron_variant CESC-US 10 69726539 69726539 single base substitution C T 3_prime_UTR_variant CESC-US 10 69726539 69726539 single base substitution C T exon_variant CESC-US 10 69726539 69726539 single base substitution C T synonymous_variant Q499Q 1497G>A CESC-US 10 69726539 69726539 single base substitution C T synonymous_variant Q609Q 1827G>A CESC-US 10 69748552 69748552 single base substitution C A 3_prime_UTR_variant CESC-US 10 69748552 69748552 single base substitution C A exon_variant CESC-US 10 69748552 69748552 single base substitution C A missense_variant K448N 1344G>T CESC-US 10 69748552 69748552 single base substitution C A missense_variant K558N 1674G>T CESC-US 10 69832930 69832930 single base substitution G A 5_prime_UTR_variant CESC-US 10 69832930 69832930 single base substitution G A exon_variant CESC-US 10 69832930 69832930 single base substitution G A upstream_gene_variant CLLE-ES 10 69714032 69714032 single base substitution A T exon_variant CLLE-ES 10 69714032 69714032 single base substitution A T intron_variant CLLE-ES 10 69732398 69732398 single base substitution G A intron_variant CLLE-ES 10 69771562 69771562 single base substitution A C intron_variant CLLE-ES 10 69774340 69774340 single base substitution G A intron_variant CLLE-ES 10 69803808 69803808 single base substitution T C intron_variant CLLE-ES 10 69803808 69803808 single base substitution T C upstream_gene_variant CLLE-ES 10 69810751 69810751 single base substitution T A intron_variant CLLE-ES 10 69819346 69819346 insertion of <=200bp - ATA intron_variant CLLE-ES 10 69819454 69819456 deletion of <=200bp ATA - intron_variant CLLE-ES 10 69823404 69823404 single base substitution A G downstream_gene_variant CLLE-ES 10 69823404 69823404 single base substitution A G intron_variant CLLE-ES 10 69824345 69824345 single base substitution G A downstream_gene_variant CLLE-ES 10 69824345 69824345 single base substitution G A intron_variant COAD-US 10 69682746 69682746 single base substitution G T 3_prime_UTR_variant COAD-US 10 69682746 69682746 single base substitution G T downstream_gene_variant COAD-US 10 69682746 69682746 single base substitution G T missense_variant T1031N 3092C>A COAD-US 10 69682746 69682746 single base substitution G T missense_variant T1039N 3116C>A COAD-US 10 69682746 69682746 single base substitution G T missense_variant T929N 2786C>A COAD-US 10 69682746 69682746 single base substitution G T missense_variant T961N 2882C>A COAD-US 10 69692354 69692354 single base substitution C T splice_region_variant COAD-US 10 69700825 69700825 single base substitution A G 3_prime_UTR_variant COAD-US 10 69700825 69700825 single base substitution A G intron_variant COAD-US 10 69700825 69700825 single base substitution A G missense_variant V690A 2069T>C COAD-US 10 69700825 69700825 single base substitution A G missense_variant V792A 2375T>C COAD-US 10 69700825 69700825 single base substitution A G missense_variant V800A 2399T>C COAD-US 10 69714420 69714420 single base substitution A T 3_prime_UTR_variant COAD-US 10 69714420 69714420 single base substitution A T exon_variant COAD-US 10 69714420 69714420 single base substitution A T missense_variant L655I 1963T>A COAD-US 10 69714420 69714420 single base substitution A T missense_variant L757I 2269T>A COAD-US 10 69714420 69714420 single base substitution A T missense_variant L765I 2293T>A COAD-US 10 69750919 69750919 single base substitution T G 3_prime_UTR_variant COAD-US 10 69750919 69750919 single base substitution T G missense_variant N327H 979A>C COAD-US 10 69750919 69750919 single base substitution T G missense_variant N437H 1309A>C COAD-US 10 69750919 69750919 single base substitution T G upstream_gene_variant COAD-US 10 69750958 69750958 insertion of <=200bp - A splice_acceptor_variant COAD-US 10 69750958 69750958 insertion of <=200bp - A upstream_gene_variant COAD-US 10 69773841 69773841 single base substitution G A 3_prime_UTR_variant COAD-US 10 69773841 69773841 single base substitution G A exon_variant COAD-US 10 69773841 69773841 single base substitution G A synonymous_variant S227S 681C>T COAD-US 10 69773841 69773841 single base substitution G A synonymous_variant S337S 1011C>T COAD-US 10 69832742 69832742 single base substitution C T downstream_gene_variant COAD-US 10 69832742 69832742 single base substitution C T exon_variant COAD-US 10 69832742 69832742 single base substitution C T missense_variant G42R 124G>A COCA-CN 10 69684858 69684858 single base substitution C A 3_prime_UTR_variant COCA-CN 10 69684858 69684858 single base substitution C A missense_variant K873N 2619G>T COCA-CN 10 69684858 69684858 single base substitution C A missense_variant K905N 2715G>T COCA-CN 10 69684858 69684858 single base substitution C A missense_variant K975N 2925G>T COCA-CN 10 69684858 69684858 single base substitution C A missense_variant K983N 2949G>T COCA-CN 10 69692309 69692309 single base substitution A T intron_variant COCA-CN 10 69700686 69700686 single base substitution T C intron_variant COCA-CN 10 69714447 69714447 single base substitution C A 3_prime_UTR_variant COCA-CN 10 69714447 69714447 single base substitution C A exon_variant COCA-CN 10 69714447 69714447 single base substitution C A stop_gained E646* 1936G>T COCA-CN 10 69714447 69714447 single base substitution C A stop_gained E748* 2242G>T COCA-CN 10 69714447 69714447 single base substitution C A stop_gained E756* 2266G>T COCA-CN 10 69716551 69716551 single base substitution A G exon_variant COCA-CN 10 69716551 69716551 single base substitution A G intron_variant COCA-CN 10 69716604 69716604 single base substitution A T exon_variant COCA-CN 10 69716604 69716604 single base substitution A T intron_variant COCA-CN 10 69742848 69742848 single base substitution C A intron_variant COCA-CN 10 69743545 69743545 single base substitution A C intron_variant COCA-CN 10 69750997 69750997 single base substitution A C intron_variant COCA-CN 10 69750997 69750997 single base substitution A C upstream_gene_variant COCA-CN 10 69770389 69770389 single base substitution T C intron_variant COCA-CN 10 69792721 69792721 single base substitution T C downstream_gene_variant COCA-CN 10 69792721 69792721 single base substitution T C intron_variant COCA-CN 10 69793644 69793644 single base substitution C T downstream_gene_variant COCA-CN 10 69793644 69793644 single base substitution C T intron_variant COCA-CN 10 69799088 69799088 single base substitution A G intron_variant COCA-CN 10 69799088 69799088 single base substitution A G upstream_gene_variant COCA-CN 10 69799112 69799112 single base substitution C T intron_variant COCA-CN 10 69799112 69799112 single base substitution C T upstream_gene_variant COCA-CN 10 69799127 69799127 single base substitution T A intron_variant COCA-CN 10 69799127 69799127 single base substitution T A upstream_gene_variant COCA-CN 10 69804428 69804428 single base substitution T G intron_variant COCA-CN 10 69804428 69804428 single base substitution T G upstream_gene_variant COCA-CN 10 69805902 69805902 single base substitution G A intron_variant COCA-CN 10 69824335 69824335 single base substitution G A downstream_gene_variant COCA-CN 10 69824335 69824335 single base substitution G A intron_variant COCA-CN 10 69824643 69824643 single base substitution C T downstream_gene_variant COCA-CN 10 69824643 69824643 single base substitution C T intron_variant EOPC-DE 10 69777023 69777023 single base substitution A G intron_variant ESAD-UK 10 69678930 69678930 single base substitution C T downstream_gene_variant ESAD-UK 10 69680891 69680891 single base substitution A G downstream_gene_variant ESAD-UK 10 69684188 69684188 single base substitution G A intron_variant ESAD-UK 10 69686180 69686180 single base substitution A T intron_variant ESAD-UK 10 69686648 69686648 single base substitution C T intron_variant ESAD-UK 10 69687479 69687479 single base substitution G C intron_variant ESAD-UK 10 69687819 69687819 single base substitution T G intron_variant ESAD-UK 10 69689490 69689490 single base substitution T G intron_variant ESAD-UK 10 69691684 69691684 single base substitution A T intron_variant ESAD-UK 10 69694735 69694735 deletion of <=200bp C - intron_variant ESAD-UK 10 69695637 69695637 single base substitution C A intron_variant ESAD-UK 10 69696319 69696319 single base substitution C G intron_variant ESAD-UK 10 69696580 69696580 single base substitution C G intron_variant ESAD-UK 10 69696870 69696870 single base substitution G C intron_variant ESAD-UK 10 69697626 69697626 single base substitution A C intron_variant ESAD-UK 10 69700320 69700320 single base substitution G C intron_variant ESAD-UK 10 69700587 69700587 single base substitution T G intron_variant ESAD-UK 10 69701517 69701517 single base substitution C T intron_variant ESAD-UK 10 69704302 69704302 single base substitution C T intron_variant ESAD-UK 10 69706744 69706744 single base substitution C T intron_variant ESAD-UK 10 69711007 69711007 single base substitution T A downstream_gene_variant ESAD-UK 10 69711007 69711007 single base substitution T A intron_variant ESAD-UK 10 69711198 69711198 single base substitution T C downstream_gene_variant ESAD-UK 10 69711198 69711198 single base substitution T C intron_variant ESAD-UK 10 69712605 69712605 single base substitution C T downstream_gene_variant ESAD-UK 10 69712605 69712605 single base substitution C T intron_variant ESAD-UK 10 69712754 69712754 single base substitution C T downstream_gene_variant ESAD-UK 10 69712754 69712754 single base substitution C T intron_variant ESAD-UK 10 69714986 69714986 single base substitution A G exon_variant ESAD-UK 10 69714986 69714986 single base substitution A G intron_variant ESAD-UK 10 69715017 69715017 single base substitution T G exon_variant ESAD-UK 10 69715017 69715017 single base substitution T G intron_variant ESAD-UK 10 69718295 69718295 single base substitution C A intron_variant ESAD-UK 10 69718295 69718295 single base substitution C A upstream_gene_variant ESAD-UK 10 69719232 69719232 single base substitution T A intron_variant ESAD-UK 10 69719232 69719232 single base substitution T A upstream_gene_variant ESAD-UK 10 69720831 69720831 single base substitution G A downstream_gene_variant ESAD-UK 10 69720831 69720831 single base substitution G A intron_variant ESAD-UK 10 69720831 69720831 single base substitution G A upstream_gene_variant ESAD-UK 10 69724696 69724696 single base substitution A C exon_variant ESAD-UK 10 69724696 69724696 single base substitution A C intron_variant ESAD-UK 10 69729224 69729224 insertion of <=200bp - G intron_variant ESAD-UK 10 69730036 69730036 single base substitution A T intron_variant ESAD-UK 10 69738785 69738785 single base substitution G A intron_variant ESAD-UK 10 69739936 69739936 single base substitution T G intron_variant ESAD-UK 10 69741994 69741994 single base substitution A G intron_variant ESAD-UK 10 69742571 69742571 single base substitution C T intron_variant ESAD-UK 10 69743057 69743057 single base substitution G A intron_variant ESAD-UK 10 69744516 69744516 deletion of <=200bp T - intron_variant ESAD-UK 10 69748434 69748434 single base substitution C A 3_prime_UTR_variant ESAD-UK 10 69748434 69748434 single base substitution C A exon_variant ESAD-UK 10 69748434 69748434 single base substitution C A stop_gained E488* 1462G>T ESAD-UK 10 69748434 69748434 single base substitution C A stop_gained E598* 1792G>T ESAD-UK 10 69753530 69753530 insertion of <=200bp - T 3_prime_UTR_variant ESAD-UK 10 69753530 69753530 insertion of <=200bp - T intron_variant ESAD-UK 10 69753530 69753530 insertion of <=200bp - T upstream_gene_variant ESAD-UK 10 69756063 69756063 single base substitution G A intron_variant ESAD-UK 10 69756470 69756470 single base substitution G A intron_variant ESAD-UK 10 69756507 69756507 single base substitution C T intron_variant ESAD-UK 10 69757978 69757978 single base substitution C T intron_variant ESAD-UK 10 69759438 69759438 single base substitution G C intron_variant ESAD-UK 10 69760221 69760233 deletion of <=200bp AGCTACTCAGGAG - intron_variant ESAD-UK 10 69762471 69762471 single base substitution T C intron_variant ESAD-UK 10 69762607 69762607 single base substitution T A intron_variant ESAD-UK 10 69764105 69764109 deletion of <=200bp TTGTT - intron_variant ESAD-UK 10 69764175 69764175 deletion of <=200bp C - intron_variant ESAD-UK 10 69764176 69764176 single base substitution T G intron_variant ESAD-UK 10 69764279 69764279 single base substitution T G intron_variant ESAD-UK 10 69764676 69764676 single base substitution G T intron_variant ESAD-UK 10 69765305 69765305 single base substitution A G intron_variant ESAD-UK 10 69766138 69766138 single base substitution T G intron_variant ESAD-UK 10 69767006 69767006 single base substitution C T intron_variant ESAD-UK 10 69768383 69768383 single base substitution G C intron_variant ESAD-UK 10 69769470 69769470 single base substitution G A intron_variant ESAD-UK 10 69770704 69770704 single base substitution T C intron_variant ESAD-UK 10 69771737 69771737 single base substitution T C intron_variant ESAD-UK 10 69773008 69773008 single base substitution A G intron_variant ESAD-UK 10 69775202 69775202 single base substitution G A intron_variant ESAD-UK 10 69776059 69776059 single base substitution G A intron_variant ESAD-UK 10 69782001 69782001 single base substitution A G intron_variant ESAD-UK 10 69786200 69786200 single base substitution A T intron_variant ESAD-UK 10 69793497 69793497 single base substitution A T downstream_gene_variant ESAD-UK 10 69793497 69793497 single base substitution A T intron_variant ESAD-UK 10 69797916 69797917 deletion of <=200bp TT - exon_variant ESAD-UK 10 69797916 69797917 deletion of <=200bp TT - frameshift_variant K79 ESAD-UK 10 69797916 69797917 deletion of <=200bp TT - frameshift_variant KS132 ESAD-UK 10 69797916 69797917 deletion of <=200bp TT - frameshift_variant KS156 ESAD-UK 10 69797916 69797917 deletion of <=200bp TT - frameshift_variant KS22 ESAD-UK 10 69798358 69798358 single base substitution C T intron_variant ESAD-UK 10 69798358 69798358 single base substitution C T upstream_gene_variant ESAD-UK 10 69802253 69802253 single base substitution G A intron_variant ESAD-UK 10 69802253 69802253 single base substitution G A upstream_gene_variant ESAD-UK 10 69806372 69806372 single base substitution A G intron_variant ESAD-UK 10 69808598 69808598 single base substitution A T intron_variant ESAD-UK 10 69812133 69812133 deletion of <=200bp T - intron_variant ESAD-UK 10 69813203 69813203 single base substitution G A intron_variant ESAD-UK 10 69815442 69815442 single base substitution A G intron_variant ESAD-UK 10 69816866 69816866 insertion of <=200bp - AT intron_variant ESAD-UK 10 69819974 69819974 single base substitution T C intron_variant ESAD-UK 10 69820361 69820361 single base substitution T C intron_variant ESAD-UK 10 69820961 69820961 single base substitution C T intron_variant ESAD-UK 10 69821487 69821487 single base substitution A C intron_variant ESAD-UK 10 69823686 69823686 single base substitution A C downstream_gene_variant ESAD-UK 10 69823686 69823686 single base substitution A C intron_variant ESAD-UK 10 69824324 69824324 single base substitution A C downstream_gene_variant ESAD-UK 10 69824324 69824324 single base substitution A C intron_variant ESAD-UK 10 69824685 69824685 single base substitution C T downstream_gene_variant ESAD-UK 10 69824685 69824685 single base substitution C T intron_variant ESAD-UK 10 69825713 69825713 single base substitution A C downstream_gene_variant ESAD-UK 10 69825713 69825713 single base substitution A C intron_variant ESAD-UK 10 69826555 69826555 single base substitution G T downstream_gene_variant ESAD-UK 10 69826555 69826555 single base substitution G T intron_variant ESAD-UK 10 69827314 69827314 single base substitution A G downstream_gene_variant ESAD-UK 10 69827314 69827314 single base substitution A G intron_variant ESAD-UK 10 69828557 69828557 single base substitution C A 3_prime_UTR_variant ESAD-UK 10 69828557 69828557 single base substitution C A downstream_gene_variant ESAD-UK 10 69828557 69828557 single base substitution C A intron_variant ESAD-UK 10 69830369 69830369 single base substitution A T downstream_gene_variant ESAD-UK 10 69830369 69830369 single base substitution A T intron_variant ESAD-UK 10 69831668 69831668 single base substitution C T downstream_gene_variant ESAD-UK 10 69831668 69831668 single base substitution C T intron_variant ESAD-UK 10 69838360 69838360 deletion of <=200bp T - upstream_gene_variant ESAD-UK 10 69838382 69838382 insertion of <=200bp - A upstream_gene_variant ESAD-UK 10 69839723 69839723 single base substitution G A upstream_gene_variant ESCA-CN 10 69700734 69700734 single base substitution G T 3_prime_UTR_variant ESCA-CN 10 69700734 69700734 single base substitution G T intron_variant ESCA-CN 10 69700734 69700734 single base substitution G T synonymous_variant S720S 2160C>A ESCA-CN 10 69700734 69700734 single base substitution G T synonymous_variant S822S 2466C>A ESCA-CN 10 69700734 69700734 single base substitution G T synonymous_variant S830S 2490C>A ESCA-CN 10 69716603 69716606 deletion of <=200bp AAAA - exon_variant ESCA-CN 10 69716603 69716606 deletion of <=200bp AAAA - intron_variant ESCA-CN 10 69785304 69785304 single base substitution G A missense_variant R193W 577C>T ESCA-CN 10 69785304 69785304 single base substitution G A missense_variant R303W 907C>T ESCA-CN 10 69785304 69785304 single base substitution G A splice_region_variant KIRC-US 10 69797906 69797908 deletion of <=200bp TCT - disruptive_inframe_deletion QI82L KIRC-US 10 69797906 69797908 deletion of <=200bp TCT - disruptive_inframe_deletion SD135S KIRC-US 10 69797906 69797908 deletion of <=200bp TCT - disruptive_inframe_deletion SD159S KIRC-US 10 69797906 69797908 deletion of <=200bp TCT - disruptive_inframe_deletion SD25S KIRC-US 10 69797906 69797908 deletion of <=200bp TCT - exon_variant KIRP-US 10 69714847 69714847 single base substitution A G 3_prime_UTR_variant KIRP-US 10 69714847 69714847 single base substitution A G exon_variant KIRP-US 10 69714847 69714847 single base substitution A G missense_variant L587P 1760T>C KIRP-US 10 69714847 69714847 single base substitution A G missense_variant L689P 2066T>C KIRP-US 10 69714847 69714847 single base substitution A G missense_variant L697P 2090T>C LAML-KR 10 69705636 69705636 single base substitution T A intron_variant LAML-KR 10 69778678 69778678 single base substitution G T intron_variant LAML-KR 10 69799092 69799092 single base substitution G A intron_variant LAML-KR 10 69799092 69799092 single base substitution G A upstream_gene_variant LAML-KR 10 69824727 69824727 single base substitution C A downstream_gene_variant LAML-KR 10 69824727 69824727 single base substitution C A intron_variant LICA-CN 10 69692370 69692370 single base substitution C T 3_prime_UTR_variant LICA-CN 10 69692370 69692370 single base substitution C T stop_gained W839* 2516G>A LICA-CN 10 69692370 69692370 single base substitution C T stop_gained W871* 2612G>A LICA-CN 10 69692370 69692370 single base substitution C T stop_gained W941* 2822G>A LICA-CN 10 69692370 69692370 single base substitution C T stop_gained W949* 2846G>A LICA-FR 10 69686166 69686166 single base substitution T A intron_variant LICA-FR 10 69691178 69691178 single base substitution A C intron_variant LICA-FR 10 69701423 69701423 single base substitution C A intron_variant LICA-FR 10 69701429 69701429 single base substitution T C intron_variant LICA-FR 10 69701468 69701468 single base substitution C T intron_variant LICA-FR 10 69727308 69727308 single base substitution G C intron_variant LICA-FR 10 69750981 69750981 single base substitution T A intron_variant LICA-FR 10 69750981 69750981 single base substitution T A upstream_gene_variant LICA-FR 10 69759493 69759493 single base substitution T A intron_variant LICA-FR 10 69802224 69802224 single base substitution T C intron_variant LICA-FR 10 69802224 69802224 single base substitution T C upstream_gene_variant LICA-FR 10 69805345 69805345 single base substitution G T intron_variant LICA-FR 10 69822355 69822355 insertion of <=200bp - A downstream_gene_variant LICA-FR 10 69822355 69822355 insertion of <=200bp - A intron_variant LICA-FR 10 69828007 69828007 single base substitution C T 3_prime_UTR_variant LICA-FR 10 69828007 69828007 single base substitution C T downstream_gene_variant LICA-FR 10 69828007 69828007 single base substitution C T intron_variant LIHC-US 10 69726472 69726472 single base substitution T C 3_prime_UTR_variant LIHC-US 10 69726472 69726472 single base substitution T C exon_variant LIHC-US 10 69726472 69726472 single base substitution T C missense_variant I522V 1564A>G LIHC-US 10 69726472 69726472 single base substitution T C missense_variant I632V 1894A>G LIHC-US 10 69785411 69785411 single base substitution C A 3_prime_UTR_variant LIHC-US 10 69785411 69785411 single base substitution C A exon_variant LIHC-US 10 69785411 69785411 single base substitution C A missense_variant G157V 470G>T LIHC-US 10 69785411 69785411 single base substitution C A missense_variant G267V 800G>T LIHC-US 10 69797855 69797855 single base substitution G C exon_variant LIHC-US 10 69797855 69797855 single base substitution G C missense_variant L100V 298C>G LIHC-US 10 69797855 69797855 single base substitution G C missense_variant S153C 458C>G LIHC-US 10 69797855 69797855 single base substitution G C missense_variant S177C 530C>G LIHC-US 10 69797855 69797855 single base substitution G C missense_variant S43C 128C>G LINC-JP 10 69682670 69682670 single base substitution A C 3_prime_UTR_variant LINC-JP 10 69682670 69682670 single base substitution A C downstream_gene_variant LINC-JP 10 69699150 69699150 single base substitution A C intron_variant LINC-JP 10 69701553 69701553 single base substitution A T intron_variant LINC-JP 10 69710128 69710128 single base substitution G T downstream_gene_variant LINC-JP 10 69710128 69710128 single base substitution G T intron_variant LINC-JP 10 69718590 69718590 single base substitution T C intron_variant LINC-JP 10 69718590 69718590 single base substitution T C upstream_gene_variant LINC-JP 10 69719125 69719125 single base substitution C A intron_variant LINC-JP 10 69719125 69719125 single base substitution C A upstream_gene_variant LINC-JP 10 69727010 69727010 single base substitution T C intron_variant LINC-JP 10 69730575 69730575 single base substitution G A intron_variant LINC-JP 10 69743932 69743932 single base substitution T C intron_variant LINC-JP 10 69748317 69748317 deletion of <=200bp T - intron_variant LINC-JP 10 69750805 69750805 single base substitution T C intron_variant LINC-JP 10 69750805 69750805 single base substitution T C upstream_gene_variant LINC-JP 10 69750921 69750921 single base substitution A G 3_prime_UTR_variant LINC-JP 10 69750921 69750921 single base substitution A G missense_variant L326P 977T>C LINC-JP 10 69750921 69750921 single base substitution A G missense_variant L436P 1307T>C LINC-JP 10 69750921 69750921 single base substitution A G upstream_gene_variant LINC-JP 10 69752130 69752130 single base substitution T A intron_variant LINC-JP 10 69752130 69752130 single base substitution T A upstream_gene_variant LINC-JP 10 69756425 69756425 single base substitution A C intron_variant LINC-JP 10 69756839 69756839 single base substitution A T intron_variant LINC-JP 10 69757520 69757520 single base substitution T A intron_variant LINC-JP 10 69769051 69769051 single base substitution C T intron_variant LINC-JP 10 69773542 69773542 single base substitution C A intron_variant LINC-JP 10 69790130 69790130 single base substitution A C downstream_gene_variant LINC-JP 10 69790130 69790130 single base substitution A C intron_variant LINC-JP 10 69798122 69798122 single base substitution A T exon_variant LINC-JP 10 69798122 69798122 single base substitution A T intron_variant LINC-JP 10 69798124 69798124 single base substitution T A intron_variant LINC-JP 10 69798124 69798124 single base substitution T A upstream_gene_variant LINC-JP 10 69804253 69804253 single base substitution C T exon_variant LINC-JP 10 69804253 69804253 single base substitution C T intron_variant LINC-JP 10 69804253 69804253 single base substitution C T synonymous_variant A98A 294G>A LINC-JP 10 69804253 69804253 single base substitution C T upstream_gene_variant LINC-JP 10 69820677 69820677 deletion of <=200bp A - intron_variant LIRI-JP 10 69678049 69678049 single base substitution A G downstream_gene_variant LIRI-JP 10 69681440 69681440 single base substitution T C downstream_gene_variant LIRI-JP 10 69682102 69682102 deletion of <=200bp T - 3_prime_UTR_variant LIRI-JP 10 69682102 69682102 deletion of <=200bp T - downstream_gene_variant LIRI-JP 10 69686137 69686137 single base substitution A G intron_variant LIRI-JP 10 69687572 69687572 single base substitution G T intron_variant LIRI-JP 10 69689915 69689915 single base substitution C T intron_variant LIRI-JP 10 69690430 69690430 single base substitution G A intron_variant LIRI-JP 10 69690577 69690577 single base substitution C T intron_variant LIRI-JP 10 69691841 69691841 single base substitution A G intron_variant LIRI-JP 10 69695932 69695932 single base substitution T G 3_prime_UTR_variant LIRI-JP 10 69695932 69695932 single base substitution T G missense_variant T776P 2326A>C LIRI-JP 10 69695932 69695932 single base substitution T G missense_variant T808P 2422A>C LIRI-JP 10 69695932 69695932 single base substitution T G missense_variant T878P 2632A>C LIRI-JP 10 69695932 69695932 single base substitution T G missense_variant T886P 2656A>C LIRI-JP 10 69696623 69696623 single base substitution G A intron_variant LIRI-JP 10 69698227 69698227 single base substitution G A intron_variant LIRI-JP 10 69698580 69698580 single base substitution A C intron_variant LIRI-JP 10 69700483 69700483 single base substitution T A intron_variant LIRI-JP 10 69701873 69701873 single base substitution A G intron_variant LIRI-JP 10 69702857 69702857 single base substitution T C intron_variant LIRI-JP 10 69702867 69702867 single base substitution A G intron_variant LIRI-JP 10 69704540 69704540 single base substitution A C intron_variant LIRI-JP 10 69704602 69704602 single base substitution G A intron_variant LIRI-JP 10 69705225 69705225 single base substitution T C intron_variant LIRI-JP 10 69706160 69706160 single base substitution C A intron_variant LIRI-JP 10 69707066 69707066 single base substitution A G intron_variant LIRI-JP 10 69707455 69707455 single base substitution T C intron_variant LIRI-JP 10 69707836 69707836 single base substitution T C intron_variant LIRI-JP 10 69710178 69710178 single base substitution G A downstream_gene_variant LIRI-JP 10 69710178 69710178 single base substitution G A intron_variant LIRI-JP 10 69711364 69711364 single base substitution G C downstream_gene_variant LIRI-JP 10 69711364 69711364 single base substitution G C intron_variant LIRI-JP 10 69711670 69711670 single base substitution C T downstream_gene_variant LIRI-JP 10 69711670 69711670 single base substitution C T intron_variant LIRI-JP 10 69711846 69711846 single base substitution T A downstream_gene_variant LIRI-JP 10 69711846 69711846 single base substitution T A intron_variant LIRI-JP 10 69713539 69713539 single base substitution C A downstream_gene_variant LIRI-JP 10 69713539 69713539 single base substitution C A intron_variant LIRI-JP 10 69714130 69714130 single base substitution C T exon_variant LIRI-JP 10 69714130 69714130 single base substitution C T intron_variant LIRI-JP 10 69715006 69715006 single base substitution A C exon_variant LIRI-JP 10 69715006 69715006 single base substitution A C intron_variant LIRI-JP 10 69715669 69715669 single base substitution T C exon_variant LIRI-JP 10 69715669 69715669 single base substitution T C intron_variant LIRI-JP 10 69715752 69715752 single base substitution G C exon_variant LIRI-JP 10 69715752 69715752 single base substitution G C intron_variant LIRI-JP 10 69717322 69717322 single base substitution C A intron_variant LIRI-JP 10 69717322 69717322 single base substitution C A upstream_gene_variant LIRI-JP 10 69717392 69717392 single base substitution A G intron_variant LIRI-JP 10 69717392 69717392 single base substitution A G upstream_gene_variant LIRI-JP 10 69718749 69718749 single base substitution T C intron_variant LIRI-JP 10 69718749 69718749 single base substitution T C upstream_gene_variant LIRI-JP 10 69719539 69719539 single base substitution A C intron_variant LIRI-JP 10 69719539 69719539 single base substitution A C upstream_gene_variant LIRI-JP 10 69720280 69720280 single base substitution T G downstream_gene_variant LIRI-JP 10 69720280 69720280 single base substitution T G intron_variant LIRI-JP 10 69720280 69720280 single base substitution T G upstream_gene_variant LIRI-JP 10 69720948 69720948 single base substitution T C downstream_gene_variant LIRI-JP 10 69720948 69720948 single base substitution T C intron_variant LIRI-JP 10 69720948 69720948 single base substitution T C upstream_gene_variant LIRI-JP 10 69721753 69721753 single base substitution T C downstream_gene_variant LIRI-JP 10 69721753 69721753 single base substitution T C intron_variant LIRI-JP 10 69722112 69722112 single base substitution T G downstream_gene_variant LIRI-JP 10 69722112 69722112 single base substitution T G intron_variant LIRI-JP 10 69724568 69724568 single base substitution C T exon_variant LIRI-JP 10 69724568 69724568 single base substitution C T intron_variant LIRI-JP 10 69730632 69730632 single base substitution T C intron_variant LIRI-JP 10 69730901 69730901 single base substitution G A intron_variant LIRI-JP 10 69732761 69732761 single base substitution T C intron_variant LIRI-JP 10 69733539 69733539 single base substitution G A intron_variant LIRI-JP 10 69736120 69736120 single base substitution C A intron_variant LIRI-JP 10 69738150 69738150 single base substitution A C intron_variant LIRI-JP 10 69740542 69740542 single base substitution C G intron_variant LIRI-JP 10 69744447 69744447 single base substitution C G intron_variant LIRI-JP 10 69745457 69745457 single base substitution T C intron_variant LIRI-JP 10 69745970 69745970 single base substitution G C intron_variant LIRI-JP 10 69747472 69747472 single base substitution A G intron_variant LIRI-JP 10 69748984 69748984 single base substitution T C intron_variant LIRI-JP 10 69751713 69751713 single base substitution G A intron_variant LIRI-JP 10 69751713 69751713 single base substitution G A upstream_gene_variant LIRI-JP 10 69754838 69754838 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 69754838 69754838 single base substitution T C intron_variant LIRI-JP 10 69754838 69754838 single base substitution T C upstream_gene_variant LIRI-JP 10 69756739 69756739 single base substitution C A intron_variant LIRI-JP 10 69766174 69766174 single base substitution G C intron_variant LIRI-JP 10 69766924 69766924 single base substitution T C intron_variant LIRI-JP 10 69767047 69767047 single base substitution C G intron_variant LIRI-JP 10 69772109 69772109 single base substitution C T intron_variant LIRI-JP 10 69773206 69773206 single base substitution T A intron_variant LIRI-JP 10 69774669 69774669 single base substitution T A intron_variant LIRI-JP 10 69775571 69775571 single base substitution A G intron_variant LIRI-JP 10 69778564 69778564 single base substitution T C intron_variant LIRI-JP 10 69779095 69779095 single base substitution A G intron_variant LIRI-JP 10 69780820 69780820 single base substitution G T intron_variant LIRI-JP 10 69783064 69783064 single base substitution A G intron_variant LIRI-JP 10 69784451 69784451 single base substitution T C intron_variant LIRI-JP 10 69787338 69787338 single base substitution T C intron_variant LIRI-JP 10 69788787 69788787 single base substitution T C downstream_gene_variant LIRI-JP 10 69788787 69788787 single base substitution T C intron_variant LIRI-JP 10 69789015 69789015 single base substitution A C downstream_gene_variant LIRI-JP 10 69789015 69789015 single base substitution A C intron_variant LIRI-JP 10 69790408 69790408 single base substitution C T downstream_gene_variant LIRI-JP 10 69790408 69790408 single base substitution C T intron_variant LIRI-JP 10 69791969 69791969 single base substitution T G downstream_gene_variant LIRI-JP 10 69791969 69791969 single base substitution T G intron_variant LIRI-JP 10 69792209 69792209 single base substitution T C downstream_gene_variant LIRI-JP 10 69792209 69792209 single base substitution T C intron_variant LIRI-JP 10 69793997 69793997 single base substitution A C intron_variant LIRI-JP 10 69796582 69796582 single base substitution T C intron_variant LIRI-JP 10 69798056 69798056 single base substitution C A exon_variant LIRI-JP 10 69798056 69798056 single base substitution C A intron_variant LIRI-JP 10 69798901 69798901 single base substitution T C intron_variant LIRI-JP 10 69798901 69798901 single base substitution T C upstream_gene_variant LIRI-JP 10 69800470 69800470 single base substitution A G intron_variant LIRI-JP 10 69800470 69800470 single base substitution A G upstream_gene_variant LIRI-JP 10 69801179 69801179 single base substitution T C intron_variant LIRI-JP 10 69801179 69801179 single base substitution T C upstream_gene_variant LIRI-JP 10 69801221 69801221 single base substitution T C intron_variant LIRI-JP 10 69801221 69801221 single base substitution T C upstream_gene_variant LIRI-JP 10 69802848 69802848 deletion of <=200bp A - intron_variant LIRI-JP 10 69802848 69802848 deletion of <=200bp A - upstream_gene_variant LIRI-JP 10 69803946 69803946 single base substitution T C intron_variant LIRI-JP 10 69803946 69803946 single base substitution T C upstream_gene_variant LIRI-JP 10 69804480 69804480 single base substitution A G intron_variant LIRI-JP 10 69804480 69804480 single base substitution A G upstream_gene_variant LIRI-JP 10 69805519 69805519 single base substitution G A intron_variant LIRI-JP 10 69805879 69805879 single base substitution C T intron_variant LIRI-JP 10 69806470 69806470 single base substitution T C intron_variant LIRI-JP 10 69808715 69808715 single base substitution A C intron_variant LIRI-JP 10 69812956 69812956 single base substitution T C intron_variant LIRI-JP 10 69813756 69813756 single base substitution C A intron_variant LIRI-JP 10 69815226 69815226 single base substitution T C intron_variant LIRI-JP 10 69815629 69815629 single base substitution C T intron_variant LIRI-JP 10 69818343 69818343 single base substitution A G intron_variant LIRI-JP 10 69818383 69818383 single base substitution G A intron_variant LIRI-JP 10 69822632 69822632 single base substitution A G downstream_gene_variant LIRI-JP 10 69822632 69822632 single base substitution A G intron_variant LIRI-JP 10 69823271 69823271 single base substitution T C downstream_gene_variant LIRI-JP 10 69823271 69823271 single base substitution T C intron_variant LIRI-JP 10 69826933 69826933 single base substitution A C downstream_gene_variant LIRI-JP 10 69826933 69826933 single base substitution A C exon_variant LIRI-JP 10 69826933 69826933 single base substitution A C intron_variant LIRI-JP 10 69830149 69830149 single base substitution A C 3_prime_UTR_variant LIRI-JP 10 69830149 69830149 single base substitution A C downstream_gene_variant LIRI-JP 10 69830149 69830149 single base substitution A C intron_variant LIRI-JP 10 69830411 69830420 deletion of <=200bp CAAAGCTGAG - downstream_gene_variant LIRI-JP 10 69830411 69830420 deletion of <=200bp CAAAGCTGAG - intron_variant LIRI-JP 10 69832436 69832436 single base substitution A G downstream_gene_variant LIRI-JP 10 69832436 69832436 single base substitution A G intron_variant LIRI-JP 10 69832500 69832500 single base substitution T C downstream_gene_variant LIRI-JP 10 69832500 69832500 single base substitution T C intron_variant LIRI-JP 10 69836635 69836635 single base substitution C T upstream_gene_variant LUSC-KR 10 69687806 69687806 single base substitution G A intron_variant LUSC-KR 10 69688578 69688578 single base substitution T A intron_variant LUSC-KR 10 69690052 69690052 single base substitution T A intron_variant LUSC-KR 10 69697456 69697456 single base substitution G T intron_variant LUSC-KR 10 69699738 69699738 single base substitution C A intron_variant LUSC-KR 10 69702296 69702296 single base substitution T C intron_variant LUSC-KR 10 69702559 69702559 single base substitution C A intron_variant LUSC-KR 10 69704333 69704333 single base substitution C A intron_variant LUSC-KR 10 69707054 69707054 single base substitution T C intron_variant LUSC-KR 10 69720870 69720870 single base substitution C T downstream_gene_variant LUSC-KR 10 69720870 69720870 single base substitution C T intron_variant LUSC-KR 10 69720870 69720870 single base substitution C T upstream_gene_variant LUSC-KR 10 69720874 69720874 single base substitution C T downstream_gene_variant LUSC-KR 10 69720874 69720874 single base substitution C T intron_variant LUSC-KR 10 69720874 69720874 single base substitution C T upstream_gene_variant LUSC-KR 10 69724817 69724817 single base substitution C G exon_variant LUSC-KR 10 69724817 69724817 single base substitution C G intron_variant LUSC-KR 10 69728222 69728222 single base substitution C A intron_variant LUSC-KR 10 69731976 69731976 single base substitution G A intron_variant LUSC-KR 10 69733828 69733828 single base substitution T A intron_variant LUSC-KR 10 69734872 69734872 single base substitution G T intron_variant LUSC-KR 10 69737476 69737476 single base substitution C G intron_variant LUSC-KR 10 69741810 69741810 single base substitution G C intron_variant LUSC-KR 10 69743478 69743478 single base substitution A C intron_variant LUSC-KR 10 69759115 69759115 single base substitution C A intron_variant LUSC-KR 10 69763155 69763155 single base substitution C A intron_variant LUSC-KR 10 69765440 69765440 single base substitution T A intron_variant LUSC-KR 10 69767228 69767228 single base substitution T G intron_variant LUSC-KR 10 69769848 69769848 single base substitution T C intron_variant LUSC-KR 10 69772646 69772646 single base substitution T C intron_variant LUSC-KR 10 69775110 69775110 single base substitution C A intron_variant LUSC-KR 10 69783318 69783318 single base substitution G C intron_variant LUSC-KR 10 69787486 69787486 single base substitution C A intron_variant LUSC-KR 10 69790427 69790427 single base substitution C A downstream_gene_variant LUSC-KR 10 69790427 69790427 single base substitution C A intron_variant LUSC-KR 10 69792555 69792555 single base substitution G C 3_prime_UTR_variant LUSC-KR 10 69792555 69792555 single base substitution G C downstream_gene_variant LUSC-KR 10 69792555 69792555 single base substitution G C exon_variant LUSC-KR 10 69792555 69792555 single base substitution G C intron_variant LUSC-KR 10 69792555 69792555 single base substitution G C missense_variant H143D 427C>G LUSC-KR 10 69792555 69792555 single base substitution G C missense_variant H253D 757C>G LUSC-KR 10 69792949 69792949 single base substitution G T downstream_gene_variant LUSC-KR 10 69792949 69792949 single base substitution G T intron_variant LUSC-KR 10 69793644 69793644 single base substitution C T downstream_gene_variant LUSC-KR 10 69793644 69793644 single base substitution C T intron_variant LUSC-KR 10 69794730 69794730 single base substitution C A intron_variant LUSC-KR 10 69797144 69797144 single base substitution C G intron_variant LUSC-KR 10 69798188 69798188 single base substitution C T intron_variant LUSC-KR 10 69798188 69798188 single base substitution C T upstream_gene_variant LUSC-KR 10 69800336 69800336 single base substitution C A intron_variant LUSC-KR 10 69800336 69800336 single base substitution C A upstream_gene_variant LUSC-KR 10 69805199 69805199 single base substitution G A intron_variant LUSC-KR 10 69805669 69805669 single base substitution T C intron_variant LUSC-KR 10 69811152 69811152 single base substitution A G intron_variant LUSC-KR 10 69822849 69822849 single base substitution T A downstream_gene_variant LUSC-KR 10 69822849 69822849 single base substitution T A intron_variant LUSC-KR 10 69824392 69824392 single base substitution T A downstream_gene_variant LUSC-KR 10 69824392 69824392 single base substitution T A intron_variant LUSC-KR 10 69830500 69830500 single base substitution C A downstream_gene_variant LUSC-KR 10 69830500 69830500 single base substitution C A intron_variant LUSC-KR 10 69838919 69838919 single base substitution G A upstream_gene_variant LUSC-US 10 69700823 69700823 single base substitution T A 3_prime_UTR_variant LUSC-US 10 69700823 69700823 single base substitution T A intron_variant LUSC-US 10 69700823 69700823 single base substitution T A missense_variant I691F 2071A>T LUSC-US 10 69700823 69700823 single base substitution T A missense_variant I793F 2377A>T LUSC-US 10 69700823 69700823 single base substitution T A missense_variant I801F 2401A>T LUSC-US 10 69804216 69804216 single base substitution C G exon_variant LUSC-US 10 69804216 69804216 single base substitution C G intron_variant LUSC-US 10 69804216 69804216 single base substitution C G missense_variant D111H 331G>C LUSC-US 10 69804216 69804216 single base substitution C G upstream_gene_variant MALY-DE 10 69681699 69681699 single base substitution T C 3_prime_UTR_variant MALY-DE 10 69681699 69681699 single base substitution T C downstream_gene_variant MALY-DE 10 69681803 69681803 single base substitution C A 3_prime_UTR_variant MALY-DE 10 69681803 69681803 single base substitution C A downstream_gene_variant MALY-DE 10 69682480 69682480 insertion of <=200bp - A 3_prime_UTR_variant MALY-DE 10 69682480 69682480 insertion of <=200bp - A downstream_gene_variant MALY-DE 10 69682505 69682505 single base substitution T C 3_prime_UTR_variant MALY-DE 10 69682505 69682505 single base substitution T C downstream_gene_variant MALY-DE 10 69682667 69682667 single base substitution T G 3_prime_UTR_variant MALY-DE 10 69682667 69682667 single base substitution T G downstream_gene_variant MALY-DE 10 69684105 69684105 single base substitution T A intron_variant MALY-DE 10 69684472 69684472 single base substitution A T intron_variant MALY-DE 10 69692302 69692302 single base substitution T C intron_variant MALY-DE 10 69700970 69700973 deletion of <=200bp AATA - intron_variant MALY-DE 10 69707215 69707215 single base substitution G A intron_variant MALY-DE 10 69707712 69707712 single base substitution G T intron_variant MALY-DE 10 69713306 69713306 single base substitution C T downstream_gene_variant MALY-DE 10 69713306 69713306 single base substitution C T intron_variant MALY-DE 10 69715244 69715244 single base substitution A T exon_variant MALY-DE 10 69715244 69715244 single base substitution A T intron_variant MALY-DE 10 69716261 69716261 single base substitution C T exon_variant MALY-DE 10 69716261 69716261 single base substitution C T intron_variant MALY-DE 10 69717226 69717226 single base substitution C T intron_variant MALY-DE 10 69717226 69717226 single base substitution C T upstream_gene_variant MALY-DE 10 69718715 69718715 single base substitution T C intron_variant MALY-DE 10 69718715 69718715 single base substitution T C upstream_gene_variant MALY-DE 10 69720445 69720445 single base substitution C T downstream_gene_variant MALY-DE 10 69720445 69720445 single base substitution C T intron_variant MALY-DE 10 69720445 69720445 single base substitution C T upstream_gene_variant MALY-DE 10 69721113 69721113 single base substitution T C downstream_gene_variant MALY-DE 10 69721113 69721113 single base substitution T C intron_variant MALY-DE 10 69721113 69721113 single base substitution T C upstream_gene_variant MALY-DE 10 69728528 69728528 insertion of <=200bp - CA intron_variant MALY-DE 10 69733154 69733154 single base substitution G C intron_variant MALY-DE 10 69735420 69735420 single base substitution T G intron_variant MALY-DE 10 69747013 69747013 single base substitution A G intron_variant MALY-DE 10 69747915 69747915 single base substitution C G intron_variant MALY-DE 10 69750668 69750668 single base substitution G C 3_prime_UTR_variant MALY-DE 10 69750668 69750668 single base substitution G C missense_variant S369C 1106C>G MALY-DE 10 69750668 69750668 single base substitution G C missense_variant S479C 1436C>G MALY-DE 10 69750668 69750668 single base substitution G C upstream_gene_variant MALY-DE 10 69753362 69753362 deletion of <=200bp T - 3_prime_UTR_variant MALY-DE 10 69753362 69753362 deletion of <=200bp T - intron_variant MALY-DE 10 69753362 69753362 deletion of <=200bp T - upstream_gene_variant MALY-DE 10 69757918 69757918 single base substitution T G intron_variant MALY-DE 10 69763982 69763982 single base substitution C A intron_variant MALY-DE 10 69767068 69767068 single base substitution C T intron_variant MALY-DE 10 69779355 69779355 single base substitution C G intron_variant MALY-DE 10 69782920 69782920 single base substitution A T intron_variant MALY-DE 10 69793865 69793865 single base substitution G A 3_prime_UTR_variant MALY-DE 10 69793865 69793865 single base substitution G A exon_variant MALY-DE 10 69793865 69793865 single base substitution G A missense_variant P181L 542C>T MALY-DE 10 69793865 69793865 single base substitution G A missense_variant P205L 614C>T MALY-DE 10 69793865 69793865 single base substitution G A missense_variant P71L 212C>T MALY-DE 10 69805522 69805522 single base substitution T G intron_variant MALY-DE 10 69805863 69805863 single base substitution C A intron_variant MALY-DE 10 69807054 69807054 single base substitution T A intron_variant MALY-DE 10 69807115 69807115 single base substitution T C intron_variant MALY-DE 10 69811419 69811419 single base substitution G A intron_variant MALY-DE 10 69812271 69812271 single base substitution C T intron_variant MALY-DE 10 69831545 69831545 single base substitution A T downstream_gene_variant MALY-DE 10 69831545 69831545 single base substitution A T intron_variant MALY-DE 10 69831905 69831905 single base substitution A C downstream_gene_variant MALY-DE 10 69831905 69831905 single base substitution A C intron_variant MALY-DE 10 69837066 69837066 single base substitution C A upstream_gene_variant MELA-AU 10 69677234 69677235 multiple base substitution (>=2bp and <=200bp) GT AA downstream_gene_variant MELA-AU 10 69678403 69678403 single base substitution G A downstream_gene_variant MELA-AU 10 69679609 69679609 single base substitution T A downstream_gene_variant MELA-AU 10 69680870 69680870 single base substitution T A downstream_gene_variant MELA-AU 10 69681229 69681229 single base substitution G A downstream_gene_variant MELA-AU 10 69681437 69681437 single base substitution G A downstream_gene_variant MELA-AU 10 69681636 69681636 single base substitution G A downstream_gene_variant MELA-AU 10 69681888 69681888 single base substitution G A 3_prime_UTR_variant MELA-AU 10 69681888 69681888 single base substitution G A downstream_gene_variant MELA-AU 10 69683610 69683610 single base substitution A T intron_variant MELA-AU 10 69683910 69683910 single base substitution G A intron_variant MELA-AU 10 69685587 69685587 single base substitution T C intron_variant MELA-AU 10 69686081 69686081 single base substitution G A intron_variant MELA-AU 10 69686911 69686911 single base substitution G A intron_variant MELA-AU 10 69688093 69688093 single base substitution C T intron_variant MELA-AU 10 69688134 69688134 single base substitution C T intron_variant MELA-AU 10 69688455 69688455 single base substitution G A intron_variant MELA-AU 10 69689373 69689373 single base substitution G A intron_variant MELA-AU 10 69689592 69689592 single base substitution G A intron_variant MELA-AU 10 69690593 69690593 single base substitution C A intron_variant MELA-AU 10 69690868 69690868 single base substitution G A intron_variant MELA-AU 10 69690928 69690928 single base substitution G A intron_variant MELA-AU 10 69691124 69691124 single base substitution A C intron_variant MELA-AU 10 69691545 69691545 single base substitution G A intron_variant MELA-AU 10 69691653 69691653 single base substitution G A intron_variant MELA-AU 10 69691849 69691849 single base substitution G A intron_variant MELA-AU 10 69692227 69692228 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 69692467 69692467 single base substitution G A 3_prime_UTR_variant MELA-AU 10 69692467 69692467 single base substitution G A missense_variant H807Y 2419C>T MELA-AU 10 69692467 69692467 single base substitution G A missense_variant H839Y 2515C>T MELA-AU 10 69692467 69692467 single base substitution G A missense_variant H909Y 2725C>T MELA-AU 10 69692467 69692467 single base substitution G A missense_variant H917Y 2749C>T MELA-AU 10 69693138 69693138 single base substitution G A intron_variant MELA-AU 10 69693986 69693986 single base substitution T C intron_variant MELA-AU 10 69694920 69694920 single base substitution T C intron_variant MELA-AU 10 69695452 69695452 single base substitution G A intron_variant MELA-AU 10 69696361 69696361 single base substitution T C intron_variant MELA-AU 10 69696568 69696568 single base substitution G A intron_variant MELA-AU 10 69697027 69697027 single base substitution G A intron_variant MELA-AU 10 69697132 69697132 single base substitution A C intron_variant MELA-AU 10 69697233 69697233 single base substitution G A intron_variant MELA-AU 10 69697366 69697366 single base substitution G A intron_variant MELA-AU 10 69697367 69697367 single base substitution G A intron_variant MELA-AU 10 69697385 69697385 single base substitution G A intron_variant MELA-AU 10 69697757 69697757 single base substitution T G intron_variant MELA-AU 10 69698142 69698142 single base substitution G A intron_variant MELA-AU 10 69698213 69698213 single base substitution A G intron_variant MELA-AU 10 69698321 69698321 single base substitution G A intron_variant MELA-AU 10 69698889 69698889 single base substitution G A intron_variant MELA-AU 10 69699245 69699245 single base substitution T A intron_variant MELA-AU 10 69699307 69699307 single base substitution G A intron_variant MELA-AU 10 69699479 69699480 deletion of <=200bp AT - intron_variant MELA-AU 10 69701105 69701105 single base substitution G A intron_variant MELA-AU 10 69701480 69701480 single base substitution G A intron_variant MELA-AU 10 69702751 69702751 single base substitution G A intron_variant MELA-AU 10 69702791 69702791 single base substitution G A intron_variant MELA-AU 10 69703624 69703624 single base substitution G A intron_variant MELA-AU 10 69703666 69703666 single base substitution G A intron_variant MELA-AU 10 69704000 69704000 single base substitution G A intron_variant MELA-AU 10 69704075 69704075 single base substitution C T intron_variant MELA-AU 10 69704359 69704359 single base substitution G A intron_variant MELA-AU 10 69704480 69704480 single base substitution T A intron_variant MELA-AU 10 69705132 69705132 single base substitution G A intron_variant MELA-AU 10 69705801 69705801 single base substitution G A intron_variant MELA-AU 10 69706527 69706528 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 69706710 69706710 single base substitution G A intron_variant MELA-AU 10 69706779 69706779 single base substitution T A intron_variant MELA-AU 10 69707022 69707022 single base substitution G A intron_variant MELA-AU 10 69707067 69707067 single base substitution G A intron_variant MELA-AU 10 69707807 69707807 single base substitution A T intron_variant MELA-AU 10 69707874 69707874 single base substitution G A intron_variant MELA-AU 10 69707963 69707963 single base substitution A G intron_variant MELA-AU 10 69708204 69708204 single base substitution G A intron_variant MELA-AU 10 69708291 69708291 single base substitution G A intron_variant MELA-AU 10 69708860 69708860 single base substitution A T intron_variant MELA-AU 10 69708968 69708968 single base substitution G A downstream_gene_variant MELA-AU 10 69708968 69708968 single base substitution G A intron_variant MELA-AU 10 69709880 69709880 single base substitution G A downstream_gene_variant MELA-AU 10 69709880 69709880 single base substitution G A intron_variant MELA-AU 10 69709912 69709912 single base substitution G A downstream_gene_variant MELA-AU 10 69709912 69709912 single base substitution G A intron_variant MELA-AU 10 69710034 69710035 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 69710034 69710035 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 69710149 69710149 single base substitution C A downstream_gene_variant MELA-AU 10 69710149 69710149 single base substitution C A intron_variant MELA-AU 10 69711096 69711096 single base substitution G A downstream_gene_variant MELA-AU 10 69711096 69711096 single base substitution G A intron_variant MELA-AU 10 69711353 69711353 single base substitution C A downstream_gene_variant MELA-AU 10 69711353 69711353 single base substitution C A intron_variant MELA-AU 10 69712631 69712631 single base substitution T C downstream_gene_variant MELA-AU 10 69712631 69712631 single base substitution T C intron_variant MELA-AU 10 69712873 69712873 single base substitution G A downstream_gene_variant MELA-AU 10 69712873 69712873 single base substitution G A intron_variant MELA-AU 10 69713152 69713152 single base substitution A T downstream_gene_variant MELA-AU 10 69713152 69713152 single base substitution A T intron_variant MELA-AU 10 69713545 69713545 single base substitution G A downstream_gene_variant MELA-AU 10 69713545 69713545 single base substitution G A intron_variant MELA-AU 10 69713862 69713862 single base substitution G A downstream_gene_variant MELA-AU 10 69713862 69713862 single base substitution G A intron_variant MELA-AU 10 69715151 69715151 single base substitution G A exon_variant MELA-AU 10 69715151 69715151 single base substitution G A intron_variant MELA-AU 10 69715515 69715515 single base substitution C T exon_variant MELA-AU 10 69715515 69715515 single base substitution C T intron_variant MELA-AU 10 69716003 69716003 single base substitution G A exon_variant MELA-AU 10 69716003 69716003 single base substitution G A intron_variant MELA-AU 10 69716200 69716200 single base substitution G A exon_variant MELA-AU 10 69716200 69716200 single base substitution G A intron_variant MELA-AU 10 69716921 69716922 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 69716921 69716922 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 69717657 69717658 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 69717657 69717658 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 69717688 69717688 single base substitution C T intron_variant MELA-AU 10 69717688 69717688 single base substitution C T upstream_gene_variant MELA-AU 10 69717737 69717737 single base substitution T G intron_variant MELA-AU 10 69717737 69717737 single base substitution T G upstream_gene_variant MELA-AU 10 69720173 69720173 single base substitution G A downstream_gene_variant MELA-AU 10 69720173 69720173 single base substitution G A intron_variant MELA-AU 10 69720173 69720173 single base substitution G A upstream_gene_variant MELA-AU 10 69721376 69721376 single base substitution G A downstream_gene_variant MELA-AU 10 69721376 69721376 single base substitution G A intron_variant MELA-AU 10 69721376 69721376 single base substitution G A upstream_gene_variant MELA-AU 10 69723487 69723488 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 69723487 69723488 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 69723771 69723771 single base substitution G A downstream_gene_variant MELA-AU 10 69723771 69723771 single base substitution G A intron_variant MELA-AU 10 69723827 69723827 single base substitution C G downstream_gene_variant MELA-AU 10 69723827 69723827 single base substitution C G intron_variant MELA-AU 10 69724549 69724549 single base substitution G A exon_variant MELA-AU 10 69724549 69724549 single base substitution G A intron_variant MELA-AU 10 69724664 69724664 single base substitution G A exon_variant MELA-AU 10 69724664 69724664 single base substitution G A intron_variant MELA-AU 10 69725009 69725009 single base substitution G A exon_variant MELA-AU 10 69725009 69725009 single base substitution G A intron_variant MELA-AU 10 69725133 69725133 single base substitution T A exon_variant MELA-AU 10 69725133 69725133 single base substitution T A intron_variant MELA-AU 10 69725306 69725306 single base substitution G A exon_variant MELA-AU 10 69725306 69725306 single base substitution G A intron_variant MELA-AU 10 69725339 69725339 single base substitution G T exon_variant MELA-AU 10 69725339 69725339 single base substitution G T intron_variant MELA-AU 10 69725922 69725922 single base substitution G A exon_variant MELA-AU 10 69725922 69725922 single base substitution G A intron_variant MELA-AU 10 69726146 69726146 single base substitution G A exon_variant MELA-AU 10 69726146 69726146 single base substitution G A intron_variant MELA-AU 10 69726185 69726185 single base substitution G A exon_variant MELA-AU 10 69726185 69726185 single base substitution G A intron_variant MELA-AU 10 69726823 69726823 single base substitution G A intron_variant MELA-AU 10 69727274 69727274 single base substitution G A intron_variant MELA-AU 10 69727326 69727326 single base substitution A G intron_variant MELA-AU 10 69727630 69727630 single base substitution A T intron_variant MELA-AU 10 69727667 69727667 single base substitution G A intron_variant MELA-AU 10 69727682 69727682 single base substitution G A intron_variant MELA-AU 10 69727710 69727710 single base substitution G A intron_variant MELA-AU 10 69728150 69728150 single base substitution G C intron_variant MELA-AU 10 69729136 69729136 single base substitution G C intron_variant MELA-AU 10 69729280 69729280 single base substitution G A intron_variant MELA-AU 10 69729430 69729430 single base substitution G A intron_variant MELA-AU 10 69729582 69729582 single base substitution G A intron_variant MELA-AU 10 69730979 69730979 single base substitution G A intron_variant MELA-AU 10 69731279 69731279 single base substitution G A intron_variant MELA-AU 10 69731280 69731280 single base substitution G A intron_variant MELA-AU 10 69731312 69731312 single base substitution G A intron_variant MELA-AU 10 69732423 69732423 single base substitution G A intron_variant MELA-AU 10 69732623 69732623 single base substitution G A intron_variant MELA-AU 10 69733571 69733571 single base substitution G A intron_variant MELA-AU 10 69734160 69734160 single base substitution C T intron_variant MELA-AU 10 69734167 69734167 single base substitution A G intron_variant MELA-AU 10 69734317 69734317 single base substitution G A intron_variant MELA-AU 10 69734870 69734870 single base substitution C G intron_variant MELA-AU 10 69734996 69734996 single base substitution A G intron_variant MELA-AU 10 69736370 69736370 single base substitution C T intron_variant MELA-AU 10 69736618 69736618 single base substitution C T intron_variant MELA-AU 10 69736619 69736619 single base substitution C T intron_variant MELA-AU 10 69736834 69736834 single base substitution T C intron_variant MELA-AU 10 69736836 69736836 single base substitution T C intron_variant MELA-AU 10 69736931 69736931 single base substitution G A intron_variant MELA-AU 10 69738072 69738072 single base substitution G T intron_variant MELA-AU 10 69738287 69738287 single base substitution G A intron_variant MELA-AU 10 69738310 69738310 single base substitution G A intron_variant MELA-AU 10 69738711 69738711 single base substitution G A intron_variant MELA-AU 10 69738983 69738983 single base substitution A T intron_variant MELA-AU 10 69739196 69739196 single base substitution A G intron_variant MELA-AU 10 69740291 69740291 single base substitution G A intron_variant MELA-AU 10 69741361 69741361 single base substitution G A intron_variant MELA-AU 10 69742367 69742367 single base substitution A T intron_variant MELA-AU 10 69742378 69742378 single base substitution G A intron_variant MELA-AU 10 69744035 69744035 single base substitution G A intron_variant MELA-AU 10 69744238 69744238 single base substitution G A intron_variant MELA-AU 10 69744256 69744256 single base substitution G A intron_variant MELA-AU 10 69744281 69744281 single base substitution G A intron_variant MELA-AU 10 69746698 69746698 single base substitution G A intron_variant MELA-AU 10 69746797 69746797 single base substitution A G intron_variant MELA-AU 10 69747475 69747475 single base substitution G A intron_variant MELA-AU 10 69749268 69749268 single base substitution T C intron_variant MELA-AU 10 69749946 69749946 single base substitution G A intron_variant MELA-AU 10 69750255 69750255 single base substitution G A intron_variant MELA-AU 10 69750255 69750255 single base substitution G A upstream_gene_variant MELA-AU 10 69750333 69750333 single base substitution G A intron_variant MELA-AU 10 69750333 69750333 single base substitution G A upstream_gene_variant MELA-AU 10 69750806 69750806 single base substitution A G intron_variant MELA-AU 10 69750806 69750806 single base substitution A G upstream_gene_variant MELA-AU 10 69751530 69751530 single base substitution G A intron_variant MELA-AU 10 69751530 69751530 single base substitution G A upstream_gene_variant MELA-AU 10 69753283 69753283 single base substitution A G 3_prime_UTR_variant MELA-AU 10 69753283 69753283 single base substitution A G intron_variant MELA-AU 10 69753283 69753283 single base substitution A G upstream_gene_variant MELA-AU 10 69753898 69753898 single base substitution T G 3_prime_UTR_variant MELA-AU 10 69753898 69753898 single base substitution T G intron_variant MELA-AU 10 69753898 69753898 single base substitution T G upstream_gene_variant MELA-AU 10 69754184 69754184 single base substitution T A 3_prime_UTR_variant MELA-AU 10 69754184 69754184 single base substitution T A intron_variant MELA-AU 10 69754184 69754184 single base substitution T A upstream_gene_variant MELA-AU 10 69754778 69754778 single base substitution G A 3_prime_UTR_variant MELA-AU 10 69754778 69754778 single base substitution G A intron_variant MELA-AU 10 69754778 69754778 single base substitution G A upstream_gene_variant MELA-AU 10 69756045 69756045 single base substitution G A intron_variant MELA-AU 10 69756107 69756107 single base substitution T G intron_variant MELA-AU 10 69757323 69757323 single base substitution T A intron_variant MELA-AU 10 69757591 69757591 single base substitution C T intron_variant MELA-AU 10 69759366 69759366 single base substitution T C intron_variant MELA-AU 10 69759461 69759461 single base substitution T C intron_variant MELA-AU 10 69760812 69760812 single base substitution G A intron_variant MELA-AU 10 69761035 69761035 single base substitution G A intron_variant MELA-AU 10 69761130 69761130 single base substitution A T intron_variant MELA-AU 10 69761993 69761993 single base substitution C T intron_variant MELA-AU 10 69762360 69762360 single base substitution T A intron_variant MELA-AU 10 69762665 69762665 single base substitution A G intron_variant MELA-AU 10 69763674 69763675 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 69764512 69764512 single base substitution G A intron_variant MELA-AU 10 69764923 69764923 single base substitution G A intron_variant MELA-AU 10 69766488 69766488 single base substitution G A intron_variant MELA-AU 10 69766744 69766744 single base substitution A C intron_variant MELA-AU 10 69767714 69767714 single base substitution G A intron_variant MELA-AU 10 69767715 69767715 single base substitution A C intron_variant MELA-AU 10 69769110 69769110 single base substitution G A intron_variant MELA-AU 10 69769998 69769998 single base substitution G A intron_variant MELA-AU 10 69771224 69771224 single base substitution A G intron_variant MELA-AU 10 69772248 69772248 single base substitution G A intron_variant MELA-AU 10 69773163 69773163 single base substitution G A intron_variant MELA-AU 10 69773458 69773458 single base substitution G A intron_variant MELA-AU 10 69774274 69774274 single base substitution C T intron_variant MELA-AU 10 69774825 69774825 single base substitution C T intron_variant MELA-AU 10 69774952 69774952 single base substitution G A intron_variant MELA-AU 10 69775938 69775938 single base substitution A T intron_variant MELA-AU 10 69776244 69776244 single base substitution G A intron_variant MELA-AU 10 69778026 69778026 single base substitution G A intron_variant MELA-AU 10 69778379 69778379 single base substitution T C intron_variant MELA-AU 10 69778543 69778543 single base substitution G A intron_variant MELA-AU 10 69779154 69779154 single base substitution G A intron_variant MELA-AU 10 69779219 69779219 single base substitution G A intron_variant MELA-AU 10 69779518 69779518 single base substitution G A intron_variant MELA-AU 10 69779768 69779768 single base substitution G A intron_variant MELA-AU 10 69780037 69780037 single base substitution G A intron_variant MELA-AU 10 69780750 69780750 single base substitution G A intron_variant MELA-AU 10 69781080 69781080 single base substitution G A intron_variant MELA-AU 10 69781166 69781166 single base substitution G A intron_variant MELA-AU 10 69781357 69781357 single base substitution G A intron_variant MELA-AU 10 69782054 69782054 single base substitution C T intron_variant MELA-AU 10 69782075 69782075 single base substitution G A intron_variant MELA-AU 10 69782151 69782151 single base substitution G A intron_variant MELA-AU 10 69782282 69782282 single base substitution A G intron_variant MELA-AU 10 69782298 69782298 single base substitution A G intron_variant MELA-AU 10 69783907 69783907 single base substitution C A intron_variant MELA-AU 10 69785622 69785622 single base substitution G A intron_variant MELA-AU 10 69785744 69785744 single base substitution G A intron_variant MELA-AU 10 69789584 69789584 single base substitution C T downstream_gene_variant MELA-AU 10 69789584 69789584 single base substitution C T intron_variant MELA-AU 10 69789630 69789630 single base substitution G A downstream_gene_variant MELA-AU 10 69789630 69789630 single base substitution G A intron_variant MELA-AU 10 69789685 69789685 single base substitution C T downstream_gene_variant MELA-AU 10 69789685 69789685 single base substitution C T intron_variant MELA-AU 10 69790406 69790406 single base substitution G A downstream_gene_variant MELA-AU 10 69790406 69790406 single base substitution G A intron_variant MELA-AU 10 69791417 69791417 single base substitution C T downstream_gene_variant MELA-AU 10 69791417 69791417 single base substitution C T intron_variant MELA-AU 10 69791810 69791810 single base substitution T G downstream_gene_variant MELA-AU 10 69791810 69791810 single base substitution T G intron_variant MELA-AU 10 69792668 69792668 single base substitution C T downstream_gene_variant MELA-AU 10 69792668 69792668 single base substitution C T intron_variant MELA-AU 10 69792983 69792983 single base substitution A T downstream_gene_variant MELA-AU 10 69792983 69792983 single base substitution A T intron_variant MELA-AU 10 69794873 69794873 single base substitution A C intron_variant MELA-AU 10 69795403 69795403 single base substitution G A intron_variant MELA-AU 10 69795632 69795632 single base substitution C T intron_variant MELA-AU 10 69795794 69795794 single base substitution G A intron_variant MELA-AU 10 69795868 69795868 single base substitution G A intron_variant MELA-AU 10 69795989 69795989 single base substitution G A intron_variant MELA-AU 10 69796062 69796062 single base substitution G A intron_variant MELA-AU 10 69796252 69796252 single base substitution G A intron_variant MELA-AU 10 69796608 69796608 single base substitution C A intron_variant MELA-AU 10 69799238 69799238 single base substitution G A 5_prime_UTR_variant MELA-AU 10 69799238 69799238 single base substitution G A intron_variant MELA-AU 10 69799238 69799238 single base substitution G A missense_variant P132S 394C>T MELA-AU 10 69799238 69799238 single base substitution G A upstream_gene_variant MELA-AU 10 69800134 69800134 single base substitution G T intron_variant MELA-AU 10 69800134 69800134 single base substitution G T upstream_gene_variant MELA-AU 10 69800780 69800780 single base substitution A G intron_variant MELA-AU 10 69800780 69800780 single base substitution A G upstream_gene_variant MELA-AU 10 69801516 69801516 single base substitution T G intron_variant MELA-AU 10 69801516 69801516 single base substitution T G upstream_gene_variant MELA-AU 10 69801952 69801952 single base substitution G T intron_variant MELA-AU 10 69801952 69801952 single base substitution G T upstream_gene_variant MELA-AU 10 69802722 69802722 single base substitution G A intron_variant MELA-AU 10 69802722 69802722 single base substitution G A upstream_gene_variant MELA-AU 10 69803222 69803222 single base substitution T C intron_variant MELA-AU 10 69803222 69803222 single base substitution T C upstream_gene_variant MELA-AU 10 69804515 69804515 single base substitution A C intron_variant MELA-AU 10 69804515 69804515 single base substitution A C upstream_gene_variant MELA-AU 10 69804827 69804827 single base substitution C T intron_variant MELA-AU 10 69805007 69805007 single base substitution G A intron_variant MELA-AU 10 69805106 69805106 single base substitution G A intron_variant MELA-AU 10 69805136 69805136 single base substitution G A intron_variant MELA-AU 10 69807659 69807659 single base substitution A G intron_variant MELA-AU 10 69809009 69809009 single base substitution C T intron_variant MELA-AU 10 69809645 69809645 single base substitution G A intron_variant MELA-AU 10 69810249 69810249 single base substitution T A intron_variant MELA-AU 10 69811777 69811777 single base substitution G A intron_variant MELA-AU 10 69811837 69811837 single base substitution G A intron_variant MELA-AU 10 69811839 69811839 single base substitution G A intron_variant MELA-AU 10 69811879 69811879 single base substitution G A intron_variant MELA-AU 10 69812538 69812538 single base substitution G A intron_variant MELA-AU 10 69813203 69813203 single base substitution G A intron_variant MELA-AU 10 69814743 69814743 single base substitution G A intron_variant MELA-AU 10 69814783 69814783 single base substitution G A intron_variant MELA-AU 10 69814825 69814825 single base substitution G A intron_variant MELA-AU 10 69815642 69815643 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 69815657 69815657 single base substitution G A intron_variant MELA-AU 10 69816222 69816222 single base substitution G A intron_variant MELA-AU 10 69816737 69816737 single base substitution G A intron_variant MELA-AU 10 69818128 69818128 single base substitution G A intron_variant MELA-AU 10 69818187 69818187 single base substitution G A intron_variant MELA-AU 10 69820061 69820061 single base substitution C T intron_variant MELA-AU 10 69820696 69820696 single base substitution A C intron_variant MELA-AU 10 69820721 69820721 single base substitution A G intron_variant MELA-AU 10 69821234 69821234 single base substitution G T intron_variant MELA-AU 10 69821390 69821390 single base substitution C T intron_variant MELA-AU 10 69821625 69821625 single base substitution G A intron_variant MELA-AU 10 69821637 69821637 single base substitution A G intron_variant MELA-AU 10 69825146 69825146 single base substitution A T downstream_gene_variant MELA-AU 10 69825146 69825146 single base substitution A T intron_variant MELA-AU 10 69825547 69825547 single base substitution G A downstream_gene_variant MELA-AU 10 69825547 69825547 single base substitution G A intron_variant MELA-AU 10 69827508 69827508 single base substitution G A 3_prime_UTR_variant MELA-AU 10 69827508 69827508 single base substitution G A intron_variant MELA-AU 10 69827707 69827707 single base substitution C T 3_prime_UTR_variant MELA-AU 10 69827707 69827707 single base substitution C T intron_variant MELA-AU 10 69827725 69827725 single base substitution G A 3_prime_UTR_variant MELA-AU 10 69827725 69827725 single base substitution G A intron_variant MELA-AU 10 69827999 69827999 single base substitution T C 3_prime_UTR_variant MELA-AU 10 69827999 69827999 single base substitution T C downstream_gene_variant MELA-AU 10 69827999 69827999 single base substitution T C intron_variant MELA-AU 10 69828152 69828152 single base substitution G A 3_prime_UTR_variant MELA-AU 10 69828152 69828152 single base substitution G A downstream_gene_variant MELA-AU 10 69828152 69828152 single base substitution G A intron_variant MELA-AU 10 69828839 69828839 single base substitution G A 3_prime_UTR_variant MELA-AU 10 69828839 69828839 single base substitution G A downstream_gene_variant MELA-AU 10 69828839 69828839 single base substitution G A intron_variant MELA-AU 10 69828840 69828840 single base substitution G A 3_prime_UTR_variant MELA-AU 10 69828840 69828840 single base substitution G A downstream_gene_variant MELA-AU 10 69828840 69828840 single base substitution G A intron_variant MELA-AU 10 69830242 69830242 single base substitution A G 3_prime_UTR_variant MELA-AU 10 69830242 69830242 single base substitution A G downstream_gene_variant MELA-AU 10 69830242 69830242 single base substitution A G intron_variant MELA-AU 10 69830338 69830338 single base substitution G A downstream_gene_variant MELA-AU 10 69830338 69830338 single base substitution G A intron_variant MELA-AU 10 69830338 69830338 single base substitution G A missense_variant P82L 245C>T MELA-AU 10 69830555 69830555 single base substitution A C downstream_gene_variant MELA-AU 10 69830555 69830555 single base substitution A C intron_variant MELA-AU 10 69831612 69831612 single base substitution G A downstream_gene_variant MELA-AU 10 69831612 69831612 single base substitution G A intron_variant MELA-AU 10 69832594 69832594 single base substitution G A downstream_gene_variant MELA-AU 10 69832594 69832594 single base substitution G A intron_variant MELA-AU 10 69834008 69834008 single base substitution T C intron_variant MELA-AU 10 69834008 69834008 single base substitution T C upstream_gene_variant MELA-AU 10 69834594 69834594 single base substitution G A exon_variant MELA-AU 10 69834594 69834594 single base substitution G A intron_variant MELA-AU 10 69834594 69834594 single base substitution G A upstream_gene_variant MELA-AU 10 69834703 69834703 single base substitution C A intron_variant MELA-AU 10 69834703 69834703 single base substitution C A upstream_gene_variant MELA-AU 10 69835100 69835100 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 10 69835100 69835100 single base substitution G A upstream_gene_variant MELA-AU 10 69836432 69836432 single base substitution C T upstream_gene_variant MELA-AU 10 69836463 69836463 single base substitution C T upstream_gene_variant MELA-AU 10 69836672 69836672 single base substitution G A upstream_gene_variant MELA-AU 10 69836777 69836777 single base substitution G A upstream_gene_variant MELA-AU 10 69836878 69836878 single base substitution C T upstream_gene_variant MELA-AU 10 69837472 69837472 single base substitution C T upstream_gene_variant MELA-AU 10 69838817 69838817 single base substitution C T upstream_gene_variant MELA-AU 10 69838849 69838849 single base substitution A G upstream_gene_variant MELA-AU 10 69839077 69839077 single base substitution C T upstream_gene_variant MELA-AU 10 69839880 69839880 single base substitution A T upstream_gene_variant ORCA-IN 10 69695578 69695578 single base substitution C G intron_variant ORCA-IN 10 69703093 69703093 single base substitution G C intron_variant ORCA-IN 10 69704976 69704976 single base substitution C G intron_variant ORCA-IN 10 69707819 69707819 single base substitution C A intron_variant ORCA-IN 10 69733274 69733274 single base substitution G A intron_variant OV-AU 10 69677951 69677951 single base substitution T C downstream_gene_variant OV-AU 10 69680821 69680821 single base substitution T C downstream_gene_variant OV-AU 10 69698203 69698203 single base substitution A G intron_variant OV-AU 10 69703351 69703351 single base substitution G T intron_variant OV-AU 10 69713684 69713684 single base substitution G A downstream_gene_variant OV-AU 10 69713684 69713684 single base substitution G A intron_variant OV-AU 10 69719587 69719587 single base substitution A G downstream_gene_variant OV-AU 10 69719587 69719587 single base substitution A G intron_variant OV-AU 10 69719587 69719587 single base substitution A G upstream_gene_variant OV-AU 10 69720553 69720553 single base substitution T C downstream_gene_variant OV-AU 10 69720553 69720553 single base substitution T C intron_variant OV-AU 10 69720553 69720553 single base substitution T C upstream_gene_variant OV-AU 10 69735872 69735872 single base substitution T G intron_variant OV-AU 10 69737659 69737659 single base substitution G C intron_variant OV-AU 10 69741434 69741434 single base substitution C A intron_variant OV-AU 10 69750305 69750305 single base substitution G C intron_variant OV-AU 10 69750305 69750305 single base substitution G C upstream_gene_variant OV-AU 10 69754570 69754570 single base substitution A G 3_prime_UTR_variant OV-AU 10 69754570 69754570 single base substitution A G intron_variant OV-AU 10 69754570 69754570 single base substitution A G upstream_gene_variant OV-AU 10 69764871 69764871 single base substitution C T intron_variant OV-AU 10 69772845 69772845 single base substitution A G intron_variant OV-AU 10 69773901 69773901 single base substitution G C 3_prime_UTR_variant OV-AU 10 69773901 69773901 single base substitution G C exon_variant OV-AU 10 69773901 69773901 single base substitution G C stop_gained Y207* 621C>G OV-AU 10 69773901 69773901 single base substitution G C stop_gained Y317* 951C>G OV-AU 10 69776354 69776354 single base substitution C A intron_variant OV-AU 10 69787438 69787438 single base substitution G T intron_variant OV-AU 10 69790060 69790060 single base substitution T A downstream_gene_variant OV-AU 10 69790060 69790060 single base substitution T A intron_variant OV-AU 10 69790803 69790803 single base substitution A C downstream_gene_variant OV-AU 10 69790803 69790803 single base substitution A C intron_variant OV-AU 10 69793118 69793118 single base substitution A T downstream_gene_variant OV-AU 10 69793118 69793118 single base substitution A T intron_variant OV-AU 10 69800235 69800235 single base substitution T A intron_variant OV-AU 10 69800235 69800235 single base substitution T A upstream_gene_variant OV-AU 10 69806055 69806055 single base substitution T A intron_variant OV-AU 10 69814060 69814060 single base substitution T C intron_variant OV-AU 10 69821250 69821250 single base substitution A G intron_variant OV-AU 10 69827450 69827450 single base substitution T C 3_prime_UTR_variant OV-AU 10 69827450 69827450 single base substitution T C intron_variant OV-AU 10 69828242 69828242 single base substitution T C 3_prime_UTR_variant OV-AU 10 69828242 69828242 single base substitution T C downstream_gene_variant OV-AU 10 69828242 69828242 single base substitution T C intron_variant OV-AU 10 69836849 69836849 single base substitution A C upstream_gene_variant OV-AU 10 69838870 69838870 single base substitution A T upstream_gene_variant OV-AU 10 69839567 69839567 single base substitution C A upstream_gene_variant PACA-AU 10 69685537 69685537 single base substitution C A intron_variant PACA-AU 10 69685923 69685923 single base substitution G A intron_variant PACA-AU 10 69699479 69699480 deletion of <=200bp AT - intron_variant PACA-AU 10 69700523 69700523 single base substitution A T intron_variant PACA-AU 10 69708784 69708784 single base substitution A G intron_variant PACA-AU 10 69710859 69710859 single base substitution T C downstream_gene_variant PACA-AU 10 69710859 69710859 single base substitution T C intron_variant PACA-AU 10 69715957 69715957 single base substitution T C exon_variant PACA-AU 10 69715957 69715957 single base substitution T C intron_variant PACA-AU 10 69716189 69716189 single base substitution C T exon_variant PACA-AU 10 69716189 69716189 single base substitution C T intron_variant PACA-AU 10 69718339 69718339 single base substitution G A intron_variant PACA-AU 10 69718339 69718339 single base substitution G A upstream_gene_variant PACA-AU 10 69720164 69720164 single base substitution C A downstream_gene_variant PACA-AU 10 69720164 69720164 single base substitution C A intron_variant PACA-AU 10 69720164 69720164 single base substitution C A upstream_gene_variant PACA-AU 10 69723128 69723128 single base substitution G A downstream_gene_variant PACA-AU 10 69723128 69723128 single base substitution G A intron_variant PACA-AU 10 69724492 69724492 single base substitution A C downstream_gene_variant PACA-AU 10 69724492 69724492 single base substitution A C intron_variant PACA-AU 10 69729201 69729201 single base substitution G A intron_variant PACA-AU 10 69730573 69730573 single base substitution A C intron_variant PACA-AU 10 69731419 69731419 single base substitution A T intron_variant PACA-AU 10 69733840 69733840 single base substitution C T intron_variant PACA-AU 10 69734113 69734116 deletion of <=200bp AAAT - intron_variant PACA-AU 10 69735389 69735389 single base substitution G A intron_variant PACA-AU 10 69736549 69736549 insertion of <=200bp - T intron_variant PACA-AU 10 69739898 69739898 single base substitution C T intron_variant PACA-AU 10 69740732 69740732 single base substitution C T intron_variant PACA-AU 10 69741622 69741622 deletion of <=200bp G - intron_variant PACA-AU 10 69745898 69745898 single base substitution A T intron_variant PACA-AU 10 69756927 69756927 single base substitution T C intron_variant PACA-AU 10 69763320 69763320 single base substitution T C intron_variant PACA-AU 10 69768026 69768026 single base substitution C T intron_variant PACA-AU 10 69780982 69780982 single base substitution A T intron_variant PACA-AU 10 69782046 69782046 single base substitution C T intron_variant PACA-AU 10 69782247 69782247 single base substitution A C intron_variant PACA-AU 10 69782258 69782258 insertion of <=200bp - AAAT intron_variant PACA-AU 10 69785847 69785847 deletion of <=200bp T - intron_variant PACA-AU 10 69786383 69786383 single base substitution G A intron_variant PACA-AU 10 69786898 69786898 single base substitution C G intron_variant PACA-AU 10 69790801 69790801 single base substitution A G downstream_gene_variant PACA-AU 10 69790801 69790801 single base substitution A G intron_variant PACA-AU 10 69792813 69792813 single base substitution G A downstream_gene_variant PACA-AU 10 69792813 69792813 single base substitution G A intron_variant PACA-AU 10 69796835 69796835 single base substitution G A intron_variant PACA-AU 10 69796842 69796842 single base substitution T C intron_variant PACA-AU 10 69811739 69811739 single base substitution A G intron_variant PACA-AU 10 69822736 69822736 single base substitution G A downstream_gene_variant PACA-AU 10 69822736 69822736 single base substitution G A intron_variant PACA-AU 10 69823141 69823141 deletion of <=200bp T - downstream_gene_variant PACA-AU 10 69823141 69823141 deletion of <=200bp T - intron_variant PACA-AU 10 69827115 69827115 single base substitution C A downstream_gene_variant PACA-AU 10 69827115 69827115 single base substitution C A intron_variant PACA-CA 10 69677147 69677147 single base substitution G A downstream_gene_variant PACA-CA 10 69679263 69679263 single base substitution G A downstream_gene_variant PACA-CA 10 69682409 69682409 single base substitution A T 3_prime_UTR_variant PACA-CA 10 69682409 69682409 single base substitution A T downstream_gene_variant PACA-CA 10 69682663 69682663 single base substitution A G 3_prime_UTR_variant PACA-CA 10 69682663 69682663 single base substitution A G downstream_gene_variant PACA-CA 10 69685867 69685867 single base substitution A G intron_variant PACA-CA 10 69687929 69687929 single base substitution G A intron_variant PACA-CA 10 69689445 69689445 single base substitution T C intron_variant PACA-CA 10 69691440 69691440 single base substitution C T intron_variant PACA-CA 10 69693323 69693323 single base substitution G T intron_variant PACA-CA 10 69693855 69693855 single base substitution A T intron_variant PACA-CA 10 69695663 69695663 single base substitution T C intron_variant PACA-CA 10 69709244 69709244 insertion of <=200bp - A downstream_gene_variant PACA-CA 10 69709244 69709244 insertion of <=200bp - A intron_variant PACA-CA 10 69709585 69709585 single base substitution G A downstream_gene_variant PACA-CA 10 69709585 69709585 single base substitution G A intron_variant PACA-CA 10 69715547 69715547 single base substitution A C exon_variant PACA-CA 10 69715547 69715547 single base substitution A C intron_variant PACA-CA 10 69715858 69715858 single base substitution G A exon_variant PACA-CA 10 69715858 69715858 single base substitution G A intron_variant PACA-CA 10 69718919 69718919 single base substitution A C intron_variant PACA-CA 10 69718919 69718919 single base substitution A C upstream_gene_variant PACA-CA 10 69723091 69723091 single base substitution A G downstream_gene_variant PACA-CA 10 69723091 69723091 single base substitution A G intron_variant PACA-CA 10 69725804 69725804 single base substitution G A exon_variant PACA-CA 10 69725804 69725804 single base substitution G A intron_variant PACA-CA 10 69730998 69730998 single base substitution T A intron_variant PACA-CA 10 69733250 69733250 single base substitution C A intron_variant PACA-CA 10 69738319 69738319 single base substitution G A intron_variant PACA-CA 10 69739457 69739457 insertion of <=200bp - A intron_variant PACA-CA 10 69740392 69740441 deletion of <=200bp AACTACTCTTAAGTAGAGAGACTATAAACAATTAACCAATCAAAAATAAC - intron_variant PACA-CA 10 69741076 69741076 single base substitution T G intron_variant PACA-CA 10 69741674 69741674 single base substitution C T intron_variant PACA-CA 10 69741761 69741761 single base substitution T A intron_variant PACA-CA 10 69741941 69741941 single base substitution G C intron_variant PACA-CA 10 69748662 69748662 single base substitution G A intron_variant PACA-CA 10 69749834 69749834 single base substitution G A intron_variant PACA-CA 10 69755057 69755057 single base substitution T C intron_variant PACA-CA 10 69755057 69755057 single base substitution T C splice_region_variant PACA-CA 10 69755900 69755900 deletion of <=200bp A - intron_variant PACA-CA 10 69755900 69755900 deletion of <=200bp A - splice_region_variant PACA-CA 10 69756817 69756817 single base substitution G A intron_variant PACA-CA 10 69757431 69757431 deletion of <=200bp T - intron_variant PACA-CA 10 69765036 69765036 single base substitution T A intron_variant PACA-CA 10 69770367 69770367 single base substitution G A intron_variant PACA-CA 10 69772262 69772262 single base substitution G A intron_variant PACA-CA 10 69773782 69773782 single base substitution C A splice_donor_variant PACA-CA 10 69782885 69782885 single base substitution T C intron_variant PACA-CA 10 69786339 69786339 single base substitution G A intron_variant PACA-CA 10 69787850 69787850 single base substitution G A downstream_gene_variant PACA-CA 10 69787850 69787850 single base substitution G A intron_variant PACA-CA 10 69791880 69791880 single base substitution A G downstream_gene_variant PACA-CA 10 69791880 69791880 single base substitution A G intron_variant PACA-CA 10 69793760 69793760 single base substitution C T 3_prime_UTR_variant PACA-CA 10 69793760 69793760 single base substitution C T exon_variant PACA-CA 10 69793760 69793760 single base substitution C T missense_variant R106H 317G>A PACA-CA 10 69793760 69793760 single base substitution C T missense_variant R216H 647G>A PACA-CA 10 69793760 69793760 single base substitution C T missense_variant R240H 719G>A PACA-CA 10 69798038 69798038 deletion of <=200bp T - exon_variant PACA-CA 10 69798038 69798038 deletion of <=200bp T - intron_variant PACA-CA 10 69800832 69800832 single base substitution A T intron_variant PACA-CA 10 69800832 69800832 single base substitution A T upstream_gene_variant PACA-CA 10 69803184 69803184 single base substitution G A intron_variant PACA-CA 10 69803184 69803184 single base substitution G A upstream_gene_variant PACA-CA 10 69803185 69803185 single base substitution A T intron_variant PACA-CA 10 69803185 69803185 single base substitution A T upstream_gene_variant PACA-CA 10 69804254 69804254 single base substitution G A exon_variant PACA-CA 10 69804254 69804254 single base substitution G A intron_variant PACA-CA 10 69804254 69804254 single base substitution G A missense_variant A98V 293C>T PACA-CA 10 69804254 69804254 single base substitution G A upstream_gene_variant PACA-CA 10 69804304 69804304 single base substitution C T exon_variant PACA-CA 10 69804304 69804304 single base substitution C T intron_variant PACA-CA 10 69804304 69804304 single base substitution C T synonymous_variant L81L 243G>A PACA-CA 10 69804304 69804304 single base substitution C T upstream_gene_variant PACA-CA 10 69805824 69805824 single base substitution A T intron_variant PACA-CA 10 69814367 69814367 single base substitution T C intron_variant PACA-CA 10 69818358 69818358 single base substitution T A intron_variant PACA-CA 10 69819656 69819656 single base substitution A G intron_variant PACA-CA 10 69820292 69820292 single base substitution A G intron_variant PACA-CA 10 69822273 69822273 deletion of <=200bp A - downstream_gene_variant PACA-CA 10 69822273 69822273 deletion of <=200bp A - intron_variant PACA-CA 10 69825607 69825607 insertion of <=200bp - A downstream_gene_variant PACA-CA 10 69825607 69825607 insertion of <=200bp - A intron_variant PACA-CA 10 69829640 69829640 single base substitution A T 3_prime_UTR_variant PACA-CA 10 69829640 69829640 single base substitution A T downstream_gene_variant PACA-CA 10 69829640 69829640 single base substitution A T intron_variant PACA-CA 10 69839156 69839156 insertion of <=200bp - A upstream_gene_variant PACA-CA 10 69839438 69839438 single base substitution G C upstream_gene_variant PAEN-AU 10 69693562 69693562 single base substitution G A intron_variant PAEN-AU 10 69743307 69743307 single base substitution T G intron_variant PAEN-AU 10 69775617 69775617 single base substitution T C intron_variant PAEN-IT 10 69803853 69803853 single base substitution C G intron_variant PAEN-IT 10 69803853 69803853 single base substitution C G upstream_gene_variant PAEN-IT 10 69810563 69810563 single base substitution C G intron_variant PAEN-IT 10 69819402 69819402 single base substitution T C intron_variant PAEN-IT 10 69827672 69827672 single base substitution C T 3_prime_UTR_variant PAEN-IT 10 69827672 69827672 single base substitution C T intron_variant PBCA-DE 10 69683340 69683340 single base substitution C T intron_variant PBCA-DE 10 69684881 69684881 single base substitution A T 3_prime_UTR_variant PBCA-DE 10 69684881 69684881 single base substitution A T missense_variant F866I 2596T>A PBCA-DE 10 69684881 69684881 single base substitution A T missense_variant F898I 2692T>A PBCA-DE 10 69684881 69684881 single base substitution A T missense_variant F968I 2902T>A PBCA-DE 10 69684881 69684881 single base substitution A T missense_variant F976I 2926T>A PBCA-DE 10 69689988 69689988 insertion of <=200bp - A intron_variant PBCA-DE 10 69692885 69692885 single base substitution C A intron_variant PBCA-DE 10 69694170 69694170 insertion of <=200bp - G intron_variant PBCA-DE 10 69697545 69697545 single base substitution C A intron_variant PBCA-DE 10 69699479 69699480 deletion of <=200bp AT - intron_variant PBCA-DE 10 69708043 69708043 single base substitution A G intron_variant PBCA-DE 10 69717524 69717524 single base substitution A G intron_variant PBCA-DE 10 69717524 69717524 single base substitution A G upstream_gene_variant PBCA-DE 10 69725418 69725418 single base substitution C G exon_variant PBCA-DE 10 69725418 69725418 single base substitution C G intron_variant PBCA-DE 10 69741536 69741536 single base substitution G A intron_variant PBCA-DE 10 69745532 69745532 single base substitution C A intron_variant PBCA-DE 10 69755566 69755566 single base substitution A C intron_variant PBCA-DE 10 69758685 69758685 single base substitution C T intron_variant PBCA-DE 10 69759699 69759699 insertion of <=200bp - A intron_variant PBCA-DE 10 69760546 69760546 single base substitution C T intron_variant PBCA-DE 10 69765874 69765874 single base substitution C A intron_variant PBCA-DE 10 69769957 69769957 single base substitution C A intron_variant PBCA-DE 10 69770026 69770030 deletion of <=200bp CAGTG - intron_variant PBCA-DE 10 69784169 69784169 single base substitution T G intron_variant PBCA-DE 10 69785319 69785320 deletion of <=200bp CA - 3_prime_UTR_variant PBCA-DE 10 69785319 69785320 deletion of <=200bp CA - exon_variant PBCA-DE 10 69785319 69785320 deletion of <=200bp CA - frameshift_variant TE187 PBCA-DE 10 69785319 69785320 deletion of <=200bp CA - frameshift_variant TE297 PBCA-DE 10 69786162 69786162 deletion of <=200bp T - intron_variant PBCA-DE 10 69797655 69797656 deletion of <=200bp GT - intron_variant PBCA-DE 10 69801476 69801476 single base substitution C T intron_variant PBCA-DE 10 69801476 69801476 single base substitution C T upstream_gene_variant PBCA-DE 10 69808841 69808842 deletion of <=200bp TA - intron_variant PBCA-DE 10 69822209 69822209 single base substitution T A downstream_gene_variant PBCA-DE 10 69822209 69822209 single base substitution T A intron_variant PBCA-DE 10 69836573 69836573 single base substitution C T upstream_gene_variant PBCA-DE 10 69838171 69838171 single base substitution C T upstream_gene_variant PRAD-CA 10 69680196 69680196 single base substitution G T downstream_gene_variant PRAD-CA 10 69681952 69681952 single base substitution T C 3_prime_UTR_variant PRAD-CA 10 69681952 69681952 single base substitution T C downstream_gene_variant PRAD-CA 10 69694194 69694194 single base substitution T A intron_variant PRAD-CA 10 69696024 69696024 single base substitution G T intron_variant PRAD-CA 10 69700003 69700003 single base substitution A C intron_variant PRAD-CA 10 69716613 69716613 single base substitution A C exon_variant PRAD-CA 10 69716613 69716613 single base substitution A C intron_variant PRAD-CA 10 69726126 69726126 single base substitution G A exon_variant PRAD-CA 10 69726126 69726126 single base substitution G A intron_variant PRAD-CA 10 69748016 69748016 single base substitution C A intron_variant PRAD-CA 10 69780320 69780320 single base substitution G T intron_variant PRAD-CA 10 69819283 69819283 single base substitution A C intron_variant PRAD-CA 10 69819535 69819535 single base substitution T C intron_variant PRAD-UK 10 69685427 69685427 single base substitution A G intron_variant PRAD-UK 10 69699839 69699839 single base substitution C T intron_variant PRAD-UK 10 69707690 69707690 single base substitution C A intron_variant PRAD-UK 10 69728874 69728874 single base substitution G C intron_variant PRAD-UK 10 69753296 69753296 single base substitution T A 3_prime_UTR_variant PRAD-UK 10 69753296 69753296 single base substitution T A intron_variant PRAD-UK 10 69753296 69753296 single base substitution T A upstream_gene_variant PRAD-UK 10 69799986 69799986 single base substitution G C intron_variant PRAD-UK 10 69799986 69799986 single base substitution G C upstream_gene_variant PRAD-UK 10 69805187 69805187 single base substitution G T intron_variant PRAD-UK 10 69808313 69808313 single base substitution T A intron_variant PRAD-UK 10 69810830 69810830 single base substitution T C intron_variant PRAD-UK 10 69819111 69819111 single base substitution C T intron_variant PRAD-UK 10 69819530 69819537 deletion of <=200bp TATATTAT - intron_variant PRAD-UK 10 69833388 69833388 single base substitution G C intron_variant PRAD-UK 10 69833388 69833388 single base substitution G C upstream_gene_variant PRAD-UK 10 69834381 69834381 single base substitution G T intron_variant PRAD-UK 10 69834381 69834381 single base substitution G T upstream_gene_variant READ-US 10 69684892 69684892 single base substitution A C 3_prime_UTR_variant READ-US 10 69684892 69684892 single base substitution A C missense_variant F862C 2585T>G READ-US 10 69684892 69684892 single base substitution A C missense_variant F894C 2681T>G READ-US 10 69684892 69684892 single base substitution A C missense_variant F964C 2891T>G READ-US 10 69684892 69684892 single base substitution A C missense_variant F972C 2915T>G RECA-EU 10 69678707 69678707 single base substitution C T downstream_gene_variant RECA-EU 10 69679093 69679093 single base substitution C T downstream_gene_variant RECA-EU 10 69689754 69689754 single base substitution G C intron_variant RECA-EU 10 69709772 69709772 single base substitution T C downstream_gene_variant RECA-EU 10 69709772 69709772 single base substitution T C intron_variant RECA-EU 10 69709773 69709773 single base substitution C T downstream_gene_variant RECA-EU 10 69709773 69709773 single base substitution C T intron_variant RECA-EU 10 69741554 69741554 single base substitution A G intron_variant RECA-EU 10 69741814 69741814 single base substitution C A intron_variant RECA-EU 10 69757918 69757918 single base substitution T C intron_variant RECA-EU 10 69757949 69757949 single base substitution C G intron_variant RECA-EU 10 69760033 69760033 single base substitution C T intron_variant RECA-EU 10 69770714 69770714 single base substitution T A intron_variant RECA-EU 10 69777996 69777996 single base substitution C G intron_variant RECA-EU 10 69800924 69800924 single base substitution A C intron_variant RECA-EU 10 69800924 69800924 single base substitution A C upstream_gene_variant RECA-EU 10 69806440 69806440 single base substitution T A intron_variant RECA-EU 10 69817417 69817417 single base substitution C T intron_variant RECA-EU 10 69824333 69824333 single base substitution A G downstream_gene_variant RECA-EU 10 69824333 69824333 single base substitution A G intron_variant SKCA-BR 10 69683616 69683616 single base substitution G A intron_variant SKCA-BR 10 69684483 69684483 single base substitution G A intron_variant SKCA-BR 10 69684878 69684878 single base substitution G A 3_prime_UTR_variant SKCA-BR 10 69684878 69684878 single base substitution G A missense_variant H867Y 2599C>T SKCA-BR 10 69684878 69684878 single base substitution G A missense_variant H899Y 2695C>T SKCA-BR 10 69684878 69684878 single base substitution G A missense_variant H969Y 2905C>T SKCA-BR 10 69684878 69684878 single base substitution G A missense_variant H977Y 2929C>T SKCA-BR 10 69684961 69684961 single base substitution C G intron_variant SKCA-BR 10 69686189 69686189 single base substitution C A intron_variant SKCA-BR 10 69686209 69686209 single base substitution G A intron_variant SKCA-BR 10 69687148 69687187 deletion of <=200bp TATATATATATATATATATATATATATATATATATATATA - intron_variant SKCA-BR 10 69687301 69687301 single base substitution G A intron_variant SKCA-BR 10 69689290 69689291 deletion of <=200bp TC - intron_variant SKCA-BR 10 69690981 69690981 single base substitution T C intron_variant SKCA-BR 10 69691660 69691660 single base substitution G A intron_variant SKCA-BR 10 69695252 69695252 single base substitution C A intron_variant SKCA-BR 10 69695253 69695253 single base substitution A C intron_variant SKCA-BR 10 69697146 69697146 single base substitution G A intron_variant SKCA-BR 10 69698477 69698477 single base substitution T G intron_variant SKCA-BR 10 69699478 69699478 insertion of <=200bp - GAT intron_variant SKCA-BR 10 69701665 69701665 single base substitution A G intron_variant SKCA-BR 10 69704238 69704238 single base substitution G A intron_variant SKCA-BR 10 69704524 69704524 single base substitution G A intron_variant SKCA-BR 10 69706398 69706398 single base substitution G T intron_variant SKCA-BR 10 69708836 69708836 single base substitution C T intron_variant SKCA-BR 10 69716107 69716107 single base substitution G A exon_variant SKCA-BR 10 69716107 69716107 single base substitution G A intron_variant SKCA-BR 10 69723771 69723771 single base substitution G A downstream_gene_variant SKCA-BR 10 69723771 69723771 single base substitution G A intron_variant SKCA-BR 10 69723783 69723783 single base substitution C A downstream_gene_variant SKCA-BR 10 69723783 69723783 single base substitution C A intron_variant SKCA-BR 10 69724132 69724132 single base substitution G A downstream_gene_variant SKCA-BR 10 69724132 69724132 single base substitution G A intron_variant SKCA-BR 10 69725450 69725450 single base substitution A G exon_variant SKCA-BR 10 69725450 69725450 single base substitution A G intron_variant SKCA-BR 10 69732211 69732211 single base substitution G A intron_variant SKCA-BR 10 69740328 69740328 single base substitution G A intron_variant SKCA-BR 10 69743545 69743545 single base substitution A C intron_variant SKCA-BR 10 69748498 69748498 single base substitution G A 3_prime_UTR_variant SKCA-BR 10 69748498 69748498 single base substitution G A exon_variant SKCA-BR 10 69748498 69748498 single base substitution G A synonymous_variant I466I 1398C>T SKCA-BR 10 69748498 69748498 single base substitution G A synonymous_variant I576I 1728C>T SKCA-BR 10 69749438 69749438 single base substitution A T intron_variant SKCA-BR 10 69756072 69756072 single base substitution A C intron_variant SKCA-BR 10 69763085 69763086 deletion of <=200bp AT - intron_variant SKCA-BR 10 69763100 69763100 single base substitution T G intron_variant SKCA-BR 10 69763102 69763102 single base substitution T G intron_variant SKCA-BR 10 69763549 69763549 single base substitution G A intron_variant SKCA-BR 10 69765517 69765517 single base substitution G A intron_variant SKCA-BR 10 69766137 69766137 insertion of <=200bp - TG intron_variant SKCA-BR 10 69767173 69767173 single base substitution C T intron_variant SKCA-BR 10 69771924 69771924 single base substitution T G intron_variant SKCA-BR 10 69776085 69776085 single base substitution G A intron_variant SKCA-BR 10 69778657 69778658 deletion of <=200bp CT - intron_variant SKCA-BR 10 69780450 69780450 single base substitution C T intron_variant SKCA-BR 10 69780474 69780474 single base substitution T C intron_variant SKCA-BR 10 69780525 69780526 deletion of <=200bp CA - intron_variant SKCA-BR 10 69781139 69781139 single base substitution A G intron_variant SKCA-BR 10 69785861 69785861 single base substitution T A intron_variant SKCA-BR 10 69796480 69796480 single base substitution A G intron_variant SKCA-BR 10 69805063 69805063 single base substitution G A intron_variant SKCA-BR 10 69805971 69805971 single base substitution A C intron_variant SKCA-BR 10 69807686 69807686 insertion of <=200bp - GT intron_variant SKCA-BR 10 69810874 69810874 single base substitution C A intron_variant SKCA-BR 10 69811359 69811359 single base substitution G C intron_variant SKCA-BR 10 69811635 69811635 single base substitution A G intron_variant SKCA-BR 10 69812121 69812121 single base substitution G A intron_variant SKCA-BR 10 69813980 69813980 single base substitution C A intron_variant SKCA-BR 10 69819216 69819216 insertion of <=200bp - AATAATATTATATATT intron_variant SKCA-BR 10 69819333 69819333 insertion of <=200bp - CATA intron_variant SKCA-BR 10 69819372 69819372 insertion of <=200bp - CATA intron_variant SKCA-BR 10 69819500 69819500 insertion of <=200bp - TA intron_variant SKCA-BR 10 69819600 69819600 insertion of <=200bp - TA intron_variant SKCA-BR 10 69822234 69822234 single base substitution G A downstream_gene_variant SKCA-BR 10 69822234 69822234 single base substitution G A intron_variant SKCA-BR 10 69822235 69822235 single base substitution G A downstream_gene_variant SKCA-BR 10 69822235 69822235 single base substitution G A intron_variant SKCA-BR 10 69833840 69833840 single base substitution C T 5_prime_UTR_variant SKCA-BR 10 69833840 69833840 single base substitution C T exon_variant SKCA-BR 10 69833840 69833840 single base substitution C T intron_variant SKCA-BR 10 69833840 69833840 single base substitution C T upstream_gene_variant SKCA-BR 10 69835179 69835179 insertion of <=200bp - GC upstream_gene_variant SKCA-BR 10 69836878 69836878 single base substitution C T upstream_gene_variant SKCA-BR 10 69839378 69839378 single base substitution G A upstream_gene_variant SKCM-US 10 69684878 69684878 single base substitution G A 3_prime_UTR_variant SKCM-US 10 69684878 69684878 single base substitution G A missense_variant H867Y 2599C>T SKCM-US 10 69684878 69684878 single base substitution G A missense_variant H899Y 2695C>T SKCM-US 10 69684878 69684878 single base substitution G A missense_variant H969Y 2905C>T SKCM-US 10 69684878 69684878 single base substitution G A missense_variant H977Y 2929C>T SKCM-US 10 69726449 69726449 single base substitution G A 3_prime_UTR_variant SKCM-US 10 69726449 69726449 single base substitution G A exon_variant SKCM-US 10 69726449 69726449 single base substitution G A synonymous_variant A529A 1587C>T SKCM-US 10 69726449 69726449 single base substitution G A synonymous_variant A639A 1917C>T SKCM-US 10 69750152 69750152 single base substitution T G 3_prime_UTR_variant SKCM-US 10 69750152 69750152 single base substitution T G synonymous_variant A373A 1119A>C SKCM-US 10 69750152 69750152 single base substitution T G synonymous_variant A483A 1449A>C SKCM-US 10 69750152 69750152 single base substitution T G upstream_gene_variant SKCM-US 10 69750933 69750933 single base substitution G A 3_prime_UTR_variant SKCM-US 10 69750933 69750933 single base substitution G A missense_variant S322F 965C>T SKCM-US 10 69750933 69750933 single base substitution G A missense_variant S432F 1295C>T SKCM-US 10 69750933 69750933 single base substitution G A upstream_gene_variant SKCM-US 10 69751987 69751987 single base substitution G A 3_prime_UTR_variant SKCM-US 10 69751987 69751987 single base substitution G A missense_variant P304S 910C>T SKCM-US 10 69751987 69751987 single base substitution G A missense_variant P414S 1240C>T SKCM-US 10 69751987 69751987 single base substitution G A upstream_gene_variant SKCM-US 10 69752044 69752044 single base substitution G A 3_prime_UTR_variant SKCM-US 10 69752044 69752044 single base substitution G A missense_variant P285S 853C>T SKCM-US 10 69752044 69752044 single base substitution G A missense_variant P395S 1183C>T SKCM-US 10 69752044 69752044 single base substitution G A upstream_gene_variant SKCM-US 10 69785421 69785421 single base substitution A G 3_prime_UTR_variant SKCM-US 10 69785421 69785421 single base substitution A G exon_variant SKCM-US 10 69785421 69785421 single base substitution A G missense_variant F154L 460T>C SKCM-US 10 69785421 69785421 single base substitution A G missense_variant F264L 790T>C STAD-US 10 69682730 69682730 single base substitution C T 3_prime_UTR_variant STAD-US 10 69682730 69682730 single base substitution C T downstream_gene_variant STAD-US 10 69682730 69682730 single base substitution C T synonymous_variant L1036L 3108G>A STAD-US 10 69682730 69682730 single base substitution C T synonymous_variant L1044L 3132G>A STAD-US 10 69682730 69682730 single base substitution C T synonymous_variant L934L 2802G>A STAD-US 10 69682730 69682730 single base substitution C T synonymous_variant L966L 2898G>A STAD-US 10 69682805 69682805 single base substitution G A 3_prime_UTR_variant STAD-US 10 69682805 69682805 single base substitution G A synonymous_variant L1011L 3033C>T STAD-US 10 69682805 69682805 single base substitution G A synonymous_variant L1019L 3057C>T STAD-US 10 69682805 69682805 single base substitution G A synonymous_variant L909L 2727C>T STAD-US 10 69682805 69682805 single base substitution G A synonymous_variant L941L 2823C>T STAD-US 10 69684937 69684937 single base substitution T G 3_prime_UTR_variant STAD-US 10 69684937 69684937 single base substitution T G missense_variant E847A 2540A>C STAD-US 10 69684937 69684937 single base substitution T G missense_variant E879A 2636A>C STAD-US 10 69684937 69684937 single base substitution T G missense_variant E949A 2846A>C STAD-US 10 69684937 69684937 single base substitution T G missense_variant E957A 2870A>C STAD-US 10 69692445 69692445 single base substitution C T 3_prime_UTR_variant STAD-US 10 69692445 69692445 single base substitution C T missense_variant C814Y 2441G>A STAD-US 10 69692445 69692445 single base substitution C T missense_variant C846Y 2537G>A STAD-US 10 69692445 69692445 single base substitution C T missense_variant C916Y 2747G>A STAD-US 10 69692445 69692445 single base substitution C T missense_variant C924Y 2771G>A STAD-US 10 69700775 69700775 single base substitution G A 3_prime_UTR_variant STAD-US 10 69700775 69700775 single base substitution G A intron_variant STAD-US 10 69700775 69700775 single base substitution G A missense_variant P707S 2119C>T STAD-US 10 69700775 69700775 single base substitution G A missense_variant P809S 2425C>T STAD-US 10 69700775 69700775 single base substitution G A missense_variant P817S 2449C>T STAD-US 10 69700806 69700806 single base substitution A C 3_prime_UTR_variant STAD-US 10 69700806 69700806 single base substitution A C intron_variant STAD-US 10 69700806 69700806 single base substitution A C missense_variant I696M 2088T>G STAD-US 10 69700806 69700806 single base substitution A C missense_variant I798M 2394T>G STAD-US 10 69700806 69700806 single base substitution A C missense_variant I806M 2418T>G STAD-US 10 69714858 69714858 single base substitution A T 3_prime_UTR_variant STAD-US 10 69714858 69714858 single base substitution A T exon_variant STAD-US 10 69714858 69714858 single base substitution A T missense_variant N583K 1749T>A STAD-US 10 69714858 69714858 single base substitution A T missense_variant N685K 2055T>A STAD-US 10 69714858 69714858 single base substitution A T missense_variant N693K 2079T>A STAD-US 10 69748461 69748461 single base substitution A C 3_prime_UTR_variant STAD-US 10 69748461 69748461 single base substitution A C exon_variant STAD-US 10 69748461 69748461 single base substitution A C missense_variant F479V 1435T>G STAD-US 10 69748461 69748461 single base substitution A C missense_variant F589V 1765T>G STAD-US 10 69750049 69750049 single base substitution C A 3_prime_UTR_variant STAD-US 10 69750049 69750049 single base substitution C A missense_variant D408Y 1222G>T STAD-US 10 69750049 69750049 single base substitution C A missense_variant D518Y 1552G>T STAD-US 10 69750049 69750049 single base substitution C A upstream_gene_variant STAD-US 10 69750775 69750775 insertion of <=200bp - A splice_region_variant STAD-US 10 69750775 69750775 insertion of <=200bp - A upstream_gene_variant STAD-US 10 69773784 69773784 single base substitution A G splice_region_variant STAD-US 10 69785304 69785304 single base substitution G A missense_variant R193W 577C>T STAD-US 10 69785304 69785304 single base substitution G A missense_variant R303W 907C>T STAD-US 10 69785304 69785304 single base substitution G A splice_region_variant STAD-US 10 69785320 69785320 single base substitution A G 3_prime_UTR_variant STAD-US 10 69785320 69785320 single base substitution A G exon_variant STAD-US 10 69785320 69785320 single base substitution A G synonymous_variant T187T 561T>C STAD-US 10 69785320 69785320 single base substitution A G synonymous_variant T297T 891T>C STAD-US 10 69785436 69785436 deletion of <=200bp A - splice_region_variant STAD-US 10 69792621 69792621 single base substitution A G 3_prime_UTR_variant STAD-US 10 69792621 69792621 single base substitution A G downstream_gene_variant STAD-US 10 69792621 69792621 single base substitution A G exon_variant STAD-US 10 69792621 69792621 single base substitution A G intron_variant STAD-US 10 69792621 69792621 single base substitution A G missense_variant Y121H 361T>C STAD-US 10 69792621 69792621 single base substitution A G missense_variant Y231H 691T>C STAD-US 10 69793738 69793738 single base substitution A G 3_prime_UTR_variant STAD-US 10 69793738 69793738 single base substitution A G downstream_gene_variant STAD-US 10 69793738 69793738 single base substitution A G exon_variant STAD-US 10 69793738 69793738 single base substitution A G synonymous_variant G113G 339T>C STAD-US 10 69793738 69793738 single base substitution A G synonymous_variant G223G 669T>C STAD-US 10 69804277 69804277 single base substitution T C exon_variant STAD-US 10 69804277 69804277 single base substitution T C intron_variant STAD-US 10 69804277 69804277 single base substitution T C synonymous_variant S90S 270A>G STAD-US 10 69804277 69804277 single base substitution T C upstream_gene_variant THCA-SA 10 69682343 69682343 single base substitution C G 3_prime_UTR_variant THCA-SA 10 69682343 69682343 single base substitution C G downstream_gene_variant THCA-SA 10 69695949 69695949 single base substitution A G 3_prime_UTR_variant THCA-SA 10 69695949 69695949 single base substitution A G missense_variant V770A 2309T>C THCA-SA 10 69695949 69695949 single base substitution A G missense_variant V802A 2405T>C THCA-SA 10 69695949 69695949 single base substitution A G missense_variant V872A 2615T>C THCA-SA 10 69695949 69695949 single base substitution A G missense_variant V880A 2639T>C THCA-SA 10 69773931 69773931 single base substitution A G 3_prime_UTR_variant THCA-SA 10 69773931 69773931 single base substitution A G exon_variant THCA-SA 10 69773931 69773931 single base substitution A G synonymous_variant S197S 591T>C THCA-SA 10 69773931 69773931 single base substitution A G synonymous_variant S307S 921T>C UCEC-US 10 69682722 69682722 single base substitution G A 3_prime_UTR_variant UCEC-US 10 69682722 69682722 single base substitution G A downstream_gene_variant UCEC-US 10 69682722 69682722 single base substitution G A missense_variant A1039V 3116C>T UCEC-US 10 69682722 69682722 single base substitution G A missense_variant A1047V 3140C>T UCEC-US 10 69682722 69682722 single base substitution G A missense_variant A937V 2810C>T UCEC-US 10 69682722 69682722 single base substitution G A missense_variant A969V 2906C>T UCEC-US 10 69692480 69692480 single base substitution T C 3_prime_UTR_variant UCEC-US 10 69692480 69692480 single base substitution T C synonymous_variant L802L 2406A>G UCEC-US 10 69692480 69692480 single base substitution T C synonymous_variant L834L 2502A>G UCEC-US 10 69692480 69692480 single base substitution T C synonymous_variant L904L 2712A>G UCEC-US 10 69692480 69692480 single base substitution T C synonymous_variant L912L 2736A>G UCEC-US 10 69699350 69699350 single base substitution A C 3_prime_UTR_variant UCEC-US 10 69699350 69699350 single base substitution A C intron_variant UCEC-US 10 69699350 69699350 single base substitution A C missense_variant F754V 2260T>G UCEC-US 10 69699350 69699350 single base substitution A C missense_variant F856V 2566T>G UCEC-US 10 69699350 69699350 single base substitution A C missense_variant F864V 2590T>G UCEC-US 10 69714447 69714447 single base substitution C A 3_prime_UTR_variant UCEC-US 10 69714447 69714447 single base substitution C A exon_variant UCEC-US 10 69714447 69714447 single base substitution C A stop_gained E646* 1936G>T UCEC-US 10 69714447 69714447 single base substitution C A stop_gained E748* 2242G>T UCEC-US 10 69714447 69714447 single base substitution C A stop_gained E756* 2266G>T UCEC-US 10 69714452 69714452 single base substitution C T 3_prime_UTR_variant UCEC-US 10 69714452 69714452 single base substitution C T exon_variant UCEC-US 10 69714452 69714452 single base substitution C T missense_variant R644H 1931G>A UCEC-US 10 69714452 69714452 single base substitution C T missense_variant R746H 2237G>A UCEC-US 10 69714452 69714452 single base substitution C T missense_variant R754H 2261G>A UCEC-US 10 69714797 69714797 single base substitution G A 3_prime_UTR_variant UCEC-US 10 69714797 69714797 single base substitution G A exon_variant UCEC-US 10 69714797 69714797 single base substitution G A missense_variant R604C 1810C>T UCEC-US 10 69714797 69714797 single base substitution G A missense_variant R706C 2116C>T UCEC-US 10 69714797 69714797 single base substitution G A missense_variant R714C 2140C>T UCEC-US 10 69716666 69716666 single base substitution A C 3_prime_UTR_variant UCEC-US 10 69716666 69716666 single base substitution A C missense_variant L563R 1688T>G UCEC-US 10 69716666 69716666 single base substitution A C missense_variant L665R 1994T>G UCEC-US 10 69716666 69716666 single base substitution A C missense_variant L673R 2018T>G UCEC-US 10 69716666 69716666 single base substitution A C upstream_gene_variant UCEC-US 10 69748511 69748511 single base substitution T G 3_prime_UTR_variant UCEC-US 10 69748511 69748511 single base substitution T G exon_variant UCEC-US 10 69748511 69748511 single base substitution T G missense_variant K462T 1385A>C UCEC-US 10 69748511 69748511 single base substitution T G missense_variant K572T 1715A>C UCEC-US 10 69750676 69750676 single base substitution C T 3_prime_UTR_variant UCEC-US 10 69750676 69750676 single base substitution C T synonymous_variant P366P 1098G>A UCEC-US 10 69750676 69750676 single base substitution C T synonymous_variant P476P 1428G>A UCEC-US 10 69750676 69750676 single base substitution C T upstream_gene_variant UCEC-US 10 69750942 69750942 single base substitution G A 3_prime_UTR_variant UCEC-US 10 69750942 69750942 single base substitution G A missense_variant T319M 956C>T UCEC-US 10 69750942 69750942 single base substitution G A missense_variant T429M 1286C>T UCEC-US 10 69750942 69750942 single base substitution G A upstream_gene_variant UCEC-US 10 69752390 69752390 single base substitution T G 3_prime_UTR_variant UCEC-US 10 69752390 69752390 single base substitution T G missense_variant Q263H 789A>C UCEC-US 10 69752390 69752390 single base substitution T G missense_variant Q373H 1119A>C UCEC-US 10 69752390 69752390 single base substitution T G upstream_gene_variant UCEC-US 10 69785361 69785361 single base substitution T G 3_prime_UTR_variant UCEC-US 10 69785361 69785361 single base substitution T G exon_variant UCEC-US 10 69785361 69785361 single base substitution T G missense_variant N174H 520A>C UCEC-US 10 69785361 69785361 single base substitution T G missense_variant N284H 850A>C UCEC-US 10 69793731 69793731 single base substitution C A 3_prime_UTR_variant UCEC-US 10 69793731 69793731 single base substitution C A downstream_gene_variant UCEC-US 10 69793731 69793731 single base substitution C A exon_variant UCEC-US 10 69793731 69793731 single base substitution C A missense_variant D116Y 346G>T UCEC-US 10 69793731 69793731 single base substitution C A missense_variant D226Y 676G>T UCEC-US 10 69832788 69832788 single base substitution T G downstream_gene_variant UCEC-US 10 69832788 69832788 single base substitution T G exon_variant UCEC-US 10 69832788 69832788 single base substitution T G missense_variant R26S 78A>C UCEC-US 10 69832808 69832808 single base substitution C A downstream_gene_variant UCEC-US 10 69832808 69832808 single base substitution C A exon_variant UCEC-US 10 69832808 69832808 single base substitution C A stop_gained E20* 58G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-GN-A266-06 COSM3439744 c.1917C>T p.A639A Substitution - coding silent 10:67966692-67966692 - SJHGG002_A COSM4968730 c.1796_1801delTACTAC p.I599_H601>N Complex - deletion inframe 10:67988668-67988673 - TCGA-CA-6717-01 COSM1348662 c.1309A>C p.N437H Substitution - Missense 10:67991162-67991162 - S0057 COSM5881933 c.2539C>A p.Q847K Substitution - Missense 10:67939644-67939644 - U2940 COSM5620952 c.2764A>G p.K922E Substitution - Missense 10:67932695-67932695 - Gp2D COSM2159075 c.1885A>C p.N629H Substitution - Missense 10:67966724-67966724 - TCGA-F5-6814-01 COSM3415186 c.2915T>G p.F972C Substitution - Missense 10:67925135-67925135 - BK0092 COSM4188813 c.2029G>C p.D677H Substitution - Missense 10:67956898-67956898 - TCGA-DS-A0VK-01 COSM458803 c.1827G>A p.Q609Q Substitution - coding silent 10:67966782-67966782 - S02351 COSM5694972 c.1346A>G p.Y449C Substitution - Missense 10:67991001-67991001 - tumor_4166706 COSM5948513 c.1436C>G p.S479C Substitution - Missense 10:67990911-67990911 - ccRCC-70 COSM1662127 c.1694A>T p.E565V Substitution - Missense 10:67988775-67988775 - Pat_06_A COSM4015221 c.907C>T p.R303W Substitution - Missense 10:68025547-68025547 - ESO-175 COSM1254138 c.863T>G p.V288G Substitution - Missense 10:68025591-68025591 - TCGA-AM-5821-01 COSM3751897 c.1011C>T p.S337S Substitution - coding silent 10:68014084-68014084 - LS180 COSM2159053 c.2756G>A p.G919D Substitution - Missense 10:67932703-67932703 - SC_9038 COSM5560853 c.702T>A p.N234K Substitution - Missense 10:68032853-68032853 - TCGA-BS-A0UF-01 COSM919633 c.58G>T p.E20* Substitution - Nonsense 10:68073051-68073051 - TCGA-D3-A3CE-06 COSM3439749 c.790T>C p.F264L Substitution - Missense 10:68025664-68025664 - T2197 COSM4690138 c.2911delA p.I971fs*21 Deletion - Frameshift 10:67925139-67925139 - PT41 COSM5924513 c.1951-4C>T p.? Unknown 10:67956980-67956980 - TCGA-HF-7132-01 COSM4015214 c.2771G>A p.C924Y Substitution - Missense 10:67932688-67932688 - TCGA-G3-A25W-01 COSM4927151 c.1894A>G p.I632V Substitution - Missense 10:67966715-67966715 - TCGA-AN-A046-01 COSM1209600 c.944G>A p.R315Q Substitution - Missense 10:68014151-68014151 - TCGA-CD-A48C-01 COSM4015213 c.2870A>C p.E957A Substitution - Missense 10:67925180-67925180 - TCGA-D1-A17Q-01 COSM919632 c.78A>C p.R26S Substitution - Missense 10:68073031-68073031 - LS174T COSM2159053 c.2756G>A p.G919D Substitution - Missense 10:67932703-67932703 - PD11366a COSM2159097 c.543G>A p.P181P Substitution - coding silent 10:68034107-68034107 - TCGA-AP-A056-01 COSM919630 c.850A>C p.N284H Substitution - Missense 10:68025604-68025604 - TCGA-A8-A0A6-01 COSM3807498 c.45T>G p.G15G Substitution - coding silent 10:68073064-68073064 - TCGA-BS-A0TC-01 COSM919622 c.2266G>T p.E756* Substitution - Nonsense 10:67954690-67954690 - PCSI_0022_Pa_P COSM216351 c.243G>A p.L81L Substitution - coding silent 10:68044547-68044547 - Gp5D COSM2159075 c.1885A>C p.N629H Substitution - Missense 10:67966724-67966724 - TCGA-HF-7136-01 COSM4015219 c.1552G>T p.D518Y Substitution - Missense 10:67990292-67990292 - 2296_T COSM3978718 c.1854A>T p.I618I Substitution - coding silent 10:67966755-67966755 - 2492700 COSM5599663 c.1526C>T p.T509I Substitution - Missense 10:67990318-67990318 - TCGA-CG-5727-01 COSM4015215 c.2449C>T p.P817S Substitution - Missense 10:67941018-67941018 - TCGA-BS-A0UM-01 COSM919623 c.2261G>A p.R754H Substitution - Missense 10:67954695-67954695 - PCSI_0084_Pa_P_526 COSM3375580 c.293C>T p.A98V Substitution - Missense 10:68044497-68044497 - Gp5D COSM2159074 c.1988T>G p.F663C Substitution - Missense 10:67956939-67956939 - LUAD_E01047 COSM390021 c.1343A>G p.H448R Substitution - Missense 10:67991004-67991004 - PT40 COSM5923878 c.1370G>A p.G457E Substitution - Missense 10:67990977-67990977 - 10748 COSM3728098 c.1577C>T p.A526V Substitution - Missense 10:67990267-67990267 - T2269 COSM4690139 c.2141G>A p.R714H Substitution - Missense 10:67955039-67955039 - 2292379 COSM4609896 c.2680C>T p.Q894* Substitution - Nonsense 10:67932779-67932779 - 585210 COSM325489 c.1548G>T p.M516I Substitution - Missense 10:67990296-67990296 - I2L-P7-Tumor-Organoid COSM5360282 c.282T>C p.A94A Substitution - coding silent 10:68044508-68044508 - TCGA-BR-8589-01 COSM4015218 c.1765T>G p.F589V Substitution - Missense 10:67988704-67988704 - KM12 COSM2159104 c.367G>A p.E123K Substitution - Missense 10:68044423-68044423 - JEKO-1 COSM1739684 c.43G>A p.G15S Substitution - Missense 10:68073066-68073066 - YUPAT COSM1686629 c.2595+1G>A p.? Unknown 10:67939587-67939587 - TCGA-BR-8680-01 COSM4015216 c.2418T>G p.I806M Substitution - Missense 10:67941049-67941049 - Case5 COSM1579484 c.2789T>C p.L930P Substitution - Missense 10:67932670-67932670 - Capan-1 COSM327972 c.778-3_778-2insT p.? Unknown 10:68025678-68025679 - PCSI_0476_Pa_P_526 COSM5031340 c.1069+1G>T p.? Unknown 10:68014025-68014025 - PTC_448 COSM5959336 c.2639T>C p.V880A Substitution - Missense 10:67936192-67936192 - UM-SCC-11B COSM4598015 c.787G>T p.V263L Substitution - Missense 10:68025667-68025667 - TCGA-AX-A0J0-01 COSM919625 c.2018T>G p.L673R Substitution - Missense 10:67956909-67956909 - 2492703 COSM5599663 c.1526C>T p.T509I Substitution - Missense 10:67990318-67990318 - TCGA-18-3416-01 COSM684632 c.331G>C p.D111H Substitution - Missense 10:68044459-68044459 - TCGA-AO-A12E-01 COSM427774 c.2754G>A p.A918A Substitution - coding silent 10:67932705-67932705 - TCGA-A5-A0VP-01 COSM919628 c.1286C>T p.T429M Substitution - Missense 10:67991185-67991185 - TCGA-F4-6856-01 COSM1348660 c.2293T>A p.L765I Substitution - Missense 10:67954663-67954663 - sysucc-311T COSM919622 c.2266G>T p.E756* Substitution - Nonsense 10:67954690-67954690 - TCGA-FV-A3I0-01 COSM4921789 c.458C>G p.S153C Substitution - Missense 10:68038098-68038098 - ATL001 COSM5703679 c.3029A>G p.Q1010R Substitution - Missense 10:67923076-67923076 - CSCC-5-T COSM4508245 c.769C>T p.L257L Substitution - coding silent 10:68032786-68032786 - HCC2157 COSM23133 c.3085C>T p.L1029L Substitution - coding silent 10:67923020-67923020 - TCGA-FU-A3HZ-01 COSM4840379 c.1674G>T p.K558N Substitution - Missense 10:67988795-67988795 - TCGA-23-2078-01 COSM71045 c.2717A>G p.N906S Substitution - Missense 10:67932742-67932742 - CHOL12 COSM194919 c.647G>A p.R216H Substitution - Missense 10:68034003-68034003 - ASHPC_0006_Pa_P COSM194919 c.647G>A p.R216H Substitution - Missense 10:68034003-68034003 - A2 COSM4179605 c.778-10C>T p.? Unknown 10:68025686-68025686 - TCGA-AP-A0LM-01 COSM919623 c.2261G>A p.R754H Substitution - Missense 10:67954695-67954695 - T3155 COSM4690141 c.230A>G p.Q77R Substitution - Missense 10:68044560-68044560 - TCGA-F1-6177-01 COSM4015217 c.2079T>A p.N693K Substitution - Missense 10:67955101-67955101 - PCSI_0022_Pa_X COSM216351 c.243G>A p.L81L Substitution - coding silent 10:68044547-68044547 - T3082 COSM4690140 c.534A>G p.Q178Q Substitution - coding silent 10:68034116-68034116 - TCGA-A8-A07C-01 COSM427776 c.9C>A p.C3* Substitution - Nonsense 10:68073100-68073100 - TCGA-CA-6718-01 COSM1348656 c.3116C>A p.T1039N Substitution - Missense 10:67922989-67922989 - 587346 COSM1209598 c.881G>A p.S294N Substitution - Missense 10:68025573-68025573 - 587342 COSM1209600 c.944G>A p.R315Q Substitution - Missense 10:68014151-68014151 - LUAD-S01315 COSM343882 c.868G>C p.E290Q Substitution - Missense 10:68025586-68025586 - TCGA-BR-8363-01 COSM4015222 c.891T>C p.T297T Substitution - coding silent 10:68025563-68025563 - S02384 COSM5698168 c.2436G>A p.V812V Substitution - coding silent 10:67941031-67941031 - TCGA-BR-8487-01 COSM4015220 c.1068T>C p.I356I Substitution - coding silent 10:68014027-68014027 - TCGA-CG-4306-01 COSM4015225 c.270A>G p.S90S Substitution - coding silent 10:68044520-68044520 - STC252 COSM5050278 c.712T>C p.S238P Substitution - Missense 10:68032843-68032843 - TCGA-BH-A0HF-01 COSM3807494 c.2440C>T p.L814F Substitution - Missense 10:67941027-67941027 - 3N35-VS-3T35 COSM4981030 c.2500T>A p.L834M Substitution - Missense 10:67940967-67940967 - TCGA-BR-7958-01 COSM4015212 c.3057C>T p.L1019L Substitution - coding silent 10:67923048-67923048 - TCGA-BS-A0UF-01 COSM919626 c.1715A>C p.K572T Substitution - Missense 10:67988754-67988754 - TCGA-DG-A2KK-01 COSM4828420 c.3046G>T p.E1016* Substitution - Nonsense 10:67923059-67923059 - TCGA-AP-A0LM-01 COSM919620 c.2736A>G p.L912L Substitution - coding silent 10:67932723-67932723 - Au2 COSM5599663 c.1526C>T p.T509I Substitution - Missense 10:67990318-67990318 - EGC15 COSM5050279 c.190G>T p.G64* Substitution - Nonsense 10:68072919-68072919 - TCGA-CA-6717-01 COSM1348657 c.2862G>A p.K954K Substitution - coding silent 10:67932597-67932597 - Gp2D COSM2159094 c.691T>A p.Y231N Substitution - Missense 10:68032864-68032864 - MZ7-mel COSM26294 c.1815G>A p.E605E Substitution - coding silent 10:67966794-67966794 - TCGA-A8-A08R-01 COSM427775 c.578_581delTGCA p.M193fs*29 Deletion - Frameshift 10:68034069-68034072 - Pat_30_A COSM3439746 c.1295C>T p.S432F Substitution - Missense 10:67991176-67991176 - LUAD-CHTN-3090346 COSM356675 c.355G>T p.V119L Substitution - Missense 10:68044435-68044435 - TCGA-BR-8680-01 COSM4015224 c.669T>C p.G223G Substitution - coding silent 10:68033981-68033981 - CSCC-49-T COSM4476778 c.2098C>T p.P700S Substitution - Missense 10:67955082-67955082 - ZZUFHECRKL-G075T COSM5440442 c.2490C>A p.S830S Substitution - coding silent 10:67940977-67940977 - TCGA-IH-A3EA-01 COSM3439746 c.1295C>T p.S432F Substitution - Missense 10:67991176-67991176 - S02275 COSM5682723 c.2682A>T p.Q894H Substitution - Missense 10:67932777-67932777 - TCGA-EE-A29B-06 COSM3439743 c.2929C>T p.H977Y Substitution - Missense 10:67925121-67925121 - TCGA-G3-A3CJ-01 COSM4914812 c.800G>T p.G267V Substitution - Missense 10:68025654-68025654 - S00945 COSM311755 c.1720T>C p.Y574H Substitution - Missense 10:67988749-67988749 - 3N44-VS-3T44 COSM4982153 c.1423C>T p.H475Y Substitution - Missense 10:67990924-67990924 - Gp5D COSM2159094 c.691T>A p.Y231N Substitution - Missense 10:68032864-68032864 - LUAD-B00915 COSM332553 c.1514G>T p.R505M Substitution - Missense 10:67990330-67990330 - TCGA-AX-A0J0-01 COSM919631 c.676G>T p.D226Y Substitution - Missense 10:68033974-68033974 - HCC107 COSM1603640 c.294G>A p.A98A Substitution - coding silent 10:68044496-68044496 - TCGA-DA-A1I5-06 COSM3439748 c.1183C>T p.P395S Substitution - Missense 10:67992287-67992287 - RK137_C01 COSM1627578 c.2656A>C p.T886P Substitution - Missense 10:67936175-67936175 - HCC018T COSM5820102 c.2846G>A p.W949* Substitution - Nonsense 10:67932613-67932613 - TCGA-AO-A0JB-01 COSM427773 c.2964G>T p.L988L Substitution - coding silent 10:67925086-67925086 - TCGA-CG-5726-01 COSM4015223 c.691T>C p.Y231H Substitution - Missense 10:68032864-68032864 - PCSI_0084_Pa_X COSM3375580 c.293C>T p.A98V Substitution - Missense 10:68044497-68044497 - LIM1899 COSM4639678 c.961C>A p.L321I Substitution - Missense 10:68014134-68014134 - TCGA-BR-4361-01 COSM4015211 c.3132G>A p.L1044L Substitution - coding silent 10:67922973-67922973 - TCGA-B5-A11H-01 COSM919624 c.2140C>T p.R714C Substitution - Missense 10:67955040-67955040 - TCGA-EE-A2A2-06 COSM3439745 c.1449A>C p.A483A Substitution - coding silent 10:67990395-67990395 - TCGA-D1-A103-01 COSM919619 c.3140C>T p.A1047V Substitution - Missense 10:67922965-67922965 - TCGA-AP-A056-01 COSM919629 c.1119A>C p.Q373H Substitution - Missense 10:67992633-67992633 - PAPNNX COSM919623 c.2261G>A p.R754H Substitution - Missense 10:67954695-67954695 - 587284 COSM1209599 c.419T>C p.V140A Substitution - Missense 10:68038137-68038137 - AOCS-166-1-2 COSM3981076 c.951C>G p.Y317* Substitution - Nonsense 10:68014144-68014144 - PCSI_0022_Pa_C COSM216351 c.243G>A p.L81L Substitution - coding silent 10:68044547-68044547 - 2492702 COSM5599663 c.1526C>T p.T509I Substitution - Missense 10:67990318-67990318 - 71 COSM5014920 c.2302C>A p.P768T Substitution - Missense 10:67954654-67954654 - TCGA-CA-6717-01 COSM1348659 c.2399T>C p.V800A Substitution - Missense 10:67941068-67941068 - TCGA-AA-3710-01 COSM293546 c.1322_1323insT p.L441fs*4 Insertion - Frameshift 10:67991148-67991149 - ESCC_136 COSM5642977 c.2087C>G p.S696C Substitution - Missense 10:67955093-67955093 - TCGA-A8-A0A6-01 COSM3807495 c.2258T>G p.V753G Substitution - Missense 10:67954698-67954698 - 041T COSM1728941 c.1099A>T p.I367F Substitution - Missense 10:67992653-67992653 - Pat_30_B COSM3439746 c.1295C>T p.S432F Substitution - Missense 10:67991176-67991176 - BD121T COSM5515348 c.2190G>T p.K730N Substitution - Missense 10:67954990-67954990 - CLL169 COSM1289398 c.690G>T p.R230S Substitution - Missense 10:68032865-68032865 - PT49 COSM5515348 c.2190G>T p.K730N Substitution - Missense 10:67954990-67954990 - ESCC_83 COSM5636234 c.1852A>G p.I618V Substitution - Missense 10:67966757-67966757 - TCGA-CG-5721-01 COSM4015221 c.907C>T p.R303W Substitution - Missense 10:68025547-68025547 - 19M COSM5578700 c.2297T>C p.L766S Substitution - Missense 10:67954659-67954659 - LUAD-S01357 COSM386283 c.477C>T p.F159F Substitution - coding silent 10:68034173-68034173 - TCGA-AP-A056-01 COSM919627 c.1428G>A p.P476P Substitution - coding silent 10:67990919-67990919 - TCGA-A8-A0A6-01 COSM3807497 c.783T>G p.G261G Substitution - coding silent 10:68025671-68025671 - TCGA-CA-6717-01 COSM1348663 c.124G>A p.G42R Substitution - Missense 10:68072985-68072985 - ESO-077 COSM1254137 c.287C>T p.T96M Substitution - Missense 10:68044503-68044503 - HCC107T COSM1603640 c.294G>A p.A98A Substitution - coding silent 10:68044496-68044496 - TCGA-E9-A1N8-01 COSM1474710 c.2671_2674delCAAA p.Q891fs*78 Deletion - Frameshift 10:67936157-67936160 - NCI-H322M COSM1683433 c.778-10_778-9insT p.? Unknown 10:68025685-68025686 - HCC105T COSM1603639 c.1307T>C p.L436P Substitution - Missense 10:67991164-67991164 - S00945 COSM311755 c.1720T>C p.Y574H Substitution - Missense 10:67988749-67988749 - PCSI0022 COSM216351 c.243G>A p.L81L Substitution - coding silent 10:68044547-68044547 - 2492701 COSM5599663 c.1526C>T p.T509I Substitution - Missense 10:67990318-67990318 - TCGA-EE-A2MU-06 COSM3439747 c.1240C>T p.P414S Substitution - Missense 10:67992230-67992230 - 4_RESISTANT COSM1724542 c.2526G>A p.G842G Substitution - coding silent 10:67940941-67940941 - TCGA-B9-5155-01 COSM3985692 c.2090T>C p.L697P Substitution - Missense 10:67955090-67955090 - YUPAT COSM1702578 c.571C>T p.P191S Substitution - Missense 10:68034079-68034079 - WA55 COSM236755 c.670_671insT p.N225fs*1 Insertion - Frameshift 10:68033979-68033980 - TCGA-AA-3663-01 COSM5826744 c.1272-3_1272-2insT p.? Unknown 10:67991201-67991202 - ZZUFHECRKL-G026T COSM4015221 c.907C>T p.R303W Substitution - Missense 10:68025547-68025547 - S0080 COSM5881931 c.3152A>C p.N1051T Substitution - Missense 10:67922953-67922953 - TCGA-18-3419-01 COSM684634 c.2401A>T p.I801F Substitution - Missense 10:67941066-67941066 - tumor_4177376 COSM3356123 c.542C>T p.P181L Substitution - Missense 10:68034108-68034108 - TCGA-B5-A0JY-01 COSM919621 c.2590T>G p.F864V Substitution - Missense 10:67939593-67939593 - TCGA-AA-A010-01 COSM281680 c.940G>T p.G314* Substitution - Nonsense 10:68014155-68014155 - C91 COSM4444311 c.1703T>C p.V568A Substitution - Missense 10:67988766-67988766 - HCC105 COSM1603639 c.1307T>C p.L436P Substitution - Missense 10:67991164-67991164 - 41 COSM3356123 c.542C>T p.P181L Substitution - Missense 10:68034108-68034108 - HT115 COSM2159100 c.494A>C p.K165T Substitution - Missense 10:68034156-68034156 - CHEWS011 COSM4573715 c.2680C>A p.Q894K Substitution - Missense 10:67932779-67932779 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.51649;Hs.51891 10q21.3 609248

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.226+5707T>G 10 69826933 HC A C Missense p.V288G c.863T>G 10 69785348 ESCA A G IntronicSNV . c.1332-17T>C 10 69750789 NSCLC A G IntronicSNV . c.387-8T>C 10 69797934 STAD A G Missense p.F264L c.790T>C 10 69785421 CM A G Missense p.Y231H c.691T>C 10 69792621 STAD A G Missense p.Y574H c.1720T>C 10 69748506 SCLC A T Missense p.N693K c.2079T>A 10 69714858 STAD C A Missense p.M516I c.1548G>T 10 69750053 SCLC C A Missense p.Q273H c.819G>T 10 69785392 LUAD C A Missense p.R230S c.690G>T 10 69792622 CLL C A Missense p.R843I c.2528G>T 10 69700696 LUAD C A Nonsense p.E756* c.2266G>T 10 69714447 UCEC C A Synonymous p.A918A c.2754G>T 10 69692462 LUAD C A Synonymous p.L988L c.2964G>T 10 69684843 BRCA C G Missense p.D111H c.331G>C 10 69804216 LUSC C T IntronicSNV . c.1926+1872G>A 10 69724568 HC C T IntronicSNV . c.2361+222G>A 10 69714130 HC C T Missense p.E756K c.2266G>A 10 69714447 LUAD C T Missense p.R754H c.2261G>A 10 69714452 UCEC C T Synonymous p.A918A c.2754G>A 10 69692462 BRCA C T Synonymous p.L411L c.1233G>A 10 69751994 BRCA C T Synonymous p.L81L c.243G>A 10 69804304 PAAD G A Missense p.H977Y c.2929C>T 10 69684878 CM G A Missense p.P395S c.1183C>T 10 69752044 CM G A Missense p.P414S c.1240C>T 10 69751987 CM G A Missense p.P817S c.2449C>T 10 69700775 STAD G A Missense p.R714C c.2140C>T 10 69714797 UCEC G A Missense p.S432F c.1295C>T 10 69750933 CM G A Missense p.T429M c.1286C>T 10 69750942 UCEC G A Missense p.T96M c.287C>T 10 69804260 ESCA G A Nonsense p.Q163* c.487C>T 10 69793920 LUAD G A Synonymous p.L110L c.330C>T 10 69804217 CM G A Synonymous p.S844S c.2532C>T 10 69699408 HNSC G C Synonymous p.L43L c.129C>G 10 69832737 LUAD G T Missense p.A669E c.2006C>A 10 69716678 LUAD G T Nonsense p.C3* c.9C>A 10 69832857 BRCA T - 3-UTRDeletion . c.3171+590delT 10 69682101 HC T A Missense p.E777V c.2330A>T 10 69714383 LUAD T A Missense p.I801F c.2401A>T 10 69700823 LUSC TATATTATAATATTATA - IntronicDeletion . c.226+13096_226+13112delTAATATTATAATATATA 10 69819530 CLL T C IntronicSNV . c.2050-782A>G 10 69715669 HC T C IntronicSNV . c.227-13637A>G 10 69817957 PIA T C Missense p.N906S c.2717A>G 10 69692499 OV T C Synonymous p.R584R c.1752A>G 10 69748474 CM TCT - InFrameDeletion p.D136delD c.405_407delAGA 10 69797906 RCCC TGCA - Frameshift p.M193Kfs*29 c.578_581delTGCA 10 69793826 BRCA T G Missense p.T886P c.2656A>C 10 69695932 HC T G Synonymous p.A483A c.1449A>C 10 69750152 CM TTTG - Frameshift p.Q891Ifs*78 c.2671_2674delCAAA 10 69695914 BRCA