Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 10 93170250 93170250 + Missense_Mutation SNP C C G TCGA-OR-A5K9-01A-11D-A29I-10 TCGA-OR-A5K9-11A-11D-A29L-10 g.chr10:93170250C>G c.55C>G c.(55-57)Ccc>Gcc p.P19A ACC 10 93170250 93170250 + Missense_Mutation SNP C C G TCGA-OR-A5KS-01A-11D-A30A-10 TCGA-OR-A5KS-10A-01D-A30A-10 g.chr10:93170250C>G c.55C>G c.(55-57)Ccc>Gcc p.P19A BLCA 10 93220240 93220240 + Missense_Mutation SNP G G C TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr10:93220240G>C c.325G>C c.(325-327)Gat>Cat p.D109H BLCA 10 93220321 93220321 + Splice_Site SNP C C T TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr10:93220321C>T c.406C>T c.(406-408)Cag>Tag p.Q136* BLCA 10 93244276 93244276 + Missense_Mutation SNP G G C TCGA-FD-A5BX-01A-11D-A26M-08 TCGA-FD-A5BX-10A-01D-A26K-08 g.chr10:93244276G>C c.834G>C c.(832-834)aaG>aaC p.K278N BLCA 10 93247480 93247481 + Frame_Shift_Ins INS - - A TCGA-XF-A9SX-01A-21D-A391-08 TCGA-XF-A9SX-10A-01D-A394-08 g.chr10:93247480_93247481insA c.1136_1137insA c.(1135-1140)gcaaaafs p.AK379fs BLCA 10 93250985 93250985 + Missense_Mutation SNP G G A TCGA-BT-A42E-01A-11D-A23U-08 TCGA-BT-A42E-10A-01D-A23U-08 g.chr10:93250985G>A c.1220G>A c.(1219-1221)aGa>aAa p.R407K BLCA 10 93252127 93252127 + Missense_Mutation SNP G G C TCGA-GD-A76B-01A-11D-A32B-08 TCGA-GD-A76B-10A-01D-A329-08 g.chr10:93252127G>C c.1318G>C c.(1318-1320)Gat>Cat p.D440H BLCA 10 93252132 93252132 + Missense_Mutation SNP G G C TCGA-FD-A3NA-01A-11D-A21A-08 TCGA-FD-A3NA-10A-01D-A21A-08 g.chr10:93252132G>C c.1323G>C c.(1321-1323)ttG>ttC p.L441F BLCA 10 93252138 93252138 + Missense_Mutation SNP G G C TCGA-E7-A97Q-01A-11D-A38G-08 TCGA-E7-A97Q-10A-01D-A38J-08 g.chr10:93252138G>C c.1329G>C c.(1327-1329)aaG>aaC p.K443N BLCA 10 93252163 93252163 + Missense_Mutation SNP G G A TCGA-ZF-AA4X-01A-11D-A38G-08 TCGA-ZF-AA4X-10A-01D-A38J-08 g.chr10:93252163G>A c.1354G>A c.(1354-1356)Gaa>Aaa p.E452K BLCA 10 93272072 93272072 + Missense_Mutation SNP G G C TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr10:93272072G>C c.2262G>C c.(2260-2262)aaG>aaC p.K754N BRCA 10 93220311 93220311 + Silent SNP G G A TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr10:93220311G>A c.396G>A c.(394-396)gtG>gtA p.V132V BRCA 10 93240885 93240885 + Missense_Mutation SNP A A T TCGA-AQ-A54N-01A-11D-A25Q-09 TCGA-AQ-A54N-10A-01D-A25Q-09 g.chr10:93240885A>T c.700A>T c.(700-702)Ata>Tta p.I234L BRCA 10 93247499 93247499 + Missense_Mutation SNP G G C TCGA-BH-A0HA-01A-11D-A12Q-09 TCGA-BH-A0HA-11A-31D-A12Q-09 g.chr10:93247499G>C c.1155G>C c.(1153-1155)caG>caC p.Q385H BRCA 10 93256090 93256090 + Silent SNP C C T TCGA-A7-A26E-01A-11D-A167-09 TCGA-A7-A26E-10A-01D-A167-09 g.chr10:93256090C>T c.1641C>T c.(1639-1641)atC>atT p.I547I BRCA 10 93257913 93257915 + In_Frame_Del DEL GAA GAA - TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr10:93257913_93257915delGAA c.1729_1731delGAA c.(1729-1731)gaadel p.E578del CESC 10 93261075 93261075 + Missense_Mutation SNP G G A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr10:93261075G>A c.2194G>A c.(2194-2196)Gaa>Aaa p.E732K COAD 10 93220255 93220255 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr10:93220255G>A c.340G>A c.(340-342)Gaa>Aaa p.E114K COAD 10 93220255 93220255 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr10:93220255G>A c.340G>A c.(340-342)Gaa>Aaa p.E114K COAD 10 93221093 93221093 + Nonsense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:93221093G>T c.490G>T c.(490-492)Gaa>Taa p.E164* COAD 10 93221924 93221924 + Missense_Mutation SNP G G A TCGA-AZ-6606-01A-11D-1835-10 TCGA-AZ-6606-11A-01D-1835-10 g.chr10:93221924G>A c.583G>A c.(583-585)Gat>Aat p.D195N COAD 10 93244350 93244350 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr10:93244350T>G c.908T>G c.(907-909)tTt>tGt p.F303C COAD 10 93245000 93245000 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr10:93245000T>G c.1034T>G c.(1033-1035)tTg>tGg p.L345W COAD 10 93245035 93245035 + Missense_Mutation SNP T T A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:93245035T>A c.1069T>A c.(1069-1071)Tgg>Agg p.W357R COAD 10 93245035 93245035 + Missense_Mutation SNP T T C TCGA-CA-5796-01A-01D-1650-10 TCGA-CA-5796-10A-01D-1650-10 g.chr10:93245035T>C c.1069T>C c.(1069-1071)Tgg>Cgg p.W357R COAD 10 93247480 93247481 + Frame_Shift_Ins INS - - A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr10:93247480_93247481insA c.1136_1137insA c.(1135-1140)gcaaaafs p.AK379fs COAD 10 93252213 93252213 + Silent SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr10:93252213A>G c.1404A>G c.(1402-1404)ctA>ctG p.L468L COAD 10 93252237 93252237 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:93252237T>G c.1428T>G c.(1426-1428)gaT>gaG p.D476E COAD 10 93258674 93258674 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:93258674C>T c.1801C>T c.(1801-1803)Ccc>Tcc p.P601S COAD 10 93260360 93260360 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr10:93260360G>A c.2052G>A c.(2050-2052)acG>acA p.T684T COAD 10 93272103 93272103 + Missense_Mutation SNP A A G TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr10:93272103A>G c.2293A>G c.(2293-2295)Att>Gtt p.I765V COADREAD 10 93220255 93220255 + Missense_Mutation SNP G G A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr10:93220255G>A c.340G>A c.(340-342)Gaa>Aaa p.E114K COADREAD 10 93220255 93220255 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr10:93220255G>A c.340G>A c.(340-342)Gaa>Aaa p.E114K COADREAD 10 93221093 93221093 + Nonsense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:93221093G>T c.490G>T c.(490-492)Gaa>Taa p.E164* COADREAD 10 93221924 93221924 + Missense_Mutation SNP G G A TCGA-AZ-6606-01A-11D-1835-10 TCGA-AZ-6606-11A-01D-1835-10 g.chr10:93221924G>A c.583G>A c.(583-585)Gat>Aat p.D195N COADREAD 10 93244317 93244317 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:93244317C>T c.875C>T c.(874-876)tCt>tTt p.S292F COADREAD 10 93244350 93244350 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr10:93244350T>G c.908T>G c.(907-909)tTt>tGt p.F303C COADREAD 10 93245000 93245000 + Missense_Mutation SNP T T G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr10:93245000T>G c.1034T>G c.(1033-1035)tTg>tGg p.L345W COADREAD 10 93245035 93245035 + Missense_Mutation SNP T T A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:93245035T>A c.1069T>A c.(1069-1071)Tgg>Agg p.W357R COADREAD 10 93245035 93245035 + Missense_Mutation SNP T T C TCGA-CA-5796-01A-01D-1650-10 TCGA-CA-5796-10A-01D-1650-10 g.chr10:93245035T>C c.1069T>C c.(1069-1071)Tgg>Cgg p.W357R COADREAD 10 93247480 93247481 + Frame_Shift_Ins INS - - A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr10:93247480_93247481insA c.1136_1137insA c.(1135-1140)gcaaaafs p.AK379fs COADREAD 10 93252213 93252213 + Silent SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr10:93252213A>G c.1404A>G c.(1402-1404)ctA>ctG p.L468L COADREAD 10 93252237 93252237 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:93252237T>G c.1428T>G c.(1426-1428)gaT>gaG p.D476E COADREAD 10 93257924 93257924 + Missense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr10:93257924C>A c.1740C>A c.(1738-1740)ttC>ttA p.F580L COADREAD 10 93258674 93258674 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:93258674C>T c.1801C>T c.(1801-1803)Ccc>Tcc p.P601S COADREAD 10 93260360 93260360 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr10:93260360G>A c.2052G>A c.(2050-2052)acG>acA p.T684T COADREAD 10 93272103 93272103 + Missense_Mutation SNP A A G TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr10:93272103A>G c.2293A>G c.(2293-2295)Att>Gtt p.I765V DLBC 10 93221018 93221018 + Missense_Mutation SNP G G A TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chr10:93221018G>A c.415G>A c.(415-417)Gta>Ata p.V139I DLBC 10 93260363 93260363 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr10:93260363C>T c.2055C>T c.(2053-2055)gaC>gaT p.D685D ESCA 10 93242782 93242783 + In_Frame_Ins INS - - AGG TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr10:93242782_93242783insAGG c.770_771insAGG c.(769-774)atagct>atAGGagct p.257_258IA>IGA ESCA 10 93250956 93250956 + Splice_Site SNP G G A TCGA-LN-A8I1-01A-11D-A36J-09 TCGA-LN-A8I1-10A-01D-A36M-09 g.chr10:93250956G>A c.e12-1 ESCA 10 93257887 93257887 + Missense_Mutation SNP A A G TCGA-2H-A9GG-01A-11D-A37C-09 TCGA-2H-A9GG-11A-11D-A37F-09 g.chr10:93257887A>G c.1703A>G c.(1702-1704)gAa>gGa p.E568G GBM 10 93244394 93244394 + Missense_Mutation SNP A A G TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr10:93244394A>G c.952A>G c.(952-954)Aaa>Gaa p.K318E GBMLGG 10 93185044 93185044 + Missense_Mutation SNP G G C TCGA-FG-A70Z-01A-12D-A33T-08 TCGA-FG-A70Z-10A-01D-A33W-08 g.chr10:93185044G>C c.145G>C c.(145-147)Gac>Cac p.D49H GBMLGG 10 93244394 93244394 + Missense_Mutation SNP A A G TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr10:93244394A>G c.952A>G c.(952-954)Aaa>Gaa p.K318E GBMLGG 10 93247529 93247529 + Silent SNP C C T TCGA-DH-A7UR-01A-11D-A33T-08 TCGA-DH-A7UR-10A-01D-A33W-08 g.chr10:93247529C>T c.1185C>T c.(1183-1185)atC>atT p.I395I GBMLGG 10 93260258 93260258 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:93260258G>T c.e19-1 GBMLGG 10 93260993 93260993 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:93260993G>T c.2112G>T c.(2110-2112)aaG>aaT p.K704N HNSC 10 93185163 93185163 + Missense_Mutation SNP G G T TCGA-BB-4217-01A-11D-2078-08 TCGA-BB-4217-10A-01D-2078-08 g.chr10:93185163G>T c.264G>T c.(262-264)aaG>aaT p.K88N HNSC 10 93221022 93221022 + Missense_Mutation SNP A A T TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chr10:93221022A>T c.419A>T c.(418-420)gAa>gTa p.E140V HNSC 10 93221090 93221090 + Missense_Mutation SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr10:93221090C>T c.487C>T c.(487-489)Cca>Tca p.P163S HNSC 10 93221098 93221098 + Missense_Mutation SNP A A C TCGA-CN-A63U-01A-11D-A30E-08 TCGA-CN-A63U-10A-01D-A30H-08 g.chr10:93221098A>C c.495A>C c.(493-495)ttA>ttC p.L165F HNSC 10 93221100 93221100 + Missense_Mutation SNP A A T TCGA-F7-7848-01A-11D-2129-08 TCGA-F7-7848-10A-01D-2129-08 g.chr10:93221100A>T c.497A>T c.(496-498)aAt>aTt p.N166I HNSC 10 93221956 93221956 + Intron SNP A A T TCGA-CQ-7064-01A-11D-2394-08 TCGA-CQ-7064-10A-01D-2394-08 g.chr10:93221956A>T HNSC 10 93242780 93242780 + Missense_Mutation SNP G G C TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr10:93242780G>C c.768G>C c.(766-768)caG>caC p.Q256H HNSC 10 93245017 93245017 + Missense_Mutation SNP A A G TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr10:93245017A>G c.1051A>G c.(1051-1053)Atg>Gtg p.M351V KIPAN 10 93220253 93220253 + Missense_Mutation SNP C C T TCGA-B0-5106-01A-01D-1421-08 TCGA-B0-5106-11A-01D-1421-08 g.chr10:93220253C>T c.338C>T c.(337-339)tCc>tTc p.S113F KIPAN 10 93252242 93252243 + Splice_Site INS - - T TCGA-A4-8310-01A-11D-2396-08 TCGA-A4-8310-10A-01D-2396-08 g.chr10:93252242_93252243insT c.e13+1 KIPAN 10 93258806 93258806 + Missense_Mutation SNP G G A TCGA-B0-5109-01A-02D-1421-08 TCGA-B0-5109-11A-01D-1421-08 g.chr10:93258806G>A c.1849G>A c.(1849-1851)Gta>Ata p.V617I KIRC 10 93220253 93220253 + Missense_Mutation SNP C C T TCGA-B0-5106-01A-01D-1421-08 TCGA-B0-5106-11A-01D-1421-08 g.chr10:93220253C>T c.338C>T c.(337-339)tCc>tTc p.S113F KIRC 10 93258806 93258806 + Missense_Mutation SNP G G A TCGA-B0-5109-01A-02D-1421-08 TCGA-B0-5109-11A-01D-1421-08 g.chr10:93258806G>A c.1849G>A c.(1849-1851)Gta>Ata p.V617I KIRP 10 93252242 93252243 + Splice_Site INS - - T TCGA-A4-8310-01A-11D-2396-08 TCGA-A4-8310-10A-01D-2396-08 g.chr10:93252242_93252243insT c.e13+1 LGG 10 93185044 93185044 + Missense_Mutation SNP G G C TCGA-FG-A70Z-01A-12D-A33T-08 TCGA-FG-A70Z-10A-01D-A33W-08 g.chr10:93185044G>C c.145G>C c.(145-147)Gac>Cac p.D49H LGG 10 93247529 93247529 + Silent SNP C C T TCGA-DH-A7UR-01A-11D-A33T-08 TCGA-DH-A7UR-10A-01D-A33W-08 g.chr10:93247529C>T c.1185C>T c.(1183-1185)atC>atT p.I395I LGG 10 93260258 93260258 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:93260258G>T c.e19-1 LGG 10 93260993 93260993 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:93260993G>T c.2112G>T c.(2110-2112)aaG>aaT p.K704N LIHC 10 93221940 93221940 + Splice_Site SNP C C T TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr10:93221940C>T c.599C>T c.(598-600)aCt>aTt p.T200I LIHC 10 93252211 93252211 + Missense_Mutation SNP C C G TCGA-CC-A7IJ-01A-11D-A33Q-10 TCGA-CC-A7IJ-10A-01D-A33Q-10 g.chr10:93252211C>G c.1402C>G c.(1402-1404)Cta>Gta p.L468V LUAD 10 93220264 93220264 + Missense_Mutation SNP G G T TCGA-50-5941-01A-11D-1753-08 TCGA-50-5941-10A-01D-1753-08 g.chr10:93220264G>T c.349G>T c.(349-351)Gcc>Tcc p.A117S LUAD 10 93220277 93220277 + Missense_Mutation SNP C C A TCGA-05-4244-01A-01D-1105-08 TCGA-05-4244-10A-01D-1105-08 g.chr10:93220277C>A c.362C>A c.(361-363)cCa>cAa p.P121Q LUAD 10 93238018 93238018 + Frame_Shift_Del DEL A A - TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chr10:93238018delA c.661delA c.(661-663)aaafs p.K221fs LUAD 10 93242723 93242723 + Splice_Site SNP G G C TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chr10:93242723G>C c.e8-1 LUAD 10 93244262 93244262 + Splice_Site SNP A A C TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr10:93244262A>C c.e9-1 LUAD 10 93256105 93256105 + Silent SNP G G T TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr10:93256105G>T c.1656G>T c.(1654-1656)gtG>gtT p.V552V LUAD 10 93258885 93258885 + Missense_Mutation SNP T T C TCGA-17-Z018-01A-01W-0746-08 TCGA-17-Z018-11A-01W-0746-08 g.chr10:93258885T>C c.1928T>C c.(1927-1929)gTg>gCg p.V643A LUAD 10 93260329 93260329 + Missense_Mutation SNP G G C TCGA-17-Z015-01A-01W-0746-08 TCGA-17-Z015-11A-01W-0746-08 g.chr10:93260329G>C c.2021G>C c.(2020-2022)aGa>aCa p.R674T LUSC 10 93244288 93244288 + Silent SNP A A G TCGA-37-5819-01A-01D-1632-08 TCGA-37-5819-10A-01D-1632-08 g.chr10:93244288A>G c.846A>G c.(844-846)caA>caG p.Q282Q LUSC 10 93252127 93252127 + Missense_Mutation SNP G G T TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr10:93252127G>T c.1318G>T c.(1318-1320)Gat>Tat p.D440Y PAAD 10 93221081 93221081 + Missense_Mutation SNP G G A TCGA-HV-A7OP-01A-11D-A33T-08 TCGA-HV-A7OP-10A-01D-A33W-08 g.chr10:93221081G>A c.478G>A c.(478-480)Gat>Aat p.D160N PAAD 10 93244323 93244323 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:93244323G>A c.881G>A c.(880-882)cGc>cAc p.R294H PAAD 10 93256087 93256087 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:93256087C>T c.1638C>T c.(1636-1638)ggC>ggT p.G546G PAAD 10 93261004 93261004 + Missense_Mutation SNP A A G TCGA-IB-AAUS-01A-12D-A38G-08 TCGA-IB-AAUS-10A-01D-A38J-08 g.chr10:93261004A>G c.2123A>G c.(2122-2124)cAt>cGt p.H708R PRAD 10 93220201 93220201 + Missense_Mutation SNP A A G TCGA-KK-A7AY-01A-11D-A33T-08 TCGA-KK-A7AY-11A-21D-A33W-08 g.chr10:93220201A>G c.286A>G c.(286-288)Att>Gtt p.I96V PRAD 10 93244322 93244322 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:93244322C>T c.880C>T c.(880-882)Cgc>Tgc p.R294C PRAD 10 93253266 93253266 + Splice_Site SNP G G A TCGA-HC-7077-01A-11D-1961-08 TCGA-HC-7077-10A-01D-1961-08 g.chr10:93253266G>A c.e14+1 READ 10 93244317 93244317 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:93244317C>T c.875C>T c.(874-876)tCt>tTt p.S292F READ 10 93257924 93257924 + Missense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr10:93257924C>A c.1740C>A c.(1738-1740)ttC>ttA p.F580L SARC 10 93220291 93220291 + Missense_Mutation SNP C C A TCGA-WP-A9GB-01A-11D-A37C-09 TCGA-WP-A9GB-10A-01D-A37F-09 g.chr10:93220291C>A c.376C>A c.(376-378)Cct>Act p.P126T SKCM 10 93185065 93185065 + Missense_Mutation SNP A A G TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr10:93185065A>G c.166A>G c.(166-168)Att>Gtt p.I56V SKCM 10 93220272 93220272 + Silent SNP C C T TCGA-EE-A2GE-06A-11D-A196-08 TCGA-EE-A2GE-10A-01D-A198-08 g.chr10:93220272C>T c.357C>T c.(355-357)gtC>gtT p.V119V SKCM 10 93220273 93220273 + Missense_Mutation SNP C C T TCGA-EE-A2GE-06A-11D-A196-08 TCGA-EE-A2GE-10A-01D-A198-08 g.chr10:93220273C>T c.358C>T c.(358-360)Ctt>Ttt p.L120F SKCM 10 93244936 93244936 + Splice_Site SNP G G T TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr10:93244936G>T c.e10-1 SKCM 10 93256117 93256117 + Silent SNP T T C TCGA-EE-A29C-06A-21D-A197-08 TCGA-EE-A29C-10A-01D-A199-08 g.chr10:93256117T>C c.1668T>C c.(1666-1668)tgT>tgC p.C556C

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 10 93221924 93221924 single base substitution G C 5_prime_UTR_variant BLCA-CN 10 93221924 93221924 single base substitution G C missense_variant D195H 583G>C BLCA-CN 10 93272136 93272136 single base substitution G C missense_variant E365Q 1093G>C BLCA-CN 10 93272136 93272136 single base substitution G C missense_variant E426Q 1276G>C BLCA-CN 10 93272136 93272136 single base substitution G C missense_variant E776Q 2326G>C BLCA-CN 10 93272136 93272136 single base substitution G C missense_variant E780Q 2338G>C BLCA-US 10 93252132 93252132 single base substitution G C downstream_gene_variant BLCA-US 10 93252132 93252132 single base substitution G C missense_variant L30F 90G>C BLCA-US 10 93252132 93252132 single base substitution G C missense_variant L441F 1323G>C BLCA-US 10 93252132 93252132 single base substitution G C missense_variant L445F 1335G>C BLCA-US 10 93252132 93252132 single base substitution G C missense_variant L91F 273G>C BOCA-FR 10 93260081 93260081 single base substitution C T intron_variant BRCA-EU 10 93166615 93166616 deletion of <=200bp GT - upstream_gene_variant BRCA-EU 10 93167100 93167100 single base substitution G T upstream_gene_variant BRCA-EU 10 93167277 93167277 single base substitution C T upstream_gene_variant BRCA-EU 10 93171083 93171083 single base substitution G T intron_variant BRCA-EU 10 93171121 93171121 single base substitution A C intron_variant BRCA-EU 10 93172975 93172975 single base substitution G T intron_variant BRCA-EU 10 93174260 93174260 insertion of <=200bp - A intron_variant BRCA-EU 10 93174778 93174778 single base substitution G C intron_variant BRCA-EU 10 93175311 93175311 single base substitution G C intron_variant BRCA-EU 10 93176434 93176434 single base substitution A G intron_variant BRCA-EU 10 93176628 93176628 single base substitution C G intron_variant BRCA-EU 10 93177088 93177088 deletion of <=200bp T - intron_variant BRCA-EU 10 93177088 93177088 insertion of <=200bp - T intron_variant BRCA-EU 10 93179041 93179041 single base substitution C A intron_variant BRCA-EU 10 93183727 93183727 single base substitution A G intron_variant BRCA-EU 10 93185201 93185201 single base substitution T C intron_variant BRCA-EU 10 93191609 93191609 single base substitution G C intron_variant BRCA-EU 10 93191981 93191981 single base substitution T G intron_variant BRCA-EU 10 93195961 93195961 single base substitution T A intron_variant BRCA-EU 10 93196117 93196117 single base substitution C T intron_variant BRCA-EU 10 93197229 93197229 single base substitution T A intron_variant BRCA-EU 10 93198834 93198834 single base substitution T G intron_variant BRCA-EU 10 93199290 93199290 single base substitution T C intron_variant BRCA-EU 10 93205096 93205096 single base substitution C G intron_variant BRCA-EU 10 93208819 93208819 single base substitution G C intron_variant BRCA-EU 10 93209286 93209286 single base substitution G A intron_variant BRCA-EU 10 93209657 93209657 single base substitution A T intron_variant BRCA-EU 10 93210731 93210731 single base substitution C T intron_variant BRCA-EU 10 93211282 93211282 single base substitution A T intron_variant BRCA-EU 10 93211355 93211355 single base substitution C G intron_variant BRCA-EU 10 93211740 93211740 single base substitution G C intron_variant BRCA-EU 10 93212787 93212787 single base substitution A C intron_variant BRCA-EU 10 93212910 93212910 single base substitution C T intron_variant BRCA-EU 10 93212994 93212994 single base substitution G A intron_variant BRCA-EU 10 93213114 93213114 single base substitution G C intron_variant BRCA-EU 10 93214190 93214190 single base substitution T C intron_variant BRCA-EU 10 93215078 93215078 single base substitution A G intron_variant BRCA-EU 10 93216177 93216177 single base substitution G C intron_variant BRCA-EU 10 93216410 93216410 single base substitution C T intron_variant BRCA-EU 10 93217859 93217859 single base substitution A G intron_variant BRCA-EU 10 93217859 93217859 single base substitution A G upstream_gene_variant BRCA-EU 10 93218756 93218756 single base substitution A G intron_variant BRCA-EU 10 93218756 93218756 single base substitution A G upstream_gene_variant BRCA-EU 10 93219805 93219805 single base substitution T C intron_variant BRCA-EU 10 93219805 93219805 single base substitution T C upstream_gene_variant BRCA-EU 10 93220462 93220462 single base substitution C G intron_variant BRCA-EU 10 93220462 93220462 single base substitution C G upstream_gene_variant BRCA-EU 10 93223894 93223894 single base substitution T C downstream_gene_variant BRCA-EU 10 93223894 93223894 single base substitution T C intron_variant BRCA-EU 10 93226111 93226111 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 93226111 93226111 deletion of <=200bp A - intron_variant BRCA-EU 10 93228533 93228533 single base substitution A T intron_variant BRCA-EU 10 93229169 93229169 single base substitution G C intron_variant BRCA-EU 10 93230361 93230361 single base substitution G A intron_variant BRCA-EU 10 93230560 93230560 single base substitution C T intron_variant BRCA-EU 10 93230686 93230686 single base substitution G A intron_variant BRCA-EU 10 93232344 93232344 deletion of <=200bp A - intron_variant BRCA-EU 10 93232487 93232487 single base substitution A T intron_variant BRCA-EU 10 93233421 93233421 single base substitution G C intron_variant BRCA-EU 10 93234018 93234020 deletion of <=200bp AGA - intron_variant BRCA-EU 10 93234689 93234689 single base substitution C T intron_variant BRCA-EU 10 93236839 93236839 single base substitution G C intron_variant BRCA-EU 10 93236956 93236956 single base substitution A C intron_variant BRCA-EU 10 93240492 93240492 single base substitution C G intron_variant BRCA-EU 10 93240492 93240492 single base substitution C G upstream_gene_variant BRCA-EU 10 93242053 93242053 single base substitution T G intron_variant BRCA-EU 10 93242053 93242053 single base substitution T G upstream_gene_variant BRCA-EU 10 93242192 93242192 single base substitution C G intron_variant BRCA-EU 10 93242192 93242192 single base substitution C G upstream_gene_variant BRCA-EU 10 93247481 93247481 insertion of <=200bp - A exon_variant BRCA-EU 10 93247481 93247481 insertion of <=200bp - A frameshift_variant A29A? BRCA-EU 10 93247481 93247481 insertion of <=200bp - A frameshift_variant A379A? BRCA-EU 10 93247481 93247481 insertion of <=200bp - A frameshift_variant A383A? BRCA-EU 10 93247481 93247481 insertion of <=200bp - A intron_variant BRCA-EU 10 93248675 93248675 single base substitution G C exon_variant BRCA-EU 10 93248675 93248675 single base substitution G C intron_variant BRCA-EU 10 93251034 93251034 single base substitution G C downstream_gene_variant BRCA-EU 10 93251034 93251034 single base substitution G C synonymous_variant R12R 36G>C BRCA-EU 10 93251034 93251034 single base substitution G C synonymous_variant R423R 1269G>C BRCA-EU 10 93251034 93251034 single base substitution G C synonymous_variant R427R 1281G>C BRCA-EU 10 93251034 93251034 single base substitution G C synonymous_variant R73R 219G>C BRCA-EU 10 93254718 93254718 insertion of <=200bp - T downstream_gene_variant BRCA-EU 10 93254718 93254718 insertion of <=200bp - T intron_variant BRCA-EU 10 93255297 93255297 single base substitution G A intron_variant BRCA-EU 10 93255592 93255592 single base substitution G C intron_variant BRCA-EU 10 93255596 93255596 single base substitution T C intron_variant BRCA-EU 10 93255716 93255716 single base substitution G C intron_variant BRCA-EU 10 93256128 93256128 single base substitution C G missense_variant P149R 446C>G BRCA-EU 10 93256128 93256128 single base substitution C G missense_variant P210R 629C>G BRCA-EU 10 93256128 93256128 single base substitution C G missense_variant P560R 1679C>G BRCA-EU 10 93256128 93256128 single base substitution C G missense_variant P564R 1691C>G BRCA-EU 10 93256503 93256503 single base substitution G A intron_variant BRCA-EU 10 93256803 93256803 single base substitution G A intron_variant BRCA-EU 10 93257570 93257570 single base substitution A G intron_variant BRCA-EU 10 93258537 93258537 deletion of <=200bp A - intron_variant BRCA-EU 10 93259928 93259928 single base substitution A G intron_variant BRCA-EU 10 93259995 93259995 single base substitution G C intron_variant BRCA-EU 10 93260598 93260598 single base substitution G T intron_variant BRCA-EU 10 93261644 93261644 single base substitution C A intron_variant BRCA-EU 10 93262756 93262756 single base substitution G A intron_variant BRCA-EU 10 93263021 93263021 single base substitution G C intron_variant BRCA-EU 10 93263647 93263647 single base substitution G C intron_variant BRCA-EU 10 93263703 93263703 single base substitution C T intron_variant BRCA-EU 10 93268763 93268763 single base substitution C A intron_variant BRCA-EU 10 93269359 93269359 deletion of <=200bp A - intron_variant BRCA-EU 10 93274331 93274331 single base substitution A G 3_prime_UTR_variant BRCA-EU 10 93274331 93274331 single base substitution A G downstream_gene_variant BRCA-EU 10 93274528 93274528 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 10 93274528 93274528 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 93274532 93274532 single base substitution T A 3_prime_UTR_variant BRCA-EU 10 93274532 93274532 single base substitution T A downstream_gene_variant BRCA-EU 10 93276190 93276190 single base substitution G A downstream_gene_variant BRCA-EU 10 93278010 93278010 single base substitution C T downstream_gene_variant BRCA-EU 10 93278408 93278408 single base substitution G C downstream_gene_variant BRCA-FR 10 93174778 93174778 single base substitution G C intron_variant BRCA-FR 10 93179041 93179041 single base substitution C A intron_variant BRCA-FR 10 93196117 93196117 single base substitution C T intron_variant BRCA-FR 10 93199290 93199290 single base substitution T C intron_variant BRCA-FR 10 93211355 93211355 single base substitution C G intron_variant BRCA-FR 10 93236956 93236956 single base substitution A C intron_variant BRCA-FR 10 93240492 93240492 single base substitution C G intron_variant BRCA-FR 10 93240492 93240492 single base substitution C G upstream_gene_variant BRCA-FR 10 93251374 93251374 single base substitution G A downstream_gene_variant BRCA-FR 10 93251374 93251374 single base substitution G A intron_variant BRCA-FR 10 93255592 93255592 single base substitution G C intron_variant BRCA-FR 10 93256803 93256803 single base substitution G A intron_variant BRCA-FR 10 93263021 93263021 single base substitution G C intron_variant BRCA-FR 10 93263647 93263647 single base substitution G C intron_variant BRCA-FR 10 93268763 93268763 single base substitution C A intron_variant BRCA-FR 10 93278794 93278794 single base substitution T A downstream_gene_variant BRCA-UK 10 93208915 93208915 single base substitution G A intron_variant BRCA-UK 10 93209516 93209516 single base substitution G C intron_variant BRCA-UK 10 93254154 93254154 single base substitution G C downstream_gene_variant BRCA-UK 10 93254154 93254154 single base substitution G C intron_variant BRCA-UK 10 93258635 93258635 single base substitution C G missense_variant Q177E 529C>G BRCA-UK 10 93258635 93258635 single base substitution C G missense_variant Q238E 712C>G BRCA-UK 10 93258635 93258635 single base substitution C G missense_variant Q588E 1762C>G BRCA-UK 10 93258635 93258635 single base substitution C G missense_variant Q592E 1774C>G BRCA-US 10 93220311 93220311 single base substitution G A synonymous_variant V132V 396G>A BRCA-US 10 93220311 93220311 single base substitution G A upstream_gene_variant BRCA-US 10 93240885 93240885 single base substitution A T 5_prime_UTR_variant BRCA-US 10 93240885 93240885 single base substitution A T missense_variant I234L 700A>T BRCA-US 10 93240885 93240885 single base substitution A T upstream_gene_variant BRCA-US 10 93247499 93247499 single base substitution G C exon_variant BRCA-US 10 93247499 93247499 single base substitution G C intron_variant BRCA-US 10 93247499 93247499 single base substitution G C missense_variant Q35H 105G>C BRCA-US 10 93247499 93247499 single base substitution G C missense_variant Q385H 1155G>C BRCA-US 10 93247499 93247499 single base substitution G C missense_variant Q389H 1167G>C BRCA-US 10 93256090 93256090 single base substitution C T synonymous_variant I136I 408C>T BRCA-US 10 93256090 93256090 single base substitution C T synonymous_variant I197I 591C>T BRCA-US 10 93256090 93256090 single base substitution C T synonymous_variant I547I 1641C>T BRCA-US 10 93256090 93256090 single base substitution C T synonymous_variant I551I 1653C>T BRCA-US 10 93257913 93257915 deletion of <=200bp GAA - inframe_deletion E166 BRCA-US 10 93257913 93257915 deletion of <=200bp GAA - inframe_deletion E227 BRCA-US 10 93257913 93257915 deletion of <=200bp GAA - inframe_deletion E577 BRCA-US 10 93257913 93257915 deletion of <=200bp GAA - inframe_deletion E581 BTCA-JP 10 93240874 93240874 single base substitution G T 5_prime_UTR_variant BTCA-JP 10 93240874 93240874 single base substitution G T missense_variant R230I 689G>T BTCA-JP 10 93240874 93240874 single base substitution G T upstream_gene_variant BTCA-JP 10 93247394 93247394 deletion of <=200bp A - exon_variant BTCA-JP 10 93247394 93247394 deletion of <=200bp A - intron_variant CESC-US 10 93249462 93249462 single base substitution G C exon_variant CESC-US 10 93249462 93249462 single base substitution G C intron_variant CESC-US 10 93261075 93261075 single base substitution G A missense_variant E321K 961G>A CESC-US 10 93261075 93261075 single base substitution G A missense_variant E382K 1144G>A CESC-US 10 93261075 93261075 single base substitution G A missense_variant E732K 2194G>A CESC-US 10 93261075 93261075 single base substitution G A missense_variant E736K 2206G>A CLLE-ES 10 93170105 93170105 single base substitution C T 5_prime_UTR_variant CLLE-ES 10 93170172 93170172 single base substitution G A 5_prime_UTR_variant CLLE-ES 10 93215062 93215062 single base substitution A G intron_variant CLLE-ES 10 93220576 93220576 single base substitution A T intron_variant CLLE-ES 10 93220576 93220576 single base substitution A T upstream_gene_variant CLLE-ES 10 93261803 93261803 single base substitution A T intron_variant CLLE-ES 10 93265471 93265471 single base substitution C T intron_variant COAD-US 10 93170250 93170250 single base substitution C G missense_variant P19A 55C>G COAD-US 10 93220255 93220255 single base substitution G A missense_variant E114K 340G>A COAD-US 10 93220255 93220255 single base substitution G A upstream_gene_variant COAD-US 10 93221018 93221018 single base substitution G A missense_variant V139I 415G>A COAD-US 10 93221018 93221018 single base substitution G A upstream_gene_variant COAD-US 10 93221093 93221093 single base substitution G T stop_gained E164* 490G>T COAD-US 10 93221093 93221093 single base substitution G T upstream_gene_variant COAD-US 10 93252237 93252237 single base substitution T G downstream_gene_variant COAD-US 10 93252237 93252237 single base substitution T G missense_variant D126E 378T>G COAD-US 10 93252237 93252237 single base substitution T G missense_variant D476E 1428T>G COAD-US 10 93252237 93252237 single base substitution T G missense_variant D480E 1440T>G COAD-US 10 93252237 93252237 single base substitution T G missense_variant D65E 195T>G COCA-CN 10 93172387 93172387 single base substitution T A intron_variant COCA-CN 10 93184985 93184985 single base substitution A C intron_variant COCA-CN 10 93185171 93185171 single base substitution A C splice_region_variant COCA-CN 10 93185177 93185177 single base substitution T G intron_variant COCA-CN 10 93188678 93188678 single base substitution C A intron_variant COCA-CN 10 93189513 93189513 single base substitution G C intron_variant COCA-CN 10 93200109 93200109 single base substitution C T intron_variant COCA-CN 10 93221904 93221904 single base substitution A C 5_prime_UTR_variant COCA-CN 10 93221904 93221904 single base substitution A C missense_variant K188T 563A>C COCA-CN 10 93238000 93238000 single base substitution A C 5_prime_UTR_variant COCA-CN 10 93238000 93238000 single base substitution A C missense_variant S215R 643A>C COCA-CN 10 93240856 93240856 single base substitution G A 5_prime_UTR_variant COCA-CN 10 93240856 93240856 single base substitution G A missense_variant R224Q 671G>A COCA-CN 10 93240856 93240856 single base substitution G A upstream_gene_variant COCA-CN 10 93243999 93243999 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 10 93243999 93243999 single base substitution C A exon_variant COCA-CN 10 93243999 93243999 single base substitution C A intron_variant COCA-CN 10 93250931 93250931 single base substitution A G downstream_gene_variant COCA-CN 10 93250931 93250931 single base substitution A G intron_variant COCA-CN 10 93257924 93257924 single base substitution C T synonymous_variant F169F 507C>T COCA-CN 10 93257924 93257924 single base substitution C T synonymous_variant F230F 690C>T COCA-CN 10 93257924 93257924 single base substitution C T synonymous_variant F580F 1740C>T COCA-CN 10 93257924 93257924 single base substitution C T synonymous_variant F584F 1752C>T COCA-CN 10 93272642 93272642 single base substitution G A 3_prime_UTR_variant EOPC-DE 10 93216502 93216502 single base substitution C T intron_variant ESAD-UK 10 93166009 93166009 single base substitution T A upstream_gene_variant ESAD-UK 10 93166980 93166987 deletion of <=200bp TTTATTTT - upstream_gene_variant ESAD-UK 10 93167300 93167300 single base substitution A C upstream_gene_variant ESAD-UK 10 93167408 93167408 single base substitution C T upstream_gene_variant ESAD-UK 10 93167592 93167592 single base substitution G A upstream_gene_variant ESAD-UK 10 93171917 93171917 single base substitution C G intron_variant ESAD-UK 10 93172388 93172388 single base substitution A T intron_variant ESAD-UK 10 93172896 93172896 single base substitution A T intron_variant ESAD-UK 10 93177585 93177585 single base substitution G A intron_variant ESAD-UK 10 93177929 93177929 single base substitution C A intron_variant ESAD-UK 10 93178541 93178541 single base substitution A T intron_variant ESAD-UK 10 93179603 93179603 single base substitution C A intron_variant ESAD-UK 10 93179994 93179994 single base substitution G T intron_variant ESAD-UK 10 93183454 93183454 single base substitution A G intron_variant ESAD-UK 10 93184492 93184492 single base substitution T C intron_variant ESAD-UK 10 93191535 93191535 single base substitution C G intron_variant ESAD-UK 10 93191862 93191862 single base substitution T G intron_variant ESAD-UK 10 93192741 93192741 single base substitution C T intron_variant ESAD-UK 10 93194508 93194508 single base substitution A G intron_variant ESAD-UK 10 93195347 93195347 single base substitution C T intron_variant ESAD-UK 10 93196299 93196299 single base substitution T C intron_variant ESAD-UK 10 93197713 93197713 single base substitution A T intron_variant ESAD-UK 10 93198898 93198898 single base substitution A C intron_variant ESAD-UK 10 93213272 93213272 single base substitution G A intron_variant ESAD-UK 10 93213866 93213866 single base substitution A G intron_variant ESAD-UK 10 93214838 93214838 single base substitution A C intron_variant ESAD-UK 10 93217263 93217263 single base substitution T G intron_variant ESAD-UK 10 93217263 93217263 single base substitution T G upstream_gene_variant ESAD-UK 10 93218541 93218541 deletion of <=200bp A - intron_variant ESAD-UK 10 93218541 93218541 deletion of <=200bp A - upstream_gene_variant ESAD-UK 10 93218541 93218541 insertion of <=200bp - A intron_variant ESAD-UK 10 93218541 93218541 insertion of <=200bp - A upstream_gene_variant ESAD-UK 10 93218640 93218640 single base substitution T C intron_variant ESAD-UK 10 93218640 93218640 single base substitution T C upstream_gene_variant ESAD-UK 10 93220016 93220016 single base substitution A C intron_variant ESAD-UK 10 93220016 93220016 single base substitution A C upstream_gene_variant ESAD-UK 10 93222871 93222871 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 93222871 93222871 single base substitution G A intron_variant ESAD-UK 10 93222960 93222960 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 93222960 93222960 single base substitution G A intron_variant ESAD-UK 10 93223335 93223335 single base substitution C G 3_prime_UTR_variant ESAD-UK 10 93223335 93223335 single base substitution C G intron_variant ESAD-UK 10 93224123 93224123 deletion of <=200bp A - downstream_gene_variant ESAD-UK 10 93224123 93224123 deletion of <=200bp A - intron_variant ESAD-UK 10 93224505 93224505 single base substitution G A downstream_gene_variant ESAD-UK 10 93224505 93224505 single base substitution G A intron_variant ESAD-UK 10 93225365 93225365 single base substitution C G downstream_gene_variant ESAD-UK 10 93225365 93225365 single base substitution C G intron_variant ESAD-UK 10 93229643 93229643 single base substitution A C intron_variant ESAD-UK 10 93230204 93230204 single base substitution A T intron_variant ESAD-UK 10 93230562 93230562 deletion of <=200bp A - intron_variant ESAD-UK 10 93232181 93232181 single base substitution A C intron_variant ESAD-UK 10 93232651 93232651 single base substitution G T intron_variant ESAD-UK 10 93237958 93237958 single base substitution C T missense_variant P201S 601C>T ESAD-UK 10 93237958 93237958 single base substitution C T splice_region_variant ESAD-UK 10 93238588 93238588 insertion of <=200bp - A intron_variant ESAD-UK 10 93239222 93239222 single base substitution T A intron_variant ESAD-UK 10 93239222 93239222 single base substitution T A upstream_gene_variant ESAD-UK 10 93239695 93239695 single base substitution A C intron_variant ESAD-UK 10 93239695 93239695 single base substitution A C upstream_gene_variant ESAD-UK 10 93240371 93240371 single base substitution A G intron_variant ESAD-UK 10 93240371 93240371 single base substitution A G upstream_gene_variant ESAD-UK 10 93240740 93240740 insertion of <=200bp - T intron_variant ESAD-UK 10 93240740 93240740 insertion of <=200bp - T upstream_gene_variant ESAD-UK 10 93241078 93241078 single base substitution G C intron_variant ESAD-UK 10 93241078 93241078 single base substitution G C upstream_gene_variant ESAD-UK 10 93241726 93241726 single base substitution A G intron_variant ESAD-UK 10 93241726 93241726 single base substitution A G upstream_gene_variant ESAD-UK 10 93244587 93244587 insertion of <=200bp - A intron_variant ESAD-UK 10 93244699 93244699 single base substitution C T intron_variant ESAD-UK 10 93245287 93245287 single base substitution C T exon_variant ESAD-UK 10 93245287 93245287 single base substitution C T intron_variant ESAD-UK 10 93247481 93247481 deletion of <=200bp A - exon_variant ESAD-UK 10 93247481 93247481 deletion of <=200bp A - frameshift_variant A29 ESAD-UK 10 93247481 93247481 deletion of <=200bp A - frameshift_variant A379 ESAD-UK 10 93247481 93247481 deletion of <=200bp A - frameshift_variant A383 ESAD-UK 10 93247481 93247481 deletion of <=200bp A - intron_variant ESAD-UK 10 93247982 93247982 single base substitution G A exon_variant ESAD-UK 10 93247982 93247982 single base substitution G A intron_variant ESAD-UK 10 93248869 93248869 insertion of <=200bp - T exon_variant ESAD-UK 10 93248869 93248869 insertion of <=200bp - T intron_variant ESAD-UK 10 93248969 93248969 single base substitution A C exon_variant ESAD-UK 10 93248969 93248969 single base substitution A C intron_variant ESAD-UK 10 93251619 93251619 single base substitution A G downstream_gene_variant ESAD-UK 10 93251619 93251619 single base substitution A G intron_variant ESAD-UK 10 93251674 93251674 single base substitution G A downstream_gene_variant ESAD-UK 10 93251674 93251674 single base substitution G A intron_variant ESAD-UK 10 93251815 93251815 single base substitution A T downstream_gene_variant ESAD-UK 10 93251815 93251815 single base substitution A T intron_variant ESAD-UK 10 93253553 93253553 single base substitution A T downstream_gene_variant ESAD-UK 10 93253553 93253553 single base substitution A T intron_variant ESAD-UK 10 93253735 93253735 single base substitution T G downstream_gene_variant ESAD-UK 10 93253735 93253735 single base substitution T G intron_variant ESAD-UK 10 93254337 93254337 single base substitution A C downstream_gene_variant ESAD-UK 10 93254337 93254337 single base substitution A C intron_variant ESAD-UK 10 93254502 93254502 single base substitution G T downstream_gene_variant ESAD-UK 10 93254502 93254502 single base substitution G T intron_variant ESAD-UK 10 93257619 93257619 single base substitution G C intron_variant ESAD-UK 10 93257819 93257819 single base substitution T G intron_variant ESAD-UK 10 93258473 93258473 single base substitution G A intron_variant ESAD-UK 10 93260455 93260455 single base substitution C G intron_variant ESAD-UK 10 93269033 93269033 deletion of <=200bp A - intron_variant ESAD-UK 10 93269041 93269041 single base substitution T A intron_variant ESAD-UK 10 93269259 93269259 single base substitution C T intron_variant ESAD-UK 10 93269456 93269456 single base substitution C T intron_variant ESAD-UK 10 93270217 93270217 single base substitution C A intron_variant ESAD-UK 10 93273265 93273265 insertion of <=200bp - T 3_prime_UTR_variant ESAD-UK 10 93273265 93273265 insertion of <=200bp - T downstream_gene_variant ESAD-UK 10 93273274 93273274 single base substitution A T 3_prime_UTR_variant ESAD-UK 10 93273274 93273274 single base substitution A T downstream_gene_variant ESAD-UK 10 93273331 93273331 insertion of <=200bp - T 3_prime_UTR_variant ESAD-UK 10 93273331 93273331 insertion of <=200bp - T downstream_gene_variant ESAD-UK 10 93273738 93273738 single base substitution C G 3_prime_UTR_variant ESAD-UK 10 93273738 93273738 single base substitution C G downstream_gene_variant ESAD-UK 10 93274066 93274066 single base substitution T G 3_prime_UTR_variant ESAD-UK 10 93274066 93274066 single base substitution T G downstream_gene_variant ESAD-UK 10 93274173 93274174 deletion of <=200bp CT - 3_prime_UTR_variant ESAD-UK 10 93274173 93274174 deletion of <=200bp CT - downstream_gene_variant ESAD-UK 10 93275380 93275380 single base substitution G A downstream_gene_variant ESAD-UK 10 93275472 93275472 single base substitution G A downstream_gene_variant ESAD-UK 10 93276021 93276021 single base substitution G A downstream_gene_variant ESAD-UK 10 93278756 93278756 insertion of <=200bp - T downstream_gene_variant ESAD-UK 10 93279137 93279137 single base substitution T C downstream_gene_variant ESCA-CN 10 93273081 93273081 single base substitution T G 3_prime_UTR_variant ESCA-CN 10 93273081 93273081 single base substitution T G downstream_gene_variant GBM-US 10 93244394 93244394 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant GBM-US 10 93244394 93244394 single base substitution A G exon_variant GBM-US 10 93244394 93244394 single base substitution A G missense_variant K318E 952A>G GBM-US 10 93244394 93244394 single base substitution A G missense_variant K322E 964A>G KIRC-US 10 93185116 93185116 single base substitution G C missense_variant A73P 217G>C KIRC-US 10 93220253 93220253 single base substitution C T missense_variant S113F 338C>T KIRC-US 10 93220253 93220253 single base substitution C T upstream_gene_variant KIRC-US 10 93258806 93258806 single base substitution G A missense_variant V206I 616G>A KIRC-US 10 93258806 93258806 single base substitution G A missense_variant V267I 799G>A KIRC-US 10 93258806 93258806 single base substitution G A missense_variant V617I 1849G>A KIRC-US 10 93258806 93258806 single base substitution G A missense_variant V621I 1861G>A KIRP-US 10 93252242 93252242 insertion of <=200bp - T downstream_gene_variant KIRP-US 10 93252242 93252242 insertion of <=200bp - T splice_donor_variant LAML-KR 10 93267358 93267358 single base substitution G A intron_variant LAML-KR 10 93268074 93268074 single base substitution C T intron_variant LICA-FR 10 93167054 93167054 single base substitution G A upstream_gene_variant LICA-FR 10 93188160 93188160 single base substitution G A intron_variant LICA-FR 10 93188994 93188994 single base substitution C T intron_variant LICA-FR 10 93189033 93189033 single base substitution G T intron_variant LICA-FR 10 93189572 93189572 single base substitution C T intron_variant LICA-FR 10 93189584 93189584 single base substitution C A intron_variant LICA-FR 10 93189885 93189885 single base substitution C T intron_variant LICA-FR 10 93190434 93190452 deletion of <=200bp TTTTATCAGAGACTAGGAT - intron_variant LICA-FR 10 93256081 93256081 single base substitution A G synonymous_variant P133P 399A>G LICA-FR 10 93256081 93256081 single base substitution A G synonymous_variant P194P 582A>G LICA-FR 10 93256081 93256081 single base substitution A G synonymous_variant P544P 1632A>G LICA-FR 10 93256081 93256081 single base substitution A G synonymous_variant P548P 1644A>G LICA-FR 10 93265422 93265422 single base substitution T G intron_variant LICA-FR 10 93266230 93266230 single base substitution C A intron_variant LICA-FR 10 93266259 93266259 single base substitution G A intron_variant LICA-FR 10 93266435 93266435 single base substitution C T intron_variant LICA-FR 10 93266648 93266648 single base substitution A C intron_variant LICA-FR 10 93266649 93266649 single base substitution C T intron_variant LICA-FR 10 93267720 93267720 single base substitution T C intron_variant LICA-FR 10 93267895 93267895 single base substitution C G intron_variant LICA-FR 10 93267902 93267902 single base substitution G A intron_variant LICA-FR 10 93267993 93267993 single base substitution C A intron_variant LIHC-US 10 93252211 93252211 single base substitution C G downstream_gene_variant LIHC-US 10 93252211 93252211 single base substitution C G missense_variant L118V 352C>G LIHC-US 10 93252211 93252211 single base substitution C G missense_variant L468V 1402C>G LIHC-US 10 93252211 93252211 single base substitution C G missense_variant L472V 1414C>G LIHC-US 10 93252211 93252211 single base substitution C G missense_variant L57V 169C>G LINC-JP 10 93170165 93170165 single base substitution G T 5_prime_UTR_variant LINC-JP 10 93171444 93171444 single base substitution A G intron_variant LINC-JP 10 93175804 93175804 single base substitution T A intron_variant LINC-JP 10 93192740 93192740 single base substitution G A intron_variant LINC-JP 10 93220880 93220880 single base substitution A G intron_variant LINC-JP 10 93220880 93220880 single base substitution A G upstream_gene_variant LINC-JP 10 93222132 93222132 single base substitution G C 3_prime_UTR_variant LINC-JP 10 93222132 93222132 single base substitution G C intron_variant LINC-JP 10 93234125 93234125 single base substitution A G intron_variant LINC-JP 10 93242775 93242775 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 10 93242775 93242775 single base substitution C T stop_gained R255* 763C>T LINC-JP 10 93242775 93242775 single base substitution C T upstream_gene_variant LINC-JP 10 93242927 93242927 single base substitution A G intron_variant LINC-JP 10 93242927 93242927 single base substitution A G upstream_gene_variant LINC-JP 10 93251108 93251108 single base substitution T C downstream_gene_variant LINC-JP 10 93251108 93251108 single base substitution T C intron_variant LINC-JP 10 93253168 93253168 deletion of <=200bp T - downstream_gene_variant LINC-JP 10 93253168 93253168 deletion of <=200bp T - intron_variant LINC-JP 10 93253376 93253376 single base substitution T C downstream_gene_variant LINC-JP 10 93253376 93253376 single base substitution T C intron_variant LINC-JP 10 93257062 93257062 single base substitution C T intron_variant LINC-JP 10 93257963 93257963 single base substitution T A intron_variant LINC-JP 10 93260475 93260475 single base substitution T C intron_variant LINC-JP 10 93261882 93261882 single base substitution T G intron_variant LIRI-JP 10 93165531 93165531 single base substitution T C upstream_gene_variant LIRI-JP 10 93168366 93168366 insertion of <=200bp - A upstream_gene_variant LIRI-JP 10 93171023 93171023 single base substitution A G intron_variant LIRI-JP 10 93172284 93172284 single base substitution T G intron_variant LIRI-JP 10 93173907 93173907 single base substitution G T intron_variant LIRI-JP 10 93174462 93174462 single base substitution G T intron_variant LIRI-JP 10 93175216 93175216 single base substitution A G intron_variant LIRI-JP 10 93185528 93185528 single base substitution T A intron_variant LIRI-JP 10 93186050 93186050 single base substitution T C intron_variant LIRI-JP 10 93194046 93194046 single base substitution C T intron_variant LIRI-JP 10 93194790 93194790 single base substitution G A intron_variant LIRI-JP 10 93198503 93198503 single base substitution C T intron_variant LIRI-JP 10 93199883 93199883 single base substitution G A intron_variant LIRI-JP 10 93200201 93200201 single base substitution A G intron_variant LIRI-JP 10 93209358 93209358 single base substitution A T intron_variant LIRI-JP 10 93209939 93209939 single base substitution A G intron_variant LIRI-JP 10 93210811 93210811 single base substitution A G intron_variant LIRI-JP 10 93212237 93212237 single base substitution T C intron_variant LIRI-JP 10 93212492 93212492 single base substitution C A intron_variant LIRI-JP 10 93216891 93216891 single base substitution T G intron_variant LIRI-JP 10 93217522 93217522 single base substitution C T intron_variant LIRI-JP 10 93217522 93217522 single base substitution C T upstream_gene_variant LIRI-JP 10 93218823 93218823 single base substitution T C intron_variant LIRI-JP 10 93218823 93218823 single base substitution T C upstream_gene_variant LIRI-JP 10 93220248 93220248 single base substitution A G synonymous_variant S111S 333A>G LIRI-JP 10 93220248 93220248 single base substitution A G upstream_gene_variant LIRI-JP 10 93220453 93220454 deletion of <=200bp TA - intron_variant LIRI-JP 10 93220453 93220454 deletion of <=200bp TA - upstream_gene_variant LIRI-JP 10 93225442 93225442 single base substitution A G downstream_gene_variant LIRI-JP 10 93225442 93225442 single base substitution A G intron_variant LIRI-JP 10 93227654 93227654 single base substitution C T downstream_gene_variant LIRI-JP 10 93227654 93227654 single base substitution C T intron_variant LIRI-JP 10 93247676 93247676 single base substitution A T exon_variant LIRI-JP 10 93247676 93247676 single base substitution A T intron_variant LIRI-JP 10 93248499 93248499 deletion of <=200bp A - exon_variant LIRI-JP 10 93248499 93248499 deletion of <=200bp A - intron_variant LIRI-JP 10 93249921 93249921 single base substitution A G downstream_gene_variant LIRI-JP 10 93249921 93249921 single base substitution A G intron_variant LIRI-JP 10 93250248 93250248 single base substitution A G downstream_gene_variant LIRI-JP 10 93250248 93250248 single base substitution A G intron_variant LIRI-JP 10 93252284 93252284 single base substitution A G downstream_gene_variant LIRI-JP 10 93252284 93252284 single base substitution A G intron_variant LIRI-JP 10 93252525 93252525 single base substitution A G downstream_gene_variant LIRI-JP 10 93252525 93252525 single base substitution A G intron_variant LIRI-JP 10 93252531 93252531 single base substitution A C downstream_gene_variant LIRI-JP 10 93252531 93252531 single base substitution A C intron_variant LIRI-JP 10 93253905 93253905 single base substitution G T downstream_gene_variant LIRI-JP 10 93253905 93253905 single base substitution G T intron_variant LIRI-JP 10 93259458 93259458 single base substitution T C intron_variant LIRI-JP 10 93260211 93260211 deletion of <=200bp A - intron_variant LIRI-JP 10 93260702 93260702 single base substitution A G intron_variant LIRI-JP 10 93260824 93260824 single base substitution T G intron_variant LIRI-JP 10 93269388 93269388 single base substitution A G intron_variant LIRI-JP 10 93272388 93272388 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 93277671 93277671 single base substitution T C downstream_gene_variant LIRI-JP 10 93277972 93277972 single base substitution T C downstream_gene_variant LUSC-KR 10 93165676 93165676 single base substitution A G upstream_gene_variant LUSC-KR 10 93168693 93168693 single base substitution G A upstream_gene_variant LUSC-KR 10 93172577 93172577 single base substitution G T intron_variant LUSC-KR 10 93175120 93175120 single base substitution A T intron_variant LUSC-KR 10 93182236 93182236 single base substitution G T intron_variant LUSC-KR 10 93187850 93187850 single base substitution A G intron_variant LUSC-KR 10 93187961 93187961 single base substitution T C intron_variant LUSC-KR 10 93188063 93188063 single base substitution A T intron_variant LUSC-KR 10 93188072 93188072 single base substitution C T intron_variant LUSC-KR 10 93191342 93191342 single base substitution A G intron_variant LUSC-KR 10 93192121 93192121 single base substitution T C intron_variant LUSC-KR 10 93193879 93193879 single base substitution G A intron_variant LUSC-KR 10 93203202 93203202 single base substitution C T intron_variant LUSC-KR 10 93204636 93204636 single base substitution G A intron_variant LUSC-KR 10 93219454 93219454 single base substitution G C intron_variant LUSC-KR 10 93219454 93219454 single base substitution G C upstream_gene_variant LUSC-KR 10 93226318 93226318 single base substitution A C downstream_gene_variant LUSC-KR 10 93226318 93226318 single base substitution A C intron_variant LUSC-KR 10 93227405 93227405 single base substitution C T downstream_gene_variant LUSC-KR 10 93227405 93227405 single base substitution C T intron_variant LUSC-KR 10 93232502 93232502 single base substitution T G intron_variant LUSC-KR 10 93232926 93232926 single base substitution G C intron_variant LUSC-KR 10 93239793 93239793 single base substitution A G intron_variant LUSC-KR 10 93239793 93239793 single base substitution A G upstream_gene_variant LUSC-KR 10 93241614 93241614 single base substitution A G intron_variant LUSC-KR 10 93241614 93241614 single base substitution A G upstream_gene_variant LUSC-KR 10 93248886 93248886 single base substitution A G exon_variant LUSC-KR 10 93248886 93248886 single base substitution A G intron_variant LUSC-KR 10 93249704 93249704 single base substitution A G exon_variant LUSC-KR 10 93249704 93249704 single base substitution A G intron_variant LUSC-KR 10 93250088 93250088 single base substitution G C downstream_gene_variant LUSC-KR 10 93250088 93250088 single base substitution G C intron_variant LUSC-KR 10 93264572 93264572 single base substitution C A intron_variant LUSC-KR 10 93264592 93264592 single base substitution C A intron_variant LUSC-KR 10 93264852 93264852 single base substitution C T intron_variant LUSC-KR 10 93264903 93264903 single base substitution C A intron_variant LUSC-KR 10 93266520 93266520 single base substitution A G intron_variant LUSC-KR 10 93267452 93267452 single base substitution C A intron_variant LUSC-KR 10 93267561 93267561 single base substitution G A intron_variant LUSC-KR 10 93267691 93267691 single base substitution G A intron_variant LUSC-KR 10 93267868 93267868 single base substitution A G intron_variant LUSC-KR 10 93267902 93267902 single base substitution G A intron_variant LUSC-KR 10 93268074 93268074 single base substitution C T intron_variant LUSC-KR 10 93268125 93268125 single base substitution A C intron_variant LUSC-KR 10 93270377 93270377 single base substitution A G intron_variant LUSC-KR 10 93276574 93276574 single base substitution A G downstream_gene_variant LUSC-KR 10 93277799 93277799 single base substitution T G downstream_gene_variant LUSC-US 10 93244288 93244288 single base substitution A G 5_prime_UTR_variant LUSC-US 10 93244288 93244288 single base substitution A G exon_variant LUSC-US 10 93244288 93244288 single base substitution A G synonymous_variant Q282Q 846A>G LUSC-US 10 93244288 93244288 single base substitution A G synonymous_variant Q286Q 858A>G LUSC-US 10 93252127 93252127 single base substitution G T downstream_gene_variant LUSC-US 10 93252127 93252127 single base substitution G T missense_variant D29Y 85G>T LUSC-US 10 93252127 93252127 single base substitution G T missense_variant D440Y 1318G>T LUSC-US 10 93252127 93252127 single base substitution G T missense_variant D444Y 1330G>T LUSC-US 10 93252127 93252127 single base substitution G T missense_variant D90Y 268G>T MALY-DE 10 93166745 93166745 deletion of <=200bp T - upstream_gene_variant MALY-DE 10 93173819 93173819 single base substitution G A intron_variant MALY-DE 10 93174951 93174952 deletion of <=200bp GT - intron_variant MALY-DE 10 93178990 93178990 single base substitution T C intron_variant MALY-DE 10 93193115 93193115 insertion of <=200bp - T intron_variant MALY-DE 10 93204897 93204897 single base substitution G A intron_variant MALY-DE 10 93212481 93212481 insertion of <=200bp - A intron_variant MALY-DE 10 93213537 93213537 insertion of <=200bp - T intron_variant MALY-DE 10 93214332 93214332 deletion of <=200bp T - intron_variant MALY-DE 10 93217219 93217219 single base substitution A G intron_variant MALY-DE 10 93217219 93217219 single base substitution A G upstream_gene_variant MALY-DE 10 93222729 93222729 single base substitution T A 3_prime_UTR_variant MALY-DE 10 93222729 93222729 single base substitution T A intron_variant MALY-DE 10 93227944 93227944 single base substitution A C downstream_gene_variant MALY-DE 10 93227944 93227944 single base substitution A C intron_variant MALY-DE 10 93233988 93233988 single base substitution G T intron_variant MALY-DE 10 93235652 93235652 single base substitution C T intron_variant MALY-DE 10 93251330 93251330 single base substitution T G downstream_gene_variant MALY-DE 10 93251330 93251330 single base substitution T G intron_variant MALY-DE 10 93258952 93258952 single base substitution T C intron_variant MALY-DE 10 93276388 93276388 single base substitution A C downstream_gene_variant MELA-AU 10 93166325 93166325 single base substitution G A upstream_gene_variant MELA-AU 10 93167873 93167873 single base substitution G A upstream_gene_variant MELA-AU 10 93168412 93168412 single base substitution G A upstream_gene_variant MELA-AU 10 93172387 93172387 single base substitution T A intron_variant MELA-AU 10 93173091 93173091 single base substitution C T intron_variant MELA-AU 10 93173895 93173895 single base substitution C A intron_variant MELA-AU 10 93178730 93178730 single base substitution T C intron_variant MELA-AU 10 93179237 93179237 single base substitution G A intron_variant MELA-AU 10 93179584 93179584 single base substitution G A intron_variant MELA-AU 10 93185365 93185365 single base substitution C T intron_variant MELA-AU 10 93185813 93185813 single base substitution A T intron_variant MELA-AU 10 93185910 93185910 single base substitution G A intron_variant MELA-AU 10 93187567 93187567 single base substitution T C intron_variant MELA-AU 10 93189366 93189366 single base substitution G A intron_variant MELA-AU 10 93190651 93190651 single base substitution C T intron_variant MELA-AU 10 93190788 93190788 single base substitution C T intron_variant MELA-AU 10 93190884 93190884 single base substitution C T intron_variant MELA-AU 10 93191628 93191628 single base substitution C T intron_variant MELA-AU 10 93191792 93191792 single base substitution C T intron_variant MELA-AU 10 93192375 93192375 single base substitution A G intron_variant MELA-AU 10 93192886 93192886 single base substitution G A intron_variant MELA-AU 10 93193285 93193285 single base substitution C T intron_variant MELA-AU 10 93193352 93193352 single base substitution A T intron_variant MELA-AU 10 93194298 93194298 single base substitution C T intron_variant MELA-AU 10 93194368 93194368 single base substitution G A intron_variant MELA-AU 10 93195614 93195615 multiple base substitution (>=2bp and <=200bp) TA GT intron_variant MELA-AU 10 93195775 93195775 single base substitution C T intron_variant MELA-AU 10 93196450 93196450 single base substitution T C intron_variant MELA-AU 10 93198333 93198333 single base substitution C T intron_variant MELA-AU 10 93198400 93198400 single base substitution G A intron_variant MELA-AU 10 93198623 93198623 single base substitution T C intron_variant MELA-AU 10 93199094 93199094 single base substitution C T intron_variant MELA-AU 10 93199098 93199098 single base substitution C T intron_variant MELA-AU 10 93200073 93200073 single base substitution C T intron_variant MELA-AU 10 93203224 93203224 single base substitution G A intron_variant MELA-AU 10 93203332 93203332 single base substitution G A intron_variant MELA-AU 10 93203346 93203346 single base substitution C T intron_variant MELA-AU 10 93204100 93204100 single base substitution G A intron_variant MELA-AU 10 93204187 93204187 single base substitution G A intron_variant MELA-AU 10 93204833 93204833 single base substitution G A intron_variant MELA-AU 10 93204878 93204878 single base substitution G A intron_variant MELA-AU 10 93204976 93204976 single base substitution G A intron_variant MELA-AU 10 93205524 93205524 single base substitution C G intron_variant MELA-AU 10 93205593 93205593 single base substitution G A intron_variant MELA-AU 10 93205732 93205732 single base substitution G A intron_variant MELA-AU 10 93205777 93205777 single base substitution G A intron_variant MELA-AU 10 93205855 93205856 multiple base substitution (>=2bp and <=200bp) GG TA intron_variant MELA-AU 10 93205876 93205876 single base substitution G A intron_variant MELA-AU 10 93210046 93210046 single base substitution T C intron_variant MELA-AU 10 93210114 93210114 single base substitution C T intron_variant MELA-AU 10 93211567 93211567 single base substitution C A intron_variant MELA-AU 10 93212615 93212615 single base substitution G T intron_variant MELA-AU 10 93214249 93214249 single base substitution C T intron_variant MELA-AU 10 93214826 93214826 single base substitution C T intron_variant MELA-AU 10 93217395 93217395 single base substitution G A intron_variant MELA-AU 10 93217395 93217395 single base substitution G A upstream_gene_variant MELA-AU 10 93217430 93217430 single base substitution G A intron_variant MELA-AU 10 93217430 93217430 single base substitution G A upstream_gene_variant MELA-AU 10 93218074 93218074 single base substitution T C intron_variant MELA-AU 10 93218074 93218074 single base substitution T C upstream_gene_variant MELA-AU 10 93218665 93218665 single base substitution C T intron_variant MELA-AU 10 93218665 93218665 single base substitution C T upstream_gene_variant MELA-AU 10 93220561 93220561 single base substitution A T intron_variant MELA-AU 10 93220561 93220561 single base substitution A T upstream_gene_variant MELA-AU 10 93221910 93221910 single base substitution T G 5_prime_UTR_variant MELA-AU 10 93221910 93221910 single base substitution T G missense_variant V190G 569T>G MELA-AU 10 93222219 93222219 single base substitution T C 3_prime_UTR_variant MELA-AU 10 93222219 93222219 single base substitution T C intron_variant MELA-AU 10 93223154 93223154 single base substitution G A 3_prime_UTR_variant MELA-AU 10 93223154 93223154 single base substitution G A intron_variant MELA-AU 10 93223381 93223381 single base substitution G A 3_prime_UTR_variant MELA-AU 10 93223381 93223381 single base substitution G A intron_variant MELA-AU 10 93223586 93223586 single base substitution C T downstream_gene_variant MELA-AU 10 93223586 93223586 single base substitution C T intron_variant MELA-AU 10 93224223 93224223 single base substitution C T downstream_gene_variant MELA-AU 10 93224223 93224223 single base substitution C T intron_variant MELA-AU 10 93225452 93225452 single base substitution G A downstream_gene_variant MELA-AU 10 93225452 93225452 single base substitution G A intron_variant MELA-AU 10 93225583 93225583 single base substitution C T downstream_gene_variant MELA-AU 10 93225583 93225583 single base substitution C T intron_variant MELA-AU 10 93226178 93226178 single base substitution T C downstream_gene_variant MELA-AU 10 93226178 93226178 single base substitution T C intron_variant MELA-AU 10 93226984 93226984 single base substitution C T downstream_gene_variant MELA-AU 10 93226984 93226984 single base substitution C T intron_variant MELA-AU 10 93227140 93227140 single base substitution G A downstream_gene_variant MELA-AU 10 93227140 93227140 single base substitution G A intron_variant MELA-AU 10 93227312 93227312 single base substitution G T downstream_gene_variant MELA-AU 10 93227312 93227312 single base substitution G T intron_variant MELA-AU 10 93228431 93228431 single base substitution G A intron_variant MELA-AU 10 93229321 93229321 single base substitution C T intron_variant MELA-AU 10 93231114 93231114 single base substitution C T intron_variant MELA-AU 10 93231354 93231354 single base substitution A G intron_variant MELA-AU 10 93233220 93233220 single base substitution G A intron_variant MELA-AU 10 93233286 93233286 single base substitution C G intron_variant MELA-AU 10 93233908 93233908 single base substitution A G intron_variant MELA-AU 10 93234557 93234557 single base substitution G A intron_variant MELA-AU 10 93235186 93235186 single base substitution A T intron_variant MELA-AU 10 93235790 93235790 single base substitution C T intron_variant MELA-AU 10 93236568 93236568 single base substitution C T intron_variant MELA-AU 10 93236913 93236913 single base substitution C T intron_variant MELA-AU 10 93237929 93237929 single base substitution A T intron_variant MELA-AU 10 93238078 93238078 single base substitution C T intron_variant MELA-AU 10 93239781 93239781 single base substitution T A intron_variant MELA-AU 10 93239781 93239781 single base substitution T A upstream_gene_variant MELA-AU 10 93239787 93239787 single base substitution T G intron_variant MELA-AU 10 93239787 93239787 single base substitution T G upstream_gene_variant MELA-AU 10 93240488 93240488 single base substitution C T intron_variant MELA-AU 10 93240488 93240488 single base substitution C T upstream_gene_variant MELA-AU 10 93241014 93241014 single base substitution G A intron_variant MELA-AU 10 93241014 93241014 single base substitution G A upstream_gene_variant MELA-AU 10 93242398 93242398 single base substitution C T intron_variant MELA-AU 10 93242398 93242398 single base substitution C T upstream_gene_variant MELA-AU 10 93243619 93243619 single base substitution G A intron_variant MELA-AU 10 93243619 93243619 single base substitution G A upstream_gene_variant MELA-AU 10 93244405 93244405 single base substitution T C 5_prime_UTR_variant MELA-AU 10 93244405 93244405 single base substitution T C exon_variant MELA-AU 10 93244405 93244405 single base substitution T C synonymous_variant A321A 963T>C MELA-AU 10 93244405 93244405 single base substitution T C synonymous_variant A325A 975T>C MELA-AU 10 93244516 93244516 single base substitution C T intron_variant MELA-AU 10 93246310 93246310 single base substitution G T exon_variant MELA-AU 10 93246310 93246310 single base substitution G T intron_variant MELA-AU 10 93246881 93246881 single base substitution T A exon_variant MELA-AU 10 93246881 93246881 single base substitution T A intron_variant MELA-AU 10 93248391 93248391 single base substitution C T exon_variant MELA-AU 10 93248391 93248391 single base substitution C T intron_variant MELA-AU 10 93248439 93248439 single base substitution G A exon_variant MELA-AU 10 93248439 93248439 single base substitution G A intron_variant MELA-AU 10 93250045 93250045 single base substitution G A downstream_gene_variant MELA-AU 10 93250045 93250045 single base substitution G A intron_variant MELA-AU 10 93250424 93250425 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 93250424 93250425 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 93251173 93251173 single base substitution C T downstream_gene_variant MELA-AU 10 93251173 93251173 single base substitution C T intron_variant MELA-AU 10 93251185 93251185 single base substitution T C downstream_gene_variant MELA-AU 10 93251185 93251185 single base substitution T C intron_variant MELA-AU 10 93251610 93251610 single base substitution T A downstream_gene_variant MELA-AU 10 93251610 93251610 single base substitution T A intron_variant MELA-AU 10 93251612 93251612 single base substitution T C downstream_gene_variant MELA-AU 10 93251612 93251612 single base substitution T C intron_variant MELA-AU 10 93251846 93251846 single base substitution T A downstream_gene_variant MELA-AU 10 93251846 93251846 single base substitution T A intron_variant MELA-AU 10 93252598 93252598 deletion of <=200bp A - downstream_gene_variant MELA-AU 10 93252598 93252598 deletion of <=200bp A - intron_variant MELA-AU 10 93252934 93252935 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 93252934 93252935 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 93253666 93253666 single base substitution C T downstream_gene_variant MELA-AU 10 93253666 93253666 single base substitution C T intron_variant MELA-AU 10 93254451 93254451 single base substitution A G downstream_gene_variant MELA-AU 10 93254451 93254451 single base substitution A G intron_variant MELA-AU 10 93255188 93255188 single base substitution G A intron_variant MELA-AU 10 93255412 93255412 single base substitution G T intron_variant MELA-AU 10 93256117 93256117 single base substitution T C synonymous_variant C145C 435T>C MELA-AU 10 93256117 93256117 single base substitution T C synonymous_variant C206C 618T>C MELA-AU 10 93256117 93256117 single base substitution T C synonymous_variant C556C 1668T>C MELA-AU 10 93256117 93256117 single base substitution T C synonymous_variant C560C 1680T>C MELA-AU 10 93256551 93256551 single base substitution G A intron_variant MELA-AU 10 93256662 93256662 single base substitution C T intron_variant MELA-AU 10 93256996 93256996 single base substitution G A intron_variant MELA-AU 10 93257099 93257099 single base substitution A T intron_variant MELA-AU 10 93259963 93259963 single base substitution G A intron_variant MELA-AU 10 93261180 93261180 single base substitution C T intron_variant MELA-AU 10 93263700 93263700 single base substitution C T intron_variant MELA-AU 10 93270238 93270238 single base substitution A G intron_variant MELA-AU 10 93270853 93270853 single base substitution G T intron_variant MELA-AU 10 93272606 93272606 single base substitution A G 3_prime_UTR_variant MELA-AU 10 93272643 93272643 single base substitution G T 3_prime_UTR_variant MELA-AU 10 93275023 93275023 single base substitution G A downstream_gene_variant MELA-AU 10 93275175 93275175 single base substitution T G downstream_gene_variant MELA-AU 10 93275732 93275732 single base substitution C T downstream_gene_variant MELA-AU 10 93276799 93276799 single base substitution C T downstream_gene_variant ORCA-IN 10 93173835 93173835 single base substitution G C intron_variant ORCA-IN 10 93176024 93176024 single base substitution G T intron_variant OV-AU 10 93175660 93175660 single base substitution A T intron_variant OV-AU 10 93194523 93194523 single base substitution C G intron_variant OV-AU 10 93205297 93205297 single base substitution G T intron_variant OV-AU 10 93216679 93216679 single base substitution A C intron_variant OV-AU 10 93217723 93217723 single base substitution G C intron_variant OV-AU 10 93217723 93217723 single base substitution G C upstream_gene_variant OV-AU 10 93217934 93217934 single base substitution A T intron_variant OV-AU 10 93217934 93217934 single base substitution A T upstream_gene_variant OV-AU 10 93219484 93219484 single base substitution A G intron_variant OV-AU 10 93219484 93219484 single base substitution A G upstream_gene_variant OV-AU 10 93230745 93230745 single base substitution A G intron_variant OV-AU 10 93230747 93230747 single base substitution G A intron_variant OV-AU 10 93240010 93240010 single base substitution A C intron_variant OV-AU 10 93240010 93240010 single base substitution A C upstream_gene_variant OV-AU 10 93246996 93246996 single base substitution T C exon_variant OV-AU 10 93246996 93246996 single base substitution T C intron_variant OV-AU 10 93249553 93249553 single base substitution A T exon_variant OV-AU 10 93249553 93249553 single base substitution A T intron_variant OV-AU 10 93266850 93266850 single base substitution C T intron_variant OV-AU 10 93270438 93270438 single base substitution G T intron_variant OV-AU 10 93270552 93270552 single base substitution G T intron_variant OV-AU 10 93272726 93272726 single base substitution G C 3_prime_UTR_variant OV-AU 10 93275103 93275103 single base substitution C G downstream_gene_variant PACA-AU 10 93180897 93180897 single base substitution C G intron_variant PACA-AU 10 93181176 93181176 single base substitution G C intron_variant PACA-AU 10 93194562 93194562 single base substitution G A intron_variant PACA-AU 10 93196890 93196890 single base substitution T G intron_variant PACA-AU 10 93197526 93197526 single base substitution C T intron_variant PACA-AU 10 93199422 93199422 single base substitution C A intron_variant PACA-AU 10 93209223 93209223 single base substitution T A intron_variant PACA-AU 10 93209231 93209231 single base substitution A T intron_variant PACA-AU 10 93213566 93213566 single base substitution G C intron_variant PACA-AU 10 93217275 93217275 single base substitution C T intron_variant PACA-AU 10 93217275 93217275 single base substitution C T upstream_gene_variant PACA-AU 10 93217916 93217916 single base substitution A T intron_variant PACA-AU 10 93217916 93217916 single base substitution A T upstream_gene_variant PACA-AU 10 93220255 93220255 single base substitution G T stop_gained E114* 340G>T PACA-AU 10 93220255 93220255 single base substitution G T upstream_gene_variant PACA-AU 10 93224851 93224851 deletion of <=200bp T - downstream_gene_variant PACA-AU 10 93224851 93224851 deletion of <=200bp T - intron_variant PACA-AU 10 93233204 93233204 single base substitution T A intron_variant PACA-AU 10 93236188 93236188 single base substitution G A intron_variant PACA-AU 10 93238645 93238645 single base substitution A G intron_variant PACA-AU 10 93240664 93240664 single base substitution C T intron_variant PACA-AU 10 93240664 93240664 single base substitution C T upstream_gene_variant PACA-AU 10 93242679 93242679 single base substitution G A intron_variant PACA-AU 10 93242679 93242679 single base substitution G A upstream_gene_variant PACA-AU 10 93244629 93244629 single base substitution G A intron_variant PACA-AU 10 93247328 93247328 single base substitution C G exon_variant PACA-AU 10 93247328 93247328 single base substitution C G intron_variant PACA-AU 10 93250415 93250415 single base substitution G A downstream_gene_variant PACA-AU 10 93250415 93250415 single base substitution G A intron_variant PACA-AU 10 93251814 93251814 single base substitution T A downstream_gene_variant PACA-AU 10 93251814 93251814 single base substitution T A intron_variant PACA-AU 10 93253168 93253168 deletion of <=200bp T - downstream_gene_variant PACA-AU 10 93253168 93253168 deletion of <=200bp T - intron_variant PACA-AU 10 93257451 93257451 single base substitution G T intron_variant PACA-AU 10 93258061 93258061 single base substitution C T intron_variant PACA-AU 10 93258537 93258537 deletion of <=200bp A - intron_variant PACA-AU 10 93260206 93260206 single base substitution C T intron_variant PACA-AU 10 93260618 93260618 single base substitution G A intron_variant PACA-AU 10 93263734 93263734 single base substitution C T intron_variant PACA-AU 10 93268836 93268836 single base substitution T A intron_variant PACA-AU 10 93268837 93268837 single base substitution C T intron_variant PACA-AU 10 93269588 93269588 single base substitution C T intron_variant PACA-AU 10 93272005 93272005 single base substitution T A intron_variant PACA-AU 10 93272629 93272629 insertion of <=200bp - TT 3_prime_UTR_variant PACA-AU 10 93273662 93273662 single base substitution C G 3_prime_UTR_variant PACA-AU 10 93273662 93273662 single base substitution C G downstream_gene_variant PACA-AU 10 93274975 93274975 single base substitution A T downstream_gene_variant PACA-AU 10 93275838 93275875 deletion of <=200bp ACTTTTTTCACTTAATATTGTCTTTTATAGATTTATTT - downstream_gene_variant PACA-AU 10 93277081 93277081 single base substitution G A downstream_gene_variant PACA-CA 10 93172399 93172399 single base substitution C A intron_variant PACA-CA 10 93173355 93173355 deletion of <=200bp G - intron_variant PACA-CA 10 93173810 93173810 single base substitution G A intron_variant PACA-CA 10 93174456 93174456 single base substitution G C intron_variant PACA-CA 10 93179041 93179041 single base substitution C T intron_variant PACA-CA 10 93179794 93179794 single base substitution C T intron_variant PACA-CA 10 93179810 93179810 deletion of <=200bp T - intron_variant PACA-CA 10 93182990 93182990 single base substitution C G intron_variant PACA-CA 10 93183740 93183740 single base substitution C T intron_variant PACA-CA 10 93184915 93184915 single base substitution C T intron_variant PACA-CA 10 93189844 93189844 single base substitution C T intron_variant PACA-CA 10 93196229 93196229 single base substitution G T intron_variant PACA-CA 10 93196254 93196254 single base substitution A G intron_variant PACA-CA 10 93196827 93196827 single base substitution T C intron_variant PACA-CA 10 93197859 93197859 single base substitution C T intron_variant PACA-CA 10 93203839 93203839 insertion of <=200bp - T intron_variant PACA-CA 10 93204250 93204250 single base substitution G T intron_variant PACA-CA 10 93204348 93204348 single base substitution G T intron_variant PACA-CA 10 93209534 93209534 single base substitution A G intron_variant PACA-CA 10 93216620 93216620 single base substitution C T intron_variant PACA-CA 10 93217430 93217430 insertion of <=200bp - A intron_variant PACA-CA 10 93217430 93217430 insertion of <=200bp - A upstream_gene_variant PACA-CA 10 93218548 93218548 single base substitution A C intron_variant PACA-CA 10 93218548 93218548 single base substitution A C upstream_gene_variant PACA-CA 10 93218796 93218796 single base substitution T C intron_variant PACA-CA 10 93218796 93218796 single base substitution T C upstream_gene_variant PACA-CA 10 93220365 93220365 single base substitution G C intron_variant PACA-CA 10 93220365 93220365 single base substitution G C upstream_gene_variant PACA-CA 10 93224851 93224851 deletion of <=200bp T - downstream_gene_variant PACA-CA 10 93224851 93224851 deletion of <=200bp T - intron_variant PACA-CA 10 93225548 93225548 single base substitution T G downstream_gene_variant PACA-CA 10 93225548 93225548 single base substitution T G intron_variant PACA-CA 10 93228818 93228818 deletion of <=200bp A - intron_variant PACA-CA 10 93231148 93231148 single base substitution T A intron_variant PACA-CA 10 93233900 93233900 insertion of <=200bp - A intron_variant PACA-CA 10 93236108 93236108 single base substitution A T intron_variant PACA-CA 10 93239870 93239870 single base substitution T G intron_variant PACA-CA 10 93239870 93239870 single base substitution T G upstream_gene_variant PACA-CA 10 93244716 93244716 single base substitution T G intron_variant PACA-CA 10 93245645 93245645 single base substitution A C exon_variant PACA-CA 10 93245645 93245645 single base substitution A C intron_variant PACA-CA 10 93254523 93254523 single base substitution G T downstream_gene_variant PACA-CA 10 93254523 93254523 single base substitution G T intron_variant PACA-CA 10 93260412 93260412 single base substitution G A intron_variant PACA-CA 10 93261770 93261770 single base substitution C A intron_variant PACA-CA 10 93263462 93263462 single base substitution C T intron_variant PACA-CA 10 93270264 93270264 single base substitution T C intron_variant PACA-CA 10 93276078 93276078 single base substitution G A downstream_gene_variant PAEN-AU 10 93166969 93166969 single base substitution T G upstream_gene_variant PAEN-AU 10 93166977 93166977 single base substitution T G upstream_gene_variant PAEN-AU 10 93170048 93170048 single base substitution G T upstream_gene_variant PAEN-AU 10 93224879 93224879 single base substitution A G downstream_gene_variant PAEN-AU 10 93224879 93224879 single base substitution A G intron_variant PAEN-AU 10 93240753 93240753 single base substitution T A intron_variant PAEN-AU 10 93240753 93240753 single base substitution T A upstream_gene_variant PAEN-IT 10 93172577 93172577 single base substitution G A intron_variant PAEN-IT 10 93183037 93183037 single base substitution A G intron_variant PAEN-IT 10 93241085 93241085 single base substitution T A intron_variant PAEN-IT 10 93241085 93241085 single base substitution T A upstream_gene_variant PBCA-DE 10 93166615 93166616 deletion of <=200bp GT - upstream_gene_variant PBCA-DE 10 93185050 93185050 single base substitution G T stop_gained G51* 151G>T PBCA-DE 10 93199190 93199191 deletion of <=200bp TA - intron_variant PBCA-DE 10 93212481 93212481 insertion of <=200bp - A intron_variant PBCA-DE 10 93230746 93230746 single base substitution C T intron_variant PBCA-DE 10 93241151 93241151 insertion of <=200bp - A intron_variant PBCA-DE 10 93241151 93241151 insertion of <=200bp - A upstream_gene_variant PBCA-DE 10 93252737 93252737 single base substitution A G downstream_gene_variant PBCA-DE 10 93252737 93252737 single base substitution A G intron_variant PBCA-DE 10 93254158 93254158 deletion of <=200bp A - downstream_gene_variant PBCA-DE 10 93254158 93254158 deletion of <=200bp A - intron_variant PBCA-DE 10 93259280 93259280 single base substitution G A intron_variant PBCA-DE 10 93261279 93261282 deletion of <=200bp ACTA - intron_variant PRAD-CA 10 93172225 93172225 single base substitution C T intron_variant PRAD-CA 10 93193805 93193805 single base substitution T G intron_variant PRAD-CA 10 93210795 93210795 single base substitution G T intron_variant PRAD-CA 10 93221562 93221562 single base substitution T A intron_variant PRAD-CA 10 93221562 93221562 single base substitution T A upstream_gene_variant PRAD-CA 10 93246581 93246581 single base substitution G C exon_variant PRAD-CA 10 93246581 93246581 single base substitution G C intron_variant PRAD-CA 10 93261181 93261181 single base substitution C T intron_variant PRAD-CA 10 93263092 93263092 single base substitution T C intron_variant PRAD-UK 10 93168356 93168356 single base substitution A C upstream_gene_variant PRAD-UK 10 93177761 93177761 single base substitution T C intron_variant PRAD-UK 10 93186025 93186025 single base substitution A T intron_variant PRAD-UK 10 93190956 93190956 single base substitution A T intron_variant PRAD-UK 10 93191466 93191466 single base substitution G A intron_variant PRAD-UK 10 93209056 93209063 deletion of <=200bp TAATTACC - intron_variant PRAD-UK 10 93209063 93209063 single base substitution C T intron_variant PRAD-UK 10 93215005 93215005 single base substitution T C intron_variant PRAD-UK 10 93215054 93215054 single base substitution T C intron_variant PRAD-UK 10 93215686 93215686 insertion of <=200bp - TATATA intron_variant PRAD-UK 10 93231039 93231039 single base substitution T G intron_variant PRAD-UK 10 93233584 93233584 single base substitution T C intron_variant PRAD-UK 10 93236712 93236712 single base substitution T C intron_variant PRAD-UK 10 93236719 93236719 single base substitution T C intron_variant PRAD-US 10 93253266 93253266 single base substitution G A downstream_gene_variant PRAD-US 10 93253266 93253266 single base substitution G A splice_donor_variant READ-US 10 93185064 93185064 single base substitution A C missense_variant Q55H 165A>C READ-US 10 93185151 93185151 single base substitution C T synonymous_variant F84F 252C>T READ-US 10 93220250 93220250 single base substitution C T missense_variant S112L 335C>T READ-US 10 93220250 93220250 single base substitution C T upstream_gene_variant READ-US 10 93220255 93220255 single base substitution G A missense_variant E114K 340G>A READ-US 10 93220255 93220255 single base substitution G A upstream_gene_variant READ-US 10 93272061 93272061 single base substitution C T missense_variant P340S 1018C>T READ-US 10 93272061 93272061 single base substitution C T missense_variant P401S 1201C>T READ-US 10 93272061 93272061 single base substitution C T missense_variant P751S 2251C>T READ-US 10 93272061 93272061 single base substitution C T missense_variant P755S 2263C>T RECA-EU 10 93165700 93165700 single base substitution C T upstream_gene_variant RECA-EU 10 93173633 93173633 single base substitution G A intron_variant RECA-EU 10 93216342 93216342 single base substitution T A intron_variant RECA-EU 10 93229783 93229783 single base substitution C A intron_variant RECA-EU 10 93243232 93243232 single base substitution C T intron_variant RECA-EU 10 93243232 93243232 single base substitution C T upstream_gene_variant RECA-EU 10 93249864 93249864 single base substitution C G downstream_gene_variant RECA-EU 10 93249864 93249864 single base substitution C G intron_variant RECA-EU 10 93260960 93260960 single base substitution T C synonymous_variant D282D 846T>C RECA-EU 10 93260960 93260960 single base substitution T C synonymous_variant D343D 1029T>C RECA-EU 10 93260960 93260960 single base substitution T C synonymous_variant D693D 2079T>C RECA-EU 10 93260960 93260960 single base substitution T C synonymous_variant D697D 2091T>C RECA-EU 10 93260961 93260961 single base substitution G T missense_variant V283F 847G>T RECA-EU 10 93260961 93260961 single base substitution G T missense_variant V344F 1030G>T RECA-EU 10 93260961 93260961 single base substitution G T missense_variant V694F 2080G>T RECA-EU 10 93260961 93260961 single base substitution G T missense_variant V698F 2092G>T RECA-EU 10 93275367 93275367 single base substitution C T downstream_gene_variant SKCA-BR 10 93174950 93174952 deletion of <=200bp AGT - intron_variant SKCA-BR 10 93188120 93188120 single base substitution C T intron_variant SKCA-BR 10 93194607 93194607 single base substitution C T intron_variant SKCA-BR 10 93201714 93201714 single base substitution A T intron_variant SKCA-BR 10 93211230 93211230 single base substitution A G intron_variant SKCA-BR 10 93214982 93214982 single base substitution G A intron_variant SKCA-BR 10 93225317 93225317 insertion of <=200bp - GT downstream_gene_variant SKCA-BR 10 93225317 93225317 insertion of <=200bp - GT intron_variant SKCA-BR 10 93228696 93228696 insertion of <=200bp - CA intron_variant SKCA-BR 10 93229377 93229377 single base substitution G A intron_variant SKCA-BR 10 93231966 93231966 single base substitution G A intron_variant SKCA-BR 10 93234521 93234521 single base substitution A G intron_variant SKCA-BR 10 93248948 93248948 single base substitution T G exon_variant SKCA-BR 10 93248948 93248948 single base substitution T G intron_variant SKCA-BR 10 93248975 93248975 single base substitution C T exon_variant SKCA-BR 10 93248975 93248975 single base substitution C T intron_variant SKCA-BR 10 93251217 93251217 single base substitution A C downstream_gene_variant SKCA-BR 10 93251217 93251217 single base substitution A C intron_variant SKCA-BR 10 93254561 93254561 single base substitution A G downstream_gene_variant SKCA-BR 10 93254561 93254561 single base substitution A G intron_variant SKCA-BR 10 93256502 93256502 single base substitution T A intron_variant SKCA-BR 10 93256503 93256503 single base substitution G C intron_variant SKCA-BR 10 93261584 93261584 single base substitution T A intron_variant SKCA-BR 10 93264321 93264321 single base substitution G A intron_variant SKCA-BR 10 93264382 93264382 single base substitution T C intron_variant SKCA-BR 10 93266401 93266401 single base substitution C A intron_variant SKCA-BR 10 93266402 93266403 deletion of <=200bp CA - intron_variant SKCA-BR 10 93266425 93266425 single base substitution G A intron_variant SKCA-BR 10 93266435 93266435 single base substitution C T intron_variant SKCA-BR 10 93267107 93267107 single base substitution T C intron_variant SKCA-BR 10 93277506 93277506 single base substitution G A downstream_gene_variant SKCA-BR 10 93278509 93278509 single base substitution G A downstream_gene_variant SKCM-US 10 93185065 93185065 single base substitution A G missense_variant I56V 166A>G SKCM-US 10 93244936 93244936 single base substitution G T splice_acceptor_variant SKCM-US 10 93256117 93256117 single base substitution T C synonymous_variant C145C 435T>C SKCM-US 10 93256117 93256117 single base substitution T C synonymous_variant C206C 618T>C SKCM-US 10 93256117 93256117 single base substitution T C synonymous_variant C556C 1668T>C SKCM-US 10 93256117 93256117 single base substitution T C synonymous_variant C560C 1680T>C STAD-US 10 93170292 93170292 deletion of <=200bp A - frameshift_variant K33 STAD-US 10 93185148 93185148 single base substitution T C synonymous_variant V83V 249T>C STAD-US 10 93221110 93221110 single base substitution T G missense_variant F169L 507T>G STAD-US 10 93221110 93221110 single base substitution T G upstream_gene_variant STAD-US 10 93242786 93242786 single base substitution T C 5_prime_UTR_variant STAD-US 10 93242786 93242786 single base substitution T C synonymous_variant A258A 774T>C STAD-US 10 93242786 93242786 single base substitution T C upstream_gene_variant STAD-US 10 93244365 93244365 single base substitution A G 5_prime_UTR_variant STAD-US 10 93244365 93244365 single base substitution A G exon_variant STAD-US 10 93244365 93244365 single base substitution A G missense_variant K308R 923A>G STAD-US 10 93244365 93244365 single base substitution A G missense_variant K312R 935A>G STAD-US 10 93244943 93244943 single base substitution C T 5_prime_UTR_variant STAD-US 10 93244943 93244943 single base substitution C T exon_variant STAD-US 10 93244943 93244943 single base substitution C T missense_variant A326V 977C>T STAD-US 10 93244943 93244943 single base substitution C T missense_variant A330V 989C>T STAD-US 10 93247481 93247481 insertion of <=200bp - A exon_variant STAD-US 10 93247481 93247481 insertion of <=200bp - A frameshift_variant A29A? STAD-US 10 93247481 93247481 insertion of <=200bp - A frameshift_variant A379A? STAD-US 10 93247481 93247481 insertion of <=200bp - A frameshift_variant A383A? STAD-US 10 93247481 93247481 insertion of <=200bp - A intron_variant STAD-US 10 93250996 93250996 single base substitution G A 5_prime_UTR_variant STAD-US 10 93250996 93250996 single base substitution G A downstream_gene_variant STAD-US 10 93250996 93250996 single base substitution G A missense_variant D411N 1231G>A STAD-US 10 93250996 93250996 single base substitution G A missense_variant D415N 1243G>A STAD-US 10 93250996 93250996 single base substitution G A missense_variant D61N 181G>A STAD-US 10 93257892 93257892 single base substitution T G missense_variant L159V 475T>G STAD-US 10 93257892 93257892 single base substitution T G missense_variant L220V 658T>G STAD-US 10 93257892 93257892 single base substitution T G missense_variant L570V 1708T>G STAD-US 10 93257892 93257892 single base substitution T G missense_variant L574V 1720T>G UCEC-US 10 93221064 93221064 single base substitution T G missense_variant F154C 461T>G UCEC-US 10 93221064 93221064 single base substitution T G upstream_gene_variant UCEC-US 10 93221942 93221942 single base substitution G C missense_variant V201L 601G>C UCEC-US 10 93221942 93221942 single base substitution G C splice_donor_variant UCEC-US 10 93242744 93242744 single base substitution A G 5_prime_UTR_variant UCEC-US 10 93242744 93242744 single base substitution A G synonymous_variant T244T 732A>G UCEC-US 10 93242744 93242744 single base substitution A G upstream_gene_variant UCEC-US 10 93242759 93242759 single base substitution C A 5_prime_UTR_variant UCEC-US 10 93242759 93242759 single base substitution C A synonymous_variant I249I 747C>A UCEC-US 10 93242759 93242759 single base substitution C A upstream_gene_variant UCEC-US 10 93244317 93244317 single base substitution C A 5_prime_UTR_variant UCEC-US 10 93244317 93244317 single base substitution C A exon_variant UCEC-US 10 93244317 93244317 single base substitution C A missense_variant S292Y 875C>A UCEC-US 10 93244317 93244317 single base substitution C A missense_variant S296Y 887C>A UCEC-US 10 93247344 93247344 single base substitution T C exon_variant UCEC-US 10 93247344 93247344 single base substitution T C intron_variant UCEC-US 10 93247526 93247526 single base substitution C T exon_variant UCEC-US 10 93247526 93247526 single base substitution C T intron_variant UCEC-US 10 93247526 93247526 single base substitution C T synonymous_variant N394N 1182C>T UCEC-US 10 93247526 93247526 single base substitution C T synonymous_variant N398N 1194C>T UCEC-US 10 93247526 93247526 single base substitution C T synonymous_variant N44N 132C>T UCEC-US 10 93251014 93251014 single base substitution C A downstream_gene_variant UCEC-US 10 93251014 93251014 single base substitution C A missense_variant L417I 1249C>A UCEC-US 10 93251014 93251014 single base substitution C A missense_variant L421I 1261C>A UCEC-US 10 93251014 93251014 single base substitution C A missense_variant L67I 199C>A UCEC-US 10 93251014 93251014 single base substitution C A missense_variant L6I 16C>A UCEC-US 10 93252196 93252196 single base substitution G T downstream_gene_variant UCEC-US 10 93252196 93252196 single base substitution G T stop_gained E113* 337G>T UCEC-US 10 93252196 93252196 single base substitution G T stop_gained E463* 1387G>T UCEC-US 10 93252196 93252196 single base substitution G T stop_gained E467* 1399G>T UCEC-US 10 93252196 93252196 single base substitution G T stop_gained E52* 154G>T UCEC-US 10 93253232 93253232 single base substitution T G downstream_gene_variant UCEC-US 10 93253232 93253232 single base substitution T G missense_variant C146W 438T>G UCEC-US 10 93253232 93253232 single base substitution T G missense_variant C496W 1488T>G UCEC-US 10 93253232 93253232 single base substitution T G missense_variant C500W 1500T>G UCEC-US 10 93253232 93253232 single base substitution T G missense_variant C85W 255T>G UCEC-US 10 93255980 93255980 single base substitution C A missense_variant L100I 298C>A UCEC-US 10 93255980 93255980 single base substitution C A missense_variant L161I 481C>A UCEC-US 10 93255980 93255980 single base substitution C A missense_variant L511I 1531C>A UCEC-US 10 93255980 93255980 single base substitution C A missense_variant L515I 1543C>A UCEC-US 10 93258692 93258692 single base substitution T G missense_variant S196A 586T>G UCEC-US 10 93258692 93258692 single base substitution T G missense_variant S257A 769T>G UCEC-US 10 93258692 93258692 single base substitution T G missense_variant S607A 1819T>G UCEC-US 10 93258692 93258692 single base substitution T G missense_variant S611A 1831T>G

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CHC1743T COSM4805668 c.1632A>G p.P544P Substitution - coding silent 10:91496324-91496324 + Gp5D COSM1969289 c.321T>G p.S107S Substitution - coding silent 10:91460479-91460479 + LN229 COSM1969328 c.1864G>T p.D622Y Substitution - Missense 10:91499064-91499064 + WSU-HN13 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + SCC-15 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + TCGA-A7-A26E-01 COSM1474860 c.1641C>T p.I547I Substitution - coding silent 10:91496333-91496333 + C0069T COSM4165565 c.2079T>C p.D693D Substitution - coding silent 10:91501203-91501203 + TCGA-HU-A4G8-01 COSM4016578 c.977C>T p.A326V Substitution - Missense 10:91485186-91485186 + TCGA-EI-6917-01 COSM3415342 c.2251C>T p.P751S Substitution - Missense 10:91512304-91512304 + TCGA-B5-A0K9-01 COSM921386 c.1182C>T p.N394N Substitution - coding silent 10:91487769-91487769 + PT50 COSM5937431 c.1006C>T p.P336S Substitution - Missense 10:91485215-91485215 + Pat_59_B COSM5837446 c.737C>T p.T246M Substitution - Missense 10:91482992-91482992 + 587332 COSM1209482 c.473C>T p.T158M Substitution - Missense 10:91461319-91461319 + TCGA-AN-A0AK-01 COSM5205791 c.1729_1731delGAA p.E578delE Deletion - In frame 10:91498156-91498158 + TCGA-AX-A05Z-01 COSM921381 c.461T>G p.F154C Substitution - Missense 10:91461307-91461307 + TCGA-AC-A5XS-01 COSM4391015 c.396G>A p.V132V Substitution - coding silent 10:91460554-91460554 + TCGA-CA-6718-01 COSM198466 c.340G>A p.E114K Substitution - Missense 10:91460498-91460498 + sysucc-311T COSM1969303 c.671G>A p.R224Q Substitution - Missense 10:91481099-91481099 + PTC-515C COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + TCGA-AP-A056-01 COSM921390 c.1488T>G p.C496W Substitution - Missense 10:91493475-91493475 + TCGA-AA-A010-01 COSM281660 c.1801C>T p.P601S Substitution - Missense 10:91498917-91498917 + 3498_T COSM3978897 c.1940A>T p.N647I Substitution - Missense 10:91499140-91499140 + B104-0 COSM1745965 c.583G>C p.D195H Substitution - Missense 10:91462167-91462167 + pfg017T COSM1603848 c.1433-9delT p.? Unknown 10:91493411-91493411 + TCGA-F4-6463-01 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + TCGA-EI-6917-01 COSM3415339 c.335C>T p.S112L Substitution - Missense 10:91460493-91460493 + TCGA-AG-3892-01 COSM257098 c.1740C>A p.F580L Substitution - Missense 10:91498167-91498167 + CRC-33T COSM5479493 c.563A>C p.K188T Substitution - Missense 10:91462147-91462147 + TCGA-B5-A0JV-01 COSM921388 c.1317C>T p.A439A Substitution - coding silent 10:91492369-91492369 + TCGA-BR-6452-01 COSM4016576 c.774T>C p.A258A Substitution - coding silent 10:91483029-91483029 + TCGA-BS-A0UJ-01 COSM921383 c.732A>G p.T244T Substitution - coding silent 10:91482987-91482987 + TCGA-FD-A3NA-01 COSM1297497 c.1323G>C p.L441F Substitution - Missense 10:91492375-91492375 + Detroit_562 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + SW1116 COSM1969333 c.2320G>A p.G774R Substitution - Missense 10:91512373-91512373 + T3038 COSM4689901 c.632G>A p.G211E Substitution - Missense 10:91478232-91478232 + SCC-25 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + B34-Tumor COSM1745966 c.2326G>C p.E776Q Substitution - Missense 10:91512379-91512379 + S02376 COSM5696854 c.971-3C>A p.? Unknown 10:91485177-91485177 + T3262 COSM4689902 c.1409G>A p.R470H Substitution - Missense 10:91492461-91492461 + EV005-R3 COSM4410759 c.424G>A p.V142I Substitution - Missense 10:91461270-91461270 + RK263_C01 COSM4779990 c.333A>G p.S111S Substitution - coding silent 10:91460491-91460491 + LIM2405 COSM4641388 c.1449C>T p.H483H Substitution - coding silent 10:91493436-91493436 + TCGA-AA-A00N-01 COSM275443 c.908T>G p.F303C Substitution - Missense 10:91484593-91484593 + ATL089 COSM1969284 c.165A>C p.Q55H Substitution - Missense 10:91425307-91425307 + WSU-HN12 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + TCGA-AA-A010-01 COSM281661 c.1681-10C>A p.? Unknown 10:91498098-91498098 + 2492730 COSM5729867 c.1275T>C p.H425H Substitution - coding silent 10:91491283-91491283 + H322T COSM1194850 c.265A>G p.N89D Substitution - Missense 10:91425407-91425407 + Pat_06_A COSM1349767 c.1137delA p.I382fs*11 Deletion - Frameshift 10:91487724-91487724 + Pat_65_A COSM5837447 c.764G>A p.R255Q Substitution - Missense 10:91483019-91483019 + 587222 COSM1209480 c.1342A>G p.T448A Substitution - Missense 10:91492394-91492394 + TCGA-BH-A0HA-01 COSM428126 c.1155G>C p.Q385H Substitution - Missense 10:91487742-91487742 + 93VU147T COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + CSCC-18-T COSM4535160 c.2160G>A p.G720G Substitution - coding silent 10:91501284-91501284 + S01578 COSM5670219 c.1204G>T p.D402Y Substitution - Missense 10:91491212-91491212 + WSU-HN8 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + LUAD-CHTN-MAD06-00668 COSM358437 c.351C>A p.A117A Substitution - coding silent 10:91460509-91460509 + TCGA-AP-A0LM-01 COSM921391 c.1531C>A p.L511I Substitution - Missense 10:91496223-91496223 + BD235T COSM5501639 c.689G>T p.R230I Substitution - Missense 10:91481117-91481117 + TCGA-B7-5818-01 COSM4016574 c.507T>G p.F169L Substitution - Missense 10:91461353-91461353 + TCGA-F5-6814-01 COSM198466 c.340G>A p.E114K Substitution - Missense 10:91460498-91460498 + TCGA-B0-5106-01 COSM466076 c.338C>T p.S113F Substitution - Missense 10:91460496-91460496 + TCGA-B5-A0JY-01 COSM921384 c.747C>A p.I249I Substitution - coding silent 10:91483002-91483002 + 462 COSM198466 c.340G>A p.E114K Substitution - Missense 10:91460498-91460498 + CSCC-41-T COSM4573151 c.989T>C p.V330A Substitution - Missense 10:91485198-91485198 + MZ7-mel COSM23123 c.1071G>A p.W357* Substitution - Nonsense 10:91485280-91485280 + TCGA-CG-5721-01 COSM4016572 c.249T>C p.V83V Substitution - coding silent 10:91425391-91425391 + TCGA-BR-6457-01 COSM1969317 c.1231G>A p.D411N Substitution - Missense 10:91491239-91491239 + SNU-175 COSM1969316 c.1198C>A p.L400M Substitution - Missense 10:91491206-91491206 + TCGA-EE-A29C-06 COSM3441482 c.1668T>C p.C556C Substitution - coding silent 10:91496360-91496360 + T3724 COSM4689903 c.1586A>C p.K529T Substitution - Missense 10:91496278-91496278 + C0069T COSM4165566 c.2080G>T p.V694F Substitution - Missense 10:91501204-91501204 + PDA_044 COSM5000404 c.2102A>G p.D701G Substitution - Missense 10:91501226-91501226 + TCGA-HU-A4GH-01 COSM4016579 c.1708T>G p.L570V Substitution - Missense 10:91498135-91498135 + S01297 COSM5667365 c.898C>G p.P300A Substitution - Missense 10:91484583-91484583 + PD4126a COSM161495 c.1762C>G p.Q588E Substitution - Missense 10:91498878-91498878 + K31 COSM249171 c.1162_1163insT p.S388fs*16 Insertion - Frameshift 10:91487749-91487750 + Gp2D COSM1969289 c.321T>G p.S107S Substitution - coding silent 10:91460479-91460479 + TCGA-ER-A19P-06 COSM3441481 c.971-1G>T p.? Unknown 10:91485179-91485179 + MO_1012 COSM1349767 c.1137delA p.I382fs*11 Deletion - Frameshift 10:91487724-91487724 + C467 COSM3415342 c.2251C>T p.P751S Substitution - Missense 10:91512304-91512304 + ACINAR06 COSM1735617 c.1109A>C p.Q370P Substitution - Missense 10:91487696-91487696 + sysucc-1317T COSM5448059 c.643A>C p.S215R Substitution - Missense 10:91478243-91478243 + TCGA-AQ-A54N-01 COSM3807971 c.700A>T p.I234L Substitution - Missense 10:91481128-91481128 + TCGA-32-4208-01 COSM3397301 c.952A>G p.K318E Substitution - Missense 10:91484637-91484637 + LUAD-F00368 COSM340894 c.2035G>A p.D679N Substitution - Missense 10:91500586-91500586 + TCGA-F5-6814-01 COSM3415337 c.252C>T p.F84F Substitution - coding silent 10:91425394-91425394 + BN24T COSM1603848 c.1433-9delT p.? Unknown 10:91493411-91493411 + TCGA-B5-A0JY-01 COSM921382 c.600+1G>C p.? Unknown 10:91462185-91462185 + TCGA-CA-6717-01 COSM1349768 c.1428T>G p.D476E Substitution - Missense 10:91492480-91492480 + TCGA-CA-6717-01 COSM1349762 c.490G>T p.E164* Substitution - Nonsense 10:91461336-91461336 + XHDG35 COSM428125 c.204G>A p.P68P Substitution - coding silent 10:91425346-91425346 + B34 COSM1745966 c.2326G>C p.E776Q Substitution - Missense 10:91512379-91512379 + CR007 COSM1969310 c.880C>T p.R294C Substitution - Missense 10:91484565-91484565 + K122 COSM249588 c.140G>T p.G47V Substitution - Missense 10:91425282-91425282 + TCGA-CC-A7IJ-01 COSM4924501 c.1402C>G p.L468V Substitution - Missense 10:91492454-91492454 + T98G COSM1969309 c.772G>T p.A258S Substitution - Missense 10:91483027-91483027 + 8057700 COSM3383081 c.340G>T p.E114* Substitution - Nonsense 10:91460498-91460498 + UM-SCC-2 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + TCGA-AM-5821-01 COSM3752050 c.415G>A p.V139I Substitution - Missense 10:91461261-91461261 + TCGA-IN-7808-01 COSM4016577 c.923A>G p.K308R Substitution - Missense 10:91484608-91484608 + MN-1054 COSM1578855 c.957G>A p.V319V Substitution - coding silent 10:91484642-91484642 + ccRCC-18 COSM1659176 c.2121A>G p.L707L Substitution - coding silent 10:91501245-91501245 + TCGA-EE-A2A0-06 COSM3441479 c.166A>G p.I56V Substitution - Missense 10:91425308-91425308 + CHC1743T COSM4805668 c.1632A>G p.P544P Substitution - coding silent 10:91496324-91496324 + T263 COSM1349766 c.1136_1137insA p.I382fs*22 Insertion - Frameshift 10:91487723-91487724 + TCGA-BS-A0UF-01 COSM921387 c.1249C>A p.L417I Substitution - Missense 10:91491257-91491257 + SCC-9 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + SNUH_G76_S1 COSM4419084 c.474G>A p.T158T Substitution - coding silent 10:91461320-91461320 + BN24 COSM1603847 c.763C>T p.R255* Substitution - Nonsense 10:91483018-91483018 + B104-0-Tumor COSM1745965 c.583G>C p.D195H Substitution - Missense 10:91462167-91462167 + TCGA-D1-A17Q-01 COSM921393 c.1819T>G p.S607A Substitution - Missense 10:91498935-91498935 + PTC-7C COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + TCGA-F5-6814-01 COSM1969284 c.165A>C p.Q55H Substitution - Missense 10:91425307-91425307 + LS513 COSM1969293 c.466C>A p.L156I Substitution - Missense 10:91461312-91461312 + TCGA-37-5819-01 COSM686101 c.846A>G p.Q282Q Substitution - coding silent 10:91484531-91484531 + LUAD-E00918 COSM364965 c.473C>G p.T158R Substitution - Missense 10:91461319-91461319 + LUAD-CHTN-MAD06-00668 COSM358438 c.354A>T p.P118P Substitution - coding silent 10:91460512-91460512 + PD9760a COSM5801993 c.1137_1138insA p.I382fs*22 Insertion - Frameshift 10:91487724-91487725 + SNU-C4 COSM4651829 c.891T>C p.P297P Substitution - coding silent 10:91484576-91484576 + NOKSI COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + TCGA-B0-4822-01 COSM3358906 c.217G>C p.A73P Substitution - Missense 10:91425359-91425359 + TCGA-HC-7077-01 COSM3670626 c.1521+1G>A p.? Unknown 10:91493509-91493509 + BN24T COSM1603847 c.763C>T p.R255* Substitution - Nonsense 10:91483018-91483018 + BZ33 COSM1349767 c.1137delA p.I382fs*11 Deletion - Frameshift 10:91487724-91487724 + TCGA-EK-A3GK-01 COSM4852662 c.2194G>A p.E732K Substitution - Missense 10:91501318-91501318 + KYSE-450 COSM1969285 c.210A>C p.K70N Substitution - Missense 10:91425352-91425352 + S02219 COSM5675550 c.810C>A p.H270Q Substitution - Missense 10:91483065-91483065 + TCGA-AA-A00N-01 COSM275444 c.1034T>G p.L345W Substitution - Missense 10:91485243-91485243 + Pat_40_B COSM1349767 c.1137delA p.I382fs*11 Deletion - Frameshift 10:91487724-91487724 + TCGA-B0-5109-01 COSM466077 c.1849G>A p.V617I Substitution - Missense 10:91499049-91499049 + TCGA-22-5473-01 COSM686100 c.1318G>T p.D440Y Substitution - Missense 10:91492370-91492370 + CAL33 COSM3752048 c.55C>G p.P19A Substitution - Missense 10:91410493-91410493 + TCGA-D1-A17Q-01 COSM921385 c.875C>A p.S292Y Substitution - Missense 10:91484560-91484560 + HCC2998 COSM1969326 c.1824T>C p.V608V Substitution - coding silent 10:91498940-91498940 + TCGA-D1-A103-01 COSM921389 c.1387G>T p.E463* Substitution - Nonsense 10:91492439-91492439 + 587222 COSM1209481 c.2271G>T p.K757N Substitution - Missense 10:91512324-91512324 + LUAD-NYU1051S COSM368487 c.923A>T p.K308M Substitution - Missense 10:91484608-91484608 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.596088;Hs.596090;Hs.596096 10q23.32

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.G222Vfs*36 c.663delA 10 93238018 LUAD A - Frameshift p.I382Sfs*11 c.1144delA 10 93247481 HNSC A - Frameshift p.K33Sfs*58 c.98delA 10 93170292 STAD A G Missense p.I124V c.370A>G 10 93220285 LUAD A G Missense p.I56V c.166A>G 10 93185065 CM A G Missense p.K318E c.952A>G 10 93244394 GBM A G Synonymous p.A635A c.1905A>G 10 93258862 BRCA A G Synonymous p.Q282Q c.846A>G 10 93244288 LUSC A - IntronicDeletion . c.1191+963delG 10 93248498 HC A T Missense p.N166I c.497A>T 10 93221100 HNSC C A Missense p.P121Q c.362C>A 10 93220277 LUAD C A Nonsense p.S582* c.1745C>A 10 93257929 CM C A Synonymous p.I395I c.1185C>A 10 93247529 LUAD CC TT Missense p.L120F c.357_358delinsTT 10 93220272 CM C G Missense p.Q588E c.1762C>G 10 93258635 BRCA C T IntronicSNV . c.822-3C>T 10 93244261 STAD C T Missense p.R423W c.1267C>T 10 93251032 STAD C T Missense p.S113F c.338C>T 10 93220253 RCCC C T Missense p.S768L c.2303C>T 10 93272113 CM C T Synonymous p.I547I c.1641C>T 10 93256090 BRCA C T Synonymous p.N394N c.1182C>T 10 93247526 UCEC C T Synonymous p.S367S c.1101C>T 10 93247445 CM G A Missense p.D411N c.1231G>A 10 93250996 STAD G A Missense p.V617I c.1849G>A 10 93258806 RCCC G A SpliceDonorSNV . c.1521+1G>A 10 93253266 PRAD G A Synonymous p.P68P c.204G>A 10 93185103 BRCA G C Missense p.A73P c.217G>C 10 93185116 RCCC G C Missense p.L441F c.1323G>C 10 93252132 BLCA G C Missense p.Q256H c.768G>C 10 93242780 HNSC G C Missense p.R674T c.2021G>C 10 93260329 LUAD G T IntronicSNV . c.822-107G>T 10 93244157 CM G T Missense p.A117S c.349G>T 10 93220264 LUAD G T Missense p.D440Y c.1318G>T 10 93252127 LUSC G T SpliceAcceptorSNV . c.971-1G>T 10 93244936 CM T C Missense p.V643A c.1928T>C 10 93258885 LUAD T C Synonymous p.C556C c.1668T>C 10 93256117 CM T G Missense p.F169L c.507T>G 10 93221110 STAD T - IntronicDeletion . c.1433-3delT 10 93253168 STAD - T IntronicInsertion . c.2211-16dupT 10 93271998 STAD