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 20 39793679 39793679 + Missense_Mutation SNP G G A TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr20:39793679G>A c.1324G>A c.(1324-1326)Gtg>Atg p.V442M ACC 20 39794128 39794128 + Missense_Mutation SNP G G T TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chr20:39794128G>T c.1548G>T c.(1546-1548)aaG>aaT p.K516N ACC 20 39794149 39794149 + Silent SNP C C A TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chr20:39794149C>A c.1569C>A c.(1567-1569)acC>acA p.T523T ACC 20 39795024 39795024 + Missense_Mutation SNP G G A TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr20:39795024G>A c.1990G>A c.(1990-1992)Gag>Aag p.E664K BLCA 20 39788556 39788556 + Nonsense_Mutation SNP G G A TCGA-FD-A6TK-01A-42D-A339-08 TCGA-FD-A6TK-10A-21D-A339-08 g.chr20:39788556G>A c.417G>A c.(415-417)tgG>tgA p.W139* BLCA 20 39792785 39792785 + Missense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr20:39792785G>T c.1161G>T c.(1159-1161)aaG>aaT p.K387N BLCA 20 39793642 39793642 + Missense_Mutation SNP C C G TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr20:39793642C>G c.1287C>G c.(1285-1287)ttC>ttG p.F429L BLCA 20 39793950 39793950 + Silent SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr20:39793950C>T c.1452C>T c.(1450-1452)aaC>aaT p.N484N BLCA 20 39794164 39794164 + Silent SNP C C T TCGA-XF-AAMF-01A-21D-A42E-08 TCGA-XF-AAMF-10A-01D-A42H-08 g.chr20:39794164C>T c.1584C>T c.(1582-1584)ggC>ggT p.G528G BLCA 20 39795196 39795196 + Missense_Mutation SNP G G A TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr20:39795196G>A c.2081G>A c.(2080-2082)cGg>cAg p.R694Q BLCA 20 39795497 39795497 + Missense_Mutation SNP G G C TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr20:39795497G>C c.2299G>C c.(2299-2301)Gct>Cct p.A767P BLCA 20 39796536 39796536 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr20:39796536C>G c.2346C>G c.(2344-2346)ttC>ttG p.F782L BLCA 20 39797452 39797452 + Missense_Mutation SNP G G A TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chr20:39797452G>A c.2425G>A c.(2425-2427)Gag>Aag p.E809K BLCA 20 39798838 39798838 + Missense_Mutation SNP G G A TCGA-C4-A0EZ-01A-21D-A10S-08 TCGA-C4-A0EZ-10A-01D-A10S-08 g.chr20:39798838G>A c.2737G>A c.(2737-2739)Gcc>Acc p.A913T BLCA 20 39798876 39798876 + Silent SNP G G A TCGA-DK-AA75-01A-11D-A391-08 TCGA-DK-AA75-10A-01D-A394-08 g.chr20:39798876G>A c.2775G>A c.(2773-2775)aaG>aaA p.K925K BLCA 20 39802161 39802161 + Missense_Mutation SNP G G C TCGA-DK-A6B5-01A-11D-A31L-08 TCGA-DK-A6B5-10A-01D-A31J-08 g.chr20:39802161G>C c.3381G>C c.(3379-3381)aaG>aaC p.K1127N BLCA 20 39802354 39802354 + Missense_Mutation SNP G G A TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr20:39802354G>A c.3457G>A c.(3457-3459)Gaa>Aaa p.E1153K BLCA 20 39802821 39802821 + Missense_Mutation SNP G G C TCGA-CF-A1HS-01A-11D-A13W-08 TCGA-CF-A1HS-10A-01D-A13W-08 g.chr20:39802821G>C c.3700G>C c.(3700-3702)Gat>Cat p.D1234H BLCA 20 39802893 39802893 + Missense_Mutation SNP G G A TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr20:39802893G>A c.3772G>A c.(3772-3774)Gag>Aag p.E1258K BRCA 20 39791131 39791131 + Silent SNP C C T TCGA-A1-A0SI-01A-11D-A142-09 TCGA-A1-A0SI-10B-01D-A142-09 g.chr20:39791131C>T c.552C>T c.(550-552)gtC>gtT p.V184V BRCA 20 39791337 39791337 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr20:39791337G>A c.653G>A c.(652-654)cGc>cAc p.R218H BRCA 20 39792360 39792360 + Silent SNP C C A TCGA-C8-A1HN-01A-11D-A135-09 TCGA-C8-A1HN-10A-01D-A135-09 g.chr20:39792360C>A c.897C>A c.(895-897)gtC>gtA p.V299V BRCA 20 39793935 39793935 + Missense_Mutation SNP G G T TCGA-BH-A18U-01A-21D-A12B-09 TCGA-BH-A18U-11A-23D-A12B-09 g.chr20:39793935G>T c.1437G>T c.(1435-1437)atG>atT p.M479I BRCA 20 39795424 39795424 + Silent SNP G G A TCGA-EW-A2FW-01A-11D-A17D-09 TCGA-EW-A2FW-10A-01D-A17D-09 g.chr20:39795424G>A c.2226G>A c.(2224-2226)gaG>gaA p.E742E BRCA 20 39796490 39796490 + Splice_Site SNP A A G TCGA-BH-A0DH-01A-11D-A099-09 TCGA-BH-A0DH-10A-01D-A099-09 g.chr20:39796490A>G c.e20-1 BRCA 20 39798164 39798164 + Missense_Mutation SNP T T A TCGA-E2-A1II-01A-11D-A142-09 TCGA-E2-A1II-10A-01D-A142-09 g.chr20:39798164T>A c.2648T>A c.(2647-2649)aTt>aAt p.I883N BRCA 20 39798809 39798809 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr20:39798809C>T c.2708C>T c.(2707-2709)tCg>tTg p.S903L BRCA 20 39800883 39800883 + Silent SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr20:39800883C>G c.2859C>G c.(2857-2859)ctC>ctG p.L953L BRCA 20 39802138 39802138 + Missense_Mutation SNP G G A TCGA-AO-A12D-01A-11D-A10Y-09 TCGA-AO-A12D-10A-01D-A110-09 g.chr20:39802138G>A c.3358G>A c.(3358-3360)Gag>Aag p.E1120K BRCA 20 39802848 39802848 + Nonsense_Mutation SNP C C T TCGA-AN-A0FY-01A-11W-A050-09 TCGA-AN-A0FY-10A-01D-A047-09 g.chr20:39802848C>T c.3727C>T c.(3727-3729)Cga>Tga p.R1243* BRCA 20 39802876 39802876 + Missense_Mutation SNP G G A TCGA-BH-A0EI-01A-11D-A10Y-09 TCGA-BH-A0EI-10A-01D-A110-09 g.chr20:39802876G>A c.3755G>A c.(3754-3756)cGc>cAc p.R1252H CESC 20 39793956 39793956 + Missense_Mutation SNP C C G TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr20:39793956C>G c.1458C>G c.(1456-1458)atC>atG p.I486M CESC 20 39794458 39794458 + Silent SNP C C G TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr20:39794458C>G c.1791C>G c.(1789-1791)ctC>ctG p.L597L CESC 20 39794982 39794982 + Missense_Mutation SNP G G C TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr20:39794982G>C c.1948G>C c.(1948-1950)Gag>Cag p.E650Q CESC 20 39795201 39795201 + Missense_Mutation SNP C C T TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr20:39795201C>T c.2086C>T c.(2086-2088)Cgg>Tgg p.R696W CHOL 20 39793975 39793975 + Missense_Mutation SNP G G A TCGA-W5-AA38-01A-11D-A417-09 TCGA-W5-AA38-10A-01D-A41A-09 g.chr20:39793975G>A c.1477G>A c.(1477-1479)Ggc>Agc p.G493S COAD 20 39788273 39788273 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr20:39788273G>A c.245G>A c.(244-246)cGc>cAc p.R82H COAD 20 39788351 39788351 + Missense_Mutation SNP T T C TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr20:39788351T>C c.323T>C c.(322-324)gTc>gCc p.V108A COAD 20 39788351 39788351 + Missense_Mutation SNP T T C TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr20:39788351T>C c.323T>C c.(322-324)gTc>gCc p.V108A COAD 20 39791294 39791294 + Missense_Mutation SNP C C T TCGA-AA-3972-01A-01W-0995-10 TCGA-AA-3972-10A-01W-0999-10 g.chr20:39791294C>T c.610C>T c.(610-612)Cgc>Tgc p.R204C COAD 20 39791858 39791858 + Silent SNP G G A TCGA-AA-3561-01A-01W-0831-10 TCGA-AA-3561-10A-01W-0831-10 g.chr20:39791858G>A c.732G>A c.(730-732)ccG>ccA p.P244P COAD 20 39792421 39792421 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr20:39792421G>A c.958G>A c.(958-960)Gac>Aac p.D320N COAD 20 39792438 39792438 + Silent SNP T T C TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr20:39792438T>C c.975T>C c.(973-975)ccT>ccC p.P325P COAD 20 39792456 39792458 + In_Frame_Del DEL CTC CTC - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr20:39792456_39792458delCTC c.993_995delCTC c.(991-996)atctcc>atc p.S334del COAD 20 39792606 39792606 + Silent SNP C C A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr20:39792606C>A c.1056C>A c.(1054-1056)gcC>gcA p.A352A COAD 20 39792626 39792626 + Missense_Mutation SNP T T C TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr20:39792626T>C c.1076T>C c.(1075-1077)aTg>aCg p.M359T COAD 20 39793963 39793963 + Missense_Mutation SNP T T C TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr20:39793963T>C c.1465T>C c.(1465-1467)Tct>Cct p.S489P COAD 20 39793963 39793963 + Missense_Mutation SNP T T C TCGA-F4-6459-01A-11D-1771-10 TCGA-F4-6459-10A-01D-1771-10 g.chr20:39793963T>C c.1465T>C c.(1465-1467)Tct>Cct p.S489P COAD 20 39793965 39793965 + Silent SNP T T C TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr20:39793965T>C c.1467T>C c.(1465-1467)tcT>tcC p.S489S COAD 20 39794411 39794411 + Missense_Mutation SNP T T C TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr20:39794411T>C c.1744T>C c.(1744-1746)Tcc>Ccc p.S582P COAD 20 39795148 39795148 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr20:39795148C>T c.2033C>T c.(2032-2034)gCt>gTt p.A678V COAD 20 39795227 39795227 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr20:39795227C>T c.2112C>T c.(2110-2112)atC>atT p.I704I COAD 20 39797439 39797439 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr20:39797439C>T c.2412C>T c.(2410-2412)gcC>gcT p.A804A COAD 20 39798114 39798114 + Frame_Shift_Del DEL C C - TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr20:39798114delC c.2598delC c.(2596-2598)agcfs p.S866fs COAD 20 39798134 39798134 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr20:39798134G>A c.2618G>A c.(2617-2619)cGg>cAg p.R873Q COAD 20 39801106 39801106 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr20:39801106C>T c.2951C>T c.(2950-2952)cCg>cTg p.P984L COAD 20 39801163 39801163 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr20:39801163A>C c.3008A>C c.(3007-3009)tAc>tCc p.Y1003S COAD 20 39801224 39801224 + Silent SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr20:39801224C>T c.3069C>T c.(3067-3069)taC>taT p.Y1023Y COAD 20 39801406 39801406 + Silent SNP G G A TCGA-AZ-6606-01A-11D-1835-10 TCGA-AZ-6606-11A-01D-1835-10 g.chr20:39801406G>A c.3168G>A c.(3166-3168)acG>acA p.T1056T COAD 20 39802571 39802571 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr20:39802571G>A c.3565G>A c.(3565-3567)Gca>Aca p.A1189T COAD 20 39802799 39802799 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr20:39802799G>A c.3678G>A c.(3676-3678)acG>acA p.T1226T COAD 20 39802903 39802903 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr20:39802903G>A c.3782G>A c.(3781-3783)cGc>cAc p.R1261H COADREAD 20 39788273 39788273 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr20:39788273G>A c.245G>A c.(244-246)cGc>cAc p.R82H COADREAD 20 39788351 39788351 + Missense_Mutation SNP T T C TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr20:39788351T>C c.323T>C c.(322-324)gTc>gCc p.V108A COADREAD 20 39788351 39788351 + Missense_Mutation SNP T T C TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr20:39788351T>C c.323T>C c.(322-324)gTc>gCc p.V108A COADREAD 20 39791294 39791294 + Missense_Mutation SNP C C T TCGA-AA-3972-01A-01W-0995-10 TCGA-AA-3972-10A-01W-0999-10 g.chr20:39791294C>T c.610C>T c.(610-612)Cgc>Tgc p.R204C COADREAD 20 39791858 39791858 + Silent SNP G G A TCGA-AA-3561-01A-01W-0831-10 TCGA-AA-3561-10A-01W-0831-10 g.chr20:39791858G>A c.732G>A c.(730-732)ccG>ccA p.P244P COADREAD 20 39792421 39792421 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr20:39792421G>A c.958G>A c.(958-960)Gac>Aac p.D320N COADREAD 20 39792438 39792438 + Silent SNP T T C TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr20:39792438T>C c.975T>C c.(973-975)ccT>ccC p.P325P COADREAD 20 39792456 39792458 + In_Frame_Del DEL CTC CTC - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr20:39792456_39792458delCTC c.993_995delCTC c.(991-996)atctcc>atc p.S334del COADREAD 20 39792606 39792606 + Silent SNP C C A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr20:39792606C>A c.1056C>A c.(1054-1056)gcC>gcA p.A352A COADREAD 20 39792626 39792626 + Missense_Mutation SNP T T C TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr20:39792626T>C c.1076T>C c.(1075-1077)aTg>aCg p.M359T COADREAD 20 39793963 39793963 + Missense_Mutation SNP T T C TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr20:39793963T>C c.1465T>C c.(1465-1467)Tct>Cct p.S489P COADREAD 20 39793963 39793963 + Missense_Mutation SNP T T C TCGA-F4-6459-01A-11D-1771-10 TCGA-F4-6459-10A-01D-1771-10 g.chr20:39793963T>C c.1465T>C c.(1465-1467)Tct>Cct p.S489P COADREAD 20 39793963 39793963 + Missense_Mutation SNP T T C TCGA-F5-6811-01A-11D-1826-10 TCGA-F5-6811-10A-01D-1826-10 g.chr20:39793963T>C c.1465T>C c.(1465-1467)Tct>Cct p.S489P COADREAD 20 39793965 39793965 + Silent SNP T T C TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr20:39793965T>C c.1467T>C c.(1465-1467)tcT>tcC p.S489S COADREAD 20 39793965 39793965 + Silent SNP T T C TCGA-CL-5917-01A-11D-1657-10 TCGA-CL-5917-10A-01D-1657-10 g.chr20:39793965T>C c.1467T>C c.(1465-1467)tcT>tcC p.S489S COADREAD 20 39794411 39794411 + Missense_Mutation SNP T T C TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr20:39794411T>C c.1744T>C c.(1744-1746)Tcc>Ccc p.S582P COADREAD 20 39795148 39795148 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr20:39795148C>T c.2033C>T c.(2032-2034)gCt>gTt p.A678V COADREAD 20 39795227 39795227 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr20:39795227C>T c.2112C>T c.(2110-2112)atC>atT p.I704I COADREAD 20 39795345 39795345 + Missense_Mutation SNP G G A TCGA-CI-6621-01A-11D-1826-10 TCGA-CI-6621-10A-01D-1826-10 g.chr20:39795345G>A c.2147G>A c.(2146-2148)cGt>cAt p.R716H COADREAD 20 39795391 39795391 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr20:39795391C>T c.2193C>T c.(2191-2193)ttC>ttT p.F731F COADREAD 20 39797439 39797439 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr20:39797439C>T c.2412C>T c.(2410-2412)gcC>gcT p.A804A COADREAD 20 39798114 39798114 + Frame_Shift_Del DEL C C - TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr20:39798114delC c.2598delC c.(2596-2598)agcfs p.S866fs COADREAD 20 39798134 39798134 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr20:39798134G>A c.2618G>A c.(2617-2619)cGg>cAg p.R873Q COADREAD 20 39801106 39801106 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr20:39801106C>T c.2951C>T c.(2950-2952)cCg>cTg p.P984L COADREAD 20 39801163 39801163 + Missense_Mutation SNP A A C TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr20:39801163A>C c.3008A>C c.(3007-3009)tAc>tCc p.Y1003S COADREAD 20 39801224 39801224 + Silent SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr20:39801224C>T c.3069C>T c.(3067-3069)taC>taT p.Y1023Y COADREAD 20 39801406 39801406 + Silent SNP G G A TCGA-AZ-6606-01A-11D-1835-10 TCGA-AZ-6606-11A-01D-1835-10 g.chr20:39801406G>A c.3168G>A c.(3166-3168)acG>acA p.T1056T COADREAD 20 39802571 39802571 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr20:39802571G>A c.3565G>A c.(3565-3567)Gca>Aca p.A1189T COADREAD 20 39802799 39802799 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr20:39802799G>A c.3678G>A c.(3676-3678)acG>acA p.T1226T COADREAD 20 39802903 39802903 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr20:39802903G>A c.3782G>A c.(3781-3783)cGc>cAc p.R1261H DLBC 20 39802374 39802374 + Silent SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr20:39802374C>T c.3477C>T c.(3475-3477)ttC>ttT p.F1159F ESCA 20 39788339 39788339 + Missense_Mutation SNP C C T TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr20:39788339C>T c.311C>T c.(310-312)tCa>tTa p.S104L ESCA 20 39794968 39794968 + Missense_Mutation SNP G G A TCGA-L5-A4OW-01A-11D-A28B-09 TCGA-L5-A4OW-11A-11D-A28E-09 g.chr20:39794968G>A c.1934G>A c.(1933-1935)cGc>cAc p.R645H ESCA 20 39795158 39795158 + Missense_Mutation SNP G G T TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr20:39795158G>T c.2043G>T c.(2041-2043)atG>atT p.M681I ESCA 20 39800921 39800922 + Frame_Shift_Ins INS - - G TCGA-LN-A4A2-01A-31D-A27G-09 TCGA-LN-A4A2-10A-01D-A27G-09 g.chr20:39800921_39800922insG c.2897_2898insG c.(2896-2901)gatgaafs p.DE966fs ESCA 20 39802094 39802094 + Missense_Mutation SNP G G A TCGA-L5-A4OT-01A-11D-A28B-09 TCGA-L5-A4OT-11A-11D-A28E-09 g.chr20:39802094G>A c.3314G>A c.(3313-3315)cGa>cAa p.R1105Q GBM 20 39788360 39788360 + Missense_Mutation SNP A A G TCGA-06-0648-01A-01W-0323-08 TCGA-06-0648-10A-01W-0323-08 g.chr20:39788360A>G c.332A>G c.(331-333)tAt>tGt p.Y111C GBM 20 39794468 39794468 + Splice_Site SNP T T C TCGA-76-6282-01A-11D-1696-08 TCGA-76-6282-10A-01D-1696-08 g.chr20:39794468T>C c.e16+2 GBM 20 39795447 39795447 + Missense_Mutation SNP T T G TCGA-06-0743-01A-01D-1492-08 TCGA-06-0743-10A-01D-1492-08 g.chr20:39795447T>G c.2249T>G c.(2248-2250)aTg>aGg p.M750R GBM 20 39795453 39795453 + Missense_Mutation SNP T T A TCGA-06-0743-01A-01D-1492-08 TCGA-06-0743-10A-01D-1492-08 g.chr20:39795453T>A c.2255T>A c.(2254-2256)cTg>cAg p.L752Q GBM 20 39801169 39801169 + Missense_Mutation SNP G G A TCGA-06-0192-01B-01W-0348-08 TCGA-06-0192-10A-01W-0348-08 g.chr20:39801169G>A c.3014G>A c.(3013-3015)cGa>cAa p.R1005Q GBM 20 39802384 39802384 + Missense_Mutation SNP G G A TCGA-06-0195-01B-01D-1491-08 TCGA-06-0195-10A-01D-1491-08 g.chr20:39802384G>A c.3487G>A c.(3487-3489)Gag>Aag p.E1163K GBMLGG 20 39788360 39788360 + Missense_Mutation SNP A A G TCGA-06-0648-01A-01W-0323-08 TCGA-06-0648-10A-01W-0323-08 g.chr20:39788360A>G c.332A>G c.(331-333)tAt>tGt p.Y111C GBMLGG 20 39793914 39793914 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:39793914C>T c.1416C>T c.(1414-1416)taC>taT p.Y472Y GBMLGG 20 39794468 39794468 + Splice_Site SNP T T C TCGA-76-6282-01A-11D-1696-08 TCGA-76-6282-10A-01D-1696-08 g.chr20:39794468T>C c.e16+2 GBMLGG 20 39794927 39794927 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:39794927C>T c.1893C>T c.(1891-1893)tcC>tcT p.S631S GBMLGG 20 39795447 39795447 + Missense_Mutation SNP T T G TCGA-06-0743-01A-01D-1492-08 TCGA-06-0743-10A-01D-1492-08 g.chr20:39795447T>G c.2249T>G c.(2248-2250)aTg>aGg p.M750R GBMLGG 20 39795452 39795452 + Missense_Mutation SNP C C G TCGA-DU-8161-01A-11D-2253-08 TCGA-DU-8161-10A-01D-2253-08 g.chr20:39795452C>G c.2254C>G c.(2254-2256)Ctg>Gtg p.L752V GBMLGG 20 39795453 39795453 + Missense_Mutation SNP T T A TCGA-06-0743-01A-01D-1492-08 TCGA-06-0743-10A-01D-1492-08 g.chr20:39795453T>A c.2255T>A c.(2254-2256)cTg>cAg p.L752Q GBMLGG 20 39795459 39795459 + Missense_Mutation SNP A A G TCGA-DU-5855-01A-11D-1705-08 TCGA-DU-5855-10A-01D-1705-08 g.chr20:39795459A>G c.2261A>G c.(2260-2262)tAt>tGt p.Y754C GBMLGG 20 39796515 39796515 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:39796515T>C c.2325T>C c.(2323-2325)taT>taC p.Y775Y GBMLGG 20 39798830 39798830 + Missense_Mutation SNP A A T TCGA-QH-A6CU-01A-11D-A31L-08 TCGA-QH-A6CU-10A-01D-A31J-08 g.chr20:39798830A>T c.2729A>T c.(2728-2730)gAt>gTt p.D910V GBMLGG 20 39801169 39801169 + Missense_Mutation SNP G G A TCGA-06-0192-01B-01W-0348-08 TCGA-06-0192-10A-01W-0348-08 g.chr20:39801169G>A c.3014G>A c.(3013-3015)cGa>cAa p.R1005Q GBMLGG 20 39802384 39802384 + Missense_Mutation SNP G G A TCGA-06-0195-01B-01D-1491-08 TCGA-06-0195-10A-01D-1491-08 g.chr20:39802384G>A c.3487G>A c.(3487-3489)Gag>Aag p.E1163K GBMLGG 20 39802384 39802384 + Missense_Mutation SNP G G A TCGA-CS-4941-01A-01D-1468-08 TCGA-CS-4941-10A-01D-1468-08 g.chr20:39802384G>A c.3487G>A c.(3487-3489)Gag>Aag p.E1163K GBMLGG 20 39802384 39802384 + Missense_Mutation SNP G G A TCGA-DU-5852-01A-11D-1705-08 TCGA-DU-5852-10A-01D-1705-08 g.chr20:39802384G>A c.3487G>A c.(3487-3489)Gag>Aag p.E1163K GBMLGG 20 39802386 39802387 + In_Frame_Ins INS - - GAAGAA TCGA-CS-5395-01A-01D-1468-08 TCGA-CS-5395-10A-01D-1468-08 g.chr20:39802386_39802387insGAAGAA c.3489_3490insGAAGAA c.(3490-3492)gaa>GAAGAAgaa p.1164_1164E>EEE HNSC 20 39788302 39788302 + Missense_Mutation SNP C C G TCGA-CV-A460-01A-21D-A25D-08 TCGA-CV-A460-10A-01D-A25E-08 g.chr20:39788302C>G c.274C>G c.(274-276)Cgc>Ggc p.R92G HNSC 20 39788394 39788394 + Silent SNP G G T TCGA-IQ-A61J-01A-11D-A30E-08 TCGA-IQ-A61J-10A-01D-A30H-08 g.chr20:39788394G>T c.366G>T c.(364-366)ctG>ctT p.L122L HNSC 20 39791883 39791883 + Missense_Mutation SNP G G C TCGA-CV-6936-01A-11D-1912-08 TCGA-CV-6936-10A-01D-1912-08 g.chr20:39791883G>C c.757G>C c.(757-759)Gag>Cag p.E253Q HNSC 20 39791907 39791907 + Missense_Mutation SNP T T C TCGA-QK-A8Z9-01B-11D-A391-08 TCGA-QK-A8Z9-10A-01D-A394-08 g.chr20:39791907T>C c.781T>C c.(781-783)Tac>Cac p.Y261H HNSC 20 39792085 39792085 + Missense_Mutation SNP G G T TCGA-CN-5373-01A-01D-1434-08 TCGA-CN-5373-10A-01D-1434-08 g.chr20:39792085G>T c.857G>T c.(856-858)cGa>cTa p.R286L HNSC 20 39793623 39793623 + Missense_Mutation SNP G G A TCGA-CV-7411-01A-11D-2078-08 TCGA-CV-7411-10A-01D-2078-08 g.chr20:39793623G>A c.1268G>A c.(1267-1269)aGa>aAa p.R423K HNSC 20 39793697 39793697 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr20:39793697G>A c.1342G>A c.(1342-1344)Ggg>Agg p.G448R HNSC 20 39794930 39794930 + Silent SNP C C G TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr20:39794930C>G c.1896C>G c.(1894-1896)ctC>ctG p.L632L HNSC 20 39797452 39797452 + Missense_Mutation SNP G G C TCGA-DQ-7588-01A-11D-2078-08 TCGA-DQ-7588-10B-01D-2078-08 g.chr20:39797452G>C c.2425G>C c.(2425-2427)Gag>Cag p.E809Q HNSC 20 39797792 39797792 + Missense_Mutation SNP G G A TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr20:39797792G>A c.2557G>A c.(2557-2559)Gtg>Atg p.V853M HNSC 20 39801217 39801217 + Missense_Mutation SNP C C G TCGA-QK-A6IG-01A-11D-A31L-08 TCGA-QK-A6IG-10A-01D-A31J-08 g.chr20:39801217C>G c.3062C>G c.(3061-3063)tCc>tGc p.S1021C KICH 20 39801085 39801085 + Missense_Mutation SNP A A G TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr20:39801085A>G c.2930A>G c.(2929-2931)tAc>tGc p.Y977C KIPAN 20 39796506 39796506 + Silent SNP G G T TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr20:39796506G>T c.2316G>T c.(2314-2316)ggG>ggT p.G772G KIPAN 20 39798840 39798840 + Silent SNP C C T TCGA-B0-4827-01A-02D-1421-08 TCGA-B0-4827-11A-01D-1421-08 g.chr20:39798840C>T c.2739C>T c.(2737-2739)gcC>gcT p.A913A KIPAN 20 39801085 39801085 + Missense_Mutation SNP A A G TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr20:39801085A>G c.2930A>G c.(2929-2931)tAc>tGc p.Y977C KIPAN 20 39802104 39802104 + Silent SNP G G A TCGA-DV-5565-01A-01D-1534-10 TCGA-DV-5565-10A-01D-1535-10 g.chr20:39802104G>A c.3324G>A c.(3322-3324)gtG>gtA p.V1108V KIRC 20 39796506 39796506 + Silent SNP G G T TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr20:39796506G>T c.2316G>T c.(2314-2316)ggG>ggT p.G772G KIRC 20 39798840 39798840 + Silent SNP C C T TCGA-B0-4827-01A-02D-1421-08 TCGA-B0-4827-11A-01D-1421-08 g.chr20:39798840C>T c.2739C>T c.(2737-2739)gcC>gcT p.A913A KIRC 20 39802104 39802104 + Silent SNP G G A TCGA-DV-5565-01A-01D-1534-10 TCGA-DV-5565-10A-01D-1535-10 g.chr20:39802104G>A c.3324G>A c.(3322-3324)gtG>gtA p.V1108V LGG 20 39793914 39793914 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:39793914C>T c.1416C>T c.(1414-1416)taC>taT p.Y472Y LGG 20 39794927 39794927 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:39794927C>T c.1893C>T c.(1891-1893)tcC>tcT p.S631S LGG 20 39795452 39795452 + Missense_Mutation SNP C C G TCGA-DU-8161-01A-11D-2253-08 TCGA-DU-8161-10A-01D-2253-08 g.chr20:39795452C>G c.2254C>G c.(2254-2256)Ctg>Gtg p.L752V LGG 20 39795459 39795459 + Missense_Mutation SNP A A G TCGA-DU-5855-01A-11D-1705-08 TCGA-DU-5855-10A-01D-1705-08 g.chr20:39795459A>G c.2261A>G c.(2260-2262)tAt>tGt p.Y754C LGG 20 39796515 39796515 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:39796515T>C c.2325T>C c.(2323-2325)taT>taC p.Y775Y LGG 20 39798830 39798830 + Missense_Mutation SNP A A T TCGA-QH-A6CU-01A-11D-A31L-08 TCGA-QH-A6CU-10A-01D-A31J-08 g.chr20:39798830A>T c.2729A>T c.(2728-2730)gAt>gTt p.D910V LGG 20 39802384 39802384 + Missense_Mutation SNP G G A TCGA-CS-4941-01A-01D-1468-08 TCGA-CS-4941-10A-01D-1468-08 g.chr20:39802384G>A c.3487G>A c.(3487-3489)Gag>Aag p.E1163K LGG 20 39802384 39802384 + Missense_Mutation SNP G G A TCGA-DU-5852-01A-11D-1705-08 TCGA-DU-5852-10A-01D-1705-08 g.chr20:39802384G>A c.3487G>A c.(3487-3489)Gag>Aag p.E1163K LGG 20 39802386 39802387 + In_Frame_Ins INS - - GAAGAA TCGA-CS-5395-01A-01D-1468-08 TCGA-CS-5395-10A-01D-1468-08 g.chr20:39802386_39802387insGAAGAA c.3489_3490insGAAGAA c.(3490-3492)gaa>GAAGAAgaa p.1164_1164E>EEE LIHC 20 39791106 39791106 + Missense_Mutation SNP A A T TCGA-CC-A9FS-01A-11D-A36X-10 TCGA-CC-A9FS-10A-01D-A370-10 g.chr20:39791106A>T c.527A>T c.(526-528)gAc>gTc p.D176V LIHC 20 39792440 39792440 + Missense_Mutation SNP T T C TCGA-G3-A6UC-01A-21D-A33K-10 TCGA-G3-A6UC-10A-01D-A33K-10 g.chr20:39792440T>C c.977T>C c.(976-978)cTt>cCt p.L326P LIHC 20 39792450 39792451 + Frame_Shift_Ins INS - - T TCGA-CC-5264-01A-01D-A12Z-10 TCGA-CC-5264-10A-01D-A12Z-10 g.chr20:39792450_39792451insT c.987_988insT c.(988-990)tggfs p.W330fs LIHC 20 39792450 39792451 + Frame_Shift_Ins INS - - T TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr20:39792450_39792451insT c.987_988insT c.(988-990)tggfs p.W330fs LIHC 20 39794969 39794969 + Silent SNP C C T TCGA-BC-A112-01A-11D-A12Z-10 TCGA-BC-A112-11A-11D-A12Z-10 g.chr20:39794969C>T c.1935C>T c.(1933-1935)cgC>cgT p.R645R LIHC 20 39798114 39798114 + Frame_Shift_Del DEL C C - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr20:39798114delC c.2598delC c.(2596-2598)agcfs p.S866fs LIHC 20 39802162 39802162 + Missense_Mutation SNP A A G TCGA-UB-A7MF-01A-11D-A33K-10 TCGA-UB-A7MF-10A-01D-A33K-10 g.chr20:39802162A>G c.3382A>G c.(3382-3384)Aca>Gca p.T1128A LIHC 20 39802780 39802780 + Missense_Mutation SNP T T G TCGA-DD-AADO-01A-11D-A40R-10 TCGA-DD-AADO-10A-01D-A40U-10 g.chr20:39802780T>G c.3659T>G c.(3658-3660)cTc>cGc p.L1220R LUAD 20 39791175 39791175 + Splice_Site SNP C C A TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr20:39791175C>A c.596C>A c.(595-597)aCg>aAg p.T199K LUAD 20 39791337 39791337 + Missense_Mutation SNP G G A TCGA-55-8207-01A-11D-2238-08 TCGA-55-8207-10A-01D-2238-08 g.chr20:39791337G>A c.653G>A c.(652-654)cGc>cAc p.R218H LUAD 20 39792419 39792419 + Missense_Mutation SNP C C G TCGA-49-6767-01A-11D-1855-08 TCGA-49-6767-11A-01D-1855-08 g.chr20:39792419C>G c.956C>G c.(955-957)cCg>cGg p.P319R LUAD 20 39793983 39793983 + Silent SNP C C G TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr20:39793983C>G c.1485C>G c.(1483-1485)ctC>ctG p.L495L LUAD 20 39794177 39794177 + Missense_Mutation SNP G G A TCGA-05-4395-01A-01D-1265-08 TCGA-05-4395-10A-01D-1265-08 g.chr20:39794177G>A c.1597G>A c.(1597-1599)Gag>Aag p.E533K LUAD 20 39794392 39794392 + Missense_Mutation SNP G G T TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr20:39794392G>T c.1725G>T c.(1723-1725)gaG>gaT p.E575D LUAD 20 39795149 39795149 + Silent SNP T T C TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr20:39795149T>C c.2034T>C c.(2032-2034)gcT>gcC p.A678A LUAD 20 39795229 39795229 + Missense_Mutation SNP C C G TCGA-05-4402-01A-01D-1265-08 TCGA-05-4402-10A-01D-1265-08 g.chr20:39795229C>G c.2114C>G c.(2113-2115)tCt>tGt p.S705C LUAD 20 39801184 39801184 + Missense_Mutation SNP G G T TCGA-64-1676-01A-01D-0969-08 TCGA-64-1676-10A-01D-0969-08 g.chr20:39801184G>T c.3029G>T c.(3028-3030)cGc>cTc p.R1010L LUSC 20 39788562 39788562 + Missense_Mutation SNP G G T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr20:39788562G>T c.423G>T c.(421-423)atG>atT p.M141I LUSC 20 39791871 39791871 + Missense_Mutation SNP G G A TCGA-66-2727-01A-01D-0983-08 TCGA-66-2727-11A-01D-0983-08 g.chr20:39791871G>A c.745G>A c.(745-747)Gtg>Atg p.V249M LUSC 20 39794432 39794432 + Missense_Mutation SNP G G C TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr20:39794432G>C c.1765G>C c.(1765-1767)Gag>Cag p.E589Q LUSC 20 39802170 39802170 + Silent SNP T T C TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr20:39802170T>C c.3390T>C c.(3388-3390)ttT>ttC p.F1130F LUSC 20 39802790 39802790 + Silent SNP C C T TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr20:39802790C>T c.3669C>T c.(3667-3669)ttC>ttT p.F1223F OV 20 39791295 39791295 + Missense_Mutation SNP G G A TCGA-61-1730-01A-01W-0639-09 TCGA-61-1730-11A-01W-0639-09 g.chr20:39791295G>A c.611G>A c.(610-612)cGc>cAc p.R204H OV 20 39794389 39794389 + Missense_Mutation SNP C C G TCGA-13-2057-01A-02D-1526-09 TCGA-13-2057-10A-01D-1526-09 g.chr20:39794389C>G c.1722C>G c.(1720-1722)atC>atG p.I574M PAAD 20 39802571 39802571 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:39802571G>A c.3565G>A c.(3565-3567)Gca>Aca p.A1189T PRAD 20 39796522 39796522 + Missense_Mutation SNP C C T TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr20:39796522C>T c.2332C>T c.(2332-2334)Cgc>Tgc p.R778C READ 20 39793963 39793963 + Missense_Mutation SNP T T C TCGA-F5-6811-01A-11D-1826-10 TCGA-F5-6811-10A-01D-1826-10 g.chr20:39793963T>C c.1465T>C c.(1465-1467)Tct>Cct p.S489P READ 20 39793965 39793965 + Silent SNP T T C TCGA-CL-5917-01A-11D-1657-10 TCGA-CL-5917-10A-01D-1657-10 g.chr20:39793965T>C c.1467T>C c.(1465-1467)tcT>tcC p.S489S READ 20 39795345 39795345 + Missense_Mutation SNP G G A TCGA-CI-6621-01A-11D-1826-10 TCGA-CI-6621-10A-01D-1826-10 g.chr20:39795345G>A c.2147G>A c.(2146-2148)cGt>cAt p.R716H READ 20 39795391 39795391 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr20:39795391C>T c.2193C>T c.(2191-2193)ttC>ttT p.F731F SARC 20 39792474 39792474 + Splice_Site SNP G G T TCGA-K1-A3PN-01A-11D-A228-09 TCGA-K1-A3PN-10A-01D-A22A-09 g.chr20:39792474G>T c.e10+1 SARC 20 39793948 39793948 + Missense_Mutation SNP A A T TCGA-DX-A6BK-01A-11D-A307-09 TCGA-DX-A6BK-10A-01D-A307-09 g.chr20:39793948A>T c.1450A>T c.(1450-1452)Aac>Tac p.N484Y SKCM 20 39788792 39788792 + Splice_Site SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr20:39788792C>T c.511C>T c.(511-513)Cgt>Tgt p.R171C SKCM 20 39791897 39791897 + Silent SNP C C T TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr20:39791897C>T c.771C>T c.(769-771)ttC>ttT p.F257F SKCM 20 39792036 39792036 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr20:39792036C>T c.808C>T c.(808-810)Cgc>Tgc p.R270C SKCM 20 39792045 39792045 + Missense_Mutation SNP G G A TCGA-D3-A1Q4-06A-11D-A196-08 TCGA-D3-A1Q4-10A-01D-A198-08 g.chr20:39792045G>A c.817G>A c.(817-819)Gtg>Atg p.V273M SKCM 20 39792068 39792068 + Silent SNP C C T TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr20:39792068C>T c.840C>T c.(838-840)ttC>ttT p.F280F SKCM 20 39792092 39792092 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr20:39792092C>T c.864C>T c.(862-864)atC>atT p.I288I SKCM 20 39792111 39792111 + Silent SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr20:39792111C>T c.883C>T c.(883-885)Ctg>Ttg p.L295L SKCM 20 39793585 39793585 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr20:39793585C>T c.1230C>T c.(1228-1230)atC>atT p.I410I SKCM 20 39793702 39793702 + Silent SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr20:39793702C>T c.1347C>T c.(1345-1347)ctC>ctT p.L449L SKCM 20 39794189 39794189 + Missense_Mutation SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr20:39794189G>A c.1609G>A c.(1609-1611)Gag>Aag p.E537K SKCM 20 39794389 39794389 + Silent SNP C C T TCGA-FS-A1Z0-06A-11D-A197-08 TCGA-FS-A1Z0-10A-01D-A199-08 g.chr20:39794389C>T c.1722C>T c.(1720-1722)atC>atT p.I574I SKCM 20 39794935 39794935 + Missense_Mutation SNP A A G TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr20:39794935A>G c.1901A>G c.(1900-1902)gAc>gGc p.D634G SKCM 20 39795007 39795007 + Missense_Mutation SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr20:39795007C>G c.1973C>G c.(1972-1974)cCa>cGa p.P658R SKCM 20 39795344 39795344 + Missense_Mutation SNP C C T TCGA-ER-A19M-06A-61D-A23B-08 TCGA-ER-A19M-10A-01D-A23B-08 g.chr20:39795344C>T c.2146C>T c.(2146-2148)Cgt>Tgt p.R716C SKCM 20 39801087 39801087 + Missense_Mutation SNP C C T TCGA-D3-A2J7-06A-11D-A196-08 TCGA-D3-A2J7-10A-01D-A198-08 g.chr20:39801087C>T c.2932C>T c.(2932-2934)Cgg>Tgg p.R978W SKCM 20 39801100 39801100 + Missense_Mutation SNP C C T TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr20:39801100C>T c.2945C>T c.(2944-2946)tCc>tTc p.S982F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 20 39797452 39797452 single base substitution G A downstream_gene_variant BLCA-US 20 39797452 39797452 single base substitution G A exon_variant BLCA-US 20 39797452 39797452 single base substitution G A missense_variant E809K 2425G>A BLCA-US 20 39797452 39797452 single base substitution G A upstream_gene_variant BLCA-US 20 39802354 39802354 single base substitution G A 3_prime_UTR_variant BLCA-US 20 39802354 39802354 single base substitution G A downstream_gene_variant BLCA-US 20 39802354 39802354 single base substitution G A exon_variant BLCA-US 20 39802354 39802354 single base substitution G A missense_variant E1153K 3457G>A BLCA-US 20 39802354 39802354 single base substitution G A upstream_gene_variant BLCA-US 20 39802821 39802821 single base substitution G C downstream_gene_variant BLCA-US 20 39802821 39802821 single base substitution G C exon_variant BLCA-US 20 39802821 39802821 single base substitution G C intron_variant BLCA-US 20 39802821 39802821 single base substitution G C missense_variant D1234H 3700G>C BLCA-US 20 39802821 39802821 single base substitution G C missense_variant D1235H 3703G>C BOCA-FR 20 39800936 39800936 single base substitution G A downstream_gene_variant BOCA-FR 20 39800936 39800936 single base substitution G A intron_variant BOCA-FR 20 39800936 39800936 single base substitution G A splice_region_variant BOCA-FR 20 39800936 39800936 single base substitution G A upstream_gene_variant BRCA-EU 20 39761880 39761880 single base substitution C A upstream_gene_variant BRCA-EU 20 39762542 39762542 single base substitution C T upstream_gene_variant BRCA-EU 20 39763104 39763104 deletion of <=200bp A - upstream_gene_variant BRCA-EU 20 39763225 39763225 single base substitution G A upstream_gene_variant BRCA-EU 20 39764986 39764986 deletion of <=200bp G - upstream_gene_variant BRCA-EU 20 39765068 39765068 single base substitution G A upstream_gene_variant BRCA-EU 20 39767007 39767007 single base substitution G C intron_variant BRCA-EU 20 39769641 39769641 single base substitution C T intron_variant BRCA-EU 20 39771873 39771873 single base substitution C G intron_variant BRCA-EU 20 39773652 39773652 single base substitution C T intron_variant BRCA-EU 20 39774505 39774505 single base substitution C A intron_variant BRCA-EU 20 39776490 39776490 single base substitution T A intron_variant BRCA-EU 20 39776653 39776653 single base substitution G A intron_variant BRCA-EU 20 39777947 39777947 single base substitution C G intron_variant BRCA-EU 20 39779034 39779034 single base substitution G A intron_variant BRCA-EU 20 39782663 39782663 single base substitution C G intron_variant BRCA-EU 20 39784220 39784220 single base substitution C G intron_variant BRCA-EU 20 39784433 39784433 single base substitution C G intron_variant BRCA-EU 20 39785328 39785328 single base substitution C T intron_variant BRCA-EU 20 39786092 39786092 single base substitution C G intron_variant BRCA-EU 20 39788327 39788327 single base substitution G A exon_variant BRCA-EU 20 39788327 39788327 single base substitution G A missense_variant R100Q 299G>A BRCA-EU 20 39788327 39788327 single base substitution G A upstream_gene_variant BRCA-EU 20 39788481 39788481 single base substitution C T downstream_gene_variant BRCA-EU 20 39788481 39788481 single base substitution C T intron_variant BRCA-EU 20 39788481 39788481 single base substitution C T upstream_gene_variant BRCA-EU 20 39788663 39788663 single base substitution C G downstream_gene_variant BRCA-EU 20 39788663 39788663 single base substitution C G intron_variant BRCA-EU 20 39788663 39788663 single base substitution C G upstream_gene_variant BRCA-EU 20 39788664 39788664 single base substitution A G downstream_gene_variant BRCA-EU 20 39788664 39788664 single base substitution A G intron_variant BRCA-EU 20 39788664 39788664 single base substitution A G upstream_gene_variant BRCA-EU 20 39789677 39789677 single base substitution G C downstream_gene_variant BRCA-EU 20 39789677 39789677 single base substitution G C intron_variant BRCA-EU 20 39789677 39789677 single base substitution G C upstream_gene_variant BRCA-EU 20 39791037 39791037 single base substitution G C downstream_gene_variant BRCA-EU 20 39791037 39791037 single base substitution G C exon_variant BRCA-EU 20 39791037 39791037 single base substitution G C intron_variant BRCA-EU 20 39791037 39791037 single base substitution G C upstream_gene_variant BRCA-EU 20 39791858 39791858 single base substitution G C downstream_gene_variant BRCA-EU 20 39791858 39791858 single base substitution G C exon_variant BRCA-EU 20 39791858 39791858 single base substitution G C synonymous_variant P244P 732G>C BRCA-EU 20 39791858 39791858 single base substitution G C upstream_gene_variant BRCA-EU 20 39796441 39796441 single base substitution C G downstream_gene_variant BRCA-EU 20 39796441 39796441 single base substitution C G exon_variant BRCA-EU 20 39796441 39796441 single base substitution C G intron_variant BRCA-EU 20 39796441 39796441 single base substitution C G upstream_gene_variant BRCA-EU 20 39797420 39797420 single base substitution C T downstream_gene_variant BRCA-EU 20 39797420 39797420 single base substitution C T exon_variant BRCA-EU 20 39797420 39797420 single base substitution C T missense_variant A798V 2393C>T BRCA-EU 20 39797420 39797420 single base substitution C T upstream_gene_variant BRCA-EU 20 39798218 39798218 single base substitution C G downstream_gene_variant BRCA-EU 20 39798218 39798218 single base substitution C G intron_variant BRCA-EU 20 39798218 39798218 single base substitution C G upstream_gene_variant BRCA-EU 20 39798267 39798267 single base substitution A G downstream_gene_variant BRCA-EU 20 39798267 39798267 single base substitution A G intron_variant BRCA-EU 20 39798267 39798267 single base substitution A G upstream_gene_variant BRCA-EU 20 39800104 39800104 single base substitution G A downstream_gene_variant BRCA-EU 20 39800104 39800104 single base substitution G A intron_variant BRCA-EU 20 39800104 39800104 single base substitution G A upstream_gene_variant BRCA-EU 20 39802642 39802642 single base substitution C A 3_prime_UTR_variant BRCA-EU 20 39802642 39802642 single base substitution C A downstream_gene_variant BRCA-EU 20 39802642 39802642 single base substitution C A exon_variant BRCA-EU 20 39802642 39802642 single base substitution C A missense_variant F1212L 3636C>A BRCA-EU 20 39806034 39806034 single base substitution G A downstream_gene_variant BRCA-EU 20 39806034 39806034 single base substitution G A intron_variant BRCA-EU 20 39806081 39806081 single base substitution C G downstream_gene_variant BRCA-EU 20 39806081 39806081 single base substitution C G intron_variant BRCA-EU 20 39806220 39806220 single base substitution G T downstream_gene_variant BRCA-EU 20 39806220 39806220 single base substitution G T intron_variant BRCA-EU 20 39806792 39806792 single base substitution C T downstream_gene_variant BRCA-EU 20 39806792 39806792 single base substitution C T intron_variant BRCA-EU 20 39807017 39807017 single base substitution C G downstream_gene_variant BRCA-EU 20 39807017 39807017 single base substitution C G intron_variant BRCA-EU 20 39809579 39809579 single base substitution G A intron_variant BRCA-EU 20 39810192 39810192 single base substitution C A intron_variant BRCA-EU 20 39810192 39810192 single base substitution C G intron_variant BRCA-EU 20 39811095 39811095 single base substitution C A intron_variant BRCA-EU 20 39811242 39811242 single base substitution G A intron_variant BRCA-EU 20 39811310 39811310 single base substitution G T intron_variant BRCA-EU 20 39812084 39812084 single base substitution G C downstream_gene_variant BRCA-EU 20 39813611 39813611 single base substitution G C downstream_gene_variant BRCA-EU 20 39815664 39815664 single base substitution A G downstream_gene_variant BRCA-EU 20 39816459 39816459 single base substitution T A downstream_gene_variant BRCA-FR 20 39771873 39771873 single base substitution C G intron_variant BRCA-FR 20 39776653 39776653 single base substitution G A intron_variant BRCA-FR 20 39779034 39779034 single base substitution G A intron_variant BRCA-FR 20 39784220 39784220 single base substitution C G intron_variant BRCA-FR 20 39806034 39806034 single base substitution G A downstream_gene_variant BRCA-FR 20 39806034 39806034 single base substitution G A intron_variant BRCA-FR 20 39806081 39806081 single base substitution C G downstream_gene_variant BRCA-FR 20 39806081 39806081 single base substitution C G intron_variant BRCA-FR 20 39811310 39811310 single base substitution G T intron_variant BRCA-FR 20 39812084 39812084 single base substitution G C downstream_gene_variant BRCA-KR 20 39798806 39798806 single base substitution C T downstream_gene_variant BRCA-KR 20 39798806 39798806 single base substitution C T exon_variant BRCA-KR 20 39798806 39798806 single base substitution C T missense_variant A902V 2705C>T BRCA-KR 20 39798806 39798806 single base substitution C T upstream_gene_variant BRCA-US 20 39791131 39791131 single base substitution C T downstream_gene_variant BRCA-US 20 39791131 39791131 single base substitution C T exon_variant BRCA-US 20 39791131 39791131 single base substitution C T synonymous_variant V184V 552C>T BRCA-US 20 39791131 39791131 single base substitution C T upstream_gene_variant BRCA-US 20 39791337 39791337 single base substitution G A downstream_gene_variant BRCA-US 20 39791337 39791337 single base substitution G A missense_variant R218H 653G>A BRCA-US 20 39791337 39791337 single base substitution G A upstream_gene_variant BRCA-US 20 39792360 39792360 single base substitution C A downstream_gene_variant BRCA-US 20 39792360 39792360 single base substitution C A exon_variant BRCA-US 20 39792360 39792360 single base substitution C A synonymous_variant V299V 897C>A BRCA-US 20 39792360 39792360 single base substitution C A upstream_gene_variant BRCA-US 20 39793935 39793935 single base substitution G T downstream_gene_variant BRCA-US 20 39793935 39793935 single base substitution G T exon_variant BRCA-US 20 39793935 39793935 single base substitution G T missense_variant M479I 1437G>T BRCA-US 20 39793935 39793935 single base substitution G T upstream_gene_variant BRCA-US 20 39795424 39795424 single base substitution G A downstream_gene_variant BRCA-US 20 39795424 39795424 single base substitution G A exon_variant BRCA-US 20 39795424 39795424 single base substitution G A synonymous_variant E742E 2226G>A BRCA-US 20 39795424 39795424 single base substitution G A upstream_gene_variant BRCA-US 20 39796490 39796490 single base substitution A G downstream_gene_variant BRCA-US 20 39796490 39796490 single base substitution A G exon_variant BRCA-US 20 39796490 39796490 single base substitution A G splice_acceptor_variant BRCA-US 20 39796490 39796490 single base substitution A G upstream_gene_variant BRCA-US 20 39798164 39798164 single base substitution T A downstream_gene_variant BRCA-US 20 39798164 39798164 single base substitution T A missense_variant I883N 2648T>A BRCA-US 20 39798164 39798164 single base substitution T A splice_region_variant BRCA-US 20 39798164 39798164 single base substitution T A upstream_gene_variant BRCA-US 20 39798809 39798809 single base substitution C T downstream_gene_variant BRCA-US 20 39798809 39798809 single base substitution C T exon_variant BRCA-US 20 39798809 39798809 single base substitution C T missense_variant S903L 2708C>T BRCA-US 20 39798809 39798809 single base substitution C T upstream_gene_variant BRCA-US 20 39800883 39800883 single base substitution C G downstream_gene_variant BRCA-US 20 39800883 39800883 single base substitution C G intron_variant BRCA-US 20 39800883 39800883 single base substitution C G synonymous_variant L953L 2859C>G BRCA-US 20 39800883 39800883 single base substitution C G upstream_gene_variant BRCA-US 20 39802138 39802138 single base substitution G A 3_prime_UTR_variant BRCA-US 20 39802138 39802138 single base substitution G A downstream_gene_variant BRCA-US 20 39802138 39802138 single base substitution G A exon_variant BRCA-US 20 39802138 39802138 single base substitution G A missense_variant E1120K 3358G>A BRCA-US 20 39802138 39802138 single base substitution G A upstream_gene_variant BRCA-US 20 39802848 39802848 single base substitution C T downstream_gene_variant BRCA-US 20 39802848 39802848 single base substitution C T exon_variant BRCA-US 20 39802848 39802848 single base substitution C T intron_variant BRCA-US 20 39802848 39802848 single base substitution C T stop_gained R1243* 3727C>T BRCA-US 20 39802848 39802848 single base substitution C T stop_gained R1244* 3730C>T BRCA-US 20 39802876 39802876 single base substitution G A downstream_gene_variant BRCA-US 20 39802876 39802876 single base substitution G A exon_variant BRCA-US 20 39802876 39802876 single base substitution G A intron_variant BRCA-US 20 39802876 39802876 single base substitution G A missense_variant R1252H 3755G>A BRCA-US 20 39802876 39802876 single base substitution G A missense_variant R1253H 3758G>A BTCA-JP 20 39766520 39766520 single base substitution C T intron_variant BTCA-JP 20 39791692 39791692 single base substitution C T downstream_gene_variant BTCA-JP 20 39791692 39791692 single base substitution C T exon_variant BTCA-JP 20 39791692 39791692 single base substitution C T intron_variant BTCA-JP 20 39791692 39791692 single base substitution C T upstream_gene_variant BTCA-JP 20 39794470 39794470 single base substitution A G downstream_gene_variant BTCA-JP 20 39794470 39794470 single base substitution A G exon_variant BTCA-JP 20 39794470 39794470 single base substitution A G splice_region_variant BTCA-JP 20 39794470 39794470 single base substitution A G upstream_gene_variant CESC-US 20 39793956 39793956 single base substitution C G downstream_gene_variant CESC-US 20 39793956 39793956 single base substitution C G exon_variant CESC-US 20 39793956 39793956 single base substitution C G missense_variant I486M 1458C>G CESC-US 20 39793956 39793956 single base substitution C G upstream_gene_variant CESC-US 20 39794458 39794458 single base substitution C G downstream_gene_variant CESC-US 20 39794458 39794458 single base substitution C G exon_variant CESC-US 20 39794458 39794458 single base substitution C G synonymous_variant L597L 1791C>G CESC-US 20 39794458 39794458 single base substitution C G upstream_gene_variant CESC-US 20 39794982 39794982 single base substitution G C downstream_gene_variant CESC-US 20 39794982 39794982 single base substitution G C exon_variant CESC-US 20 39794982 39794982 single base substitution G C missense_variant E650Q 1948G>C CESC-US 20 39794982 39794982 single base substitution G C upstream_gene_variant CESC-US 20 39795201 39795201 single base substitution C T downstream_gene_variant CESC-US 20 39795201 39795201 single base substitution C T exon_variant CESC-US 20 39795201 39795201 single base substitution C T missense_variant R696W 2086C>T CESC-US 20 39795201 39795201 single base substitution C T upstream_gene_variant CLLE-ES 20 39764555 39764555 single base substitution A G upstream_gene_variant CLLE-ES 20 39792094 39792094 single base substitution A G downstream_gene_variant CLLE-ES 20 39792094 39792094 single base substitution A G exon_variant CLLE-ES 20 39792094 39792094 single base substitution A G missense_variant E289G 866A>G CLLE-ES 20 39792094 39792094 single base substitution A G upstream_gene_variant COAD-US 20 39788273 39788273 single base substitution G A exon_variant COAD-US 20 39788273 39788273 single base substitution G A missense_variant R82H 245G>A COAD-US 20 39788273 39788273 single base substitution G A upstream_gene_variant COAD-US 20 39792421 39792421 single base substitution G A downstream_gene_variant COAD-US 20 39792421 39792421 single base substitution G A exon_variant COAD-US 20 39792421 39792421 single base substitution G A missense_variant D320N 958G>A COAD-US 20 39792421 39792421 single base substitution G A upstream_gene_variant COAD-US 20 39792456 39792458 deletion of <=200bp CTC - downstream_gene_variant COAD-US 20 39792456 39792458 deletion of <=200bp CTC - exon_variant COAD-US 20 39792456 39792458 deletion of <=200bp CTC - inframe_deletion IS331I COAD-US 20 39792456 39792458 deletion of <=200bp CTC - upstream_gene_variant COAD-US 20 39792606 39792606 single base substitution C A downstream_gene_variant COAD-US 20 39792606 39792606 single base substitution C A exon_variant COAD-US 20 39792606 39792606 single base substitution C A synonymous_variant A352A 1056C>A COAD-US 20 39792606 39792606 single base substitution C A upstream_gene_variant COAD-US 20 39795148 39795148 single base substitution C T downstream_gene_variant COAD-US 20 39795148 39795148 single base substitution C T exon_variant COAD-US 20 39795148 39795148 single base substitution C T missense_variant A678V 2033C>T COAD-US 20 39795148 39795148 single base substitution C T upstream_gene_variant COAD-US 20 39795227 39795227 single base substitution C T downstream_gene_variant COAD-US 20 39795227 39795227 single base substitution C T exon_variant COAD-US 20 39795227 39795227 single base substitution C T synonymous_variant I704I 2112C>T COAD-US 20 39795227 39795227 single base substitution C T upstream_gene_variant COAD-US 20 39797439 39797439 single base substitution C T downstream_gene_variant COAD-US 20 39797439 39797439 single base substitution C T exon_variant COAD-US 20 39797439 39797439 single base substitution C T synonymous_variant A804A 2412C>T COAD-US 20 39797439 39797439 single base substitution C T upstream_gene_variant COAD-US 20 39798893 39798893 single base substitution A T downstream_gene_variant COAD-US 20 39798893 39798893 single base substitution A T exon_variant COAD-US 20 39798893 39798893 single base substitution A T missense_variant Q931L 2792A>T COAD-US 20 39798893 39798893 single base substitution A T upstream_gene_variant COAD-US 20 39801106 39801106 single base substitution C T downstream_gene_variant COAD-US 20 39801106 39801106 single base substitution C T exon_variant COAD-US 20 39801106 39801106 single base substitution C T missense_variant P984L 2951C>T COAD-US 20 39801106 39801106 single base substitution C T upstream_gene_variant COAD-US 20 39801163 39801163 single base substitution A C 3_prime_UTR_variant COAD-US 20 39801163 39801163 single base substitution A C downstream_gene_variant COAD-US 20 39801163 39801163 single base substitution A C exon_variant COAD-US 20 39801163 39801163 single base substitution A C missense_variant Y1003S 3008A>C COAD-US 20 39801163 39801163 single base substitution A C upstream_gene_variant COAD-US 20 39802571 39802571 single base substitution G A 3_prime_UTR_variant COAD-US 20 39802571 39802571 single base substitution G A downstream_gene_variant COAD-US 20 39802571 39802571 single base substitution G A exon_variant COAD-US 20 39802571 39802571 single base substitution G A missense_variant A1189T 3565G>A COAD-US 20 39802944 39802944 single base substitution G A downstream_gene_variant COAD-US 20 39802944 39802944 single base substitution G A exon_variant COAD-US 20 39802944 39802944 single base substitution G A intron_variant COAD-US 20 39802944 39802944 single base substitution G A missense_variant E1275K 3823G>A COAD-US 20 39802944 39802944 single base substitution G A missense_variant E1276K 3826G>A COCA-CN 20 39766404 39766404 single base substitution G T exon_variant COCA-CN 20 39766404 39766404 single base substitution G T missense_variant K41N 123G>T COCA-CN 20 39791162 39791162 single base substitution C T downstream_gene_variant COCA-CN 20 39791162 39791162 single base substitution C T exon_variant COCA-CN 20 39791162 39791162 single base substitution C T stop_gained R195* 583C>T COCA-CN 20 39791162 39791162 single base substitution C T upstream_gene_variant COCA-CN 20 39791229 39791229 single base substitution C A downstream_gene_variant COCA-CN 20 39791229 39791229 single base substitution C A intron_variant COCA-CN 20 39791229 39791229 single base substitution C A upstream_gene_variant COCA-CN 20 39791295 39791295 single base substitution G A downstream_gene_variant COCA-CN 20 39791295 39791295 single base substitution G A missense_variant R204H 611G>A COCA-CN 20 39791295 39791295 single base substitution G A upstream_gene_variant COCA-CN 20 39791299 39791299 single base substitution C T downstream_gene_variant COCA-CN 20 39791299 39791299 single base substitution C T synonymous_variant S205S 615C>T COCA-CN 20 39791299 39791299 single base substitution C T upstream_gene_variant COCA-CN 20 39793694 39793694 single base substitution G A downstream_gene_variant COCA-CN 20 39793694 39793694 single base substitution G A missense_variant D447N 1339G>A COCA-CN 20 39793694 39793694 single base substitution G A upstream_gene_variant COCA-CN 20 39793710 39793710 single base substitution C A downstream_gene_variant COCA-CN 20 39793710 39793710 single base substitution C A missense_variant P452H 1355C>A COCA-CN 20 39793710 39793710 single base substitution C A upstream_gene_variant COCA-CN 20 39793976 39793976 single base substitution G T downstream_gene_variant COCA-CN 20 39793976 39793976 single base substitution G T exon_variant COCA-CN 20 39793976 39793976 single base substitution G T missense_variant G493V 1478G>T COCA-CN 20 39793976 39793976 single base substitution G T upstream_gene_variant COCA-CN 20 39794446 39794446 single base substitution C T downstream_gene_variant COCA-CN 20 39794446 39794446 single base substitution C T exon_variant COCA-CN 20 39794446 39794446 single base substitution C T synonymous_variant G593G 1779C>T COCA-CN 20 39794446 39794446 single base substitution C T upstream_gene_variant COCA-CN 20 39794859 39794859 single base substitution C T downstream_gene_variant COCA-CN 20 39794859 39794859 single base substitution C T exon_variant COCA-CN 20 39794859 39794859 single base substitution C T missense_variant R609C 1825C>T COCA-CN 20 39794859 39794859 single base substitution C T upstream_gene_variant COCA-CN 20 39794945 39794945 single base substitution G A downstream_gene_variant COCA-CN 20 39794945 39794945 single base substitution G A exon_variant COCA-CN 20 39794945 39794945 single base substitution G A synonymous_variant T637T 1911G>A COCA-CN 20 39794945 39794945 single base substitution G A upstream_gene_variant COCA-CN 20 39797941 39797941 single base substitution G A downstream_gene_variant COCA-CN 20 39797941 39797941 single base substitution G A intron_variant COCA-CN 20 39797941 39797941 single base substitution G A upstream_gene_variant COCA-CN 20 39798133 39798133 single base substitution C T downstream_gene_variant COCA-CN 20 39798133 39798133 single base substitution C T exon_variant COCA-CN 20 39798133 39798133 single base substitution C T missense_variant R873W 2617C>T COCA-CN 20 39798133 39798133 single base substitution C T upstream_gene_variant COCA-CN 20 39798979 39798979 single base substitution C A downstream_gene_variant COCA-CN 20 39798979 39798979 single base substitution C A exon_variant COCA-CN 20 39798979 39798979 single base substitution C A intron_variant COCA-CN 20 39798979 39798979 single base substitution C A upstream_gene_variant COCA-CN 20 39801485 39801485 single base substitution C T 3_prime_UTR_variant COCA-CN 20 39801485 39801485 single base substitution C T downstream_gene_variant COCA-CN 20 39801485 39801485 single base substitution C T exon_variant COCA-CN 20 39801485 39801485 single base substitution C T missense_variant R1083C 3247C>T COCA-CN 20 39801485 39801485 single base substitution C T upstream_gene_variant COCA-CN 20 39802052 39802052 single base substitution G A downstream_gene_variant COCA-CN 20 39802052 39802052 single base substitution G A splice_region_variant COCA-CN 20 39802052 39802052 single base substitution G A upstream_gene_variant COCA-CN 20 39803232 39803232 single base substitution C T 3_prime_UTR_variant COCA-CN 20 39803232 39803232 single base substitution C T downstream_gene_variant COCA-CN 20 39803232 39803232 single base substitution C T intron_variant EOPC-DE 20 39765489 39765489 single base substitution C G upstream_gene_variant EOPC-DE 20 39778990 39778990 single base substitution G T intron_variant ESAD-UK 20 39760949 39760949 single base substitution C G upstream_gene_variant ESAD-UK 20 39762803 39762803 single base substitution C G upstream_gene_variant ESAD-UK 20 39764023 39764023 single base substitution A G upstream_gene_variant ESAD-UK 20 39764181 39764181 single base substitution C T upstream_gene_variant ESAD-UK 20 39768383 39768383 single base substitution T C intron_variant ESAD-UK 20 39773454 39773454 single base substitution G T intron_variant ESAD-UK 20 39780468 39780468 single base substitution C T intron_variant ESAD-UK 20 39780564 39780564 single base substitution A G intron_variant ESAD-UK 20 39780907 39780907 single base substitution C T intron_variant ESAD-UK 20 39782114 39782114 insertion of <=200bp - T intron_variant ESAD-UK 20 39782153 39782153 single base substitution G T intron_variant ESAD-UK 20 39785329 39785329 single base substitution G A intron_variant ESAD-UK 20 39785568 39785568 single base substitution G A intron_variant ESAD-UK 20 39786571 39786571 single base substitution G A intron_variant ESAD-UK 20 39788059 39788059 single base substitution T G intron_variant ESAD-UK 20 39788059 39788059 single base substitution T G upstream_gene_variant ESAD-UK 20 39795338 39795338 single base substitution C T downstream_gene_variant ESAD-UK 20 39795338 39795338 single base substitution C T exon_variant ESAD-UK 20 39795338 39795338 single base substitution C T missense_variant H714Y 2140C>T ESAD-UK 20 39795338 39795338 single base substitution C T upstream_gene_variant ESAD-UK 20 39797954 39797954 single base substitution T C downstream_gene_variant ESAD-UK 20 39797954 39797954 single base substitution T C intron_variant ESAD-UK 20 39797954 39797954 single base substitution T C upstream_gene_variant ESAD-UK 20 39798134 39798134 single base substitution G A downstream_gene_variant ESAD-UK 20 39798134 39798134 single base substitution G A exon_variant ESAD-UK 20 39798134 39798134 single base substitution G A missense_variant R873Q 2618G>A ESAD-UK 20 39798134 39798134 single base substitution G A upstream_gene_variant ESAD-UK 20 39802596 39802596 single base substitution G A 3_prime_UTR_variant ESAD-UK 20 39802596 39802596 single base substitution G A downstream_gene_variant ESAD-UK 20 39802596 39802596 single base substitution G A exon_variant ESAD-UK 20 39802596 39802596 single base substitution G A missense_variant S1197N 3590G>A ESAD-UK 20 39802889 39802889 single base substitution G A downstream_gene_variant ESAD-UK 20 39802889 39802889 single base substitution G A exon_variant ESAD-UK 20 39802889 39802889 single base substitution G A intron_variant ESAD-UK 20 39802889 39802889 single base substitution G A synonymous_variant P1256P 3768G>A ESAD-UK 20 39802889 39802889 single base substitution G A synonymous_variant P1257P 3771G>A ESAD-UK 20 39806805 39806805 single base substitution G A downstream_gene_variant ESAD-UK 20 39806805 39806805 single base substitution G A intron_variant ESAD-UK 20 39806985 39806985 single base substitution T C downstream_gene_variant ESAD-UK 20 39806985 39806985 single base substitution T C intron_variant ESAD-UK 20 39807052 39807052 insertion of <=200bp - T downstream_gene_variant ESAD-UK 20 39807052 39807052 insertion of <=200bp - T intron_variant ESAD-UK 20 39808088 39808088 single base substitution A G downstream_gene_variant ESAD-UK 20 39808088 39808088 single base substitution A G intron_variant ESAD-UK 20 39808379 39808379 single base substitution C G downstream_gene_variant ESAD-UK 20 39808379 39808379 single base substitution C G intron_variant ESAD-UK 20 39809462 39809462 single base substitution C T intron_variant ESAD-UK 20 39811284 39811284 single base substitution C G intron_variant ESAD-UK 20 39811680 39811680 single base substitution C T downstream_gene_variant ESAD-UK 20 39811824 39811825 deletion of <=200bp TA - downstream_gene_variant ESAD-UK 20 39815459 39815459 single base substitution G T downstream_gene_variant ESAD-UK 20 39816227 39816227 single base substitution C T downstream_gene_variant ESCA-CN 20 39766383 39766383 single base substitution C G exon_variant ESCA-CN 20 39766383 39766383 single base substitution C G synonymous_variant V34V 102C>G ESCA-CN 20 39794440 39794440 single base substitution C T downstream_gene_variant ESCA-CN 20 39794440 39794440 single base substitution C T exon_variant ESCA-CN 20 39794440 39794440 single base substitution C T synonymous_variant F591F 1773C>T ESCA-CN 20 39794440 39794440 single base substitution C T upstream_gene_variant ESCA-CN 20 39802343 39802343 single base substitution T A 3_prime_UTR_variant ESCA-CN 20 39802343 39802343 single base substitution T A downstream_gene_variant ESCA-CN 20 39802343 39802343 single base substitution T A exon_variant ESCA-CN 20 39802343 39802343 single base substitution T A missense_variant I1149N 3446T>A ESCA-CN 20 39802343 39802343 single base substitution T A upstream_gene_variant GBM-US 20 39788360 39788360 single base substitution A G exon_variant GBM-US 20 39788360 39788360 single base substitution A G missense_variant Y111C 332A>G GBM-US 20 39788360 39788360 single base substitution A G upstream_gene_variant GBM-US 20 39794468 39794468 single base substitution T C downstream_gene_variant GBM-US 20 39794468 39794468 single base substitution T C exon_variant GBM-US 20 39794468 39794468 single base substitution T C splice_donor_variant GBM-US 20 39794468 39794468 single base substitution T C upstream_gene_variant GBM-US 20 39795447 39795447 single base substitution T G downstream_gene_variant GBM-US 20 39795447 39795447 single base substitution T G exon_variant GBM-US 20 39795447 39795447 single base substitution T G missense_variant M750R 2249T>G GBM-US 20 39795447 39795447 single base substitution T G upstream_gene_variant GBM-US 20 39795453 39795453 single base substitution T A downstream_gene_variant GBM-US 20 39795453 39795453 single base substitution T A exon_variant GBM-US 20 39795453 39795453 single base substitution T A missense_variant L752Q 2255T>A GBM-US 20 39795453 39795453 single base substitution T A upstream_gene_variant GBM-US 20 39801169 39801169 single base substitution G A 3_prime_UTR_variant GBM-US 20 39801169 39801169 single base substitution G A downstream_gene_variant GBM-US 20 39801169 39801169 single base substitution G A exon_variant GBM-US 20 39801169 39801169 single base substitution G A missense_variant R1005Q 3014G>A GBM-US 20 39801169 39801169 single base substitution G A upstream_gene_variant GBM-US 20 39802384 39802384 single base substitution G A 3_prime_UTR_variant GBM-US 20 39802384 39802384 single base substitution G A downstream_gene_variant GBM-US 20 39802384 39802384 single base substitution G A exon_variant GBM-US 20 39802384 39802384 single base substitution G A missense_variant E1163K 3487G>A GBM-US 20 39802384 39802384 single base substitution G A upstream_gene_variant KIRC-US 20 39796506 39796506 single base substitution G T downstream_gene_variant KIRC-US 20 39796506 39796506 single base substitution G T exon_variant KIRC-US 20 39796506 39796506 single base substitution G T synonymous_variant G772G 2316G>T KIRC-US 20 39796506 39796506 single base substitution G T upstream_gene_variant KIRC-US 20 39798840 39798840 single base substitution C T downstream_gene_variant KIRC-US 20 39798840 39798840 single base substitution C T exon_variant KIRC-US 20 39798840 39798840 single base substitution C T synonymous_variant A913A 2739C>T KIRC-US 20 39798840 39798840 single base substitution C T upstream_gene_variant KIRC-US 20 39802104 39802104 single base substitution G A 3_prime_UTR_variant KIRC-US 20 39802104 39802104 single base substitution G A downstream_gene_variant KIRC-US 20 39802104 39802104 single base substitution G A exon_variant KIRC-US 20 39802104 39802104 single base substitution G A synonymous_variant V1108V 3324G>A KIRC-US 20 39802104 39802104 single base substitution G A upstream_gene_variant LAML-KR 20 39798618 39798618 single base substitution C G downstream_gene_variant LAML-KR 20 39798618 39798618 single base substitution C G intron_variant LAML-KR 20 39798618 39798618 single base substitution C G upstream_gene_variant LAML-KR 20 39815212 39815212 single base substitution G A downstream_gene_variant LGG-US 20 39795459 39795459 single base substitution A G downstream_gene_variant LGG-US 20 39795459 39795459 single base substitution A G exon_variant LGG-US 20 39795459 39795459 single base substitution A G missense_variant Y754C 2261A>G LGG-US 20 39795459 39795459 single base substitution A G upstream_gene_variant LGG-US 20 39802384 39802384 single base substitution G A 3_prime_UTR_variant LGG-US 20 39802384 39802384 single base substitution G A downstream_gene_variant LGG-US 20 39802384 39802384 single base substitution G A exon_variant LGG-US 20 39802384 39802384 single base substitution G A missense_variant E1163K 3487G>A LGG-US 20 39802384 39802384 single base substitution G A upstream_gene_variant LGG-US 20 39802386 39802386 insertion of <=200bp - GAAGAA 3_prime_UTR_variant LGG-US 20 39802386 39802386 insertion of <=200bp - GAAGAA downstream_gene_variant LGG-US 20 39802386 39802386 insertion of <=200bp - GAAGAA exon_variant LGG-US 20 39802386 39802386 insertion of <=200bp - GAAGAA inframe_insertion E1163EKK LGG-US 20 39802386 39802386 insertion of <=200bp - GAAGAA upstream_gene_variant LICA-FR 20 39761291 39761291 deletion of <=200bp A - upstream_gene_variant LICA-FR 20 39780216 39780216 single base substitution A C intron_variant LICA-FR 20 39785845 39785845 insertion of <=200bp - TGTGTGTG intron_variant LICA-FR 20 39792091 39792091 single base substitution T G downstream_gene_variant LICA-FR 20 39792091 39792091 single base substitution T G exon_variant LICA-FR 20 39792091 39792091 single base substitution T G missense_variant I288S 863T>G LICA-FR 20 39792091 39792091 single base substitution T G upstream_gene_variant LICA-FR 20 39794368 39794368 single base substitution C T downstream_gene_variant LICA-FR 20 39794368 39794368 single base substitution C T exon_variant LICA-FR 20 39794368 39794368 single base substitution C T synonymous_variant R567R 1701C>T LICA-FR 20 39794368 39794368 single base substitution C T upstream_gene_variant LICA-FR 20 39810074 39810074 single base substitution A G intron_variant LIHC-US 20 39792440 39792440 single base substitution T C downstream_gene_variant LIHC-US 20 39792440 39792440 single base substitution T C exon_variant LIHC-US 20 39792440 39792440 single base substitution T C missense_variant L326P 977T>C LIHC-US 20 39792440 39792440 single base substitution T C upstream_gene_variant LIHC-US 20 39792450 39792450 insertion of <=200bp - T downstream_gene_variant LIHC-US 20 39792450 39792450 insertion of <=200bp - T exon_variant LIHC-US 20 39792450 39792450 insertion of <=200bp - T frameshift_variant Y329Y? LIHC-US 20 39792450 39792450 insertion of <=200bp - T upstream_gene_variant LIHC-US 20 39794969 39794969 single base substitution C T downstream_gene_variant LIHC-US 20 39794969 39794969 single base substitution C T exon_variant LIHC-US 20 39794969 39794969 single base substitution C T synonymous_variant R645R 1935C>T LIHC-US 20 39794969 39794969 single base substitution C T upstream_gene_variant LIHC-US 20 39802162 39802162 single base substitution A G 3_prime_UTR_variant LIHC-US 20 39802162 39802162 single base substitution A G downstream_gene_variant LIHC-US 20 39802162 39802162 single base substitution A G exon_variant LIHC-US 20 39802162 39802162 single base substitution A G missense_variant T1128A 3382A>G LIHC-US 20 39802162 39802162 single base substitution A G upstream_gene_variant LINC-JP 20 39760769 39760769 single base substitution G C upstream_gene_variant LINC-JP 20 39788170 39788170 single base substitution A T intron_variant LINC-JP 20 39788170 39788170 single base substitution A T upstream_gene_variant LINC-JP 20 39788437 39788437 single base substitution G C exon_variant LINC-JP 20 39788437 39788437 single base substitution G C intron_variant LINC-JP 20 39788437 39788437 single base substitution G C upstream_gene_variant LINC-JP 20 39788674 39788674 single base substitution T G downstream_gene_variant LINC-JP 20 39788674 39788674 single base substitution T G intron_variant LINC-JP 20 39788674 39788674 single base substitution T G upstream_gene_variant LINC-JP 20 39792107 39792107 single base substitution C A downstream_gene_variant LINC-JP 20 39792107 39792107 single base substitution C A exon_variant LINC-JP 20 39792107 39792107 single base substitution C A missense_variant F293L 879C>A LINC-JP 20 39792107 39792107 single base substitution C A upstream_gene_variant LINC-JP 20 39792150 39792150 insertion of <=200bp - A downstream_gene_variant LINC-JP 20 39792150 39792150 insertion of <=200bp - A intron_variant LINC-JP 20 39792150 39792150 insertion of <=200bp - A upstream_gene_variant LINC-JP 20 39793989 39793989 single base substitution G A downstream_gene_variant LINC-JP 20 39793989 39793989 single base substitution G A exon_variant LINC-JP 20 39793989 39793989 single base substitution G A synonymous_variant L497L 1491G>A LINC-JP 20 39793989 39793989 single base substitution G A upstream_gene_variant LINC-JP 20 39794630 39794630 single base substitution A C downstream_gene_variant LINC-JP 20 39794630 39794630 single base substitution A C intron_variant LINC-JP 20 39794630 39794630 single base substitution A C upstream_gene_variant LINC-JP 20 39796512 39796512 single base substitution G A downstream_gene_variant LINC-JP 20 39796512 39796512 single base substitution G A exon_variant LINC-JP 20 39796512 39796512 single base substitution G A synonymous_variant L774L 2322G>A LINC-JP 20 39796512 39796512 single base substitution G A upstream_gene_variant LINC-JP 20 39798796 39798796 single base substitution A G downstream_gene_variant LINC-JP 20 39798796 39798796 single base substitution A G exon_variant LINC-JP 20 39798796 39798796 single base substitution A G missense_variant I899V 2695A>G LINC-JP 20 39798796 39798796 single base substitution A G upstream_gene_variant LINC-JP 20 39809844 39809844 single base substitution T C intron_variant LINC-JP 20 39813707 39813707 single base substitution C T downstream_gene_variant LIRI-JP 20 39760764 39760764 single base substitution G A upstream_gene_variant LIRI-JP 20 39762958 39762958 single base substitution A G upstream_gene_variant LIRI-JP 20 39764815 39764815 single base substitution A G upstream_gene_variant LIRI-JP 20 39766998 39766998 single base substitution G A intron_variant LIRI-JP 20 39767529 39767529 single base substitution C T intron_variant LIRI-JP 20 39770128 39770128 single base substitution A G intron_variant LIRI-JP 20 39770709 39770709 single base substitution A G intron_variant LIRI-JP 20 39773378 39773378 single base substitution G A intron_variant LIRI-JP 20 39773379 39773379 single base substitution G T intron_variant LIRI-JP 20 39777814 39777814 single base substitution A G intron_variant LIRI-JP 20 39777875 39777875 single base substitution T G intron_variant LIRI-JP 20 39785766 39785766 single base substitution T G intron_variant LIRI-JP 20 39787361 39787361 single base substitution T G intron_variant LIRI-JP 20 39787361 39787361 single base substitution T G upstream_gene_variant LIRI-JP 20 39791493 39791493 single base substitution T G downstream_gene_variant LIRI-JP 20 39791493 39791493 single base substitution T G intron_variant LIRI-JP 20 39791493 39791493 single base substitution T G upstream_gene_variant LIRI-JP 20 39794543 39794543 single base substitution T C downstream_gene_variant LIRI-JP 20 39794543 39794543 single base substitution T C intron_variant LIRI-JP 20 39794543 39794543 single base substitution T C upstream_gene_variant LIRI-JP 20 39794946 39794946 single base substitution C T downstream_gene_variant LIRI-JP 20 39794946 39794946 single base substitution C T exon_variant LIRI-JP 20 39794946 39794946 single base substitution C T missense_variant H638Y 1912C>T LIRI-JP 20 39794946 39794946 single base substitution C T upstream_gene_variant LIRI-JP 20 39796241 39796241 single base substitution G C downstream_gene_variant LIRI-JP 20 39796241 39796241 single base substitution G C intron_variant LIRI-JP 20 39796241 39796241 single base substitution G C upstream_gene_variant LIRI-JP 20 39796372 39796372 single base substitution C A downstream_gene_variant LIRI-JP 20 39796372 39796372 single base substitution C A exon_variant LIRI-JP 20 39796372 39796372 single base substitution C A intron_variant LIRI-JP 20 39796372 39796372 single base substitution C A upstream_gene_variant LIRI-JP 20 39797705 39797705 single base substitution T C downstream_gene_variant LIRI-JP 20 39797705 39797705 single base substitution T C intron_variant LIRI-JP 20 39797705 39797705 single base substitution T C upstream_gene_variant LIRI-JP 20 39798375 39798375 single base substitution G A downstream_gene_variant LIRI-JP 20 39798375 39798375 single base substitution G A intron_variant LIRI-JP 20 39798375 39798375 single base substitution G A upstream_gene_variant LIRI-JP 20 39801516 39801516 single base substitution A C downstream_gene_variant LIRI-JP 20 39801516 39801516 single base substitution A C missense_variant E1093A 3278A>C LIRI-JP 20 39801516 39801516 single base substitution A C splice_region_variant LIRI-JP 20 39801516 39801516 single base substitution A C upstream_gene_variant LIRI-JP 20 39803373 39803373 single base substitution T C 3_prime_UTR_variant LIRI-JP 20 39803373 39803373 single base substitution T C downstream_gene_variant LIRI-JP 20 39803373 39803373 single base substitution T C intron_variant LIRI-JP 20 39804743 39804743 single base substitution C G downstream_gene_variant LIRI-JP 20 39804743 39804743 single base substitution C G intron_variant LIRI-JP 20 39805429 39805429 single base substitution T G downstream_gene_variant LIRI-JP 20 39805429 39805429 single base substitution T G intron_variant LIRI-JP 20 39806273 39806273 single base substitution G A downstream_gene_variant LIRI-JP 20 39806273 39806273 single base substitution G A intron_variant LIRI-JP 20 39806409 39806409 single base substitution A G downstream_gene_variant LIRI-JP 20 39806409 39806409 single base substitution A G intron_variant LIRI-JP 20 39812876 39812876 single base substitution C T downstream_gene_variant LUSC-KR 20 39766179 39766179 single base substitution G T 5_prime_UTR_variant LUSC-KR 20 39766179 39766179 single base substitution G T upstream_gene_variant LUSC-KR 20 39779625 39779625 single base substitution G C intron_variant LUSC-KR 20 39779995 39779995 single base substitution G C intron_variant LUSC-KR 20 39789248 39789248 single base substitution G A downstream_gene_variant LUSC-KR 20 39789248 39789248 single base substitution G A intron_variant LUSC-KR 20 39789248 39789248 single base substitution G A upstream_gene_variant LUSC-KR 20 39790343 39790343 single base substitution G T downstream_gene_variant LUSC-KR 20 39790343 39790343 single base substitution G T intron_variant LUSC-KR 20 39790343 39790343 single base substitution G T upstream_gene_variant LUSC-KR 20 39795959 39795959 single base substitution G A downstream_gene_variant LUSC-KR 20 39795959 39795959 single base substitution G A intron_variant LUSC-KR 20 39795959 39795959 single base substitution G A upstream_gene_variant LUSC-KR 20 39798223 39798223 single base substitution T C downstream_gene_variant LUSC-KR 20 39798223 39798223 single base substitution T C intron_variant LUSC-KR 20 39798223 39798223 single base substitution T C upstream_gene_variant LUSC-KR 20 39801766 39801766 single base substitution G A downstream_gene_variant LUSC-KR 20 39801766 39801766 single base substitution G A intron_variant LUSC-KR 20 39801766 39801766 single base substitution G A upstream_gene_variant LUSC-KR 20 39815299 39815299 single base substitution C G downstream_gene_variant LUSC-US 20 39788562 39788562 single base substitution G T downstream_gene_variant LUSC-US 20 39788562 39788562 single base substitution G T exon_variant LUSC-US 20 39788562 39788562 single base substitution G T missense_variant M141I 423G>T LUSC-US 20 39788562 39788562 single base substitution G T upstream_gene_variant LUSC-US 20 39791871 39791871 single base substitution G A downstream_gene_variant LUSC-US 20 39791871 39791871 single base substitution G A exon_variant LUSC-US 20 39791871 39791871 single base substitution G A missense_variant V249M 745G>A LUSC-US 20 39791871 39791871 single base substitution G A upstream_gene_variant LUSC-US 20 39794432 39794432 single base substitution G C downstream_gene_variant LUSC-US 20 39794432 39794432 single base substitution G C exon_variant LUSC-US 20 39794432 39794432 single base substitution G C missense_variant E589Q 1765G>C LUSC-US 20 39794432 39794432 single base substitution G C upstream_gene_variant LUSC-US 20 39802170 39802170 single base substitution T C 3_prime_UTR_variant LUSC-US 20 39802170 39802170 single base substitution T C downstream_gene_variant LUSC-US 20 39802170 39802170 single base substitution T C exon_variant LUSC-US 20 39802170 39802170 single base substitution T C synonymous_variant F1130F 3390T>C LUSC-US 20 39802170 39802170 single base substitution T C upstream_gene_variant LUSC-US 20 39802790 39802790 single base substitution C T downstream_gene_variant LUSC-US 20 39802790 39802790 single base substitution C T exon_variant LUSC-US 20 39802790 39802790 single base substitution C T intron_variant LUSC-US 20 39802790 39802790 single base substitution C T synonymous_variant F1223F 3669C>T LUSC-US 20 39802790 39802790 single base substitution C T synonymous_variant F1224F 3672C>T MALY-DE 20 39762972 39762972 single base substitution C A upstream_gene_variant MALY-DE 20 39766573 39766573 single base substitution C T intron_variant MALY-DE 20 39775614 39775614 single base substitution A G intron_variant MALY-DE 20 39775762 39775762 single base substitution T C intron_variant MALY-DE 20 39781796 39781796 single base substitution C T intron_variant MALY-DE 20 39786455 39786455 single base substitution G A intron_variant MALY-DE 20 39795469 39795469 single base substitution C T downstream_gene_variant MALY-DE 20 39795469 39795469 single base substitution C T exon_variant MALY-DE 20 39795469 39795469 single base substitution C T synonymous_variant N757N 2271C>T MALY-DE 20 39795469 39795469 single base substitution C T upstream_gene_variant MALY-DE 20 39804921 39804921 single base substitution C T downstream_gene_variant MALY-DE 20 39804921 39804921 single base substitution C T intron_variant MALY-DE 20 39814835 39814835 single base substitution A G downstream_gene_variant MALY-DE 20 39816220 39816220 single base substitution A T downstream_gene_variant MELA-AU 20 39761173 39761173 single base substitution C G upstream_gene_variant MELA-AU 20 39761929 39761930 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 20 39761993 39761993 single base substitution C T upstream_gene_variant MELA-AU 20 39762438 39762438 single base substitution C T upstream_gene_variant MELA-AU 20 39762501 39762501 single base substitution C T upstream_gene_variant MELA-AU 20 39763206 39763206 single base substitution C T upstream_gene_variant MELA-AU 20 39764459 39764459 single base substitution G A upstream_gene_variant MELA-AU 20 39764738 39764738 single base substitution C T upstream_gene_variant MELA-AU 20 39765258 39765258 single base substitution C T upstream_gene_variant MELA-AU 20 39765260 39765260 single base substitution C T upstream_gene_variant MELA-AU 20 39766430 39766430 single base substitution C A exon_variant MELA-AU 20 39766430 39766430 single base substitution C A missense_variant T50N 149C>A MELA-AU 20 39766722 39766722 single base substitution G A intron_variant MELA-AU 20 39768870 39768870 single base substitution T C intron_variant MELA-AU 20 39769432 39769432 single base substitution T A intron_variant MELA-AU 20 39769483 39769483 single base substitution G A intron_variant MELA-AU 20 39770386 39770386 single base substitution C T intron_variant MELA-AU 20 39770947 39770947 single base substitution A G intron_variant MELA-AU 20 39770998 39770998 single base substitution G A intron_variant MELA-AU 20 39771683 39771683 single base substitution C T intron_variant MELA-AU 20 39771751 39771751 single base substitution C T intron_variant MELA-AU 20 39772431 39772431 single base substitution C T intron_variant MELA-AU 20 39772649 39772649 single base substitution C T intron_variant MELA-AU 20 39772841 39772841 single base substitution C T intron_variant MELA-AU 20 39774325 39774325 single base substitution G T intron_variant MELA-AU 20 39774713 39774713 single base substitution C T intron_variant MELA-AU 20 39774902 39774902 single base substitution C T intron_variant MELA-AU 20 39776120 39776120 single base substitution G A intron_variant MELA-AU 20 39776315 39776315 single base substitution C T intron_variant MELA-AU 20 39776956 39776956 single base substitution C G intron_variant MELA-AU 20 39777091 39777091 single base substitution C T intron_variant MELA-AU 20 39777219 39777219 single base substitution C T intron_variant MELA-AU 20 39777234 39777234 single base substitution G A intron_variant MELA-AU 20 39777848 39777848 single base substitution T C intron_variant MELA-AU 20 39778127 39778127 single base substitution G A intron_variant MELA-AU 20 39778623 39778623 single base substitution C T intron_variant MELA-AU 20 39778745 39778745 single base substitution C T intron_variant MELA-AU 20 39778854 39778854 single base substitution C T intron_variant MELA-AU 20 39779096 39779096 single base substitution C T intron_variant MELA-AU 20 39779486 39779486 single base substitution C T intron_variant MELA-AU 20 39779980 39779980 single base substitution C T intron_variant MELA-AU 20 39780038 39780038 single base substitution C T intron_variant MELA-AU 20 39780039 39780039 single base substitution C G intron_variant MELA-AU 20 39780140 39780140 single base substitution C T intron_variant MELA-AU 20 39780931 39780931 single base substitution C T intron_variant MELA-AU 20 39781106 39781106 single base substitution C A intron_variant MELA-AU 20 39781321 39781321 single base substitution C T intron_variant MELA-AU 20 39781730 39781730 single base substitution G A intron_variant MELA-AU 20 39783670 39783670 single base substitution C T intron_variant MELA-AU 20 39783998 39783998 single base substitution C T intron_variant MELA-AU 20 39784300 39784300 single base substitution C T intron_variant MELA-AU 20 39785251 39785251 single base substitution C T intron_variant MELA-AU 20 39785289 39785289 single base substitution G A intron_variant MELA-AU 20 39786156 39786156 single base substitution C T intron_variant MELA-AU 20 39786178 39786178 single base substitution C T intron_variant MELA-AU 20 39787166 39787166 single base substitution C T intron_variant MELA-AU 20 39787166 39787166 single base substitution C T upstream_gene_variant MELA-AU 20 39788005 39788006 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 20 39788005 39788006 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 20 39788059 39788059 single base substitution T G intron_variant MELA-AU 20 39788059 39788059 single base substitution T G upstream_gene_variant MELA-AU 20 39788241 39788241 single base substitution C T intron_variant MELA-AU 20 39788241 39788241 single base substitution C T splice_region_variant MELA-AU 20 39788241 39788241 single base substitution C T upstream_gene_variant MELA-AU 20 39788783 39788783 single base substitution C T downstream_gene_variant MELA-AU 20 39788783 39788783 single base substitution C T exon_variant MELA-AU 20 39788783 39788783 single base substitution C T missense_variant R168C 502C>T MELA-AU 20 39788783 39788783 single base substitution C T upstream_gene_variant MELA-AU 20 39789045 39789045 single base substitution G A downstream_gene_variant MELA-AU 20 39789045 39789045 single base substitution G A intron_variant MELA-AU 20 39789045 39789045 single base substitution G A upstream_gene_variant MELA-AU 20 39789221 39789221 single base substitution G A downstream_gene_variant MELA-AU 20 39789221 39789221 single base substitution G A intron_variant MELA-AU 20 39789221 39789221 single base substitution G A upstream_gene_variant MELA-AU 20 39789298 39789298 single base substitution T G downstream_gene_variant MELA-AU 20 39789298 39789298 single base substitution T G intron_variant MELA-AU 20 39789298 39789298 single base substitution T G upstream_gene_variant MELA-AU 20 39789846 39789846 single base substitution C T downstream_gene_variant MELA-AU 20 39789846 39789846 single base substitution C T intron_variant MELA-AU 20 39789846 39789846 single base substitution C T upstream_gene_variant MELA-AU 20 39789895 39789895 single base substitution C T downstream_gene_variant MELA-AU 20 39789895 39789895 single base substitution C T intron_variant MELA-AU 20 39789895 39789895 single base substitution C T upstream_gene_variant MELA-AU 20 39790170 39790170 single base substitution C T downstream_gene_variant MELA-AU 20 39790170 39790170 single base substitution C T intron_variant MELA-AU 20 39790170 39790170 single base substitution C T upstream_gene_variant MELA-AU 20 39790622 39790622 single base substitution C T downstream_gene_variant MELA-AU 20 39790622 39790622 single base substitution C T intron_variant MELA-AU 20 39790622 39790622 single base substitution C T upstream_gene_variant MELA-AU 20 39790796 39790796 single base substitution C T downstream_gene_variant MELA-AU 20 39790796 39790796 single base substitution C T intron_variant MELA-AU 20 39790796 39790796 single base substitution C T upstream_gene_variant MELA-AU 20 39791087 39791087 single base substitution C T downstream_gene_variant MELA-AU 20 39791087 39791087 single base substitution C T exon_variant MELA-AU 20 39791087 39791087 single base substitution C T splice_region_variant MELA-AU 20 39791087 39791087 single base substitution C T upstream_gene_variant MELA-AU 20 39791300 39791301 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 20 39791300 39791301 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant G206K 616GG>AA MELA-AU 20 39791300 39791301 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 20 39791492 39791492 single base substitution C T downstream_gene_variant MELA-AU 20 39791492 39791492 single base substitution C T intron_variant MELA-AU 20 39791492 39791492 single base substitution C T upstream_gene_variant MELA-AU 20 39791592 39791592 single base substitution C T downstream_gene_variant MELA-AU 20 39791592 39791592 single base substitution C T splice_region_variant MELA-AU 20 39791592 39791592 single base substitution C T upstream_gene_variant MELA-AU 20 39791749 39791749 single base substitution G A downstream_gene_variant MELA-AU 20 39791749 39791749 single base substitution G A exon_variant MELA-AU 20 39791749 39791749 single base substitution G A intron_variant MELA-AU 20 39791749 39791749 single base substitution G A upstream_gene_variant MELA-AU 20 39791863 39791863 single base substitution T C downstream_gene_variant MELA-AU 20 39791863 39791863 single base substitution T C exon_variant MELA-AU 20 39791863 39791863 single base substitution T C missense_variant L246P 737T>C MELA-AU 20 39791863 39791863 single base substitution T C upstream_gene_variant MELA-AU 20 39792085 39792085 single base substitution G A downstream_gene_variant MELA-AU 20 39792085 39792085 single base substitution G A exon_variant MELA-AU 20 39792085 39792085 single base substitution G A missense_variant R286Q 857G>A MELA-AU 20 39792085 39792085 single base substitution G A upstream_gene_variant MELA-AU 20 39792138 39792139 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 20 39792138 39792139 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 20 39792138 39792139 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 20 39792139 39792139 single base substitution C T downstream_gene_variant MELA-AU 20 39792139 39792139 single base substitution C T intron_variant MELA-AU 20 39792139 39792139 single base substitution C T upstream_gene_variant MELA-AU 20 39792252 39792252 single base substitution C T downstream_gene_variant MELA-AU 20 39792252 39792252 single base substitution C T intron_variant MELA-AU 20 39792252 39792252 single base substitution C T upstream_gene_variant MELA-AU 20 39793033 39793033 deletion of <=200bp T - downstream_gene_variant MELA-AU 20 39793033 39793033 deletion of <=200bp T - intron_variant MELA-AU 20 39793033 39793033 deletion of <=200bp T - upstream_gene_variant MELA-AU 20 39793387 39793387 single base substitution C T downstream_gene_variant MELA-AU 20 39793387 39793387 single base substitution C T intron_variant MELA-AU 20 39793387 39793387 single base substitution C T upstream_gene_variant MELA-AU 20 39793689 39793689 single base substitution C T downstream_gene_variant MELA-AU 20 39793689 39793689 single base substitution C T missense_variant S445F 1334C>T MELA-AU 20 39793689 39793689 single base substitution C T upstream_gene_variant MELA-AU 20 39794757 39794757 single base substitution C T downstream_gene_variant MELA-AU 20 39794757 39794757 single base substitution C T exon_variant MELA-AU 20 39794757 39794757 single base substitution C T intron_variant MELA-AU 20 39794757 39794757 single base substitution C T upstream_gene_variant MELA-AU 20 39795608 39795608 single base substitution C T downstream_gene_variant MELA-AU 20 39795608 39795608 single base substitution C T intron_variant MELA-AU 20 39795608 39795608 single base substitution C T upstream_gene_variant MELA-AU 20 39796371 39796371 single base substitution C T downstream_gene_variant MELA-AU 20 39796371 39796371 single base substitution C T exon_variant MELA-AU 20 39796371 39796371 single base substitution C T intron_variant MELA-AU 20 39796371 39796371 single base substitution C T upstream_gene_variant MELA-AU 20 39796505 39796505 single base substitution G A downstream_gene_variant MELA-AU 20 39796505 39796505 single base substitution G A exon_variant MELA-AU 20 39796505 39796505 single base substitution G A missense_variant G772E 2315G>A MELA-AU 20 39796505 39796505 single base substitution G A upstream_gene_variant MELA-AU 20 39796789 39796789 single base substitution C T downstream_gene_variant MELA-AU 20 39796789 39796789 single base substitution C T intron_variant MELA-AU 20 39796789 39796789 single base substitution C T upstream_gene_variant MELA-AU 20 39797297 39797297 single base substitution C T downstream_gene_variant MELA-AU 20 39797297 39797297 single base substitution C T intron_variant MELA-AU 20 39797297 39797297 single base substitution C T upstream_gene_variant MELA-AU 20 39797804 39797804 single base substitution C T downstream_gene_variant MELA-AU 20 39797804 39797804 single base substitution C T exon_variant MELA-AU 20 39797804 39797804 single base substitution C T missense_variant P857S 2569C>T MELA-AU 20 39797804 39797804 single base substitution C T upstream_gene_variant MELA-AU 20 39798328 39798328 single base substitution C T downstream_gene_variant MELA-AU 20 39798328 39798328 single base substitution C T intron_variant MELA-AU 20 39798328 39798328 single base substitution C T upstream_gene_variant MELA-AU 20 39800244 39800244 single base substitution A G downstream_gene_variant MELA-AU 20 39800244 39800244 single base substitution A G intron_variant MELA-AU 20 39800244 39800244 single base substitution A G upstream_gene_variant MELA-AU 20 39801751 39801751 single base substitution C T downstream_gene_variant MELA-AU 20 39801751 39801751 single base substitution C T intron_variant MELA-AU 20 39801751 39801751 single base substitution C T upstream_gene_variant MELA-AU 20 39801945 39801946 multiple base substitution (>=2bp and <=200bp) GG AT downstream_gene_variant MELA-AU 20 39801945 39801946 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 20 39801945 39801946 multiple base substitution (>=2bp and <=200bp) GG AT upstream_gene_variant MELA-AU 20 39802413 39802413 single base substitution C T 3_prime_UTR_variant MELA-AU 20 39802413 39802413 single base substitution C T downstream_gene_variant MELA-AU 20 39802413 39802413 single base substitution C T exon_variant MELA-AU 20 39802413 39802413 single base substitution C T synonymous_variant F1172F 3516C>T MELA-AU 20 39802413 39802413 single base substitution C T upstream_gene_variant MELA-AU 20 39803168 39803168 single base substitution G A 3_prime_UTR_variant MELA-AU 20 39803168 39803168 single base substitution G A downstream_gene_variant MELA-AU 20 39803168 39803168 single base substitution G A exon_variant MELA-AU 20 39803168 39803168 single base substitution G A intron_variant MELA-AU 20 39803504 39803504 single base substitution G A 3_prime_UTR_variant MELA-AU 20 39803504 39803504 single base substitution G A downstream_gene_variant MELA-AU 20 39803504 39803504 single base substitution G A intron_variant MELA-AU 20 39803689 39803689 single base substitution C T 3_prime_UTR_variant MELA-AU 20 39803689 39803689 single base substitution C T downstream_gene_variant MELA-AU 20 39803689 39803689 single base substitution C T intron_variant MELA-AU 20 39804711 39804711 single base substitution G T downstream_gene_variant MELA-AU 20 39804711 39804711 single base substitution G T intron_variant MELA-AU 20 39805186 39805186 single base substitution A G downstream_gene_variant MELA-AU 20 39805186 39805186 single base substitution A G intron_variant MELA-AU 20 39806206 39806206 single base substitution C G downstream_gene_variant MELA-AU 20 39806206 39806206 single base substitution C G intron_variant MELA-AU 20 39807081 39807081 single base substitution C T downstream_gene_variant MELA-AU 20 39807081 39807081 single base substitution C T intron_variant MELA-AU 20 39808871 39808871 single base substitution G A downstream_gene_variant MELA-AU 20 39808871 39808871 single base substitution G A intron_variant MELA-AU 20 39809343 39809343 single base substitution C T downstream_gene_variant MELA-AU 20 39809343 39809343 single base substitution C T intron_variant MELA-AU 20 39810227 39810227 single base substitution C T intron_variant MELA-AU 20 39811965 39811966 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 20 39812959 39812959 single base substitution C A downstream_gene_variant MELA-AU 20 39813715 39813716 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 20 39813785 39813786 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 20 39814171 39814171 single base substitution G A downstream_gene_variant MELA-AU 20 39815059 39815060 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 20 39815153 39815153 single base substitution G A downstream_gene_variant MELA-AU 20 39815272 39815272 single base substitution C T downstream_gene_variant MELA-AU 20 39816271 39816271 single base substitution T G downstream_gene_variant MELA-AU 20 39816607 39816607 single base substitution T C downstream_gene_variant NBL-US 20 39802312 39802312 single base substitution G T 3_prime_UTR_variant NBL-US 20 39802312 39802312 single base substitution G T downstream_gene_variant NBL-US 20 39802312 39802312 single base substitution G T exon_variant NBL-US 20 39802312 39802312 single base substitution G T missense_variant V1139L 3415G>T NBL-US 20 39802312 39802312 single base substitution G T upstream_gene_variant ORCA-IN 20 39766440 39766440 single base substitution C T exon_variant ORCA-IN 20 39766440 39766440 single base substitution C T synonymous_variant V53V 159C>T ORCA-IN 20 39791421 39791421 single base substitution C G downstream_gene_variant ORCA-IN 20 39791421 39791421 single base substitution C G intron_variant ORCA-IN 20 39791421 39791421 single base substitution C G upstream_gene_variant ORCA-IN 20 39799962 39799962 single base substitution C G downstream_gene_variant ORCA-IN 20 39799962 39799962 single base substitution C G intron_variant ORCA-IN 20 39799962 39799962 single base substitution C G upstream_gene_variant ORCA-IN 20 39802881 39802881 single base substitution C A downstream_gene_variant ORCA-IN 20 39802881 39802881 single base substitution C A exon_variant ORCA-IN 20 39802881 39802881 single base substitution C A intron_variant ORCA-IN 20 39802881 39802881 single base substitution C A missense_variant Q1254K 3760C>A ORCA-IN 20 39802881 39802881 single base substitution C A missense_variant Q1255K 3763C>A ORCA-IN 20 39807417 39807417 single base substitution G C downstream_gene_variant ORCA-IN 20 39807417 39807417 single base substitution G C intron_variant ORCA-IN 20 39807637 39807637 single base substitution G A downstream_gene_variant ORCA-IN 20 39807637 39807637 single base substitution G A intron_variant OV-AU 20 39763304 39763304 single base substitution A T upstream_gene_variant OV-AU 20 39769342 39769342 single base substitution G T intron_variant OV-AU 20 39774501 39774501 single base substitution T A intron_variant OV-AU 20 39775218 39775218 single base substitution G A intron_variant OV-AU 20 39775792 39775792 single base substitution C A intron_variant OV-AU 20 39776354 39776354 single base substitution T C intron_variant OV-AU 20 39777361 39777361 single base substitution T G intron_variant OV-AU 20 39790757 39790757 single base substitution C T downstream_gene_variant OV-AU 20 39790757 39790757 single base substitution C T intron_variant OV-AU 20 39790757 39790757 single base substitution C T upstream_gene_variant OV-AU 20 39797874 39797874 single base substitution C T downstream_gene_variant OV-AU 20 39797874 39797874 single base substitution C T intron_variant OV-AU 20 39797874 39797874 single base substitution C T upstream_gene_variant OV-AU 20 39798883 39798883 single base substitution G A downstream_gene_variant OV-AU 20 39798883 39798883 single base substitution G A exon_variant OV-AU 20 39798883 39798883 single base substitution G A missense_variant E928K 2782G>A OV-AU 20 39798883 39798883 single base substitution G A upstream_gene_variant OV-AU 20 39810984 39810984 single base substitution T A intron_variant PACA-AU 20 39763083 39763083 single base substitution C T upstream_gene_variant PACA-AU 20 39766722 39766722 single base substitution G T intron_variant PACA-AU 20 39770515 39770515 single base substitution C G intron_variant PACA-AU 20 39770516 39770516 single base substitution T A intron_variant PACA-AU 20 39778689 39778689 single base substitution G A intron_variant PACA-AU 20 39785185 39785185 single base substitution C T intron_variant PACA-AU 20 39790971 39790971 single base substitution T C downstream_gene_variant PACA-AU 20 39790971 39790971 single base substitution T C intron_variant PACA-AU 20 39790971 39790971 single base substitution T C upstream_gene_variant PACA-AU 20 39794432 39794432 single base substitution G A downstream_gene_variant PACA-AU 20 39794432 39794432 single base substitution G A exon_variant PACA-AU 20 39794432 39794432 single base substitution G A missense_variant E589K 1765G>A PACA-AU 20 39794432 39794432 single base substitution G A upstream_gene_variant PACA-AU 20 39801038 39801038 single base substitution A C downstream_gene_variant PACA-AU 20 39801038 39801038 single base substitution A C intron_variant PACA-AU 20 39801038 39801038 single base substitution A C upstream_gene_variant PACA-AU 20 39802078 39802078 single base substitution C G 3_prime_UTR_variant PACA-AU 20 39802078 39802078 single base substitution C G downstream_gene_variant PACA-AU 20 39802078 39802078 single base substitution C G exon_variant PACA-AU 20 39802078 39802078 single base substitution C G missense_variant L1100V 3298C>G PACA-AU 20 39802078 39802078 single base substitution C G upstream_gene_variant PACA-AU 20 39803623 39803623 single base substitution C T 3_prime_UTR_variant PACA-AU 20 39803623 39803623 single base substitution C T downstream_gene_variant PACA-AU 20 39803623 39803623 single base substitution C T intron_variant PACA-AU 20 39806757 39806757 single base substitution C G downstream_gene_variant PACA-AU 20 39806757 39806757 single base substitution C G intron_variant PACA-AU 20 39808427 39808427 single base substitution G A downstream_gene_variant PACA-AU 20 39808427 39808427 single base substitution G A intron_variant PACA-AU 20 39809067 39809067 single base substitution C T downstream_gene_variant PACA-AU 20 39809067 39809067 single base substitution C T intron_variant PACA-AU 20 39811840 39811840 single base substitution A T downstream_gene_variant PACA-AU 20 39815786 39815786 single base substitution C A downstream_gene_variant PACA-CA 20 39763641 39763641 single base substitution T A upstream_gene_variant PACA-CA 20 39776256 39776256 single base substitution C G intron_variant PACA-CA 20 39787182 39787182 single base substitution G A intron_variant PACA-CA 20 39787182 39787182 single base substitution G A upstream_gene_variant PACA-CA 20 39789458 39789458 single base substitution G A downstream_gene_variant PACA-CA 20 39789458 39789458 single base substitution G A intron_variant PACA-CA 20 39789458 39789458 single base substitution G A upstream_gene_variant PACA-CA 20 39790555 39790555 single base substitution G T downstream_gene_variant PACA-CA 20 39790555 39790555 single base substitution G T intron_variant PACA-CA 20 39790555 39790555 single base substitution G T upstream_gene_variant PACA-CA 20 39790757 39790757 single base substitution C T downstream_gene_variant PACA-CA 20 39790757 39790757 single base substitution C T intron_variant PACA-CA 20 39790757 39790757 single base substitution C T upstream_gene_variant PACA-CA 20 39794409 39794409 single base substitution G A downstream_gene_variant PACA-CA 20 39794409 39794409 single base substitution G A exon_variant PACA-CA 20 39794409 39794409 single base substitution G A missense_variant G581D 1742G>A PACA-CA 20 39794409 39794409 single base substitution G A upstream_gene_variant PACA-CA 20 39797700 39797700 single base substitution C T downstream_gene_variant PACA-CA 20 39797700 39797700 single base substitution C T intron_variant PACA-CA 20 39797700 39797700 single base substitution C T upstream_gene_variant PACA-CA 20 39804382 39804382 single base substitution C T downstream_gene_variant PACA-CA 20 39804382 39804382 single base substitution C T intron_variant PACA-CA 20 39806760 39806760 single base substitution C T downstream_gene_variant PACA-CA 20 39806760 39806760 single base substitution C T intron_variant PACA-CA 20 39808943 39808943 single base substitution T G downstream_gene_variant PACA-CA 20 39808943 39808943 single base substitution T G intron_variant PACA-CA 20 39809666 39809666 single base substitution G C intron_variant PACA-CA 20 39811809 39811809 insertion of <=200bp - TA downstream_gene_variant PACA-CA 20 39811823 39811823 single base substitution G A downstream_gene_variant PACA-CA 20 39812110 39812110 single base substitution G A downstream_gene_variant PACA-CA 20 39814315 39814315 single base substitution T A downstream_gene_variant PACA-CA 20 39816581 39816581 single base substitution G C downstream_gene_variant PAEN-IT 20 39763718 39763718 single base substitution C A upstream_gene_variant PAEN-IT 20 39788639 39788639 single base substitution C A downstream_gene_variant PAEN-IT 20 39788639 39788639 single base substitution C A intron_variant PAEN-IT 20 39788639 39788639 single base substitution C A upstream_gene_variant PBCA-DE 20 39790931 39790931 single base substitution G C downstream_gene_variant PBCA-DE 20 39790931 39790931 single base substitution G C intron_variant PBCA-DE 20 39790931 39790931 single base substitution G C upstream_gene_variant PBCA-DE 20 39803938 39803938 single base substitution G A 3_prime_UTR_variant PBCA-DE 20 39803938 39803938 single base substitution G A downstream_gene_variant PBCA-DE 20 39803938 39803938 single base substitution G A intron_variant PRAD-CA 20 39775894 39775894 single base substitution G C intron_variant PRAD-CA 20 39776849 39776849 single base substitution T G intron_variant PRAD-CA 20 39781285 39781285 single base substitution C G intron_variant PRAD-CA 20 39801164 39801164 single base substitution C A 3_prime_UTR_variant PRAD-CA 20 39801164 39801164 single base substitution C A downstream_gene_variant PRAD-CA 20 39801164 39801164 single base substitution C A exon_variant PRAD-CA 20 39801164 39801164 single base substitution C A stop_gained Y1003* 3009C>A PRAD-CA 20 39801164 39801164 single base substitution C A upstream_gene_variant PRAD-CA 20 39812946 39812946 single base substitution T A downstream_gene_variant PRAD-UK 20 39765622 39765622 single base substitution G A 5_prime_UTR_variant PRAD-UK 20 39765622 39765622 single base substitution G A upstream_gene_variant PRAD-UK 20 39784200 39784200 single base substitution C A intron_variant PRAD-UK 20 39800793 39800793 single base substitution G A downstream_gene_variant PRAD-UK 20 39800793 39800793 single base substitution G A intron_variant PRAD-UK 20 39800793 39800793 single base substitution G A upstream_gene_variant PRAD-US 20 39796522 39796522 single base substitution C T downstream_gene_variant PRAD-US 20 39796522 39796522 single base substitution C T exon_variant PRAD-US 20 39796522 39796522 single base substitution C T missense_variant R778C 2332C>T PRAD-US 20 39796522 39796522 single base substitution C T upstream_gene_variant READ-US 20 39795345 39795345 single base substitution G A downstream_gene_variant READ-US 20 39795345 39795345 single base substitution G A exon_variant READ-US 20 39795345 39795345 single base substitution G A missense_variant R716H 2147G>A READ-US 20 39795345 39795345 single base substitution G A upstream_gene_variant RECA-EU 20 39766387 39766387 single base substitution A C exon_variant RECA-EU 20 39766387 39766387 single base substitution A C missense_variant T36P 106A>C RECA-EU 20 39812312 39812312 single base substitution C T downstream_gene_variant RECA-EU 20 39816029 39816029 single base substitution C T downstream_gene_variant SKCA-BR 20 39762292 39762292 insertion of <=200bp - CAA upstream_gene_variant SKCA-BR 20 39763121 39763121 single base substitution G A upstream_gene_variant SKCA-BR 20 39763990 39763990 single base substitution A G upstream_gene_variant SKCA-BR 20 39764025 39764025 single base substitution A C upstream_gene_variant SKCA-BR 20 39765581 39765581 single base substitution G C upstream_gene_variant SKCA-BR 20 39765592 39765592 single base substitution T C upstream_gene_variant SKCA-BR 20 39766302 39766302 single base substitution T C exon_variant SKCA-BR 20 39766302 39766302 single base substitution T C synonymous_variant P7P 21T>C SKCA-BR 20 39766302 39766302 single base substitution T C upstream_gene_variant SKCA-BR 20 39767136 39767136 single base substitution C T intron_variant SKCA-BR 20 39767459 39767459 single base substitution A C intron_variant SKCA-BR 20 39776459 39776459 single base substitution G A intron_variant SKCA-BR 20 39781510 39781510 single base substitution G T intron_variant SKCA-BR 20 39781838 39781838 single base substitution C T intron_variant SKCA-BR 20 39786190 39786190 single base substitution C T intron_variant SKCA-BR 20 39789715 39789715 single base substitution A G downstream_gene_variant SKCA-BR 20 39789715 39789715 single base substitution A G intron_variant SKCA-BR 20 39789715 39789715 single base substitution A G upstream_gene_variant SKCA-BR 20 39790874 39790875 deletion of <=200bp TG - downstream_gene_variant SKCA-BR 20 39790874 39790875 deletion of <=200bp TG - intron_variant SKCA-BR 20 39790874 39790875 deletion of <=200bp TG - upstream_gene_variant SKCA-BR 20 39790875 39790875 single base substitution G T downstream_gene_variant SKCA-BR 20 39790875 39790875 single base substitution G T intron_variant SKCA-BR 20 39790875 39790875 single base substitution G T upstream_gene_variant SKCA-BR 20 39796112 39796112 single base substitution T G downstream_gene_variant SKCA-BR 20 39796112 39796112 single base substitution T G intron_variant SKCA-BR 20 39796112 39796112 single base substitution T G upstream_gene_variant SKCA-BR 20 39796117 39796117 single base substitution A G downstream_gene_variant SKCA-BR 20 39796117 39796117 single base substitution A G intron_variant SKCA-BR 20 39796117 39796117 single base substitution A G upstream_gene_variant SKCA-BR 20 39797002 39797002 single base substitution A T downstream_gene_variant SKCA-BR 20 39797002 39797002 single base substitution A T intron_variant SKCA-BR 20 39797002 39797002 single base substitution A T upstream_gene_variant SKCA-BR 20 39797003 39797003 single base substitution C T downstream_gene_variant SKCA-BR 20 39797003 39797003 single base substitution C T intron_variant SKCA-BR 20 39797003 39797003 single base substitution C T upstream_gene_variant SKCA-BR 20 39797532 39797532 single base substitution C T downstream_gene_variant SKCA-BR 20 39797532 39797532 single base substitution C T intron_variant SKCA-BR 20 39797532 39797532 single base substitution C T upstream_gene_variant SKCA-BR 20 39803883 39803883 single base substitution C G 3_prime_UTR_variant SKCA-BR 20 39803883 39803883 single base substitution C G downstream_gene_variant SKCA-BR 20 39803883 39803883 single base substitution C G intron_variant SKCA-BR 20 39808740 39808740 single base substitution T G downstream_gene_variant SKCA-BR 20 39808740 39808740 single base substitution T G intron_variant SKCA-BR 20 39815697 39815697 single base substitution T C downstream_gene_variant SKCA-BR 20 39815780 39815780 single base substitution A G downstream_gene_variant SKCM-US 20 39788792 39788792 single base substitution C T downstream_gene_variant SKCM-US 20 39788792 39788792 single base substitution C T missense_variant R171C 511C>T SKCM-US 20 39788792 39788792 single base substitution C T splice_region_variant SKCM-US 20 39788792 39788792 single base substitution C T upstream_gene_variant SKCM-US 20 39791897 39791897 single base substitution C T downstream_gene_variant SKCM-US 20 39791897 39791897 single base substitution C T exon_variant SKCM-US 20 39791897 39791897 single base substitution C T synonymous_variant F257F 771C>T SKCM-US 20 39791897 39791897 single base substitution C T upstream_gene_variant SKCM-US 20 39792036 39792036 single base substitution C T downstream_gene_variant SKCM-US 20 39792036 39792036 single base substitution C T exon_variant SKCM-US 20 39792036 39792036 single base substitution C T missense_variant R270C 808C>T SKCM-US 20 39792036 39792036 single base substitution C T upstream_gene_variant SKCM-US 20 39792045 39792045 single base substitution G A downstream_gene_variant SKCM-US 20 39792045 39792045 single base substitution G A exon_variant SKCM-US 20 39792045 39792045 single base substitution G A missense_variant V273M 817G>A SKCM-US 20 39792045 39792045 single base substitution G A upstream_gene_variant SKCM-US 20 39792068 39792068 single base substitution C T downstream_gene_variant SKCM-US 20 39792068 39792068 single base substitution C T exon_variant SKCM-US 20 39792068 39792068 single base substitution C T synonymous_variant F280F 840C>T SKCM-US 20 39792068 39792068 single base substitution C T upstream_gene_variant SKCM-US 20 39792092 39792092 single base substitution C T downstream_gene_variant SKCM-US 20 39792092 39792092 single base substitution C T exon_variant SKCM-US 20 39792092 39792092 single base substitution C T synonymous_variant I288I 864C>T SKCM-US 20 39792092 39792092 single base substitution C T upstream_gene_variant SKCM-US 20 39792111 39792111 single base substitution C T downstream_gene_variant SKCM-US 20 39792111 39792111 single base substitution C T exon_variant SKCM-US 20 39792111 39792111 single base substitution C T synonymous_variant L295L 883C>T SKCM-US 20 39792111 39792111 single base substitution C T upstream_gene_variant SKCM-US 20 39793585 39793585 single base substitution C T downstream_gene_variant SKCM-US 20 39793585 39793585 single base substitution C T synonymous_variant I410I 1230C>T SKCM-US 20 39793585 39793585 single base substitution C T upstream_gene_variant SKCM-US 20 39793702 39793702 single base substitution C T downstream_gene_variant SKCM-US 20 39793702 39793702 single base substitution C T synonymous_variant L449L 1347C>T SKCM-US 20 39793702 39793702 single base substitution C T upstream_gene_variant SKCM-US 20 39794189 39794189 single base substitution G A downstream_gene_variant SKCM-US 20 39794189 39794189 single base substitution G A missense_variant E537K 1609G>A SKCM-US 20 39794189 39794189 single base substitution G A splice_region_variant SKCM-US 20 39794189 39794189 single base substitution G A upstream_gene_variant SKCM-US 20 39794389 39794389 single base substitution C T downstream_gene_variant SKCM-US 20 39794389 39794389 single base substitution C T exon_variant SKCM-US 20 39794389 39794389 single base substitution C T synonymous_variant I574I 1722C>T SKCM-US 20 39794389 39794389 single base substitution C T upstream_gene_variant SKCM-US 20 39794419 39794419 single base substitution C T downstream_gene_variant SKCM-US 20 39794419 39794419 single base substitution C T exon_variant SKCM-US 20 39794419 39794419 single base substitution C T synonymous_variant L584L 1752C>T SKCM-US 20 39794419 39794419 single base substitution C T upstream_gene_variant SKCM-US 20 39794935 39794935 single base substitution A G downstream_gene_variant SKCM-US 20 39794935 39794935 single base substitution A G exon_variant SKCM-US 20 39794935 39794935 single base substitution A G missense_variant D634G 1901A>G SKCM-US 20 39794935 39794935 single base substitution A G upstream_gene_variant SKCM-US 20 39795344 39795344 single base substitution C T downstream_gene_variant SKCM-US 20 39795344 39795344 single base substitution C T exon_variant SKCM-US 20 39795344 39795344 single base substitution C T missense_variant R716C 2146C>T SKCM-US 20 39795344 39795344 single base substitution C T upstream_gene_variant SKCM-US 20 39801087 39801087 single base substitution C T downstream_gene_variant SKCM-US 20 39801087 39801087 single base substitution C T exon_variant SKCM-US 20 39801087 39801087 single base substitution C T missense_variant R978W 2932C>T SKCM-US 20 39801087 39801087 single base substitution C T upstream_gene_variant SKCM-US 20 39801100 39801100 single base substitution C T downstream_gene_variant SKCM-US 20 39801100 39801100 single base substitution C T exon_variant SKCM-US 20 39801100 39801100 single base substitution C T missense_variant S982F 2945C>T SKCM-US 20 39801100 39801100 single base substitution C T upstream_gene_variant SKCM-US 20 39801155 39801155 single base substitution C T 3_prime_UTR_variant SKCM-US 20 39801155 39801155 single base substitution C T downstream_gene_variant SKCM-US 20 39801155 39801155 single base substitution C T exon_variant SKCM-US 20 39801155 39801155 single base substitution C T synonymous_variant F1000F 3000C>T SKCM-US 20 39801155 39801155 single base substitution C T upstream_gene_variant STAD-US 20 39788754 39788754 single base substitution G A downstream_gene_variant STAD-US 20 39788754 39788754 single base substitution G A exon_variant STAD-US 20 39788754 39788754 single base substitution G A missense_variant R158Q 473G>A STAD-US 20 39788754 39788754 single base substitution G A upstream_gene_variant STAD-US 20 39788762 39788762 single base substitution T C downstream_gene_variant STAD-US 20 39788762 39788762 single base substitution T C exon_variant STAD-US 20 39788762 39788762 single base substitution T C missense_variant F161L 481T>C STAD-US 20 39788762 39788762 single base substitution T C upstream_gene_variant STAD-US 20 39788775 39788775 single base substitution A T downstream_gene_variant STAD-US 20 39788775 39788775 single base substitution A T exon_variant STAD-US 20 39788775 39788775 single base substitution A T missense_variant D165V 494A>T STAD-US 20 39788775 39788775 single base substitution A T upstream_gene_variant STAD-US 20 39791294 39791294 single base substitution C T downstream_gene_variant STAD-US 20 39791294 39791294 single base substitution C T missense_variant R204C 610C>T STAD-US 20 39791294 39791294 single base substitution C T upstream_gene_variant STAD-US 20 39791298 39791298 single base substitution G A downstream_gene_variant STAD-US 20 39791298 39791298 single base substitution G A missense_variant S205N 614G>A STAD-US 20 39791298 39791298 single base substitution G A upstream_gene_variant STAD-US 20 39791353 39791353 single base substitution C T downstream_gene_variant STAD-US 20 39791353 39791353 single base substitution C T synonymous_variant S223S 669C>T STAD-US 20 39791353 39791353 single base substitution C T upstream_gene_variant STAD-US 20 39791364 39791364 single base substitution C T downstream_gene_variant STAD-US 20 39791364 39791364 single base substitution C T missense_variant T227M 680C>T STAD-US 20 39791364 39791364 single base substitution C T upstream_gene_variant STAD-US 20 39791907 39791907 single base substitution T C downstream_gene_variant STAD-US 20 39791907 39791907 single base substitution T C exon_variant STAD-US 20 39791907 39791907 single base substitution T C missense_variant Y261H 781T>C STAD-US 20 39791907 39791907 single base substitution T C upstream_gene_variant STAD-US 20 39792036 39792036 single base substitution C T downstream_gene_variant STAD-US 20 39792036 39792036 single base substitution C T exon_variant STAD-US 20 39792036 39792036 single base substitution C T missense_variant R270C 808C>T STAD-US 20 39792036 39792036 single base substitution C T upstream_gene_variant STAD-US 20 39792073 39792073 single base substitution G A downstream_gene_variant STAD-US 20 39792073 39792073 single base substitution G A exon_variant STAD-US 20 39792073 39792073 single base substitution G A missense_variant R282Q 845G>A STAD-US 20 39792073 39792073 single base substitution G A upstream_gene_variant STAD-US 20 39792749 39792749 single base substitution G A downstream_gene_variant STAD-US 20 39792749 39792749 single base substitution G A missense_variant M375I 1125G>A STAD-US 20 39792749 39792749 single base substitution G A upstream_gene_variant STAD-US 20 39792806 39792806 single base substitution G A downstream_gene_variant STAD-US 20 39792806 39792806 single base substitution G A synonymous_variant L394L 1182G>A STAD-US 20 39792806 39792806 single base substitution G A upstream_gene_variant STAD-US 20 39793674 39793674 single base substitution A G downstream_gene_variant STAD-US 20 39793674 39793674 single base substitution A G missense_variant K440R 1319A>G STAD-US 20 39793674 39793674 single base substitution A G upstream_gene_variant STAD-US 20 39793708 39793708 single base substitution A C downstream_gene_variant STAD-US 20 39793708 39793708 single base substitution A C synonymous_variant S451S 1353A>C STAD-US 20 39793708 39793708 single base substitution A C upstream_gene_variant STAD-US 20 39794342 39794342 single base substitution C T downstream_gene_variant STAD-US 20 39794342 39794342 single base substitution C T exon_variant STAD-US 20 39794342 39794342 single base substitution C T missense_variant R559C 1675C>T STAD-US 20 39794342 39794342 single base substitution C T upstream_gene_variant STAD-US 20 39794919 39794919 single base substitution T G downstream_gene_variant STAD-US 20 39794919 39794919 single base substitution T G exon_variant STAD-US 20 39794919 39794919 single base substitution T G missense_variant F629V 1885T>G STAD-US 20 39794919 39794919 single base substitution T G upstream_gene_variant STAD-US 20 39794988 39794988 single base substitution C T downstream_gene_variant STAD-US 20 39794988 39794988 single base substitution C T exon_variant STAD-US 20 39794988 39794988 single base substitution C T stop_gained R652* 1954C>T STAD-US 20 39794988 39794988 single base substitution C T upstream_gene_variant STAD-US 20 39798806 39798806 single base substitution C T downstream_gene_variant STAD-US 20 39798806 39798806 single base substitution C T exon_variant STAD-US 20 39798806 39798806 single base substitution C T missense_variant A902V 2705C>T STAD-US 20 39798806 39798806 single base substitution C T upstream_gene_variant STAD-US 20 39798904 39798904 single base substitution G A downstream_gene_variant STAD-US 20 39798904 39798904 single base substitution G A exon_variant STAD-US 20 39798904 39798904 single base substitution G A missense_variant A935T 2803G>A STAD-US 20 39798904 39798904 single base substitution G A upstream_gene_variant STAD-US 20 39800838 39800838 single base substitution T C downstream_gene_variant STAD-US 20 39800838 39800838 single base substitution T C intron_variant STAD-US 20 39800838 39800838 single base substitution T C synonymous_variant T938T 2814T>C STAD-US 20 39800838 39800838 single base substitution T C upstream_gene_variant STAD-US 20 39801247 39801247 single base substitution G A 3_prime_UTR_variant STAD-US 20 39801247 39801247 single base substitution G A downstream_gene_variant STAD-US 20 39801247 39801247 single base substitution G A exon_variant STAD-US 20 39801247 39801247 single base substitution G A missense_variant C1031Y 3092G>A STAD-US 20 39801247 39801247 single base substitution G A upstream_gene_variant STAD-US 20 39801287 39801287 single base substitution T C downstream_gene_variant STAD-US 20 39801287 39801287 single base substitution T C splice_donor_variant STAD-US 20 39801287 39801287 single base substitution T C upstream_gene_variant UCEC-US 20 39792069 39792069 single base substitution C A downstream_gene_variant UCEC-US 20 39792069 39792069 single base substitution C A exon_variant UCEC-US 20 39792069 39792069 single base substitution C A missense_variant L281I 841C>A UCEC-US 20 39792069 39792069 single base substitution C A upstream_gene_variant UCEC-US 20 39792735 39792735 single base substitution G A downstream_gene_variant UCEC-US 20 39792735 39792735 single base substitution G A missense_variant G371S 1111G>A UCEC-US 20 39792735 39792735 single base substitution G A upstream_gene_variant UCEC-US 20 39794302 39794302 single base substitution C T downstream_gene_variant UCEC-US 20 39794302 39794302 single base substitution C T exon_variant UCEC-US 20 39794302 39794302 single base substitution C T synonymous_variant H545H 1635C>T UCEC-US 20 39794302 39794302 single base substitution C T upstream_gene_variant UCEC-US 20 39794395 39794395 single base substitution C T downstream_gene_variant UCEC-US 20 39794395 39794395 single base substitution C T exon_variant UCEC-US 20 39794395 39794395 single base substitution C T synonymous_variant T576T 1728C>T UCEC-US 20 39794395 39794395 single base substitution C T upstream_gene_variant UCEC-US 20 39794454 39794454 single base substitution C T downstream_gene_variant UCEC-US 20 39794454 39794454 single base substitution C T exon_variant UCEC-US 20 39794454 39794454 single base substitution C T missense_variant T596M 1787C>T UCEC-US 20 39794454 39794454 single base substitution C T upstream_gene_variant UCEC-US 20 39794947 39794947 single base substitution A G downstream_gene_variant UCEC-US 20 39794947 39794947 single base substitution A G exon_variant UCEC-US 20 39794947 39794947 single base substitution A G missense_variant H638R 1913A>G UCEC-US 20 39794947 39794947 single base substitution A G upstream_gene_variant UCEC-US 20 39795391 39795391 single base substitution C T downstream_gene_variant UCEC-US 20 39795391 39795391 single base substitution C T exon_variant UCEC-US 20 39795391 39795391 single base substitution C T synonymous_variant F731F 2193C>T UCEC-US 20 39795391 39795391 single base substitution C T upstream_gene_variant UCEC-US 20 39795437 39795437 single base substitution T C downstream_gene_variant UCEC-US 20 39795437 39795437 single base substitution T C exon_variant UCEC-US 20 39795437 39795437 single base substitution T C missense_variant Y747H 2239T>C UCEC-US 20 39795437 39795437 single base substitution T C upstream_gene_variant UCEC-US 20 39798786 39798786 single base substitution C T downstream_gene_variant UCEC-US 20 39798786 39798786 single base substitution C T exon_variant UCEC-US 20 39798786 39798786 single base substitution C T synonymous_variant F895F 2685C>T UCEC-US 20 39798786 39798786 single base substitution C T upstream_gene_variant UCEC-US 20 39800903 39800903 single base substitution G A downstream_gene_variant UCEC-US 20 39800903 39800903 single base substitution G A intron_variant UCEC-US 20 39800903 39800903 single base substitution G A missense_variant C960Y 2879G>A UCEC-US 20 39800903 39800903 single base substitution G A upstream_gene_variant UCEC-US 20 39801087 39801087 single base substitution C T downstream_gene_variant UCEC-US 20 39801087 39801087 single base substitution C T exon_variant UCEC-US 20 39801087 39801087 single base substitution C T missense_variant R978W 2932C>T UCEC-US 20 39801087 39801087 single base substitution C T upstream_gene_variant UCEC-US 20 39801188 39801188 single base substitution C G 3_prime_UTR_variant UCEC-US 20 39801188 39801188 single base substitution C G downstream_gene_variant UCEC-US 20 39801188 39801188 single base substitution C G exon_variant UCEC-US 20 39801188 39801188 single base substitution C G missense_variant I1011M 3033C>G UCEC-US 20 39801188 39801188 single base substitution C G upstream_gene_variant UCEC-US 20 39801481 39801481 single base substitution C T 3_prime_UTR_variant UCEC-US 20 39801481 39801481 single base substitution C T downstream_gene_variant UCEC-US 20 39801481 39801481 single base substitution C T exon_variant UCEC-US 20 39801481 39801481 single base substitution C T synonymous_variant S1081S 3243C>T UCEC-US 20 39801481 39801481 single base substitution C T upstream_gene_variant UCEC-US 20 39802358 39802358 single base substitution T G 3_prime_UTR_variant UCEC-US 20 39802358 39802358 single base substitution T G downstream_gene_variant UCEC-US 20 39802358 39802358 single base substitution T G exon_variant UCEC-US 20 39802358 39802358 single base substitution T G missense_variant F1154C 3461T>G UCEC-US 20 39802358 39802358 single base substitution T G upstream_gene_variant UCEC-US 20 39802889 39802889 single base substitution G A downstream_gene_variant UCEC-US 20 39802889 39802889 single base substitution G A exon_variant UCEC-US 20 39802889 39802889 single base substitution G A intron_variant UCEC-US 20 39802889 39802889 single base substitution G A synonymous_variant P1256P 3768G>A UCEC-US 20 39802889 39802889 single base substitution G A synonymous_variant P1257P 3771G>A UCEC-US 20 39802942 39802942 single base substitution G A downstream_gene_variant UCEC-US 20 39802942 39802942 single base substitution G A exon_variant UCEC-US 20 39802942 39802942 single base substitution G A intron_variant UCEC-US 20 39802942 39802942 single base substitution G A missense_variant R1274Q 3821G>A UCEC-US 20 39802942 39802942 single base substitution G A missense_variant R1275Q 3824G>A UCEC-US 20 39802951 39802951 single base substitution G A downstream_gene_variant UCEC-US 20 39802951 39802951 single base substitution G A exon_variant UCEC-US 20 39802951 39802951 single base substitution G A intron_variant UCEC-US 20 39802951 39802951 single base substitution G A missense_variant R1277K 3830G>A UCEC-US 20 39802951 39802951 single base substitution G A missense_variant R1278K 3833G>A UCEC-US 20 39802951 39802951 single base substitution G A splice_region_variant UCEC-US 20 39813832 39813832 single base substitution C A downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ATL011 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL050 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-A1-A0SI-01 COSM1483633 c.552C>T p.V184V Substitution - coding silent 20:41162491-41162491 + TCGA-C4-A0EZ-01 COSM419402 c.2737G>A p.A913T Substitution - Missense 20:41170198-41170198 + OSCC-GB_00800111 COSM4887883 c.159C>T p.V53V Substitution - coding silent 20:41137800-41137800 + ATL175 COSM5707441 c.3512_3514delATT p.N1171_F1172>I Complex - deletion inframe 20:41173769-41173771 + TCGA-AA-3663-01 COSM1411788 c.958G>A p.D320N Substitution - Missense 20:41163781-41163781 + TCGA-D1-A174-01 COSM1026802 c.2879G>A p.C960Y Substitution - Missense 20:41172263-41172263 + ATL098 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + CHC2034T COSM4789847 c.863T>G p.I288S Substitution - Missense 20:41163451-41163451 + TCGA-D5-6930-01 COSM1411786 c.245G>A p.R82H Substitution - Missense 20:41159633-41159633 + YUGAFFE COSM1713470 c.2945C>T p.S982F Substitution - Missense 20:41172460-41172460 + NCI-H2009 COSM18204 c.1466C>G p.S489C Substitution - Missense 20:41165324-41165324 + 2273188 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + CHC2034T COSM4789847 c.863T>G p.I288S Substitution - Missense 20:41163451-41163451 + PD13764a COSM5773579 c.732G>C p.P244P Substitution - coding silent 20:41163218-41163218 + ATL182 COSM5707427 c.3047A>G p.Q1016R Substitution - Missense 20:41172562-41172562 + Pat_01_B COSM5198245 c.1324G>A p.V442M Substitution - Missense 20:41165039-41165039 + ESCC_41 COSM5629584 c.807T>A p.D269E Substitution - Missense 20:41163395-41163395 + 2402372 COSM5049787 c.1025A>G p.D342G Substitution - Missense 20:41163935-41163935 + TCGA-BR-7703-01 COSM4098395 c.1954C>T p.R652* Substitution - Nonsense 20:41166348-41166348 + TCGA-AA-3972-01 COSM297321 c.610C>T p.R204C Substitution - Missense 20:41162654-41162654 + ATL104 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + KM12 COSM3291374 c.2139G>A p.K713K Substitution - coding silent 20:41166697-41166697 + ATL346 COSM5707425 c.2615T>G p.L872R Substitution - Missense 20:41169491-41169491 + 8014573 COSM3389747 c.3298C>G p.L1100V Substitution - Missense 20:41173438-41173438 + KPOPBR-03-T COSM4098396 c.2705C>T p.A902V Substitution - Missense 20:41170166-41170166 + TCGA-AP-A056-01 COSM1026806 c.3461T>G p.F1154C Substitution - Missense 20:41173718-41173718 + TCGA-BR-6452-01 COSM4098396 c.2705C>T p.A902V Substitution - Missense 20:41170166-41170166 + ATL370 COSM3291378 c.2332C>T p.R778C Substitution - Missense 20:41167882-41167882 + ATL020 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + 2153020 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ZZUFHECRKL-G045T COSM5437951 c.3446T>A p.I1149N Substitution - Missense 20:41173703-41173703 + LOVO COSM3291407 c.3680C>T p.T1227M Substitution - Missense 20:41174158-41174158 + sysucc-1370T COSM5471206 c.1355C>A p.P452H Substitution - Missense 20:41165070-41165070 + ATL288 COSM5707417 c.2242C>G p.R748G Substitution - Missense 20:41166800-41166800 + ATL140 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + WSU-HN8 COSM4590998 c.1921C>A p.Q641K Substitution - Missense 20:41166315-41166315 + TCGA-BR-4362-01 COSM4098382 c.481T>C p.F161L Substitution - Missense 20:41160122-41160122 + TCGA-AP-A0LD-01 COSM1026794 c.1111G>A p.G371S Substitution - Missense 20:41164095-41164095 + TCGA-CA-6717-01 COSM1411797 c.2412C>T p.A804A Substitution - coding silent 20:41168799-41168799 + EGC15 COSM5057305 c.1084C>T p.R362C Substitution - Missense 20:41163994-41163994 + DM16 COSM5609951 c.1137C>T p.Y379Y Substitution - coding silent 20:41164121-41164121 + ATL330 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + Au4 COSM5604520 c.2569C>T p.P857S Substitution - Missense 20:41169164-41169164 + TARGET-30-PASTKC COSM1287209 c.3415G>T p.V1139L Substitution - Missense 20:41173672-41173672 + TCGA-DU-5852-01 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + 2273185 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL009 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL326 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL018 COSM5707408 c.139G>A p.E47K Substitution - Missense 20:41137780-41137780 + ATL167 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + pfg118T COSM4753317 c.2406C>G p.Y802* Substitution - Nonsense 20:41168793-41168793 + 61 COSM443826 c.3758G>A p.R1253H Substitution - Missense 20:41174236-41174236 + 2296_T COSM3963564 c.2319C>A p.A773A Substitution - coding silent 20:41167869-41167869 + TCGA-D3-A2J7-06 COSM1026803 c.2932C>T p.R978W Substitution - Missense 20:41172447-41172447 + ATL273 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-F4-6856-01 COSM1411790 c.993_995delCTC p.S334delS Deletion - In frame 20:41163816-41163818 + PD9605a COSM5138634 c.299G>A p.R100Q Substitution - Missense 20:41159687-41159687 + ATL252 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL005 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL402 COSM3734686 c.1559C>T p.S520F Substitution - Missense 20:41165499-41165499 + BICR_22 COSM4590998 c.1921C>A p.Q641K Substitution - Missense 20:41166315-41166315 + SC_9026 COSM5565747 c.1072C>T p.R358W Substitution - Missense 20:41163982-41163982 + Pat_05_A COSM3291377 c.2272G>A p.E758K Substitution - Missense 20:41166830-41166830 + ATL327 COSM5707418 c.2242C>T p.R748C Substitution - Missense 20:41166800-41166800 + YUGOE COSM1713468 c.2439C>T p.I813I Substitution - coding silent 20:41168826-41168826 + T55 COSM4715090 c.979T>C p.S327P Substitution - Missense 20:41163802-41163802 + HCT116 COSM3291388 c.2657G>A p.R886H Substitution - Missense 20:41170118-41170118 + 115T COSM1725397 c.2179G>A p.G727R Substitution - Missense 20:41166737-41166737 + PD12797a COSM3769785 c.2120G>A p.R707Q Substitution - Missense 20:41166595-41166595 + ATL261 COSM5707438 c.3509A>G p.Q1170R Substitution - Missense 20:41173766-41173766 + TCGA-A6-6653-01 COSM1411802 c.3565G>A p.A1189T Substitution - Missense 20:41173931-41173931 + ATL313 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + TCGA-06-0743-01 COSM3405076 c.2249T>G p.M750R Substitution - Missense 20:41166807-41166807 + ATL418 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL277 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + 66 COSM5744045 c.1780G>A p.D594N Substitution - Missense 20:41165807-41165807 + ATL403 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + PD4261a COSM5771417 c.2393C>T p.A798V Substitution - Missense 20:41168780-41168780 + ATL039 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + TCGA-AP-A059-01 COSM1026796 c.1635C>T p.H545H Substitution - coding silent 20:41165662-41165662 + ATL298 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + LP6007523-DNA_A01 COSM5035859 c.2140C>T p.H714Y Substitution - Missense 20:41166698-41166698 + ATL328 COSM5707441 c.3512_3514delATT p.N1171_F1172>I Complex - deletion inframe 20:41173769-41173771 + pfg008T COSM1641344 c.789+1G>A p.? Unknown 20:41163276-41163276 + TCGA-76-6282-01 COSM3405075 c.1799+2T>C p.? Unknown 20:41165828-41165828 + CSCC-45-T COSM4549601 c.477G>A p.K159K Substitution - coding silent 20:41160118-41160118 + TCGA-CW-6093-01 COSM478153 c.2316G>T p.G772G Substitution - coding silent 20:41167866-41167866 + 2466116 COSM3769785 c.2120G>A p.R707Q Substitution - Missense 20:41166595-41166595 + ESO-131 COSM1262380 c.589C>T p.R197W Substitution - Missense 20:41162528-41162528 + TCGA-ER-A19M-06 COSM3546315 c.2146C>T p.R716C Substitution - Missense 20:41166704-41166704 + SC_9093 COSM5569410 c.596C>T p.T199M Substitution - Missense 20:41162535-41162535 + TCGA-B7-5816-01 COSM4098394 c.1885T>G p.F629V Substitution - Missense 20:41166279-41166279 + STC252 COSM5057308 c.2751G>A p.E917E Substitution - coding silent 20:41170212-41170212 + ATL235 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL280 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL354 COSM5707430 c.3487_3489delGAG p.E1164delE Deletion - In frame 20:41173744-41173746 + CSCC-31-T COSM4497446 c.496C>T p.R166W Substitution - Missense 20:41160137-41160137 + SH-7032 COSM4134539 c.835A>G p.S279G Substitution - Missense 20:41163423-41163423 + 587284 COSM1220947 c.1753G>A p.V585M Substitution - Missense 20:41165780-41165780 + TCGA-66-2754-01 COSM723672 c.3672C>T p.F1224F Substitution - coding silent 20:41174150-41174150 + 587278 COSM1220948 c.3223G>A p.D1075N Substitution - Missense 20:41172821-41172821 + ATL019 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL326 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + STC252 COSM5057306 c.2086C>T p.R696W Substitution - Missense 20:41166561-41166561 + YUKAT COSM5392057 c.2989G>A p.G997S Substitution - Missense 20:41172504-41172504 + BN43 COSM3707759 c.2695A>G p.I899V Substitution - Missense 20:41170156-41170156 + ATL138 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL090 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + ATL257 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + ATL053 COSM5707424 c.2606G>T p.G869V Substitution - Missense 20:41169482-41169482 + BN43T COSM3707759 c.2695A>G p.I899V Substitution - Missense 20:41170156-41170156 + ATL354 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL073 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-06-0648-01 COSM2151410 c.332A>G p.Y111C Substitution - Missense 20:41159720-41159720 + AOCS-145-1-6 COSM4136888 c.2782G>A p.E928K Substitution - Missense 20:41170243-41170243 + SH-3458 COSM4134539 c.835A>G p.S279G Substitution - Missense 20:41163423-41163423 + ATL051 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + 93VU147T COSM4590998 c.1921C>A p.Q641K Substitution - Missense 20:41166315-41166315 + 2250162 COSM5029967 c.2905+7G>A p.? Unknown 20:41172296-41172296 + sysucc-311T COSM5464928 c.2617C>T p.R873W Substitution - Missense 20:41169493-41169493 + CSCC-31-T COSM4523497 c.1218G>A p.E406E Substitution - coding silent 20:41164933-41164933 + TCGA-B0-4827-01 COSM478154 c.2739C>T p.A913A Substitution - coding silent 20:41170200-41170200 + 2153048 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL039 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-AP-A059-01 COSM1026798 c.1787C>T p.T596M Substitution - Missense 20:41165814-41165814 + ATL172 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + TCGA-BR-8591-01 COSM4098393 c.1675C>T p.R559C Substitution - Missense 20:41165702-41165702 + ATL306 COSM5707428 c.3047A>T p.Q1016L Substitution - Missense 20:41172562-41172562 + HCC1395 COSM18203 c.1745C>G p.S582C Substitution - Missense 20:41165772-41165772 + TCGA-AZ-4615-01 COSM3693495 c.2792A>T p.Q931L Substitution - Missense 20:41170253-41170253 + 19 COSM5748166 c.3540delA p.G1182fs*2 Deletion - Frameshift 20:41173797-41173797 + TCGA-EE-A29V-06 COSM3546307 c.771C>T p.F257F Substitution - coding silent 20:41163257-41163257 + 3N56-VS-3T56 COSM4983809 c.1784A>G p.Y595C Substitution - Missense 20:41165811-41165811 + TCGA-AA-3561-01 COSM292513 c.732G>A p.P244P Substitution - coding silent 20:41163218-41163218 + LAU63 COSM233121 c.2837G>A p.R946K Substitution - Missense 20:41172221-41172221 + Pat_24_B COSM3911298 c.808C>T p.R270C Substitution - Missense 20:41163396-41163396 + BK0043 COSM4187613 c.2011G>T p.A671S Substitution - Missense 20:41166486-41166486 + LUAD-CHTN-Z4716A COSM362125 c.2686G>A p.V896I Substitution - Missense 20:41170147-41170147 + ATL016 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + CP66-MEL COSM18201 c.973C>T p.P325S Substitution - Missense 20:41163796-41163796 + TCGA-FW-A3R5-06 COSM3911300 c.1230C>T p.I410I Substitution - coding silent 20:41164945-41164945 + ATL094 COSM5707423 c.2600C>G p.P867R Substitution - Missense 20:41169476-41169476 + ATL050 COSM5707423 c.2600C>G p.P867R Substitution - Missense 20:41169476-41169476 + ATL251 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL324 COSM5707413 c.1817A>G p.Q606R Substitution - Missense 20:41166211-41166211 + cSCCP4 COSM139187 c.2890C>T p.P964S Substitution - Missense 20:41172274-41172274 + TCGA-HU-A4H3-01 COSM4098387 c.781T>C p.Y261H Substitution - Missense 20:41163267-41163267 + TCGA-A5-A0R7-01 COSM1026795 c.1574G>C p.S525T Substitution - Missense 20:41165514-41165514 + ATL083 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL093 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL168 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + sysucc-1397T COSM5474282 c.3280-8G>A p.? Unknown 20:41173412-41173412 + 2273186 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL253 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + S0029 COSM5883560 c.1603C>T p.P535S Substitution - Missense 20:41165543-41165543 + 193 COSM145783 c.866A>G p.E289G Substitution - Missense 20:41163454-41163454 + TCGA-EE-A181-06 COSM3546306 c.511C>T p.R171C Substitution - Missense 20:41160152-41160152 + ATL019 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + RKO COSM4648399 c.944A>C p.D315A Substitution - Missense 20:41163767-41163767 + TCGA-AP-A059-01 COSM1026793 c.841C>A p.L281I Substitution - Missense 20:41163429-41163429 + SH-5693 COSM4134539 c.835A>G p.S279G Substitution - Missense 20:41163423-41163423 + CAL33 COSM4590998 c.1921C>A p.Q641K Substitution - Missense 20:41166315-41166315 + ATL401 COSM5707428 c.3047A>T p.Q1016L Substitution - Missense 20:41172562-41172562 + TCGA-AY-6197-01 COSM1411791 c.1056C>A p.A352A Substitution - coding silent 20:41163966-41163966 + ATL308 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL316 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + QC2-35-T2 COSM5655167 c.3028C>T p.R1010C Substitution - Missense 20:41172543-41172543 + RK100_C01 COSM1632293 c.3278A>C p.E1093A Substitution - Missense 20:41172876-41172876 + 2521259 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + TCGA-BR-8487-01 COSM4098385 c.669C>T p.S223S Substitution - coding silent 20:41162713-41162713 + 2273192 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL216 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL183 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ESCC_BICR_016T COSM5439545 c.102C>G p.V34V Substitution - coding silent 20:41137743-41137743 + TCGA-13-2057-01 COSM1326740 c.1722C>G p.I574M Substitution - Missense 20:41165749-41165749 + TCGA-HU-A4GQ-01 COSM4098388 c.845G>A p.R282Q Substitution - Missense 20:41163433-41163433 + T3225 COSM4715092 c.2053G>A p.V685I Substitution - Missense 20:41166528-41166528 + NOKSI COSM4590998 c.1921C>A p.Q641K Substitution - Missense 20:41166315-41166315 + HCC1395 COSM18203 c.1745C>G p.S582C Substitution - Missense 20:41165772-41165772 + SS6003314 COSM1026807 c.3771G>A p.P1257P Substitution - coding silent 20:41174249-41174249 + ATL343 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL221 COSM5707419 c.2248A>G p.M750V Substitution - Missense 20:41166806-41166806 + TCGA-B5-A0JZ-01 COSM1026808 c.3824G>A p.R1275Q Substitution - Missense 20:41174302-41174302 + ATL156 COSM5707410 c.1523A>G p.H508R Substitution - Missense 20:41165463-41165463 + HCC13 COSM1615592 c.879C>A p.F293L Substitution - Missense 20:41163467-41163467 + ccRCC-40 COSM1663547 c.2197A>G p.S733G Substitution - Missense 20:41166755-41166755 + PD7341a COSM5782043 c.3636C>A p.F1212L Substitution - Missense 20:41174002-41174002 + ATL257 COSM5707413 c.1817A>G p.Q606R Substitution - Missense 20:41166211-41166211 + ATL122 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL102 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL295 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-B5-A0JY-01 COSM176472 c.2193C>T p.F731F Substitution - coding silent 20:41166751-41166751 + Pat_41_B COSM5857865 c.1769C>T p.T590I Substitution - Missense 20:41165796-41165796 + TCGA-FP-A4BE-01 COSM4098381 c.473G>A p.R158Q Substitution - Missense 20:41160114-41160114 + TCGA-IH-A3EA-01 COSM3546314 c.1752C>T p.L584L Substitution - coding silent 20:41165779-41165779 + TCGA-BR-6452-01 COSM3911298 c.808C>T p.R270C Substitution - Missense 20:41163396-41163396 + ATL288 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + DM6 COSM5609954 c.837C>T p.S279S Substitution - coding silent 20:41163425-41163425 + DM10 COSM5609950 c.3770C>A p.P1257Q Substitution - Missense 20:41174248-41174248 + Patient_2 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL277 COSM5707426 c.2818G>A p.G940R Substitution - Missense 20:41172202-41172202 + TCGA-AX-A063-01 COSM1026799 c.1913A>G p.H638R Substitution - Missense 20:41166307-41166307 + 22T COSM106333 c.2601C>T p.P867P Substitution - coding silent 20:41169477-41169477 + ATL053 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + Pat_24_A COSM3911298 c.808C>T p.R270C Substitution - Missense 20:41163396-41163396 + ATL165 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + sysucc-1577T COSM5764767 c.3247C>T p.R1083C Substitution - Missense 20:41172845-41172845 + ATL075 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL346 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + KM12 COSM3291366 c.1736C>T p.P579L Substitution - Missense 20:41165763-41165763 + ATL233 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL222 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-BR-4184-01 COSM4098397 c.2803G>A p.A935T Substitution - Missense 20:41170264-41170264 + T578 COSM176472 c.2193C>T p.F731F Substitution - coding silent 20:41166751-41166751 + Pat_59_A COSM5857864 c.488C>T p.S163L Substitution - Missense 20:41160129-41160129 + ATL046 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL003 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL346 COSM5707423 c.2600C>G p.P867R Substitution - Missense 20:41169476-41169476 + TCGA-BR-7707-01 COSM4098384 c.614G>A p.S205N Substitution - Missense 20:41162658-41162658 + HT55 COSM3291372 c.2030A>G p.Q677R Substitution - Missense 20:41166505-41166505 + BD118T COSM5507512 c.1799+4A>G p.? Unknown 20:41165830-41165830 + ATL216 COSM5707408 c.139G>A p.E47K Substitution - Missense 20:41137780-41137780 + HCC93T COSM3707758 c.2322G>A p.L774L Substitution - coding silent 20:41167872-41167872 + SH-8559 COSM5020784 c.3696G>T p.R1232R Substitution - coding silent 20:41174174-41174174 + ATL213 COSM5707441 c.3512_3514delATT p.N1171_F1172>I Complex - deletion inframe 20:41173769-41173771 + TCGA-66-2727-01 COSM723676 c.745G>A p.V249M Substitution - Missense 20:41163231-41163231 + ATL128 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL060 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL023 COSM5707422 c.2598C>G p.S866R Substitution - Missense 20:41169474-41169474 + ATL176 COSM5707413 c.1817A>G p.Q606R Substitution - Missense 20:41166211-41166211 + ATL156 COSM5707415 c.2193_2195delCGA p.D732delD Deletion - In frame 20:41166751-41166753 + ATL317 COSM5707434 c.3499T>A p.F1167I Substitution - Missense 20:41173756-41173756 + cSCCP7 COSM143688 c.2723_2724CC>TT p.S908F Substitution - Missense 20:41170184-41170185 + TCGA-Q1-A73O-01 COSM4834409 c.1458C>G p.I486M Substitution - Missense 20:41165316-41165316 + PTC-10C COSM4134539 c.835A>G p.S279G Substitution - Missense 20:41163423-41163423 + SS84 COSM3734686 c.1559C>T p.S520F Substitution - Missense 20:41165499-41165499 + DM74 COSM5609955 c.1161G>A p.K387K Substitution - coding silent 20:41164145-41164145 + ATL295 COSM5707412 c.1561_1563delGAG p.E522delE Deletion - In frame 20:41165501-41165503 + SSG01 COSM5574251 c.3473G>A p.R1158H Substitution - Missense 20:41173730-41173730 + T3670 COSM4715097 c.3823C>T p.R1275* Substitution - Nonsense 20:41174301-41174301 + TCGA-EB-A41A-01 COSM3546316 c.3000C>T p.F1000F Substitution - coding silent 20:41172515-41172515 + ATL003 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + PT52 COSM5941027 c.737T>A p.L246H Substitution - Missense 20:41163223-41163223 + TCGA-D1-A17R-01 COSM1026800 c.2239T>C p.Y747H Substitution - Missense 20:41166797-41166797 + TCGA-BH-A0DH-01 COSM443822 c.2302-2A>G p.? Unknown 20:41167850-41167850 + ATL403 COSM5707418 c.2242C>T p.R748C Substitution - Missense 20:41166800-41166800 + ATL117 COSM5707433 c.3494A>T p.D1165V Substitution - Missense 20:41173751-41173751 + ATL023 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ACINAR27 COSM1734453 c.791A>T p.E264V Substitution - Missense 20:41163379-41163379 + TCGA-06-0195-01 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + TCGA-61-1730-01 COSM1326741 c.611G>A p.R204H Substitution - Missense 20:41162655-41162655 + ATL177 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL170 COSM5707439 c.3509_3511delAGA p.Q1170_N1171>H Complex - deletion inframe 20:41173766-41173768 + TCGA-37-3783-01 COSM723675 c.1765G>C p.E589Q Substitution - Missense 20:41165792-41165792 + ATL421 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-EE-A3JE-06 COSM3911299 c.840C>T p.F280F Substitution - coding silent 20:41163428-41163428 + TCGA-AO-A12D-01 COSM443824 c.3358G>A p.E1120K Substitution - Missense 20:41173498-41173498 + TCGA-EE-A29D-06 COSM3546309 c.864C>T p.I288I Substitution - coding silent 20:41163452-41163452 + TCGA-D1-A103-01 COSM1026797 c.1728C>T p.T576T Substitution - coding silent 20:41165755-41165755 + ATL081 COSM5707439 c.3509_3511delAGA p.Q1170_N1171>H Complex - deletion inframe 20:41173766-41173768 + ATL116 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + sysucc-1370T COSM5471204 c.583C>T p.R195* Substitution - Nonsense 20:41162522-41162522 + YULETA COSM5392056 c.976C>T p.L326F Substitution - Missense 20:41163799-41163799 + ATL161 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + TCGA-EE-A2MI-06 COSM3546310 c.883C>T p.L295L Substitution - coding silent 20:41163471-41163471 + TCGA-EW-A2FW-01 COSM3841005 c.2226G>A p.E742E Substitution - coding silent 20:41166784-41166784 + ATL403 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + SS31 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL092 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + CSCC-44-T COSM4508419 c.775C>G p.L259V Substitution - Missense 20:41163261-41163261 + S0029 COSM5883561 c.1604C>T p.P535L Substitution - Missense 20:41165544-41165544 + ATL051 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + TCGA-G3-A6UC-01 COSM4929742 c.977T>C p.L326P Substitution - Missense 20:41163800-41163800 + 2402410 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + SH-6055 COSM5020502 c.2973C>T p.Y991Y Substitution - coding silent 20:41172488-41172488 + ESCC_72 COSM5634349 c.3630C>T p.D1210D Substitution - coding silent 20:41173996-41173996 + SH-1362 COSM4134539 c.835A>G p.S279G Substitution - Missense 20:41163423-41163423 + ATL261 COSM5707436 c.3506A>G p.D1169G Substitution - Missense 20:41173763-41173763 + ATL102 COSM5707411 c.1524C>G p.H508Q Substitution - Missense 20:41165464-41165464 + pfg316T COSM4753314 c.652C>T p.R218C Substitution - Missense 20:41162696-41162696 + Patient_2 COSM5414376 c.1035C>T p.S345S Substitution - coding silent 20:41163945-41163945 + MedB-1 COSM5621536 c.782A>G p.Y261C Substitution - Missense 20:41163268-41163268 + HCC2218 COSM21858 c.2983G>C p.A995P Substitution - Missense 20:41172498-41172498 + ATL424 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + CAL27 COSM4590998 c.1921C>A p.Q641K Substitution - Missense 20:41166315-41166315 + TCGA-CD-A4MG-01 COSM297321 c.610C>T p.R204C Substitution - Missense 20:41162654-41162654 + ATL217 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + sysucc-1370T COSM5471205 c.1339G>A p.D447N Substitution - Missense 20:41165054-41165054 + SS9 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + CSCC-62-T COSM4464210 c.1322C>T p.P441L Substitution - Missense 20:41165037-41165037 + pfg008T COSM1641344 c.789+1G>A p.? Unknown 20:41163276-41163276 + ATL402 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + HCC1395 COSM18203 c.1745C>G p.S582C Substitution - Missense 20:41165772-41165772 + TCGA-ER-A193-06 COSM3546312 c.1609G>A p.E537K Substitution - Missense 20:41165549-41165549 + DM17 COSM5609952 c.1519C>T p.P507S Substitution - Missense 20:41165459-41165459 + TCGA-BH-A0EI-01 COSM443826 c.3758G>A p.R1253H Substitution - Missense 20:41174236-41174236 + ASHPC_0006_Pa_P COSM3785395 c.1742G>A p.G581D Substitution - Missense 20:41165769-41165769 + BCM723T COSM4956180 c.1701C>T p.R567R Substitution - coding silent 20:41165728-41165728 + TCGA-BS-A0UV-01 COSM1026801 c.2685C>T p.F895F Substitution - coding silent 20:41170146-41170146 + TCGA-KK-A59V-01 COSM3291378 c.2332C>T p.R778C Substitution - Missense 20:41167882-41167882 + 2273183 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + 2153016 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL295 COSM5707414 c.1873G>T p.D625Y Substitution - Missense 20:41166267-41166267 + SH-2871 COSM5019650 c.2553C>T p.N851N Substitution - coding silent 20:41169148-41169148 + TCGA-BS-A0UV-01 COSM1026808 c.3824G>A p.R1275Q Substitution - Missense 20:41174302-41174302 + MO_1114 COSM5564893 c.590G>T p.R197L Substitution - Missense 20:41162529-41162529 + SH-1679 COSM4134539 c.835A>G p.S279G Substitution - Missense 20:41163423-41163423 + TCGA-DR-A0ZM-01 COSM459750 c.1791C>G p.L597L Substitution - coding silent 20:41165818-41165818 + STC263 COSM3291367 c.1788G>A p.T596T Substitution - coding silent 20:41165815-41165815 + ATL326 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + ATL289 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + TCGA-DK-A1A6-01 COSM1307392 c.2425G>A p.E809K Substitution - Missense 20:41168812-41168812 + T3225 COSM4715093 c.2779C>T p.R927C Substitution - Missense 20:41170240-41170240 + ATL076 COSM3734686 c.1559C>T p.S520F Substitution - Missense 20:41165499-41165499 + ATL223 COSM5707428 c.3047A>T p.Q1016L Substitution - Missense 20:41172562-41172562 + ATL011 COSM5707429 c.3056A>T p.D1019V Substitution - Missense 20:41172571-41172571 + ATL247 COSM5707432 c.3494A>G p.D1165G Substitution - Missense 20:41173751-41173751 + TCGA-DV-5565-01 COSM3363247 c.3324G>A p.V1108V Substitution - coding silent 20:41173464-41173464 + 16640 COSM48681 c.322G>A p.V108I Substitution - Missense 20:41159710-41159710 + 2153042 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL275 COSM3734686 c.1559C>T p.S520F Substitution - Missense 20:41165499-41165499 + TCGA-AX-A0J0-01 COSM1026805 c.3243C>T p.S1081S Substitution - coding silent 20:41172841-41172841 + TCGA-06-0743-01 COSM3405077 c.2255T>A p.L752Q Substitution - Missense 20:41166813-41166813 + ATL265 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + 2243933 COSM3769785 c.2120G>A p.R707Q Substitution - Missense 20:41166595-41166595 + 2273184 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL370 COSM5707435 c.3505G>C p.D1169H Substitution - Missense 20:41173762-41173762 + ATL278 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-D1-A160-01 COSM1026803 c.2932C>T p.R978W Substitution - Missense 20:41172447-41172447 + ATL008 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + ATL412 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + 2273193 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL130 COSM5707440 c.3511_3513delAAT p.N1171delN Deletion - In frame 20:41173768-41173770 + Pat_24_A COSM5857868 c.2536G>A p.V846M Substitution - Missense 20:41169131-41169131 + 2153022 COSM3734686 c.1559C>T p.S520F Substitution - Missense 20:41165499-41165499 + sysucc-880T COSM5462962 c.615C>T p.S205S Substitution - coding silent 20:41162659-41162659 + ATL415 COSM5707442 c.3514_3516delTTC p.F1172delF Deletion - In frame 20:41173771-41173773 + SNU-175 COSM3291411 c.3805G>A p.A1269T Substitution - Missense 20:41174283-41174283 + NCI-H2009 COSM18204 c.1466C>G p.S489C Substitution - Missense 20:41165324-41165324 + 2273187 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + TCGA-BR-4362-01 COSM4098398 c.2814T>C p.T938T Substitution - coding silent 20:41172198-41172198 + ATL034 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL314 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + ESCC-249T COSM3939349 c.1773C>T p.F591F Substitution - coding silent 20:41165800-41165800 + ATL316 COSM1411792 c.1465T>C p.S489P Substitution - Missense 20:41165323-41165323 + TCGA-AD-6964-01 COSM3693496 c.3826G>A p.E1276K Substitution - Missense 20:41174304-41174304 + ATL023 COSM5707421 c.2549T>C p.V850A Substitution - Missense 20:41169144-41169144 + TCGA-CF-A1HS-01 COSM419401 c.3703G>C p.D1235H Substitution - Missense 20:41174181-41174181 + TCGA-A6-6781-01 COSM1411798 c.2951C>T p.P984L Substitution - Missense 20:41172466-41172466 + CP66-MEL COSM18201 c.973C>T p.P325S Substitution - Missense 20:41163796-41163796 + 3206A7_009_T COSM5041262 c.2552A>G p.N851S Substitution - Missense 20:41169147-41169147 + 1115202 COSM5569410 c.596C>T p.T199M Substitution - Missense 20:41162535-41162535 + HCC93 COSM3707758 c.2322G>A p.L774L Substitution - coding silent 20:41167872-41167872 + BCM723T COSM4956180 c.1701C>T p.R567R Substitution - coding silent 20:41165728-41165728 + TCGA-33-6737-01 COSM723673 c.3390T>C p.F1130F Substitution - coding silent 20:41173530-41173530 + H2009 COSM18204 c.1466C>G p.S489C Substitution - Missense 20:41165324-41165324 + TCGA-FW-A3R5-06 COSM3911298 c.808C>T p.R270C Substitution - Missense 20:41163396-41163396 + TCGA-85-6561-01 COSM723678 c.423G>T p.M141I Substitution - Missense 20:41159922-41159922 + ATL018 COSM3734686 c.1559C>T p.S520F Substitution - Missense 20:41165499-41165499 + Pat_59_A COSM5857867 c.2194G>A p.D732N Substitution - Missense 20:41166752-41166752 + 8033523 COSM3389746 c.1765G>A p.E589K Substitution - Missense 20:41165792-41165792 + 2273182 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + Pat_16_B COSM4497446 c.496C>T p.R166W Substitution - Missense 20:41160137-41160137 + ATL156 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL242 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + 2324292 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL005 COSM5707420 c.2258G>A p.R753H Substitution - Missense 20:41166816-41166816 + Pat_02_B COSM5857866 c.2002T>G p.W668G Substitution - Missense 20:41166477-41166477 + ATL017 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-HU-A4G8-01 COSM4098390 c.1182G>A p.L394L Substitution - coding silent 20:41164166-41164166 + 2153064 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + LS513 COSM4646926 c.43G>T p.G15C Substitution - Missense 20:41137684-41137684 + DM6 COSM5609953 c.643C>T p.Q215* Substitution - Nonsense 20:41162687-41162687 + T26 COSM4134539 c.835A>G p.S279G Substitution - Missense 20:41163423-41163423 + ATL162 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-HU-A4G9-01 COSM4098400 c.3130+2T>C p.? Unknown 20:41172647-41172647 + 100695 COSM96136 c.3366C>T p.D1122D Substitution - coding silent 20:41173506-41173506 + 188 COSM1741616 c.2484-7C>T p.? Unknown 20:41169072-41169072 + TCGA-B5-A11E-01 COSM1026809 c.3833G>A p.R1278K Substitution - Missense 20:41174311-41174311 + ATL317 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + sysucc-966T COSM1326741 c.611G>A p.R204H Substitution - Missense 20:41162655-41162655 + ATL417 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + T3088 COSM1026803 c.2932C>T p.R978W Substitution - Missense 20:41172447-41172447 + TCGA-AN-A046-01 COSM3291349 c.653G>A p.R218H Substitution - Missense 20:41162697-41162697 + ATL312 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + 2153044 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL399 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL425 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + 8012675 COSM1168953 c.717G>A p.R239R Substitution - coding silent 20:41163203-41163203 + TCGA-AP-A051-01 COSM1026797 c.1728C>T p.T576T Substitution - coding silent 20:41165755-41165755 + ATL421 COSM5707416 c.2201T>G p.L734R Substitution - Missense 20:41166759-41166759 + ATL106 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + S0051 COSM5883562 c.1985C>G p.A662G Substitution - Missense 20:41166379-41166379 + 2153029 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + HCC2218 COSM21858 c.2983G>C p.A995P Substitution - Missense 20:41172498-41172498 + 2246938 COSM4413515 c.2112C>G p.I704M Substitution - Missense 20:41166587-41166587 + 298 COSM3291407 c.3680C>T p.T1227M Substitution - Missense 20:41174158-41174158 + TCGA-CG-5733-01 COSM4098386 c.680C>T p.T227M Substitution - Missense 20:41162724-41162724 + PD7192a COSM3769785 c.2120G>A p.R707Q Substitution - Missense 20:41166595-41166595 + 2273191 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + TCGA-06-0192 COSM2150662 c.3014G>A p.R1005Q Substitution - Missense 20:41172529-41172529 + ATL342 COSM5707437 c.3506_3508delACC p.D1169_Q1170>E Complex - deletion inframe 20:41173763-41173765 + NCI-H2009 COSM18204 c.1466C>G p.S489C Substitution - Missense 20:41165324-41165324 + TCGA-D1-A17M-01 COSM443825 c.3730C>T p.R1244* Substitution - Nonsense 20:41174208-41174208 + SS26 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL225 COSM3734686 c.1559C>T p.S520F Substitution - Missense 20:41165499-41165499 + ATL002 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL054 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + 2273189 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + TCGA-06-0192-01 COSM2150662 c.3014G>A p.R1005Q Substitution - Missense 20:41172529-41172529 + ATL337 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + ATL044 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + PD18285a COSM3769785 c.2120G>A p.R707Q Substitution - Missense 20:41166595-41166595 + ATL150 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + SH-1439 COSM5020784 c.3696G>T p.R1232R Substitution - coding silent 20:41174174-41174174 + Au4 COSM5604519 c.857G>A p.R286Q Substitution - Missense 20:41163445-41163445 + ATL048 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-EE-A3J4-06 COSM3911301 c.1901A>G p.D634G Substitution - Missense 20:41166295-41166295 + TCGA-BS-A0UA-01 COSM1026808 c.3824G>A p.R1275Q Substitution - Missense 20:41174302-41174302 + ATL135 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-HU-A4GH-01 COSM4098391 c.1319A>G p.K440R Substitution - Missense 20:41165034-41165034 + ATL283 COSM5707439 c.3509_3511delAGA p.Q1170_N1171>H Complex - deletion inframe 20:41173766-41173768 + ATL358 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + ATL135 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + pfg146T COSM4753315 c.730C>T p.P244S Substitution - Missense 20:41163216-41163216 + HCC2218 COSM21858 c.2983G>C p.A995P Substitution - Missense 20:41172498-41172498 + ATL154 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL293 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + TCGA-AZ-4315-01 COSM1411796 c.2112C>T p.I704I Substitution - coding silent 20:41166587-41166587 + TCGA-CS-4941-01 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + TCGA-BR-8680-01 COSM4098392 c.1353A>C p.S451S Substitution - coding silent 20:41165068-41165068 + TCGA-D1-A17Q-01 COSM1026807 c.3771G>A p.P1257P Substitution - coding silent 20:41174249-41174249 + pfg068T COSM4753316 c.1073G>A p.R358Q Substitution - Missense 20:41163983-41163983 + TCGA-C8-A1HN-01 COSM443820 c.897C>A p.V299V Substitution - coding silent 20:41163720-41163720 + YUZINO COSM1713467 c.1892C>T p.S631F Substitution - Missense 20:41166286-41166286 + ATL139 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL113 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + sysucc-1370T COSM5471207 c.1779C>T p.G593G Substitution - coding silent 20:41165806-41165806 + TCGA-BR-A4QL-01 COSM4098397 c.2803G>A p.A935T Substitution - Missense 20:41170264-41170264 + CP66-MEL COSM18201 c.973C>T p.P325S Substitution - Missense 20:41163796-41163796 + TCGA-AC-A23H-01 COSM3841006 c.2708C>T p.S903L Substitution - Missense 20:41170169-41170169 + TCGA-AZ-4315-01 COSM1411799 c.3008A>C p.Y1003S Substitution - Missense 20:41172523-41172523 + STC291 COSM5057307 c.2748G>A p.Q916Q Substitution - coding silent 20:41170209-41170209 + ATL356 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + 2273194 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + TCGA-D3-A1Q4-06 COSM3546308 c.817G>A p.V273M Substitution - Missense 20:41163405-41163405 + TCGA-AC-A23H-01 COSM3841007 c.2859C>G p.L953L Substitution - coding silent 20:41172243-41172243 + ATL035 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + cSCCP7 COSM140265 c.3667C>T p.P1223S Substitution - Missense 20:41174145-41174145 + 2153028 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL044 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL302 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + SH-9248 COSM5020502 c.2973C>T p.Y991Y Substitution - coding silent 20:41172488-41172488 + T2963 COSM4715096 c.3477C>T p.F1159F Substitution - coding silent 20:41173734-41173734 + MO_1410 COSM5555759 c.1729G>A p.G577R Substitution - Missense 20:41165756-41165756 + ATL370 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + TCGA-UB-A7MF-01 COSM4918911 c.3382A>G p.T1128A Substitution - Missense 20:41173522-41173522 + ATL241 COSM5707436 c.3506A>G p.D1169G Substitution - Missense 20:41173763-41173763 + ATL037 COSM5707431 c.3493G>C p.D1165H Substitution - Missense 20:41173750-41173750 + ATL414 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + T3091 COSM3291375 c.2154G>A p.Q718Q Substitution - coding silent 20:41166712-41166712 + TCGA-DA-A3F8-06 COSM1713470 c.2945C>T p.S982F Substitution - Missense 20:41172460-41172460 + 2243929 COSM3769785 c.2120G>A p.R707Q Substitution - Missense 20:41166595-41166595 + HX27T COSM3707757 c.1491G>A p.L497L Substitution - coding silent 20:41165349-41165349 + ATL267 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL425 COSM3405078 c.3487G>A p.E1163K Substitution - Missense 20:41173744-41173744 + ATL241 COSM5707432 c.3494A>G p.D1165G Substitution - Missense 20:41173751-41173751 + TCGA-BR-4361-01 COSM4098383 c.494A>T p.D165V Substitution - Missense 20:41160135-41160135 + ATL231 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-EK-A3GK-01 COSM4854051 c.1948G>C p.E650Q Substitution - Missense 20:41166342-41166342 + YUPORCH COSM1713469 c.2669A>G p.K890R Substitution - Missense 20:41170130-41170130 + ATL215 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL062 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + T1154 COSM4715089 c.530T>C p.L177P Substitution - Missense 20:41162469-41162469 + TCGA-CD-A4MJ-01 COSM4098399 c.3092G>A p.C1031Y Substitution - Missense 20:41172607-41172607 + ATL333 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + PT48 COSM5934032 c.2630A>T p.D877V Substitution - Missense 20:41169506-41169506 + 19M COSM5579332 c.750C>T p.S250S Substitution - coding silent 20:41163236-41163236 + ATL094 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + MedB-1 COSM5621537 c.3207G>A p.M1069I Substitution - Missense 20:41172805-41172805 + HCC13T COSM1615592 c.879C>A p.F293L Substitution - Missense 20:41163467-41163467 + 38-4 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + T407 COSM4715095 c.2952G>A p.P984P Substitution - coding silent 20:41172467-41172467 + 193-01-1TD COSM145783 c.866A>G p.E289G Substitution - Missense 20:41163454-41163454 + 10-P1058 COSM4581811 c.1574G>T p.S525I Substitution - Missense 20:41165514-41165514 + TCGA-B5-A11R-01 COSM1026804 c.3033C>G p.I1011M Substitution - Missense 20:41172548-41172548 + TCGA-AN-A0FY-01 COSM443825 c.3730C>T p.R1244* Substitution - Nonsense 20:41174208-41174208 + TCGA-E2-A1II-01 COSM1483634 c.2648T>A p.I883N Substitution - Missense 20:41169524-41169524 + ATL327 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + 2492730 COSM292513 c.732G>A p.P244P Substitution - coding silent 20:41163218-41163218 + TCGA-DU-5855-01 COSM3972555 c.2261A>G p.Y754C Substitution - Missense 20:41166819-41166819 + CSCC-44-T COSM4470079 c.1638C>T p.S546S Substitution - coding silent 20:41165665-41165665 + TCGA-BC-A112-01 COSM4936582 c.1935C>T p.R645R Substitution - coding silent 20:41166329-41166329 + CSCC-35-T COSM4489818 c.3535C>T p.P1179S Substitution - Missense 20:41173792-41173792 + TCGA-FS-A1Z0-06 COSM3546313 c.1722C>T p.I574I Substitution - coding silent 20:41165749-41165749 + WSU-HN12 COSM4590998 c.1921C>A p.Q641K Substitution - Missense 20:41166315-41166315 + ATL278 COSM5707418 c.2242C>T p.R748C Substitution - Missense 20:41166800-41166800 + TCGA-G2-A3IE-01 COSM1307393 c.3457G>A p.E1153K Substitution - Missense 20:41173714-41173714 + TCGA-06-0648 COSM2151410 c.332A>G p.Y111C Substitution - Missense 20:41159720-41159720 + ATL093 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + HCC2218 COSM21858 c.2983G>C p.A995P Substitution - Missense 20:41172498-41172498 + ATL255 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + T3498 COSM4715088 c.443C>A p.P148H Substitution - Missense 20:41159942-41159942 + TCGA-BR-4361-01 COSM4098389 c.1125G>A p.M375I Substitution - Missense 20:41164109-41164109 + DM79 COSM5609956 c.2057C>T p.P686L Substitution - Missense 20:41166532-41166532 + ATL244 COSM5707443 c.3515_3517delTCC p.F1172delF Deletion - In frame 20:41173772-41173774 + TCGA-EE-A29E-06 COSM3546311 c.1347C>T p.L449L Substitution - coding silent 20:41165062-41165062 + PDA_012 COSM18203 c.1745C>G p.S582C Substitution - Missense 20:41165772-41165772 + SNU-283 COSM4650928 c.182C>T p.T61M Substitution - Missense 20:41137823-41137823 + OSCC-GB_00910111 COSM4888175 c.3763C>A p.Q1255K Substitution - Missense 20:41174241-41174241 + TCGA-BH-A18U-01 COSM443821 c.1437G>T p.M479I Substitution - Missense 20:41165295-41165295 + TCGA-CM-6171-01 COSM1411795 c.2033C>T p.A678V Substitution - Missense 20:41166508-41166508 + RK308_C01 COSM3740135 c.1912C>T p.H638Y Substitution - Missense 20:41166306-41166306 + PT52 COSM5941026 c.736C>T p.L246F Substitution - Missense 20:41163222-41163222 + ATL221 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + PD13802a COSM5025037 c.1726A>G p.T576A Substitution - Missense 20:41165753-41165753 + ccRCC-17 COSM1663546 c.1994G>T p.S665I Substitution - Missense 20:41166388-41166388 + C0080T COSM4164720 c.106A>C p.T36P Substitution - Missense 20:41137747-41137747 + ATL264 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + ATL121 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + T3306 COSM4715091 c.1825C>T p.R609C Substitution - Missense 20:41166219-41166219 + 2273190 COSM3734685 c.1034C>T p.S345F Substitution - Missense 20:41163944-41163944 + 2243935 COSM3769785 c.2120G>A p.R707Q Substitution - Missense 20:41166595-41166595 + sysucc-880T COSM5462963 c.1478G>T p.G493V Substitution - Missense 20:41165336-41165336 + 6115114 COSM5552304 c.1577A>T p.D526V Substitution - Missense 20:41165517-41165517 + 2402409 COSM5049788 c.1024G>A p.D342N Substitution - Missense 20:41163934-41163934 + ATL210 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + ATL280 COSM5707409 c.142C>T p.R48W Substitution - Missense 20:41137783-41137783 + TCGA-CI-6621-01 COSM1565783 c.2147G>A p.R716H Substitution - Missense 20:41166705-41166705 + SS86 COSM5574252 c.3482_3496del15 p.Y1162_M1166delYEEDM Deletion - In frame 20:41173739-41173753 + ATL177 COSM5707423 c.2600C>G p.P867R Substitution - Missense 20:41169476-41169476 + T351 COSM4715094 c.2802C>T p.D934D Substitution - coding silent 20:41170263-41170263 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.268177 20q12-q13.1 172420

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.E1093A c.3278A>C 20 39801516 HC A G Missense p.D634G c.1901A>G 20 39794935 CM A G Missense p.H638R c.1913A>G 20 39794947 UCEC A G Missense p.Y111C c.332A>G 20 39788360 GBM A G Missense p.Y754C c.2261A>G 20 39795459 LGG A G SpliceAcceptorSNV . c.2302-2A>G 20 39796490 BRCA C A Synonymous p.V299V c.897C>A 20 39792360 BRCA CC TA Synonymous p.(=) c.471_472delinsTA 20 39788752 CM C G Missense p.I1011M c.3033C>G 20 39801188 UCEC C G Missense p.L752V c.2254C>G 20 39795452 LGG C G Missense p.P319R c.956C>G 20 39792419 LUAD C G Missense p.P658R c.1973C>G 20 39795007 CM C G Missense p.R88G c.262C>G 20 39788290 BRCA C G Missense p.S705C c.2114C>G 20 39795229 LUAD C - IntronicDeletion . c.1799+174delC 20 39794631 CM C T IntronicSNV . c.1800-107C>T 20 39794727 CM C T Missense p.R171C c.511C>T 20 39788792 CM C T Missense p.R204C c.610C>T 20 39791294 COREAD C T Missense p.R978W c.2932C>T 20 39801087 CM C T Missense p.R978W c.2932C>T 20 39801087 UCEC C T Missense p.S982F c.2945C>T 20 39801100 CM C T Missense p.T227M c.680C>T 20 39791364 STAD C T Nonsense p.R1244* c.3730C>T 20 39802848 BRCA C T Synonymous p.A913A c.2739C>T 20 39798840 RCCC C T Synonymous p.F1224F c.3672C>T 20 39802790 LUSC C T Synonymous p.F257F c.771C>T 20 39791897 CM C T Synonymous p.F280F c.840C>T 20 39792068 CM C T Synonymous p.I574I c.1722C>T 20 39794389 CM C T Synonymous p.L295L c.883C>T 20 39792111 CM C T Synonymous p.L584L c.1752C>T 20 39794419 CM C T Synonymous p.V184V c.552C>T 20 39791131 BRCA - GAAGAA MultiAAMissense p.E1164delinsGRK c.3490_3491insGAAGAA 20 39802387 LGG G A IntronicSNV . c.2302-34G>A 20 39796458 CM G A Missense p.A913T c.2737G>A 20 39798838 BLCA G A Missense p.A935T c.2803G>A 20 39798904 STAD G A Missense p.C960Y c.2879G>A 20 39800903 UCEC G A Missense p.E1120K c.3358G>A 20 39802138 BRCA G A Missense p.E1153K c.3457G>A 20 39802354 BLCA G A Missense p.E1163K c.3487G>A 20 39802384 GBM G A Missense p.E1163K c.3487G>A 20 39802384 LGG G A Missense p.E533K c.1597G>A 20 39794177 LUAD G A Missense p.E537K c.1609G>A 20 39794189 CM G A Missense p.E809K c.2425G>A 20 39797452 BLCA G A Missense p.G371S c.1111G>A 20 39792735 UCEC G A Missense p.M113I c.339G>A 20 39788367 CM G A Missense p.R1005Q c.3014G>A 20 39801169 GBM G A Missense p.R1253H c.3758G>A 20 39802876 BRCA G A Missense p.R1275Q c.3824G>A 20 39802942 UCEC G A Missense p.R423K c.1268G>A 20 39793623 HNSC G A Missense p.V108I c.322G>A 20 39788350 LUAD G A Missense p.V249M c.745G>A 20 39791871 LUSC G A Missense p.V273M c.817G>A 20 39792045 CM G A SpliceDonorSNV . c.789+1G>A 20 39791916 STAD G A Synonymous p.P244P c.732G>A 20 39791858 COREAD G A Synonymous p.R239R c.717G>A 20 39791843 PAAD G A Synonymous p.V1108V c.3324G>A 20 39802104 RCCC G C IntronicSNV . c.2808+44G>C 20 39798953 CM G C Missense p.A995P c.2983G>C 20 39801138 BRCA G C Missense p.D1235H c.3703G>C 20 39802821 BLCA G C Missense p.E253Q c.757G>C 20 39791883 HNSC G C Missense p.E589Q c.1765G>C 20 39794432 LUSC G C Missense p.E809Q c.2425G>C 20 39797452 HNSC G T Missense p.E575D c.1725G>T 20 39794392 LUAD G T Missense p.M141I c.423G>T 20 39788562 LUSC G T Missense p.M479I c.1437G>T 20 39793935 BRCA G T Missense p.R1010L c.3029G>T 20 39801184 LUAD G T Missense p.R286L c.857G>T 20 39792085 HNSC G T Missense p.V1139L c.3415G>T 20 39802312 NB G T Synonymous p.G772G c.2316G>T 20 39796506 RCCC T A Missense p.I883N c.2648T>A 20 39798164 BRCA T A Missense p.L752Q c.2255T>A 20 39795453 GBM T C 3-UTRSNV . c.3873+227T>C 20 39803373 HC T C Missense p.Y747H c.2239T>C 20 39795437 UCEC T C SpliceDonorSNV . c.1799+2T>C 20 39794468 GBM T C Synonymous p.F1130F c.3390T>C 20 39802170 LUSC T G Missense p.F629V c.1885T>G 20 39794919 STAD T G Missense p.M750R c.2249T>G 20 39795447 GBM - T IntronicInsertion . c.513-197dupT 20 39790876 CM