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 14 24031492 24031495 + Splice_Site DEL CTTA CTTA - TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr14:24031492_24031495delCTTA c.e15+1 BLCA 14 24029009 24029009 + Silent SNP C C T TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr14:24029009C>T c.2307G>A c.(2305-2307)tcG>tcA p.S769S BLCA 14 24029581 24029581 + Silent SNP C C A TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr14:24029581C>A c.2040G>T c.(2038-2040)ctG>ctT p.L680L BLCA 14 24030568 24030568 + Missense_Mutation SNP C C A TCGA-XF-AAMZ-01A-11D-A42E-08 TCGA-XF-AAMZ-10A-01D-A42H-08 g.chr14:24030568C>A c.1930G>T c.(1930-1932)Gac>Tac p.D644Y BLCA 14 24034889 24034889 + Missense_Mutation SNP T T C TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr14:24034889T>C c.667A>G c.(667-669)Atc>Gtc p.I223V BLCA 14 24035801 24035801 + Missense_Mutation SNP G G T TCGA-FD-A5BX-01A-11D-A26M-08 TCGA-FD-A5BX-10A-01D-A26K-08 g.chr14:24035801G>T c.299C>A c.(298-300)gCc>gAc p.A100D BLCA 14 24035814 24035814 + Missense_Mutation SNP C C T TCGA-PQ-A6FI-01A-11D-A31L-08 TCGA-PQ-A6FI-10A-01D-A31J-08 g.chr14:24035814C>T c.286G>A c.(286-288)Gag>Aag p.E96K BLCA 14 24036487 24036487 + Missense_Mutation SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr14:24036487C>T c.37G>A c.(37-39)Gaa>Aaa p.E13K BLCA 14 24036510 24036510 + Missense_Mutation SNP G G A TCGA-E7-A5KF-01A-11D-A289-08 TCGA-E7-A5KF-10A-01D-A289-08 g.chr14:24036510G>A c.14C>T c.(13-15)tCg>tTg p.S5L BRCA 14 24028968 24028968 + Missense_Mutation SNP G G A TCGA-E9-A1R6-01A-11D-A14G-09 TCGA-E9-A1R6-10A-01D-A14G-09 g.chr14:24028968G>A c.2348C>T c.(2347-2349)tCg>tTg p.S783L BRCA 14 24030620 24030620 + Silent SNP C C T TCGA-AC-A2FG-01A-11D-A17D-09 TCGA-AC-A2FG-11A-22D-A17D-09 g.chr14:24030620C>T c.1878G>A c.(1876-1878)ctG>ctA p.L626L BRCA 14 24032653 24032654 + Frame_Shift_Ins INS - - C TCGA-A8-A08X-01A-21W-A019-09 TCGA-A8-A08X-10A-01W-A021-09 g.chr14:24032653_24032654insC c.1345_1346insG c.(1345-1347)gccfs p.A449fs BRCA 14 24032994 24032994 + Missense_Mutation SNP G G T TCGA-EW-A1PH-01A-11D-A14K-09 TCGA-EW-A1PH-10A-01D-A14K-09 g.chr14:24032994G>T c.1163C>A c.(1162-1164)gCc>gAc p.A388D BRCA 14 24035346 24035346 + Missense_Mutation SNP C C T TCGA-B6-A0IN-01A-11W-A050-09 TCGA-B6-A0IN-10A-01W-A055-09 g.chr14:24035346C>T c.495G>A c.(493-495)atG>atA p.M165I BRCA 14 24035526 24035526 + Missense_Mutation SNP C C G TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr14:24035526C>G c.432G>C c.(430-432)gaG>gaC p.E144D BRCA 14 24035549 24035549 + Nonsense_Mutation SNP G G A TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr14:24035549G>A c.409C>T c.(409-411)Cga>Tga p.R137* BRCA 14 24035577 24035577 + Missense_Mutation SNP C C G TCGA-AC-A3BB-01A-21D-A19Y-09 TCGA-AC-A3BB-10A-01D-A19Y-09 g.chr14:24035577C>G c.381G>C c.(379-381)ttG>ttC p.L127F BRCA 14 24035597 24035597 + Missense_Mutation SNP C C T TCGA-A2-A04Y-01A-21W-A050-09 TCGA-A2-A04Y-10A-01W-A055-09 g.chr14:24035597C>T c.361G>A c.(361-363)Ggc>Agc p.G121S COAD 14 24029546 24029546 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr14:24029546G>A c.2075C>T c.(2074-2076)gCt>gTt p.A692V COAD 14 24029552 24029552 + Frame_Shift_Del DEL T T - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr14:24029552delT c.2069delA c.(2068-2070)aacfs p.N690fs COAD 14 24030796 24030796 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr14:24030796C>A c.1782G>T c.(1780-1782)caG>caT p.Q594H COAD 14 24030824 24030825 + Frame_Shift_Ins INS - - T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr14:24030824_24030825insT c.1753_1754insA c.(1753-1755)atgfs p.M585fs COAD 14 24030825 24030825 + Frame_Shift_Del DEL T T - TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr14:24030825delT c.1753delA c.(1753-1755)atgfs p.M585fs COAD 14 24032653 24032654 + Frame_Shift_Ins INS - - C TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr14:24032653_24032654insC c.1345_1346insG c.(1345-1347)gccfs p.A449fs COAD 14 24032794 24032794 + Splice_Site SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr14:24032794G>A c.1286C>T c.(1285-1287)aCg>aTg p.T429M COAD 14 24032996 24032996 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr14:24032996C>A c.1161G>T c.(1159-1161)caG>caT p.Q387H COAD 14 24035341 24035341 + Missense_Mutation SNP C C T TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr14:24035341C>T c.500G>A c.(499-501)cGg>cAg p.R167Q COAD 14 24035342 24035342 + Missense_Mutation SNP G G A TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr14:24035342G>A c.499C>T c.(499-501)Cgg>Tgg p.R167W COAD 14 24035494 24035494 + Missense_Mutation SNP C C T TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr14:24035494C>T c.464G>A c.(463-465)cGc>cAc p.R155H COAD 14 24035527 24035527 + Missense_Mutation SNP T T C TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr14:24035527T>C c.431A>G c.(430-432)gAg>gGg p.E144G COAD 14 24035828 24035828 + Missense_Mutation SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr14:24035828A>G c.272T>C c.(271-273)aTg>aCg p.M91T COAD 14 24036471 24036471 + Missense_Mutation SNP G G T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr14:24036471G>T c.53C>A c.(52-54)gCc>gAc p.A18D COADREAD 14 24029037 24029037 + Missense_Mutation SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr14:24029037C>T c.2279G>A c.(2278-2280)cGc>cAc p.R760H COADREAD 14 24029546 24029546 + Missense_Mutation SNP G G A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr14:24029546G>A c.2075C>T c.(2074-2076)gCt>gTt p.A692V COADREAD 14 24029552 24029552 + Frame_Shift_Del DEL T T - TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr14:24029552delT c.2069delA c.(2068-2070)aacfs p.N690fs COADREAD 14 24030796 24030796 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr14:24030796C>A c.1782G>T c.(1780-1782)caG>caT p.Q594H COADREAD 14 24030824 24030825 + Frame_Shift_Ins INS - - T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr14:24030824_24030825insT c.1753_1754insA c.(1753-1755)atgfs p.M585fs COADREAD 14 24030825 24030825 + Frame_Shift_Del DEL T T - TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr14:24030825delT c.1753delA c.(1753-1755)atgfs p.M585fs COADREAD 14 24032653 24032654 + Frame_Shift_Ins INS - - C TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr14:24032653_24032654insC c.1345_1346insG c.(1345-1347)gccfs p.A449fs COADREAD 14 24032794 24032794 + Splice_Site SNP G G A TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr14:24032794G>A c.1286C>T c.(1285-1287)aCg>aTg p.T429M COADREAD 14 24032996 24032996 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr14:24032996C>A c.1161G>T c.(1159-1161)caG>caT p.Q387H COADREAD 14 24033579 24033579 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:24033579G>T c.940C>A c.(940-942)Ctt>Att p.L314I COADREAD 14 24033844 24033844 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:24033844C>T c.848G>A c.(847-849)cGa>cAa p.R283Q COADREAD 14 24035341 24035341 + Missense_Mutation SNP C C T TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr14:24035341C>T c.500G>A c.(499-501)cGg>cAg p.R167Q COADREAD 14 24035342 24035342 + Missense_Mutation SNP G G A TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr14:24035342G>A c.499C>T c.(499-501)Cgg>Tgg p.R167W COADREAD 14 24035494 24035494 + Missense_Mutation SNP C C T TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr14:24035494C>T c.464G>A c.(463-465)cGc>cAc p.R155H COADREAD 14 24035527 24035527 + Missense_Mutation SNP T T C TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr14:24035527T>C c.431A>G c.(430-432)gAg>gGg p.E144G COADREAD 14 24035828 24035828 + Missense_Mutation SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr14:24035828A>G c.272T>C c.(271-273)aTg>aCg p.M91T COADREAD 14 24036471 24036471 + Missense_Mutation SNP G G T TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr14:24036471G>T c.53C>A c.(52-54)gCc>gAc p.A18D ESCA 14 24031497 24031499 + Splice_Site DEL TTG TTG - TCGA-IG-A3YB-01A-11D-A247-09 TCGA-IG-A3YB-10A-01D-A247-09 g.chr14:24031497_24031499delTTG c.1626_1628delCAA c.(1624-1629)aacaac>aac p.542_543NN>N ESCA 14 24035498 24035498 + Missense_Mutation SNP C C T TCGA-IG-A3YB-01A-11D-A247-09 TCGA-IG-A3YB-10A-01D-A247-09 g.chr14:24035498C>T c.460G>A c.(460-462)Gtg>Atg p.V154M GBMLGG 14 24031799 24031799 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr14:24031799G>A c.1414C>T c.(1414-1416)Cca>Tca p.P472S GBMLGG 14 24034396 24034396 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr14:24034396G>A c.754C>T c.(754-756)Cgt>Tgt p.R252C GBMLGG 14 24035874 24035874 + Missense_Mutation SNP C C T TCGA-HT-7467-01A-11D-2024-08 TCGA-HT-7467-10A-01D-2024-08 g.chr14:24035874C>T c.226G>A c.(226-228)Gcc>Acc p.A76T HNSC 14 24030798 24030798 + Nonsense_Mutation SNP G G A TCGA-CR-7390-01A-11D-2012-08 TCGA-CR-7390-10A-01D-2013-08 g.chr14:24030798G>A c.1780C>T c.(1780-1782)Cag>Tag p.Q594* HNSC 14 24032660 24032660 + Missense_Mutation SNP C C T TCGA-IQ-A61O-01A-11D-A30E-08 TCGA-IQ-A61O-10A-01D-A30H-08 g.chr14:24032660C>T c.1339G>A c.(1339-1341)Ggg>Agg p.G447R HNSC 14 24034829 24034829 + Missense_Mutation SNP C C T TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr14:24034829C>T c.727G>A c.(727-729)Gac>Aac p.D243N HNSC 14 24034829 24034829 + Missense_Mutation SNP C C T TCGA-CV-6948-01A-11D-1912-08 TCGA-CV-6948-10A-01D-1912-08 g.chr14:24034829C>T c.727G>A c.(727-729)Gac>Aac p.D243N KIPAN 14 24032848 24032848 + Splice_Site SNP C C T TCGA-A4-8098-01A-11D-2396-08 TCGA-A4-8098-10A-01D-2396-08 g.chr14:24032848C>T c.e12-1 KIPAN 14 24033327 24033327 + Missense_Mutation SNP T T C TCGA-B0-5692-01A-11D-1534-10 TCGA-B0-5692-11A-01D-1534-10 g.chr14:24033327T>C c.1019A>G c.(1018-1020)gAt>gGt p.D340G KIPAN 14 24035342 24035342 + Missense_Mutation SNP G G A TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chr14:24035342G>A c.499C>T c.(499-501)Cgg>Tgg p.R167W KIPAN 14 24036472 24036472 + Frame_Shift_Del DEL C C - TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr14:24036472delC c.52delG c.(52-54)gccfs p.A18fs KIRC 14 24033327 24033327 + Missense_Mutation SNP T T C TCGA-B0-5692-01A-11D-1534-10 TCGA-B0-5692-11A-01D-1534-10 g.chr14:24033327T>C c.1019A>G c.(1018-1020)gAt>gGt p.D340G KIRC 14 24035342 24035342 + Missense_Mutation SNP G G A TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chr14:24035342G>A c.499C>T c.(499-501)Cgg>Tgg p.R167W KIRP 14 24032848 24032848 + Splice_Site SNP C C T TCGA-A4-8098-01A-11D-2396-08 TCGA-A4-8098-10A-01D-2396-08 g.chr14:24032848C>T c.e12-1 KIRP 14 24036472 24036472 + Frame_Shift_Del DEL C C - TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr14:24036472delC c.52delG c.(52-54)gccfs p.A18fs LAML 14 24033309 24033309 + Missense_Mutation SNP C C T TCGA-AB-3009-03A-01D-0739-09 TCGA-AB-3009-11A-01D-0739-09 g.chr14:24033309C>T c.1037G>A c.(1036-1038)cGg>cAg p.R346Q LGG 14 24031799 24031799 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr14:24031799G>A c.1414C>T c.(1414-1416)Cca>Tca p.P472S LGG 14 24034396 24034396 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr14:24034396G>A c.754C>T c.(754-756)Cgt>Tgt p.R252C LGG 14 24035874 24035874 + Missense_Mutation SNP C C T TCGA-HT-7467-01A-11D-2024-08 TCGA-HT-7467-10A-01D-2024-08 g.chr14:24035874C>T c.226G>A c.(226-228)Gcc>Acc p.A76T LIHC 14 24031766 24031766 + Frame_Shift_Del DEL C C - TCGA-G3-A3CK-01A-11D-A20W-10 TCGA-G3-A3CK-10A-01D-A20W-10 g.chr14:24031766delC c.1447delG c.(1447-1449)gagfs p.E483fs LIHC 14 24035857 24035857 + Silent SNP T T A TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr14:24035857T>A c.243A>T c.(241-243)acA>acT p.T81T LUAD 14 24028973 24028973 + Silent SNP C C T TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr14:24028973C>T c.2343G>A c.(2341-2343)gtG>gtA p.V781V LUAD 14 24030508 24030508 + Missense_Mutation SNP G G C TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr14:24030508G>C c.1990C>G c.(1990-1992)Cca>Gca p.P664A LUAD 14 24030622 24030622 + Missense_Mutation SNP G G C TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr14:24030622G>C c.1876C>G c.(1876-1878)Ctg>Gtg p.L626V LUAD 14 24031721 24031721 + Missense_Mutation SNP G G C TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr14:24031721G>C c.1492C>G c.(1492-1494)Ccc>Gcc p.P498A LUAD 14 24032623 24032623 + Missense_Mutation SNP C C T TCGA-17-Z032-01A-01W-0746-08 TCGA-17-Z032-11A-01W-0746-08 g.chr14:24032623C>T c.1376G>A c.(1375-1377)cGc>cAc p.R459H LUAD 14 24034374 24034374 + Missense_Mutation SNP C C T TCGA-55-8207-01A-11D-2238-08 TCGA-55-8207-10A-01D-2238-08 g.chr14:24034374C>T c.776G>A c.(775-777)cGg>cAg p.R259Q LUAD 14 24035553 24035553 + Missense_Mutation SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr14:24035553C>A c.405G>T c.(403-405)atG>atT p.M135I LUSC 14 24030804 24030804 + Missense_Mutation SNP C C T TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr14:24030804C>T c.1774G>A c.(1774-1776)Ggc>Agc p.G592S OV 14 24030606 24030606 + Missense_Mutation SNP T T C TCGA-29-2432-01A-01D-1526-09 TCGA-29-2432-10A-01D-1526-09 g.chr14:24030606T>C c.1892A>G c.(1891-1893)gAt>gGt p.D631G OV 14 24032597 24032597 + Missense_Mutation SNP T T A TCGA-29-1703-01A-01W-0633-09 TCGA-29-1703-10A-01W-0633-09 g.chr14:24032597T>A c.1402A>T c.(1402-1404)Att>Ttt p.I468F OV 14 24035342 24035342 + Missense_Mutation SNP G G A TCGA-25-2396-01A-01W-0799-08 TCGA-25-2396-10A-01W-0799-08 g.chr14:24035342G>A c.499C>T c.(499-501)Cgg>Tgg p.R167W OV 14 24036403 24036403 + Missense_Mutation SNP C C T TCGA-61-1915-01A-01W-0639-09 TCGA-61-1915-11A-01W-0640-09 g.chr14:24036403C>T c.121G>A c.(121-123)Gac>Aac p.D41N OV 14 24036406 24036406 + Missense_Mutation SNP G G A TCGA-09-1674-01A-01W-0633-09 TCGA-09-1674-10A-01W-0633-09 g.chr14:24036406G>A c.118C>T c.(118-120)Cgc>Tgc p.R40C PAAD 14 24033058 24033058 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:24033058G>T c.1099C>A c.(1099-1101)Ctg>Atg p.L367M PAAD 14 24033572 24033572 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:24033572C>T c.947G>A c.(946-948)cGc>cAc p.R316H PAAD 14 24033838 24033838 + Missense_Mutation SNP G G A TCGA-FZ-5921-01A-11D-1609-08 TCGA-FZ-5921-11A-01D-1609-08 g.chr14:24033838G>A c.854C>T c.(853-855)gCc>gTc p.A285V PRAD 14 24031220 24031220 + Nonsense_Mutation SNP G G A TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr14:24031220G>A c.1684C>T c.(1684-1686)Cag>Tag p.Q562* PRAD 14 24033829 24033829 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr14:24033829G>A c.863C>T c.(862-864)gCg>gTg p.A288V PRAD 14 24035556 24035556 + Silent SNP C C T TCGA-VN-A88L-01A-11D-A34U-08 TCGA-VN-A88L-10A-01D-A34X-08 g.chr14:24035556C>T c.402G>A c.(400-402)gaG>gaA p.E134E READ 14 24029037 24029037 + Missense_Mutation SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr14:24029037C>T c.2279G>A c.(2278-2280)cGc>cAc p.R760H READ 14 24033579 24033579 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:24033579G>T c.940C>A c.(940-942)Ctt>Att p.L314I READ 14 24033844 24033844 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr14:24033844C>T c.848G>A c.(847-849)cGa>cAa p.R283Q SARC 14 24033590 24033590 + Missense_Mutation SNP G G C TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr14:24033590G>C c.929C>G c.(928-930)gCt>gGt p.A310G SKCM 14 24031578 24031578 + Missense_Mutation SNP G G A TCGA-GN-A4U7-06A-21D-A32N-08 TCGA-GN-A4U7-10B-01D-A32N-08 g.chr14:24031578G>A c.1547C>T c.(1546-1548)tCc>tTc p.S516F SKCM 14 24031768 24031768 + Missense_Mutation SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr14:24031768C>T c.1445G>A c.(1444-1446)gGg>gAg p.G482E SKCM 14 24033266 24033266 + Silent SNP G G A TCGA-EE-A29B-06A-11D-A197-08 TCGA-EE-A29B-10A-01D-A199-08 g.chr14:24033266G>A c.1080C>T c.(1078-1080)gcC>gcT p.A360A SKCM 14 24033353 24033353 + Silent SNP T T C TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr14:24033353T>C c.993A>G c.(991-993)acA>acG p.T331T SKCM 14 24034858 24034858 + Missense_Mutation SNP G G A TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr14:24034858G>A c.698C>T c.(697-699)tCc>tTc p.S233F SKCM 14 24035517 24035517 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr14:24035517G>A c.441C>T c.(439-441)ctC>ctT p.L147L SKCM 14 24036410 24036410 + Silent SNP G G A TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr14:24036410G>A c.114C>T c.(112-114)tcC>tcT p.S38S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 14 24026493 24026493 single base substitution A G downstream_gene_variant BLCA-US 14 24028017 24028017 single base substitution G A downstream_gene_variant BLCA-US 14 24029009 24029009 single base substitution C T downstream_gene_variant BLCA-US 14 24029009 24029009 single base substitution C T exon_variant BLCA-US 14 24029009 24029009 single base substitution C T synonymous_variant S769S 2307G>A BLCA-US 14 24034889 24034889 single base substitution T C 3_prime_UTR_variant BLCA-US 14 24034889 24034889 single base substitution T C downstream_gene_variant BLCA-US 14 24034889 24034889 single base substitution T C exon_variant BLCA-US 14 24034889 24034889 single base substitution T C missense_variant I223V 667A>G BLCA-US 14 24034889 24034889 single base substitution T C upstream_gene_variant BLCA-US 14 24036487 24036487 single base substitution C T exon_variant BLCA-US 14 24036487 24036487 single base substitution C T missense_variant E13K 37G>A BLCA-US 14 24036487 24036487 single base substitution C T upstream_gene_variant BRCA-EU 14 24024385 24024385 single base substitution C T downstream_gene_variant BRCA-EU 14 24027603 24027603 single base substitution C G downstream_gene_variant BRCA-EU 14 24028003 24028003 single base substitution G C downstream_gene_variant BRCA-EU 14 24028819 24028819 single base substitution G A 3_prime_UTR_variant BRCA-EU 14 24028819 24028819 single base substitution G A downstream_gene_variant BRCA-EU 14 24028819 24028819 single base substitution G A exon_variant BRCA-EU 14 24029936 24029936 single base substitution C T downstream_gene_variant BRCA-EU 14 24029936 24029936 single base substitution C T intron_variant BRCA-EU 14 24029936 24029936 single base substitution C T upstream_gene_variant BRCA-EU 14 24031150 24031150 single base substitution G A downstream_gene_variant BRCA-EU 14 24031150 24031150 single base substitution G A exon_variant BRCA-EU 14 24031150 24031150 single base substitution G A intron_variant BRCA-EU 14 24031150 24031150 single base substitution G A upstream_gene_variant BRCA-EU 14 24031606 24031606 single base substitution G C downstream_gene_variant BRCA-EU 14 24031606 24031606 single base substitution G C exon_variant BRCA-EU 14 24031606 24031606 single base substitution G C missense_variant L4V 10C>G BRCA-EU 14 24031606 24031606 single base substitution G C missense_variant L507V 1519C>G BRCA-EU 14 24031606 24031606 single base substitution G C upstream_gene_variant BRCA-EU 14 24032763 24032763 single base substitution G A downstream_gene_variant BRCA-EU 14 24032763 24032763 single base substitution G A exon_variant BRCA-EU 14 24032763 24032763 single base substitution G A intron_variant BRCA-EU 14 24032763 24032763 single base substitution G A upstream_gene_variant BRCA-EU 14 24036063 24036063 single base substitution G A downstream_gene_variant BRCA-EU 14 24036063 24036063 single base substitution G A exon_variant BRCA-EU 14 24036063 24036063 single base substitution G A intron_variant BRCA-EU 14 24036063 24036063 single base substitution G A upstream_gene_variant BRCA-EU 14 24036219 24036219 single base substitution T C downstream_gene_variant BRCA-EU 14 24036219 24036219 single base substitution T C exon_variant BRCA-EU 14 24036219 24036219 single base substitution T C intron_variant BRCA-EU 14 24036219 24036219 single base substitution T C upstream_gene_variant BRCA-EU 14 24036404 24036404 single base substitution G C exon_variant BRCA-EU 14 24036404 24036404 single base substitution G C intron_variant BRCA-EU 14 24036404 24036404 single base substitution G C synonymous_variant R40R 120C>G BRCA-EU 14 24036404 24036404 single base substitution G C upstream_gene_variant BRCA-EU 14 24036564 24036564 single base substitution T A 5_prime_UTR_variant BRCA-EU 14 24036564 24036564 single base substitution T A intron_variant BRCA-EU 14 24036564 24036564 single base substitution T A upstream_gene_variant BRCA-EU 14 24037093 24037093 single base substitution G A 5_prime_UTR_variant BRCA-EU 14 24037093 24037093 single base substitution G A upstream_gene_variant BRCA-EU 14 24037374 24037374 single base substitution G A upstream_gene_variant BRCA-EU 14 24038026 24038029 deletion of <=200bp AGAA - upstream_gene_variant BRCA-EU 14 24039688 24039688 single base substitution C T upstream_gene_variant BRCA-EU 14 24040178 24040178 single base substitution C A upstream_gene_variant BRCA-EU 14 24040280 24040280 single base substitution G T upstream_gene_variant BRCA-EU 14 24041780 24041780 single base substitution G A upstream_gene_variant BRCA-FR 14 24027979 24027979 single base substitution G A downstream_gene_variant BRCA-FR 14 24028819 24028819 single base substitution G A 3_prime_UTR_variant BRCA-FR 14 24028819 24028819 single base substitution G A downstream_gene_variant BRCA-FR 14 24028819 24028819 single base substitution G A exon_variant BRCA-FR 14 24032343 24032343 single base substitution G A downstream_gene_variant BRCA-FR 14 24032343 24032343 single base substitution G A exon_variant BRCA-FR 14 24032343 24032343 single base substitution G A intron_variant BRCA-FR 14 24032343 24032343 single base substitution G A upstream_gene_variant BRCA-FR 14 24036063 24036063 single base substitution G A downstream_gene_variant BRCA-FR 14 24036063 24036063 single base substitution G A exon_variant BRCA-FR 14 24036063 24036063 single base substitution G A intron_variant BRCA-FR 14 24036063 24036063 single base substitution G A upstream_gene_variant BRCA-UK 14 24041780 24041780 single base substitution G A upstream_gene_variant BRCA-US 14 24026073 24026073 single base substitution G A downstream_gene_variant BRCA-US 14 24026219 24026219 single base substitution G A downstream_gene_variant BRCA-US 14 24026483 24026483 single base substitution G C downstream_gene_variant BRCA-US 14 24028236 24028236 single base substitution C T downstream_gene_variant BRCA-US 14 24028968 24028968 single base substitution G A downstream_gene_variant BRCA-US 14 24028968 24028968 single base substitution G A exon_variant BRCA-US 14 24028968 24028968 single base substitution G A missense_variant S783L 2348C>T BRCA-US 14 24030620 24030620 single base substitution C T downstream_gene_variant BRCA-US 14 24030620 24030620 single base substitution C T exon_variant BRCA-US 14 24030620 24030620 single base substitution C T synonymous_variant L626L 1878G>A BRCA-US 14 24030620 24030620 single base substitution C T synonymous_variant L88L 264G>A BRCA-US 14 24030620 24030620 single base substitution C T upstream_gene_variant BRCA-US 14 24032653 24032653 insertion of <=200bp - C 3_prime_UTR_variant BRCA-US 14 24032653 24032653 insertion of <=200bp - C downstream_gene_variant BRCA-US 14 24032653 24032653 insertion of <=200bp - C exon_variant BRCA-US 14 24032653 24032653 insertion of <=200bp - C frameshift_variant A449A? BRCA-US 14 24032653 24032653 insertion of <=200bp - C upstream_gene_variant BRCA-US 14 24032994 24032994 single base substitution G T downstream_gene_variant BRCA-US 14 24032994 24032994 single base substitution G T exon_variant BRCA-US 14 24032994 24032994 single base substitution G T missense_variant A388D 1163C>A BRCA-US 14 24032994 24032994 single base substitution G T upstream_gene_variant BRCA-US 14 24035107 24035107 single base substitution G T downstream_gene_variant BRCA-US 14 24035107 24035107 single base substitution G T exon_variant BRCA-US 14 24035107 24035107 single base substitution G T intron_variant BRCA-US 14 24035107 24035107 single base substitution G T splice_region_variant BRCA-US 14 24035107 24035107 single base substitution G T upstream_gene_variant BRCA-US 14 24035346 24035346 single base substitution C T 3_prime_UTR_variant BRCA-US 14 24035346 24035346 single base substitution C T downstream_gene_variant BRCA-US 14 24035346 24035346 single base substitution C T exon_variant BRCA-US 14 24035346 24035346 single base substitution C T missense_variant M165I 495G>A BRCA-US 14 24035346 24035346 single base substitution C T upstream_gene_variant BRCA-US 14 24035526 24035526 single base substitution C G 3_prime_UTR_variant BRCA-US 14 24035526 24035526 single base substitution C G downstream_gene_variant BRCA-US 14 24035526 24035526 single base substitution C G exon_variant BRCA-US 14 24035526 24035526 single base substitution C G missense_variant E144D 432G>C BRCA-US 14 24035526 24035526 single base substitution C G upstream_gene_variant BRCA-US 14 24035549 24035549 single base substitution G A 3_prime_UTR_variant BRCA-US 14 24035549 24035549 single base substitution G A downstream_gene_variant BRCA-US 14 24035549 24035549 single base substitution G A exon_variant BRCA-US 14 24035549 24035549 single base substitution G A stop_gained R137* 409C>T BRCA-US 14 24035549 24035549 single base substitution G A synonymous_variant ?137 BRCA-US 14 24035549 24035549 single base substitution G A upstream_gene_variant BRCA-US 14 24035577 24035577 single base substitution C G 3_prime_UTR_variant BRCA-US 14 24035577 24035577 single base substitution C G downstream_gene_variant BRCA-US 14 24035577 24035577 single base substitution C G exon_variant BRCA-US 14 24035577 24035577 single base substitution C G missense_variant L127F 381G>C BRCA-US 14 24035577 24035577 single base substitution C G upstream_gene_variant BRCA-US 14 24035597 24035597 single base substitution C T 3_prime_UTR_variant BRCA-US 14 24035597 24035597 single base substitution C T downstream_gene_variant BRCA-US 14 24035597 24035597 single base substitution C T exon_variant BRCA-US 14 24035597 24035597 single base substitution C T missense_variant G121S 361G>A BRCA-US 14 24035597 24035597 single base substitution C T upstream_gene_variant BRCA-US 14 24040435 24040435 insertion of <=200bp - C upstream_gene_variant BRCA-US 14 24040436 24040436 deletion of <=200bp C - upstream_gene_variant BRCA-US 14 24040653 24040653 single base substitution C A upstream_gene_variant BRCA-US 14 24041029 24041029 single base substitution G A upstream_gene_variant BTCA-JP 14 24026296 24026296 single base substitution G A downstream_gene_variant BTCA-JP 14 24030793 24030793 single base substitution A T downstream_gene_variant BTCA-JP 14 24030793 24030793 single base substitution A T exon_variant BTCA-JP 14 24030793 24030793 single base substitution A T synonymous_variant A57A 171T>A BTCA-JP 14 24030793 24030793 single base substitution A T synonymous_variant A595A 1785T>A BTCA-JP 14 24030793 24030793 single base substitution A T upstream_gene_variant BTCA-JP 14 24031615 24031615 single base substitution C G downstream_gene_variant BTCA-JP 14 24031615 24031615 single base substitution C G exon_variant BTCA-JP 14 24031615 24031615 single base substitution C G missense_variant E1Q 1G>C BTCA-JP 14 24031615 24031615 single base substitution C G missense_variant E504Q 1510G>C BTCA-JP 14 24031615 24031615 single base substitution C G upstream_gene_variant BTCA-JP 14 24032884 24032884 single base substitution G A downstream_gene_variant BTCA-JP 14 24032884 24032884 single base substitution G A exon_variant BTCA-JP 14 24032884 24032884 single base substitution G A intron_variant BTCA-JP 14 24032884 24032884 single base substitution G A upstream_gene_variant BTCA-JP 14 24035080 24035080 single base substitution G A 3_prime_UTR_variant BTCA-JP 14 24035080 24035080 single base substitution G A downstream_gene_variant BTCA-JP 14 24035080 24035080 single base substitution G A exon_variant BTCA-JP 14 24035080 24035080 single base substitution G A intron_variant BTCA-JP 14 24035080 24035080 single base substitution G A missense_variant T197M 590C>T BTCA-JP 14 24035080 24035080 single base substitution G A upstream_gene_variant BTCA-JP 14 24040538 24040538 single base substitution G A upstream_gene_variant CESC-US 14 24030408 24030408 single base substitution G A downstream_gene_variant CESC-US 14 24030408 24030408 single base substitution G A intron_variant CESC-US 14 24030408 24030408 single base substitution G A upstream_gene_variant CESC-US 14 24030665 24030665 single base substitution G A downstream_gene_variant CESC-US 14 24030665 24030665 single base substitution G A intron_variant CESC-US 14 24030665 24030665 single base substitution G A upstream_gene_variant CESC-US 14 24034779 24034779 single base substitution C T downstream_gene_variant CESC-US 14 24034779 24034779 single base substitution C T exon_variant CESC-US 14 24034779 24034779 single base substitution C T intron_variant CESC-US 14 24034779 24034779 single base substitution C T upstream_gene_variant CESC-US 14 24036583 24036583 single base substitution C T 5_prime_UTR_variant CESC-US 14 24036583 24036583 single base substitution C T intron_variant CESC-US 14 24036583 24036583 single base substitution C T upstream_gene_variant CLLE-ES 14 24041816 24041816 deletion of <=200bp G - upstream_gene_variant COAD-US 14 24027955 24027955 single base substitution G A downstream_gene_variant COAD-US 14 24029552 24029552 deletion of <=200bp T - downstream_gene_variant COAD-US 14 24029552 24029552 deletion of <=200bp T - exon_variant COAD-US 14 24029552 24029552 deletion of <=200bp T - frameshift_variant N152 COAD-US 14 24029552 24029552 deletion of <=200bp T - frameshift_variant N690 COAD-US 14 24029552 24029552 deletion of <=200bp T - upstream_gene_variant COAD-US 14 24030801 24030801 insertion of <=200bp - GCCA downstream_gene_variant COAD-US 14 24030801 24030801 insertion of <=200bp - GCCA exon_variant COAD-US 14 24030801 24030801 insertion of <=200bp - GCCA frameshift_variant P55LA? COAD-US 14 24030801 24030801 insertion of <=200bp - GCCA frameshift_variant P593LA? COAD-US 14 24030801 24030801 insertion of <=200bp - GCCA upstream_gene_variant COAD-US 14 24030824 24030824 insertion of <=200bp - T downstream_gene_variant COAD-US 14 24030824 24030824 insertion of <=200bp - T exon_variant COAD-US 14 24030824 24030824 insertion of <=200bp - T frameshift_variant M47I? COAD-US 14 24030824 24030824 insertion of <=200bp - T frameshift_variant M585I? COAD-US 14 24030824 24030824 insertion of <=200bp - T upstream_gene_variant COAD-US 14 24032653 24032653 insertion of <=200bp - C 3_prime_UTR_variant COAD-US 14 24032653 24032653 insertion of <=200bp - C downstream_gene_variant COAD-US 14 24032653 24032653 insertion of <=200bp - C exon_variant COAD-US 14 24032653 24032653 insertion of <=200bp - C frameshift_variant A449A? COAD-US 14 24032653 24032653 insertion of <=200bp - C upstream_gene_variant COAD-US 14 24036471 24036471 single base substitution G T exon_variant COAD-US 14 24036471 24036471 single base substitution G T missense_variant A18D 53C>A COAD-US 14 24036471 24036471 single base substitution G T upstream_gene_variant COAD-US 14 24040238 24040238 single base substitution C T upstream_gene_variant COAD-US 14 24040358 24040358 single base substitution C T upstream_gene_variant COAD-US 14 24040436 24040436 deletion of <=200bp C - upstream_gene_variant COCA-CN 14 24026080 24026080 single base substitution C A downstream_gene_variant COCA-CN 14 24026083 24026083 single base substitution C T downstream_gene_variant COCA-CN 14 24029155 24029155 single base substitution G A downstream_gene_variant COCA-CN 14 24029155 24029155 single base substitution G A exon_variant COCA-CN 14 24029155 24029155 single base substitution G A missense_variant P750S 2248C>T COCA-CN 14 24031267 24031267 single base substitution C T downstream_gene_variant COCA-CN 14 24031267 24031267 single base substitution C T exon_variant COCA-CN 14 24031267 24031267 single base substitution C T intron_variant COCA-CN 14 24031267 24031267 single base substitution C T missense_variant R546H 1637G>A COCA-CN 14 24031267 24031267 single base substitution C T upstream_gene_variant COCA-CN 14 24033018 24033018 single base substitution C T downstream_gene_variant COCA-CN 14 24033018 24033018 single base substitution C T exon_variant COCA-CN 14 24033018 24033018 single base substitution C T missense_variant R380Q 1139G>A COCA-CN 14 24033018 24033018 single base substitution C T upstream_gene_variant COCA-CN 14 24035281 24035281 single base substitution C T 3_prime_UTR_variant COCA-CN 14 24035281 24035281 single base substitution C T downstream_gene_variant COCA-CN 14 24035281 24035281 single base substitution C T exon_variant COCA-CN 14 24035281 24035281 single base substitution C T missense_variant R187H 560G>A COCA-CN 14 24035281 24035281 single base substitution C T upstream_gene_variant COCA-CN 14 24040154 24040154 single base substitution C T upstream_gene_variant COCA-CN 14 24040449 24040449 single base substitution C A upstream_gene_variant ESAD-UK 14 24028364 24028364 insertion of <=200bp - C downstream_gene_variant ESAD-UK 14 24029133 24029133 single base substitution C T downstream_gene_variant ESAD-UK 14 24029133 24029133 single base substitution C T intron_variant ESAD-UK 14 24030673 24030673 single base substitution T C downstream_gene_variant ESAD-UK 14 24030673 24030673 single base substitution T C intron_variant ESAD-UK 14 24030673 24030673 single base substitution T C upstream_gene_variant ESAD-UK 14 24030847 24030847 single base substitution G C downstream_gene_variant ESAD-UK 14 24030847 24030847 single base substitution G C exon_variant ESAD-UK 14 24030847 24030847 single base substitution G C splice_region_variant ESAD-UK 14 24030847 24030847 single base substitution G C upstream_gene_variant ESAD-UK 14 24031937 24031937 insertion of <=200bp - C downstream_gene_variant ESAD-UK 14 24031937 24031937 insertion of <=200bp - C exon_variant ESAD-UK 14 24031937 24031937 insertion of <=200bp - C intron_variant ESAD-UK 14 24031937 24031937 insertion of <=200bp - C upstream_gene_variant ESAD-UK 14 24033397 24033397 single base substitution A G downstream_gene_variant ESAD-UK 14 24033397 24033397 single base substitution A G exon_variant ESAD-UK 14 24033397 24033397 single base substitution A G intron_variant ESAD-UK 14 24033397 24033397 single base substitution A G upstream_gene_variant ESAD-UK 14 24034279 24034279 single base substitution G A downstream_gene_variant ESAD-UK 14 24034279 24034279 single base substitution G A exon_variant ESAD-UK 14 24034279 24034279 single base substitution G A intron_variant ESAD-UK 14 24034279 24034279 single base substitution G A upstream_gene_variant ESAD-UK 14 24035498 24035498 single base substitution C T 3_prime_UTR_variant ESAD-UK 14 24035498 24035498 single base substitution C T downstream_gene_variant ESAD-UK 14 24035498 24035498 single base substitution C T exon_variant ESAD-UK 14 24035498 24035498 single base substitution C T missense_variant V154M 460G>A ESAD-UK 14 24035498 24035498 single base substitution C T upstream_gene_variant ESAD-UK 14 24035593 24035593 single base substitution A G 3_prime_UTR_variant ESAD-UK 14 24035593 24035593 single base substitution A G downstream_gene_variant ESAD-UK 14 24035593 24035593 single base substitution A G exon_variant ESAD-UK 14 24035593 24035593 single base substitution A G missense_variant L122P 365T>C ESAD-UK 14 24035593 24035593 single base substitution A G upstream_gene_variant ESAD-UK 14 24037003 24037003 single base substitution C G 5_prime_UTR_variant ESAD-UK 14 24037003 24037003 single base substitution C G exon_variant ESAD-UK 14 24037003 24037003 single base substitution C G upstream_gene_variant ESAD-UK 14 24039879 24039879 single base substitution G A upstream_gene_variant ESAD-UK 14 24042075 24042075 single base substitution G A upstream_gene_variant ESCA-CN 14 24031695 24031695 deletion of <=200bp C - downstream_gene_variant ESCA-CN 14 24031695 24031695 deletion of <=200bp C - intron_variant ESCA-CN 14 24031695 24031695 deletion of <=200bp C - upstream_gene_variant ESCA-CN 14 24040471 24040471 single base substitution G C upstream_gene_variant GBM-US 14 24040215 24040215 single base substitution C T upstream_gene_variant KIRC-US 14 24033327 24033327 single base substitution T C downstream_gene_variant KIRC-US 14 24033327 24033327 single base substitution T C exon_variant KIRC-US 14 24033327 24033327 single base substitution T C missense_variant D340G 1019A>G KIRC-US 14 24033327 24033327 single base substitution T C upstream_gene_variant KIRC-US 14 24035342 24035342 single base substitution G A 3_prime_UTR_variant KIRC-US 14 24035342 24035342 single base substitution G A downstream_gene_variant KIRC-US 14 24035342 24035342 single base substitution G A exon_variant KIRC-US 14 24035342 24035342 single base substitution G A missense_variant R167W 499C>T KIRC-US 14 24035342 24035342 single base substitution G A upstream_gene_variant KIRP-US 14 24030557 24030557 single base substitution T C downstream_gene_variant KIRP-US 14 24030557 24030557 single base substitution T C exon_variant KIRP-US 14 24030557 24030557 single base substitution T C synonymous_variant P109P 327A>G KIRP-US 14 24030557 24030557 single base substitution T C synonymous_variant P647P 1941A>G KIRP-US 14 24030557 24030557 single base substitution T C upstream_gene_variant KIRP-US 14 24032848 24032848 single base substitution C T downstream_gene_variant KIRP-US 14 24032848 24032848 single base substitution C T exon_variant KIRP-US 14 24032848 24032848 single base substitution C T intron_variant KIRP-US 14 24032848 24032848 single base substitution C T splice_acceptor_variant KIRP-US 14 24032848 24032848 single base substitution C T upstream_gene_variant KIRP-US 14 24036472 24036472 deletion of <=200bp C - exon_variant KIRP-US 14 24036472 24036472 deletion of <=200bp C - frameshift_variant A18 KIRP-US 14 24036472 24036472 deletion of <=200bp C - upstream_gene_variant KIRP-US 14 24040204 24040204 single base substitution C G upstream_gene_variant LGG-US 14 24035874 24035874 single base substitution C T downstream_gene_variant LGG-US 14 24035874 24035874 single base substitution C T exon_variant LGG-US 14 24035874 24035874 single base substitution C T intron_variant LGG-US 14 24035874 24035874 single base substitution C T missense_variant A76T 226G>A LGG-US 14 24035874 24035874 single base substitution C T upstream_gene_variant LGG-US 14 24040638 24040638 single base substitution G A upstream_gene_variant LICA-CN 14 24026347 24026347 single base substitution C A downstream_gene_variant LICA-CN 14 24033563 24033563 single base substitution A T downstream_gene_variant LICA-CN 14 24033563 24033563 single base substitution A T exon_variant LICA-CN 14 24033563 24033563 single base substitution A T missense_variant L319H 956T>A LICA-CN 14 24033563 24033563 single base substitution A T upstream_gene_variant LICA-FR 14 24026085 24026085 single base substitution A G downstream_gene_variant LICA-FR 14 24026505 24026505 single base substitution G A downstream_gene_variant LICA-FR 14 24029227 24029227 single base substitution G A downstream_gene_variant LICA-FR 14 24029227 24029227 single base substitution G A exon_variant LICA-FR 14 24029227 24029227 single base substitution G A stop_gained Q188* 562C>T LICA-FR 14 24029227 24029227 single base substitution G A stop_gained Q726* 2176C>T LICA-FR 14 24031178 24031178 single base substitution G A downstream_gene_variant LICA-FR 14 24031178 24031178 single base substitution G A exon_variant LICA-FR 14 24031178 24031178 single base substitution G A intron_variant LICA-FR 14 24031178 24031178 single base substitution G A missense_variant H576Y 1726C>T LICA-FR 14 24031178 24031178 single base substitution G A upstream_gene_variant LICA-FR 14 24033930 24033930 deletion of <=200bp A - downstream_gene_variant LICA-FR 14 24033930 24033930 deletion of <=200bp A - exon_variant LICA-FR 14 24033930 24033930 deletion of <=200bp A - intron_variant LICA-FR 14 24033930 24033930 deletion of <=200bp A - upstream_gene_variant LICA-FR 14 24035594 24035594 single base substitution G A 3_prime_UTR_variant LICA-FR 14 24035594 24035594 single base substitution G A downstream_gene_variant LICA-FR 14 24035594 24035594 single base substitution G A exon_variant LICA-FR 14 24035594 24035594 single base substitution G A synonymous_variant L122L 364C>T LICA-FR 14 24035594 24035594 single base substitution G A upstream_gene_variant LICA-FR 14 24040436 24040436 deletion of <=200bp C - upstream_gene_variant LIHC-US 14 24031766 24031766 deletion of <=200bp C - downstream_gene_variant LIHC-US 14 24031766 24031766 deletion of <=200bp C - exon_variant LIHC-US 14 24031766 24031766 deletion of <=200bp C - frameshift_variant E483 LIHC-US 14 24031766 24031766 deletion of <=200bp C - upstream_gene_variant LIHC-US 14 24032935 24032935 single base substitution C G downstream_gene_variant LIHC-US 14 24032935 24032935 single base substitution C G exon_variant LIHC-US 14 24032935 24032935 single base substitution C G missense_variant A408P 1222G>C LIHC-US 14 24032935 24032935 single base substitution C G upstream_gene_variant LIHC-US 14 24040535 24040535 single base substitution G A upstream_gene_variant LINC-JP 14 24025100 24025100 single base substitution T A downstream_gene_variant LINC-JP 14 24027828 24027828 single base substitution G A downstream_gene_variant LINC-JP 14 24029037 24029037 single base substitution C T downstream_gene_variant LINC-JP 14 24029037 24029037 single base substitution C T exon_variant LINC-JP 14 24029037 24029037 single base substitution C T missense_variant R760H 2279G>A LINC-JP 14 24029302 24029302 single base substitution C T downstream_gene_variant LINC-JP 14 24029302 24029302 single base substitution C T exon_variant LINC-JP 14 24029302 24029302 single base substitution C T intron_variant LINC-JP 14 24030622 24030622 single base substitution G T downstream_gene_variant LINC-JP 14 24030622 24030622 single base substitution G T exon_variant LINC-JP 14 24030622 24030622 single base substitution G T missense_variant L626M 1876C>A LINC-JP 14 24030622 24030622 single base substitution G T missense_variant L88M 262C>A LINC-JP 14 24030622 24030622 single base substitution G T upstream_gene_variant LINC-JP 14 24031186 24031186 insertion of <=200bp - C downstream_gene_variant LINC-JP 14 24031186 24031186 insertion of <=200bp - C exon_variant LINC-JP 14 24031186 24031186 insertion of <=200bp - C frameshift_variant K573K? LINC-JP 14 24031186 24031186 insertion of <=200bp - C intron_variant LINC-JP 14 24031186 24031186 insertion of <=200bp - C upstream_gene_variant LINC-JP 14 24031571 24031571 single base substitution C T downstream_gene_variant LINC-JP 14 24031571 24031571 single base substitution C T exon_variant LINC-JP 14 24031571 24031571 single base substitution C T missense_variant M15I 45G>A LINC-JP 14 24031571 24031571 single base substitution C T missense_variant M518I 1554G>A LINC-JP 14 24031571 24031571 single base substitution C T upstream_gene_variant LINC-JP 14 24033081 24033081 single base substitution G A downstream_gene_variant LINC-JP 14 24033081 24033081 single base substitution G A exon_variant LINC-JP 14 24033081 24033081 single base substitution G A intron_variant LINC-JP 14 24033081 24033081 single base substitution G A upstream_gene_variant LINC-JP 14 24034729 24034729 single base substitution G C downstream_gene_variant LINC-JP 14 24034729 24034729 single base substitution G C exon_variant LINC-JP 14 24034729 24034729 single base substitution G C intron_variant LINC-JP 14 24034729 24034729 single base substitution G C upstream_gene_variant LINC-JP 14 24035832 24035832 single base substitution C T downstream_gene_variant LINC-JP 14 24035832 24035832 single base substitution C T exon_variant LINC-JP 14 24035832 24035832 single base substitution C T intron_variant LINC-JP 14 24035832 24035832 single base substitution C T missense_variant A90T 268G>A LINC-JP 14 24035832 24035832 single base substitution C T upstream_gene_variant LINC-JP 14 24040509 24040509 single base substitution C A upstream_gene_variant LINC-JP 14 24040560 24040560 single base substitution C T upstream_gene_variant LIRI-JP 14 24027961 24027961 single base substitution G A downstream_gene_variant LIRI-JP 14 24028659 24028659 single base substitution C T downstream_gene_variant LIRI-JP 14 24031081 24031081 single base substitution A T downstream_gene_variant LIRI-JP 14 24031081 24031081 single base substitution A T exon_variant LIRI-JP 14 24031081 24031081 single base substitution A T intron_variant LIRI-JP 14 24031081 24031081 single base substitution A T upstream_gene_variant LIRI-JP 14 24031784 24031784 single base substitution C G downstream_gene_variant LIRI-JP 14 24031784 24031784 single base substitution C G exon_variant LIRI-JP 14 24031784 24031784 single base substitution C G missense_variant A477P 1429G>C LIRI-JP 14 24031784 24031784 single base substitution C G upstream_gene_variant LIRI-JP 14 24033370 24033370 single base substitution T C downstream_gene_variant LIRI-JP 14 24033370 24033370 single base substitution T C exon_variant LIRI-JP 14 24033370 24033370 single base substitution T C splice_acceptor_variant LIRI-JP 14 24033370 24033370 single base substitution T C upstream_gene_variant LIRI-JP 14 24033386 24033386 single base substitution G C downstream_gene_variant LIRI-JP 14 24033386 24033386 single base substitution G C exon_variant LIRI-JP 14 24033386 24033386 single base substitution G C intron_variant LIRI-JP 14 24033386 24033386 single base substitution G C upstream_gene_variant LIRI-JP 14 24033423 24033423 single base substitution G A downstream_gene_variant LIRI-JP 14 24033423 24033423 single base substitution G A exon_variant LIRI-JP 14 24033423 24033423 single base substitution G A intron_variant LIRI-JP 14 24033423 24033423 single base substitution G A upstream_gene_variant LIRI-JP 14 24034702 24034702 single base substitution C T downstream_gene_variant LIRI-JP 14 24034702 24034702 single base substitution C T exon_variant LIRI-JP 14 24034702 24034702 single base substitution C T intron_variant LIRI-JP 14 24034702 24034702 single base substitution C T upstream_gene_variant LIRI-JP 14 24036177 24036177 single base substitution G C downstream_gene_variant LIRI-JP 14 24036177 24036177 single base substitution G C exon_variant LIRI-JP 14 24036177 24036177 single base substitution G C intron_variant LIRI-JP 14 24036177 24036177 single base substitution G C upstream_gene_variant LIRI-JP 14 24036261 24036261 deletion of <=200bp T - downstream_gene_variant LIRI-JP 14 24036261 24036261 deletion of <=200bp T - exon_variant LIRI-JP 14 24036261 24036261 deletion of <=200bp T - intron_variant LIRI-JP 14 24036261 24036261 deletion of <=200bp T - upstream_gene_variant LIRI-JP 14 24039738 24039738 single base substitution G A upstream_gene_variant LIRI-JP 14 24040436 24040436 insertion of <=200bp - C upstream_gene_variant LIRI-JP 14 24040846 24040846 single base substitution C T upstream_gene_variant LIRI-JP 14 24041761 24041761 single base substitution A G upstream_gene_variant LUSC-KR 14 24024337 24024337 single base substitution C A downstream_gene_variant LUSC-KR 14 24025363 24025363 single base substitution C G downstream_gene_variant LUSC-KR 14 24025914 24025914 single base substitution G T downstream_gene_variant LUSC-KR 14 24026493 24026493 single base substitution A G downstream_gene_variant LUSC-KR 14 24033070 24033070 single base substitution C T downstream_gene_variant LUSC-KR 14 24033070 24033070 single base substitution C T exon_variant LUSC-KR 14 24033070 24033070 single base substitution C T splice_region_variant LUSC-KR 14 24033070 24033070 single base substitution C T upstream_gene_variant LUSC-KR 14 24039164 24039164 single base substitution C T upstream_gene_variant LUSC-KR 14 24040774 24040774 single base substitution G A upstream_gene_variant LUSC-US 14 24030804 24030804 single base substitution C T downstream_gene_variant LUSC-US 14 24030804 24030804 single base substitution C T exon_variant LUSC-US 14 24030804 24030804 single base substitution C T missense_variant G54S 160G>A LUSC-US 14 24030804 24030804 single base substitution C T missense_variant G592S 1774G>A LUSC-US 14 24030804 24030804 single base substitution C T upstream_gene_variant LUSC-US 14 24040344 24040344 single base substitution G T upstream_gene_variant LUSC-US 14 24040504 24040504 single base substitution G A upstream_gene_variant LUSC-US 14 24040570 24040570 single base substitution G C upstream_gene_variant LUSC-US 14 24041127 24041127 single base substitution G T upstream_gene_variant MALY-DE 14 24024295 24024295 single base substitution C G downstream_gene_variant MALY-DE 14 24031975 24031975 single base substitution G A downstream_gene_variant MALY-DE 14 24031975 24031975 single base substitution G A exon_variant MALY-DE 14 24031975 24031975 single base substitution G A intron_variant MALY-DE 14 24031975 24031975 single base substitution G A upstream_gene_variant MALY-DE 14 24036899 24036899 insertion of <=200bp - CAGCGGCAGCGGCAGCGA 5_prime_UTR_variant MALY-DE 14 24036899 24036899 insertion of <=200bp - CAGCGGCAGCGGCAGCGA intron_variant MALY-DE 14 24036899 24036899 insertion of <=200bp - CAGCGGCAGCGGCAGCGA upstream_gene_variant MALY-DE 14 24042030 24042030 single base substitution A G upstream_gene_variant MELA-AU 14 24023838 24023838 single base substitution C T downstream_gene_variant MELA-AU 14 24026263 24026263 single base substitution C T downstream_gene_variant MELA-AU 14 24028601 24028601 single base substitution G A downstream_gene_variant MELA-AU 14 24028912 24028912 single base substitution C A 3_prime_UTR_variant MELA-AU 14 24028912 24028912 single base substitution C A downstream_gene_variant MELA-AU 14 24028912 24028912 single base substitution C A exon_variant MELA-AU 14 24030561 24030561 single base substitution G A downstream_gene_variant MELA-AU 14 24030561 24030561 single base substitution G A exon_variant MELA-AU 14 24030561 24030561 single base substitution G A missense_variant S108F 323C>T MELA-AU 14 24030561 24030561 single base substitution G A missense_variant S646F 1937C>T MELA-AU 14 24030561 24030561 single base substitution G A upstream_gene_variant MELA-AU 14 24031955 24031955 single base substitution T A downstream_gene_variant MELA-AU 14 24031955 24031955 single base substitution T A exon_variant MELA-AU 14 24031955 24031955 single base substitution T A intron_variant MELA-AU 14 24031955 24031955 single base substitution T A upstream_gene_variant MELA-AU 14 24031971 24031971 single base substitution G A downstream_gene_variant MELA-AU 14 24031971 24031971 single base substitution G A exon_variant MELA-AU 14 24031971 24031971 single base substitution G A intron_variant MELA-AU 14 24031971 24031971 single base substitution G A upstream_gene_variant MELA-AU 14 24031975 24031975 single base substitution G A downstream_gene_variant MELA-AU 14 24031975 24031975 single base substitution G A exon_variant MELA-AU 14 24031975 24031975 single base substitution G A intron_variant MELA-AU 14 24031975 24031975 single base substitution G A upstream_gene_variant MELA-AU 14 24033513 24033513 single base substitution C G downstream_gene_variant MELA-AU 14 24033513 24033513 single base substitution C G intron_variant MELA-AU 14 24033513 24033513 single base substitution C G upstream_gene_variant MELA-AU 14 24033828 24033828 single base substitution C T downstream_gene_variant MELA-AU 14 24033828 24033828 single base substitution C T exon_variant MELA-AU 14 24033828 24033828 single base substitution C T synonymous_variant A288A 864G>A MELA-AU 14 24033828 24033828 single base substitution C T upstream_gene_variant MELA-AU 14 24034664 24034664 single base substitution G A downstream_gene_variant MELA-AU 14 24034664 24034664 single base substitution G A exon_variant MELA-AU 14 24034664 24034664 single base substitution G A intron_variant MELA-AU 14 24034664 24034664 single base substitution G A upstream_gene_variant MELA-AU 14 24034887 24034887 single base substitution G A 3_prime_UTR_variant MELA-AU 14 24034887 24034887 single base substitution G A downstream_gene_variant MELA-AU 14 24034887 24034887 single base substitution G A exon_variant MELA-AU 14 24034887 24034887 single base substitution G A synonymous_variant I223I 669C>T MELA-AU 14 24034887 24034887 single base substitution G A upstream_gene_variant MELA-AU 14 24035249 24035249 single base substitution G A downstream_gene_variant MELA-AU 14 24035249 24035249 single base substitution G A exon_variant MELA-AU 14 24035249 24035249 single base substitution G A intron_variant MELA-AU 14 24035249 24035249 single base substitution G A upstream_gene_variant MELA-AU 14 24035563 24035563 single base substitution G A 3_prime_UTR_variant MELA-AU 14 24035563 24035563 single base substitution G A downstream_gene_variant MELA-AU 14 24035563 24035563 single base substitution G A exon_variant MELA-AU 14 24035563 24035563 single base substitution G A missense_variant S132F 395C>T MELA-AU 14 24035563 24035563 single base substitution G A upstream_gene_variant MELA-AU 14 24035581 24035581 single base substitution G A 3_prime_UTR_variant MELA-AU 14 24035581 24035581 single base substitution G A downstream_gene_variant MELA-AU 14 24035581 24035581 single base substitution G A exon_variant MELA-AU 14 24035581 24035581 single base substitution G A missense_variant T126I 377C>T MELA-AU 14 24035581 24035581 single base substitution G A upstream_gene_variant MELA-AU 14 24036899 24036899 insertion of <=200bp - CAGCGGCAGCGGCAGCGA 5_prime_UTR_variant MELA-AU 14 24036899 24036899 insertion of <=200bp - CAGCGGCAGCGGCAGCGA intron_variant MELA-AU 14 24036899 24036899 insertion of <=200bp - CAGCGGCAGCGGCAGCGA upstream_gene_variant MELA-AU 14 24037417 24037417 single base substitution G A upstream_gene_variant MELA-AU 14 24037488 24037488 single base substitution C T upstream_gene_variant MELA-AU 14 24037580 24037580 single base substitution G A upstream_gene_variant MELA-AU 14 24038229 24038229 single base substitution G A upstream_gene_variant MELA-AU 14 24038502 24038502 single base substitution G A upstream_gene_variant MELA-AU 14 24038590 24038590 single base substitution A G upstream_gene_variant MELA-AU 14 24038657 24038657 single base substitution G A upstream_gene_variant MELA-AU 14 24038693 24038693 single base substitution A C upstream_gene_variant MELA-AU 14 24038913 24038913 single base substitution G A upstream_gene_variant MELA-AU 14 24038941 24038942 multiple base substitution (>=2bp and <=200bp) GG CA upstream_gene_variant MELA-AU 14 24039050 24039050 single base substitution C T upstream_gene_variant MELA-AU 14 24039410 24039410 single base substitution G A upstream_gene_variant MELA-AU 14 24039644 24039644 single base substitution G A upstream_gene_variant MELA-AU 14 24039805 24039805 single base substitution G A upstream_gene_variant MELA-AU 14 24039851 24039851 single base substitution G A upstream_gene_variant MELA-AU 14 24039938 24039938 single base substitution G A upstream_gene_variant MELA-AU 14 24040189 24040189 single base substitution C T upstream_gene_variant MELA-AU 14 24040606 24040606 single base substitution C T upstream_gene_variant MELA-AU 14 24040771 24040771 single base substitution C T upstream_gene_variant MELA-AU 14 24040832 24040832 single base substitution C T upstream_gene_variant MELA-AU 14 24040927 24040927 single base substitution G A upstream_gene_variant MELA-AU 14 24041113 24041113 single base substitution G A upstream_gene_variant MELA-AU 14 24041320 24041320 single base substitution C T upstream_gene_variant MELA-AU 14 24041460 24041460 single base substitution C T upstream_gene_variant MELA-AU 14 24041929 24041929 single base substitution C T upstream_gene_variant ORCA-IN 14 24029601 24029601 single base substitution C G downstream_gene_variant ORCA-IN 14 24029601 24029601 single base substitution C G exon_variant ORCA-IN 14 24029601 24029601 single base substitution C G missense_variant E136Q 406G>C ORCA-IN 14 24029601 24029601 single base substitution C G missense_variant E674Q 2020G>C ORCA-IN 14 24029601 24029601 single base substitution C G upstream_gene_variant ORCA-IN 14 24033262 24033262 single base substitution G T downstream_gene_variant ORCA-IN 14 24033262 24033262 single base substitution G T exon_variant ORCA-IN 14 24033262 24033262 single base substitution G T missense_variant L362I 1084C>A ORCA-IN 14 24033262 24033262 single base substitution G T upstream_gene_variant ORCA-IN 14 24040204 24040204 single base substitution C A upstream_gene_variant OV-AU 14 24029038 24029038 single base substitution G A downstream_gene_variant OV-AU 14 24029038 24029038 single base substitution G A exon_variant OV-AU 14 24029038 24029038 single base substitution G A missense_variant R760C 2278C>T OV-AU 14 24030741 24030741 single base substitution G A downstream_gene_variant OV-AU 14 24030741 24030741 single base substitution G A exon_variant OV-AU 14 24030741 24030741 single base substitution G A missense_variant P613S 1837C>T OV-AU 14 24030741 24030741 single base substitution G A missense_variant P75S 223C>T OV-AU 14 24030741 24030741 single base substitution G A upstream_gene_variant OV-AU 14 24039501 24039501 single base substitution T G upstream_gene_variant OV-AU 14 24040024 24040024 single base substitution G A upstream_gene_variant PACA-AU 14 24023909 24023909 single base substitution C G downstream_gene_variant PACA-AU 14 24031937 24031938 deletion of <=200bp CC - downstream_gene_variant PACA-AU 14 24031937 24031938 deletion of <=200bp CC - exon_variant PACA-AU 14 24031937 24031938 deletion of <=200bp CC - intron_variant PACA-AU 14 24031937 24031938 deletion of <=200bp CC - upstream_gene_variant PACA-AU 14 24031955 24031955 single base substitution T A downstream_gene_variant PACA-AU 14 24031955 24031955 single base substitution T A exon_variant PACA-AU 14 24031955 24031955 single base substitution T A intron_variant PACA-AU 14 24031955 24031955 single base substitution T A upstream_gene_variant PACA-AU 14 24037671 24037671 single base substitution G C upstream_gene_variant PACA-AU 14 24038107 24038107 single base substitution G A upstream_gene_variant PACA-AU 14 24038546 24038546 single base substitution G T upstream_gene_variant PACA-AU 14 24038822 24038822 single base substitution G A upstream_gene_variant PACA-AU 14 24040007 24040007 single base substitution G A upstream_gene_variant PACA-CA 14 24025028 24025028 single base substitution T G downstream_gene_variant PACA-CA 14 24025529 24025529 single base substitution G A downstream_gene_variant PACA-CA 14 24027646 24027646 single base substitution C T downstream_gene_variant PACA-CA 14 24030790 24030790 single base substitution A G downstream_gene_variant PACA-CA 14 24030790 24030790 single base substitution A G exon_variant PACA-CA 14 24030790 24030790 single base substitution A G synonymous_variant D58D 174T>C PACA-CA 14 24030790 24030790 single base substitution A G synonymous_variant D596D 1788T>C PACA-CA 14 24030790 24030790 single base substitution A G upstream_gene_variant PACA-CA 14 24031936 24031936 insertion of <=200bp - C downstream_gene_variant PACA-CA 14 24031936 24031936 insertion of <=200bp - C exon_variant PACA-CA 14 24031936 24031936 insertion of <=200bp - C intron_variant PACA-CA 14 24031936 24031936 insertion of <=200bp - C upstream_gene_variant PACA-CA 14 24037021 24037021 single base substitution C T 5_prime_UTR_variant PACA-CA 14 24037021 24037021 single base substitution C T exon_variant PACA-CA 14 24037021 24037021 single base substitution C T upstream_gene_variant PACA-CA 14 24037367 24037367 single base substitution G T upstream_gene_variant PBCA-DE 14 24024236 24024236 single base substitution G A downstream_gene_variant PBCA-DE 14 24031955 24031955 single base substitution T A downstream_gene_variant PBCA-DE 14 24031955 24031955 single base substitution T A exon_variant PBCA-DE 14 24031955 24031955 single base substitution T A intron_variant PBCA-DE 14 24031955 24031955 single base substitution T A upstream_gene_variant PBCA-DE 14 24031975 24031975 single base substitution G A downstream_gene_variant PBCA-DE 14 24031975 24031975 single base substitution G A exon_variant PBCA-DE 14 24031975 24031975 single base substitution G A intron_variant PBCA-DE 14 24031975 24031975 single base substitution G A upstream_gene_variant PBCA-DE 14 24032425 24032425 single base substitution G T downstream_gene_variant PBCA-DE 14 24032425 24032425 single base substitution G T exon_variant PBCA-DE 14 24032425 24032425 single base substitution G T intron_variant PBCA-DE 14 24032425 24032425 single base substitution G T upstream_gene_variant PBCA-DE 14 24040983 24040983 single base substitution G T upstream_gene_variant PRAD-CA 14 24036380 24036380 single base substitution G C exon_variant PRAD-CA 14 24036380 24036380 single base substitution G C intron_variant PRAD-CA 14 24036380 24036380 single base substitution G C missense_variant H48Q 144C>G PRAD-CA 14 24036380 24036380 single base substitution G C upstream_gene_variant PRAD-UK 14 24031534 24031534 single base substitution G C downstream_gene_variant PRAD-UK 14 24031534 24031534 single base substitution G C exon_variant PRAD-UK 14 24031534 24031534 single base substitution G C missense_variant L28V 82C>G PRAD-UK 14 24031534 24031534 single base substitution G C missense_variant L531V 1591C>G PRAD-UK 14 24031534 24031534 single base substitution G C upstream_gene_variant PRAD-US 14 24026160 24026160 single base substitution A G downstream_gene_variant PRAD-US 14 24027979 24027979 single base substitution G A downstream_gene_variant PRAD-US 14 24031220 24031220 single base substitution G A downstream_gene_variant PRAD-US 14 24031220 24031220 single base substitution G A exon_variant PRAD-US 14 24031220 24031220 single base substitution G A intron_variant PRAD-US 14 24031220 24031220 single base substitution G A stop_gained Q562* 1684C>T PRAD-US 14 24031220 24031220 single base substitution G A upstream_gene_variant PRAD-US 14 24040359 24040359 single base substitution G A upstream_gene_variant PRAD-US 14 24040525 24040525 single base substitution C T upstream_gene_variant READ-US 14 24029037 24029037 single base substitution C T downstream_gene_variant READ-US 14 24029037 24029037 single base substitution C T exon_variant READ-US 14 24029037 24029037 single base substitution C T missense_variant R760H 2279G>A RECA-EU 14 24025562 24025562 single base substitution G C downstream_gene_variant RECA-EU 14 24026589 24026589 single base substitution G T downstream_gene_variant RECA-EU 14 24028436 24028436 single base substitution T C downstream_gene_variant RECA-EU 14 24029118 24029118 single base substitution C T downstream_gene_variant RECA-EU 14 24029118 24029118 single base substitution C T intron_variant RECA-EU 14 24041643 24041643 single base substitution T G upstream_gene_variant SKCA-BR 14 24024899 24024899 single base substitution A C downstream_gene_variant SKCA-BR 14 24034450 24034450 single base substitution G A downstream_gene_variant SKCA-BR 14 24034450 24034450 single base substitution G A exon_variant SKCA-BR 14 24034450 24034450 single base substitution G A intron_variant SKCA-BR 14 24034450 24034450 single base substitution G A upstream_gene_variant SKCA-BR 14 24037008 24037008 single base substitution A G 5_prime_UTR_variant SKCA-BR 14 24037008 24037008 single base substitution A G exon_variant SKCA-BR 14 24037008 24037008 single base substitution A G upstream_gene_variant SKCA-BR 14 24037033 24037033 single base substitution T C 5_prime_UTR_variant SKCA-BR 14 24037033 24037033 single base substitution T C exon_variant SKCA-BR 14 24037033 24037033 single base substitution T C upstream_gene_variant SKCA-BR 14 24037039 24037039 single base substitution T C 5_prime_UTR_variant SKCA-BR 14 24037039 24037039 single base substitution T C exon_variant SKCA-BR 14 24037039 24037039 single base substitution T C upstream_gene_variant SKCA-BR 14 24039150 24039150 single base substitution C T upstream_gene_variant SKCA-BR 14 24039151 24039151 single base substitution C T upstream_gene_variant SKCA-BR 14 24040081 24040081 single base substitution G A upstream_gene_variant SKCA-BR 14 24042046 24042046 single base substitution C T upstream_gene_variant SKCM-US 14 24030569 24030569 single base substitution C T downstream_gene_variant SKCM-US 14 24030569 24030569 single base substitution C T exon_variant SKCM-US 14 24030569 24030569 single base substitution C T synonymous_variant L105L 315G>A SKCM-US 14 24030569 24030569 single base substitution C T synonymous_variant L643L 1929G>A SKCM-US 14 24030569 24030569 single base substitution C T upstream_gene_variant SKCM-US 14 24031768 24031768 single base substitution C T downstream_gene_variant SKCM-US 14 24031768 24031768 single base substitution C T exon_variant SKCM-US 14 24031768 24031768 single base substitution C T missense_variant G482E 1445G>A SKCM-US 14 24031768 24031768 single base substitution C T upstream_gene_variant SKCM-US 14 24033266 24033266 single base substitution G A downstream_gene_variant SKCM-US 14 24033266 24033266 single base substitution G A exon_variant SKCM-US 14 24033266 24033266 single base substitution G A synonymous_variant A360A 1080C>T SKCM-US 14 24033266 24033266 single base substitution G A upstream_gene_variant SKCM-US 14 24033353 24033353 single base substitution T C downstream_gene_variant SKCM-US 14 24033353 24033353 single base substitution T C exon_variant SKCM-US 14 24033353 24033353 single base substitution T C synonymous_variant T331T 993A>G SKCM-US 14 24033353 24033353 single base substitution T C upstream_gene_variant SKCM-US 14 24034858 24034858 single base substitution G A 3_prime_UTR_variant SKCM-US 14 24034858 24034858 single base substitution G A downstream_gene_variant SKCM-US 14 24034858 24034858 single base substitution G A exon_variant SKCM-US 14 24034858 24034858 single base substitution G A missense_variant S233F 698C>T SKCM-US 14 24034858 24034858 single base substitution G A upstream_gene_variant SKCM-US 14 24035517 24035517 single base substitution G A 3_prime_UTR_variant SKCM-US 14 24035517 24035517 single base substitution G A downstream_gene_variant SKCM-US 14 24035517 24035517 single base substitution G A exon_variant SKCM-US 14 24035517 24035517 single base substitution G A synonymous_variant L147L 441C>T SKCM-US 14 24035517 24035517 single base substitution G A upstream_gene_variant SKCM-US 14 24035813 24035813 single base substitution T C downstream_gene_variant SKCM-US 14 24035813 24035813 single base substitution T C exon_variant SKCM-US 14 24035813 24035813 single base substitution T C intron_variant SKCM-US 14 24035813 24035813 single base substitution T C missense_variant E96G 287A>G SKCM-US 14 24035813 24035813 single base substitution T C upstream_gene_variant SKCM-US 14 24036410 24036410 single base substitution G A exon_variant SKCM-US 14 24036410 24036410 single base substitution G A intron_variant SKCM-US 14 24036410 24036410 single base substitution G A synonymous_variant S38S 114C>T SKCM-US 14 24036410 24036410 single base substitution G A upstream_gene_variant SKCM-US 14 24040151 24040151 single base substitution T C upstream_gene_variant SKCM-US 14 24040243 24040243 single base substitution G A upstream_gene_variant SKCM-US 14 24040471 24040471 single base substitution G A upstream_gene_variant SKCM-US 14 24040512 24040512 single base substitution G A upstream_gene_variant SKCM-US 14 24040602 24040602 single base substitution T A upstream_gene_variant SKCM-US 14 24040606 24040606 single base substitution C T upstream_gene_variant STAD-US 14 24026212 24026213 deletion of <=200bp CA - downstream_gene_variant STAD-US 14 24026387 24026387 single base substitution C G downstream_gene_variant STAD-US 14 24031515 24031515 single base substitution C T downstream_gene_variant STAD-US 14 24031515 24031515 single base substitution C T exon_variant STAD-US 14 24031515 24031515 single base substitution C T missense_variant R34H 101G>A STAD-US 14 24031515 24031515 single base substitution C T missense_variant R537H 1610G>A STAD-US 14 24031515 24031515 single base substitution C T upstream_gene_variant STAD-US 14 24032638 24032638 single base substitution G A 3_prime_UTR_variant STAD-US 14 24032638 24032638 single base substitution G A downstream_gene_variant STAD-US 14 24032638 24032638 single base substitution G A exon_variant STAD-US 14 24032638 24032638 single base substitution G A missense_variant A454V 1361C>T STAD-US 14 24032638 24032638 single base substitution G A upstream_gene_variant STAD-US 14 24032709 24032709 single base substitution C T downstream_gene_variant STAD-US 14 24032709 24032709 single base substitution C T exon_variant STAD-US 14 24032709 24032709 single base substitution C T splice_region_variant STAD-US 14 24032709 24032709 single base substitution C T upstream_gene_variant STAD-US 14 24033302 24033302 single base substitution C T downstream_gene_variant STAD-US 14 24033302 24033302 single base substitution C T exon_variant STAD-US 14 24033302 24033302 single base substitution C T synonymous_variant R348R 1044G>A STAD-US 14 24033302 24033302 single base substitution C T upstream_gene_variant STAD-US 14 24033782 24033782 single base substitution C T downstream_gene_variant STAD-US 14 24033782 24033782 single base substitution C T exon_variant STAD-US 14 24033782 24033782 single base substitution C T missense_variant A304T 910G>A STAD-US 14 24033782 24033782 single base substitution C T upstream_gene_variant STAD-US 14 24033828 24033828 single base substitution C A downstream_gene_variant STAD-US 14 24033828 24033828 single base substitution C A exon_variant STAD-US 14 24033828 24033828 single base substitution C A synonymous_variant A288A 864G>T STAD-US 14 24033828 24033828 single base substitution C A upstream_gene_variant STAD-US 14 24034396 24034396 single base substitution G A 3_prime_UTR_variant STAD-US 14 24034396 24034396 single base substitution G A downstream_gene_variant STAD-US 14 24034396 24034396 single base substitution G A exon_variant STAD-US 14 24034396 24034396 single base substitution G A missense_variant R252C 754C>T STAD-US 14 24034396 24034396 single base substitution G A upstream_gene_variant STAD-US 14 24036397 24036397 deletion of <=200bp C - exon_variant STAD-US 14 24036397 24036397 deletion of <=200bp C - frameshift_variant D43 STAD-US 14 24036397 24036397 deletion of <=200bp C - intron_variant STAD-US 14 24036397 24036397 deletion of <=200bp C - upstream_gene_variant STAD-US 14 24040144 24040144 single base substitution G A upstream_gene_variant STAD-US 14 24040254 24040254 single base substitution C T upstream_gene_variant STAD-US 14 24040511 24040511 single base substitution G A upstream_gene_variant STAD-US 14 24040545 24040545 single base substitution G T upstream_gene_variant STAD-US 14 24040633 24040633 single base substitution G A upstream_gene_variant STAD-US 14 24041061 24041061 single base substitution C T upstream_gene_variant UCEC-US 14 24026149 24026149 single base substitution A G downstream_gene_variant UCEC-US 14 24028255 24028255 single base substitution G A downstream_gene_variant UCEC-US 14 24029197 24029197 single base substitution G A downstream_gene_variant UCEC-US 14 24029197 24029197 single base substitution G A exon_variant UCEC-US 14 24029197 24029197 single base substitution G A missense_variant R736W 2206C>T UCEC-US 14 24029197 24029197 single base substitution G A synonymous_variant ?198 UCEC-US 14 24030804 24030804 single base substitution C T downstream_gene_variant UCEC-US 14 24030804 24030804 single base substitution C T exon_variant UCEC-US 14 24030804 24030804 single base substitution C T missense_variant G54S 160G>A UCEC-US 14 24030804 24030804 single base substitution C T missense_variant G592S 1774G>A UCEC-US 14 24030804 24030804 single base substitution C T upstream_gene_variant UCEC-US 14 24031573 24031573 single base substitution T C downstream_gene_variant UCEC-US 14 24031573 24031573 single base substitution T C exon_variant UCEC-US 14 24031573 24031573 single base substitution T C missense_variant M15V 43A>G UCEC-US 14 24031573 24031573 single base substitution T C missense_variant M518V 1552A>G UCEC-US 14 24031573 24031573 single base substitution T C upstream_gene_variant UCEC-US 14 24032946 24032946 single base substitution C T downstream_gene_variant UCEC-US 14 24032946 24032946 single base substitution C T exon_variant UCEC-US 14 24032946 24032946 single base substitution C T missense_variant G404D 1211G>A UCEC-US 14 24032946 24032946 single base substitution C T upstream_gene_variant UCEC-US 14 24033004 24033004 single base substitution C A downstream_gene_variant UCEC-US 14 24033004 24033004 single base substitution C A exon_variant UCEC-US 14 24033004 24033004 single base substitution C A stop_gained E385* 1153G>T UCEC-US 14 24033004 24033004 single base substitution C A upstream_gene_variant UCEC-US 14 24033799 24033799 single base substitution A G downstream_gene_variant UCEC-US 14 24033799 24033799 single base substitution A G exon_variant UCEC-US 14 24033799 24033799 single base substitution A G missense_variant M298T 893T>C UCEC-US 14 24033799 24033799 single base substitution A G upstream_gene_variant UCEC-US 14 24033844 24033844 single base substitution C T downstream_gene_variant UCEC-US 14 24033844 24033844 single base substitution C T exon_variant UCEC-US 14 24033844 24033844 single base substitution C T missense_variant R283Q 848G>A UCEC-US 14 24033844 24033844 single base substitution C T upstream_gene_variant UCEC-US 14 24035052 24035052 single base substitution G A 3_prime_UTR_variant UCEC-US 14 24035052 24035052 single base substitution G A downstream_gene_variant UCEC-US 14 24035052 24035052 single base substitution G A exon_variant UCEC-US 14 24035052 24035052 single base substitution G A intron_variant UCEC-US 14 24035052 24035052 single base substitution G A synonymous_variant S206S 618C>T UCEC-US 14 24035052 24035052 single base substitution G A upstream_gene_variant UCEC-US 14 24035116 24035116 single base substitution G A downstream_gene_variant UCEC-US 14 24035116 24035116 single base substitution G A exon_variant UCEC-US 14 24035116 24035116 single base substitution G A intron_variant UCEC-US 14 24035116 24035116 single base substitution G A upstream_gene_variant UCEC-US 14 24035308 24035311 deletion of <=200bp GGGA - 3_prime_UTR_variant UCEC-US 14 24035308 24035311 deletion of <=200bp GGGA - downstream_gene_variant UCEC-US 14 24035308 24035311 deletion of <=200bp GGGA - exon_variant UCEC-US 14 24035308 24035311 deletion of <=200bp GGGA - frameshift_variant LP177 UCEC-US 14 24035308 24035311 deletion of <=200bp GGGA - upstream_gene_variant UCEC-US 14 24035764 24035764 single base substitution C A downstream_gene_variant UCEC-US 14 24035764 24035764 single base substitution C A exon_variant UCEC-US 14 24035764 24035764 single base substitution C A intron_variant UCEC-US 14 24035764 24035764 single base substitution C A splice_region_variant UCEC-US 14 24035764 24035764 single base substitution C A upstream_gene_variant UCEC-US 14 24035773 24035773 single base substitution C A downstream_gene_variant UCEC-US 14 24035773 24035773 single base substitution C A exon_variant UCEC-US 14 24035773 24035773 single base substitution C A intron_variant UCEC-US 14 24035773 24035773 single base substitution C A missense_variant K109N 327G>T UCEC-US 14 24035773 24035773 single base substitution C A splice_region_variant UCEC-US 14 24035773 24035773 single base substitution C A upstream_gene_variant UCEC-US 14 24036171 24036171 single base substitution A G downstream_gene_variant UCEC-US 14 24036171 24036171 single base substitution A G exon_variant UCEC-US 14 24036171 24036171 single base substitution A G intron_variant UCEC-US 14 24036171 24036171 single base substitution A G upstream_gene_variant UCEC-US 14 24040169 24040169 single base substitution C T upstream_gene_variant UCEC-US 14 24040212 24040212 single base substitution G T upstream_gene_variant UCEC-US 14 24040238 24040238 single base substitution C T upstream_gene_variant UCEC-US 14 24040430 24040430 single base substitution C T upstream_gene_variant UCEC-US 14 24041119 24041119 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand LC_C21 COSM1188778 c.97G>T p.A33S Substitution - Missense 14:23567218-23567218 - TCGA-EE-A2MR-06 COSM3495274 c.441C>T p.L147L Substitution - coding silent 14:23566308-23566308 - TCGA-AB-3009-03 COSM158678 c.1037G>A p.R346Q Substitution - Missense 14:23564100-23564100 - SS6003121 COSM3980104 c.460G>A p.V154M Substitution - Missense 14:23566289-23566289 - 313 COSM1741976 c.40G>C p.E14Q Substitution - Missense 14:23567275-23567275 - pfg043T COSM4751300 c.1812A>C p.E604D Substitution - Missense 14:23561557-23561557 - HCC105T COSM1607537 c.1554G>A p.M518I Substitution - Missense 14:23562362-23562362 - LOVO COSM2032109 c.933C>T p.V311V Substitution - coding silent 14:23564377-23564377 - BD72T COSM5513028 c.590C>T p.T197M Substitution - Missense 14:23565871-23565871 - CHC1598T COSM4788905 c.2176C>T p.Q726* Substitution - Nonsense 14:23560018-23560018 - LIM1899 COSM4639956 c.304C>T p.L102L Substitution - coding silent 14:23566587-23566587 - 76 COSM5015209 c.1453G>A p.G485R Substitution - Missense 14:23562551-23562551 - TCGA-A8-A0A6-01 COSM3814570 c.409C>T p.R137* Substitution - Nonsense 14:23566340-23566340 - TCGA-D3-A2JD-06 COSM3495276 c.114C>T p.S38S Substitution - coding silent 14:23567201-23567201 - TCGA-CJ-4881-01 COSM69679 c.499C>T p.R167W Substitution - Missense 14:23566133-23566133 - TCGA-B5-A0JR-01 COSM954813 c.893T>C p.M298T Substitution - Missense 14:23564590-23564590 - TCGA-29-2432-01 COSM1323548 c.1892A>G p.D631G Substitution - Missense 14:23561397-23561397 - HCA7 COSM1369248 c.1345delG p.A449fs*84 Deletion - Frameshift 14:23563445-23563445 - SC_9026 COSM5568240 c.112T>A p.S38T Substitution - Missense 14:23567203-23567203 - TCGA-EW-A1PH-01 COSM1477486 c.1163C>A p.A388D Substitution - Missense 14:23563785-23563785 - TCGA-A2-A04Y-01 COSM432916 c.361G>A p.G121S Substitution - Missense 14:23566388-23566388 - TCGA-EE-A2A2-06 COSM3495270 c.993A>G p.T331T Substitution - coding silent 14:23564144-23564144 - TCGA-BR-4201-01 COSM4050094 c.1361C>T p.A454V Substitution - Missense 14:23563429-23563429 - TCGA-AO-A03M-01 COSM3814569 c.432G>C p.E144D Substitution - Missense 14:23566317-23566317 - TCGA-D3-A3MR-06 COSM3495266 c.1445G>A p.G482E Substitution - Missense 14:23562559-23562559 - OSCC-GB_01100111 COSM4888377 c.1084C>A p.L362I Substitution - Missense 14:23564053-23564053 - TCGA-GL-A59R-01 COSM3987588 c.1941A>G p.P647P Substitution - coding silent 14:23561348-23561348 - TCGA-61-1915-01 COSM1323546 c.121G>A p.D41N Substitution - Missense 14:23567194-23567194 - TCGA-AC-A3BB-01 COSM3814571 c.381G>C p.L127F Substitution - Missense 14:23566368-23566368 - TCGA-D1-A16X-01 COSM954818 c.327G>T p.K109N Substitution - Missense 14:23566564-23566564 - 2497767 COSM183334 c.1286C>T p.T429M Substitution - Missense 14:23563585-23563585 - CRC-19T COSM5481166 c.1139G>A p.R380Q Substitution - Missense 14:23563809-23563809 - CSCC-27-T COSM4464118 c.1319C>T p.A440V Substitution - Missense 14:23563471-23563471 - DLD1 COSM4611598 c.2263delC p.L755fs*3 Deletion - Frameshift 14:23559844-23559844 - TCGA-BR-8679-01 COSM4050102 c.864G>T p.A288A Substitution - coding silent 14:23564619-23564619 - TCGA-09-1674-01 COSM1323545 c.118C>T p.R40C Substitution - Missense 14:23567197-23567197 - 193 COSM3720816 c.808G>C p.D270H Substitution - Missense 14:23565133-23565133 - TCGA-A6-6780-01 COSM1369247 c.1345_1346insG p.A449fs*49 Insertion - Frameshift 14:23563444-23563445 - DLBCL832 COSM1580508 c.2018T>G p.F673C Substitution - Missense 14:23560394-23560394 - AOCS-166-1-2 COSM3983200 c.1837C>T p.P613S Substitution - Missense 14:23561532-23561532 - HX17T COSM1607536 c.1718_1719insG p.Y574fs*23 Insertion - Frameshift 14:23561976-23561977 - CSCC-40-T COSM4469280 c.1591C>T p.L531F Substitution - Missense 14:23562325-23562325 - PCSI_0017_Pa_P COSM216319 c.1788T>C p.D596D Substitution - coding silent 14:23561581-23561581 - TCGA-D1-A0ZU-01 COSM954815 c.530_533delTCCC p.L177fs*21 Deletion - Frameshift 14:23566099-23566102 - T2269 COSM4662219 c.1752A>C p.K584N Substitution - Missense 14:23561617-23561617 - TCGA-AC-A2FG-01 COSM3814567 c.1878G>A p.L626L Substitution - coding silent 14:23561411-23561411 - 262T COSM3968749 c.226G>A p.A76T Substitution - Missense 14:23566665-23566665 - SNU-C2B COSM2032104 c.1089C>T p.S363S Substitution - coding silent 14:23564048-23564048 - T3090 COSM266012 c.1753delA p.M585fs*43 Deletion - Frameshift 14:23561616-23561616 - S00829 COSM5659935 c.735C>T p.F245F Substitution - coding silent 14:23565612-23565612 - TCGA-AS-3778-01 COSM469835 c.848G>T p.R283L Substitution - Missense 14:23564635-23564635 - sysucc-1370T COSM2032120 c.560G>A p.R187H Substitution - Missense 14:23566072-23566072 - SNUH_G35_S1 COSM3999229 c.1162G>A p.A388T Substitution - Missense 14:23563786-23563786 - RKO COSM2032117 c.598A>G p.T200A Substitution - Missense 14:23565863-23565863 - TCGA-BR-4256-01 COSM4050100 c.910G>A p.A304T Substitution - Missense 14:23564573-23564573 - CHC892T COSM4960321 c.1726C>T p.H576Y Substitution - Missense 14:23561969-23561969 - LUAD-S01320 COSM346169 c.891C>T p.I297I Substitution - coding silent 14:23564592-23564592 - HCC99 COSM147749 c.2279G>A p.R760H Substitution - Missense 14:23559828-23559828 - RK285_C01 COSM4778962 c.1429G>C p.A477P Substitution - Missense 14:23562575-23562575 - TCGA-D1-A17Q-01 COSM954814 c.618C>T p.S206S Substitution - coding silent 14:23565843-23565843 - 1517_CLM COSM5754562 c.2098G>A p.A700T Substitution - Missense 14:23560314-23560314 - TCGA-AX-A062-01 COSM954809 c.1552A>G p.M518V Substitution - Missense 14:23562364-23562364 - HCC93 COSM3706209 c.268G>A p.A90T Substitution - Missense 14:23566623-23566623 - T3724 COSM4662215 c.1845C>T p.P615P Substitution - coding silent 14:23561524-23561524 - PD11380a COSM5773118 c.1519C>G p.L507V Substitution - Missense 14:23562397-23562397 - TCGA-29-1703-01 COSM1323547 c.1402A>T p.I468F Substitution - Missense 14:23563388-23563388 - TCGA-AA-3966-01 COSM272342 c.272T>C p.M91T Substitution - Missense 14:23566619-23566619 - TCGA-AO-A0JB-01 COSM432914 c.569-6C>A p.? Unknown 14:23565898-23565898 - OSCC-GB_00860111 COSM4885406 c.2020G>C p.E674Q Substitution - Missense 14:23560392-23560392 - 18195 COSM1300523 c.2307G>A p.S769S Substitution - coding silent 14:23559800-23559800 - T3262 COSM183333 c.1782G>T p.Q594H Substitution - Missense 14:23561587-23561587 - TCGA-E5-A2PC-01 COSM1300523 c.2307G>A p.S769S Substitution - coding silent 14:23559800-23559800 - SJHGG066_A COSM4971247 c.1734-4T>A p.? Unknown 14:23561639-23561639 - TCGA-A6-6781-01 COSM1369246 c.1753_1754insA p.M585fs*12 Insertion - Frameshift 14:23561615-23561616 - LP6005500-DNA_F02 COSM5037031 c.1734-3C>G p.? Unknown 14:23561638-23561638 - CSCC-27-T COSM4504933 c.679C>T p.L227L Substitution - coding silent 14:23565668-23565668 - S02219 COSM5675599 c.295G>C p.D99H Substitution - Missense 14:23566596-23566596 - TCGA-EI-6507-01 COSM147749 c.2279G>A p.R760H Substitution - Missense 14:23559828-23559828 - TCGA-AA-3672-01 COSM266012 c.1753delA p.M585fs*43 Deletion - Frameshift 14:23561616-23561616 - TCGA-HT-7467-01 COSM3968749 c.226G>A p.A76T Substitution - Missense 14:23566665-23566665 - TCGA-GN-A269-01 COSM3495264 c.1929G>A p.L643L Substitution - coding silent 14:23561360-23561360 - SC_9003 COSM5566777 c.2266C>T p.R756W Substitution - Missense 14:23559841-23559841 - pfg025T COSM1640053 c.294C>T p.H98H Substitution - coding silent 14:23566597-23566597 - TCGA-HU-A4GU-01 COSM4050092 c.1610G>A p.R537H Substitution - Missense 14:23562306-23562306 - TCGA-B5-A11E-01 COSM954817 c.329+7G>T p.? Unknown 14:23566555-23566555 - TCGA-G3-A25V-01 COSM4914532 c.1222G>C p.A408P Substitution - Missense 14:23563726-23563726 - TCGA-AS-3777-01 COSM1493253 c.902G>A p.R301H Substitution - Missense 14:23564581-23564581 - RK062_C01 COSM1629257 c.978-2A>G p.? Unknown 14:23564161-23564161 - TCGA-CM-5861-01 COSM1369245 c.2069delA p.N690fs*6 Deletion - Frameshift 14:23560343-23560343 - CSCC-49-T COSM4498709 c.525C>T p.V175V Substitution - coding silent 14:23566107-23566107 - GC8_T COSM147749 c.2279G>A p.R760H Substitution - Missense 14:23559828-23559828 - TCGA-J9-A52C-01 COSM4877587 c.1684C>T p.Q562* Substitution - Nonsense 14:23562011-23562011 - SNUH_G08_S1 COSM147749 c.2279G>A p.R760H Substitution - Missense 14:23559828-23559828 - S00936 COSM309181 c.1138C>T p.R380* Substitution - Nonsense 14:23563810-23563810 - CHC892T COSM4797021 c.364C>T p.L122L Substitution - coding silent 14:23566385-23566385 - HCC96T COSM3706206 c.1876C>A p.L626M Substitution - Missense 14:23561413-23561413 - PD18283a COSM3770466 c.2226C>G p.T742T Substitution - coding silent 14:23559968-23559968 - CHC892T COSM4960321 c.1726C>T p.H576Y Substitution - Missense 14:23561969-23561969 - LN18 COSM2032103 c.1142C>A p.A381D Substitution - Missense 14:23563806-23563806 - SNU-175 COSM2032124 c.418G>T p.A140S Substitution - Missense 14:23566331-23566331 - I2L-P19Ta-Tumor-Biopsy COSM5362461 c.2135T>C p.I712T Substitution - Missense 14:23560277-23560277 - HCC074T COSM5810119 c.956T>A p.L319H Substitution - Missense 14:23564354-23564354 - SNUH_G35_S1 COSM147749 c.2279G>A p.R760H Substitution - Missense 14:23559828-23559828 - 0066_CRUK_PC_0066_T1_DNA COSM5421268 c.1591C>G p.L531V Substitution - Missense 14:23562325-23562325 - 1517_PT COSM5754562 c.2098G>A p.A700T Substitution - Missense 14:23560314-23560314 - TCGA-AB-2878-03 COSM1317875 c.1339G>T p.G447W Substitution - Missense 14:23563451-23563451 - TCGA-BR-8680-01 COSM4050098 c.1044G>A p.R348R Substitution - coding silent 14:23564093-23564093 - DLBCL922 COSM1580507 c.2317A>T p.I773F Substitution - Missense 14:23559790-23559790 - 3N07-VS-3T07 COSM4978897 c.99C>T p.A33A Substitution - coding silent 14:23567216-23567216 - PCSI_0017_Pa_X COSM216319 c.1788T>C p.D596D Substitution - coding silent 14:23561581-23561581 - TCGA-AP-A05N-01 COSM954811 c.1153G>T p.E385* Substitution - Nonsense 14:23563795-23563795 - CHC322T COSM3765750 c.1092-5G>A p.? Unknown 14:23563861-23563861 - CPCG0260-F1 COSM4880294 c.144C>G p.H48Q Substitution - Missense 14:23567171-23567171 - TCGA-G4-6299-01 COSM1369250 c.53C>A p.A18D Substitution - Missense 14:23567262-23567262 - ESCC_143 COSM4464118 c.1319C>T p.A440V Substitution - Missense 14:23563471-23563471 - TCGA-25-2396-01 COSM69679 c.499C>T p.R167W Substitution - Missense 14:23566133-23566133 - DLD1 COSM4622923 c.1927C>A p.L643M Substitution - Missense 14:23561362-23561362 - TCGA-AX-A05Z-01 COSM698138 c.1774G>A p.G592S Substitution - Missense 14:23561595-23561595 - RKO COSM1369248 c.1345delG p.A449fs*84 Deletion - Frameshift 14:23563445-23563445 - TCGA-AP-A059-01 COSM954810 c.1211G>A p.G404D Substitution - Missense 14:23563737-23563737 - TCGA-EE-A29B-06 COSM3495268 c.1080C>T p.A360A Substitution - coding silent 14:23564057-23564057 - 587226 COSM1183105 c.1565C>T p.A522V Substitution - Missense 14:23562351-23562351 - H_KA-869586G-S_16427 COSM158678 c.1037G>A p.R346Q Substitution - Missense 14:23564100-23564100 - TCGA-A8-A08X-01 COSM1369247 c.1345_1346insG p.A449fs*49 Insertion - Frameshift 14:23563444-23563445 - 587388 COSM1183108 c.127G>A p.D43N Substitution - Missense 14:23567188-23567188 - 05-P8068 COSM4577780 c.783C>T p.H261H Substitution - coding silent 14:23565158-23565158 - TCGA-B0-5692-01 COSM469834 c.1019A>G p.D340G Substitution - Missense 14:23564118-23564118 - PD5944a COSM5796511 c.120C>G p.R40R Substitution - coding silent 14:23567195-23567195 - TCGA-DK-A1AC-01 COSM1300525 c.37G>A p.E13K Substitution - Missense 14:23567278-23567278 - TCGA-66-2785-01 COSM698138 c.1774G>A p.G592S Substitution - Missense 14:23561595-23561595 - CSCC-49-T COSM4561013 c.865G>A p.V289I Substitution - Missense 14:23564618-23564618 - 587284 COSM1183106 c.856G>A p.G286R Substitution - Missense 14:23564627-23564627 - LP6007504-DNA_A01 COSM5037318 c.365T>C p.L122P Substitution - Missense 14:23566384-23566384 - BD98T COSM5520729 c.1510G>C p.E504Q Substitution - Missense 14:23562406-23562406 - TCGA-AP-A05N-01 COSM954816 c.352C>T p.P118S Substitution - Missense 14:23566397-23566397 - HCC96 COSM3706206 c.1876C>A p.L626M Substitution - Missense 14:23561413-23561413 - 869586 COSM158678 c.1037G>A p.R346Q Substitution - Missense 14:23564100-23564100 - I2L-P19Ta-Tumor-Organoid COSM5362461 c.2135T>C p.I712T Substitution - Missense 14:23560277-23560277 - 1115161 COSM5573501 c.978-6G>A p.? Unknown 14:23564165-23564165 - TCGA-F1-6177-01 COSM4050096 c.1290G>A p.A430A Substitution - coding silent 14:23563500-23563500 - 587222 COSM954818 c.327G>T p.K109N Substitution - Missense 14:23566564-23566564 - TCGA-BR-8680-01 COSM4050104 c.754C>T p.R252C Substitution - Missense 14:23565187-23565187 - AOCS-124-1-X COSM3983198 c.2278C>T p.R760C Substitution - Missense 14:23559829-23559829 - TCGA-AM-5820-01 COSM5828086 c.1776_1777insTGGC p.P593fs*5 Insertion - Frameshift 14:23561592-23561593 - TCGA-BG-A0M4-01 COSM954812 c.946C>T p.R316C Substitution - Missense 14:23564364-23564364 - HCC99T COSM147749 c.2279G>A p.R760H Substitution - Missense 14:23559828-23559828 - H650 COSM1194359 c.2026G>A p.E676K Substitution - Missense 14:23560386-23560386 - EGC15 COSM5053878 c.1687C>T p.R563W Substitution - Missense 14:23562008-23562008 - HCC2998 COSM2032128 c.327G>A p.K109K Substitution - coding silent 14:23566564-23566564 - TCGA-D3-A1Q6-06 COSM3495272 c.698C>T p.S233F Substitution - Missense 14:23565649-23565649 - SNU-C4 COSM4652469 c.1249C>T p.R417C Substitution - Missense 14:23563622-23563622 - HCC93T COSM3706209 c.268G>A p.A90T Substitution - Missense 14:23566623-23566623 - CHC892T COSM4797021 c.364C>T p.L122L Substitution - coding silent 14:23566385-23566385 - sysucc-311T COSM5478660 c.1637G>A p.R546H Substitution - Missense 14:23562058-23562058 - WSU-HN12 COSM4601091 c.1984C>A p.P662T Substitution - Missense 14:23561305-23561305 - TCGA-B6-A0IN-01 COSM432915 c.495G>A p.M165I Substitution - Missense 14:23566137-23566137 - HCC105 COSM1607537 c.1554G>A p.M518I Substitution - Missense 14:23562362-23562362 - Ly19 COSM1580509 c.374G>A p.C125Y Substitution - Missense 14:23566375-23566375 - TCGA-BS-A0UF-01 COSM170137 c.848G>A p.R283Q Substitution - Missense 14:23564635-23564635 - TCGA-A4-8098-01 COSM3987590 c.1233-1G>A p.? Unknown 14:23563639-23563639 - CHC1598T COSM4788905 c.2176C>T p.Q726* Substitution - Nonsense 14:23560018-23560018 - TCGA-AA-A00A-01 COSM298220 c.431A>G p.E144G Substitution - Missense 14:23566318-23566318 - TCGA-EB-A4OZ-01 COSM3495275 c.287A>G p.E96G Substitution - Missense 14:23566604-23566604 - TCGA-E9-A1R6-01 COSM1477485 c.2348C>T p.S783L Substitution - Missense 14:23559759-23559759 - TCGA-G2-A2ES-01 COSM1300524 c.667A>G p.I223V Substitution - Missense 14:23565680-23565680 - 587388 COSM1183107 c.233C>T p.S78F Substitution - Missense 14:23566658-23566658 - TCGA-B5-A0JY-01 COSM954808 c.2206C>T p.R736W Substitution - Missense 14:23559988-23559988 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.342412;Hs.342943;Hs.343198;Hs.343244 14q11.2 603534

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.M298T c.893T>C 14 24033799 UCEC A G Synonymous p.D596D c.1788T>C 14 24030790 PAAD A T IntronicSNV . c.1733+90T>A 14 24031081 HC C A Missense p.M135I c.405G>T 14 24035553 LUAD C A Nonsense p.E385* c.1153G>T 14 24033004 UCEC C T Missense p.A304T c.910G>A 14 24033782 STAD C T Missense p.A76T c.226G>A 14 24035874 LGG C T Missense p.D243N c.727G>A 14 24034829 HNSC C T Missense p.G121S c.361G>A 14 24035597 BRCA C T Missense p.G482E c.1445G>A 14 24031768 CM C T Missense p.M165I c.495G>A 14 24035346 BRCA C T Missense p.R346Q c.1037G>A 14 24033309 AML C T Missense p.R459H c.1376G>A 14 24032623 LUAD C T Missense p.R590Q c.1769G>A 14 24030809 BRCA C T SpliceAcceptorSNV . c.472-1G>A 14 24035370 CM C T Synonymous p.A430A c.1290G>A 14 24032709 STAD C T Synonymous p.L643L c.1929G>A 14 24030569 CM C T Synonymous p.R398R c.1194G>A 14 24032963 CM G A IntronicSNV . c.1092-7C>T 14 24033072 CM G A IntronicSNV . c.1993+179C>T 14 24030326 CM G A IntronicSNV . c.569-15C>T 14 24035116 UCEC G A IntronicSNV . c.978-55C>T 14 24033423 HC G A Missense p.A454V c.1361C>T 14 24032638 STAD G A Missense p.R167W c.499C>T 14 24035342 OV G A Missense p.R167W c.499C>T 14 24035342 RCCC G A Missense p.R301C c.901C>T 14 24033791 BRCA G A Missense p.S233F c.698C>T 14 24034858 CM G A Missense p.S783L c.2348C>T 14 24028968 BRCA G A Missense p.T429M c.1286C>T 14 24032794 COREAD G A Nonsense p.Q594* c.1780C>T 14 24030798 HNSC G A Nonsense p.R380* c.1138C>T 14 24033019 SCLC G A Nonsense p.R380* c.1138C>T 14 24033019 STAD G A Synonymous p.A360A c.1080C>T 14 24033266 CM G A Synonymous p.H98H c.294C>T 14 24035806 STAD G A Synonymous p.S377S c.1131C>T 14 24033026 CM G A Synonymous p.S38S c.114C>T 14 24036410 CM G C Missense p.L626V c.1876C>G 14 24030622 LUAD GG AA IntronicBlockSubstitution . c.1628+49_1628+50delinsTT 14 24031447 CM GGGA - Frameshift p.L177Hfs*21 c.530_533delTCCC 14 24035308 UCEC G T IntronicSNV . c.1410+164C>A 14 24032425 MB G T IntronicSNV . c.569-6C>A 14 24035107 BRCA G T Missense p.A388D c.1163C>A 14 24032994 BRCA T C Missense p.D340G c.1019A>G 14 24033327 RCCC T C Missense p.E144G c.431A>G 14 24035527 COREAD T C Missense p.I223V c.667A>G 14 24034889 BLCA T C Missense p.M518V c.1552A>G 14 24031573 UCEC T C Synonymous p.T331T c.993A>G 14 24033353 CM