Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 19 872058 872058 + Silent SNP G G T TCGA-G2-A2ES-01A-11D-A17V-08 TCGA-G2-A2ES-11A-31D-A17V-08 g.chr19:872058G>T c.1966C>A c.(1966-1968)Cgg>Agg p.R656R BLCA 19 872088 872088 + Silent SNP G G A TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr19:872088G>A c.1936C>T c.(1936-1938)Ctg>Ttg p.L646L BLCA 19 875330 875330 + Missense_Mutation SNP G G A TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr19:875330G>A c.1685C>T c.(1684-1686)tCg>tTg p.S562L BLCA 19 876999 876999 + Missense_Mutation SNP G G T TCGA-FD-A3SN-01A-12D-A22Z-08 TCGA-FD-A3SN-10A-01D-A22Z-08 g.chr19:876999G>T c.1535C>A c.(1534-1536)aCg>aAg p.T512K BLCA 19 877138 877138 + Missense_Mutation SNP C C T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr19:877138C>T c.1396G>A c.(1396-1398)Gag>Aag p.E466K BLCA 19 881651 881651 + Missense_Mutation SNP C C T TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr19:881651C>T c.1049G>A c.(1048-1050)cGt>cAt p.R350H BLCA 19 884913 884913 + Silent SNP G G A TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr19:884913G>A c.975C>T c.(973-975)atC>atT p.I325I BLCA 19 886012 886012 + Missense_Mutation SNP C C T TCGA-GC-A3RB-01A-12D-A21Z-08 TCGA-GC-A3RB-10A-01D-A21Z-08 g.chr19:886012C>T c.637G>A c.(637-639)Gtg>Atg p.V213M BLCA 19 886120 886120 + Nonsense_Mutation SNP C C A TCGA-K4-A5RI-01A-11D-A289-08 TCGA-K4-A5RI-10A-01D-A289-08 g.chr19:886120C>A c.529G>T c.(529-531)Gag>Tag p.E177* BRCA 19 875294 875295 + Frame_Shift_Del DEL TT TT - TCGA-E9-A1R2-01A-11D-A14G-09 TCGA-E9-A1R2-10A-01D-A14G-09 g.chr19:875294_875295delTT c.1720_1721delAA c.(1720-1722)aagfs p.K574fs BRCA 19 875298 875298 + Missense_Mutation SNP C C A TCGA-AC-A5EH-01A-11D-A28B-09 TCGA-AC-A5EH-10A-01D-A28E-09 g.chr19:875298C>A c.1717G>T c.(1717-1719)Gac>Tac p.D573Y BRCA 19 881682 881682 + Missense_Mutation SNP G G A TCGA-PE-A5DE-01A-11D-A27P-09 TCGA-PE-A5DE-10A-01D-A27P-09 g.chr19:881682G>A c.1018C>T c.(1018-1020)Cgg>Tgg p.R340W BRCA 19 884973 884973 + Missense_Mutation SNP G G C TCGA-AO-A0J6-01A-11W-A050-09 TCGA-AO-A0J6-10A-01W-A055-09 g.chr19:884973G>C c.915C>G c.(913-915)atC>atG p.I305M BRCA 19 891096 891096 + Missense_Mutation SNP C C T TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr19:891096C>T c.36G>A c.(34-36)atG>atA p.M12I CESC 19 872088 872088 + Silent SNP G G A TCGA-EK-A2PG-01A-11D-A18J-09 TCGA-EK-A2PG-10A-01D-A18J-09 g.chr19:872088G>A c.1936C>T c.(1936-1938)Ctg>Ttg p.L646L CESC 19 879963 879963 + Silent SNP G G A TCGA-DG-A2KL-01A-11D-A17W-09 TCGA-DG-A2KL-10A-01D-A17W-09 g.chr19:879963G>A c.1327C>T c.(1327-1329)Ctg>Ttg p.L443L CESC 19 881596 881596 + Silent SNP G G C TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr19:881596G>C c.1104C>G c.(1102-1104)ctC>ctG p.L368L CHOL 19 875282 875282 + Missense_Mutation SNP T T C TCGA-3X-AAVE-01A-11D-A417-09 TCGA-3X-AAVE-10A-01D-A41A-09 g.chr19:875282T>C c.1733A>G c.(1732-1734)gAc>gGc p.D578G COAD 19 879943 879943 + Missense_Mutation SNP G G C TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q COAD 19 884936 884936 + Frame_Shift_Del DEL C C - TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr19:884936delC c.952delG c.(952-954)gtgfs p.V318fs COAD 19 885862 885862 + Missense_Mutation SNP G G T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr19:885862G>T c.787C>A c.(787-789)Ctg>Atg p.L263M COAD 19 885913 885913 + Missense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr19:885913C>T c.736G>A c.(736-738)Gtg>Atg p.V246M COAD 19 885944 885944 + Missense_Mutation SNP G G C TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr19:885944G>C c.705C>G c.(703-705)agC>agG p.S235R COAD 19 890170 890170 + Missense_Mutation SNP C C T TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr19:890170C>T c.244G>A c.(244-246)Gag>Aag p.E82K COAD 19 890996 890996 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr19:890996C>T c.136G>A c.(136-138)Gcc>Acc p.A46T COADREAD 19 879943 879943 + Missense_Mutation SNP G G C TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q COADREAD 19 884936 884936 + Frame_Shift_Del DEL C C - TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr19:884936delC c.952delG c.(952-954)gtgfs p.V318fs COADREAD 19 885862 885862 + Missense_Mutation SNP G G T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr19:885862G>T c.787C>A c.(787-789)Ctg>Atg p.L263M COADREAD 19 885913 885913 + Missense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr19:885913C>T c.736G>A c.(736-738)Gtg>Atg p.V246M COADREAD 19 885944 885944 + Missense_Mutation SNP G G C TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr19:885944G>C c.705C>G c.(703-705)agC>agG p.S235R COADREAD 19 890170 890170 + Missense_Mutation SNP C C T TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr19:890170C>T c.244G>A c.(244-246)Gag>Aag p.E82K COADREAD 19 890996 890996 + Missense_Mutation SNP C C T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr19:890996C>T c.136G>A c.(136-138)Gcc>Acc p.A46T DLBC 19 879943 879943 + Missense_Mutation SNP G G C TCGA-FF-8042-01A-11D-2210-10 TCGA-FF-8042-10A-01D-2210-10 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q DLBC 19 880103 880103 + Missense_Mutation SNP C C T TCGA-FF-A7CX-01A-12D-A382-10 TCGA-FF-A7CX-10A-01D-A385-10 g.chr19:880103C>T c.1187G>A c.(1186-1188)cGg>cAg p.R396Q ESCA 19 875405 875405 + Missense_Mutation SNP G G A TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr19:875405G>A c.1610C>T c.(1609-1611)tCg>tTg p.S537L ESCA 19 885801 885801 + Missense_Mutation SNP A A G TCGA-2H-A9GO-01A-11D-A37C-09 TCGA-2H-A9GO-11A-11D-A37F-09 g.chr19:885801A>G c.848T>C c.(847-849)cTc>cCc p.L283P GBM 19 868170 868170 + Silent SNP C C T TCGA-32-5222-01A-01D-1486-08 TCGA-32-5222-10A-01D-1486-08 g.chr19:868170C>T c.2565G>A c.(2563-2565)ccG>ccA p.P855P GBMLGG 19 868170 868170 + Silent SNP C C T TCGA-32-5222-01A-01D-1486-08 TCGA-32-5222-10A-01D-1486-08 g.chr19:868170C>T c.2565G>A c.(2563-2565)ccG>ccA p.P855P GBMLGG 19 877046 877046 + Missense_Mutation SNP C C A TCGA-S9-A6TV-01A-12D-A34J-08 TCGA-S9-A6TV-10B-01D-A34M-08 g.chr19:877046C>A c.1488G>T c.(1486-1488)caG>caT p.Q496H GBMLGG 19 885908 885908 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:885908G>A c.741C>T c.(739-741)agC>agT p.S247S GBMLGG 19 885978 885978 + Missense_Mutation SNP C C G TCGA-FG-A713-01A-11D-A32B-08 TCGA-FG-A713-10A-01D-A329-08 g.chr19:885978C>G c.671G>C c.(670-672)gGc>gCc p.G224A GBMLGG 19 891130 891131 + Start_Codon_Del DEL AT AT - TCGA-S9-A6WP-01A-12D-A34A-08 TCGA-S9-A6WP-10A-01D-A34A-08 g.chr19:891130_891131delAT HNSC 19 868422 868422 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr19:868422T>C c.2477A>G c.(2476-2478)aAc>aGc p.N826S HNSC 19 873494 873494 + Missense_Mutation SNP C C G TCGA-CV-7236-01A-11D-2012-08 TCGA-CV-7236-10A-01D-2013-08 g.chr19:873494C>G c.1860G>C c.(1858-1860)tgG>tgC p.W620C HNSC 19 873569 873569 + Silent SNP G G C TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr19:873569G>C c.1785C>G c.(1783-1785)gtC>gtG p.V595V HNSC 19 877178 877178 + Silent SNP C C T TCGA-T3-A92M-01A-31D-A391-08 TCGA-T3-A92M-10A-01D-A394-08 g.chr19:877178C>T c.1356G>A c.(1354-1356)ctG>ctA p.L452L HNSC 19 879973 879973 + Silent SNP C C T TCGA-UF-A7JO-01A-11D-A34J-08 TCGA-UF-A7JO-10A-01D-A34M-08 g.chr19:879973C>T c.1317G>A c.(1315-1317)acG>acA p.T439T HNSC 19 880111 880111 + Silent SNP G G A TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr19:880111G>A c.1179C>T c.(1177-1179)atC>atT p.I393I HNSC 19 881615 881615 + Missense_Mutation SNP G G A TCGA-CQ-5333-01A-01D-2394-08 TCGA-CQ-5333-10A-01D-2394-08 g.chr19:881615G>A c.1085C>T c.(1084-1086)tCg>tTg p.S362L HNSC 19 881689 881689 + Silent SNP G G C TCGA-F7-A61S-01A-11D-A28R-08 TCGA-F7-A61S-10A-01D-A28U-08 g.chr19:881689G>C c.1011C>G c.(1009-1011)ctC>ctG p.L337L HNSC 19 885883 885883 + Missense_Mutation SNP C C T TCGA-BA-6868-01B-12D-1912-08 TCGA-BA-6868-10A-01D-1912-08 g.chr19:885883C>T c.766G>A c.(766-768)Gac>Aac p.D256N HNSC 19 889662 889662 + Silent SNP C C T TCGA-CV-A45U-01A-12D-A24D-08 TCGA-CV-A45U-10A-01D-A24F-08 g.chr19:889662C>T c.423G>A c.(421-423)gtG>gtA p.V141V KICH 19 871135 871135 + Silent SNP A A G TCGA-KN-8419-01A-11D-2310-10 TCGA-KN-8419-11A-01D-2310-10 g.chr19:871135A>G c.2217T>C c.(2215-2217)gtT>gtC p.V739V KIPAN 19 871135 871135 + Silent SNP A A G TCGA-KN-8419-01A-11D-2310-10 TCGA-KN-8419-11A-01D-2310-10 g.chr19:871135A>G c.2217T>C c.(2215-2217)gtT>gtC p.V739V KIPAN 19 879943 879943 + Missense_Mutation SNP G G C TCGA-BQ-5890-01A-11D-1589-08 TCGA-BQ-5890-11A-01D-1589-08 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q KIPAN 19 879943 879943 + Missense_Mutation SNP G G C TCGA-G7-6789-01A-11D-1961-08 TCGA-G7-6789-10A-01D-1962-08 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q KIPAN 19 879943 879943 + Missense_Mutation SNP G G C TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q KIPAN 19 884992 884992 + Missense_Mutation SNP G G A TCGA-CZ-5986-01A-11D-1669-08 TCGA-CZ-5986-11A-01D-1669-08 g.chr19:884992G>A c.896C>T c.(895-897)tCc>tTc p.S299F KIRC 19 884992 884992 + Missense_Mutation SNP G G A TCGA-CZ-5986-01A-11D-1669-08 TCGA-CZ-5986-11A-01D-1669-08 g.chr19:884992G>A c.896C>T c.(895-897)tCc>tTc p.S299F KIRP 19 879943 879943 + Missense_Mutation SNP G G C TCGA-BQ-5890-01A-11D-1589-08 TCGA-BQ-5890-11A-01D-1589-08 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q KIRP 19 879943 879943 + Missense_Mutation SNP G G C TCGA-G7-6789-01A-11D-1961-08 TCGA-G7-6789-10A-01D-1962-08 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q KIRP 19 879943 879943 + Missense_Mutation SNP G G C TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr19:879943G>C c.1347C>G c.(1345-1347)caC>caG p.H449Q LGG 19 877046 877046 + Missense_Mutation SNP C C A TCGA-S9-A6TV-01A-12D-A34J-08 TCGA-S9-A6TV-10B-01D-A34M-08 g.chr19:877046C>A c.1488G>T c.(1486-1488)caG>caT p.Q496H LGG 19 885908 885908 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:885908G>A c.741C>T c.(739-741)agC>agT p.S247S LGG 19 885978 885978 + Missense_Mutation SNP C C G TCGA-FG-A713-01A-11D-A32B-08 TCGA-FG-A713-10A-01D-A329-08 g.chr19:885978C>G c.671G>C c.(670-672)gGc>gCc p.G224A LGG 19 891130 891131 + Start_Codon_Del DEL AT AT - TCGA-S9-A6WP-01A-12D-A34A-08 TCGA-S9-A6WP-10A-01D-A34A-08 g.chr19:891130_891131delAT LIHC 19 868154 868154 + Missense_Mutation SNP A A G TCGA-G3-A3CG-01A-11D-A20W-10 TCGA-G3-A3CG-10A-01D-A20W-10 g.chr19:868154A>G c.2581T>C c.(2581-2583)Tct>Cct p.S861P LIHC 19 868161 868161 + Silent SNP T T A TCGA-DD-AACK-01A-11D-A40R-10 TCGA-DD-AACK-10A-01D-A40U-10 g.chr19:868161T>A c.2574A>T c.(2572-2574)acA>acT p.T858T LIHC 19 873468 873468 + Missense_Mutation SNP A A G TCGA-DD-A39X-01A-11D-A20W-10 TCGA-DD-A39X-11A-11D-A20W-10 g.chr19:873468A>G c.1886T>C c.(1885-1887)cTg>cCg p.L629P LIHC 19 890977 890977 + Missense_Mutation SNP C C T TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr19:890977C>T c.155G>A c.(154-156)cGc>cAc p.R52H LUAD 19 871946 871946 + Missense_Mutation SNP A A G TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr19:871946A>G c.2078T>C c.(2077-2079)cTc>cCc p.L693P LUAD 19 872020 872020 + Silent SNP C C T TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr19:872020C>T c.2004G>A c.(2002-2004)ctG>ctA p.L668L LUAD 19 872078 872078 + Missense_Mutation SNP C C T TCGA-91-6831-01A-11D-1855-08 TCGA-91-6831-11A-02D-1855-08 g.chr19:872078C>T c.1946G>A c.(1945-1947)gGc>gAc p.G649D LUAD 19 873486 873486 + Missense_Mutation SNP T T A TCGA-49-6761-01A-31D-1945-08 TCGA-49-6761-11A-01D-1945-08 g.chr19:873486T>A c.1868A>T c.(1867-1869)gAc>gTc p.D623V LUAD 19 877041 877041 + Missense_Mutation SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr19:877041C>A c.1493G>T c.(1492-1494)aGt>aTt p.S498I LUAD 19 881567 881567 + Missense_Mutation SNP G G C TCGA-MP-A4TH-01A-31D-A25L-08 TCGA-MP-A4TH-10A-01D-A25L-08 g.chr19:881567G>C c.1133C>G c.(1132-1134)cCt>cGt p.P378R LUAD 19 881589 881589 + Missense_Mutation SNP C C A TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr19:881589C>A c.1111G>T c.(1111-1113)Gcc>Tcc p.A371S LUAD 19 881704 881704 + Silent SNP T T C TCGA-73-4670-01A-01D-1265-08 TCGA-73-4670-11A-01D-1265-08 g.chr19:881704T>C c.996A>G c.(994-996)aaA>aaG p.K332K LUAD 19 884906 884906 + Missense_Mutation SNP C C A TCGA-99-8028-01A-11D-2238-08 TCGA-99-8028-10A-01D-2238-08 g.chr19:884906C>A c.982G>T c.(982-984)Gtg>Ttg p.V328L LUAD 19 885978 885978 + Missense_Mutation SNP C C T TCGA-86-8674-01A-21D-2393-08 TCGA-86-8674-10A-01D-2393-08 g.chr19:885978C>T c.671G>A c.(670-672)gGc>gAc p.G224D LUAD 19 886117 886117 + Missense_Mutation SNP C C A TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chr19:886117C>A c.532G>T c.(532-534)Ggc>Tgc p.G178C LUAD 19 886165 886165 + Missense_Mutation SNP C C T TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr19:886165C>T c.484G>A c.(484-486)Gtc>Atc p.V162I LUAD 19 889717 889717 + Frame_Shift_Del DEL C C - TCGA-78-7537-01A-11D-2063-08 TCGA-78-7537-10A-01D-2063-08 g.chr19:889717delC c.368delG c.(367-369)ggcfs p.G123fs LUSC 19 872083 872083 + Silent SNP C C A TCGA-43-3394-01A-01D-0983-08 TCGA-43-3394-10A-01D-0983-08 g.chr19:872083C>A c.1941G>T c.(1939-1941)cgG>cgT p.R647R LUSC 19 875362 875362 + Silent SNP G G C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr19:875362G>C c.1653C>G c.(1651-1653)ctC>ctG p.L551L LUSC 19 875420 875420 + Missense_Mutation SNP G G A TCGA-34-5240-01A-01D-1441-08 TCGA-34-5240-10A-01D-1441-08 g.chr19:875420G>A c.1595C>T c.(1594-1596)tCg>tTg p.S532L OV 19 871095 871095 + Missense_Mutation SNP C C G TCGA-23-2649-01A-01D-1526-09 TCGA-23-2649-10A-01D-1526-09 g.chr19:871095C>G c.2257G>C c.(2257-2259)Ggc>Cgc p.G753R PAAD 19 868430 868430 + Nonsense_Mutation SNP C C T TCGA-US-A77E-01A-11D-A32N-08 TCGA-US-A77E-11A-11D-A32N-08 g.chr19:868430C>T c.2469G>A c.(2467-2469)tgG>tgA p.W823* PRAD 19 881676 881676 + Missense_Mutation SNP G G T TCGA-CH-5752-01A-11D-1576-08 TCGA-CH-5752-10A-01D-1576-08 g.chr19:881676G>T c.1024C>A c.(1024-1026)Cta>Ata p.L342I SARC 19 871225 871225 + Silent SNP C C T TCGA-MB-A8JL-01A-11D-A36J-09 TCGA-MB-A8JL-10A-01D-A36M-09 g.chr19:871225C>T c.2127G>A c.(2125-2127)ccG>ccA p.P709P SKCM 19 868150 868150 + Missense_Mutation SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr19:868150G>A c.2585C>T c.(2584-2586)cCc>cTc p.P862L SKCM 19 868150 868150 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:868150G>A c.2585C>T c.(2584-2586)cCc>cTc p.P862L SKCM 19 868157 868157 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr19:868157G>A c.2578C>T c.(2578-2580)Cac>Tac p.H860Y SKCM 19 868158 868158 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr19:868158G>A c.2577C>T c.(2575-2577)caC>caT p.H859H SKCM 19 873482 873482 + Silent SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr19:873482G>A c.1872C>T c.(1870-1872)ttC>ttT p.F624F SKCM 19 873506 873506 + Silent SNP C C T TCGA-EE-A2MG-06A-11D-A197-08 TCGA-EE-A2MG-10A-01D-A199-08 g.chr19:873506C>T c.1848G>A c.(1846-1848)caG>caA p.Q616Q SKCM 19 875301 875301 + Missense_Mutation SNP G G A TCGA-EE-A180-06A-11D-A21A-08 TCGA-EE-A180-10B-01D-A21A-08 g.chr19:875301G>A c.1714C>T c.(1714-1716)Cct>Tct p.P572S SKCM 19 875447 875447 + Missense_Mutation SNP G G A TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr19:875447G>A c.1568C>T c.(1567-1569)tCc>tTc p.S523F SKCM 19 880010 880010 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr19:880010G>A c.1280C>T c.(1279-1281)cCc>cTc p.P427L SKCM 19 880116 880116 + Missense_Mutation SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr19:880116G>A c.1174C>T c.(1174-1176)Cac>Tac p.H392Y SKCM 19 880117 880117 + Silent SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr19:880117G>A c.1173C>T c.(1171-1173)gtC>gtT p.V391V SKCM 19 885838 885838 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr19:885838G>A c.811C>T c.(811-813)Ctc>Ttc p.L271F

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 19 891068 891068 single base substitution C T exon_variant BLCA-CN 19 891068 891068 single base substitution C T intron_variant BLCA-CN 19 891068 891068 single base substitution C T missense_variant E22K 64G>A BLCA-US 19 872058 872058 single base substitution G T 3_prime_UTR_variant BLCA-US 19 872058 872058 single base substitution G T downstream_gene_variant BLCA-US 19 872058 872058 single base substitution G T intron_variant BLCA-US 19 872058 872058 single base substitution G T synonymous_variant R656R 1966C>A BLCA-US 19 875330 875330 single base substitution G A exon_variant BLCA-US 19 875330 875330 single base substitution G A missense_variant S315L 944C>T BLCA-US 19 875330 875330 single base substitution G A missense_variant S418L 1253C>T BLCA-US 19 875330 875330 single base substitution G A missense_variant S493L 1478C>T BLCA-US 19 875330 875330 single base substitution G A missense_variant S562L 1685C>T BLCA-US 19 876999 876999 single base substitution G T exon_variant BLCA-US 19 876999 876999 single base substitution G T intron_variant BLCA-US 19 876999 876999 single base substitution G T missense_variant T265K 794C>A BLCA-US 19 876999 876999 single base substitution G T missense_variant T368K 1103C>A BLCA-US 19 876999 876999 single base substitution G T missense_variant T512K 1535C>A BLCA-US 19 886012 886012 single base substitution C T 3_prime_UTR_variant BLCA-US 19 886012 886012 single base substitution C T downstream_gene_variant BLCA-US 19 886012 886012 single base substitution C T exon_variant BLCA-US 19 886012 886012 single base substitution C T intron_variant BLCA-US 19 886012 886012 single base substitution C T missense_variant V213M 637G>A BLCA-US 19 886012 886012 single base substitution C T upstream_gene_variant BOCA-FR 19 876894 876894 single base substitution G A intron_variant BOCA-FR 19 877845 877845 single base substitution C A intron_variant BRCA-EU 19 864058 864058 single base substitution A G downstream_gene_variant BRCA-EU 19 864507 864507 single base substitution T A downstream_gene_variant BRCA-EU 19 864626 864626 single base substitution C A downstream_gene_variant BRCA-EU 19 866454 866454 single base substitution C T downstream_gene_variant BRCA-EU 19 866608 866608 single base substitution G A downstream_gene_variant BRCA-EU 19 867041 867041 single base substitution C G downstream_gene_variant BRCA-EU 19 867180 867180 single base substitution T A downstream_gene_variant BRCA-EU 19 869814 869814 single base substitution C T downstream_gene_variant BRCA-EU 19 869814 869814 single base substitution C T intron_variant BRCA-EU 19 870337 870337 single base substitution G A downstream_gene_variant BRCA-EU 19 870337 870337 single base substitution G A intron_variant BRCA-EU 19 870753 870753 single base substitution G A downstream_gene_variant BRCA-EU 19 870753 870753 single base substitution G A intron_variant BRCA-EU 19 870888 870932 deletion of <=200bp GGGCAGGACATGGAGGCGGGGAGCCGTGTGGATTCGGGGGGACCT - downstream_gene_variant BRCA-EU 19 870888 870932 deletion of <=200bp GGGCAGGACATGGAGGCGGGGAGCCGTGTGGATTCGGGGGGACCT - intron_variant BRCA-EU 19 872407 872407 single base substitution G A downstream_gene_variant BRCA-EU 19 872407 872407 single base substitution G A intron_variant BRCA-EU 19 872839 872839 single base substitution G C downstream_gene_variant BRCA-EU 19 872839 872839 single base substitution G C intron_variant BRCA-EU 19 873077 873077 single base substitution G C downstream_gene_variant BRCA-EU 19 873077 873077 single base substitution G C intron_variant BRCA-EU 19 873583 873583 single base substitution C G splice_acceptor_variant BRCA-EU 19 873770 873770 deletion of <=200bp C - intron_variant BRCA-EU 19 874152 874152 single base substitution C T intron_variant BRCA-EU 19 875416 875416 single base substitution G C exon_variant BRCA-EU 19 875416 875416 single base substitution G C intron_variant BRCA-EU 19 875416 875416 single base substitution G C synonymous_variant L286L 858C>G BRCA-EU 19 875416 875416 single base substitution G C synonymous_variant L389L 1167C>G BRCA-EU 19 875416 875416 single base substitution G C synonymous_variant L464L 1392C>G BRCA-EU 19 875416 875416 single base substitution G C synonymous_variant L533L 1599C>G BRCA-EU 19 877566 877566 single base substitution G A intron_variant BRCA-EU 19 878513 878513 single base substitution C G intron_variant BRCA-EU 19 878805 878805 single base substitution C A intron_variant BRCA-EU 19 879606 879606 single base substitution T G intron_variant BRCA-EU 19 880107 880107 single base substitution G A exon_variant BRCA-EU 19 880107 880107 single base substitution G A intron_variant BRCA-EU 19 880107 880107 single base substitution G A missense_variant H148Y 442C>T BRCA-EU 19 880107 880107 single base substitution G A missense_variant H251Y 751C>T BRCA-EU 19 880107 880107 single base substitution G A missense_variant H395Y 1183C>T BRCA-EU 19 883322 883322 single base substitution G T downstream_gene_variant BRCA-EU 19 883322 883322 single base substitution G T intron_variant BRCA-EU 19 883708 883708 single base substitution T A downstream_gene_variant BRCA-EU 19 883708 883708 single base substitution T A intron_variant BRCA-EU 19 885282 885282 single base substitution G A downstream_gene_variant BRCA-EU 19 885282 885282 single base substitution G A intron_variant BRCA-EU 19 885422 885422 single base substitution C T downstream_gene_variant BRCA-EU 19 885422 885422 single base substitution C T intron_variant BRCA-EU 19 885588 885588 single base substitution C T downstream_gene_variant BRCA-EU 19 885588 885588 single base substitution C T intron_variant BRCA-EU 19 887322 887322 single base substitution T C downstream_gene_variant BRCA-EU 19 887322 887322 single base substitution T C intron_variant BRCA-EU 19 887322 887322 single base substitution T C upstream_gene_variant BRCA-EU 19 887390 887390 single base substitution G A downstream_gene_variant BRCA-EU 19 887390 887390 single base substitution G A intron_variant BRCA-EU 19 887390 887390 single base substitution G A upstream_gene_variant BRCA-EU 19 887697 887697 single base substitution G A downstream_gene_variant BRCA-EU 19 887697 887697 single base substitution G A intron_variant BRCA-EU 19 887697 887697 single base substitution G A upstream_gene_variant BRCA-EU 19 888846 888846 single base substitution C T downstream_gene_variant BRCA-EU 19 888846 888846 single base substitution C T intron_variant BRCA-EU 19 888846 888846 single base substitution C T upstream_gene_variant BRCA-EU 19 889860 889860 single base substitution C T downstream_gene_variant BRCA-EU 19 889860 889860 single base substitution C T intron_variant BRCA-EU 19 889860 889860 single base substitution C T upstream_gene_variant BRCA-EU 19 889861 889861 single base substitution G A downstream_gene_variant BRCA-EU 19 889861 889861 single base substitution G A intron_variant BRCA-EU 19 889861 889861 single base substitution G A upstream_gene_variant BRCA-EU 19 890294 890294 single base substitution C T 3_prime_UTR_variant BRCA-EU 19 890294 890294 single base substitution C T downstream_gene_variant BRCA-EU 19 890294 890294 single base substitution C T intron_variant BRCA-EU 19 890294 890294 single base substitution C T upstream_gene_variant BRCA-EU 19 890746 890746 single base substitution C T downstream_gene_variant BRCA-EU 19 890746 890746 single base substitution C T intron_variant BRCA-EU 19 890746 890746 single base substitution C T upstream_gene_variant BRCA-EU 19 891930 891930 single base substitution A T intron_variant BRCA-EU 19 891930 891930 single base substitution A T upstream_gene_variant BRCA-EU 19 892042 892042 single base substitution T A intron_variant BRCA-EU 19 892042 892042 single base substitution T A upstream_gene_variant BRCA-EU 19 892792 892792 single base substitution C T 5_prime_UTR_variant BRCA-EU 19 892792 892792 single base substitution C T intron_variant BRCA-EU 19 892792 892792 single base substitution C T upstream_gene_variant BRCA-EU 19 893031 893031 single base substitution G A intron_variant BRCA-EU 19 893031 893031 single base substitution G A upstream_gene_variant BRCA-EU 19 893032 893032 single base substitution G A intron_variant BRCA-EU 19 893032 893032 single base substitution G A upstream_gene_variant BRCA-EU 19 893316 893316 single base substitution G T upstream_gene_variant BRCA-EU 19 893444 893444 single base substitution T C upstream_gene_variant BRCA-EU 19 893455 893455 single base substitution T C upstream_gene_variant BRCA-EU 19 893456 893456 single base substitution A C upstream_gene_variant BRCA-EU 19 893457 893457 single base substitution A C upstream_gene_variant BRCA-EU 19 893460 893460 single base substitution A G upstream_gene_variant BRCA-EU 19 893494 893494 single base substitution C A upstream_gene_variant BRCA-EU 19 893496 893496 single base substitution G A upstream_gene_variant BRCA-EU 19 893516 893516 single base substitution G T upstream_gene_variant BRCA-EU 19 893731 893731 single base substitution G T upstream_gene_variant BRCA-EU 19 893956 893956 single base substitution G C upstream_gene_variant BRCA-EU 19 895019 895019 single base substitution G C upstream_gene_variant BRCA-EU 19 896628 896628 single base substitution G T upstream_gene_variant BRCA-FR 19 875335 875335 single base substitution C G exon_variant BRCA-FR 19 875335 875335 single base substitution C G synonymous_variant L313L 939G>C BRCA-FR 19 875335 875335 single base substitution C G synonymous_variant L416L 1248G>C BRCA-FR 19 875335 875335 single base substitution C G synonymous_variant L491L 1473G>C BRCA-FR 19 875335 875335 single base substitution C G synonymous_variant L560L 1680G>C BRCA-FR 19 883708 883708 single base substitution T A downstream_gene_variant BRCA-FR 19 883708 883708 single base substitution T A intron_variant BRCA-FR 19 887322 887322 single base substitution T C downstream_gene_variant BRCA-FR 19 887322 887322 single base substitution T C intron_variant BRCA-FR 19 887322 887322 single base substitution T C upstream_gene_variant BRCA-UK 19 877843 877843 single base substitution A G intron_variant BRCA-US 19 875294 875295 deletion of <=200bp TT - exon_variant BRCA-US 19 875294 875295 deletion of <=200bp TT - frameshift_variant K327 BRCA-US 19 875294 875295 deletion of <=200bp TT - frameshift_variant K430 BRCA-US 19 875294 875295 deletion of <=200bp TT - frameshift_variant K505 BRCA-US 19 875294 875295 deletion of <=200bp TT - frameshift_variant K574 BRCA-US 19 884973 884973 single base substitution G C downstream_gene_variant BRCA-US 19 884973 884973 single base substitution G C exon_variant BRCA-US 19 884973 884973 single base substitution G C intron_variant BRCA-US 19 884973 884973 single base substitution G C missense_variant I161M 483C>G BRCA-US 19 884973 884973 single base substitution G C missense_variant I305M 915C>G BRCA-US 19 884973 884973 single base substitution G C missense_variant I58M 174C>G BRCA-US 19 891096 891096 single base substitution C T exon_variant BRCA-US 19 891096 891096 single base substitution C T intron_variant BRCA-US 19 891096 891096 single base substitution C T missense_variant M12I 36G>A BTCA-JP 19 868031 868031 single base substitution C T 3_prime_UTR_variant BTCA-JP 19 871270 871270 single base substitution C A downstream_gene_variant BTCA-JP 19 871270 871270 single base substitution C A intron_variant BTCA-JP 19 886014 886014 single base substitution C T 3_prime_UTR_variant BTCA-JP 19 886014 886014 single base substitution C T downstream_gene_variant BTCA-JP 19 886014 886014 single base substitution C T exon_variant BTCA-JP 19 886014 886014 single base substitution C T intron_variant BTCA-JP 19 886014 886014 single base substitution C T missense_variant R212H 635G>A BTCA-JP 19 886014 886014 single base substitution C T upstream_gene_variant CESC-US 19 872088 872088 single base substitution G A 3_prime_UTR_variant CESC-US 19 872088 872088 single base substitution G A downstream_gene_variant CESC-US 19 872088 872088 single base substitution G A intron_variant CESC-US 19 872088 872088 single base substitution G A synonymous_variant L646L 1936C>T CESC-US 19 879963 879963 single base substitution G A exon_variant CESC-US 19 879963 879963 single base substitution G A intron_variant CESC-US 19 879963 879963 single base substitution G A synonymous_variant L196L 586C>T CESC-US 19 879963 879963 single base substitution G A synonymous_variant L299L 895C>T CESC-US 19 879963 879963 single base substitution G A synonymous_variant L443L 1327C>T CESC-US 19 881596 881596 single base substitution G C downstream_gene_variant CESC-US 19 881596 881596 single base substitution G C exon_variant CESC-US 19 881596 881596 single base substitution G C intron_variant CESC-US 19 881596 881596 single base substitution G C synonymous_variant L121L 363C>G CESC-US 19 881596 881596 single base substitution G C synonymous_variant L224L 672C>G CESC-US 19 881596 881596 single base substitution G C synonymous_variant L368L 1104C>G CLLE-ES 19 876562 876562 single base substitution G T intron_variant CLLE-ES 19 877577 877577 insertion of <=200bp - G intron_variant CLLE-ES 19 878158 878158 single base substitution C T intron_variant CLLE-ES 19 882207 882207 single base substitution G T downstream_gene_variant CLLE-ES 19 882207 882207 single base substitution G T intron_variant CLLE-ES 19 893445 893445 single base substitution C G upstream_gene_variant COAD-US 19 868236 868236 single base substitution A G 3_prime_UTR_variant COAD-US 19 868236 868236 single base substitution A G synonymous_variant R833R 2499T>C COAD-US 19 871135 871135 single base substitution A G 3_prime_UTR_variant COAD-US 19 871135 871135 single base substitution A G downstream_gene_variant COAD-US 19 871135 871135 single base substitution A G missense_variant L428S 1283T>C COAD-US 19 871135 871135 single base substitution A G missense_variant L675S 2024T>C COAD-US 19 871135 871135 single base substitution A G synonymous_variant V739V 2217T>C COAD-US 19 871135 871135 single base substitution A G synonymous_variant V758V 2274T>C COAD-US 19 871171 871171 single base substitution G A 3_prime_UTR_variant COAD-US 19 871171 871171 single base substitution G A downstream_gene_variant COAD-US 19 871171 871171 single base substitution G A missense_variant P416L 1247C>T COAD-US 19 871171 871171 single base substitution G A missense_variant P663L 1988C>T COAD-US 19 871171 871171 single base substitution G A synonymous_variant P727P 2181C>T COAD-US 19 871171 871171 single base substitution G A synonymous_variant P746P 2238C>T COAD-US 19 871222 871222 single base substitution G A 3_prime_UTR_variant COAD-US 19 871222 871222 single base substitution G A downstream_gene_variant COAD-US 19 871222 871222 single base substitution G A missense_variant T399M 1196C>T COAD-US 19 871222 871222 single base substitution G A missense_variant T646M 1937C>T COAD-US 19 871222 871222 single base substitution G A synonymous_variant D710D 2130C>T COAD-US 19 871222 871222 single base substitution G A synonymous_variant D729D 2187C>T COAD-US 19 872089 872089 single base substitution A G 3_prime_UTR_variant COAD-US 19 872089 872089 single base substitution A G downstream_gene_variant COAD-US 19 872089 872089 single base substitution A G intron_variant COAD-US 19 872089 872089 single base substitution A G synonymous_variant F645F 1935T>C COAD-US 19 884936 884936 deletion of <=200bp C - downstream_gene_variant COAD-US 19 884936 884936 deletion of <=200bp C - exon_variant COAD-US 19 884936 884936 deletion of <=200bp C - frameshift_variant V174 COAD-US 19 884936 884936 deletion of <=200bp C - frameshift_variant V318 COAD-US 19 884936 884936 deletion of <=200bp C - frameshift_variant V71 COAD-US 19 884936 884936 deletion of <=200bp C - intron_variant COAD-US 19 885818 885818 single base substitution A G downstream_gene_variant COAD-US 19 885818 885818 single base substitution A G exon_variant COAD-US 19 885818 885818 single base substitution A G intron_variant COAD-US 19 885818 885818 single base substitution A G synonymous_variant F277F 831T>C COAD-US 19 885818 885818 single base substitution A G synonymous_variant F30F 90T>C COAD-US 19 885913 885913 single base substitution C T 3_prime_UTR_variant COAD-US 19 885913 885913 single base substitution C T exon_variant COAD-US 19 885913 885913 single base substitution C T intron_variant COAD-US 19 885913 885913 single base substitution C T missense_variant V246M 736G>A COAD-US 19 885913 885913 single base substitution C T upstream_gene_variant COAD-US 19 885944 885944 single base substitution G C 3_prime_UTR_variant COAD-US 19 885944 885944 single base substitution G C exon_variant COAD-US 19 885944 885944 single base substitution G C intron_variant COAD-US 19 885944 885944 single base substitution G C missense_variant S235R 705C>G COAD-US 19 885944 885944 single base substitution G C upstream_gene_variant COAD-US 19 890170 890170 single base substitution C T 3_prime_UTR_variant COAD-US 19 890170 890170 single base substitution C T downstream_gene_variant COAD-US 19 890170 890170 single base substitution C T exon_variant COAD-US 19 890170 890170 single base substitution C T intron_variant COAD-US 19 890170 890170 single base substitution C T missense_variant E82K 244G>A COAD-US 19 890170 890170 single base substitution C T upstream_gene_variant COAD-US 19 890996 890996 single base substitution C T exon_variant COAD-US 19 890996 890996 single base substitution C T intron_variant COAD-US 19 890996 890996 single base substitution C T missense_variant A46T 136G>A COCA-CN 19 863127 863127 single base substitution G A downstream_gene_variant COCA-CN 19 868555 868555 single base substitution C T downstream_gene_variant COCA-CN 19 868555 868555 single base substitution C T intron_variant COCA-CN 19 872660 872660 single base substitution T G downstream_gene_variant COCA-CN 19 872660 872660 single base substitution T G intron_variant COCA-CN 19 876893 876893 single base substitution C T intron_variant COCA-CN 19 876911 876911 single base substitution G A intron_variant COCA-CN 19 876967 876967 single base substitution C G intron_variant COCA-CN 19 876967 876967 single base substitution C G splice_region_variant COCA-CN 19 878805 878805 single base substitution C T intron_variant COCA-CN 19 879615 879615 single base substitution C A intron_variant COCA-CN 19 879743 879743 single base substitution C G intron_variant COCA-CN 19 880005 880005 single base substitution C T exon_variant COCA-CN 19 880005 880005 single base substitution C T intron_variant COCA-CN 19 880005 880005 single base substitution C T missense_variant V182I 544G>A COCA-CN 19 880005 880005 single base substitution C T missense_variant V285I 853G>A COCA-CN 19 880005 880005 single base substitution C T missense_variant V429I 1285G>A COCA-CN 19 885706 885706 single base substitution G C downstream_gene_variant COCA-CN 19 885706 885706 single base substitution G C intron_variant COCA-CN 19 885853 885853 single base substitution G A 3_prime_UTR_variant COCA-CN 19 885853 885853 single base substitution G A exon_variant COCA-CN 19 885853 885853 single base substitution G A intron_variant COCA-CN 19 885853 885853 single base substitution G A missense_variant R19C 55C>T COCA-CN 19 885853 885853 single base substitution G A missense_variant R266C 796C>T COCA-CN 19 885959 885959 single base substitution C T 3_prime_UTR_variant COCA-CN 19 885959 885959 single base substitution C T exon_variant COCA-CN 19 885959 885959 single base substitution C T intron_variant COCA-CN 19 885959 885959 single base substitution C T synonymous_variant T230T 690G>A COCA-CN 19 885959 885959 single base substitution C T upstream_gene_variant COCA-CN 19 886230 886230 single base substitution G C downstream_gene_variant COCA-CN 19 886230 886230 single base substitution G C intron_variant COCA-CN 19 886230 886230 single base substitution G C upstream_gene_variant COCA-CN 19 890975 890975 single base substitution T C downstream_gene_variant COCA-CN 19 890975 890975 single base substitution T C exon_variant COCA-CN 19 890975 890975 single base substitution T C intron_variant COCA-CN 19 890975 890975 single base substitution T C missense_variant S53G 157A>G EOPC-DE 19 872481 872481 single base substitution G A downstream_gene_variant EOPC-DE 19 872481 872481 single base substitution G A intron_variant EOPC-DE 19 883220 883220 single base substitution T C downstream_gene_variant EOPC-DE 19 883220 883220 single base substitution T C intron_variant EOPC-DE 19 883221 883221 single base substitution A G downstream_gene_variant EOPC-DE 19 883221 883221 single base substitution A G intron_variant ESAD-UK 19 863525 863525 single base substitution G A downstream_gene_variant ESAD-UK 19 864895 864895 single base substitution G A downstream_gene_variant ESAD-UK 19 865311 865311 single base substitution G T downstream_gene_variant ESAD-UK 19 865570 865570 single base substitution G A downstream_gene_variant ESAD-UK 19 868374 868374 single base substitution C T 3_prime_UTR_variant ESAD-UK 19 868374 868374 single base substitution C T intron_variant ESAD-UK 19 868374 868374 single base substitution C T stop_retained_variant *842* 2525G>A ESAD-UK 19 868374 868374 single base substitution C T stop_retained_variant *861* 2582G>A ESAD-UK 19 870332 870332 single base substitution A G downstream_gene_variant ESAD-UK 19 870332 870332 single base substitution A G intron_variant ESAD-UK 19 872332 872332 single base substitution G A downstream_gene_variant ESAD-UK 19 872332 872332 single base substitution G A intron_variant ESAD-UK 19 874109 874109 single base substitution C T intron_variant ESAD-UK 19 877400 877400 single base substitution G A intron_variant ESAD-UK 19 881541 881541 single base substitution C T downstream_gene_variant ESAD-UK 19 881541 881541 single base substitution C T intron_variant ESAD-UK 19 882233 882233 single base substitution C T downstream_gene_variant ESAD-UK 19 882233 882233 single base substitution C T intron_variant ESAD-UK 19 884996 884996 single base substitution C T downstream_gene_variant ESAD-UK 19 884996 884996 single base substitution C T exon_variant ESAD-UK 19 884996 884996 single base substitution C T intron_variant ESAD-UK 19 884996 884996 single base substitution C T missense_variant A154T 460G>A ESAD-UK 19 884996 884996 single base substitution C T missense_variant A298T 892G>A ESAD-UK 19 884996 884996 single base substitution C T missense_variant A51T 151G>A ESAD-UK 19 885665 885665 single base substitution C T downstream_gene_variant ESAD-UK 19 885665 885665 single base substitution C T intron_variant ESAD-UK 19 885833 885833 single base substitution G T 3_prime_UTR_variant ESAD-UK 19 885833 885833 single base substitution G T exon_variant ESAD-UK 19 885833 885833 single base substitution G T intron_variant ESAD-UK 19 885833 885833 single base substitution G T missense_variant N25K 75C>A ESAD-UK 19 885833 885833 single base substitution G T missense_variant N272K 816C>A ESAD-UK 19 885898 885898 single base substitution C T 3_prime_UTR_variant ESAD-UK 19 885898 885898 single base substitution C T exon_variant ESAD-UK 19 885898 885898 single base substitution C T intron_variant ESAD-UK 19 885898 885898 single base substitution C T missense_variant E251K 751G>A ESAD-UK 19 885898 885898 single base substitution C T missense_variant E4K 10G>A ESAD-UK 19 888785 888785 single base substitution G A downstream_gene_variant ESAD-UK 19 888785 888785 single base substitution G A intron_variant ESAD-UK 19 888785 888785 single base substitution G A upstream_gene_variant ESAD-UK 19 889204 889204 single base substitution C T downstream_gene_variant ESAD-UK 19 889204 889204 single base substitution C T intron_variant ESAD-UK 19 889204 889204 single base substitution C T upstream_gene_variant ESAD-UK 19 889368 889368 single base substitution C T downstream_gene_variant ESAD-UK 19 889368 889368 single base substitution C T intron_variant ESAD-UK 19 889368 889368 single base substitution C T upstream_gene_variant ESAD-UK 19 889861 889861 single base substitution G A downstream_gene_variant ESAD-UK 19 889861 889861 single base substitution G A intron_variant ESAD-UK 19 889861 889861 single base substitution G A upstream_gene_variant ESAD-UK 19 893481 893481 single base substitution T C upstream_gene_variant ESAD-UK 19 896469 896469 single base substitution G T upstream_gene_variant ESCA-CN 19 871865 871865 single base substitution G C downstream_gene_variant ESCA-CN 19 871865 871865 single base substitution G C intron_variant ESCA-CN 19 885818 885818 single base substitution A G downstream_gene_variant ESCA-CN 19 885818 885818 single base substitution A G exon_variant ESCA-CN 19 885818 885818 single base substitution A G intron_variant ESCA-CN 19 885818 885818 single base substitution A G synonymous_variant F277F 831T>C ESCA-CN 19 885818 885818 single base substitution A G synonymous_variant F30F 90T>C ESCA-CN 19 897446 897446 single base substitution C T upstream_gene_variant GBM-US 19 868170 868170 single base substitution C T 3_prime_UTR_variant GBM-US 19 868170 868170 single base substitution C T synonymous_variant P855P 2565G>A KIRC-US 19 871987 871987 single base substitution G A 3_prime_UTR_variant KIRC-US 19 871987 871987 single base substitution G A downstream_gene_variant KIRC-US 19 871987 871987 single base substitution G A intron_variant KIRC-US 19 871987 871987 single base substitution G A synonymous_variant T679T 2037C>T KIRC-US 19 884992 884992 single base substitution G A downstream_gene_variant KIRC-US 19 884992 884992 single base substitution G A exon_variant KIRC-US 19 884992 884992 single base substitution G A intron_variant KIRC-US 19 884992 884992 single base substitution G A missense_variant S155F 464C>T KIRC-US 19 884992 884992 single base substitution G A missense_variant S299F 896C>T KIRC-US 19 884992 884992 single base substitution G A missense_variant S52F 155C>T LAML-KR 19 864956 864956 single base substitution T C downstream_gene_variant LAML-KR 19 873035 873035 single base substitution G A downstream_gene_variant LAML-KR 19 873035 873035 single base substitution G A intron_variant LAML-KR 19 877693 877693 single base substitution C G intron_variant LAML-KR 19 879776 879776 single base substitution G A intron_variant LAML-KR 19 879935 879935 single base substitution A G intron_variant LAML-KR 19 879935 879935 single base substitution A G splice_donor_variant LAML-KR 19 880066 880066 single base substitution G A exon_variant LAML-KR 19 880066 880066 single base substitution G A intron_variant LAML-KR 19 880066 880066 single base substitution G A synonymous_variant S161S 483C>T LAML-KR 19 880066 880066 single base substitution G A synonymous_variant S264S 792C>T LAML-KR 19 880066 880066 single base substitution G A synonymous_variant S408S 1224C>T LGG-US 19 879947 879947 single base substitution C T exon_variant LGG-US 19 879947 879947 single base substitution C T intron_variant LGG-US 19 879947 879947 single base substitution C T missense_variant S201N 602G>A LGG-US 19 879947 879947 single base substitution C T missense_variant S304N 911G>A LGG-US 19 879947 879947 single base substitution C T missense_variant S448N 1343G>A LICA-FR 19 867293 867308 deletion of <=200bp GGGGGCCTTAAAGTGG - downstream_gene_variant LICA-FR 19 868252 868252 single base substitution C T 3_prime_UTR_variant LICA-FR 19 868252 868252 single base substitution C T splice_acceptor_variant LICA-FR 19 877577 877577 insertion of <=200bp - AGGGGCTGGCG intron_variant LICA-FR 19 877685 877685 single base substitution G A intron_variant LICA-FR 19 878485 878485 single base substitution C T intron_variant LICA-FR 19 878550 878550 single base substitution C T intron_variant LICA-FR 19 879399 879399 single base substitution A G intron_variant LICA-FR 19 881955 881955 single base substitution T A downstream_gene_variant LICA-FR 19 881955 881955 single base substitution T A intron_variant LICA-FR 19 882373 882373 single base substitution G C downstream_gene_variant LICA-FR 19 882373 882373 single base substitution G C intron_variant LICA-FR 19 885802 885802 single base substitution G T downstream_gene_variant LICA-FR 19 885802 885802 single base substitution G T exon_variant LICA-FR 19 885802 885802 single base substitution G T intron_variant LICA-FR 19 885802 885802 single base substitution G T missense_variant L283I 847C>A LICA-FR 19 885802 885802 single base substitution G T missense_variant L36I 106C>A LICA-FR 19 895447 895447 single base substitution G A upstream_gene_variant LICA-FR 19 897488 897488 single base substitution A C upstream_gene_variant LIHC-US 19 873468 873468 single base substitution A G downstream_gene_variant LIHC-US 19 873468 873468 single base substitution A G exon_variant LIHC-US 19 873468 873468 single base substitution A G missense_variant L382P 1145T>C LIHC-US 19 873468 873468 single base substitution A G missense_variant L629P 1886T>C LIHC-US 19 890977 890977 single base substitution C T downstream_gene_variant LIHC-US 19 890977 890977 single base substitution C T exon_variant LIHC-US 19 890977 890977 single base substitution C T intron_variant LIHC-US 19 890977 890977 single base substitution C T missense_variant R52H 155G>A LINC-JP 19 866277 866277 insertion of <=200bp - C downstream_gene_variant LINC-JP 19 868364 868364 single base substitution C T 3_prime_UTR_variant LINC-JP 19 868364 868364 single base substitution C T intron_variant LINC-JP 19 875387 875387 single base substitution C T exon_variant LINC-JP 19 875387 875387 single base substitution C T intron_variant LINC-JP 19 875387 875387 single base substitution C T missense_variant R296H 887G>A LINC-JP 19 875387 875387 single base substitution C T missense_variant R399H 1196G>A LINC-JP 19 875387 875387 single base substitution C T missense_variant R474H 1421G>A LINC-JP 19 875387 875387 single base substitution C T missense_variant R543H 1628G>A LINC-JP 19 879681 879681 single base substitution G A intron_variant LINC-JP 19 879776 879776 single base substitution G A intron_variant LINC-JP 19 879784 879784 single base substitution G A intron_variant LINC-JP 19 879803 879803 single base substitution C T intron_variant LINC-JP 19 879811 879811 single base substitution C G intron_variant LINC-JP 19 879855 879855 single base substitution C G intron_variant LINC-JP 19 879872 879872 single base substitution G C intron_variant LINC-JP 19 885660 885660 single base substitution C T downstream_gene_variant LINC-JP 19 885660 885660 single base substitution C T intron_variant LIRI-JP 19 868032 868032 deletion of <=200bp G - 3_prime_UTR_variant LIRI-JP 19 881413 881413 single base substitution A G downstream_gene_variant LIRI-JP 19 881413 881413 single base substitution A G intron_variant LIRI-JP 19 889538 889538 single base substitution A C downstream_gene_variant LIRI-JP 19 889538 889538 single base substitution A C intron_variant LIRI-JP 19 889538 889538 single base substitution A C upstream_gene_variant LIRI-JP 19 893417 893417 single base substitution A C upstream_gene_variant LIRI-JP 19 893447 893447 single base substitution A G upstream_gene_variant LIRI-JP 19 893455 893455 single base substitution T C upstream_gene_variant LIRI-JP 19 893456 893456 single base substitution A C upstream_gene_variant LIRI-JP 19 893457 893457 single base substitution A C upstream_gene_variant LIRI-JP 19 896640 896643 deletion of <=200bp CTAT - upstream_gene_variant LIRI-JP 19 896757 896757 single base substitution A G upstream_gene_variant LIRI-JP 19 897121 897121 single base substitution C G upstream_gene_variant LIRI-JP 19 897349 897349 single base substitution T C upstream_gene_variant LUSC-KR 19 863516 863516 single base substitution G A downstream_gene_variant LUSC-KR 19 865617 865617 single base substitution T A downstream_gene_variant LUSC-KR 19 865640 865640 single base substitution G A downstream_gene_variant LUSC-KR 19 866608 866608 single base substitution G A downstream_gene_variant LUSC-KR 19 870246 870246 single base substitution G A downstream_gene_variant LUSC-KR 19 870246 870246 single base substitution G A intron_variant LUSC-KR 19 870443 870443 single base substitution C G downstream_gene_variant LUSC-KR 19 870443 870443 single base substitution C G intron_variant LUSC-KR 19 870807 870807 single base substitution T G downstream_gene_variant LUSC-KR 19 870807 870807 single base substitution T G intron_variant LUSC-KR 19 870904 870904 single base substitution C G downstream_gene_variant LUSC-KR 19 870904 870904 single base substitution C G intron_variant LUSC-KR 19 873023 873023 single base substitution C G downstream_gene_variant LUSC-KR 19 873023 873023 single base substitution C G intron_variant LUSC-KR 19 873211 873211 single base substitution A C downstream_gene_variant LUSC-KR 19 873211 873211 single base substitution A C intron_variant LUSC-KR 19 873330 873330 single base substitution C T downstream_gene_variant LUSC-KR 19 873330 873330 single base substitution C T intron_variant LUSC-KR 19 873482 873482 single base substitution G A downstream_gene_variant LUSC-KR 19 873482 873482 single base substitution G A exon_variant LUSC-KR 19 873482 873482 single base substitution G A synonymous_variant F377F 1131C>T LUSC-KR 19 873482 873482 single base substitution G A synonymous_variant F624F 1872C>T LUSC-KR 19 878069 878069 single base substitution C T intron_variant LUSC-KR 19 879343 879343 single base substitution A G intron_variant LUSC-KR 19 879348 879348 single base substitution C A intron_variant LUSC-KR 19 879715 879715 single base substitution T C intron_variant LUSC-KR 19 883298 883298 single base substitution T G downstream_gene_variant LUSC-KR 19 883298 883298 single base substitution T G intron_variant LUSC-KR 19 883326 883326 single base substitution A G downstream_gene_variant LUSC-KR 19 883326 883326 single base substitution A G intron_variant LUSC-KR 19 884465 884465 single base substitution G A downstream_gene_variant LUSC-KR 19 884465 884465 single base substitution G A intron_variant LUSC-KR 19 889580 889580 single base substitution T G downstream_gene_variant LUSC-KR 19 889580 889580 single base substitution T G intron_variant LUSC-KR 19 889580 889580 single base substitution T G upstream_gene_variant LUSC-KR 19 889588 889588 single base substitution T G downstream_gene_variant LUSC-KR 19 889588 889588 single base substitution T G intron_variant LUSC-KR 19 889588 889588 single base substitution T G upstream_gene_variant LUSC-KR 19 890358 890358 single base substitution A G 3_prime_UTR_variant LUSC-KR 19 890358 890358 single base substitution A G downstream_gene_variant LUSC-KR 19 890358 890358 single base substitution A G intron_variant LUSC-KR 19 890358 890358 single base substitution A G upstream_gene_variant LUSC-KR 19 892042 892042 single base substitution T A intron_variant LUSC-KR 19 892042 892042 single base substitution T A upstream_gene_variant LUSC-KR 19 892043 892043 single base substitution T C intron_variant LUSC-KR 19 892043 892043 single base substitution T C upstream_gene_variant LUSC-KR 19 893544 893544 single base substitution C A upstream_gene_variant LUSC-KR 19 896717 896717 single base substitution T C upstream_gene_variant LUSC-US 19 872083 872083 single base substitution C A 3_prime_UTR_variant LUSC-US 19 872083 872083 single base substitution C A downstream_gene_variant LUSC-US 19 872083 872083 single base substitution C A intron_variant LUSC-US 19 872083 872083 single base substitution C A synonymous_variant R647R 1941G>T LUSC-US 19 875362 875362 single base substitution G C exon_variant LUSC-US 19 875362 875362 single base substitution G C intron_variant LUSC-US 19 875362 875362 single base substitution G C synonymous_variant L304L 912C>G LUSC-US 19 875362 875362 single base substitution G C synonymous_variant L407L 1221C>G LUSC-US 19 875362 875362 single base substitution G C synonymous_variant L482L 1446C>G LUSC-US 19 875362 875362 single base substitution G C synonymous_variant L551L 1653C>G LUSC-US 19 875420 875420 single base substitution G A exon_variant LUSC-US 19 875420 875420 single base substitution G A intron_variant LUSC-US 19 875420 875420 single base substitution G A missense_variant S285L 854C>T LUSC-US 19 875420 875420 single base substitution G A missense_variant S388L 1163C>T LUSC-US 19 875420 875420 single base substitution G A missense_variant S463L 1388C>T LUSC-US 19 875420 875420 single base substitution G A missense_variant S532L 1595C>T LUSC-US 19 879947 879947 single base substitution C T exon_variant LUSC-US 19 879947 879947 single base substitution C T intron_variant LUSC-US 19 879947 879947 single base substitution C T missense_variant S201N 602G>A LUSC-US 19 879947 879947 single base substitution C T missense_variant S304N 911G>A LUSC-US 19 879947 879947 single base substitution C T missense_variant S448N 1343G>A MALY-DE 19 865999 865999 single base substitution G C downstream_gene_variant MALY-DE 19 866950 866950 single base substitution A G downstream_gene_variant MALY-DE 19 867584 867584 single base substitution G C downstream_gene_variant MALY-DE 19 873811 873811 single base substitution T C intron_variant MALY-DE 19 893456 893456 single base substitution A G upstream_gene_variant MALY-DE 19 893469 893469 insertion of <=200bp - TAT upstream_gene_variant MALY-DE 19 897404 897404 single base substitution C T upstream_gene_variant MELA-AU 19 864043 864043 insertion of <=200bp - CACACACACACACACACACA downstream_gene_variant MELA-AU 19 864433 864433 single base substitution G A downstream_gene_variant MELA-AU 19 864455 864455 single base substitution C T downstream_gene_variant MELA-AU 19 864457 864457 single base substitution C T downstream_gene_variant MELA-AU 19 864845 864846 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 865046 865046 single base substitution G A downstream_gene_variant MELA-AU 19 865116 865116 single base substitution T C downstream_gene_variant MELA-AU 19 865290 865290 single base substitution G A downstream_gene_variant MELA-AU 19 865443 865443 single base substitution G A downstream_gene_variant MELA-AU 19 865735 865735 single base substitution T C downstream_gene_variant MELA-AU 19 865898 865898 single base substitution G A downstream_gene_variant MELA-AU 19 865926 865926 single base substitution G A downstream_gene_variant MELA-AU 19 867040 867040 single base substitution C T downstream_gene_variant MELA-AU 19 867293 867294 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 867293 867308 deletion of <=200bp GGGGGCCTTAAAGTGG - downstream_gene_variant MELA-AU 19 867767 867767 single base substitution G A downstream_gene_variant MELA-AU 19 868044 868044 single base substitution G A 3_prime_UTR_variant MELA-AU 19 868060 868060 single base substitution C T 3_prime_UTR_variant MELA-AU 19 868284 868284 single base substitution G A 3_prime_UTR_variant MELA-AU 19 868284 868284 single base substitution G A intron_variant MELA-AU 19 868836 868836 single base substitution G A downstream_gene_variant MELA-AU 19 868836 868836 single base substitution G A intron_variant MELA-AU 19 868925 868925 single base substitution G A 3_prime_UTR_variant MELA-AU 19 868925 868925 single base substitution G A downstream_gene_variant MELA-AU 19 868925 868925 single base substitution G A missense_variant S468L 1403C>T MELA-AU 19 868925 868925 single base substitution G A missense_variant S715L 2144C>T MELA-AU 19 868925 868925 single base substitution G A synonymous_variant I779I 2337C>T MELA-AU 19 868925 868925 single base substitution G A synonymous_variant I798I 2394C>T MELA-AU 19 870139 870139 single base substitution T C downstream_gene_variant MELA-AU 19 870139 870139 single base substitution T C intron_variant MELA-AU 19 870264 870264 single base substitution G A downstream_gene_variant MELA-AU 19 870264 870264 single base substitution G A intron_variant MELA-AU 19 871106 871106 single base substitution C A 3_prime_UTR_variant MELA-AU 19 871106 871106 single base substitution C A downstream_gene_variant MELA-AU 19 871106 871106 single base substitution C A missense_variant R749L 2246G>T MELA-AU 19 871106 871106 single base substitution C A missense_variant R768L 2303G>T MELA-AU 19 871106 871106 single base substitution C A missense_variant V438F 1312G>T MELA-AU 19 871106 871106 single base substitution C A missense_variant V685F 2053G>T MELA-AU 19 872205 872205 single base substitution C T downstream_gene_variant MELA-AU 19 872205 872205 single base substitution C T intron_variant MELA-AU 19 873574 873574 single base substitution T A exon_variant MELA-AU 19 873574 873574 single base substitution T A stop_gained K347* 1039A>T MELA-AU 19 873574 873574 single base substitution T A stop_gained K450* 1348A>T MELA-AU 19 873574 873574 single base substitution T A stop_gained K525* 1573A>T MELA-AU 19 873574 873574 single base substitution T A stop_gained K594* 1780A>T MELA-AU 19 873779 873779 single base substitution G A intron_variant MELA-AU 19 874426 874426 single base substitution G T intron_variant MELA-AU 19 874927 874927 single base substitution C T intron_variant MELA-AU 19 875176 875176 single base substitution A T intron_variant MELA-AU 19 875384 875384 single base substitution A T exon_variant MELA-AU 19 875384 875384 single base substitution A T intron_variant MELA-AU 19 875384 875384 single base substitution A T missense_variant V297E 890T>A MELA-AU 19 875384 875384 single base substitution A T missense_variant V400E 1199T>A MELA-AU 19 875384 875384 single base substitution A T missense_variant V475E 1424T>A MELA-AU 19 875384 875384 single base substitution A T missense_variant V544E 1631T>A MELA-AU 19 875685 875685 single base substitution C T intron_variant MELA-AU 19 876011 876011 single base substitution G A intron_variant MELA-AU 19 876134 876134 single base substitution G A intron_variant MELA-AU 19 876214 876214 single base substitution C A intron_variant MELA-AU 19 876511 876512 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 19 876512 876512 single base substitution G A intron_variant MELA-AU 19 876571 876571 single base substitution G A intron_variant MELA-AU 19 876736 876736 single base substitution G A intron_variant MELA-AU 19 877204 877204 single base substitution G A intron_variant MELA-AU 19 877243 877243 single base substitution G A intron_variant MELA-AU 19 880052 880052 single base substitution G A exon_variant MELA-AU 19 880052 880052 single base substitution G A intron_variant MELA-AU 19 880052 880052 single base substitution G A missense_variant P166L 497C>T MELA-AU 19 880052 880052 single base substitution G A missense_variant P269L 806C>T MELA-AU 19 880052 880052 single base substitution G A missense_variant P413L 1238C>T MELA-AU 19 880058 880059 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 19 880058 880059 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 880058 880059 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P164L 490CC>TT MELA-AU 19 880058 880059 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P267L 799CC>TT MELA-AU 19 880058 880059 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P411L 1231CC>TT MELA-AU 19 880111 880111 single base substitution G A exon_variant MELA-AU 19 880111 880111 single base substitution G A intron_variant MELA-AU 19 880111 880111 single base substitution G A synonymous_variant I146I 438C>T MELA-AU 19 880111 880111 single base substitution G A synonymous_variant I249I 747C>T MELA-AU 19 880111 880111 single base substitution G A synonymous_variant I393I 1179C>T MELA-AU 19 880944 880944 single base substitution A G downstream_gene_variant MELA-AU 19 880944 880944 single base substitution A G intron_variant MELA-AU 19 881083 881083 single base substitution G A downstream_gene_variant MELA-AU 19 881083 881083 single base substitution G A intron_variant MELA-AU 19 881813 881814 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 19 881813 881814 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 882284 882284 single base substitution G A downstream_gene_variant MELA-AU 19 882284 882284 single base substitution G A intron_variant MELA-AU 19 882926 882926 single base substitution G A downstream_gene_variant MELA-AU 19 882926 882926 single base substitution G A intron_variant MELA-AU 19 883590 883590 single base substitution G A downstream_gene_variant MELA-AU 19 883590 883590 single base substitution G A intron_variant MELA-AU 19 883897 883897 single base substitution G A downstream_gene_variant MELA-AU 19 883897 883897 single base substitution G A intron_variant MELA-AU 19 883902 883902 single base substitution G A downstream_gene_variant MELA-AU 19 883902 883902 single base substitution G A intron_variant MELA-AU 19 884102 884102 single base substitution C T downstream_gene_variant MELA-AU 19 884102 884102 single base substitution C T intron_variant MELA-AU 19 884311 884311 single base substitution G A downstream_gene_variant MELA-AU 19 884311 884311 single base substitution G A intron_variant MELA-AU 19 884499 884499 single base substitution G A downstream_gene_variant MELA-AU 19 884499 884499 single base substitution G A intron_variant MELA-AU 19 885016 885016 single base substitution G A downstream_gene_variant MELA-AU 19 885016 885016 single base substitution G A intron_variant MELA-AU 19 885016 885016 single base substitution G A splice_region_variant MELA-AU 19 885466 885466 single base substitution G A downstream_gene_variant MELA-AU 19 885466 885466 single base substitution G A intron_variant MELA-AU 19 885706 885706 single base substitution G A downstream_gene_variant MELA-AU 19 885706 885706 single base substitution G A intron_variant MELA-AU 19 885842 885843 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 19 885842 885843 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 19 885842 885843 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 885842 885843 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant T22I 65CC>TT MELA-AU 19 885842 885843 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant T269I 806CC>TT MELA-AU 19 886132 886132 single base substitution C T 3_prime_UTR_variant MELA-AU 19 886132 886132 single base substitution C T downstream_gene_variant MELA-AU 19 886132 886132 single base substitution C T exon_variant MELA-AU 19 886132 886132 single base substitution C T intron_variant MELA-AU 19 886132 886132 single base substitution C T missense_variant G173S 517G>A MELA-AU 19 886132 886132 single base substitution C T upstream_gene_variant MELA-AU 19 886222 886222 single base substitution G A downstream_gene_variant MELA-AU 19 886222 886222 single base substitution G A intron_variant MELA-AU 19 886222 886222 single base substitution G A upstream_gene_variant MELA-AU 19 886428 886428 single base substitution G A downstream_gene_variant MELA-AU 19 886428 886428 single base substitution G A intron_variant MELA-AU 19 886428 886428 single base substitution G A upstream_gene_variant MELA-AU 19 886488 886488 single base substitution G A downstream_gene_variant MELA-AU 19 886488 886488 single base substitution G A intron_variant MELA-AU 19 886488 886488 single base substitution G A upstream_gene_variant MELA-AU 19 886993 886993 single base substitution T A downstream_gene_variant MELA-AU 19 886993 886993 single base substitution T A intron_variant MELA-AU 19 886993 886993 single base substitution T A upstream_gene_variant MELA-AU 19 887391 887391 single base substitution G A downstream_gene_variant MELA-AU 19 887391 887391 single base substitution G A intron_variant MELA-AU 19 887391 887391 single base substitution G A upstream_gene_variant MELA-AU 19 887883 887883 single base substitution G A downstream_gene_variant MELA-AU 19 887883 887883 single base substitution G A intron_variant MELA-AU 19 887883 887883 single base substitution G A upstream_gene_variant MELA-AU 19 887975 887975 single base substitution G A downstream_gene_variant MELA-AU 19 887975 887975 single base substitution G A intron_variant MELA-AU 19 887975 887975 single base substitution G A upstream_gene_variant MELA-AU 19 889244 889244 single base substitution G A downstream_gene_variant MELA-AU 19 889244 889244 single base substitution G A intron_variant MELA-AU 19 889244 889244 single base substitution G A upstream_gene_variant MELA-AU 19 889563 889563 single base substitution G A downstream_gene_variant MELA-AU 19 889563 889563 single base substitution G A intron_variant MELA-AU 19 889563 889563 single base substitution G A upstream_gene_variant MELA-AU 19 890295 890295 single base substitution G A 3_prime_UTR_variant MELA-AU 19 890295 890295 single base substitution G A downstream_gene_variant MELA-AU 19 890295 890295 single base substitution G A intron_variant MELA-AU 19 890295 890295 single base substitution G A upstream_gene_variant MELA-AU 19 890840 890840 single base substitution G A downstream_gene_variant MELA-AU 19 890840 890840 single base substitution G A intron_variant MELA-AU 19 890840 890840 single base substitution G A upstream_gene_variant MELA-AU 19 891040 891040 single base substitution G A exon_variant MELA-AU 19 891040 891040 single base substitution G A intron_variant MELA-AU 19 891040 891040 single base substitution G A missense_variant P31L 92C>T MELA-AU 19 891156 891156 single base substitution G A intron_variant MELA-AU 19 891156 891156 single base substitution G A splice_region_variant MELA-AU 19 891156 891156 single base substitution G A upstream_gene_variant MELA-AU 19 891537 891537 single base substitution G A intron_variant MELA-AU 19 891537 891537 single base substitution G A upstream_gene_variant MELA-AU 19 892347 892347 single base substitution C T intron_variant MELA-AU 19 892347 892347 single base substitution C T splice_region_variant MELA-AU 19 892347 892347 single base substitution C T upstream_gene_variant MELA-AU 19 892462 892463 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 19 892462 892463 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 892462 892463 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 893037 893038 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 19 893037 893038 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 893435 893435 single base substitution G A upstream_gene_variant MELA-AU 19 893448 893448 single base substitution G A upstream_gene_variant MELA-AU 19 893470 893470 single base substitution G A upstream_gene_variant MELA-AU 19 893471 893471 single base substitution G A upstream_gene_variant MELA-AU 19 893521 893521 single base substitution G A upstream_gene_variant MELA-AU 19 893529 893529 single base substitution G A upstream_gene_variant MELA-AU 19 893545 893546 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 893555 893555 single base substitution G A upstream_gene_variant MELA-AU 19 893561 893561 single base substitution A G upstream_gene_variant MELA-AU 19 893570 893570 single base substitution C T upstream_gene_variant MELA-AU 19 893573 893573 single base substitution G A upstream_gene_variant MELA-AU 19 893840 893840 single base substitution C T upstream_gene_variant MELA-AU 19 894120 894120 single base substitution C T upstream_gene_variant MELA-AU 19 894881 894881 single base substitution C T upstream_gene_variant MELA-AU 19 895293 895293 single base substitution C T upstream_gene_variant MELA-AU 19 895431 895431 single base substitution G C upstream_gene_variant MELA-AU 19 896499 896499 single base substitution C T upstream_gene_variant MELA-AU 19 896750 896750 single base substitution G A upstream_gene_variant MELA-AU 19 896897 896897 single base substitution C T upstream_gene_variant MELA-AU 19 897326 897326 single base substitution G A upstream_gene_variant MELA-AU 19 897574 897574 single base substitution G A upstream_gene_variant ORCA-IN 19 863221 863221 single base substitution G T downstream_gene_variant ORCA-IN 19 868415 868415 single base substitution C A 3_prime_UTR_variant ORCA-IN 19 868415 868415 single base substitution C A splice_donor_variant ORCA-IN 19 868415 868415 single base substitution C A synonymous_variant L828L 2484G>T ORCA-IN 19 868415 868415 single base substitution C A synonymous_variant L847L 2541G>T ORCA-IN 19 877013 877013 single base substitution C A exon_variant ORCA-IN 19 877013 877013 single base substitution C A intron_variant ORCA-IN 19 877013 877013 single base substitution C A synonymous_variant L260L 780G>T ORCA-IN 19 877013 877013 single base substitution C A synonymous_variant L363L 1089G>T ORCA-IN 19 877013 877013 single base substitution C A synonymous_variant L507L 1521G>T ORCA-IN 19 888158 888158 single base substitution C T downstream_gene_variant ORCA-IN 19 888158 888158 single base substitution C T intron_variant ORCA-IN 19 888158 888158 single base substitution C T upstream_gene_variant ORCA-IN 19 890094 890094 single base substitution G A downstream_gene_variant ORCA-IN 19 890094 890094 single base substitution G A intron_variant ORCA-IN 19 890094 890094 single base substitution G A upstream_gene_variant ORCA-IN 19 890308 890308 single base substitution C T 3_prime_UTR_variant ORCA-IN 19 890308 890308 single base substitution C T downstream_gene_variant ORCA-IN 19 890308 890308 single base substitution C T intron_variant ORCA-IN 19 890308 890308 single base substitution C T upstream_gene_variant OV-AU 19 867931 867931 single base substitution G C downstream_gene_variant OV-AU 19 869430 869430 single base substitution G T downstream_gene_variant OV-AU 19 869430 869430 single base substitution G T intron_variant OV-AU 19 879821 879821 single base substitution G C intron_variant OV-AU 19 886197 886197 single base substitution C T 3_prime_UTR_variant OV-AU 19 886197 886197 single base substitution C T downstream_gene_variant OV-AU 19 886197 886197 single base substitution C T exon_variant OV-AU 19 886197 886197 single base substitution C T intron_variant OV-AU 19 886197 886197 single base substitution C T missense_variant G151D 452G>A OV-AU 19 886197 886197 single base substitution C T upstream_gene_variant OV-AU 19 888963 888963 single base substitution G C downstream_gene_variant OV-AU 19 888963 888963 single base substitution G C intron_variant OV-AU 19 888963 888963 single base substitution G C upstream_gene_variant OV-AU 19 894782 894782 single base substitution C G upstream_gene_variant OV-AU 19 896346 896346 single base substitution C T upstream_gene_variant OV-AU 19 896894 896894 single base substitution G A upstream_gene_variant PACA-AU 19 867042 867042 insertion of <=200bp - ACCCCCGTGGCGGCTGG downstream_gene_variant PACA-AU 19 867293 867308 deletion of <=200bp GGGGGCCTTAAAGTGG - downstream_gene_variant PACA-AU 19 868277 868277 single base substitution C T 3_prime_UTR_variant PACA-AU 19 868277 868277 single base substitution C T intron_variant PACA-AU 19 868430 868430 single base substitution C T 3_prime_UTR_variant PACA-AU 19 868430 868430 single base substitution C T stop_gained W823* 2469G>A PACA-AU 19 868430 868430 single base substitution C T stop_gained W842* 2526G>A PACA-AU 19 874921 874931 deletion of <=200bp AGGAGGCCGAG - intron_variant PACA-AU 19 880464 880464 single base substitution C G intron_variant PACA-AU 19 880765 880765 single base substitution C G intron_variant PACA-AU 19 883345 883345 single base substitution C T downstream_gene_variant PACA-AU 19 883345 883345 single base substitution C T intron_variant PACA-AU 19 884095 884095 single base substitution A C downstream_gene_variant PACA-AU 19 884095 884095 single base substitution A C intron_variant PACA-AU 19 884645 884645 single base substitution C T downstream_gene_variant PACA-AU 19 884645 884645 single base substitution C T intron_variant PACA-AU 19 884836 884836 single base substitution C T downstream_gene_variant PACA-AU 19 884836 884836 single base substitution C T intron_variant PACA-AU 19 890200 890200 single base substitution C A 3_prime_UTR_variant PACA-AU 19 890200 890200 single base substitution C A downstream_gene_variant PACA-AU 19 890200 890200 single base substitution C A exon_variant PACA-AU 19 890200 890200 single base substitution C A intron_variant PACA-AU 19 890200 890200 single base substitution C A missense_variant D72Y 214G>T PACA-AU 19 890200 890200 single base substitution C A upstream_gene_variant PACA-AU 19 890261 890261 single base substitution T C 3_prime_UTR_variant PACA-AU 19 890261 890261 single base substitution T C downstream_gene_variant PACA-AU 19 890261 890261 single base substitution T C intron_variant PACA-AU 19 890261 890261 single base substitution T C upstream_gene_variant PACA-AU 19 892656 892685 deletion of <=200bp TCTCCAGGCCCCGCACCGATAACCCCGCAG - 5_prime_UTR_variant PACA-AU 19 892656 892685 deletion of <=200bp TCTCCAGGCCCCGCACCGATAACCCCGCAG - intron_variant PACA-AU 19 892656 892685 deletion of <=200bp TCTCCAGGCCCCGCACCGATAACCCCGCAG - upstream_gene_variant PACA-AU 19 893421 893421 single base substitution G A upstream_gene_variant PACA-AU 19 894435 894435 single base substitution T G upstream_gene_variant PACA-CA 19 866797 866797 single base substitution A C downstream_gene_variant PACA-CA 19 866797 866797 single base substitution A G downstream_gene_variant PACA-CA 19 866908 866908 single base substitution G A downstream_gene_variant PACA-CA 19 868066 868066 single base substitution C T 3_prime_UTR_variant PACA-CA 19 868319 868319 single base substitution C T 3_prime_UTR_variant PACA-CA 19 868319 868319 single base substitution C T intron_variant PACA-CA 19 869147 869147 single base substitution C T downstream_gene_variant PACA-CA 19 869147 869147 single base substitution C T intron_variant PACA-CA 19 870584 870584 single base substitution G A downstream_gene_variant PACA-CA 19 870584 870584 single base substitution G A intron_variant PACA-CA 19 872626 872626 single base substitution A G downstream_gene_variant PACA-CA 19 872626 872626 single base substitution A G intron_variant PACA-CA 19 876327 876327 single base substitution G A intron_variant PACA-CA 19 877170 877170 single base substitution A C exon_variant PACA-CA 19 877170 877170 single base substitution A C intron_variant PACA-CA 19 877170 877170 single base substitution A C missense_variant L208R 623T>G PACA-CA 19 877170 877170 single base substitution A C missense_variant L311R 932T>G PACA-CA 19 877170 877170 single base substitution A C missense_variant L455R 1364T>G PACA-CA 19 877891 877891 single base substitution G T intron_variant PACA-CA 19 879399 879399 single base substitution A G intron_variant PACA-CA 19 882346 882346 deletion of <=200bp A - downstream_gene_variant PACA-CA 19 882346 882346 deletion of <=200bp A - intron_variant PACA-CA 19 885137 885137 single base substitution C T downstream_gene_variant PACA-CA 19 885137 885137 single base substitution C T intron_variant PACA-CA 19 887389 887389 single base substitution C T downstream_gene_variant PACA-CA 19 887389 887389 single base substitution C T intron_variant PACA-CA 19 887389 887389 single base substitution C T upstream_gene_variant PACA-CA 19 889418 889418 single base substitution C A downstream_gene_variant PACA-CA 19 889418 889418 single base substitution C A intron_variant PACA-CA 19 889418 889418 single base substitution C A upstream_gene_variant PACA-CA 19 896365 896365 single base substitution C T upstream_gene_variant PAEN-AU 19 893506 893506 single base substitution T C upstream_gene_variant PAEN-IT 19 867955 867955 single base substitution C T downstream_gene_variant PBCA-DE 19 865458 865458 insertion of <=200bp - T downstream_gene_variant PBCA-DE 19 871106 871106 single base substitution C G 3_prime_UTR_variant PBCA-DE 19 871106 871106 single base substitution C G downstream_gene_variant PBCA-DE 19 871106 871106 single base substitution C G missense_variant R749P 2246G>C PBCA-DE 19 871106 871106 single base substitution C G missense_variant R768P 2303G>C PBCA-DE 19 871106 871106 single base substitution C G missense_variant V438L 1312G>C PBCA-DE 19 871106 871106 single base substitution C G missense_variant V685L 2053G>C PBCA-DE 19 873174 873174 single base substitution A C downstream_gene_variant PBCA-DE 19 873174 873174 single base substitution A C intron_variant PBCA-DE 19 873175 873175 single base substitution G C downstream_gene_variant PBCA-DE 19 873175 873175 single base substitution G C intron_variant PBCA-DE 19 873178 873178 single base substitution A G downstream_gene_variant PBCA-DE 19 873178 873178 single base substitution A G intron_variant PBCA-DE 19 876691 876691 single base substitution A C intron_variant PBCA-DE 19 876898 876898 insertion of <=200bp - C intron_variant PBCA-DE 19 879227 879230 deletion of <=200bp AGCC - intron_variant PBCA-DE 19 879235 879238 deletion of <=200bp CCCA - intron_variant PBCA-DE 19 879433 879440 deletion of <=200bp GCCCCACG - intron_variant PBCA-DE 19 879480 879480 single base substitution C G intron_variant PBCA-DE 19 879511 879511 single base substitution G A intron_variant PBCA-DE 19 879534 879534 single base substitution T C intron_variant PBCA-DE 19 879545 879545 single base substitution C T intron_variant PBCA-DE 19 879591 879591 single base substitution A G intron_variant PBCA-DE 19 879599 879599 single base substitution G C intron_variant PBCA-DE 19 879659 879659 single base substitution T C intron_variant PBCA-DE 19 880937 880938 deletion of <=200bp AA - downstream_gene_variant PBCA-DE 19 880937 880938 deletion of <=200bp AA - intron_variant PBCA-DE 19 884782 884782 single base substitution C G downstream_gene_variant PBCA-DE 19 884782 884782 single base substitution C G intron_variant PBCA-DE 19 888061 888061 single base substitution G A downstream_gene_variant PBCA-DE 19 888061 888061 single base substitution G A intron_variant PBCA-DE 19 888061 888061 single base substitution G A upstream_gene_variant PBCA-DE 19 892656 892685 deletion of <=200bp TCTCCAGGCCCCGCACCGATAACCCCGCAG - 5_prime_UTR_variant PBCA-DE 19 892656 892685 deletion of <=200bp TCTCCAGGCCCCGCACCGATAACCCCGCAG - intron_variant PBCA-DE 19 892656 892685 deletion of <=200bp TCTCCAGGCCCCGCACCGATAACCCCGCAG - upstream_gene_variant PRAD-CA 19 866899 866899 single base substitution A G downstream_gene_variant PRAD-CA 19 866908 866908 single base substitution G A downstream_gene_variant PRAD-CA 19 876910 876910 single base substitution C T intron_variant PRAD-CA 19 880936 880936 single base substitution G A downstream_gene_variant PRAD-CA 19 880936 880936 single base substitution G A intron_variant PRAD-UK 19 866491 866491 single base substitution G A downstream_gene_variant PRAD-UK 19 869221 869221 single base substitution C T downstream_gene_variant PRAD-UK 19 869221 869221 single base substitution C T intron_variant PRAD-UK 19 875928 875928 single base substitution G A intron_variant PRAD-UK 19 893479 893479 single base substitution T A upstream_gene_variant PRAD-UK 19 894325 894325 single base substitution C T upstream_gene_variant PRAD-US 19 881676 881676 single base substitution G T downstream_gene_variant PRAD-US 19 881676 881676 single base substitution G T exon_variant PRAD-US 19 881676 881676 single base substitution G T intron_variant PRAD-US 19 881676 881676 single base substitution G T missense_variant L198I 592C>A PRAD-US 19 881676 881676 single base substitution G T missense_variant L342I 1024C>A PRAD-US 19 881676 881676 single base substitution G T missense_variant L95I 283C>A RECA-EU 19 863817 863817 single base substitution G A downstream_gene_variant RECA-EU 19 867808 867808 single base substitution C T downstream_gene_variant RECA-EU 19 880327 880327 single base substitution T C intron_variant RECA-EU 19 884954 884954 single base substitution G A downstream_gene_variant RECA-EU 19 884954 884954 single base substitution G A exon_variant RECA-EU 19 884954 884954 single base substitution G A intron_variant RECA-EU 19 884954 884954 single base substitution G A missense_variant R168C 502C>T RECA-EU 19 884954 884954 single base substitution G A missense_variant R312C 934C>T RECA-EU 19 884954 884954 single base substitution G A missense_variant R65C 193C>T RECA-EU 19 888904 888904 single base substitution G C downstream_gene_variant RECA-EU 19 888904 888904 single base substitution G C intron_variant RECA-EU 19 888904 888904 single base substitution G C upstream_gene_variant RECA-EU 19 889726 889726 single base substitution C G downstream_gene_variant RECA-EU 19 889726 889726 single base substitution C G exon_variant RECA-EU 19 889726 889726 single base substitution C G intron_variant RECA-EU 19 889726 889726 single base substitution C G missense_variant S120T 359G>C RECA-EU 19 889726 889726 single base substitution C G upstream_gene_variant SKCA-BR 19 864725 864725 single base substitution T G downstream_gene_variant SKCA-BR 19 864889 864889 single base substitution T C downstream_gene_variant SKCA-BR 19 864906 864906 single base substitution G A downstream_gene_variant SKCA-BR 19 866104 866104 single base substitution T G downstream_gene_variant SKCA-BR 19 866923 866923 single base substitution G A downstream_gene_variant SKCA-BR 19 867042 867042 single base substitution G A downstream_gene_variant SKCA-BR 19 867774 867774 single base substitution G A downstream_gene_variant SKCA-BR 19 867872 867872 single base substitution G A downstream_gene_variant SKCA-BR 19 868044 868044 single base substitution G A 3_prime_UTR_variant SKCA-BR 19 872174 872174 single base substitution A G downstream_gene_variant SKCA-BR 19 872174 872174 single base substitution A G intron_variant SKCA-BR 19 876882 876882 single base substitution C A intron_variant SKCA-BR 19 876910 876910 single base substitution C T intron_variant SKCA-BR 19 877277 877305 deletion of <=200bp TCTGTGTGCGCGCACGCCCGTGTGTGGGC - intron_variant SKCA-BR 19 877617 877617 single base substitution G C intron_variant SKCA-BR 19 879399 879399 single base substitution A G intron_variant SKCA-BR 19 879427 879427 single base substitution A G intron_variant SKCA-BR 19 879483 879483 single base substitution G A intron_variant SKCA-BR 19 879534 879534 single base substitution T C intron_variant SKCA-BR 19 879545 879545 single base substitution C T intron_variant SKCA-BR 19 879830 879830 single base substitution A C intron_variant SKCA-BR 19 880201 880201 single base substitution C G intron_variant SKCA-BR 19 881909 881909 single base substitution G A downstream_gene_variant SKCA-BR 19 881909 881909 single base substitution G A intron_variant SKCA-BR 19 882055 882055 single base substitution G A downstream_gene_variant SKCA-BR 19 882055 882055 single base substitution G A intron_variant SKCA-BR 19 883284 883284 single base substitution A G downstream_gene_variant SKCA-BR 19 883284 883284 single base substitution A G intron_variant SKCA-BR 19 888276 888276 single base substitution C T downstream_gene_variant SKCA-BR 19 888276 888276 single base substitution C T intron_variant SKCA-BR 19 888276 888276 single base substitution C T upstream_gene_variant SKCA-BR 19 888854 888854 single base substitution C T downstream_gene_variant SKCA-BR 19 888854 888854 single base substitution C T intron_variant SKCA-BR 19 888854 888854 single base substitution C T upstream_gene_variant SKCA-BR 19 889051 889051 insertion of <=200bp - TC downstream_gene_variant SKCA-BR 19 889051 889051 insertion of <=200bp - TC intron_variant SKCA-BR 19 889051 889051 insertion of <=200bp - TC upstream_gene_variant SKCA-BR 19 890255 890255 single base substitution G A 3_prime_UTR_variant SKCA-BR 19 890255 890255 single base substitution G A downstream_gene_variant SKCA-BR 19 890255 890255 single base substitution G A intron_variant SKCA-BR 19 890255 890255 single base substitution G A upstream_gene_variant SKCA-BR 19 892245 892245 single base substitution A C intron_variant SKCA-BR 19 892245 892245 single base substitution A C upstream_gene_variant SKCA-BR 19 892916 892916 single base substitution C A intron_variant SKCA-BR 19 892916 892916 single base substitution C A upstream_gene_variant SKCA-BR 19 893388 893388 single base substitution G A upstream_gene_variant SKCA-BR 19 893581 893581 single base substitution C A upstream_gene_variant SKCA-BR 19 894748 894748 single base substitution G A upstream_gene_variant SKCA-BR 19 895472 895472 single base substitution G A upstream_gene_variant SKCA-BR 19 895881 895881 single base substitution A C upstream_gene_variant SKCA-BR 19 896265 896265 single base substitution A C upstream_gene_variant SKCM-US 19 868150 868150 single base substitution G A 3_prime_UTR_variant SKCM-US 19 868150 868150 single base substitution G A missense_variant P862L 2585C>T SKCM-US 19 873482 873482 single base substitution G A downstream_gene_variant SKCM-US 19 873482 873482 single base substitution G A exon_variant SKCM-US 19 873482 873482 single base substitution G A synonymous_variant F377F 1131C>T SKCM-US 19 873482 873482 single base substitution G A synonymous_variant F624F 1872C>T SKCM-US 19 873506 873506 single base substitution C T downstream_gene_variant SKCM-US 19 873506 873506 single base substitution C T exon_variant SKCM-US 19 873506 873506 single base substitution C T synonymous_variant Q369Q 1107G>A SKCM-US 19 873506 873506 single base substitution C T synonymous_variant Q616Q 1848G>A SKCM-US 19 875301 875301 single base substitution G A exon_variant SKCM-US 19 875301 875301 single base substitution G A missense_variant P325S 973C>T SKCM-US 19 875301 875301 single base substitution G A missense_variant P428S 1282C>T SKCM-US 19 875301 875301 single base substitution G A missense_variant P503S 1507C>T SKCM-US 19 875301 875301 single base substitution G A missense_variant P572S 1714C>T SKCM-US 19 875447 875447 single base substitution G A exon_variant SKCM-US 19 875447 875447 single base substitution G A intron_variant SKCM-US 19 875447 875447 single base substitution G A missense_variant S276F 827C>T SKCM-US 19 875447 875447 single base substitution G A missense_variant S379F 1136C>T SKCM-US 19 875447 875447 single base substitution G A missense_variant S454F 1361C>T SKCM-US 19 875447 875447 single base substitution G A missense_variant S523F 1568C>T SKCM-US 19 880010 880010 single base substitution G A exon_variant SKCM-US 19 880010 880010 single base substitution G A intron_variant SKCM-US 19 880010 880010 single base substitution G A missense_variant P180L 539C>T SKCM-US 19 880010 880010 single base substitution G A missense_variant P283L 848C>T SKCM-US 19 880010 880010 single base substitution G A missense_variant P427L 1280C>T SKCM-US 19 885838 885838 single base substitution G A 3_prime_UTR_variant SKCM-US 19 885838 885838 single base substitution G A exon_variant SKCM-US 19 885838 885838 single base substitution G A intron_variant SKCM-US 19 885838 885838 single base substitution G A missense_variant L24F 70C>T SKCM-US 19 885838 885838 single base substitution G A missense_variant L271F 811C>T SKCM-US 19 886159 886159 single base substitution A G 3_prime_UTR_variant SKCM-US 19 886159 886159 single base substitution A G downstream_gene_variant SKCM-US 19 886159 886159 single base substitution A G exon_variant SKCM-US 19 886159 886159 single base substitution A G intron_variant SKCM-US 19 886159 886159 single base substitution A G missense_variant F164L 490T>C SKCM-US 19 886159 886159 single base substitution A G upstream_gene_variant STAD-US 19 871999 871999 single base substitution C T 3_prime_UTR_variant STAD-US 19 871999 871999 single base substitution C T downstream_gene_variant STAD-US 19 871999 871999 single base substitution C T intron_variant STAD-US 19 871999 871999 single base substitution C T synonymous_variant V675V 2025G>A STAD-US 19 872114 872114 single base substitution G A 3_prime_UTR_variant STAD-US 19 872114 872114 single base substitution G A downstream_gene_variant STAD-US 19 872114 872114 single base substitution G A intron_variant STAD-US 19 872114 872114 single base substitution G A missense_variant S637F 1910C>T STAD-US 19 873537 873537 single base substitution A C exon_variant STAD-US 19 873537 873537 single base substitution A C missense_variant L359R 1076T>G STAD-US 19 873537 873537 single base substitution A C missense_variant L462R 1385T>G STAD-US 19 873537 873537 single base substitution A C missense_variant L537R 1610T>G STAD-US 19 873537 873537 single base substitution A C missense_variant L606R 1817T>G STAD-US 19 873579 873579 single base substitution A G exon_variant STAD-US 19 873579 873579 single base substitution A G missense_variant I345T 1034T>C STAD-US 19 873579 873579 single base substitution A G missense_variant I448T 1343T>C STAD-US 19 873579 873579 single base substitution A G missense_variant I523T 1568T>C STAD-US 19 873579 873579 single base substitution A G missense_variant I592T 1775T>C STAD-US 19 876999 876999 single base substitution G A exon_variant STAD-US 19 876999 876999 single base substitution G A intron_variant STAD-US 19 876999 876999 single base substitution G A missense_variant T265M 794C>T STAD-US 19 876999 876999 single base substitution G A missense_variant T368M 1103C>T STAD-US 19 876999 876999 single base substitution G A missense_variant T512M 1535C>T STAD-US 19 877065 877065 single base substitution T G exon_variant STAD-US 19 877065 877065 single base substitution T G intron_variant STAD-US 19 877065 877065 single base substitution T G missense_variant D243A 728A>C STAD-US 19 877065 877065 single base substitution T G missense_variant D346A 1037A>C STAD-US 19 877065 877065 single base substitution T G missense_variant D490A 1469A>C STAD-US 19 877145 877145 single base substitution G A exon_variant STAD-US 19 877145 877145 single base substitution G A intron_variant STAD-US 19 877145 877145 single base substitution G A synonymous_variant H216H 648C>T STAD-US 19 877145 877145 single base substitution G A synonymous_variant H319H 957C>T STAD-US 19 877145 877145 single base substitution G A synonymous_variant H463H 1389C>T STAD-US 19 879980 879980 single base substitution G A exon_variant STAD-US 19 879980 879980 single base substitution G A intron_variant STAD-US 19 879980 879980 single base substitution G A missense_variant S190L 569C>T STAD-US 19 879980 879980 single base substitution G A missense_variant S293L 878C>T STAD-US 19 879980 879980 single base substitution G A missense_variant S437L 1310C>T STAD-US 19 881601 881601 single base substitution C T downstream_gene_variant STAD-US 19 881601 881601 single base substitution C T exon_variant STAD-US 19 881601 881601 single base substitution C T intron_variant STAD-US 19 881601 881601 single base substitution C T missense_variant D120N 358G>A STAD-US 19 881601 881601 single base substitution C T missense_variant D223N 667G>A STAD-US 19 881601 881601 single base substitution C T missense_variant D367N 1099G>A STAD-US 19 881679 881679 single base substitution T G downstream_gene_variant STAD-US 19 881679 881679 single base substitution T G exon_variant STAD-US 19 881679 881679 single base substitution T G intron_variant STAD-US 19 881679 881679 single base substitution T G missense_variant I197L 589A>C STAD-US 19 881679 881679 single base substitution T G missense_variant I341L 1021A>C STAD-US 19 881679 881679 single base substitution T G missense_variant I94L 280A>C STAD-US 19 886015 886015 single base substitution G A 3_prime_UTR_variant STAD-US 19 886015 886015 single base substitution G A downstream_gene_variant STAD-US 19 886015 886015 single base substitution G A exon_variant STAD-US 19 886015 886015 single base substitution G A intron_variant STAD-US 19 886015 886015 single base substitution G A missense_variant R212C 634C>T STAD-US 19 886015 886015 single base substitution G A upstream_gene_variant STAD-US 19 889762 889762 single base substitution C T downstream_gene_variant STAD-US 19 889762 889762 single base substitution C T exon_variant STAD-US 19 889762 889762 single base substitution C T intron_variant STAD-US 19 889762 889762 single base substitution C T stop_gained W108* 323G>A STAD-US 19 889762 889762 single base substitution C T upstream_gene_variant THCA-SA 19 863356 863356 single base substitution C T downstream_gene_variant THCA-SA 19 872116 872116 insertion of <=200bp - C downstream_gene_variant THCA-SA 19 872116 872116 insertion of <=200bp - C frameshift_variant G636G? THCA-SA 19 872116 872116 insertion of <=200bp - C intron_variant THCA-SA 19 872116 872116 insertion of <=200bp - C splice_region_variant THCA-SA 19 880066 880066 single base substitution G A exon_variant THCA-SA 19 880066 880066 single base substitution G A intron_variant THCA-SA 19 880066 880066 single base substitution G A synonymous_variant S161S 483C>T THCA-SA 19 880066 880066 single base substitution G A synonymous_variant S264S 792C>T THCA-SA 19 880066 880066 single base substitution G A synonymous_variant S408S 1224C>T THCA-US 19 889754 889754 single base substitution C T downstream_gene_variant THCA-US 19 889754 889754 single base substitution C T exon_variant THCA-US 19 889754 889754 single base substitution C T intron_variant THCA-US 19 889754 889754 single base substitution C T missense_variant A111T 331G>A THCA-US 19 889754 889754 single base substitution C T upstream_gene_variant UCEC-US 19 868892 868892 single base substitution G A 3_prime_UTR_variant UCEC-US 19 868892 868892 single base substitution G A downstream_gene_variant UCEC-US 19 868892 868892 single base substitution G A missense_variant A479V 1436C>T UCEC-US 19 868892 868892 single base substitution G A missense_variant A726V 2177C>T UCEC-US 19 868892 868892 single base substitution G A synonymous_variant C790C 2370C>T UCEC-US 19 868892 868892 single base substitution G A synonymous_variant C809C 2427C>T UCEC-US 19 873487 873514 deletion of <=200bp CGCCCACCCACTGCAAGAGCTGCTGCAG - downstream_gene_variant UCEC-US 19 873487 873514 deletion of <=200bp CGCCCACCCACTGCAAGAGCTGCTGCAG - exon_variant UCEC-US 19 873487 873514 deletion of <=200bp CGCCCACCCACTGCAAGAGCTGCTGCAG - frameshift_variant LQQLLQWVGD367 UCEC-US 19 873487 873514 deletion of <=200bp CGCCCACCCACTGCAAGAGCTGCTGCAG - frameshift_variant LQQLLQWVGD614 UCEC-US 19 875396 875396 single base substitution G A exon_variant UCEC-US 19 875396 875396 single base substitution G A intron_variant UCEC-US 19 875396 875396 single base substitution G A missense_variant T293M 878C>T UCEC-US 19 875396 875396 single base substitution G A missense_variant T396M 1187C>T UCEC-US 19 875396 875396 single base substitution G A missense_variant T471M 1412C>T UCEC-US 19 875396 875396 single base substitution G A missense_variant T540M 1619C>T UCEC-US 19 885852 885852 single base substitution C T 3_prime_UTR_variant UCEC-US 19 885852 885852 single base substitution C T exon_variant UCEC-US 19 885852 885852 single base substitution C T intron_variant UCEC-US 19 885852 885852 single base substitution C T missense_variant R19H 56G>A UCEC-US 19 885852 885852 single base substitution C T missense_variant R266H 797G>A UCEC-US 19 893586 893588 deletion of <=200bp TTT - upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-GC-A3RB-01 COSM1305337 c.637G>A p.V213M Substitution - Missense 19:886012-886012 - 12T COSM3713104 c.1521G>T p.L507L Substitution - coding silent 19:877013-877013 - ZZUFHECRKL-G057T COSM3757449 c.831T>C p.F277F Substitution - coding silent 19:885818-885818 - 49M COSM5591828 c.765C>T p.I255I Substitution - coding silent 19:885884-885884 - TCGA-G4-6586-01 COSM1397763 c.136G>A p.A46T Substitution - Missense 19:890996-890996 - PTC-6C COSM715596 c.1343G>A p.S448N Substitution - Missense 19:879947-879947 - YURAY COSM5391232 c.816C>T p.N272N Substitution - coding silent 19:885833-885833 - 4_RESISTANT COSM1724576 c.1736_1740delGGCTG p.R579fs*13 Deletion - Frameshift 19:875275-875279 - TCGA-FD-A3SN-01 COSM3797721 c.1535C>A p.T512K Substitution - Missense 19:876999-876999 - CSCC-49-T COSM4458548 c.108C>T p.A36A Substitution - coding silent 19:891024-891024 - RMS1_ COSM4985603 c.700A>G p.S234G Substitution - Missense 19:885949-885949 - DLD1 COSM4624178 c.641C>T p.A214V Substitution - Missense 19:886008-886008 - LAU165 COSM233996 c.880-8C>T p.? Unknown 19:885016-885016 - G6 COSM1192036 c.1768_1771+1delGTCGG p.? Unknown 19:875243-875247 - Pat_65_A COSM5857177 c.304G>A p.D102N Substitution - Missense 19:889781-889781 - sysucc-274T COSM5476139 c.157A>G p.S53G Substitution - Missense 19:890975-890975 - B22 COSM1745104 c.1546_1550delGCTGC p.A516fs*56 Deletion - Frameshift 19:876984-876988 - CHC892T COSM4797841 c.2484-1G>A p.? Unknown 19:868252-868252 - HDC54 COSM4636379 c.2245C>T p.R749C Substitution - Missense 19:871107-871107 - TCGA-DB-A64X-01 COSM715596 c.1343G>A p.S448N Substitution - Missense 19:879947-879947 - T3080 COSM4701496 c.706G>A p.A236T Substitution - Missense 19:885943-885943 - STC232 COSM5057108 c.283C>T p.R95W Substitution - Missense 19:889802-889802 - YUROG COSM5391234 c.678C>T p.I226I Substitution - coding silent 19:885971-885971 - PD18751a COSM5774078 c.1183C>T p.H395Y Substitution - Missense 19:880107-880107 - TCGA-D7-6525-01 COSM4083099 c.1910C>T p.S637F Substitution - Missense 19:872114-872114 - TCGA-AA-3662-01 COSM3757445 c.2130C>T p.D710D Substitution - coding silent 19:871222-871222 - CN-AML-CR-20-Dx COSM440702 c.1224C>T p.S408S Substitution - coding silent 19:880066-880066 - CH-54-T2 COSM5651056 c.12G>A p.L4L Substitution - coding silent 19:891120-891120 - S02342 COSM5692696 c.95C>T p.S32L Substitution - Missense 19:891037-891037 - 587338 COSM1214839 c.1366C>A p.R456S Substitution - Missense 19:877168-877168 - 1_PRE-TREATMENT COSM1719484 c.1613C>T p.P538L Substitution - Missense 19:875402-875402 - TCGA-AZ-6603-01 COSM3757445 c.2130C>T p.D710D Substitution - coding silent 19:871222-871222 - C008 COSM5523101 c.930C>T p.S310S Substitution - coding silent 19:884958-884958 - TCGA-B5-A11E-01 COSM1003608 c.2370C>T p.C790C Substitution - coding silent 19:868892-868892 - CSCC-31-T COSM4485136 c.289C>T p.L97L Substitution - coding silent 19:889796-889796 - ME037T COSM227914 c.1763C>T p.T588I Substitution - Missense 19:875252-875252 - Pat_24_A COSM4701496 c.706G>A p.A236T Substitution - Missense 19:885943-885943 - TCGA-23-2649-01 COSM1326083 c.2257G>C p.G753R Substitution - Missense 19:871095-871095 - 8053106 COSM4389615 c.2469G>A p.W823* Substitution - Nonsense 19:868430-868430 - TCGA-DA-A3F8-06 COSM1711555 c.1568C>T p.S523F Substitution - Missense 19:875447-875447 - ESCC_167 COSM5648601 c.1574G>T p.R525L Substitution - Missense 19:875441-875441 - sysucc-880T COSM5462934 c.690G>A p.T230T Substitution - coding silent 19:885959-885959 - YUKAT COSM5391219 c.2560G>A p.G854S Substitution - Missense 19:868175-868175 - S02351 COSM5695083 c.517G>C p.G173R Substitution - Missense 19:886132-886132 - Pat_06_B COSM5857173 c.1373C>G p.S458* Substitution - Nonsense 19:877161-877161 - 2492703 COSM5599911 c.2483+6G>A p.? Unknown 19:868410-868410 - LUAD-RT-S01699 COSM378250 c.1410G>A p.A470A Substitution - coding silent 19:877124-877124 - T613 COSM4701494 c.818G>A p.R273H Substitution - Missense 19:885831-885831 - CSCC-29-T COSM4456847 c.1024C>T p.L342L Substitution - coding silent 19:881676-881676 - PTC-53C COSM3773927 c.2037C>T p.T679T Substitution - coding silent 19:871987-871987 - PTC-7C COSM4132816 c.1626C>T p.T542T Substitution - coding silent 19:875389-875389 - PTC-28C COSM440701 c.2217T>C p.V739V Substitution - coding silent 19:871135-871135 - CSCC-31-T COSM4466316 c.1428C>T p.F476F Substitution - coding silent 19:877106-877106 - TCGA-CG-4441-01 COSM4083111 c.1310C>T p.S437L Substitution - Missense 19:879980-879980 - TCGA-34-5240-01 COSM715597 c.1595C>T p.S532L Substitution - Missense 19:875420-875420 - TCGA-EE-A2MG-06 COSM3541715 c.1848G>A p.Q616Q Substitution - coding silent 19:873506-873506 - PTC-53C COSM715596 c.1343G>A p.S448N Substitution - Missense 19:879947-879947 - TCGA-ES-A2HT-01 COSM4938614 c.155G>A p.R52H Substitution - Missense 19:890977-890977 - DLD1 COSM4624180 c.400C>A p.L134M Substitution - Missense 19:889685-889685 - TCGA-CG-5721-01 COSM4083124 c.1021A>C p.I341L Substitution - Missense 19:881679-881679 - YUSIM COSM5391220 c.1676C>T p.T559I Substitution - Missense 19:875339-875339 - RKO COSM2730750 c.502C>T p.L168F Substitution - Missense 19:886147-886147 - TCGA-FS-A1ZZ-06 COSM3541761 c.811C>T p.L271F Substitution - Missense 19:885838-885838 - CSCC-55-T COSM4492915 c.405C>T p.S135S Substitution - coding silent 19:889680-889680 - 1_RESISTANT COSM1719484 c.1613C>T p.P538L Substitution - Missense 19:875402-875402 - PTC-50C COSM4132819 c.1335G>C p.G445G Substitution - coding silent 19:879955-879955 - AML_14y_07_DX COSM1613119 c.1353+2T>C p.? Unknown 19:879935-879935 - TCGA-HU-A4GQ-01 COSM2730744 c.634C>T p.R212C Substitution - Missense 19:886015-886015 - B66-Tumor COSM1751276 c.64G>A p.E22K Substitution - Missense 19:891068-891068 - HCC105T COSM1613120 c.1326C>G p.A442A Substitution - coding silent 19:879964-879964 - CCK81 COSM2730755 c.125G>A p.R42Q Substitution - Missense 19:891007-891007 - 477 COSM4438754 c.315C>T p.I105I Substitution - coding silent 19:889770-889770 - J30_T COSM3960734 c.878A>T p.Q293L Substitution - Missense 19:885771-885771 - T3118 COSM4701502 c.454G>A p.A152T Substitution - Missense 19:886195-886195 - TCGA-AO-A0J6-01 COSM440706 c.915C>G p.I305M Substitution - Missense 19:884973-884973 - PTC-53C COSM4132821 c.1325C>G p.A442G Substitution - Missense 19:879965-879965 - TCGA-BR-8487-01 COSM4083105 c.1535C>T p.T512M Substitution - Missense 19:876999-876999 - I2L-P19Tb-Tumor-Organoid COSM5365196 c.303C>T p.A101A Substitution - coding silent 19:889782-889782 - pfg008T COSM1214840 c.2099-1G>T p.? Unknown 19:871254-871254 - PR-00-1165 COSM245646 c.1771G>A p.D591N Substitution - Missense 19:875244-875244 - TCGA-FW-A3R5-06 COSM3541713 c.2585C>T p.P862L Substitution - Missense 19:868150-868150 - RMS80_ COSM4988641 c.2239C>T p.P747S Substitution - Missense 19:871113-871113 - SC_9022 COSM5566731 c.2334G>A p.K778K Substitution - coding silent 19:868928-868928 - 5_PRE-TREATMENT COSM1724576 c.1736_1740delGGCTG p.R579fs*13 Deletion - Frameshift 19:875275-875279 - TCGA-AA-3712-01 COSM3757445 c.2130C>T p.D710D Substitution - coding silent 19:871222-871222 - 2492709 COSM5718452 c.1173C>T p.V391V Substitution - coding silent 19:880117-880117 - ATL065 COSM5707325 c.497C>A p.P166Q Substitution - Missense 19:886152-886152 - CHC892T COSM4797841 c.2484-1G>A p.? Unknown 19:868252-868252 - PD4199a COSM5794551 c.1599C>G p.L533L Substitution - coding silent 19:875416-875416 - PTC-53C COSM440701 c.2217T>C p.V739V Substitution - coding silent 19:871135-871135 - 61 COSM5741314 c.1415G>A p.R472Q Substitution - Missense 19:877119-877119 - TCGA-18-3408-01 COSM715596 c.1343G>A p.S448N Substitution - Missense 19:879947-879947 - TCGA-AM-5820-01 COSM3757445 c.2130C>T p.D710D Substitution - coding silent 19:871222-871222 - HCC108T COSM1613119 c.1353+2T>C p.? Unknown 19:879935-879935 - 2217534 COSM4421723 c.1729G>A p.G577S Substitution - Missense 19:875286-875286 - T55 COSM4701498 c.670G>A p.G224S Substitution - Missense 19:885979-885979 - TCGA-H4-A2HQ-01 COSM362767 c.1685C>T p.S562L Substitution - Missense 19:875330-875330 - LUAD-S01482 COSM392577 c.1632_1639delGTGCGACT p.C545fs*26 Deletion - Frameshift 19:875376-875383 - I2L-P19Tb-Tumor-Biopsy COSM5365196 c.303C>T p.A101A Substitution - coding silent 19:889782-889782 - BD124T COSM5493747 c.635G>A p.R212H Substitution - Missense 19:886014-886014 - TCGA-32-5222-01 COSM3404815 c.2565G>A p.P855P Substitution - coding silent 19:868170-868170 - CSCC-7-T COSM4531584 c.1803G>A p.T601T Substitution - coding silent 19:873551-873551 - TCGA-EK-A2PG-01 COSM4819524 c.1936C>T p.L646L Substitution - coding silent 19:872088-872088 - TCGA-G4-6298-01 COSM3693254 c.2181C>T p.P727P Substitution - coding silent 19:871171-871171 - 2497767 COSM5750093 c.1719C>G p.D573E Substitution - Missense 19:875296-875296 - S02277 COSM5683166 c.1339G>C p.D447H Substitution - Missense 19:879951-879951 - B66 COSM1751276 c.64G>A p.E22K Substitution - Missense 19:891068-891068 - 2492702 COSM5599911 c.2483+6G>A p.? Unknown 19:868410-868410 - 43 COSM5734093 c.862C>T p.R288W Substitution - Missense 19:885787-885787 - 9583_CLM COSM2730647 c.2441C>T p.T814M Substitution - Missense 19:868458-868458 - HCT15 COSM4624178 c.641C>T p.A214V Substitution - Missense 19:886008-886008 - TCGA-G4-6298-01 COSM440701 c.2217T>C p.V739V Substitution - coding silent 19:871135-871135 - TCGA-CK-5914-01 COSM1397762 c.244G>A p.E82K Substitution - Missense 19:890170-890170 - TCGA-BR-6566-01 COSM4083109 c.1389C>T p.H463H Substitution - coding silent 19:877145-877145 - TCGA-AU-6004-01 COSM1397756 c.736G>A p.V246M Substitution - Missense 19:885913-885913 - SMS-CTR COSM4989511 c.1736G>T p.R579L Substitution - Missense 19:875279-875279 - HCC61T COSM1613118 c.1672T>C p.S558P Substitution - Missense 19:875343-875343 - TCGA-AA-3713-01 COSM1397755 c.952delG p.V318fs*1 Deletion - Frameshift 19:884936-884936 - PCSI_0594_Pa_P_526 COSM5761110 c.1364T>G p.L455R Substitution - Missense 19:877170-877170 - OSCC-GB_00120111 COSM3713104 c.1521G>T p.L507L Substitution - coding silent 19:877013-877013 - ESCC_46 COSM4132825 c.30T>G p.G10G Substitution - coding silent 19:891102-891102 - TCGA-BS-A0UF-01 COSM1003609 c.1840_1867del28 p.L614fs*17 Deletion - Frameshift 19:873487-873514 - T3021 COSM4701492 c.1306C>A p.L436I Substitution - Missense 19:879984-879984 - 8014573 COSM3389529 c.214G>T p.D72Y Substitution - Missense 19:890200-890200 - TCGA-CH-5752-01 COSM1129668 c.1024C>A p.L342I Substitution - Missense 19:881676-881676 - TCGA-DG-A2KL-01 COSM4851527 c.1327C>T p.L443L Substitution - coding silent 19:879963-879963 - AOCS-093-1-9 COSM4128020 c.452G>A p.G151D Substitution - Missense 19:886197-886197 - EGC3 COSM5057107 c.2627G>A p.R876H Substitution - Missense 19:868108-868108 - YURAY COSM5391230 c.915C>T p.I305I Substitution - coding silent 19:884973-884973 - CHC326T COSM4806030 c.847C>A p.L283I Substitution - Missense 19:885802-885802 - TCGA-AM-5820-01 COSM3757447 c.1935T>C p.F645F Substitution - coding silent 19:872089-872089 - PTC-7C COSM3757449 c.831T>C p.F277F Substitution - coding silent 19:885818-885818 - A5 COSM568941 c.1560+7G>C p.? Unknown 19:876967-876967 - T3024 COSM4701490 c.1324G>A p.A442T Substitution - Missense 19:879966-879966 - TCGA-F4-6703-01 COSM440701 c.2217T>C p.V739V Substitution - coding silent 19:871135-871135 - PTC-6C COSM1397753 c.1347C>G p.H449Q Substitution - Missense 19:879943-879943 - LUAD-D00147 COSM362767 c.1685C>T p.S562L Substitution - Missense 19:875330-875330 - S02294 COSM5688792 c.1236G>T p.R412S Substitution - Missense 19:880054-880054 - TCGA-CG-5721-01 COSM4083122 c.1099G>A p.D367N Substitution - Missense 19:881601-881601 - TCGA-DM-A1D0-01 COSM1397757 c.705C>G p.S235R Substitution - Missense 19:885944-885944 - TCGA-CG-4442-01 COSM4083133 c.323G>A p.W108* Substitution - Nonsense 19:889762-889762 - LIM2405 COSM4642403 c.2603T>C p.L868P Substitution - Missense 19:868132-868132 - T578 COSM4701500 c.465C>T p.F155F Substitution - coding silent 19:886184-886184 - TCGA-D1-A17Q-01 COSM1003623 c.797G>A p.R266H Substitution - Missense 19:885852-885852 - CT-TC COSM4989511 c.1736G>T p.R579L Substitution - Missense 19:875279-875279 - PD14441a COSM5767800 c.1772-1G>C p.? Unknown 19:873583-873583 - PTC_285 COSM5958961 c.1907_1908insG p.S637fs*67 Insertion - Frameshift 19:872116-872117 - TCGA-CJ-4892-01 COSM3773927 c.2037C>T p.T679T Substitution - coding silent 19:871987-871987 - TCGA-DR-A0ZM-01 COSM459812 c.1104C>G p.L368L Substitution - coding silent 19:881596-881596 - 2492701 COSM5599911 c.2483+6G>A p.? Unknown 19:868410-868410 - PTC-7C COSM3773927 c.2037C>T p.T679T Substitution - coding silent 19:871987-871987 - 46M COSM5391234 c.678C>T p.I226I Substitution - coding silent 19:885971-885971 - 5_RESISTANT COSM1724576 c.1736_1740delGGCTG p.R579fs*13 Deletion - Frameshift 19:875275-875279 - LIM2405 COSM4642404 c.2572A>G p.T858A Substitution - Missense 19:868163-868163 - T4 COSM4132816 c.1626C>T p.T542T Substitution - coding silent 19:875389-875389 - TCGA-E9-A1R2-01 COSM1481692 c.1720_1721delAA p.K574fs*19 Deletion - Frameshift 19:875294-875295 - Pat_15_B COSM5057108 c.283C>T p.R95W Substitution - Missense 19:889802-889802 - 1517_PT COSM5755530 c.2346G>A p.L782L Substitution - coding silent 19:868916-868916 - TCGA-DJ-A1QE-01 COSM3371569 c.331G>A p.A111T Substitution - Missense 19:889754-889754 - SCMC_RM2_ COSM4989151 c.247G>A p.A83T Substitution - Missense 19:890167-890167 - HN_00443 COSM121180 c.576G>A p.L192L Substitution - coding silent 19:886073-886073 - ESO-0059 COSM1257568 c.2631G>A p.P877P Substitution - coding silent 19:868104-868104 - S02289 COSM5686047 c.2143G>A p.D715N Substitution - Missense 19:871209-871209 - TCGA-BR-A4QL-01 COSM4083097 c.2025G>A p.V675V Substitution - coding silent 19:871999-871999 - J90_T COSM2730655 c.1872C>T p.F624F Substitution - coding silent 19:873482-873482 - HCC20T COSM1613121 c.1147G>T p.A383S Substitution - Missense 19:880143-880143 - Pat_01_A COSM715597 c.1595C>T p.S532L Substitution - Missense 19:875420-875420 - C0065T COSM4154431 c.359G>C p.S120T Substitution - Missense 19:889726-889726 - S02277 COSM5683168 c.1243G>T p.D415Y Substitution - Missense 19:880047-880047 - C0088T COSM4154429 c.934C>T p.R312C Substitution - Missense 19:884954-884954 - 40M COSM5585761 c.1058C>T p.A353V Substitution - Missense 19:881642-881642 - S02246 COSM5678967 c.1959C>T p.G653G Substitution - coding silent 19:872065-872065 - CHC326T COSM4806030 c.847C>A p.L283I Substitution - Missense 19:885802-885802 - TCGA-AM-5820-01 COSM3693253 c.2499T>C p.R833R Substitution - coding silent 19:868236-868236 - HCT15 COSM4624180 c.400C>A p.L134M Substitution - Missense 19:889685-889685 - 2492708 COSM5718452 c.1173C>T p.V391V Substitution - coding silent 19:880117-880117 - TCGA-DD-A39X-01 COSM4940806 c.1886T>C p.L629P Substitution - Missense 19:873468-873468 - BN38 COSM3707549 c.1628G>A p.R543H Substitution - Missense 19:875387-875387 - PTC-1C COSM4132819 c.1335G>C p.G445G Substitution - coding silent 19:879955-879955 - BK0095 COSM715596 c.1343G>A p.S448N Substitution - Missense 19:879947-879947 - TCGA-A3-3316-01 COSM1494548 c.2403C>T p.C801C Substitution - coding silent 19:868496-868496 - TCGA-AO-A03M-01 COSM3836211 c.36G>A p.M12I Substitution - Missense 19:891096-891096 - CSB19 COSM5028448 c.1697C>A p.P566H Substitution - Missense 19:875318-875318 - YUKLAB COSM1711557 c.903G>C p.Q301H Substitution - Missense 19:884985-884985 - 2492710 COSM5718452 c.1173C>T p.V391V Substitution - coding silent 19:880117-880117 - TCGA-CZ-5986-01 COSM475518 c.896C>T p.S299F Substitution - Missense 19:884992-884992 - PTC-50C COSM4132821 c.1325C>G p.A442G Substitution - Missense 19:879965-879965 - SC_9034 COSM5567767 c.702C>T p.S234S Substitution - coding silent 19:885947-885947 - TCGA-GN-A266-06 COSM3541720 c.1280C>T p.P427L Substitution - Missense 19:880010-880010 - TCGA-G2-A2ES-01 COSM1305335 c.1966C>A p.R656R Substitution - coding silent 19:872058-872058 - S02120 COSM2730676 c.1260G>A p.K420K Substitution - coding silent 19:880030-880030 - TCGA-EE-A180-06 COSM3541717 c.1714C>T p.P572S Substitution - Missense 19:875301-875301 - TCGA-EB-A430-01 COSM3541763 c.490T>C p.F164L Substitution - Missense 19:886159-886159 - sysucc-1135T COSM568941 c.1560+7G>C p.? Unknown 19:876967-876967 - TCGA-BR-4256-01 COSM4083103 c.1775T>C p.I592T Substitution - Missense 19:873579-873579 - PTC-46C COSM4132825 c.30T>G p.G10G Substitution - coding silent 19:891102-891102 - BN28T COSM1613117 c.2168A>T p.Q723L Substitution - Missense 19:871184-871184 - TCGA-AM-5820-01 COSM3757449 c.831T>C p.F277F Substitution - coding silent 19:885818-885818 - Au2 COSM5599911 c.2483+6G>A p.? Unknown 19:868410-868410 - 2492700 COSM5599911 c.2483+6G>A p.? Unknown 19:868410-868410 - TCGA-60-2698-01 COSM715598 c.1653C>G p.L551L Substitution - coding silent 19:875362-875362 - BN38T COSM3707549 c.1628G>A p.R543H Substitution - Missense 19:875387-875387 - TCGA-AA-3697-01 COSM3757445 c.2130C>T p.D710D Substitution - coding silent 19:871222-871222 - OSCC-GB_00920111 COSM4881776 c.2483+1G>T p.? Unknown 19:868415-868415 - 462 COSM4436822 c.1368C>T p.R456R Substitution - coding silent 19:877166-877166 - 2290930 COSM4440582 c.1697C>T p.P566L Substitution - Missense 19:875318-875318 - HSJD_DIPG002 COSM715596 c.1343G>A p.S448N Substitution - Missense 19:879947-879947 - YUGAFFE COSM1711555 c.1568C>T p.S523F Substitution - Missense 19:875447-875447 - TCGA-EE-A3J5-06 COSM3541713 c.2585C>T p.P862L Substitution - Missense 19:868150-868150 - 587342 COSM1214840 c.2099-1G>T p.? Unknown 19:871254-871254 - ESO-752 COSM1257569 c.1136G>C p.G379A Substitution - Missense 19:881564-881564 - YURAY COSM5391222 c.1578C>T p.I526I Substitution - coding silent 19:875437-875437 - CADO-ES1 COSM2730647 c.2441C>T p.T814M Substitution - Missense 19:868458-868458 - TCGA-43-3394-01 COSM715601 c.1941G>T p.R647R Substitution - coding silent 19:872083-872083 - TCGA-CG-5723-01 COSM4083107 c.1469A>C p.D490A Substitution - Missense 19:877065-877065 - PTC-7C COSM715596 c.1343G>A p.S448N Substitution - Missense 19:879947-879947 - 234 COSM3731232 c.1030G>A p.A344T Substitution - Missense 19:881670-881670 - ccRCC-61 COSM1662737 c.2434A>T p.R812* Substitution - Nonsense 19:868465-868465 - sysucc-1247T COSM5764547 c.796C>T p.R266C Substitution - Missense 19:885853-885853 - TCGA-EE-A29E-06 COSM2730655 c.1872C>T p.F624F Substitution - coding silent 19:873482-873482 - PA285 COSM1163209 c.1505G>A p.S502N Substitution - Missense 19:877029-877029 - TCGA-HU-A4H3-01 COSM4083101 c.1817T>G p.L606R Substitution - Missense 19:873537-873537 - YUZINO COSM1711556 c.1097C>T p.T366I Substitution - Missense 19:881603-881603 - TCGA-D1-A168-01 COSM1003610 c.1619C>T p.T540M Substitution - Missense 19:875396-875396 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.365163;Hs.365177;Hs.365207 19p13.3 604062 2421113|CGAP|BC004554|A/G|non-coding||2915|Validated; 2421113|CGAP|BC011841|A/G|non-coding||2915|Validated; 2421113|CGAP|BC017282|A/G|non-coding||2966|Validated; 2421116|CGAP|BC004554|C/T|coding|Ala83Ala|380|Validated; 2421116|CGAP|BC011841|C/T|coding|Ala83Ala|380|Validated; 2421116|CGAP|BC017282|C/T|coding|Ala83Ala|374|Validated; 2421119|CGAP|BC004554|C/T|coding|Phe277Phe|962|Validated; 2421119|CGAP|BC011841|C/T|coding|Phe277Phe|962|Validated; 2421119|CGAP|BC017282|C/T|coding|Phe277Phe|956|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.I592T c.1775T>C 19 873579 STAD C A Missense p.A371S c.1111G>T 19 881589 LUAD C A Missense p.M654I c.1962G>T 19 872062 CM C A Synonymous p.R647R c.1941G>T 19 872083 LUSC C G Missense p.G379A c.1136G>C 19 881564 ESCA C G Missense p.W620C c.1860G>C 19 873494 HNSC C T CdsStopSNV . c.2631G>A 19 868104 ESCA C T Missense p.A111T c.331G>A 19 889754 THCA C T Missense p.D256N c.766G>A 19 885883 HNSC C T Missense p.G649D c.1946G>A 19 872078 LUAD C T Missense p.V162I c.484G>A 19 886165 LUAD C T Missense p.V213M c.637G>A 19 886012 BLCA C T Synonymous p.L192L c.576G>A 19 886073 HNSC C T Synonymous p.P855P c.2565G>A 19 868170 GBM C T Synonymous p.Q616Q c.1848G>A 19 873506 CM G A Missense p.L271F c.811C>T 19 885838 CM G A Missense p.P464S c.1390C>T 19 877144 CM G A Missense p.P572S c.1714C>T 19 875301 CM G A Missense p.P862L c.2585C>T 19 868150 CM G A Missense p.S299F c.896C>T 19 884992 RCCC G A Missense p.S437L c.1310C>T 19 879980 STAD G A Missense p.S523F c.1568C>T 19 875447 CM G A Missense p.S532L c.1595C>T 19 875420 LUSC G A Missense p.S562L c.1685C>T 19 875330 BLCA G A Missense p.S637F c.1910C>T 19 872114 STAD G A Missense p.T540M c.1619C>T 19 875396 UCEC G A Missense p.T588I c.1763C>T 19 875252 CM GCCCCAGCCCCACGT - IntronicDeletion . c.1354-1335_1354-1321delACGTGGGGCTGGGGC 19 878501 CM G C Missense p.I305M c.915C>G 19 884973 BRCA G C Synonymous p.V595V c.1785C>G 19 873569 HNSC GG AA Missense p.H392Y c.1173_1174delinsTT 19 880116 CM GG AA Missense p.H860Y c.2577_2578delinsTT 19 868157 CM G T Missense p.L342I c.1024C>A 19 881676 PRAD G T Missense p.P566H c.1697C>A 19 875318 BRCA G T Synonymous p.R656R c.1966C>A 19 872058 BLCA G T Synonymous p.T366T c.1098C>A 19 881602 STAD T C Synonymous p.K332K c.996A>G 19 881704 LUAD TT - Frameshift p.K574Efs*19 c.1720_1721delAA 19 875294 BRCA