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 9 26905570 26905570 + Missense_Mutation SNP G G A TCGA-FD-A43P-01A-31D-A23U-08 TCGA-FD-A43P-10A-01D-A23U-08 g.chr9:26905570G>A c.2327C>T c.(2326-2328)tCc>tTc p.S776F BLCA 9 26905860 26905860 + Missense_Mutation SNP C C G TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr9:26905860C>G c.2037G>C c.(2035-2037)caG>caC p.Q679H BLCA 9 26920233 26920233 + Nonsense_Mutation SNP C C A TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr9:26920233C>A c.1189G>T c.(1189-1191)Gaa>Taa p.E397* BLCA 9 26935120 26935120 + Silent SNP G G A TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chr9:26935120G>A c.234C>T c.(232-234)gaC>gaT p.D78D BRCA 9 26905603 26905603 + Missense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr9:26905603G>C c.2294C>G c.(2293-2295)tCt>tGt p.S765C BRCA 9 26907965 26907965 + Frame_Shift_Del DEL A A - TCGA-E2-A1II-01A-11D-A142-09 TCGA-E2-A1II-10A-01D-A142-09 g.chr9:26907965delA c.1689delT c.(1687-1689)cctfs p.P563fs BRCA 9 26917106 26917106 + Missense_Mutation SNP T T C TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr9:26917106T>C c.1475A>G c.(1474-1476)gAt>gGt p.D492G COAD 9 26905911 26905911 + Silent SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:26905911A>C c.1986T>G c.(1984-1986)acT>acG p.T662T COAD 9 26907897 26907897 + Missense_Mutation SNP C C G TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr9:26907897C>G c.1757G>C c.(1756-1758)aGt>aCt p.S586T COAD 9 26910389 26910392 + Frame_Shift_Del DEL AAAT AAAT - TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr9:26910389_26910392delAAAT c.1601_1604delATTT c.(1600-1605)tatttcfs p.YF534fs COAD 9 26913896 26913896 + Silent SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr9:26913896G>A c.1536C>T c.(1534-1536)gcC>gcT p.A512A COAD 9 26917136 26917136 + Missense_Mutation SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr9:26917136G>A c.1445C>T c.(1444-1446)tCg>tTg p.S482L COAD 9 26920307 26920307 + Missense_Mutation SNP C C T TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr9:26920307C>T c.1115G>A c.(1114-1116)gGg>gAg p.G372E COAD 9 26926410 26926410 + Silent SNP G G T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr9:26926410G>T c.714C>A c.(712-714)tcC>tcA p.S238S COAD 9 26926493 26926493 + Missense_Mutation SNP C C A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr9:26926493C>A c.631G>T c.(631-633)Gat>Tat p.D211Y COADREAD 9 26905911 26905911 + Silent SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:26905911A>C c.1986T>G c.(1984-1986)acT>acG p.T662T COADREAD 9 26906045 26906045 + Missense_Mutation SNP G G A TCGA-F5-6812-01A-11D-1826-10 TCGA-F5-6812-10A-01D-1826-10 g.chr9:26906045G>A c.1852C>T c.(1852-1854)Cgg>Tgg p.R618W COADREAD 9 26907897 26907897 + Missense_Mutation SNP C C G TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr9:26907897C>G c.1757G>C c.(1756-1758)aGt>aCt p.S586T COADREAD 9 26910389 26910392 + Frame_Shift_Del DEL AAAT AAAT - TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr9:26910389_26910392delAAAT c.1601_1604delATTT c.(1600-1605)tatttcfs p.YF534fs COADREAD 9 26913896 26913896 + Silent SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr9:26913896G>A c.1536C>T c.(1534-1536)gcC>gcT p.A512A COADREAD 9 26917136 26917136 + Missense_Mutation SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr9:26917136G>A c.1445C>T c.(1444-1446)tCg>tTg p.S482L COADREAD 9 26920307 26920307 + Missense_Mutation SNP C C T TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr9:26920307C>T c.1115G>A c.(1114-1116)gGg>gAg p.G372E COADREAD 9 26926410 26926410 + Silent SNP G G T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr9:26926410G>T c.714C>A c.(712-714)tcC>tcA p.S238S COADREAD 9 26926493 26926493 + Missense_Mutation SNP C C A TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr9:26926493C>A c.631G>T c.(631-633)Gat>Tat p.D211Y COADREAD 9 26935019 26935019 + Missense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr9:26935019T>G c.335A>C c.(334-336)aAa>aCa p.K112T ESCA 9 26947000 26947000 + Missense_Mutation SNP C C T TCGA-VR-A8EZ-01A-11D-A36J-09 TCGA-VR-A8EZ-10A-01D-A36M-09 g.chr9:26947000C>T c.44G>A c.(43-45)cGg>cAg p.R15Q GBMLGG 9 26905915 26905915 + Missense_Mutation SNP C C T TCGA-CS-6666-01A-11D-1893-08 TCGA-CS-6666-10A-01D-1893-08 g.chr9:26905915C>T c.1982G>A c.(1981-1983)aGg>aAg p.R661K GBMLGG 9 26919311 26919311 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:26919311T>C c.1414A>G c.(1414-1416)Aca>Gca p.T472A HNSC 9 26905576 26905576 + Missense_Mutation SNP T T A TCGA-CN-6010-01A-11D-1683-08 TCGA-CN-6010-10A-01D-1683-08 g.chr9:26905576T>A c.2321A>T c.(2320-2322)aAg>aTg p.K774M HNSC 9 26905634 26905634 + Missense_Mutation SNP C C T TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr9:26905634C>T c.2263G>A c.(2263-2265)Gat>Aat p.D755N HNSC 9 26905641 26905641 + Silent SNP A A G TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr9:26905641A>G c.2256T>C c.(2254-2256)ctT>ctC p.L752L HNSC 9 26905734 26905734 + Silent SNP C C G TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr9:26905734C>G c.2163G>C c.(2161-2163)ggG>ggC p.G721G HNSC 9 26910396 26910396 + Missense_Mutation SNP T T C TCGA-CV-A460-01A-21D-A25D-08 TCGA-CV-A460-10A-01D-A25E-08 g.chr9:26910396T>C c.1597A>G c.(1597-1599)Att>Gtt p.I533V HNSC 9 26910414 26910414 + Missense_Mutation SNP C C T TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr9:26910414C>T c.1579G>A c.(1579-1581)Gca>Aca p.A527T HNSC 9 26913936 26913936 + Missense_Mutation SNP C C A TCGA-CN-5359-01A-01D-1434-08 TCGA-CN-5359-10A-01D-1434-08 g.chr9:26913936C>A c.1496G>T c.(1495-1497)cGt>cTt p.R499L HNSC 9 26925866 26925866 + Missense_Mutation SNP A A G TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr9:26925866A>G c.826T>C c.(826-828)Tgc>Cgc p.C276R HNSC 9 26935110 26935110 + Missense_Mutation SNP G G A TCGA-CQ-A4C6-01A-11D-A25D-08 TCGA-CQ-A4C6-10A-01D-A25E-08 g.chr9:26935110G>A c.244C>T c.(244-246)Cat>Tat p.H82Y KICH 9 26905845 26905845 + Missense_Mutation SNP C C T TCGA-KL-8329-01A-11D-2310-10 TCGA-KL-8329-11A-01D-2310-10 g.chr9:26905845C>T c.2052G>A c.(2050-2052)atG>atA p.M684I KIPAN 9 26905845 26905845 + Missense_Mutation SNP C C T TCGA-KL-8329-01A-11D-2310-10 TCGA-KL-8329-11A-01D-2310-10 g.chr9:26905845C>T c.2052G>A c.(2050-2052)atG>atA p.M684I KIPAN 9 26925951 26925951 + Silent SNP C C A TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr9:26925951C>A c.741G>T c.(739-741)gtG>gtT p.V247V KIRP 9 26925951 26925951 + Silent SNP C C A TCGA-P4-A5EB-01A-11D-A28G-10 TCGA-P4-A5EB-11A-11D-A28G-10 g.chr9:26925951C>A c.741G>T c.(739-741)gtG>gtT p.V247V LGG 9 26905915 26905915 + Missense_Mutation SNP C C T TCGA-CS-6666-01A-11D-1893-08 TCGA-CS-6666-10A-01D-1893-08 g.chr9:26905915C>T c.1982G>A c.(1981-1983)aGg>aAg p.R661K LGG 9 26919311 26919311 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:26919311T>C c.1414A>G c.(1414-1416)Aca>Gca p.T472A LIHC 9 26905635 26905635 + Silent SNP A A G TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chr9:26905635A>G c.2262T>C c.(2260-2262)agT>agC p.S754S LIHC 9 26905887 26905887 + Missense_Mutation SNP C C G TCGA-BC-A69H-01A-11D-A30V-10 TCGA-BC-A69H-10A-01D-A30V-10 g.chr9:26905887C>G c.2010G>C c.(2008-2010)caG>caC p.Q670H LIHC 9 26923264 26923264 + Silent SNP C C A TCGA-DD-A1EB-01A-11D-A12Z-10 TCGA-DD-A1EB-10A-01D-A12Z-10 g.chr9:26923264C>A c.951G>T c.(949-951)ctG>ctT p.L317L LUAD 9 26905785 26905785 + Silent SNP T T C TCGA-44-7667-01A-31D-2063-08 TCGA-44-7667-10A-01D-2063-08 g.chr9:26905785T>C c.2112A>G c.(2110-2112)acA>acG p.T704T LUAD 9 26920328 26920328 + Missense_Mutation SNP T T C TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr9:26920328T>C c.1094A>G c.(1093-1095)tAt>tGt p.Y365C LUAD 9 26926558 26926558 + Splice_Site SNP C C A TCGA-78-7162-01A-21D-2063-08 TCGA-78-7162-11A-01D-2063-08 g.chr9:26926558C>A c.566G>T c.(565-567)gGg>gTg p.G189V LUAD 9 26928119 26928119 + Missense_Mutation SNP T T C TCGA-91-6829-01A-21D-1855-08 TCGA-91-6829-11A-01D-1855-08 g.chr9:26928119T>C c.544A>G c.(544-546)Aga>Gga p.R182G LUSC 9 26928209 26928209 + Missense_Mutation SNP C C A TCGA-18-4721-01A-01D-1441-08 TCGA-18-4721-11A-01D-1441-08 g.chr9:26928209C>A c.454G>T c.(454-456)Gct>Tct p.A152S OV 9 26906068 26906068 + Missense_Mutation SNP A A G TCGA-29-1768-01A-01W-0633-09 TCGA-29-1768-10A-01W-0634-09 g.chr9:26906068A>G c.1829T>C c.(1828-1830)gTc>gCc p.V610A OV 9 26919314 26919314 + Missense_Mutation SNP A A T TCGA-13-2059-01A-01D-1526-09 TCGA-13-2059-10A-01D-1526-09 g.chr9:26919314A>T c.1411T>A c.(1411-1413)Ttt>Att p.F471I OV 9 26919332 26919332 + Missense_Mutation SNP G G A TCGA-23-2645-01A-01W-1091-09 TCGA-23-2645-10A-01W-1091-09 g.chr9:26919332G>A c.1393C>T c.(1393-1395)Ccc>Tcc p.P465S PAAD 9 26905793 26905793 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:26905793G>A c.2104C>T c.(2104-2106)Ctg>Ttg p.L702L PAAD 9 26910348 26910348 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:26910348T>C c.1645A>G c.(1645-1647)Aca>Gca p.T549A PAAD 9 26919394 26919394 + Missense_Mutation SNP A A G TCGA-2L-AAQL-01A-11D-A38G-08 TCGA-2L-AAQL-11A-11D-A38J-08 g.chr9:26919394A>G c.1331T>C c.(1330-1332)cTg>cCg p.L444P PRAD 9 26905927 26905927 + Missense_Mutation SNP A A G TCGA-HC-A6AL-01A-11D-A30E-08 TCGA-HC-A6AL-10A-01D-A30H-08 g.chr9:26905927A>G c.1970T>C c.(1969-1971)cTg>cCg p.L657P PRAD 9 26907936 26907936 + Missense_Mutation SNP A A G TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:26907936A>G c.1718T>C c.(1717-1719)tTg>tCg p.L573S PRAD 9 26923257 26923257 + Missense_Mutation SNP C C A TCGA-YL-A9WI-01A-11D-A377-08 TCGA-YL-A9WI-10A-01D-A37A-08 g.chr9:26923257C>A c.958G>T c.(958-960)Gca>Tca p.A320S PRAD 9 26923257 26923257 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:26923257C>T c.958G>A c.(958-960)Gca>Aca p.A320T PRAD 9 26925851 26925851 + Missense_Mutation SNP C C T TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr9:26925851C>T c.841G>A c.(841-843)Gac>Aac p.D281N PRAD 9 26926460 26926460 + Missense_Mutation SNP C C T TCGA-KK-A6E4-01A-11D-A30E-08 TCGA-KK-A6E4-11A-11D-A30H-08 g.chr9:26926460C>T c.664G>A c.(664-666)Gag>Aag p.E222K READ 9 26906045 26906045 + Missense_Mutation SNP G G A TCGA-F5-6812-01A-11D-1826-10 TCGA-F5-6812-10A-01D-1826-10 g.chr9:26906045G>A c.1852C>T c.(1852-1854)Cgg>Tgg p.R618W READ 9 26935019 26935019 + Missense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr9:26935019T>G c.335A>C c.(334-336)aAa>aCa p.K112T SKCM 9 26910388 26910388 + Silent SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr9:26910388G>A c.1605C>T c.(1603-1605)ttC>ttT p.F535F SKCM 9 26913921 26913921 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr9:26913921G>A c.1511C>T c.(1510-1512)tCt>tTt p.S504F SKCM 9 26913937 26913937 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr9:26913937G>A c.1495C>T c.(1495-1497)Cgt>Tgt p.R499C SKCM 9 26919513 26919513 + Silent SNP A A T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr9:26919513A>T c.1212T>A c.(1210-1212)gtT>gtA p.V404V SKCM 9 26920318 26920318 + Missense_Mutation SNP A A C TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr9:26920318A>C c.1104T>G c.(1102-1104)agT>agG p.S368R SKCM 9 26925890 26925890 + Nonsense_Mutation SNP G G A TCGA-FR-A44A-06A-11D-A24R-08 TCGA-FR-A44A-10A-01D-A24R-08 g.chr9:26925890G>A c.802C>T c.(802-804)Cga>Tga p.R268* SKCM 9 26925891 26925891 + Silent SNP G G A TCGA-FR-A44A-06A-11D-A24R-08 TCGA-FR-A44A-10A-01D-A24R-08 g.chr9:26925891G>A c.801C>T c.(799-801)atC>atT p.I267I SKCM 9 26925929 26925929 + Silent SNP G G A TCGA-EE-A2MK-06A-11D-A196-08 TCGA-EE-A2MK-10A-01D-A198-08 g.chr9:26925929G>A c.763C>T c.(763-765)Ctg>Ttg p.L255L SKCM 9 26926415 26926415 + Missense_Mutation SNP T T A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr9:26926415T>A c.709A>T c.(709-711)Ata>Tta p.I237L SKCM 9 26928394 26928394 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:26928394G>A c.356C>T c.(355-357)tCa>tTa p.S119L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 9 26905860 26905860 single base substitution C G downstream_gene_variant BLCA-US 9 26905860 26905860 single base substitution C G missense_variant Q679H 2037G>C BRCA-EU 9 26899404 26899404 deletion of <=200bp A - downstream_gene_variant BRCA-EU 9 26900032 26900032 single base substitution C T downstream_gene_variant BRCA-EU 9 26901571 26901571 single base substitution G C downstream_gene_variant BRCA-EU 9 26904317 26904317 single base substitution G C 3_prime_UTR_variant BRCA-EU 9 26904317 26904317 single base substitution G C downstream_gene_variant BRCA-EU 9 26908649 26908649 single base substitution G C intron_variant BRCA-EU 9 26909531 26909533 deletion of <=200bp ACA - intron_variant BRCA-EU 9 26909769 26909769 single base substitution C T intron_variant BRCA-EU 9 26910963 26910963 single base substitution T C intron_variant BRCA-EU 9 26911799 26911853 deletion of <=200bp TTAAGATATTGTGCAAAAATATGAATAAAAGATTTATCTTAATATTCTGATTACA - downstream_gene_variant BRCA-EU 9 26911799 26911853 deletion of <=200bp TTAAGATATTGTGCAAAAATATGAATAAAAGATTTATCTTAATATTCTGATTACA - intron_variant BRCA-EU 9 26915611 26915611 single base substitution T C downstream_gene_variant BRCA-EU 9 26915611 26915611 single base substitution T C intron_variant BRCA-EU 9 26915890 26915890 single base substitution A C downstream_gene_variant BRCA-EU 9 26915890 26915890 single base substitution A C intron_variant BRCA-EU 9 26917737 26917737 single base substitution G A downstream_gene_variant BRCA-EU 9 26917737 26917737 single base substitution G A intron_variant BRCA-EU 9 26917800 26917800 insertion of <=200bp - A downstream_gene_variant BRCA-EU 9 26917800 26917800 insertion of <=200bp - A intron_variant BRCA-EU 9 26918427 26918427 single base substitution G A downstream_gene_variant BRCA-EU 9 26918427 26918427 single base substitution G A intron_variant BRCA-EU 9 26919079 26919079 single base substitution A G downstream_gene_variant BRCA-EU 9 26919079 26919079 single base substitution A G intron_variant BRCA-EU 9 26919521 26919521 single base substitution C G exon_variant BRCA-EU 9 26919521 26919521 single base substitution C G missense_variant D402H 1204G>C BRCA-EU 9 26919521 26919521 single base substitution C G missense_variant D74H 220G>C BRCA-EU 9 26919521 26919521 single base substitution C G upstream_gene_variant BRCA-EU 9 26919693 26919693 single base substitution C T intron_variant BRCA-EU 9 26919693 26919693 single base substitution C T upstream_gene_variant BRCA-EU 9 26920014 26920014 single base substitution T A intron_variant BRCA-EU 9 26920014 26920014 single base substitution T A upstream_gene_variant BRCA-EU 9 26920354 26920354 single base substitution G A synonymous_variant I28I 84C>T BRCA-EU 9 26920354 26920354 single base substitution G A synonymous_variant I356I 1068C>T BRCA-EU 9 26920354 26920354 single base substitution G A upstream_gene_variant BRCA-EU 9 26922114 26922114 single base substitution C A downstream_gene_variant BRCA-EU 9 26922114 26922114 single base substitution C A intron_variant BRCA-EU 9 26922114 26922114 single base substitution C A upstream_gene_variant BRCA-EU 9 26922637 26922637 single base substitution C G downstream_gene_variant BRCA-EU 9 26922637 26922637 single base substitution C G intron_variant BRCA-EU 9 26922637 26922637 single base substitution C G upstream_gene_variant BRCA-EU 9 26927856 26927856 single base substitution A G intron_variant BRCA-EU 9 26927856 26927856 single base substitution A G upstream_gene_variant BRCA-EU 9 26927859 26927859 single base substitution T G intron_variant BRCA-EU 9 26927859 26927859 single base substitution T G upstream_gene_variant BRCA-EU 9 26929112 26929112 single base substitution G T intron_variant BRCA-EU 9 26929629 26929629 single base substitution G C intron_variant BRCA-EU 9 26929852 26929852 single base substitution G A intron_variant BRCA-EU 9 26930937 26930937 single base substitution G A intron_variant BRCA-EU 9 26931745 26931745 single base substitution T C intron_variant BRCA-EU 9 26932034 26932034 single base substitution G A intron_variant BRCA-EU 9 26933297 26933297 single base substitution G T intron_variant BRCA-EU 9 26933703 26933703 single base substitution C T intron_variant BRCA-EU 9 26934070 26934070 single base substitution G A intron_variant BRCA-EU 9 26935493 26935493 single base substitution C T intron_variant BRCA-EU 9 26935803 26935803 deletion of <=200bp A - intron_variant BRCA-EU 9 26935986 26935986 single base substitution C T intron_variant BRCA-EU 9 26943852 26943852 single base substitution G A intron_variant BRCA-EU 9 26948275 26948275 single base substitution C G upstream_gene_variant BRCA-EU 9 26948593 26948593 single base substitution T C upstream_gene_variant BRCA-EU 9 26948969 26948969 single base substitution C G upstream_gene_variant BRCA-EU 9 26949145 26949145 single base substitution G A upstream_gene_variant BRCA-EU 9 26949685 26949685 single base substitution C G upstream_gene_variant BRCA-EU 9 26950075 26950075 single base substitution C T upstream_gene_variant BRCA-EU 9 26950772 26950772 single base substitution C A upstream_gene_variant BRCA-EU 9 26950980 26950980 single base substitution A G upstream_gene_variant BRCA-EU 9 26951588 26951588 deletion of <=200bp A - upstream_gene_variant BRCA-EU 9 26951622 26951622 single base substitution C T upstream_gene_variant BRCA-EU 9 26951673 26951673 single base substitution G C upstream_gene_variant BRCA-EU 9 26951762 26951762 single base substitution T C upstream_gene_variant BRCA-EU 9 26951781 26951781 single base substitution C T upstream_gene_variant BRCA-EU 9 26952133 26952133 single base substitution C A upstream_gene_variant BRCA-FR 9 26904317 26904317 single base substitution G C 3_prime_UTR_variant BRCA-FR 9 26904317 26904317 single base substitution G C downstream_gene_variant BRCA-FR 9 26908000 26908000 single base substitution G T intron_variant BRCA-FR 9 26908000 26908000 single base substitution G T splice_region_variant BRCA-FR 9 26919079 26919079 single base substitution A G downstream_gene_variant BRCA-FR 9 26919079 26919079 single base substitution A G intron_variant BRCA-FR 9 26922637 26922637 single base substitution C G downstream_gene_variant BRCA-FR 9 26922637 26922637 single base substitution C G intron_variant BRCA-FR 9 26922637 26922637 single base substitution C G upstream_gene_variant BRCA-FR 9 26922767 26922767 single base substitution C G downstream_gene_variant BRCA-FR 9 26922767 26922767 single base substitution C G intron_variant BRCA-FR 9 26922767 26922767 single base substitution C G upstream_gene_variant BRCA-FR 9 26930937 26930937 single base substitution G A intron_variant BRCA-FR 9 26933703 26933703 single base substitution C T intron_variant BRCA-FR 9 26934070 26934070 single base substitution G A intron_variant BRCA-FR 9 26949685 26949685 single base substitution C G upstream_gene_variant BRCA-FR 9 26950980 26950980 single base substitution A G upstream_gene_variant BRCA-FR 9 26951587 26951587 single base substitution G A upstream_gene_variant BRCA-FR 9 26951781 26951781 single base substitution C T upstream_gene_variant BRCA-UK 9 26900032 26900032 single base substitution C T downstream_gene_variant BRCA-UK 9 26911958 26911958 single base substitution G C downstream_gene_variant BRCA-UK 9 26911958 26911958 single base substitution G C intron_variant BRCA-UK 9 26919521 26919521 single base substitution C G exon_variant BRCA-UK 9 26919521 26919521 single base substitution C G missense_variant D402H 1204G>C BRCA-UK 9 26919521 26919521 single base substitution C G missense_variant D74H 220G>C BRCA-UK 9 26919521 26919521 single base substitution C G upstream_gene_variant BRCA-UK 9 26927102 26927102 single base substitution C T intron_variant BRCA-UK 9 26927102 26927102 single base substitution C T upstream_gene_variant BRCA-UK 9 26931243 26931243 single base substitution C G intron_variant BRCA-US 9 26905603 26905603 single base substitution G C downstream_gene_variant BRCA-US 9 26905603 26905603 single base substitution G C missense_variant S765C 2294C>G BRCA-US 9 26907965 26907965 deletion of <=200bp A - frameshift_variant P563 BRCA-US 9 26907965 26907965 deletion of <=200bp A - frameshift_variant P89 BRCA-US 9 26907965 26907965 deletion of <=200bp A - intron_variant BRCA-US 9 26917106 26917106 single base substitution T C downstream_gene_variant BRCA-US 9 26917106 26917106 single base substitution T C exon_variant BRCA-US 9 26917106 26917106 single base substitution T C intron_variant BRCA-US 9 26917106 26917106 single base substitution T C missense_variant D164G 491A>G BRCA-US 9 26917106 26917106 single base substitution T C missense_variant D492G 1475A>G BTCA-JP 9 26907799 26907799 single base substitution T C 3_prime_UTR_variant BTCA-JP 9 26907799 26907799 single base substitution T C downstream_gene_variant BTCA-JP 9 26907799 26907799 single base substitution T C intron_variant BTCA-JP 9 26913970 26913971 deletion of <=200bp AA - downstream_gene_variant BTCA-JP 9 26913970 26913971 deletion of <=200bp AA - intron_variant BTCA-JP 9 26923234 26923234 single base substitution G A downstream_gene_variant BTCA-JP 9 26923234 26923234 single base substitution G A synonymous_variant G327G 981C>T BTCA-JP 9 26923234 26923234 single base substitution G A upstream_gene_variant CLLE-ES 9 26910894 26910894 single base substitution C G intron_variant CLLE-ES 9 26938528 26938528 single base substitution C T intron_variant CLLE-ES 9 26950300 26950300 single base substitution C A upstream_gene_variant COAD-US 9 26910389 26910392 deletion of <=200bp AAAT - frameshift_variant YF206 COAD-US 9 26910389 26910392 deletion of <=200bp AAAT - frameshift_variant YF534 COAD-US 9 26910389 26910392 deletion of <=200bp AAAT - frameshift_variant YF60 COAD-US 9 26913896 26913896 single base substitution G A downstream_gene_variant COAD-US 9 26913896 26913896 single base substitution G A synonymous_variant A184A 552C>T COAD-US 9 26913896 26913896 single base substitution G A synonymous_variant A38A 114C>T COAD-US 9 26913896 26913896 single base substitution G A synonymous_variant A512A 1536C>T COAD-US 9 26917136 26917136 single base substitution G A downstream_gene_variant COAD-US 9 26917136 26917136 single base substitution G A exon_variant COAD-US 9 26917136 26917136 single base substitution G A intron_variant COAD-US 9 26917136 26917136 single base substitution G A missense_variant S154L 461C>T COAD-US 9 26917136 26917136 single base substitution G A missense_variant S482L 1445C>T COAD-US 9 26920307 26920307 single base substitution C T exon_variant COAD-US 9 26920307 26920307 single base substitution C T missense_variant G372E 1115G>A COAD-US 9 26920307 26920307 single base substitution C T missense_variant G44E 131G>A COAD-US 9 26920307 26920307 single base substitution C T upstream_gene_variant COAD-US 9 26926410 26926410 single base substitution G T synonymous_variant S214S 642C>A COAD-US 9 26926410 26926410 single base substitution G T synonymous_variant S238S 714C>A COAD-US 9 26926410 26926410 single base substitution G T upstream_gene_variant COAD-US 9 26928309 26928309 single base substitution C T synonymous_variant L123L 369G>A COAD-US 9 26928309 26928309 single base substitution C T synonymous_variant L147L 441G>A COCA-CN 9 26907961 26907961 single base substitution C A intron_variant COCA-CN 9 26907961 26907961 single base substitution C A stop_gained E565* 1693G>T COCA-CN 9 26907961 26907961 single base substitution C A stop_gained E91* 271G>T COCA-CN 9 26914730 26914730 single base substitution C A downstream_gene_variant COCA-CN 9 26914730 26914730 single base substitution C A intron_variant COCA-CN 9 26920133 26920133 single base substitution A G intron_variant COCA-CN 9 26920133 26920133 single base substitution A G upstream_gene_variant COCA-CN 9 26923147 26923147 single base substitution T A downstream_gene_variant COCA-CN 9 26923147 26923147 single base substitution T A intron_variant COCA-CN 9 26923147 26923147 single base substitution T A upstream_gene_variant COCA-CN 9 26924328 26924328 single base substitution C T downstream_gene_variant COCA-CN 9 26924328 26924328 single base substitution C T intron_variant COCA-CN 9 26924328 26924328 single base substitution C T upstream_gene_variant COCA-CN 9 26926080 26926080 single base substitution T G intron_variant COCA-CN 9 26926080 26926080 single base substitution T G upstream_gene_variant COCA-CN 9 26932410 26932410 single base substitution C T intron_variant COCA-CN 9 26948332 26948332 single base substitution G A upstream_gene_variant EOPC-DE 9 26949880 26949880 single base substitution G A upstream_gene_variant ESAD-UK 9 26900022 26900022 deletion of <=200bp T - downstream_gene_variant ESAD-UK 9 26901199 26901199 single base substitution C G downstream_gene_variant ESAD-UK 9 26902584 26902584 single base substitution T A downstream_gene_variant ESAD-UK 9 26903153 26903153 single base substitution A T downstream_gene_variant ESAD-UK 9 26905606 26905606 single base substitution T G downstream_gene_variant ESAD-UK 9 26905606 26905606 single base substitution T G missense_variant K764T 2291A>C ESAD-UK 9 26912702 26912702 single base substitution T A downstream_gene_variant ESAD-UK 9 26912702 26912702 single base substitution T A intron_variant ESAD-UK 9 26913156 26913156 single base substitution T C downstream_gene_variant ESAD-UK 9 26913156 26913156 single base substitution T C intron_variant ESAD-UK 9 26913775 26913775 single base substitution T C downstream_gene_variant ESAD-UK 9 26913775 26913775 single base substitution T C intron_variant ESAD-UK 9 26916119 26916119 single base substitution G C downstream_gene_variant ESAD-UK 9 26916119 26916119 single base substitution G C intron_variant ESAD-UK 9 26916682 26916682 single base substitution G A downstream_gene_variant ESAD-UK 9 26916682 26916682 single base substitution G A exon_variant ESAD-UK 9 26916682 26916682 single base substitution G A intron_variant ESAD-UK 9 26918635 26918635 single base substitution G A downstream_gene_variant ESAD-UK 9 26918635 26918635 single base substitution G A intron_variant ESAD-UK 9 26919016 26919016 single base substitution A T downstream_gene_variant ESAD-UK 9 26919016 26919016 single base substitution A T intron_variant ESAD-UK 9 26919746 26919746 single base substitution T A intron_variant ESAD-UK 9 26919746 26919746 single base substitution T A upstream_gene_variant ESAD-UK 9 26920087 26920087 deletion of <=200bp A - intron_variant ESAD-UK 9 26920087 26920087 deletion of <=200bp A - upstream_gene_variant ESAD-UK 9 26920685 26920685 single base substitution G C intron_variant ESAD-UK 9 26920685 26920685 single base substitution G C upstream_gene_variant ESAD-UK 9 26921272 26921272 single base substitution G A downstream_gene_variant ESAD-UK 9 26921272 26921272 single base substitution G A intron_variant ESAD-UK 9 26921272 26921272 single base substitution G A upstream_gene_variant ESAD-UK 9 26922124 26922150 deletion of <=200bp AGACACCACAGTATTTTGACTTACTTT - downstream_gene_variant ESAD-UK 9 26922124 26922150 deletion of <=200bp AGACACCACAGTATTTTGACTTACTTT - intron_variant ESAD-UK 9 26922124 26922150 deletion of <=200bp AGACACCACAGTATTTTGACTTACTTT - upstream_gene_variant ESAD-UK 9 26923800 26923800 deletion of <=200bp A - downstream_gene_variant ESAD-UK 9 26923800 26923800 deletion of <=200bp A - intron_variant ESAD-UK 9 26923800 26923800 deletion of <=200bp A - upstream_gene_variant ESAD-UK 9 26925791 26925791 single base substitution T A downstream_gene_variant ESAD-UK 9 26925791 26925791 single base substitution T A intron_variant ESAD-UK 9 26925791 26925791 single base substitution T A upstream_gene_variant ESAD-UK 9 26926411 26926411 single base substitution G A missense_variant S214F 641C>T ESAD-UK 9 26926411 26926411 single base substitution G A missense_variant S238F 713C>T ESAD-UK 9 26926411 26926411 single base substitution G A upstream_gene_variant ESAD-UK 9 26930588 26930588 single base substitution T G intron_variant ESAD-UK 9 26931805 26931805 single base substitution C T intron_variant ESAD-UK 9 26932357 26932357 deletion of <=200bp T - intron_variant ESAD-UK 9 26932595 26932595 single base substitution G A intron_variant ESAD-UK 9 26933863 26933863 single base substitution G T intron_variant ESAD-UK 9 26935404 26935404 single base substitution T C intron_variant ESAD-UK 9 26939149 26939149 single base substitution G A intron_variant ESAD-UK 9 26939603 26939603 single base substitution T G intron_variant ESAD-UK 9 26943357 26943357 single base substitution G T intron_variant ESAD-UK 9 26944603 26944603 deletion of <=200bp A - intron_variant ESAD-UK 9 26945084 26945084 single base substitution C T intron_variant ESAD-UK 9 26946349 26946349 single base substitution G A intron_variant ESAD-UK 9 26947365 26947365 single base substitution G A 5_prime_UTR_variant ESAD-UK 9 26947365 26947365 single base substitution G A upstream_gene_variant ESAD-UK 9 26952267 26952267 deletion of <=200bp T - upstream_gene_variant ESAD-UK 9 26952297 26952297 single base substitution C T upstream_gene_variant ESCA-CN 9 26925888 26925888 single base substitution T C downstream_gene_variant ESCA-CN 9 26925888 26925888 single base substitution T C synonymous_variant R268R 804A>G ESCA-CN 9 26925888 26925888 single base substitution T C upstream_gene_variant ESCA-CN 9 26925890 26925890 single base substitution G A downstream_gene_variant ESCA-CN 9 26925890 26925890 single base substitution G A stop_gained R268* 802C>T ESCA-CN 9 26925890 26925890 single base substitution G A upstream_gene_variant ESCA-CN 9 26935126 26935126 single base substitution T A synonymous_variant S52S 156A>T ESCA-CN 9 26935126 26935126 single base substitution T A synonymous_variant S76S 228A>T KIRP-US 9 26925951 26925951 single base substitution C A synonymous_variant V223V 669G>T KIRP-US 9 26925951 26925951 single base substitution C A synonymous_variant V247V 741G>T KIRP-US 9 26925951 26925951 single base substitution C A upstream_gene_variant LAML-KR 9 26952293 26952293 single base substitution G T upstream_gene_variant LGG-US 9 26905915 26905915 single base substitution C T downstream_gene_variant LGG-US 9 26905915 26905915 single base substitution C T missense_variant R278K 833G>A LGG-US 9 26905915 26905915 single base substitution C T missense_variant R661K 1982G>A LICA-FR 9 26916821 26916821 single base substitution T C downstream_gene_variant LICA-FR 9 26916821 26916821 single base substitution T C intron_variant LICA-FR 9 26921479 26921479 single base substitution C T downstream_gene_variant LICA-FR 9 26921479 26921479 single base substitution C T intron_variant LICA-FR 9 26921479 26921479 single base substitution C T upstream_gene_variant LICA-FR 9 26929484 26929484 insertion of <=200bp - A intron_variant LICA-FR 9 26948775 26948775 single base substitution A G upstream_gene_variant LIHC-US 9 26905635 26905635 single base substitution A G downstream_gene_variant LIHC-US 9 26905635 26905635 single base substitution A G synonymous_variant S754S 2262T>C LIHC-US 9 26905887 26905887 single base substitution C G downstream_gene_variant LIHC-US 9 26905887 26905887 single base substitution C G missense_variant Q287H 861G>C LIHC-US 9 26905887 26905887 single base substitution C G missense_variant Q670H 2010G>C LIHC-US 9 26923264 26923264 single base substitution C A downstream_gene_variant LIHC-US 9 26923264 26923264 single base substitution C A synonymous_variant L317L 951G>T LIHC-US 9 26923264 26923264 single base substitution C A upstream_gene_variant LINC-JP 9 26903549 26903549 single base substitution G T downstream_gene_variant LINC-JP 9 26909153 26909153 single base substitution C A intron_variant LINC-JP 9 26913245 26913245 single base substitution T C downstream_gene_variant LINC-JP 9 26913245 26913245 single base substitution T C intron_variant LINC-JP 9 26913970 26913971 deletion of <=200bp AA - downstream_gene_variant LINC-JP 9 26913970 26913971 deletion of <=200bp AA - intron_variant LINC-JP 9 26925893 26925893 single base substitution T C missense_variant I243V 727A>G LINC-JP 9 26925893 26925893 single base substitution T C missense_variant I267V 799A>G LINC-JP 9 26925893 26925893 single base substitution T C upstream_gene_variant LINC-JP 9 26927137 26927137 single base substitution G T intron_variant LINC-JP 9 26927137 26927137 single base substitution G T upstream_gene_variant LINC-JP 9 26929053 26929053 single base substitution T C intron_variant LINC-JP 9 26932988 26932988 single base substitution C T intron_variant LIRI-JP 9 26900215 26900215 single base substitution G A downstream_gene_variant LIRI-JP 9 26904094 26904094 single base substitution T A 3_prime_UTR_variant LIRI-JP 9 26904094 26904094 single base substitution T A downstream_gene_variant LIRI-JP 9 26904694 26904694 single base substitution T C 3_prime_UTR_variant LIRI-JP 9 26904694 26904694 single base substitution T C downstream_gene_variant LIRI-JP 9 26905370 26905370 single base substitution C A 3_prime_UTR_variant LIRI-JP 9 26905370 26905370 single base substitution C A downstream_gene_variant LIRI-JP 9 26906220 26906221 deletion of <=200bp AT - downstream_gene_variant LIRI-JP 9 26906220 26906221 deletion of <=200bp AT - intron_variant LIRI-JP 9 26906614 26906614 single base substitution C T downstream_gene_variant LIRI-JP 9 26906614 26906614 single base substitution C T intron_variant LIRI-JP 9 26910482 26910482 single base substitution A C intron_variant LIRI-JP 9 26914678 26914678 single base substitution T C downstream_gene_variant LIRI-JP 9 26914678 26914678 single base substitution T C intron_variant LIRI-JP 9 26916000 26916000 single base substitution T C downstream_gene_variant LIRI-JP 9 26916000 26916000 single base substitution T C intron_variant LIRI-JP 9 26916074 26916074 single base substitution G T downstream_gene_variant LIRI-JP 9 26916074 26916074 single base substitution G T intron_variant LIRI-JP 9 26918366 26918366 single base substitution T A downstream_gene_variant LIRI-JP 9 26918366 26918366 single base substitution T A intron_variant LIRI-JP 9 26918863 26918863 single base substitution C A downstream_gene_variant LIRI-JP 9 26918863 26918863 single base substitution C A intron_variant LIRI-JP 9 26919248 26919248 single base substitution T C exon_variant LIRI-JP 9 26919248 26919248 single base substitution T C intron_variant LIRI-JP 9 26922316 26922316 single base substitution T C downstream_gene_variant LIRI-JP 9 26922316 26922316 single base substitution T C intron_variant LIRI-JP 9 26922316 26922316 single base substitution T C upstream_gene_variant LIRI-JP 9 26922857 26922857 single base substitution T C downstream_gene_variant LIRI-JP 9 26922857 26922857 single base substitution T C intron_variant LIRI-JP 9 26922857 26922857 single base substitution T C upstream_gene_variant LIRI-JP 9 26924254 26924254 single base substitution G A downstream_gene_variant LIRI-JP 9 26924254 26924254 single base substitution G A intron_variant LIRI-JP 9 26924254 26924254 single base substitution G A upstream_gene_variant LIRI-JP 9 26925460 26925460 single base substitution C A downstream_gene_variant LIRI-JP 9 26925460 26925460 single base substitution C A intron_variant LIRI-JP 9 26925460 26925460 single base substitution C A upstream_gene_variant LIRI-JP 9 26927084 26927084 single base substitution T C intron_variant LIRI-JP 9 26927084 26927084 single base substitution T C upstream_gene_variant LIRI-JP 9 26930431 26930431 single base substitution T C intron_variant LIRI-JP 9 26931019 26931019 single base substitution A G intron_variant LIRI-JP 9 26934086 26934086 single base substitution T C intron_variant LIRI-JP 9 26934164 26934164 single base substitution T C intron_variant LIRI-JP 9 26934974 26934974 single base substitution T G intron_variant LIRI-JP 9 26936102 26936102 single base substitution G A intron_variant LIRI-JP 9 26936431 26936431 single base substitution T C intron_variant LIRI-JP 9 26940900 26940900 single base substitution C T intron_variant LIRI-JP 9 26941337 26941337 single base substitution C T intron_variant LIRI-JP 9 26942523 26942523 single base substitution T C intron_variant LIRI-JP 9 26942712 26942712 single base substitution C G intron_variant LIRI-JP 9 26944942 26944942 single base substitution A G intron_variant LIRI-JP 9 26945182 26945182 single base substitution C T intron_variant LIRI-JP 9 26946848 26946848 single base substitution C A intron_variant LIRI-JP 9 26947861 26947861 single base substitution G T upstream_gene_variant LIRI-JP 9 26951537 26951537 single base substitution A G upstream_gene_variant LIRI-JP 9 26951565 26951565 single base substitution A G upstream_gene_variant LUSC-KR 9 26903659 26903659 single base substitution T C downstream_gene_variant LUSC-KR 9 26904972 26904972 single base substitution T C 3_prime_UTR_variant LUSC-KR 9 26904972 26904972 single base substitution T C downstream_gene_variant LUSC-KR 9 26905183 26905183 single base substitution T G 3_prime_UTR_variant LUSC-KR 9 26905183 26905183 single base substitution T G downstream_gene_variant LUSC-KR 9 26905588 26905588 single base substitution G C downstream_gene_variant LUSC-KR 9 26905588 26905588 single base substitution G C missense_variant S770C 2309C>G LUSC-KR 9 26906445 26906445 single base substitution G T downstream_gene_variant LUSC-KR 9 26906445 26906445 single base substitution G T intron_variant LUSC-KR 9 26908805 26908805 single base substitution T G intron_variant LUSC-KR 9 26913829 26913829 single base substitution C T downstream_gene_variant LUSC-KR 9 26913829 26913829 single base substitution C T intron_variant LUSC-KR 9 26914151 26914151 single base substitution G A downstream_gene_variant LUSC-KR 9 26914151 26914151 single base substitution G A intron_variant LUSC-KR 9 26918384 26918384 single base substitution C A downstream_gene_variant LUSC-KR 9 26918384 26918384 single base substitution C A intron_variant LUSC-KR 9 26919917 26919917 single base substitution C A intron_variant LUSC-KR 9 26919917 26919917 single base substitution C A upstream_gene_variant LUSC-KR 9 26923016 26923016 single base substitution G A downstream_gene_variant LUSC-KR 9 26923016 26923016 single base substitution G A intron_variant LUSC-KR 9 26923016 26923016 single base substitution G A upstream_gene_variant LUSC-KR 9 26925851 26925851 single base substitution C G downstream_gene_variant LUSC-KR 9 26925851 26925851 single base substitution C G missense_variant D281H 841G>C LUSC-KR 9 26925851 26925851 single base substitution C G upstream_gene_variant LUSC-KR 9 26926678 26926678 single base substitution G A intron_variant LUSC-KR 9 26926678 26926678 single base substitution G A upstream_gene_variant LUSC-KR 9 26928422 26928422 single base substitution C T intron_variant LUSC-KR 9 26928427 26928427 single base substitution G T intron_variant LUSC-KR 9 26932085 26932085 single base substitution C T intron_variant LUSC-KR 9 26940505 26940505 single base substitution G C intron_variant LUSC-KR 9 26949611 26949611 single base substitution G T upstream_gene_variant LUSC-KR 9 26951456 26951456 single base substitution A G upstream_gene_variant LUSC-KR 9 26951472 26951472 single base substitution A T upstream_gene_variant LUSC-US 9 26928209 26928209 single base substitution C A missense_variant A128S 382G>T LUSC-US 9 26928209 26928209 single base substitution C A missense_variant A152S 454G>T LUSC-US 9 26928209 26928209 single base substitution C A upstream_gene_variant MALY-DE 9 26906135 26906135 single base substitution G A downstream_gene_variant MALY-DE 9 26906135 26906135 single base substitution G A intron_variant MALY-DE 9 26921702 26921702 single base substitution A G downstream_gene_variant MALY-DE 9 26921702 26921702 single base substitution A G intron_variant MALY-DE 9 26921702 26921702 single base substitution A G upstream_gene_variant MALY-DE 9 26922296 26922296 single base substitution A G downstream_gene_variant MALY-DE 9 26922296 26922296 single base substitution A G intron_variant MALY-DE 9 26922296 26922296 single base substitution A G upstream_gene_variant MALY-DE 9 26923014 26923014 single base substitution A G downstream_gene_variant MALY-DE 9 26923014 26923014 single base substitution A G intron_variant MALY-DE 9 26923014 26923014 single base substitution A G upstream_gene_variant MALY-DE 9 26923638 26923638 single base substitution C G downstream_gene_variant MALY-DE 9 26923638 26923638 single base substitution C G intron_variant MALY-DE 9 26923638 26923638 single base substitution C G upstream_gene_variant MALY-DE 9 26924651 26924651 single base substitution G A downstream_gene_variant MALY-DE 9 26924651 26924651 single base substitution G A intron_variant MALY-DE 9 26924651 26924651 single base substitution G A upstream_gene_variant MALY-DE 9 26934880 26934880 single base substitution G A intron_variant MALY-DE 9 26940579 26940579 single base substitution T G intron_variant MALY-DE 9 26950662 26950662 single base substitution G T upstream_gene_variant MELA-AU 9 26899195 26899195 single base substitution G A downstream_gene_variant MELA-AU 9 26899569 26899569 single base substitution C T downstream_gene_variant MELA-AU 9 26899824 26899824 single base substitution C T downstream_gene_variant MELA-AU 9 26900846 26900846 single base substitution G A downstream_gene_variant MELA-AU 9 26901503 26901503 single base substitution T C downstream_gene_variant MELA-AU 9 26902078 26902078 single base substitution G A downstream_gene_variant MELA-AU 9 26902314 26902314 single base substitution G T downstream_gene_variant MELA-AU 9 26903000 26903000 single base substitution A C downstream_gene_variant MELA-AU 9 26903942 26903942 single base substitution G A downstream_gene_variant MELA-AU 9 26905015 26905015 single base substitution G A 3_prime_UTR_variant MELA-AU 9 26905015 26905015 single base substitution G A downstream_gene_variant MELA-AU 9 26905267 26905267 single base substitution G A 3_prime_UTR_variant MELA-AU 9 26905267 26905267 single base substitution G A downstream_gene_variant MELA-AU 9 26908427 26908428 multiple base substitution (>=2bp and <=200bp) GT AG intron_variant MELA-AU 9 26910069 26910070 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 26911030 26911030 single base substitution G A intron_variant MELA-AU 9 26911144 26911144 single base substitution G A intron_variant MELA-AU 9 26911298 26911298 single base substitution G A intron_variant MELA-AU 9 26911312 26911312 single base substitution G A intron_variant MELA-AU 9 26911325 26911325 single base substitution A C intron_variant MELA-AU 9 26911784 26911784 single base substitution T C downstream_gene_variant MELA-AU 9 26911784 26911784 single base substitution T C intron_variant MELA-AU 9 26912070 26912070 single base substitution G A downstream_gene_variant MELA-AU 9 26912070 26912070 single base substitution G A intron_variant MELA-AU 9 26913345 26913345 single base substitution G A downstream_gene_variant MELA-AU 9 26913345 26913345 single base substitution G A intron_variant MELA-AU 9 26913921 26913921 single base substitution G A downstream_gene_variant MELA-AU 9 26913921 26913921 single base substitution G A missense_variant S176F 527C>T MELA-AU 9 26913921 26913921 single base substitution G A missense_variant S30F 89C>T MELA-AU 9 26913921 26913921 single base substitution G A missense_variant S504F 1511C>T MELA-AU 9 26914224 26914224 single base substitution C T downstream_gene_variant MELA-AU 9 26914224 26914224 single base substitution C T intron_variant MELA-AU 9 26914553 26914553 single base substitution C T downstream_gene_variant MELA-AU 9 26914553 26914553 single base substitution C T intron_variant MELA-AU 9 26915337 26915337 single base substitution C T downstream_gene_variant MELA-AU 9 26915337 26915337 single base substitution C T intron_variant MELA-AU 9 26915433 26915433 single base substitution G A downstream_gene_variant MELA-AU 9 26915433 26915433 single base substitution G A intron_variant MELA-AU 9 26915775 26915775 single base substitution G A downstream_gene_variant MELA-AU 9 26915775 26915775 single base substitution G A intron_variant MELA-AU 9 26916050 26916050 single base substitution A C downstream_gene_variant MELA-AU 9 26916050 26916050 single base substitution A C intron_variant MELA-AU 9 26916277 26916277 single base substitution C T downstream_gene_variant MELA-AU 9 26916277 26916277 single base substitution C T intron_variant MELA-AU 9 26916960 26916960 single base substitution G A downstream_gene_variant MELA-AU 9 26916960 26916960 single base substitution G A intron_variant MELA-AU 9 26917336 26917336 single base substitution G A downstream_gene_variant MELA-AU 9 26917336 26917336 single base substitution G A intron_variant MELA-AU 9 26917338 26917338 single base substitution A G downstream_gene_variant MELA-AU 9 26917338 26917338 single base substitution A G intron_variant MELA-AU 9 26917693 26917693 single base substitution G A downstream_gene_variant MELA-AU 9 26917693 26917693 single base substitution G A intron_variant MELA-AU 9 26918552 26918552 single base substitution G A downstream_gene_variant MELA-AU 9 26918552 26918552 single base substitution G A intron_variant MELA-AU 9 26919135 26919135 single base substitution A G downstream_gene_variant MELA-AU 9 26919135 26919135 single base substitution A G intron_variant MELA-AU 9 26919404 26919404 single base substitution G A exon_variant MELA-AU 9 26919404 26919404 single base substitution G A missense_variant P113S 337C>T MELA-AU 9 26919404 26919404 single base substitution G A missense_variant P441S 1321C>T MELA-AU 9 26919404 26919404 single base substitution G A upstream_gene_variant MELA-AU 9 26919871 26919871 single base substitution A G intron_variant MELA-AU 9 26919871 26919871 single base substitution A G upstream_gene_variant MELA-AU 9 26920086 26920086 single base substitution G A intron_variant MELA-AU 9 26920086 26920086 single base substitution G A upstream_gene_variant MELA-AU 9 26920402 26920402 single base substitution G A intron_variant MELA-AU 9 26920402 26920402 single base substitution G A upstream_gene_variant MELA-AU 9 26920532 26920532 single base substitution A G intron_variant MELA-AU 9 26920532 26920532 single base substitution A G upstream_gene_variant MELA-AU 9 26920747 26920747 single base substitution C T intron_variant MELA-AU 9 26920747 26920747 single base substitution C T upstream_gene_variant MELA-AU 9 26921061 26921061 single base substitution G A downstream_gene_variant MELA-AU 9 26921061 26921061 single base substitution G A intron_variant MELA-AU 9 26921061 26921061 single base substitution G A upstream_gene_variant MELA-AU 9 26921428 26921428 single base substitution G A downstream_gene_variant MELA-AU 9 26921428 26921428 single base substitution G A intron_variant MELA-AU 9 26921428 26921428 single base substitution G A upstream_gene_variant MELA-AU 9 26922198 26922198 single base substitution A C downstream_gene_variant MELA-AU 9 26922198 26922198 single base substitution A C intron_variant MELA-AU 9 26922198 26922198 single base substitution A C upstream_gene_variant MELA-AU 9 26923352 26923352 single base substitution G A downstream_gene_variant MELA-AU 9 26923352 26923352 single base substitution G A splice_region_variant MELA-AU 9 26923352 26923352 single base substitution G A upstream_gene_variant MELA-AU 9 26924148 26924148 single base substitution G A downstream_gene_variant MELA-AU 9 26924148 26924148 single base substitution G A intron_variant MELA-AU 9 26924148 26924148 single base substitution G A upstream_gene_variant MELA-AU 9 26924352 26924352 single base substitution G A downstream_gene_variant MELA-AU 9 26924352 26924352 single base substitution G A intron_variant MELA-AU 9 26924352 26924352 single base substitution G A upstream_gene_variant MELA-AU 9 26925120 26925120 single base substitution G T downstream_gene_variant MELA-AU 9 26925120 26925120 single base substitution G T intron_variant MELA-AU 9 26925120 26925120 single base substitution G T upstream_gene_variant MELA-AU 9 26925929 26925929 single base substitution G A synonymous_variant L231L 691C>T MELA-AU 9 26925929 26925929 single base substitution G A synonymous_variant L255L 763C>T MELA-AU 9 26925929 26925929 single base substitution G A upstream_gene_variant MELA-AU 9 26927488 26927488 single base substitution G A intron_variant MELA-AU 9 26927488 26927488 single base substitution G A upstream_gene_variant MELA-AU 9 26927504 26927504 single base substitution G A intron_variant MELA-AU 9 26927504 26927504 single base substitution G A upstream_gene_variant MELA-AU 9 26930107 26930107 single base substitution T A intron_variant MELA-AU 9 26930108 26930108 single base substitution T A intron_variant MELA-AU 9 26930315 26930315 single base substitution G A intron_variant MELA-AU 9 26930946 26930946 single base substitution G A intron_variant MELA-AU 9 26930971 26930971 single base substitution A T intron_variant MELA-AU 9 26933378 26933378 single base substitution G A intron_variant MELA-AU 9 26933479 26933479 single base substitution A T intron_variant MELA-AU 9 26934051 26934051 single base substitution C T intron_variant MELA-AU 9 26934052 26934052 single base substitution C T intron_variant MELA-AU 9 26934980 26934980 single base substitution T C intron_variant MELA-AU 9 26936375 26936375 single base substitution T A intron_variant MELA-AU 9 26937115 26937115 single base substitution G A intron_variant MELA-AU 9 26937861 26937861 single base substitution A T intron_variant MELA-AU 9 26938477 26938477 single base substitution G A intron_variant MELA-AU 9 26939071 26939071 single base substitution G A intron_variant MELA-AU 9 26939545 26939545 single base substitution G A intron_variant MELA-AU 9 26940269 26940269 single base substitution G A intron_variant MELA-AU 9 26941359 26941359 single base substitution A T intron_variant MELA-AU 9 26942671 26942671 single base substitution G A intron_variant MELA-AU 9 26944944 26944944 single base substitution G A intron_variant MELA-AU 9 26945035 26945035 single base substitution G A intron_variant MELA-AU 9 26945109 26945109 single base substitution G A intron_variant MELA-AU 9 26945524 26945524 single base substitution G A intron_variant MELA-AU 9 26946220 26946220 single base substitution G A intron_variant MELA-AU 9 26946235 26946235 single base substitution A C intron_variant MELA-AU 9 26946611 26946611 single base substitution G A intron_variant MELA-AU 9 26946623 26946623 single base substitution C T intron_variant MELA-AU 9 26947415 26947415 single base substitution C T 5_prime_UTR_variant MELA-AU 9 26947415 26947415 single base substitution C T upstream_gene_variant MELA-AU 9 26947462 26947462 single base substitution G A upstream_gene_variant MELA-AU 9 26947478 26947478 single base substitution G A upstream_gene_variant MELA-AU 9 26947524 26947524 single base substitution C T upstream_gene_variant MELA-AU 9 26947525 26947525 single base substitution C T upstream_gene_variant MELA-AU 9 26948442 26948442 single base substitution C T upstream_gene_variant MELA-AU 9 26948499 26948499 single base substitution C T upstream_gene_variant MELA-AU 9 26948689 26948689 single base substitution C T upstream_gene_variant MELA-AU 9 26948708 26948708 single base substitution C T upstream_gene_variant MELA-AU 9 26949652 26949652 single base substitution G A upstream_gene_variant MELA-AU 9 26950007 26950007 single base substitution C T upstream_gene_variant MELA-AU 9 26950106 26950106 single base substitution C T upstream_gene_variant MELA-AU 9 26950544 26950544 single base substitution A G upstream_gene_variant MELA-AU 9 26951407 26951407 single base substitution C T upstream_gene_variant MELA-AU 9 26951549 26951549 single base substitution T G upstream_gene_variant MELA-AU 9 26951560 26951560 single base substitution T C upstream_gene_variant MELA-AU 9 26951725 26951725 single base substitution C T upstream_gene_variant ORCA-IN 9 26899318 26899318 single base substitution G T downstream_gene_variant ORCA-IN 9 26926396 26926396 single base substitution C A missense_variant C219F 656G>T ORCA-IN 9 26926396 26926396 single base substitution C A missense_variant C243F 728G>T ORCA-IN 9 26926396 26926396 single base substitution C A upstream_gene_variant ORCA-IN 9 26930714 26930714 single base substitution T A intron_variant ORCA-IN 9 26940380 26940380 single base substitution G A intron_variant ORCA-IN 9 26948082 26948082 single base substitution C A upstream_gene_variant OV-AU 9 26901057 26901057 single base substitution A G downstream_gene_variant OV-AU 9 26915945 26915945 single base substitution A G downstream_gene_variant OV-AU 9 26915945 26915945 single base substitution A G intron_variant OV-AU 9 26930923 26930923 single base substitution C A intron_variant OV-AU 9 26935903 26935903 single base substitution T A intron_variant OV-AU 9 26942344 26942344 single base substitution G A intron_variant OV-AU 9 26949673 26949673 single base substitution G T upstream_gene_variant OV-AU 9 26949970 26949970 single base substitution T G upstream_gene_variant PACA-AU 9 26901781 26901781 single base substitution T C downstream_gene_variant PACA-AU 9 26904654 26904654 insertion of <=200bp - T 3_prime_UTR_variant PACA-AU 9 26904654 26904654 insertion of <=200bp - T downstream_gene_variant PACA-AU 9 26924848 26924848 single base substitution C T downstream_gene_variant PACA-AU 9 26924848 26924848 single base substitution C T intron_variant PACA-AU 9 26924848 26924848 single base substitution C T upstream_gene_variant PACA-AU 9 26932273 26932273 single base substitution C T intron_variant PACA-AU 9 26938388 26938388 deletion of <=200bp T - intron_variant PACA-AU 9 26941451 26941451 single base substitution C A intron_variant PACA-AU 9 26945635 26945635 single base substitution C T intron_variant PACA-CA 9 26903201 26903201 single base substitution C T downstream_gene_variant PACA-CA 9 26907801 26907801 single base substitution C T 3_prime_UTR_variant PACA-CA 9 26907801 26907801 single base substitution C T intron_variant PACA-CA 9 26910715 26910715 single base substitution G A intron_variant PACA-CA 9 26918942 26918942 single base substitution T C downstream_gene_variant PACA-CA 9 26918942 26918942 single base substitution T C intron_variant PACA-CA 9 26925308 26925308 single base substitution C T downstream_gene_variant PACA-CA 9 26925308 26925308 single base substitution C T intron_variant PACA-CA 9 26925308 26925308 single base substitution C T upstream_gene_variant PACA-CA 9 26929200 26929200 single base substitution T A intron_variant PACA-CA 9 26932136 26932136 single base substitution T C intron_variant PACA-CA 9 26932627 26932627 single base substitution C T intron_variant PACA-CA 9 26933299 26933299 single base substitution G T intron_variant PACA-CA 9 26933555 26933555 single base substitution G A intron_variant PACA-CA 9 26936837 26936837 single base substitution G C intron_variant PACA-CA 9 26937291 26937291 single base substitution G T intron_variant PACA-CA 9 26942086 26942086 single base substitution A G intron_variant PACA-CA 9 26942439 26942439 single base substitution A G intron_variant PACA-CA 9 26949169 26949169 single base substitution C T upstream_gene_variant PACA-CA 9 26950478 26950478 single base substitution C T upstream_gene_variant PAEN-IT 9 26932353 26932353 single base substitution A T intron_variant PBCA-DE 9 26905099 26905099 single base substitution G A 3_prime_UTR_variant PBCA-DE 9 26905099 26905099 single base substitution G A downstream_gene_variant PBCA-DE 9 26907307 26907307 single base substitution C G downstream_gene_variant PBCA-DE 9 26907307 26907307 single base substitution C G intron_variant PBCA-DE 9 26908727 26908727 single base substitution C T intron_variant PBCA-DE 9 26911178 26911178 insertion of <=200bp - TTT intron_variant PBCA-DE 9 26911185 26911185 deletion of <=200bp C - intron_variant PBCA-DE 9 26929201 26929201 insertion of <=200bp - A intron_variant PBCA-DE 9 26939715 26939715 single base substitution T C intron_variant PBCA-DE 9 26940651 26940651 single base substitution T A intron_variant PRAD-CA 9 26904713 26904713 single base substitution T C 3_prime_UTR_variant PRAD-CA 9 26904713 26904713 single base substitution T C downstream_gene_variant PRAD-UK 9 26900708 26900708 single base substitution G A downstream_gene_variant PRAD-UK 9 26908195 26908195 insertion of <=200bp - GACT intron_variant PRAD-UK 9 26925841 26925841 single base substitution T G downstream_gene_variant PRAD-UK 9 26925841 26925841 single base substitution T G missense_variant D284A 851A>C PRAD-UK 9 26925841 26925841 single base substitution T G upstream_gene_variant PRAD-UK 9 26939086 26939086 single base substitution T C intron_variant PRAD-US 9 26905927 26905927 single base substitution A G downstream_gene_variant PRAD-US 9 26905927 26905927 single base substitution A G missense_variant L274P 821T>C PRAD-US 9 26905927 26905927 single base substitution A G missense_variant L657P 1970T>C PRAD-US 9 26925851 26925851 single base substitution C T downstream_gene_variant PRAD-US 9 26925851 26925851 single base substitution C T missense_variant D281N 841G>A PRAD-US 9 26925851 26925851 single base substitution C T upstream_gene_variant PRAD-US 9 26926460 26926460 single base substitution C T missense_variant E198K 592G>A PRAD-US 9 26926460 26926460 single base substitution C T missense_variant E222K 664G>A PRAD-US 9 26926460 26926460 single base substitution C T upstream_gene_variant READ-US 9 26906045 26906045 single base substitution G A downstream_gene_variant READ-US 9 26906045 26906045 single base substitution G A missense_variant R235W 703C>T READ-US 9 26906045 26906045 single base substitution G A missense_variant R618W 1852C>T READ-US 9 26910421 26910421 single base substitution T G synonymous_variant R196R 588A>C READ-US 9 26910421 26910421 single base substitution T G synonymous_variant R50R 150A>C READ-US 9 26910421 26910421 single base substitution T G synonymous_variant R524R 1572A>C RECA-EU 9 26916877 26916877 single base substitution T C downstream_gene_variant RECA-EU 9 26916877 26916877 single base substitution T C intron_variant RECA-EU 9 26916915 26916915 single base substitution C A downstream_gene_variant RECA-EU 9 26916915 26916915 single base substitution C A intron_variant RECA-EU 9 26920307 26920307 single base substitution C G exon_variant RECA-EU 9 26920307 26920307 single base substitution C G missense_variant G372A 1115G>C RECA-EU 9 26920307 26920307 single base substitution C G missense_variant G44A 131G>C RECA-EU 9 26920307 26920307 single base substitution C G upstream_gene_variant RECA-EU 9 26930107 26930107 single base substitution T A intron_variant SKCA-BR 9 26902637 26902637 single base substitution G A downstream_gene_variant SKCA-BR 9 26906079 26906079 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 9 26906079 26906079 insertion of <=200bp - TA intron_variant SKCA-BR 9 26908144 26908144 single base substitution G A intron_variant SKCA-BR 9 26908165 26908166 deletion of <=200bp CT - intron_variant SKCA-BR 9 26914578 26914578 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 9 26914578 26914578 insertion of <=200bp - CA intron_variant SKCA-BR 9 26915268 26915268 single base substitution C T downstream_gene_variant SKCA-BR 9 26915268 26915268 single base substitution C T intron_variant SKCA-BR 9 26918286 26918286 single base substitution A T downstream_gene_variant SKCA-BR 9 26918286 26918286 single base substitution A T intron_variant SKCA-BR 9 26919175 26919175 single base substitution G A downstream_gene_variant SKCA-BR 9 26919175 26919175 single base substitution G A intron_variant SKCA-BR 9 26922497 26922497 single base substitution G A downstream_gene_variant SKCA-BR 9 26922497 26922497 single base substitution G A intron_variant SKCA-BR 9 26922497 26922497 single base substitution G A upstream_gene_variant SKCA-BR 9 26924142 26924142 single base substitution C T downstream_gene_variant SKCA-BR 9 26924142 26924142 single base substitution C T intron_variant SKCA-BR 9 26924142 26924142 single base substitution C T upstream_gene_variant SKCA-BR 9 26929601 26929601 single base substitution G A intron_variant SKCA-BR 9 26930579 26930580 deletion of <=200bp AT - intron_variant SKCA-BR 9 26933276 26933276 single base substitution A C intron_variant SKCA-BR 9 26934745 26934745 single base substitution G A intron_variant SKCA-BR 9 26938552 26938553 deletion of <=200bp TA - intron_variant SKCA-BR 9 26939639 26939639 single base substitution G A intron_variant SKCA-BR 9 26941818 26941818 single base substitution G A intron_variant SKCA-BR 9 26941832 26941832 single base substitution G A intron_variant SKCA-BR 9 26946576 26946576 single base substitution C G intron_variant SKCA-BR 9 26948448 26948448 insertion of <=200bp - TATTATTA upstream_gene_variant SKCM-US 9 26910388 26910388 single base substitution G A synonymous_variant F207F 621C>T SKCM-US 9 26910388 26910388 single base substitution G A synonymous_variant F535F 1605C>T SKCM-US 9 26910388 26910388 single base substitution G A synonymous_variant F61F 183C>T SKCM-US 9 26913921 26913921 single base substitution G A downstream_gene_variant SKCM-US 9 26913921 26913921 single base substitution G A missense_variant S176F 527C>T SKCM-US 9 26913921 26913921 single base substitution G A missense_variant S30F 89C>T SKCM-US 9 26913921 26913921 single base substitution G A missense_variant S504F 1511C>T SKCM-US 9 26913937 26913937 single base substitution G A downstream_gene_variant SKCM-US 9 26913937 26913937 single base substitution G A missense_variant R171C 511C>T SKCM-US 9 26913937 26913937 single base substitution G A missense_variant R25C 73C>T SKCM-US 9 26913937 26913937 single base substitution G A missense_variant R499C 1495C>T SKCM-US 9 26919485 26919485 single base substitution G C exon_variant SKCM-US 9 26919485 26919485 single base substitution G C missense_variant P414A 1240C>G SKCM-US 9 26919485 26919485 single base substitution G C missense_variant P86A 256C>G SKCM-US 9 26919485 26919485 single base substitution G C upstream_gene_variant SKCM-US 9 26919513 26919513 single base substitution A T exon_variant SKCM-US 9 26919513 26919513 single base substitution A T synonymous_variant V404V 1212T>A SKCM-US 9 26919513 26919513 single base substitution A T synonymous_variant V76V 228T>A SKCM-US 9 26919513 26919513 single base substitution A T upstream_gene_variant SKCM-US 9 26920318 26920318 single base substitution A C exon_variant SKCM-US 9 26920318 26920318 single base substitution A C missense_variant S368R 1104T>G SKCM-US 9 26920318 26920318 single base substitution A C missense_variant S40R 120T>G SKCM-US 9 26920318 26920318 single base substitution A C upstream_gene_variant SKCM-US 9 26925929 26925929 single base substitution G A synonymous_variant L231L 691C>T SKCM-US 9 26925929 26925929 single base substitution G A synonymous_variant L255L 763C>T SKCM-US 9 26925929 26925929 single base substitution G A upstream_gene_variant SKCM-US 9 26926415 26926415 single base substitution T A missense_variant I213L 637A>T SKCM-US 9 26926415 26926415 single base substitution T A missense_variant I237L 709A>T SKCM-US 9 26926415 26926415 single base substitution T A upstream_gene_variant SKCM-US 9 26928394 26928394 single base substitution G A missense_variant S119L 356C>T SKCM-US 9 26928394 26928394 single base substitution G A missense_variant S95L 284C>T STAD-US 9 26910403 26910403 single base substitution T C synonymous_variant T202T 606A>G STAD-US 9 26910403 26910403 single base substitution T C synonymous_variant T530T 1590A>G STAD-US 9 26910403 26910403 single base substitution T C synonymous_variant T56T 168A>G STAD-US 9 26919401 26919401 single base substitution T C exon_variant STAD-US 9 26919401 26919401 single base substitution T C missense_variant M114V 340A>G STAD-US 9 26919401 26919401 single base substitution T C missense_variant M442V 1324A>G STAD-US 9 26919401 26919401 single base substitution T C upstream_gene_variant STAD-US 9 26919405 26919405 single base substitution A T exon_variant STAD-US 9 26919405 26919405 single base substitution A T missense_variant N112K 336T>A STAD-US 9 26919405 26919405 single base substitution A T missense_variant N440K 1320T>A STAD-US 9 26919405 26919405 single base substitution A T upstream_gene_variant STAD-US 9 26920381 26920381 single base substitution A G splice_region_variant STAD-US 9 26920381 26920381 single base substitution A G upstream_gene_variant STAD-US 9 26935065 26935065 single base substitution A G missense_variant F73L 217T>C STAD-US 9 26935065 26935065 single base substitution A G missense_variant F97L 289T>C STAD-US 9 26935204 26935204 single base substitution A G intron_variant STAD-US 9 26935204 26935204 single base substitution A G splice_region_variant UCEC-US 9 26905614 26905614 single base substitution T G downstream_gene_variant UCEC-US 9 26905614 26905614 single base substitution T G missense_variant Q761H 2283A>C UCEC-US 9 26905646 26905646 single base substitution T C downstream_gene_variant UCEC-US 9 26905646 26905646 single base substitution T C missense_variant T751A 2251A>G UCEC-US 9 26905722 26905722 single base substitution A G downstream_gene_variant UCEC-US 9 26905722 26905722 single base substitution A G synonymous_variant C725C 2175T>C UCEC-US 9 26905751 26905751 single base substitution C T downstream_gene_variant UCEC-US 9 26905751 26905751 single base substitution C T missense_variant D716N 2146G>A UCEC-US 9 26905837 26905837 single base substitution G A downstream_gene_variant UCEC-US 9 26905837 26905837 single base substitution G A missense_variant A687V 2060C>T UCEC-US 9 26905933 26905933 single base substitution T G downstream_gene_variant UCEC-US 9 26905933 26905933 single base substitution T G missense_variant N272T 815A>C UCEC-US 9 26905933 26905933 single base substitution T G missense_variant N655T 1964A>C UCEC-US 9 26910336 26910336 single base substitution C A missense_variant D225Y 673G>T UCEC-US 9 26910336 26910336 single base substitution C A missense_variant G553C 1657G>T UCEC-US 9 26910336 26910336 single base substitution C A missense_variant G79C 235G>T UCEC-US 9 26923269 26923269 single base substitution C A downstream_gene_variant UCEC-US 9 26923269 26923269 single base substitution C A stop_gained E316* 946G>T UCEC-US 9 26923269 26923269 single base substitution C A upstream_gene_variant UCEC-US 9 26923308 26923308 single base substitution G A downstream_gene_variant UCEC-US 9 26923308 26923308 single base substitution G A stop_gained R303* 907C>T UCEC-US 9 26923308 26923308 single base substitution G A upstream_gene_variant UCEC-US 9 26923312 26923312 single base substitution T G downstream_gene_variant UCEC-US 9 26923312 26923312 single base substitution T G missense_variant E301D 903A>C UCEC-US 9 26923312 26923312 single base substitution T G upstream_gene_variant UCEC-US 9 26925944 26925944 single base substitution C T missense_variant A226T 676G>A UCEC-US 9 26925944 26925944 single base substitution C T missense_variant A250T 748G>A UCEC-US 9 26925944 26925944 single base substitution C T upstream_gene_variant UCEC-US 9 26928172 26928172 single base substitution C T missense_variant G140D 419G>A UCEC-US 9 26928172 26928172 single base substitution C T missense_variant G164D 491G>A UCEC-US 9 26928172 26928172 single base substitution C T upstream_gene_variant UCEC-US 9 26928189 26928189 single base substitution C A missense_variant K134N 402G>T UCEC-US 9 26928189 26928189 single base substitution C A missense_variant K158N 474G>T UCEC-US 9 26928189 26928189 single base substitution C A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-CG-5733-01 COSM3906690 c.1153A>G p.M385V Substitution - Missense 9:26919403-26919403 - TCGA-D1-A17U-01 COSM1107927 c.1841C>T p.A614V Substitution - Missense 9:26905887-26905887 - TCGA-D1-A17M-01 COSM4865077 c.748G>A p.A250T Substitution - Missense 9:26925946-26925946 - TCGA-DM-A282-01 COSM1461840 c.944G>A p.G315E Substitution - Missense 9:26920309-26920309 - ESO-179 COSM1262338 c.1198G>A p.G400S Substitution - Missense 9:26919358-26919358 - TCGA-EE-A2MJ-06 COSM3656686 c.1434C>T p.F478F Substitution - coding silent 9:26910390-26910390 - DN14065 COSM5962838 c.1487-4C>A p.? Unknown 9:26908002-26908002 - B35 COSM1756111 c.392C>T p.S131L Substitution - Missense 9:26928102-26928102 - TCGA-BS-A0UF-01 COSM1107923 c.2080A>G p.T694A Substitution - Missense 9:26905648-26905648 - S02382 COSM5698051 c.2203G>A p.V735I Substitution - Missense 9:26905696-26905696 - 23T COSM3716280 c.557G>T p.C186F Substitution - Missense 9:26926398-26926398 - TCGA-HC-A6AL-01 COSM3675314 c.1799T>C p.L600P Substitution - Missense 9:26905929-26905929 - J90_T COSM3952640 c.2138C>G p.S713C Substitution - Missense 9:26905590-26905590 - TCGA-BC-A69H-01 COSM4919093 c.2010G>C p.Q670H Substitution - Missense 9:26905889-26905889 - TCGA-EE-A2MJ-06 COSM3656690 c.1041T>A p.V347V Substitution - coding silent 9:26919515-26919515 - TCGA-23-2645-01 COSM1331597 c.1222C>T p.P408S Substitution - Missense 9:26919334-26919334 - TCGA-CM-5861-01 COSM4787234 c.1536C>T p.A512A Substitution - coding silent 9:26913898-26913898 - TCGA-CG-5721-01 COSM3906692 c.870T>C p.G290G Substitution - coding silent 9:26920383-26920383 - TCGA-BS-A0TA-01 COSM1107932 c.736C>T p.R246* Substitution - Nonsense 9:26923310-26923310 - TCGA-F5-6812-01 COSM1569307 c.1681C>T p.R561W Substitution - Missense 9:26906047-26906047 - TCGA-D5-6540-01 COSM4783047 c.1445C>T p.S482L Substitution - Missense 9:26917138-26917138 - TCGA-EE-A2MK-06 COSM4892106 c.763C>T p.L255L Substitution - coding silent 9:26925931-26925931 - TCGA-G2-A2EO-01 COSM1314735 c.1866G>C p.Q622H Substitution - Missense 9:26905862-26905862 - TCGA-D5-6540-01 COSM1461839 c.1274C>T p.S425L Substitution - Missense 9:26917138-26917138 - TCGA-D1-A17M-01 COSM4865066 c.2175T>C p.C725C Substitution - coding silent 9:26905724-26905724 - TCGA-CM-5861-01 COSM1461838 c.1365C>T p.A455A Substitution - coding silent 9:26913898-26913898 - TCGA-BS-A0UV-01 COSM4864594 c.2146G>A p.D716N Substitution - Missense 9:26905753-26905753 - TCGA-DD-A1EB-01 COSM4928746 c.951G>T p.L317L Substitution - coding silent 9:26923266-26923266 - TCGA-AX-A0J0-01 COSM1107928 c.1793A>C p.N598T Substitution - Missense 9:26905935-26905935 - PD4005a COSM4809410 c.1204G>C p.D402H Substitution - Missense 9:26919523-26919523 - BRC16 COSM5027056 c.2211G>A p.L737L Substitution - coding silent 9:26905517-26905517 - TCGA-BS-A0UF-01 COSM4875915 c.946G>T p.E316* Substitution - Nonsense 9:26923271-26923271 - TCGA-HC-A6AL-01 COSM4876800 c.1970T>C p.L657P Substitution - Missense 9:26905929-26905929 - 360_T COSM3952641 c.1809C>T p.L603L Substitution - coding silent 9:26905919-26905919 - TCGA-A5-A0GP-01 COSM1107922 c.2112A>C p.Q704H Substitution - Missense 9:26905616-26905616 - PCSI_0114_Pa_P COSM4965804 c.126C>A p.T42T Substitution - coding silent 9:26946920-26946920 - TCGA-FS-A1ZK-06 COSM3926648 c.933T>G p.S311R Substitution - Missense 9:26920320-26920320 - TCGA-BC-A3KF-01 COSM4927798 c.2091T>C p.S697S Substitution - coding silent 9:26905637-26905637 - ESCC-154T COSM3942997 c.631C>T p.R211* Substitution - Nonsense 9:26925892-26925892 - ESCC_170 COSM5649586 c.1360A>G p.M454V Substitution - Missense 9:26913903-26913903 - TCGA-BS-A0UV-01 COSM1107925 c.1975G>A p.D659N Substitution - Missense 9:26905753-26905753 - TCGA-BG-A0M4-01 COSM1107935 c.320G>A p.G107D Substitution - Missense 9:26928174-26928174 - RKO COSM4373479 c.2078G>A p.G693E Substitution - Missense 9:26905821-26905821 - TCGA-BR-4361-01 COSM3906694 c.150T>C p.S50S Substitution - coding silent 9:26935206-26935206 - C125 COSM4616969 c.2338G>C p.E780Q Substitution - Missense 9:26905561-26905561 - T3498 COSM4714936 c.1810A>T p.R604W Substitution - Missense 9:26905918-26905918 - TCGA-CM-6162-01 COSM4949211 c.714C>A p.S238S Substitution - coding silent 9:26926412-26926412 - TCGA-P4-A5EB-01 COSM4908311 c.741G>T p.V247V Substitution - coding silent 9:26925953-26925953 - OSCC-GB_00230111 COSM3716280 c.557G>T p.C186F Substitution - Missense 9:26926398-26926398 - TCGA-AC-A23H-01 COSM4815455 c.2294C>G p.S765C Substitution - Missense 9:26905605-26905605 - TCGA-EE-A2MD-06 COSM3656687 c.1340C>T p.S447F Substitution - Missense 9:26913923-26913923 - TCGA-BR-6452-01 COSM4907454 c.289T>C p.F97L Substitution - Missense 9:26935067-26935067 - TCGA-CS-6666-01 COSM3930005 c.1811G>A p.R604K Substitution - Missense 9:26905917-26905917 - TCGA-EE-A29M-06 COSM3656688 c.1324C>T p.R442C Substitution - Missense 9:26913939-26913939 - TCGA-DM-A282-01 COSM4784480 c.1115G>A p.G372E Substitution - Missense 9:26920309-26920309 - TCGA-E2-A1II-01 COSM5228895 c.1689delT p.E564fs*5 Deletion - Frameshift 9:26907967-26907967 - OSCC-GB_00230111 COSM4889900 c.728G>T p.C243F Substitution - Missense 9:26926398-26926398 - BD87T COSM2771334 c.810C>T p.G270G Substitution - coding silent 9:26923236-26923236 - YUKAT COSM5410942 c.120C>T p.D40D Substitution - coding silent 9:26946926-26946926 - TCGA-EJ-7782-01 COSM4879263 c.841G>A p.D281N Substitution - Missense 9:26925853-26925853 - TCGA-FW-A3R5-06 COSM3926649 c.185C>T p.S62L Substitution - Missense 9:26928396-26928396 - TCGA-BS-A0UF-01 COSM1107931 c.775G>T p.E259* Substitution - Nonsense 9:26923271-26923271 - TCGA-KK-A6E4-01 COSM4876473 c.493G>A p.E165K Substitution - Missense 9:26926462-26926462 - TCGA-D1-A103-01 COSM1107929 c.1486G>T p.G496C Substitution - Missense 9:26910338-26910338 - HCC97 COSM1624884 c.628A>G p.I210V Substitution - Missense 9:26925895-26925895 - LUAD-E01317 COSM403875 c.1866G>A p.Q622Q Substitution - coding silent 9:26905862-26905862 - C0042T COSM4138919 c.944G>C p.G315A Substitution - Missense 9:26920309-26920309 - TCGA-CS-6666-01 COSM4908702 c.1982G>A p.R661K Substitution - Missense 9:26905917-26905917 - TCGA-HU-A4H4-01 COSM4907776 c.1590A>G p.T530T Substitution - coding silent 9:26910405-26910405 - TCGA-EJ-7782-01 COSM3784225 c.670G>A p.D224N Substitution - Missense 9:26925853-26925853 - PT14_1 COSM3656688 c.1324C>T p.R442C Substitution - Missense 9:26913939-26913939 - TCGA-BR-6452-01 COSM3906691 c.1149T>A p.N383K Substitution - Missense 9:26919407-26919407 - QC2-22-T2 COSM5653023 c.2059G>T p.A687S Substitution - Missense 9:26905840-26905840 - CSCC-20-T COSM4454281 c.280A>G p.T94A Substitution - Missense 9:26928214-26928214 - TCGA-G2-A2EO-01 COSM4811998 c.2037G>C p.Q679H Substitution - Missense 9:26905862-26905862 - TCGA-EE-A2MJ-06 COSM4892080 c.1605C>T p.F535F Substitution - coding silent 9:26910390-26910390 - TCGA-EE-A2MD-06 COSM4899274 c.1511C>T p.S504F Substitution - Missense 9:26913923-26913923 - PD4005a COSM219293 c.1033G>C p.D345H Substitution - Missense 9:26919523-26919523 - TCGA-EB-A1NK-01 COSM3656689 c.1069C>G p.P357A Substitution - Missense 9:26919487-26919487 - T3498 COSM4714935 c.1981A>T p.R661W Substitution - Missense 9:26905918-26905918 - TCGA-AC-A23H-01 COSM3848276 c.2123C>G p.S708C Substitution - Missense 9:26905605-26905605 - PD4005a COSM219293 c.1033G>C p.D345H Substitution - Missense 9:26919523-26919523 - ESCC-154T COSM4909111 c.802C>T p.R268* Substitution - Nonsense 9:26925892-26925892 - 0057_CRUK_PC_0057_T1_DNA COSM5422703 c.851A>C p.D284A Substitution - Missense 9:26925843-26925843 - TCGA-D8-A1XK-01 COSM3848277 c.1304A>G p.D435G Substitution - Missense 9:26917108-26917108 - SJOS010_D COSM5023228 c.272A>G p.D91G Substitution - Missense 9:26935084-26935084 - CSCC-27-T COSM4463642 c.129C>T p.T43T Substitution - coding silent 9:26946917-26946917 - LUAD-NYU284 COSM373371 c.759C>T p.I253I Substitution - coding silent 9:26923287-26923287 - HCT116 COSM2771323 c.1569G>A p.L523L Substitution - coding silent 9:26907916-26907916 - ESCC_BICR_010T COSM5436073 c.228A>T p.S76S Substitution - coding silent 9:26935128-26935128 - TCGA-B5-A11O-01 COSM1107937 c.69C>A p.Y23* Substitution - Nonsense 9:26935116-26935116 - 19 COSM5746969 c.341C>T p.A114V Substitution - Missense 9:26928153-26928153 - GCT27 COSM5749445 c.1292T>C p.L431P Substitution - Missense 9:26917120-26917120 - TCGA-CK-5916-01 COSM3699299 c.270G>A p.L90L Substitution - coding silent 9:26928311-26928311 - TCGA-D1-A17M-01 COSM1107924 c.2004T>C p.C668C Substitution - coding silent 9:26905724-26905724 - TCGA-AP-A0LM-01 COSM1107936 c.303G>T p.K101N Substitution - Missense 9:26928191-26928191 - TCGA-BS-A0UF-01 COSM4875973 c.2251A>G p.T751A Substitution - Missense 9:26905648-26905648 - J75_T COSM5762394 c.670G>C p.D224H Substitution - Missense 9:26925853-26925853 - TCGA-FS-A1ZK-06 COSM4892179 c.1104T>G p.S368R Substitution - Missense 9:26920320-26920320 - TCGA-CK-5916-01 COSM4948020 c.441G>A p.L147L Substitution - coding silent 9:26928311-26928311 - TCGA-18-4721-01 COSM753709 c.283G>T p.A95S Substitution - Missense 9:26928211-26928211 - TCGA-EE-A29M-06 COSM4897450 c.1495C>T p.R499C Substitution - Missense 9:26913939-26913939 - ZZUFHECRKL-G072T COSM5432929 c.804A>G p.R268R Substitution - coding silent 9:26925890-26925890 - HCC97T COSM4781392 c.799A>G p.I267V Substitution - Missense 9:26925895-26925895 - TCGA-D1-A103-01 COSM4874703 c.1657G>T p.G553C Substitution - Missense 9:26910338-26910338 - RKO COSM2771321 c.1907G>A p.G636E Substitution - Missense 9:26905821-26905821 - TCGA-BG-A0M4-01 COSM4868136 c.491G>A p.G164D Substitution - Missense 9:26928174-26928174 - TCGA-EB-A1NK-01 COSM4899207 c.1240C>G p.P414A Substitution - Missense 9:26919487-26919487 - TCGA-AX-A0J1-01 COSM1107926 c.1889C>T p.A630V Substitution - Missense 9:26905839-26905839 - J75_T COSM5762393 c.841G>C p.D281H Substitution - Missense 9:26925853-26925853 - TCGA-AD-6895-01 COSM1461837 c.1430_1433delATTT p.Y477fs*18 Deletion - Frameshift 9:26910391-26910394 - 3N44-VS-3T44 COSM4982340 c.1129A>G p.I377V Substitution - Missense 9:26920295-26920295 - HCC4T COSM1624883 c.1652-6delT p.? Unknown 9:26906082-26906082 - TCGA-AK-3429-01 COSM487333 c.1622T>C p.I541T Substitution - Missense 9:26907863-26907863 - P09-1372 COSM246622 c.695C>T p.A232V Substitution - Missense 9:26925828-26925828 - TCGA-BC-A3KF-01 COSM4927797 c.2262T>C p.S754S Substitution - coding silent 9:26905637-26905637 - T75 COSM1177699 c.1422G>A p.M474I Substitution - Missense 9:26910402-26910402 - TCGA-AD-6895-01 COSM5130044 c.1601_1604delATTT p.Y534fs*18 Deletion - Frameshift 9:26910391-26910394 - TCGA-CG-5733-01 COSM4906530 c.1324A>G p.M442V Substitution - Missense 9:26919403-26919403 - YUWHIM COSM1700997 c.1601C>T p.P534L Substitution - Missense 9:26907884-26907884 - TCGA-AX-A0J0-01 COSM4867228 c.1964A>C p.N655T Substitution - Missense 9:26905935-26905935 - PD13418a COSM5794882 c.1068C>T p.I356I Substitution - coding silent 9:26920356-26920356 - PD13418a COSM5794883 c.897C>T p.I299I Substitution - coding silent 9:26920356-26920356 - TCGA-GN-A266-06 COSM3656692 c.538A>T p.I180L Substitution - Missense 9:26926417-26926417 - STC291 COSM5063862 c.538G>A p.A180T Substitution - Missense 9:26928127-26928127 - TCGA-AP-A0LM-01 COSM1107933 c.732A>C p.E244D Substitution - Missense 9:26923314-26923314 - TCGA-D1-A17M-01 COSM1107934 c.577G>A p.A193T Substitution - Missense 9:26925946-26925946 - TCGA-AP-A0LM-01 COSM4873832 c.474G>T p.K158N Substitution - Missense 9:26928191-26928191 - C0042T COSM4138918 c.1115G>C p.G372A Substitution - Missense 9:26920309-26920309 - TCGA-BS-A0TA-01 COSM4873964 c.907C>T p.R303* Substitution - Nonsense 9:26923310-26923310 - TCGA-HU-A4H4-01 COSM3906689 c.1419A>G p.T473T Substitution - coding silent 9:26910405-26910405 - NCI-H720 COSM4373503 c.569A>T p.H190L Substitution - Missense 9:26926557-26926557 - TCGA-BR-6452-01 COSM4907484 c.1320T>A p.N440K Substitution - Missense 9:26919407-26919407 - ESCC_BICR_010T COSM5436074 c.57A>T p.S19S Substitution - coding silent 9:26935128-26935128 - ESCC_170 COSM5649585 c.1531A>G p.M511V Substitution - Missense 9:26913903-26913903 - 2492722 COSM5724528 c.1546C>A p.P516T Substitution - Missense 9:26913888-26913888 - TCGA-F5-6814-01 COSM3433078 c.1401A>C p.R467R Substitution - coding silent 9:26910423-26910423 - TCGA-B2-3924-01 COSM487334 c.1400G>T p.R467L Substitution - Missense 9:26910424-26910424 - 0057_CRUK_PC_0057_T1_DNA COSM5422704 c.680A>C p.D227A Substitution - Missense 9:26925843-26925843 - PT14_1 COSM4897450 c.1495C>T p.R499C Substitution - Missense 9:26913939-26913939 - DN14065 COSM5962837 c.1658-4C>A p.? Unknown 9:26908002-26908002 - TCGA-DD-A1EB-01 COSM4928747 c.780G>T p.L260L Substitution - coding silent 9:26923266-26923266 - TCGA-13-2059-01 COSM1331598 c.1240T>A p.F414I Substitution - Missense 9:26919316-26919316 - NCI-H720 COSM2771343 c.398A>T p.H133L Substitution - Missense 9:26926557-26926557 - TCGA-F5-6812-01 COSM4782614 c.1852C>T p.R618W Substitution - Missense 9:26906047-26906047 - TCGA-KK-A6E4-01 COSM4876472 c.664G>A p.E222K Substitution - Missense 9:26926462-26926462 - HCC97T COSM1624884 c.628A>G p.I210V Substitution - Missense 9:26925895-26925895 - TCGA-18-4721-01 COSM4859948 c.454G>T p.A152S Substitution - Missense 9:26928211-26928211 - TCGA-CG-5721-01 COSM4906790 c.1041T>C p.G347G Substitution - coding silent 9:26920383-26920383 - TCGA-GN-A266-06 COSM4893652 c.709A>T p.I237L Substitution - Missense 9:26926417-26926417 - S02382 COSM5698052 c.2032G>A p.V678I Substitution - Missense 9:26905696-26905696 - STC291 COSM5063863 c.367G>A p.A123T Substitution - Missense 9:26928127-26928127 - TCGA-AP-A0LM-01 COSM4873753 c.903A>C p.E301D Substitution - Missense 9:26923314-26923314 - TCGA-BR-6452-01 COSM3906693 c.118T>C p.F40L Substitution - Missense 9:26935067-26935067 - HCC125T COSM1624882 c.1652-6_1652-5insT p.? Unknown 9:26906081-26906082 - TCGA-D8-A1XK-01 COSM4814046 c.1475A>G p.D492G Substitution - Missense 9:26917108-26917108 - TCGA-EE-A2MJ-06 COSM4892095 c.1212T>A p.V404V Substitution - coding silent 9:26919515-26919515 - TCGA-P4-A5EB-01 COSM3996498 c.570G>T p.V190V Substitution - coding silent 9:26925953-26925953 - QC2-22-T2 COSM5653024 c.1888G>T p.A630S Substitution - Missense 9:26905840-26905840 - TCGA-F5-6814-01 COSM4782411 c.1572A>C p.R524R Substitution - coding silent 9:26910423-26910423 - BD87T COSM4373494 c.981C>T p.G327G Substitution - coding silent 9:26923236-26923236 - ZZUFHECRKL-G072T COSM5432930 c.633A>G p.R211R Substitution - coding silent 9:26925890-26925890 - TCGA-EE-A2MK-06 COSM3656691 c.592C>T p.L198L Substitution - coding silent 9:26925931-26925931 - TCGA-AG-3892-01 COSM257744 c.164A>C p.K55T Substitution - Missense 9:26935021-26935021 - 2492722 COSM5724529 c.1375C>A p.P459T Substitution - Missense 9:26913888-26913888 - CSCC-20-T COSM4454280 c.451A>G p.T151A Substitution - Missense 9:26928214-26928214 - LUAD-5V8LT COSM403079 c.1525A>T p.K509* Substitution - Nonsense 9:26907960-26907960 - TCGA-A5-A0GP-01 COSM4865919 c.2283A>C p.Q761H Substitution - Missense 9:26905616-26905616 - C125 COSM4616970 c.2167G>C p.E723Q Substitution - Missense 9:26905561-26905561 - BRC16 COSM5027055 c.2382G>A p.L794L Substitution - coding silent 9:26905517-26905517 - TCGA-CM-6162-01 COSM1461841 c.543C>A p.S181S Substitution - coding silent 9:26926412-26926412 - TCGA-E2-A1II-01 COSM5228896 c.1518delT p.E507fs*5 Deletion - Frameshift 9:26907967-26907967 - TCGA-AP-A0LO-01 COSM1107930 c.1411T>C p.S471P Substitution - Missense 9:26910413-26910413 - TCGA-BC-A69H-01 COSM4919094 c.1839G>C p.Q613H Substitution - Missense 9:26905889-26905889 - SJOS010_D COSM5023229 c.101A>G p.D34G Substitution - Missense 9:26935084-26935084 - GCT27 COSM5749444 c.1463T>C p.L488P Substitution - Missense 9:26917120-26917120 - 19 COSM5746968 c.512C>T p.A171V Substitution - Missense 9:26928153-26928153 - TCGA-29-1768-01 COSM1331599 c.1658T>C p.V553A Substitution - Missense 9:26906070-26906070 - HCT116 COSM4373481 c.1740G>A p.L580L Substitution - coding silent 9:26907916-26907916 - PD4005a COSM4809410 c.1204G>C p.D402H Substitution - Missense 9:26919523-26919523 - 3N44-VS-3T44 COSM4982341 c.958A>G p.I320V Substitution - Missense 9:26920295-26920295 - TCGA-AX-A0J1-01 COSM4867603 c.2060C>T p.A687V Substitution - Missense 9:26905839-26905839 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.27182 9p21 603873 1531352|dbSNP|BC032551|A/C|coding|Thr592Pro|1880|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.S368R c.1104T>G 9 26920318 CM A G Missense p.C276R c.826T>C 9 26925866 HNSC A G Missense p.L657P c.1970T>C 9 26905927 PRAD A G Synonymous p.C725C c.2175T>C 9 26905722 UCEC A T Synonymous p.V404V c.1212T>A 9 26919513 CM C A Missense p.A152S c.454G>T 9 26928209 LUSC C G Missense p.Q679H c.2037G>C 9 26905860 BLCA C G SpliceAcceptorSNV . c.1823-1G>C 9 26906075 STAD C T 3-UTRSNV . c.2385+21G>A 9 26905491 ESCA C T Missense p.A250T c.748G>A 9 26925944 UCEC C T Missense p.E222K c.664G>A 9 26926460 PRAD C T Missense p.G164D c.491G>A 9 26928172 UCEC C T Missense p.G457S c.1369G>A 9 26919356 ESCA C T Missense p.G475S c.1423G>A 9 26917158 CM C T Missense p.R661K c.1982G>A 9 26905915 LGG C T Synonymous p.L794L c.2382G>A 9 26905515 BRCA G A Missense p.R499C c.1495C>T 9 26913937 CM G A Missense p.S504F c.1511C>T 9 26913921 CM G A Nonsense p.R303* c.907C>T 9 26923308 UCEC G A Synonymous p.F535F c.1605C>T 9 26910388 CM G A Synonymous p.L255L c.763C>T 9 26925929 CM G C Missense p.P414A c.1240C>G 9 26919485 CM T A Missense p.H699L c.2096A>T 9 26905801 CM T A Missense p.K774M c.2321A>T 9 26905576 HNSC TCAAAAAAAAAAAAAAAAAAAAAAAAA - IntronicDeletion . c.343+1200_343+1226delTTTTTTTTTTTTTTTTTTTTTTTTTGA 9 26933785 CLL T C Missense p.M442V c.1324A>G 9 26919401 STAD T C Missense p.R182G c.544A>G 9 26928119 LUAD T G Missense p.Q761H c.2283A>C 9 26905614 UCEC