Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 17 1371412 1371412 + Silent SNP C C T TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr17:1371412C>T c.2661G>A c.(2659-2661)gcG>gcA p.A887A BLCA 17 1370776 1370776 + Silent SNP G G A TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chr17:1370776G>A c.2958C>T c.(2956-2958)ggC>ggT p.G986G BLCA 17 1371362 1371362 + Missense_Mutation SNP T T C TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr17:1371362T>C c.2711A>G c.(2710-2712)cAg>cGg p.Q904R BLCA 17 1374391 1374391 + Missense_Mutation SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr17:1374391G>A c.2081C>T c.(2080-2082)gCc>gTc p.A694V BLCA 17 1375225 1375225 + Missense_Mutation SNP C C T TCGA-C4-A0F7-01A-11D-A10S-08 TCGA-C4-A0F7-10A-01D-A10S-08 g.chr17:1375225C>T c.1892G>A c.(1891-1893)cGc>cAc p.R631H BLCA 17 1375308 1375308 + Silent SNP G G A TCGA-4Z-AA7S-01A-11D-A391-08 TCGA-4Z-AA7S-10A-01D-A394-08 g.chr17:1375308G>A c.1809C>T c.(1807-1809)gaC>gaT p.D603D BLCA 17 1375431 1375431 + Missense_Mutation SNP T T A TCGA-XF-AAN4-01A-11D-A42E-08 TCGA-XF-AAN4-10A-01D-A42H-08 g.chr17:1375431T>A c.1784A>T c.(1783-1785)gAt>gTt p.D595V BLCA 17 1378124 1378124 + Silent SNP G G T TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr17:1378124G>T c.1593C>A c.(1591-1593)ctC>ctA p.L531L BLCA 17 1381474 1381474 + Silent SNP G G A TCGA-E5-A2PC-01A-11D-A202-08 TCGA-E5-A2PC-10B-01D-A202-08 g.chr17:1381474G>A c.1203C>T c.(1201-1203)ttC>ttT p.F401F BLCA 17 1381931 1381931 + Silent SNP G G A TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr17:1381931G>A c.1086C>T c.(1084-1086)atC>atT p.I362I BLCA 17 1386204 1386204 + Missense_Mutation SNP C C T TCGA-FD-A3B6-01A-21D-A20D-08 TCGA-FD-A3B6-10A-01D-A20D-08 g.chr17:1386204C>T c.392G>A c.(391-393)cGc>cAc p.R131H BLCA 17 1387516 1387516 + Missense_Mutation SNP G G T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr17:1387516G>T c.52C>A c.(52-54)Ctg>Atg p.L18M BRCA 17 1374587 1374587 + Missense_Mutation SNP G G A TCGA-D8-A1XM-01A-21D-A14K-09 TCGA-D8-A1XM-10A-01D-A14K-09 g.chr17:1374587G>A c.1960C>T c.(1960-1962)Cgg>Tgg p.R654W BRCA 17 1383839 1383839 + Silent SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr17:1383839G>A c.783C>T c.(781-783)ttC>ttT p.F261F CESC 17 1370785 1370785 + Silent SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr17:1370785G>A c.2949C>T c.(2947-2949)atC>atT p.I983I CESC 17 1371352 1371352 + Silent SNP G G C TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr17:1371352G>C c.2721C>G c.(2719-2721)ctC>ctG p.L907L CESC 17 1377928 1377928 + Silent SNP G G A TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr17:1377928G>A c.1668C>T c.(1666-1668)ctC>ctT p.L556L CESC 17 1381435 1381435 + Silent SNP G G A TCGA-EK-A2RB-01A-11D-A18J-09 TCGA-EK-A2RB-10A-01D-A18J-09 g.chr17:1381435G>A c.1242C>T c.(1240-1242)ttC>ttT p.F414F CHOL 17 1384109 1384109 + Missense_Mutation SNP C C A TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr17:1384109C>A c.593G>T c.(592-594)gGg>gTg p.G198V COAD 17 1369024 1369024 + Missense_Mutation SNP C C A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr17:1369024C>A c.3083G>T c.(3082-3084)cGg>cTg p.R1028L COAD 17 1372854 1372854 + Missense_Mutation SNP G G A TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr17:1372854G>A c.2476C>T c.(2476-2478)Cgg>Tgg p.R826W COAD 17 1373557 1373557 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr17:1373557C>T c.2333G>A c.(2332-2334)cGc>cAc p.R778H COAD 17 1373564 1373564 + Missense_Mutation SNP G G T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:1373564G>T c.2326C>A c.(2326-2328)Cat>Aat p.H776N COAD 17 1375229 1375229 + Missense_Mutation SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr17:1375229G>A c.1888C>T c.(1888-1890)Cgc>Tgc p.R630C COAD 17 1377974 1377974 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:1377974C>T c.1622G>A c.(1621-1623)aGc>aAc p.S541N COAD 17 1378233 1378233 + Splice_Site SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr17:1378233G>A c.1563C>T c.(1561-1563)acC>acT p.T521T COAD 17 1381979 1381979 + Silent SNP G G A TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr17:1381979G>A c.1038C>T c.(1036-1038)ctC>ctT p.L346L COAD 17 1381997 1381997 + Silent SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr17:1381997C>T c.1020G>A c.(1018-1020)gcG>gcA p.A340A COAD 17 1382900 1382900 + Missense_Mutation SNP T T C TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr17:1382900T>C c.901A>G c.(901-903)Aag>Gag p.K301E COAD 17 1382944 1382944 + Missense_Mutation SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr17:1382944G>A c.857C>T c.(856-858)gCc>gTc p.A286V COAD 17 1385799 1385799 + Silent SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr17:1385799C>T c.495G>A c.(493-495)aaG>aaA p.K165K COAD 17 1386205 1386205 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr17:1386205G>A c.391C>T c.(391-393)Cgc>Tgc p.R131C COAD 17 1386346 1386346 + Missense_Mutation SNP C C T TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr17:1386346C>T c.250G>A c.(250-252)Gtg>Atg p.V84M COADREAD 17 1369024 1369024 + Missense_Mutation SNP C C A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr17:1369024C>A c.3083G>T c.(3082-3084)cGg>cTg p.R1028L COADREAD 17 1372854 1372854 + Missense_Mutation SNP G G A TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr17:1372854G>A c.2476C>T c.(2476-2478)Cgg>Tgg p.R826W COADREAD 17 1373557 1373557 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr17:1373557C>T c.2333G>A c.(2332-2334)cGc>cAc p.R778H COADREAD 17 1373564 1373564 + Missense_Mutation SNP G G T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:1373564G>T c.2326C>A c.(2326-2328)Cat>Aat p.H776N COADREAD 17 1375229 1375229 + Missense_Mutation SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr17:1375229G>A c.1888C>T c.(1888-1890)Cgc>Tgc p.R630C COADREAD 17 1377974 1377974 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:1377974C>T c.1622G>A c.(1621-1623)aGc>aAc p.S541N COADREAD 17 1378233 1378233 + Splice_Site SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr17:1378233G>A c.1563C>T c.(1561-1563)acC>acT p.T521T COADREAD 17 1381979 1381979 + Silent SNP G G A TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr17:1381979G>A c.1038C>T c.(1036-1038)ctC>ctT p.L346L COADREAD 17 1381997 1381997 + Silent SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr17:1381997C>T c.1020G>A c.(1018-1020)gcG>gcA p.A340A COADREAD 17 1382900 1382900 + Missense_Mutation SNP T T C TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr17:1382900T>C c.901A>G c.(901-903)Aag>Gag p.K301E COADREAD 17 1382944 1382944 + Missense_Mutation SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr17:1382944G>A c.857C>T c.(856-858)gCc>gTc p.A286V COADREAD 17 1385799 1385799 + Silent SNP C C T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr17:1385799C>T c.495G>A c.(493-495)aaG>aaA p.K165K COADREAD 17 1386205 1386205 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr17:1386205G>A c.391C>T c.(391-393)Cgc>Tgc p.R131C COADREAD 17 1386346 1386346 + Missense_Mutation SNP C C T TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr17:1386346C>T c.250G>A c.(250-252)Gtg>Atg p.V84M DLBC 17 1382889 1382889 + Silent SNP G G A TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr17:1382889G>A c.912C>T c.(910-912)acC>acT p.T304T ESCA 17 1378125 1378125 + Missense_Mutation SNP A A G TCGA-LN-A4A3-01A-11D-A27G-09 TCGA-LN-A4A3-10A-01D-A27G-09 g.chr17:1378125A>G c.1592T>C c.(1591-1593)cTc>cCc p.L531P ESCA 17 1382889 1382889 + Silent SNP G G A TCGA-ZR-A9CJ-01B-11D-A387-09 TCGA-ZR-A9CJ-10A-01D-A38A-09 g.chr17:1382889G>A c.912C>T c.(910-912)acC>acT p.T304T ESCA 17 1386153 1386153 + Splice_Site SNP A A C TCGA-IC-A6RF-01A-13D-A33E-09 TCGA-IC-A6RF-10A-21D-A33H-09 g.chr17:1386153A>C c.e4+1 ESCA 17 1386310 1386310 + Missense_Mutation SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr17:1386310G>A c.286C>T c.(286-288)Cgt>Tgt p.R96C GBMLGG 17 1371366 1371366 + Missense_Mutation SNP G G A TCGA-DU-A76K-01A-11D-A33T-08 TCGA-DU-A76K-10A-01D-A33W-08 g.chr17:1371366G>A c.2707C>T c.(2707-2709)Cgg>Tgg p.R903W GBMLGG 17 1375272 1375272 + Silent SNP C C T TCGA-S9-A6U5-01A-12D-A33T-08 TCGA-S9-A6U5-10A-01D-A33W-08 g.chr17:1375272C>T c.1845G>A c.(1843-1845)ggG>ggA p.G615G GBMLGG 17 1380798 1380798 + Splice_Site SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1380798C>T c.e14+1 GBMLGG 17 1380819 1380819 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1380819C>T c.1449G>A c.(1447-1449)aaG>aaA p.K483K GBMLGG 17 1384090 1384090 + Silent SNP G G T TCGA-S9-A7QZ-01A-12D-A34J-08 TCGA-S9-A7QZ-10A-01D-A34M-08 g.chr17:1384090G>T c.612C>A c.(610-612)atC>atA p.I204I GBMLGG 17 1387545 1387545 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1387545C>T c.23G>A c.(22-24)cGt>cAt p.R8H HNSC 17 1373933 1373933 + Missense_Mutation SNP G G T TCGA-CV-7414-01A-11D-2078-08 TCGA-CV-7414-10A-01D-2078-08 g.chr17:1373933G>T c.2158C>A c.(2158-2160)Ctc>Atc p.L720I HNSC 17 1374583 1374583 + Missense_Mutation SNP G G A TCGA-CR-5250-01A-01D-1512-08 TCGA-CR-5250-10A-01D-1512-08 g.chr17:1374583G>A c.1964C>T c.(1963-1965)cCg>cTg p.P655L HNSC 17 1375218 1375218 + Silent SNP G G A TCGA-CV-7429-01A-11D-2129-08 TCGA-CV-7429-10A-01D-2129-08 g.chr17:1375218G>A c.1899C>T c.(1897-1899)taC>taT p.Y633Y HNSC 17 1375249 1375249 + Missense_Mutation SNP C C G TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr17:1375249C>G c.1868G>C c.(1867-1869)cGc>cCc p.R623P HNSC 17 1375450 1375450 + Missense_Mutation SNP G G A TCGA-CV-7101-01A-11D-2012-08 TCGA-CV-7101-10A-01D-2013-08 g.chr17:1375450G>A c.1765C>T c.(1765-1767)Cgc>Tgc p.R589C HNSC 17 1381744 1381744 + Missense_Mutation SNP G G A TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chr17:1381744G>A c.1150C>T c.(1150-1152)Ctc>Ttc p.L384F HNSC 17 1386207 1386207 + Missense_Mutation SNP T T G TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr17:1386207T>G c.389A>C c.(388-390)gAg>gCg p.E130A HNSC 17 1386278 1386278 + Missense_Mutation SNP C C G TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr17:1386278C>G c.318G>C c.(316-318)gaG>gaC p.E106D HNSC 17 1386944 1386944 + Missense_Mutation SNP G G A TCGA-CV-6962-01A-11D-1912-08 TCGA-CV-6962-10A-01D-1912-08 g.chr17:1386944G>A c.202C>T c.(202-204)Cgt>Tgt p.R68C HNSC 17 1387008 1387008 + Silent SNP G G A TCGA-CV-6955-01A-11D-2012-08 TCGA-CV-6955-10A-01D-2013-08 g.chr17:1387008G>A c.138C>T c.(136-138)ggC>ggT p.G46G HNSC 17 1387540 1387540 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr17:1387540G>A c.28C>T c.(28-30)Cgg>Tgg p.R10W HNSC 17 1387541 1387541 + Silent SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr17:1387541G>A c.27C>T c.(25-27)gaC>gaT p.D9D HNSC 17 1387576 1387576 + Missense_Mutation SNP G G A TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chr17:1387576G>A c.97C>T c.(97-99)Cgg>Tgg p.R33W KIPAN 17 1370772 1370772 + Splice_Site SNP A A C TCGA-A4-7734-01A-11D-2136-08 TCGA-A4-7734-10A-01D-2136-08 g.chr17:1370772A>C c.e30+1 KIPAN 17 1382903 1382903 + Frame_Shift_Del DEL G G - TCGA-CZ-5451-01A-01D-1501-10 TCGA-CZ-5451-11A-01D-1501-10 g.chr17:1382903delG c.898delC c.(898-900)ctcfs p.L300fs KIPAN 17 1386297 1386297 + Missense_Mutation SNP G G C TCGA-DW-7836-01A-11D-2136-08 TCGA-DW-7836-10A-01D-2136-08 g.chr17:1386297G>C c.299C>G c.(298-300)gCt>gGt p.A100G KIRC 17 1382903 1382903 + Frame_Shift_Del DEL G G - TCGA-CZ-5451-01A-01D-1501-10 TCGA-CZ-5451-11A-01D-1501-10 g.chr17:1382903delG c.898delC c.(898-900)ctcfs p.L300fs KIRP 17 1370772 1370772 + Splice_Site SNP A A C TCGA-A4-7734-01A-11D-2136-08 TCGA-A4-7734-10A-01D-2136-08 g.chr17:1370772A>C c.e30+1 KIRP 17 1386297 1386297 + Missense_Mutation SNP G G C TCGA-DW-7836-01A-11D-2136-08 TCGA-DW-7836-10A-01D-2136-08 g.chr17:1386297G>C c.299C>G c.(298-300)gCt>gGt p.A100G LGG 17 1371366 1371366 + Missense_Mutation SNP G G A TCGA-DU-A76K-01A-11D-A33T-08 TCGA-DU-A76K-10A-01D-A33W-08 g.chr17:1371366G>A c.2707C>T c.(2707-2709)Cgg>Tgg p.R903W LGG 17 1375272 1375272 + Silent SNP C C T TCGA-S9-A6U5-01A-12D-A33T-08 TCGA-S9-A6U5-10A-01D-A33W-08 g.chr17:1375272C>T c.1845G>A c.(1843-1845)ggG>ggA p.G615G LGG 17 1380798 1380798 + Splice_Site SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1380798C>T c.e14+1 LGG 17 1380819 1380819 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1380819C>T c.1449G>A c.(1447-1449)aaG>aaA p.K483K LGG 17 1384090 1384090 + Silent SNP G G T TCGA-S9-A7QZ-01A-12D-A34J-08 TCGA-S9-A7QZ-10A-01D-A34M-08 g.chr17:1384090G>T c.612C>A c.(610-612)atC>atA p.I204I LGG 17 1387545 1387545 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1387545C>T c.23G>A c.(22-24)cGt>cAt p.R8H LIHC 17 1371776 1371776 + Silent SNP G G C TCGA-DD-AACP-01A-11D-A40R-10 TCGA-DD-AACP-10A-01D-A40U-10 g.chr17:1371776G>C c.2520C>G c.(2518-2520)gcC>gcG p.A840A LIHC 17 1378257 1378257 + Silent SNP C C A TCGA-DD-AADQ-01A-11D-A40R-10 TCGA-DD-AADQ-10A-01D-A40U-10 g.chr17:1378257C>A c.1539G>T c.(1537-1539)gcG>gcT p.A513A LIHC 17 1381960 1381960 + Missense_Mutation SNP G G A TCGA-G3-A5SK-01A-11D-A27I-10 TCGA-G3-A5SK-10A-01D-A27I-10 g.chr17:1381960G>A c.1057C>T c.(1057-1059)Cgc>Tgc p.R353C LIHC 17 1383903 1383903 + Missense_Mutation SNP A A G TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr17:1383903A>G c.719T>C c.(718-720)gTc>gCc p.V240A LIHC 17 1384146 1384146 + Missense_Mutation SNP G G C TCGA-DD-AADS-01A-11D-A40R-10 TCGA-DD-AADS-10A-01D-A40U-10 g.chr17:1384146G>C c.556C>G c.(556-558)Ctc>Gtc p.L186V LUAD 17 1369047 1369047 + Splice_Site SNP C C T TCGA-67-6215-01A-11D-1753-08 TCGA-67-6215-10A-01D-1753-08 g.chr17:1369047C>T c.e32-1 LUAD 17 1370595 1370595 + Missense_Mutation SNP C C T TCGA-50-5939-01A-11D-1625-08 TCGA-50-5939-11A-01D-1625-08 g.chr17:1370595C>T c.3001G>A c.(3001-3003)Gac>Aac p.D1001N LUAD 17 1371352 1371352 + Silent SNP G G A TCGA-91-6830-01A-11D-1945-08 TCGA-91-6830-11A-01D-1945-08 g.chr17:1371352G>A c.2721C>T c.(2719-2721)ctC>ctT p.L907L LUAD 17 1371772 1371772 + Missense_Mutation SNP C C A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr17:1371772C>A c.2524G>T c.(2524-2526)Gct>Tct p.A842S LUAD 17 1377914 1377914 + Missense_Mutation SNP C C A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr17:1377914C>A c.1682G>T c.(1681-1683)cGg>cTg p.R561L LUAD 17 1381978 1381978 + Missense_Mutation SNP C C A TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr17:1381978C>A c.1039G>T c.(1039-1041)Gcc>Tcc p.A347S LUAD 17 1384168 1384168 + Silent SNP C C A TCGA-55-6985-01A-11D-1945-08 TCGA-55-6985-11A-01D-1945-08 g.chr17:1384168C>A c.534G>T c.(532-534)gtG>gtT p.V178V LUAD 17 1384169 1384169 + Missense_Mutation SNP A A G TCGA-55-6985-01A-11D-1945-08 TCGA-55-6985-11A-01D-1945-08 g.chr17:1384169A>G c.533T>C c.(532-534)gTg>gCg p.V178A LUAD 17 1386344 1386344 + Silent SNP C C A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr17:1386344C>A c.252G>T c.(250-252)gtG>gtT p.V84V LUSC 17 1382019 1382019 + Missense_Mutation SNP G G A TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr17:1382019G>A c.998C>T c.(997-999)cCg>cTg p.P333L PAAD 17 1381256 1381256 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:1381256C>T c.1306G>A c.(1306-1308)Gtc>Atc p.V436I PAAD 17 1381754 1381754 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:1381754C>T c.1140G>A c.(1138-1140)acG>acA p.T380T PCPG 17 1381197 1381197 + Silent SNP G G A TCGA-QR-A70C-01A-21D-A35D-08 TCGA-QR-A70C-10A-01D-A35B-08 g.chr17:1381197G>A c.1365C>T c.(1363-1365)atC>atT p.I455I PRAD 17 1386310 1386310 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:1386310G>A c.286C>T c.(286-288)Cgt>Tgt p.R96C SARC 17 1370618 1370618 + Missense_Mutation SNP C C G TCGA-3B-A9HT-01A-11D-A38Z-09 TCGA-3B-A9HT-10A-01D-A38Z-09 g.chr17:1370618C>G c.2978G>C c.(2977-2979)gGc>gCc p.G993A SKCM 17 1371150 1371150 + Missense_Mutation SNP G G A TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr17:1371150G>A c.2846C>T c.(2845-2847)gCg>gTg p.A949V SKCM 17 1371284 1371284 + Missense_Mutation SNP G G A TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr17:1371284G>A c.2789C>T c.(2788-2790)aCc>aTc p.T930I SKCM 17 1371776 1371776 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr17:1371776G>A c.2520C>T c.(2518-2520)gcC>gcT p.A840A SKCM 17 1372852 1372852 + Silent SNP C C T TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr17:1372852C>T c.2478G>A c.(2476-2478)cgG>cgA p.R826R SKCM 17 1373566 1373566 + Missense_Mutation SNP T T C TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr17:1373566T>C c.2324A>G c.(2323-2325)gAc>gGc p.D775G SKCM 17 1374529 1374529 + Missense_Mutation SNP T T A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr17:1374529T>A c.2018A>T c.(2017-2019)tAc>tTc p.Y673F SKCM 17 1375289 1375289 + Nonsense_Mutation SNP G G A TCGA-D3-A2J8-06A-11D-A196-08 TCGA-D3-A2J8-10A-01D-A198-08 g.chr17:1375289G>A c.1828C>T c.(1828-1830)Cag>Tag p.Q610* SKCM 17 1378283 1378284 + Frame_Shift_Ins INS - - T TCGA-FW-A3I3-06A-11D-A21A-08 TCGA-FW-A3I3-10A-01D-A21A-08 g.chr17:1378283_1378284insT c.1512_1513insA c.(1510-1515)cgagggfs p.G505fs SKCM 17 1381191 1381191 + Silent SNP C C A TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr17:1381191C>A c.1371G>T c.(1369-1371)tcG>tcT p.S457S SKCM 17 1384026 1384026 + Missense_Mutation SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr17:1384026G>A c.676C>T c.(676-678)Ccc>Tcc p.P226S SKCM 17 1384095 1384095 + Missense_Mutation SNP G G A TCGA-EE-A2MK-06A-11D-A196-08 TCGA-EE-A2MK-10A-01D-A198-08 g.chr17:1384095G>A c.607C>T c.(607-609)Cac>Tac p.H203Y SKCM 17 1386255 1386255 + Missense_Mutation SNP G G A TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr17:1386255G>A c.341C>T c.(340-342)gCc>gTc p.A114V SKCM 17 1386285 1386285 + Missense_Mutation SNP G G T TCGA-ER-A19E-06A-11D-A197-08 TCGA-ER-A19E-10A-01D-A199-08 g.chr17:1386285G>T c.311C>A c.(310-312)tCt>tAt p.S104Y BLCA 15 59429625 59429625 + Missense_Mutation SNP C C T TCGA-2F-A9KT-01A-11D-A38G-08 TCGA-2F-A9KT-10A-01D-A38J-08 g.chr15:59429625C>T c.3281G>A c.(3280-3282)cGa>cAa p.R1094Q BLCA 15 59430525 59430527 + In_Frame_Del DEL CCC CCC - TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr15:59430525_59430527delCCC c.3120_3122delGGG c.(3118-3123)gggggc>ggc p.1040_1041GG>G BLCA 15 59445944 59445944 + Silent SNP G G T TCGA-DK-AA76-01A-11D-A391-08 TCGA-DK-AA76-10A-01D-A394-08 g.chr15:59445944G>T c.2925C>A c.(2923-2925)ccC>ccA p.P975P BLCA 15 59455471 59455471 + Missense_Mutation SNP C C T TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr15:59455471C>T c.2512G>A c.(2512-2514)Gag>Aag p.E838K BLCA 15 59465948 59465948 + Missense_Mutation SNP G G C TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr15:59465948G>C c.2331C>G c.(2329-2331)ttC>ttG p.F777L BLCA 15 59466040 59466040 + Missense_Mutation SNP C C G TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr15:59466040C>G c.2239G>C c.(2239-2241)Ggg>Cgg p.G747R BLCA 15 59466098 59466098 + Missense_Mutation SNP C C G TCGA-2F-A9KP-01A-11D-A38G-08 TCGA-2F-A9KP-10A-01D-A38J-08 g.chr15:59466098C>G c.2181G>C c.(2179-2181)ttG>ttC p.L727F BLCA 15 59466419 59466419 + Missense_Mutation SNP C C T TCGA-FD-A62P-01A-32D-A30E-08 TCGA-FD-A62P-10A-01D-A30H-08 g.chr15:59466419C>T c.2070G>A c.(2068-2070)atG>atA p.M690I BLCA 15 59500904 59500904 + Silent SNP G G A TCGA-DK-A3IQ-01A-31D-A20D-08 TCGA-DK-A3IQ-10A-01D-A20D-08 g.chr15:59500904G>A c.1506C>T c.(1504-1506)ttC>ttT p.F502F BLCA 15 59500964 59500964 + Silent SNP G G A TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr15:59500964G>A c.1446C>T c.(1444-1446)ctC>ctT p.L482L BLCA 15 59501033 59501033 + Silent SNP G G A TCGA-E5-A4TZ-01A-11D-A31L-08 TCGA-E5-A4TZ-10B-01D-A31J-08 g.chr15:59501033G>A c.1377C>T c.(1375-1377)atC>atT p.I459I BLCA 15 59502740 59502740 + Silent SNP G G A TCGA-DK-A1A5-01A-11D-A13W-08 TCGA-DK-A1A5-10A-01D-A13W-08 g.chr15:59502740G>A c.1335C>T c.(1333-1335)atC>atT p.I445I BLCA 15 59548521 59548521 + Silent SNP G G A TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr15:59548521G>A c.294C>T c.(292-294)aaC>aaT p.N98N BRCA 15 59445902 59445902 + Silent SNP G G A TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr15:59445902G>A c.2967C>T c.(2965-2967)taC>taT p.Y989Y BRCA 15 59470680 59470680 + Missense_Mutation SNP C C A TCGA-A8-A085-01A-11W-A019-09 TCGA-A8-A085-10A-01W-A021-09 g.chr15:59470680C>A c.1961G>T c.(1960-1962)gGc>gTc p.G654V BRCA 15 59500992 59500992 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr15:59500992A>C c.1418T>G c.(1417-1419)gTg>gGg p.V473G BRCA 15 59502732 59502732 + Missense_Mutation SNP T T C TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr15:59502732T>C c.1343A>G c.(1342-1344)gAc>gGc p.D448G BRCA 15 59515261 59515261 + Missense_Mutation SNP C C G TCGA-C8-A1HM-01A-12D-A135-09 TCGA-C8-A1HM-10A-01D-A135-09 g.chr15:59515261C>G c.907G>C c.(907-909)Gag>Cag p.E303Q BRCA 15 59519659 59519660 + Splice_Site DEL TG TG - TCGA-A8-A09B-01A-11W-A019-09 TCGA-A8-A09B-10A-01W-A021-09 g.chr15:59519659_59519660delTG c.640_641delCA c.(640-642)cag>g p.Q214fs CESC 15 59430493 59430493 + Nonsense_Mutation SNP G G A TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr15:59430493G>A c.3154C>T c.(3154-3156)Cag>Tag p.Q1052* CESC 15 59553670 59553670 + Missense_Mutation SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr15:59553670G>C c.186C>G c.(184-186)ttC>ttG p.F62L CESC 15 59553683 59553683 + Nonsense_Mutation SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr15:59553683G>C c.173C>G c.(172-174)tCa>tGa p.S58* COAD 15 59445908 59445908 + Silent SNP G G A TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr15:59445908G>A c.2961C>T c.(2959-2961)agC>agT p.S987S COAD 15 59453296 59453296 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:59453296C>T c.2761G>A c.(2761-2763)Gga>Aga p.G921R COAD 15 59455418 59455418 + Silent SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr15:59455418G>A c.2565C>T c.(2563-2565)agC>agT p.S855S COAD 15 59466390 59466390 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr15:59466390C>T c.2099G>A c.(2098-2100)cGa>cAa p.R700Q COAD 15 59470603 59470603 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:59470603C>T c.2038G>A c.(2038-2040)Gcc>Acc p.A680T COAD 15 59470679 59470679 + Silent SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr15:59470679G>A c.1962C>T c.(1960-1962)ggC>ggT p.G654G COAD 15 59501014 59501014 + Missense_Mutation SNP C C A TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr15:59501014C>A c.1396G>T c.(1396-1398)Gtg>Ttg p.V466L COAD 15 59510094 59510094 + Missense_Mutation SNP A A C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr15:59510094A>C c.1103T>G c.(1102-1104)gTa>gGa p.V368G COAD 15 59510113 59510113 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:59510113G>A c.1084C>T c.(1084-1086)Cgg>Tgg p.R362W COAD 15 59510143 59510143 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr15:59510143G>A c.1054C>T c.(1054-1056)Cgg>Tgg p.R352W COAD 15 59510159 59510159 + Silent SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr15:59510159C>T c.1038G>A c.(1036-1038)gaG>gaA p.E346E COAD 15 59516946 59516946 + Missense_Mutation SNP A A C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr15:59516946A>C c.719T>G c.(718-720)cTc>cGc p.L240R COAD 15 59519757 59519757 + Silent SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr15:59519757A>G c.543T>C c.(541-543)ggT>ggC p.G181G COAD 15 59523927 59523927 + Missense_Mutation SNP C C T TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr15:59523927C>T c.484G>A c.(484-486)Gtc>Atc p.V162I COAD 15 59523958 59523958 + Silent SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr15:59523958C>T c.453G>A c.(451-453)ccG>ccA p.P151P COAD 15 59564585 59564585 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:59564585C>T c.67G>A c.(67-69)Gac>Aac p.D23N COADREAD 15 59445908 59445908 + Silent SNP G G A TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr15:59445908G>A c.2961C>T c.(2959-2961)agC>agT p.S987S COADREAD 15 59453296 59453296 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr15:59453296C>T c.2761G>A c.(2761-2763)Gga>Aga p.G921R COADREAD 15 59455418 59455418 + Silent SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr15:59455418G>A c.2565C>T c.(2563-2565)agC>agT p.S855S COADREAD 15 59455418 59455418 + Silent SNP G G A TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr15:59455418G>A c.2565C>T c.(2563-2565)agC>agT p.S855S COADREAD 15 59464132 59464132 + Missense_Mutation SNP T T A TCGA-AG-3727-01A-01W-0899-10 TCGA-AG-3727-10A-01W-0901-10 g.chr15:59464132T>A c.2444A>T c.(2443-2445)aAa>aTa p.K815I COADREAD 15 59466390 59466390 + Missense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr15:59466390C>T c.2099G>A c.(2098-2100)cGa>cAa p.R700Q COADREAD 15 59470603 59470603 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:59470603C>T c.2038G>A c.(2038-2040)Gcc>Acc p.A680T COADREAD 15 59470679 59470679 + Silent SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr15:59470679G>A c.1962C>T c.(1960-1962)ggC>ggT p.G654G COADREAD 15 59480399 59480399 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:59480399C>T c.1822G>A c.(1822-1824)Gaa>Aaa p.E608K COADREAD 15 59487694 59487694 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:59487694C>T c.1771G>A c.(1771-1773)Gaa>Aaa p.E591K COADREAD 15 59501014 59501014 + Missense_Mutation SNP C C A TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr15:59501014C>A c.1396G>T c.(1396-1398)Gtg>Ttg p.V466L COADREAD 15 59510094 59510094 + Missense_Mutation SNP A A C TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr15:59510094A>C c.1103T>G c.(1102-1104)gTa>gGa p.V368G COADREAD 15 59510113 59510113 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:59510113G>A c.1084C>T c.(1084-1086)Cgg>Tgg p.R362W COADREAD 15 59510143 59510143 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr15:59510143G>A c.1054C>T c.(1054-1056)Cgg>Tgg p.R352W COADREAD 15 59510159 59510159 + Silent SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr15:59510159C>T c.1038G>A c.(1036-1038)gaG>gaA p.E346E COADREAD 15 59516946 59516946 + Missense_Mutation SNP A A C TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr15:59516946A>C c.719T>G c.(718-720)cTc>cGc p.L240R COADREAD 15 59519757 59519757 + Silent SNP A A G TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr15:59519757A>G c.543T>C c.(541-543)ggT>ggC p.G181G COADREAD 15 59523927 59523927 + Missense_Mutation SNP C C T TCGA-CM-6677-01A-11D-1835-10 TCGA-CM-6677-10A-01D-1835-10 g.chr15:59523927C>T c.484G>A c.(484-486)Gtc>Atc p.V162I COADREAD 15 59523958 59523958 + Silent SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr15:59523958C>T c.453G>A c.(451-453)ccG>ccA p.P151P COADREAD 15 59564585 59564585 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:59564585C>T c.67G>A c.(67-69)Gac>Aac p.D23N DLBC 15 59500970 59500970 + Silent SNP C C T TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr15:59500970C>T c.1440G>A c.(1438-1440)acG>acA p.T480T DLBC 15 59506886 59506886 + Nonsense_Mutation SNP C C A TCGA-FA-A7Q1-01A-11D-A382-10 TCGA-FA-A7Q1-10A-01D-A385-10 g.chr15:59506886C>A c.1141G>T c.(1141-1143)Gaa>Taa p.E381* DLBC 15 59517011 59517011 + Silent SNP G G A TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr15:59517011G>A c.654C>T c.(652-654)ggC>ggT p.G218G ESCA 15 59506906 59506906 + Missense_Mutation SNP G G T TCGA-RE-A7BO-01A-11D-A33E-09 TCGA-RE-A7BO-10A-01D-A33H-09 g.chr15:59506906G>T c.1121C>A c.(1120-1122)gCc>gAc p.A374D GBM 15 59502739 59502739 + Missense_Mutation SNP C C G TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr15:59502739C>G c.1336G>C c.(1336-1338)Gta>Cta p.V446L GBMLGG 15 59445849 59445849 + Missense_Mutation SNP C C A TCGA-HT-7880-01A-11D-2395-08 TCGA-HT-7880-10A-01D-2396-08 g.chr15:59445849C>A c.3020G>T c.(3019-3021)cGa>cTa p.R1007L GBMLGG 15 59453404 59453404 + Missense_Mutation SNP T T C TCGA-E1-A7Z3-01A-11D-A34J-08 TCGA-E1-A7Z3-10A-01D-A34M-08 g.chr15:59453404T>C c.2653A>G c.(2653-2655)Aac>Gac p.N885D GBMLGG 15 59487690 59487690 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:59487690G>A c.1775C>T c.(1774-1776)aCc>aTc p.T592I GBMLGG 15 59502739 59502739 + Missense_Mutation SNP C C G TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr15:59502739C>G c.1336G>C c.(1336-1338)Gta>Cta p.V446L HNSC 15 59445837 59445837 + Missense_Mutation SNP G G A TCGA-CN-6988-01A-11D-1912-08 TCGA-CN-6988-10A-01D-1912-08 g.chr15:59445837G>A c.3032C>T c.(3031-3033)aCg>aTg p.T1011M HNSC 15 59455404 59455404 + Missense_Mutation SNP C C T TCGA-CR-6487-01A-11D-1870-08 TCGA-CR-6487-10A-01D-1870-08 g.chr15:59455404C>T c.2579G>A c.(2578-2580)cGt>cAt p.R860H HNSC 15 59494582 59494582 + Silent SNP C C T TCGA-IQ-A61H-01A-11D-A30E-08 TCGA-IQ-A61H-10A-01D-A30H-08 g.chr15:59494582C>T c.1641G>A c.(1639-1641)ccG>ccA p.P547P HNSC 15 59500990 59500990 + Missense_Mutation SNP C C T TCGA-CV-A6JN-01A-11D-A31L-08 TCGA-CV-A6JN-10A-01D-A31J-08 g.chr15:59500990C>T c.1420G>A c.(1420-1422)Ggt>Agt p.G474S KICH 15 59466112 59466112 + Missense_Mutation SNP A A G TCGA-KL-8328-01A-11D-2310-10 TCGA-KL-8328-11A-01D-2310-10 g.chr15:59466112A>G c.2167T>C c.(2167-2169)Tca>Cca p.S723P KIPAN 15 59464119 59464119 + Missense_Mutation SNP T T A TCGA-B8-5163-01A-01D-1421-08 TCGA-B8-5163-10A-01D-1421-08 g.chr15:59464119T>A c.2457A>T c.(2455-2457)gaA>gaT p.E819D KIPAN 15 59466112 59466112 + Missense_Mutation SNP A A G TCGA-KL-8328-01A-11D-2310-10 TCGA-KL-8328-11A-01D-2310-10 g.chr15:59466112A>G c.2167T>C c.(2167-2169)Tca>Cca p.S723P KIPAN 15 59466345 59466345 + Missense_Mutation SNP T T C TCGA-2Z-A9JE-01A-11D-A42J-10 TCGA-2Z-A9JE-10A-01D-A42M-10 g.chr15:59466345T>C c.2144A>G c.(2143-2145)tAc>tGc p.Y715C KIPAN 15 59470597 59470597 + Missense_Mutation SNP C C G TCGA-BP-4967-01A-01D-1462-08 TCGA-BP-4967-11A-01D-1462-08 g.chr15:59470597C>G c.2044G>C c.(2044-2046)Gag>Cag p.E682Q KIPAN 15 59501015 59501015 + Silent SNP G G A TCGA-BQ-7061-01A-11D-1961-08 TCGA-BQ-7061-11A-01D-1961-08 g.chr15:59501015G>A c.1395C>T c.(1393-1395)gaC>gaT p.D465D KIPAN 15 59506883 59506883 + Missense_Mutation SNP A A G TCGA-BP-4986-01A-01D-1462-08 TCGA-BP-4986-11A-01D-1462-08 g.chr15:59506883A>G c.1144T>C c.(1144-1146)Tac>Cac p.Y382H KIPAN 15 59528837 59528837 + Missense_Mutation SNP T T C TCGA-AK-3431-01A-02D-1361-10 TCGA-AK-3431-10A-01D-1361-10 g.chr15:59528837T>C c.367A>G c.(367-369)Aaa>Gaa p.K123E KIRC 15 59464119 59464119 + Missense_Mutation SNP T T A TCGA-B8-5163-01A-01D-1421-08 TCGA-B8-5163-10A-01D-1421-08 g.chr15:59464119T>A c.2457A>T c.(2455-2457)gaA>gaT p.E819D KIRC 15 59470597 59470597 + Missense_Mutation SNP C C G TCGA-BP-4967-01A-01D-1462-08 TCGA-BP-4967-11A-01D-1462-08 g.chr15:59470597C>G c.2044G>C c.(2044-2046)Gag>Cag p.E682Q KIRC 15 59506883 59506883 + Missense_Mutation SNP A A G TCGA-BP-4986-01A-01D-1462-08 TCGA-BP-4986-11A-01D-1462-08 g.chr15:59506883A>G c.1144T>C c.(1144-1146)Tac>Cac p.Y382H KIRC 15 59528837 59528837 + Missense_Mutation SNP T T C TCGA-AK-3431-01A-02D-1361-10 TCGA-AK-3431-10A-01D-1361-10 g.chr15:59528837T>C c.367A>G c.(367-369)Aaa>Gaa p.K123E KIRP 15 59466345 59466345 + Missense_Mutation SNP T T C TCGA-2Z-A9JE-01A-11D-A42J-10 TCGA-2Z-A9JE-10A-01D-A42M-10 g.chr15:59466345T>C c.2144A>G c.(2143-2145)tAc>tGc p.Y715C KIRP 15 59501015 59501015 + Silent SNP G G A TCGA-BQ-7061-01A-11D-1961-08 TCGA-BQ-7061-11A-01D-1961-08 g.chr15:59501015G>A c.1395C>T c.(1393-1395)gaC>gaT p.D465D LGG 15 59445849 59445849 + Missense_Mutation SNP C C A TCGA-HT-7880-01A-11D-2395-08 TCGA-HT-7880-10A-01D-2396-08 g.chr15:59445849C>A c.3020G>T c.(3019-3021)cGa>cTa p.R1007L LGG 15 59453404 59453404 + Missense_Mutation SNP T T C TCGA-E1-A7Z3-01A-11D-A34J-08 TCGA-E1-A7Z3-10A-01D-A34M-08 g.chr15:59453404T>C c.2653A>G c.(2653-2655)Aac>Gac p.N885D LGG 15 59487690 59487690 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:59487690G>A c.1775C>T c.(1774-1776)aCc>aTc p.T592I LIHC 15 59445837 59445837 + Missense_Mutation SNP G G A TCGA-CC-A9FW-01A-11D-A36X-10 TCGA-CC-A9FW-10A-01D-A370-10 g.chr15:59445837G>A c.3032C>T c.(3031-3033)aCg>aTg p.T1011M LIHC 15 59450529 59450529 + Silent SNP A A C TCGA-BC-A216-01A-11D-A152-10 TCGA-BC-A216-11A-11D-A152-10 g.chr15:59450529A>C c.2835T>G c.(2833-2835)acT>acG p.T945T LIHC 15 59464100 59464100 + Missense_Mutation SNP G G A TCGA-DD-A11A-01A-11D-A12Z-10 TCGA-DD-A11A-10A-01D-A12Z-10 g.chr15:59464100G>A c.2476C>T c.(2476-2478)Ctc>Ttc p.L826F LIHC 15 59466403 59466403 + Missense_Mutation SNP C C G TCGA-2V-A95S-01A-11D-A36X-10 TCGA-2V-A95S-10D-01D-A370-10 g.chr15:59466403C>G c.2086G>C c.(2086-2088)Gat>Cat p.D696H LIHC 15 59480390 59480390 + Missense_Mutation SNP C C T TCGA-WJ-A86L-01A-12D-A45V-10 TCGA-WJ-A86L-10A-01D-A38X-10 g.chr15:59480390C>T c.1831G>A c.(1831-1833)Ggt>Agt p.G611S LIHC 15 59500993 59500993 + Missense_Mutation SNP C C A TCGA-QA-A7B7-01A-11D-A32G-10 TCGA-QA-A7B7-10A-01D-A32G-10 g.chr15:59500993C>A c.1417G>T c.(1417-1419)Gtg>Ttg p.V473L LIHC 15 59502718 59502718 + Missense_Mutation SNP T T G TCGA-CC-A3MC-01A-11D-A22F-10 TCGA-CC-A3MC-10A-01D-A22F-10 g.chr15:59502718T>G c.1357A>C c.(1357-1359)Aaa>Caa p.K453Q LUAD 15 59470690 59470690 + Missense_Mutation SNP C C T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr15:59470690C>T c.1951G>A c.(1951-1953)Gag>Aag p.E651K LUAD 15 59480399 59480399 + Nonsense_Mutation SNP C C A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr15:59480399C>A c.1822G>T c.(1822-1824)Gaa>Taa p.E608* LUAD 15 59487661 59487661 + Splice_Site SNP T T A TCGA-55-8514-01A-11D-2393-08 TCGA-55-8514-10A-01D-2393-08 g.chr15:59487661T>A c.1804A>T c.(1804-1806)Agg>Tgg p.R602W LUAD 15 59494582 59494582 + Silent SNP C C G TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr15:59494582C>G c.1641G>C c.(1639-1641)ccG>ccC p.P547P LUAD 15 59494582 59494582 + Silent SNP C C G TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr15:59494582C>G c.1641G>C c.(1639-1641)ccG>ccC p.P547P LUAD 15 59494607 59494607 + Splice_Site SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr15:59494607C>A c.e16-1 LUAD 15 59502771 59502771 + Missense_Mutation SNP C C G TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr15:59502771C>G c.1304G>C c.(1303-1305)tGg>tCg p.W435S LUAD 15 59515350 59515350 + Missense_Mutation SNP G G A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr15:59515350G>A c.818C>T c.(817-819)aCg>aTg p.T273M LUAD 15 59519758 59519758 + Missense_Mutation SNP C C A TCGA-95-7562-01A-11D-2238-08 TCGA-95-7562-10B-01D-2238-08 g.chr15:59519758C>A c.542G>T c.(541-543)gGt>gTt p.G181V LUAD 15 59523934 59523934 + Silent SNP G G A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr15:59523934G>A c.477C>T c.(475-477)gcC>gcT p.A159A LUAD 15 59548495 59548495 + Missense_Mutation SNP C C A TCGA-55-7570-01A-11D-2036-08 TCGA-55-7570-10A-01D-2036-08 g.chr15:59548495C>A c.320G>T c.(319-321)tGc>tTc p.C107F LUAD 15 59553679 59553679 + Silent SNP G G A TCGA-17-Z033-01A-01W-0746-08 TCGA-17-Z033-11A-01W-0746-08 g.chr15:59553679G>A c.177C>T c.(175-177)gtC>gtT p.V59V LUAD 15 59553681 59553681 + Missense_Mutation SNP C C A TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chr15:59553681C>A c.175G>T c.(175-177)Gtc>Ttc p.V59F LUSC 15 59506474 59506474 + Missense_Mutation SNP C C T TCGA-22-5491-01A-01D-1632-08 TCGA-22-5491-11A-01D-1632-08 g.chr15:59506474C>T c.1228G>A c.(1228-1230)Gaa>Aaa p.E410K LUSC 15 59516905 59516905 + Nonsense_Mutation SNP C C A TCGA-60-2720-01A-01D-1522-08 TCGA-60-2720-11A-01D-1522-08 g.chr15:59516905C>A c.760G>T c.(760-762)Gag>Tag p.E254* LUSC 15 59519708 59519708 + Missense_Mutation SNP T T C TCGA-22-4604-01A-01D-1267-08 TCGA-22-4604-11A-01D-1267-08 g.chr15:59519708T>C c.592A>G c.(592-594)Agg>Ggg p.R198G LUSC 15 59519720 59519720 + Missense_Mutation SNP G G C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr15:59519720G>C c.580C>G c.(580-582)Ctg>Gtg p.L194V OV 15 59470658 59470658 + Silent SNP C C G TCGA-29-1777-01A-01W-0639-09 TCGA-29-1777-10A-01W-0639-09 g.chr15:59470658C>G c.1983G>C c.(1981-1983)tcG>tcC p.S661S PAAD 15 59519753 59519753 + Missense_Mutation SNP C C T TCGA-2J-AABP-01A-11D-A40W-08 TCGA-2J-AABP-10A-01D-A40W-08 g.chr15:59519753C>T c.547G>A c.(547-549)Gaa>Aaa p.E183K PRAD 15 59480400 59480400 + Silent SNP G G A TCGA-ZG-A9L1-01A-11D-A41K-08 TCGA-ZG-A9L1-10A-01D-A41N-08 g.chr15:59480400G>A c.1821C>T c.(1819-1821)gtC>gtT p.V607V PRAD 15 59500983 59500983 + Missense_Mutation SNP C C T TCGA-YL-A8SB-01A-31D-A377-08 TCGA-YL-A8SB-10A-01D-A37A-08 g.chr15:59500983C>T c.1427G>A c.(1426-1428)gGg>gAg p.G476E PRAD 15 59506877 59506877 + Missense_Mutation SNP T T A TCGA-M7-A723-01A-12D-A32B-08 TCGA-M7-A723-10A-01D-A329-08 g.chr15:59506877T>A c.1150A>T c.(1150-1152)Att>Ttt p.I384F PRAD 15 59564611 59564611 + Missense_Mutation SNP T T G TCGA-CH-5761-01A-11D-1576-08 TCGA-CH-5761-11A-01D-1576-08 g.chr15:59564611T>G c.41A>C c.(40-42)cAc>cCc p.H14P READ 15 59455418 59455418 + Silent SNP G G A TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr15:59455418G>A c.2565C>T c.(2563-2565)agC>agT p.S855S READ 15 59464132 59464132 + Missense_Mutation SNP T T A TCGA-AG-3727-01A-01W-0899-10 TCGA-AG-3727-10A-01W-0901-10 g.chr15:59464132T>A c.2444A>T c.(2443-2445)aAa>aTa p.K815I READ 15 59480399 59480399 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:59480399C>T c.1822G>A c.(1822-1824)Gaa>Aaa p.E608K READ 15 59487694 59487694 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:59487694C>T c.1771G>A c.(1771-1773)Gaa>Aaa p.E591K SARC 15 59470648 59470648 + Missense_Mutation SNP C C A TCGA-DX-A8BN-01A-11D-A37C-09 TCGA-DX-A8BN-11A-22D-A37F-09 g.chr15:59470648C>A c.1993G>T c.(1993-1995)Gac>Tac p.D665Y SKCM 15 59466410 59466411 + Frame_Shift_Del DEL TC TC - TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr15:59466410_59466411delTC c.2078_2079delGA c.(2077-2079)agafs p.R693fs SKCM 15 59466433 59466433 + Missense_Mutation SNP G G A TCGA-EE-A185-06A-11D-A196-08 TCGA-EE-A185-10A-01D-A198-08 g.chr15:59466433G>A c.2056C>T c.(2056-2058)Ctt>Ttt p.L686F SKCM 15 59470628 59470628 + Silent SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr15:59470628C>T c.2013G>A c.(2011-2013)ctG>ctA p.L671L SKCM 15 59494600 59494600 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr15:59494600G>A c.1623C>T c.(1621-1623)ttC>ttT p.F541F SKCM 15 59497637 59497637 + Silent SNP A A G TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr15:59497637A>G c.1578T>C c.(1576-1578)ctT>ctC p.L526L SKCM 15 59510172 59510172 + Missense_Mutation SNP G G A TCGA-EE-A29B-06A-11D-A197-08 TCGA-EE-A29B-10A-01D-A199-08 g.chr15:59510172G>A c.1025C>T c.(1024-1026)aCc>aTc p.T342I SKCM 15 59516941 59516941 + Missense_Mutation SNP C C T TCGA-EE-A20B-06A-11D-A196-08 TCGA-EE-A20B-10A-01D-A198-08 g.chr15:59516941C>T c.724G>A c.(724-726)Ggc>Agc p.G242S SKCM 15 59523928 59523928 + Silent SNP G G T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr15:59523928G>T c.483C>A c.(481-483)acC>acA p.T161T SKCM 15 59548558 59548558 + Missense_Mutation SNP G G A TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr15:59548558G>A c.257C>T c.(256-258)cCa>cTa p.P86L SKCM 15 59564525 59564525 + Missense_Mutation SNP A A C TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr15:59564525A>C c.127T>G c.(127-129)Tac>Gac p.Y43D

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 15 59499840 59499840 single base substitution G T downstream_gene_variant BLCA-CN 15 59499840 59499840 single base substitution G T intron_variant BLCA-CN 15 59499840 59499840 single base substitution G T upstream_gene_variant BLCA-US 15 59466040 59466040 single base substitution C G downstream_gene_variant BLCA-US 15 59466040 59466040 single base substitution C G intron_variant BLCA-US 15 59466040 59466040 single base substitution C G missense_variant G237R 709G>C BLCA-US 15 59466040 59466040 single base substitution C G missense_variant G747R 2239G>C BLCA-US 15 59499546 59499546 single base substitution C G downstream_gene_variant BLCA-US 15 59499546 59499546 single base substitution C G intron_variant BLCA-US 15 59499546 59499546 single base substitution C G upstream_gene_variant BLCA-US 15 59500904 59500904 single base substitution G A downstream_gene_variant BLCA-US 15 59500904 59500904 single base substitution G A exon_variant BLCA-US 15 59500904 59500904 single base substitution G A intron_variant BLCA-US 15 59500904 59500904 single base substitution G A synonymous_variant F25F 75C>T BLCA-US 15 59500904 59500904 single base substitution G A synonymous_variant F502F 1506C>T BLCA-US 15 59500904 59500904 single base substitution G A upstream_gene_variant BLCA-US 15 59502740 59502740 single base substitution G A intron_variant BLCA-US 15 59502740 59502740 single base substitution G A synonymous_variant I165I 495C>T BLCA-US 15 59502740 59502740 single base substitution G A synonymous_variant I445I 1335C>T BLCA-US 15 59502740 59502740 single base substitution G A upstream_gene_variant BLCA-US 15 59548521 59548521 single base substitution G A exon_variant BLCA-US 15 59548521 59548521 single base substitution G A synonymous_variant N98N 294C>T BOCA-FR 15 59499025 59499025 single base substitution G T downstream_gene_variant BOCA-FR 15 59499025 59499025 single base substitution G T intron_variant BOCA-FR 15 59499025 59499025 single base substitution G T upstream_gene_variant BOCA-FR 15 59559793 59559793 single base substitution C T downstream_gene_variant BOCA-FR 15 59559793 59559793 single base substitution C T intron_variant BOCA-FR 15 59559793 59559793 single base substitution C T upstream_gene_variant BOCA-FR 15 59599201 59599201 single base substitution C T intron_variant BOCA-FR 15 59642597 59642597 single base substitution T G intron_variant BOCA-UK 15 59499949 59499949 single base substitution T A downstream_gene_variant BOCA-UK 15 59499949 59499949 single base substitution T A intron_variant BOCA-UK 15 59499949 59499949 single base substitution T A upstream_gene_variant BRCA-EU 15 59422835 59422835 single base substitution C G downstream_gene_variant BRCA-EU 15 59423606 59423606 single base substitution C A downstream_gene_variant BRCA-EU 15 59424958 59424958 single base substitution C G downstream_gene_variant BRCA-EU 15 59425925 59425925 single base substitution G A downstream_gene_variant BRCA-EU 15 59428553 59428555 deletion of <=200bp AAG - 3_prime_UTR_variant BRCA-EU 15 59428553 59428555 deletion of <=200bp AAG - downstream_gene_variant BRCA-EU 15 59433429 59433429 single base substitution G A intron_variant BRCA-EU 15 59433512 59433512 single base substitution C T intron_variant BRCA-EU 15 59436335 59436335 single base substitution C G intron_variant BRCA-EU 15 59437268 59437268 single base substitution C G intron_variant BRCA-EU 15 59437787 59437787 single base substitution C T intron_variant BRCA-EU 15 59438074 59438074 single base substitution A T intron_variant BRCA-EU 15 59439351 59439351 single base substitution C G intron_variant BRCA-EU 15 59439565 59439565 single base substitution G A intron_variant BRCA-EU 15 59439783 59439783 single base substitution G A intron_variant BRCA-EU 15 59443642 59443642 deletion of <=200bp C - intron_variant BRCA-EU 15 59445589 59445589 deletion of <=200bp T - intron_variant BRCA-EU 15 59445694 59445694 single base substitution C A intron_variant BRCA-EU 15 59447404 59447404 single base substitution T A intron_variant BRCA-EU 15 59447404 59447404 single base substitution T A upstream_gene_variant BRCA-EU 15 59447603 59447603 single base substitution A T intron_variant BRCA-EU 15 59447603 59447603 single base substitution A T upstream_gene_variant BRCA-EU 15 59447691 59447691 insertion of <=200bp - T intron_variant BRCA-EU 15 59447691 59447691 insertion of <=200bp - T upstream_gene_variant BRCA-EU 15 59449496 59449496 insertion of <=200bp - T intron_variant BRCA-EU 15 59449496 59449496 insertion of <=200bp - T upstream_gene_variant BRCA-EU 15 59451142 59451142 single base substitution C T downstream_gene_variant BRCA-EU 15 59451142 59451142 single base substitution C T intron_variant BRCA-EU 15 59451530 59451530 single base substitution G T downstream_gene_variant BRCA-EU 15 59451530 59451530 single base substitution G T intron_variant BRCA-EU 15 59454289 59454289 single base substitution G A downstream_gene_variant BRCA-EU 15 59454289 59454289 single base substitution G A intron_variant BRCA-EU 15 59456094 59456094 single base substitution C T intron_variant BRCA-EU 15 59456655 59456655 single base substitution A C intron_variant BRCA-EU 15 59457463 59457463 single base substitution C T intron_variant BRCA-EU 15 59459856 59459856 single base substitution C A downstream_gene_variant BRCA-EU 15 59459856 59459856 single base substitution C A intron_variant BRCA-EU 15 59461765 59461765 deletion of <=200bp T - downstream_gene_variant BRCA-EU 15 59461765 59461765 deletion of <=200bp T - intron_variant BRCA-EU 15 59462798 59462798 insertion of <=200bp - A downstream_gene_variant BRCA-EU 15 59462798 59462798 insertion of <=200bp - A intron_variant BRCA-EU 15 59463031 59463031 single base substitution A C downstream_gene_variant BRCA-EU 15 59463031 59463031 single base substitution A C intron_variant BRCA-EU 15 59466964 59466964 single base substitution C T downstream_gene_variant BRCA-EU 15 59466964 59466964 single base substitution C T intron_variant BRCA-EU 15 59467101 59467101 single base substitution C G downstream_gene_variant BRCA-EU 15 59467101 59467101 single base substitution C G intron_variant BRCA-EU 15 59468710 59468710 single base substitution G A downstream_gene_variant BRCA-EU 15 59468710 59468710 single base substitution G A intron_variant BRCA-EU 15 59469103 59469103 single base substitution G T downstream_gene_variant BRCA-EU 15 59469103 59469103 single base substitution G T intron_variant BRCA-EU 15 59469891 59469891 single base substitution C T downstream_gene_variant BRCA-EU 15 59469891 59469891 single base substitution C T intron_variant BRCA-EU 15 59470634 59470634 single base substitution G A exon_variant BRCA-EU 15 59470634 59470634 single base substitution G A intron_variant BRCA-EU 15 59470634 59470634 single base substitution G A synonymous_variant F159F 477C>T BRCA-EU 15 59470634 59470634 single base substitution G A synonymous_variant F669F 2007C>T BRCA-EU 15 59470792 59470792 single base substitution C G intron_variant BRCA-EU 15 59471214 59471214 single base substitution C T intron_variant BRCA-EU 15 59472291 59472291 single base substitution A G intron_variant BRCA-EU 15 59472609 59472609 single base substitution A C intron_variant BRCA-EU 15 59473060 59473060 single base substitution A T intron_variant BRCA-EU 15 59473318 59473318 single base substitution C T intron_variant BRCA-EU 15 59474448 59474448 single base substitution G C intron_variant BRCA-EU 15 59475263 59475263 single base substitution G A intron_variant BRCA-EU 15 59476031 59476031 single base substitution C A intron_variant BRCA-EU 15 59476670 59476670 single base substitution C A intron_variant BRCA-EU 15 59477583 59477583 single base substitution C T intron_variant BRCA-EU 15 59478387 59478387 single base substitution C A intron_variant BRCA-EU 15 59478604 59478605 deletion of <=200bp TA - intron_variant BRCA-EU 15 59479604 59479618 deletion of <=200bp TCACTAGGATGGTTA - intron_variant BRCA-EU 15 59480018 59480018 single base substitution G C intron_variant BRCA-EU 15 59484681 59484681 single base substitution G A downstream_gene_variant BRCA-EU 15 59484681 59484681 single base substitution G A intron_variant BRCA-EU 15 59486489 59486489 single base substitution G C downstream_gene_variant BRCA-EU 15 59486489 59486489 single base substitution G C intron_variant BRCA-EU 15 59488069 59488069 single base substitution A T intron_variant BRCA-EU 15 59490554 59490554 single base substitution C T intron_variant BRCA-EU 15 59490745 59490745 single base substitution C T intron_variant BRCA-EU 15 59492577 59492577 single base substitution T G intron_variant BRCA-EU 15 59492860 59492860 single base substitution G A intron_variant BRCA-EU 15 59493137 59493137 single base substitution C T intron_variant BRCA-EU 15 59494349 59494349 single base substitution C G intron_variant BRCA-EU 15 59496604 59496604 single base substitution T A downstream_gene_variant BRCA-EU 15 59496604 59496604 single base substitution T A intron_variant BRCA-EU 15 59497947 59497947 single base substitution G A downstream_gene_variant BRCA-EU 15 59497947 59497947 single base substitution G A intron_variant BRCA-EU 15 59498868 59498868 single base substitution C T downstream_gene_variant BRCA-EU 15 59498868 59498868 single base substitution C T intron_variant BRCA-EU 15 59499202 59499202 single base substitution C T downstream_gene_variant BRCA-EU 15 59499202 59499202 single base substitution C T intron_variant BRCA-EU 15 59499202 59499202 single base substitution C T upstream_gene_variant BRCA-EU 15 59500055 59500055 single base substitution G A downstream_gene_variant BRCA-EU 15 59500055 59500055 single base substitution G A intron_variant BRCA-EU 15 59500055 59500055 single base substitution G A upstream_gene_variant BRCA-EU 15 59500728 59500728 single base substitution A G downstream_gene_variant BRCA-EU 15 59500728 59500728 single base substitution A G intron_variant BRCA-EU 15 59500728 59500728 single base substitution A G upstream_gene_variant BRCA-EU 15 59500856 59500856 single base substitution C T downstream_gene_variant BRCA-EU 15 59500856 59500856 single base substitution C T intron_variant BRCA-EU 15 59500856 59500856 single base substitution C T upstream_gene_variant BRCA-EU 15 59503140 59503140 single base substitution T A intron_variant BRCA-EU 15 59503140 59503140 single base substitution T A upstream_gene_variant BRCA-EU 15 59504678 59504678 single base substitution C T intron_variant BRCA-EU 15 59504678 59504678 single base substitution C T upstream_gene_variant BRCA-EU 15 59506760 59506760 single base substitution C T intron_variant BRCA-EU 15 59506817 59506818 deletion of <=200bp TA - intron_variant BRCA-EU 15 59506872 59506872 single base substitution G A intron_variant BRCA-EU 15 59506872 59506872 single base substitution G A synonymous_variant G105G 315C>T BRCA-EU 15 59506872 59506872 single base substitution G A synonymous_variant G385G 1155C>T BRCA-EU 15 59507249 59507249 single base substitution A G intron_variant BRCA-EU 15 59507633 59507633 single base substitution G A intron_variant BRCA-EU 15 59508049 59508049 single base substitution G C intron_variant BRCA-EU 15 59512380 59512380 single base substitution G A downstream_gene_variant BRCA-EU 15 59512380 59512380 single base substitution G A intron_variant BRCA-EU 15 59512380 59512380 single base substitution G A upstream_gene_variant BRCA-EU 15 59517211 59517211 single base substitution T C downstream_gene_variant BRCA-EU 15 59517211 59517211 single base substitution T C intron_variant BRCA-EU 15 59517574 59517574 deletion of <=200bp T - downstream_gene_variant BRCA-EU 15 59517574 59517574 deletion of <=200bp T - intron_variant BRCA-EU 15 59518187 59518187 single base substitution C G downstream_gene_variant BRCA-EU 15 59518187 59518187 single base substitution C G intron_variant BRCA-EU 15 59519552 59519552 single base substitution C T downstream_gene_variant BRCA-EU 15 59519552 59519552 single base substitution C T intron_variant BRCA-EU 15 59519593 59519593 single base substitution T A downstream_gene_variant BRCA-EU 15 59519593 59519593 single base substitution T A intron_variant BRCA-EU 15 59519871 59519871 single base substitution T G intron_variant BRCA-EU 15 59519871 59519871 single base substitution T G upstream_gene_variant BRCA-EU 15 59520493 59520493 single base substitution C T intron_variant BRCA-EU 15 59520493 59520493 single base substitution C T upstream_gene_variant BRCA-EU 15 59521358 59521358 single base substitution G A intron_variant BRCA-EU 15 59521358 59521358 single base substitution G A upstream_gene_variant BRCA-EU 15 59522073 59522073 insertion of <=200bp - A intron_variant BRCA-EU 15 59522073 59522073 insertion of <=200bp - A upstream_gene_variant BRCA-EU 15 59522282 59522282 single base substitution C T intron_variant BRCA-EU 15 59522282 59522282 single base substitution C T upstream_gene_variant BRCA-EU 15 59523325 59523325 single base substitution G A intron_variant BRCA-EU 15 59523325 59523325 single base substitution G A upstream_gene_variant BRCA-EU 15 59524330 59524330 single base substitution G C intron_variant BRCA-EU 15 59524330 59524330 single base substitution G C upstream_gene_variant BRCA-EU 15 59525315 59525315 deletion of <=200bp T - intron_variant BRCA-EU 15 59525607 59525607 single base substitution G A intron_variant BRCA-EU 15 59527256 59527256 single base substitution C T intron_variant BRCA-EU 15 59527331 59527331 single base substitution C A intron_variant BRCA-EU 15 59527487 59527487 single base substitution C T intron_variant BRCA-EU 15 59527892 59527892 single base substitution C T intron_variant BRCA-EU 15 59527954 59527954 single base substitution C A intron_variant BRCA-EU 15 59529491 59529491 single base substitution G C intron_variant BRCA-EU 15 59531058 59531058 single base substitution C T intron_variant BRCA-EU 15 59531776 59531776 single base substitution G C intron_variant BRCA-EU 15 59532058 59532058 single base substitution G C intron_variant BRCA-EU 15 59532291 59532292 deletion of <=200bp AC - intron_variant BRCA-EU 15 59532586 59532586 single base substitution G T intron_variant BRCA-EU 15 59533246 59533246 single base substitution G A intron_variant BRCA-EU 15 59533319 59533319 single base substitution G C intron_variant BRCA-EU 15 59533667 59533667 single base substitution G A intron_variant BRCA-EU 15 59535331 59535331 single base substitution T G intron_variant BRCA-EU 15 59535547 59535547 single base substitution T C intron_variant BRCA-EU 15 59535669 59535669 single base substitution G A intron_variant BRCA-EU 15 59535873 59535873 single base substitution G A intron_variant BRCA-EU 15 59536801 59536801 single base substitution C T intron_variant BRCA-EU 15 59538288 59538288 single base substitution C A intron_variant BRCA-EU 15 59538452 59538452 single base substitution G T intron_variant BRCA-EU 15 59539778 59539778 single base substitution A G intron_variant BRCA-EU 15 59544418 59544418 single base substitution G A intron_variant BRCA-EU 15 59544518 59544518 single base substitution G A intron_variant BRCA-EU 15 59544637 59544637 single base substitution G T intron_variant BRCA-EU 15 59545580 59545580 single base substitution A G intron_variant BRCA-EU 15 59546163 59546163 single base substitution C T intron_variant BRCA-EU 15 59546646 59546646 single base substitution T C intron_variant BRCA-EU 15 59548174 59548174 single base substitution C T intron_variant BRCA-EU 15 59548305 59548305 single base substitution C G intron_variant BRCA-EU 15 59549188 59549188 deletion of <=200bp A - intron_variant BRCA-EU 15 59549568 59549568 single base substitution G A intron_variant BRCA-EU 15 59550069 59550069 single base substitution G T intron_variant BRCA-EU 15 59550185 59550185 single base substitution T G intron_variant BRCA-EU 15 59550812 59550812 single base substitution G A intron_variant BRCA-EU 15 59553120 59553120 single base substitution C T intron_variant BRCA-EU 15 59553638 59553638 single base substitution A G exon_variant BRCA-EU 15 59553638 59553638 single base substitution A G intron_variant BRCA-EU 15 59553638 59553638 single base substitution A G missense_variant I73T 218T>C BRCA-EU 15 59561863 59561863 single base substitution C T downstream_gene_variant BRCA-EU 15 59561863 59561863 single base substitution C T intron_variant BRCA-EU 15 59561863 59561863 single base substitution C T upstream_gene_variant BRCA-EU 15 59562091 59562091 single base substitution G A downstream_gene_variant BRCA-EU 15 59562091 59562091 single base substitution G A intron_variant BRCA-EU 15 59562091 59562091 single base substitution G A upstream_gene_variant BRCA-EU 15 59563184 59563184 single base substitution A G downstream_gene_variant BRCA-EU 15 59563184 59563184 single base substitution A G intron_variant BRCA-EU 15 59563506 59563506 single base substitution T C downstream_gene_variant BRCA-EU 15 59563506 59563506 single base substitution T C intron_variant BRCA-EU 15 59563586 59563586 single base substitution C T downstream_gene_variant BRCA-EU 15 59563586 59563586 single base substitution C T intron_variant BRCA-EU 15 59563960 59563960 single base substitution T G downstream_gene_variant BRCA-EU 15 59563960 59563960 single base substitution T G intron_variant BRCA-EU 15 59564013 59564013 single base substitution G A downstream_gene_variant BRCA-EU 15 59564013 59564013 single base substitution G A intron_variant BRCA-EU 15 59564156 59564156 single base substitution G A downstream_gene_variant BRCA-EU 15 59564156 59564156 single base substitution G A intron_variant BRCA-EU 15 59564232 59564232 single base substitution C T downstream_gene_variant BRCA-EU 15 59564232 59564232 single base substitution C T intron_variant BRCA-EU 15 59567563 59567563 single base substitution C T intron_variant BRCA-EU 15 59567578 59567578 single base substitution A G intron_variant BRCA-EU 15 59568752 59568752 single base substitution C G intron_variant BRCA-EU 15 59568755 59568755 single base substitution A G intron_variant BRCA-EU 15 59569401 59569401 single base substitution T A intron_variant BRCA-EU 15 59571807 59571807 insertion of <=200bp - C intron_variant BRCA-EU 15 59573766 59573766 single base substitution C T intron_variant BRCA-EU 15 59576226 59576226 single base substitution A T intron_variant BRCA-EU 15 59576841 59576841 single base substitution T A intron_variant BRCA-EU 15 59578150 59578150 single base substitution C A intron_variant BRCA-EU 15 59578379 59578379 single base substitution G C intron_variant BRCA-EU 15 59578484 59578484 single base substitution G C intron_variant BRCA-EU 15 59578738 59578738 single base substitution A G intron_variant BRCA-EU 15 59580038 59580038 single base substitution G A intron_variant BRCA-EU 15 59580863 59580863 single base substitution C T intron_variant BRCA-EU 15 59582152 59582152 single base substitution A G intron_variant BRCA-EU 15 59583812 59583812 single base substitution A C intron_variant BRCA-EU 15 59584129 59584129 deletion of <=200bp A - intron_variant BRCA-EU 15 59584147 59584147 single base substitution G A intron_variant BRCA-EU 15 59586132 59586132 single base substitution C T intron_variant BRCA-EU 15 59587454 59587454 deletion of <=200bp A - intron_variant BRCA-EU 15 59587454 59587454 insertion of <=200bp - A intron_variant BRCA-EU 15 59588511 59588511 single base substitution A T intron_variant BRCA-EU 15 59590593 59590593 single base substitution G A intron_variant BRCA-EU 15 59591080 59591080 single base substitution C T intron_variant BRCA-EU 15 59592011 59592011 single base substitution T C intron_variant BRCA-EU 15 59593141 59593141 single base substitution A G intron_variant BRCA-EU 15 59593278 59593278 single base substitution G A intron_variant BRCA-EU 15 59594423 59594423 single base substitution C G intron_variant BRCA-EU 15 59595562 59595562 single base substitution G A intron_variant BRCA-EU 15 59596479 59596479 single base substitution G A intron_variant BRCA-EU 15 59597845 59597845 single base substitution C A intron_variant BRCA-EU 15 59598318 59598318 single base substitution C T intron_variant BRCA-EU 15 59598593 59598593 single base substitution G A intron_variant BRCA-EU 15 59600252 59600252 single base substitution T C intron_variant BRCA-EU 15 59602186 59602186 single base substitution C T intron_variant BRCA-EU 15 59604590 59604590 single base substitution G C intron_variant BRCA-EU 15 59607656 59607656 single base substitution G A intron_variant BRCA-EU 15 59608744 59608744 single base substitution G T intron_variant BRCA-EU 15 59609840 59609840 single base substitution G T intron_variant BRCA-EU 15 59612491 59612491 single base substitution G A intron_variant BRCA-EU 15 59614470 59614470 single base substitution C T intron_variant BRCA-EU 15 59614679 59614679 single base substitution C T intron_variant BRCA-EU 15 59615287 59615287 single base substitution G A intron_variant BRCA-EU 15 59616276 59616276 single base substitution G C intron_variant BRCA-EU 15 59617384 59617384 single base substitution G A intron_variant BRCA-EU 15 59617418 59617419 deletion of <=200bp AG - intron_variant BRCA-EU 15 59617981 59617981 single base substitution G A intron_variant BRCA-EU 15 59618731 59618731 single base substitution T C intron_variant BRCA-EU 15 59618778 59618778 single base substitution G C intron_variant BRCA-EU 15 59619847 59619847 single base substitution G C intron_variant BRCA-EU 15 59621352 59621352 single base substitution G T intron_variant BRCA-EU 15 59621360 59621360 single base substitution C T intron_variant BRCA-EU 15 59622367 59622367 single base substitution C T intron_variant BRCA-EU 15 59625058 59625058 single base substitution G C intron_variant BRCA-EU 15 59626178 59626178 single base substitution G T intron_variant BRCA-EU 15 59627424 59627424 single base substitution G C intron_variant BRCA-EU 15 59627506 59627506 single base substitution A G intron_variant BRCA-EU 15 59627615 59627615 single base substitution G A intron_variant BRCA-EU 15 59628204 59628204 single base substitution C A intron_variant BRCA-EU 15 59630047 59630047 single base substitution T G intron_variant BRCA-EU 15 59630674 59630674 single base substitution T A intron_variant BRCA-EU 15 59630956 59630956 single base substitution C A intron_variant BRCA-EU 15 59630997 59630997 single base substitution C G intron_variant BRCA-EU 15 59631481 59631481 single base substitution A G intron_variant BRCA-EU 15 59631515 59631515 single base substitution A C intron_variant BRCA-EU 15 59632508 59632508 deletion of <=200bp A - intron_variant BRCA-EU 15 59632730 59632730 deletion of <=200bp T - intron_variant BRCA-EU 15 59633203 59633203 single base substitution G A intron_variant BRCA-EU 15 59635025 59635025 single base substitution C G intron_variant BRCA-EU 15 59635156 59635156 single base substitution T C intron_variant BRCA-EU 15 59636814 59636814 single base substitution C T intron_variant BRCA-EU 15 59637442 59637442 single base substitution G A intron_variant BRCA-EU 15 59639501 59639501 single base substitution C G intron_variant BRCA-EU 15 59640154 59640154 single base substitution G T intron_variant BRCA-EU 15 59641708 59641708 single base substitution C T intron_variant BRCA-EU 15 59644035 59644035 single base substitution C T intron_variant BRCA-EU 15 59645061 59645061 single base substitution T C intron_variant BRCA-EU 15 59645137 59645137 single base substitution G C intron_variant BRCA-EU 15 59647865 59647865 single base substitution C T intron_variant BRCA-EU 15 59652435 59652435 single base substitution C T intron_variant BRCA-EU 15 59654130 59654130 single base substitution G T intron_variant BRCA-EU 15 59654873 59654873 single base substitution G A intron_variant BRCA-EU 15 59655128 59655128 deletion of <=200bp T - intron_variant BRCA-EU 15 59658646 59658646 single base substitution G A intron_variant BRCA-EU 15 59659116 59659116 insertion of <=200bp - A intron_variant BRCA-EU 15 59660178 59660178 single base substitution G C intron_variant BRCA-EU 15 59661583 59661583 insertion of <=200bp - A intron_variant BRCA-EU 15 59662724 59662724 single base substitution C A intron_variant BRCA-EU 15 59662938 59662938 single base substitution A C intron_variant BRCA-EU 15 59664491 59664491 single base substitution T G intron_variant BRCA-EU 15 59664770 59664770 deletion of <=200bp C - 5_prime_UTR_variant BRCA-EU 15 59664770 59664770 deletion of <=200bp C - exon_variant BRCA-EU 15 59664770 59664770 deletion of <=200bp C - upstream_gene_variant BRCA-EU 15 59667428 59667428 single base substitution T C upstream_gene_variant BRCA-EU 15 59667629 59667629 single base substitution C T upstream_gene_variant BRCA-EU 15 59667951 59667951 single base substitution C T upstream_gene_variant BRCA-EU 15 59668458 59668458 single base substitution T C upstream_gene_variant BRCA-EU 15 59669434 59669434 single base substitution G A upstream_gene_variant BRCA-EU 15 59669918 59669918 single base substitution G A upstream_gene_variant BRCA-FR 15 59433429 59433429 single base substitution G A intron_variant BRCA-FR 15 59439351 59439351 single base substitution C G intron_variant BRCA-FR 15 59439488 59439488 single base substitution C G intron_variant BRCA-FR 15 59439887 59439887 single base substitution C G intron_variant BRCA-FR 15 59467124 59467124 single base substitution C T downstream_gene_variant BRCA-FR 15 59467124 59467124 single base substitution C T intron_variant BRCA-FR 15 59470338 59470338 single base substitution G A downstream_gene_variant BRCA-FR 15 59470338 59470338 single base substitution G A intron_variant BRCA-FR 15 59471214 59471214 single base substitution C T intron_variant BRCA-FR 15 59501832 59501832 single base substitution G A intron_variant BRCA-FR 15 59501832 59501832 single base substitution G A upstream_gene_variant BRCA-FR 15 59507633 59507633 single base substitution G A intron_variant BRCA-FR 15 59508049 59508049 single base substitution G C intron_variant BRCA-FR 15 59517211 59517211 single base substitution T C downstream_gene_variant BRCA-FR 15 59517211 59517211 single base substitution T C intron_variant BRCA-FR 15 59518187 59518187 single base substitution C G downstream_gene_variant BRCA-FR 15 59518187 59518187 single base substitution C G intron_variant BRCA-FR 15 59519552 59519552 single base substitution C T downstream_gene_variant BRCA-FR 15 59519552 59519552 single base substitution C T intron_variant BRCA-FR 15 59520493 59520493 single base substitution C T intron_variant BRCA-FR 15 59520493 59520493 single base substitution C T upstream_gene_variant BRCA-FR 15 59523325 59523325 single base substitution G A intron_variant BRCA-FR 15 59523325 59523325 single base substitution G A upstream_gene_variant BRCA-FR 15 59524330 59524330 single base substitution G C intron_variant BRCA-FR 15 59524330 59524330 single base substitution G C upstream_gene_variant BRCA-FR 15 59525472 59525472 single base substitution C T intron_variant BRCA-FR 15 59527892 59527892 single base substitution C T intron_variant BRCA-FR 15 59527954 59527954 single base substitution C A intron_variant BRCA-FR 15 59530336 59530336 single base substitution G C intron_variant BRCA-FR 15 59531776 59531776 single base substitution G C intron_variant BRCA-FR 15 59532586 59532586 single base substitution G T intron_variant BRCA-FR 15 59533319 59533319 single base substitution G C intron_variant BRCA-FR 15 59535669 59535669 single base substitution G A intron_variant BRCA-FR 15 59550812 59550812 single base substitution G A intron_variant BRCA-FR 15 59553120 59553120 single base substitution C T intron_variant BRCA-FR 15 59563506 59563506 single base substitution T C downstream_gene_variant BRCA-FR 15 59563506 59563506 single base substitution T C intron_variant BRCA-FR 15 59580863 59580863 single base substitution C T intron_variant BRCA-FR 15 59584147 59584147 single base substitution G A intron_variant BRCA-FR 15 59586031 59586031 single base substitution T C intron_variant BRCA-FR 15 59594423 59594423 single base substitution C G intron_variant BRCA-FR 15 59612491 59612491 single base substitution G A intron_variant BRCA-FR 15 59614679 59614679 single base substitution C T intron_variant BRCA-FR 15 59615287 59615287 single base substitution G A intron_variant BRCA-FR 15 59619847 59619847 single base substitution G C intron_variant BRCA-FR 15 59621360 59621360 single base substitution C T intron_variant BRCA-FR 15 59636814 59636814 single base substitution C T intron_variant BRCA-FR 15 59647933 59647933 single base substitution G A intron_variant BRCA-FR 15 59669243 59669243 single base substitution T G upstream_gene_variant BRCA-UK 15 59456655 59456655 single base substitution A C intron_variant BRCA-UK 15 59464137 59464137 single base substitution C A missense_variant K234N 702G>T BRCA-UK 15 59464137 59464137 single base substitution C A missense_variant K303N 909G>T BRCA-UK 15 59464137 59464137 single base substitution C A missense_variant K813N 2439G>T BRCA-UK 15 59466964 59466964 single base substitution C T downstream_gene_variant BRCA-UK 15 59466964 59466964 single base substitution C T intron_variant BRCA-UK 15 59493137 59493137 single base substitution C T intron_variant BRCA-UK 15 59504502 59504502 single base substitution C G intron_variant BRCA-UK 15 59504502 59504502 single base substitution C G upstream_gene_variant BRCA-UK 15 59532028 59532028 single base substitution C G intron_variant BRCA-UK 15 59561863 59561863 single base substitution C T downstream_gene_variant BRCA-UK 15 59561863 59561863 single base substitution C T intron_variant BRCA-UK 15 59561863 59561863 single base substitution C T upstream_gene_variant BRCA-UK 15 59611499 59611499 single base substitution G A intron_variant BRCA-UK 15 59652309 59652309 single base substitution C G intron_variant BRCA-US 15 59428908 59428908 single base substitution G T 3_prime_UTR_variant BRCA-US 15 59428908 59428908 single base substitution G T synonymous_variant G66G 198C>A BRCA-US 15 59445902 59445902 single base substitution G A synonymous_variant Y989Y 2967C>T BRCA-US 15 59445902 59445902 single base substitution G A upstream_gene_variant BRCA-US 15 59470680 59470680 single base substitution C A exon_variant BRCA-US 15 59470680 59470680 single base substitution C A intron_variant BRCA-US 15 59470680 59470680 single base substitution C A missense_variant G144V 431G>T BRCA-US 15 59470680 59470680 single base substitution C A missense_variant G654V 1961G>T BRCA-US 15 59500992 59500992 single base substitution A C downstream_gene_variant BRCA-US 15 59500992 59500992 single base substitution A C exon_variant BRCA-US 15 59500992 59500992 single base substitution A C intron_variant BRCA-US 15 59500992 59500992 single base substitution A C missense_variant V473G 1418T>G BRCA-US 15 59500992 59500992 single base substitution A C upstream_gene_variant BRCA-US 15 59502732 59502732 single base substitution T C intron_variant BRCA-US 15 59502732 59502732 single base substitution T C missense_variant D168G 503A>G BRCA-US 15 59502732 59502732 single base substitution T C missense_variant D448G 1343A>G BRCA-US 15 59502732 59502732 single base substitution T C upstream_gene_variant BRCA-US 15 59515261 59515261 single base substitution C G downstream_gene_variant BRCA-US 15 59515261 59515261 single base substitution C G exon_variant BRCA-US 15 59515261 59515261 single base substitution C G missense_variant E133Q 397G>C BRCA-US 15 59515261 59515261 single base substitution C G missense_variant E303Q 907G>C BRCA-US 15 59515261 59515261 single base substitution C G upstream_gene_variant BRCA-US 15 59516993 59516993 single base substitution T G downstream_gene_variant BRCA-US 15 59516993 59516993 single base substitution T G exon_variant BRCA-US 15 59516993 59516993 single base substitution T G missense_variant K224N 672A>C BRCA-US 15 59516993 59516993 single base substitution T G missense_variant K54N 162A>C BRCA-US 15 59519659 59519660 deletion of <=200bp TG - downstream_gene_variant BRCA-US 15 59519659 59519660 deletion of <=200bp TG - frameshift_variant Q214 BRCA-US 15 59519659 59519660 deletion of <=200bp TG - frameshift_variant Q44 BRCA-US 15 59519659 59519660 deletion of <=200bp TG - splice_region_variant BTCA-JP 15 59466318 59466318 insertion of <=200bp - A downstream_gene_variant BTCA-JP 15 59466318 59466318 insertion of <=200bp - A intron_variant BTCA-JP 15 59466318 59466318 insertion of <=200bp - A splice_region_variant BTCA-JP 15 59499164 59499164 single base substitution C T downstream_gene_variant BTCA-JP 15 59499164 59499164 single base substitution C T intron_variant BTCA-JP 15 59499164 59499164 single base substitution C T upstream_gene_variant BTCA-JP 15 59500964 59500964 single base substitution G C downstream_gene_variant BTCA-JP 15 59500964 59500964 single base substitution G C exon_variant BTCA-JP 15 59500964 59500964 single base substitution G C intron_variant BTCA-JP 15 59500964 59500964 single base substitution G C synonymous_variant L482L 1446C>G BTCA-JP 15 59500964 59500964 single base substitution G C synonymous_variant L5L 15C>G BTCA-JP 15 59500964 59500964 single base substitution G C upstream_gene_variant BTCA-JP 15 59502737 59502737 single base substitution T C intron_variant BTCA-JP 15 59502737 59502737 single base substitution T C synonymous_variant V166V 498A>G BTCA-JP 15 59502737 59502737 single base substitution T C synonymous_variant V446V 1338A>G BTCA-JP 15 59502737 59502737 single base substitution T C upstream_gene_variant BTCA-JP 15 59506717 59506717 insertion of <=200bp - T intron_variant BTCA-JP 15 59510372 59510372 single base substitution G A downstream_gene_variant BTCA-JP 15 59510372 59510372 single base substitution G A intron_variant BTCA-JP 15 59529005 59529005 single base substitution T A intron_variant BTCA-JP 15 59548614 59548614 single base substitution T C intron_variant CESC-US 15 59430493 59430493 single base substitution G A stop_gained Q1052* 3154C>T CESC-US 15 59430493 59430493 single base substitution G A stop_gained Q43* 127C>T CESC-US 15 59443250 59443250 single base substitution G A intron_variant CESC-US 15 59500058 59500058 single base substitution G A downstream_gene_variant CESC-US 15 59500058 59500058 single base substitution G A intron_variant CESC-US 15 59500058 59500058 single base substitution G A upstream_gene_variant CESC-US 15 59553670 59553670 single base substitution G C exon_variant CESC-US 15 59553670 59553670 single base substitution G C intron_variant CESC-US 15 59553670 59553670 single base substitution G C missense_variant F62L 186C>G CESC-US 15 59553683 59553683 single base substitution G C exon_variant CESC-US 15 59553683 59553683 single base substitution G C intron_variant CESC-US 15 59553683 59553683 single base substitution G C stop_gained S58* 173C>G CLLE-ES 15 59426148 59426148 single base substitution G A downstream_gene_variant CLLE-ES 15 59438341 59438341 single base substitution T C intron_variant CLLE-ES 15 59449666 59449666 single base substitution A T intron_variant CLLE-ES 15 59449666 59449666 single base substitution A T upstream_gene_variant CLLE-ES 15 59449865 59449865 single base substitution G A intron_variant CLLE-ES 15 59449865 59449865 single base substitution G A upstream_gene_variant CLLE-ES 15 59464004 59464004 single base substitution C T downstream_gene_variant CLLE-ES 15 59464004 59464004 single base substitution C T intron_variant CLLE-ES 15 59490583 59490583 single base substitution G C intron_variant CLLE-ES 15 59503915 59503915 single base substitution T A intron_variant CLLE-ES 15 59503915 59503915 single base substitution T A upstream_gene_variant CLLE-ES 15 59518375 59518375 single base substitution T A downstream_gene_variant CLLE-ES 15 59518375 59518375 single base substitution T A intron_variant CLLE-ES 15 59645563 59645563 single base substitution A G intron_variant CLLE-ES 15 59647272 59647272 single base substitution T C intron_variant CLLE-ES 15 59657011 59657011 single base substitution G A intron_variant CLLE-ES 15 59661474 59661474 single base substitution G A intron_variant CLLE-ES 15 59664115 59664115 single base substitution C T intron_variant CLLE-ES 15 59664588 59664588 single base substitution C T intron_variant CLLE-ES 15 59664701 59664701 single base substitution G C 5_prime_UTR_variant CLLE-ES 15 59664701 59664701 single base substitution G C exon_variant COAD-US 15 59455454 59455454 single base substitution A T missense_variant S264R 792T>A COAD-US 15 59455454 59455454 single base substitution A T missense_variant S843R 2529T>A COAD-US 15 59470679 59470679 single base substitution G A exon_variant COAD-US 15 59470679 59470679 single base substitution G A intron_variant COAD-US 15 59470679 59470679 single base substitution G A synonymous_variant G144G 432C>T COAD-US 15 59470679 59470679 single base substitution G A synonymous_variant G654G 1962C>T COAD-US 15 59499164 59499164 single base substitution C T downstream_gene_variant COAD-US 15 59499164 59499164 single base substitution C T intron_variant COAD-US 15 59499164 59499164 single base substitution C T upstream_gene_variant COAD-US 15 59499212 59499212 single base substitution G A downstream_gene_variant COAD-US 15 59499212 59499212 single base substitution G A intron_variant COAD-US 15 59499212 59499212 single base substitution G A upstream_gene_variant COAD-US 15 59499228 59499228 single base substitution C T downstream_gene_variant COAD-US 15 59499228 59499228 single base substitution C T intron_variant COAD-US 15 59499228 59499228 single base substitution C T upstream_gene_variant COAD-US 15 59499329 59499329 single base substitution G A downstream_gene_variant COAD-US 15 59499329 59499329 single base substitution G A intron_variant COAD-US 15 59499329 59499329 single base substitution G A upstream_gene_variant COAD-US 15 59499648 59499648 single base substitution T A downstream_gene_variant COAD-US 15 59499648 59499648 single base substitution T A intron_variant COAD-US 15 59499648 59499648 single base substitution T A upstream_gene_variant COAD-US 15 59499780 59499781 deletion of <=200bp TG - downstream_gene_variant COAD-US 15 59499780 59499781 deletion of <=200bp TG - intron_variant COAD-US 15 59499780 59499781 deletion of <=200bp TG - upstream_gene_variant COAD-US 15 59500923 59500923 single base substitution T C downstream_gene_variant COAD-US 15 59500923 59500923 single base substitution T C exon_variant COAD-US 15 59500923 59500923 single base substitution T C intron_variant COAD-US 15 59500923 59500923 single base substitution T C missense_variant N19S 56A>G COAD-US 15 59500923 59500923 single base substitution T C missense_variant N496S 1487A>G COAD-US 15 59500923 59500923 single base substitution T C upstream_gene_variant COAD-US 15 59510113 59510113 single base substitution G A missense_variant R192W 574C>T COAD-US 15 59510113 59510113 single base substitution G A missense_variant R362W 1084C>T COAD-US 15 59510113 59510113 single base substitution G A missense_variant R82W 244C>T COAD-US 15 59510143 59510143 single base substitution G A missense_variant R182W 544C>T COAD-US 15 59510143 59510143 single base substitution G A missense_variant R352W 1054C>T COAD-US 15 59510143 59510143 single base substitution G A missense_variant R72W 214C>T COAD-US 15 59510159 59510159 single base substitution C T synonymous_variant E176E 528G>A COAD-US 15 59510159 59510159 single base substitution C T synonymous_variant E346E 1038G>A COAD-US 15 59510159 59510159 single base substitution C T synonymous_variant E66E 198G>A COAD-US 15 59516946 59516946 single base substitution A C downstream_gene_variant COAD-US 15 59516946 59516946 single base substitution A C exon_variant COAD-US 15 59516946 59516946 single base substitution A C missense_variant L240R 719T>G COAD-US 15 59516946 59516946 single base substitution A C missense_variant L70R 209T>G COAD-US 15 59523927 59523927 single base substitution C T 3_prime_UTR_variant COAD-US 15 59523927 59523927 single base substitution C T exon_variant COAD-US 15 59523927 59523927 single base substitution C T missense_variant V162I 484G>A COAD-US 15 59523927 59523927 single base substitution C T upstream_gene_variant COAD-US 15 59564585 59564585 single base substitution C T exon_variant COAD-US 15 59564585 59564585 single base substitution C T missense_variant D23N 67G>A COCA-CN 15 59429637 59429637 single base substitution G A intron_variant COCA-CN 15 59429637 59429637 single base substitution G A missense_variant T1090M 3269C>T COCA-CN 15 59464190 59464190 single base substitution G A stop_gained R217* 649C>T COCA-CN 15 59464190 59464190 single base substitution G A stop_gained R286* 856C>T COCA-CN 15 59464190 59464190 single base substitution G A stop_gained R796* 2386C>T COCA-CN 15 59466484 59466484 single base substitution A G downstream_gene_variant COCA-CN 15 59466484 59466484 single base substitution A G intron_variant COCA-CN 15 59500971 59500971 single base substitution G A downstream_gene_variant COCA-CN 15 59500971 59500971 single base substitution G A exon_variant COCA-CN 15 59500971 59500971 single base substitution G A intron_variant COCA-CN 15 59500971 59500971 single base substitution G A missense_variant T3M 8C>T COCA-CN 15 59500971 59500971 single base substitution G A missense_variant T480M 1439C>T COCA-CN 15 59500971 59500971 single base substitution G A upstream_gene_variant COCA-CN 15 59502956 59502956 single base substitution A G intron_variant COCA-CN 15 59502956 59502956 single base substitution A G upstream_gene_variant COCA-CN 15 59524108 59524108 single base substitution G A intron_variant COCA-CN 15 59524108 59524108 single base substitution G A upstream_gene_variant COCA-CN 15 59528710 59528710 single base substitution C A intron_variant COCA-CN 15 59528749 59528749 single base substitution A G intron_variant COCA-CN 15 59548349 59548349 single base substitution T C intron_variant COCA-CN 15 59551315 59551315 single base substitution A G intron_variant COCA-CN 15 59564556 59564556 single base substitution C T exon_variant COCA-CN 15 59564556 59564556 single base substitution C T synonymous_variant E32E 96G>A COCA-CN 15 59658499 59658499 single base substitution C T intron_variant EOPC-DE 15 59424127 59424127 single base substitution C T downstream_gene_variant EOPC-DE 15 59473969 59473969 single base substitution T C intron_variant EOPC-DE 15 59512868 59512868 single base substitution G A downstream_gene_variant EOPC-DE 15 59512868 59512868 single base substitution G A intron_variant EOPC-DE 15 59512868 59512868 single base substitution G A upstream_gene_variant EOPC-DE 15 59537512 59537512 single base substitution T G intron_variant EOPC-DE 15 59544978 59544978 single base substitution A G intron_variant EOPC-DE 15 59544999 59544999 single base substitution C T intron_variant EOPC-DE 15 59551850 59551850 single base substitution G C intron_variant EOPC-DE 15 59580054 59580054 single base substitution G C intron_variant EOPC-DE 15 59586110 59586110 single base substitution C T intron_variant EOPC-DE 15 59616851 59616851 single base substitution C T intron_variant ESAD-UK 15 59422585 59422585 single base substitution T C downstream_gene_variant ESAD-UK 15 59424707 59424707 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 59425386 59425386 single base substitution C G downstream_gene_variant ESAD-UK 15 59430624 59430624 single base substitution C T intron_variant ESAD-UK 15 59433696 59433696 insertion of <=200bp - TT intron_variant ESAD-UK 15 59436253 59436253 single base substitution C T intron_variant ESAD-UK 15 59437204 59437204 single base substitution G A intron_variant ESAD-UK 15 59443241 59443250 deletion of <=200bp CACACACACG - intron_variant ESAD-UK 15 59444079 59444079 single base substitution C G intron_variant ESAD-UK 15 59445883 59445883 single base substitution G C missense_variant P996A 2986C>G ESAD-UK 15 59445883 59445883 single base substitution G C upstream_gene_variant ESAD-UK 15 59446199 59446199 single base substitution G T intron_variant ESAD-UK 15 59446199 59446199 single base substitution G T upstream_gene_variant ESAD-UK 15 59450583 59450583 single base substitution A C downstream_gene_variant ESAD-UK 15 59450583 59450583 single base substitution A C splice_region_variant ESAD-UK 15 59450583 59450583 single base substitution A C upstream_gene_variant ESAD-UK 15 59450904 59450904 single base substitution C T downstream_gene_variant ESAD-UK 15 59450904 59450904 single base substitution C T intron_variant ESAD-UK 15 59451588 59451588 single base substitution G A downstream_gene_variant ESAD-UK 15 59451588 59451588 single base substitution G A intron_variant ESAD-UK 15 59452256 59452256 single base substitution A T downstream_gene_variant ESAD-UK 15 59452256 59452256 single base substitution A T intron_variant ESAD-UK 15 59456038 59456038 single base substitution G A intron_variant ESAD-UK 15 59456281 59456281 single base substitution G A intron_variant ESAD-UK 15 59457673 59457673 single base substitution C T intron_variant ESAD-UK 15 59460335 59460335 single base substitution G A downstream_gene_variant ESAD-UK 15 59460335 59460335 single base substitution G A intron_variant ESAD-UK 15 59463024 59463024 single base substitution G C downstream_gene_variant ESAD-UK 15 59463024 59463024 single base substitution G C intron_variant ESAD-UK 15 59464056 59464056 single base substitution C T downstream_gene_variant ESAD-UK 15 59464056 59464056 single base substitution C T intron_variant ESAD-UK 15 59465183 59465183 single base substitution C T intron_variant ESAD-UK 15 59465415 59465415 single base substitution C A intron_variant ESAD-UK 15 59467444 59467444 single base substitution G T downstream_gene_variant ESAD-UK 15 59467444 59467444 single base substitution G T intron_variant ESAD-UK 15 59469808 59469808 single base substitution G A downstream_gene_variant ESAD-UK 15 59469808 59469808 single base substitution G A intron_variant ESAD-UK 15 59472745 59472745 single base substitution T C intron_variant ESAD-UK 15 59475341 59475341 single base substitution T C intron_variant ESAD-UK 15 59477281 59477281 deletion of <=200bp T - intron_variant ESAD-UK 15 59478854 59478854 single base substitution T A intron_variant ESAD-UK 15 59478886 59478886 single base substitution A C intron_variant ESAD-UK 15 59483760 59483760 single base substitution G C downstream_gene_variant ESAD-UK 15 59483760 59483760 single base substitution G C intron_variant ESAD-UK 15 59485730 59485730 single base substitution G A downstream_gene_variant ESAD-UK 15 59485730 59485730 single base substitution G A intron_variant ESAD-UK 15 59486827 59486827 single base substitution C A downstream_gene_variant ESAD-UK 15 59486827 59486827 single base substitution C A intron_variant ESAD-UK 15 59490666 59490666 single base substitution T C intron_variant ESAD-UK 15 59490708 59490708 single base substitution A T intron_variant ESAD-UK 15 59496808 59496808 single base substitution G A downstream_gene_variant ESAD-UK 15 59496808 59496808 single base substitution G A intron_variant ESAD-UK 15 59505187 59505187 single base substitution T G intron_variant ESAD-UK 15 59505187 59505187 single base substitution T G upstream_gene_variant ESAD-UK 15 59507972 59507972 deletion of <=200bp A - intron_variant ESAD-UK 15 59509409 59509409 single base substitution G C intron_variant ESAD-UK 15 59512756 59512756 single base substitution T G downstream_gene_variant ESAD-UK 15 59512756 59512756 single base substitution T G intron_variant ESAD-UK 15 59512756 59512756 single base substitution T G upstream_gene_variant ESAD-UK 15 59512783 59512783 single base substitution G C downstream_gene_variant ESAD-UK 15 59512783 59512783 single base substitution G C intron_variant ESAD-UK 15 59512783 59512783 single base substitution G C upstream_gene_variant ESAD-UK 15 59514607 59514607 single base substitution C T downstream_gene_variant ESAD-UK 15 59514607 59514607 single base substitution C T intron_variant ESAD-UK 15 59514607 59514607 single base substitution C T upstream_gene_variant ESAD-UK 15 59515611 59515611 single base substitution A G downstream_gene_variant ESAD-UK 15 59515611 59515611 single base substitution A G intron_variant ESAD-UK 15 59516056 59516056 single base substitution C T downstream_gene_variant ESAD-UK 15 59516056 59516056 single base substitution C T intron_variant ESAD-UK 15 59516253 59516253 single base substitution G C downstream_gene_variant ESAD-UK 15 59516253 59516253 single base substitution G C intron_variant ESAD-UK 15 59516318 59516318 single base substitution G C downstream_gene_variant ESAD-UK 15 59516318 59516318 single base substitution G C intron_variant ESAD-UK 15 59518427 59518427 single base substitution A G downstream_gene_variant ESAD-UK 15 59518427 59518427 single base substitution A G intron_variant ESAD-UK 15 59520050 59520050 single base substitution T C intron_variant ESAD-UK 15 59520050 59520050 single base substitution T C upstream_gene_variant ESAD-UK 15 59520413 59520413 single base substitution G A intron_variant ESAD-UK 15 59520413 59520413 single base substitution G A upstream_gene_variant ESAD-UK 15 59520660 59520661 deletion of <=200bp CT - intron_variant ESAD-UK 15 59520660 59520661 deletion of <=200bp CT - upstream_gene_variant ESAD-UK 15 59522292 59522292 single base substitution C T intron_variant ESAD-UK 15 59522292 59522292 single base substitution C T upstream_gene_variant ESAD-UK 15 59522399 59522399 insertion of <=200bp - GA intron_variant ESAD-UK 15 59522399 59522399 insertion of <=200bp - GA upstream_gene_variant ESAD-UK 15 59525312 59525314 deletion of <=200bp ATC - intron_variant ESAD-UK 15 59527134 59527134 single base substitution T C intron_variant ESAD-UK 15 59527188 59527188 single base substitution T C intron_variant ESAD-UK 15 59528016 59528016 single base substitution T G intron_variant ESAD-UK 15 59528765 59528765 single base substitution T A intron_variant ESAD-UK 15 59530569 59530569 single base substitution C T intron_variant ESAD-UK 15 59530998 59530998 single base substitution G A intron_variant ESAD-UK 15 59531324 59531324 single base substitution G A intron_variant ESAD-UK 15 59533462 59533462 single base substitution T G intron_variant ESAD-UK 15 59534665 59534665 single base substitution G A intron_variant ESAD-UK 15 59535142 59535142 single base substitution G A intron_variant ESAD-UK 15 59536719 59536719 single base substitution G T intron_variant ESAD-UK 15 59537680 59537680 single base substitution G C intron_variant ESAD-UK 15 59538503 59538503 single base substitution G C intron_variant ESAD-UK 15 59540228 59540228 single base substitution G A intron_variant ESAD-UK 15 59540823 59540823 single base substitution C T intron_variant ESAD-UK 15 59541711 59541711 single base substitution G A intron_variant ESAD-UK 15 59541884 59541884 single base substitution T A intron_variant ESAD-UK 15 59543528 59543528 deletion of <=200bp T - intron_variant ESAD-UK 15 59543530 59543534 deletion of <=200bp TAAAT - intron_variant ESAD-UK 15 59544229 59544229 single base substitution A C intron_variant ESAD-UK 15 59544682 59544682 single base substitution G A intron_variant ESAD-UK 15 59547513 59547513 single base substitution C T intron_variant ESAD-UK 15 59547902 59547902 deletion of <=200bp A - intron_variant ESAD-UK 15 59548440 59548440 single base substitution G A intron_variant ESAD-UK 15 59551650 59551650 single base substitution T C intron_variant ESAD-UK 15 59551657 59551657 single base substitution C G intron_variant ESAD-UK 15 59553788 59553788 single base substitution G A intron_variant ESAD-UK 15 59555270 59555270 single base substitution C A intron_variant ESAD-UK 15 59556263 59556263 insertion of <=200bp - T intron_variant ESAD-UK 15 59556595 59556595 single base substitution C A intron_variant ESAD-UK 15 59557116 59557116 single base substitution G A exon_variant ESAD-UK 15 59557116 59557116 single base substitution G A intron_variant ESAD-UK 15 59558339 59558339 single base substitution G T intron_variant ESAD-UK 15 59558339 59558339 single base substitution G T upstream_gene_variant ESAD-UK 15 59559078 59559078 single base substitution T A intron_variant ESAD-UK 15 59559078 59559078 single base substitution T A upstream_gene_variant ESAD-UK 15 59559571 59559571 single base substitution G A downstream_gene_variant ESAD-UK 15 59559571 59559571 single base substitution G A intron_variant ESAD-UK 15 59559571 59559571 single base substitution G A upstream_gene_variant ESAD-UK 15 59562625 59562625 single base substitution C G downstream_gene_variant ESAD-UK 15 59562625 59562625 single base substitution C G intron_variant ESAD-UK 15 59565214 59565214 single base substitution T C intron_variant ESAD-UK 15 59567075 59567075 deletion of <=200bp G - intron_variant ESAD-UK 15 59570353 59570353 single base substitution G A intron_variant ESAD-UK 15 59570929 59570929 single base substitution G A intron_variant ESAD-UK 15 59572486 59572486 single base substitution C T intron_variant ESAD-UK 15 59573620 59573620 single base substitution G C intron_variant ESAD-UK 15 59574269 59574269 single base substitution C T intron_variant ESAD-UK 15 59576642 59576642 single base substitution A T intron_variant ESAD-UK 15 59576760 59576760 single base substitution C T intron_variant ESAD-UK 15 59577788 59577788 single base substitution T C intron_variant ESAD-UK 15 59578092 59578092 single base substitution C T intron_variant ESAD-UK 15 59581914 59581914 single base substitution G A intron_variant ESAD-UK 15 59583229 59583229 single base substitution C G intron_variant ESAD-UK 15 59584142 59584143 deletion of <=200bp AA - intron_variant ESAD-UK 15 59584644 59584644 single base substitution C T intron_variant ESAD-UK 15 59587041 59587041 single base substitution T A intron_variant ESAD-UK 15 59588012 59588012 single base substitution A C intron_variant ESAD-UK 15 59593668 59593668 single base substitution G A intron_variant ESAD-UK 15 59595885 59595885 single base substitution T G intron_variant ESAD-UK 15 59598985 59598985 single base substitution G T intron_variant ESAD-UK 15 59599011 59599011 single base substitution A G intron_variant ESAD-UK 15 59600261 59600261 insertion of <=200bp - A intron_variant ESAD-UK 15 59601181 59601181 single base substitution G A intron_variant ESAD-UK 15 59601618 59601618 single base substitution G T intron_variant ESAD-UK 15 59604161 59604161 single base substitution A G intron_variant ESAD-UK 15 59604739 59604739 single base substitution G A intron_variant ESAD-UK 15 59604862 59604862 single base substitution G T intron_variant ESAD-UK 15 59607538 59607538 single base substitution A T intron_variant ESAD-UK 15 59611691 59611691 insertion of <=200bp - GCTATCAG intron_variant ESAD-UK 15 59612049 59612049 single base substitution C T intron_variant ESAD-UK 15 59612509 59612509 deletion of <=200bp A - intron_variant ESAD-UK 15 59618778 59618778 single base substitution G T intron_variant ESAD-UK 15 59622122 59622122 single base substitution G A intron_variant ESAD-UK 15 59623892 59623892 single base substitution A C intron_variant ESAD-UK 15 59625431 59625431 single base substitution T C intron_variant ESAD-UK 15 59627299 59627299 single base substitution A G intron_variant ESAD-UK 15 59627508 59627508 single base substitution G A intron_variant ESAD-UK 15 59628130 59628130 single base substitution C A intron_variant ESAD-UK 15 59629225 59629225 single base substitution T A intron_variant ESAD-UK 15 59630183 59630183 deletion of <=200bp T - intron_variant ESAD-UK 15 59632832 59632832 deletion of <=200bp T - intron_variant ESAD-UK 15 59634992 59634992 single base substitution A G intron_variant ESAD-UK 15 59637356 59637356 single base substitution C T intron_variant ESAD-UK 15 59637948 59637948 single base substitution G A intron_variant ESAD-UK 15 59649564 59649564 single base substitution C T intron_variant ESAD-UK 15 59651595 59651595 single base substitution G A intron_variant ESAD-UK 15 59651596 59651596 single base substitution G A intron_variant ESAD-UK 15 59652839 59652839 single base substitution T C intron_variant ESAD-UK 15 59654177 59654177 single base substitution G A intron_variant ESAD-UK 15 59654851 59654851 single base substitution T G intron_variant ESAD-UK 15 59659647 59659647 single base substitution G C intron_variant ESAD-UK 15 59662293 59662293 single base substitution A C intron_variant ESAD-UK 15 59668458 59668458 single base substitution T C upstream_gene_variant ESAD-UK 15 59668459 59668459 single base substitution T C upstream_gene_variant ESCA-CN 15 59515446 59515446 single base substitution C G downstream_gene_variant ESCA-CN 15 59515446 59515446 single base substitution C G intron_variant ESCA-CN 15 59515446 59515446 single base substitution C G upstream_gene_variant GBM-US 15 59502739 59502739 single base substitution C G intron_variant GBM-US 15 59502739 59502739 single base substitution C G missense_variant V166L 496G>C GBM-US 15 59502739 59502739 single base substitution C G missense_variant V446L 1336G>C GBM-US 15 59502739 59502739 single base substitution C G upstream_gene_variant KIRC-US 15 59464119 59464119 single base substitution T A missense_variant E240D 720A>T KIRC-US 15 59464119 59464119 single base substitution T A missense_variant E309D 927A>T KIRC-US 15 59464119 59464119 single base substitution T A missense_variant E819D 2457A>T KIRC-US 15 59470597 59470597 single base substitution C G downstream_gene_variant KIRC-US 15 59470597 59470597 single base substitution C G intron_variant KIRC-US 15 59470597 59470597 single base substitution C G missense_variant E172Q 514G>C KIRC-US 15 59470597 59470597 single base substitution C G missense_variant E682Q 2044G>C KIRC-US 15 59506883 59506883 single base substitution A G intron_variant KIRC-US 15 59506883 59506883 single base substitution A G missense_variant Y102H 304T>C KIRC-US 15 59506883 59506883 single base substitution A G missense_variant Y382H 1144T>C KIRC-US 15 59528837 59528837 single base substitution T C exon_variant KIRC-US 15 59528837 59528837 single base substitution T C intron_variant KIRC-US 15 59528837 59528837 single base substitution T C missense_variant K123E 367A>G KIRP-US 15 59501015 59501015 single base substitution G A exon_variant KIRP-US 15 59501015 59501015 single base substitution G A intron_variant KIRP-US 15 59501015 59501015 single base substitution G A synonymous_variant D185D 555C>T KIRP-US 15 59501015 59501015 single base substitution G A synonymous_variant D465D 1395C>T KIRP-US 15 59501015 59501015 single base substitution G A upstream_gene_variant KIRP-US 15 59515313 59515313 single base substitution C G downstream_gene_variant KIRP-US 15 59515313 59515313 single base substitution C G exon_variant KIRP-US 15 59515313 59515313 single base substitution C G synonymous_variant L115L 345G>C KIRP-US 15 59515313 59515313 single base substitution C G synonymous_variant L285L 855G>C KIRP-US 15 59515313 59515313 single base substitution C G upstream_gene_variant LAML-KR 15 59429779 59429779 single base substitution T C intron_variant LAML-KR 15 59434196 59434196 single base substitution T C intron_variant LAML-KR 15 59453121 59453121 single base substitution A G downstream_gene_variant LAML-KR 15 59453121 59453121 single base substitution A G intron_variant LAML-KR 15 59464211 59464211 single base substitution T C missense_variant K210E 628A>G LAML-KR 15 59464211 59464211 single base substitution T C missense_variant K279E 835A>G LAML-KR 15 59464211 59464211 single base substitution T C missense_variant K789E 2365A>G LAML-KR 15 59476640 59476640 single base substitution G A intron_variant LAML-KR 15 59569763 59569763 single base substitution A C intron_variant LAML-KR 15 59660628 59660628 single base substitution T C intron_variant LGG-US 15 59499792 59499792 single base substitution G A downstream_gene_variant LGG-US 15 59499792 59499792 single base substitution G A intron_variant LGG-US 15 59499792 59499792 single base substitution G A upstream_gene_variant LICA-CN 15 59445911 59445911 single base substitution T G missense_variant K986N 2958A>C LICA-CN 15 59445911 59445911 single base substitution T G upstream_gene_variant LICA-FR 15 59444736 59444736 single base substitution T C intron_variant LICA-FR 15 59462433 59462433 single base substitution C T downstream_gene_variant LICA-FR 15 59462433 59462433 single base substitution C T intron_variant LICA-FR 15 59483425 59483425 single base substitution C T downstream_gene_variant LICA-FR 15 59483425 59483425 single base substitution C T intron_variant LICA-FR 15 59495584 59495584 insertion of <=200bp - T intron_variant LICA-FR 15 59499033 59499033 single base substitution A C downstream_gene_variant LICA-FR 15 59499033 59499033 single base substitution A C intron_variant LICA-FR 15 59499033 59499033 single base substitution A C upstream_gene_variant LICA-FR 15 59527038 59527038 single base substitution A C intron_variant LICA-FR 15 59543503 59543503 single base substitution G C intron_variant LICA-FR 15 59564623 59564623 single base substitution T C exon_variant LICA-FR 15 59564623 59564623 single base substitution T C missense_variant H10R 29A>G LICA-FR 15 59600988 59600988 single base substitution T A intron_variant LICA-FR 15 59655627 59655627 single base substitution T C intron_variant LIHC-US 15 59450529 59450529 single base substitution A C downstream_gene_variant LIHC-US 15 59450529 59450529 single base substitution A C synonymous_variant T945T 2835T>G LIHC-US 15 59450529 59450529 single base substitution A C upstream_gene_variant LIHC-US 15 59464100 59464100 single base substitution G A missense_variant L247F 739C>T LIHC-US 15 59464100 59464100 single base substitution G A missense_variant L316F 946C>T LIHC-US 15 59464100 59464100 single base substitution G A missense_variant L826F 2476C>T LIHC-US 15 59470655 59470655 single base substitution G T exon_variant LIHC-US 15 59470655 59470655 single base substitution G T intron_variant LIHC-US 15 59470655 59470655 single base substitution G T synonymous_variant V152V 456C>A LIHC-US 15 59470655 59470655 single base substitution G T synonymous_variant V662V 1986C>A LIHC-US 15 59499173 59499173 single base substitution C A downstream_gene_variant LIHC-US 15 59499173 59499173 single base substitution C A intron_variant LIHC-US 15 59499173 59499173 single base substitution C A upstream_gene_variant LIHC-US 15 59500993 59500993 single base substitution C A downstream_gene_variant LIHC-US 15 59500993 59500993 single base substitution C A exon_variant LIHC-US 15 59500993 59500993 single base substitution C A intron_variant LIHC-US 15 59500993 59500993 single base substitution C A missense_variant V473L 1417G>T LIHC-US 15 59500993 59500993 single base substitution C A upstream_gene_variant LIHC-US 15 59502718 59502718 single base substitution T G intron_variant LIHC-US 15 59502718 59502718 single base substitution T G missense_variant K173Q 517A>C LIHC-US 15 59502718 59502718 single base substitution T G missense_variant K453Q 1357A>C LIHC-US 15 59502718 59502718 single base substitution T G upstream_gene_variant LINC-JP 15 59433008 59433008 single base substitution G A intron_variant LINC-JP 15 59441100 59441100 single base substitution T C intron_variant LINC-JP 15 59445234 59445234 single base substitution T C intron_variant LINC-JP 15 59464300 59464300 single base substitution A T intron_variant LINC-JP 15 59470611 59470611 single base substitution A C downstream_gene_variant LINC-JP 15 59470611 59470611 single base substitution A C intron_variant LINC-JP 15 59470611 59470611 single base substitution A C missense_variant F167C 500T>G LINC-JP 15 59470611 59470611 single base substitution A C missense_variant F677C 2030T>G LINC-JP 15 59488262 59488262 single base substitution A C intron_variant LINC-JP 15 59494817 59494817 single base substitution A G intron_variant LINC-JP 15 59497102 59497102 single base substitution A T downstream_gene_variant LINC-JP 15 59497102 59497102 single base substitution A T intron_variant LINC-JP 15 59504887 59504887 single base substitution T C intron_variant LINC-JP 15 59504887 59504887 single base substitution T C upstream_gene_variant LINC-JP 15 59508793 59508793 single base substitution G A intron_variant LINC-JP 15 59514833 59514833 single base substitution T C downstream_gene_variant LINC-JP 15 59514833 59514833 single base substitution T C intron_variant LINC-JP 15 59514833 59514833 single base substitution T C upstream_gene_variant LINC-JP 15 59516274 59516274 single base substitution C A downstream_gene_variant LINC-JP 15 59516274 59516274 single base substitution C A intron_variant LINC-JP 15 59523752 59523752 single base substitution T C intron_variant LINC-JP 15 59523752 59523752 single base substitution T C upstream_gene_variant LINC-JP 15 59524140 59524140 single base substitution T C intron_variant LINC-JP 15 59524140 59524140 single base substitution T C upstream_gene_variant LINC-JP 15 59527702 59527702 single base substitution T C intron_variant LINC-JP 15 59529217 59529217 single base substitution A C intron_variant LINC-JP 15 59531431 59531431 single base substitution T A intron_variant LINC-JP 15 59531432 59531432 single base substitution A T intron_variant LINC-JP 15 59532535 59532535 single base substitution A G intron_variant LINC-JP 15 59547896 59547896 single base substitution G A intron_variant LINC-JP 15 59567434 59567434 insertion of <=200bp - TT intron_variant LINC-JP 15 59568334 59568334 single base substitution C T intron_variant LINC-JP 15 59570259 59570259 single base substitution G A intron_variant LINC-JP 15 59597685 59597685 single base substitution C T intron_variant LINC-JP 15 59604082 59604082 single base substitution T C intron_variant LINC-JP 15 59604524 59604524 single base substitution T C intron_variant LINC-JP 15 59617100 59617100 single base substitution A G intron_variant LINC-JP 15 59618253 59618253 single base substitution T C intron_variant LINC-JP 15 59623608 59623608 single base substitution T C intron_variant LINC-JP 15 59630136 59630136 single base substitution T C intron_variant LINC-JP 15 59639123 59639123 single base substitution G A intron_variant LINC-JP 15 59653749 59653749 single base substitution A G intron_variant LIRI-JP 15 59427151 59427151 single base substitution T C 3_prime_UTR_variant LIRI-JP 15 59427151 59427151 single base substitution T C downstream_gene_variant LIRI-JP 15 59432560 59432560 single base substitution T C intron_variant LIRI-JP 15 59439179 59439179 single base substitution A G intron_variant LIRI-JP 15 59440255 59440255 single base substitution T C intron_variant LIRI-JP 15 59441472 59441472 single base substitution G T intron_variant LIRI-JP 15 59444575 59444575 single base substitution G A intron_variant LIRI-JP 15 59446061 59446061 single base substitution T C intron_variant LIRI-JP 15 59446061 59446061 single base substitution T C upstream_gene_variant LIRI-JP 15 59446304 59446304 single base substitution G A intron_variant LIRI-JP 15 59446304 59446304 single base substitution G A upstream_gene_variant LIRI-JP 15 59446577 59446577 single base substitution C T intron_variant LIRI-JP 15 59446577 59446577 single base substitution C T upstream_gene_variant LIRI-JP 15 59450722 59450722 single base substitution G A downstream_gene_variant LIRI-JP 15 59450722 59450722 single base substitution G A intron_variant LIRI-JP 15 59450722 59450722 single base substitution G A upstream_gene_variant LIRI-JP 15 59453374 59453374 single base substitution G A downstream_gene_variant LIRI-JP 15 59453374 59453374 single base substitution G A missense_variant R895W 2683C>T LIRI-JP 15 59454560 59454560 single base substitution A T downstream_gene_variant LIRI-JP 15 59454560 59454560 single base substitution A T intron_variant LIRI-JP 15 59455028 59455028 single base substitution C A downstream_gene_variant LIRI-JP 15 59455028 59455028 single base substitution C A intron_variant LIRI-JP 15 59457212 59457212 single base substitution C T intron_variant LIRI-JP 15 59461216 59461216 single base substitution T C downstream_gene_variant LIRI-JP 15 59461216 59461216 single base substitution T C intron_variant LIRI-JP 15 59461997 59461997 single base substitution C T downstream_gene_variant LIRI-JP 15 59461997 59461997 single base substitution C T intron_variant LIRI-JP 15 59463055 59463055 single base substitution C T downstream_gene_variant LIRI-JP 15 59463055 59463055 single base substitution C T intron_variant LIRI-JP 15 59465226 59465226 single base substitution T G intron_variant LIRI-JP 15 59466407 59466407 single base substitution C G downstream_gene_variant LIRI-JP 15 59466407 59466407 single base substitution C G intron_variant LIRI-JP 15 59466407 59466407 single base substitution C G missense_variant K184N 552G>C LIRI-JP 15 59466407 59466407 single base substitution C G missense_variant K694N 2082G>C LIRI-JP 15 59466518 59466518 single base substitution G C downstream_gene_variant LIRI-JP 15 59466518 59466518 single base substitution G C intron_variant LIRI-JP 15 59469051 59469051 single base substitution G C downstream_gene_variant LIRI-JP 15 59469051 59469051 single base substitution G C intron_variant LIRI-JP 15 59469491 59469491 single base substitution A T downstream_gene_variant LIRI-JP 15 59469491 59469491 single base substitution A T intron_variant LIRI-JP 15 59470878 59470878 single base substitution C T intron_variant LIRI-JP 15 59472317 59472317 single base substitution C A intron_variant LIRI-JP 15 59473369 59473369 single base substitution T C intron_variant LIRI-JP 15 59477109 59477109 single base substitution C A intron_variant LIRI-JP 15 59478293 59478293 single base substitution T G intron_variant LIRI-JP 15 59478547 59478547 single base substitution T C intron_variant LIRI-JP 15 59480176 59480176 single base substitution T A intron_variant LIRI-JP 15 59483202 59483202 single base substitution G A downstream_gene_variant LIRI-JP 15 59483202 59483202 single base substitution G A intron_variant LIRI-JP 15 59483479 59483479 single base substitution C A downstream_gene_variant LIRI-JP 15 59483479 59483479 single base substitution C A intron_variant LIRI-JP 15 59486053 59486053 single base substitution T C downstream_gene_variant LIRI-JP 15 59486053 59486053 single base substitution T C intron_variant LIRI-JP 15 59486540 59486540 single base substitution T C downstream_gene_variant LIRI-JP 15 59486540 59486540 single base substitution T C intron_variant LIRI-JP 15 59487402 59487402 single base substitution T C downstream_gene_variant LIRI-JP 15 59487402 59487402 single base substitution T C intron_variant LIRI-JP 15 59488185 59488185 single base substitution T C intron_variant LIRI-JP 15 59489486 59489486 single base substitution C G intron_variant LIRI-JP 15 59491796 59491796 single base substitution T C intron_variant LIRI-JP 15 59494821 59494821 single base substitution A C intron_variant LIRI-JP 15 59498058 59498058 single base substitution C T downstream_gene_variant LIRI-JP 15 59498058 59498058 single base substitution C T intron_variant LIRI-JP 15 59498509 59498509 single base substitution G A downstream_gene_variant LIRI-JP 15 59498509 59498509 single base substitution G A intron_variant LIRI-JP 15 59499879 59499879 single base substitution T C downstream_gene_variant LIRI-JP 15 59499879 59499879 single base substitution T C intron_variant LIRI-JP 15 59499879 59499879 single base substitution T C upstream_gene_variant LIRI-JP 15 59501065 59501065 single base substitution G A exon_variant LIRI-JP 15 59501065 59501065 single base substitution G A intron_variant LIRI-JP 15 59501065 59501065 single base substitution G A upstream_gene_variant LIRI-JP 15 59501992 59501992 single base substitution T C intron_variant LIRI-JP 15 59501992 59501992 single base substitution T C upstream_gene_variant LIRI-JP 15 59506401 59506401 single base substitution A G intron_variant LIRI-JP 15 59511227 59511227 deletion of <=200bp A - downstream_gene_variant LIRI-JP 15 59511227 59511227 deletion of <=200bp A - intron_variant LIRI-JP 15 59511227 59511227 deletion of <=200bp A - upstream_gene_variant LIRI-JP 15 59514560 59514560 single base substitution A G downstream_gene_variant LIRI-JP 15 59514560 59514560 single base substitution A G intron_variant LIRI-JP 15 59514560 59514560 single base substitution A G upstream_gene_variant LIRI-JP 15 59517039 59517039 single base substitution C G downstream_gene_variant LIRI-JP 15 59517039 59517039 single base substitution C G intron_variant LIRI-JP 15 59519206 59519206 single base substitution C T downstream_gene_variant LIRI-JP 15 59519206 59519206 single base substitution C T intron_variant LIRI-JP 15 59520119 59520119 single base substitution C T intron_variant LIRI-JP 15 59520119 59520119 single base substitution C T upstream_gene_variant LIRI-JP 15 59520234 59520234 single base substitution T A intron_variant LIRI-JP 15 59520234 59520234 single base substitution T A upstream_gene_variant LIRI-JP 15 59520557 59520557 single base substitution C G intron_variant LIRI-JP 15 59520557 59520557 single base substitution C G upstream_gene_variant LIRI-JP 15 59520896 59520896 single base substitution G A intron_variant LIRI-JP 15 59520896 59520896 single base substitution G A upstream_gene_variant LIRI-JP 15 59523707 59523707 single base substitution T A intron_variant LIRI-JP 15 59523707 59523707 single base substitution T A upstream_gene_variant LIRI-JP 15 59524011 59524011 single base substitution G T intron_variant LIRI-JP 15 59524011 59524011 single base substitution G T upstream_gene_variant LIRI-JP 15 59525305 59525308 deletion of <=200bp TCTT - intron_variant LIRI-JP 15 59525649 59525649 single base substitution G A intron_variant LIRI-JP 15 59526536 59526536 single base substitution A G intron_variant LIRI-JP 15 59527693 59527693 single base substitution T C intron_variant LIRI-JP 15 59530316 59530316 single base substitution C G intron_variant LIRI-JP 15 59535066 59535066 single base substitution C A intron_variant LIRI-JP 15 59537443 59537443 single base substitution T C intron_variant LIRI-JP 15 59540475 59540475 single base substitution G A intron_variant LIRI-JP 15 59542609 59542609 single base substitution T C intron_variant LIRI-JP 15 59545303 59545303 single base substitution T A intron_variant LIRI-JP 15 59545766 59545766 single base substitution T C intron_variant LIRI-JP 15 59546931 59546931 single base substitution T C intron_variant LIRI-JP 15 59547013 59547013 single base substitution A G intron_variant LIRI-JP 15 59548320 59548320 insertion of <=200bp - A intron_variant LIRI-JP 15 59550463 59550463 single base substitution T A intron_variant LIRI-JP 15 59552386 59552386 single base substitution C T intron_variant LIRI-JP 15 59554626 59554626 single base substitution G A intron_variant LIRI-JP 15 59554977 59554977 single base substitution C T intron_variant LIRI-JP 15 59556707 59556707 single base substitution G T intron_variant LIRI-JP 15 59559781 59559781 single base substitution T C downstream_gene_variant LIRI-JP 15 59559781 59559781 single base substitution T C intron_variant LIRI-JP 15 59559781 59559781 single base substitution T C upstream_gene_variant LIRI-JP 15 59560040 59560040 single base substitution G C downstream_gene_variant LIRI-JP 15 59560040 59560040 single base substitution G C intron_variant LIRI-JP 15 59560040 59560040 single base substitution G C upstream_gene_variant LIRI-JP 15 59562570 59562570 single base substitution G C downstream_gene_variant LIRI-JP 15 59562570 59562570 single base substitution G C intron_variant LIRI-JP 15 59566950 59566950 single base substitution C A intron_variant LIRI-JP 15 59567006 59567006 single base substitution G A intron_variant LIRI-JP 15 59567249 59567249 single base substitution T C intron_variant LIRI-JP 15 59569136 59569136 single base substitution T C intron_variant LIRI-JP 15 59569474 59569474 single base substitution G C intron_variant LIRI-JP 15 59571882 59571882 single base substitution T C intron_variant LIRI-JP 15 59573063 59573063 single base substitution T A intron_variant LIRI-JP 15 59576189 59576189 single base substitution A T intron_variant LIRI-JP 15 59577178 59577178 single base substitution T G intron_variant LIRI-JP 15 59577637 59577637 single base substitution A G intron_variant LIRI-JP 15 59581506 59581506 single base substitution T C intron_variant LIRI-JP 15 59582388 59582388 single base substitution A G intron_variant LIRI-JP 15 59583274 59583274 single base substitution G A intron_variant LIRI-JP 15 59583491 59583491 deletion of <=200bp A - intron_variant LIRI-JP 15 59583761 59583761 single base substitution G A intron_variant LIRI-JP 15 59584348 59584348 single base substitution A C intron_variant LIRI-JP 15 59586317 59586317 single base substitution G A intron_variant LIRI-JP 15 59586449 59586449 single base substitution G A intron_variant LIRI-JP 15 59586768 59586768 single base substitution C T intron_variant LIRI-JP 15 59586828 59586828 single base substitution C T intron_variant LIRI-JP 15 59587202 59587202 single base substitution G C intron_variant LIRI-JP 15 59594996 59594996 single base substitution A T intron_variant LIRI-JP 15 59595341 59595341 single base substitution C G intron_variant LIRI-JP 15 59595616 59595616 single base substitution T C intron_variant LIRI-JP 15 59596567 59596567 single base substitution C T intron_variant LIRI-JP 15 59598427 59598427 single base substitution T C intron_variant LIRI-JP 15 59599319 59599319 single base substitution G C intron_variant LIRI-JP 15 59607685 59607685 single base substitution T C intron_variant LIRI-JP 15 59609791 59609791 single base substitution T C intron_variant LIRI-JP 15 59611443 59611443 single base substitution G C intron_variant LIRI-JP 15 59611990 59611990 single base substitution T C intron_variant LIRI-JP 15 59613688 59613688 single base substitution T C intron_variant LIRI-JP 15 59614883 59614883 single base substitution T C intron_variant LIRI-JP 15 59614923 59614923 single base substitution T C intron_variant LIRI-JP 15 59615395 59615395 single base substitution C T intron_variant LIRI-JP 15 59617380 59617380 single base substitution G A intron_variant LIRI-JP 15 59619282 59619282 single base substitution A C intron_variant LIRI-JP 15 59620197 59620197 single base substitution A G intron_variant LIRI-JP 15 59620842 59620842 single base substitution T C intron_variant LIRI-JP 15 59621021 59621021 single base substitution C T intron_variant LIRI-JP 15 59628035 59628035 single base substitution C A intron_variant LIRI-JP 15 59629096 59629096 single base substitution T C intron_variant LIRI-JP 15 59629957 59629957 single base substitution G T intron_variant LIRI-JP 15 59632613 59632613 single base substitution G T intron_variant LIRI-JP 15 59633764 59633764 single base substitution T C intron_variant LIRI-JP 15 59635688 59635688 single base substitution T C intron_variant LIRI-JP 15 59636000 59636000 single base substitution G A intron_variant LIRI-JP 15 59637096 59637096 single base substitution A C intron_variant LIRI-JP 15 59639425 59639425 single base substitution G C intron_variant LIRI-JP 15 59642153 59642153 single base substitution T A intron_variant LIRI-JP 15 59642614 59642620 deletion of <=200bp AGAATGT - intron_variant LIRI-JP 15 59643072 59643072 insertion of <=200bp - T intron_variant LIRI-JP 15 59643630 59643630 single base substitution G C intron_variant LIRI-JP 15 59643904 59643904 single base substitution G C intron_variant LIRI-JP 15 59648470 59648470 single base substitution T C intron_variant LIRI-JP 15 59650131 59650131 single base substitution G T intron_variant LIRI-JP 15 59655782 59655782 single base substitution G C intron_variant LIRI-JP 15 59656451 59656451 single base substitution A G intron_variant LIRI-JP 15 59658095 59658095 single base substitution C A intron_variant LIRI-JP 15 59658263 59658263 single base substitution C T intron_variant LIRI-JP 15 59661013 59661013 single base substitution C A intron_variant LIRI-JP 15 59661268 59661268 single base substitution A G intron_variant LIRI-JP 15 59665467 59665467 single base substitution G A upstream_gene_variant LUSC-KR 15 59428555 59428555 single base substitution G A 3_prime_UTR_variant LUSC-KR 15 59428555 59428555 single base substitution G A downstream_gene_variant LUSC-KR 15 59429160 59429160 single base substitution G A 3_prime_UTR_variant LUSC-KR 15 59429160 59429160 single base substitution G A intron_variant LUSC-KR 15 59431619 59431619 single base substitution C A intron_variant LUSC-KR 15 59445444 59445444 single base substitution C A intron_variant LUSC-KR 15 59453067 59453067 single base substitution A G downstream_gene_variant LUSC-KR 15 59453067 59453067 single base substitution A G intron_variant LUSC-KR 15 59464039 59464039 single base substitution G A downstream_gene_variant LUSC-KR 15 59464039 59464039 single base substitution G A intron_variant LUSC-KR 15 59481964 59481964 single base substitution C T intron_variant LUSC-KR 15 59485940 59485940 single base substitution T A downstream_gene_variant LUSC-KR 15 59485940 59485940 single base substitution T A intron_variant LUSC-KR 15 59495327 59495327 single base substitution T A intron_variant LUSC-KR 15 59496772 59496772 single base substitution C A downstream_gene_variant LUSC-KR 15 59496772 59496772 single base substitution C A intron_variant LUSC-KR 15 59500543 59500543 single base substitution G C downstream_gene_variant LUSC-KR 15 59500543 59500543 single base substitution G C intron_variant LUSC-KR 15 59500543 59500543 single base substitution G C upstream_gene_variant LUSC-KR 15 59508571 59508571 single base substitution G A intron_variant LUSC-KR 15 59526803 59526803 single base substitution C T intron_variant LUSC-KR 15 59532484 59532484 single base substitution C T intron_variant LUSC-KR 15 59533659 59533659 single base substitution G A intron_variant LUSC-KR 15 59534040 59534040 single base substitution T A intron_variant LUSC-KR 15 59535096 59535096 single base substitution C G intron_variant LUSC-KR 15 59540365 59540365 single base substitution G A intron_variant LUSC-KR 15 59543699 59543699 single base substitution C G intron_variant LUSC-KR 15 59545700 59545700 single base substitution G T intron_variant LUSC-KR 15 59545946 59545946 single base substitution C A intron_variant LUSC-KR 15 59551774 59551774 single base substitution C T intron_variant LUSC-KR 15 59555045 59555045 single base substitution C A intron_variant LUSC-KR 15 59562532 59562532 single base substitution C T downstream_gene_variant LUSC-KR 15 59562532 59562532 single base substitution C T intron_variant LUSC-KR 15 59566141 59566141 single base substitution C A intron_variant LUSC-KR 15 59577754 59577754 single base substitution G C intron_variant LUSC-KR 15 59580656 59580656 single base substitution G A intron_variant LUSC-KR 15 59592156 59592156 single base substitution G C intron_variant LUSC-KR 15 59592682 59592682 single base substitution C T intron_variant LUSC-KR 15 59595826 59595826 single base substitution C A intron_variant LUSC-KR 15 59601524 59601524 single base substitution T C intron_variant LUSC-KR 15 59607173 59607173 single base substitution C A intron_variant LUSC-KR 15 59611887 59611887 single base substitution G A intron_variant LUSC-KR 15 59613332 59613332 single base substitution G A intron_variant LUSC-KR 15 59617097 59617097 single base substitution T A intron_variant LUSC-KR 15 59619508 59619508 single base substitution C T intron_variant LUSC-KR 15 59625078 59625078 single base substitution T A intron_variant LUSC-KR 15 59634371 59634371 single base substitution T A intron_variant LUSC-KR 15 59634700 59634700 single base substitution C T intron_variant LUSC-KR 15 59635864 59635864 single base substitution T C intron_variant LUSC-KR 15 59638669 59638669 single base substitution C T intron_variant LUSC-KR 15 59643449 59643449 single base substitution C G intron_variant LUSC-KR 15 59649714 59649714 single base substitution C A intron_variant LUSC-KR 15 59649715 59649715 single base substitution C G intron_variant LUSC-KR 15 59662526 59662526 single base substitution T C intron_variant LUSC-KR 15 59664751 59664751 single base substitution G T 5_prime_UTR_variant LUSC-KR 15 59664751 59664751 single base substitution G T exon_variant LUSC-KR 15 59664751 59664751 single base substitution G T upstream_gene_variant LUSC-KR 15 59665878 59665878 single base substitution C T upstream_gene_variant LUSC-KR 15 59665967 59665967 single base substitution G C upstream_gene_variant LUSC-KR 15 59667006 59667006 single base substitution G A upstream_gene_variant LUSC-KR 15 59668679 59668679 single base substitution G A upstream_gene_variant LUSC-US 15 59499206 59499206 single base substitution T A downstream_gene_variant LUSC-US 15 59499206 59499206 single base substitution T A intron_variant LUSC-US 15 59499206 59499206 single base substitution T A upstream_gene_variant LUSC-US 15 59499577 59499577 single base substitution T A downstream_gene_variant LUSC-US 15 59499577 59499577 single base substitution T A intron_variant LUSC-US 15 59499577 59499577 single base substitution T A upstream_gene_variant LUSC-US 15 59506474 59506474 single base substitution C T intron_variant LUSC-US 15 59506474 59506474 single base substitution C T missense_variant E130K 388G>A LUSC-US 15 59506474 59506474 single base substitution C T missense_variant E410K 1228G>A LUSC-US 15 59516905 59516905 single base substitution C A downstream_gene_variant LUSC-US 15 59516905 59516905 single base substitution C A exon_variant LUSC-US 15 59516905 59516905 single base substitution C A stop_gained E254* 760G>T LUSC-US 15 59516905 59516905 single base substitution C A stop_gained E84* 250G>T LUSC-US 15 59519708 59519708 single base substitution T C 3_prime_UTR_variant LUSC-US 15 59519708 59519708 single base substitution T C exon_variant LUSC-US 15 59519708 59519708 single base substitution T C missense_variant R198G 592A>G LUSC-US 15 59519708 59519708 single base substitution T C missense_variant R28G 82A>G LUSC-US 15 59519720 59519720 single base substitution G C 3_prime_UTR_variant LUSC-US 15 59519720 59519720 single base substitution G C exon_variant LUSC-US 15 59519720 59519720 single base substitution G C missense_variant L194V 580C>G LUSC-US 15 59519720 59519720 single base substitution G C missense_variant L24V 70C>G MALY-DE 15 59431451 59431451 single base substitution C T intron_variant MALY-DE 15 59443649 59443649 single base substitution C A intron_variant MALY-DE 15 59444089 59444090 deletion of <=200bp AC - intron_variant MALY-DE 15 59447107 59447107 insertion of <=200bp - G intron_variant MALY-DE 15 59447107 59447107 insertion of <=200bp - G upstream_gene_variant MALY-DE 15 59447654 59447654 single base substitution G A intron_variant MALY-DE 15 59447654 59447654 single base substitution G A upstream_gene_variant MALY-DE 15 59450730 59450730 single base substitution G C downstream_gene_variant MALY-DE 15 59450730 59450730 single base substitution G C intron_variant MALY-DE 15 59450730 59450730 single base substitution G C upstream_gene_variant MALY-DE 15 59453237 59453237 single base substitution G A downstream_gene_variant MALY-DE 15 59453237 59453237 single base substitution G A intron_variant MALY-DE 15 59462594 59462594 single base substitution G A downstream_gene_variant MALY-DE 15 59462594 59462594 single base substitution G A intron_variant MALY-DE 15 59463138 59463138 single base substitution T A downstream_gene_variant MALY-DE 15 59463138 59463138 single base substitution T A intron_variant MALY-DE 15 59472677 59472677 single base substitution G A intron_variant MALY-DE 15 59480409 59480409 single base substitution C T exon_variant MALY-DE 15 59480409 59480409 single base substitution C T intron_variant MALY-DE 15 59480409 59480409 single base substitution C T synonymous_variant K604K 1812G>A MALY-DE 15 59485307 59485307 single base substitution T C downstream_gene_variant MALY-DE 15 59485307 59485307 single base substitution T C intron_variant MALY-DE 15 59485558 59485558 deletion of <=200bp T - downstream_gene_variant MALY-DE 15 59485558 59485558 deletion of <=200bp T - intron_variant MALY-DE 15 59508867 59508867 single base substitution A G intron_variant MALY-DE 15 59508886 59508886 single base substitution C T intron_variant MALY-DE 15 59513220 59513220 single base substitution A T downstream_gene_variant MALY-DE 15 59513220 59513220 single base substitution A T intron_variant MALY-DE 15 59513220 59513220 single base substitution A T upstream_gene_variant MALY-DE 15 59515730 59515730 single base substitution G A downstream_gene_variant MALY-DE 15 59515730 59515730 single base substitution G A intron_variant MALY-DE 15 59531106 59531106 insertion of <=200bp - T intron_variant MALY-DE 15 59543331 59543331 single base substitution A G intron_variant MALY-DE 15 59543464 59543464 single base substitution A C intron_variant MALY-DE 15 59544119 59544119 single base substitution A G intron_variant MALY-DE 15 59544393 59544393 single base substitution G C intron_variant MALY-DE 15 59545462 59545462 single base substitution T G intron_variant MALY-DE 15 59548875 59548875 single base substitution C G intron_variant MALY-DE 15 59554423 59554423 single base substitution A G intron_variant MALY-DE 15 59563017 59563017 single base substitution C T downstream_gene_variant MALY-DE 15 59563017 59563017 single base substitution C T intron_variant MALY-DE 15 59564665 59564665 single base substitution T A intron_variant MALY-DE 15 59564682 59564682 single base substitution T G intron_variant MALY-DE 15 59568096 59568096 single base substitution A G intron_variant MALY-DE 15 59568662 59568662 single base substitution A T intron_variant MALY-DE 15 59582367 59582367 single base substitution T C intron_variant MALY-DE 15 59587803 59587803 single base substitution G A intron_variant MALY-DE 15 59589437 59589437 single base substitution T C intron_variant MALY-DE 15 59589678 59589678 single base substitution T A intron_variant MALY-DE 15 59590719 59590719 single base substitution A C intron_variant MALY-DE 15 59592024 59592024 single base substitution A T intron_variant MALY-DE 15 59594802 59594802 single base substitution A C intron_variant MALY-DE 15 59601378 59601378 single base substitution A T intron_variant MALY-DE 15 59601907 59601907 single base substitution T A intron_variant MALY-DE 15 59603556 59603556 single base substitution G A intron_variant MALY-DE 15 59603684 59603684 single base substitution A G intron_variant MALY-DE 15 59605058 59605058 insertion of <=200bp - AAT intron_variant MALY-DE 15 59608823 59608823 single base substitution G A intron_variant MALY-DE 15 59610270 59610270 single base substitution G A intron_variant MALY-DE 15 59610502 59610502 single base substitution G A intron_variant MALY-DE 15 59620353 59620353 single base substitution A C intron_variant MALY-DE 15 59620744 59620744 single base substitution A T intron_variant MALY-DE 15 59622222 59622222 single base substitution A G intron_variant MALY-DE 15 59622647 59622647 single base substitution T A intron_variant MALY-DE 15 59625951 59625951 single base substitution T C intron_variant MALY-DE 15 59626157 59626157 single base substitution A C intron_variant MALY-DE 15 59633686 59633686 single base substitution T A intron_variant MALY-DE 15 59635599 59635599 single base substitution G A intron_variant MALY-DE 15 59651862 59651862 single base substitution T C intron_variant MALY-DE 15 59652180 59652180 single base substitution G A intron_variant MALY-DE 15 59652320 59652320 single base substitution T A intron_variant MALY-DE 15 59660541 59660541 single base substitution A G intron_variant MALY-DE 15 59663379 59663379 single base substitution T G intron_variant MALY-DE 15 59663526 59663526 single base substitution T C intron_variant MALY-DE 15 59663650 59663650 single base substitution T C intron_variant MALY-DE 15 59663681 59663681 single base substitution T A intron_variant MALY-DE 15 59664445 59664445 single base substitution G A intron_variant MALY-DE 15 59664491 59664491 single base substitution T A intron_variant MALY-DE 15 59664494 59664494 single base substitution A T intron_variant MALY-DE 15 59664518 59664518 single base substitution T G intron_variant MALY-DE 15 59664521 59664521 single base substitution C T intron_variant MALY-DE 15 59664532 59664532 single base substitution G A intron_variant MALY-DE 15 59664533 59664533 single base substitution G C intron_variant MALY-DE 15 59664540 59664540 single base substitution G A intron_variant MALY-DE 15 59664558 59664558 single base substitution G C intron_variant MALY-DE 15 59664560 59664560 single base substitution G C intron_variant MALY-DE 15 59664564 59664564 single base substitution G A intron_variant MALY-DE 15 59664586 59664586 single base substitution C T intron_variant MALY-DE 15 59664588 59664588 single base substitution C T intron_variant MALY-DE 15 59664612 59664612 single base substitution G A intron_variant MALY-DE 15 59664630 59664630 single base substitution C A intron_variant MALY-DE 15 59664675 59664675 single base substitution G C intron_variant MALY-DE 15 59664691 59664691 single base substitution A G intron_variant MALY-DE 15 59664733 59664733 single base substitution T C 5_prime_UTR_variant MALY-DE 15 59664733 59664733 single base substitution T C exon_variant MALY-DE 15 59664733 59664733 single base substitution T C upstream_gene_variant MALY-DE 15 59664791 59664791 single base substitution G C 5_prime_UTR_variant MALY-DE 15 59664791 59664791 single base substitution G C exon_variant MALY-DE 15 59664791 59664791 single base substitution G C upstream_gene_variant MALY-DE 15 59664795 59664795 single base substitution C A 5_prime_UTR_variant MALY-DE 15 59664795 59664795 single base substitution C A exon_variant MALY-DE 15 59664795 59664795 single base substitution C A upstream_gene_variant MALY-DE 15 59666052 59666052 single base substitution C T upstream_gene_variant MELA-AU 15 59422301 59422301 single base substitution G A downstream_gene_variant MELA-AU 15 59423155 59423155 single base substitution C T downstream_gene_variant MELA-AU 15 59423728 59423728 single base substitution G A downstream_gene_variant MELA-AU 15 59424352 59424352 single base substitution G A downstream_gene_variant MELA-AU 15 59426171 59426171 single base substitution C T downstream_gene_variant MELA-AU 15 59427142 59427142 single base substitution A T 3_prime_UTR_variant MELA-AU 15 59427142 59427142 single base substitution A T downstream_gene_variant MELA-AU 15 59427145 59427145 single base substitution G A 3_prime_UTR_variant MELA-AU 15 59427145 59427145 single base substitution G A downstream_gene_variant MELA-AU 15 59427378 59427378 single base substitution G A 3_prime_UTR_variant MELA-AU 15 59427378 59427378 single base substitution G A downstream_gene_variant MELA-AU 15 59428339 59428339 single base substitution G A 3_prime_UTR_variant MELA-AU 15 59428339 59428339 single base substitution G A downstream_gene_variant MELA-AU 15 59431397 59431397 single base substitution C T intron_variant MELA-AU 15 59431701 59431701 single base substitution T C intron_variant MELA-AU 15 59433300 59433300 single base substitution G A intron_variant MELA-AU 15 59433943 59433943 single base substitution G T intron_variant MELA-AU 15 59433945 59433945 single base substitution C T intron_variant MELA-AU 15 59434319 59434319 single base substitution T A intron_variant MELA-AU 15 59434333 59434333 single base substitution C T intron_variant MELA-AU 15 59435567 59435567 single base substitution G A intron_variant MELA-AU 15 59436794 59436795 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 59436859 59436859 single base substitution G A intron_variant MELA-AU 15 59437443 59437443 single base substitution G A intron_variant MELA-AU 15 59437539 59437539 single base substitution C T intron_variant MELA-AU 15 59439144 59439144 insertion of <=200bp - T intron_variant MELA-AU 15 59439172 59439179 deletion of <=200bp AACCCAGA - intron_variant MELA-AU 15 59439337 59439337 single base substitution G A intron_variant MELA-AU 15 59439514 59439515 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59440552 59440552 single base substitution C A intron_variant MELA-AU 15 59441098 59441098 single base substitution G A intron_variant MELA-AU 15 59441135 59441135 single base substitution C T intron_variant MELA-AU 15 59441207 59441207 single base substitution G A intron_variant MELA-AU 15 59441951 59441951 single base substitution G A intron_variant MELA-AU 15 59443032 59443032 single base substitution T C intron_variant MELA-AU 15 59443179 59443179 single base substitution C T intron_variant MELA-AU 15 59443353 59443353 single base substitution C T intron_variant MELA-AU 15 59443423 59443423 single base substitution G A intron_variant MELA-AU 15 59443602 59443602 single base substitution C T intron_variant MELA-AU 15 59444064 59444064 single base substitution G A intron_variant MELA-AU 15 59444679 59444679 single base substitution G A intron_variant MELA-AU 15 59445750 59445750 single base substitution G A intron_variant MELA-AU 15 59446583 59446583 single base substitution C T intron_variant MELA-AU 15 59446583 59446583 single base substitution C T upstream_gene_variant MELA-AU 15 59446856 59446856 single base substitution G A intron_variant MELA-AU 15 59446856 59446856 single base substitution G A upstream_gene_variant MELA-AU 15 59446873 59446873 single base substitution C T intron_variant MELA-AU 15 59446873 59446873 single base substitution C T upstream_gene_variant MELA-AU 15 59448526 59448526 single base substitution G A intron_variant MELA-AU 15 59448526 59448526 single base substitution G A upstream_gene_variant MELA-AU 15 59449004 59449004 single base substitution G A intron_variant MELA-AU 15 59449004 59449004 single base substitution G A upstream_gene_variant MELA-AU 15 59449352 59449352 single base substitution G A intron_variant MELA-AU 15 59449352 59449352 single base substitution G A upstream_gene_variant MELA-AU 15 59449821 59449821 single base substitution T A intron_variant MELA-AU 15 59449821 59449821 single base substitution T A upstream_gene_variant MELA-AU 15 59450064 59450065 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 59450064 59450065 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 59450620 59450620 single base substitution G A downstream_gene_variant MELA-AU 15 59450620 59450620 single base substitution G A intron_variant MELA-AU 15 59450620 59450620 single base substitution G A upstream_gene_variant MELA-AU 15 59451127 59451127 single base substitution G A downstream_gene_variant MELA-AU 15 59451127 59451127 single base substitution G A intron_variant MELA-AU 15 59451275 59451275 single base substitution G A downstream_gene_variant MELA-AU 15 59451275 59451275 single base substitution G A intron_variant MELA-AU 15 59451283 59451283 single base substitution G A downstream_gene_variant MELA-AU 15 59451283 59451283 single base substitution G A intron_variant MELA-AU 15 59452209 59452209 single base substitution A G downstream_gene_variant MELA-AU 15 59452209 59452209 single base substitution A G intron_variant MELA-AU 15 59452508 59452508 single base substitution G A downstream_gene_variant MELA-AU 15 59452508 59452508 single base substitution G A intron_variant MELA-AU 15 59452989 59452989 single base substitution G A downstream_gene_variant MELA-AU 15 59452989 59452989 single base substitution G A intron_variant MELA-AU 15 59454184 59454184 single base substitution T C downstream_gene_variant MELA-AU 15 59454184 59454184 single base substitution T C intron_variant MELA-AU 15 59454330 59454330 single base substitution G A downstream_gene_variant MELA-AU 15 59454330 59454330 single base substitution G A intron_variant MELA-AU 15 59454548 59454548 single base substitution G A downstream_gene_variant MELA-AU 15 59454548 59454548 single base substitution G A intron_variant MELA-AU 15 59456237 59456237 single base substitution G A intron_variant MELA-AU 15 59456253 59456253 single base substitution A G intron_variant MELA-AU 15 59457040 59457040 single base substitution C T intron_variant MELA-AU 15 59457118 59457118 single base substitution G A intron_variant MELA-AU 15 59457302 59457302 single base substitution C G intron_variant MELA-AU 15 59457352 59457352 single base substitution C T intron_variant MELA-AU 15 59458098 59458098 single base substitution A C intron_variant MELA-AU 15 59458470 59458470 single base substitution C T intron_variant MELA-AU 15 59459144 59459144 single base substitution G A downstream_gene_variant MELA-AU 15 59459144 59459144 single base substitution G A intron_variant MELA-AU 15 59460404 59460404 single base substitution G A downstream_gene_variant MELA-AU 15 59460404 59460404 single base substitution G A intron_variant MELA-AU 15 59460412 59460412 single base substitution G A downstream_gene_variant MELA-AU 15 59460412 59460412 single base substitution G A intron_variant MELA-AU 15 59460429 59460429 single base substitution G A downstream_gene_variant MELA-AU 15 59460429 59460429 single base substitution G A intron_variant MELA-AU 15 59460430 59460430 single base substitution G A downstream_gene_variant MELA-AU 15 59460430 59460430 single base substitution G A intron_variant MELA-AU 15 59461283 59461283 single base substitution T C downstream_gene_variant MELA-AU 15 59461283 59461283 single base substitution T C intron_variant MELA-AU 15 59462287 59462287 single base substitution G T downstream_gene_variant MELA-AU 15 59462287 59462287 single base substitution G T intron_variant MELA-AU 15 59462289 59462289 single base substitution G A downstream_gene_variant MELA-AU 15 59462289 59462289 single base substitution G A intron_variant MELA-AU 15 59462773 59462773 single base substitution G A downstream_gene_variant MELA-AU 15 59462773 59462773 single base substitution G A intron_variant MELA-AU 15 59463325 59463325 single base substitution C T downstream_gene_variant MELA-AU 15 59463325 59463325 single base substitution C T intron_variant MELA-AU 15 59463514 59463514 single base substitution G A downstream_gene_variant MELA-AU 15 59463514 59463514 single base substitution G A intron_variant MELA-AU 15 59463535 59463536 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 59463535 59463536 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59463677 59463677 single base substitution G A downstream_gene_variant MELA-AU 15 59463677 59463677 single base substitution G A intron_variant MELA-AU 15 59464100 59464101 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant SL246SF MELA-AU 15 59464100 59464101 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant SL315SF MELA-AU 15 59464100 59464101 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant SL825SF MELA-AU 15 59464798 59464799 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59465286 59465286 single base substitution G A intron_variant MELA-AU 15 59466433 59466433 single base substitution G A downstream_gene_variant MELA-AU 15 59466433 59466433 single base substitution G A intron_variant MELA-AU 15 59466433 59466433 single base substitution G A missense_variant L176F 526C>T MELA-AU 15 59466433 59466433 single base substitution G A missense_variant L686F 2056C>T MELA-AU 15 59467493 59467493 single base substitution G A downstream_gene_variant MELA-AU 15 59467493 59467493 single base substitution G A intron_variant MELA-AU 15 59467729 59467729 single base substitution G A downstream_gene_variant MELA-AU 15 59467729 59467729 single base substitution G A intron_variant MELA-AU 15 59467743 59467743 single base substitution C T downstream_gene_variant MELA-AU 15 59467743 59467743 single base substitution C T intron_variant MELA-AU 15 59470121 59470121 single base substitution C T downstream_gene_variant MELA-AU 15 59470121 59470121 single base substitution C T intron_variant MELA-AU 15 59470851 59470851 single base substitution G A intron_variant MELA-AU 15 59471046 59471046 single base substitution G A intron_variant MELA-AU 15 59471249 59471249 single base substitution A T intron_variant MELA-AU 15 59471299 59471299 single base substitution G A intron_variant MELA-AU 15 59471607 59471607 single base substitution A C intron_variant MELA-AU 15 59471701 59471701 single base substitution G A intron_variant MELA-AU 15 59472532 59472532 single base substitution G A intron_variant MELA-AU 15 59473037 59473037 single base substitution G A intron_variant MELA-AU 15 59474807 59474807 single base substitution G A intron_variant MELA-AU 15 59474909 59474909 single base substitution G A intron_variant MELA-AU 15 59476112 59476112 single base substitution C T intron_variant MELA-AU 15 59476837 59476837 single base substitution G A intron_variant MELA-AU 15 59476940 59476940 single base substitution C A intron_variant MELA-AU 15 59477054 59477054 single base substitution G A intron_variant MELA-AU 15 59478601 59478601 deletion of <=200bp T - intron_variant MELA-AU 15 59479011 59479011 single base substitution A C intron_variant MELA-AU 15 59480324 59480325 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 15 59480324 59480325 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59480324 59480325 multiple base substitution (>=2bp and <=200bp) GG AA synonymous_variant FL632 MELA-AU 15 59480613 59480613 single base substitution G C intron_variant MELA-AU 15 59481227 59481227 single base substitution A G intron_variant MELA-AU 15 59481427 59481427 single base substitution T C intron_variant MELA-AU 15 59482190 59482190 single base substitution G A intron_variant MELA-AU 15 59482686 59482686 single base substitution G A intron_variant MELA-AU 15 59482847 59482847 single base substitution G A downstream_gene_variant MELA-AU 15 59482847 59482847 single base substitution G A intron_variant MELA-AU 15 59483748 59483748 single base substitution C T downstream_gene_variant MELA-AU 15 59483748 59483748 single base substitution C T intron_variant MELA-AU 15 59485107 59485107 single base substitution G A downstream_gene_variant MELA-AU 15 59485107 59485107 single base substitution G A intron_variant MELA-AU 15 59485340 59485340 single base substitution G A downstream_gene_variant MELA-AU 15 59485340 59485340 single base substitution G A intron_variant MELA-AU 15 59485462 59485462 single base substitution G A downstream_gene_variant MELA-AU 15 59485462 59485462 single base substitution G A intron_variant MELA-AU 15 59485595 59485595 single base substitution G A downstream_gene_variant MELA-AU 15 59485595 59485595 single base substitution G A intron_variant MELA-AU 15 59485733 59485733 single base substitution G A downstream_gene_variant MELA-AU 15 59485733 59485733 single base substitution G A intron_variant MELA-AU 15 59486158 59486158 single base substitution G A downstream_gene_variant MELA-AU 15 59486158 59486158 single base substitution G A intron_variant MELA-AU 15 59486293 59486293 single base substitution A G downstream_gene_variant MELA-AU 15 59486293 59486293 single base substitution A G intron_variant MELA-AU 15 59486535 59486535 single base substitution G A downstream_gene_variant MELA-AU 15 59486535 59486535 single base substitution G A intron_variant MELA-AU 15 59486652 59486652 single base substitution G A downstream_gene_variant MELA-AU 15 59486652 59486652 single base substitution G A intron_variant MELA-AU 15 59486721 59486721 single base substitution G A downstream_gene_variant MELA-AU 15 59486721 59486721 single base substitution G A intron_variant MELA-AU 15 59486748 59486748 single base substitution G A downstream_gene_variant MELA-AU 15 59486748 59486748 single base substitution G A intron_variant MELA-AU 15 59486946 59486946 single base substitution G A downstream_gene_variant MELA-AU 15 59486946 59486946 single base substitution G A intron_variant MELA-AU 15 59487272 59487272 single base substitution C T downstream_gene_variant MELA-AU 15 59487272 59487272 single base substitution C T intron_variant MELA-AU 15 59487464 59487464 single base substitution T C downstream_gene_variant MELA-AU 15 59487464 59487464 single base substitution T C intron_variant MELA-AU 15 59487618 59487618 single base substitution G A downstream_gene_variant MELA-AU 15 59487618 59487618 single base substitution G A intron_variant MELA-AU 15 59487644 59487644 single base substitution C T downstream_gene_variant MELA-AU 15 59487644 59487644 single base substitution C T intron_variant MELA-AU 15 59489390 59489390 single base substitution C T intron_variant MELA-AU 15 59489853 59489853 single base substitution G A intron_variant MELA-AU 15 59489934 59489934 single base substitution G A intron_variant MELA-AU 15 59489954 59489954 single base substitution G A intron_variant MELA-AU 15 59490164 59490164 single base substitution G A intron_variant MELA-AU 15 59490436 59490436 single base substitution G A intron_variant MELA-AU 15 59491250 59491250 single base substitution G A intron_variant MELA-AU 15 59494083 59494084 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59494691 59494691 single base substitution G A intron_variant MELA-AU 15 59495642 59495642 single base substitution G A intron_variant MELA-AU 15 59497167 59497167 single base substitution G A downstream_gene_variant MELA-AU 15 59497167 59497167 single base substitution G A intron_variant MELA-AU 15 59497190 59497190 single base substitution G A downstream_gene_variant MELA-AU 15 59497190 59497190 single base substitution G A intron_variant MELA-AU 15 59499089 59499090 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 59499089 59499090 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59499089 59499090 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 59499090 59499090 single base substitution G A downstream_gene_variant MELA-AU 15 59499090 59499090 single base substitution G A intron_variant MELA-AU 15 59499090 59499090 single base substitution G A upstream_gene_variant MELA-AU 15 59500206 59500206 single base substitution A G downstream_gene_variant MELA-AU 15 59500206 59500206 single base substitution A G intron_variant MELA-AU 15 59500206 59500206 single base substitution A G upstream_gene_variant MELA-AU 15 59500320 59500320 single base substitution G A downstream_gene_variant MELA-AU 15 59500320 59500320 single base substitution G A intron_variant MELA-AU 15 59500320 59500320 single base substitution G A upstream_gene_variant MELA-AU 15 59500820 59500820 single base substitution A G downstream_gene_variant MELA-AU 15 59500820 59500820 single base substitution A G intron_variant MELA-AU 15 59500820 59500820 single base substitution A G upstream_gene_variant MELA-AU 15 59501097 59501097 single base substitution G A exon_variant MELA-AU 15 59501097 59501097 single base substitution G A intron_variant MELA-AU 15 59501097 59501097 single base substitution G A upstream_gene_variant MELA-AU 15 59501327 59501327 single base substitution A G intron_variant MELA-AU 15 59501327 59501327 single base substitution A G upstream_gene_variant MELA-AU 15 59504024 59504024 single base substitution A C intron_variant MELA-AU 15 59504024 59504024 single base substitution A C upstream_gene_variant MELA-AU 15 59504111 59504111 single base substitution A G intron_variant MELA-AU 15 59504111 59504111 single base substitution A G upstream_gene_variant MELA-AU 15 59504904 59504904 insertion of <=200bp - A intron_variant MELA-AU 15 59504904 59504904 insertion of <=200bp - A upstream_gene_variant MELA-AU 15 59505931 59505931 single base substitution A C intron_variant MELA-AU 15 59505931 59505931 single base substitution A C upstream_gene_variant MELA-AU 15 59506337 59506337 single base substitution C A intron_variant MELA-AU 15 59506517 59506517 single base substitution G A intron_variant MELA-AU 15 59506517 59506517 single base substitution G A splice_region_variant MELA-AU 15 59507265 59507265 single base substitution G A intron_variant MELA-AU 15 59507813 59507813 single base substitution G A intron_variant MELA-AU 15 59508379 59508380 multiple base substitution (>=2bp and <=200bp) GG TA intron_variant MELA-AU 15 59508831 59508831 single base substitution G A intron_variant MELA-AU 15 59508865 59508865 single base substitution G A intron_variant MELA-AU 15 59508869 59508869 single base substitution A G intron_variant MELA-AU 15 59508871 59508871 single base substitution A G intron_variant MELA-AU 15 59509021 59509021 single base substitution C T intron_variant MELA-AU 15 59510547 59510547 single base substitution G A downstream_gene_variant MELA-AU 15 59510547 59510547 single base substitution G A intron_variant MELA-AU 15 59510547 59510547 single base substitution G A upstream_gene_variant MELA-AU 15 59510632 59510632 single base substitution G A downstream_gene_variant MELA-AU 15 59510632 59510632 single base substitution G A intron_variant MELA-AU 15 59510632 59510632 single base substitution G A upstream_gene_variant MELA-AU 15 59511643 59511643 single base substitution A T downstream_gene_variant MELA-AU 15 59511643 59511643 single base substitution A T intron_variant MELA-AU 15 59511643 59511643 single base substitution A T upstream_gene_variant MELA-AU 15 59511851 59511851 single base substitution G A downstream_gene_variant MELA-AU 15 59511851 59511851 single base substitution G A intron_variant MELA-AU 15 59511851 59511851 single base substitution G A upstream_gene_variant MELA-AU 15 59513401 59513401 single base substitution G A downstream_gene_variant MELA-AU 15 59513401 59513401 single base substitution G A intron_variant MELA-AU 15 59513401 59513401 single base substitution G A upstream_gene_variant MELA-AU 15 59513486 59513486 single base substitution G A downstream_gene_variant MELA-AU 15 59513486 59513486 single base substitution G A intron_variant MELA-AU 15 59513486 59513486 single base substitution G A upstream_gene_variant MELA-AU 15 59513895 59513896 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 59513895 59513896 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59513895 59513896 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 59514690 59514690 single base substitution T G downstream_gene_variant MELA-AU 15 59514690 59514690 single base substitution T G intron_variant MELA-AU 15 59514690 59514690 single base substitution T G upstream_gene_variant MELA-AU 15 59514877 59514877 single base substitution G A downstream_gene_variant MELA-AU 15 59514877 59514877 single base substitution G A intron_variant MELA-AU 15 59514877 59514877 single base substitution G A upstream_gene_variant MELA-AU 15 59515092 59515092 single base substitution G A downstream_gene_variant MELA-AU 15 59515092 59515092 single base substitution G A intron_variant MELA-AU 15 59515092 59515092 single base substitution G A upstream_gene_variant MELA-AU 15 59515703 59515703 single base substitution G A downstream_gene_variant MELA-AU 15 59515703 59515703 single base substitution G A intron_variant MELA-AU 15 59518067 59518067 single base substitution G A downstream_gene_variant MELA-AU 15 59518067 59518067 single base substitution G A intron_variant MELA-AU 15 59518099 59518099 single base substitution C A downstream_gene_variant MELA-AU 15 59518099 59518099 single base substitution C A intron_variant MELA-AU 15 59518556 59518556 single base substitution G A downstream_gene_variant MELA-AU 15 59518556 59518556 single base substitution G A intron_variant MELA-AU 15 59518976 59518976 single base substitution A G downstream_gene_variant MELA-AU 15 59518976 59518976 single base substitution A G intron_variant MELA-AU 15 59519724 59519724 single base substitution G A 3_prime_UTR_variant MELA-AU 15 59519724 59519724 single base substitution G A exon_variant MELA-AU 15 59519724 59519724 single base substitution G A synonymous_variant F192F 576C>T MELA-AU 15 59519724 59519724 single base substitution G A synonymous_variant F22F 66C>T MELA-AU 15 59520025 59520025 single base substitution G A intron_variant MELA-AU 15 59520025 59520025 single base substitution G A upstream_gene_variant MELA-AU 15 59520074 59520074 single base substitution C A intron_variant MELA-AU 15 59520074 59520074 single base substitution C A upstream_gene_variant MELA-AU 15 59520144 59520144 single base substitution C T intron_variant MELA-AU 15 59520144 59520144 single base substitution C T upstream_gene_variant MELA-AU 15 59520332 59520332 single base substitution G A intron_variant MELA-AU 15 59520332 59520332 single base substitution G A upstream_gene_variant MELA-AU 15 59521708 59521708 single base substitution G A intron_variant MELA-AU 15 59521708 59521708 single base substitution G A upstream_gene_variant MELA-AU 15 59521709 59521709 single base substitution G A intron_variant MELA-AU 15 59521709 59521709 single base substitution G A upstream_gene_variant MELA-AU 15 59522161 59522161 single base substitution A G intron_variant MELA-AU 15 59522161 59522161 single base substitution A G upstream_gene_variant MELA-AU 15 59522969 59522970 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 59522969 59522970 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 59523196 59523196 single base substitution T C intron_variant MELA-AU 15 59523196 59523196 single base substitution T C upstream_gene_variant MELA-AU 15 59523535 59523535 single base substitution G A intron_variant MELA-AU 15 59523535 59523535 single base substitution G A upstream_gene_variant MELA-AU 15 59523866 59523866 single base substitution C T intron_variant MELA-AU 15 59523866 59523866 single base substitution C T upstream_gene_variant MELA-AU 15 59524302 59524302 single base substitution G A intron_variant MELA-AU 15 59524302 59524302 single base substitution G A upstream_gene_variant MELA-AU 15 59525349 59525349 single base substitution T C intron_variant MELA-AU 15 59526455 59526455 single base substitution G A intron_variant MELA-AU 15 59527143 59527143 single base substitution G A intron_variant MELA-AU 15 59529985 59529985 single base substitution C T intron_variant MELA-AU 15 59529999 59529999 single base substitution G A intron_variant MELA-AU 15 59530520 59530543 deletion of <=200bp AATGTAAACATTCAAGAATATTGG - intron_variant MELA-AU 15 59530986 59530986 single base substitution G A intron_variant MELA-AU 15 59531502 59531502 single base substitution C T intron_variant MELA-AU 15 59532782 59532782 single base substitution A G intron_variant MELA-AU 15 59532976 59532976 single base substitution C T intron_variant MELA-AU 15 59533257 59533257 single base substitution G A intron_variant MELA-AU 15 59533507 59533507 single base substitution C A intron_variant MELA-AU 15 59533666 59533666 single base substitution G A intron_variant MELA-AU 15 59534267 59534267 single base substitution A T intron_variant MELA-AU 15 59534595 59534595 single base substitution G A intron_variant MELA-AU 15 59536962 59536962 single base substitution G A intron_variant MELA-AU 15 59537235 59537236 deletion of <=200bp AT - intron_variant MELA-AU 15 59537607 59537607 single base substitution C T intron_variant MELA-AU 15 59537653 59537653 single base substitution C A intron_variant MELA-AU 15 59538450 59538450 single base substitution G A intron_variant MELA-AU 15 59539258 59539258 single base substitution G A intron_variant MELA-AU 15 59540137 59540137 single base substitution A C intron_variant MELA-AU 15 59541013 59541013 single base substitution G A intron_variant MELA-AU 15 59541455 59541455 single base substitution T C intron_variant MELA-AU 15 59541810 59541810 single base substitution G A intron_variant MELA-AU 15 59543230 59543230 single base substitution G A intron_variant MELA-AU 15 59544735 59544735 single base substitution G A intron_variant MELA-AU 15 59545226 59545226 single base substitution G A intron_variant MELA-AU 15 59545438 59545438 single base substitution C T intron_variant MELA-AU 15 59546257 59546257 single base substitution G A intron_variant MELA-AU 15 59546591 59546591 single base substitution T A intron_variant MELA-AU 15 59547160 59547160 single base substitution G A intron_variant MELA-AU 15 59547509 59547509 single base substitution G A intron_variant MELA-AU 15 59547573 59547573 single base substitution G A intron_variant MELA-AU 15 59547886 59547886 single base substitution G A intron_variant MELA-AU 15 59548220 59548220 single base substitution G A intron_variant MELA-AU 15 59548801 59548801 single base substitution G A intron_variant MELA-AU 15 59549973 59549973 single base substitution A G intron_variant MELA-AU 15 59550039 59550039 single base substitution G A intron_variant MELA-AU 15 59552385 59552385 single base substitution A T intron_variant MELA-AU 15 59552487 59552487 single base substitution A C intron_variant MELA-AU 15 59552889 59552889 single base substitution A G intron_variant MELA-AU 15 59553378 59553378 single base substitution G A intron_variant MELA-AU 15 59553510 59553510 single base substitution A G intron_variant MELA-AU 15 59553674 59553674 single base substitution G C exon_variant MELA-AU 15 59553674 59553674 single base substitution G C intron_variant MELA-AU 15 59553674 59553674 single base substitution G C missense_variant P61R 182C>G MELA-AU 15 59554591 59554591 single base substitution G A intron_variant MELA-AU 15 59554758 59554758 single base substitution C T intron_variant MELA-AU 15 59554971 59554971 single base substitution G A intron_variant MELA-AU 15 59555274 59555274 single base substitution G A intron_variant MELA-AU 15 59555526 59555526 single base substitution A G intron_variant MELA-AU 15 59556468 59556468 single base substitution G A intron_variant MELA-AU 15 59557060 59557060 single base substitution A T intron_variant MELA-AU 15 59557268 59557268 single base substitution G A intron_variant MELA-AU 15 59557268 59557268 single base substitution G A upstream_gene_variant MELA-AU 15 59557688 59557688 single base substitution G A intron_variant MELA-AU 15 59557688 59557688 single base substitution G A upstream_gene_variant MELA-AU 15 59558197 59558197 single base substitution A G intron_variant MELA-AU 15 59558197 59558197 single base substitution A G upstream_gene_variant MELA-AU 15 59558223 59558223 single base substitution A G intron_variant MELA-AU 15 59558223 59558223 single base substitution A G upstream_gene_variant MELA-AU 15 59559085 59559085 single base substitution C T intron_variant MELA-AU 15 59559085 59559085 single base substitution C T upstream_gene_variant MELA-AU 15 59559109 59559109 single base substitution C T intron_variant MELA-AU 15 59559109 59559109 single base substitution C T upstream_gene_variant MELA-AU 15 59559294 59559294 single base substitution G A intron_variant MELA-AU 15 59559294 59559294 single base substitution G A upstream_gene_variant MELA-AU 15 59559756 59559756 single base substitution G A downstream_gene_variant MELA-AU 15 59559756 59559756 single base substitution G A intron_variant MELA-AU 15 59559756 59559756 single base substitution G A upstream_gene_variant MELA-AU 15 59559796 59559796 single base substitution G A downstream_gene_variant MELA-AU 15 59559796 59559796 single base substitution G A intron_variant MELA-AU 15 59559796 59559796 single base substitution G A upstream_gene_variant MELA-AU 15 59559887 59559887 single base substitution G A downstream_gene_variant MELA-AU 15 59559887 59559887 single base substitution G A intron_variant MELA-AU 15 59559887 59559887 single base substitution G A upstream_gene_variant MELA-AU 15 59560103 59560103 single base substitution G A downstream_gene_variant MELA-AU 15 59560103 59560103 single base substitution G A intron_variant MELA-AU 15 59560103 59560103 single base substitution G A upstream_gene_variant MELA-AU 15 59560907 59560907 single base substitution G A downstream_gene_variant MELA-AU 15 59560907 59560907 single base substitution G A intron_variant MELA-AU 15 59560907 59560907 single base substitution G A upstream_gene_variant MELA-AU 15 59561462 59561462 single base substitution G A downstream_gene_variant MELA-AU 15 59561462 59561462 single base substitution G A intron_variant MELA-AU 15 59561462 59561462 single base substitution G A upstream_gene_variant MELA-AU 15 59562588 59562588 insertion of <=200bp - A downstream_gene_variant MELA-AU 15 59562588 59562588 insertion of <=200bp - A intron_variant MELA-AU 15 59563381 59563381 single base substitution G A downstream_gene_variant MELA-AU 15 59563381 59563381 single base substitution G A intron_variant MELA-AU 15 59564092 59564092 single base substitution G A downstream_gene_variant MELA-AU 15 59564092 59564092 single base substitution G A intron_variant MELA-AU 15 59564100 59564100 single base substitution T C downstream_gene_variant MELA-AU 15 59564100 59564100 single base substitution T C intron_variant MELA-AU 15 59564698 59564698 single base substitution G A intron_variant MELA-AU 15 59565118 59565118 single base substitution G A intron_variant MELA-AU 15 59565125 59565125 single base substitution G A intron_variant MELA-AU 15 59565577 59565577 single base substitution G A intron_variant MELA-AU 15 59565810 59565810 single base substitution G A intron_variant MELA-AU 15 59566399 59566399 single base substitution G A intron_variant MELA-AU 15 59566837 59566837 single base substitution G A intron_variant MELA-AU 15 59566899 59566899 single base substitution C G intron_variant MELA-AU 15 59567025 59567025 single base substitution A C intron_variant MELA-AU 15 59567873 59567873 single base substitution G A intron_variant MELA-AU 15 59568255 59568255 single base substitution C T intron_variant MELA-AU 15 59568924 59568925 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59569712 59569712 single base substitution C T intron_variant MELA-AU 15 59570505 59570505 single base substitution C T intron_variant MELA-AU 15 59570601 59570601 single base substitution G A intron_variant MELA-AU 15 59570852 59570852 single base substitution G A intron_variant MELA-AU 15 59571403 59571403 single base substitution C T intron_variant MELA-AU 15 59571809 59571809 single base substitution C T intron_variant MELA-AU 15 59571815 59571815 single base substitution G A intron_variant MELA-AU 15 59573713 59573713 single base substitution G A intron_variant MELA-AU 15 59574174 59574174 single base substitution G A intron_variant MELA-AU 15 59574206 59574206 single base substitution C T intron_variant MELA-AU 15 59574214 59574214 single base substitution G A intron_variant MELA-AU 15 59574660 59574660 single base substitution C T intron_variant MELA-AU 15 59576489 59576490 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 59576494 59576494 single base substitution G T intron_variant MELA-AU 15 59577919 59577919 single base substitution G A intron_variant MELA-AU 15 59578829 59578829 single base substitution G A intron_variant MELA-AU 15 59578858 59578858 single base substitution G A intron_variant MELA-AU 15 59579351 59579351 single base substitution G A intron_variant MELA-AU 15 59579355 59579355 single base substitution G A intron_variant MELA-AU 15 59579586 59579586 single base substitution C T intron_variant MELA-AU 15 59579660 59579660 single base substitution G A intron_variant MELA-AU 15 59580079 59580079 single base substitution G A intron_variant MELA-AU 15 59580393 59580393 single base substitution G A intron_variant MELA-AU 15 59580917 59580917 deletion of <=200bp T - intron_variant MELA-AU 15 59581570 59581570 single base substitution A T intron_variant MELA-AU 15 59581665 59581665 single base substitution T G intron_variant MELA-AU 15 59582010 59582010 single base substitution G A intron_variant MELA-AU 15 59582944 59582944 single base substitution G A intron_variant MELA-AU 15 59582956 59582956 single base substitution G A intron_variant MELA-AU 15 59583270 59583270 single base substitution G A intron_variant MELA-AU 15 59583480 59583480 single base substitution C T intron_variant MELA-AU 15 59583593 59583593 single base substitution A G intron_variant MELA-AU 15 59585611 59585611 single base substitution G A intron_variant MELA-AU 15 59586305 59586305 single base substitution G A intron_variant MELA-AU 15 59586430 59586431 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59587255 59587255 single base substitution G A intron_variant MELA-AU 15 59587395 59587395 single base substitution G A intron_variant MELA-AU 15 59588672 59588672 single base substitution G A intron_variant MELA-AU 15 59589808 59589808 single base substitution C T intron_variant MELA-AU 15 59589989 59589989 single base substitution C G intron_variant MELA-AU 15 59590958 59590958 single base substitution G A intron_variant MELA-AU 15 59591036 59591036 single base substitution A G intron_variant MELA-AU 15 59592054 59592054 single base substitution T C intron_variant MELA-AU 15 59592512 59592512 single base substitution C G intron_variant MELA-AU 15 59592514 59592514 single base substitution G C intron_variant MELA-AU 15 59592516 59592516 single base substitution C G intron_variant MELA-AU 15 59593201 59593201 single base substitution G A intron_variant MELA-AU 15 59593835 59593835 single base substitution C T intron_variant MELA-AU 15 59595755 59595755 single base substitution G A intron_variant MELA-AU 15 59595938 59595938 single base substitution G A intron_variant MELA-AU 15 59596316 59596316 single base substitution G A intron_variant MELA-AU 15 59596966 59596966 single base substitution T C intron_variant MELA-AU 15 59597380 59597380 single base substitution C T intron_variant MELA-AU 15 59598141 59598141 single base substitution G A intron_variant MELA-AU 15 59598231 59598231 single base substitution A G intron_variant MELA-AU 15 59598819 59598819 single base substitution G A intron_variant MELA-AU 15 59598935 59598935 single base substitution C G intron_variant MELA-AU 15 59599633 59599633 single base substitution G A intron_variant MELA-AU 15 59600669 59600669 single base substitution G A intron_variant MELA-AU 15 59600825 59600825 single base substitution T C intron_variant MELA-AU 15 59601037 59601037 single base substitution C A intron_variant MELA-AU 15 59602705 59602705 single base substitution C T intron_variant MELA-AU 15 59603401 59603401 single base substitution G A intron_variant MELA-AU 15 59603746 59603746 single base substitution G A intron_variant MELA-AU 15 59604018 59604018 single base substitution G A intron_variant MELA-AU 15 59604729 59604729 single base substitution A G intron_variant MELA-AU 15 59604791 59604791 single base substitution G A intron_variant MELA-AU 15 59604878 59604878 single base substitution G A intron_variant MELA-AU 15 59605446 59605446 single base substitution G A intron_variant MELA-AU 15 59605831 59605831 single base substitution A C intron_variant MELA-AU 15 59606107 59606107 single base substitution G A intron_variant MELA-AU 15 59606457 59606457 single base substitution C T intron_variant MELA-AU 15 59606563 59606563 single base substitution G A intron_variant MELA-AU 15 59606871 59606871 single base substitution G A intron_variant MELA-AU 15 59607176 59607176 single base substitution G A intron_variant MELA-AU 15 59607389 59607389 single base substitution G A intron_variant MELA-AU 15 59608249 59608249 single base substitution G A intron_variant MELA-AU 15 59608457 59608457 single base substitution T A intron_variant MELA-AU 15 59609200 59609200 single base substitution G A intron_variant MELA-AU 15 59609542 59609542 single base substitution G A intron_variant MELA-AU 15 59610352 59610352 single base substitution G A intron_variant MELA-AU 15 59610559 59610559 single base substitution G A intron_variant MELA-AU 15 59611238 59611238 single base substitution G A intron_variant MELA-AU 15 59611675 59611676 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59611835 59611835 single base substitution G A intron_variant MELA-AU 15 59612979 59612979 single base substitution G A intron_variant MELA-AU 15 59613648 59613648 single base substitution G A intron_variant MELA-AU 15 59613712 59613712 single base substitution G A intron_variant MELA-AU 15 59614218 59614218 single base substitution G A intron_variant MELA-AU 15 59615070 59615070 single base substitution G A intron_variant MELA-AU 15 59615570 59615570 single base substitution G A intron_variant MELA-AU 15 59616179 59616179 single base substitution G A intron_variant MELA-AU 15 59617337 59617337 single base substitution G A intron_variant MELA-AU 15 59617553 59617553 single base substitution G A intron_variant MELA-AU 15 59617934 59617934 single base substitution G A intron_variant MELA-AU 15 59618071 59618071 single base substitution G A intron_variant MELA-AU 15 59618939 59618939 single base substitution G A intron_variant MELA-AU 15 59619490 59619490 single base substitution T C intron_variant MELA-AU 15 59619563 59619563 single base substitution T C intron_variant MELA-AU 15 59619593 59619593 single base substitution G A intron_variant MELA-AU 15 59620061 59620061 single base substitution G A intron_variant MELA-AU 15 59620176 59620176 single base substitution G A intron_variant MELA-AU 15 59620460 59620460 single base substitution G A intron_variant MELA-AU 15 59621052 59621053 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59621166 59621167 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59622132 59622132 single base substitution A G intron_variant MELA-AU 15 59622152 59622152 single base substitution G A intron_variant MELA-AU 15 59622223 59622223 single base substitution A C intron_variant MELA-AU 15 59622596 59622596 single base substitution C T intron_variant MELA-AU 15 59622862 59622862 single base substitution T C intron_variant MELA-AU 15 59624221 59624221 single base substitution C T intron_variant MELA-AU 15 59624493 59624493 single base substitution G A intron_variant MELA-AU 15 59624534 59624534 single base substitution G A intron_variant MELA-AU 15 59625465 59625465 single base substitution G A intron_variant MELA-AU 15 59625928 59625928 single base substitution T G intron_variant MELA-AU 15 59628437 59628437 single base substitution G A intron_variant MELA-AU 15 59629217 59629217 single base substitution C T intron_variant MELA-AU 15 59629925 59629925 single base substitution G A intron_variant MELA-AU 15 59629929 59629929 single base substitution G A intron_variant MELA-AU 15 59630934 59630934 single base substitution G A intron_variant MELA-AU 15 59630984 59630984 single base substitution G A intron_variant MELA-AU 15 59631106 59631106 single base substitution G A intron_variant MELA-AU 15 59631979 59631979 single base substitution G A intron_variant MELA-AU 15 59632180 59632180 single base substitution G A intron_variant MELA-AU 15 59634923 59634923 single base substitution G A intron_variant MELA-AU 15 59636139 59636139 single base substitution C T intron_variant MELA-AU 15 59637265 59637265 single base substitution G A intron_variant MELA-AU 15 59637841 59637841 single base substitution G A intron_variant MELA-AU 15 59638103 59638103 single base substitution G A intron_variant MELA-AU 15 59638282 59638282 single base substitution C T intron_variant MELA-AU 15 59638400 59638400 single base substitution G A intron_variant MELA-AU 15 59638466 59638466 single base substitution C T intron_variant MELA-AU 15 59638585 59638585 single base substitution C T intron_variant MELA-AU 15 59639093 59639093 single base substitution G A intron_variant MELA-AU 15 59639788 59639788 single base substitution C T intron_variant MELA-AU 15 59640956 59640956 single base substitution G A intron_variant MELA-AU 15 59641218 59641218 single base substitution G A intron_variant MELA-AU 15 59641280 59641280 single base substitution G A intron_variant MELA-AU 15 59641322 59641322 single base substitution G A intron_variant MELA-AU 15 59641351 59641351 single base substitution G A intron_variant MELA-AU 15 59641427 59641427 single base substitution C T intron_variant MELA-AU 15 59641520 59641520 single base substitution G A intron_variant MELA-AU 15 59642394 59642394 single base substitution C T intron_variant MELA-AU 15 59643320 59643320 single base substitution G A intron_variant MELA-AU 15 59643909 59643909 single base substitution G A intron_variant MELA-AU 15 59644029 59644029 single base substitution G A intron_variant MELA-AU 15 59644226 59644226 single base substitution G A intron_variant MELA-AU 15 59644343 59644343 single base substitution G A intron_variant MELA-AU 15 59645794 59645794 single base substitution A G intron_variant MELA-AU 15 59645882 59645883 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 59645950 59645950 single base substitution C T intron_variant MELA-AU 15 59645966 59645966 single base substitution A G intron_variant MELA-AU 15 59646291 59646291 single base substitution G A intron_variant MELA-AU 15 59647663 59647663 single base substitution C T intron_variant MELA-AU 15 59647768 59647768 single base substitution G A intron_variant MELA-AU 15 59647780 59647780 single base substitution C T intron_variant MELA-AU 15 59648107 59648107 single base substitution G C intron_variant MELA-AU 15 59648293 59648293 single base substitution G A intron_variant MELA-AU 15 59648558 59648558 single base substitution G A intron_variant MELA-AU 15 59649917 59649918 multiple base substitution (>=2bp and <=200bp) GG TA intron_variant MELA-AU 15 59650866 59650866 single base substitution G A intron_variant MELA-AU 15 59651525 59651525 single base substitution A T intron_variant MELA-AU 15 59651527 59651527 single base substitution T A intron_variant MELA-AU 15 59652557 59652557 single base substitution G A intron_variant MELA-AU 15 59652986 59652986 single base substitution G A intron_variant MELA-AU 15 59653196 59653196 single base substitution G A intron_variant MELA-AU 15 59654414 59654414 single base substitution G T intron_variant MELA-AU 15 59656108 59656108 single base substitution G A intron_variant MELA-AU 15 59657591 59657592 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 59658925 59658925 single base substitution T A intron_variant MELA-AU 15 59659692 59659692 single base substitution G A intron_variant MELA-AU 15 59659903 59659903 single base substitution G A intron_variant MELA-AU 15 59660297 59660297 single base substitution G A intron_variant MELA-AU 15 59660783 59660783 single base substitution A T intron_variant MELA-AU 15 59661087 59661087 single base substitution G A intron_variant MELA-AU 15 59661737 59661737 single base substitution G A intron_variant MELA-AU 15 59662964 59662964 single base substitution G A intron_variant MELA-AU 15 59664508 59664508 single base substitution C T intron_variant MELA-AU 15 59666272 59666272 single base substitution C T upstream_gene_variant MELA-AU 15 59666326 59666326 single base substitution A G upstream_gene_variant MELA-AU 15 59666559 59666559 single base substitution G A upstream_gene_variant MELA-AU 15 59667691 59667691 single base substitution C T upstream_gene_variant MELA-AU 15 59668011 59668011 single base substitution C T upstream_gene_variant MELA-AU 15 59668321 59668321 single base substitution C T upstream_gene_variant MELA-AU 15 59668364 59668364 single base substitution C T upstream_gene_variant MELA-AU 15 59668653 59668653 single base substitution C T upstream_gene_variant MELA-AU 15 59669324 59669325 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 59669599 59669599 single base substitution G A upstream_gene_variant ORCA-IN 15 59429200 59429200 single base substitution C A 3_prime_UTR_variant ORCA-IN 15 59429200 59429200 single base substitution C A intron_variant ORCA-IN 15 59456334 59456334 insertion of <=200bp - A intron_variant ORCA-IN 15 59457175 59457175 single base substitution T A intron_variant ORCA-IN 15 59469692 59469692 single base substitution G C downstream_gene_variant ORCA-IN 15 59469692 59469692 single base substitution G C intron_variant ORCA-IN 15 59470318 59470318 single base substitution C T downstream_gene_variant ORCA-IN 15 59470318 59470318 single base substitution C T intron_variant ORCA-IN 15 59477198 59477198 single base substitution C T intron_variant ORCA-IN 15 59480385 59480385 single base substitution C A exon_variant ORCA-IN 15 59480385 59480385 single base substitution C A intron_variant ORCA-IN 15 59480385 59480385 single base substitution C A synonymous_variant L612L 1836G>T ORCA-IN 15 59487543 59487543 single base substitution G A downstream_gene_variant ORCA-IN 15 59487543 59487543 single base substitution G A intron_variant ORCA-IN 15 59508920 59508920 single base substitution C T intron_variant ORCA-IN 15 59534254 59534254 single base substitution G C intron_variant ORCA-IN 15 59545959 59545959 single base substitution C G intron_variant ORCA-IN 15 59584182 59584182 single base substitution C T intron_variant ORCA-IN 15 59598410 59598410 single base substitution A G intron_variant ORCA-IN 15 59653558 59653558 single base substitution G C intron_variant ORCA-IN 15 59663870 59663870 single base substitution T A intron_variant OV-AU 15 59426113 59426113 single base substitution A T downstream_gene_variant OV-AU 15 59430396 59430396 single base substitution C T intron_variant OV-AU 15 59430396 59430396 single base substitution C T splice_donor_variant OV-AU 15 59436539 59436539 single base substitution T C intron_variant OV-AU 15 59437079 59437079 single base substitution G C intron_variant OV-AU 15 59446222 59446222 single base substitution T C intron_variant OV-AU 15 59446222 59446222 single base substitution T C upstream_gene_variant OV-AU 15 59452277 59452277 single base substitution C T downstream_gene_variant OV-AU 15 59452277 59452277 single base substitution C T intron_variant OV-AU 15 59461908 59461908 single base substitution G C downstream_gene_variant OV-AU 15 59461908 59461908 single base substitution G C intron_variant OV-AU 15 59468358 59468358 single base substitution C G downstream_gene_variant OV-AU 15 59468358 59468358 single base substitution C G intron_variant OV-AU 15 59473525 59473525 single base substitution C G intron_variant OV-AU 15 59481253 59481253 single base substitution C G intron_variant OV-AU 15 59483703 59483703 single base substitution G T downstream_gene_variant OV-AU 15 59483703 59483703 single base substitution G T intron_variant OV-AU 15 59487022 59487022 single base substitution C G downstream_gene_variant OV-AU 15 59487022 59487022 single base substitution C G intron_variant OV-AU 15 59489331 59489331 single base substitution A C intron_variant OV-AU 15 59493338 59493338 single base substitution G A intron_variant OV-AU 15 59493544 59493544 single base substitution C G intron_variant OV-AU 15 59497598 59497605 deletion of <=200bp CAGCTCGC - downstream_gene_variant OV-AU 15 59497598 59497605 deletion of <=200bp CAGCTCGC - frameshift_variant SEL537 OV-AU 15 59497598 59497605 deletion of <=200bp CAGCTCGC - frameshift_variant SEL60 OV-AU 15 59497598 59497605 deletion of <=200bp CAGCTCGC - intron_variant OV-AU 15 59497598 59497605 deletion of <=200bp CAGCTCGC - splice_donor_variant OV-AU 15 59499177 59499187 deletion of <=200bp GAGTGAGCTCG - downstream_gene_variant OV-AU 15 59499177 59499187 deletion of <=200bp GAGTGAGCTCG - intron_variant OV-AU 15 59499177 59499187 deletion of <=200bp GAGTGAGCTCG - upstream_gene_variant OV-AU 15 59532131 59532131 single base substitution T A intron_variant OV-AU 15 59539667 59539667 single base substitution G C intron_variant OV-AU 15 59554827 59554827 single base substitution G T intron_variant OV-AU 15 59556149 59556149 single base substitution G A intron_variant OV-AU 15 59565036 59565036 single base substitution C G intron_variant OV-AU 15 59579508 59579508 single base substitution T C intron_variant OV-AU 15 59589458 59589458 single base substitution T A intron_variant OV-AU 15 59594262 59594262 single base substitution G A intron_variant OV-AU 15 59594888 59594888 single base substitution G C intron_variant OV-AU 15 59595073 59595073 single base substitution G T intron_variant OV-AU 15 59610270 59610270 single base substitution G A intron_variant OV-AU 15 59614149 59614149 single base substitution G C intron_variant OV-AU 15 59614751 59614751 single base substitution G C intron_variant OV-AU 15 59618979 59618979 single base substitution C A intron_variant OV-AU 15 59623059 59623059 single base substitution C T intron_variant OV-AU 15 59633197 59633197 single base substitution C G intron_variant OV-AU 15 59636223 59636223 single base substitution A C intron_variant OV-AU 15 59649067 59649067 single base substitution C T intron_variant OV-AU 15 59651361 59651361 single base substitution T C intron_variant OV-AU 15 59655775 59655775 single base substitution C G intron_variant OV-AU 15 59657379 59657379 single base substitution C T intron_variant PACA-AU 15 59424829 59424829 single base substitution G A downstream_gene_variant PACA-AU 15 59436387 59436387 single base substitution A G intron_variant PACA-AU 15 59436947 59436947 single base substitution A C intron_variant PACA-AU 15 59440707 59440707 deletion of <=200bp A - intron_variant PACA-AU 15 59443470 59443470 single base substitution A C intron_variant PACA-AU 15 59444474 59444474 single base substitution C T intron_variant PACA-AU 15 59450074 59450074 insertion of <=200bp - G intron_variant PACA-AU 15 59450074 59450074 insertion of <=200bp - G upstream_gene_variant PACA-AU 15 59461321 59461321 single base substitution T A downstream_gene_variant PACA-AU 15 59461321 59461321 single base substitution T A intron_variant PACA-AU 15 59464653 59464653 single base substitution T A intron_variant PACA-AU 15 59478601 59478601 deletion of <=200bp T - intron_variant PACA-AU 15 59487925 59487925 single base substitution G A intron_variant PACA-AU 15 59498540 59498540 single base substitution G T downstream_gene_variant PACA-AU 15 59498540 59498540 single base substitution G T intron_variant PACA-AU 15 59508103 59508103 single base substitution C T intron_variant PACA-AU 15 59510200 59510200 single base substitution C T missense_variant G163R 487G>A PACA-AU 15 59510200 59510200 single base substitution C T missense_variant G333R 997G>A PACA-AU 15 59510200 59510200 single base substitution C T missense_variant G53R 157G>A PACA-AU 15 59517530 59517530 single base substitution G A downstream_gene_variant PACA-AU 15 59517530 59517530 single base substitution G A intron_variant PACA-AU 15 59519229 59519229 single base substitution G C downstream_gene_variant PACA-AU 15 59519229 59519229 single base substitution G C intron_variant PACA-AU 15 59527180 59527180 single base substitution G A intron_variant PACA-AU 15 59529060 59529060 single base substitution G T intron_variant PACA-AU 15 59532305 59532305 single base substitution A T intron_variant PACA-AU 15 59533431 59533431 single base substitution G A intron_variant PACA-AU 15 59534617 59534617 single base substitution T C intron_variant PACA-AU 15 59534626 59534626 single base substitution G A intron_variant PACA-AU 15 59539025 59539030 deletion of <=200bp CTCTTG - intron_variant PACA-AU 15 59550929 59550929 single base substitution G T intron_variant PACA-AU 15 59554807 59554807 single base substitution G A intron_variant PACA-AU 15 59557708 59557708 single base substitution C A intron_variant PACA-AU 15 59557708 59557708 single base substitution C A upstream_gene_variant PACA-AU 15 59561794 59561794 single base substitution C T downstream_gene_variant PACA-AU 15 59561794 59561794 single base substitution C T intron_variant PACA-AU 15 59561794 59561794 single base substitution C T upstream_gene_variant PACA-AU 15 59565912 59565912 insertion of <=200bp - A intron_variant PACA-AU 15 59571249 59571249 single base substitution C G intron_variant PACA-AU 15 59577089 59577089 single base substitution A T intron_variant PACA-AU 15 59578920 59578920 single base substitution G A intron_variant PACA-AU 15 59584138 59584138 single base substitution T A intron_variant PACA-AU 15 59593151 59593151 single base substitution C T intron_variant PACA-AU 15 59599411 59599411 single base substitution G A intron_variant PACA-AU 15 59628062 59628062 single base substitution G A intron_variant PACA-AU 15 59629684 59629684 single base substitution C A intron_variant PACA-AU 15 59636321 59636321 single base substitution A G intron_variant PACA-AU 15 59640571 59640571 single base substitution G C intron_variant PACA-AU 15 59646764 59646764 single base substitution T G intron_variant PACA-AU 15 59646833 59646833 single base substitution C A intron_variant PACA-AU 15 59659315 59659315 single base substitution A T intron_variant PACA-AU 15 59665010 59665010 single base substitution G A 5_prime_UTR_variant PACA-AU 15 59665010 59665010 single base substitution G A exon_variant PACA-AU 15 59665010 59665010 single base substitution G A upstream_gene_variant PACA-AU 15 59666959 59666959 single base substitution C A upstream_gene_variant PACA-AU 15 59668458 59668458 single base substitution T C upstream_gene_variant PACA-CA 15 59427233 59427233 single base substitution T C 3_prime_UTR_variant PACA-CA 15 59427233 59427233 single base substitution T C downstream_gene_variant PACA-CA 15 59427255 59427255 single base substitution G T 3_prime_UTR_variant PACA-CA 15 59427255 59427255 single base substitution G T downstream_gene_variant PACA-CA 15 59429446 59429446 single base substitution G A 3_prime_UTR_variant PACA-CA 15 59429446 59429446 single base substitution G A intron_variant PACA-CA 15 59432116 59432116 single base substitution C G intron_variant PACA-CA 15 59437947 59437947 single base substitution G T intron_variant PACA-CA 15 59439573 59439573 single base substitution C T intron_variant PACA-CA 15 59443641 59443641 insertion of <=200bp - C intron_variant PACA-CA 15 59443650 59443650 single base substitution A C intron_variant PACA-CA 15 59444513 59444513 single base substitution G A intron_variant PACA-CA 15 59447319 59447321 deletion of <=200bp AGG - intron_variant PACA-CA 15 59447319 59447321 deletion of <=200bp AGG - upstream_gene_variant PACA-CA 15 59449329 59449329 single base substitution G A intron_variant PACA-CA 15 59449329 59449329 single base substitution G A upstream_gene_variant PACA-CA 15 59452789 59452789 insertion of <=200bp - T downstream_gene_variant PACA-CA 15 59452789 59452789 insertion of <=200bp - T intron_variant PACA-CA 15 59453297 59453297 single base substitution G A downstream_gene_variant PACA-CA 15 59453297 59453297 single base substitution G A synonymous_variant I920I 2760C>T PACA-CA 15 59453500 59453500 single base substitution C T downstream_gene_variant PACA-CA 15 59453500 59453500 single base substitution C T intron_variant PACA-CA 15 59455129 59455129 single base substitution A G downstream_gene_variant PACA-CA 15 59455129 59455129 single base substitution A G intron_variant PACA-CA 15 59468406 59468406 single base substitution C T downstream_gene_variant PACA-CA 15 59468406 59468406 single base substitution C T intron_variant PACA-CA 15 59468554 59468554 single base substitution C T downstream_gene_variant PACA-CA 15 59468554 59468554 single base substitution C T intron_variant PACA-CA 15 59475695 59475695 single base substitution G A intron_variant PACA-CA 15 59478604 59478605 deletion of <=200bp TA - intron_variant PACA-CA 15 59481634 59481634 single base substitution T G intron_variant PACA-CA 15 59484292 59484292 single base substitution G C downstream_gene_variant PACA-CA 15 59484292 59484292 single base substitution G C intron_variant PACA-CA 15 59489039 59489039 single base substitution A T intron_variant PACA-CA 15 59495019 59495019 single base substitution C T intron_variant PACA-CA 15 59495365 59495365 single base substitution G A intron_variant PACA-CA 15 59496265 59496265 single base substitution G C downstream_gene_variant PACA-CA 15 59496265 59496265 single base substitution G C intron_variant PACA-CA 15 59502558 59502558 single base substitution C T intron_variant PACA-CA 15 59502558 59502558 single base substitution C T upstream_gene_variant PACA-CA 15 59502870 59502870 single base substitution T C intron_variant PACA-CA 15 59502870 59502870 single base substitution T C upstream_gene_variant PACA-CA 15 59506244 59506244 single base substitution C T intron_variant PACA-CA 15 59511258 59511258 single base substitution G C downstream_gene_variant PACA-CA 15 59511258 59511258 single base substitution G C intron_variant PACA-CA 15 59511258 59511258 single base substitution G C upstream_gene_variant PACA-CA 15 59512466 59512466 single base substitution G A downstream_gene_variant PACA-CA 15 59512466 59512466 single base substitution G A intron_variant PACA-CA 15 59512466 59512466 single base substitution G A upstream_gene_variant PACA-CA 15 59512864 59512864 single base substitution A G downstream_gene_variant PACA-CA 15 59512864 59512864 single base substitution A G intron_variant PACA-CA 15 59512864 59512864 single base substitution A G upstream_gene_variant PACA-CA 15 59514461 59514461 single base substitution T C downstream_gene_variant PACA-CA 15 59514461 59514461 single base substitution T C intron_variant PACA-CA 15 59514461 59514461 single base substitution T C upstream_gene_variant PACA-CA 15 59520866 59520866 single base substitution G C intron_variant PACA-CA 15 59520866 59520866 single base substitution G C upstream_gene_variant PACA-CA 15 59529853 59529853 single base substitution G A intron_variant PACA-CA 15 59534571 59534571 single base substitution T G intron_variant PACA-CA 15 59536775 59536775 single base substitution T C intron_variant PACA-CA 15 59547282 59547282 single base substitution C T intron_variant PACA-CA 15 59550182 59550200 deletion of <=200bp AGATTCACAGAGCCTCCAG - intron_variant PACA-CA 15 59552208 59552208 single base substitution T C intron_variant PACA-CA 15 59553412 59553412 single base substitution T A intron_variant PACA-CA 15 59553599 59553599 single base substitution T A intron_variant PACA-CA 15 59554078 59554078 single base substitution G T intron_variant PACA-CA 15 59557834 59557834 single base substitution A G intron_variant PACA-CA 15 59557834 59557834 single base substitution A G upstream_gene_variant PACA-CA 15 59558650 59558650 single base substitution C T intron_variant PACA-CA 15 59558650 59558650 single base substitution C T upstream_gene_variant PACA-CA 15 59561502 59561502 single base substitution C T downstream_gene_variant PACA-CA 15 59561502 59561502 single base substitution C T intron_variant PACA-CA 15 59561502 59561502 single base substitution C T upstream_gene_variant PACA-CA 15 59562126 59562126 single base substitution A C downstream_gene_variant PACA-CA 15 59562126 59562126 single base substitution A C intron_variant PACA-CA 15 59562126 59562126 single base substitution A C upstream_gene_variant PACA-CA 15 59571191 59571191 single base substitution C A intron_variant PACA-CA 15 59571316 59571316 single base substitution C G intron_variant PACA-CA 15 59575584 59575584 single base substitution C T intron_variant PACA-CA 15 59576085 59576085 single base substitution T A intron_variant PACA-CA 15 59580319 59580319 single base substitution C T intron_variant PACA-CA 15 59580357 59580357 deletion of <=200bp T - intron_variant PACA-CA 15 59581779 59581779 single base substitution T C intron_variant PACA-CA 15 59586004 59586004 single base substitution G A intron_variant PACA-CA 15 59586435 59586435 single base substitution G C intron_variant PACA-CA 15 59586741 59586741 single base substitution C A intron_variant PACA-CA 15 59587889 59587889 single base substitution G C intron_variant PACA-CA 15 59601744 59601744 single base substitution C A intron_variant PACA-CA 15 59602817 59602817 single base substitution A G intron_variant PACA-CA 15 59602841 59602841 single base substitution C T intron_variant PACA-CA 15 59604713 59604713 deletion of <=200bp T - intron_variant PACA-CA 15 59609693 59609693 single base substitution C A intron_variant PACA-CA 15 59616020 59616020 single base substitution G C intron_variant PACA-CA 15 59618700 59618700 single base substitution G A intron_variant PACA-CA 15 59621352 59621352 single base substitution G A intron_variant PACA-CA 15 59623608 59623608 single base substitution T G intron_variant PACA-CA 15 59626710 59626710 single base substitution C T intron_variant PACA-CA 15 59628111 59628111 single base substitution G A intron_variant PACA-CA 15 59632875 59632875 single base substitution A G intron_variant PACA-CA 15 59634739 59634741 deletion of <=200bp TCC - intron_variant PACA-CA 15 59643118 59643118 single base substitution C T intron_variant PACA-CA 15 59647000 59647000 single base substitution C T intron_variant PACA-CA 15 59649178 59649178 single base substitution C T intron_variant PACA-CA 15 59652738 59652738 single base substitution C T intron_variant PACA-CA 15 59656906 59656906 single base substitution C T intron_variant PACA-CA 15 59657580 59657580 single base substitution T C intron_variant PACA-CA 15 59658458 59658458 single base substitution G A intron_variant PAEN-AU 15 59431631 59431631 single base substitution A C intron_variant PAEN-AU 15 59431958 59431958 single base substitution G A intron_variant PAEN-AU 15 59514124 59514124 single base substitution G T downstream_gene_variant PAEN-AU 15 59514124 59514124 single base substitution G T intron_variant PAEN-AU 15 59514124 59514124 single base substitution G T upstream_gene_variant PAEN-AU 15 59525856 59525856 single base substitution C T intron_variant PAEN-AU 15 59536350 59536350 single base substitution T C intron_variant PAEN-AU 15 59538042 59538042 single base substitution G T intron_variant PAEN-AU 15 59570595 59570595 single base substitution A T intron_variant PAEN-AU 15 59647863 59647863 single base substitution T A intron_variant PAEN-IT 15 59430082 59430082 single base substitution G A intron_variant PAEN-IT 15 59477409 59477409 single base substitution A G intron_variant PAEN-IT 15 59519185 59519185 single base substitution C T downstream_gene_variant PAEN-IT 15 59519185 59519185 single base substitution C T intron_variant PAEN-IT 15 59532887 59532887 single base substitution C G intron_variant PAEN-IT 15 59614983 59614983 single base substitution A G intron_variant PBCA-DE 15 59444089 59444090 deletion of <=200bp AC - intron_variant PBCA-DE 15 59458877 59458877 single base substitution G A intron_variant PBCA-DE 15 59475361 59475361 single base substitution C T intron_variant PBCA-DE 15 59476762 59476762 single base substitution G A intron_variant PBCA-DE 15 59483213 59483213 single base substitution G T downstream_gene_variant PBCA-DE 15 59483213 59483213 single base substitution G T intron_variant PBCA-DE 15 59500346 59500346 single base substitution C T downstream_gene_variant PBCA-DE 15 59500346 59500346 single base substitution C T intron_variant PBCA-DE 15 59500346 59500346 single base substitution C T upstream_gene_variant PBCA-DE 15 59507827 59507827 single base substitution C T intron_variant PBCA-DE 15 59512508 59512508 single base substitution C T downstream_gene_variant PBCA-DE 15 59512508 59512508 single base substitution C T intron_variant PBCA-DE 15 59512508 59512508 single base substitution C T upstream_gene_variant PBCA-DE 15 59517318 59517318 single base substitution G A downstream_gene_variant PBCA-DE 15 59517318 59517318 single base substitution G A intron_variant PBCA-DE 15 59532586 59532586 single base substitution G T intron_variant PBCA-DE 15 59540921 59540921 single base substitution G A intron_variant PBCA-DE 15 59555751 59555751 insertion of <=200bp - T intron_variant PBCA-DE 15 59562052 59562052 insertion of <=200bp - A downstream_gene_variant PBCA-DE 15 59562052 59562052 insertion of <=200bp - A intron_variant PBCA-DE 15 59562052 59562052 insertion of <=200bp - A upstream_gene_variant PBCA-DE 15 59583247 59583247 single base substitution A G intron_variant PBCA-DE 15 59589475 59589475 deletion of <=200bp T - intron_variant PBCA-DE 15 59592156 59592156 single base substitution G C intron_variant PBCA-DE 15 59592362 59592362 single base substitution G C intron_variant PBCA-DE 15 59592496 59592497 deletion of <=200bp CA - intron_variant PBCA-DE 15 59594454 59594454 single base substitution G A intron_variant PBCA-DE 15 59604351 59604351 single base substitution A T intron_variant PBCA-DE 15 59604855 59604855 single base substitution T C intron_variant PBCA-DE 15 59605058 59605058 insertion of <=200bp - AAT intron_variant PBCA-DE 15 59620440 59620440 single base substitution C T intron_variant PBCA-DE 15 59637513 59637513 single base substitution A C intron_variant PBCA-DE 15 59637684 59637684 single base substitution G A intron_variant PBCA-DE 15 59657487 59657487 single base substitution G C intron_variant PBCA-DE 15 59662089 59662089 insertion of <=200bp - CA intron_variant PRAD-CA 15 59431454 59431454 single base substitution A G intron_variant PRAD-CA 15 59432287 59432287 single base substitution A T intron_variant PRAD-CA 15 59445070 59445070 single base substitution T A intron_variant PRAD-CA 15 59458739 59458739 single base substitution T A intron_variant PRAD-CA 15 59468665 59468665 single base substitution C T downstream_gene_variant PRAD-CA 15 59468665 59468665 single base substitution C T intron_variant PRAD-CA 15 59470597 59470597 single base substitution C T downstream_gene_variant PRAD-CA 15 59470597 59470597 single base substitution C T intron_variant PRAD-CA 15 59470597 59470597 single base substitution C T missense_variant E172K 514G>A PRAD-CA 15 59470597 59470597 single base substitution C T missense_variant E682K 2044G>A PRAD-CA 15 59507136 59507136 single base substitution A G intron_variant PRAD-CA 15 59508890 59508890 single base substitution T C intron_variant PRAD-CA 15 59515849 59515849 single base substitution G A downstream_gene_variant PRAD-CA 15 59515849 59515849 single base substitution G A intron_variant PRAD-CA 15 59537108 59537108 single base substitution G C intron_variant PRAD-CA 15 59557329 59557329 single base substitution G A intron_variant PRAD-CA 15 59557329 59557329 single base substitution G A upstream_gene_variant PRAD-CA 15 59562031 59562031 single base substitution G C downstream_gene_variant PRAD-CA 15 59562031 59562031 single base substitution G C intron_variant PRAD-CA 15 59562031 59562031 single base substitution G C upstream_gene_variant PRAD-CA 15 59564942 59564942 single base substitution A C intron_variant PRAD-CA 15 59568408 59568408 single base substitution T C intron_variant PRAD-CA 15 59577711 59577711 single base substitution C T intron_variant PRAD-CA 15 59666326 59666326 single base substitution A G upstream_gene_variant PRAD-UK 15 59435221 59435221 single base substitution A G intron_variant PRAD-UK 15 59444880 59444880 single base substitution G C intron_variant PRAD-UK 15 59450284 59450284 single base substitution C T intron_variant PRAD-UK 15 59450284 59450284 single base substitution C T upstream_gene_variant PRAD-UK 15 59450468 59450468 single base substitution G C downstream_gene_variant PRAD-UK 15 59450468 59450468 single base substitution G C intron_variant PRAD-UK 15 59450468 59450468 single base substitution G C upstream_gene_variant PRAD-UK 15 59465184 59465184 single base substitution G A intron_variant PRAD-UK 15 59473353 59473353 single base substitution A G intron_variant PRAD-UK 15 59483570 59483570 insertion of <=200bp - AG downstream_gene_variant PRAD-UK 15 59483570 59483570 insertion of <=200bp - AG intron_variant PRAD-UK 15 59484160 59484160 single base substitution C T downstream_gene_variant PRAD-UK 15 59484160 59484160 single base substitution C T intron_variant PRAD-UK 15 59484209 59484211 deletion of <=200bp AAC - downstream_gene_variant PRAD-UK 15 59484209 59484211 deletion of <=200bp AAC - intron_variant PRAD-UK 15 59494444 59494444 single base substitution C A intron_variant PRAD-UK 15 59497733 59497733 insertion of <=200bp - TCATTGAACAAAATGTAATT downstream_gene_variant PRAD-UK 15 59497733 59497733 insertion of <=200bp - TCATTGAACAAAATGTAATT intron_variant PRAD-UK 15 59507437 59507456 deletion of <=200bp TGAATTGATAATAGAAGCAG - intron_variant PRAD-UK 15 59521279 59521279 single base substitution C T intron_variant PRAD-UK 15 59521279 59521279 single base substitution C T upstream_gene_variant PRAD-UK 15 59521280 59521280 single base substitution A G intron_variant PRAD-UK 15 59521280 59521280 single base substitution A G upstream_gene_variant PRAD-UK 15 59537326 59537326 single base substitution T C intron_variant PRAD-UK 15 59556742 59556742 single base substitution G A intron_variant PRAD-UK 15 59574187 59574187 single base substitution G T intron_variant PRAD-UK 15 59579323 59579323 single base substitution T C intron_variant PRAD-UK 15 59648628 59648628 single base substitution A G intron_variant PRAD-UK 15 59658093 59658093 single base substitution G C intron_variant PRAD-UK 15 59660089 59660089 single base substitution C T intron_variant PRAD-US 15 59564611 59564611 single base substitution T G exon_variant PRAD-US 15 59564611 59564611 single base substitution T G missense_variant H14P 41A>C READ-US 15 59497652 59497652 single base substitution C T downstream_gene_variant READ-US 15 59497652 59497652 single base substitution C T exon_variant READ-US 15 59497652 59497652 single base substitution C T intron_variant READ-US 15 59497652 59497652 single base substitution C T synonymous_variant R44R 132G>A READ-US 15 59497652 59497652 single base substitution C T synonymous_variant R521R 1563G>A READ-US 15 59499375 59499375 single base substitution C T downstream_gene_variant READ-US 15 59499375 59499375 single base substitution C T intron_variant READ-US 15 59499375 59499375 single base substitution C T upstream_gene_variant READ-US 15 59500187 59500187 single base substitution A G downstream_gene_variant READ-US 15 59500187 59500187 single base substitution A G intron_variant READ-US 15 59500187 59500187 single base substitution A G upstream_gene_variant READ-US 15 59510236 59510236 single base substitution C A stop_gained E151* 451G>T READ-US 15 59510236 59510236 single base substitution C A stop_gained E321* 961G>T READ-US 15 59510236 59510236 single base substitution C A stop_gained E41* 121G>T RECA-EU 15 59427467 59427467 single base substitution G A 3_prime_UTR_variant RECA-EU 15 59427467 59427467 single base substitution G A downstream_gene_variant RECA-EU 15 59427482 59427482 single base substitution C G 3_prime_UTR_variant RECA-EU 15 59427482 59427482 single base substitution C G downstream_gene_variant RECA-EU 15 59428124 59428124 single base substitution T C 3_prime_UTR_variant RECA-EU 15 59428124 59428124 single base substitution T C downstream_gene_variant RECA-EU 15 59439411 59439411 single base substitution A T intron_variant RECA-EU 15 59449521 59449521 single base substitution C A intron_variant RECA-EU 15 59449521 59449521 single base substitution C A upstream_gene_variant RECA-EU 15 59451229 59451229 single base substitution T A downstream_gene_variant RECA-EU 15 59451229 59451229 single base substitution T A intron_variant RECA-EU 15 59495949 59495949 single base substitution C T intron_variant RECA-EU 15 59499424 59499424 single base substitution T C downstream_gene_variant RECA-EU 15 59499424 59499424 single base substitution T C intron_variant RECA-EU 15 59499424 59499424 single base substitution T C upstream_gene_variant RECA-EU 15 59500478 59500478 single base substitution T A downstream_gene_variant RECA-EU 15 59500478 59500478 single base substitution T A intron_variant RECA-EU 15 59500478 59500478 single base substitution T A upstream_gene_variant RECA-EU 15 59503131 59503131 single base substitution T C intron_variant RECA-EU 15 59503131 59503131 single base substitution T C upstream_gene_variant RECA-EU 15 59516086 59516086 single base substitution G A downstream_gene_variant RECA-EU 15 59516086 59516086 single base substitution G A intron_variant RECA-EU 15 59518812 59518812 single base substitution C G downstream_gene_variant RECA-EU 15 59518812 59518812 single base substitution C G intron_variant RECA-EU 15 59563797 59563797 single base substitution C A downstream_gene_variant RECA-EU 15 59563797 59563797 single base substitution C A intron_variant RECA-EU 15 59568019 59568019 single base substitution C A intron_variant RECA-EU 15 59569752 59569752 single base substitution A C intron_variant RECA-EU 15 59571326 59571326 single base substitution C G intron_variant RECA-EU 15 59575388 59575388 single base substitution C T intron_variant RECA-EU 15 59584801 59584801 single base substitution G A intron_variant RECA-EU 15 59596807 59596807 single base substitution T C intron_variant RECA-EU 15 59608303 59608303 single base substitution C T intron_variant RECA-EU 15 59608890 59608890 single base substitution G A intron_variant RECA-EU 15 59609356 59609356 single base substitution T C intron_variant RECA-EU 15 59621983 59621983 single base substitution T A intron_variant RECA-EU 15 59622068 59622068 single base substitution T C intron_variant SKCA-BR 15 59426612 59426612 single base substitution G A downstream_gene_variant SKCA-BR 15 59427593 59427593 single base substitution C T 3_prime_UTR_variant SKCA-BR 15 59427593 59427593 single base substitution C T downstream_gene_variant SKCA-BR 15 59429445 59429445 single base substitution G A 3_prime_UTR_variant SKCA-BR 15 59429445 59429445 single base substitution G A intron_variant SKCA-BR 15 59431433 59431467 deletion of <=200bp TCCCTCATTATTACTCCTCACACTTCCCTCCCACC - intron_variant SKCA-BR 15 59431453 59431453 single base substitution C G intron_variant SKCA-BR 15 59431454 59431454 single base substitution A G intron_variant SKCA-BR 15 59431499 59431499 single base substitution A C intron_variant SKCA-BR 15 59431699 59431699 insertion of <=200bp - CTCA intron_variant SKCA-BR 15 59434278 59434278 single base substitution C T intron_variant SKCA-BR 15 59435154 59435154 single base substitution G A intron_variant SKCA-BR 15 59441259 59441259 single base substitution T G intron_variant SKCA-BR 15 59441261 59441261 single base substitution T G intron_variant SKCA-BR 15 59442875 59442875 single base substitution G A intron_variant SKCA-BR 15 59443250 59443250 single base substitution G A intron_variant SKCA-BR 15 59447130 59447130 single base substitution T C intron_variant SKCA-BR 15 59447130 59447130 single base substitution T C upstream_gene_variant SKCA-BR 15 59451785 59451785 single base substitution T C downstream_gene_variant SKCA-BR 15 59451785 59451785 single base substitution T C intron_variant SKCA-BR 15 59453463 59453463 single base substitution G A downstream_gene_variant SKCA-BR 15 59453463 59453463 single base substitution G A intron_variant SKCA-BR 15 59456200 59456200 single base substitution G A intron_variant SKCA-BR 15 59465179 59465179 single base substitution T C intron_variant SKCA-BR 15 59467419 59467419 single base substitution C T downstream_gene_variant SKCA-BR 15 59467419 59467419 single base substitution C T intron_variant SKCA-BR 15 59469195 59469195 insertion of <=200bp - GA downstream_gene_variant SKCA-BR 15 59469195 59469195 insertion of <=200bp - GA intron_variant SKCA-BR 15 59473691 59473691 single base substitution G A intron_variant SKCA-BR 15 59474605 59474605 single base substitution T G intron_variant SKCA-BR 15 59476649 59476649 single base substitution T C intron_variant SKCA-BR 15 59477388 59477388 single base substitution A G intron_variant SKCA-BR 15 59478603 59478603 insertion of <=200bp - TAA intron_variant SKCA-BR 15 59479393 59479393 single base substitution G A intron_variant SKCA-BR 15 59480746 59480746 single base substitution T A intron_variant SKCA-BR 15 59481205 59481205 single base substitution C T intron_variant SKCA-BR 15 59481703 59481703 insertion of <=200bp - TTTTC intron_variant SKCA-BR 15 59486535 59486535 single base substitution G A downstream_gene_variant SKCA-BR 15 59486535 59486535 single base substitution G A intron_variant SKCA-BR 15 59487712 59487712 single base substitution G A exon_variant SKCA-BR 15 59487712 59487712 single base substitution G A intron_variant SKCA-BR 15 59487712 59487712 single base substitution G A missense_variant R108C 322C>T SKCA-BR 15 59487712 59487712 single base substitution G A missense_variant R585C 1753C>T SKCA-BR 15 59493590 59493590 single base substitution G A intron_variant SKCA-BR 15 59495554 59495554 single base substitution C T intron_variant SKCA-BR 15 59501241 59501241 single base substitution G A intron_variant SKCA-BR 15 59501241 59501241 single base substitution G A upstream_gene_variant SKCA-BR 15 59501829 59501829 single base substitution G A intron_variant SKCA-BR 15 59501829 59501829 single base substitution G A upstream_gene_variant SKCA-BR 15 59505335 59505341 deletion of <=200bp TTTATTA - intron_variant SKCA-BR 15 59505335 59505341 deletion of <=200bp TTTATTA - upstream_gene_variant SKCA-BR 15 59508791 59508791 insertion of <=200bp - GTATCTATCTATCTA intron_variant SKCA-BR 15 59508793 59508793 single base substitution G C intron_variant SKCA-BR 15 59508855 59508855 single base substitution G C intron_variant SKCA-BR 15 59508861 59508861 single base substitution A G intron_variant SKCA-BR 15 59513066 59513067 deletion of <=200bp AT - downstream_gene_variant SKCA-BR 15 59513066 59513067 deletion of <=200bp AT - intron_variant SKCA-BR 15 59513066 59513067 deletion of <=200bp AT - upstream_gene_variant SKCA-BR 15 59513147 59513147 single base substitution G A downstream_gene_variant SKCA-BR 15 59513147 59513147 single base substitution G A intron_variant SKCA-BR 15 59513147 59513147 single base substitution G A upstream_gene_variant SKCA-BR 15 59513224 59513224 insertion of <=200bp - TTA downstream_gene_variant SKCA-BR 15 59513224 59513224 insertion of <=200bp - TTA intron_variant SKCA-BR 15 59513224 59513224 insertion of <=200bp - TTA upstream_gene_variant SKCA-BR 15 59513235 59513235 insertion of <=200bp - TTA downstream_gene_variant SKCA-BR 15 59513235 59513235 insertion of <=200bp - TTA intron_variant SKCA-BR 15 59513235 59513235 insertion of <=200bp - TTA upstream_gene_variant SKCA-BR 15 59517109 59517109 single base substitution G A downstream_gene_variant SKCA-BR 15 59517109 59517109 single base substitution G A intron_variant SKCA-BR 15 59519257 59519257 single base substitution T C downstream_gene_variant SKCA-BR 15 59519257 59519257 single base substitution T C intron_variant SKCA-BR 15 59519637 59519637 single base substitution G A downstream_gene_variant SKCA-BR 15 59519637 59519637 single base substitution G A intron_variant SKCA-BR 15 59519710 59519710 single base substitution G A 3_prime_UTR_variant SKCA-BR 15 59519710 59519710 single base substitution G A exon_variant SKCA-BR 15 59519710 59519710 single base substitution G A missense_variant S197F 590C>T SKCA-BR 15 59519710 59519710 single base substitution G A missense_variant S27F 80C>T SKCA-BR 15 59520455 59520455 single base substitution T G intron_variant SKCA-BR 15 59520455 59520455 single base substitution T G upstream_gene_variant SKCA-BR 15 59525865 59525865 insertion of <=200bp - AAT intron_variant SKCA-BR 15 59527143 59527143 single base substitution G A intron_variant SKCA-BR 15 59531163 59531163 single base substitution G T intron_variant SKCA-BR 15 59531423 59531424 deletion of <=200bp AT - intron_variant SKCA-BR 15 59531604 59531604 single base substitution T C intron_variant SKCA-BR 15 59532629 59532629 single base substitution A T intron_variant SKCA-BR 15 59534244 59534244 single base substitution C T intron_variant SKCA-BR 15 59537280 59537280 single base substitution G A intron_variant SKCA-BR 15 59541090 59541090 single base substitution C T intron_variant SKCA-BR 15 59542755 59542755 single base substitution G A intron_variant SKCA-BR 15 59545662 59545662 single base substitution G A intron_variant SKCA-BR 15 59547029 59547029 insertion of <=200bp - CT intron_variant SKCA-BR 15 59553541 59553541 single base substitution C T intron_variant SKCA-BR 15 59554764 59554764 single base substitution T G intron_variant SKCA-BR 15 59556509 59556509 single base substitution G T intron_variant SKCA-BR 15 59557223 59557223 single base substitution G A intron_variant SKCA-BR 15 59557223 59557223 single base substitution G A upstream_gene_variant SKCA-BR 15 59557992 59557992 single base substitution A T intron_variant SKCA-BR 15 59557992 59557992 single base substitution A T upstream_gene_variant SKCA-BR 15 59558851 59558851 single base substitution G T intron_variant SKCA-BR 15 59558851 59558851 single base substitution G T upstream_gene_variant SKCA-BR 15 59561996 59561996 single base substitution G A downstream_gene_variant SKCA-BR 15 59561996 59561996 single base substitution G A intron_variant SKCA-BR 15 59561996 59561996 single base substitution G A upstream_gene_variant SKCA-BR 15 59563017 59563017 single base substitution C T downstream_gene_variant SKCA-BR 15 59563017 59563017 single base substitution C T intron_variant SKCA-BR 15 59563831 59563831 single base substitution C T downstream_gene_variant SKCA-BR 15 59563831 59563831 single base substitution C T intron_variant SKCA-BR 15 59565294 59565294 single base substitution G A intron_variant SKCA-BR 15 59567933 59567933 single base substitution A C intron_variant SKCA-BR 15 59568219 59568219 single base substitution G A intron_variant SKCA-BR 15 59569751 59569751 insertion of <=200bp - ACAAAAAAAAAAC intron_variant SKCA-BR 15 59569756 59569756 single base substitution A C intron_variant SKCA-BR 15 59574687 59574687 single base substitution C T intron_variant SKCA-BR 15 59577913 59577913 single base substitution A G intron_variant SKCA-BR 15 59582285 59582285 single base substitution G A intron_variant SKCA-BR 15 59583910 59583912 deletion of <=200bp AAG - intron_variant SKCA-BR 15 59583911 59583912 deletion of <=200bp AG - intron_variant SKCA-BR 15 59588767 59588767 single base substitution C T intron_variant SKCA-BR 15 59589261 59589261 single base substitution C G intron_variant SKCA-BR 15 59589273 59589273 single base substitution G A intron_variant SKCA-BR 15 59589558 59589558 single base substitution C T intron_variant SKCA-BR 15 59599733 59599733 single base substitution G A intron_variant SKCA-BR 15 59599807 59599813 deletion of <=200bp TTTTTGG - intron_variant SKCA-BR 15 59600735 59600735 single base substitution G A intron_variant SKCA-BR 15 59602200 59602200 single base substitution A G intron_variant SKCA-BR 15 59606586 59606586 single base substitution G A intron_variant SKCA-BR 15 59607748 59607748 insertion of <=200bp - TTA intron_variant SKCA-BR 15 59611235 59611235 single base substitution T G intron_variant SKCA-BR 15 59611778 59611778 single base substitution T A intron_variant SKCA-BR 15 59614153 59614153 single base substitution A G intron_variant SKCA-BR 15 59614218 59614218 single base substitution G A intron_variant SKCA-BR 15 59616052 59616052 single base substitution G A intron_variant SKCA-BR 15 59616248 59616248 single base substitution G A intron_variant SKCA-BR 15 59616514 59616514 single base substitution G A intron_variant SKCA-BR 15 59621166 59621166 single base substitution G A intron_variant SKCA-BR 15 59621703 59621703 single base substitution A G intron_variant SKCA-BR 15 59622501 59622501 single base substitution G A intron_variant SKCA-BR 15 59624747 59624747 single base substitution G A intron_variant SKCA-BR 15 59628957 59628957 single base substitution T C intron_variant SKCA-BR 15 59630359 59630359 insertion of <=200bp - TA intron_variant SKCA-BR 15 59631960 59631960 single base substitution G A intron_variant SKCA-BR 15 59639123 59639124 deletion of <=200bp GA - intron_variant SKCA-BR 15 59645568 59645573 deletion of <=200bp AAAAAG - intron_variant SKCA-BR 15 59645573 59645573 single base substitution G A intron_variant SKCA-BR 15 59645956 59645957 deletion of <=200bp CA - intron_variant SKCA-BR 15 59645971 59645972 deletion of <=200bp AC - intron_variant SKCA-BR 15 59645980 59645980 single base substitution G A intron_variant SKCA-BR 15 59647280 59647280 single base substitution T G intron_variant SKCA-BR 15 59647596 59647596 single base substitution G T intron_variant SKCA-BR 15 59648882 59648895 deletion of <=200bp TCCTCCCACATAAG - intron_variant SKCA-BR 15 59648960 59648960 single base substitution T G intron_variant SKCA-BR 15 59652647 59652647 single base substitution G A intron_variant SKCA-BR 15 59653725 59653725 single base substitution T C intron_variant SKCA-BR 15 59655175 59655175 insertion of <=200bp - CTT intron_variant SKCA-BR 15 59656499 59656499 single base substitution A G intron_variant SKCA-BR 15 59658497 59658497 single base substitution C T intron_variant SKCA-BR 15 59659194 59659199 deletion of <=200bp CGCAAA - intron_variant SKCA-BR 15 59659196 59659201 deletion of <=200bp CAAAAA - intron_variant SKCA-BR 15 59659201 59659201 single base substitution A C intron_variant SKCA-BR 15 59660199 59660199 single base substitution T A intron_variant SKCA-BR 15 59661180 59661180 single base substitution C T intron_variant SKCA-BR 15 59662301 59662301 single base substitution C T intron_variant SKCA-BR 15 59665397 59665397 single base substitution C T upstream_gene_variant SKCA-BR 15 59666310 59666315 deletion of <=200bp AAGAAG - upstream_gene_variant SKCA-BR 15 59666605 59666605 single base substitution G A upstream_gene_variant SKCA-BR 15 59667696 59667696 single base substitution G A upstream_gene_variant SKCA-BR 15 59668192 59668194 deletion of <=200bp TAA - upstream_gene_variant SKCM-US 15 59466410 59466411 deletion of <=200bp TC - downstream_gene_variant SKCM-US 15 59466410 59466411 deletion of <=200bp TC - frameshift_variant R183 SKCM-US 15 59466410 59466411 deletion of <=200bp TC - frameshift_variant R693 SKCM-US 15 59466410 59466411 deletion of <=200bp TC - intron_variant SKCM-US 15 59466433 59466433 single base substitution G A downstream_gene_variant SKCM-US 15 59466433 59466433 single base substitution G A intron_variant SKCM-US 15 59466433 59466433 single base substitution G A missense_variant L176F 526C>T SKCM-US 15 59466433 59466433 single base substitution G A missense_variant L686F 2056C>T SKCM-US 15 59470628 59470628 single base substitution C T exon_variant SKCM-US 15 59470628 59470628 single base substitution C T intron_variant SKCM-US 15 59470628 59470628 single base substitution C T synonymous_variant L161L 483G>A SKCM-US 15 59470628 59470628 single base substitution C T synonymous_variant L671L 2013G>A SKCM-US 15 59494600 59494600 single base substitution G A exon_variant SKCM-US 15 59494600 59494600 single base substitution G A intron_variant SKCM-US 15 59494600 59494600 single base substitution G A synonymous_variant F541F 1623C>T SKCM-US 15 59494600 59494600 single base substitution G A synonymous_variant F64F 192C>T SKCM-US 15 59497637 59497637 single base substitution A G downstream_gene_variant SKCM-US 15 59497637 59497637 single base substitution A G exon_variant SKCM-US 15 59497637 59497637 single base substitution A G intron_variant SKCM-US 15 59497637 59497637 single base substitution A G synonymous_variant L49L 147T>C SKCM-US 15 59497637 59497637 single base substitution A G synonymous_variant L526L 1578T>C SKCM-US 15 59499502 59499502 single base substitution G A downstream_gene_variant SKCM-US 15 59499502 59499502 single base substitution G A intron_variant SKCM-US 15 59499502 59499502 single base substitution G A upstream_gene_variant SKCM-US 15 59499593 59499593 single base substitution G A downstream_gene_variant SKCM-US 15 59499593 59499593 single base substitution G A intron_variant SKCM-US 15 59499593 59499593 single base substitution G A upstream_gene_variant SKCM-US 15 59499621 59499621 single base substitution G A downstream_gene_variant SKCM-US 15 59499621 59499621 single base substitution G A intron_variant SKCM-US 15 59499621 59499621 single base substitution G A upstream_gene_variant SKCM-US 15 59499966 59499966 single base substitution G A downstream_gene_variant SKCM-US 15 59499966 59499966 single base substitution G A intron_variant SKCM-US 15 59499966 59499966 single base substitution G A upstream_gene_variant SKCM-US 15 59500176 59500176 single base substitution A G downstream_gene_variant SKCM-US 15 59500176 59500176 single base substitution A G intron_variant SKCM-US 15 59500176 59500176 single base substitution A G upstream_gene_variant SKCM-US 15 59500206 59500206 single base substitution A G downstream_gene_variant SKCM-US 15 59500206 59500206 single base substitution A G intron_variant SKCM-US 15 59500206 59500206 single base substitution A G upstream_gene_variant SKCM-US 15 59510172 59510172 single base substitution G A missense_variant T172I 515C>T SKCM-US 15 59510172 59510172 single base substitution G A missense_variant T342I 1025C>T SKCM-US 15 59510172 59510172 single base substitution G A missense_variant T62I 185C>T SKCM-US 15 59516941 59516941 single base substitution C T downstream_gene_variant SKCM-US 15 59516941 59516941 single base substitution C T exon_variant SKCM-US 15 59516941 59516941 single base substitution C T missense_variant G242S 724G>A SKCM-US 15 59516941 59516941 single base substitution C T missense_variant G72S 214G>A SKCM-US 15 59523928 59523928 single base substitution G T 3_prime_UTR_variant SKCM-US 15 59523928 59523928 single base substitution G T exon_variant SKCM-US 15 59523928 59523928 single base substitution G T synonymous_variant T161T 483C>A SKCM-US 15 59523928 59523928 single base substitution G T upstream_gene_variant SKCM-US 15 59548558 59548558 single base substitution G A exon_variant SKCM-US 15 59548558 59548558 single base substitution G A missense_variant P86L 257C>T SKCM-US 15 59564525 59564525 single base substitution A C exon_variant SKCM-US 15 59564525 59564525 single base substitution A C missense_variant Y43D 127T>G STAD-US 15 59430514 59430514 single base substitution G A missense_variant P1045S 3133C>T STAD-US 15 59430514 59430514 single base substitution G A missense_variant P36S 106C>T STAD-US 15 59499212 59499212 single base substitution G T downstream_gene_variant STAD-US 15 59499212 59499212 single base substitution G T intron_variant STAD-US 15 59499212 59499212 single base substitution G T upstream_gene_variant STAD-US 15 59499250 59499250 single base substitution G A downstream_gene_variant STAD-US 15 59499250 59499250 single base substitution G A intron_variant STAD-US 15 59499250 59499250 single base substitution G A upstream_gene_variant STAD-US 15 59499291 59499291 single base substitution C T downstream_gene_variant STAD-US 15 59499291 59499291 single base substitution C T intron_variant STAD-US 15 59499291 59499291 single base substitution C T upstream_gene_variant STAD-US 15 59499489 59499489 single base substitution G A downstream_gene_variant STAD-US 15 59499489 59499489 single base substitution G A intron_variant STAD-US 15 59499489 59499489 single base substitution G A upstream_gene_variant STAD-US 15 59499582 59499582 single base substitution G A downstream_gene_variant STAD-US 15 59499582 59499582 single base substitution G A intron_variant STAD-US 15 59499582 59499582 single base substitution G A upstream_gene_variant STAD-US 15 59499721 59499721 single base substitution T C downstream_gene_variant STAD-US 15 59499721 59499721 single base substitution T C intron_variant STAD-US 15 59499721 59499721 single base substitution T C upstream_gene_variant STAD-US 15 59499969 59499969 single base substitution A G downstream_gene_variant STAD-US 15 59499969 59499969 single base substitution A G intron_variant STAD-US 15 59499969 59499969 single base substitution A G upstream_gene_variant STAD-US 15 59500962 59500962 single base substitution T C downstream_gene_variant STAD-US 15 59500962 59500962 single base substitution T C exon_variant STAD-US 15 59500962 59500962 single base substitution T C intron_variant STAD-US 15 59500962 59500962 single base substitution T C missense_variant Q483R 1448A>G STAD-US 15 59500962 59500962 single base substitution T C missense_variant Q6R 17A>G STAD-US 15 59500962 59500962 single base substitution T C upstream_gene_variant STAD-US 15 59500995 59500995 single base substitution G A downstream_gene_variant STAD-US 15 59500995 59500995 single base substitution G A exon_variant STAD-US 15 59500995 59500995 single base substitution G A intron_variant STAD-US 15 59500995 59500995 single base substitution G A missense_variant A472V 1415C>T STAD-US 15 59500995 59500995 single base substitution G A upstream_gene_variant STAD-US 15 59501008 59501008 single base substitution C T exon_variant STAD-US 15 59501008 59501008 single base substitution C T intron_variant STAD-US 15 59501008 59501008 single base substitution C T missense_variant A468T 1402G>A STAD-US 15 59501008 59501008 single base substitution C T synonymous_variant ?188 STAD-US 15 59501008 59501008 single base substitution C T upstream_gene_variant STAD-US 15 59506484 59506484 single base substitution A C intron_variant STAD-US 15 59506484 59506484 single base substitution A C missense_variant N126K 378T>G STAD-US 15 59506484 59506484 single base substitution A C missense_variant N406K 1218T>G STAD-US 15 59506509 59506509 deletion of <=200bp T - frameshift_variant N118 STAD-US 15 59506509 59506509 deletion of <=200bp T - frameshift_variant N398 STAD-US 15 59506509 59506509 deletion of <=200bp T - intron_variant STAD-US 15 59506895 59506895 single base substitution C T intron_variant STAD-US 15 59506895 59506895 single base substitution C T missense_variant D378N 1132G>A STAD-US 15 59506895 59506895 single base substitution C T missense_variant D98N 292G>A STAD-US 15 59548485 59548485 single base substitution G T splice_region_variant STAD-US 15 59553620 59553620 single base substitution G A intron_variant STAD-US 15 59553620 59553620 single base substitution G A missense_variant A79V 236C>T STAD-US 15 59553620 59553620 single base substitution G A splice_region_variant STAD-US 15 59553637 59553637 single base substitution A C exon_variant STAD-US 15 59553637 59553637 single base substitution A C intron_variant STAD-US 15 59553637 59553637 single base substitution A C missense_variant I73M 219T>G THCA-SA 15 59429160 59429160 single base substitution G A 3_prime_UTR_variant THCA-SA 15 59429160 59429160 single base substitution G A intron_variant THCA-US 15 59510196 59510196 single base substitution C T missense_variant G164D 491G>A THCA-US 15 59510196 59510196 single base substitution C T missense_variant G334D 1001G>A THCA-US 15 59510196 59510196 single base substitution C T missense_variant G54D 161G>A UCEC-US 15 59430410 59430410 single base substitution A G intron_variant UCEC-US 15 59430410 59430410 single base substitution A G synonymous_variant D1079D 3237T>C UCEC-US 15 59445850 59445850 single base substitution G A stop_gained R1007* 3019C>T UCEC-US 15 59445850 59445850 single base substitution G A upstream_gene_variant UCEC-US 15 59455405 59455405 single base substitution G A downstream_gene_variant UCEC-US 15 59455405 59455405 single base substitution G A missense_variant R860C 2578C>T UCEC-US 15 59464114 59464114 single base substitution A G missense_variant I242T 725T>C UCEC-US 15 59464114 59464114 single base substitution A G missense_variant I311T 932T>C UCEC-US 15 59464114 59464114 single base substitution A G missense_variant I821T 2462T>C UCEC-US 15 59466008 59466008 single base substitution G A downstream_gene_variant UCEC-US 15 59466008 59466008 single base substitution G A intron_variant UCEC-US 15 59466008 59466008 single base substitution G A synonymous_variant F247F 741C>T UCEC-US 15 59466008 59466008 single base substitution G A synonymous_variant F757F 2271C>T UCEC-US 15 59466362 59466362 single base substitution G A downstream_gene_variant UCEC-US 15 59466362 59466362 single base substitution G A intron_variant UCEC-US 15 59466362 59466362 single base substitution G A synonymous_variant F199F 597C>T UCEC-US 15 59466362 59466362 single base substitution G A synonymous_variant F709F 2127C>T UCEC-US 15 59466393 59466393 single base substitution G A downstream_gene_variant UCEC-US 15 59466393 59466393 single base substitution G A intron_variant UCEC-US 15 59466393 59466393 single base substitution G A missense_variant A189V 566C>T UCEC-US 15 59466393 59466393 single base substitution G A missense_variant A699V 2096C>T UCEC-US 15 59466433 59466433 single base substitution G T downstream_gene_variant UCEC-US 15 59466433 59466433 single base substitution G T intron_variant UCEC-US 15 59466433 59466433 single base substitution G T missense_variant L176I 526C>A UCEC-US 15 59466433 59466433 single base substitution G T missense_variant L686I 2056C>A UCEC-US 15 59470659 59470659 single base substitution G A exon_variant UCEC-US 15 59470659 59470659 single base substitution G A intron_variant UCEC-US 15 59470659 59470659 single base substitution G A missense_variant S151L 452C>T UCEC-US 15 59470659 59470659 single base substitution G A missense_variant S661L 1982C>T UCEC-US 15 59480341 59480341 single base substitution C T exon_variant UCEC-US 15 59480341 59480341 single base substitution C T intron_variant UCEC-US 15 59480341 59480341 single base substitution C T missense_variant R627H 1880G>A UCEC-US 15 59480414 59480414 single base substitution C A intron_variant UCEC-US 15 59480414 59480414 single base substitution C A missense_variant V603L 1807G>T UCEC-US 15 59480414 59480414 single base substitution C A splice_region_variant UCEC-US 15 59494553 59494553 single base substitution C T exon_variant UCEC-US 15 59494553 59494553 single base substitution C T intron_variant UCEC-US 15 59494553 59494553 single base substitution C T missense_variant R557H 1670G>A UCEC-US 15 59494553 59494553 single base substitution C T missense_variant R80H 239G>A UCEC-US 15 59499241 59499241 single base substitution G A downstream_gene_variant UCEC-US 15 59499241 59499241 single base substitution G A intron_variant UCEC-US 15 59499241 59499241 single base substitution G A upstream_gene_variant UCEC-US 15 59499308 59499308 single base substitution C A downstream_gene_variant UCEC-US 15 59499308 59499308 single base substitution C A intron_variant UCEC-US 15 59499308 59499308 single base substitution C A upstream_gene_variant UCEC-US 15 59499421 59499421 single base substitution T C downstream_gene_variant UCEC-US 15 59499421 59499421 single base substitution T C intron_variant UCEC-US 15 59499421 59499421 single base substitution T C upstream_gene_variant UCEC-US 15 59499541 59499541 single base substitution C T downstream_gene_variant UCEC-US 15 59499541 59499541 single base substitution C T intron_variant UCEC-US 15 59499541 59499541 single base substitution C T upstream_gene_variant UCEC-US 15 59499603 59499603 single base substitution G A downstream_gene_variant UCEC-US 15 59499603 59499603 single base substitution G A intron_variant UCEC-US 15 59499603 59499603 single base substitution G A upstream_gene_variant UCEC-US 15 59500924 59500924 single base substitution T C downstream_gene_variant UCEC-US 15 59500924 59500924 single base substitution T C exon_variant UCEC-US 15 59500924 59500924 single base substitution T C intron_variant UCEC-US 15 59500924 59500924 single base substitution T C missense_variant N19D 55A>G UCEC-US 15 59500924 59500924 single base substitution T C missense_variant N496D 1486A>G UCEC-US 15 59500924 59500924 single base substitution T C upstream_gene_variant UCEC-US 15 59501033 59501033 single base substitution G T exon_variant UCEC-US 15 59501033 59501033 single base substitution G T intron_variant UCEC-US 15 59501033 59501033 single base substitution G T synonymous_variant I179I 537C>A UCEC-US 15 59501033 59501033 single base substitution G T synonymous_variant I459I 1377C>A UCEC-US 15 59501033 59501033 single base substitution G T upstream_gene_variant UCEC-US 15 59502775 59502775 single base substitution T G intron_variant UCEC-US 15 59502775 59502775 single base substitution T G synonymous_variant R154R 460A>C UCEC-US 15 59502775 59502775 single base substitution T G synonymous_variant R434R 1300A>C UCEC-US 15 59502775 59502775 single base substitution T G upstream_gene_variant UCEC-US 15 59510099 59510099 single base substitution G A synonymous_variant F196F 588C>T UCEC-US 15 59510099 59510099 single base substitution G A synonymous_variant F366F 1098C>T UCEC-US 15 59510099 59510099 single base substitution G A synonymous_variant F86F 258C>T UCEC-US 15 59516939 59516939 single base substitution G A downstream_gene_variant UCEC-US 15 59516939 59516939 single base substitution G A exon_variant UCEC-US 15 59516939 59516939 single base substitution G A synonymous_variant G242G 726C>T UCEC-US 15 59516939 59516939 single base substitution G A synonymous_variant G72G 216C>T UCEC-US 15 59523959 59523959 single base substitution G A 3_prime_UTR_variant UCEC-US 15 59523959 59523959 single base substitution G A exon_variant UCEC-US 15 59523959 59523959 single base substitution G A missense_variant P151L 452C>T UCEC-US 15 59523959 59523959 single base substitution G A upstream_gene_variant UCEC-US 15 59548563 59548563 single base substitution G T exon_variant UCEC-US 15 59548563 59548563 single base substitution G T missense_variant N84K 252C>A UCEC-US 15 59548571 59548571 single base substitution A G exon_variant UCEC-US 15 59548571 59548571 single base substitution A G missense_variant Y82H 244T>C UCEC-US 15 59553643 59553643 single base substitution C A exon_variant UCEC-US 15 59553643 59553643 single base substitution C A intron_variant UCEC-US 15 59553643 59553643 single base substitution C A missense_variant K71N 213G>T UCEC-US 15 59564546 59564546 single base substitution C T exon_variant UCEC-US 15 59564546 59564546 single base substitution C T missense_variant V36M 106G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand H1155 COSM1195160 c.1589T>A p.L530H Substitution - Missense 15:59205427-59205427 - CRC-19T COSM5481343 c.2471A>G p.Y824C Substitution - Missense 17:1469565-1469565 - TCGA-BR-8366-01 COSM4055937 c.330C>A p.I110I Substitution - coding silent 15:59256286-59256286 - TCGA-BC-A216-01 COSM4911389 c.2835T>G p.T945T Substitution - coding silent 15:59158330-59158330 - TCGA-DD-A11A-01 COSM4940352 c.2476C>T p.L826F Substitution - Missense 15:59171901-59171901 - TCGA-G3-A25T-01 COSM4941734 c.9T>G p.S3R Substitution - Missense 17:1484265-1484265 - LUAD-RT-S01703 COSM379615 c.1035C>T p.A345A Substitution - coding silent 17:1478688-1478688 - 029T COSM1728254 c.2756G>T p.S919I Substitution - Missense 15:59161102-59161102 - 226 COSM3730079 c.3141C>T p.P1047P Substitution - coding silent 15:59138307-59138307 - I2L-P19Tb-Tumor-Organoid COSM5364181 c.242+2T>C p.? Unknown 17:1483608-1483608 - SC_9008 COSM5548174 c.1805+10delG p.? Unknown 15:59195451-59195451 - HCT15 COSM1678504 c.1693A>T p.I565L Substitution - Missense 15:59202331-59202331 - TCGA-G3-A25S-01 COSM4926752 c.1986C>A p.V662V Substitution - coding silent 15:59178456-59178456 - 3765_T COSM3958032 c.1615A>T p.M539L Substitution - Missense 17:1474687-1474687 - H1703 COSM1196558 c.889G>T p.A297S Substitution - Missense 15:59223080-59223080 - TCGA-BS-A0UJ-01 COSM963446 c.252C>A p.N84K Substitution - Missense 15:59256364-59256364 - Ad1 COSM4440781 c.1439C>T p.T480M Substitution - Missense 15:59208772-59208772 - TCGA-BR-8589-01 COSM4055933 c.1448A>G p.Q483R Substitution - Missense 15:59208763-59208763 - TCGA-AX-A05Z-01 COSM963442 c.1300A>C p.R434R Substitution - coding silent 15:59210576-59210576 - C91 COSM4444508 c.2883C>A p.Y961* Substitution - Nonsense 15:59153787-59153787 - ESCC_45 COSM5630286 c.679C>T p.L227F Substitution - Missense 15:59224787-59224787 - Gp5D COSM2738080 c.2568T>C p.S856S Substitution - coding silent 17:1468434-1468434 - Patient_4 COSM5414461 c.441+2T>G p.? Unknown 17:1482859-1482859 - CCK81 COSM1216381 c.620G>A p.R207Q Substitution - Missense 15:59227481-59227481 - TCGA-AX-A0J0-01 COSM963440 c.1486A>G p.N496D Substitution - Missense 15:59208725-59208725 - CSCC-54-T COSM4480999 c.2474C>T p.S825F Substitution - Missense 15:59171903-59171903 - 8012432 COSM218481 c.2099G>A p.R700Q Substitution - Missense 15:59174191-59174191 - ML_97_T_01 COSM5038369 c.66C>T p.F22F Substitution - coding silent 17:1484208-1484208 - CSCC-44-T COSM4487266 c.3056C>T p.A1019V Substitution - Missense 17:1467246-1467246 - AOCS-090-1-0 COSM3983261 c.1306G>A p.V436I Substitution - Missense 17:1477962-1477962 - TCGA-60-2698-01 COSM700827 c.580C>G p.L194V Substitution - Missense 15:59227521-59227521 - TCGA-BS-A0UF-01 COSM963426 c.2271C>T p.F757F Substitution - coding silent 15:59173809-59173809 - 2461404 COSM5415859 c.3136C>A p.Q1046K Substitution - Missense 15:59138312-59138312 - HCC162T COSM3717185 c.2172A>G p.R724R Substitution - coding silent 17:1470625-1470625 - TCGA-EE-A185-06 COSM3502798 c.2056C>T p.L686F Substitution - Missense 15:59174234-59174234 - 8066503 COSM3771268 c.467G>A p.R156Q Substitution - Missense 17:1482533-1482533 - TCGA-AX-A0J1-01 COSM963421 c.3237T>C p.D1079D Substitution - coding silent 15:59138211-59138211 - TCGA-60-2720-01 COSM700829 c.760G>T p.E254* Substitution - Nonsense 15:59224706-59224706 - RKO COSM2738140 c.137G>A p.G46D Substitution - Missense 17:1483715-1483715 - CHEWS027 COSM4578380 c.1951_1953delGAG p.E651delE Deletion - In frame 15:59178489-59178491 - 468 COSM4437445 c.45T>A p.D15E Substitution - Missense 17:1484229-1484229 - AOCS-106-1-1 COSM3983259 c.1470-7C>G p.? Unknown 17:1475039-1475039 - PTC-7C COSM436052 c.2372A>G p.Q791R Substitution - Missense 17:1470224-1470224 - TCGA-F5-6814-01 COSM3420487 c.961G>T p.E321* Substitution - Nonsense 15:59218037-59218037 - YUROC COSM5385730 c.2091C>T p.V697V Substitution - coding silent 17:1471087-1471087 - SNU-175 COSM2738102 c.1689G>A p.E563E Substitution - coding silent 17:1474613-1474613 - TCGA-EE-A20B-06 COSM3502808 c.724G>A p.G242S Substitution - Missense 15:59224742-59224742 - YULETA COSM3502810 c.257C>T p.P86L Substitution - Missense 15:59256359-59256359 - 1N54-VS-1T54 COSM4976990 c.779A>G p.D260G Substitution - Missense 17:1480549-1480549 - CRC-14T COSM5452105 c.3269C>T p.T1090M Substitution - Missense 15:59137438-59137438 - CHC322T COSM251263 c.707_719del13 p.Q236fs*17 Deletion - Frameshift 17:1480609-1480621 - Pat_76_B COSM5849461 c.576_577CC>TT p.L193F Substitution - Missense 15:59227524-59227525 - TCGA-G9-6351-01 COSM3672077 c.1641G>T p.P547P Substitution - coding silent 15:59202383-59202383 - TCGA-AX-A0J1-01 COSM963429 c.2096C>T p.A699V Substitution - Missense 15:59174194-59174194 - TCGA-29-1777-01 COSM1323919 c.1983G>C p.S661S Substitution - coding silent 15:59178459-59178459 - Gp5D COSM2738086 c.2351A>G p.N784S Substitution - Missense 17:1470245-1470245 - sysucc-1317T COSM3514431 c.2846C>T p.A949V Substitution - Missense 17:1467856-1467856 - OSCC-GB_00640111 COSM4885281 c.2691C>A p.G897G Substitution - coding silent 17:1468088-1468088 - HCC27T COSM3706654 c.2030T>G p.F677C Substitution - Missense 15:59178412-59178412 - TCGA-E5-A2PC-01 COSM1302419 c.1203C>T p.F401F Substitution - coding silent 17:1478180-1478180 - PCSI_0139_Pa_X COSM3378084 c.2961-4C>A p.? Unknown 17:1467345-1467345 - DLD1 COSM1678505 c.487C>T p.R163W Substitution - Missense 15:59231725-59231725 - TCGA-AP-A059-01 COSM963422 c.3019C>T p.R1007* Substitution - Nonsense 15:59153651-59153651 - TCGA-A4-8310-01 COSM3988027 c.855G>C p.L285L Substitution - coding silent 15:59223114-59223114 - HCC27 COSM3706654 c.2030T>G p.F677C Substitution - Missense 15:59178412-59178412 - 18195 COSM1302419 c.1203C>T p.F401F Substitution - coding silent 17:1478180-1478180 - TCGA-AA-3660-01 COSM1380982 c.1888C>T p.R630C Substitution - Missense 17:1471935-1471935 - ESO-752 COSM1258539 c.725delG p.G242fs*21 Deletion - Frameshift 15:59224741-59224741 - Gp5D COSM2219713 c.2502delT p.F834fs*21 Deletion - Frameshift 15:59163282-59163282 - TCGA-CA-6717-01 COSM1373827 c.67G>A p.D23N Substitution - Missense 15:59272386-59272386 - C004 COSM5521761 c.1423C>T p.L475L Substitution - coding silent 17:1477551-1477551 - UM-SCC-17B COSM4598884 c.214G>T p.V72F Substitution - Missense 17:1483638-1483638 - TCGA-DI-A0WH-01 COSM963427 c.2204A>G p.N735S Substitution - Missense 15:59173876-59173876 - TCGA-BS-A0UJ-01 COSM975645 c.998C>A p.P333Q Substitution - Missense 17:1478725-1478725 - CPCG0388-F1 COSM4966623 c.2044G>A p.E682K Substitution - Missense 15:59178398-59178398 - PD4102a COSM162747 c.2439G>T p.K813N Substitution - Missense 15:59171938-59171938 - TCGA-AP-A0LM-01 COSM963434 c.1670G>A p.R557H Substitution - Missense 15:59202354-59202354 - TCGA-ER-A2NC-06 COSM3514433 c.2789C>T p.T930I Substitution - Missense 17:1467990-1467990 - TCGA-D5-6928-01 COSM1373812 c.1962C>T p.G654G Substitution - coding silent 15:59178480-59178480 - CSCC-15-T COSM4462702 c.1152C>T p.L384L Substitution - coding silent 17:1478448-1478448 - HT-29 COSM1683483 c.2871_2872insC p.G960fs*104 Insertion - Frameshift 15:59158293-59158294 - T3724 COSM4704902 c.2477G>A p.R826Q Substitution - Missense 17:1469559-1469559 - CHC361TA COSM3667776 c.29A>G p.H10R Substitution - Missense 15:59272424-59272424 - TCGA-AP-A056-01 COSM963428 c.2127C>T p.F709F Substitution - coding silent 15:59174163-59174163 - TCGA-AX-A063-01 COSM975641 c.2901G>A p.T967T Substitution - coding silent 17:1467539-1467539 - TCGA-BT-A3PH-01 COSM1302418 c.1593C>A p.L531L Substitution - coding silent 17:1474830-1474830 - SNUH_G76_S1 COSM2738077 c.2742C>T p.I914I Substitution - coding silent 17:1468037-1468037 - PD8969a COSM5789416 c.1943G>T p.W648L Substitution - Missense 17:1471310-1471310 - 587256 COSM1216372 c.1033G>A p.A345T Substitution - Missense 17:1478690-1478690 - ICGC_0029 COSM218482 c.997G>A p.G333R Substitution - Missense 15:59218001-59218001 - 5_PRE-TREATMENT COSM1724800 c.848_849insT p.H284fs*19 Insertion - Frameshift 15:59223120-59223121 - TCGA-C4-A0F7-01 COSM417186 c.1892G>A p.R631H Substitution - Missense 17:1471931-1471931 - 8012854 COSM218482 c.997G>A p.G333R Substitution - Missense 15:59218001-59218001 - TCGA-AA-3715-01 COSM269670 c.2038G>A p.A680T Substitution - Missense 15:59178404-59178404 - 46M COSM5588378 c.1116G>A p.E372E Substitution - coding silent 17:1478484-1478484 - TCGA-33-4566-01 COSM704967 c.998C>T p.P333L Substitution - Missense 17:1478725-1478725 - 35M COSM5581784 c.2219G>A p.R740K Substitution - Missense 17:1470477-1470477 - TCGA-CH-5761-01 COSM1129164 c.41A>C p.H14P Substitution - Missense 15:59272412-59272412 - CHC205T COSM3765988 c.3054G>T p.L1018L Substitution - coding silent 17:1467248-1467248 - 394 COSM3722673 c.2006A>T p.K669M Substitution - Missense 17:1471247-1471247 - TCGA-AZ-6598-01 COSM1380981 c.2326C>A p.H776N Substitution - Missense 17:1470270-1470270 - PD4105a COSM162745 c.1032C>T p.D344D Substitution - coding silent 17:1478691-1478691 - TCGA-BR-8361-01 COSM4055936 c.1132G>A p.D378N Substitution - Missense 15:59214696-59214696 - HCC97T COSM3717187 c.442-4C>G p.? Unknown 17:1482562-1482562 - HCT8 COSM1678504 c.1693A>T p.I565L Substitution - Missense 15:59202331-59202331 - TCGA-CD-5813-01 COSM4055935 c.1218T>G p.N406K Substitution - Missense 15:59214285-59214285 - SNUH_G10_S1 COSM4000015 c.1377+9T>G p.? Unknown 17:1477882-1477882 - TCGA-G3-A5SK-01 COSM4927516 c.1057C>T p.R353C Substitution - Missense 17:1478666-1478666 - CHC322T COSM251263 c.707_719del13 p.Q236fs*17 Deletion - Frameshift 17:1480609-1480621 - SNU-C1 COSM2738077 c.2742C>T p.I914I Substitution - coding silent 17:1468037-1468037 - TCGA-BR-8078-01 COSM4064055 c.79G>A p.A27T Substitution - Missense 17:1484195-1484195 - 06-P036 COSM4578379 c.3235G>A p.D1079N Substitution - Missense 15:59138213-59138213 - TCGA-CK-5913-01 COSM1380986 c.1020G>A p.A340A Substitution - coding silent 17:1478703-1478703 - T2269 COSM4704924 c.250A>C p.N84H Substitution - Missense 15:59256366-59256366 - RMS2114 COSM5881098 c.1165G>T p.G389C Substitution - Missense 17:1478435-1478435 - TCGA-CG-5733-01 COSM4064045 c.1589T>C p.L530P Substitution - Missense 17:1474834-1474834 - PTC-515C COSM4128312 c.2673A>G p.A891A Substitution - coding silent 15:59161185-59161185 - YUMER COSM1709541 c.1754C>T p.P585L Substitution - Missense 17:1472167-1472167 - TCGA-A8-A085-01 COSM434093 c.1961G>T p.G654V Substitution - Missense 15:59178481-59178481 - CSCC-29-T COSM4469754 c.1619C>T p.P540L Substitution - Missense 15:59202405-59202405 - LUAD-E00934 COSM393255 c.1754G>A p.R585H Substitution - Missense 15:59195512-59195512 - ATL033 COSM5706295 c.14T>C p.L5P Substitution - Missense 17:1484260-1484260 - TCGA-EE-A2MR-06 COSM3502800 c.1623C>T p.F541F Substitution - coding silent 15:59202401-59202401 - TCGA-FD-A3B6-01 COSM1302420 c.392G>A p.R131H Substitution - Missense 17:1482910-1482910 - HCC057T COSM5807866 c.2958A>C p.K986N Substitution - Missense 15:59153712-59153712 - E13 COSM1666397 c.2334+5G>A p.? Unknown 15:59173741-59173741 - C086 COSM5535077 c.1074C>T p.A358A Substitution - coding silent 15:59217924-59217924 - TCGA-AZ-6598-01 COSM1380983 c.1622G>A p.S541N Substitution - Missense 17:1474680-1474680 - 587278 COSM1216370 c.386C>A p.P129H Substitution - Missense 17:1482916-1482916 - PTC-7C COSM4129575 c.2544C>A p.G848G Substitution - coding silent 17:1468458-1468458 - PTC-10C COSM4129573 c.2652T>G p.I884M Substitution - Missense 17:1468256-1468256 - ESO-0129 COSM1258534 c.2092C>T p.R698W Substitution - Missense 17:1471086-1471086 - TCGA-FR-A3R1-01 COSM3514429 c.2980C>T p.P994S Substitution - Missense 17:1467322-1467322 - STC252 COSM5054382 c.183T>C p.P61P Substitution - coding silent 15:59261474-59261474 - SNU-175 COSM2738132 c.520A>G p.K174E Substitution - Missense 17:1482480-1482480 - CHEWS033 COSM4579450 c.387C>T p.P129P Substitution - coding silent 17:1482915-1482915 - TCGA-AA-3510-01 COSM1373822 c.1038G>A p.E346E Substitution - coding silent 15:59217960-59217960 - TCGA-FW-A3R5-06 COSM3889338 c.2520C>T p.A840A Substitution - coding silent 17:1468482-1468482 - TCGA-BR-4361-01 COSM4064050 c.368C>T p.A123V Substitution - Missense 17:1482934-1482934 - SJBALL020939_D1 COSM4993907 c.2285G>A p.R762H Substitution - Missense 17:1470311-1470311 - PD24207a COSM5768214 c.1155C>T p.G385G Substitution - coding silent 15:59214673-59214673 - TCGA-BS-A0UJ-01 COSM963447 c.244T>C p.Y82H Substitution - Missense 15:59256372-59256372 - TCGA-BR-8487-01 COSM4055926 c.3133C>T p.P1045S Substitution - Missense 15:59138315-59138315 - TCGA-AP-A056-01 COSM963431 c.1982C>T p.S661L Substitution - Missense 15:59178460-59178460 - SNUH_G14_S1 COSM3680080 c.251T>G p.V84G Substitution - Missense 17:1483051-1483051 - TCGA-FK-A3SD-01 COSM3370618 c.1121C>T p.P374L Substitution - Missense 17:1478479-1478479 - 413LT COSM4386377 c.1177T>C p.F393L Substitution - Missense 17:1478423-1478423 - PCSI_0329_Pa_P_526 COSM4962461 c.2760C>T p.I920I Substitution - coding silent 15:59161098-59161098 - Br27P COSM40355 c.542G>C p.G181A Substitution - Missense 15:59227559-59227559 - TCGA-BP-4967-01 COSM470896 c.2044G>C p.E682Q Substitution - Missense 15:59178398-59178398 - TCGA-D7-6519-01 COSM4064048 c.731A>G p.N244S Substitution - Missense 17:1480597-1480597 - YUKAT COSM5385732 c.842A>G p.N281S Substitution - Missense 17:1479665-1479665 - TCGA-EE-A2MS-06 COSM3502799 c.2013G>A p.L671L Substitution - coding silent 15:59178429-59178429 - CSCC-41-T COSM4468337 c.48C>T p.F16F Substitution - coding silent 17:1484226-1484226 - T684 COSM4704914 c.72C>T p.S24S Substitution - coding silent 17:1484202-1484202 - TCGA-32-4208-01 COSM3401852 c.1336G>C p.V446L Substitution - Missense 15:59210540-59210540 - VACO4S COSM4657145 c.1062G>A p.A354A Substitution - coding silent 15:59217936-59217936 - TCGA-BR-8589-01 COSM4055939 c.219T>G p.I73M Substitution - Missense 15:59261438-59261438 - T3174 COSM4704908 c.1027C>T p.R343* Substitution - Nonsense 17:1478696-1478696 - TCGA-BQ-7061-01 COSM3988026 c.1395C>T p.D465D Substitution - coding silent 15:59208816-59208816 - T407 COSM4704912 c.472G>A p.D158N Substitution - Missense 17:1482528-1482528 - NPC8D COSM4995709 c.793G>A p.E265K Substitution - Missense 17:1480535-1480535 - TCGA-D1-A174-01 COSM975646 c.973G>A p.A325T Substitution - Missense 17:1479445-1479445 - TCGA-EE-A2GP-06 COSM3514435 c.2324A>G p.D775G Substitution - Missense 17:1470272-1470272 - LUAD-U6SJ7 COSM400179 c.1195G>C p.E399Q Substitution - Missense 17:1478188-1478188 - TCGA-EJ-7123-01 COSM3672078 c.1055G>T p.R352L Substitution - Missense 15:59217943-59217943 - BD10T COSM5514561 c.1338A>G p.V446V Substitution - coding silent 15:59210538-59210538 - C086 COSM5535076 c.1876C>T p.R626W Substitution - Missense 15:59188146-59188146 - TCGA-Q1-A73O-01 COSM4834829 c.3154C>T p.Q1052* Substitution - Nonsense 15:59138294-59138294 - SNU-C4 COSM4652610 c.119A>G p.K40R Substitution - Missense 15:59272334-59272334 - HCC97 COSM3717187 c.442-4C>G p.? Unknown 17:1482562-1482562 - TCGA-AA-3663-01 COSM1380988 c.495G>A p.K165K Substitution - coding silent 17:1482505-1482505 - 2461402 COSM5415859 c.3136C>A p.Q1046K Substitution - Missense 15:59138312-59138312 - TCGA-DA-A1I1-06 COSM3502810 c.257C>T p.P86L Substitution - Missense 15:59256359-59256359 - TCGA-HU-A4GQ-01 COSM4064039 c.3018G>A p.S1006S Substitution - coding silent 17:1467284-1467284 - BD236T COSM5519428 c.442-4C>A p.? Unknown 17:1482562-1482562 - 31231321 COSM1582291 c.147+5C>T p.? Unknown 15:59272301-59272301 - TCGA-JW-A5VL-01 COSM4846988 c.186C>G p.F62L Substitution - Missense 15:59261471-59261471 - TCGA-D1-A168-01 COSM963445 c.452C>T p.P151L Substitution - Missense 15:59231760-59231760 - TCGA-A3-3363-01 COSM1493481 c.1820T>C p.V607A Substitution - Missense 15:59188202-59188202 - 8067509 COSM4406519 c.1107+2T>G p.? Unknown 17:1478614-1478614 - TCGA-A8-A0A6-01 COSM3816460 c.1418T>G p.V473G Substitution - Missense 15:59208793-59208793 - TCGA-D5-6931-01 COSM1380985 c.1038C>T p.L346L Substitution - coding silent 17:1478685-1478685 - DLD1 COSM4623136 c.1162G>T p.D388Y Substitution - Missense 15:59214666-59214666 - PT49 COSM5936332 c.2053C>T p.P685S Substitution - Missense 17:1471125-1471125 - SNUH_G76_S1 COSM3755263 c.1653T>C p.F551F Substitution - coding silent 17:1474649-1474649 - TCGA-JX-A3Q0-01 COSM4824019 c.2949C>T p.I983I Substitution - coding silent 17:1467491-1467491 - HX33T COSM3706654 c.2030T>G p.F677C Substitution - Missense 15:59178412-59178412 - TCGA-EE-A2MS-06 COSM3502801 c.1578T>C p.L526L Substitution - coding silent 15:59205438-59205438 - Pat_76_A COSM5849461 c.576_577CC>TT p.L193F Substitution - Missense 15:59227524-59227525 - HCC084T COSM5822337 c.2043C>G p.F681L Substitution - Missense 17:1471135-1471135 - TCGA-DJ-A13X-01 COSM3370215 c.1001G>A p.G334D Substitution - Missense 15:59217997-59217997 - TCGA-EE-A181-06 COSM3502809 c.483C>A p.T161T Substitution - coding silent 15:59231729-59231729 - BRC41 COSM5027986 c.1057G>A p.D353N Substitution - Missense 15:59217941-59217941 - L13 COSM5369096 c.734A>C p.K245T Substitution - Missense 15:59224732-59224732 - I2L-P7-Tumor-Organoid COSM5363856 c.982delG p.E328fs*4 Deletion - Frameshift 17:1479436-1479436 - TCGA-BG-A0M6-01 COSM963425 c.2277C>A p.G759G Substitution - coding silent 15:59173803-59173803 - TCGA-D8-A1XM-01 COSM1479245 c.1960C>T p.R654W Substitution - Missense 17:1471293-1471293 - T2940 COSM4630266 c.825C>T p.S275S Substitution - coding silent 17:1479682-1479682 - 587380 COSM1216371 c.1883C>T p.A628V Substitution - Missense 17:1471940-1471940 - TCGA-HU-A4G9-01 COSM2738114 c.1295C>T p.A432V Substitution - Missense 17:1478088-1478088 - sysucc-1317T COSM5448938 c.1762G>A p.V588I Substitution - Missense 17:1472159-1472159 - TCGA-B8-5163-01 COSM470895 c.2457A>T p.E819D Substitution - Missense 15:59171920-59171920 - LOVO COSM2219733 c.1581delT p.F527fs*16 Deletion - Frameshift 15:59205435-59205435 - SJRHB036A COSM3738009 c.2618C>T p.P873L Substitution - Missense 17:1468290-1468290 - OSCC-GB_00410111 COSM3711835 c.1836G>T p.L612L Substitution - coding silent 15:59188186-59188186 - TCGA-AC-A23H-01 COSM3818854 c.783C>T p.F261F Substitution - coding silent 17:1480545-1480545 - SNUH_G10_S1 COSM4000017 c.729C>T p.I243I Substitution - coding silent 17:1480599-1480599 - NB-0462 COSM1286448 c.83delT p.F28fs*74 Deletion - Frameshift 17:1484191-1484191 - pfg008T COSM1640308 c.147delT p.F49fs*4 Deletion - Frameshift 15:59272306-59272306 - TCGA-CK-5916-01 COSM3690459 c.2529T>A p.S843R Substitution - Missense 15:59163255-59163255 - pfg008T COSM1640591 c.2746G>T p.E916* Substitution - Nonsense 17:1468033-1468033 - Gp2D COSM2738080 c.2568T>C p.S856S Substitution - coding silent 17:1468434-1468434 - ICGC_0022 COSM218481 c.2099G>A p.R700Q Substitution - Missense 15:59174191-59174191 - PTC-54C COSM4000017 c.729C>T p.I243I Substitution - coding silent 17:1480599-1480599 - AOCS-106-1-1 COSM3983263 c.127-8G>T p.? Unknown 17:1483733-1483733 - PD4833a COSM5787604 c.2007C>T p.F669F Substitution - coding silent 15:59178435-59178435 - TCGA-CM-5861-01 COSM1380984 c.1563C>T p.T521T Substitution - coding silent 17:1474939-1474939 - L363 COSM1236085 c.2089G>A p.G697R Substitution - Missense 15:59174201-59174201 - TCGA-DK-A3X1-01 COSM3795279 c.2081C>T p.A694V Substitution - Missense 17:1471097-1471097 - SC_9047 COSM5557375 c.1752T>G p.I584M Substitution - Missense 15:59195514-59195514 - HCT-15 COSM1678505 c.487C>T p.R163W Substitution - Missense 15:59231725-59231725 - 587350 COSM1216383 c.1589T>G p.L530R Substitution - Missense 15:59205427-59205427 - TCGA-22-5491-01 COSM700830 c.1228G>A p.E410K Substitution - Missense 15:59214275-59214275 - AOCS-147-1-1 COSM3983257 c.1692G>A p.T564T Substitution - coding silent 17:1474610-1474610 - YURAY COSM5383612 c.1849C>T p.R617* Substitution - Nonsense 15:59188173-59188173 - pfg008T COSM1640591 c.2746G>T p.E916* Substitution - Nonsense 17:1468033-1468033 - ESCC_11 COSM5624338 c.2679C>T p.Y893Y Substitution - coding silent 17:1468100-1468100 - RK144_C01 COSM3744683 c.2683C>T p.R895W Substitution - Missense 15:59161175-59161175 - A9 COSM5350274 c.1612G>A p.E538K Substitution - Missense 15:59205404-59205404 - TCGA-FS-A1ZP-06 COSM3514439 c.1371G>T p.S457S Substitution - coding silent 17:1477897-1477897 - CSCC-55-T COSM4513403 c.832C>T p.H278Y Substitution - Missense 17:1479675-1479675 - CSCC-27-T COSM4468115 c.1422C>T p.F474F Substitution - coding silent 17:1477552-1477552 - TCGA-A6-6653-01 COSM1373820 c.1084C>T p.R362W Substitution - Missense 15:59217914-59217914 - TCGA-D5-6928-01 COSM1380989 c.391C>T p.R131C Substitution - Missense 17:1482911-1482911 - MS4 COSM1165408 c.3062C>T p.P1021L Substitution - Missense 15:59153608-59153608 - 721LT COSM4381649 c.2581T>A p.F861I Substitution - Missense 17:1468421-1468421 - PD7443a COSM3720241 c.1188+8C>G p.? Unknown 15:59214632-59214632 - 254891 COSM3724808 c.1116G>C p.E372D Substitution - Missense 17:1478484-1478484 - TCGA-A4-7734-01 COSM3988774 c.2960+2T>G p.? Unknown 17:1467478-1467478 - AOCS-078-1-9 COSM2738083 c.2505+5G>A p.? Unknown 17:1469526-1469526 - HCC162 COSM3717185 c.2172A>G p.R724R Substitution - coding silent 17:1470625-1470625 - sysucc-867T COSM5486872 c.2386C>T p.R796* Substitution - Nonsense 15:59171991-59171991 - TCGA-QB-A6FS-06 COSM3889340 c.2478G>A p.R826R Substitution - coding silent 17:1469558-1469558 - Gp2D COSM2738086 c.2351A>G p.N784S Substitution - Missense 17:1470245-1470245 - PTC_341 COSM5960369 c.276G>T p.L92L Substitution - coding silent 17:1483026-1483026 - RK306_C01 COSM4779507 c.2082G>C p.K694N Substitution - Missense 15:59174208-59174208 - TCGA-BS-A0UF-01 COSM963441 c.1377C>A p.I459I Substitution - coding silent 15:59208834-59208834 - 41T COSM3711835 c.1836G>T p.L612L Substitution - coding silent 15:59188186-59188186 - Gp2D COSM4627329 c.196C>T p.P66S Substitution - Missense 15:59261461-59261461 - TCGA-B2-5641-01 COSM470899 c.792G>C p.V264V Substitution - coding silent 15:59223177-59223177 - TCGA-GL-7773-01 COSM3988776 c.1899C>T p.Y633Y Substitution - coding silent 17:1471924-1471924 - LUAD-F00121 COSM365683 c.1695A>G p.I565M Substitution - Missense 15:59202329-59202329 - Pat_44_B COSM5138211 c.1739C>T p.T580M Substitution - Missense 15:59195527-59195527 - ESCC_18 COSM5626070 c.1401C>T p.C467C Substitution - coding silent 15:59208810-59208810 - TCGA-BG-A0LX-01 COSM963444 c.726C>T p.G242G Substitution - coding silent 15:59224740-59224740 - T19 COSM5342593 c.933G>T p.L311L Substitution - coding silent 15:59218065-59218065 - TCGA-D5-6928-01 COSM3755261 c.1990C>T p.R664* Substitution - Nonsense 17:1471263-1471263 - TCGA-BP-5186-01 COSM472321 c.1469C>A p.T490K Substitution - Missense 17:1477505-1477505 - TCGA-QA-A7B7-01 COSM4909953 c.1417G>T p.V473L Substitution - Missense 15:59208794-59208794 - P106 COSM1736367 c.2653A>G p.N885D Substitution - Missense 15:59161205-59161205 - TCGA-F4-6703-01 COSM1380990 c.250G>A p.V84M Substitution - Missense 17:1483052-1483052 - TCGA-DK-A3WW-01 COSM3794275 c.2239G>C p.G747R Substitution - Missense 15:59173841-59173841 - 8068539 COSM218482 c.997G>A p.G333R Substitution - Missense 15:59218001-59218001 - 5_RESISTANT COSM1724928 c.854_855insC p.N287fs*16 Insertion - Frameshift 15:59223114-59223115 - pfg008T COSM1640308 c.147delT p.F49fs*4 Deletion - Frameshift 15:59272306-59272306 - T276 COSM4704904 c.1681C>T p.R561W Substitution - Missense 17:1474621-1474621 - TCGA-AX-A05Z-01 COSM963430 c.2056C>A p.L686I Substitution - Missense 15:59174234-59174234 - TCGA-AO-A128-01 COSM3816461 c.1343A>G p.D448G Substitution - Missense 15:59210533-59210533 - 169 COSM3728813 c.1530+6G>T p.? Unknown 15:59208675-59208675 - TCGA-C8-A1HM-01 COSM434094 c.907G>C p.E303Q Substitution - Missense 15:59223062-59223062 - TCGA-AP-A0LM-01 COSM963433 c.1807G>T p.V603L Substitution - Missense 15:59188215-59188215 - CSCC-27-T COSM4469754 c.1619C>T p.P540L Substitution - Missense 15:59202405-59202405 - TCGA-BP-4986-01 COSM470898 c.1144T>C p.Y382H Substitution - Missense 15:59214684-59214684 - TCGA-HF-7132-01 COSM2738136 c.321C>T p.S107S Substitution - coding silent 17:1482981-1482981 - TCGA-CC-A3MC-01 COSM4919482 c.1357A>C p.K453Q Substitution - Missense 15:59210519-59210519 - TCGA-22-4604-01 COSM700828 c.592A>G p.R198G Substitution - Missense 15:59227509-59227509 - RK096_C01 COSM1630061 c.944G>A p.R315Q Substitution - Missense 17:1479474-1479474 - T3038 COSM4704922 c.1770C>T p.N590N Substitution - coding silent 15:59195496-59195496 - TCGA-IR-A3LA-01 COSM1258535 c.2721C>G p.L907L Substitution - coding silent 17:1468058-1468058 - CSCC-16-T COSM4539586 c.2704G>A p.G902R Substitution - Missense 15:59161154-59161154 - TCGA-G4-6588-01 COSM1380987 c.857C>T p.A286V Substitution - Missense 17:1479650-1479650 - T47D COSM1679352 c.1039G>A p.A347T Substitution - Missense 17:1478684-1478684 - 389 COSM4427591 c.3255T>A p.P1085P Substitution - coding silent 15:59137452-59137452 - T3094 COSM4704906 c.1580delA p.N527fs*21 Deletion - Frameshift 17:1474843-1474843 - T2938 COSM4704914 c.72C>T p.S24S Substitution - coding silent 17:1484202-1484202 - TCGA-IR-A3LK-01 COSM4817633 c.1668C>T p.L556L Substitution - coding silent 17:1474634-1474634 - CX-1 COSM4611562 c.2876_2877insC p.G960fs*104 Insertion - Frameshift 15:59158288-59158289 - SH-0622 COSM5018390 c.3113delC p.P1038fs*68 Deletion - Frameshift 15:59138335-59138335 - Pat_76_A COSM5851847 c.1442C>T p.T481I Substitution - Missense 17:1477532-1477532 - 2461403 COSM5415859 c.3136C>A p.Q1046K Substitution - Missense 15:59138312-59138312 - TCGA-FD-A3N5-01 COSM1301273 c.294C>T p.N98N Substitution - coding silent 15:59256322-59256322 - TCGA-A6-6780-01 COSM1373821 c.1054C>T p.R352W Substitution - Missense 15:59217944-59217944 - NCI-H727 COSM2738074 c.2869G>A p.V957M Substitution - Missense 17:1467571-1467571 - ESCC_81 COSM5635867 c.475G>T p.A159S Substitution - Missense 15:59231737-59231737 - HX11T COSM1609857 c.1297-7C>T p.? Unknown 17:1477978-1477978 - 12586 COSM5616894 c.2814C>T p.S938S Substitution - coding silent 17:1467888-1467888 - C91 COSM4444567 c.287G>A p.R96H Substitution - Missense 17:1483015-1483015 - I2L-P19Ta-Tumor-Biopsy COSM5364002 c.2684G>A p.R895H Substitution - Missense 17:1468095-1468095 - TCGA-G9-6342-01 COSM3672353 c.1078G>T p.G360W Substitution - Missense 17:1478645-1478645 - EGC15 COSM5054381 c.1794G>A p.W598* Substitution - Nonsense 15:59195472-59195472 - TCGA-EE-A29B-06 COSM3502807 c.1025C>T p.T342I Substitution - Missense 15:59217973-59217973 - BD175T COSM5507896 c.1446C>G p.L482L Substitution - coding silent 15:59208765-59208765 - S0004 COSM5882598 c.722C>G p.S241W Substitution - Missense 15:59224744-59224744 - TCGA-DK-A1A5-01 COSM416877 c.1335C>T p.I445I Substitution - coding silent 15:59210541-59210541 - TCGA-EE-A3JI-06 COSM3514431 c.2846C>T p.A949V Substitution - Missense 17:1467856-1467856 - ML_77_T_01 COSM5034020 c.289C>T p.R97W Substitution - Missense 17:1483013-1483013 - CN-AML-NR-08-Dx COSM5426040 c.2365A>G p.K789E Substitution - Missense 15:59172012-59172012 - Pat_59_B COSM5849460 c.758G>A p.R253Q Substitution - Missense 15:59224708-59224708 - 587228 COSM1216380 c.285G>A p.M95I Substitution - Missense 15:59256331-59256331 - 587338 COSM1216381 c.620G>A p.R207Q Substitution - Missense 15:59227481-59227481 - C0013T COSM4151473 c.459G>A p.K153K Substitution - coding silent 17:1482541-1482541 - TCGA-DD-A1EB-01 COSM4928838 c.1196A>G p.E399G Substitution - Missense 17:1478187-1478187 - TCGA-EK-A2RB-01 COSM4820084 c.1242C>T p.F414F Substitution - coding silent 17:1478141-1478141 - PTC-7C COSM4129578 c.636T>C p.G212G Substitution - coding silent DLD1 COSM1678504 c.1693A>T p.I565L Substitution - Missense 15:59202331-59202331 - TCGA-ER-A19E-06 COSM3514445 c.311C>A p.S104Y Substitution - Missense 17:1482991-1482991 - TCGA-EE-A3JA-06 COSM3514443 c.341C>T p.A114V Substitution - Missense 17:1482961-1482961 - TCGA-AK-3431-01 COSM2219786 c.367A>G p.K123E Substitution - Missense 15:59236638-59236638 - OSCC-GB_01060111 COSM4882542 c.58G>T p.E20* Substitution - Nonsense 17:1484216-1484216 - HCT8 COSM1678505 c.487C>T p.R163W Substitution - Missense 15:59231725-59231725 - TCGA-AX-A0J0-01 COSM963443 c.1098C>T p.F366F Substitution - coding silent 15:59217900-59217900 - TCGA-BR-8382-01 COSM4064053 c.213C>T p.G71G Substitution - coding silent 17:1483639-1483639 - 587342 COSM1216384 c.2146G>A p.V716I Substitution - Missense 15:59174144-59174144 - pfg217T COSM1479245 c.1960C>T p.R654W Substitution - Missense 17:1471293-1471293 - 522_T COSM3956785 c.2684G>T p.R895L Substitution - Missense 15:59161174-59161174 - 8036161 COSM3387718 c.1539G>T p.A513A Substitution - coding silent 17:1474963-1474963 - Gp2D COSM2219713 c.2502delT p.F834fs*21 Deletion - Frameshift 15:59163282-59163282 - BD124T COSM5493292 c.2164+6_2164+7insT p.? Unknown 15:59174119-59174120 - SMYM-PRGP COSM3727653 c.187C>T p.R63W Substitution - Missense 17:1483665-1483665 - T2941 COSM4704923 c.750C>T p.D250D Substitution - coding silent 15:59224716-59224716 - TP_2064 COSM5550544 c.2243C>T p.A748V Substitution - Missense 17:1470453-1470453 - TCGA-AA-3663-01 COSM1373823 c.719T>G p.L240R Substitution - Missense 15:59224747-59224747 - TCGA-AX-A0J0-01 COSM975644 c.1663G>A p.E555K Substitution - Missense 17:1474639-1474639 - TCGA-AP-A0LM-01 COSM963449 c.106G>A p.V36M Substitution - Missense 15:59272347-59272347 - TCGA-DK-A3IQ-01 COSM1301272 c.1506C>T p.F502F Substitution - coding silent 15:59208705-59208705 - TCGA-EE-A3JI-06 COSM3502811 c.127T>G p.Y43D Substitution - Missense 15:59272326-59272326 - T3094 COSM4704900 c.3063C>T p.V1021V Substitution - coding silent 17:1465750-1465750 - TCGA-BS-A0TJ-01 COSM963448 c.213G>T p.K71N Substitution - Missense 15:59261444-59261444 - PD4613a COSM5768481 c.218T>C p.I73T Substitution - Missense 15:59261439-59261439 - TCGA-BF-A3DL-01 COSM4904430 c.606C>T p.F202F Substitution - coding silent 17:1480802-1480802 - 2246940 COSM4413491 c.2417G>A p.G806D Substitution - Missense 15:59171960-59171960 - HF-19967 COSM1192982 c.3141_3142CA>T p.K1048fs*58 Complex - frameshift 15:59138306-59138307 - TCGA-BR-8680-01 COSM2219768 c.1402G>A p.A468T Substitution - Missense 15:59208809-59208809 - YUIRI COSM1708239 c.161C>G p.S54C Substitution - Missense 15:59261496-59261496 - TCGA-AN-A0AK-01 COSM3816459 c.2967C>T p.Y989Y Substitution - coding silent 15:59153703-59153703 - sysucc-1397T COSM975643 c.1822C>T p.R608C Substitution - Missense 17:1472001-1472001 - TCGA-CM-5861-01 COSM1380979 c.3083G>T p.R1028L Substitution - Missense 17:1465730-1465730 - 37T COSM3733924 c.142A>G p.I48V Substitution - Missense 15:59272311-59272311 - HCC10T COSM131195 c.2693A>G p.Y898C Substitution - Missense 17:1468086-1468086 - TCGA-EE-A2MK-06 COSM3514441 c.607C>T p.H203Y Substitution - Missense 17:1480801-1480801 - HCA7 COSM4630266 c.825C>T p.S275S Substitution - coding silent 17:1479682-1479682 - SS6003149 COSM3983032 c.2786-5T>G p.? Unknown 15:59158384-59158384 - AOCS-135-8-X COSM3981584 c.3250+1G>A p.? Unknown 15:59138197-59138197 - TCGA-F1-A448-01 COSM4055938 c.236C>T p.A79V Substitution - Missense 15:59261421-59261421 - 4_RESISTANT COSM1724147 c.48C>T p.V16V Substitution - coding silent 15:59272405-59272405 - TCGA-IR-A3LK-01 COSM4816465 c.173C>G p.S58* Substitution - Nonsense 15:59261484-59261484 - TCGA-F5-6814-01 COSM3420484 c.1563G>A p.R521R Substitution - coding silent 15:59205453-59205453 - TCGA-DK-A1A3-01 COSM417187 c.2711A>G p.Q904R Substitution - Missense 17:1468068-1468068 - TCGA-BH-A18V-06 COSM3816462 c.672A>C p.K224N Substitution - Missense 15:59224794-59224794 - TCGA-AP-A051-01 COSM963423 c.2578C>T p.R860C Substitution - Missense 15:59163206-59163206 - 4_PRE-TREATMENT COSM1724147 c.48C>T p.V16V Substitution - coding silent 15:59272405-59272405 - BD57T COSM5510861 c.2284C>T p.R762C Substitution - Missense 17:1470312-1470312 - SNUH_G26_S1 COSM3999575 c.1008C>T p.S336S Substitution - coding silent 15:59217990-59217990 - LC_C27 COSM1189353 c.2417G>A p.R806H Substitution - Missense 17:1470179-1470179 - TCGA-G4-6586-01 COSM1380980 c.2476C>T p.R826W Substitution - Missense 17:1469560-1469560 - TCGA-A6-5659-01 COSM3690460 c.1487A>G p.N496S Substitution - Missense 15:59208724-59208724 - TCGA-A8-A09B-01 COSM5832929 c.640_641delCA p.Q214fs*33 Deletion - Frameshift 15:59227460-59227461 - HCT15 COSM1678505 c.487C>T p.R163W Substitution - Missense 15:59231725-59231725 - 585260 COSM321889 c.757C>G p.R253G Substitution - Missense 15:59224709-59224709 - TCGA-EE-A3AF-06 COSM3514437 c.2018A>T p.Y673F Substitution - Missense 17:1471235-1471235 - CN-AML-08-T COSM5426040 c.2365A>G p.K789E Substitution - Missense 15:59172012-59172012 - TCGA-AP-A059-01 COSM975642 c.2134G>T p.G712C Substitution - Missense 17:1470663-1470663 - Pat_14_A COSM5849459 c.2475_2476delCC p.L826fs*6 Deletion - Frameshift 15:59171901-59171902 - T3 COSM5619202 c.2697G>A p.K899K Substitution - coding silent 17:1468082-1468082 - 522_T COSM3958034 c.635G>C p.G212A Substitution - Missense 17:1480773-1480773 - I2L-P19Ta-Tumor-Organoid COSM5364002 c.2684G>A p.R895H Substitution - Missense 17:1468095-1468095 - 587278 COSM1216369 c.3013G>A p.G1005S Substitution - Missense 17:1467289-1467289 - CHC361TA COSM3667776 c.29A>G p.H10R Substitution - Missense 15:59272424-59272424 - TCGA-CG-4305-01 COSM4064041 c.2839C>T p.Q947* Substitution - Nonsense 17:1467863-1467863 - sysucc-1370T COSM4440781 c.1439C>T p.T480M Substitution - Missense 15:59208772-59208772 - TCGA-CG-5728-01 COSM4064043 c.2400G>A p.T800T Substitution - coding silent 17:1470196-1470196 - T3064 COSM2738079 c.2708G>A p.R903Q Substitution - Missense 17:1468071-1468071 - ESO-117 COSM1258535 c.2721C>G p.L907L Substitution - coding silent 17:1468058-1468058 - TCGA-AX-A0J0-01 COSM963424 c.2462T>C p.I821T Substitution - Missense 15:59171915-59171915 - ccRCC-60 COSM1662966 c.1783C>A p.P595T Substitution - Missense 15:59195483-59195483 - HCT-15 COSM1678504 c.1693A>T p.I565L Substitution - Missense 15:59202331-59202331 - TCGA-A3-3374-01 COSM1493479 c.513A>G p.G171G Substitution - coding silent 15:59227588-59227588 - TCGA-GV-A3JX-01 COSM1302417 c.2958C>T p.G986G Substitution - coding silent 17:1467482-1467482 - RK189_C01 COSM1630060 c.1823G>C p.R608P Substitution - Missense 17:1472000-1472000 - 1920_T COSM3956786 c.1945G>T p.G649* Substitution - Nonsense 15:59178497-59178497 - CCK81 COSM2219722 c.1993G>A p.D665N Substitution - Missense 15:59178449-59178449 - HCT8 COSM4634157 c.2412C>T p.A804A Substitution - coding silent 17:1470184-1470184 - Pat_63_B COSM5849458 c.3110C>T p.P1037L Substitution - Missense 15:59138338-59138338 - ESCC_BICR_018T COSM5429062 c.1866G>A p.V622V Substitution - coding silent 17:1471957-1471957 - 2012_Recurrent COSM5346071 c.968T>C p.I323T Substitution - Missense 17:1479450-1479450 - HT29 COSM4611562 c.2876_2877insC p.G960fs*104 Insertion - Frameshift 15:59158288-59158289 - SWE-40 COSM1179933 c.3068C>A p.P1023Q Substitution - Missense 17:1465745-1465745 - 587338 COSM1216382 c.30C>A p.H10Q Substitution - Missense 15:59272423-59272423 - TCGA-AM-5820-01 COSM3755263 c.1653T>C p.F551F Substitution - coding silent 17:1474649-1474649 - T3724 COSM4704921 c.2627+1G>A p.? Unknown 15:59163156-59163156 - ESCC-134T COSM3937259 c.2450T>C p.I817T Substitution - Missense 17:1469586-1469586 - CSCC-29-T COSM4467671 c.1396C>T p.P466S Substitution - Missense 17:1477578-1477578 - AOCS-135-3-1 COSM3981584 c.3250+1G>A p.? Unknown 15:59138197-59138197 - TCGA-BR-6452-01 COSM4055934 c.1415C>T p.A472V Substitution - Missense 15:59208796-59208796 - TCGA-AX-A0J1-01 COSM963432 c.1880G>A p.R627H Substitution - Missense 15:59188142-59188142 - TCGA-CM-6677-01 COSM1373825 c.484G>A p.V162I Substitution - Missense 15:59231728-59231728 - 469 COSM4437570 c.862G>A p.E288K Substitution - Missense 17:1479645-1479645 - 1604875 COSM143370 c.290_291GG>AA p.R97Q Substitution - Missense 17:1483011-1483012 - QC2-30-T2 COSM5653717 c.1889A>T p.Q630L Substitution - Missense 15:59188133-59188133 - TCGA-D9-A6EC-06 COSM4401573 c.676C>T p.P226S Substitution - Missense 17:1480732-1480732 - TCGA-B5-A0K9-01 COSM975643 c.1822C>T p.R608C Substitution - Missense 17:1472001-1472001 - ZZUFHECRKL-G071T COSM5438916 c.255G>T p.A85A Substitution - coding silent 17:1483047-1483047 - T3021 COSM4704910 c.554A>G p.Y185C Substitution - Missense 17:1480854-1480854 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.286226 17p13.3 606538 2424602|CGAP|BC044891|A/G|coding|Arg793Gln|2377|Candidate; 2424602|CGAP|BC068013|A/G|coding|Arg791Gln|2690|Candidate; 266704|dbSNP|BC044891|C/T|non-coding||3912|Candidate; 266704|dbSNP|BC068013|C/T|non-coding||4225|Candidate; 617821|dbSNP|BC044891|C/T|non-coding||3912|Candidate; 617821|dbSNP|BC068013|C/T|non-coding||4225|Candidate Hs.654506 15q21-q22 601479 2416510|CGAP|BC098392|A/C|non-coding||4597|Validated; 2416514|CGAP|BC098392|C/G|non-coding||4618|Confirmed; 2416516|CGAP|BC098392|C/T|non-coding||4462|Candidate; 1526216|dbSNP|BC098392|A/T|coding|Ala1039Ala|3487|Candidate; 1526218|dbSNP|BC098392|G/T|non-coding||3750|Candidate; 1526219|dbSNP|BC098392|G/T|non-coding||3766|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.F63Sfs*74 c.188delT 17 1387485 NB A G Missense p.L565P c.1694T>C 17 1378128 STAD C A Nonsense p.E951* c.2851G>T 17 1371327 STAD C A Synonymous p.L964L c.2892G>T 17 1371286 LUAD C A Synonymous p.S492S c.1476G>T 17 1381191 CM C T Missense p.D1036N c.3106G>A 17 1370595 LUAD C T Missense p.R166H c.497G>A 17 1386204 BLCA C T Missense p.R666H c.1997G>A 17 1375225 BLCA C T Synonymous p.T1002T c.3006G>A 17 1370833 UCEC C T Synonymous p.T835T c.2505G>A 17 1373490 STAD G A 3-UTRSNV . c.3189+27C>T 17 1368996 CM G A 3-UTRSNV . c.3189+58C>T 17 1368965 CM G A Missense p.A149V c.446C>T 17 1386255 CM G A Missense p.A984V c.2951C>T 17 1371150 CM G A Missense p.H238Y c.712C>T 17 1384095 CM G A Missense p.L419F c.1255C>T 17 1381744 HNSC G A Missense p.P409L c.1226C>T 17 1381773 THCA G A Missense p.R103C c.307C>T 17 1386944 HNSC G A Missense p.R33W c.97C>T 17 1387576 HNSC G A Missense p.R624C c.1870C>T 17 1375450 HNSC G A Missense p.R643C c.1927C>T 17 1375295 UCEC G A Missense p.R689W c.2065C>T 17 1374587 BRCA G A Missense p.R733W c.2197C>T 17 1374380 ESCA G A Missense p.T965I c.2894C>T 17 1371284 CM G A Nonsense p.Q982* c.2944C>T 17 1371157 STAD G A Synonymous p.D379D c.1137C>T 17 1381985 BRCA G A Synonymous p.F237F c.711C>T 17 1384096 CM G A Synonymous p.F436F c.1308C>T 17 1381474 BLCA G A Synonymous p.G1021G c.3063C>T 17 1370776 BLCA G A Synonymous p.G81G c.243C>T 17 1387008 HNSC G A Synonymous p.L393L c.1179C>T 17 1381943 CM G A Synonymous p.S973S c.2919C>T 17 1371182 NSCLC G C Synonymous p.L942L c.2826C>G 17 1371352 ESCA G - Frameshift p.L335Sfs*4 c.1003delC 17 1382903 RCCC GGGCCTGGGTGCTGA - IntronicDeletion . c.76-157_76-143delTCAGCACCCAGGCCC 17 1387740 CM G T Missense p.L755I c.2263C>A 17 1373933 HNSC G T Missense p.S139Y c.416C>A 17 1386285 CM G T Synonymous p.L566L c.1698C>A 17 1378124 BLCA T A Missense p.S196C c.586A>T 17 1385813 LUAD T A Missense p.Y708F c.2123A>T 17 1374529 CM T C Missense p.D810G c.2429A>G 17 1373566 CM T C Missense p.N279S c.836A>G 17 1383891 STAD T C Missense p.Q939R c.2816A>G 17 1371362 BLCA - T Frameshift p.G540Rfs*25 c.1617dupA 17 1378284 CM A C Missense p.N406K c.1218T>G 15 59506484 STAD A C Missense p.Y43D c.127T>G 15 59564525 CM A - Frameshift p.F49Lfs*4 c.147delT 15 59564505 STAD AG - IntronicDeletion . c.2627+482_2627+483delCT 15 59454873 CLL A G Missense p.Y382H c.1144T>C 15 59506883 RCCC A G Synonymous p.L526L c.1578T>C 15 59497637 CM - A IntronicInsertion . c.333-102dupT 15 59528973 ESCA A T Missense p.N875K c.2625T>A 15 59455358 CM C A Missense p.G157V c.470G>T 15 59523941 BRCA C A Missense p.G654V c.1961G>T 15 59470680 BRCA C A Missense p.K71N c.213G>T 15 59553643 UCEC C A Missense p.K813N c.2439G>T 15 59464137 BRCA C A Missense p.V466L c.1396G>T 15 59501014 COREAD C A Missense p.V59F c.175G>T 15 59553681 LUAD C A Nonsense p.E254* c.760G>T 15 59516905 LUSC C A Nonsense p.E608* c.1822G>T 15 59480399 LUAD C A SpliceAcceptorSNV . c.1617-1G>T 15 59494607 LUAD CC TT IntronicBlockSubstitution . c.1363-108_1363-107delinsAA 15 59501154 CM C - Frameshift p.G242Afs*21 c.725delG 15 59516940 ESCA C G Missense p.E682Q c.2044G>C 15 59470597 RCCC C G Missense p.V446L c.1336G>C 15 59502739 GBM C T IntronicSNV . c.2785+413G>A 15 59452859 PIA C T Missense p.A561T c.1681G>A 15 59494542 CM C T Missense p.D353N c.1057G>A 15 59510140 BRCA C T Missense p.E410K c.1228G>A 15 59506474 LUSC C T Missense p.G242S c.724G>A 15 59516941 CM C T Missense p.G333R c.997G>A 15 59510200 PAAD C T Missense p.G334D c.1001G>A 15 59510196 THCA C T Missense p.M375I c.1125G>A 15 59506902 CM C T Missense p.R700Q c.2099G>A 15 59466390 PAAD C T Missense p.R860H c.2579G>A 15 59455404 HNSC C T Missense p.V162I c.484G>A 15 59523927 COREAD C T Synonymous p.L671L c.2013G>A 15 59470628 CM GAGCTG - SpliceAcceptorDeletion . c.643-3_645delCAGCTC 15 59517020 MM G A IntronicSNV . c.1363-18C>T 15 59501065 HC G A Missense p.L686F c.2056C>T 15 59466433 CM G A Missense p.P151L c.452C>T 15 59523959 UCEC G A Missense p.P180L c.539C>T 15 59519761 CM G A Missense p.P86L c.257C>T 15 59548558 CM G A Missense p.R814W c.2440C>T 15 59464136 STAD G A Missense p.T1011M c.3032C>T 15 59445837 HNSC G A Missense p.T342I c.1025C>T 15 59510172 CM G A Synonymous p.F502F c.1506C>T 15 59500904 BLCA G A Synonymous p.G242G c.726C>T 15 59516939 UCEC G A Synonymous p.I445I c.1335C>T 15 59502740 BLCA G A Synonymous p.N98N c.294C>T 15 59548521 BLCA G A Synonymous p.V59V c.177C>T 15 59553679 LUAD G C 5-UTRSNV . c.1-2C>G 15 59664701 CLL G C Missense p.G181A c.542G>C 15 59519758 GBM G C Missense p.R253G c.757C>G 15 59516908 SCLC G T IntronicSNV . c.147+43C>A 15 59564462 STAD G T Synonymous p.T161T c.483C>A 15 59523928 CM T A Missense p.E819D c.2457A>T 15 59464119 RCCC T A Missense p.K815I c.2444A>T 15 59464132 COREAD TC - Frameshift p.R693Kfs*3 c.2078_2079delGA 15 59466410 CM T C IntronicSNV . c.3+17425A>G 15 59647272 CLL T C Missense p.K123E c.367A>G 15 59528837 RCCC T C Missense p.R198G c.592A>G 15 59519708 LUSC T C Synonymous p.L56L c.168A>G 15 59553688 HNSC T G Missense p.H14P c.41A>C 15 59564611 PRAD