Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 13 36878631 36878631 + Silent SNP G G A TCGA-GU-AATP-01A-11D-A391-08 TCGA-GU-AATP-10A-01D-A394-08 g.chr13:36878631G>A c.1872C>T c.(1870-1872)ctC>ctT p.L624L BLCA 13 36888365 36888365 + Splice_Site SNP C C G TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr13:36888365C>G c.1482G>C c.(1480-1482)ctG>ctC p.L494L BLCA 13 36900832 36900832 + Missense_Mutation SNP T T C TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr13:36900832T>C c.1168A>G c.(1168-1170)Aaa>Gaa p.K390E BLCA 13 36903500 36903500 + Splice_Site SNP C C T TCGA-DK-A6B2-01A-11D-A30E-08 TCGA-DK-A6B2-10A-01D-A30H-08 g.chr13:36903500C>T c.1163G>A c.(1162-1164)aGg>aAg p.R388K BLCA 13 36903569 36903569 + Missense_Mutation SNP G G C TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr13:36903569G>C c.1094C>G c.(1093-1095)tCt>tGt p.S365C BLCA 13 36905578 36905578 + Silent SNP G G C TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr13:36905578G>C c.966C>G c.(964-966)ctC>ctG p.L322L BLCA 13 36909157 36909157 + Splice_Site SNP C C G TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr13:36909157C>G c.e2+1 BLCA 13 36909198 36909198 + Missense_Mutation SNP G G C TCGA-FD-A3SR-01A-11D-A22Z-08 TCGA-FD-A3SR-10A-01D-A22Z-08 g.chr13:36909198G>C c.770C>G c.(769-771)tCt>tGt p.S257C BLCA 13 36909299 36909299 + Silent SNP C C T TCGA-ZF-AA54-01A-11D-A391-08 TCGA-ZF-AA54-10A-01D-A394-08 g.chr13:36909299C>T c.669G>A c.(667-669)ttG>ttA p.L223L BLCA 13 36909384 36909384 + Nonsense_Mutation SNP G G T TCGA-4Z-AA81-01A-11D-A391-08 TCGA-4Z-AA81-10A-01D-A394-08 g.chr13:36909384G>T c.584C>A c.(583-585)tCa>tAa p.S195* BRCA 13 36878665 36878665 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr13:36878665A>C c.1838T>G c.(1837-1839)gTg>gGg p.V613G BRCA 13 36886475 36886475 + Silent SNP T T G TCGA-B6-A0RI-01A-11W-A071-09 TCGA-B6-A0RI-10A-01W-A071-09 g.chr13:36886475T>G c.1623A>C c.(1621-1623)gtA>gtC p.V541V BRCA 13 36886528 36886528 + Missense_Mutation SNP A A G TCGA-AR-A0U1-01A-11D-A10Y-09 TCGA-AR-A0U1-10A-01D-A110-09 g.chr13:36886528A>G c.1570T>C c.(1570-1572)Tct>Cct p.S524P BRCA 13 36886556 36886556 + Silent SNP C C T TCGA-D8-A1JN-01A-11D-A13L-09 TCGA-D8-A1JN-10A-01D-A13O-09 g.chr13:36886556C>T c.1542G>A c.(1540-1542)aaG>aaA p.K514K BRCA 13 36886599 36886599 + Missense_Mutation SNP G G C TCGA-A8-A07C-01A-11D-A045-09 TCGA-A8-A07C-10A-01W-A055-09 g.chr13:36886599G>C c.1499C>G c.(1498-1500)aCt>aGt p.T500S BRCA 13 36903599 36903599 + Missense_Mutation SNP C C G TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr13:36903599C>G c.1064G>C c.(1063-1065)aGa>aCa p.R355T BRCA 13 36905608 36905608 + Silent SNP G G T TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr13:36905608G>T c.936C>A c.(934-936)tcC>tcA p.S312S BRCA 13 36909960 36909960 + Missense_Mutation SNP T T G TCGA-C8-A27B-01A-11D-A167-09 TCGA-C8-A27B-10A-01D-A167-09 g.chr13:36909960T>G c.8A>C c.(7-9)cAa>cCa p.Q3P CESC 13 36878517 36878517 + Silent SNP C C T TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr13:36878517C>T c.1986G>A c.(1984-1986)aaG>aaA p.K662K CESC 13 36909405 36909405 + Missense_Mutation SNP C C T TCGA-C5-A3HE-01A-21D-A22X-09 TCGA-C5-A3HE-10A-01D-A22X-09 g.chr13:36909405C>T c.563G>A c.(562-564)gGa>gAa p.G188E COAD 13 36878538 36878538 + Silent SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:36878538C>T c.1965G>A c.(1963-1965)acG>acA p.T655T COAD 13 36878539 36878539 + Frame_Shift_Del DEL G G - TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr13:36878539delG c.1964delC c.(1963-1965)acgfs p.T655fs COAD 13 36886325 36886325 + Missense_Mutation SNP C C T TCGA-A6-3810-01A-01W-0995-10 TCGA-A6-3810-11A-01W-0995-10 g.chr13:36886325C>T c.1690G>A c.(1690-1692)Gtt>Att p.V564I COAD 13 36886522 36886522 + Nonsense_Mutation SNP T T A TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr13:36886522T>A c.1576A>T c.(1576-1578)Aaa>Taa p.K526* COAD 13 36886585 36886585 + Missense_Mutation SNP C C T TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr13:36886585C>T c.1513G>A c.(1513-1515)Gtt>Att p.V505I COAD 13 36886585 36886585 + Missense_Mutation SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr13:36886585C>T c.1513G>A c.(1513-1515)Gtt>Att p.V505I COAD 13 36886586 36886586 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:36886586G>A c.1512C>T c.(1510-1512)tgC>tgT p.C504C COAD 13 36888392 36888392 + Silent SNP T T G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr13:36888392T>G c.1455A>C c.(1453-1455)ggA>ggC p.G485G COAD 13 36900769 36900769 + Missense_Mutation SNP C C G TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr13:36900769C>G c.1231G>C c.(1231-1233)Gaa>Caa p.E411Q COAD 13 36903594 36903594 + Missense_Mutation SNP A A C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr13:36903594A>C c.1069T>G c.(1069-1071)Tcc>Gcc p.S357A COAD 13 36903599 36903599 + Missense_Mutation SNP C C A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr13:36903599C>A c.1064G>T c.(1063-1065)aGa>aTa p.R355I COAD 13 36905585 36905585 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:36905585C>A c.959G>T c.(958-960)aGa>aTa p.R320I COAD 13 36905624 36905624 + Missense_Mutation SNP A A G TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr13:36905624A>G c.920T>C c.(919-921)gTg>gCg p.V307A COAD 13 36905692 36905692 + Silent SNP C C T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr13:36905692C>T c.852G>A c.(850-852)ccG>ccA p.P284P COAD 13 36909170 36909170 + Silent SNP G G T TCGA-AA-3837-01A-01W-0900-09 TCGA-AA-3837-10A-01W-0900-09 g.chr13:36909170G>T c.798C>A c.(796-798)ccC>ccA p.P266P COAD 13 36909193 36909193 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:36909193C>T c.775G>A c.(775-777)Gat>Aat p.D259N COAD 13 36909222 36909222 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:36909222C>T c.746G>A c.(745-747)cGa>cAa p.R249Q COAD 13 36909271 36909272 + Frame_Shift_Ins INS - - A TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr13:36909271_36909272insA c.696_697insT c.(694-699)tttgtafs p.V233fs COAD 13 36909276 36909276 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:36909276A>C c.692T>G c.(691-693)tTt>tGt p.F231C COAD 13 36909342 36909342 + Missense_Mutation SNP G G A TCGA-F4-6854-01A-11D-1924-10 TCGA-F4-6854-10A-01D-1924-10 g.chr13:36909342G>A c.626C>T c.(625-627)cCg>cTg p.P209L COAD 13 36909379 36909379 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr13:36909379C>T c.589G>A c.(589-591)Gtt>Att p.V197I COAD 13 36909685 36909685 + Missense_Mutation SNP G G T TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr13:36909685G>T c.283C>A c.(283-285)Cta>Ata p.L95I COADREAD 13 36878538 36878538 + Silent SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr13:36878538C>T c.1965G>A c.(1963-1965)acG>acA p.T655T COADREAD 13 36878539 36878539 + Frame_Shift_Del DEL G G - TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr13:36878539delG c.1964delC c.(1963-1965)acgfs p.T655fs COADREAD 13 36878765 36878765 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:36878765C>T c.1738G>A c.(1738-1740)Gga>Aga p.G580R COADREAD 13 36878766 36878766 + Silent SNP G G A TCGA-AG-3583-01A-01W-0831-10 TCGA-AG-3583-10A-01W-0831-10 g.chr13:36878766G>A c.1737C>T c.(1735-1737)taC>taT p.Y579Y COADREAD 13 36886325 36886325 + Missense_Mutation SNP C C T TCGA-A6-3810-01A-01W-0995-10 TCGA-A6-3810-11A-01W-0995-10 g.chr13:36886325C>T c.1690G>A c.(1690-1692)Gtt>Att p.V564I COADREAD 13 36886522 36886522 + Nonsense_Mutation SNP T T A TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr13:36886522T>A c.1576A>T c.(1576-1578)Aaa>Taa p.K526* COADREAD 13 36886585 36886585 + Missense_Mutation SNP C C T TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr13:36886585C>T c.1513G>A c.(1513-1515)Gtt>Att p.V505I COADREAD 13 36886585 36886585 + Missense_Mutation SNP C C T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr13:36886585C>T c.1513G>A c.(1513-1515)Gtt>Att p.V505I COADREAD 13 36886586 36886586 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:36886586G>A c.1512C>T c.(1510-1512)tgC>tgT p.C504C COADREAD 13 36888392 36888392 + Silent SNP T T G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr13:36888392T>G c.1455A>C c.(1453-1455)ggA>ggC p.G485G COADREAD 13 36888471 36888471 + Missense_Mutation SNP C C T TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chr13:36888471C>T c.1376G>A c.(1375-1377)cGg>cAg p.R459Q COADREAD 13 36900769 36900769 + Missense_Mutation SNP C C G TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr13:36900769C>G c.1231G>C c.(1231-1233)Gaa>Caa p.E411Q COADREAD 13 36903594 36903594 + Missense_Mutation SNP A A C TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr13:36903594A>C c.1069T>G c.(1069-1071)Tcc>Gcc p.S357A COADREAD 13 36903599 36903599 + Missense_Mutation SNP C C A TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr13:36903599C>A c.1064G>T c.(1063-1065)aGa>aTa p.R355I COADREAD 13 36903630 36903630 + Nonsense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr13:36903630C>A c.1033G>T c.(1033-1035)Gaa>Taa p.E345* COADREAD 13 36905585 36905585 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr13:36905585C>A c.959G>T c.(958-960)aGa>aTa p.R320I COADREAD 13 36905624 36905624 + Missense_Mutation SNP A A G TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr13:36905624A>G c.920T>C c.(919-921)gTg>gCg p.V307A COADREAD 13 36905692 36905692 + Silent SNP C C T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr13:36905692C>T c.852G>A c.(850-852)ccG>ccA p.P284P COADREAD 13 36909170 36909170 + Silent SNP G G T TCGA-AA-3837-01A-01W-0900-09 TCGA-AA-3837-10A-01W-0900-09 g.chr13:36909170G>T c.798C>A c.(796-798)ccC>ccA p.P266P COADREAD 13 36909193 36909193 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:36909193C>T c.775G>A c.(775-777)Gat>Aat p.D259N COADREAD 13 36909193 36909193 + Missense_Mutation SNP C C T TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr13:36909193C>T c.775G>A c.(775-777)Gat>Aat p.D259N COADREAD 13 36909222 36909222 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr13:36909222C>T c.746G>A c.(745-747)cGa>cAa p.R249Q COADREAD 13 36909271 36909272 + Frame_Shift_Ins INS - - A TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr13:36909271_36909272insA c.696_697insT c.(694-699)tttgtafs p.V233fs COADREAD 13 36909276 36909276 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr13:36909276A>C c.692T>G c.(691-693)tTt>tGt p.F231C COADREAD 13 36909342 36909342 + Missense_Mutation SNP G G A TCGA-F4-6854-01A-11D-1924-10 TCGA-F4-6854-10A-01D-1924-10 g.chr13:36909342G>A c.626C>T c.(625-627)cCg>cTg p.P209L COADREAD 13 36909379 36909379 + Missense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr13:36909379C>T c.589G>A c.(589-591)Gtt>Att p.V197I COADREAD 13 36909685 36909685 + Missense_Mutation SNP G G T TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr13:36909685G>T c.283C>A c.(283-285)Cta>Ata p.L95I ESCA 13 36900758 36900758 + Missense_Mutation SNP T T G TCGA-RE-A7BO-01A-11D-A33E-09 TCGA-RE-A7BO-10A-01D-A33H-09 g.chr13:36900758T>G c.1242A>C c.(1240-1242)aaA>aaC p.K414N ESCA 13 36900829 36900829 + Missense_Mutation SNP C C A TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr13:36900829C>A c.1171G>T c.(1171-1173)Gat>Tat p.D391Y ESCA 13 36909223 36909223 + Nonsense_Mutation SNP G G A TCGA-2H-A9GM-01A-11D-A37C-09 TCGA-2H-A9GM-11A-11D-A37F-09 g.chr13:36909223G>A c.745C>T c.(745-747)Cga>Tga p.R249* ESCA 13 36909527 36909527 + Silent SNP A A G TCGA-IG-A4QS-01A-11D-A27G-09 TCGA-IG-A4QS-10A-01D-A27G-09 g.chr13:36909527A>G c.441T>C c.(439-441)acT>acC p.T147T GBM 13 36909291 36909291 + Missense_Mutation SNP T T C TCGA-76-6660-01A-11D-1845-08 TCGA-76-6660-10A-01D-1845-08 g.chr13:36909291T>C c.677A>G c.(676-678)aAt>aGt p.N226S GBMLGG 13 36886330 36886330 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:36886330C>T c.1685G>A c.(1684-1686)tGc>tAc p.C562Y GBMLGG 13 36888512 36888512 + Silent SNP A A G TCGA-FG-A6IZ-01A-11D-A31L-08 TCGA-FG-A6IZ-10A-01D-A31J-08 g.chr13:36888512A>G c.1335T>C c.(1333-1335)acT>acC p.T445T GBMLGG 13 36909272 36909272 + Frame_Shift_Del DEL A A - TCGA-S9-A7IZ-01A-11D-A34A-08 TCGA-S9-A7IZ-10A-01D-A34A-08 g.chr13:36909272delA c.696delT c.(694-696)tttfs p.F232fs GBMLGG 13 36909291 36909291 + Missense_Mutation SNP T T C TCGA-76-6660-01A-11D-1845-08 TCGA-76-6660-10A-01D-1845-08 g.chr13:36909291T>C c.677A>G c.(676-678)aAt>aGt p.N226S GBMLGG 13 36909330 36909330 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:36909330G>A c.638C>T c.(637-639)aCc>aTc p.T213I GBMLGG 13 36909834 36909834 + Missense_Mutation SNP T T A TCGA-E1-A7Z4-01A-11D-A34J-08 TCGA-E1-A7Z4-10A-01D-A34M-08 g.chr13:36909834T>A c.134A>T c.(133-135)tAc>tTc p.Y45F HNSC 13 36909222 36909222 + Missense_Mutation SNP C C T TCGA-CN-4741-01A-01D-1434-08 TCGA-CN-4741-10A-01D-1434-08 g.chr13:36909222C>T c.746G>A c.(745-747)cGa>cAa p.R249Q HNSC 13 36909285 36909285 + Missense_Mutation SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr13:36909285A>G c.683T>C c.(682-684)gTa>gCa p.V228A HNSC 13 36909740 36909740 + Missense_Mutation SNP C C A TCGA-HD-7753-01A-11D-2078-08 TCGA-HD-7753-10A-01D-2078-08 g.chr13:36909740C>A c.228G>T c.(226-228)caG>caT p.Q76H KICH 13 36909383 36909383 + Silent SNP T T C TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr13:36909383T>C c.585A>G c.(583-585)tcA>tcG p.S195S KIPAN 13 36909383 36909383 + Silent SNP T T C TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr13:36909383T>C c.585A>G c.(583-585)tcA>tcG p.S195S LGG 13 36886330 36886330 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:36886330C>T c.1685G>A c.(1684-1686)tGc>tAc p.C562Y LGG 13 36888512 36888512 + Silent SNP A A G TCGA-FG-A6IZ-01A-11D-A31L-08 TCGA-FG-A6IZ-10A-01D-A31J-08 g.chr13:36888512A>G c.1335T>C c.(1333-1335)acT>acC p.T445T LGG 13 36909272 36909272 + Frame_Shift_Del DEL A A - TCGA-S9-A7IZ-01A-11D-A34A-08 TCGA-S9-A7IZ-10A-01D-A34A-08 g.chr13:36909272delA c.696delT c.(694-696)tttfs p.F232fs LGG 13 36909330 36909330 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr13:36909330G>A c.638C>T c.(637-639)aCc>aTc p.T213I LGG 13 36909834 36909834 + Missense_Mutation SNP T T A TCGA-E1-A7Z4-01A-11D-A34J-08 TCGA-E1-A7Z4-10A-01D-A34M-08 g.chr13:36909834T>A c.134A>T c.(133-135)tAc>tTc p.Y45F LIHC 13 36878657 36878657 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr13:36878657delT c.1846delA c.(1846-1848)actfs p.T616fs LIHC 13 36905735 36905735 + Splice_Site SNP T T C TCGA-WX-AA46-01A-11D-A38X-10 TCGA-WX-AA46-10A-01D-A38X-10 g.chr13:36905735T>C c.e3-2 LUAD 13 36888510 36888510 + Missense_Mutation SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr13:36888510C>A c.1337G>T c.(1336-1338)gGt>gTt p.G446V LUAD 13 36900714 36900714 + Missense_Mutation SNP G G A TCGA-55-7570-01A-11D-2036-08 TCGA-55-7570-10A-01D-2036-08 g.chr13:36900714G>A c.1286C>T c.(1285-1287)tCa>tTa p.S429L LUAD 13 36903531 36903531 + Missense_Mutation SNP C C A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr13:36903531C>A c.1132G>T c.(1132-1134)Gat>Tat p.D378Y LUAD 13 36903546 36903546 + Missense_Mutation SNP C C G TCGA-17-Z047-01A-01W-0747-08 TCGA-17-Z047-11A-01W-0746-08 g.chr13:36903546C>G c.1117G>C c.(1117-1119)Gac>Cac p.D373H LUAD 13 36909299 36909299 + Missense_Mutation SNP C C G TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr13:36909299C>G c.669G>C c.(667-669)ttG>ttC p.L223F LUAD 13 36909550 36909550 + Nonsense_Mutation SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr13:36909550C>A c.418G>T c.(418-420)Gaa>Taa p.E140* LUAD 13 36909680 36909680 + Missense_Mutation SNP C C A TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr13:36909680C>A c.288G>T c.(286-288)gaG>gaT p.E96D LUAD 13 36909703 36909703 + Missense_Mutation SNP G G A TCGA-55-8087-01A-11D-2238-08 TCGA-55-8087-10A-01D-2238-08 g.chr13:36909703G>A c.265C>T c.(265-267)Cgc>Tgc p.R89C LUAD 13 36909909 36909909 + Missense_Mutation SNP T T G TCGA-91-8497-01A-11D-2393-08 TCGA-91-8497-10A-01D-2393-08 g.chr13:36909909T>G c.59A>C c.(58-60)tAt>tCt p.Y20S LUAD 13 36909952 36909952 + Missense_Mutation SNP G G C TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chr13:36909952G>C c.16C>G c.(16-18)Caa>Gaa p.Q6E LUSC 13 36878767 36878767 + Missense_Mutation SNP T T G TCGA-66-2757-01A-01D-1522-08 TCGA-66-2757-11A-01D-1522-08 g.chr13:36878767T>G c.1736A>C c.(1735-1737)tAc>tCc p.Y579S LUSC 13 36909559 36909559 + Nonsense_Mutation SNP G G A TCGA-66-2789-01A-01D-0983-08 TCGA-66-2789-11A-01D-0983-08 g.chr13:36909559G>A c.409C>T c.(409-411)Cag>Tag p.Q137* LUSC 13 36909772 36909772 + Missense_Mutation SNP G G C TCGA-22-5471-01A-01D-1632-08 TCGA-22-5471-11A-01D-1632-08 g.chr13:36909772G>C c.196C>G c.(196-198)Cac>Gac p.H66D PAAD 13 36878678 36878678 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:36878678T>C c.1825A>G c.(1825-1827)Atc>Gtc p.I609V PAAD 13 36878745 36878745 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:36878745A>G c.1758T>C c.(1756-1758)gcT>gcC p.A586A PAAD 13 36886315 36886315 + Missense_Mutation SNP A A G TCGA-OE-A75W-01A-12D-A32N-08 TCGA-OE-A75W-10A-01D-A32N-08 g.chr13:36886315A>G c.1700T>C c.(1699-1701)gTt>gCt p.V567A PAAD 13 36900795 36900795 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:36900795A>G c.1205T>C c.(1204-1206)aTt>aCt p.I402T PAAD 13 36905734 36905734 + Splice_Site SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr13:36905734C>A c.e3-1 PRAD 13 36886567 36886567 + Missense_Mutation SNP G G A TCGA-EJ-5527-01A-01D-1576-08 TCGA-EJ-5527-10A-01D-1577-08 g.chr13:36886567G>A c.1531C>T c.(1531-1533)Cca>Tca p.P511S READ 13 36878765 36878765 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr13:36878765C>T c.1738G>A c.(1738-1740)Gga>Aga p.G580R READ 13 36878766 36878766 + Silent SNP G G A TCGA-AG-3583-01A-01W-0831-10 TCGA-AG-3583-10A-01W-0831-10 g.chr13:36878766G>A c.1737C>T c.(1735-1737)taC>taT p.Y579Y READ 13 36888471 36888471 + Missense_Mutation SNP C C T TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chr13:36888471C>T c.1376G>A c.(1375-1377)cGg>cAg p.R459Q READ 13 36903630 36903630 + Nonsense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr13:36903630C>A c.1033G>T c.(1033-1035)Gaa>Taa p.E345* READ 13 36909193 36909193 + Missense_Mutation SNP C C T TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr13:36909193C>T c.775G>A c.(775-777)Gat>Aat p.D259N SKCM 13 36888536 36888536 + Silent SNP A A G TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr13:36888536A>G c.1311T>C c.(1309-1311)ggT>ggC p.G437G SKCM 13 36888548 36888548 + Missense_Mutation SNP C C A TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr13:36888548C>A c.1299G>T c.(1297-1299)tgG>tgT p.W433C SKCM 13 36909172 36909172 + Missense_Mutation SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr13:36909172G>A c.796C>T c.(796-798)Ccc>Tcc p.P266S SKCM 13 36909302 36909302 + Silent SNP A A T TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr13:36909302A>T c.666T>A c.(664-666)atT>atA p.I222I SKCM 13 36909411 36909411 + Missense_Mutation SNP G G A TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chr13:36909411G>A c.557C>T c.(556-558)tCc>tTc p.S186F SKCM 13 36909789 36909789 + Missense_Mutation SNP G G A TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr13:36909789G>A c.179C>T c.(178-180)tCa>tTa p.S60L

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 13 36909745 36909745 single base substitution T A exon_variant BLCA-CN 13 36909745 36909745 single base substitution T A stop_gained R75* 223A>T BLCA-US 13 36909157 36909157 single base substitution C G downstream_gene_variant BLCA-US 13 36909157 36909157 single base substitution C G splice_donor_variant BLCA-US 13 36909198 36909198 single base substitution G C downstream_gene_variant BLCA-US 13 36909198 36909198 single base substitution G C exon_variant BLCA-US 13 36909198 36909198 single base substitution G C missense_variant S257C 770C>G BRCA-EU 13 36871067 36871067 single base substitution T C downstream_gene_variant BRCA-EU 13 36871387 36871387 single base substitution C T downstream_gene_variant BRCA-EU 13 36871992 36871992 single base substitution C G downstream_gene_variant BRCA-EU 13 36871995 36871995 single base substitution A T downstream_gene_variant BRCA-EU 13 36872112 36872112 single base substitution C G downstream_gene_variant BRCA-EU 13 36873384 36873384 single base substitution C G downstream_gene_variant BRCA-EU 13 36873451 36873451 single base substitution G A downstream_gene_variant BRCA-EU 13 36873956 36873956 single base substitution A G downstream_gene_variant BRCA-EU 13 36875644 36875644 single base substitution A G downstream_gene_variant BRCA-EU 13 36876362 36876362 single base substitution T G 3_prime_UTR_variant BRCA-EU 13 36876362 36876362 single base substitution T G downstream_gene_variant BRCA-EU 13 36877684 36877684 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 13 36877684 36877684 deletion of <=200bp T - downstream_gene_variant BRCA-EU 13 36878750 36878750 single base substitution C T exon_variant BRCA-EU 13 36878750 36878750 single base substitution C T missense_variant E585K 1753G>A BRCA-EU 13 36881677 36881677 single base substitution C G downstream_gene_variant BRCA-EU 13 36881677 36881677 single base substitution C G intron_variant BRCA-EU 13 36883201 36883201 single base substitution G C downstream_gene_variant BRCA-EU 13 36883201 36883201 single base substitution G C intron_variant BRCA-EU 13 36884342 36884342 single base substitution C G downstream_gene_variant BRCA-EU 13 36884342 36884342 single base substitution C G intron_variant BRCA-EU 13 36884559 36884559 single base substitution A T downstream_gene_variant BRCA-EU 13 36884559 36884559 single base substitution A T intron_variant BRCA-EU 13 36884973 36884973 single base substitution C G downstream_gene_variant BRCA-EU 13 36884973 36884973 single base substitution C G intron_variant BRCA-EU 13 36886369 36886369 single base substitution A G exon_variant BRCA-EU 13 36886369 36886369 single base substitution A G missense_variant F549S 1646T>C BRCA-EU 13 36886502 36886502 single base substitution T C exon_variant BRCA-EU 13 36886502 36886502 single base substitution T C synonymous_variant K532K 1596A>G BRCA-EU 13 36888256 36888256 single base substitution C A intron_variant BRCA-EU 13 36888256 36888256 single base substitution C A upstream_gene_variant BRCA-EU 13 36889330 36889330 single base substitution G T intron_variant BRCA-EU 13 36889330 36889330 single base substitution G T upstream_gene_variant BRCA-EU 13 36890029 36890029 single base substitution T C intron_variant BRCA-EU 13 36890029 36890029 single base substitution T C upstream_gene_variant BRCA-EU 13 36890328 36890328 single base substitution C G intron_variant BRCA-EU 13 36890328 36890328 single base substitution C G upstream_gene_variant BRCA-EU 13 36894833 36894833 single base substitution G C intron_variant BRCA-EU 13 36895804 36895804 single base substitution C T downstream_gene_variant BRCA-EU 13 36895804 36895804 single base substitution C T intron_variant BRCA-EU 13 36896307 36896307 single base substitution C T downstream_gene_variant BRCA-EU 13 36896307 36896307 single base substitution C T intron_variant BRCA-EU 13 36896570 36896570 single base substitution C G downstream_gene_variant BRCA-EU 13 36896570 36896570 single base substitution C G intron_variant BRCA-EU 13 36897366 36897366 single base substitution C G downstream_gene_variant BRCA-EU 13 36897366 36897366 single base substitution C G intron_variant BRCA-EU 13 36897884 36897884 single base substitution C G downstream_gene_variant BRCA-EU 13 36897884 36897884 single base substitution C G intron_variant BRCA-EU 13 36897985 36897985 single base substitution A G downstream_gene_variant BRCA-EU 13 36897985 36897985 single base substitution A G intron_variant BRCA-EU 13 36898095 36898095 single base substitution C G downstream_gene_variant BRCA-EU 13 36898095 36898095 single base substitution C G intron_variant BRCA-EU 13 36898124 36898124 single base substitution C G downstream_gene_variant BRCA-EU 13 36898124 36898124 single base substitution C G intron_variant BRCA-EU 13 36898636 36898636 single base substitution G A downstream_gene_variant BRCA-EU 13 36898636 36898636 single base substitution G A intron_variant BRCA-EU 13 36901936 36901936 single base substitution C G intron_variant BRCA-EU 13 36901936 36901936 single base substitution C G upstream_gene_variant BRCA-EU 13 36902306 36902306 single base substitution A T intron_variant BRCA-EU 13 36902306 36902306 single base substitution A T upstream_gene_variant BRCA-EU 13 36902934 36902934 insertion of <=200bp - A intron_variant BRCA-EU 13 36902934 36902934 insertion of <=200bp - A upstream_gene_variant BRCA-EU 13 36902971 36902971 insertion of <=200bp - A intron_variant BRCA-EU 13 36902971 36902971 insertion of <=200bp - A upstream_gene_variant BRCA-EU 13 36906101 36906101 single base substitution C G downstream_gene_variant BRCA-EU 13 36906101 36906101 single base substitution C G intron_variant BRCA-EU 13 36906305 36906305 single base substitution A G downstream_gene_variant BRCA-EU 13 36906305 36906305 single base substitution A G intron_variant BRCA-EU 13 36906541 36906541 single base substitution T C downstream_gene_variant BRCA-EU 13 36906541 36906541 single base substitution T C intron_variant BRCA-EU 13 36907158 36907159 deletion of <=200bp TC - downstream_gene_variant BRCA-EU 13 36907158 36907159 deletion of <=200bp TC - intron_variant BRCA-EU 13 36907570 36907570 single base substitution T A downstream_gene_variant BRCA-EU 13 36907570 36907570 single base substitution T A intron_variant BRCA-EU 13 36908105 36908105 single base substitution G C downstream_gene_variant BRCA-EU 13 36908105 36908105 single base substitution G C intron_variant BRCA-EU 13 36910184 36910184 single base substitution C G intron_variant BRCA-EU 13 36911379 36911379 single base substitution T C intron_variant BRCA-EU 13 36917004 36917004 single base substitution G C intron_variant BRCA-EU 13 36918814 36918814 deletion of <=200bp A - intron_variant BRCA-EU 13 36921454 36921454 single base substitution C A intron_variant BRCA-EU 13 36921454 36921454 single base substitution C A upstream_gene_variant BRCA-EU 13 36922030 36922030 single base substitution A G intron_variant BRCA-EU 13 36922030 36922030 single base substitution A G upstream_gene_variant BRCA-EU 13 36923167 36923167 single base substitution G A intron_variant BRCA-EU 13 36923167 36923167 single base substitution G A upstream_gene_variant BRCA-EU 13 36926313 36926313 single base substitution T C intron_variant BRCA-EU 13 36926381 36926381 single base substitution T G intron_variant BRCA-EU 13 36926873 36926873 single base substitution C G intron_variant BRCA-EU 13 36927015 36927015 single base substitution C G intron_variant BRCA-EU 13 36927096 36927096 single base substitution C G intron_variant BRCA-EU 13 36931814 36931814 single base substitution A G intron_variant BRCA-EU 13 36932258 36932258 deletion of <=200bp A - intron_variant BRCA-EU 13 36932328 36932328 deletion of <=200bp A - intron_variant BRCA-EU 13 36932385 36932385 single base substitution C T intron_variant BRCA-EU 13 36933250 36933250 single base substitution G A intron_variant BRCA-EU 13 36934425 36934425 single base substitution G C intron_variant BRCA-EU 13 36935125 36935125 single base substitution C A intron_variant BRCA-EU 13 36936458 36936458 single base substitution C T intron_variant BRCA-EU 13 36936493 36936493 single base substitution A C intron_variant BRCA-EU 13 36937033 36937033 single base substitution C A intron_variant BRCA-EU 13 36937157 36937157 single base substitution A T intron_variant BRCA-EU 13 36937833 36937833 single base substitution G A intron_variant BRCA-EU 13 36938555 36938555 single base substitution C T intron_variant BRCA-EU 13 36938788 36938788 single base substitution C T intron_variant BRCA-EU 13 36938912 36938912 single base substitution G C intron_variant BRCA-EU 13 36939850 36939850 insertion of <=200bp - T intron_variant BRCA-EU 13 36940681 36940681 single base substitution G A intron_variant BRCA-EU 13 36941176 36941176 single base substitution G A intron_variant BRCA-EU 13 36941399 36941399 single base substitution C A intron_variant BRCA-EU 13 36941517 36941517 single base substitution A C intron_variant BRCA-EU 13 36941563 36941563 single base substitution A G intron_variant BRCA-EU 13 36941636 36941636 single base substitution C T intron_variant BRCA-EU 13 36942157 36942157 deletion of <=200bp A - intron_variant BRCA-EU 13 36943147 36943147 single base substitution A G intron_variant BRCA-EU 13 36944184 36944184 single base substitution G A intron_variant BRCA-EU 13 36946140 36946140 single base substitution G T upstream_gene_variant BRCA-EU 13 36946423 36946423 single base substitution T C upstream_gene_variant BRCA-EU 13 36947445 36947445 single base substitution C T upstream_gene_variant BRCA-EU 13 36948086 36948086 single base substitution G A upstream_gene_variant BRCA-EU 13 36948161 36948161 single base substitution T G upstream_gene_variant BRCA-EU 13 36948953 36948953 single base substitution G A upstream_gene_variant BRCA-EU 13 36948955 36948955 single base substitution T A upstream_gene_variant BRCA-FR 13 36873956 36873956 single base substitution A G downstream_gene_variant BRCA-FR 13 36876362 36876362 single base substitution T G 3_prime_UTR_variant BRCA-FR 13 36876362 36876362 single base substitution T G downstream_gene_variant BRCA-FR 13 36881677 36881677 single base substitution C G downstream_gene_variant BRCA-FR 13 36881677 36881677 single base substitution C G intron_variant BRCA-FR 13 36883201 36883201 single base substitution G C downstream_gene_variant BRCA-FR 13 36883201 36883201 single base substitution G C intron_variant BRCA-FR 13 36892751 36892751 single base substitution G C intron_variant BRCA-FR 13 36892751 36892751 single base substitution G C upstream_gene_variant BRCA-FR 13 36893459 36893459 single base substitution C A intron_variant BRCA-FR 13 36893459 36893459 single base substitution C A upstream_gene_variant BRCA-FR 13 36912693 36912693 single base substitution T G intron_variant BRCA-FR 13 36920560 36920560 single base substitution C A 5_prime_UTR_variant BRCA-FR 13 36920560 36920560 single base substitution C A intron_variant BRCA-FR 13 36920560 36920560 single base substitution C A upstream_gene_variant BRCA-FR 13 36932385 36932385 single base substitution C T intron_variant BRCA-FR 13 36934171 36934171 single base substitution G T intron_variant BRCA-FR 13 36934425 36934425 single base substitution G C intron_variant BRCA-FR 13 36934481 36934481 single base substitution G C intron_variant BRCA-FR 13 36936458 36936458 single base substitution C T intron_variant BRCA-FR 13 36937142 36937142 single base substitution C T intron_variant BRCA-FR 13 36938013 36938013 single base substitution G T intron_variant BRCA-FR 13 36938555 36938555 single base substitution C T intron_variant BRCA-FR 13 36940681 36940681 single base substitution G A intron_variant BRCA-FR 13 36941176 36941176 single base substitution G A intron_variant BRCA-FR 13 36941636 36941636 single base substitution C T intron_variant BRCA-FR 13 36948953 36948953 single base substitution G A upstream_gene_variant BRCA-FR 13 36948955 36948955 single base substitution T A upstream_gene_variant BRCA-UK 13 36884342 36884342 single base substitution C G downstream_gene_variant BRCA-UK 13 36884342 36884342 single base substitution C G intron_variant BRCA-UK 13 36889129 36889129 single base substitution C G intron_variant BRCA-UK 13 36889129 36889129 single base substitution C G upstream_gene_variant BRCA-UK 13 36890029 36890029 single base substitution T C intron_variant BRCA-UK 13 36890029 36890029 single base substitution T C upstream_gene_variant BRCA-UK 13 36911683 36911683 single base substitution C T intron_variant BRCA-UK 13 36937157 36937157 single base substitution A T intron_variant BRCA-US 13 36878665 36878665 single base substitution A C exon_variant BRCA-US 13 36878665 36878665 single base substitution A C missense_variant V613G 1838T>G BRCA-US 13 36886475 36886475 single base substitution T G exon_variant BRCA-US 13 36886475 36886475 single base substitution T G synonymous_variant V541V 1623A>C BRCA-US 13 36886528 36886528 single base substitution A G exon_variant BRCA-US 13 36886528 36886528 single base substitution A G missense_variant S524P 1570T>C BRCA-US 13 36886556 36886556 single base substitution C T exon_variant BRCA-US 13 36886556 36886556 single base substitution C T synonymous_variant K514K 1542G>A BRCA-US 13 36886556 36886556 single base substitution C T upstream_gene_variant BRCA-US 13 36886599 36886599 single base substitution G C exon_variant BRCA-US 13 36886599 36886599 single base substitution G C missense_variant T500S 1499C>G BRCA-US 13 36886599 36886599 single base substitution G C upstream_gene_variant BRCA-US 13 36888569 36888569 single base substitution G T exon_variant BRCA-US 13 36888569 36888569 single base substitution G T intron_variant BRCA-US 13 36888569 36888569 single base substitution G T upstream_gene_variant BRCA-US 13 36900603 36900603 single base substitution C G exon_variant BRCA-US 13 36900603 36900603 single base substitution C G intron_variant BRCA-US 13 36903599 36903599 single base substitution C G exon_variant BRCA-US 13 36903599 36903599 single base substitution C G missense_variant R355T 1064G>C BRCA-US 13 36903599 36903599 single base substitution C G upstream_gene_variant BRCA-US 13 36905608 36905608 single base substitution G T downstream_gene_variant BRCA-US 13 36905608 36905608 single base substitution G T exon_variant BRCA-US 13 36905608 36905608 single base substitution G T synonymous_variant S312S 936C>A BRCA-US 13 36905608 36905608 single base substitution G T upstream_gene_variant BRCA-US 13 36909960 36909960 single base substitution T G exon_variant BRCA-US 13 36909960 36909960 single base substitution T G missense_variant Q3P 8A>C BTCA-JP 13 36878598 36878598 single base substitution C G exon_variant BTCA-JP 13 36878598 36878598 single base substitution C G missense_variant Q635H 1905G>C BTCA-JP 13 36878766 36878766 single base substitution G A exon_variant BTCA-JP 13 36878766 36878766 single base substitution G A synonymous_variant Y579Y 1737C>T BTCA-JP 13 36886516 36886516 single base substitution C A exon_variant BTCA-JP 13 36886516 36886516 single base substitution C A missense_variant D528Y 1582G>T BTCA-JP 13 36900829 36900829 single base substitution C A exon_variant BTCA-JP 13 36900829 36900829 single base substitution C A missense_variant D391Y 1171G>T BTCA-JP 13 36900829 36900829 single base substitution C A upstream_gene_variant BTCA-JP 13 36909369 36909369 single base substitution T C downstream_gene_variant BTCA-JP 13 36909369 36909369 single base substitution T C exon_variant BTCA-JP 13 36909369 36909369 single base substitution T C missense_variant E200G 599A>G BTCA-JP 13 36909719 36909719 single base substitution T G exon_variant BTCA-JP 13 36909719 36909719 single base substitution T G missense_variant E83D 249A>C BTCA-JP 13 36939726 36939726 single base substitution G A intron_variant CESC-US 13 36878517 36878517 single base substitution C T downstream_gene_variant CESC-US 13 36878517 36878517 single base substitution C T exon_variant CESC-US 13 36878517 36878517 single base substitution C T synonymous_variant K662K 1986G>A CESC-US 13 36909405 36909405 single base substitution C T downstream_gene_variant CESC-US 13 36909405 36909405 single base substitution C T exon_variant CESC-US 13 36909405 36909405 single base substitution C T missense_variant G188E 563G>A CLLE-ES 13 36880212 36880212 single base substitution C T intron_variant CLLE-ES 13 36884186 36884186 single base substitution T C downstream_gene_variant CLLE-ES 13 36884186 36884186 single base substitution T C intron_variant CLLE-ES 13 36884731 36884731 single base substitution G A downstream_gene_variant CLLE-ES 13 36884731 36884731 single base substitution G A intron_variant CLLE-ES 13 36887124 36887124 single base substitution A C intron_variant CLLE-ES 13 36887124 36887124 single base substitution A C upstream_gene_variant CLLE-ES 13 36897353 36897353 single base substitution G A downstream_gene_variant CLLE-ES 13 36897353 36897353 single base substitution G A intron_variant CLLE-ES 13 36900689 36900689 single base substitution A C exon_variant CLLE-ES 13 36900689 36900689 single base substitution A C intron_variant CLLE-ES 13 36904249 36904249 single base substitution G A intron_variant CLLE-ES 13 36904249 36904249 single base substitution G A upstream_gene_variant CLLE-ES 13 36907246 36907246 single base substitution A T downstream_gene_variant CLLE-ES 13 36907246 36907246 single base substitution A T intron_variant CLLE-ES 13 36915985 36915985 single base substitution G A intron_variant CLLE-ES 13 36945759 36945759 single base substitution C A upstream_gene_variant CLLE-ES 13 36945881 36945881 single base substitution T C upstream_gene_variant CLLE-ES 13 36946962 36946962 single base substitution T G upstream_gene_variant COAD-US 13 36871781 36871781 single base substitution G A downstream_gene_variant COAD-US 13 36878538 36878538 single base substitution C T downstream_gene_variant COAD-US 13 36878538 36878538 single base substitution C T exon_variant COAD-US 13 36878538 36878538 single base substitution C T synonymous_variant T655T 1965G>A COAD-US 13 36878539 36878539 deletion of <=200bp G - downstream_gene_variant COAD-US 13 36878539 36878539 deletion of <=200bp G - exon_variant COAD-US 13 36878539 36878539 deletion of <=200bp G - frameshift_variant T655 COAD-US 13 36886469 36886469 single base substitution T C exon_variant COAD-US 13 36886469 36886469 single base substitution T C synonymous_variant A543A 1629A>G COAD-US 13 36886522 36886522 single base substitution T A exon_variant COAD-US 13 36886522 36886522 single base substitution T A stop_gained K526* 1576A>T COAD-US 13 36886585 36886585 single base substitution C T exon_variant COAD-US 13 36886585 36886585 single base substitution C T missense_variant V505I 1513G>A COAD-US 13 36886585 36886585 single base substitution C T upstream_gene_variant COAD-US 13 36886586 36886586 single base substitution G A exon_variant COAD-US 13 36886586 36886586 single base substitution G A synonymous_variant C504C 1512C>T COAD-US 13 36886586 36886586 single base substitution G A upstream_gene_variant COAD-US 13 36900769 36900769 single base substitution C G exon_variant COAD-US 13 36900769 36900769 single base substitution C G missense_variant E411Q 1231G>C COAD-US 13 36900769 36900769 single base substitution C G upstream_gene_variant COAD-US 13 36903594 36903594 single base substitution A C exon_variant COAD-US 13 36903594 36903594 single base substitution A C missense_variant S357A 1069T>G COAD-US 13 36903594 36903594 single base substitution A C upstream_gene_variant COAD-US 13 36905692 36905692 single base substitution C T downstream_gene_variant COAD-US 13 36905692 36905692 single base substitution C T exon_variant COAD-US 13 36905692 36905692 single base substitution C T synonymous_variant P284P 852G>A COAD-US 13 36905692 36905692 single base substitution C T upstream_gene_variant COAD-US 13 36909222 36909222 single base substitution C T downstream_gene_variant COAD-US 13 36909222 36909222 single base substitution C T exon_variant COAD-US 13 36909222 36909222 single base substitution C T missense_variant R249Q 746G>A COAD-US 13 36909342 36909342 single base substitution G A downstream_gene_variant COAD-US 13 36909342 36909342 single base substitution G A exon_variant COAD-US 13 36909342 36909342 single base substitution G A missense_variant P209L 626C>T COAD-US 13 36909379 36909379 single base substitution C T downstream_gene_variant COAD-US 13 36909379 36909379 single base substitution C T exon_variant COAD-US 13 36909379 36909379 single base substitution C T missense_variant V197I 589G>A COAD-US 13 36909685 36909685 single base substitution G T downstream_gene_variant COAD-US 13 36909685 36909685 single base substitution G T exon_variant COAD-US 13 36909685 36909685 single base substitution G T missense_variant L95I 283C>A COCA-CN 13 36878906 36878906 single base substitution A C intron_variant COCA-CN 13 36883623 36883623 single base substitution G A downstream_gene_variant COCA-CN 13 36883623 36883623 single base substitution G A intron_variant COCA-CN 13 36884092 36884092 single base substitution T A downstream_gene_variant COCA-CN 13 36884092 36884092 single base substitution T A intron_variant COCA-CN 13 36888471 36888471 single base substitution C T exon_variant COCA-CN 13 36888471 36888471 single base substitution C T missense_variant R459Q 1376G>A COCA-CN 13 36888471 36888471 single base substitution C T upstream_gene_variant COCA-CN 13 36893875 36893875 single base substitution T C intron_variant COCA-CN 13 36893881 36893881 single base substitution G C intron_variant COCA-CN 13 36894130 36894130 single base substitution A G intron_variant COCA-CN 13 36895064 36895064 single base substitution C T downstream_gene_variant COCA-CN 13 36895064 36895064 single base substitution C T intron_variant COCA-CN 13 36903477 36903477 single base substitution C T intron_variant COCA-CN 13 36903477 36903477 single base substitution C T upstream_gene_variant COCA-CN 13 36903569 36903569 single base substitution G T exon_variant COCA-CN 13 36903569 36903569 single base substitution G T missense_variant S365Y 1094C>A COCA-CN 13 36903569 36903569 single base substitution G T upstream_gene_variant COCA-CN 13 36903639 36903639 single base substitution C T exon_variant COCA-CN 13 36903639 36903639 single base substitution C T missense_variant A342T 1024G>A COCA-CN 13 36903639 36903639 single base substitution C T upstream_gene_variant COCA-CN 13 36909198 36909198 single base substitution G T downstream_gene_variant COCA-CN 13 36909198 36909198 single base substitution G T exon_variant COCA-CN 13 36909198 36909198 single base substitution G T missense_variant S257Y 770C>A COCA-CN 13 36909341 36909341 single base substitution C T downstream_gene_variant COCA-CN 13 36909341 36909341 single base substitution C T exon_variant COCA-CN 13 36909341 36909341 single base substitution C T synonymous_variant P209P 627G>A COCA-CN 13 36909384 36909384 single base substitution G A downstream_gene_variant COCA-CN 13 36909384 36909384 single base substitution G A exon_variant COCA-CN 13 36909384 36909384 single base substitution G A missense_variant S195L 584C>T COCA-CN 13 36909533 36909533 single base substitution G C downstream_gene_variant COCA-CN 13 36909533 36909533 single base substitution G C exon_variant COCA-CN 13 36909533 36909533 single base substitution G C synonymous_variant T145T 435C>G COCA-CN 13 36909721 36909721 single base substitution C A exon_variant COCA-CN 13 36909721 36909721 single base substitution C A stop_gained E83* 247G>T COCA-CN 13 36909901 36909901 single base substitution C T exon_variant COCA-CN 13 36909901 36909901 single base substitution C T missense_variant A23T 67G>A COCA-CN 13 36934100 36934100 single base substitution A T intron_variant COCA-CN 13 36940014 36940014 single base substitution C T intron_variant ESAD-UK 13 36870995 36870995 single base substitution G C downstream_gene_variant ESAD-UK 13 36871075 36871075 single base substitution A G downstream_gene_variant ESAD-UK 13 36871257 36871257 single base substitution G A downstream_gene_variant ESAD-UK 13 36871277 36871277 single base substitution C A downstream_gene_variant ESAD-UK 13 36871526 36871526 single base substitution A G downstream_gene_variant ESAD-UK 13 36871653 36871653 single base substitution C T downstream_gene_variant ESAD-UK 13 36871756 36871756 single base substitution C T downstream_gene_variant ESAD-UK 13 36872184 36872184 single base substitution A T downstream_gene_variant ESAD-UK 13 36872332 36872332 single base substitution A G downstream_gene_variant ESAD-UK 13 36872589 36872589 single base substitution G C downstream_gene_variant ESAD-UK 13 36873110 36873110 single base substitution A C downstream_gene_variant ESAD-UK 13 36873110 36873110 single base substitution A T downstream_gene_variant ESAD-UK 13 36873131 36873131 single base substitution A C downstream_gene_variant ESAD-UK 13 36873627 36873627 single base substitution T C downstream_gene_variant ESAD-UK 13 36873650 36873650 single base substitution T G downstream_gene_variant ESAD-UK 13 36873667 36873667 single base substitution T G downstream_gene_variant ESAD-UK 13 36873843 36873843 single base substitution C T downstream_gene_variant ESAD-UK 13 36873882 36873882 single base substitution T G downstream_gene_variant ESAD-UK 13 36873968 36873968 single base substitution A C downstream_gene_variant ESAD-UK 13 36874084 36874084 single base substitution G A downstream_gene_variant ESAD-UK 13 36874104 36874104 single base substitution A G downstream_gene_variant ESAD-UK 13 36874425 36874425 single base substitution T C downstream_gene_variant ESAD-UK 13 36874818 36874818 single base substitution G T downstream_gene_variant ESAD-UK 13 36874996 36874996 single base substitution C T downstream_gene_variant ESAD-UK 13 36875593 36875593 single base substitution G C downstream_gene_variant ESAD-UK 13 36875894 36875894 single base substitution T G 3_prime_UTR_variant ESAD-UK 13 36875894 36875894 single base substitution T G downstream_gene_variant ESAD-UK 13 36876022 36876022 single base substitution A C 3_prime_UTR_variant ESAD-UK 13 36876022 36876022 single base substitution A C downstream_gene_variant ESAD-UK 13 36876192 36876192 single base substitution G T 3_prime_UTR_variant ESAD-UK 13 36876192 36876192 single base substitution G T downstream_gene_variant ESAD-UK 13 36876218 36876218 single base substitution A C 3_prime_UTR_variant ESAD-UK 13 36876218 36876218 single base substitution A C downstream_gene_variant ESAD-UK 13 36876515 36876515 single base substitution A C 3_prime_UTR_variant ESAD-UK 13 36876515 36876515 single base substitution A C downstream_gene_variant ESAD-UK 13 36877176 36877176 single base substitution T A 3_prime_UTR_variant ESAD-UK 13 36877176 36877176 single base substitution T A downstream_gene_variant ESAD-UK 13 36877684 36877684 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 13 36877684 36877684 deletion of <=200bp T - downstream_gene_variant ESAD-UK 13 36877685 36877685 insertion of <=200bp - A 3_prime_UTR_variant ESAD-UK 13 36877685 36877685 insertion of <=200bp - A downstream_gene_variant ESAD-UK 13 36878375 36878375 single base substitution A C 3_prime_UTR_variant ESAD-UK 13 36878375 36878375 single base substitution A C downstream_gene_variant ESAD-UK 13 36878680 36878680 single base substitution C A exon_variant ESAD-UK 13 36878680 36878680 single base substitution C A missense_variant G608V 1823G>T ESAD-UK 13 36878997 36878997 single base substitution A T intron_variant ESAD-UK 13 36879123 36879123 single base substitution A G intron_variant ESAD-UK 13 36880016 36880016 single base substitution T G intron_variant ESAD-UK 13 36880814 36880814 single base substitution T C intron_variant ESAD-UK 13 36880990 36880990 single base substitution T G intron_variant ESAD-UK 13 36881007 36881007 insertion of <=200bp - A intron_variant ESAD-UK 13 36881217 36881217 single base substitution T C intron_variant ESAD-UK 13 36881506 36881506 single base substitution A T downstream_gene_variant ESAD-UK 13 36881506 36881506 single base substitution A T intron_variant ESAD-UK 13 36881540 36881540 single base substitution A C downstream_gene_variant ESAD-UK 13 36881540 36881540 single base substitution A C intron_variant ESAD-UK 13 36881584 36881584 single base substitution T G downstream_gene_variant ESAD-UK 13 36881584 36881584 single base substitution T G intron_variant ESAD-UK 13 36882673 36882673 single base substitution A C downstream_gene_variant ESAD-UK 13 36882673 36882673 single base substitution A C intron_variant ESAD-UK 13 36883077 36883077 single base substitution A C downstream_gene_variant ESAD-UK 13 36883077 36883077 single base substitution A C intron_variant ESAD-UK 13 36883230 36883230 single base substitution A C downstream_gene_variant ESAD-UK 13 36883230 36883230 single base substitution A C intron_variant ESAD-UK 13 36883694 36883694 deletion of <=200bp A - downstream_gene_variant ESAD-UK 13 36883694 36883694 deletion of <=200bp A - intron_variant ESAD-UK 13 36883825 36883825 single base substitution G A downstream_gene_variant ESAD-UK 13 36883825 36883825 single base substitution G A intron_variant ESAD-UK 13 36884028 36884028 single base substitution T C downstream_gene_variant ESAD-UK 13 36884028 36884028 single base substitution T C intron_variant ESAD-UK 13 36884355 36884355 single base substitution T A downstream_gene_variant ESAD-UK 13 36884355 36884355 single base substitution T A intron_variant ESAD-UK 13 36884422 36884422 single base substitution T C downstream_gene_variant ESAD-UK 13 36884422 36884422 single base substitution T C intron_variant ESAD-UK 13 36884664 36884664 single base substitution A C downstream_gene_variant ESAD-UK 13 36884664 36884664 single base substitution A C intron_variant ESAD-UK 13 36884835 36884835 single base substitution C T downstream_gene_variant ESAD-UK 13 36884835 36884835 single base substitution C T intron_variant ESAD-UK 13 36885334 36885334 single base substitution G A downstream_gene_variant ESAD-UK 13 36885334 36885334 single base substitution G A intron_variant ESAD-UK 13 36885660 36885660 single base substitution C T downstream_gene_variant ESAD-UK 13 36885660 36885660 single base substitution C T intron_variant ESAD-UK 13 36885802 36885802 single base substitution A G downstream_gene_variant ESAD-UK 13 36885802 36885802 single base substitution A G intron_variant ESAD-UK 13 36885834 36885834 single base substitution T G downstream_gene_variant ESAD-UK 13 36885834 36885834 single base substitution T G intron_variant ESAD-UK 13 36885997 36885997 single base substitution G T downstream_gene_variant ESAD-UK 13 36885997 36885997 single base substitution G T intron_variant ESAD-UK 13 36886202 36886202 single base substitution C A downstream_gene_variant ESAD-UK 13 36886202 36886202 single base substitution C A intron_variant ESAD-UK 13 36886320 36886320 single base substitution G C exon_variant ESAD-UK 13 36886320 36886320 single base substitution G C missense_variant N565K 1695C>G ESAD-UK 13 36886325 36886325 single base substitution C T exon_variant ESAD-UK 13 36886325 36886325 single base substitution C T missense_variant V564I 1690G>A ESAD-UK 13 36886338 36886338 single base substitution T A exon_variant ESAD-UK 13 36886338 36886338 single base substitution T A synonymous_variant A559A 1677A>T ESAD-UK 13 36886394 36886394 single base substitution C T intron_variant ESAD-UK 13 36886452 36886452 single base substitution T G intron_variant ESAD-UK 13 36886452 36886452 single base substitution T G splice_region_variant ESAD-UK 13 36886539 36886539 single base substitution A C exon_variant ESAD-UK 13 36886539 36886539 single base substitution A C missense_variant L520R 1559T>G ESAD-UK 13 36886641 36886641 single base substitution T G exon_variant ESAD-UK 13 36886641 36886641 single base substitution T G intron_variant ESAD-UK 13 36886641 36886641 single base substitution T G upstream_gene_variant ESAD-UK 13 36886815 36886815 single base substitution A C intron_variant ESAD-UK 13 36886815 36886815 single base substitution A C upstream_gene_variant ESAD-UK 13 36887398 36887398 single base substitution A C intron_variant ESAD-UK 13 36887398 36887398 single base substitution A C upstream_gene_variant ESAD-UK 13 36887398 36887398 single base substitution A T intron_variant ESAD-UK 13 36887398 36887398 single base substitution A T upstream_gene_variant ESAD-UK 13 36887568 36887568 single base substitution A C intron_variant ESAD-UK 13 36887568 36887568 single base substitution A C upstream_gene_variant ESAD-UK 13 36887677 36887677 single base substitution T G intron_variant ESAD-UK 13 36887677 36887677 single base substitution T G upstream_gene_variant ESAD-UK 13 36888160 36888160 single base substitution A C exon_variant ESAD-UK 13 36888160 36888160 single base substitution A C intron_variant ESAD-UK 13 36888160 36888160 single base substitution A C upstream_gene_variant ESAD-UK 13 36888190 36888190 single base substitution C T exon_variant ESAD-UK 13 36888190 36888190 single base substitution C T intron_variant ESAD-UK 13 36888190 36888190 single base substitution C T upstream_gene_variant ESAD-UK 13 36888209 36888209 single base substitution C T exon_variant ESAD-UK 13 36888209 36888209 single base substitution C T intron_variant ESAD-UK 13 36888209 36888209 single base substitution C T upstream_gene_variant ESAD-UK 13 36888371 36888371 single base substitution C A exon_variant ESAD-UK 13 36888371 36888371 single base substitution C A missense_variant Q492H 1476G>T ESAD-UK 13 36888371 36888371 single base substitution C A upstream_gene_variant ESAD-UK 13 36888580 36888580 single base substitution A C intron_variant ESAD-UK 13 36888580 36888580 single base substitution A C upstream_gene_variant ESAD-UK 13 36889318 36889318 single base substitution C A intron_variant ESAD-UK 13 36889318 36889318 single base substitution C A upstream_gene_variant ESAD-UK 13 36889512 36889512 single base substitution T G intron_variant ESAD-UK 13 36889512 36889512 single base substitution T G upstream_gene_variant ESAD-UK 13 36889988 36889988 single base substitution A C intron_variant ESAD-UK 13 36889988 36889988 single base substitution A C upstream_gene_variant ESAD-UK 13 36890258 36890258 single base substitution T G intron_variant ESAD-UK 13 36890258 36890258 single base substitution T G upstream_gene_variant ESAD-UK 13 36890381 36890381 single base substitution C A intron_variant ESAD-UK 13 36890381 36890381 single base substitution C A upstream_gene_variant ESAD-UK 13 36890702 36890702 single base substitution T G intron_variant ESAD-UK 13 36890702 36890702 single base substitution T G upstream_gene_variant ESAD-UK 13 36890824 36890824 single base substitution A G intron_variant ESAD-UK 13 36890824 36890824 single base substitution A G upstream_gene_variant ESAD-UK 13 36890970 36890970 single base substitution T C intron_variant ESAD-UK 13 36890970 36890970 single base substitution T C upstream_gene_variant ESAD-UK 13 36891246 36891246 single base substitution G A intron_variant ESAD-UK 13 36891246 36891246 single base substitution G A upstream_gene_variant ESAD-UK 13 36891718 36891718 single base substitution T C intron_variant ESAD-UK 13 36891718 36891718 single base substitution T C upstream_gene_variant ESAD-UK 13 36894338 36894338 single base substitution C T intron_variant ESAD-UK 13 36894895 36894895 single base substitution A G intron_variant ESAD-UK 13 36895235 36895235 single base substitution G A downstream_gene_variant ESAD-UK 13 36895235 36895235 single base substitution G A intron_variant ESAD-UK 13 36896280 36896280 single base substitution T G downstream_gene_variant ESAD-UK 13 36896280 36896280 single base substitution T G intron_variant ESAD-UK 13 36896557 36896557 single base substitution T G downstream_gene_variant ESAD-UK 13 36896557 36896557 single base substitution T G intron_variant ESAD-UK 13 36896646 36896646 insertion of <=200bp - AA downstream_gene_variant ESAD-UK 13 36896646 36896646 insertion of <=200bp - AA intron_variant ESAD-UK 13 36896669 36896669 single base substitution T G downstream_gene_variant ESAD-UK 13 36896669 36896669 single base substitution T G intron_variant ESAD-UK 13 36896766 36896766 single base substitution T A downstream_gene_variant ESAD-UK 13 36896766 36896766 single base substitution T A intron_variant ESAD-UK 13 36896777 36896777 single base substitution T C downstream_gene_variant ESAD-UK 13 36896777 36896777 single base substitution T C intron_variant ESAD-UK 13 36896789 36896789 single base substitution A G downstream_gene_variant ESAD-UK 13 36896789 36896789 single base substitution A G intron_variant ESAD-UK 13 36897163 36897163 insertion of <=200bp - A downstream_gene_variant ESAD-UK 13 36897163 36897163 insertion of <=200bp - A intron_variant ESAD-UK 13 36897295 36897295 single base substitution T C downstream_gene_variant ESAD-UK 13 36897295 36897295 single base substitution T C intron_variant ESAD-UK 13 36897550 36897550 single base substitution A C downstream_gene_variant ESAD-UK 13 36897550 36897550 single base substitution A C intron_variant ESAD-UK 13 36897550 36897550 single base substitution A G downstream_gene_variant ESAD-UK 13 36897550 36897550 single base substitution A G intron_variant ESAD-UK 13 36898004 36898004 single base substitution A C downstream_gene_variant ESAD-UK 13 36898004 36898004 single base substitution A C intron_variant ESAD-UK 13 36898502 36898502 single base substitution A C downstream_gene_variant ESAD-UK 13 36898502 36898502 single base substitution A C intron_variant ESAD-UK 13 36898609 36898609 single base substitution T G downstream_gene_variant ESAD-UK 13 36898609 36898609 single base substitution T G intron_variant ESAD-UK 13 36898637 36898637 single base substitution A C downstream_gene_variant ESAD-UK 13 36898637 36898637 single base substitution A C intron_variant ESAD-UK 13 36898908 36898908 single base substitution G A downstream_gene_variant ESAD-UK 13 36898908 36898908 single base substitution G A intron_variant ESAD-UK 13 36899155 36899155 single base substitution A G downstream_gene_variant ESAD-UK 13 36899155 36899155 single base substitution A G intron_variant ESAD-UK 13 36899286 36899286 single base substitution T G downstream_gene_variant ESAD-UK 13 36899286 36899286 single base substitution T G intron_variant ESAD-UK 13 36899913 36899913 single base substitution A G downstream_gene_variant ESAD-UK 13 36899913 36899913 single base substitution A G intron_variant ESAD-UK 13 36900687 36900687 insertion of <=200bp - A exon_variant ESAD-UK 13 36900687 36900687 insertion of <=200bp - A intron_variant ESAD-UK 13 36901035 36901035 single base substitution T C intron_variant ESAD-UK 13 36901035 36901035 single base substitution T C upstream_gene_variant ESAD-UK 13 36901187 36901187 single base substitution G A intron_variant ESAD-UK 13 36901187 36901187 single base substitution G A upstream_gene_variant ESAD-UK 13 36901487 36901487 single base substitution T G intron_variant ESAD-UK 13 36901487 36901487 single base substitution T G upstream_gene_variant ESAD-UK 13 36901628 36901628 single base substitution T G intron_variant ESAD-UK 13 36901628 36901628 single base substitution T G upstream_gene_variant ESAD-UK 13 36901939 36901939 single base substitution A T intron_variant ESAD-UK 13 36901939 36901939 single base substitution A T upstream_gene_variant ESAD-UK 13 36902152 36902152 single base substitution A C intron_variant ESAD-UK 13 36902152 36902152 single base substitution A C upstream_gene_variant ESAD-UK 13 36902185 36902185 single base substitution A G intron_variant ESAD-UK 13 36902185 36902185 single base substitution A G upstream_gene_variant ESAD-UK 13 36902268 36902268 single base substitution C A intron_variant ESAD-UK 13 36902268 36902268 single base substitution C A upstream_gene_variant ESAD-UK 13 36902426 36902426 single base substitution T C intron_variant ESAD-UK 13 36902426 36902426 single base substitution T C upstream_gene_variant ESAD-UK 13 36902463 36902463 single base substitution G T intron_variant ESAD-UK 13 36902463 36902463 single base substitution G T upstream_gene_variant ESAD-UK 13 36902477 36902477 single base substitution A C intron_variant ESAD-UK 13 36902477 36902477 single base substitution A C upstream_gene_variant ESAD-UK 13 36902521 36902521 single base substitution T C intron_variant ESAD-UK 13 36902521 36902521 single base substitution T C upstream_gene_variant ESAD-UK 13 36902738 36902738 single base substitution G A intron_variant ESAD-UK 13 36902738 36902738 single base substitution G A upstream_gene_variant ESAD-UK 13 36903441 36903441 single base substitution A G intron_variant ESAD-UK 13 36903441 36903441 single base substitution A G upstream_gene_variant ESAD-UK 13 36903556 36903556 single base substitution C G exon_variant ESAD-UK 13 36903556 36903556 single base substitution C G synonymous_variant V369V 1107G>C ESAD-UK 13 36903556 36903556 single base substitution C G upstream_gene_variant ESAD-UK 13 36903599 36903599 single base substitution C G exon_variant ESAD-UK 13 36903599 36903599 single base substitution C G missense_variant R355T 1064G>C ESAD-UK 13 36903599 36903599 single base substitution C G upstream_gene_variant ESAD-UK 13 36903638 36903638 single base substitution G A exon_variant ESAD-UK 13 36903638 36903638 single base substitution G A missense_variant A342V 1025C>T ESAD-UK 13 36903638 36903638 single base substitution G A upstream_gene_variant ESAD-UK 13 36903812 36903812 single base substitution T G intron_variant ESAD-UK 13 36903812 36903812 single base substitution T G upstream_gene_variant ESAD-UK 13 36903843 36903843 single base substitution A G intron_variant ESAD-UK 13 36903843 36903843 single base substitution A G upstream_gene_variant ESAD-UK 13 36904125 36904125 single base substitution A C intron_variant ESAD-UK 13 36904125 36904125 single base substitution A C upstream_gene_variant ESAD-UK 13 36904126 36904126 single base substitution A C intron_variant ESAD-UK 13 36904126 36904126 single base substitution A C upstream_gene_variant ESAD-UK 13 36904158 36904158 single base substitution T G intron_variant ESAD-UK 13 36904158 36904158 single base substitution T G upstream_gene_variant ESAD-UK 13 36904178 36904178 single base substitution A C intron_variant ESAD-UK 13 36904178 36904178 single base substitution A C upstream_gene_variant ESAD-UK 13 36904292 36904292 single base substitution T G intron_variant ESAD-UK 13 36904292 36904292 single base substitution T G upstream_gene_variant ESAD-UK 13 36905174 36905174 single base substitution G C downstream_gene_variant ESAD-UK 13 36905174 36905174 single base substitution G C intron_variant ESAD-UK 13 36905174 36905174 single base substitution G C upstream_gene_variant ESAD-UK 13 36905311 36905311 single base substitution A C downstream_gene_variant ESAD-UK 13 36905311 36905311 single base substitution A C intron_variant ESAD-UK 13 36905311 36905311 single base substitution A C upstream_gene_variant ESAD-UK 13 36905586 36905586 single base substitution T C downstream_gene_variant ESAD-UK 13 36905586 36905586 single base substitution T C exon_variant ESAD-UK 13 36905586 36905586 single base substitution T C missense_variant R320G 958A>G ESAD-UK 13 36905586 36905586 single base substitution T C upstream_gene_variant ESAD-UK 13 36905675 36905675 single base substitution G A downstream_gene_variant ESAD-UK 13 36905675 36905675 single base substitution G A exon_variant ESAD-UK 13 36905675 36905675 single base substitution G A missense_variant A290V 869C>T ESAD-UK 13 36905675 36905675 single base substitution G A upstream_gene_variant ESAD-UK 13 36905867 36905867 single base substitution A G downstream_gene_variant ESAD-UK 13 36905867 36905867 single base substitution A G intron_variant ESAD-UK 13 36906310 36906310 single base substitution C A downstream_gene_variant ESAD-UK 13 36906310 36906310 single base substitution C A intron_variant ESAD-UK 13 36906486 36906486 single base substitution T G downstream_gene_variant ESAD-UK 13 36906486 36906486 single base substitution T G intron_variant ESAD-UK 13 36907116 36907116 single base substitution T G downstream_gene_variant ESAD-UK 13 36907116 36907116 single base substitution T G intron_variant ESAD-UK 13 36907133 36907133 single base substitution T G downstream_gene_variant ESAD-UK 13 36907133 36907133 single base substitution T G intron_variant ESAD-UK 13 36907217 36907217 single base substitution T G downstream_gene_variant ESAD-UK 13 36907217 36907217 single base substitution T G intron_variant ESAD-UK 13 36907593 36907593 single base substitution A G downstream_gene_variant ESAD-UK 13 36907593 36907593 single base substitution A G intron_variant ESAD-UK 13 36908068 36908068 single base substitution A G downstream_gene_variant ESAD-UK 13 36908068 36908068 single base substitution A G intron_variant ESAD-UK 13 36908162 36908162 single base substitution G T downstream_gene_variant ESAD-UK 13 36908162 36908162 single base substitution G T intron_variant ESAD-UK 13 36908525 36908525 single base substitution T A downstream_gene_variant ESAD-UK 13 36908525 36908525 single base substitution T A intron_variant ESAD-UK 13 36908638 36908638 single base substitution C G downstream_gene_variant ESAD-UK 13 36908638 36908638 single base substitution C G intron_variant ESAD-UK 13 36908774 36908774 single base substitution T G downstream_gene_variant ESAD-UK 13 36908774 36908774 single base substitution T G intron_variant ESAD-UK 13 36909169 36909169 single base substitution C G downstream_gene_variant ESAD-UK 13 36909169 36909169 single base substitution C G exon_variant ESAD-UK 13 36909169 36909169 single base substitution C G missense_variant G267R 799G>C ESAD-UK 13 36909323 36909323 single base substitution C G downstream_gene_variant ESAD-UK 13 36909323 36909323 single base substitution C G exon_variant ESAD-UK 13 36909323 36909323 single base substitution C G synonymous_variant G215G 645G>C ESAD-UK 13 36909381 36909381 single base substitution G A downstream_gene_variant ESAD-UK 13 36909381 36909381 single base substitution G A exon_variant ESAD-UK 13 36909381 36909381 single base substitution G A missense_variant S196L 587C>T ESAD-UK 13 36909428 36909428 single base substitution T G downstream_gene_variant ESAD-UK 13 36909428 36909428 single base substitution T G exon_variant ESAD-UK 13 36909428 36909428 single base substitution T G missense_variant E180D 540A>C ESAD-UK 13 36909503 36909503 single base substitution T C downstream_gene_variant ESAD-UK 13 36909503 36909503 single base substitution T C exon_variant ESAD-UK 13 36909503 36909503 single base substitution T C synonymous_variant A155A 465A>G ESAD-UK 13 36909926 36909926 single base substitution C A exon_variant ESAD-UK 13 36909926 36909926 single base substitution C A missense_variant K14N 42G>T ESAD-UK 13 36910612 36910612 single base substitution C T intron_variant ESAD-UK 13 36910959 36910959 insertion of <=200bp - A intron_variant ESAD-UK 13 36911316 36911316 single base substitution T G intron_variant ESAD-UK 13 36911578 36911578 single base substitution G T intron_variant ESAD-UK 13 36911644 36911644 single base substitution A C intron_variant ESAD-UK 13 36911756 36911756 single base substitution G A intron_variant ESAD-UK 13 36911967 36911967 single base substitution A C intron_variant ESAD-UK 13 36912001 36912001 single base substitution T G intron_variant ESAD-UK 13 36912103 36912103 single base substitution A G intron_variant ESAD-UK 13 36912122 36912122 single base substitution G T intron_variant ESAD-UK 13 36912147 36912147 single base substitution T C intron_variant ESAD-UK 13 36912147 36912147 single base substitution T G intron_variant ESAD-UK 13 36912177 36912177 single base substitution T G intron_variant ESAD-UK 13 36912281 36912281 single base substitution T G intron_variant ESAD-UK 13 36912783 36912783 single base substitution A T intron_variant ESAD-UK 13 36912852 36912852 single base substitution A T intron_variant ESAD-UK 13 36912871 36912871 single base substitution T G intron_variant ESAD-UK 13 36912948 36912948 single base substitution G A intron_variant ESAD-UK 13 36913023 36913023 single base substitution A G intron_variant ESAD-UK 13 36913300 36913300 single base substitution G T intron_variant ESAD-UK 13 36913617 36913617 single base substitution A G intron_variant ESAD-UK 13 36913978 36913978 single base substitution A T intron_variant ESAD-UK 13 36914041 36914041 single base substitution A G intron_variant ESAD-UK 13 36914058 36914058 single base substitution T C intron_variant ESAD-UK 13 36914087 36914087 single base substitution T C intron_variant ESAD-UK 13 36915504 36915504 single base substitution C A intron_variant ESAD-UK 13 36915548 36915548 single base substitution A T intron_variant ESAD-UK 13 36915739 36915739 single base substitution T C intron_variant ESAD-UK 13 36915749 36915749 single base substitution T C intron_variant ESAD-UK 13 36915768 36915768 single base substitution T G intron_variant ESAD-UK 13 36915783 36915783 single base substitution A G intron_variant ESAD-UK 13 36915903 36915903 single base substitution T G intron_variant ESAD-UK 13 36916112 36916112 single base substitution A G intron_variant ESAD-UK 13 36916416 36916416 single base substitution A G intron_variant ESAD-UK 13 36916513 36916513 single base substitution A C intron_variant ESAD-UK 13 36916817 36916817 single base substitution T G intron_variant ESAD-UK 13 36917231 36917231 single base substitution T G intron_variant ESAD-UK 13 36917660 36917660 single base substitution G A intron_variant ESAD-UK 13 36918452 36918452 single base substitution G A intron_variant ESAD-UK 13 36919656 36919656 single base substitution G T intron_variant ESAD-UK 13 36921072 36921072 single base substitution G C intron_variant ESAD-UK 13 36921072 36921072 single base substitution G C upstream_gene_variant ESAD-UK 13 36921322 36921322 single base substitution G T intron_variant ESAD-UK 13 36921322 36921322 single base substitution G T upstream_gene_variant ESAD-UK 13 36921420 36921420 single base substitution A T intron_variant ESAD-UK 13 36921420 36921420 single base substitution A T upstream_gene_variant ESAD-UK 13 36921690 36921690 single base substitution T C intron_variant ESAD-UK 13 36921690 36921690 single base substitution T C upstream_gene_variant ESAD-UK 13 36921703 36921703 single base substitution A C intron_variant ESAD-UK 13 36921703 36921703 single base substitution A C upstream_gene_variant ESAD-UK 13 36921913 36921913 single base substitution T A intron_variant ESAD-UK 13 36921913 36921913 single base substitution T A upstream_gene_variant ESAD-UK 13 36922250 36922250 single base substitution C T intron_variant ESAD-UK 13 36922250 36922250 single base substitution C T upstream_gene_variant ESAD-UK 13 36922814 36922814 single base substitution C T intron_variant ESAD-UK 13 36922814 36922814 single base substitution C T upstream_gene_variant ESAD-UK 13 36922925 36922925 single base substitution G A intron_variant ESAD-UK 13 36922925 36922925 single base substitution G A upstream_gene_variant ESAD-UK 13 36922937 36922937 single base substitution G A intron_variant ESAD-UK 13 36922937 36922937 single base substitution G A upstream_gene_variant ESAD-UK 13 36923166 36923166 single base substitution C A intron_variant ESAD-UK 13 36923166 36923166 single base substitution C A upstream_gene_variant ESAD-UK 13 36923213 36923213 single base substitution C G intron_variant ESAD-UK 13 36923213 36923213 single base substitution C G upstream_gene_variant ESAD-UK 13 36923588 36923588 single base substitution C T intron_variant ESAD-UK 13 36923588 36923588 single base substitution C T upstream_gene_variant ESAD-UK 13 36923652 36923652 single base substitution G A intron_variant ESAD-UK 13 36923652 36923652 single base substitution G A upstream_gene_variant ESAD-UK 13 36924135 36924135 single base substitution T G intron_variant ESAD-UK 13 36924135 36924135 single base substitution T G upstream_gene_variant ESAD-UK 13 36924431 36924431 single base substitution T C intron_variant ESAD-UK 13 36924431 36924431 single base substitution T C upstream_gene_variant ESAD-UK 13 36924723 36924723 single base substitution A C intron_variant ESAD-UK 13 36924723 36924723 single base substitution A C upstream_gene_variant ESAD-UK 13 36924781 36924781 single base substitution C G intron_variant ESAD-UK 13 36924781 36924781 single base substitution C G upstream_gene_variant ESAD-UK 13 36924973 36924973 single base substitution T C intron_variant ESAD-UK 13 36924973 36924973 single base substitution T C upstream_gene_variant ESAD-UK 13 36925234 36925234 single base substitution T A intron_variant ESAD-UK 13 36925234 36925234 single base substitution T A upstream_gene_variant ESAD-UK 13 36925286 36925286 single base substitution C A intron_variant ESAD-UK 13 36925286 36925286 single base substitution C A upstream_gene_variant ESAD-UK 13 36925371 36925371 single base substitution C G intron_variant ESAD-UK 13 36925371 36925371 single base substitution C G upstream_gene_variant ESAD-UK 13 36925392 36925392 single base substitution A G intron_variant ESAD-UK 13 36925392 36925392 single base substitution A G upstream_gene_variant ESAD-UK 13 36925712 36925712 single base substitution C T intron_variant ESAD-UK 13 36925712 36925712 single base substitution C T upstream_gene_variant ESAD-UK 13 36925943 36925943 single base substitution T G intron_variant ESAD-UK 13 36926025 36926025 single base substitution A T intron_variant ESAD-UK 13 36926060 36926060 single base substitution G T intron_variant ESAD-UK 13 36926115 36926115 single base substitution A G intron_variant ESAD-UK 13 36926301 36926301 single base substitution T C intron_variant ESAD-UK 13 36926311 36926311 single base substitution T C intron_variant ESAD-UK 13 36926380 36926380 single base substitution T C intron_variant ESAD-UK 13 36926419 36926419 single base substitution T G intron_variant ESAD-UK 13 36926877 36926877 single base substitution A C intron_variant ESAD-UK 13 36927258 36927258 insertion of <=200bp - A intron_variant ESAD-UK 13 36927282 36927282 single base substitution T C intron_variant ESAD-UK 13 36927659 36927659 single base substitution C A intron_variant ESAD-UK 13 36928080 36928080 single base substitution C A intron_variant ESAD-UK 13 36928176 36928176 single base substitution T G intron_variant ESAD-UK 13 36928364 36928364 single base substitution C A intron_variant ESAD-UK 13 36928550 36928550 single base substitution C A intron_variant ESAD-UK 13 36928759 36928759 single base substitution T C intron_variant ESAD-UK 13 36929030 36929030 single base substitution T C intron_variant ESAD-UK 13 36929969 36929969 single base substitution A C intron_variant ESAD-UK 13 36930736 36930736 single base substitution T C intron_variant ESAD-UK 13 36930778 36930778 single base substitution T C intron_variant ESAD-UK 13 36930870 36930870 single base substitution T A intron_variant ESAD-UK 13 36930963 36930963 single base substitution A C intron_variant ESAD-UK 13 36930983 36930983 single base substitution A G intron_variant ESAD-UK 13 36931210 36931210 single base substitution T G intron_variant ESAD-UK 13 36931370 36931370 single base substitution G T intron_variant ESAD-UK 13 36931482 36931482 single base substitution G A intron_variant ESAD-UK 13 36932312 36932312 single base substitution T G intron_variant ESAD-UK 13 36932764 36932764 single base substitution A G intron_variant ESAD-UK 13 36932767 36932767 single base substitution G T intron_variant ESAD-UK 13 36932856 36932856 single base substitution T C intron_variant ESAD-UK 13 36933100 36933100 single base substitution T G intron_variant ESAD-UK 13 36933732 36933732 single base substitution T C intron_variant ESAD-UK 13 36934489 36934489 single base substitution A T intron_variant ESAD-UK 13 36934872 36934872 single base substitution A C intron_variant ESAD-UK 13 36935254 36935254 single base substitution A C intron_variant ESAD-UK 13 36935342 36935342 single base substitution T C intron_variant ESAD-UK 13 36935578 36935578 single base substitution G C intron_variant ESAD-UK 13 36936629 36936629 single base substitution T G intron_variant ESAD-UK 13 36936839 36936839 single base substitution G C intron_variant ESAD-UK 13 36936851 36936851 single base substitution A C intron_variant ESAD-UK 13 36936876 36936876 single base substitution C T intron_variant ESAD-UK 13 36936968 36936968 single base substitution C G intron_variant ESAD-UK 13 36937157 36937157 single base substitution A T intron_variant ESAD-UK 13 36937344 36937344 single base substitution C A intron_variant ESAD-UK 13 36937774 36937774 single base substitution A G intron_variant ESAD-UK 13 36937871 36937871 single base substitution A C intron_variant ESAD-UK 13 36937961 36937961 single base substitution A C intron_variant ESAD-UK 13 36938453 36938453 single base substitution T G intron_variant ESAD-UK 13 36939153 36939153 single base substitution A C intron_variant ESAD-UK 13 36939258 36939258 single base substitution T A intron_variant ESAD-UK 13 36939388 36939388 single base substitution A G intron_variant ESAD-UK 13 36939479 36939479 single base substitution T G intron_variant ESAD-UK 13 36939553 36939553 single base substitution T G intron_variant ESAD-UK 13 36939575 36939575 single base substitution T G intron_variant ESAD-UK 13 36940835 36940835 single base substitution C G intron_variant ESAD-UK 13 36940944 36940944 single base substitution G A intron_variant ESAD-UK 13 36941161 36941161 single base substitution C T intron_variant ESAD-UK 13 36941176 36941176 single base substitution G A intron_variant ESAD-UK 13 36941264 36941264 single base substitution A C intron_variant ESAD-UK 13 36941268 36941268 single base substitution T G intron_variant ESAD-UK 13 36941307 36941307 single base substitution G T intron_variant ESAD-UK 13 36941640 36941640 single base substitution T A intron_variant ESAD-UK 13 36941767 36941767 single base substitution T G intron_variant ESAD-UK 13 36941995 36941995 single base substitution A G intron_variant ESAD-UK 13 36942723 36942723 single base substitution G A intron_variant ESAD-UK 13 36943010 36943010 single base substitution C T intron_variant ESAD-UK 13 36943053 36943053 single base substitution T C intron_variant ESAD-UK 13 36943170 36943170 single base substitution A C intron_variant ESAD-UK 13 36943366 36943366 single base substitution A C intron_variant ESAD-UK 13 36943754 36943754 single base substitution T C intron_variant ESAD-UK 13 36944070 36944070 single base substitution G A intron_variant ESAD-UK 13 36944229 36944229 single base substitution A C 5_prime_UTR_variant ESAD-UK 13 36944388 36944388 single base substitution T A upstream_gene_variant ESAD-UK 13 36944543 36944543 single base substitution A C upstream_gene_variant ESAD-UK 13 36944603 36944603 single base substitution T G upstream_gene_variant ESAD-UK 13 36944902 36944902 single base substitution T C upstream_gene_variant ESAD-UK 13 36944902 36944902 single base substitution T G upstream_gene_variant ESAD-UK 13 36944941 36944941 single base substitution A C upstream_gene_variant ESAD-UK 13 36944942 36944942 single base substitution A T upstream_gene_variant ESAD-UK 13 36944963 36944963 single base substitution T A upstream_gene_variant ESAD-UK 13 36945219 36945219 single base substitution G T upstream_gene_variant ESAD-UK 13 36945945 36945945 single base substitution T G upstream_gene_variant ESAD-UK 13 36946146 36946146 single base substitution A G upstream_gene_variant ESAD-UK 13 36946266 36946266 single base substitution A T upstream_gene_variant ESAD-UK 13 36947065 36947065 single base substitution G A upstream_gene_variant ESAD-UK 13 36947366 36947366 single base substitution G T upstream_gene_variant ESAD-UK 13 36947370 36947370 single base substitution C A upstream_gene_variant ESAD-UK 13 36947443 36947443 single base substitution C T upstream_gene_variant ESAD-UK 13 36947558 36947558 single base substitution C G upstream_gene_variant ESAD-UK 13 36948489 36948489 single base substitution A C upstream_gene_variant ESAD-UK 13 36948563 36948563 single base substitution A C upstream_gene_variant ESAD-UK 13 36948733 36948733 single base substitution T G upstream_gene_variant ESAD-UK 13 36949145 36949145 single base substitution T G upstream_gene_variant ESAD-UK 13 36949300 36949300 single base substitution G C upstream_gene_variant ESCA-CN 13 36909849 36909849 single base substitution T A exon_variant ESCA-CN 13 36909849 36909849 single base substitution T A missense_variant E40V 119A>T ESCA-CN 13 36939673 36939673 single base substitution T G intron_variant LAML-KR 13 36907583 36907583 single base substitution G T downstream_gene_variant LAML-KR 13 36907583 36907583 single base substitution G T intron_variant LAML-KR 13 36940123 36940123 single base substitution T C intron_variant LAML-KR 13 36942453 36942453 single base substitution T C intron_variant LICA-FR 13 36880887 36880887 single base substitution A G intron_variant LICA-FR 13 36885124 36885124 single base substitution G A downstream_gene_variant LICA-FR 13 36885124 36885124 single base substitution G A intron_variant LICA-FR 13 36895753 36895753 single base substitution C T downstream_gene_variant LICA-FR 13 36895753 36895753 single base substitution C T intron_variant LICA-FR 13 36900197 36900197 single base substitution T C exon_variant LICA-FR 13 36900197 36900197 single base substitution T C intron_variant LICA-FR 13 36902565 36902565 single base substitution C A intron_variant LICA-FR 13 36902565 36902565 single base substitution C A upstream_gene_variant LICA-FR 13 36916840 36916840 single base substitution C A intron_variant LICA-FR 13 36916867 36916867 single base substitution G C intron_variant LICA-FR 13 36926344 36926344 single base substitution A T intron_variant LICA-FR 13 36937526 36937526 single base substitution G T intron_variant LIHC-US 13 36939921 36939921 single base substitution G C intron_variant LINC-JP 13 36872655 36872655 single base substitution T C downstream_gene_variant LINC-JP 13 36873596 36873596 single base substitution A G downstream_gene_variant LINC-JP 13 36877541 36877541 single base substitution T C 3_prime_UTR_variant LINC-JP 13 36877541 36877541 single base substitution T C downstream_gene_variant LINC-JP 13 36882854 36882854 single base substitution A T downstream_gene_variant LINC-JP 13 36882854 36882854 single base substitution A T intron_variant LINC-JP 13 36885126 36885126 single base substitution T A downstream_gene_variant LINC-JP 13 36885126 36885126 single base substitution T A intron_variant LINC-JP 13 36886346 36886346 single base substitution C A exon_variant LINC-JP 13 36886346 36886346 single base substitution C A stop_gained E557* 1669G>T LINC-JP 13 36887657 36887657 single base substitution G A intron_variant LINC-JP 13 36887657 36887657 single base substitution G A upstream_gene_variant LINC-JP 13 36900913 36900913 single base substitution T C intron_variant LINC-JP 13 36900913 36900913 single base substitution T C upstream_gene_variant LINC-JP 13 36902246 36902246 single base substitution C A intron_variant LINC-JP 13 36902246 36902246 single base substitution C A upstream_gene_variant LINC-JP 13 36909834 36909834 single base substitution T C exon_variant LINC-JP 13 36909834 36909834 single base substitution T C missense_variant Y45C 134A>G LINC-JP 13 36913764 36913764 single base substitution C A intron_variant LINC-JP 13 36916300 36916300 single base substitution A T intron_variant LINC-JP 13 36918913 36918913 single base substitution C A intron_variant LINC-JP 13 36928068 36928068 single base substitution T C intron_variant LINC-JP 13 36932458 36932458 single base substitution A G intron_variant LINC-JP 13 36935712 36935712 single base substitution T C intron_variant LINC-JP 13 36940023 36940023 single base substitution A T intron_variant LINC-JP 13 36941017 36941017 single base substitution G A intron_variant LINC-JP 13 36942603 36942603 single base substitution A C intron_variant LIRI-JP 13 36871271 36871271 single base substitution T A downstream_gene_variant LIRI-JP 13 36874384 36874384 single base substitution T C downstream_gene_variant LIRI-JP 13 36875851 36875851 deletion of <=200bp A - 3_prime_UTR_variant LIRI-JP 13 36875851 36875851 deletion of <=200bp A - downstream_gene_variant LIRI-JP 13 36876478 36876478 single base substitution C G 3_prime_UTR_variant LIRI-JP 13 36876478 36876478 single base substitution C G downstream_gene_variant LIRI-JP 13 36877918 36877918 single base substitution G T 3_prime_UTR_variant LIRI-JP 13 36877918 36877918 single base substitution G T downstream_gene_variant LIRI-JP 13 36878511 36878511 single base substitution T C downstream_gene_variant LIRI-JP 13 36878511 36878511 single base substitution T C exon_variant LIRI-JP 13 36878511 36878511 single base substitution T C synonymous_variant K664K 1992A>G LIRI-JP 13 36880027 36880027 single base substitution C T intron_variant LIRI-JP 13 36881729 36881729 single base substitution A T downstream_gene_variant LIRI-JP 13 36881729 36881729 single base substitution A T intron_variant LIRI-JP 13 36881859 36881859 single base substitution T C downstream_gene_variant LIRI-JP 13 36881859 36881859 single base substitution T C intron_variant LIRI-JP 13 36883229 36883229 single base substitution A C downstream_gene_variant LIRI-JP 13 36883229 36883229 single base substitution A C intron_variant LIRI-JP 13 36884089 36884089 single base substitution T C downstream_gene_variant LIRI-JP 13 36884089 36884089 single base substitution T C intron_variant LIRI-JP 13 36884092 36884092 single base substitution T G downstream_gene_variant LIRI-JP 13 36884092 36884092 single base substitution T G intron_variant LIRI-JP 13 36884914 36884914 single base substitution G A downstream_gene_variant LIRI-JP 13 36884914 36884914 single base substitution G A intron_variant LIRI-JP 13 36885061 36885061 single base substitution G A downstream_gene_variant LIRI-JP 13 36885061 36885061 single base substitution G A intron_variant LIRI-JP 13 36885394 36885394 single base substitution T C downstream_gene_variant LIRI-JP 13 36885394 36885394 single base substitution T C intron_variant LIRI-JP 13 36886299 36886299 single base substitution T C exon_variant LIRI-JP 13 36886299 36886299 single base substitution T C synonymous_variant V572V 1716A>G LIRI-JP 13 36886334 36886334 single base substitution T C exon_variant LIRI-JP 13 36886334 36886334 single base substitution T C missense_variant K561E 1681A>G LIRI-JP 13 36886544 36886544 single base substitution G T exon_variant LIRI-JP 13 36886544 36886544 single base substitution G T missense_variant S518R 1554C>A LIRI-JP 13 36886745 36886745 single base substitution G T intron_variant LIRI-JP 13 36886745 36886745 single base substitution G T upstream_gene_variant LIRI-JP 13 36887281 36887281 single base substitution A G intron_variant LIRI-JP 13 36887281 36887281 single base substitution A G upstream_gene_variant LIRI-JP 13 36887834 36887834 single base substitution G T intron_variant LIRI-JP 13 36887834 36887834 single base substitution G T upstream_gene_variant LIRI-JP 13 36888337 36888337 single base substitution A G intron_variant LIRI-JP 13 36888337 36888337 single base substitution A G upstream_gene_variant LIRI-JP 13 36889061 36889061 single base substitution T C intron_variant LIRI-JP 13 36889061 36889061 single base substitution T C upstream_gene_variant LIRI-JP 13 36890090 36890090 single base substitution T C intron_variant LIRI-JP 13 36890090 36890090 single base substitution T C upstream_gene_variant LIRI-JP 13 36890188 36890188 single base substitution A G intron_variant LIRI-JP 13 36890188 36890188 single base substitution A G upstream_gene_variant LIRI-JP 13 36890593 36890593 single base substitution A G intron_variant LIRI-JP 13 36890593 36890593 single base substitution A G upstream_gene_variant LIRI-JP 13 36890677 36890677 single base substitution T G intron_variant LIRI-JP 13 36890677 36890677 single base substitution T G upstream_gene_variant LIRI-JP 13 36890950 36890950 single base substitution A T intron_variant LIRI-JP 13 36890950 36890950 single base substitution A T upstream_gene_variant LIRI-JP 13 36892462 36892462 single base substitution T C intron_variant LIRI-JP 13 36892462 36892462 single base substitution T C upstream_gene_variant LIRI-JP 13 36892953 36892953 single base substitution T A intron_variant LIRI-JP 13 36892953 36892953 single base substitution T A upstream_gene_variant LIRI-JP 13 36894736 36894736 single base substitution G C intron_variant LIRI-JP 13 36897307 36897307 single base substitution A C downstream_gene_variant LIRI-JP 13 36897307 36897307 single base substitution A C intron_variant LIRI-JP 13 36897319 36897319 single base substitution A T downstream_gene_variant LIRI-JP 13 36897319 36897319 single base substitution A T intron_variant LIRI-JP 13 36897681 36897681 single base substitution C T downstream_gene_variant LIRI-JP 13 36897681 36897681 single base substitution C T intron_variant LIRI-JP 13 36898202 36898202 single base substitution G T downstream_gene_variant LIRI-JP 13 36898202 36898202 single base substitution G T intron_variant LIRI-JP 13 36898428 36898428 single base substitution T C downstream_gene_variant LIRI-JP 13 36898428 36898428 single base substitution T C intron_variant LIRI-JP 13 36899347 36899347 single base substitution C T downstream_gene_variant LIRI-JP 13 36899347 36899347 single base substitution C T intron_variant LIRI-JP 13 36899377 36899377 single base substitution A T downstream_gene_variant LIRI-JP 13 36899377 36899377 single base substitution A T intron_variant LIRI-JP 13 36900734 36900734 deletion of <=200bp T - exon_variant LIRI-JP 13 36900734 36900734 deletion of <=200bp T - frameshift_variant K422 LIRI-JP 13 36901431 36901431 single base substitution T G intron_variant LIRI-JP 13 36901431 36901431 single base substitution T G upstream_gene_variant LIRI-JP 13 36901987 36901987 single base substitution C T intron_variant LIRI-JP 13 36901987 36901987 single base substitution C T upstream_gene_variant LIRI-JP 13 36902564 36902564 single base substitution T C intron_variant LIRI-JP 13 36902564 36902564 single base substitution T C upstream_gene_variant LIRI-JP 13 36903055 36903055 single base substitution T C intron_variant LIRI-JP 13 36903055 36903055 single base substitution T C upstream_gene_variant LIRI-JP 13 36903409 36903409 single base substitution A C intron_variant LIRI-JP 13 36903409 36903409 single base substitution A C upstream_gene_variant LIRI-JP 13 36903898 36903898 single base substitution G C intron_variant LIRI-JP 13 36903898 36903898 single base substitution G C upstream_gene_variant LIRI-JP 13 36903912 36903912 single base substitution G T intron_variant LIRI-JP 13 36903912 36903912 single base substitution G T upstream_gene_variant LIRI-JP 13 36904017 36904017 single base substitution T C intron_variant LIRI-JP 13 36904017 36904017 single base substitution T C upstream_gene_variant LIRI-JP 13 36904218 36904218 single base substitution T C intron_variant LIRI-JP 13 36904218 36904218 single base substitution T C upstream_gene_variant LIRI-JP 13 36905077 36905077 single base substitution C G downstream_gene_variant LIRI-JP 13 36905077 36905077 single base substitution C G intron_variant LIRI-JP 13 36905077 36905077 single base substitution C G upstream_gene_variant LIRI-JP 13 36905849 36905849 single base substitution A G downstream_gene_variant LIRI-JP 13 36905849 36905849 single base substitution A G intron_variant LIRI-JP 13 36906914 36906914 single base substitution T C downstream_gene_variant LIRI-JP 13 36906914 36906914 single base substitution T C intron_variant LIRI-JP 13 36906985 36906985 single base substitution A G downstream_gene_variant LIRI-JP 13 36906985 36906985 single base substitution A G intron_variant LIRI-JP 13 36909844 36909844 single base substitution C T exon_variant LIRI-JP 13 36909844 36909844 single base substitution C T missense_variant A42T 124G>A LIRI-JP 13 36910473 36910473 single base substitution C A 5_prime_UTR_variant LIRI-JP 13 36910473 36910473 single base substitution C A intron_variant LIRI-JP 13 36910912 36910912 single base substitution A G intron_variant LIRI-JP 13 36911644 36911644 single base substitution A G intron_variant LIRI-JP 13 36912348 36912348 single base substitution A G intron_variant LIRI-JP 13 36912939 36912939 single base substitution T A intron_variant LIRI-JP 13 36914113 36914113 single base substitution G A intron_variant LIRI-JP 13 36914213 36914213 single base substitution T C intron_variant LIRI-JP 13 36914655 36914655 single base substitution G T intron_variant LIRI-JP 13 36915041 36915041 single base substitution C T intron_variant LIRI-JP 13 36915529 36915529 single base substitution A C intron_variant LIRI-JP 13 36915653 36915653 single base substitution G A intron_variant LIRI-JP 13 36917539 36917539 single base substitution G T intron_variant LIRI-JP 13 36917659 36917659 single base substitution C T intron_variant LIRI-JP 13 36920806 36920806 single base substitution C T 5_prime_UTR_variant LIRI-JP 13 36920806 36920806 single base substitution C T exon_variant LIRI-JP 13 36920806 36920806 single base substitution C T intron_variant LIRI-JP 13 36920806 36920806 single base substitution C T upstream_gene_variant LIRI-JP 13 36921197 36921197 single base substitution G C intron_variant LIRI-JP 13 36921197 36921197 single base substitution G C upstream_gene_variant LIRI-JP 13 36921768 36921768 single base substitution T C intron_variant LIRI-JP 13 36921768 36921768 single base substitution T C upstream_gene_variant LIRI-JP 13 36921869 36921869 single base substitution A G intron_variant LIRI-JP 13 36921869 36921869 single base substitution A G upstream_gene_variant LIRI-JP 13 36922102 36922102 single base substitution G A intron_variant LIRI-JP 13 36922102 36922102 single base substitution G A upstream_gene_variant LIRI-JP 13 36922202 36922202 single base substitution C T intron_variant LIRI-JP 13 36922202 36922202 single base substitution C T upstream_gene_variant LIRI-JP 13 36922415 36922415 single base substitution C A intron_variant LIRI-JP 13 36922415 36922415 single base substitution C A upstream_gene_variant LIRI-JP 13 36922776 36922776 single base substitution G A intron_variant LIRI-JP 13 36922776 36922776 single base substitution G A upstream_gene_variant LIRI-JP 13 36923274 36923274 single base substitution C A intron_variant LIRI-JP 13 36923274 36923274 single base substitution C A upstream_gene_variant LIRI-JP 13 36923496 36923496 single base substitution T A intron_variant LIRI-JP 13 36923496 36923496 single base substitution T A upstream_gene_variant LIRI-JP 13 36927461 36927461 single base substitution T A intron_variant LIRI-JP 13 36927607 36927607 single base substitution T C intron_variant LIRI-JP 13 36927671 36927671 single base substitution G T intron_variant LIRI-JP 13 36927739 36927739 single base substitution C T intron_variant LIRI-JP 13 36929771 36929771 single base substitution T A intron_variant LIRI-JP 13 36929786 36929786 single base substitution A G intron_variant LIRI-JP 13 36930532 36930532 single base substitution C T intron_variant LIRI-JP 13 36931086 36931095 deletion of <=200bp TTAAAGACAG - intron_variant LIRI-JP 13 36931246 36931246 single base substitution C A intron_variant LIRI-JP 13 36931349 36931349 single base substitution G A intron_variant LIRI-JP 13 36934287 36934287 single base substitution C G intron_variant LIRI-JP 13 36934417 36934417 single base substitution A G intron_variant LIRI-JP 13 36934787 36934787 single base substitution T C intron_variant LIRI-JP 13 36935750 36935750 single base substitution A T intron_variant LIRI-JP 13 36936230 36936230 single base substitution G A intron_variant LIRI-JP 13 36936445 36936445 single base substitution C G intron_variant LIRI-JP 13 36936518 36936518 single base substitution G T intron_variant LIRI-JP 13 36936712 36936712 single base substitution C A intron_variant LIRI-JP 13 36936818 36936818 single base substitution C A intron_variant LIRI-JP 13 36937961 36937961 single base substitution A G intron_variant LIRI-JP 13 36938106 36938106 single base substitution T C intron_variant LIRI-JP 13 36938493 36938493 single base substitution A G intron_variant LIRI-JP 13 36938703 36938703 single base substitution T C intron_variant LIRI-JP 13 36939623 36939623 single base substitution T G intron_variant LIRI-JP 13 36939945 36939945 single base substitution C T intron_variant LIRI-JP 13 36941774 36941774 single base substitution G T intron_variant LIRI-JP 13 36942084 36942084 single base substitution C A intron_variant LIRI-JP 13 36943151 36943151 single base substitution A C intron_variant LIRI-JP 13 36943173 36943173 single base substitution A G intron_variant LIRI-JP 13 36943633 36943633 single base substitution G T intron_variant LIRI-JP 13 36943753 36943753 single base substitution C G intron_variant LIRI-JP 13 36944244 36944244 single base substitution G T 5_prime_UTR_variant LIRI-JP 13 36945684 36945684 single base substitution T C upstream_gene_variant LIRI-JP 13 36945814 36945814 single base substitution G A upstream_gene_variant LIRI-JP 13 36946756 36946756 single base substitution C G upstream_gene_variant LIRI-JP 13 36946995 36946995 single base substitution G A upstream_gene_variant LIRI-JP 13 36947476 36947476 single base substitution T C upstream_gene_variant LIRI-JP 13 36948198 36948198 single base substitution G T upstream_gene_variant LIRI-JP 13 36949128 36949128 single base substitution C A upstream_gene_variant LUSC-KR 13 36873124 36873124 single base substitution C A downstream_gene_variant LUSC-KR 13 36874084 36874084 single base substitution G A downstream_gene_variant LUSC-KR 13 36877771 36877771 single base substitution T C 3_prime_UTR_variant LUSC-KR 13 36877771 36877771 single base substitution T C downstream_gene_variant LUSC-KR 13 36881584 36881584 single base substitution T G downstream_gene_variant LUSC-KR 13 36881584 36881584 single base substitution T G intron_variant LUSC-KR 13 36887427 36887427 single base substitution G A intron_variant LUSC-KR 13 36887427 36887427 single base substitution G A upstream_gene_variant LUSC-KR 13 36888636 36888636 single base substitution C A intron_variant LUSC-KR 13 36888636 36888636 single base substitution C A upstream_gene_variant LUSC-KR 13 36889293 36889293 single base substitution C A intron_variant LUSC-KR 13 36889293 36889293 single base substitution C A upstream_gene_variant LUSC-KR 13 36893168 36893168 single base substitution C T intron_variant LUSC-KR 13 36893168 36893168 single base substitution C T upstream_gene_variant LUSC-KR 13 36893183 36893183 single base substitution C T intron_variant LUSC-KR 13 36893183 36893183 single base substitution C T upstream_gene_variant LUSC-KR 13 36893193 36893193 single base substitution G A intron_variant LUSC-KR 13 36893193 36893193 single base substitution G A upstream_gene_variant LUSC-KR 13 36893505 36893505 single base substitution A G intron_variant LUSC-KR 13 36893505 36893505 single base substitution A G upstream_gene_variant LUSC-KR 13 36895431 36895431 single base substitution C T downstream_gene_variant LUSC-KR 13 36895431 36895431 single base substitution C T intron_variant LUSC-KR 13 36895493 36895493 single base substitution G A downstream_gene_variant LUSC-KR 13 36895493 36895493 single base substitution G A intron_variant LUSC-KR 13 36895751 36895751 single base substitution C A downstream_gene_variant LUSC-KR 13 36895751 36895751 single base substitution C A intron_variant LUSC-KR 13 36896047 36896047 single base substitution T G downstream_gene_variant LUSC-KR 13 36896047 36896047 single base substitution T G intron_variant LUSC-KR 13 36898268 36898268 single base substitution C A downstream_gene_variant LUSC-KR 13 36898268 36898268 single base substitution C A intron_variant LUSC-KR 13 36898269 36898269 single base substitution C A downstream_gene_variant LUSC-KR 13 36898269 36898269 single base substitution C A intron_variant LUSC-KR 13 36898786 36898786 single base substitution G C downstream_gene_variant LUSC-KR 13 36898786 36898786 single base substitution G C intron_variant LUSC-KR 13 36907274 36907274 single base substitution C T downstream_gene_variant LUSC-KR 13 36907274 36907274 single base substitution C T intron_variant LUSC-KR 13 36907583 36907583 single base substitution G T downstream_gene_variant LUSC-KR 13 36907583 36907583 single base substitution G T intron_variant LUSC-KR 13 36911480 36911480 single base substitution G A intron_variant LUSC-KR 13 36912162 36912162 single base substitution G A intron_variant LUSC-KR 13 36914149 36914149 single base substitution G A intron_variant LUSC-KR 13 36930279 36930279 single base substitution A T intron_variant LUSC-KR 13 36933683 36933683 single base substitution C T intron_variant LUSC-KR 13 36939490 36939490 single base substitution C T intron_variant LUSC-US 13 36878767 36878767 single base substitution T G missense_variant Y579S 1736A>C LUSC-US 13 36878767 36878767 single base substitution T G splice_region_variant LUSC-US 13 36909559 36909559 single base substitution G A downstream_gene_variant LUSC-US 13 36909559 36909559 single base substitution G A exon_variant LUSC-US 13 36909559 36909559 single base substitution G A stop_gained Q137* 409C>T LUSC-US 13 36909772 36909772 single base substitution G C exon_variant LUSC-US 13 36909772 36909772 single base substitution G C missense_variant H66D 196C>G MALY-DE 13 36876094 36876094 single base substitution G A 3_prime_UTR_variant MALY-DE 13 36876094 36876094 single base substitution G A downstream_gene_variant MALY-DE 13 36877559 36877559 single base substitution T A 3_prime_UTR_variant MALY-DE 13 36877559 36877559 single base substitution T A downstream_gene_variant MALY-DE 13 36878094 36878094 single base substitution C A 3_prime_UTR_variant MALY-DE 13 36878094 36878094 single base substitution C A downstream_gene_variant MALY-DE 13 36878676 36878676 single base substitution G C exon_variant MALY-DE 13 36878676 36878676 single base substitution G C missense_variant I609M 1827C>G MALY-DE 13 36880075 36880075 single base substitution A C intron_variant MALY-DE 13 36880393 36880393 single base substitution G C intron_variant MALY-DE 13 36881540 36881540 single base substitution A C downstream_gene_variant MALY-DE 13 36881540 36881540 single base substitution A C intron_variant MALY-DE 13 36883044 36883044 single base substitution G T downstream_gene_variant MALY-DE 13 36883044 36883044 single base substitution G T intron_variant MALY-DE 13 36884751 36884751 single base substitution C G downstream_gene_variant MALY-DE 13 36884751 36884751 single base substitution C G intron_variant MALY-DE 13 36887552 36887552 single base substitution A C intron_variant MALY-DE 13 36887552 36887552 single base substitution A C upstream_gene_variant MALY-DE 13 36889668 36889668 single base substitution A G intron_variant MALY-DE 13 36889668 36889668 single base substitution A G upstream_gene_variant MALY-DE 13 36890927 36890927 single base substitution G C intron_variant MALY-DE 13 36890927 36890927 single base substitution G C upstream_gene_variant MALY-DE 13 36892305 36892305 single base substitution C A intron_variant MALY-DE 13 36892305 36892305 single base substitution C A upstream_gene_variant MALY-DE 13 36897164 36897164 single base substitution A C downstream_gene_variant MALY-DE 13 36897164 36897164 single base substitution A C intron_variant MALY-DE 13 36897562 36897562 single base substitution T C downstream_gene_variant MALY-DE 13 36897562 36897562 single base substitution T C intron_variant MALY-DE 13 36898091 36898091 single base substitution A C downstream_gene_variant MALY-DE 13 36898091 36898091 single base substitution A C intron_variant MALY-DE 13 36898611 36898611 single base substitution A G downstream_gene_variant MALY-DE 13 36898611 36898611 single base substitution A G intron_variant MALY-DE 13 36900404 36900404 single base substitution C A exon_variant MALY-DE 13 36900404 36900404 single base substitution C A intron_variant MALY-DE 13 36901445 36901445 single base substitution A C intron_variant MALY-DE 13 36901445 36901445 single base substitution A C upstream_gene_variant MALY-DE 13 36901987 36901987 single base substitution C T intron_variant MALY-DE 13 36901987 36901987 single base substitution C T upstream_gene_variant MALY-DE 13 36902226 36902226 single base substitution G A intron_variant MALY-DE 13 36902226 36902226 single base substitution G A upstream_gene_variant MALY-DE 13 36904287 36904287 single base substitution T C intron_variant MALY-DE 13 36904287 36904287 single base substitution T C upstream_gene_variant MALY-DE 13 36907570 36907570 single base substitution T A downstream_gene_variant MALY-DE 13 36907570 36907570 single base substitution T A intron_variant MALY-DE 13 36908862 36908862 single base substitution A C downstream_gene_variant MALY-DE 13 36908862 36908862 single base substitution A C intron_variant MALY-DE 13 36909063 36909063 single base substitution T C downstream_gene_variant MALY-DE 13 36909063 36909063 single base substitution T C intron_variant MALY-DE 13 36910959 36910959 insertion of <=200bp - A intron_variant MALY-DE 13 36917592 36917592 single base substitution G T intron_variant MALY-DE 13 36918814 36918814 insertion of <=200bp - A intron_variant MALY-DE 13 36919793 36919793 single base substitution C A intron_variant MALY-DE 13 36919793 36919793 single base substitution C A upstream_gene_variant MALY-DE 13 36919875 36919875 deletion of <=200bp G - intron_variant MALY-DE 13 36919875 36919875 deletion of <=200bp G - upstream_gene_variant MALY-DE 13 36920881 36920881 single base substitution C T 5_prime_UTR_variant MALY-DE 13 36920881 36920881 single base substitution C T exon_variant MALY-DE 13 36920881 36920881 single base substitution C T intron_variant MALY-DE 13 36920881 36920881 single base substitution C T upstream_gene_variant MALY-DE 13 36922232 36922232 single base substitution G T intron_variant MALY-DE 13 36922232 36922232 single base substitution G T upstream_gene_variant MALY-DE 13 36922694 36922694 single base substitution T C intron_variant MALY-DE 13 36922694 36922694 single base substitution T C upstream_gene_variant MALY-DE 13 36923581 36923581 single base substitution A G intron_variant MALY-DE 13 36923581 36923581 single base substitution A G upstream_gene_variant MALY-DE 13 36926957 36926957 single base substitution C A intron_variant MALY-DE 13 36927249 36927249 single base substitution C A intron_variant MALY-DE 13 36928991 36928991 single base substitution T C intron_variant MALY-DE 13 36932258 36932258 deletion of <=200bp A - intron_variant MALY-DE 13 36932410 36932410 single base substitution C G intron_variant MALY-DE 13 36932446 36932446 single base substitution T A intron_variant MALY-DE 13 36943131 36943131 single base substitution T A intron_variant MALY-DE 13 36944698 36944698 single base substitution G A upstream_gene_variant MALY-DE 13 36946511 36946511 single base substitution A T upstream_gene_variant MALY-DE 13 36946645 36946645 single base substitution A G upstream_gene_variant MALY-DE 13 36948089 36948089 single base substitution A T upstream_gene_variant MELA-AU 13 36870954 36870954 single base substitution T G downstream_gene_variant MELA-AU 13 36871104 36871104 single base substitution G A downstream_gene_variant MELA-AU 13 36871386 36871387 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 13 36871535 36871535 single base substitution G A downstream_gene_variant MELA-AU 13 36871838 36871838 single base substitution A T downstream_gene_variant MELA-AU 13 36871958 36871958 single base substitution C T downstream_gene_variant MELA-AU 13 36873158 36873158 single base substitution C T downstream_gene_variant MELA-AU 13 36873791 36873791 single base substitution G A downstream_gene_variant MELA-AU 13 36873961 36873961 single base substitution G A downstream_gene_variant MELA-AU 13 36873986 36873986 single base substitution G A downstream_gene_variant MELA-AU 13 36874036 36874036 single base substitution G A downstream_gene_variant MELA-AU 13 36874255 36874255 single base substitution A G downstream_gene_variant MELA-AU 13 36875239 36875239 single base substitution A C downstream_gene_variant MELA-AU 13 36876271 36876271 single base substitution G A 3_prime_UTR_variant MELA-AU 13 36876271 36876271 single base substitution G A downstream_gene_variant MELA-AU 13 36876606 36876607 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 13 36876606 36876607 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 13 36879810 36879810 single base substitution G A intron_variant MELA-AU 13 36880381 36880381 single base substitution G A intron_variant MELA-AU 13 36881336 36881336 single base substitution G A downstream_gene_variant MELA-AU 13 36881336 36881336 single base substitution G A intron_variant MELA-AU 13 36881799 36881799 single base substitution G A downstream_gene_variant MELA-AU 13 36881799 36881799 single base substitution G A intron_variant MELA-AU 13 36882160 36882160 single base substitution T A downstream_gene_variant MELA-AU 13 36882160 36882160 single base substitution T A intron_variant MELA-AU 13 36882163 36882163 single base substitution C T downstream_gene_variant MELA-AU 13 36882163 36882163 single base substitution C T intron_variant MELA-AU 13 36882973 36882973 single base substitution G A downstream_gene_variant MELA-AU 13 36882973 36882973 single base substitution G A intron_variant MELA-AU 13 36883728 36883728 single base substitution G A downstream_gene_variant MELA-AU 13 36883728 36883728 single base substitution G A intron_variant MELA-AU 13 36887959 36887959 single base substitution A G intron_variant MELA-AU 13 36887959 36887959 single base substitution A G upstream_gene_variant MELA-AU 13 36889826 36889826 single base substitution A G intron_variant MELA-AU 13 36889826 36889826 single base substitution A G upstream_gene_variant MELA-AU 13 36889976 36889976 single base substitution G A intron_variant MELA-AU 13 36889976 36889976 single base substitution G A upstream_gene_variant MELA-AU 13 36890829 36890829 single base substitution G C intron_variant MELA-AU 13 36890829 36890829 single base substitution G C upstream_gene_variant MELA-AU 13 36892216 36892216 single base substitution C T intron_variant MELA-AU 13 36892216 36892216 single base substitution C T upstream_gene_variant MELA-AU 13 36893775 36893775 single base substitution T C intron_variant MELA-AU 13 36894735 36894735 single base substitution G A intron_variant MELA-AU 13 36895875 36895875 single base substitution G A downstream_gene_variant MELA-AU 13 36895875 36895875 single base substitution G A intron_variant MELA-AU 13 36896249 36896249 single base substitution C T downstream_gene_variant MELA-AU 13 36896249 36896249 single base substitution C T intron_variant MELA-AU 13 36896318 36896318 single base substitution G A downstream_gene_variant MELA-AU 13 36896318 36896318 single base substitution G A intron_variant MELA-AU 13 36897142 36897142 single base substitution C T downstream_gene_variant MELA-AU 13 36897142 36897142 single base substitution C T intron_variant MELA-AU 13 36898018 36898018 single base substitution T C downstream_gene_variant MELA-AU 13 36898018 36898018 single base substitution T C intron_variant MELA-AU 13 36898226 36898226 single base substitution G A downstream_gene_variant MELA-AU 13 36898226 36898226 single base substitution G A intron_variant MELA-AU 13 36898296 36898296 single base substitution G A downstream_gene_variant MELA-AU 13 36898296 36898296 single base substitution G A intron_variant MELA-AU 13 36898846 36898846 single base substitution A G downstream_gene_variant MELA-AU 13 36898846 36898846 single base substitution A G intron_variant MELA-AU 13 36898953 36898953 single base substitution G A downstream_gene_variant MELA-AU 13 36898953 36898953 single base substitution G A intron_variant MELA-AU 13 36899087 36899087 single base substitution A T downstream_gene_variant MELA-AU 13 36899087 36899087 single base substitution A T intron_variant MELA-AU 13 36899290 36899290 single base substitution G A downstream_gene_variant MELA-AU 13 36899290 36899290 single base substitution G A intron_variant MELA-AU 13 36899587 36899587 single base substitution G A downstream_gene_variant MELA-AU 13 36899587 36899587 single base substitution G A intron_variant MELA-AU 13 36899638 36899638 single base substitution G A downstream_gene_variant MELA-AU 13 36899638 36899638 single base substitution G A intron_variant MELA-AU 13 36899919 36899919 single base substitution A C downstream_gene_variant MELA-AU 13 36899919 36899919 single base substitution A C intron_variant MELA-AU 13 36899989 36899989 single base substitution G A downstream_gene_variant MELA-AU 13 36899989 36899989 single base substitution G A intron_variant MELA-AU 13 36900238 36900238 single base substitution G A exon_variant MELA-AU 13 36900238 36900238 single base substitution G A intron_variant MELA-AU 13 36900686 36900686 single base substitution G A exon_variant MELA-AU 13 36900686 36900686 single base substitution G A intron_variant MELA-AU 13 36901038 36901038 single base substitution A G intron_variant MELA-AU 13 36901038 36901038 single base substitution A G upstream_gene_variant MELA-AU 13 36901897 36901897 single base substitution G A intron_variant MELA-AU 13 36901897 36901897 single base substitution G A upstream_gene_variant MELA-AU 13 36902868 36902868 single base substitution G A intron_variant MELA-AU 13 36902868 36902868 single base substitution G A upstream_gene_variant MELA-AU 13 36903449 36903449 single base substitution G A intron_variant MELA-AU 13 36903449 36903449 single base substitution G A upstream_gene_variant MELA-AU 13 36904072 36904072 single base substitution T C intron_variant MELA-AU 13 36904072 36904072 single base substitution T C upstream_gene_variant MELA-AU 13 36904421 36904421 single base substitution T C downstream_gene_variant MELA-AU 13 36904421 36904421 single base substitution T C intron_variant MELA-AU 13 36904421 36904421 single base substitution T C upstream_gene_variant MELA-AU 13 36904743 36904743 single base substitution G A downstream_gene_variant MELA-AU 13 36904743 36904743 single base substitution G A intron_variant MELA-AU 13 36904743 36904743 single base substitution G A upstream_gene_variant MELA-AU 13 36907262 36907262 single base substitution T C downstream_gene_variant MELA-AU 13 36907262 36907262 single base substitution T C intron_variant MELA-AU 13 36907723 36907723 single base substitution A C downstream_gene_variant MELA-AU 13 36907723 36907723 single base substitution A C intron_variant MELA-AU 13 36908573 36908573 single base substitution G A downstream_gene_variant MELA-AU 13 36908573 36908573 single base substitution G A intron_variant MELA-AU 13 36908843 36908843 single base substitution A T downstream_gene_variant MELA-AU 13 36908843 36908843 single base substitution A T intron_variant MELA-AU 13 36909172 36909172 single base substitution G A downstream_gene_variant MELA-AU 13 36909172 36909172 single base substitution G A exon_variant MELA-AU 13 36909172 36909172 single base substitution G A missense_variant P266S 796C>T MELA-AU 13 36909265 36909265 single base substitution G T downstream_gene_variant MELA-AU 13 36909265 36909265 single base substitution G T exon_variant MELA-AU 13 36909265 36909265 single base substitution G T missense_variant P235T 703C>A MELA-AU 13 36910066 36910066 single base substitution T G intron_variant MELA-AU 13 36910631 36910631 single base substitution A T intron_variant MELA-AU 13 36911632 36911632 single base substitution G A intron_variant MELA-AU 13 36913338 36913338 single base substitution A G intron_variant MELA-AU 13 36913703 36913703 single base substitution G A intron_variant MELA-AU 13 36913886 36913886 single base substitution G A intron_variant MELA-AU 13 36914672 36914672 single base substitution G A intron_variant MELA-AU 13 36914749 36914749 single base substitution C G intron_variant MELA-AU 13 36915129 36915129 single base substitution G A intron_variant MELA-AU 13 36915304 36915304 single base substitution G A intron_variant MELA-AU 13 36915757 36915757 single base substitution A G intron_variant MELA-AU 13 36917348 36917348 single base substitution G A intron_variant MELA-AU 13 36918428 36918428 single base substitution C T intron_variant MELA-AU 13 36920231 36920231 single base substitution A G intron_variant MELA-AU 13 36920231 36920231 single base substitution A G upstream_gene_variant MELA-AU 13 36921669 36921669 single base substitution C T intron_variant MELA-AU 13 36921669 36921669 single base substitution C T upstream_gene_variant MELA-AU 13 36922088 36922088 single base substitution C T intron_variant MELA-AU 13 36922088 36922088 single base substitution C T upstream_gene_variant MELA-AU 13 36923341 36923341 single base substitution C T intron_variant MELA-AU 13 36923341 36923341 single base substitution C T upstream_gene_variant MELA-AU 13 36923893 36923893 single base substitution C T intron_variant MELA-AU 13 36923893 36923893 single base substitution C T upstream_gene_variant MELA-AU 13 36924019 36924019 single base substitution T A intron_variant MELA-AU 13 36924019 36924019 single base substitution T A upstream_gene_variant MELA-AU 13 36924624 36924624 single base substitution C T intron_variant MELA-AU 13 36924624 36924624 single base substitution C T upstream_gene_variant MELA-AU 13 36926566 36926567 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 13 36926619 36926619 single base substitution T A intron_variant MELA-AU 13 36926916 36926916 single base substitution C T intron_variant MELA-AU 13 36927793 36927793 single base substitution T C intron_variant MELA-AU 13 36928995 36928995 single base substitution C T intron_variant MELA-AU 13 36929986 36929986 deletion of <=200bp C - intron_variant MELA-AU 13 36930168 36930168 single base substitution C T intron_variant MELA-AU 13 36931123 36931123 single base substitution T G intron_variant MELA-AU 13 36931212 36931212 single base substitution C T intron_variant MELA-AU 13 36932283 36932283 single base substitution T G intron_variant MELA-AU 13 36932607 36932607 single base substitution C T intron_variant MELA-AU 13 36932711 36932711 single base substitution T C intron_variant MELA-AU 13 36934655 36934655 single base substitution G A intron_variant MELA-AU 13 36935736 36935737 multiple base substitution (>=2bp and <=200bp) TC AT intron_variant MELA-AU 13 36936946 36936946 single base substitution G C intron_variant MELA-AU 13 36937021 36937021 single base substitution C T intron_variant MELA-AU 13 36937106 36937106 single base substitution C T intron_variant MELA-AU 13 36937345 36937345 deletion of <=200bp T - intron_variant MELA-AU 13 36937584 36937584 single base substitution C G intron_variant MELA-AU 13 36938050 36938050 single base substitution C T intron_variant MELA-AU 13 36938198 36938198 single base substitution C T intron_variant MELA-AU 13 36939078 36939078 single base substitution C T intron_variant MELA-AU 13 36939824 36939824 single base substitution G A intron_variant MELA-AU 13 36940139 36940139 single base substitution C T intron_variant MELA-AU 13 36940240 36940240 single base substitution C T intron_variant MELA-AU 13 36940289 36940289 single base substitution C T intron_variant MELA-AU 13 36940934 36940934 single base substitution T C intron_variant MELA-AU 13 36941104 36941104 single base substitution C T intron_variant MELA-AU 13 36941161 36941161 single base substitution C T intron_variant MELA-AU 13 36941199 36941199 single base substitution C T intron_variant MELA-AU 13 36941405 36941405 single base substitution C T intron_variant MELA-AU 13 36942026 36942026 single base substitution C T intron_variant MELA-AU 13 36942369 36942369 single base substitution G A intron_variant MELA-AU 13 36942800 36942800 single base substitution C T intron_variant MELA-AU 13 36943680 36943680 single base substitution C A intron_variant MELA-AU 13 36943999 36943999 single base substitution T C intron_variant MELA-AU 13 36944216 36944216 single base substitution C T intron_variant MELA-AU 13 36944381 36944382 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 13 36944407 36944407 single base substitution C T upstream_gene_variant MELA-AU 13 36944442 36944442 single base substitution C T upstream_gene_variant MELA-AU 13 36944459 36944459 single base substitution C T upstream_gene_variant MELA-AU 13 36944599 36944599 single base substitution A G upstream_gene_variant MELA-AU 13 36944601 36944601 single base substitution A C upstream_gene_variant MELA-AU 13 36944837 36944837 single base substitution C T upstream_gene_variant MELA-AU 13 36945005 36945005 single base substitution C T upstream_gene_variant MELA-AU 13 36945007 36945007 single base substitution T C upstream_gene_variant MELA-AU 13 36945378 36945378 single base substitution C T upstream_gene_variant MELA-AU 13 36945585 36945585 single base substitution G A upstream_gene_variant MELA-AU 13 36945749 36945749 single base substitution C A upstream_gene_variant MELA-AU 13 36945826 36945826 single base substitution T C upstream_gene_variant MELA-AU 13 36945878 36945878 single base substitution C T upstream_gene_variant MELA-AU 13 36947138 36947138 single base substitution G A upstream_gene_variant MELA-AU 13 36947721 36947721 single base substitution C T upstream_gene_variant MELA-AU 13 36947823 36947823 single base substitution C T upstream_gene_variant MELA-AU 13 36948402 36948402 single base substitution C T upstream_gene_variant ORCA-IN 13 36894409 36894409 single base substitution C T intron_variant ORCA-IN 13 36899142 36899142 single base substitution C G downstream_gene_variant ORCA-IN 13 36899142 36899142 single base substitution C G intron_variant ORCA-IN 13 36914922 36914922 single base substitution T C intron_variant OV-AU 13 36877607 36877607 single base substitution T A 3_prime_UTR_variant OV-AU 13 36877607 36877607 single base substitution T A downstream_gene_variant OV-AU 13 36880159 36880159 single base substitution G A intron_variant OV-AU 13 36886070 36886070 single base substitution A C downstream_gene_variant OV-AU 13 36886070 36886070 single base substitution A C intron_variant OV-AU 13 36888210 36888210 single base substitution G C exon_variant OV-AU 13 36888210 36888210 single base substitution G C intron_variant OV-AU 13 36888210 36888210 single base substitution G C upstream_gene_variant OV-AU 13 36890286 36890286 single base substitution C T intron_variant OV-AU 13 36890286 36890286 single base substitution C T upstream_gene_variant OV-AU 13 36894313 36894313 single base substitution C A intron_variant OV-AU 13 36896281 36896281 single base substitution T G downstream_gene_variant OV-AU 13 36896281 36896281 single base substitution T G intron_variant OV-AU 13 36896874 36896874 single base substitution G A downstream_gene_variant OV-AU 13 36896874 36896874 single base substitution G A intron_variant OV-AU 13 36903588 36903588 single base substitution C A exon_variant OV-AU 13 36903588 36903588 single base substitution C A missense_variant D359Y 1075G>T OV-AU 13 36903588 36903588 single base substitution C A upstream_gene_variant OV-AU 13 36905355 36905355 single base substitution C T downstream_gene_variant OV-AU 13 36905355 36905355 single base substitution C T intron_variant OV-AU 13 36905355 36905355 single base substitution C T upstream_gene_variant OV-AU 13 36914033 36914033 single base substitution C G intron_variant OV-AU 13 36915726 36915726 single base substitution T G intron_variant OV-AU 13 36916264 36916264 single base substitution T A intron_variant OV-AU 13 36917469 36917469 single base substitution G A intron_variant OV-AU 13 36923964 36923964 single base substitution A C intron_variant OV-AU 13 36923964 36923964 single base substitution A C upstream_gene_variant OV-AU 13 36926704 36926704 single base substitution A C intron_variant OV-AU 13 36937789 36937789 single base substitution A C intron_variant OV-AU 13 36944190 36944190 single base substitution A C intron_variant OV-AU 13 36948927 36948927 single base substitution G A upstream_gene_variant PACA-AU 13 36871131 36871131 single base substitution C T downstream_gene_variant PACA-AU 13 36871712 36871712 single base substitution T A downstream_gene_variant PACA-AU 13 36875373 36875373 single base substitution G A downstream_gene_variant PACA-AU 13 36877632 36877632 single base substitution G A 3_prime_UTR_variant PACA-AU 13 36877632 36877632 single base substitution G A downstream_gene_variant PACA-AU 13 36881184 36881184 single base substitution C A intron_variant PACA-AU 13 36881531 36881531 single base substitution T G downstream_gene_variant PACA-AU 13 36881531 36881531 single base substitution T G intron_variant PACA-AU 13 36882147 36882147 single base substitution T C downstream_gene_variant PACA-AU 13 36882147 36882147 single base substitution T C intron_variant PACA-AU 13 36883940 36883940 single base substitution C A downstream_gene_variant PACA-AU 13 36883940 36883940 single base substitution C A intron_variant PACA-AU 13 36884419 36884419 insertion of <=200bp - T downstream_gene_variant PACA-AU 13 36884419 36884419 insertion of <=200bp - T intron_variant PACA-AU 13 36885963 36885963 single base substitution G A downstream_gene_variant PACA-AU 13 36885963 36885963 single base substitution G A intron_variant PACA-AU 13 36886585 36886585 single base substitution C T exon_variant PACA-AU 13 36886585 36886585 single base substitution C T missense_variant V505I 1513G>A PACA-AU 13 36886585 36886585 single base substitution C T upstream_gene_variant PACA-AU 13 36889136 36889136 single base substitution G A intron_variant PACA-AU 13 36889136 36889136 single base substitution G A upstream_gene_variant PACA-AU 13 36890022 36890022 single base substitution A C intron_variant PACA-AU 13 36890022 36890022 single base substitution A C upstream_gene_variant PACA-AU 13 36890080 36890082 deletion of <=200bp AAT - intron_variant PACA-AU 13 36890080 36890082 deletion of <=200bp AAT - upstream_gene_variant PACA-AU 13 36890108 36890108 single base substitution C T intron_variant PACA-AU 13 36890108 36890108 single base substitution C T upstream_gene_variant PACA-AU 13 36890798 36890798 single base substitution T A intron_variant PACA-AU 13 36890798 36890798 single base substitution T A upstream_gene_variant PACA-AU 13 36892532 36892532 single base substitution G A intron_variant PACA-AU 13 36892532 36892532 single base substitution G A upstream_gene_variant PACA-AU 13 36893099 36893099 single base substitution C T intron_variant PACA-AU 13 36893099 36893099 single base substitution C T upstream_gene_variant PACA-AU 13 36893354 36893354 insertion of <=200bp - TT intron_variant PACA-AU 13 36893354 36893354 insertion of <=200bp - TT upstream_gene_variant PACA-AU 13 36894459 36894459 single base substitution C A intron_variant PACA-AU 13 36894582 36894582 single base substitution G T intron_variant PACA-AU 13 36895078 36895078 single base substitution C A downstream_gene_variant PACA-AU 13 36895078 36895078 single base substitution C A intron_variant PACA-AU 13 36895089 36895089 single base substitution G T downstream_gene_variant PACA-AU 13 36895089 36895089 single base substitution G T intron_variant PACA-AU 13 36895235 36895235 single base substitution G A downstream_gene_variant PACA-AU 13 36895235 36895235 single base substitution G A intron_variant PACA-AU 13 36896211 36896211 single base substitution C A downstream_gene_variant PACA-AU 13 36896211 36896211 single base substitution C A intron_variant PACA-AU 13 36896316 36896316 single base substitution C T downstream_gene_variant PACA-AU 13 36896316 36896316 single base substitution C T intron_variant PACA-AU 13 36897170 36897170 single base substitution G T downstream_gene_variant PACA-AU 13 36897170 36897170 single base substitution G T intron_variant PACA-AU 13 36898647 36898647 single base substitution G A downstream_gene_variant PACA-AU 13 36898647 36898647 single base substitution G A intron_variant PACA-AU 13 36899025 36899025 single base substitution A C downstream_gene_variant PACA-AU 13 36899025 36899025 single base substitution A C intron_variant PACA-AU 13 36906002 36906002 single base substitution A T downstream_gene_variant PACA-AU 13 36906002 36906002 single base substitution A T intron_variant PACA-AU 13 36910967 36910967 single base substitution T A intron_variant PACA-AU 13 36918864 36918864 single base substitution C T intron_variant PACA-AU 13 36919038 36919038 deletion of <=200bp T - intron_variant PACA-AU 13 36919551 36919551 single base substitution T C intron_variant PACA-AU 13 36919771 36919771 single base substitution C G exon_variant PACA-AU 13 36919771 36919771 single base substitution C G intron_variant PACA-AU 13 36920746 36920746 single base substitution C T 5_prime_UTR_variant PACA-AU 13 36920746 36920746 single base substitution C T exon_variant PACA-AU 13 36920746 36920746 single base substitution C T intron_variant PACA-AU 13 36920746 36920746 single base substitution C T upstream_gene_variant PACA-AU 13 36921610 36921610 single base substitution G C intron_variant PACA-AU 13 36921610 36921610 single base substitution G C upstream_gene_variant PACA-AU 13 36929986 36929986 deletion of <=200bp C - intron_variant PACA-AU 13 36929987 36929987 single base substitution C A intron_variant PACA-AU 13 36932549 36932549 single base substitution G T intron_variant PACA-AU 13 36933827 36933827 single base substitution G T intron_variant PACA-AU 13 36936801 36936801 single base substitution G T intron_variant PACA-AU 13 36937268 36937268 single base substitution G A intron_variant PACA-AU 13 36938679 36938679 single base substitution C T intron_variant PACA-AU 13 36939573 36939573 single base substitution T G intron_variant PACA-AU 13 36940047 36940047 single base substitution T G intron_variant PACA-AU 13 36942267 36942267 single base substitution C T intron_variant PACA-AU 13 36942623 36942623 single base substitution C G intron_variant PACA-AU 13 36944902 36944902 single base substitution T G upstream_gene_variant PACA-AU 13 36945759 36945759 single base substitution C A upstream_gene_variant PACA-AU 13 36946197 36946197 single base substitution A T upstream_gene_variant PACA-AU 13 36947222 36947222 single base substitution G T upstream_gene_variant PACA-AU 13 36947995 36947995 single base substitution G A upstream_gene_variant PACA-CA 13 36871873 36871873 single base substitution C A downstream_gene_variant PACA-CA 13 36872993 36872993 single base substitution G A downstream_gene_variant PACA-CA 13 36873640 36873640 single base substitution G C downstream_gene_variant PACA-CA 13 36874854 36874854 single base substitution T C downstream_gene_variant PACA-CA 13 36874926 36874926 single base substitution T G downstream_gene_variant PACA-CA 13 36875217 36875217 single base substitution C T downstream_gene_variant PACA-CA 13 36876783 36876783 single base substitution A C 3_prime_UTR_variant PACA-CA 13 36876783 36876783 single base substitution A C downstream_gene_variant PACA-CA 13 36877772 36877772 single base substitution G A 3_prime_UTR_variant PACA-CA 13 36877772 36877772 single base substitution G A downstream_gene_variant PACA-CA 13 36878112 36878112 single base substitution A C 3_prime_UTR_variant PACA-CA 13 36878112 36878112 single base substitution A C downstream_gene_variant PACA-CA 13 36885725 36885725 single base substitution T A downstream_gene_variant PACA-CA 13 36885725 36885725 single base substitution T A intron_variant PACA-CA 13 36886327 36886327 single base substitution A G exon_variant PACA-CA 13 36886327 36886327 single base substitution A G missense_variant I563T 1688T>C PACA-CA 13 36887713 36887713 single base substitution C T intron_variant PACA-CA 13 36887713 36887713 single base substitution C T upstream_gene_variant PACA-CA 13 36888662 36888662 single base substitution T A intron_variant PACA-CA 13 36888662 36888662 single base substitution T A upstream_gene_variant PACA-CA 13 36891323 36891323 single base substitution C T intron_variant PACA-CA 13 36891323 36891323 single base substitution C T upstream_gene_variant PACA-CA 13 36893353 36893353 insertion of <=200bp - TT intron_variant PACA-CA 13 36893353 36893353 insertion of <=200bp - TT upstream_gene_variant PACA-CA 13 36894656 36894656 single base substitution C A intron_variant PACA-CA 13 36896297 36896297 single base substitution G A downstream_gene_variant PACA-CA 13 36896297 36896297 single base substitution G A intron_variant PACA-CA 13 36896554 36896554 single base substitution G A downstream_gene_variant PACA-CA 13 36896554 36896554 single base substitution G A intron_variant PACA-CA 13 36897511 36897511 single base substitution C T downstream_gene_variant PACA-CA 13 36897511 36897511 single base substitution C T intron_variant PACA-CA 13 36901743 36901743 single base substitution C A intron_variant PACA-CA 13 36901743 36901743 single base substitution C A upstream_gene_variant PACA-CA 13 36902511 36902511 single base substitution T G intron_variant PACA-CA 13 36902511 36902511 single base substitution T G upstream_gene_variant PACA-CA 13 36903121 36903121 single base substitution T C intron_variant PACA-CA 13 36903121 36903121 single base substitution T C upstream_gene_variant PACA-CA 13 36905355 36905355 single base substitution C T downstream_gene_variant PACA-CA 13 36905355 36905355 single base substitution C T intron_variant PACA-CA 13 36905355 36905355 single base substitution C T upstream_gene_variant PACA-CA 13 36905616 36905616 single base substitution C A downstream_gene_variant PACA-CA 13 36905616 36905616 single base substitution C A exon_variant PACA-CA 13 36905616 36905616 single base substitution C A missense_variant V310F 928G>T PACA-CA 13 36905616 36905616 single base substitution C A upstream_gene_variant PACA-CA 13 36907832 36907832 deletion of <=200bp T - downstream_gene_variant PACA-CA 13 36907832 36907832 deletion of <=200bp T - intron_variant PACA-CA 13 36908734 36908734 single base substitution G A downstream_gene_variant PACA-CA 13 36908734 36908734 single base substitution G A intron_variant PACA-CA 13 36908762 36908762 single base substitution G A downstream_gene_variant PACA-CA 13 36908762 36908762 single base substitution G A intron_variant PACA-CA 13 36910253 36910253 single base substitution T C intron_variant PACA-CA 13 36911718 36911718 single base substitution C T intron_variant PACA-CA 13 36912717 36912717 single base substitution C T intron_variant PACA-CA 13 36913571 36913571 single base substitution A G intron_variant PACA-CA 13 36914373 36914373 single base substitution G A intron_variant PACA-CA 13 36914633 36914633 single base substitution G T intron_variant PACA-CA 13 36917334 36917334 single base substitution A G intron_variant PACA-CA 13 36918214 36918214 single base substitution T G intron_variant PACA-CA 13 36919818 36919818 single base substitution G A intron_variant PACA-CA 13 36919818 36919818 single base substitution G A upstream_gene_variant PACA-CA 13 36924040 36924040 single base substitution C T intron_variant PACA-CA 13 36924040 36924040 single base substitution C T upstream_gene_variant PACA-CA 13 36924041 36924041 single base substitution G A intron_variant PACA-CA 13 36924041 36924041 single base substitution G A upstream_gene_variant PACA-CA 13 36924786 36924786 insertion of <=200bp - A intron_variant PACA-CA 13 36924786 36924786 insertion of <=200bp - A upstream_gene_variant PACA-CA 13 36926122 36926122 single base substitution T A intron_variant PACA-CA 13 36926906 36926906 single base substitution C A intron_variant PACA-CA 13 36927523 36927523 single base substitution G T intron_variant PACA-CA 13 36928309 36928309 single base substitution C A intron_variant PACA-CA 13 36929790 36929790 single base substitution G T intron_variant PACA-CA 13 36929978 36929978 deletion of <=200bp A - intron_variant PACA-CA 13 36931343 36931343 single base substitution G T intron_variant PACA-CA 13 36931910 36931910 single base substitution G C intron_variant PACA-CA 13 36931913 36931913 single base substitution C T intron_variant PACA-CA 13 36932304 36932304 single base substitution G A intron_variant PACA-CA 13 36932499 36932499 single base substitution C T intron_variant PACA-CA 13 36933253 36933253 single base substitution C T intron_variant PACA-CA 13 36933268 36933268 single base substitution C T intron_variant PACA-CA 13 36933509 36933509 single base substitution C G intron_variant PACA-CA 13 36935571 36935571 single base substitution C T intron_variant PACA-CA 13 36935653 36935653 single base substitution C T intron_variant PACA-CA 13 36936100 36936100 single base substitution G T intron_variant PACA-CA 13 36936760 36936760 single base substitution G A intron_variant PACA-CA 13 36936941 36936941 single base substitution T A intron_variant PACA-CA 13 36937155 36937155 single base substitution T A intron_variant PACA-CA 13 36938145 36938145 single base substitution C T intron_variant PACA-CA 13 36939850 36939850 deletion of <=200bp T - intron_variant PACA-CA 13 36940283 36940283 single base substitution C T intron_variant PACA-CA 13 36941036 36941036 single base substitution T G intron_variant PACA-CA 13 36941289 36941289 single base substitution G A intron_variant PACA-CA 13 36941789 36941789 single base substitution T C intron_variant PACA-CA 13 36942189 36942189 single base substitution T C intron_variant PACA-CA 13 36942398 36942398 single base substitution T C intron_variant PACA-CA 13 36942585 36942585 single base substitution A T intron_variant PACA-CA 13 36942652 36942652 single base substitution C A intron_variant PACA-CA 13 36943466 36943466 single base substitution T C intron_variant PACA-CA 13 36944960 36944961 deletion of <=200bp CT - upstream_gene_variant PACA-CA 13 36945368 36945368 single base substitution C T upstream_gene_variant PACA-CA 13 36946194 36946194 single base substitution T A upstream_gene_variant PACA-CA 13 36946765 36946765 single base substitution T A upstream_gene_variant PACA-CA 13 36948558 36948558 single base substitution T A upstream_gene_variant PACA-CA 13 36948825 36948825 single base substitution G A upstream_gene_variant PAEN-AU 13 36927101 36927101 single base substitution A G intron_variant PAEN-AU 13 36932030 36932030 single base substitution A G intron_variant PAEN-IT 13 36883306 36883306 single base substitution G T downstream_gene_variant PAEN-IT 13 36883306 36883306 single base substitution G T intron_variant PAEN-IT 13 36883702 36883702 single base substitution G A downstream_gene_variant PAEN-IT 13 36883702 36883702 single base substitution G A intron_variant PAEN-IT 13 36902423 36902423 single base substitution C T intron_variant PAEN-IT 13 36902423 36902423 single base substitution C T upstream_gene_variant PAEN-IT 13 36932803 36932803 single base substitution C A intron_variant PBCA-DE 13 36892098 36892098 single base substitution T C intron_variant PBCA-DE 13 36892098 36892098 single base substitution T C upstream_gene_variant PBCA-DE 13 36903307 36903307 single base substitution T A intron_variant PBCA-DE 13 36903307 36903307 single base substitution T A upstream_gene_variant PBCA-DE 13 36904567 36904568 deletion of <=200bp AC - downstream_gene_variant PBCA-DE 13 36904567 36904568 deletion of <=200bp AC - intron_variant PBCA-DE 13 36904567 36904568 deletion of <=200bp AC - upstream_gene_variant PBCA-DE 13 36912984 36912984 single base substitution G T intron_variant PBCA-DE 13 36925047 36925047 single base substitution T A intron_variant PBCA-DE 13 36925047 36925047 single base substitution T A upstream_gene_variant PBCA-DE 13 36933030 36933030 single base substitution T A intron_variant PBCA-DE 13 36936930 36936930 insertion of <=200bp - T intron_variant PBCA-DE 13 36937489 36937490 deletion of <=200bp TC - intron_variant PBCA-DE 13 36938942 36938942 single base substitution C G intron_variant PBCA-DE 13 36939245 36939245 single base substitution T A intron_variant PBCA-DE 13 36942578 36942578 single base substitution C A intron_variant PRAD-CA 13 36897377 36897377 single base substitution G C downstream_gene_variant PRAD-CA 13 36897377 36897377 single base substitution G C intron_variant PRAD-CA 13 36906234 36906234 single base substitution G C downstream_gene_variant PRAD-CA 13 36906234 36906234 single base substitution G C intron_variant PRAD-CA 13 36909752 36909752 single base substitution T A exon_variant PRAD-CA 13 36909752 36909752 single base substitution T A missense_variant E72D 216A>T PRAD-CA 13 36930452 36930452 single base substitution C G intron_variant PRAD-CA 13 36945757 36945757 single base substitution A C upstream_gene_variant PRAD-UK 13 36904243 36904243 single base substitution C G intron_variant PRAD-UK 13 36904243 36904243 single base substitution C G upstream_gene_variant PRAD-UK 13 36915956 36915956 single base substitution C T intron_variant PRAD-UK 13 36919764 36919764 single base substitution C T exon_variant PRAD-UK 13 36919764 36919764 single base substitution C T intron_variant PRAD-UK 13 36937202 36937202 single base substitution A T intron_variant PRAD-US 13 36886567 36886567 single base substitution G A exon_variant PRAD-US 13 36886567 36886567 single base substitution G A missense_variant P511S 1531C>T PRAD-US 13 36886567 36886567 single base substitution G A upstream_gene_variant READ-US 13 36878522 36878522 single base substitution C A downstream_gene_variant READ-US 13 36878522 36878522 single base substitution C A exon_variant READ-US 13 36878522 36878522 single base substitution C A missense_variant A661S 1981G>T READ-US 13 36886586 36886586 single base substitution G A exon_variant READ-US 13 36886586 36886586 single base substitution G A synonymous_variant C504C 1512C>T READ-US 13 36886586 36886586 single base substitution G A upstream_gene_variant READ-US 13 36888471 36888471 single base substitution C T exon_variant READ-US 13 36888471 36888471 single base substitution C T missense_variant R459Q 1376G>A READ-US 13 36888471 36888471 single base substitution C T upstream_gene_variant READ-US 13 36909193 36909193 single base substitution C T downstream_gene_variant READ-US 13 36909193 36909193 single base substitution C T exon_variant READ-US 13 36909193 36909193 single base substitution C T missense_variant D259N 775G>A READ-US 13 36909247 36909247 single base substitution C T downstream_gene_variant READ-US 13 36909247 36909247 single base substitution C T exon_variant READ-US 13 36909247 36909247 single base substitution C T missense_variant A241T 721G>A RECA-EU 13 36874574 36874574 single base substitution T C downstream_gene_variant RECA-EU 13 36890270 36890270 single base substitution T C intron_variant RECA-EU 13 36890270 36890270 single base substitution T C upstream_gene_variant RECA-EU 13 36897102 36897102 single base substitution C G downstream_gene_variant RECA-EU 13 36897102 36897102 single base substitution C G intron_variant RECA-EU 13 36902865 36902865 single base substitution T C intron_variant RECA-EU 13 36902865 36902865 single base substitution T C upstream_gene_variant RECA-EU 13 36906886 36906886 single base substitution A T downstream_gene_variant RECA-EU 13 36906886 36906886 single base substitution A T intron_variant RECA-EU 13 36918255 36918255 single base substitution C T intron_variant RECA-EU 13 36919293 36919293 single base substitution A C intron_variant RECA-EU 13 36931846 36931846 single base substitution G T intron_variant RECA-EU 13 36948417 36948417 single base substitution A T upstream_gene_variant SKCA-BR 13 36871057 36871057 single base substitution T C downstream_gene_variant SKCA-BR 13 36871745 36871745 single base substitution A C downstream_gene_variant SKCA-BR 13 36872062 36872062 single base substitution G A downstream_gene_variant SKCA-BR 13 36874881 36874881 single base substitution C A downstream_gene_variant SKCA-BR 13 36876371 36876375 deletion of <=200bp TTATC - 3_prime_UTR_variant SKCA-BR 13 36876371 36876375 deletion of <=200bp TTATC - downstream_gene_variant SKCA-BR 13 36876375 36876379 deletion of <=200bp CTATA - 3_prime_UTR_variant SKCA-BR 13 36876375 36876379 deletion of <=200bp CTATA - downstream_gene_variant SKCA-BR 13 36876379 36876379 single base substitution A G 3_prime_UTR_variant SKCA-BR 13 36876379 36876379 single base substitution A G downstream_gene_variant SKCA-BR 13 36886469 36886469 single base substitution T C exon_variant SKCA-BR 13 36886469 36886469 single base substitution T C synonymous_variant A543A 1629A>G SKCA-BR 13 36890722 36890722 single base substitution T C intron_variant SKCA-BR 13 36890722 36890722 single base substitution T C upstream_gene_variant SKCA-BR 13 36890723 36890723 single base substitution G A intron_variant SKCA-BR 13 36890723 36890723 single base substitution G A upstream_gene_variant SKCA-BR 13 36890724 36890724 single base substitution A C intron_variant SKCA-BR 13 36890724 36890724 single base substitution A C upstream_gene_variant SKCA-BR 13 36893753 36893753 single base substitution A C intron_variant SKCA-BR 13 36893782 36893782 single base substitution A C intron_variant SKCA-BR 13 36893943 36893943 single base substitution A G intron_variant SKCA-BR 13 36893953 36893953 single base substitution T A intron_variant SKCA-BR 13 36897285 36897285 single base substitution C T downstream_gene_variant SKCA-BR 13 36897285 36897285 single base substitution C T intron_variant SKCA-BR 13 36910792 36910792 single base substitution C T intron_variant SKCA-BR 13 36915569 36915569 single base substitution G A intron_variant SKCA-BR 13 36918173 36918173 insertion of <=200bp - AT intron_variant SKCA-BR 13 36919103 36919103 single base substitution A T intron_variant SKCA-BR 13 36923902 36923902 single base substitution A T intron_variant SKCA-BR 13 36923902 36923902 single base substitution A T upstream_gene_variant SKCA-BR 13 36924184 36924184 single base substitution G C intron_variant SKCA-BR 13 36924184 36924184 single base substitution G C upstream_gene_variant SKCA-BR 13 36926923 36926923 insertion of <=200bp - CA intron_variant SKCA-BR 13 36933079 36933080 deletion of <=200bp TG - intron_variant SKCA-BR 13 36937488 36937488 insertion of <=200bp - ATC intron_variant SKCA-BR 13 36939282 36939282 single base substitution C T intron_variant SKCA-BR 13 36940293 36940293 single base substitution C T intron_variant SKCA-BR 13 36940943 36940943 single base substitution C A intron_variant SKCA-BR 13 36941849 36941849 single base substitution C T intron_variant SKCA-BR 13 36942572 36942572 single base substitution A C intron_variant SKCA-BR 13 36942584 36942584 single base substitution T A intron_variant SKCA-BR 13 36942596 36942596 single base substitution G A intron_variant SKCA-BR 13 36945749 36945749 insertion of <=200bp - CACAA upstream_gene_variant SKCA-BR 13 36945753 36945753 single base substitution C A upstream_gene_variant SKCA-BR 13 36945753 36945757 deletion of <=200bp CACAA - upstream_gene_variant SKCA-BR 13 36945757 36945757 single base substitution A C upstream_gene_variant SKCA-BR 13 36947684 36947684 single base substitution C T upstream_gene_variant SKCM-US 13 36888536 36888536 single base substitution A G exon_variant SKCM-US 13 36888536 36888536 single base substitution A G synonymous_variant G437G 1311T>C SKCM-US 13 36888536 36888536 single base substitution A G upstream_gene_variant SKCM-US 13 36909302 36909302 single base substitution A T downstream_gene_variant SKCM-US 13 36909302 36909302 single base substitution A T exon_variant SKCM-US 13 36909302 36909302 single base substitution A T synonymous_variant I222I 666T>A SKCM-US 13 36909411 36909411 single base substitution G A downstream_gene_variant SKCM-US 13 36909411 36909411 single base substitution G A exon_variant SKCM-US 13 36909411 36909411 single base substitution G A missense_variant S186F 557C>T SKCM-US 13 36909789 36909789 single base substitution G A exon_variant SKCM-US 13 36909789 36909789 single base substitution G A missense_variant S60L 179C>T STAD-US 13 36878523 36878523 single base substitution C T downstream_gene_variant STAD-US 13 36878523 36878523 single base substitution C T exon_variant STAD-US 13 36878523 36878523 single base substitution C T synonymous_variant E660E 1980G>A STAD-US 13 36878539 36878539 single base substitution G A downstream_gene_variant STAD-US 13 36878539 36878539 single base substitution G A exon_variant STAD-US 13 36878539 36878539 single base substitution G A missense_variant T655M 1964C>T STAD-US 13 36878722 36878722 single base substitution G T exon_variant STAD-US 13 36878722 36878722 single base substitution G T missense_variant A594E 1781C>A STAD-US 13 36888405 36888405 single base substitution T G exon_variant STAD-US 13 36888405 36888405 single base substitution T G missense_variant K481T 1442A>C STAD-US 13 36888405 36888405 single base substitution T G upstream_gene_variant STAD-US 13 36888425 36888425 single base substitution G T exon_variant STAD-US 13 36888425 36888425 single base substitution G T synonymous_variant T474T 1422C>A STAD-US 13 36888425 36888425 single base substitution G T upstream_gene_variant STAD-US 13 36888456 36888456 single base substitution T C exon_variant STAD-US 13 36888456 36888456 single base substitution T C missense_variant E464G 1391A>G STAD-US 13 36888456 36888456 single base substitution T C upstream_gene_variant STAD-US 13 36888472 36888472 single base substitution G A exon_variant STAD-US 13 36888472 36888472 single base substitution G A missense_variant R459W 1375C>T STAD-US 13 36888472 36888472 single base substitution G A upstream_gene_variant STAD-US 13 36888477 36888477 single base substitution C T exon_variant STAD-US 13 36888477 36888477 single base substitution C T missense_variant R457Q 1370G>A STAD-US 13 36888477 36888477 single base substitution C T upstream_gene_variant STAD-US 13 36900787 36900787 single base substitution A G exon_variant STAD-US 13 36900787 36900787 single base substitution A G missense_variant C405R 1213T>C STAD-US 13 36900787 36900787 single base substitution A G upstream_gene_variant STAD-US 13 36905566 36905566 single base substitution C A downstream_gene_variant STAD-US 13 36905566 36905566 single base substitution C A exon_variant STAD-US 13 36905566 36905566 single base substitution C A synonymous_variant L326L 978G>T STAD-US 13 36905566 36905566 single base substitution C A upstream_gene_variant STAD-US 13 36905589 36905589 single base substitution C A downstream_gene_variant STAD-US 13 36905589 36905589 single base substitution C A exon_variant STAD-US 13 36905589 36905589 single base substitution C A missense_variant D319Y 955G>T STAD-US 13 36905589 36905589 single base substitution C A upstream_gene_variant STAD-US 13 36905729 36905729 single base substitution C A downstream_gene_variant STAD-US 13 36905729 36905729 single base substitution C A exon_variant STAD-US 13 36905729 36905729 single base substitution C A missense_variant C272F 815G>T STAD-US 13 36905729 36905729 single base substitution C A upstream_gene_variant STAD-US 13 36909169 36909169 single base substitution C T downstream_gene_variant STAD-US 13 36909169 36909169 single base substitution C T exon_variant STAD-US 13 36909169 36909169 single base substitution C T missense_variant G267R 799G>A STAD-US 13 36909272 36909272 deletion of <=200bp A - downstream_gene_variant STAD-US 13 36909272 36909272 deletion of <=200bp A - exon_variant STAD-US 13 36909272 36909272 deletion of <=200bp A - frameshift_variant F232 STAD-US 13 36909272 36909272 insertion of <=200bp - A downstream_gene_variant STAD-US 13 36909272 36909272 insertion of <=200bp - A exon_variant STAD-US 13 36909272 36909272 insertion of <=200bp - A frameshift_variant F232F? STAD-US 13 36909285 36909285 single base substitution A G downstream_gene_variant STAD-US 13 36909285 36909285 single base substitution A G exon_variant STAD-US 13 36909285 36909285 single base substitution A G missense_variant V228A 683T>C STAD-US 13 36909408 36909408 single base substitution T C downstream_gene_variant STAD-US 13 36909408 36909408 single base substitution T C exon_variant STAD-US 13 36909408 36909408 single base substitution T C missense_variant Y187C 560A>G STAD-US 13 36909426 36909426 deletion of <=200bp C - downstream_gene_variant STAD-US 13 36909426 36909426 deletion of <=200bp C - exon_variant STAD-US 13 36909426 36909426 deletion of <=200bp C - frameshift_variant G181 STAD-US 13 36909438 36909438 single base substitution T C downstream_gene_variant STAD-US 13 36909438 36909438 single base substitution T C exon_variant STAD-US 13 36909438 36909438 single base substitution T C missense_variant Q177R 530A>G THCA-SA 13 36871810 36871810 single base substitution C T downstream_gene_variant THCA-SA 13 36877578 36877578 single base substitution G T 3_prime_UTR_variant THCA-SA 13 36877578 36877578 single base substitution G T downstream_gene_variant THCA-SA 13 36877685 36877685 single base substitution T A 3_prime_UTR_variant THCA-SA 13 36877685 36877685 single base substitution T A downstream_gene_variant THCA-SA 13 36877894 36877894 single base substitution G A 3_prime_UTR_variant THCA-SA 13 36877894 36877894 single base substitution G A downstream_gene_variant THCA-SA 13 36877978 36877978 single base substitution T C 3_prime_UTR_variant THCA-SA 13 36877978 36877978 single base substitution T C downstream_gene_variant THCA-SA 13 36886469 36886469 single base substitution T C exon_variant THCA-SA 13 36886469 36886469 single base substitution T C synonymous_variant A543A 1629A>G THCA-SA 13 36909893 36909893 single base substitution T C exon_variant THCA-SA 13 36909893 36909893 single base substitution T C synonymous_variant L25L 75A>G THCA-SA 13 36920504 36920504 single base substitution C T 5_prime_UTR_variant THCA-SA 13 36920504 36920504 single base substitution C T intron_variant THCA-SA 13 36920504 36920504 single base substitution C T upstream_gene_variant THCA-SA 13 36920918 36920918 single base substitution C G 5_prime_UTR_variant THCA-SA 13 36920918 36920918 single base substitution C G intron_variant THCA-SA 13 36920918 36920918 single base substitution C G upstream_gene_variant THCA-US 13 36903501 36903501 single base substitution T C missense_variant R388G 1162A>G THCA-US 13 36903501 36903501 single base substitution T C splice_region_variant THCA-US 13 36903501 36903501 single base substitution T C upstream_gene_variant UCEC-US 13 36878616 36878616 single base substitution C A exon_variant UCEC-US 13 36878616 36878616 single base substitution C A missense_variant Q629H 1887G>T UCEC-US 13 36886510 36886510 single base substitution C A exon_variant UCEC-US 13 36886510 36886510 single base substitution C A missense_variant D530Y 1588G>T UCEC-US 13 36886531 36886531 single base substitution C A exon_variant UCEC-US 13 36886531 36886531 single base substitution C A stop_gained E523* 1567G>T UCEC-US 13 36886576 36886576 single base substitution C A exon_variant UCEC-US 13 36886576 36886576 single base substitution C A stop_gained E508* 1522G>T UCEC-US 13 36886576 36886576 single base substitution C A upstream_gene_variant UCEC-US 13 36900723 36900723 single base substitution T C exon_variant UCEC-US 13 36900723 36900723 single base substitution T C missense_variant N426S 1277A>G UCEC-US 13 36903576 36903576 single base substitution C A exon_variant UCEC-US 13 36903576 36903576 single base substitution C A stop_gained E363* 1087G>T UCEC-US 13 36903576 36903576 single base substitution C A upstream_gene_variant UCEC-US 13 36903584 36903584 single base substitution T C exon_variant UCEC-US 13 36903584 36903584 single base substitution T C missense_variant Q360R 1079A>G UCEC-US 13 36903584 36903584 single base substitution T C upstream_gene_variant UCEC-US 13 36905640 36905640 single base substitution C T downstream_gene_variant UCEC-US 13 36905640 36905640 single base substitution C T exon_variant UCEC-US 13 36905640 36905640 single base substitution C T missense_variant A302T 904G>A UCEC-US 13 36905640 36905640 single base substitution C T upstream_gene_variant UCEC-US 13 36905644 36905644 single base substitution T C downstream_gene_variant UCEC-US 13 36905644 36905644 single base substitution T C exon_variant UCEC-US 13 36905644 36905644 single base substitution T C synonymous_variant L300L 900A>G UCEC-US 13 36905644 36905644 single base substitution T C upstream_gene_variant UCEC-US 13 36909222 36909222 single base substitution C T downstream_gene_variant UCEC-US 13 36909222 36909222 single base substitution C T exon_variant UCEC-US 13 36909222 36909222 single base substitution C T missense_variant R249Q 746G>A UCEC-US 13 36909288 36909288 single base substitution C A downstream_gene_variant UCEC-US 13 36909288 36909288 single base substitution C A exon_variant UCEC-US 13 36909288 36909288 single base substitution C A missense_variant G227V 680G>T UCEC-US 13 36909305 36909305 single base substitution C A downstream_gene_variant UCEC-US 13 36909305 36909305 single base substitution C A exon_variant UCEC-US 13 36909305 36909305 single base substitution C A missense_variant L221F 663G>T UCEC-US 13 36909466 36909466 single base substitution C T downstream_gene_variant UCEC-US 13 36909466 36909466 single base substitution C T exon_variant UCEC-US 13 36909466 36909466 single base substitution C T missense_variant A168T 502G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-BR-6458-01 COSM4047366 c.1442A>C p.K481T Substitution - Missense 13:36314268-36314268 - ESO-0133 COSM1266625 c.340T>C p.Y114H Substitution - Missense 13:36335491-36335491 - TCGA-BR-4256-01 COSM4047373 c.955G>T p.D319Y Substitution - Missense 13:36331452-36331452 - TCGA-AK-3458-01 COSM469388 c.1760C>A p.T587N Substitution - Missense 13:36304606-36304606 - TCGA-AP-A051-01 COSM947140 c.904G>A p.A302T Substitution - Missense 13:36331503-36331503 - TCGA-HU-A4G2-01 COSM551209 c.560A>G p.Y187C Substitution - Missense 13:36335271-36335271 - Pat_46_B COSM5842463 c.886C>T p.P296S Substitution - Missense 13:36331521-36331521 - pfg180T COSM4752892 c.1032A>C p.E344D Substitution - Missense 13:36329494-36329494 - HCC2998 COSM2072535 c.73T>C p.L25L Substitution - coding silent 13:36335758-36335758 - EGC3 COSM4047364 c.1964C>T p.T655M Substitution - Missense 13:36304402-36304402 - ESCC_13 COSM5625111 c.1876G>C p.E626Q Substitution - Missense 13:36304490-36304490 - TCGA-F4-6854-01 COSM1366678 c.626C>T p.P209L Substitution - Missense 13:36335205-36335205 - T3111 COSM4729578 c.704C>T p.P235L Substitution - Missense 13:36335127-36335127 - PCSI_0075_Pa_P COSM3376539 c.1688T>C p.I563T Substitution - Missense 13:36312190-36312190 - TCGA-EJ-5527-01 COSM1128382 c.1531C>T p.P511S Substitution - Missense 13:36312430-36312430 - Pat_60_B COSM2072519 c.1162delA p.R388fs*12 Deletion - Frameshift 13:36329364-36329364 - SS6003320 COSM3980201 c.465A>G p.A155A Substitution - coding silent 13:36335366-36335366 - RK308_C01 COSM3744150 c.124G>A p.A42T Substitution - Missense 13:36335707-36335707 - 587376 COSM1227346 c.617C>A p.S206Y Substitution - Missense 13:36335214-36335214 - CR007 COSM4994643 c.810+7G>A p.? Unknown 13:36335014-36335014 - TCGA-F5-6465-01 COSM277459 c.775G>A p.D259N Substitution - Missense 13:36335056-36335056 - TCGA-EI-6917-01 COSM3417566 c.721G>A p.A241T Substitution - Missense 13:36335110-36335110 - TCGA-DJ-A3UN-01 COSM2072520 c.1162A>G p.R388G Substitution - Missense 13:36329364-36329364 - HCC144T COSM3704614 c.1669G>T p.E557* Substitution - Nonsense 13:36312209-36312209 - TCGA-EI-6882-01 COSM1366670 c.1512C>T p.C504C Substitution - coding silent 13:36312449-36312449 - pfg181T COSM4752877 c.1952A>C p.K651T Substitution - Missense 13:36304414-36304414 - ESO-137 COSM1266628 c.1389A>C p.E463D Substitution - Missense 13:36314321-36314321 - TCGA-AR-A0U1-01 COSM432358 c.1570T>C p.S524P Substitution - Missense 13:36312391-36312391 - TCGA-CM-6162-01 COSM1366669 c.1513G>A p.V505I Substitution - Missense 13:36312448-36312448 - ATL045 COSM5704702 c.1085A>T p.K362I Substitution - Missense 13:36329441-36329441 - CLL079 COSM1289897 c.674C>A p.P225Q Substitution - Missense 13:36335157-36335157 - T578 COSM4729576 c.1131G>T p.K377N Substitution - Missense 13:36329395-36329395 - sysucc-1370T COSM5470171 c.67G>A p.A23T Substitution - Missense 13:36335764-36335764 - HCC144 COSM3704614 c.1669G>T p.E557* Substitution - Nonsense 13:36312209-36312209 - BD14T COSM5517188 c.1171G>T p.D391Y Substitution - Missense 13:36326692-36326692 - 82 COSM5014044 c.546C>A p.H182Q Substitution - Missense 13:36335285-36335285 - PTC-7C COSM3753671 c.1629A>G p.A543A Substitution - coding silent 13:36312332-36312332 - C008 COSM5523904 c.206C>T p.P69L Substitution - Missense 13:36335625-36335625 - TCGA-AA-3662-01 COSM1366676 c.852G>A p.P284P Substitution - coding silent 13:36331555-36331555 - TCGA-BR-8591-01 COSM4047364 c.1964C>T p.T655M Substitution - Missense 13:36304402-36304402 - CRC-03T COSM1562268 c.1376G>A p.R459Q Substitution - Missense 13:36314334-36314334 - SJOS001105_D1 COSM5023144 c.361G>A p.D121N Substitution - Missense 13:36335470-36335470 - pfg060T COSM4752893 c.278A>G p.E93G Substitution - Missense 13:36335553-36335553 - TCGA-AX-A0J0-01 COSM947135 c.1522G>T p.E508* Substitution - Nonsense 13:36312439-36312439 - HT55 COSM2072506 c.1781C>T p.A594V Substitution - Missense 13:36304585-36304585 - ESO-157 COSM1266629 c.1242A>C p.K414N Substitution - Missense 13:36326621-36326621 - TCGA-BR-6457-01 COSM4047365 c.1781C>A p.A594E Substitution - Missense 13:36304585-36304585 - TCGA-D5-6931-01 COSM1366668 c.1576A>T p.K526* Substitution - Nonsense 13:36312385-36312385 - T1154 COSM2072509 c.1581delA p.D528fs*14 Deletion - Frameshift 13:36312380-36312380 - H23 COSM1196487 c.1039G>A p.E347K Substitution - Missense 13:36329487-36329487 - TCGA-EI-6506-01 COSM1562268 c.1376G>A p.R459Q Substitution - Missense 13:36314334-36314334 - 587222 COSM1227345 c.1217A>C p.E406A Substitution - Missense 13:36326646-36326646 - TCGA-AA-3511-01 COSM1366669 c.1513G>A p.V505I Substitution - Missense 13:36312448-36312448 - TCGA-AG-3892-01 COSM258086 c.1033G>T p.E345* Substitution - Nonsense 13:36329493-36329493 - ESCC-248T COSM3936312 c.119A>T p.E40V Substitution - Missense 13:36335712-36335712 - LS174T COSM2072519 c.1162delA p.R388fs*12 Deletion - Frameshift 13:36329364-36329364 - RK305_C01 COSM4943805 c.1681A>G p.K561E Substitution - Missense 13:36312197-36312197 - HCC5T COSM3704615 c.134A>G p.Y45C Substitution - Missense 13:36335697-36335697 - XHDG59C COSM4767770 c.103G>A p.E35K Substitution - Missense 13:36335728-36335728 - ESO-708 COSM1266630 c.1188A>C p.E396D Substitution - Missense 13:36326675-36326675 - T3091 COSM1366677 c.696_697insT p.V233fs*8 Insertion - Frameshift 13:36335134-36335135 - BD112T COSM5490867 c.1582G>T p.D528Y Substitution - Missense 13:36312379-36312379 - ESO-682 COSM1266628 c.1389A>C p.E463D Substitution - Missense 13:36314321-36314321 - TCGA-FW-A3TU-06 COSM3468626 c.666T>A p.I222I Substitution - coding silent 13:36335165-36335165 - TCGA-BS-A0UM-01 COSM947137 c.1139G>A p.R380H Substitution - Missense 13:36329387-36329387 - B65 COSM1747426 c.223A>T p.R75* Substitution - Nonsense 13:36335608-36335608 - C008 COSM5523903 c.205C>T p.P69S Substitution - Missense 13:36335626-36335626 - PD9585a COSM5779576 c.1646T>C p.F549S Substitution - Missense 13:36312232-36312232 - pfg057T COSM4765705 c.697_698insT p.N234fs*7 Insertion - Frameshift 13:36335133-36335134 - CRC-09T COSM5452822 c.435C>G p.T145T Substitution - coding silent 13:36335396-36335396 - TCGA-HU-A4H3-01 COSM4047374 c.815G>T p.C272F Substitution - Missense 13:36331592-36331592 - T155 COSM277459 c.775G>A p.D259N Substitution - Missense 13:36335056-36335056 - TCGA-AZ-4315-01 COSM1366670 c.1512C>T p.C504C Substitution - coding silent 13:36312449-36312449 - 61 COSM2072511 c.1337G>A p.G446D Substitution - Missense 13:36314373-36314373 - RK306_C01 COSM4944097 c.1554C>A p.S518R Substitution - Missense 13:36312407-36312407 - TCGA-HU-A4GT-01 COSM4047376 c.683T>C p.V228A Substitution - Missense 13:36335148-36335148 - TCGA-CA-6718-01 COSM1366666 c.1965G>A p.T655T Substitution - coding silent 13:36304401-36304401 - TCGA-B5-A0JY-01 COSM947138 c.1087G>T p.E363* Substitution - Nonsense 13:36329439-36329439 - tumor_4115001 COSM5947581 c.1827C>G p.I609M Substitution - Missense 13:36304539-36304539 - 587278 COSM1180799 c.185_186delAA p.K62fs*3 Deletion - Frameshift 13:36335645-36335646 - cSCCP7 COSM139993 c.515C>T p.P172L Substitution - Missense 13:36335316-36335316 - 2 COSM4172099 c.469G>C p.A157P Substitution - Missense 13:36335362-36335362 - TCGA-A5-A0VQ-01 COSM947145 c.502G>A p.A168T Substitution - Missense 13:36335329-36335329 - TCGA-C8-A26Y-01 COSM3813764 c.1064G>C p.R355T Substitution - Missense 13:36329462-36329462 - TCGA-66-2789-01 COSM696658 c.409C>T p.Q137* Substitution - Nonsense 13:36335422-36335422 - OST102PT COSM1732553 c.946C>A p.P316T Substitution - Missense 13:36331461-36331461 - pfg122T COSM4765705 c.697_698insT p.N234fs*7 Insertion - Frameshift 13:36335133-36335134 - TCGA-AX-A05Z-01 COSM947142 c.746G>A p.R249Q Substitution - Missense 13:36335085-36335085 - TCGA-AP-A0LM-01 COSM947141 c.900A>G p.L300L Substitution - coding silent 13:36331507-36331507 - TCGA-CM-4743-01 COSM1366679 c.589G>A p.V197I Substitution - Missense 13:36335242-36335242 - TCGA-BR-A4QL-01 COSM4047369 c.1375C>T p.R459W Substitution - Missense 13:36314335-36314335 - TCGA-BR-6452-01 COSM4047375 c.799G>A p.G267R Substitution - Missense 13:36335032-36335032 - B65-Tumor COSM1747426 c.223A>T p.R75* Substitution - Nonsense 13:36335608-36335608 - CSCC-44-T COSM4523956 c.1243G>C p.E415Q Substitution - Missense 13:36326620-36326620 - ESO-0009 COSM1266624 c.1469T>C p.V490A Substitution - Missense 13:36314241-36314241 - 4132_T COSM3955558 c.1022G>A p.R341K Substitution - Missense 13:36329504-36329504 - YUROC COSM5376712 c.1372G>A p.E458K Substitution - Missense 13:36314338-36314338 - TCGA-AG-3583-01 COSM287901 c.1737C>T p.Y579Y Substitution - coding silent 13:36304629-36304629 - pfg108T COSM4752883 c.1645T>G p.F549V Substitution - Missense 13:36312233-36312233 - SW1417 COSM2072503 c.1950G>T p.E650D Substitution - Missense 13:36304416-36304416 - SM-4AX85 COSM5035063 c.645G>C p.G215G Substitution - coding silent 13:36335186-36335186 - TCGA-D8-A1JN-01 COSM1477216 c.1542G>A p.K514K Substitution - coding silent 13:36312419-36312419 - NCI-H23 COSM1196487 c.1039G>A p.E347K Substitution - Missense 13:36329487-36329487 - PR-09-2517 COSM247559 c.729G>A p.S243S Substitution - coding silent 13:36335102-36335102 - TCGA-IR-A3LK-01 COSM4816535 c.1986G>A p.K662K Substitution - coding silent 13:36304380-36304380 - QC2-09-T2 COSM5652199 c.731A>G p.Y244C Substitution - Missense 13:36335100-36335100 - T578 COSM4729574 c.1997A>C p.K666T Substitution - Missense 13:36304369-36304369 - TCGA-BR-4201-01 COSM4047370 c.1370G>A p.R457Q Substitution - Missense 13:36314340-36314340 - sysucc-311T COSM5478513 c.247G>T p.E83* Substitution - Nonsense 13:36335584-36335584 - TCGA-BR-4257-01 COSM4047377 c.530A>G p.Q177R Substitution - Missense 13:36335301-36335301 - TCGA-AM-5821-01 COSM3753671 c.1629A>G p.A543A Substitution - coding silent 13:36312332-36312332 - TCGA-C8-A27B-01 COSM1477217 c.8A>C p.Q3P Substitution - Missense 13:36335823-36335823 - RDES COSM4575919 c.363C>T p.D121D Substitution - coding silent 13:36335468-36335468 - LUAD-S01357 COSM386585 c.489A>T p.S163S Substitution - coding silent 13:36335342-36335342 - HCC5 COSM3704615 c.134A>G p.Y45C Substitution - Missense 13:36335697-36335697 - T98G COSM947139 c.1079A>G p.Q360R Substitution - Missense 13:36329447-36329447 - TCGA-D5-6541-01 COSM1366672 c.1231G>C p.E411Q Substitution - Missense 13:36326632-36326632 - HDC82 COSM4636604 c.1697A>G p.N566S Substitution - Missense 13:36312181-36312181 - TCGA-AP-A0LM-01 COSM947142 c.746G>A p.R249Q Substitution - Missense 13:36335085-36335085 - TCGA-BR-8687-01 COSM4047367 c.1422C>A p.T474T Substitution - coding silent 13:36314288-36314288 - TCGA-BS-A0UV-01 COSM947144 c.663G>T p.L221F Substitution - Missense 13:36335168-36335168 - BRC38 COSM5027756 c.577G>A p.E193K Substitution - Missense 13:36335254-36335254 - ESO-0950 COSM1266626 c.1564C>G p.P522A Substitution - Missense 13:36312397-36312397 - TCGA-AP-A054-01 COSM947139 c.1079A>G p.Q360R Substitution - Missense 13:36329447-36329447 - TCGA-GN-A26A-06 COSM3468627 c.557C>T p.S186F Substitution - Missense 13:36335274-36335274 - AOCS-092-1-6 COSM3957198 c.1075G>T p.D359Y Substitution - Missense 13:36329451-36329451 - SM-4AX84 COSM4412903 c.1823G>T p.G608V Substitution - Missense 13:36304543-36304543 - 134398 COSM323566 c.1499C>T p.T500I Substitution - Missense 13:36312462-36312462 - TCGA-DK-A1AC-01 COSM1300174 c.810+1G>C p.? Unknown 13:36335020-36335020 - RK236_C01 COSM4945028 c.1716A>G p.V572V Substitution - coding silent 13:36312162-36312162 - TCGA-A8-A0A6-01 COSM3813763 c.1838T>G p.V613G Substitution - Missense 13:36304528-36304528 - TCGA-EI-6513-01 COSM3417565 c.1981G>T p.A661S Substitution - Missense 13:36304385-36304385 - T207 COSM4729577 c.760T>C p.L254L Substitution - coding silent 13:36335071-36335071 - CSCC-40-T COSM4568144 c.1004T>C p.L335P Substitution - Missense 13:36331403-36331403 - AOCS-092-3-3 COSM3957198 c.1075G>T p.D359Y Substitution - Missense 13:36329451-36329451 - LS180 COSM2072519 c.1162delA p.R388fs*12 Deletion - Frameshift 13:36329364-36329364 - ESO-0125 COSM1266623 c.1581_1582insA p.D528fs*18 Insertion - Frameshift 13:36312379-36312380 - TCGA-D1-A103-01 COSM947143 c.680G>T p.G227V Substitution - Missense 13:36335151-36335151 - TCGA-D1-A17Q-01 COSM947134 c.1567G>T p.E523* Substitution - Nonsense 13:36312394-36312394 - PTC-14C COSM4147698 c.1946G>T p.G649V Substitution - Missense 13:36304420-36304420 - TCGA-B6-A0RI-01 COSM432357 c.1623A>C p.V541V Substitution - coding silent 13:36312338-36312338 - TCGA-BR-4369-01 COSM4047368 c.1391A>G p.E464G Substitution - Missense 13:36314319-36314319 - Pat_26_B COSM5842464 c.437C>T p.S146L Substitution - Missense 13:36335394-36335394 - TCGA-AZ-6605-01 COSM1366680 c.283C>A p.L95I Substitution - Missense 13:36335548-36335548 - Pat_14_A COSM2072519 c.1162delA p.R388fs*12 Deletion - Frameshift 13:36329364-36329364 - LUAD_E00522 COSM352485 c.22G>T p.G8* Substitution - Nonsense 13:36335809-36335809 - HN_63048 COSM121937 c.1539C>T p.V513V Substitution - coding silent 13:36312422-36312422 - TCGA-A8-A09Z-01 COSM3813765 c.936C>A p.S312S Substitution - coding silent 13:36331471-36331471 - I2L-P7-Tumor-Organoid COSM5362273 c.706G>A p.A236T Substitution - Missense 13:36335125-36335125 - ESO-732 COSM1266631 c.1559T>G p.L520R Substitution - Missense 13:36312402-36312402 - LS411 COSM2072527 c.696delT p.F232fs*2 Deletion - Frameshift 13:36335135-36335135 - TCGA-FD-A3SR-01 COSM3793267 c.770C>G p.S257C Substitution - Missense 13:36335061-36335061 - TCGA-66-2757-01 COSM696659 c.1736A>C p.Y579S Substitution - Missense 13:36304630-36304630 - PD14471a COSM5770757 c.1753G>A p.E585K Substitution - Missense 13:36304613-36304613 - TCGA-D3-A3ML-06 COSM3468628 c.179C>T p.S60L Substitution - Missense 13:36335652-36335652 - LUAD-YINHD COSM348828 c.505G>A p.E169K Substitution - Missense 13:36335326-36335326 - TCGA-D3-A2JH-06 COSM3468625 c.1311T>C p.G437G Substitution - coding silent 13:36314399-36314399 - TCGA-AA-A00N-01 COSM277460 c.692T>G p.F231C Substitution - Missense 13:36335139-36335139 - CSCC-55-T COSM4558810 c.780G>A p.T260T Substitution - coding silent 13:36335051-36335051 - Pat_26_A COSM5842464 c.437C>T p.S146L Substitution - Missense 13:36335394-36335394 - LUAD-YINHD COSM348829 c.382G>C p.E128Q Substitution - Missense 13:36335449-36335449 - D-05 COSM4766484 c.1512C>A p.C504* Substitution - Nonsense 13:36312449-36312449 - CSCC-31-T COSM4458225 c.1077C>T p.D359D Substitution - coding silent 13:36329449-36329449 - TCGA-A8-A07C-01 COSM432359 c.1499C>G p.T500S Substitution - Missense 13:36312462-36312462 - T578 COSM4729575 c.1390G>T p.E464* Substitution - Nonsense 13:36314320-36314320 - TCGA-G4-6299-01 COSM1366667 c.1964delC p.T655fs*4 Deletion - Frameshift 13:36304402-36304402 - SS6003314 COSM3980202 c.42G>T p.K14N Substitution - Missense 13:36335789-36335789 - ESCC_83 COSM5636259 c.1742A>G p.Y581C Substitution - Missense 13:36304624-36304624 - TCGA-AP-A059-01 COSM947132 c.1887G>T p.Q629H Substitution - Missense 13:36304479-36304479 - PD5946a COSM5774626 c.1596A>G p.K532K Substitution - coding silent 13:36312365-36312365 - HN_62652 COSM126938 c.1649C>G p.S550* Substitution - Nonsense 13:36312229-36312229 - TCGA-AA-A00N-01 COSM277459 c.775G>A p.D259N Substitution - Missense 13:36335056-36335056 - 8066449 COSM1366669 c.1513G>A p.V505I Substitution - Missense 13:36312448-36312448 - Pat_46_A COSM5842463 c.886C>T p.P296S Substitution - Missense 13:36331521-36331521 - RK001_C01 COSM1629084 c.1992A>G p.K664K Substitution - coding silent 13:36304374-36304374 - TCGA-CG-5723-01 COSM4047371 c.1213T>C p.C405R Substitution - Missense 13:36326650-36326650 - Pat_59_B COSM5842462 c.1058G>A p.R353K Substitution - Missense 13:36329468-36329468 - TCGA-AA-3837-01 COSM295193 c.798C>A p.P266P Substitution - coding silent 13:36335033-36335033 - TCGA-22-5471-01 COSM696657 c.196C>G p.H66D Substitution - Missense 13:36335635-36335635 - TCGA-AX-A0J1-01 COSM947136 c.1277A>G p.N426S Substitution - Missense 13:36326586-36326586 - D21 COSM2072529 c.627G>A p.P209P Substitution - coding silent 13:36335204-36335204 - ESO-1059 COSM1266627 c.430A>G p.N144D Substitution - Missense 13:36335401-36335401 - TCGA-CA-6717-01 COSM947142 c.746G>A p.R249Q Substitution - Missense 13:36335085-36335085 - TCGA-CM-5861-01 COSM1366673 c.1069T>G p.S357A Substitution - Missense 13:36329457-36329457 - C84 COSM4611313 c.1717_1721delCAAAC p.Q573fs*8 Deletion - Frameshift 13:36312157-36312161 - TCGA-BR-4184-01 COSM4047363 c.1980G>A p.E660E Substitution - coding silent 13:36304386-36304386 - pfg068T COSM4765704 c.1582_1583insA p.D528fs*18 Insertion - Frameshift 13:36312378-36312379 - SNU-C4 COSM2072527 c.696delT p.F232fs*2 Deletion - Frameshift 13:36335135-36335135 - CRC-10T COSM5457672 c.584C>T p.S195L Substitution - Missense 13:36335247-36335247 - TCGA-C5-A3HE-01 COSM4827658 c.563G>A p.G188E Substitution - Missense 13:36335268-36335268 - TCGA-BS-A0UV-01 COSM947133 c.1588G>T p.D530Y Substitution - Missense 13:36312373-36312373 - ATL008 COSM5704703 c.298G>T p.A100S Substitution - Missense 13:36335533-36335533 - TCGA-HU-A4GN-01 COSM4047372 c.978G>T p.L326L Substitution - coding silent 13:36331429-36331429 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.440407;Hs.440408;Hs.440414 13q13.3 607111

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - 3-UTRDeletion . c.1998+2655delC 13 36875850 HC A C IntronicSNV . c.1484-510T>G 13 36887124 CLL A C Missense p.L520R c.1559T>G 13 36886539 ESCA A G Missense p.S524P c.1570T>C 13 36886528 BRCA A G Missense p.V490A c.1469T>C 13 36888378 ESCA A G Missense p.Y114H c.340T>C 13 36909628 ESCA A G Synonymous p.G437G c.1311T>C 13 36888536 CM A G Synonymous p.N256N c.768T>C 13 36909200 CM A T Missense p.C123S c.367T>A 13 36909601 CM C A Missense p.D319Y c.955G>T 13 36905589 STAD C A Missense p.G446V c.1337G>T 13 36888510 LUAD C A Missense p.Q229H c.687G>T 13 36909281 BRCA C A Missense p.Q76H c.228G>T 13 36909740 HNSC C T IntronicSNV . c.1734-1443G>A 13 36880212 CLL C T Missense p.A168T c.502G>A 13 36909466 UCEC C T Missense p.E193K c.577G>A 13 36909391 BRCA C T Missense p.R249Q c.746G>A 13 36909222 HNSC C T Missense p.R457Q c.1370G>A 13 36888477 STAD C T Missense p.V564I c.1690G>A 13 36886325 COREAD C T Synonymous p.K514K c.1542G>A 13 36886556 BRCA G A 3-UTRSNV . c.1998+2411C>T 13 36876094 DLBCL G A Missense p.P266S c.796C>T 13 36909172 CM G A Missense p.P511S c.1531C>T 13 36886567 PRAD G A Missense p.S186F c.557C>T 13 36909411 CM G A Missense p.S60L c.179C>T 13 36909789 CM G A Missense p.T500I c.1499C>T 13 36886599 SCLC G A Nonsense p.Q137* c.409C>T 13 36909559 LUSC G A Synonymous p.V513V c.1539C>T 13 36886559 HNSC G A Synonymous p.Y579Y c.1737C>T 13 36878766 COREAD G C Missense p.H66D c.196C>G 13 36909772 LUSC G C Missense p.P522A c.1564C>G 13 36886534 ESCA G C Missense p.Q6E c.16C>G 13 36909952 LUAD G C Missense p.T500S c.1499C>G 13 36886599 BRCA G C Nonsense p.S550* c.1649C>G 13 36886366 HNSC G T Missense p.A594E c.1781C>A 13 36878722 STAD G T Missense p.P225Q c.674C>A 13 36909294 CLL G T Synonymous p.P266P c.798C>A 13 36909170 COREAD T C Missense p.E464G c.1391A>G 13 36888456 STAD T C Missense p.N144D c.430A>G 13 36909538 ESCA T C Missense p.N226S c.677A>G 13 36909291 GBM T C Missense p.Q177R c.530A>G 13 36909438 STAD T C Missense p.Q360R c.1079A>G 13 36903584 UCEC T C Missense p.R388G c.1162A>G 13 36903501 THCA T C Missense p.Y187C c.560A>G 13 36909408 LUAD T C Synonymous p.K664K c.1992A>G 13 36878511 HC - T Frameshift p.D528Rfs*18 c.1581dupA 13 36886517 ESCA T G Missense p.E396D c.1188A>C 13 36900812 ESCA T G Missense p.E463D c.1389A>C 13 36888458 ESCA T G Missense p.K414N c.1242A>C 13 36900758 ESCA T G Missense p.K481T c.1442A>C 13 36888405 STAD T G Missense p.Q3P c.8A>C 13 36909960 BRCA T G Missense p.Y579S c.1736A>C 13 36878767 LUSC T G Synonymous p.V541V c.1623A>C 13 36886475 BRCA