Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 9 35059068 35059068 + Missense_Mutation SNP G G A TCGA-BT-A42F-01A-11D-A23U-08 TCGA-BT-A42F-10A-01D-A23U-08 g.chr9:35059068G>A c.2153C>T c.(2152-2154)tCa>tTa p.S718L BLCA 9 35059694 35059694 + Silent SNP G G A TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr9:35059694G>A c.1800C>T c.(1798-1800)gtC>gtT p.V600V BLCA 9 35061056 35061056 + Missense_Mutation SNP C C A TCGA-FD-A6TE-01A-12D-A339-08 TCGA-FD-A6TE-10A-21D-A339-08 g.chr9:35061056C>A c.1315G>T c.(1315-1317)Gcc>Tcc p.A439S BLCA 9 35061086 35061086 + Missense_Mutation SNP G G A TCGA-GC-A3BM-01A-11D-A22Z-08 TCGA-GC-A3BM-10A-01D-A22Z-08 g.chr9:35061086G>A c.1285C>T c.(1285-1287)Ctc>Ttc p.L429F BLCA 9 35062058 35062058 + Silent SNP C C T TCGA-GC-A3OO-01A-11D-A22Z-08 TCGA-GC-A3OO-10C-01D-A22Z-08 g.chr9:35062058C>T c.1023G>A c.(1021-1023)gtG>gtA p.V341V BLCA 9 35062088 35062088 + Silent SNP G G A TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr9:35062088G>A c.993C>T c.(991-993)ctC>ctT p.L331L BLCA 9 35065378 35065378 + Splice_Site SNP C C G TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr9:35065378C>G c.446G>C c.(445-447)gGa>gCa p.G149A BRCA 9 35057429 35057429 + Silent SNP C C T TCGA-A2-A0YG-01A-21D-A10G-09 TCGA-A2-A0YG-10A-01D-A10G-09 g.chr9:35057429C>T c.2259G>A c.(2257-2259)cgG>cgA p.R753R BRCA 9 35059573 35059573 + Nonsense_Mutation SNP G G A TCGA-AR-A0TX-01A-11D-A099-09 TCGA-AR-A0TX-10A-01D-A099-09 g.chr9:35059573G>A c.1921C>T c.(1921-1923)Cag>Tag p.Q641* BRCA 9 35061169 35061169 + Missense_Mutation SNP T T C TCGA-AO-A12E-01A-11D-A10M-09 TCGA-AO-A12E-10A-01D-A10M-09 g.chr9:35061169T>C c.1202A>G c.(1201-1203)aAt>aGt p.N401S BRCA 9 35064200 35064200 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr9:35064200A>C c.659T>G c.(658-660)gTg>gGg p.V220G BRCA 9 35065250 35065250 + Missense_Mutation SNP C C G TCGA-A8-A095-01A-11W-A019-09 TCGA-A8-A095-10A-01W-A021-09 g.chr9:35065250C>G c.574G>C c.(574-576)Gag>Cag p.E192Q CESC 9 35064274 35064274 + Missense_Mutation SNP T T A TCGA-EA-A1QS-01A-61D-A22X-09 TCGA-EA-A1QS-10A-01D-A22X-09 g.chr9:35064274T>A c.585A>T c.(583-585)gaA>gaT p.E195D CHOL 9 35060888 35060888 + Silent SNP C C T TCGA-4G-AAZT-01A-11D-A417-09 TCGA-4G-AAZT-10A-01D-A41A-09 g.chr9:35060888C>T c.1392G>A c.(1390-1392)ctG>ctA p.L464L COAD 9 35057429 35057429 + Silent SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr9:35057429C>T c.2259G>A c.(2257-2259)cgG>cgA p.R753R COAD 9 35059581 35059581 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr9:35059581C>T c.1913G>A c.(1912-1914)cGt>cAt p.R638H COAD 9 35060498 35060498 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:35060498A>C c.1507T>G c.(1507-1509)Ttc>Gtc p.F503V COAD 9 35061100 35061100 + Missense_Mutation SNP C C T TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr9:35061100C>T c.1271G>A c.(1270-1272)cGc>cAc p.R424H COAD 9 35062005 35062005 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:35062005C>T c.1076G>A c.(1075-1077)cGa>cAa p.R359Q COAD 9 35062026 35062026 + Missense_Mutation SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr9:35062026C>T c.1055G>A c.(1054-1056)aGc>aAc p.S352N COAD 9 35062244 35062244 + Silent SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr9:35062244C>T c.915G>A c.(913-915)gaG>gaA p.E305E COAD 9 35062983 35062985 + In_Frame_Del DEL AAG AAG - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr9:35062983_35062985delAAG c.801_803delCTT c.(799-804)ttcttg>ttg p.F267del COADREAD 9 35057429 35057429 + Silent SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr9:35057429C>T c.2259G>A c.(2257-2259)cgG>cgA p.R753R COADREAD 9 35059581 35059581 + Missense_Mutation SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr9:35059581C>T c.1913G>A c.(1912-1914)cGt>cAt p.R638H COADREAD 9 35060498 35060498 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:35060498A>C c.1507T>G c.(1507-1509)Ttc>Gtc p.F503V COADREAD 9 35061100 35061100 + Missense_Mutation SNP C C T TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr9:35061100C>T c.1271G>A c.(1270-1272)cGc>cAc p.R424H COADREAD 9 35062005 35062005 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:35062005C>T c.1076G>A c.(1075-1077)cGa>cAa p.R359Q COADREAD 9 35062026 35062026 + Missense_Mutation SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr9:35062026C>T c.1055G>A c.(1054-1056)aGc>aAc p.S352N COADREAD 9 35062244 35062244 + Silent SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr9:35062244C>T c.915G>A c.(913-915)gaG>gaA p.E305E COADREAD 9 35062983 35062985 + In_Frame_Del DEL AAG AAG - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr9:35062983_35062985delAAG c.801_803delCTT c.(799-804)ttcttg>ttg p.F267del COADREAD 9 35066724 35066724 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:35066724G>A c.393C>T c.(391-393)ttC>ttT p.F131F ESCA 9 35059171 35059171 + Nonsense_Mutation SNP C C A TCGA-R6-A6Y2-01B-11D-A33E-09 TCGA-R6-A6Y2-10A-01D-A33H-09 g.chr9:35059171C>A c.2050G>T c.(2050-2052)Gga>Tga p.G684* ESCA 9 35059557 35059557 + Missense_Mutation SNP G G T TCGA-LN-A49P-01A-11D-A247-09 TCGA-LN-A49P-10A-01D-A247-09 g.chr9:35059557G>T c.1937C>A c.(1936-1938)cCa>cAa p.P646Q ESCA 9 35059646 35059647 + Frame_Shift_Ins INS - - T TCGA-2H-A9GM-01A-11D-A37C-09 TCGA-2H-A9GM-11A-11D-A37F-09 g.chr9:35059646_35059647insT c.1847_1848insA c.(1846-1848)aatfs p.N616fs ESCA 9 35059646 35059647 + Frame_Shift_Ins INS - - T TCGA-L5-A88Z-01A-11D-A36J-09 TCGA-L5-A88Z-11A-11D-A36M-09 g.chr9:35059646_35059647insT c.1847_1848insA c.(1846-1848)aatfs p.N616fs ESCA 9 35060315 35060315 + Missense_Mutation SNP C C T TCGA-VR-A8EX-01A-11D-A36J-09 TCGA-VR-A8EX-10A-01D-A36M-09 g.chr9:35060315C>T c.1690G>A c.(1690-1692)Gac>Aac p.D564N ESCA 9 35060387 35060387 + Missense_Mutation SNP T T C TCGA-RE-A7BO-01A-11D-A33E-09 TCGA-RE-A7BO-10A-01D-A33H-09 g.chr9:35060387T>C c.1618A>G c.(1618-1620)Atc>Gtc p.I540V ESCA 9 35062127 35062127 + Silent SNP G G T TCGA-KH-A6WC-01A-11D-A33E-09 TCGA-KH-A6WC-10B-01D-A33H-09 g.chr9:35062127G>T c.954C>A c.(952-954)ggC>ggA p.G318G ESCA 9 35062276 35062276 + Missense_Mutation SNP T T C TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr9:35062276T>C c.883A>G c.(883-885)Aag>Gag p.K295E ESCA 9 35067909 35067909 + Missense_Mutation SNP A A G TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr9:35067909A>G c.281T>C c.(280-282)gTa>gCa p.V94A ESCA 9 35067938 35067938 + Missense_Mutation SNP C C T TCGA-LN-A4A9-01A-11D-A28B-09 TCGA-LN-A4A9-10A-01D-A28E-09 g.chr9:35067938C>T c.252G>A c.(250-252)atG>atA p.M84I GBM 9 35059646 35059647 + Frame_Shift_Ins INS - - T TCGA-06-0124-01A-01D-1490-08 TCGA-06-0124-10A-01D-1490-08 g.chr9:35059646_35059647insT c.1847_1848insA c.(1846-1848)aatfs p.N616fs GBMLGG 9 35059646 35059647 + Frame_Shift_Ins INS - - T TCGA-06-0124-01A-01D-1490-08 TCGA-06-0124-10A-01D-1490-08 g.chr9:35059646_35059647insT c.1847_1848insA c.(1846-1848)aatfs p.N616fs GBMLGG 9 35060873 35060873 + Silent SNP T T G TCGA-S9-A6WL-01A-21D-A33T-08 TCGA-S9-A6WL-10A-01D-A33W-08 g.chr9:35060873T>G c.1407A>C c.(1405-1407)gtA>gtC p.V469V GBMLGG 9 35066787 35066787 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:35066787G>A c.330C>T c.(328-330)taC>taT p.Y110Y GBMLGG 9 35068295 35068295 + Missense_Mutation SNP C C G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:35068295C>G c.82G>C c.(82-84)Gtt>Ctt p.V28L HNSC 9 35059087 35059087 + Missense_Mutation SNP C C T TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chr9:35059087C>T c.2134G>A c.(2134-2136)Gag>Aag p.E712K HNSC 9 35059572 35059572 + Missense_Mutation SNP T T A TCGA-P3-A5Q6-01A-11D-A28R-08 TCGA-P3-A5Q6-10A-01D-A28U-08 g.chr9:35059572T>A c.1922A>T c.(1921-1923)cAg>cTg p.Q641L HNSC 9 35059698 35059698 + Missense_Mutation SNP C C T TCGA-CN-6023-01A-11D-1683-08 TCGA-CN-6023-10A-01D-1683-08 g.chr9:35059698C>T c.1796G>A c.(1795-1797)cGa>cAa p.R599Q HNSC 9 35060329 35060329 + Missense_Mutation SNP A A C TCGA-CV-7253-01A-11D-2012-08 TCGA-CV-7253-10A-01D-2013-08 g.chr9:35060329A>C c.1676T>G c.(1675-1677)gTc>gGc p.V559G HNSC 9 35061050 35061050 + Missense_Mutation SNP C C A TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr9:35061050C>A c.1321G>T c.(1321-1323)Gtc>Ttc p.V441F HNSC 9 35061120 35061120 + Silent SNP C C T TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr9:35061120C>T c.1251G>A c.(1249-1251)gaG>gaA p.E417E HNSC 9 35061622 35061622 + Silent SNP C C T TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr9:35061622C>T c.1146G>A c.(1144-1146)caG>caA p.Q382Q HNSC 9 35061650 35061650 + Missense_Mutation SNP T T A TCGA-CN-6023-01A-11D-1683-08 TCGA-CN-6023-10A-01D-1683-08 g.chr9:35061650T>A c.1118A>T c.(1117-1119)gAt>gTt p.D373V HNSC 9 35062342 35062342 + Missense_Mutation SNP C C G TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr9:35062342C>G c.817G>C c.(817-819)Gag>Cag p.E273Q KIPAN 9 35059494 35059494 + Missense_Mutation SNP G G A TCGA-BP-4346-01A-01D-1366-10 TCGA-BP-4346-11A-01D-1366-10 g.chr9:35059494G>A c.2000C>T c.(1999-2001)gCc>gTc p.A667V KIPAN 9 35061057 35061057 + Silent SNP A A G TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr9:35061057A>G c.1314T>C c.(1312-1314)gaT>gaC p.D438D KIPAN 9 35061687 35061687 + Splice_Site SNP C C G TCGA-BP-4330-01A-01D-1366-10 TCGA-BP-4330-11A-01D-1366-10 g.chr9:35061687C>G c.e10-1 KIPAN 9 35062023 35062023 + Missense_Mutation SNP A A T TCGA-BP-4160-01A-02D-1366-10 TCGA-BP-4160-11A-01D-1806-10 g.chr9:35062023A>T c.1058T>A c.(1057-1059)aTt>aAt p.I353N KIPAN 9 35066717 35066717 + Missense_Mutation SNP A A T TCGA-UZ-A9PR-01A-11D-A42J-10 TCGA-UZ-A9PR-10A-01D-A42M-10 g.chr9:35066717A>T c.400T>A c.(400-402)Tac>Aac p.Y134N KIPAN 9 35068351 35068351 + Missense_Mutation SNP C C A TCGA-CJ-4637-01A-02D-1386-10 TCGA-CJ-4637-11A-01D-1251-10 g.chr9:35068351C>A c.26G>T c.(25-27)gGt>gTt p.G9V KIRC 9 35059494 35059494 + Missense_Mutation SNP G G A TCGA-BP-4346-01A-01D-1366-10 TCGA-BP-4346-11A-01D-1366-10 g.chr9:35059494G>A c.2000C>T c.(1999-2001)gCc>gTc p.A667V KIRC 9 35061687 35061687 + Splice_Site SNP C C G TCGA-BP-4330-01A-01D-1366-10 TCGA-BP-4330-11A-01D-1366-10 g.chr9:35061687C>G c.e10-1 KIRC 9 35062023 35062023 + Missense_Mutation SNP A A T TCGA-BP-4160-01A-02D-1366-10 TCGA-BP-4160-11A-01D-1806-10 g.chr9:35062023A>T c.1058T>A c.(1057-1059)aTt>aAt p.I353N KIRC 9 35068351 35068351 + Missense_Mutation SNP C C A TCGA-CJ-4637-01A-02D-1386-10 TCGA-CJ-4637-11A-01D-1251-10 g.chr9:35068351C>A c.26G>T c.(25-27)gGt>gTt p.G9V KIRP 9 35061057 35061057 + Silent SNP A A G TCGA-DZ-6133-01A-11D-1961-08 TCGA-DZ-6133-10A-01D-1962-08 g.chr9:35061057A>G c.1314T>C c.(1312-1314)gaT>gaC p.D438D KIRP 9 35066717 35066717 + Missense_Mutation SNP A A T TCGA-UZ-A9PR-01A-11D-A42J-10 TCGA-UZ-A9PR-10A-01D-A42M-10 g.chr9:35066717A>T c.400T>A c.(400-402)Tac>Aac p.Y134N LGG 9 35060873 35060873 + Silent SNP T T G TCGA-S9-A6WL-01A-21D-A33T-08 TCGA-S9-A6WL-10A-01D-A33W-08 g.chr9:35060873T>G c.1407A>C c.(1405-1407)gtA>gtC p.V469V LGG 9 35066787 35066787 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:35066787G>A c.330C>T c.(328-330)taC>taT p.Y110Y LGG 9 35068295 35068295 + Missense_Mutation SNP C C G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:35068295C>G c.82G>C c.(82-84)Gtt>Ctt p.V28L LIHC 9 35060881 35060881 + Missense_Mutation SNP T T C TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr9:35060881T>C c.1399A>G c.(1399-1401)Acc>Gcc p.T467A LIHC 9 35063004 35063004 + Missense_Mutation SNP T T A TCGA-DD-AAD8-01A-11D-A40R-10 TCGA-DD-AAD8-10A-01D-A40U-10 g.chr9:35063004T>A c.782A>T c.(781-783)gAg>gTg p.E261V LIHC 9 35068306 35068306 + Missense_Mutation SNP T T G TCGA-DD-AACA-01A-11D-A40R-10 TCGA-DD-AACA-10A-01D-A40U-10 g.chr9:35068306T>G c.71A>C c.(70-72)aAt>aCt p.N24T LIHC 9 35068346 35068346 + Missense_Mutation SNP C C T TCGA-CC-A7II-01A-11D-A33K-10 TCGA-CC-A7II-10A-01D-A33K-10 g.chr9:35068346C>T c.31G>A c.(31-33)Gac>Aac p.D11N LUAD 9 35057457 35057457 + Missense_Mutation SNP C C A TCGA-17-Z045-01A-01W-0746-08 TCGA-17-Z045-11A-01W-0747-08 g.chr9:35057457C>A c.2231G>T c.(2230-2232)cGc>cTc p.R744L LUAD 9 35059077 35059077 + Missense_Mutation SNP G G A TCGA-44-7662-01A-11D-2063-08 TCGA-44-7662-10A-01D-2063-08 g.chr9:35059077G>A c.2144C>T c.(2143-2145)aCa>aTa p.T715I LUAD 9 35059603 35059603 + Missense_Mutation SNP G G C TCGA-86-6562-01A-11D-1753-08 TCGA-86-6562-10A-01D-1753-08 g.chr9:35059603G>C c.1891C>G c.(1891-1893)Cct>Gct p.P631A LUAD 9 35059646 35059647 + Frame_Shift_Ins INS - - T TCGA-86-8280-01A-11D-2284-08 TCGA-86-8280-10A-01D-2284-08 g.chr9:35059646_35059647insT c.1847_1848insA c.(1846-1848)aatfs p.N616fs LUAD 9 35060352 35060352 + Nonsense_Mutation SNP C C T TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr9:35060352C>T c.1653G>A c.(1651-1653)tgG>tgA p.W551* LUAD 9 35061014 35061014 + Frame_Shift_Del DEL G G - TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr9:35061014delG c.1357delC c.(1357-1359)cggfs p.R453fs LUAD 9 35061054 35061054 + Silent SNP G G A TCGA-38-4625-01A-01D-1553-08 TCGA-38-4625-11A-01D-1553-08 g.chr9:35061054G>A c.1317C>T c.(1315-1317)gcC>gcT p.A439A LUAD 9 35062999 35062999 + Nonsense_Mutation SNP C C A TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr9:35062999C>A c.787G>T c.(787-789)Gga>Tga p.G263* LUAD 9 35065277 35065277 + Missense_Mutation SNP G G A TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr9:35065277G>A c.547C>T c.(547-549)Cac>Tac p.H183Y LUAD 9 35068309 35068309 + Missense_Mutation SNP G G A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr9:35068309G>A c.68C>T c.(67-69)cCc>cTc p.P23L LUSC 9 35061053 35061053 + Nonsense_Mutation SNP C C A TCGA-46-3768-01A-01D-0983-08 TCGA-46-3768-10A-01D-0983-08 g.chr9:35061053C>A c.1318G>T c.(1318-1320)Gag>Tag p.E440* LUSC 9 35066808 35066808 + Silent SNP C C T TCGA-51-4079-01A-01D-1458-08 TCGA-51-4079-11A-01D-1458-08 g.chr9:35066808C>T c.309G>A c.(307-309)caG>caA p.Q103Q OV 9 35067954 35067954 + Missense_Mutation SNP T T A TCGA-29-1688-01A-01W-0633-09 TCGA-29-1688-10A-01W-0633-09 g.chr9:35067954T>A c.236A>T c.(235-237)gAt>gTt p.D79V PCPG 9 35057381 35057381 + Silent SNP G G A TCGA-WB-A81E-01A-11D-A35I-08 TCGA-WB-A81E-10A-01D-A35G-08 g.chr9:35057381G>A c.2307C>T c.(2305-2307)ggC>ggT p.G769G PCPG 9 35060506 35060506 + Missense_Mutation SNP G G A TCGA-QR-A708-01A-11D-A35D-08 TCGA-QR-A708-10A-01D-A35B-08 g.chr9:35060506G>A c.1499C>T c.(1498-1500)cCa>cTa p.P500L PRAD 9 35062992 35062992 + Missense_Mutation SNP A A G TCGA-KC-A7FD-01A-11D-A33T-08 TCGA-KC-A7FD-10A-01D-A33W-08 g.chr9:35062992A>G c.794T>C c.(793-795)tTc>tCc p.F265S PRAD 9 35062993 35062993 + Missense_Mutation SNP A A C TCGA-KC-A7FD-01A-11D-A33T-08 TCGA-KC-A7FD-10A-01D-A33W-08 g.chr9:35062993A>C c.793T>G c.(793-795)Ttc>Gtc p.F265V READ 9 35066724 35066724 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:35066724G>A c.393C>T c.(391-393)ttC>ttT p.F131F SARC 9 35060455 35060455 + Missense_Mutation SNP T T C TCGA-SG-A6Z7-01A-12D-A32I-09 TCGA-SG-A6Z7-11A-21D-A32I-09 g.chr9:35060455T>C c.1550A>G c.(1549-1551)tAt>tGt p.Y517C SKCM 9 35060446 35060446 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:35060446G>A c.1559C>T c.(1558-1560)cCt>cTt p.P520L SKCM 9 35061054 35061054 + Silent SNP G G A TCGA-D9-A148-06A-11D-A19A-08 TCGA-D9-A148-10A-01D-A19A-08 g.chr9:35061054G>A c.1317C>T c.(1315-1317)gcC>gcT p.A439A SKCM 9 35061055 35061055 + Missense_Mutation SNP G G A TCGA-D9-A148-06A-11D-A19A-08 TCGA-D9-A148-10A-01D-A19A-08 g.chr9:35061055G>A c.1316C>T c.(1315-1317)gCc>gTc p.A439V SKCM 9 35065361 35065361 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr9:35065361G>A c.463C>T c.(463-465)Cgt>Tgt p.R155C SKCM 9 35066696 35066696 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr9:35066696C>T c.421G>A c.(421-423)Gaa>Aaa p.E141K SKCM 9 35066718 35066718 + Silent SNP T T C TCGA-EE-A2GT-06A-12D-A197-08 TCGA-EE-A2GT-10A-01D-A199-08 g.chr9:35066718T>C c.399A>G c.(397-399)gtA>gtG p.V133V SKCM 9 35068289 35068289 + Missense_Mutation SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr9:35068289C>T c.88G>A c.(88-90)Gaa>Aaa p.E30K

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 9 35062292 35062292 single base substitution G C downstream_gene_variant BLCA-CN 9 35062292 35062292 single base substitution G C exon_variant BLCA-CN 9 35062292 35062292 single base substitution G C synonymous_variant A289A 867C>G BLCA-CN 9 35062292 35062292 single base substitution G C upstream_gene_variant BLCA-US 9 35059694 35059694 single base substitution G A downstream_gene_variant BLCA-US 9 35059694 35059694 single base substitution G A exon_variant BLCA-US 9 35059694 35059694 single base substitution G A synonymous_variant V600V 1800C>T BLCA-US 9 35059694 35059694 single base substitution G A upstream_gene_variant BLCA-US 9 35061086 35061086 single base substitution G A downstream_gene_variant BLCA-US 9 35061086 35061086 single base substitution G A exon_variant BLCA-US 9 35061086 35061086 single base substitution G A missense_variant L429F 1285C>T BLCA-US 9 35061086 35061086 single base substitution G A upstream_gene_variant BLCA-US 9 35062058 35062058 single base substitution C T downstream_gene_variant BLCA-US 9 35062058 35062058 single base substitution C T exon_variant BLCA-US 9 35062058 35062058 single base substitution C T synonymous_variant V341V 1023G>A BLCA-US 9 35062058 35062058 single base substitution C T upstream_gene_variant BLCA-US 9 35076535 35076535 single base substitution C G upstream_gene_variant BLCA-US 9 35077090 35077090 single base substitution C G upstream_gene_variant BRCA-EU 9 35051648 35051648 single base substitution G T downstream_gene_variant BRCA-EU 9 35052819 35052819 single base substitution T C downstream_gene_variant BRCA-EU 9 35053099 35053099 single base substitution G C downstream_gene_variant BRCA-EU 9 35053210 35053210 single base substitution C T downstream_gene_variant BRCA-EU 9 35053309 35053309 single base substitution G T downstream_gene_variant BRCA-EU 9 35054096 35054096 single base substitution G T downstream_gene_variant BRCA-EU 9 35055402 35055402 single base substitution T C downstream_gene_variant BRCA-EU 9 35055874 35055874 deletion of <=200bp C - downstream_gene_variant BRCA-EU 9 35056243 35056243 single base substitution C A 3_prime_UTR_variant BRCA-EU 9 35056243 35056243 single base substitution C A downstream_gene_variant BRCA-EU 9 35057498 35057498 single base substitution C G downstream_gene_variant BRCA-EU 9 35057498 35057498 single base substitution C G exon_variant BRCA-EU 9 35057498 35057498 single base substitution C G missense_variant E730D 2190G>C BRCA-EU 9 35057690 35057690 insertion of <=200bp - C downstream_gene_variant BRCA-EU 9 35057690 35057690 insertion of <=200bp - C exon_variant BRCA-EU 9 35057690 35057690 insertion of <=200bp - C intron_variant BRCA-EU 9 35059144 35059144 single base substitution G A downstream_gene_variant BRCA-EU 9 35059144 35059144 single base substitution G A exon_variant BRCA-EU 9 35059144 35059144 single base substitution G A missense_variant R693C 2077C>T BRCA-EU 9 35059144 35059144 single base substitution G A upstream_gene_variant BRCA-EU 9 35065615 35065615 single base substitution G A intron_variant BRCA-EU 9 35065615 35065615 single base substitution G A upstream_gene_variant BRCA-EU 9 35066122 35066122 single base substitution C A intron_variant BRCA-EU 9 35066122 35066122 single base substitution C A upstream_gene_variant BRCA-EU 9 35068472 35068472 single base substitution A T intron_variant BRCA-EU 9 35069541 35069541 single base substitution C A intron_variant BRCA-EU 9 35069773 35069773 single base substitution C A intron_variant BRCA-EU 9 35071763 35071763 single base substitution C T 5_prime_UTR_variant BRCA-EU 9 35071763 35071763 single base substitution C T intron_variant BRCA-EU 9 35075588 35075588 single base substitution T A upstream_gene_variant BRCA-EU 9 35076363 35076363 single base substitution G C upstream_gene_variant BRCA-EU 9 35077542 35077542 single base substitution C G upstream_gene_variant BRCA-EU 9 35077604 35077604 deletion of <=200bp A - upstream_gene_variant BRCA-EU 9 35077944 35077944 single base substitution A G upstream_gene_variant BRCA-FR 9 35056402 35056402 single base substitution G A 3_prime_UTR_variant BRCA-FR 9 35056402 35056402 single base substitution G A downstream_gene_variant BRCA-FR 9 35069773 35069773 single base substitution C A intron_variant BRCA-FR 9 35071763 35071763 single base substitution C T 5_prime_UTR_variant BRCA-FR 9 35071763 35071763 single base substitution C T intron_variant BRCA-UK 9 35057455 35057455 single base substitution G A downstream_gene_variant BRCA-UK 9 35057455 35057455 single base substitution G A exon_variant BRCA-UK 9 35057455 35057455 single base substitution G A missense_variant R745C 2233C>T BRCA-UK 9 35075545 35075545 single base substitution G C upstream_gene_variant BRCA-US 9 35057429 35057429 single base substitution C T downstream_gene_variant BRCA-US 9 35057429 35057429 single base substitution C T exon_variant BRCA-US 9 35057429 35057429 single base substitution C T synonymous_variant R753R 2259G>A BRCA-US 9 35059573 35059573 single base substitution G A downstream_gene_variant BRCA-US 9 35059573 35059573 single base substitution G A exon_variant BRCA-US 9 35059573 35059573 single base substitution G A stop_gained Q641* 1921C>T BRCA-US 9 35059573 35059573 single base substitution G A upstream_gene_variant BRCA-US 9 35061169 35061169 single base substitution T C downstream_gene_variant BRCA-US 9 35061169 35061169 single base substitution T C exon_variant BRCA-US 9 35061169 35061169 single base substitution T C missense_variant N401S 1202A>G BRCA-US 9 35061169 35061169 single base substitution T C upstream_gene_variant BRCA-US 9 35064200 35064200 single base substitution A C downstream_gene_variant BRCA-US 9 35064200 35064200 single base substitution A C exon_variant BRCA-US 9 35064200 35064200 single base substitution A C missense_variant V220G 659T>G BRCA-US 9 35064200 35064200 single base substitution A C upstream_gene_variant BRCA-US 9 35065250 35065250 single base substitution C G downstream_gene_variant BRCA-US 9 35065250 35065250 single base substitution C G missense_variant E147Q 439G>C BRCA-US 9 35065250 35065250 single base substitution C G missense_variant E192Q 574G>C BRCA-US 9 35065250 35065250 single base substitution C G splice_region_variant BRCA-US 9 35065250 35065250 single base substitution C G upstream_gene_variant BRCA-US 9 35074432 35074432 single base substitution C T upstream_gene_variant BRCA-US 9 35075528 35075528 single base substitution T G upstream_gene_variant BRCA-US 9 35076497 35076497 single base substitution T C upstream_gene_variant BRCA-US 9 35077299 35077299 single base substitution A G upstream_gene_variant BRCA-US 9 35078182 35078182 single base substitution G C upstream_gene_variant BTCA-JP 9 35064031 35064031 insertion of <=200bp - C downstream_gene_variant BTCA-JP 9 35064031 35064031 insertion of <=200bp - C intron_variant BTCA-JP 9 35064031 35064031 insertion of <=200bp - C upstream_gene_variant BTCA-JP 9 35075485 35075485 single base substitution T G upstream_gene_variant CESC-US 9 35064274 35064274 single base substitution T A downstream_gene_variant CESC-US 9 35064274 35064274 single base substitution T A exon_variant CESC-US 9 35064274 35064274 single base substitution T A missense_variant E150D 450A>T CESC-US 9 35064274 35064274 single base substitution T A missense_variant E195D 585A>T CESC-US 9 35064274 35064274 single base substitution T A upstream_gene_variant CLLE-ES 9 35068375 35068375 single base substitution G T intron_variant CLLE-ES 9 35071166 35071166 single base substitution T G intron_variant CLLE-ES 9 35077824 35077824 single base substitution G A upstream_gene_variant COAD-US 9 35057429 35057429 single base substitution C T downstream_gene_variant COAD-US 9 35057429 35057429 single base substitution C T exon_variant COAD-US 9 35057429 35057429 single base substitution C T synonymous_variant R753R 2259G>A COAD-US 9 35059581 35059581 single base substitution C T downstream_gene_variant COAD-US 9 35059581 35059581 single base substitution C T exon_variant COAD-US 9 35059581 35059581 single base substitution C T missense_variant R638H 1913G>A COAD-US 9 35059581 35059581 single base substitution C T upstream_gene_variant COAD-US 9 35060498 35060498 single base substitution A C downstream_gene_variant COAD-US 9 35060498 35060498 single base substitution A C exon_variant COAD-US 9 35060498 35060498 single base substitution A C missense_variant F503V 1507T>G COAD-US 9 35060498 35060498 single base substitution A C upstream_gene_variant COAD-US 9 35061100 35061100 single base substitution C T downstream_gene_variant COAD-US 9 35061100 35061100 single base substitution C T exon_variant COAD-US 9 35061100 35061100 single base substitution C T missense_variant R424H 1271G>A COAD-US 9 35061100 35061100 single base substitution C T upstream_gene_variant COAD-US 9 35074206 35074206 single base substitution G T upstream_gene_variant COAD-US 9 35075292 35075292 single base substitution A G upstream_gene_variant COAD-US 9 35076791 35076791 single base substitution T C upstream_gene_variant COCA-CN 9 35061503 35061503 single base substitution T C downstream_gene_variant COCA-CN 9 35061503 35061503 single base substitution T C intron_variant COCA-CN 9 35061503 35061503 single base substitution T C upstream_gene_variant COCA-CN 9 35065272 35065272 single base substitution G A downstream_gene_variant COCA-CN 9 35065272 35065272 single base substitution G A exon_variant COCA-CN 9 35065272 35065272 single base substitution G A synonymous_variant C139C 417C>T COCA-CN 9 35065272 35065272 single base substitution G A synonymous_variant C184C 552C>T COCA-CN 9 35065272 35065272 single base substitution G A upstream_gene_variant COCA-CN 9 35067772 35067772 single base substitution C T intron_variant COCA-CN 9 35068313 35068313 single base substitution G T 5_prime_UTR_variant COCA-CN 9 35068313 35068313 single base substitution G T exon_variant COCA-CN 9 35068313 35068313 single base substitution G T missense_variant R22S 64C>A COCA-CN 9 35075453 35075453 single base substitution C T upstream_gene_variant COCA-CN 9 35076962 35076962 single base substitution C A upstream_gene_variant EOPC-DE 9 35059266 35059266 single base substitution T C downstream_gene_variant EOPC-DE 9 35059266 35059266 single base substitution T C intron_variant EOPC-DE 9 35059266 35059266 single base substitution T C upstream_gene_variant EOPC-DE 9 35066890 35066890 single base substitution A C intron_variant ESAD-UK 9 35051484 35051484 single base substitution C T downstream_gene_variant ESAD-UK 9 35054361 35054361 single base substitution G C downstream_gene_variant ESAD-UK 9 35054475 35054475 single base substitution C T downstream_gene_variant ESAD-UK 9 35059116 35059116 single base substitution G T downstream_gene_variant ESAD-UK 9 35059116 35059116 single base substitution G T exon_variant ESAD-UK 9 35059116 35059116 single base substitution G T missense_variant S702Y 2105C>A ESAD-UK 9 35059116 35059116 single base substitution G T upstream_gene_variant ESAD-UK 9 35061087 35061087 single base substitution A T downstream_gene_variant ESAD-UK 9 35061087 35061087 single base substitution A T exon_variant ESAD-UK 9 35061087 35061087 single base substitution A T missense_variant D428E 1284T>A ESAD-UK 9 35061087 35061087 single base substitution A T upstream_gene_variant ESAD-UK 9 35062877 35062877 single base substitution G A downstream_gene_variant ESAD-UK 9 35062877 35062877 single base substitution G A intron_variant ESAD-UK 9 35062877 35062877 single base substitution G A upstream_gene_variant ESAD-UK 9 35063912 35063912 single base substitution A G downstream_gene_variant ESAD-UK 9 35063912 35063912 single base substitution A G intron_variant ESAD-UK 9 35063912 35063912 single base substitution A G upstream_gene_variant ESAD-UK 9 35064778 35064778 single base substitution A G downstream_gene_variant ESAD-UK 9 35064778 35064778 single base substitution A G intron_variant ESAD-UK 9 35064778 35064778 single base substitution A G upstream_gene_variant ESAD-UK 9 35066082 35066082 single base substitution C A intron_variant ESAD-UK 9 35066082 35066082 single base substitution C A upstream_gene_variant ESAD-UK 9 35068023 35068023 single base substitution G A exon_variant ESAD-UK 9 35068023 35068023 single base substitution G A missense_variant T11I 32C>T ESAD-UK 9 35068023 35068023 single base substitution G A missense_variant T56I 167C>T ESAD-UK 9 35069575 35069575 single base substitution G A intron_variant ESAD-UK 9 35073192 35073192 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant ESAD-UK 9 35073192 35073192 single base substitution A T upstream_gene_variant ESAD-UK 9 35078013 35078013 single base substitution G C upstream_gene_variant ESCA-CN 9 35061659 35061659 single base substitution C G downstream_gene_variant ESCA-CN 9 35061659 35061659 single base substitution C G exon_variant ESCA-CN 9 35061659 35061659 single base substitution C G missense_variant G370A 1109G>C ESCA-CN 9 35061659 35061659 single base substitution C G upstream_gene_variant ESCA-CN 9 35074978 35074978 single base substitution C T upstream_gene_variant ESCA-CN 9 35077366 35077366 single base substitution G A upstream_gene_variant GACA-CN 9 35059664 35059664 single base substitution G A downstream_gene_variant GACA-CN 9 35059664 35059664 single base substitution G A exon_variant GACA-CN 9 35059664 35059664 single base substitution G A synonymous_variant G610G 1830C>T GACA-CN 9 35059664 35059664 single base substitution G A upstream_gene_variant GBM-US 9 35059646 35059646 insertion of <=200bp - T downstream_gene_variant GBM-US 9 35059646 35059646 insertion of <=200bp - T exon_variant GBM-US 9 35059646 35059646 insertion of <=200bp - T frameshift_variant N616N? GBM-US 9 35059646 35059646 insertion of <=200bp - T upstream_gene_variant KIRC-US 9 35059494 35059494 single base substitution G A downstream_gene_variant KIRC-US 9 35059494 35059494 single base substitution G A exon_variant KIRC-US 9 35059494 35059494 single base substitution G A missense_variant A667V 2000C>T KIRC-US 9 35059494 35059494 single base substitution G A upstream_gene_variant KIRC-US 9 35061687 35061687 single base substitution C G downstream_gene_variant KIRC-US 9 35061687 35061687 single base substitution C G splice_acceptor_variant KIRC-US 9 35061687 35061687 single base substitution C G upstream_gene_variant KIRC-US 9 35062023 35062023 single base substitution A T downstream_gene_variant KIRC-US 9 35062023 35062023 single base substitution A T exon_variant KIRC-US 9 35062023 35062023 single base substitution A T missense_variant I353N 1058T>A KIRC-US 9 35062023 35062023 single base substitution A T upstream_gene_variant KIRC-US 9 35068351 35068351 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant KIRC-US 9 35068351 35068351 single base substitution C A exon_variant KIRC-US 9 35068351 35068351 single base substitution C A missense_variant G9V 26G>T KIRC-US 9 35075002 35075002 single base substitution G A upstream_gene_variant KIRC-US 9 35075004 35075004 single base substitution C G upstream_gene_variant KIRC-US 9 35078167 35078167 single base substitution A T upstream_gene_variant KIRP-US 9 35061057 35061057 single base substitution A G downstream_gene_variant KIRP-US 9 35061057 35061057 single base substitution A G exon_variant KIRP-US 9 35061057 35061057 single base substitution A G synonymous_variant D438D 1314T>C KIRP-US 9 35061057 35061057 single base substitution A G upstream_gene_variant KIRP-US 9 35077002 35077002 single base substitution A G upstream_gene_variant LICA-CN 9 35059668 35059668 single base substitution T C downstream_gene_variant LICA-CN 9 35059668 35059668 single base substitution T C exon_variant LICA-CN 9 35059668 35059668 single base substitution T C missense_variant D609G 1826A>G LICA-CN 9 35059668 35059668 single base substitution T C upstream_gene_variant LICA-FR 9 35060840 35060840 single base substitution C A downstream_gene_variant LICA-FR 9 35060840 35060840 single base substitution C A exon_variant LICA-FR 9 35060840 35060840 single base substitution C A synonymous_variant G480G 1440G>T LICA-FR 9 35060840 35060840 single base substitution C A upstream_gene_variant LICA-FR 9 35066709 35066709 single base substitution C T exon_variant LICA-FR 9 35066709 35066709 single base substitution C T synonymous_variant K136K 408G>A LICA-FR 9 35066709 35066709 single base substitution C T synonymous_variant K91K 273G>A LIHC-US 9 35068346 35068346 single base substitution C T 5_prime_UTR_variant LIHC-US 9 35068346 35068346 single base substitution C T exon_variant LIHC-US 9 35068346 35068346 single base substitution C T missense_variant D11N 31G>A LINC-JP 9 35053255 35053255 single base substitution T C downstream_gene_variant LINC-JP 9 35057188 35057188 single base substitution G T downstream_gene_variant LINC-JP 9 35057188 35057188 single base substitution G T exon_variant LINC-JP 9 35057188 35057188 single base substitution G T missense_variant P783T 2347C>A LINC-JP 9 35060448 35060448 single base substitution A T downstream_gene_variant LINC-JP 9 35060448 35060448 single base substitution A T exon_variant LINC-JP 9 35060448 35060448 single base substitution A T synonymous_variant P519P 1557T>A LINC-JP 9 35060448 35060448 single base substitution A T upstream_gene_variant LINC-JP 9 35060610 35060610 single base substitution T C downstream_gene_variant LINC-JP 9 35060610 35060610 single base substitution T C exon_variant LINC-JP 9 35060610 35060610 single base substitution T C intron_variant LINC-JP 9 35060610 35060610 single base substitution T C upstream_gene_variant LINC-JP 9 35060862 35060862 single base substitution T A downstream_gene_variant LINC-JP 9 35060862 35060862 single base substitution T A exon_variant LINC-JP 9 35060862 35060862 single base substitution T A missense_variant Q473L 1418A>T LINC-JP 9 35060862 35060862 single base substitution T A upstream_gene_variant LINC-JP 9 35062130 35062130 single base substitution A G downstream_gene_variant LINC-JP 9 35062130 35062130 single base substitution A G exon_variant LINC-JP 9 35062130 35062130 single base substitution A G synonymous_variant H317H 951T>C LINC-JP 9 35062130 35062130 single base substitution A G upstream_gene_variant LIRI-JP 9 35051838 35051838 single base substitution T C downstream_gene_variant LIRI-JP 9 35054384 35054384 single base substitution T C downstream_gene_variant LIRI-JP 9 35055522 35055522 single base substitution T C downstream_gene_variant LIRI-JP 9 35056064 35056064 single base substitution T C 3_prime_UTR_variant LIRI-JP 9 35056064 35056064 single base substitution T C downstream_gene_variant LIRI-JP 9 35057466 35057466 single base substitution C T downstream_gene_variant LIRI-JP 9 35057466 35057466 single base substitution C T exon_variant LIRI-JP 9 35057466 35057466 single base substitution C T missense_variant R741H 2222G>A LIRI-JP 9 35059074 35059074 single base substitution T C downstream_gene_variant LIRI-JP 9 35059074 35059074 single base substitution T C exon_variant LIRI-JP 9 35059074 35059074 single base substitution T C missense_variant N716S 2147A>G LIRI-JP 9 35059074 35059074 single base substitution T C upstream_gene_variant LIRI-JP 9 35059647 35059647 deletion of <=200bp T - downstream_gene_variant LIRI-JP 9 35059647 35059647 deletion of <=200bp T - exon_variant LIRI-JP 9 35059647 35059647 deletion of <=200bp T - frameshift_variant N616 LIRI-JP 9 35059647 35059647 deletion of <=200bp T - upstream_gene_variant LIRI-JP 9 35059682 35059682 single base substitution G A downstream_gene_variant LIRI-JP 9 35059682 35059682 single base substitution G A exon_variant LIRI-JP 9 35059682 35059682 single base substitution G A synonymous_variant I604I 1812C>T LIRI-JP 9 35059682 35059682 single base substitution G A upstream_gene_variant LIRI-JP 9 35060653 35060653 single base substitution C G downstream_gene_variant LIRI-JP 9 35060653 35060653 single base substitution C G exon_variant LIRI-JP 9 35060653 35060653 single base substitution C G intron_variant LIRI-JP 9 35060653 35060653 single base substitution C G upstream_gene_variant LIRI-JP 9 35061003 35061003 single base substitution G A downstream_gene_variant LIRI-JP 9 35061003 35061003 single base substitution G A intron_variant LIRI-JP 9 35061003 35061003 single base substitution G A upstream_gene_variant LIRI-JP 9 35061846 35061846 single base substitution G T downstream_gene_variant LIRI-JP 9 35061846 35061846 single base substitution G T intron_variant LIRI-JP 9 35061846 35061846 single base substitution G T upstream_gene_variant LIRI-JP 9 35062046 35062046 single base substitution T A downstream_gene_variant LIRI-JP 9 35062046 35062046 single base substitution T A exon_variant LIRI-JP 9 35062046 35062046 single base substitution T A synonymous_variant A345A 1035A>T LIRI-JP 9 35062046 35062046 single base substitution T A upstream_gene_variant LIRI-JP 9 35062490 35062490 single base substitution C G downstream_gene_variant LIRI-JP 9 35062490 35062490 single base substitution C G intron_variant LIRI-JP 9 35062490 35062490 single base substitution C G upstream_gene_variant LIRI-JP 9 35062784 35062784 single base substitution G A downstream_gene_variant LIRI-JP 9 35062784 35062784 single base substitution G A intron_variant LIRI-JP 9 35062784 35062784 single base substitution G A upstream_gene_variant LIRI-JP 9 35063710 35063710 single base substitution T G downstream_gene_variant LIRI-JP 9 35063710 35063710 single base substitution T G intron_variant LIRI-JP 9 35063710 35063710 single base substitution T G upstream_gene_variant LIRI-JP 9 35063789 35063789 single base substitution T G downstream_gene_variant LIRI-JP 9 35063789 35063789 single base substitution T G intron_variant LIRI-JP 9 35063789 35063789 single base substitution T G upstream_gene_variant LIRI-JP 9 35064263 35064263 single base substitution T C downstream_gene_variant LIRI-JP 9 35064263 35064263 single base substitution T C exon_variant LIRI-JP 9 35064263 35064263 single base substitution T C missense_variant N154S 461A>G LIRI-JP 9 35064263 35064263 single base substitution T C missense_variant N199S 596A>G LIRI-JP 9 35064263 35064263 single base substitution T C upstream_gene_variant LIRI-JP 9 35064389 35064391 deletion of <=200bp AAG - downstream_gene_variant LIRI-JP 9 35064389 35064391 deletion of <=200bp AAG - intron_variant LIRI-JP 9 35064389 35064391 deletion of <=200bp AAG - upstream_gene_variant LIRI-JP 9 35066211 35066211 single base substitution T A intron_variant LIRI-JP 9 35066211 35066211 single base substitution T A upstream_gene_variant LIRI-JP 9 35067532 35067532 single base substitution C A intron_variant LIRI-JP 9 35067965 35067965 single base substitution A C exon_variant LIRI-JP 9 35067965 35067965 single base substitution A C missense_variant D30E 90T>G LIRI-JP 9 35067965 35067965 single base substitution A C missense_variant D75E 225T>G LIRI-JP 9 35068525 35068525 single base substitution A G intron_variant LIRI-JP 9 35068729 35068729 single base substitution T C intron_variant LIRI-JP 9 35069292 35069292 single base substitution C T intron_variant LIRI-JP 9 35070973 35070973 single base substitution T C intron_variant LIRI-JP 9 35071249 35071249 single base substitution G A intron_variant LIRI-JP 9 35075408 35075408 deletion of <=200bp A - upstream_gene_variant LIRI-JP 9 35076713 35076713 single base substitution T G upstream_gene_variant LUSC-KR 9 35052335 35052335 single base substitution T A downstream_gene_variant LUSC-KR 9 35053369 35053369 single base substitution C A downstream_gene_variant LUSC-KR 9 35055968 35055968 single base substitution C A downstream_gene_variant LUSC-KR 9 35061503 35061503 single base substitution T C downstream_gene_variant LUSC-KR 9 35061503 35061503 single base substitution T C intron_variant LUSC-KR 9 35061503 35061503 single base substitution T C upstream_gene_variant LUSC-KR 9 35064506 35064506 single base substitution T A downstream_gene_variant LUSC-KR 9 35064506 35064506 single base substitution T A intron_variant LUSC-KR 9 35064506 35064506 single base substitution T A upstream_gene_variant LUSC-KR 9 35072571 35072571 single base substitution C T 5_prime_UTR_variant LUSC-KR 9 35072571 35072571 single base substitution C T upstream_gene_variant LUSC-KR 9 35075226 35075226 single base substitution C G upstream_gene_variant LUSC-KR 9 35076131 35076131 single base substitution G A upstream_gene_variant LUSC-US 9 35061053 35061053 single base substitution C A downstream_gene_variant LUSC-US 9 35061053 35061053 single base substitution C A exon_variant LUSC-US 9 35061053 35061053 single base substitution C A stop_gained E440* 1318G>T LUSC-US 9 35061053 35061053 single base substitution C A upstream_gene_variant LUSC-US 9 35066808 35066808 single base substitution C T exon_variant LUSC-US 9 35066808 35066808 single base substitution C T synonymous_variant Q103Q 309G>A LUSC-US 9 35066808 35066808 single base substitution C T synonymous_variant Q58Q 174G>A LUSC-US 9 35076575 35076575 single base substitution C G upstream_gene_variant MALY-DE 9 35051219 35051219 single base substitution C A downstream_gene_variant MALY-DE 9 35052968 35052968 single base substitution T C downstream_gene_variant MALY-DE 9 35064306 35064306 single base substitution A C downstream_gene_variant MALY-DE 9 35064306 35064306 single base substitution A C intron_variant MALY-DE 9 35064306 35064306 single base substitution A C upstream_gene_variant MALY-DE 9 35069499 35069499 single base substitution G C intron_variant MALY-DE 9 35072040 35072040 single base substitution G C intron_variant MALY-DE 9 35072040 35072040 single base substitution G C upstream_gene_variant MELA-AU 9 35051114 35051114 single base substitution C T downstream_gene_variant MELA-AU 9 35051596 35051596 single base substitution A C downstream_gene_variant MELA-AU 9 35052552 35052552 single base substitution G A downstream_gene_variant MELA-AU 9 35053727 35053727 single base substitution C A downstream_gene_variant MELA-AU 9 35053973 35053973 single base substitution G A downstream_gene_variant MELA-AU 9 35054104 35054104 single base substitution G A downstream_gene_variant MELA-AU 9 35055869 35055869 single base substitution G A downstream_gene_variant MELA-AU 9 35056267 35056267 single base substitution G A 3_prime_UTR_variant MELA-AU 9 35056267 35056267 single base substitution G A downstream_gene_variant MELA-AU 9 35056320 35056320 single base substitution G A 3_prime_UTR_variant MELA-AU 9 35056320 35056320 single base substitution G A downstream_gene_variant MELA-AU 9 35056321 35056321 single base substitution G A 3_prime_UTR_variant MELA-AU 9 35056321 35056321 single base substitution G A downstream_gene_variant MELA-AU 9 35056342 35056342 single base substitution G A 3_prime_UTR_variant MELA-AU 9 35056342 35056342 single base substitution G A downstream_gene_variant MELA-AU 9 35056897 35056897 single base substitution C T 3_prime_UTR_variant MELA-AU 9 35056897 35056897 single base substitution C T downstream_gene_variant MELA-AU 9 35056897 35056897 single base substitution C T exon_variant MELA-AU 9 35058257 35058257 single base substitution G A downstream_gene_variant MELA-AU 9 35058257 35058257 single base substitution G A intron_variant MELA-AU 9 35058257 35058257 single base substitution G A upstream_gene_variant MELA-AU 9 35060142 35060142 single base substitution G A downstream_gene_variant MELA-AU 9 35060142 35060142 single base substitution G A intron_variant MELA-AU 9 35060142 35060142 single base substitution G A upstream_gene_variant MELA-AU 9 35060234 35060234 single base substitution A G downstream_gene_variant MELA-AU 9 35060234 35060234 single base substitution A G intron_variant MELA-AU 9 35060234 35060234 single base substitution A G upstream_gene_variant MELA-AU 9 35060934 35060934 single base substitution G A downstream_gene_variant MELA-AU 9 35060934 35060934 single base substitution G A intron_variant MELA-AU 9 35060934 35060934 single base substitution G A upstream_gene_variant MELA-AU 9 35061348 35061348 single base substitution G A downstream_gene_variant MELA-AU 9 35061348 35061348 single base substitution G A intron_variant MELA-AU 9 35061348 35061348 single base substitution G A upstream_gene_variant MELA-AU 9 35061686 35061687 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 9 35061686 35061687 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant G361D 1082G>A MELA-AU 9 35061686 35061687 multiple base substitution (>=2bp and <=200bp) CC TT splice_acceptor_variant MELA-AU 9 35061686 35061687 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 35062354 35062354 single base substitution G A downstream_gene_variant MELA-AU 9 35062354 35062354 single base substitution G A splice_region_variant MELA-AU 9 35062354 35062354 single base substitution G A upstream_gene_variant MELA-AU 9 35062743 35062743 single base substitution C T downstream_gene_variant MELA-AU 9 35062743 35062743 single base substitution C T intron_variant MELA-AU 9 35062743 35062743 single base substitution C T upstream_gene_variant MELA-AU 9 35064018 35064018 single base substitution G A downstream_gene_variant MELA-AU 9 35064018 35064018 single base substitution G A intron_variant MELA-AU 9 35064018 35064018 single base substitution G A upstream_gene_variant MELA-AU 9 35064067 35064067 single base substitution G A downstream_gene_variant MELA-AU 9 35064067 35064067 single base substitution G A intron_variant MELA-AU 9 35064067 35064067 single base substitution G A upstream_gene_variant MELA-AU 9 35064074 35064074 single base substitution G A downstream_gene_variant MELA-AU 9 35064074 35064074 single base substitution G A intron_variant MELA-AU 9 35064074 35064074 single base substitution G A upstream_gene_variant MELA-AU 9 35064142 35064142 single base substitution G A downstream_gene_variant MELA-AU 9 35064142 35064142 single base substitution G A intron_variant MELA-AU 9 35064142 35064142 single base substitution G A upstream_gene_variant MELA-AU 9 35064174 35064174 single base substitution G A downstream_gene_variant MELA-AU 9 35064174 35064174 single base substitution G A exon_variant MELA-AU 9 35064174 35064174 single base substitution G A missense_variant L229F 685C>T MELA-AU 9 35064174 35064174 single base substitution G A upstream_gene_variant MELA-AU 9 35064295 35064295 single base substitution G A downstream_gene_variant MELA-AU 9 35064295 35064295 single base substitution G A intron_variant MELA-AU 9 35064295 35064295 single base substitution G A upstream_gene_variant MELA-AU 9 35065056 35065056 single base substitution G A downstream_gene_variant MELA-AU 9 35065056 35065056 single base substitution G A intron_variant MELA-AU 9 35065056 35065056 single base substitution G A upstream_gene_variant MELA-AU 9 35065781 35065781 single base substitution G A intron_variant MELA-AU 9 35065781 35065781 single base substitution G A upstream_gene_variant MELA-AU 9 35066494 35066494 single base substitution G A intron_variant MELA-AU 9 35066494 35066494 single base substitution G A upstream_gene_variant MELA-AU 9 35066819 35066819 single base substitution G A splice_region_variant MELA-AU 9 35067025 35067025 single base substitution A G intron_variant MELA-AU 9 35067633 35067633 single base substitution A T intron_variant MELA-AU 9 35069395 35069395 single base substitution G A intron_variant MELA-AU 9 35070446 35070446 single base substitution T G intron_variant MELA-AU 9 35071390 35071390 single base substitution G A intron_variant MELA-AU 9 35073973 35073974 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 35074394 35074394 single base substitution A C upstream_gene_variant MELA-AU 9 35074582 35074582 single base substitution G A upstream_gene_variant MELA-AU 9 35076144 35076144 single base substitution G A upstream_gene_variant MELA-AU 9 35077633 35077633 single base substitution G A upstream_gene_variant MELA-AU 9 35077753 35077753 single base substitution A T upstream_gene_variant NBL-US 9 35074957 35074957 single base substitution G C upstream_gene_variant ORCA-IN 9 35062249 35062249 single base substitution C T downstream_gene_variant ORCA-IN 9 35062249 35062249 single base substitution C T exon_variant ORCA-IN 9 35062249 35062249 single base substitution C T missense_variant D304N 910G>A ORCA-IN 9 35062249 35062249 single base substitution C T upstream_gene_variant ORCA-IN 9 35073729 35073729 single base substitution C G upstream_gene_variant ORCA-IN 9 35075044 35075044 single base substitution C A upstream_gene_variant ORCA-IN 9 35078185 35078185 single base substitution G A upstream_gene_variant OV-AU 9 35060183 35060183 single base substitution A C downstream_gene_variant OV-AU 9 35060183 35060183 single base substitution A C intron_variant OV-AU 9 35060183 35060183 single base substitution A C upstream_gene_variant OV-AU 9 35072819 35072819 single base substitution G T 5_prime_UTR_variant OV-AU 9 35072819 35072819 single base substitution G T upstream_gene_variant PACA-AU 9 35060129 35060130 deletion of <=200bp AG - downstream_gene_variant PACA-AU 9 35060129 35060130 deletion of <=200bp AG - intron_variant PACA-AU 9 35060129 35060130 deletion of <=200bp AG - upstream_gene_variant PACA-AU 9 35067344 35067344 single base substitution T G intron_variant PACA-AU 9 35070501 35070501 single base substitution C T intron_variant PACA-AU 9 35076947 35076947 single base substitution C T upstream_gene_variant PACA-CA 9 35051405 35051405 single base substitution T C downstream_gene_variant PACA-CA 9 35055282 35055285 deletion of <=200bp TGTG - downstream_gene_variant PACA-CA 9 35055293 35055295 deletion of <=200bp ATT - downstream_gene_variant PACA-CA 9 35060452 35060452 single base substitution C A downstream_gene_variant PACA-CA 9 35060452 35060452 single base substitution C A exon_variant PACA-CA 9 35060452 35060452 single base substitution C A missense_variant G518V 1553G>T PACA-CA 9 35060452 35060452 single base substitution C A upstream_gene_variant PACA-CA 9 35070852 35070852 insertion of <=200bp - C intron_variant PACA-CA 9 35072542 35072542 single base substitution G A 5_prime_UTR_variant PACA-CA 9 35072542 35072542 single base substitution G A exon_variant PACA-CA 9 35072542 35072542 single base substitution G A upstream_gene_variant PACA-CA 9 35074093 35074093 single base substitution A C upstream_gene_variant PBCA-DE 9 35058381 35058381 single base substitution C T downstream_gene_variant PBCA-DE 9 35058381 35058381 single base substitution C T intron_variant PBCA-DE 9 35058381 35058381 single base substitution C T upstream_gene_variant PBCA-DE 9 35066123 35066123 insertion of <=200bp - A intron_variant PBCA-DE 9 35066123 35066123 insertion of <=200bp - A upstream_gene_variant PBCA-DE 9 35072184 35072184 single base substitution A T intron_variant PBCA-DE 9 35072184 35072184 single base substitution A T upstream_gene_variant PRAD-CA 9 35061401 35061401 single base substitution C T downstream_gene_variant PRAD-CA 9 35061401 35061401 single base substitution C T intron_variant PRAD-CA 9 35061401 35061401 single base substitution C T upstream_gene_variant PRAD-UK 9 35051692 35051692 single base substitution T C downstream_gene_variant PRAD-UK 9 35054447 35054447 single base substitution T C downstream_gene_variant PRAD-UK 9 35068149 35068149 single base substitution C T intron_variant PRAD-UK 9 35074319 35074319 single base substitution T A upstream_gene_variant PRAD-US 9 35076446 35076446 single base substitution C A upstream_gene_variant RECA-EU 9 35053912 35053912 single base substitution A G downstream_gene_variant RECA-EU 9 35071199 35071199 single base substitution T G intron_variant RECA-EU 9 35073400 35073400 single base substitution A G upstream_gene_variant RECA-EU 9 35073957 35073957 single base substitution G A upstream_gene_variant SKCA-BR 9 35051914 35051914 insertion of <=200bp - AT downstream_gene_variant SKCA-BR 9 35054242 35054242 single base substitution C T downstream_gene_variant SKCA-BR 9 35054803 35054803 single base substitution C A downstream_gene_variant SKCA-BR 9 35059539 35059539 single base substitution G A downstream_gene_variant SKCA-BR 9 35059539 35059539 single base substitution G A exon_variant SKCA-BR 9 35059539 35059539 single base substitution G A missense_variant S652F 1955C>T SKCA-BR 9 35059539 35059539 single base substitution G A upstream_gene_variant SKCA-BR 9 35060039 35060039 single base substitution G A downstream_gene_variant SKCA-BR 9 35060039 35060039 single base substitution G A intron_variant SKCA-BR 9 35060039 35060039 single base substitution G A upstream_gene_variant SKCA-BR 9 35062489 35062489 single base substitution A C downstream_gene_variant SKCA-BR 9 35062489 35062489 single base substitution A C intron_variant SKCA-BR 9 35062489 35062489 single base substitution A C upstream_gene_variant SKCA-BR 9 35067976 35067976 single base substitution G A exon_variant SKCA-BR 9 35067976 35067976 single base substitution G A missense_variant L27F 79C>T SKCA-BR 9 35067976 35067976 single base substitution G A missense_variant L72F 214C>T SKCA-BR 9 35068506 35068506 single base substitution G A intron_variant SKCA-BR 9 35075214 35075214 single base substitution G A upstream_gene_variant SKCA-BR 9 35076239 35076239 single base substitution A G upstream_gene_variant SKCA-BR 9 35077020 35077020 single base substitution C T upstream_gene_variant SKCM-US 9 35060446 35060446 single base substitution G A downstream_gene_variant SKCM-US 9 35060446 35060446 single base substitution G A exon_variant SKCM-US 9 35060446 35060446 single base substitution G A missense_variant P520L 1559C>T SKCM-US 9 35060446 35060446 single base substitution G A upstream_gene_variant SKCM-US 9 35065361 35065361 single base substitution G A exon_variant SKCM-US 9 35065361 35065361 single base substitution G A missense_variant R110C 328C>T SKCM-US 9 35065361 35065361 single base substitution G A missense_variant R155C 463C>T SKCM-US 9 35065361 35065361 single base substitution G A upstream_gene_variant SKCM-US 9 35066696 35066696 single base substitution C T exon_variant SKCM-US 9 35066696 35066696 single base substitution C T missense_variant E141K 421G>A SKCM-US 9 35066696 35066696 single base substitution C T missense_variant E96K 286G>A SKCM-US 9 35066718 35066718 single base substitution T C exon_variant SKCM-US 9 35066718 35066718 single base substitution T C synonymous_variant V133V 399A>G SKCM-US 9 35066718 35066718 single base substitution T C synonymous_variant V88V 264A>G SKCM-US 9 35068289 35068289 single base substitution C T 5_prime_UTR_variant SKCM-US 9 35068289 35068289 single base substitution C T exon_variant SKCM-US 9 35068289 35068289 single base substitution C T missense_variant E30K 88G>A SKCM-US 9 35074161 35074161 single base substitution G A upstream_gene_variant SKCM-US 9 35074167 35074167 single base substitution A T upstream_gene_variant SKCM-US 9 35074205 35074205 single base substitution G A upstream_gene_variant SKCM-US 9 35076968 35076968 single base substitution C T upstream_gene_variant SKCM-US 9 35077033 35077033 single base substitution C T upstream_gene_variant STAD-US 9 35059577 35059577 single base substitution A G downstream_gene_variant STAD-US 9 35059577 35059577 single base substitution A G exon_variant STAD-US 9 35059577 35059577 single base substitution A G synonymous_variant L639L 1917T>C STAD-US 9 35059577 35059577 single base substitution A G upstream_gene_variant STAD-US 9 35059794 35059794 single base substitution C T downstream_gene_variant STAD-US 9 35059794 35059794 single base substitution C T exon_variant STAD-US 9 35059794 35059794 single base substitution C T missense_variant R567H 1700G>A STAD-US 9 35059794 35059794 single base substitution C T upstream_gene_variant STAD-US 9 35062112 35062112 single base substitution G A downstream_gene_variant STAD-US 9 35062112 35062112 single base substitution G A exon_variant STAD-US 9 35062112 35062112 single base substitution G A synonymous_variant R323R 969C>T STAD-US 9 35062112 35062112 single base substitution G A upstream_gene_variant STAD-US 9 35062113 35062113 single base substitution C T downstream_gene_variant STAD-US 9 35062113 35062113 single base substitution C T exon_variant STAD-US 9 35062113 35062113 single base substitution C T missense_variant R323H 968G>A STAD-US 9 35062113 35062113 single base substitution C T upstream_gene_variant STAD-US 9 35065361 35065361 single base substitution G A exon_variant STAD-US 9 35065361 35065361 single base substitution G A missense_variant R110C 328C>T STAD-US 9 35065361 35065361 single base substitution G A missense_variant R155C 463C>T STAD-US 9 35065361 35065361 single base substitution G A upstream_gene_variant STAD-US 9 35066769 35066769 single base substitution C T exon_variant STAD-US 9 35066769 35066769 single base substitution C T synonymous_variant V116V 348G>A STAD-US 9 35066769 35066769 single base substitution C T synonymous_variant V71V 213G>A STAD-US 9 35067913 35067913 single base substitution G A exon_variant STAD-US 9 35067913 35067913 single base substitution G A missense_variant R48C 142C>T STAD-US 9 35067913 35067913 single base substitution G A missense_variant R93C 277C>T STAD-US 9 35074153 35074153 single base substitution G T upstream_gene_variant STAD-US 9 35075485 35075485 deletion of <=200bp T - upstream_gene_variant STAD-US 9 35077266 35077266 single base substitution C T upstream_gene_variant THCA-US 9 35065309 35065309 single base substitution G A downstream_gene_variant THCA-US 9 35065309 35065309 single base substitution G A exon_variant THCA-US 9 35065309 35065309 single base substitution G A missense_variant P127L 380C>T THCA-US 9 35065309 35065309 single base substitution G A missense_variant P172L 515C>T THCA-US 9 35065309 35065309 single base substitution G A upstream_gene_variant UCEC-US 9 35057147 35057147 single base substitution G A downstream_gene_variant UCEC-US 9 35057147 35057147 single base substitution G A exon_variant UCEC-US 9 35057147 35057147 single base substitution G A synonymous_variant Y796Y 2388C>T UCEC-US 9 35059111 35059111 single base substitution C T downstream_gene_variant UCEC-US 9 35059111 35059111 single base substitution C T exon_variant UCEC-US 9 35059111 35059111 single base substitution C T missense_variant E704K 2110G>A UCEC-US 9 35059111 35059111 single base substitution C T upstream_gene_variant UCEC-US 9 35059202 35059202 single base substitution C T downstream_gene_variant UCEC-US 9 35059202 35059202 single base substitution C T exon_variant UCEC-US 9 35059202 35059202 single base substitution C T synonymous_variant E673E 2019G>A UCEC-US 9 35059202 35059202 single base substitution C T upstream_gene_variant UCEC-US 9 35059707 35059707 single base substitution G A downstream_gene_variant UCEC-US 9 35059707 35059707 single base substitution G A exon_variant UCEC-US 9 35059707 35059707 single base substitution G A missense_variant A596V 1787C>T UCEC-US 9 35059707 35059707 single base substitution G A upstream_gene_variant UCEC-US 9 35060843 35060843 single base substitution G A downstream_gene_variant UCEC-US 9 35060843 35060843 single base substitution G A exon_variant UCEC-US 9 35060843 35060843 single base substitution G A synonymous_variant I479I 1437C>T UCEC-US 9 35060843 35060843 single base substitution G A upstream_gene_variant UCEC-US 9 35061638 35061638 single base substitution C T downstream_gene_variant UCEC-US 9 35061638 35061638 single base substitution C T exon_variant UCEC-US 9 35061638 35061638 single base substitution C T missense_variant R377H 1130G>A UCEC-US 9 35061638 35061638 single base substitution C T upstream_gene_variant UCEC-US 9 35062231 35062231 single base substitution C T downstream_gene_variant UCEC-US 9 35062231 35062231 single base substitution C T exon_variant UCEC-US 9 35062231 35062231 single base substitution C T missense_variant A310T 928G>A UCEC-US 9 35062231 35062231 single base substitution C T upstream_gene_variant UCEC-US 9 35063019 35063019 single base substitution C T downstream_gene_variant UCEC-US 9 35063019 35063019 single base substitution C T exon_variant UCEC-US 9 35063019 35063019 single base substitution C T missense_variant R256Q 767G>A UCEC-US 9 35063019 35063019 single base substitution C T upstream_gene_variant UCEC-US 9 35064180 35064180 single base substitution G T downstream_gene_variant UCEC-US 9 35064180 35064180 single base substitution G T exon_variant UCEC-US 9 35064180 35064180 single base substitution G T missense_variant P227T 679C>A UCEC-US 9 35064180 35064180 single base substitution G T upstream_gene_variant UCEC-US 9 35067942 35067942 single base substitution C T exon_variant UCEC-US 9 35067942 35067942 single base substitution C T missense_variant R38Q 113G>A UCEC-US 9 35067942 35067942 single base substitution C T missense_variant R83Q 248G>A UCEC-US 9 35067943 35067943 single base substitution G A exon_variant UCEC-US 9 35067943 35067943 single base substitution G A missense_variant R38W 112C>T UCEC-US 9 35067943 35067943 single base substitution G A missense_variant R83W 247C>T UCEC-US 9 35067979 35067979 single base substitution C T exon_variant UCEC-US 9 35067979 35067979 single base substitution C T missense_variant V26I 76G>A UCEC-US 9 35067979 35067979 single base substitution C T missense_variant V71I 211G>A UCEC-US 9 35067983 35067983 single base substitution G A exon_variant UCEC-US 9 35067983 35067983 single base substitution G A synonymous_variant C24C 72C>T UCEC-US 9 35067983 35067983 single base substitution G A synonymous_variant C69C 207C>T UCEC-US 9 35068312 35068312 single base substitution C T 5_prime_UTR_variant UCEC-US 9 35068312 35068312 single base substitution C T exon_variant UCEC-US 9 35068312 35068312 single base substitution C T missense_variant R22H 65G>A UCEC-US 9 35074161 35074161 single base substitution G A upstream_gene_variant UCEC-US 9 35074941 35074941 single base substitution C T upstream_gene_variant UCEC-US 9 35075315 35075315 single base substitution C T upstream_gene_variant UCEC-US 9 35075493 35075493 single base substitution C T upstream_gene_variant UCEC-US 9 35075722 35075722 single base substitution G T upstream_gene_variant UCEC-US 9 35076819 35076819 single base substitution C T upstream_gene_variant UCEC-US 9 35077266 35077266 single base substitution C T upstream_gene_variant UCEC-US 9 35077285 35077285 single base substitution G T upstream_gene_variant UCEC-US 9 35077293 35077293 single base substitution T C upstream_gene_variant UCEC-US 9 35077382 35077382 single base substitution C A upstream_gene_variant UCEC-US 9 35077397 35077397 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand EGC8 COSM5063932 c.430C>T p.R144* Substitution - Nonsense 9:35066690-35066690 - SC_9080 COSM5554252 c.1517T>A p.F506Y Substitution - Missense 9:35060491-35060491 - HCC135 COSM3664324 c.1557T>A p.P519P Substitution - coding silent 9:35060451-35060451 - RK106_C01 COSM1636175 c.225T>G p.D75E Substitution - Missense 9:35067968-35067968 - TCGA-BK-A0C9-01 COSM1108577 c.211G>A p.V71I Substitution - Missense 9:35067982-35067982 - 2521243 COSM5886651 c.130-6C>T p.? Unknown 9:35068069-35068069 - TCGA-AP-A056-01 COSM1108575 c.247C>T p.R83W Substitution - Missense 9:35067946-35067946 - RK130_C01 COSM1636173 c.2147A>G p.N716S Substitution - Missense 9:35059077-35059077 - T3090 COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - TCGA-EA-A1QS-01 COSM4831003 c.585A>T p.E195D Substitution - Missense 9:35064277-35064277 - TCGA-A6-6781-01 COSM1462184 c.1913G>A p.R638H Substitution - Missense 9:35059584-35059584 - TCGA-AA-3518-01 COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - Pat_29_A COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - TCGA-AP-A051-01 COSM1108579 c.207C>T p.C69C Substitution - coding silent 9:35067986-35067986 - TCGA-AO-A12E-01 COSM1270181 c.1202A>G p.N401S Substitution - Missense 9:35061172-35061172 - ccRCC-21 COSM1664945 c.361G>A p.D121N Substitution - Missense 9:35066759-35066759 - TCGA-A8-A0A6-01 COSM3848449 c.659T>G p.V220G Substitution - Missense 9:35064203-35064203 - LC_C9 COSM1187701 c.920A>T p.D307V Substitution - Missense 9:35062242-35062242 - TCGA-AP-A059-01 COSM1108559 c.2019G>A p.E673E Substitution - coding silent 9:35059205-35059205 - HCC128T COSM1624938 c.1418A>T p.Q473L Substitution - Missense 9:35060865-35060865 - 2492720 COSM5721304 c.2105C>T p.S702F Substitution - Missense 9:35059119-35059119 - TCGA-CG-5723-01 COSM3907078 c.277C>T p.R93C Substitution - Missense 9:35067916-35067916 - TCGA-CA-6717-01 COSM1462185 c.1507T>G p.F503V Substitution - Missense 9:35060501-35060501 - 587222 COSM1232240 c.1725C>A p.F575L Substitution - Missense 9:35059772-35059772 - TCGA-46-3768-01 COSM753542 c.1318G>T p.E440* Substitution - Nonsense 9:35061056-35061056 - HCC149T COSM3664325 c.951T>C p.H317H Substitution - coding silent 9:35062133-35062133 - PT49 COSM5935527 c.1991C>T p.S664F Substitution - Missense 9:35059506-35059506 - 2492721 COSM5721304 c.2105C>T p.S702F Substitution - Missense 9:35059119-35059119 - TCGA-AP-A059-01 COSM1108565 c.1130G>A p.R377H Substitution - Missense 9:35061641-35061641 - CHC1556T COSM4787693 c.408G>A p.K136K Substitution - coding silent 9:35066712-35066712 - HCC149 COSM3664325 c.951T>C p.H317H Substitution - coding silent 9:35062133-35062133 - TCGA-BR-8372-01 COSM2773890 c.968G>A p.R323H Substitution - Missense 9:35062116-35062116 - TCGA-FW-A3R5-06 COSM3926748 c.1559C>T p.P520L Substitution - Missense 9:35060449-35060449 - HCT15 COSM2773883 c.1198G>T p.A400S Substitution - Missense 9:35061176-35061176 - pfg122T COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - B96 COSM1756153 c.867C>G p.A289A Substitution - coding silent 9:35062295-35062295 - PCSI_0079_Pa_P COSM3382524 c.1553G>T p.G518V Substitution - Missense 9:35060455-35060455 - SNUH_G10_S1 COSM150600 c.811+3G>A p.? Unknown 9:35062975-35062975 - HX17T COSM1624937 c.2347C>A p.P783T Substitution - Missense 9:35057191-35057191 - SNU-175 COSM2773865 c.2410C>A p.L804M Substitution - Missense 9:35057128-35057128 - TCGA-EE-A2GI-06 COSM3657096 c.463C>T p.R155C Substitution - Missense 9:35065364-35065364 - SNUH_G45_S1 COSM2773894 c.812-7C>G p.? Unknown 9:35062357-35062357 - GC8_T COSM150600 c.811+3G>A p.? Unknown 9:35062975-35062975 - 2521259 COSM5890464 c.2029A>G p.K677E Substitution - Missense 9:35059195-35059195 - TCGA-DZ-6133-01 COSM3996531 c.1314T>C p.D438D Substitution - coding silent 9:35061060-35061060 - sysucc-1397T COSM5475289 c.64C>A p.R22S Substitution - Missense 9:35068316-35068316 - TCGA-GC-A3BM-01 COSM3779988 c.1285C>T p.L429F Substitution - Missense 9:35061089-35061089 - TCGA-12-0707 COSM2154555 c.441G>C p.R147R Substitution - coding silent 9:35066679-35066679 - PD8964a COSM5782149 c.2190G>C p.E730D Substitution - Missense 9:35057501-35057501 - T3610 COSM4740252 c.1847_1848insA p.N616fs*12 Insertion - Frameshift 9:35059649-35059650 - TCGA-A2-A0YG-01 COSM455889 c.2259G>A p.R753R Substitution - coding silent 9:35057432-35057432 - TCGA-DS-A1OC-01 COSM1294463 c.85G>C p.D29H Substitution - Missense 9:35068295-35068295 - T207 COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - TCGA-12-0707 COSM2154466 c.442A>T p.K148* Substitution - Nonsense 9:35066678-35066678 - RK159_C01 COSM1636174 c.1812C>T p.I604I Substitution - coding silent 9:35059685-35059685 - Pat_06_A COSM1462188 c.801_803delCTT p.F267delF Deletion - In frame 9:35062986-35062988 - TCGA-GC-A3OO-01 COSM3779989 c.1023G>A p.V341V Substitution - coding silent 9:35062061-35062061 - CSCC-17-T COSM4479404 c.2320C>T p.P774S Substitution - Missense 9:35057218-35057218 - TCGA-BP-4330-01 COSM3367700 c.1082-1G>C p.? Unknown 9:35061690-35061690 - SNU-175 COSM2773890 c.968G>A p.R323H Substitution - Missense 9:35062116-35062116 - TCGA-HU-A4H3-01 COSM3907075 c.1700G>A p.R567H Substitution - Missense 9:35059797-35059797 - TCGA-51-4079-01 COSM753541 c.309G>A p.Q103Q Substitution - coding silent 9:35066811-35066811 - LUAD-E00918 COSM365438 c.580G>A p.E194K Substitution - Missense 9:35064282-35064282 - S02403 COSM5700598 c.391T>C p.F131L Substitution - Missense 9:35066729-35066729 - TCGA-B5-A0JZ-01 COSM1108561 c.1787C>T p.A596V Substitution - Missense 9:35059710-35059710 - TCGA-CM-5861-01 COSM1462186 c.1271G>A p.R424H Substitution - Missense 9:35061103-35061103 - PT55 COSM5942306 c.67C>T p.P23S Substitution - Missense 9:35068313-35068313 - RK257_C01 COSM4779244 c.1035A>T p.A345A Substitution - coding silent 9:35062049-35062049 - OSCC-GB_00690111 COSM4886937 c.910G>A p.D304N Substitution - Missense 9:35062252-35062252 - S00829 COSM5660185 c.361G>C p.D121H Substitution - Missense 9:35066759-35066759 - TCGA-DJ-A2Q8-01 COSM3375236 c.515C>T p.P172L Substitution - Missense 9:35065312-35065312 - pfg016T COSM1643817 c.1337C>T p.A446V Substitution - Missense 9:35061037-35061037 - 169 COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - 587376 COSM1232241 c.1191A>C p.E397D Substitution - Missense 9:35061580-35061580 - SJACT060_D COSM4968175 c.1278G>C p.K426N Substitution - Missense 9:35061096-35061096 - TCGA-B5-A11N-01 COSM1108573 c.248G>A p.R83Q Substitution - Missense 9:35067945-35067945 - 3 COSM4166666 c.2371A>C p.T791P Substitution - Missense 9:35057167-35057167 - CHEWS031 COSM4588804 c.2214A>G p.E738E Substitution - coding silent 9:35057477-35057477 - SC_9081 COSM5549415 c.889G>A p.A297T Substitution - Missense 9:35062273-35062273 - ESO-1059 COSM1270180 c.1904G>C p.R635T Substitution - Missense 9:35059593-35059593 - Pat_65_A COSM1462188 c.801_803delCTT p.F267delF Deletion - In frame 9:35062986-35062988 - TCGA-BT-A3PJ-01 COSM3779987 c.1800C>T p.V600V Substitution - coding silent 9:35059697-35059697 - TCGA-BR-8363-01 COSM3907077 c.348G>A p.V116V Substitution - coding silent 9:35066772-35066772 - TCGA-29-1688-01 COSM1331567 c.236A>T p.D79V Substitution - Missense 9:35067957-35067957 - T1743 COSM4740254 c.303-2A>T p.? Unknown 9:35066819-35066819 - TCGA-BR-4362-01 COSM3657096 c.463C>T p.R155C Substitution - Missense 9:35065364-35065364 - CRC-02T COSM5455779 c.552C>T p.C184C Substitution - coding silent 9:35065275-35065275 - ESO-0067 COSM1270179 c.1275G>T p.K425N Substitution - Missense 9:35061099-35061099 - TCGA-HU-A4GT-01 COSM3907076 c.969C>T p.R323R Substitution - coding silent 9:35062115-35062115 - TCGA-BR-7851-01 COSM3907075 c.1700G>A p.R567H Substitution - Missense 9:35059797-35059797 - TCGA-EE-A2GT-06 COSM3657098 c.399A>G p.V133V Substitution - coding silent 9:35066721-35066721 - 2492722 COSM5721304 c.2105C>T p.S702F Substitution - Missense 9:35059119-35059119 - TCGA-AR-A0TX-01 COSM455890 c.1921C>T p.Q641* Substitution - Nonsense 9:35059576-35059576 - cSCCP4 COSM138708 c.1711C>T p.P571S Substitution - Missense 9:35059786-35059786 - MO_1232 COSM5557123 c.899T>C p.I300T Substitution - Missense 9:35062263-35062263 - RK245_C01 COSM4945137 c.1359+9C>T p.? Unknown 9:35061006-35061006 - LUAD-B01811 COSM334938 c.1400C>T p.T467I Substitution - Missense 9:35060883-35060883 - 2492721 COSM5721305 c.157C>T p.R53* Substitution - Nonsense 9:35068036-35068036 - S40_pre COSM5575079 c.1848_1849insA p.V617fs*11 Insertion - Frameshift 9:35059648-35059649 - CSCC-29-T COSM4546267 c.396G>A p.E132E Substitution - coding silent 9:35066724-35066724 - HCT8 COSM2773883 c.1198G>T p.A400S Substitution - Missense 9:35061176-35061176 - Pat_53_A COSM4740252 c.1847_1848insA p.N616fs*12 Insertion - Frameshift 9:35059649-35059650 - T3174 COSM4740253 c.1401C>T p.T467T Substitution - coding silent 9:35060882-35060882 - 1517_PT COSM5757368 c.1163T>C p.M388T Substitution - Missense 9:35061608-35061608 - ACINAR01 COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - CHC1556T COSM4787693 c.408G>A p.K136K Substitution - coding silent 9:35066712-35066712 - HCC129T COSM5817028 c.1826A>G p.D609G Substitution - Missense 9:35059671-35059671 - 1 COSM4166563 c.766C>T p.R256* Substitution - Nonsense 9:35063023-35063023 - STC291 COSM5063931 c.710C>A p.P237H Substitution - Missense 9:35063079-35063079 - TCGA-AP-A059-01 COSM1108571 c.679C>A p.P227T Substitution - Missense 9:35064183-35064183 - pfg205T COSM4752637 c.2098C>T p.R700C Substitution - Missense 9:35059126-35059126 - TCGA-AP-A059-01 COSM1108581 c.65G>A p.R22H Substitution - Missense 9:35068315-35068315 - TCGA-CC-A7II-01 COSM4937708 c.31G>A p.D11N Substitution - Missense 9:35068349-35068349 - TCGA-D1-A103-01 COSM1108557 c.2110G>A p.E704K Substitution - Missense 9:35059114-35059114 - S02065 COSM5672994 c.964C>T p.R322W Substitution - Missense 9:35062120-35062120 - T3202 COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - B96-Tumor COSM1756153 c.867C>G p.A289A Substitution - coding silent 9:35062295-35062295 - GC1_T COSM150599 c.1830C>T p.G610G Substitution - coding silent 9:35059667-35059667 - CHC1704T COSM4803910 c.1440G>T p.G480G Substitution - coding silent 9:35060843-35060843 - LP6005935-DNA_G03 COSM5032238 c.2105C>A p.S702Y Substitution - Missense 9:35059119-35059119 - PT13 COSM5896029 c.1316C>T p.A439V Substitution - Missense 9:35061058-35061058 - 2492729 COSM5726349 c.1981C>T p.L661L Substitution - coding silent 9:35059516-35059516 - 388 COSM98359 c.1105A>G p.I369V Substitution - Missense 9:35061666-35061666 - RK076_C01 COSM3703549 c.2222G>A p.R741H Substitution - Missense 9:35057469-35057469 - TCGA-CJ-4637-01 COSM1137995 c.26G>T p.G9V Substitution - Missense 9:35068354-35068354 - T3094 COSM4740252 c.1847_1848insA p.N616fs*12 Insertion - Frameshift 9:35059649-35059650 - SNU-175 COSM2773877 c.1743G>A p.S581S Substitution - coding silent 9:35059754-35059754 - TCGA-AP-A056-01 COSM1108569 c.767G>A p.R256Q Substitution - Missense 9:35063022-35063022 - TCGA-BP-4160-01 COSM3774383 c.1058T>A p.I353N Substitution - Missense 9:35062026-35062026 - MSK-PCa3_organoid COSM5423679 c.2306G>C p.G769A Substitution - Missense 9:35057385-35057385 - YUWAND COSM1701063 c.1936C>T p.P646S Substitution - Missense 9:35059561-35059561 - PAPNNX COSM5005197 c.577-6_577-5insGG p.? Unknown 9:35064290-35064291 - TCGA-BP-4346-01 COSM3367699 c.2000C>T p.A667V Substitution - Missense 9:35059497-35059497 - TCGA-AX-A0J1-01 COSM1108555 c.2388C>T p.Y796Y Substitution - coding silent 9:35057150-35057150 - ccRCC-35 COSM1664944 c.552C>A p.C184* Substitution - Nonsense 9:35065275-35065275 - TCGA-EE-A29M-06 COSM3657097 c.421G>A p.E141K Substitution - Missense 9:35066699-35066699 - TCGA-12-0707 COSM2154554 c.440G>C p.R147P Substitution - Missense 9:35066680-35066680 - T3724 COSM291710 c.1847delA p.N616fs*63 Deletion - Frameshift 9:35059650-35059650 - Pat_16_B COSM5876181 c.2078G>A p.R693H Substitution - Missense 9:35059146-35059146 - TCGA-CM-4743-01 COSM455889 c.2259G>A p.R753R Substitution - coding silent 9:35057432-35057432 - CSCC-31-T COSM4479404 c.2320C>T p.P774S Substitution - Missense 9:35057218-35057218 - 2492720 COSM5721305 c.157C>T p.R53* Substitution - Nonsense 9:35068036-35068036 - 2492722 COSM5721305 c.157C>T p.R53* Substitution - Nonsense 9:35068036-35068036 - T2944 COSM4740251 c.2179C>A p.P727T Substitution - Missense 9:35057512-35057512 - 2492723 COSM5721305 c.157C>T p.R53* Substitution - Nonsense 9:35068036-35068036 - DLD1 COSM2773883 c.1198G>T p.A400S Substitution - Missense 9:35061176-35061176 - HCC135T COSM3664324 c.1557T>A p.P519P Substitution - coding silent 9:35060451-35060451 - T3064 COSM4740250 c.2297G>A p.R766Q Substitution - Missense 9:35057394-35057394 - PT52 COSM5939982 c.892C>T p.P298S Substitution - Missense 9:35062270-35062270 - CHC1704T COSM4803910 c.1440G>T p.G480G Substitution - coding silent 9:35060843-35060843 - SJHGG041_D COSM4969682 c.2395G>T p.D799Y Substitution - Missense 9:35057143-35057143 - STC291 COSM5063930 c.1321G>A p.V441I Substitution - Missense 9:35061053-35061053 - I2L-P19Ta-Tumor-Organoid COSM5359244 c.193C>T p.R65* Substitution - Nonsense 9:35068000-35068000 - ESO-717 COSM1242993 c.1755T>C p.A585A Substitution - coding silent 9:35059742-35059742 - ZZUFHECRKL-G071T COSM5439025 c.1109G>C p.G370A Substitution - Missense 9:35061662-35061662 - 388 COSM98359 c.1105A>G p.I369V Substitution - Missense 9:35061666-35061666 - HCC128 COSM1624938 c.1418A>T p.Q473L Substitution - Missense 9:35060865-35060865 - TCGA-D1-A103-01 COSM1108567 c.928G>A p.A310T Substitution - Missense 9:35062234-35062234 - TCGA-HU-A4G8-01 COSM3907074 c.1917T>C p.L639L Substitution - coding silent 9:35059580-35059580 - LUAD-NYU1219 COSM370297 c.811G>T p.G271C Substitution - Missense 9:35062978-35062978 - TCGA-D1-A103-01 COSM1108563 c.1437C>T p.I479I Substitution - coding silent 9:35060846-35060846 - RK298_C01 COSM3703550 c.596A>G p.N199S Substitution - Missense 9:35064266-35064266 - pfg043T COSM4752638 c.1366T>G p.L456V Substitution - Missense 9:35060917-35060917 - T2643 COSM4740252 c.1847_1848insA p.N616fs*12 Insertion - Frameshift 9:35059649-35059650 - TCGA-A8-A095-01 COSM455892 c.574G>C p.E192Q Substitution - Missense 9:35065253-35065253 - TCGA-EE-A182-06 COSM3657099 c.88G>A p.E30K Substitution - Missense 9:35068292-35068292 - ESO-1163 COSM1270181 c.1202A>G p.N401S Substitution - Missense 9:35061172-35061172 - I2L-P19Ta-Tumor-Biopsy COSM5359244 c.193C>T p.R65* Substitution - Nonsense 9:35068000-35068000 - 2492723 COSM5721304 c.2105C>T p.S702F Substitution - Missense 9:35059119-35059119 - CSCC-59-T COSM4452433 c.185A>C p.K62T Substitution - Missense 9:35068008-35068008 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.529782 9p13.3 601023 2482724|CGAP|BC110913|G/T|non-coding||2772|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.D75E c.225T>G 9 35067965 HC A C Missense p.V559G c.1676T>G 9 35060329 HNSC A T Missense p.I353N c.1058T>A 9 35062023 RCCC C A Missense p.G9V c.26G>T 9 35068351 RCCC C A Missense p.K425N c.1275G>T 9 35061096 ESCA C A Missense p.R25L c.74G>T 9 35068303 STAD C A Missense p.R744L c.2231G>T 9 35057457 LUAD C A Nonsense p.E440* c.1318G>T 9 35061053 LUSC C A Nonsense p.G263* c.787G>T 9 35062999 LUAD C G Missense p.E192Q c.574G>C 9 35065250 BRCA C G Missense p.E273Q c.817G>C 9 35062342 HNSC C G Missense p.R635T c.1904G>C 9 35059590 ESCA C G SpliceAcceptorSNV . c.1082-1G>C 9 35061687 RCCC C T Missense p.E141K c.421G>A 9 35066696 CM C T Missense p.E30K c.88G>A 9 35068289 CM C T Missense p.E712K c.2134G>A 9 35059087 HNSC C T Missense p.R599Q c.1796G>A 9 35059698 HNSC C T Missense p.V71I c.211G>A 9 35067979 UCEC C T Synonymous p.Q103Q c.309G>A 9 35066808 LUSC C T Synonymous p.R753R c.2259G>A 9 35057429 BRCA G A Missense p.A446V c.1337C>T 9 35061034 STAD G A Missense p.A596V c.1787C>T 9 35059707 UCEC G A Missense p.A667V c.2000C>T 9 35059494 RCCC G A Missense p.H340Y c.1018C>T 9 35062063 CM G A Missense p.P172L c.515C>T 9 35065309 THCA G A Missense p.P23L c.68C>T 9 35068309 CM G A Missense p.P774L c.2321C>T 9 35057214 CM G A Missense p.R155C c.463C>T 9 35065361 CM G A Synonymous p.A439A c.1317C>T 9 35061054 LUAD G A Synonymous p.F771F c.2313C>T 9 35057375 MM G A Synonymous p.I114I c.342C>T 9 35066775 CM G A Synonymous p.V600V c.1800C>T 9 35059694 BLCA G C Missense p.P631A c.1891C>G 9 35059603 LUAD GG AA Missense p.A439V c.1316_1317delinsTT 9 35061054 CM G T Missense p.P646Q c.1937C>A 9 35059557 LUAD T A Missense p.D373V c.1118A>T 9 35061650 HNSC T C Missense p.N716S c.2147A>G 9 35059074 HC T C Synonymous p.V133V c.399A>G 9 35066718 CM - T Frameshift p.N616Kfs*12 c.1847dupA 9 35059647 CM - T Frameshift p.N616Kfs*12 c.1847dupA 9 35059647 GBM