Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 9 132637739 132637739 + Silent SNP C C T TCGA-OR-A5L2-01A-11D-A30A-10 TCGA-OR-A5L2-10A-01D-A30A-10 g.chr9:132637739C>T c.2199C>T c.(2197-2199)acC>acT p.T733T BLCA 9 132614875 132614875 + Missense_Mutation SNP T T G TCGA-BT-A20Q-01A-11D-A14W-08 TCGA-BT-A20Q-11A-11D-A14W-08 g.chr9:132614875T>G c.41T>G c.(40-42)aTa>aGa p.I14R BLCA 9 132618639 132618639 + Splice_Site SNP G G A TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr9:132618639G>A c.135G>A c.(133-135)caG>caA p.Q45Q BLCA 9 132620365 132620365 + Missense_Mutation SNP G G A TCGA-CF-A3MI-01A-11D-A20D-08 TCGA-CF-A3MI-10A-01D-A20D-08 g.chr9:132620365G>A c.172G>A c.(172-174)Gct>Act p.A58T BLCA 9 132620767 132620767 + Missense_Mutation SNP G G A TCGA-K4-AAQO-01A-11D-A38G-08 TCGA-K4-AAQO-10A-01D-A38J-08 g.chr9:132620767G>A c.220G>A c.(220-222)Gtg>Atg p.V74M BLCA 9 132630421 132630421 + Silent SNP G G C TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr9:132630421G>C c.828G>C c.(826-828)cgG>cgC p.R276R BLCA 9 132630629 132630629 + Missense_Mutation SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr9:132630629G>A c.1036G>A c.(1036-1038)Gag>Aag p.E346K BLCA 9 132637006 132637006 + Missense_Mutation SNP C C T TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr9:132637006C>T c.1892C>T c.(1891-1893)tCg>tTg p.S631L BLCA 9 132637007 132637007 + Silent SNP G G A TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr9:132637007G>A c.1893G>A c.(1891-1893)tcG>tcA p.S631S BLCA 9 132641854 132641854 + Frame_Shift_Del DEL C C - TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr9:132641854delC c.2515delC c.(2515-2517)cccfs p.P840fs BLCA 9 132642525 132642525 + Silent SNP G G A TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr9:132642525G>A c.2718G>A c.(2716-2718)aaG>aaA p.K906K BRCA 9 132623252 132623253 + Frame_Shift_Del DEL CC CC - TCGA-AR-A0TY-01A-12W-A12T-09 TCGA-AR-A0TY-10A-01D-A110-09 g.chr9:132623252_132623253delCC c.367_368delCC c.(367-369)cctfs p.P123fs BRCA 9 132637217 132637217 + Silent SNP C C A TCGA-E9-A2JS-01A-11D-A17W-09 TCGA-E9-A2JS-10A-01D-A17W-09 g.chr9:132637217C>A c.2031C>A c.(2029-2031)ggC>ggA p.G677G BRCA 9 132637592 132637592 + Silent SNP G G A TCGA-BH-A18P-01A-11D-A12B-09 TCGA-BH-A18P-11A-43D-A12B-09 g.chr9:132637592G>A c.2052G>A c.(2050-2052)aaG>aaA p.K684K BRCA 9 132637681 132637681 + Missense_Mutation SNP G G A TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr9:132637681G>A c.2141G>A c.(2140-2142)cGc>cAc p.R714H CESC 9 132627642 132627642 + Missense_Mutation SNP C C G TCGA-EK-A2PM-01A-11D-A18J-09 TCGA-EK-A2PM-10A-01D-A18J-09 g.chr9:132627642C>G c.672C>G c.(670-672)ttC>ttG p.F224L CESC 9 132631176 132631176 + Missense_Mutation SNP C C T TCGA-EK-A2RJ-01A-11D-A18J-09 TCGA-EK-A2RJ-10A-01D-A18J-09 g.chr9:132631176C>T c.1171C>T c.(1171-1173)Cgc>Tgc p.R391C CESC 9 132637226 132637226 + Silent SNP C C G TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr9:132637226C>G c.2040C>G c.(2038-2040)ctC>ctG p.L680L CESC 9 132637870 132637870 + Missense_Mutation SNP C C A TCGA-DS-A7WF-01A-11D-A351-09 TCGA-DS-A7WF-10A-01D-A351-09 g.chr9:132637870C>A c.2250C>A c.(2248-2250)gaC>gaA p.D750E CESC 9 132640638 132640638 + Missense_Mutation SNP G G A TCGA-EK-A2PM-01A-11D-A18J-09 TCGA-EK-A2PM-10A-01D-A18J-09 g.chr9:132640638G>A c.2431G>A c.(2431-2433)Gag>Aag p.E811K CHOL 9 132642541 132642541 + Missense_Mutation SNP C C T TCGA-W5-AA2R-01A-11D-A417-09 TCGA-W5-AA2R-10A-01D-A41A-09 g.chr9:132642541C>T c.2734C>T c.(2734-2736)Cgg>Tgg p.R912W COAD 9 132620779 132620779 + Missense_Mutation SNP A A C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:132620779A>C c.232A>C c.(232-234)Acg>Ccg p.T78P COAD 9 132623282 132623282 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr9:132623282G>A c.397G>A c.(397-399)Gag>Aag p.E133K COAD 9 132630354 132630354 + Missense_Mutation SNP C C T TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr9:132630354C>T c.761C>T c.(760-762)aCg>aTg p.T254M COAD 9 132630366 132630366 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:132630366C>T c.773C>T c.(772-774)aCg>aTg p.T258M COAD 9 132630548 132630548 + Nonsense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr9:132630548C>T c.955C>T c.(955-957)Cga>Tga p.R319* COAD 9 132631176 132631176 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr9:132631176C>T c.1171C>T c.(1171-1173)Cgc>Tgc p.R391C COAD 9 132642413 132642413 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:132642413C>T c.2606C>T c.(2605-2607)tCg>tTg p.S869L COADREAD 9 132620356 132620356 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:132620356G>T c.163G>T c.(163-165)Gaa>Taa p.E55* COADREAD 9 132620779 132620779 + Missense_Mutation SNP A A C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:132620779A>C c.232A>C c.(232-234)Acg>Ccg p.T78P COADREAD 9 132623282 132623282 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr9:132623282G>A c.397G>A c.(397-399)Gag>Aag p.E133K COADREAD 9 132630302 132630302 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:132630302C>T c.709C>T c.(709-711)Cgc>Tgc p.R237C COADREAD 9 132630354 132630354 + Missense_Mutation SNP C C T TCGA-AA-3833-01A-01W-0900-09 TCGA-AA-3833-10A-01W-0900-09 g.chr9:132630354C>T c.761C>T c.(760-762)aCg>aTg p.T254M COADREAD 9 132630366 132630366 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:132630366C>T c.773C>T c.(772-774)aCg>aTg p.T258M COADREAD 9 132630548 132630548 + Nonsense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr9:132630548C>T c.955C>T c.(955-957)Cga>Tga p.R319* COADREAD 9 132631176 132631176 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr9:132631176C>T c.1171C>T c.(1171-1173)Cgc>Tgc p.R391C COADREAD 9 132642413 132642413 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:132642413C>T c.2606C>T c.(2605-2607)tCg>tTg p.S869L COADREAD 9 132642547 132642547 + Missense_Mutation SNP G G A TCGA-AG-3883-01A-02W-0899-10 TCGA-AG-3883-10A-01W-0901-10 g.chr9:132642547G>A c.2740G>A c.(2740-2742)Gtg>Atg p.V914M ESCA 9 132632775 132632775 + Missense_Mutation SNP G G T TCGA-2H-A9GK-01A-11D-A37C-09 TCGA-2H-A9GK-11A-11D-A37F-09 g.chr9:132632775G>T c.1609G>T c.(1609-1611)Gtc>Ttc p.V537F ESCA 9 132637912 132637912 + Silent SNP G G T TCGA-L5-A8NE-01A-11D-A37C-09 TCGA-L5-A8NE-11A-11D-A37F-09 g.chr9:132637912G>T c.2292G>T c.(2290-2292)ctG>ctT p.L764L GBM 9 132625554 132625555 + Frame_Shift_Del DEL TC TC - TCGA-14-0817-01A-01W-0424-08 TCGA-14-0817-10A-01W-0424-08 g.chr9:132625554_132625555delTC c.587_588delTC c.(586-588)gtcfs p.V196fs GBM 9 132638480 132638480 + Missense_Mutation SNP C C T TCGA-12-3649-01A-01D-1495-08 TCGA-12-3649-10A-01D-1495-08 g.chr9:132638480C>T c.2372C>T c.(2371-2373)gCc>gTc p.A791V GBMLGG 9 132620334 132620334 + Silent SNP C C T TCGA-S9-A7QW-01A-11D-A34A-08 TCGA-S9-A7QW-10A-01D-A34A-08 g.chr9:132620334C>T c.141C>T c.(139-141)gcC>gcT p.A47A GBMLGG 9 132620353 132620353 + Missense_Mutation SNP G G A TCGA-S9-A7R7-01A-11D-A34J-08 TCGA-S9-A7R7-10A-01D-A34M-08 g.chr9:132620353G>A c.160G>A c.(160-162)Gga>Aga p.G54R GBMLGG 9 132625554 132625555 + Frame_Shift_Del DEL TC TC - TCGA-14-0817-01A-01W-0424-08 TCGA-14-0817-10A-01W-0424-08 g.chr9:132625554_132625555delTC c.587_588delTC c.(586-588)gtcfs p.V196fs GBMLGG 9 132630508 132630508 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:132630508G>A c.915G>A c.(913-915)tcG>tcA p.S305S GBMLGG 9 132631191 132631191 + Missense_Mutation SNP G G A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr9:132631191G>A c.1186G>A c.(1186-1188)Gtc>Atc p.V396I GBMLGG 9 132631651 132631651 + Missense_Mutation SNP G G T TCGA-DU-7010-01A-11D-2024-08 TCGA-DU-7010-10A-01D-2024-08 g.chr9:132631651G>T c.1339G>T c.(1339-1341)Gac>Tac p.D447Y GBMLGG 9 132632081 132632081 + Missense_Mutation SNP C C G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:132632081C>G c.1523C>G c.(1522-1524)gCc>gGc p.A508G GBMLGG 9 132636916 132636916 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:132636916G>T c.1802G>T c.(1801-1803)aGc>aTc p.S601I GBMLGG 9 132638480 132638480 + Missense_Mutation SNP C C T TCGA-12-3649-01A-01D-1495-08 TCGA-12-3649-10A-01D-1495-08 g.chr9:132638480C>T c.2372C>T c.(2371-2373)gCc>gTc p.A791V GBMLGG 9 132642504 132642504 + Missense_Mutation SNP G G T TCGA-DU-A76K-01A-11D-A33T-08 TCGA-DU-A76K-10A-01D-A33W-08 g.chr9:132642504G>T c.2697G>T c.(2695-2697)gaG>gaT p.E899D HNSC 9 132630581 132630581 + Missense_Mutation SNP C C A TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr9:132630581C>A c.988C>A c.(988-990)Cgc>Agc p.R330S HNSC 9 132637139 132637139 + Silent SNP G G A TCGA-P3-A5Q5-01A-11D-A28R-08 TCGA-P3-A5Q5-10A-01D-A28U-08 g.chr9:132637139G>A c.1953G>A c.(1951-1953)gtG>gtA p.V651V HNSC 9 132637882 132637882 + Silent SNP C C T TCGA-CR-7401-01A-11D-2012-08 TCGA-CR-7401-10A-01D-2013-08 g.chr9:132637882C>T c.2262C>T c.(2260-2262)gtC>gtT p.V754V KIPAN 9 132618631 132618631 + Missense_Mutation SNP T T A TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr9:132618631T>A c.127T>A c.(127-129)Tgt>Agt p.C43S KIPAN 9 132623219 132623219 + Missense_Mutation SNP T T C TCGA-A4-7584-01A-11D-2136-08 TCGA-A4-7584-10A-01D-2136-08 g.chr9:132623219T>C c.334T>C c.(334-336)Tcc>Ccc p.S112P KIPAN 9 132625464 132625464 + Splice_Site SNP G G T TCGA-2Z-A9J6-01A-11D-A382-10 TCGA-2Z-A9J6-10A-01D-A385-10 g.chr9:132625464G>T c.e9-1 KIPAN 9 132630512 132630512 + Missense_Mutation SNP G G C TCGA-UZ-A9PR-01A-11D-A42J-10 TCGA-UZ-A9PR-10A-01D-A42M-10 g.chr9:132630512G>C c.919G>C c.(919-921)Gcc>Ccc p.A307P KIPAN 9 132636882 132636883 + Frame_Shift_Ins INS - - T TCGA-CJ-5684-01A-11D-1534-10 TCGA-CJ-5684-11A-01D-1535-10 g.chr9:132636882_132636883insT c.1768_1769insT c.(1768-1770)cggfs p.R590fs KIPAN 9 132636883 132636883 + Missense_Mutation SNP G G T TCGA-CJ-5684-01A-11D-1534-10 TCGA-CJ-5684-11A-01D-1535-10 g.chr9:132636883G>T c.1769G>T c.(1768-1770)cGg>cTg p.R590L KIPAN 9 132638511 132638511 + Silent SNP C C T TCGA-SX-A7SM-01A-11D-A34Z-10 TCGA-SX-A7SM-10A-01D-A34Z-10 g.chr9:132638511C>T c.2403C>T c.(2401-2403)ttC>ttT p.F801F KIRC 9 132636882 132636883 + Frame_Shift_Ins INS - - T TCGA-CJ-5684-01A-11D-1534-10 TCGA-CJ-5684-11A-01D-1535-10 g.chr9:132636882_132636883insT c.1768_1769insT c.(1768-1770)cggfs p.R590fs KIRC 9 132636883 132636883 + Missense_Mutation SNP G G T TCGA-CJ-5684-01A-11D-1534-10 TCGA-CJ-5684-11A-01D-1535-10 g.chr9:132636883G>T c.1769G>T c.(1768-1770)cGg>cTg p.R590L KIRP 9 132618631 132618631 + Missense_Mutation SNP T T A TCGA-EV-5903-01A-11D-1589-08 TCGA-EV-5903-10A-01D-1589-08 g.chr9:132618631T>A c.127T>A c.(127-129)Tgt>Agt p.C43S KIRP 9 132623219 132623219 + Missense_Mutation SNP T T C TCGA-A4-7584-01A-11D-2136-08 TCGA-A4-7584-10A-01D-2136-08 g.chr9:132623219T>C c.334T>C c.(334-336)Tcc>Ccc p.S112P KIRP 9 132625464 132625464 + Splice_Site SNP G G T TCGA-2Z-A9J6-01A-11D-A382-10 TCGA-2Z-A9J6-10A-01D-A385-10 g.chr9:132625464G>T c.e9-1 KIRP 9 132630512 132630512 + Missense_Mutation SNP G G C TCGA-UZ-A9PR-01A-11D-A42J-10 TCGA-UZ-A9PR-10A-01D-A42M-10 g.chr9:132630512G>C c.919G>C c.(919-921)Gcc>Ccc p.A307P KIRP 9 132638511 132638511 + Silent SNP C C T TCGA-SX-A7SM-01A-11D-A34Z-10 TCGA-SX-A7SM-10A-01D-A34Z-10 g.chr9:132638511C>T c.2403C>T c.(2401-2403)ttC>ttT p.F801F LGG 9 132620334 132620334 + Silent SNP C C T TCGA-S9-A7QW-01A-11D-A34A-08 TCGA-S9-A7QW-10A-01D-A34A-08 g.chr9:132620334C>T c.141C>T c.(139-141)gcC>gcT p.A47A LGG 9 132620353 132620353 + Missense_Mutation SNP G G A TCGA-S9-A7R7-01A-11D-A34J-08 TCGA-S9-A7R7-10A-01D-A34M-08 g.chr9:132620353G>A c.160G>A c.(160-162)Gga>Aga p.G54R LGG 9 132630508 132630508 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:132630508G>A c.915G>A c.(913-915)tcG>tcA p.S305S LGG 9 132631191 132631191 + Missense_Mutation SNP G G A TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr9:132631191G>A c.1186G>A c.(1186-1188)Gtc>Atc p.V396I LGG 9 132631651 132631651 + Missense_Mutation SNP G G T TCGA-DU-7010-01A-11D-2024-08 TCGA-DU-7010-10A-01D-2024-08 g.chr9:132631651G>T c.1339G>T c.(1339-1341)Gac>Tac p.D447Y LGG 9 132632081 132632081 + Missense_Mutation SNP C C G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:132632081C>G c.1523C>G c.(1522-1524)gCc>gGc p.A508G LGG 9 132636916 132636916 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:132636916G>T c.1802G>T c.(1801-1803)aGc>aTc p.S601I LGG 9 132642504 132642504 + Missense_Mutation SNP G G T TCGA-DU-A76K-01A-11D-A33T-08 TCGA-DU-A76K-10A-01D-A33W-08 g.chr9:132642504G>T c.2697G>T c.(2695-2697)gaG>gaT p.E899D LIHC 9 132614914 132614914 + Splice_Site SNP A A G TCGA-G3-AAV4-01A-11D-A382-10 TCGA-G3-AAV4-10A-01D-A385-10 g.chr9:132614914A>G c.80A>G c.(79-81)aAg>aGg p.K27R LIHC 9 132630495 132630495 + Missense_Mutation SNP G G T TCGA-DD-AADB-01A-11D-A40R-10 TCGA-DD-AADB-10A-01D-A40U-10 g.chr9:132630495G>T c.902G>T c.(901-903)gGc>gTc p.G301V LIHC 9 132632035 132632035 + Missense_Mutation SNP T T C TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chr9:132632035T>C c.1477T>C c.(1477-1479)Tac>Cac p.Y493H LIHC 9 132632793 132632793 + Missense_Mutation SNP C C T TCGA-KR-A7K0-01A-12D-A33Q-10 TCGA-KR-A7K0-10A-01D-A33Q-10 g.chr9:132632793C>T c.1627C>T c.(1627-1629)Ctt>Ttt p.L543F LIHC 9 132636872 132636872 + Silent SNP A A T TCGA-G3-A7M5-01A-11D-A33Q-10 TCGA-G3-A7M5-10A-01D-A33Q-10 g.chr9:132636872A>T c.1758A>T c.(1756-1758)ctA>ctT p.L586L LIHC 9 132637022 132637022 + Silent SNP C C T TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr9:132637022C>T c.1908C>T c.(1906-1908)caC>caT p.H636H LIHC 9 132638408 132638408 + Splice_Site SNP G G T TCGA-DD-AADQ-01A-11D-A40R-10 TCGA-DD-AADQ-10A-01D-A40U-10 g.chr9:132638408G>T c.e22-1 LIHC 9 132642472 132642472 + Missense_Mutation SNP C C A TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr9:132642472C>A c.2665C>A c.(2665-2667)Cgc>Agc p.R889S LUAD 9 132620750 132620750 + Missense_Mutation SNP A A G TCGA-53-A4EZ-01A-12D-A24P-08 TCGA-53-A4EZ-10A-01D-A24P-08 g.chr9:132620750A>G c.203A>G c.(202-204)aAa>aGa p.K68R LUAD 9 132620769 132620769 + Silent SNP G G T TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr9:132620769G>T c.222G>T c.(220-222)gtG>gtT p.V74V LUAD 9 132620784 132620784 + Silent SNP C C T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr9:132620784C>T c.237C>T c.(235-237)ttC>ttT p.F79F LUAD 9 132623839 132623839 + Missense_Mutation SNP A A T TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr9:132623839A>T c.445A>T c.(445-447)Aac>Tac p.N149Y LUAD 9 132630289 132630289 + Silent SNP C C T TCGA-62-8399-01A-21D-2323-08 TCGA-62-8399-10A-01D-2323-08 g.chr9:132630289C>T c.696C>T c.(694-696)acC>acT p.T232T LUAD 9 132630324 132630324 + Missense_Mutation SNP A A G TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr9:132630324A>G c.731A>G c.(730-732)cAc>cGc p.H244R LUAD 9 132630558 132630558 + Missense_Mutation SNP C C T TCGA-86-8054-01A-11D-2238-08 TCGA-86-8054-10A-01D-2238-08 g.chr9:132630558C>T c.965C>T c.(964-966)tCt>tTt p.S322F LUAD 9 132630679 132630679 + Silent SNP G G T TCGA-49-6743-01A-11D-1855-08 TCGA-49-6743-11A-01D-1855-08 g.chr9:132630679G>T c.1086G>T c.(1084-1086)gcG>gcT p.A362A LUAD 9 132632069 132632069 + Missense_Mutation SNP G G A TCGA-MP-A4T2-01A-11D-A24P-08 TCGA-MP-A4T2-10A-01D-A24P-08 g.chr9:132632069G>A c.1511G>A c.(1510-1512)gGg>gAg p.G504E LUAD 9 132632799 132632799 + Missense_Mutation SNP G G T TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr9:132632799G>T c.1633G>T c.(1633-1635)Gcc>Tcc p.A545S LUAD 9 132637028 132637028 + Silent SNP G G A TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chr9:132637028G>A c.1914G>A c.(1912-1914)acG>acA p.T638T LUAD 9 132637174 132637175 + Frame_Shift_Ins INS - - G TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr9:132637174_132637175insG c.1988_1989insG c.(1987-1992)tacgtcfs p.YV663fs LUAD 9 132637221 132637221 + Missense_Mutation SNP G G C TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr9:132637221G>C c.2035G>C c.(2035-2037)Gta>Cta p.V679L LUAD 9 132637634 132637634 + Silent SNP C C T TCGA-05-4425-01A-01D-1753-08 TCGA-05-4425-10A-01D-1753-08 g.chr9:132637634C>T c.2094C>T c.(2092-2094)tcC>tcT p.S698S LUAD 9 132637849 132637849 + Silent SNP C C T TCGA-17-Z055-01A-01W-0747-08 TCGA-17-Z055-11A-01W-0747-08 g.chr9:132637849C>T c.2229C>T c.(2227-2229)ccC>ccT p.P743P LUAD 9 132637912 132637912 + Silent SNP G G T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr9:132637912G>T c.2292G>T c.(2290-2292)ctG>ctT p.L764L LUSC 9 132623876 132623876 + Missense_Mutation SNP A A C TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr9:132623876A>C c.482A>C c.(481-483)cAg>cCg p.Q161P LUSC 9 132642449 132642449 + Missense_Mutation SNP G G C TCGA-70-6722-01A-11D-1817-08 TCGA-70-6722-10A-01D-1817-08 g.chr9:132642449G>C c.2642G>C c.(2641-2643)gGa>gCa p.G881A OV 9 132632056 132632056 + Missense_Mutation SNP C C T TCGA-25-2401-01A-01W-0799-08 TCGA-25-2401-10A-01W-0799-08 g.chr9:132632056C>T c.1498C>T c.(1498-1500)Cca>Tca p.P500S OV 9 132632062 132632062 + Missense_Mutation SNP G G A TCGA-29-1776-01A-01W-0639-09 TCGA-29-1776-10A-01W-0639-09 g.chr9:132632062G>A c.1504G>A c.(1504-1506)Gcc>Acc p.A502T PAAD 9 132623286 132623286 + Nonsense_Mutation SNP C C A TCGA-HZ-A8P0-01A-11D-A36O-08 TCGA-HZ-A8P0-10A-01D-A367-08 g.chr9:132623286C>A c.401C>A c.(400-402)tCa>tAa p.S134* PAAD 9 132631614 132631614 + Silent SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:132631614G>T c.1302G>T c.(1300-1302)cgG>cgT p.R434R PAAD 9 132642473 132642473 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:132642473G>A c.2666G>A c.(2665-2667)cGc>cAc p.R889H PRAD 9 132630711 132630711 + Missense_Mutation SNP G G T TCGA-WW-A8ZI-01A-11D-A377-08 TCGA-WW-A8ZI-10A-01D-A37A-08 g.chr9:132630711G>T c.1118G>T c.(1117-1119)aGc>aTc p.S373I PRAD 9 132641857 132641857 + Missense_Mutation SNP C C T TCGA-EJ-5502-01A-01D-1576-08 TCGA-EJ-5502-10A-01D-1577-08 g.chr9:132641857C>T c.2518C>T c.(2518-2520)Ccc>Tcc p.P840S READ 9 132620356 132620356 + Nonsense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:132620356G>T c.163G>T c.(163-165)Gaa>Taa p.E55* READ 9 132630302 132630302 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:132630302C>T c.709C>T c.(709-711)Cgc>Tgc p.R237C READ 9 132642547 132642547 + Missense_Mutation SNP G G A TCGA-AG-3883-01A-02W-0899-10 TCGA-AG-3883-10A-01W-0901-10 g.chr9:132642547G>A c.2740G>A c.(2740-2742)Gtg>Atg p.V914M SARC 9 132637674 132637674 + Missense_Mutation SNP G G A TCGA-DX-AB2H-01A-11D-A38Z-09 TCGA-DX-AB2H-10A-01D-A38Z-09 g.chr9:132637674G>A c.2134G>A c.(2134-2136)Gtg>Atg p.V712M SKCM 9 132618591 132618591 + Silent SNP C C T TCGA-EE-A3J8-06A-11D-A20D-08 TCGA-EE-A3J8-10A-01D-A20D-08 g.chr9:132618591C>T c.87C>T c.(85-87)acC>acT p.T29T SKCM 9 132623221 132623221 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:132623221C>T c.336C>T c.(334-336)tcC>tcT p.S112S SKCM 9 132627616 132627616 + Missense_Mutation SNP G G A TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr9:132627616G>A c.646G>A c.(646-648)Ggg>Agg p.G216R SKCM 9 132630713 132630713 + Missense_Mutation SNP C C T TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr9:132630713C>T c.1120C>T c.(1120-1122)Ccc>Tcc p.P374S SKCM 9 132630714 132630714 + Missense_Mutation SNP C C T TCGA-EE-A3JE-06A-11D-A20D-08 TCGA-EE-A3JE-10A-01D-A20D-08 g.chr9:132630714C>T c.1121C>T c.(1120-1122)cCc>cTc p.P374L SKCM 9 132632009 132632009 + Missense_Mutation SNP A A G TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr9:132632009A>G c.1451A>G c.(1450-1452)gAc>gGc p.D484G SKCM 9 132632120 132632120 + Missense_Mutation SNP G G T TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr9:132632120G>T c.1562G>T c.(1561-1563)cGa>cTa p.R521L SKCM 9 132637876 132637876 + Silent SNP G G A TCGA-FS-A4FC-06A-11D-A24R-08 TCGA-FS-A4FC-10A-01D-A24R-08 g.chr9:132637876G>A c.2256G>A c.(2254-2256)ctG>ctA p.L752L SKCM 9 132641892 132641892 + Silent SNP C C T TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr9:132641892C>T c.2553C>T c.(2551-2553)gtC>gtT p.V851V SKCM 9 132641904 132641904 + Silent SNP C C T TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr9:132641904C>T c.2565C>T c.(2563-2565)ggC>ggT p.G855G SKCM 9 132641905 132641905 + Missense_Mutation SNP C C T TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr9:132641905C>T c.2566C>T c.(2566-2568)Cat>Tat p.H856Y

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 9 132630419 132630419 single base substitution C T missense_variant R276W 826C>T AML-US 9 132630419 132630419 single base substitution C T upstream_gene_variant BLCA-CN 9 132594181 132594181 single base substitution G A upstream_gene_variant BLCA-US 9 132614875 132614875 single base substitution T G exon_variant BLCA-US 9 132614875 132614875 single base substitution T G missense_variant I14R 41T>G BLCA-US 9 132620365 132620365 single base substitution G A exon_variant BLCA-US 9 132620365 132620365 single base substitution G A missense_variant A58T 172G>A BLCA-US 9 132630421 132630421 single base substitution G C synonymous_variant R276R 828G>C BLCA-US 9 132630421 132630421 single base substitution G C upstream_gene_variant BLCA-US 9 132630629 132630629 single base substitution G A exon_variant BLCA-US 9 132630629 132630629 single base substitution G A missense_variant E346K 1036G>A BLCA-US 9 132630629 132630629 single base substitution G A upstream_gene_variant BLCA-US 9 132637006 132637006 single base substitution C T downstream_gene_variant BLCA-US 9 132637006 132637006 single base substitution C T exon_variant BLCA-US 9 132637006 132637006 single base substitution C T missense_variant S631L 1892C>T BLCA-US 9 132637006 132637006 single base substitution C T upstream_gene_variant BOCA-UK 9 132597457 132597457 single base substitution G C intron_variant BOCA-UK 9 132597457 132597457 single base substitution G C upstream_gene_variant BRCA-EU 9 132595299 132595299 insertion of <=200bp - TATGTGTATATACATG upstream_gene_variant BRCA-EU 9 132597993 132597994 deletion of <=200bp CT - intron_variant BRCA-EU 9 132602670 132602670 single base substitution G A intron_variant BRCA-EU 9 132604700 132604700 single base substitution G A intron_variant BRCA-EU 9 132605318 132605318 single base substitution A T intron_variant BRCA-EU 9 132607465 132607465 single base substitution C G intron_variant BRCA-EU 9 132607899 132607903 deletion of <=200bp AGCTT - intron_variant BRCA-EU 9 132608031 132608031 single base substitution G C intron_variant BRCA-EU 9 132608165 132608165 single base substitution T G intron_variant BRCA-EU 9 132610762 132610762 single base substitution A C intron_variant BRCA-EU 9 132612364 132612364 single base substitution T C intron_variant BRCA-EU 9 132612672 132612672 single base substitution C T intron_variant BRCA-EU 9 132613111 132613111 single base substitution T G intron_variant BRCA-EU 9 132613894 132613894 single base substitution C T intron_variant BRCA-EU 9 132613907 132613907 single base substitution C T intron_variant BRCA-EU 9 132613930 132613930 single base substitution C T intron_variant BRCA-EU 9 132614241 132614241 single base substitution T C intron_variant BRCA-EU 9 132618613 132618613 single base substitution G A downstream_gene_variant BRCA-EU 9 132618613 132618613 single base substitution G A exon_variant BRCA-EU 9 132618613 132618613 single base substitution G A missense_variant G37R 109G>A BRCA-EU 9 132618958 132618958 single base substitution G C downstream_gene_variant BRCA-EU 9 132618958 132618958 single base substitution G C intron_variant BRCA-EU 9 132624513 132624513 single base substitution G A downstream_gene_variant BRCA-EU 9 132624513 132624513 single base substitution G A intron_variant BRCA-EU 9 132625846 132625846 single base substitution C G intron_variant BRCA-EU 9 132625846 132625846 single base substitution C G upstream_gene_variant BRCA-EU 9 132626168 132626168 single base substitution C T intron_variant BRCA-EU 9 132626168 132626168 single base substitution C T upstream_gene_variant BRCA-EU 9 132626845 132626845 single base substitution G C intron_variant BRCA-EU 9 132626845 132626845 single base substitution G C upstream_gene_variant BRCA-EU 9 132626972 132626972 single base substitution G C intron_variant BRCA-EU 9 132626972 132626972 single base substitution G C upstream_gene_variant BRCA-EU 9 132627383 132627383 single base substitution G A intron_variant BRCA-EU 9 132627383 132627383 single base substitution G A upstream_gene_variant BRCA-EU 9 132628567 132628567 single base substitution G A intron_variant BRCA-EU 9 132628567 132628567 single base substitution G A upstream_gene_variant BRCA-EU 9 132630069 132630069 single base substitution T C intron_variant BRCA-EU 9 132630069 132630069 single base substitution T C upstream_gene_variant BRCA-EU 9 132630496 132630496 single base substitution C T synonymous_variant G301G 903C>T BRCA-EU 9 132630496 132630496 single base substitution C T upstream_gene_variant BRCA-EU 9 132631127 132631127 single base substitution C T intron_variant BRCA-EU 9 132631564 132631564 single base substitution G A intron_variant BRCA-EU 9 132632351 132632351 single base substitution G A exon_variant BRCA-EU 9 132632351 132632351 single base substitution G A intron_variant BRCA-EU 9 132634064 132634064 single base substitution C T downstream_gene_variant BRCA-EU 9 132634064 132634064 single base substitution C T intron_variant BRCA-EU 9 132634064 132634064 single base substitution C T upstream_gene_variant BRCA-EU 9 132637282 132637282 single base substitution C A downstream_gene_variant BRCA-EU 9 132637282 132637282 single base substitution C A intron_variant BRCA-EU 9 132637282 132637282 single base substitution C A upstream_gene_variant BRCA-EU 9 132638425 132638425 single base substitution G A exon_variant BRCA-EU 9 132638425 132638425 single base substitution G A missense_variant A773T 2317G>A BRCA-EU 9 132638425 132638425 single base substitution G A upstream_gene_variant BRCA-EU 9 132638867 132638867 single base substitution G C intron_variant BRCA-EU 9 132638867 132638867 single base substitution G C upstream_gene_variant BRCA-EU 9 132640947 132640967 deletion of <=200bp CTCCACTCCCTGCCATGCCCA - downstream_gene_variant BRCA-EU 9 132640947 132640967 deletion of <=200bp CTCCACTCCCTGCCATGCCCA - intron_variant BRCA-EU 9 132640947 132640967 deletion of <=200bp CTCCACTCCCTGCCATGCCCA - upstream_gene_variant BRCA-EU 9 132640967 132640967 single base substitution A T downstream_gene_variant BRCA-EU 9 132640967 132640967 single base substitution A T intron_variant BRCA-EU 9 132640967 132640967 single base substitution A T upstream_gene_variant BRCA-EU 9 132641626 132641626 single base substitution C T downstream_gene_variant BRCA-EU 9 132641626 132641626 single base substitution C T intron_variant BRCA-EU 9 132641626 132641626 single base substitution C T upstream_gene_variant BRCA-EU 9 132642848 132642848 single base substitution T C 3_prime_UTR_variant BRCA-EU 9 132642848 132642848 single base substitution T C downstream_gene_variant BRCA-EU 9 132642848 132642848 single base substitution T C exon_variant BRCA-EU 9 132643383 132643383 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 132643383 132643383 single base substitution G A downstream_gene_variant BRCA-EU 9 132643383 132643383 single base substitution G A exon_variant BRCA-EU 9 132644472 132644472 single base substitution C T downstream_gene_variant BRCA-EU 9 132648503 132648503 single base substitution C T downstream_gene_variant BRCA-EU 9 132648779 132648779 single base substitution C G downstream_gene_variant BRCA-FR 9 132597457 132597457 single base substitution G A intron_variant BRCA-FR 9 132597457 132597457 single base substitution G A upstream_gene_variant BRCA-FR 9 132608576 132608576 single base substitution C G intron_variant BRCA-FR 9 132612949 132612949 single base substitution T G intron_variant BRCA-FR 9 132613894 132613894 single base substitution C T intron_variant BRCA-FR 9 132626972 132626972 single base substitution G C intron_variant BRCA-FR 9 132626972 132626972 single base substitution G C upstream_gene_variant BRCA-FR 9 132628567 132628567 single base substitution G A intron_variant BRCA-FR 9 132628567 132628567 single base substitution G A upstream_gene_variant BRCA-FR 9 132630496 132630496 single base substitution C T synonymous_variant G301G 903C>T BRCA-FR 9 132630496 132630496 single base substitution C T upstream_gene_variant BRCA-FR 9 132646794 132646794 single base substitution G T downstream_gene_variant BRCA-FR 9 132648503 132648503 single base substitution C T downstream_gene_variant BRCA-KR 9 132637106 132637106 single base substitution A T downstream_gene_variant BRCA-KR 9 132637106 132637106 single base substitution A T splice_acceptor_variant BRCA-KR 9 132637106 132637106 single base substitution A T upstream_gene_variant BRCA-UK 9 132599786 132599786 single base substitution G A intron_variant BRCA-UK 9 132607465 132607465 single base substitution C G intron_variant BRCA-US 9 132595746 132595746 single base substitution C T upstream_gene_variant BRCA-US 9 132623252 132623253 deletion of <=200bp CC - downstream_gene_variant BRCA-US 9 132623252 132623253 deletion of <=200bp CC - frameshift_variant P123 BRCA-US 9 132637217 132637217 single base substitution C A downstream_gene_variant BRCA-US 9 132637217 132637217 single base substitution C A exon_variant BRCA-US 9 132637217 132637217 single base substitution C A synonymous_variant G677G 2031C>A BRCA-US 9 132637217 132637217 single base substitution C A upstream_gene_variant BRCA-US 9 132637592 132637592 single base substitution G A exon_variant BRCA-US 9 132637592 132637592 single base substitution G A synonymous_variant K684K 2052G>A BRCA-US 9 132637592 132637592 single base substitution G A upstream_gene_variant BRCA-US 9 132637681 132637681 single base substitution G A exon_variant BRCA-US 9 132637681 132637681 single base substitution G A missense_variant R714H 2141G>A BRCA-US 9 132637681 132637681 single base substitution G A upstream_gene_variant BTCA-JP 9 132593034 132593034 single base substitution C T upstream_gene_variant BTCA-JP 9 132623253 132623253 single base substitution C T downstream_gene_variant BTCA-JP 9 132623253 132623253 single base substitution C T missense_variant P123L 368C>T BTCA-JP 9 132631953 132631953 single base substitution A G intron_variant BTCA-JP 9 132631953 132631953 single base substitution A G splice_region_variant BTCA-JP 9 132637683 132637683 single base substitution G A exon_variant BTCA-JP 9 132637683 132637683 single base substitution G A missense_variant E715K 2143G>A BTCA-JP 9 132637683 132637683 single base substitution G A upstream_gene_variant BTCA-JP 9 132638297 132638297 single base substitution G A intron_variant BTCA-JP 9 132638297 132638297 single base substitution G A upstream_gene_variant BTCA-JP 9 132638394 132638394 single base substitution C A intron_variant BTCA-JP 9 132638394 132638394 single base substitution C A upstream_gene_variant BTCA-JP 9 132638479 132638479 single base substitution G A exon_variant BTCA-JP 9 132638479 132638479 single base substitution G A missense_variant A791T 2371G>A BTCA-JP 9 132638479 132638479 single base substitution G A upstream_gene_variant BTCA-JP 9 132641755 132641755 single base substitution C G downstream_gene_variant BTCA-JP 9 132641755 132641755 single base substitution C G exon_variant BTCA-JP 9 132641755 132641755 single base substitution C G intron_variant CESC-US 9 132596001 132596001 deletion of <=200bp A - upstream_gene_variant CESC-US 9 132597032 132597032 single base substitution C T exon_variant CESC-US 9 132597032 132597032 single base substitution C T upstream_gene_variant CESC-US 9 132627642 132627642 single base substitution C G missense_variant F224L 672C>G CESC-US 9 132627642 132627642 single base substitution C G upstream_gene_variant CESC-US 9 132631176 132631176 single base substitution C T exon_variant CESC-US 9 132631176 132631176 single base substitution C T intron_variant CESC-US 9 132631176 132631176 single base substitution C T missense_variant R391C 1171C>T CESC-US 9 132637226 132637226 single base substitution C G downstream_gene_variant CESC-US 9 132637226 132637226 single base substitution C G exon_variant CESC-US 9 132637226 132637226 single base substitution C G synonymous_variant L680L 2040C>G CESC-US 9 132637226 132637226 single base substitution C G upstream_gene_variant CESC-US 9 132637870 132637870 single base substitution C A exon_variant CESC-US 9 132637870 132637870 single base substitution C A missense_variant D750E 2250C>A CESC-US 9 132637870 132637870 single base substitution C A upstream_gene_variant CESC-US 9 132640638 132640638 single base substitution G A exon_variant CESC-US 9 132640638 132640638 single base substitution G A missense_variant E811K 2431G>A CESC-US 9 132640638 132640638 single base substitution G A upstream_gene_variant CESC-US 9 132641781 132641781 single base substitution G A downstream_gene_variant CESC-US 9 132641781 132641781 single base substitution G A exon_variant CESC-US 9 132641781 132641781 single base substitution G A intron_variant CLLE-ES 9 132598786 132598786 single base substitution A G intron_variant CLLE-ES 9 132624560 132624560 single base substitution C T downstream_gene_variant CLLE-ES 9 132624560 132624560 single base substitution C T intron_variant CLLE-ES 9 132630361 132630361 single base substitution G A synonymous_variant A256A 768G>A CLLE-ES 9 132630361 132630361 single base substitution G A upstream_gene_variant CLLE-ES 9 132640689 132640689 single base substitution T C exon_variant CLLE-ES 9 132640689 132640689 single base substitution T C missense_variant W828R 2482T>C CLLE-ES 9 132640689 132640689 single base substitution T C upstream_gene_variant CLLE-ES 9 132644161 132644161 single base substitution G C downstream_gene_variant COAD-US 9 132593277 132593277 single base substitution G T upstream_gene_variant COAD-US 9 132620779 132620779 single base substitution A C exon_variant COAD-US 9 132620779 132620779 single base substitution A C missense_variant T78P 232A>C COAD-US 9 132623282 132623282 single base substitution G A downstream_gene_variant COAD-US 9 132623282 132623282 single base substitution G A missense_variant E133K 397G>A COAD-US 9 132630366 132630366 single base substitution C T missense_variant T258M 773C>T COAD-US 9 132630366 132630366 single base substitution C T upstream_gene_variant COAD-US 9 132630548 132630548 single base substitution C T stop_gained R319* 955C>T COAD-US 9 132630548 132630548 single base substitution C T upstream_gene_variant COAD-US 9 132637691 132637691 single base substitution C T exon_variant COAD-US 9 132637691 132637691 single base substitution C T synonymous_variant L717L 2151C>T COAD-US 9 132637691 132637691 single base substitution C T upstream_gene_variant COAD-US 9 132642413 132642413 single base substitution C T downstream_gene_variant COAD-US 9 132642413 132642413 single base substitution C T exon_variant COAD-US 9 132642413 132642413 single base substitution C T missense_variant S869L 2606C>T COCA-CN 9 132602208 132602208 single base substitution A T intron_variant COCA-CN 9 132614629 132614629 single base substitution A G intron_variant COCA-CN 9 132620786 132620786 single base substitution G A exon_variant COCA-CN 9 132620786 132620786 single base substitution G A missense_variant R80Q 239G>A COCA-CN 9 132625541 132625541 single base substitution T C downstream_gene_variant COCA-CN 9 132625541 132625541 single base substitution T C missense_variant Y192H 574T>C COCA-CN 9 132630581 132630581 single base substitution C T missense_variant R330C 988C>T COCA-CN 9 132630581 132630581 single base substitution C T upstream_gene_variant COCA-CN 9 132630668 132630668 single base substitution G C exon_variant COCA-CN 9 132630668 132630668 single base substitution G C missense_variant D359H 1075G>C COCA-CN 9 132630670 132630670 single base substitution C G exon_variant COCA-CN 9 132630670 132630670 single base substitution C G missense_variant D359E 1077C>G COCA-CN 9 132632815 132632815 single base substitution A C downstream_gene_variant COCA-CN 9 132632815 132632815 single base substitution A C intron_variant COCA-CN 9 132632815 132632815 single base substitution A C missense_variant D550A 1649A>C COCA-CN 9 132635784 132635784 single base substitution C T downstream_gene_variant COCA-CN 9 132635784 132635784 single base substitution C T intron_variant COCA-CN 9 132635784 132635784 single base substitution C T missense_variant R562W 1684C>T COCA-CN 9 132635784 132635784 single base substitution C T upstream_gene_variant COCA-CN 9 132636888 132636888 single base substitution G A downstream_gene_variant COCA-CN 9 132636888 132636888 single base substitution G A intron_variant COCA-CN 9 132636888 132636888 single base substitution G A missense_variant E592K 1774G>A COCA-CN 9 132636888 132636888 single base substitution G A upstream_gene_variant COCA-CN 9 132636935 132636935 single base substitution C T downstream_gene_variant COCA-CN 9 132636935 132636935 single base substitution C T splice_region_variant COCA-CN 9 132636935 132636935 single base substitution C T synonymous_variant L607L 1821C>T COCA-CN 9 132636935 132636935 single base substitution C T upstream_gene_variant COCA-CN 9 132637710 132637710 single base substitution G A exon_variant COCA-CN 9 132637710 132637710 single base substitution G A missense_variant A724T 2170G>A COCA-CN 9 132637710 132637710 single base substitution G A upstream_gene_variant COCA-CN 9 132638332 132638332 single base substitution A G intron_variant COCA-CN 9 132638332 132638332 single base substitution A G upstream_gene_variant COCA-CN 9 132638412 132638412 single base substitution C T exon_variant COCA-CN 9 132638412 132638412 single base substitution C T synonymous_variant F768F 2304C>T COCA-CN 9 132638412 132638412 single base substitution C T upstream_gene_variant COCA-CN 9 132638544 132638544 single base substitution C T intron_variant COCA-CN 9 132638544 132638544 single base substitution C T upstream_gene_variant COCA-CN 9 132642472 132642472 single base substitution C T downstream_gene_variant COCA-CN 9 132642472 132642472 single base substitution C T exon_variant COCA-CN 9 132642472 132642472 single base substitution C T missense_variant R889C 2665C>T EOPC-DE 9 132611881 132611881 single base substitution A G intron_variant ESAD-UK 9 132592448 132592448 single base substitution G A upstream_gene_variant ESAD-UK 9 132592837 132592837 single base substitution G C upstream_gene_variant ESAD-UK 9 132595251 132595251 single base substitution T G upstream_gene_variant ESAD-UK 9 132595573 132595573 single base substitution C T upstream_gene_variant ESAD-UK 9 132597686 132597686 single base substitution T C intron_variant ESAD-UK 9 132597686 132597686 single base substitution T C upstream_gene_variant ESAD-UK 9 132601751 132601751 single base substitution C T intron_variant ESAD-UK 9 132602902 132602902 single base substitution A G intron_variant ESAD-UK 9 132605215 132605215 single base substitution C T intron_variant ESAD-UK 9 132607661 132607661 single base substitution T C intron_variant ESAD-UK 9 132607963 132607963 single base substitution G A intron_variant ESAD-UK 9 132608188 132608188 deletion of <=200bp T - intron_variant ESAD-UK 9 132609668 132609668 single base substitution G A intron_variant ESAD-UK 9 132609700 132609700 single base substitution A G intron_variant ESAD-UK 9 132609831 132609831 single base substitution C T intron_variant ESAD-UK 9 132612904 132612904 single base substitution G T intron_variant ESAD-UK 9 132614214 132614214 single base substitution G A intron_variant ESAD-UK 9 132616958 132616958 single base substitution A T downstream_gene_variant ESAD-UK 9 132616958 132616958 single base substitution A T intron_variant ESAD-UK 9 132619346 132619346 single base substitution A C downstream_gene_variant ESAD-UK 9 132619346 132619346 single base substitution A C intron_variant ESAD-UK 9 132621055 132621055 single base substitution C G downstream_gene_variant ESAD-UK 9 132621055 132621055 single base substitution C G intron_variant ESAD-UK 9 132623560 132623560 single base substitution C T downstream_gene_variant ESAD-UK 9 132623560 132623560 single base substitution C T intron_variant ESAD-UK 9 132623663 132623663 single base substitution G A downstream_gene_variant ESAD-UK 9 132623663 132623663 single base substitution G A intron_variant ESAD-UK 9 132623992 132623992 single base substitution T C downstream_gene_variant ESAD-UK 9 132623992 132623992 single base substitution T C intron_variant ESAD-UK 9 132624383 132624385 deletion of <=200bp CTC - downstream_gene_variant ESAD-UK 9 132624383 132624385 deletion of <=200bp CTC - intron_variant ESAD-UK 9 132625160 132625160 single base substitution G T downstream_gene_variant ESAD-UK 9 132625160 132625160 single base substitution G T intron_variant ESAD-UK 9 132626505 132626505 single base substitution T G intron_variant ESAD-UK 9 132626505 132626505 single base substitution T G upstream_gene_variant ESAD-UK 9 132627677 132627677 single base substitution G T intron_variant ESAD-UK 9 132627677 132627677 single base substitution G T upstream_gene_variant ESAD-UK 9 132630342 132630342 single base substitution C T missense_variant P250L 749C>T ESAD-UK 9 132630342 132630342 single base substitution C T upstream_gene_variant ESAD-UK 9 132638103 132638103 single base substitution G A intron_variant ESAD-UK 9 132638103 132638103 single base substitution G A upstream_gene_variant ESAD-UK 9 132638521 132638521 single base substitution C T splice_region_variant ESAD-UK 9 132638521 132638521 single base substitution C T upstream_gene_variant ESAD-UK 9 132638961 132638961 single base substitution G A intron_variant ESAD-UK 9 132638961 132638961 single base substitution G A upstream_gene_variant ESAD-UK 9 132642105 132642105 single base substitution C T downstream_gene_variant ESAD-UK 9 132642105 132642105 single base substitution C T intron_variant ESAD-UK 9 132642765 132642765 single base substitution C T 3_prime_UTR_variant ESAD-UK 9 132642765 132642765 single base substitution C T downstream_gene_variant ESAD-UK 9 132642765 132642765 single base substitution C T exon_variant ESAD-UK 9 132643086 132643086 single base substitution C T 3_prime_UTR_variant ESAD-UK 9 132643086 132643086 single base substitution C T downstream_gene_variant ESAD-UK 9 132643086 132643086 single base substitution C T exon_variant ESAD-UK 9 132643111 132643111 single base substitution C T 3_prime_UTR_variant ESAD-UK 9 132643111 132643111 single base substitution C T downstream_gene_variant ESAD-UK 9 132643111 132643111 single base substitution C T exon_variant ESAD-UK 9 132643889 132643889 single base substitution C G 3_prime_UTR_variant ESAD-UK 9 132643889 132643889 single base substitution C G downstream_gene_variant ESAD-UK 9 132643889 132643889 single base substitution C G exon_variant ESAD-UK 9 132644125 132644125 single base substitution G A downstream_gene_variant ESAD-UK 9 132644378 132644378 single base substitution G T downstream_gene_variant ESAD-UK 9 132644587 132644587 single base substitution C T downstream_gene_variant ESAD-UK 9 132647485 132647485 single base substitution C T downstream_gene_variant ESCA-CN 9 132631268 132631268 single base substitution C T exon_variant ESCA-CN 9 132631268 132631268 single base substitution C T intron_variant ESCA-CN 9 132631268 132631268 single base substitution C T synonymous_variant Y421Y 1263C>T ESCA-CN 9 132632784 132632784 single base substitution G A downstream_gene_variant ESCA-CN 9 132632784 132632784 single base substitution G A intron_variant ESCA-CN 9 132632784 132632784 single base substitution G A missense_variant E540K 1618G>A ESCA-CN 9 132637170 132637170 single base substitution C T downstream_gene_variant ESCA-CN 9 132637170 132637170 single base substitution C T exon_variant ESCA-CN 9 132637170 132637170 single base substitution C T stop_gained Q662* 1984C>T ESCA-CN 9 132637170 132637170 single base substitution C T upstream_gene_variant ESCA-CN 9 132640632 132640632 single base substitution C T exon_variant ESCA-CN 9 132640632 132640632 single base substitution C T stop_gained Q809* 2425C>T ESCA-CN 9 132640632 132640632 single base substitution C T upstream_gene_variant GBM-US 9 132625554 132625555 deletion of <=200bp TC - downstream_gene_variant GBM-US 9 132625554 132625555 deletion of <=200bp TC - frameshift_variant V196 GBM-US 9 132638480 132638480 single base substitution C T exon_variant GBM-US 9 132638480 132638480 single base substitution C T missense_variant A791V 2372C>T GBM-US 9 132638480 132638480 single base substitution C T upstream_gene_variant KIRC-US 9 132636882 132636882 insertion of <=200bp - T downstream_gene_variant KIRC-US 9 132636882 132636882 insertion of <=200bp - T frameshift_variant R590S? KIRC-US 9 132636882 132636882 insertion of <=200bp - T intron_variant KIRC-US 9 132636882 132636882 insertion of <=200bp - T upstream_gene_variant KIRC-US 9 132636883 132636883 single base substitution G T downstream_gene_variant KIRC-US 9 132636883 132636883 single base substitution G T intron_variant KIRC-US 9 132636883 132636883 single base substitution G T missense_variant R590L 1769G>T KIRC-US 9 132636883 132636883 single base substitution G T upstream_gene_variant KIRP-US 9 132593305 132593305 single base substitution G T upstream_gene_variant KIRP-US 9 132618631 132618631 single base substitution T A downstream_gene_variant KIRP-US 9 132618631 132618631 single base substitution T A exon_variant KIRP-US 9 132618631 132618631 single base substitution T A missense_variant C43S 127T>A KIRP-US 9 132623219 132623219 single base substitution T C downstream_gene_variant KIRP-US 9 132623219 132623219 single base substitution T C missense_variant S112P 334T>C LAML-KR 9 132591992 132591992 single base substitution T C upstream_gene_variant LAML-KR 9 132596071 132596071 single base substitution C T upstream_gene_variant LAML-KR 9 132605666 132605666 single base substitution G A intron_variant LGG-US 9 132631191 132631191 single base substitution G A exon_variant LGG-US 9 132631191 132631191 single base substitution G A intron_variant LGG-US 9 132631191 132631191 single base substitution G A missense_variant V396I 1186G>A LGG-US 9 132631651 132631651 single base substitution G T exon_variant LGG-US 9 132631651 132631651 single base substitution G T intron_variant LGG-US 9 132631651 132631651 single base substitution G T missense_variant D447Y 1339G>T LICA-CN 9 132640633 132640633 single base substitution A C exon_variant LICA-CN 9 132640633 132640633 single base substitution A C missense_variant Q809P 2426A>C LICA-CN 9 132640633 132640633 single base substitution A C upstream_gene_variant LICA-FR 9 132595797 132595797 single base substitution C T upstream_gene_variant LICA-FR 9 132603046 132603047 deletion of <=200bp TT - intron_variant LICA-FR 9 132606796 132606796 single base substitution T A intron_variant LICA-FR 9 132608902 132608902 deletion of <=200bp T - intron_variant LICA-FR 9 132628389 132628402 deletion of <=200bp GCCTGGGCTTTCAT - intron_variant LICA-FR 9 132628389 132628402 deletion of <=200bp GCCTGGGCTTTCAT - upstream_gene_variant LICA-FR 9 132630750 132630750 single base substitution C T intron_variant LIHC-US 9 132632035 132632035 single base substitution T C exon_variant LIHC-US 9 132632035 132632035 single base substitution T C intron_variant LIHC-US 9 132632035 132632035 single base substitution T C missense_variant Y493H 1477T>C LIHC-US 9 132632793 132632793 single base substitution C T downstream_gene_variant LIHC-US 9 132632793 132632793 single base substitution C T intron_variant LIHC-US 9 132632793 132632793 single base substitution C T missense_variant L543F 1627C>T LIHC-US 9 132636872 132636872 single base substitution A T downstream_gene_variant LIHC-US 9 132636872 132636872 single base substitution A T intron_variant LIHC-US 9 132636872 132636872 single base substitution A T synonymous_variant L586L 1758A>T LIHC-US 9 132636872 132636872 single base substitution A T upstream_gene_variant LIHC-US 9 132636968 132636968 single base substitution G A downstream_gene_variant LIHC-US 9 132636968 132636968 single base substitution G A exon_variant LIHC-US 9 132636968 132636968 single base substitution G A synonymous_variant K618K 1854G>A LIHC-US 9 132636968 132636968 single base substitution G A upstream_gene_variant LIHC-US 9 132642472 132642472 single base substitution C A downstream_gene_variant LIHC-US 9 132642472 132642472 single base substitution C A exon_variant LIHC-US 9 132642472 132642472 single base substitution C A missense_variant R889S 2665C>A LINC-JP 9 132594379 132594379 insertion of <=200bp - G upstream_gene_variant LINC-JP 9 132595793 132595793 single base substitution C T upstream_gene_variant LINC-JP 9 132596001 132596001 deletion of <=200bp A - upstream_gene_variant LINC-JP 9 132597630 132597630 single base substitution C T intron_variant LINC-JP 9 132597630 132597630 single base substitution C T upstream_gene_variant LINC-JP 9 132597678 132597678 single base substitution G T intron_variant LINC-JP 9 132597678 132597678 single base substitution G T upstream_gene_variant LINC-JP 9 132603392 132603392 single base substitution A C intron_variant LINC-JP 9 132611170 132611170 single base substitution G A intron_variant LINC-JP 9 132623518 132623518 single base substitution C T downstream_gene_variant LINC-JP 9 132623518 132623518 single base substitution C T intron_variant LINC-JP 9 132627656 132627656 single base substitution A T missense_variant Q229L 686A>T LINC-JP 9 132627656 132627656 single base substitution A T upstream_gene_variant LINC-JP 9 132632452 132632452 single base substitution C G downstream_gene_variant LINC-JP 9 132632452 132632452 single base substitution C G intron_variant LINC-JP 9 132632774 132632774 single base substitution C T downstream_gene_variant LINC-JP 9 132632774 132632774 single base substitution C T intron_variant LINC-JP 9 132632774 132632774 single base substitution C T synonymous_variant V536V 1608C>T LINC-JP 9 132641987 132641987 single base substitution A G downstream_gene_variant LINC-JP 9 132641987 132641987 single base substitution A G intron_variant LINC-JP 9 132647953 132647953 insertion of <=200bp - GCA downstream_gene_variant LIRI-JP 9 132600252 132600252 single base substitution A G intron_variant LIRI-JP 9 132602480 132602480 single base substitution C G intron_variant LIRI-JP 9 132605018 132605018 single base substitution A C intron_variant LIRI-JP 9 132605519 132605519 single base substitution G A intron_variant LIRI-JP 9 132606583 132606583 single base substitution A T intron_variant LIRI-JP 9 132607852 132607852 single base substitution G T intron_variant LIRI-JP 9 132611511 132611511 single base substitution A T intron_variant LIRI-JP 9 132614944 132614944 single base substitution G T downstream_gene_variant LIRI-JP 9 132614944 132614944 single base substitution G T intron_variant LIRI-JP 9 132615676 132615676 single base substitution C A downstream_gene_variant LIRI-JP 9 132615676 132615676 single base substitution C A intron_variant LIRI-JP 9 132616605 132616605 single base substitution G A downstream_gene_variant LIRI-JP 9 132616605 132616605 single base substitution G A intron_variant LIRI-JP 9 132616973 132616974 deletion of <=200bp GA - downstream_gene_variant LIRI-JP 9 132616973 132616974 deletion of <=200bp GA - intron_variant LIRI-JP 9 132620490 132620490 single base substitution A G intron_variant LIRI-JP 9 132621532 132621533 deletion of <=200bp CC - downstream_gene_variant LIRI-JP 9 132621532 132621533 deletion of <=200bp CC - intron_variant LIRI-JP 9 132622294 132622294 single base substitution A G downstream_gene_variant LIRI-JP 9 132622294 132622294 single base substitution A G intron_variant LIRI-JP 9 132622380 132622380 single base substitution C T downstream_gene_variant LIRI-JP 9 132622380 132622380 single base substitution C T intron_variant LIRI-JP 9 132623454 132623454 single base substitution A T downstream_gene_variant LIRI-JP 9 132623454 132623454 single base substitution A T intron_variant LIRI-JP 9 132624756 132624756 single base substitution C T downstream_gene_variant LIRI-JP 9 132624756 132624756 single base substitution C T intron_variant LIRI-JP 9 132625953 132625953 single base substitution G C intron_variant LIRI-JP 9 132625953 132625953 single base substitution G C upstream_gene_variant LIRI-JP 9 132627394 132627394 single base substitution G T intron_variant LIRI-JP 9 132627394 132627394 single base substitution G T upstream_gene_variant LIRI-JP 9 132632133 132632133 single base substitution C G exon_variant LIRI-JP 9 132632133 132632133 single base substitution C G intron_variant LIRI-JP 9 132635429 132635429 single base substitution C T downstream_gene_variant LIRI-JP 9 132635429 132635429 single base substitution C T intron_variant LIRI-JP 9 132635429 132635429 single base substitution C T upstream_gene_variant LIRI-JP 9 132637681 132637681 single base substitution G T exon_variant LIRI-JP 9 132637681 132637681 single base substitution G T missense_variant R714L 2141G>T LIRI-JP 9 132637681 132637681 single base substitution G T upstream_gene_variant LUSC-KR 9 132597464 132597464 single base substitution C T intron_variant LUSC-KR 9 132597464 132597464 single base substitution C T upstream_gene_variant LUSC-KR 9 132606902 132606902 single base substitution C A intron_variant LUSC-KR 9 132610095 132610095 single base substitution C G intron_variant LUSC-KR 9 132610221 132610221 single base substitution A G intron_variant LUSC-KR 9 132615750 132615750 single base substitution A G downstream_gene_variant LUSC-KR 9 132615750 132615750 single base substitution A G intron_variant LUSC-KR 9 132623512 132623512 single base substitution C G downstream_gene_variant LUSC-KR 9 132623512 132623512 single base substitution C G intron_variant LUSC-KR 9 132630191 132630191 single base substitution G T intron_variant LUSC-KR 9 132630191 132630191 single base substitution G T upstream_gene_variant LUSC-KR 9 132641626 132641626 single base substitution C G downstream_gene_variant LUSC-KR 9 132641626 132641626 single base substitution C G intron_variant LUSC-KR 9 132641626 132641626 single base substitution C G upstream_gene_variant LUSC-KR 9 132647746 132647746 single base substitution G T downstream_gene_variant LUSC-US 9 132593188 132593188 single base substitution C G upstream_gene_variant LUSC-US 9 132595737 132595737 single base substitution C A upstream_gene_variant LUSC-US 9 132597006 132597006 single base substitution C A exon_variant LUSC-US 9 132597006 132597006 single base substitution C A upstream_gene_variant LUSC-US 9 132623876 132623876 single base substitution A C downstream_gene_variant LUSC-US 9 132623876 132623876 single base substitution A C missense_variant Q161P 482A>C LUSC-US 9 132642449 132642449 single base substitution G C downstream_gene_variant LUSC-US 9 132642449 132642449 single base substitution G C exon_variant LUSC-US 9 132642449 132642449 single base substitution G C missense_variant G881A 2642G>C MALY-DE 9 132601248 132601248 single base substitution C A intron_variant MALY-DE 9 132603981 132603981 single base substitution C T intron_variant MALY-DE 9 132609089 132609089 single base substitution A G intron_variant MALY-DE 9 132609091 132609091 single base substitution A T intron_variant MALY-DE 9 132618343 132618343 single base substitution T G downstream_gene_variant MALY-DE 9 132618343 132618343 single base substitution T G intron_variant MALY-DE 9 132625470 132625470 single base substitution C A downstream_gene_variant MALY-DE 9 132625470 132625470 single base substitution C A missense_variant P168Q 503C>A MALY-DE 9 132635171 132635171 insertion of <=200bp - C downstream_gene_variant MALY-DE 9 132635171 132635171 insertion of <=200bp - C intron_variant MALY-DE 9 132635171 132635171 insertion of <=200bp - C upstream_gene_variant MALY-DE 9 132646413 132646413 single base substitution T C downstream_gene_variant MELA-AU 9 132592264 132592264 single base substitution G A upstream_gene_variant MELA-AU 9 132592420 132592425 deletion of <=200bp GAACAT - upstream_gene_variant MELA-AU 9 132592624 132592624 single base substitution G A upstream_gene_variant MELA-AU 9 132592944 132592945 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 132593287 132593287 single base substitution C T upstream_gene_variant MELA-AU 9 132593726 132593726 single base substitution G A upstream_gene_variant MELA-AU 9 132595231 132595231 single base substitution G A upstream_gene_variant MELA-AU 9 132595477 132595477 single base substitution G A upstream_gene_variant MELA-AU 9 132596027 132596027 single base substitution G A upstream_gene_variant MELA-AU 9 132597084 132597084 single base substitution T A exon_variant MELA-AU 9 132597084 132597084 single base substitution T A upstream_gene_variant MELA-AU 9 132597229 132597229 single base substitution G A exon_variant MELA-AU 9 132597229 132597229 single base substitution G A upstream_gene_variant MELA-AU 9 132597641 132597641 single base substitution C T intron_variant MELA-AU 9 132597641 132597641 single base substitution C T upstream_gene_variant MELA-AU 9 132597643 132597643 single base substitution C T intron_variant MELA-AU 9 132597643 132597643 single base substitution C T upstream_gene_variant MELA-AU 9 132597644 132597644 single base substitution C T intron_variant MELA-AU 9 132597644 132597644 single base substitution C T upstream_gene_variant MELA-AU 9 132597655 132597655 single base substitution C T intron_variant MELA-AU 9 132597655 132597655 single base substitution C T upstream_gene_variant MELA-AU 9 132597657 132597657 single base substitution C T intron_variant MELA-AU 9 132597657 132597657 single base substitution C T upstream_gene_variant MELA-AU 9 132597676 132597676 single base substitution G A intron_variant MELA-AU 9 132597676 132597676 single base substitution G A upstream_gene_variant MELA-AU 9 132597678 132597678 single base substitution G A intron_variant MELA-AU 9 132597678 132597678 single base substitution G A upstream_gene_variant MELA-AU 9 132597990 132597990 single base substitution C T intron_variant MELA-AU 9 132598867 132598867 single base substitution C A intron_variant MELA-AU 9 132601159 132601159 single base substitution C T intron_variant MELA-AU 9 132603175 132603175 single base substitution G A intron_variant MELA-AU 9 132603629 132603629 single base substitution C T intron_variant MELA-AU 9 132604100 132604100 single base substitution C T intron_variant MELA-AU 9 132604192 132604192 single base substitution C T intron_variant MELA-AU 9 132605105 132605105 single base substitution C A intron_variant MELA-AU 9 132605168 132605169 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 132605248 132605248 single base substitution T A intron_variant MELA-AU 9 132605250 132605250 single base substitution A T intron_variant MELA-AU 9 132606084 132606084 single base substitution T A intron_variant MELA-AU 9 132606937 132606937 single base substitution C T intron_variant MELA-AU 9 132607022 132607022 single base substitution C T intron_variant MELA-AU 9 132609289 132609289 single base substitution C T intron_variant MELA-AU 9 132609807 132609807 single base substitution C T intron_variant MELA-AU 9 132610977 132610977 single base substitution C T intron_variant MELA-AU 9 132611493 132611494 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 132611965 132611965 single base substitution C T intron_variant MELA-AU 9 132612230 132612230 single base substitution C A intron_variant MELA-AU 9 132613246 132613246 single base substitution T C intron_variant MELA-AU 9 132613899 132613899 single base substitution G A intron_variant MELA-AU 9 132614275 132614275 single base substitution C T intron_variant MELA-AU 9 132614509 132614509 single base substitution C T intron_variant MELA-AU 9 132614761 132614761 single base substitution C T intron_variant MELA-AU 9 132617226 132617227 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 132617226 132617227 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 132617241 132617241 single base substitution C T downstream_gene_variant MELA-AU 9 132617241 132617241 single base substitution C T intron_variant MELA-AU 9 132618115 132618115 single base substitution T C downstream_gene_variant MELA-AU 9 132618115 132618115 single base substitution T C intron_variant MELA-AU 9 132618333 132618333 single base substitution C T downstream_gene_variant MELA-AU 9 132618333 132618333 single base substitution C T intron_variant MELA-AU 9 132618403 132618403 single base substitution C T downstream_gene_variant MELA-AU 9 132618403 132618403 single base substitution C T intron_variant MELA-AU 9 132618445 132618445 single base substitution T G downstream_gene_variant MELA-AU 9 132618445 132618445 single base substitution T G intron_variant MELA-AU 9 132618705 132618705 single base substitution C T downstream_gene_variant MELA-AU 9 132618705 132618705 single base substitution C T intron_variant MELA-AU 9 132620187 132620187 single base substitution C T intron_variant MELA-AU 9 132620462 132620462 single base substitution C T intron_variant MELA-AU 9 132621115 132621115 single base substitution C T downstream_gene_variant MELA-AU 9 132621115 132621115 single base substitution C T intron_variant MELA-AU 9 132621266 132621266 single base substitution C T downstream_gene_variant MELA-AU 9 132621266 132621266 single base substitution C T intron_variant MELA-AU 9 132622154 132622154 single base substitution A T downstream_gene_variant MELA-AU 9 132622154 132622154 single base substitution A T intron_variant MELA-AU 9 132622372 132622372 single base substitution G A downstream_gene_variant MELA-AU 9 132622372 132622372 single base substitution G A intron_variant MELA-AU 9 132622608 132622608 single base substitution C T downstream_gene_variant MELA-AU 9 132622608 132622608 single base substitution C T intron_variant MELA-AU 9 132622954 132622954 single base substitution G A downstream_gene_variant MELA-AU 9 132622954 132622954 single base substitution G A intron_variant MELA-AU 9 132622956 132622956 single base substitution T A downstream_gene_variant MELA-AU 9 132622956 132622956 single base substitution T A intron_variant MELA-AU 9 132624433 132624433 single base substitution G A downstream_gene_variant MELA-AU 9 132624433 132624433 single base substitution G A intron_variant MELA-AU 9 132627585 132627585 single base substitution A T synonymous_variant P205P 615A>T MELA-AU 9 132627585 132627585 single base substitution A T upstream_gene_variant MELA-AU 9 132628184 132628184 single base substitution C T intron_variant MELA-AU 9 132628184 132628184 single base substitution C T upstream_gene_variant MELA-AU 9 132628957 132628957 single base substitution C T intron_variant MELA-AU 9 132628957 132628957 single base substitution C T upstream_gene_variant MELA-AU 9 132629085 132629085 single base substitution G A intron_variant MELA-AU 9 132629085 132629085 single base substitution G A upstream_gene_variant MELA-AU 9 132629886 132629886 single base substitution C T intron_variant MELA-AU 9 132629886 132629886 single base substitution C T upstream_gene_variant MELA-AU 9 132630100 132630100 single base substitution C T intron_variant MELA-AU 9 132630100 132630100 single base substitution C T upstream_gene_variant MELA-AU 9 132630147 132630147 single base substitution G A intron_variant MELA-AU 9 132630147 132630147 single base substitution G A upstream_gene_variant MELA-AU 9 132630815 132630815 single base substitution C T intron_variant MELA-AU 9 132631361 132631361 single base substitution C T intron_variant MELA-AU 9 132631672 132631672 single base substitution C T exon_variant MELA-AU 9 132631672 132631672 single base substitution C T intron_variant MELA-AU 9 132631672 132631672 single base substitution C T missense_variant L454F 1360C>T MELA-AU 9 132631944 132631944 single base substitution C T intron_variant MELA-AU 9 132631944 132631944 single base substitution C T splice_region_variant MELA-AU 9 132632103 132632103 single base substitution C T exon_variant MELA-AU 9 132632103 132632103 single base substitution C T intron_variant MELA-AU 9 132632103 132632103 single base substitution C T synonymous_variant F515F 1545C>T MELA-AU 9 132632416 132632416 single base substitution G A exon_variant MELA-AU 9 132632416 132632416 single base substitution G A intron_variant MELA-AU 9 132632838 132632838 single base substitution G T downstream_gene_variant MELA-AU 9 132632838 132632838 single base substitution G T intron_variant MELA-AU 9 132633110 132633110 single base substitution C T downstream_gene_variant MELA-AU 9 132633110 132633110 single base substitution C T intron_variant MELA-AU 9 132633110 132633110 single base substitution C T upstream_gene_variant MELA-AU 9 132633305 132633305 single base substitution A G downstream_gene_variant MELA-AU 9 132633305 132633305 single base substitution A G intron_variant MELA-AU 9 132633305 132633305 single base substitution A G upstream_gene_variant MELA-AU 9 132634358 132634358 single base substitution T C downstream_gene_variant MELA-AU 9 132634358 132634358 single base substitution T C intron_variant MELA-AU 9 132634358 132634358 single base substitution T C upstream_gene_variant MELA-AU 9 132634920 132634920 single base substitution G C downstream_gene_variant MELA-AU 9 132634920 132634920 single base substitution G C intron_variant MELA-AU 9 132634920 132634920 single base substitution G C upstream_gene_variant MELA-AU 9 132635862 132635862 single base substitution C T downstream_gene_variant MELA-AU 9 132635862 132635862 single base substitution C T intron_variant MELA-AU 9 132635862 132635862 single base substitution C T upstream_gene_variant MELA-AU 9 132638370 132638370 single base substitution C T intron_variant MELA-AU 9 132638370 132638370 single base substitution C T upstream_gene_variant MELA-AU 9 132639243 132639243 single base substitution C T intron_variant MELA-AU 9 132639243 132639243 single base substitution C T upstream_gene_variant MELA-AU 9 132639383 132639383 single base substitution G A intron_variant MELA-AU 9 132639383 132639383 single base substitution G A upstream_gene_variant MELA-AU 9 132639404 132639404 single base substitution C T intron_variant MELA-AU 9 132639404 132639404 single base substitution C T upstream_gene_variant MELA-AU 9 132640147 132640147 single base substitution G A intron_variant MELA-AU 9 132640147 132640147 single base substitution G A upstream_gene_variant MELA-AU 9 132640515 132640515 single base substitution C T intron_variant MELA-AU 9 132640515 132640515 single base substitution C T upstream_gene_variant MELA-AU 9 132641986 132641986 single base substitution C T downstream_gene_variant MELA-AU 9 132641986 132641986 single base substitution C T intron_variant MELA-AU 9 132642310 132642310 single base substitution C T downstream_gene_variant MELA-AU 9 132642310 132642310 single base substitution C T intron_variant MELA-AU 9 132642778 132642778 single base substitution T C 3_prime_UTR_variant MELA-AU 9 132642778 132642778 single base substitution T C downstream_gene_variant MELA-AU 9 132642778 132642778 single base substitution T C exon_variant MELA-AU 9 132643450 132643450 single base substitution G A 3_prime_UTR_variant MELA-AU 9 132643450 132643450 single base substitution G A downstream_gene_variant MELA-AU 9 132643450 132643450 single base substitution G A exon_variant MELA-AU 9 132643470 132643470 single base substitution C T 3_prime_UTR_variant MELA-AU 9 132643470 132643470 single base substitution C T downstream_gene_variant MELA-AU 9 132643470 132643470 single base substitution C T exon_variant MELA-AU 9 132643925 132643925 single base substitution C T 3_prime_UTR_variant MELA-AU 9 132643925 132643925 single base substitution C T downstream_gene_variant MELA-AU 9 132643925 132643925 single base substitution C T exon_variant MELA-AU 9 132643934 132643934 single base substitution G C 3_prime_UTR_variant MELA-AU 9 132643934 132643934 single base substitution G C downstream_gene_variant MELA-AU 9 132643934 132643934 single base substitution G C exon_variant MELA-AU 9 132644337 132644337 single base substitution C T downstream_gene_variant MELA-AU 9 132644341 132644341 single base substitution G A downstream_gene_variant MELA-AU 9 132644644 132644644 single base substitution C A downstream_gene_variant MELA-AU 9 132646415 132646415 single base substitution G A downstream_gene_variant MELA-AU 9 132646602 132646602 single base substitution G A downstream_gene_variant MELA-AU 9 132648148 132648149 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant ORCA-IN 9 132609285 132609285 single base substitution A G intron_variant ORCA-IN 9 132624843 132624843 deletion of <=200bp G - downstream_gene_variant ORCA-IN 9 132624843 132624843 deletion of <=200bp G - intron_variant ORCA-IN 9 132626371 132626371 single base substitution G A intron_variant ORCA-IN 9 132626371 132626371 single base substitution G A upstream_gene_variant ORCA-IN 9 132630549 132630549 single base substitution G A missense_variant R319Q 956G>A ORCA-IN 9 132630549 132630549 single base substitution G A upstream_gene_variant ORCA-IN 9 132637415 132637415 single base substitution C T downstream_gene_variant ORCA-IN 9 132637415 132637415 single base substitution C T intron_variant ORCA-IN 9 132637415 132637415 single base substitution C T upstream_gene_variant ORCA-IN 9 132648779 132648779 single base substitution C T downstream_gene_variant OV-AU 9 132597419 132597419 single base substitution G C intron_variant OV-AU 9 132597419 132597419 single base substitution G C upstream_gene_variant OV-AU 9 132611570 132611570 single base substitution C A intron_variant OV-AU 9 132615878 132615878 single base substitution G C downstream_gene_variant OV-AU 9 132615878 132615878 single base substitution G C intron_variant OV-AU 9 132622280 132622280 single base substitution C T downstream_gene_variant OV-AU 9 132622280 132622280 single base substitution C T intron_variant OV-AU 9 132628238 132628238 single base substitution A T intron_variant OV-AU 9 132628238 132628238 single base substitution A T upstream_gene_variant OV-AU 9 132633179 132633179 single base substitution C T downstream_gene_variant OV-AU 9 132633179 132633179 single base substitution C T intron_variant OV-AU 9 132633179 132633179 single base substitution C T upstream_gene_variant OV-AU 9 132636021 132636021 single base substitution G A downstream_gene_variant OV-AU 9 132636021 132636021 single base substitution G A intron_variant OV-AU 9 132636021 132636021 single base substitution G A missense_variant E580K 1738G>A OV-AU 9 132636021 132636021 single base substitution G A upstream_gene_variant OV-AU 9 132636753 132636753 single base substitution T C downstream_gene_variant OV-AU 9 132636753 132636753 single base substitution T C intron_variant OV-AU 9 132636753 132636753 single base substitution T C upstream_gene_variant OV-AU 9 132637065 132637065 single base substitution C T downstream_gene_variant OV-AU 9 132637065 132637065 single base substitution C T intron_variant OV-AU 9 132637065 132637065 single base substitution C T upstream_gene_variant PACA-AU 9 132592800 132592800 single base substitution T C upstream_gene_variant PACA-AU 9 132595292 132595292 single base substitution G A upstream_gene_variant PACA-AU 9 132596122 132596122 single base substitution C T upstream_gene_variant PACA-AU 9 132605443 132605443 single base substitution G A intron_variant PACA-AU 9 132608082 132608082 single base substitution G T intron_variant PACA-AU 9 132618816 132618816 single base substitution G A downstream_gene_variant PACA-AU 9 132618816 132618816 single base substitution G A intron_variant PACA-AU 9 132628597 132628597 insertion of <=200bp - T intron_variant PACA-AU 9 132628597 132628597 insertion of <=200bp - T upstream_gene_variant PACA-AU 9 132631269 132631269 single base substitution G A exon_variant PACA-AU 9 132631269 132631269 single base substitution G A intron_variant PACA-AU 9 132631269 132631269 single base substitution G A missense_variant V422M 1264G>A PACA-AU 9 132635171 132635171 insertion of <=200bp - C downstream_gene_variant PACA-AU 9 132635171 132635171 insertion of <=200bp - C intron_variant PACA-AU 9 132635171 132635171 insertion of <=200bp - C upstream_gene_variant PACA-AU 9 132635351 132635353 deletion of <=200bp TTC - downstream_gene_variant PACA-AU 9 132635351 132635353 deletion of <=200bp TTC - intron_variant PACA-AU 9 132635351 132635353 deletion of <=200bp TTC - upstream_gene_variant PACA-CA 9 132592625 132592625 single base substitution A G upstream_gene_variant PACA-CA 9 132595278 132595278 single base substitution G A upstream_gene_variant PACA-CA 9 132595572 132595572 single base substitution T A upstream_gene_variant PACA-CA 9 132595849 132595849 single base substitution A T upstream_gene_variant PACA-CA 9 132612026 132612026 single base substitution G A intron_variant PACA-CA 9 132613023 132613023 single base substitution C A intron_variant PACA-CA 9 132616685 132616685 single base substitution T A downstream_gene_variant PACA-CA 9 132616685 132616685 single base substitution T A intron_variant PACA-CA 9 132616957 132616957 single base substitution G C downstream_gene_variant PACA-CA 9 132616957 132616957 single base substitution G C intron_variant PACA-CA 9 132622402 132622402 single base substitution G A downstream_gene_variant PACA-CA 9 132622402 132622402 single base substitution G A intron_variant PACA-CA 9 132625060 132625060 single base substitution C T downstream_gene_variant PACA-CA 9 132625060 132625060 single base substitution C T intron_variant PACA-CA 9 132625676 132625676 single base substitution G A downstream_gene_variant PACA-CA 9 132625676 132625676 single base substitution G A intron_variant PACA-CA 9 132625676 132625676 single base substitution G A upstream_gene_variant PACA-CA 9 132626112 132626112 single base substitution C T intron_variant PACA-CA 9 132626112 132626112 single base substitution C T upstream_gene_variant PACA-CA 9 132628238 132628238 single base substitution A T intron_variant PACA-CA 9 132628238 132628238 single base substitution A T upstream_gene_variant PACA-CA 9 132630134 132630134 single base substitution G A intron_variant PACA-CA 9 132630134 132630134 single base substitution G A upstream_gene_variant PACA-CA 9 132630765 132630765 single base substitution C T intron_variant PACA-CA 9 132632562 132632562 single base substitution C T downstream_gene_variant PACA-CA 9 132632562 132632562 single base substitution C T intron_variant PACA-CA 9 132633219 132633219 single base substitution G T downstream_gene_variant PACA-CA 9 132633219 132633219 single base substitution G T intron_variant PACA-CA 9 132633219 132633219 single base substitution G T upstream_gene_variant PACA-CA 9 132635610 132635610 single base substitution G A downstream_gene_variant PACA-CA 9 132635610 132635610 single base substitution G A intron_variant PACA-CA 9 132635610 132635610 single base substitution G A upstream_gene_variant PACA-CA 9 132637682 132637682 single base substitution C T exon_variant PACA-CA 9 132637682 132637682 single base substitution C T synonymous_variant R714R 2142C>T PACA-CA 9 132637682 132637682 single base substitution C T upstream_gene_variant PACA-CA 9 132640182 132640182 single base substitution G A intron_variant PACA-CA 9 132640182 132640182 single base substitution G A upstream_gene_variant PACA-CA 9 132640438 132640438 single base substitution A G intron_variant PACA-CA 9 132640438 132640438 single base substitution A G upstream_gene_variant PACA-CA 9 132647072 132647072 single base substitution A T downstream_gene_variant PAEN-AU 9 132595296 132595296 single base substitution A G upstream_gene_variant PAEN-AU 9 132604929 132604929 single base substitution A G intron_variant PAEN-AU 9 132641863 132641863 single base substitution C G downstream_gene_variant PAEN-AU 9 132641863 132641863 single base substitution C G exon_variant PAEN-AU 9 132641863 132641863 single base substitution C G missense_variant P842A 2524C>G PAEN-IT 9 132601751 132601751 single base substitution C T intron_variant PAEN-IT 9 132602193 132602193 single base substitution G A intron_variant PAEN-IT 9 132624147 132624147 single base substitution G C downstream_gene_variant PAEN-IT 9 132624147 132624147 single base substitution G C intron_variant PBCA-DE 9 132596001 132596001 insertion of <=200bp - A upstream_gene_variant PBCA-DE 9 132602599 132602599 single base substitution G A intron_variant PBCA-DE 9 132605555 132605555 insertion of <=200bp - A intron_variant PBCA-DE 9 132605569 132605571 deletion of <=200bp TGT - intron_variant PBCA-DE 9 132608825 132608825 deletion of <=200bp C - intron_variant PBCA-DE 9 132626697 132626697 single base substitution C T intron_variant PBCA-DE 9 132626697 132626697 single base substitution C T upstream_gene_variant PBCA-DE 9 132637280 132637280 deletion of <=200bp C - downstream_gene_variant PBCA-DE 9 132637280 132637280 deletion of <=200bp C - intron_variant PBCA-DE 9 132637280 132637280 deletion of <=200bp C - upstream_gene_variant PBCA-DE 9 132648563 132648563 single base substitution T C downstream_gene_variant PRAD-CA 9 132592721 132592721 single base substitution C T upstream_gene_variant PRAD-CA 9 132597414 132597414 single base substitution G A intron_variant PRAD-CA 9 132597414 132597414 single base substitution G A upstream_gene_variant PRAD-CA 9 132602024 132602024 single base substitution G T intron_variant PRAD-CA 9 132630492 132630492 single base substitution G C missense_variant R300P 899G>C PRAD-CA 9 132630492 132630492 single base substitution G C upstream_gene_variant PRAD-CA 9 132637088 132637088 single base substitution C T downstream_gene_variant PRAD-CA 9 132637088 132637088 single base substitution C T intron_variant PRAD-CA 9 132637088 132637088 single base substitution C T upstream_gene_variant PRAD-CA 9 132643117 132643117 single base substitution C T 3_prime_UTR_variant PRAD-CA 9 132643117 132643117 single base substitution C T downstream_gene_variant PRAD-CA 9 132643117 132643117 single base substitution C T exon_variant PRAD-UK 9 132624658 132624658 single base substitution C A downstream_gene_variant PRAD-UK 9 132624658 132624658 single base substitution C A intron_variant PRAD-UK 9 132635171 132635171 insertion of <=200bp - C downstream_gene_variant PRAD-UK 9 132635171 132635171 insertion of <=200bp - C intron_variant PRAD-UK 9 132635171 132635171 insertion of <=200bp - C upstream_gene_variant PRAD-UK 9 132635179 132635179 insertion of <=200bp - C downstream_gene_variant PRAD-UK 9 132635179 132635179 insertion of <=200bp - C intron_variant PRAD-UK 9 132635179 132635179 insertion of <=200bp - C upstream_gene_variant PRAD-UK 9 132644287 132644287 single base substitution G A downstream_gene_variant PRAD-US 9 132641857 132641857 single base substitution C T downstream_gene_variant PRAD-US 9 132641857 132641857 single base substitution C T exon_variant PRAD-US 9 132641857 132641857 single base substitution C T missense_variant P840S 2518C>T RECA-EU 9 132596773 132596773 single base substitution C T upstream_gene_variant RECA-EU 9 132600817 132600817 single base substitution C T intron_variant RECA-EU 9 132606564 132606564 single base substitution A C intron_variant RECA-EU 9 132619708 132619708 single base substitution G A downstream_gene_variant RECA-EU 9 132619708 132619708 single base substitution G A intron_variant RECA-EU 9 132625647 132625647 single base substitution G A downstream_gene_variant RECA-EU 9 132625647 132625647 single base substitution G A intron_variant RECA-EU 9 132625647 132625647 single base substitution G A upstream_gene_variant RECA-EU 9 132628051 132628051 single base substitution G A intron_variant RECA-EU 9 132628051 132628051 single base substitution G A upstream_gene_variant RECA-EU 9 132643789 132643789 single base substitution A G 3_prime_UTR_variant RECA-EU 9 132643789 132643789 single base substitution A G downstream_gene_variant RECA-EU 9 132643789 132643789 single base substitution A G exon_variant SKCA-BR 9 132592536 132592536 insertion of <=200bp - CTT upstream_gene_variant SKCA-BR 9 132597421 132597421 single base substitution A C intron_variant SKCA-BR 9 132597421 132597421 single base substitution A C upstream_gene_variant SKCA-BR 9 132603045 132603045 insertion of <=200bp - CT intron_variant SKCA-BR 9 132603914 132603914 single base substitution G C intron_variant SKCA-BR 9 132604071 132604071 single base substitution G A intron_variant SKCA-BR 9 132605396 132605396 insertion of <=200bp - ATT intron_variant SKCA-BR 9 132609195 132609195 single base substitution C T intron_variant SKCA-BR 9 132610176 132610176 insertion of <=200bp - AT intron_variant SKCA-BR 9 132613100 132613100 single base substitution A T intron_variant SKCA-BR 9 132613232 132613232 single base substitution C T intron_variant SKCA-BR 9 132613291 132613291 single base substitution G A intron_variant SKCA-BR 9 132615934 132615934 single base substitution C T downstream_gene_variant SKCA-BR 9 132615934 132615934 single base substitution C T intron_variant SKCA-BR 9 132617713 132617714 deletion of <=200bp AC - downstream_gene_variant SKCA-BR 9 132617713 132617714 deletion of <=200bp AC - intron_variant SKCA-BR 9 132619072 132619072 single base substitution T C downstream_gene_variant SKCA-BR 9 132619072 132619072 single base substitution T C intron_variant SKCA-BR 9 132622614 132622614 insertion of <=200bp - GA downstream_gene_variant SKCA-BR 9 132622614 132622614 insertion of <=200bp - GA intron_variant SKCA-BR 9 132625451 132625451 single base substitution T C downstream_gene_variant SKCA-BR 9 132625451 132625451 single base substitution T C intron_variant SKCA-BR 9 132629582 132629582 single base substitution T G intron_variant SKCA-BR 9 132629582 132629582 single base substitution T G upstream_gene_variant SKCA-BR 9 132629583 132629583 single base substitution G C intron_variant SKCA-BR 9 132629583 132629583 single base substitution G C upstream_gene_variant SKCA-BR 9 132633696 132633696 single base substitution C T downstream_gene_variant SKCA-BR 9 132633696 132633696 single base substitution C T intron_variant SKCA-BR 9 132633696 132633696 single base substitution C T upstream_gene_variant SKCA-BR 9 132634411 132634411 single base substitution T C downstream_gene_variant SKCA-BR 9 132634411 132634411 single base substitution T C intron_variant SKCA-BR 9 132634411 132634411 single base substitution T C upstream_gene_variant SKCA-BR 9 132635086 132635086 single base substitution C G downstream_gene_variant SKCA-BR 9 132635086 132635086 single base substitution C G intron_variant SKCA-BR 9 132635086 132635086 single base substitution C G upstream_gene_variant SKCA-BR 9 132637277 132637277 single base substitution C T downstream_gene_variant SKCA-BR 9 132637277 132637277 single base substitution C T intron_variant SKCA-BR 9 132637277 132637277 single base substitution C T upstream_gene_variant SKCA-BR 9 132638250 132638250 single base substitution C T intron_variant SKCA-BR 9 132638250 132638250 single base substitution C T upstream_gene_variant SKCA-BR 9 132640233 132640233 single base substitution C T intron_variant SKCA-BR 9 132640233 132640233 single base substitution C T upstream_gene_variant SKCA-BR 9 132641860 132641860 single base substitution G C downstream_gene_variant SKCA-BR 9 132641860 132641860 single base substitution G C exon_variant SKCA-BR 9 132641860 132641860 single base substitution G C missense_variant G841R 2521G>C SKCA-BR 9 132648484 132648484 single base substitution T G downstream_gene_variant SKCM-US 9 132593232 132593232 single base substitution G A upstream_gene_variant SKCM-US 9 132595788 132595788 single base substitution G A upstream_gene_variant SKCM-US 9 132618591 132618591 single base substitution C T downstream_gene_variant SKCM-US 9 132618591 132618591 single base substitution C T exon_variant SKCM-US 9 132618591 132618591 single base substitution C T synonymous_variant T29T 87C>T SKCM-US 9 132623221 132623221 single base substitution C T downstream_gene_variant SKCM-US 9 132623221 132623221 single base substitution C T synonymous_variant S112S 336C>T SKCM-US 9 132627616 132627616 single base substitution G A missense_variant G216R 646G>A SKCM-US 9 132627616 132627616 single base substitution G A upstream_gene_variant SKCM-US 9 132632009 132632009 single base substitution A G exon_variant SKCM-US 9 132632009 132632009 single base substitution A G intron_variant SKCM-US 9 132632009 132632009 single base substitution A G missense_variant D484G 1451A>G SKCM-US 9 132632120 132632120 single base substitution G T exon_variant SKCM-US 9 132632120 132632120 single base substitution G T intron_variant SKCM-US 9 132632120 132632120 single base substitution G T missense_variant R521L 1562G>T SKCM-US 9 132637876 132637876 single base substitution G A exon_variant SKCM-US 9 132637876 132637876 single base substitution G A synonymous_variant L752L 2256G>A SKCM-US 9 132637876 132637876 single base substitution G A upstream_gene_variant SKCM-US 9 132638502 132638502 single base substitution C T exon_variant SKCM-US 9 132638502 132638502 single base substitution C T synonymous_variant I798I 2394C>T SKCM-US 9 132638502 132638502 single base substitution C T upstream_gene_variant SKCM-US 9 132640700 132640700 single base substitution C T exon_variant SKCM-US 9 132640700 132640700 single base substitution C T synonymous_variant F831F 2493C>T SKCM-US 9 132640700 132640700 single base substitution C T upstream_gene_variant SKCM-US 9 132641892 132641892 single base substitution C T downstream_gene_variant SKCM-US 9 132641892 132641892 single base substitution C T exon_variant SKCM-US 9 132641892 132641892 single base substitution C T synonymous_variant V851V 2553C>T SKCM-US 9 132641905 132641905 single base substitution C T downstream_gene_variant SKCM-US 9 132641905 132641905 single base substitution C T exon_variant SKCM-US 9 132641905 132641905 single base substitution C T missense_variant H856Y 2566C>T STAD-US 9 132618599 132618599 single base substitution C T downstream_gene_variant STAD-US 9 132618599 132618599 single base substitution C T exon_variant STAD-US 9 132618599 132618599 single base substitution C T missense_variant S32L 95C>T STAD-US 9 132620767 132620767 single base substitution G A exon_variant STAD-US 9 132620767 132620767 single base substitution G A missense_variant V74M 220G>A STAD-US 9 132630544 132630544 single base substitution G A synonymous_variant A317A 951G>A STAD-US 9 132630544 132630544 single base substitution G A upstream_gene_variant STAD-US 9 132630616 132630616 single base substitution G A exon_variant STAD-US 9 132630616 132630616 single base substitution G A synonymous_variant S341S 1023G>A STAD-US 9 132630616 132630616 single base substitution G A upstream_gene_variant STAD-US 9 132630629 132630629 single base substitution G A exon_variant STAD-US 9 132630629 132630629 single base substitution G A missense_variant E346K 1036G>A STAD-US 9 132630629 132630629 single base substitution G A upstream_gene_variant STAD-US 9 132636012 132636012 single base substitution C T downstream_gene_variant STAD-US 9 132636012 132636012 single base substitution C T intron_variant STAD-US 9 132636012 132636012 single base substitution C T missense_variant R577W 1729C>T STAD-US 9 132636012 132636012 single base substitution C T upstream_gene_variant STAD-US 9 132636952 132636952 single base substitution G A downstream_gene_variant STAD-US 9 132636952 132636952 single base substitution G A exon_variant STAD-US 9 132636952 132636952 single base substitution G A missense_variant R613H 1838G>A STAD-US 9 132636952 132636952 single base substitution G A upstream_gene_variant STAD-US 9 132637006 132637006 single base substitution C T downstream_gene_variant STAD-US 9 132637006 132637006 single base substitution C T exon_variant STAD-US 9 132637006 132637006 single base substitution C T missense_variant S631L 1892C>T STAD-US 9 132637006 132637006 single base substitution C T upstream_gene_variant STAD-US 9 132637208 132637208 single base substitution C T downstream_gene_variant STAD-US 9 132637208 132637208 single base substitution C T exon_variant STAD-US 9 132637208 132637208 single base substitution C T synonymous_variant N674N 2022C>T STAD-US 9 132637208 132637208 single base substitution C T upstream_gene_variant STAD-US 9 132637711 132637711 single base substitution C T exon_variant STAD-US 9 132637711 132637711 single base substitution C T missense_variant A724V 2171C>T STAD-US 9 132637711 132637711 single base substitution C T upstream_gene_variant STAD-US 9 132640637 132640637 single base substitution C T exon_variant STAD-US 9 132640637 132640637 single base substitution C T synonymous_variant A810A 2430C>T STAD-US 9 132640637 132640637 single base substitution C T upstream_gene_variant THCA-SA 9 132636920 132636920 single base substitution C T downstream_gene_variant THCA-SA 9 132636920 132636920 single base substitution C T intron_variant THCA-SA 9 132636920 132636920 single base substitution C T synonymous_variant H602H 1806C>T THCA-SA 9 132636920 132636920 single base substitution C T upstream_gene_variant THCA-US 9 132631703 132631703 single base substitution G A intron_variant THCA-US 9 132631703 132631703 single base substitution G A missense_variant R464Q 1391G>A THCA-US 9 132631703 132631703 single base substitution G A splice_region_variant UCEC-US 9 132597419 132597419 single base substitution G T intron_variant UCEC-US 9 132597419 132597419 single base substitution G T upstream_gene_variant UCEC-US 9 132625468 132625468 single base substitution G A downstream_gene_variant UCEC-US 9 132625468 132625468 single base substitution G A synonymous_variant P167P 501G>A UCEC-US 9 132630483 132630483 single base substitution G A missense_variant G297E 890G>A UCEC-US 9 132630483 132630483 single base substitution G A upstream_gene_variant UCEC-US 9 132630665 132630667 deletion of <=200bp GAC - exon_variant UCEC-US 9 132630665 132630667 deletion of <=200bp GAC - inframe_deletion D358 UCEC-US 9 132631681 132631681 single base substitution G A exon_variant UCEC-US 9 132631681 132631681 single base substitution G A intron_variant UCEC-US 9 132631681 132631681 single base substitution G A missense_variant V457M 1369G>A UCEC-US 9 132631997 132631997 single base substitution C A exon_variant UCEC-US 9 132631997 132631997 single base substitution C A intron_variant UCEC-US 9 132631997 132631997 single base substitution C A missense_variant P480H 1439C>A UCEC-US 9 132632094 132632094 single base substitution G A exon_variant UCEC-US 9 132632094 132632094 single base substitution G A intron_variant UCEC-US 9 132632094 132632094 single base substitution G A stop_gained W512* 1536G>A UCEC-US 9 132632804 132632804 single base substitution C A downstream_gene_variant UCEC-US 9 132632804 132632804 single base substitution C A intron_variant UCEC-US 9 132632804 132632804 single base substitution C A missense_variant F546L 1638C>A UCEC-US 9 132635786 132635786 single base substitution G A downstream_gene_variant UCEC-US 9 132635786 132635786 single base substitution G A intron_variant UCEC-US 9 132635786 132635786 single base substitution G A synonymous_variant R562R 1686G>A UCEC-US 9 132635786 132635786 single base substitution G A upstream_gene_variant UCEC-US 9 132636908 132636908 single base substitution G T downstream_gene_variant UCEC-US 9 132636908 132636908 single base substitution G T intron_variant UCEC-US 9 132636908 132636908 single base substitution G T missense_variant K598N 1794G>T UCEC-US 9 132636908 132636908 single base substitution G T upstream_gene_variant UCEC-US 9 132636941 132636941 single base substitution G A downstream_gene_variant UCEC-US 9 132636941 132636941 single base substitution G A splice_region_variant UCEC-US 9 132636941 132636941 single base substitution G A synonymous_variant G609G 1827G>A UCEC-US 9 132636941 132636941 single base substitution G A upstream_gene_variant UCEC-US 9 132636948 132636948 single base substitution C A downstream_gene_variant UCEC-US 9 132636948 132636948 single base substitution C A exon_variant UCEC-US 9 132636948 132636948 single base substitution C A missense_variant L612M 1834C>A UCEC-US 9 132636948 132636948 single base substitution C A upstream_gene_variant UCEC-US 9 132637029 132637029 single base substitution G A downstream_gene_variant UCEC-US 9 132637029 132637029 single base substitution G A exon_variant UCEC-US 9 132637029 132637029 single base substitution G A missense_variant A639T 1915G>A UCEC-US 9 132637029 132637029 single base substitution G A upstream_gene_variant UCEC-US 9 132641862 132641862 single base substitution G A downstream_gene_variant UCEC-US 9 132641862 132641862 single base substitution G A exon_variant UCEC-US 9 132641862 132641862 single base substitution G A synonymous_variant G841G 2523G>A UCEC-US 9 132641901 132641901 single base substitution C T downstream_gene_variant UCEC-US 9 132641901 132641901 single base substitution C T exon_variant UCEC-US 9 132641901 132641901 single base substitution C T synonymous_variant S854S 2562C>T UCEC-US 9 132642504 132642504 single base substitution G T downstream_gene_variant UCEC-US 9 132642504 132642504 single base substitution G T exon_variant UCEC-US 9 132642504 132642504 single base substitution G T missense_variant E899D 2697G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 044-05-01TD COSM3328596 c.768G>A p.A256A Substitution - coding silent 9:129868082-129868082 + TCGA-CF-A3MI-01 COSM1314560 c.172G>A p.A58T Substitution - Missense 9:129858086-129858086 + TCGA-KR-A7K0-01 COSM4918124 c.1627C>T p.L543F Substitution - Missense 9:129870514-129870514 + CACO2 COSM3328604 c.774G>A p.T258T Substitution - coding silent 9:129868088-129868088 + HCC041T COSM5809572 c.2426A>C p.Q809P Substitution - Missense 9:129878354-129878354 + TCGA-EV-5903-01 COSM3996365 c.127T>A p.C43S Substitution - Missense 9:129856352-129856352 + TCGA-29-1776-01 COSM1330696 c.1504G>A p.A502T Substitution - Missense 9:129869783-129869783 + LS174T COSM3328713 c.1814_1815insC p.L607fs*54 Insertion - Frameshift 9:129874649-129874650 + TCGA-AZ-4315-01 COSM1460457 c.2606C>T p.S869L Substitution - Missense 9:129880134-129880134 + PD7240a COSM5781904 c.2317G>A p.A773T Substitution - Missense 9:129876146-129876146 + TCGA-BS-A0UF-01 COSM1105907 c.1638C>A p.F546L Substitution - Missense 9:129870525-129870525 + 8044606 COSM3395617 c.1264G>A p.V422M Substitution - Missense 9:129868990-129868990 + ESCC-098T COSM3942918 c.1618G>A p.E540K Substitution - Missense 9:129870505-129870505 + PT28 COSM5906358 c.805G>A p.D269N Substitution - Missense 9:129868119-129868119 + RK001_C01 COSM1636061 c.2141G>T p.R714L Substitution - Missense 9:129875402-129875402 + I2L-P28-Tumor-Organoid COSM5359501 c.2278G>A p.V760I Substitution - Missense 9:129875619-129875619 + TCGA-EK-A2RJ-01 COSM1460454 c.1171C>T p.R391C Substitution - Missense 9:129868897-129868897 + TCGA-CG-5721-01 COSM3904737 c.220G>A p.V74M Substitution - Missense 9:129858488-129858488 + RMS80_ COSM4988756 c.1990G>A p.V664I Substitution - Missense 9:129874897-129874897 + sysucc-1370T COSM5472677 c.1684C>T p.R562W Substitution - Missense 9:129873505-129873505 + I2L-P19Ta-Tumor-Biopsy COSM5359256 c.2335G>A p.V779M Substitution - Missense 9:129876164-129876164 + 587336 COSM1231999 c.757G>A p.A253T Substitution - Missense 9:129868071-129868071 + HCT-15 COSM1674892 c.1306C>T p.R436W Substitution - Missense 9:129869339-129869339 + sysucc-1397T COSM5475229 c.2665C>T p.R889C Substitution - Missense 9:129880193-129880193 + KM12 COSM3328601 c.769C>T p.L257L Substitution - coding silent 9:129868083-129868083 + TCGA-CG-5721-01 COSM3904740 c.951G>A p.A317A Substitution - coding silent 9:129868265-129868265 + TARGET-20-PABLDZ-09A-02D COSM5487228 c.826C>T p.R276W Substitution - Missense 9:129868140-129868140 + TCGA-AG-3891-01 COSM5069296 c.676G>A p.G226S Substitution - Missense 9:129865367-129865367 + TCGA-D1-A17M-01 COSM1105885 c.501G>A p.P167P Substitution - coding silent 9:129863189-129863189 + HT115 COSM3328617 c.976C>T p.R326W Substitution - Missense 9:129868290-129868290 + TCGA-EE-A3AB-06 COSM3654841 c.1451A>G p.D484G Substitution - Missense 9:129869730-129869730 + TCGA-AP-A0LM-01 COSM1105933 c.2562C>T p.S854S Substitution - coding silent 9:129879622-129879622 + TCGA-D1-A103-01 COSM1105929 c.2523G>A p.G841G Substitution - coding silent 9:129879583-129879583 + CSCC-7-T COSM4485570 c.294C>T p.A98A Substitution - coding silent 9:129858562-129858562 + LN18 COSM1105893 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + 587238 COSM1231990 c.1837C>T p.R613C Substitution - Missense 9:129874672-129874672 + 044-05-01TD COSM3328598 c.768G>A p.A256A Substitution - coding silent 9:129868082-129868082 + PTC-28C COSM4163411 c.575A>T p.Y192F Substitution - Missense 9:129863263-129863263 + TCGA-AM-5820-01 COSM3763673 c.2151C>T p.L717L Substitution - coding silent 9:129875412-129875412 + 2521249 COSM5888066 c.1067C>T p.A356V Substitution - Missense 9:129868381-129868381 + TCGA-AU-6004-01 COSM1460449 c.955C>T p.R319* Substitution - Nonsense 9:129868269-129868269 + TCGA-D1-A17R-01 COSM1105896 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + ESO-1145 COSM1270053 c.1780_1781insTG p.Y595fs*58 Insertion - Frameshift 9:129874615-129874616 + DLD1 COSM1674890 c.1306C>T p.R436W Substitution - Missense 9:129869339-129869339 + PTC-14C COSM4163422 c.2093C>G p.S698C Substitution - Missense 9:129875354-129875354 + S02382 COSM5460377 c.1075G>C p.D359H Substitution - Missense 9:129868389-129868389 + DF01 COSM5759491 c.919G>T p.A307S Substitution - Missense 9:129868233-129868233 + ASHPC_0010_Pa_P COSM4964781 c.2142C>T p.R714R Substitution - coding silent 9:129875403-129875403 + ATL089 COSM5711161 c.950C>T p.A317V Substitution - Missense 9:129868264-129868264 + CACO2 COSM3328602 c.774G>A p.T258T Substitution - coding silent 9:129868088-129868088 + CSCC-40-T COSM4455205 c.698A>G p.Q233R Substitution - Missense 9:129868012-129868012 + BL1 COSM1161776 c.503C>A p.P168Q Substitution - Missense 9:129863191-129863191 + ASHPC_0010_Pa_P COSM4964780 c.2142C>T p.R714R Substitution - coding silent 9:129875403-129875403 + TCGA-EB-A44P-01 COSM3654853 c.2493C>T p.F831F Substitution - coding silent 9:129878421-129878421 + PT28 COSM5906360 c.805G>A p.D269N Substitution - Missense 9:129868119-129868119 + Pat_45_B COSM5875665 c.2189C>T p.T730I Substitution - Missense 9:129875450-129875450 + GCT27 COSM5749459 c.199G>A p.A67T Substitution - Missense 9:129858467-129858467 + TCGA-AP-A051-01 COSM1105923 c.1915G>A p.A639T Substitution - Missense 9:129874750-129874750 + DN11120 COSM5780055 c.903C>T p.G301G Substitution - coding silent 9:129868217-129868217 + STC291 COSM5063675 c.767C>T p.A256V Substitution - Missense 9:129868081-129868081 + TCGA-D3-A3ML-06 COSM3654844 c.1562G>T p.R521L Substitution - Missense 9:129869841-129869841 + TCGA-CG-4300-01 COSM3904753 c.2171C>T p.A724V Substitution - Missense 9:129875432-129875432 + T2197 COSM4739708 c.2514_2515insC p.G841fs*4 Insertion - Frameshift 9:129879574-129879575 + TCGA-BH-A18G-01 COSM3328737 c.2141G>A p.R714H Substitution - Missense 9:129875402-129875402 + PTC-54C COSM4163417 c.2068A>G p.M690V Substitution - Missense 9:129875329-129875329 + TCGA-BH-A18P-01 COSM455468 c.2052G>A p.K684K Substitution - coding silent 9:129875313-129875313 + TCGA-BR-8081-01 COSM3904741 c.1023G>A p.S341S Substitution - coding silent 9:129868337-129868337 + TCGA-D1-A15X-01 COSM1105916 c.1827G>A p.G609G Substitution - coding silent 9:129874662-129874662 + YUKAT COSM5410523 c.597C>T p.V199V Substitution - coding silent 9:129863285-129863285 + 61 COSM5738760 c.532G>A p.G178S Substitution - Missense 9:129863220-129863220 + TCGA-BR-4201-01 COSM3779733 c.1036G>A p.E346K Substitution - Missense 9:129868350-129868350 + I2L-P7-Tumor-Organoid COSM5036357 c.749C>T p.P250L Substitution - Missense 9:129868063-129868063 + TCGA-D1-A17Q-01 COSM1105902 c.1439C>A p.P480H Substitution - Missense 9:129869718-129869718 + TCGA-HT-8564-01 COSM3328655 c.1186G>A p.V396I Substitution - Missense 9:129868912-129868912 + TCGA-AU-6004-01 COSM1460451 c.955C>T p.R319* Substitution - Nonsense 9:129868269-129868269 + CRC-02T COSM5455734 c.574T>C p.Y192H Substitution - Missense 9:129863262-129863262 + TCGA-AY-6197-01 COSM1460440 c.232A>C p.T78P Substitution - Missense 9:129858500-129858500 + C99 COSM4620542 c.1710G>A p.V570V Substitution - coding silent 9:129873714-129873714 + TCGA-EV-5903-01 COSM3996363 c.127T>A p.C43S Substitution - Missense 9:129856352-129856352 + TCGA-AR-A0TY-01 COSM455463 c.367_368delCC p.P123fs*5 Deletion - Frameshift 9:129860973-129860974 + TCGA-EB-A44P-01 COSM3654854 c.2493C>T p.F831F Substitution - coding silent 9:129878421-129878421 + OSCC-GB_00450111 COSM3716226 c.956G>A p.R319Q Substitution - Missense 9:129868270-129868270 + ESCC-248T COSM3942915 c.1263C>T p.Y421Y Substitution - coding silent 9:129868989-129868989 + T3174 COSM4739691 c.102G>A p.G34G Substitution - coding silent 9:129856327-129856327 + BD112T COSM5490852 c.1395A>G p.V465V Substitution - coding silent 9:129869674-129869674 + PTC-54C COSM3982751 c.2172G>A p.A724A Substitution - coding silent 9:129875433-129875433 + STC291 COSM5063677 c.767C>T p.A256V Substitution - Missense 9:129868081-129868081 + sysucc-773T COSM5460379 c.1075G>C p.D359H Substitution - Missense 9:129868389-129868389 + TCGA-JX-A3Q0-01 COSM4824831 c.2040C>G p.L680L Substitution - coding silent 9:129874947-129874947 + PTC-28C COSM4163414 c.1496A>T p.K499M Substitution - Missense 9:129869775-129869775 + TCGA-BH-A18G-01 COSM3328739 c.2141G>A p.R714H Substitution - Missense 9:129875402-129875402 + S02382 COSM5460379 c.1075G>C p.D359H Substitution - Missense 9:129868389-129868389 + ESO-105 COSM1270058 c.1737C>T p.P579P Substitution - coding silent 9:129873741-129873741 + TCGA-D5-6928-01 COSM1460448 c.773C>T p.T258M Substitution - Missense 9:129868087-129868087 + LN229 COSM1105896 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + PD13602a COSM5780055 c.903C>T p.G301G Substitution - coding silent 9:129868217-129868217 + BL1 COSM1161778 c.503C>A p.P168Q Substitution - Missense 9:129863191-129863191 + CSCC-7-T COSM4485568 c.294C>T p.A98A Substitution - coding silent 9:129858562-129858562 + KPOPBR-39-T COSM5964549 c.1922-2A>T p.? Unknown 9:129874827-129874827 + SNU-175 COSM3328724 c.2005G>A p.E669K Substitution - Missense 9:129874912-129874912 + TCGA-D1-A103-01 COSM1105906 c.1536G>A p.W512* Substitution - Nonsense 9:129869815-129869815 + HCT15 COSM1674892 c.1306C>T p.R436W Substitution - Missense 9:129869339-129869339 + SNU-C2B COSM4651663 c.542G>A p.R181H Substitution - Missense 9:129863230-129863230 + TCGA-EK-A2PM-01 COSM3328743 c.2431G>A p.E811K Substitution - Missense 9:129878359-129878359 + TCGA-G4-6304-01 COSM5175973 c.2513-1G>T p.? Unknown 9:129879572-129879572 + TCGA-EP-A2KA-01 COSM4917306 c.2665C>A p.R889S Substitution - Missense 9:129880193-129880193 + TCGA-D1-A17Q-01 COSM1105900 c.1439C>A p.P480H Substitution - Missense 9:129869718-129869718 + sysucc-773T COSM5460382 c.1077C>G p.D359E Substitution - Missense 9:129868391-129868391 + TCGA-EK-A2RJ-01 COSM1460452 c.1171C>T p.R391C Substitution - Missense 9:129868897-129868897 + TCGA-DS-A7WF-01 COSM4821659 c.2250C>A p.D750E Substitution - Missense 9:129875591-129875591 + TCGA-E9-A2JS-01 COSM3847840 c.2031C>A p.G677G Substitution - coding silent 9:129874938-129874938 + PTC-28C COSM4163416 c.1496A>T p.K499M Substitution - Missense 9:129869775-129869775 + BD19T COSM5499736 c.368C>T p.P123L Substitution - Missense 9:129860974-129860974 + NB2272T COSM1236663 c.136-3C>A p.? Unknown 9:129858047-129858047 + CSCC-40-T COSM4472973 c.1819C>T p.L607F Substitution - Missense 9:129874654-129874654 + BN38 COSM3664146 c.1608C>T p.V536V Substitution - coding silent 9:129870495-129870495 + TCGA-AM-5820-01 COSM3763672 c.2151C>T p.L717L Substitution - coding silent 9:129875412-129875412 + TCGA-KR-A7K0-01 COSM4918122 c.1627C>T p.L543F Substitution - Missense 9:129870514-129870514 + TARGET-30-PASCJJ COSM1288847 c.118C>T p.L40L Substitution - coding silent 9:129856343-129856343 + MO_1176 COSM5572863 c.252C>T p.Y84Y Substitution - coding silent 9:129858520-129858520 + 1265T COSM5762575 c.2524C>G p.P842A Substitution - Missense 9:129879584-129879584 + TCGA-EJ-5502-01 COSM1472165 c.2518C>T p.P840S Substitution - Missense 9:129879578-129879578 + Pa29C COSM87491 c.1378C>G p.L460V Substitution - Missense 9:129869411-129869411 + T98G COSM1105896 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + TCGA-DK-A2I4-01 COSM3779735 c.1036G>A p.E346K Substitution - Missense 9:129868350-129868350 + Pat_06_B COSM5875670 c.2266C>A p.L756M Substitution - Missense 9:129875607-129875607 + 86323 COSM96262 c.477C>T p.A159A Substitution - coding silent 9:129861592-129861592 + TCGA-EE-A3AB-06 COSM3654842 c.1451A>G p.D484G Substitution - Missense 9:129869730-129869730 + SNU-C2B COSM1105888 c.501G>A p.P167P Substitution - coding silent 9:129863189-129863189 + TCGA-AA-3833-01 COSM271593 c.761C>T p.T254M Substitution - Missense 9:129868075-129868075 + U373 COSM1105893 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + 1N40-VS-1T40 COSM3654853 c.2493C>T p.F831F Substitution - coding silent 9:129878421-129878421 + TCGA-DD-A3A9-01 COSM4920772 c.1477T>C p.Y493H Substitution - Missense 9:129869756-129869756 + ESO17T COSM1173453 c.1172G>A p.R391H Substitution - Missense 9:129868898-129868898 + TCGA-H4-A2HQ-01 COSM1314563 c.1892C>T p.S631L Substitution - Missense 9:129874727-129874727 + TCGA-CD-A4MG-01 COSM3904744 c.1729C>T p.R577W Substitution - Missense 9:129873733-129873733 + PD13602a COSM5780056 c.903C>T p.G301G Substitution - coding silent 9:129868217-129868217 + TCGA-FR-A3R1-01 COSM3654851 c.2394C>T p.I798I Substitution - coding silent 9:129876223-129876223 + sysucc-773T COSM5460380 c.1077C>G p.D359E Substitution - Missense 9:129868391-129868391 + HCT8 COSM1674890 c.1306C>T p.R436W Substitution - Missense 9:129869339-129869339 + SNU-C2B COSM1105885 c.501G>A p.P167P Substitution - coding silent 9:129863189-129863189 + TCGA-AZ-4315-01 COSM1460455 c.2606C>T p.S869L Substitution - Missense 9:129880134-129880134 + Au5 COSM5606179 c.673C>T p.R225* Substitution - Nonsense 9:129865364-129865364 + YULOCUS COSM5410528 c.2700C>T p.N900N Substitution - coding silent 9:129880228-129880228 + TCGA-AP-A0LM-01 COSM1105934 c.2697G>T p.E899D Substitution - Missense 9:129880225-129880225 + TCGA-12-3649-01 COSM3413378 c.2372C>T p.A791V Substitution - Missense 9:129876201-129876201 + TCGA-B5-A11E-01 COSM1105892 c.890G>A p.G297E Substitution - Missense 9:129868204-129868204 + HCT-15 COSM1674890 c.1306C>T p.R436W Substitution - Missense 9:129869339-129869339 + I2L-P19Ta-Tumor-Organoid COSM5359256 c.2335G>A p.V779M Substitution - Missense 9:129876164-129876164 + I2L-P19Ta-Tumor-Organoid COSM5359254 c.2335G>A p.V779M Substitution - Missense 9:129876164-129876164 + pfg122T COSM4761497 c.46G>T p.E16* Substitution - Nonsense 9:129852601-129852601 + SNU-175 COSM1231988 c.1837C>T p.R613C Substitution - Missense 9:129874672-129874672 + 587238 COSM1231988 c.1837C>T p.R613C Substitution - Missense 9:129874672-129874672 + Gp5D COSM3328749 c.2444G>A p.G815D Substitution - Missense 9:129878372-129878372 + TARGET-20-PABLDZ-09A-02D COSM5487226 c.826C>T p.R276W Substitution - Missense 9:129868140-129868140 + U87 COSM1105893 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + PTC-7C COSM4163408 c.171T>C p.F57F Substitution - coding silent 9:129858085-129858085 + TCGA-F1-A448-01 COSM3904756 c.2430C>T p.A810A Substitution - coding silent 9:129878358-129878358 + TCGA-AA-3663-01 COSM1460443 c.397G>A p.E133K Substitution - Missense 9:129861003-129861003 + TCGA-A4-7584-01 COSM3996368 c.334T>C p.S112P Substitution - Missense 9:129860940-129860940 + TCGA-G3-A7M5-01 COSM4941964 c.1758A>T p.L586L Substitution - coding silent 9:129874593-129874593 + LN229 COSM1105893 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + sysucc-834T COSM5486717 c.2170G>A p.A724T Substitution - Missense 9:129875431-129875431 + SH-0622 COSM3328722 c.2005G>A p.E669K Substitution - Missense 9:129874912-129874912 + OSCC-GB_00450111 COSM3716227 c.956G>A p.R319Q Substitution - Missense 9:129868270-129868270 + PTC-54C COSM4163419 c.2068A>G p.M690V Substitution - Missense 9:129875329-129875329 + RMS80_ COSM4988758 c.1990G>A p.V664I Substitution - Missense 9:129874897-129874897 + DN11120 COSM5780056 c.903C>T p.G301G Substitution - coding silent 9:129868217-129868217 + TCGA-F1-A448-01 COSM3904758 c.2430C>T p.A810A Substitution - coding silent 9:129878358-129878358 + TCGA-AX-A05S-01 COSM1105922 c.1834C>A p.L612M Substitution - Missense 9:129874669-129874669 + TCGA-AP-A0LM-01 COSM1105936 c.2697G>T p.E899D Substitution - Missense 9:129880225-129880225 + BD112T COSM5490850 c.1395A>G p.V465V Substitution - coding silent 9:129869674-129869674 + TCGA-06-0130 COSM2149539 c.290_291delCA p.A97fs*12 Deletion - Frameshift 9:129858558-129858559 + T1154 COSM4739694 c.467T>C p.M156T Substitution - Missense 9:129861582-129861582 + PT52 COSM5939979 c.1438C>T p.P480S Substitution - Missense 9:129869717-129869717 + T3202 COSM4739705 c.2035G>A p.V679I Substitution - Missense 9:129874942-129874942 + 86323 COSM96261 c.477C>T p.A159A Substitution - coding silent 9:129861592-129861592 + TCGA-70-6722-01 COSM752563 c.2642G>C p.G881A Substitution - Missense 9:129880170-129880170 + PTC-54C COSM3982749 c.2172G>A p.A724A Substitution - coding silent 9:129875433-129875433 + ESOSCC157T COSM1173455 c.2666G>A p.R889H Substitution - Missense 9:129880194-129880194 + 587336 COSM1231997 c.757G>A p.A253T Substitution - Missense 9:129868071-129868071 + 8015109 COSM3395617 c.1264G>A p.V422M Substitution - Missense 9:129868990-129868990 + TCGA-H4-A2HQ-01 COSM1314561 c.1892C>T p.S631L Substitution - Missense 9:129874727-129874727 + 3101B7_032_T COSM5043199 c.1441G>T p.G481* Substitution - Nonsense 9:129869720-129869720 + S01297 COSM5667810 c.1929C>G p.H643Q Substitution - Missense 9:129874836-129874836 + HCC041T COSM5809570 c.2426A>C p.Q809P Substitution - Missense 9:129878354-129878354 + TCGA-AG-3891-01 COSM5069298 c.676G>A p.G226S Substitution - Missense 9:129865367-129865367 + CSCC-31-T COSM4152097 c.1738G>A p.E580K Substitution - Missense 9:129873742-129873742 + Au5 COSM5606177 c.673C>T p.R225* Substitution - Nonsense 9:129865364-129865364 + CSCC-55-T COSM4565612 c.2305_2306GG>AA p.G769K Substitution - Missense 9:129876134-129876135 + Au3 COSM5602578 c.1845C>T p.F615F Substitution - coding silent 9:129874680-129874680 + TCGA-CK-4951-01 COSM5153239 c.1267C>A p.L423I Substitution - Missense 9:129868993-129868993 + TCGA-CG-5721-01 COSM3904735 c.220G>A p.V74M Substitution - Missense 9:129858488-129858488 + CSCC-31-T COSM4529990 c.1659G>A p.K553K Substitution - coding silent 9:129870546-129870546 + TCGA-DK-A2I4-01 COSM3779730 c.828G>C p.R276R Substitution - coding silent 9:129868142-129868142 + ESCC_BICR_045T COSM5441810 c.2425C>T p.Q809* Substitution - Nonsense 9:129878353-129878353 + TCGA-HU-A4GP-01 COSM1314561 c.1892C>T p.S631L Substitution - Missense 9:129874727-129874727 + BD72T COSM5512621 c.2143G>A p.E715K Substitution - Missense 9:129875404-129875404 + TCGA-D3-A51G-06 COSM3654838 c.646G>A p.G216R Substitution - Missense 9:129865337-129865337 + TCGA-D5-6530-01 COSM5163181 c.976C>A p.R326R Substitution - coding silent 9:129868290-129868290 + H1703 COSM1196635 c.1831G>A p.D611N Substitution - Missense 9:129874666-129874666 + BD72T COSM5512619 c.2143G>A p.E715K Substitution - Missense 9:129875404-129875404 + AOCS-155-3-5 COSM4152095 c.1738G>A p.E580K Substitution - Missense 9:129873742-129873742 + TCGA-D1-A103-01 COSM1105903 c.1536G>A p.W512* Substitution - Nonsense 9:129869815-129869815 + ATL089 COSM5711163 c.950C>T p.A317V Substitution - Missense 9:129868264-129868264 + DF01 COSM5759493 c.919G>T p.A307S Substitution - Missense 9:129868233-129868233 + TCGA-DU-7010-01 COSM3929848 c.1339G>T p.D447Y Substitution - Missense 9:129869372-129869372 + TCGA-BR-4184-01 COSM3904747 c.1838G>A p.R613H Substitution - Missense 9:129874673-129874673 + T1154 COSM4739693 c.467T>C p.M156T Substitution - Missense 9:129861582-129861582 + PT52 COSM5939981 c.1438C>T p.P480S Substitution - Missense 9:129869717-129869717 + SNUH_G16_S1 COSM3982749 c.2172G>A p.A724A Substitution - coding silent 9:129875433-129875433 + ESCC-069T COSM3942919 c.1984C>T p.Q662* Substitution - Nonsense 9:129874891-129874891 + sysucc-1370T COSM5472675 c.1684C>T p.R562W Substitution - Missense 9:129873505-129873505 + TCGA-CJ-5684-01 COSM3367583 c.1769G>T p.R590L Substitution - Missense 9:129874604-129874604 + TCGA-AP-A051-01 COSM1105926 c.1915G>A p.A639T Substitution - Missense 9:129874750-129874750 + TCGA-D3-A3ML-06 COSM3654845 c.1562G>T p.R521L Substitution - Missense 9:129869841-129869841 + sysucc-834T COSM5486715 c.2170G>A p.A724T Substitution - Missense 9:129875431-129875431 + T98G COSM1105893 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + BN38T COSM3664146 c.1608C>T p.V536V Substitution - coding silent 9:129870495-129870495 + TCGA-CD-A4MG-01 COSM3904746 c.1729C>T p.R577W Substitution - Missense 9:129873733-129873733 + TCGA-BR-8081-01 COSM3904743 c.1023G>A p.S341S Substitution - coding silent 9:129868337-129868337 + 19M COSM5579956 c.648G>A p.G216G Substitution - coding silent 9:129865339-129865339 + HCC16 COSM1624622 c.686A>T p.Q229L Substitution - Missense 9:129865377-129865377 + SK-OV-3 COSM1674896 c.2235A>T p.K745N Substitution - Missense 9:129875576-129875576 + TCGA-D1-A103-01 COSM1105915 c.1794G>T p.K598N Substitution - Missense 9:129874629-129874629 + TCGA-DK-A2I4-01 COSM3779732 c.828G>C p.R276R Substitution - coding silent 9:129868142-129868142 + NB2272T COSM1236661 c.136-3C>A p.? Unknown 9:129858047-129858047 + TCGA-FS-A4FC-06 COSM3654848 c.2256G>A p.L752L Substitution - coding silent 9:129875597-129875597 + TCGA-D9-A1JW-06 COSM3654857 c.2553C>T p.V851V Substitution - coding silent 9:129879613-129879613 + 3101B7_032_T COSM5043201 c.1441G>T p.G481* Substitution - Nonsense 9:129869720-129869720 + H322T COSM1194860 c.830G>A p.S277N Substitution - Missense 9:129868144-129868144 + TCGA-AX-A0J1-01 COSM1105910 c.1686G>A p.R562R Substitution - coding silent 9:129873507-129873507 + TCGA-D1-A15X-01 COSM1105918 c.1827G>A p.G609G Substitution - coding silent 9:129874662-129874662 + TCGA-EE-A3J8-06 COSM3654835 c.87C>T p.T29T Substitution - coding silent 9:129856312-129856312 + TCGA-EE-A3AF-06 COSM3654859 c.2566C>T p.H856Y Substitution - Missense 9:129879626-129879626 + T3064 COSM4739702 c.1150G>A p.A384T Substitution - Missense 9:129868876-129868876 + TCGA-AA-3663-01 COSM1460445 c.397G>A p.E133K Substitution - Missense 9:129861003-129861003 + TCGA-29-1776-01 COSM1330694 c.1504G>A p.A502T Substitution - Missense 9:129869783-129869783 + TCGA-12-3649-01 COSM3413377 c.2372C>T p.A791V Substitution - Missense 9:129876201-129876201 + TCGA-AG-A002-01 COSM289808 c.163G>T p.E55* Substitution - Nonsense 9:129858077-129858077 + SNU-C2B COSM4651662 c.542G>A p.R181H Substitution - Missense 9:129863230-129863230 + Pat_53_B COSM5487226 c.826C>T p.R276W Substitution - Missense 9:129868140-129868140 + TCGA-D5-6530-01 COSM5163183 c.976C>A p.R326R Substitution - coding silent 9:129868290-129868290 + U87 COSM1105896 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + sysucc-311T COSM5467622 c.1774G>A p.E592K Substitution - Missense 9:129874609-129874609 + YULOCUS COSM5410529 c.2701C>T p.L901L Substitution - coding silent 9:129880229-129880229 + TCGA-BT-A20Q-01 COSM421937 c.41T>G p.I14R Substitution - Missense 9:129852596-129852596 + TCGA-46-3769-01 COSM752566 c.482A>C p.Q161P Substitution - Missense 9:129861597-129861597 + T3024 COSM4739711 c.2652C>T p.P884P Substitution - coding silent 9:129880180-129880180 + TCGA-EP-A2KA-01 COSM4917308 c.2665C>A p.R889S Substitution - Missense 9:129880193-129880193 + CPCG0248-F1 COSM4966771 c.899G>C p.R300P Substitution - Missense 9:129868213-129868213 + TCGA-AX-A0J1-01 COSM1105912 c.1686G>A p.R562R Substitution - coding silent 9:129873507-129873507 + HCC16T COSM1624622 c.686A>T p.Q229L Substitution - Missense 9:129865377-129865377 + Gp5D COSM3328751 c.2444G>A p.G815D Substitution - Missense 9:129878372-129878372 + C709 COSM4444162 c.1490C>T p.P497L Substitution - Missense 9:129869769-129869769 + TCGA-G3-A7M5-01 COSM4941962 c.1758A>T p.L586L Substitution - coding silent 9:129874593-129874593 + TCGA-BR-4184-01 COSM3904749 c.1838G>A p.R613H Substitution - Missense 9:129874673-129874673 + ESO-105 COSM1270056 c.1737C>T p.P579P Substitution - coding silent 9:129873741-129873741 + TCGA-BR-8680-01 COSM3328553 c.95C>T p.S32L Substitution - Missense 9:129856320-129856320 + TCGA-DK-A2I4-01 COSM3779733 c.1036G>A p.E346K Substitution - Missense 9:129868350-129868350 + TCGA-A4-7584-01 COSM3996366 c.334T>C p.S112P Substitution - Missense 9:129860940-129860940 + TCGA-CC-5261-01 COSM4933564 c.1854G>A p.K618K Substitution - coding silent 9:129874689-129874689 + T3064 COSM4739699 c.904delG p.G303fs*10 Deletion - Frameshift 9:129868218-129868218 + TCGA-FW-A3R5-06 COSM3926283 c.336C>T p.S112S Substitution - coding silent 9:129860942-129860942 + TCGA-CG-4300-01 COSM3904755 c.2171C>T p.A724V Substitution - Missense 9:129875432-129875432 + 45T COSM3716226 c.956G>A p.R319Q Substitution - Missense 9:129868270-129868270 + Au3 COSM5602576 c.1845C>T p.F615F Substitution - coding silent 9:129874680-129874680 + TCGA-25-2401-01 COSM86770 c.1498C>T p.P500S Substitution - Missense 9:129869777-129869777 + sysucc-1237T COSM5764539 c.1821C>T p.L607L Substitution - coding silent 9:129874656-129874656 + DLD1 COSM1674892 c.1306C>T p.R436W Substitution - Missense 9:129869339-129869339 + MO_1176 COSM5572862 c.252C>T p.Y84Y Substitution - coding silent 9:129858520-129858520 + TCGA-FW-A3R5-06 COSM3926285 c.336C>T p.S112S Substitution - coding silent 9:129860942-129860942 + TARGET-30-PASCJJ COSM1288849 c.118C>T p.L40L Substitution - coding silent 9:129856343-129856343 + I2L-P19Ta-Tumor-Biopsy COSM5359254 c.2335G>A p.V779M Substitution - Missense 9:129876164-129876164 + TCGA-AG-A002-01 COSM289807 c.163G>T p.E55* Substitution - Nonsense 9:129858077-129858077 + H322T COSM1194862 c.830G>A p.S277N Substitution - Missense 9:129868144-129868144 + S01297 COSM5667808 c.1929C>G p.H643Q Substitution - Missense 9:129874836-129874836 + YUKAT COSM5410525 c.597C>T p.V199V Substitution - coding silent 9:129863285-129863285 + LUAD-F00057 COSM339541 c.163G>A p.E55K Substitution - Missense 9:129858077-129858077 + ESO-1145 COSM1270055 c.1780_1781insTG p.Y595fs*58 Insertion - Frameshift 9:129874615-129874616 + TCGA-FR-A3R1-01 COSM3654850 c.2394C>T p.I798I Substitution - coding silent 9:129876223-129876223 + CSCC-41-T COSM4461905 c.1225C>T p.P409S Substitution - Missense 9:129868951-129868951 + 753-01-5TD COSM5419021 c.2482T>C p.W828R Substitution - Missense 9:129878410-129878410 + SNU-175 COSM3328722 c.2005G>A p.E669K Substitution - Missense 9:129874912-129874912 + TCGA-G4-6302-01 COSM5175136 c.2409+4C>T p.? Unknown 9:129876242-129876242 + 19M COSM5579954 c.648G>A p.G216G Substitution - coding silent 9:129865339-129865339 + Pat_73_B COSM5875671 c.2567A>G p.H856R Substitution - Missense 9:129879627-129879627 + TCGA-DS-A7WF-01 COSM4821657 c.2250C>A p.D750E Substitution - Missense 9:129875591-129875591 + CSCC-55-T COSM4565614 c.2305_2306GG>AA p.G769K Substitution - Missense 9:129876134-129876135 + PD7240a COSM5781905 c.2317G>A p.A773T Substitution - Missense 9:129876146-129876146 + H1155 COSM1173455 c.2666G>A p.R889H Substitution - Missense 9:129880194-129880194 + TCGA-EJ-5502-01 COSM1472167 c.2518C>T p.P840S Substitution - Missense 9:129879578-129879578 + HT115 COSM3328619 c.976C>T p.R326W Substitution - Missense 9:129868290-129868290 + LUAD-F00057 COSM339543 c.163G>A p.E55K Substitution - Missense 9:129858077-129858077 + TCGA-AG-A002-01 COSM264596 c.709C>T p.R237C Substitution - Missense 9:129868023-129868023 + TCGA-D1-A174-01 COSM1105937 c.2734C>T p.R912W Substitution - Missense 9:129880262-129880262 + TCGA-FY-A3R6-01 COSM3375125 c.1391G>A p.R464Q Substitution - Missense 9:129869424-129869424 + tumor_4182393 COSM1161778 c.503C>A p.P168Q Substitution - Missense 9:129863191-129863191 + TCGA-EE-A3J8-06 COSM3654836 c.87C>T p.T29T Substitution - coding silent 9:129856312-129856312 + sysucc-771T COSM5446810 c.2304C>T p.F768F Substitution - coding silent 9:129876133-129876133 + SNU-175 COSM3328712 c.1783T>C p.Y595H Substitution - Missense 9:129874618-129874618 + TCGA-JX-A3Q0-01 COSM4824833 c.2040C>G p.L680L Substitution - coding silent 9:129874947-129874947 + TCGA-CG-5723-01 COSM3904752 c.2022C>T p.N674N Substitution - coding silent 9:129874929-129874929 + PD11336a COSM5797542 c.109G>A p.G37R Substitution - Missense 9:129856334-129856334 + TCGA-G4-6304-01 COSM5175971 c.2513-1G>T p.? Unknown 9:129879572-129879572 + Pat_45_B COSM5875667 c.2189C>T p.T730I Substitution - Missense 9:129875450-129875450 + I2L-P7-Tumor-Organoid COSM5036355 c.749C>T p.P250L Substitution - Missense 9:129868063-129868063 + 461 COSM1314558 c.172G>A p.A58T Substitution - Missense 9:129858086-129858086 + U373 COSM1105896 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + ESCC_BICR_045T COSM5441808 c.2425C>T p.Q809* Substitution - Nonsense 9:129878353-129878353 + TCGA-D3-A51G-06 COSM3654839 c.646G>A p.G216R Substitution - Missense 9:129865337-129865337 + CRC-02T COSM5455736 c.574T>C p.Y192H Substitution - Missense 9:129863262-129863262 + 8015109 COSM3395616 c.1264G>A p.V422M Substitution - Missense 9:129868990-129868990 + TCGA-D5-6928-01 COSM1460446 c.773C>T p.T258M Substitution - Missense 9:129868087-129868087 + MOLT-4 COSM1674895 c.2041T>C p.F681L Substitution - Missense 9:129874948-129874948 + RK021_C01 COSM1636058 c.1565+10C>G p.? Unknown 9:129869854-129869854 + GCT27 COSM5749461 c.199G>A p.A67T Substitution - Missense 9:129858467-129858467 + YULOCUS COSM5410526 c.2700C>T p.N900N Substitution - coding silent 9:129880228-129880228 + sysucc-771T COSM5446808 c.2304C>T p.F768F Substitution - coding silent 9:129876133-129876133 + TCGA-AR-A0TY-01 COSM455465 c.367_368delCC p.P123fs*5 Deletion - Frameshift 9:129860973-129860974 + CPCG0248-F1 COSM4966770 c.899G>C p.R300P Substitution - Missense 9:129868213-129868213 + TCGA-G4-6302-01 COSM5175134 c.2409+4C>T p.? Unknown 9:129876242-129876242 + TCGA-CK-4951-01 COSM5153237 c.1267C>A p.L423I Substitution - Missense 9:129868993-129868993 + SH-0622 COSM3328724 c.2005G>A p.E669K Substitution - Missense 9:129874912-129874912 + sysucc-1237T COSM5764537 c.1821C>T p.L607L Substitution - coding silent 9:129874656-129874656 + GHE0436 COSM5713768 c.2720T>A p.I907N Substitution - Missense 9:129880248-129880248 + 107702 COSM95741 c.427+1G>C p.? Unknown 9:129861034-129861034 + TCGA-B5-A11E-01 COSM1105889 c.890G>A p.G297E Substitution - Missense 9:129868204-129868204 + PT49 COSM5935524 c.1822G>A p.E608K Substitution - Missense 9:129874657-129874657 + SNU-175 COSM3328710 c.1783T>C p.Y595H Substitution - Missense 9:129874618-129874618 + TCGA-AP-A0LM-01 COSM1105930 c.2562C>T p.S854S Substitution - coding silent 9:129879622-129879622 + TCGA-AA-3833-01 COSM271592 c.761C>T p.T254M Substitution - Missense 9:129868075-129868075 + 45T COSM3716227 c.956G>A p.R319Q Substitution - Missense 9:129868270-129868270 + I2L-P28-Tumor-Biopsy COSM5359501 c.2278G>A p.V760I Substitution - Missense 9:129875619-129875619 + KPOPBR-39-T COSM5964550 c.1922-2A>T p.? Unknown 9:129874827-129874827 + TCGA-HU-A4GP-01 COSM1314563 c.1892C>T p.S631L Substitution - Missense 9:129874727-129874727 + TCGA-AG-A002-01 COSM264597 c.709C>T p.R237C Substitution - Missense 9:129868023-129868023 + ESCC-069T COSM3942921 c.1984C>T p.Q662* Substitution - Nonsense 9:129874891-129874891 + CSCC-41-T COSM4538017 c.2494G>C p.V832L Substitution - Missense 9:129878422-129878422 + TCGA-EE-A3AF-06 COSM3654860 c.2566C>T p.H856Y Substitution - Missense 9:129879626-129879626 + TCGA-BH-A18P-01 COSM1489730 c.2052G>A p.K684K Substitution - coding silent 9:129875313-129875313 + TCGA-D1-A17M-01 COSM1105888 c.501G>A p.P167P Substitution - coding silent 9:129863189-129863189 + TCGA-DD-A3A9-01 COSM4920770 c.1477T>C p.Y493H Substitution - Missense 9:129869756-129869756 + RK001_C01 COSM1636062 c.2141G>T p.R714L Substitution - Missense 9:129875402-129875402 + TCGA-CG-5721-01 COSM3904738 c.951G>A p.A317A Substitution - coding silent 9:129868265-129868265 + TCGA-D9-A1JW-06 COSM3654856 c.2553C>T p.V851V Substitution - coding silent 9:129879613-129879613 + 107702 COSM95742 c.427+1G>C p.? Unknown 9:129861034-129861034 + T3266 COSM4739697 c.827G>A p.R276Q Substitution - Missense 9:129868141-129868141 + TCGA-EK-A2PM-01 COSM4831360 c.672C>G p.F224L Substitution - Missense 9:129865363-129865363 + T3202 COSM4739706 c.2035G>A p.V679I Substitution - Missense 9:129874942-129874942 + 8044606 COSM3395616 c.1264G>A p.V422M Substitution - Missense 9:129868990-129868990 + TCGA-EK-A2PM-01 COSM4831362 c.672C>G p.F224L Substitution - Missense 9:129865363-129865363 + TCGA-CC-5261-01 COSM4933562 c.1854G>A p.K618K Substitution - coding silent 9:129874689-129874689 + TCGA-DU-7010-01 COSM3929846 c.1339G>T p.D447Y Substitution - Missense 9:129869372-129869372 + PD11336a COSM5797544 c.109G>A p.G37R Substitution - Missense 9:129856334-129856334 + TCGA-CF-A3MI-01 COSM1314558 c.172G>A p.A58T Substitution - Missense 9:129858086-129858086 + U343 COSM1105893 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + U343 COSM1105896 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + TCGA-D1-A103-01 COSM1105913 c.1794G>T p.K598N Substitution - Missense 9:129874629-129874629 + TCGA-CJ-5684-01 COSM3367582 c.1769G>T p.R590L Substitution - Missense 9:129874604-129874604 + T3064 COSM4739700 c.904delG p.G303fs*10 Deletion - Frameshift 9:129868218-129868218 + ESCC-098T COSM3942916 c.1618G>A p.E540K Substitution - Missense 9:129870505-129870505 + 2521249 COSM5888068 c.1067C>T p.A356V Substitution - Missense 9:129868381-129868381 + TCGA-06-0130 COSM2149541 c.290_291delCA p.A97fs*12 Deletion - Frameshift 9:129858558-129858559 + TCGA-BR-4201-01 COSM3779735 c.1036G>A p.E346K Substitution - Missense 9:129868350-129868350 + TCGA-BT-A20Q-01 COSM421935 c.41T>G p.I14R Substitution - Missense 9:129852596-129852596 + HCT8 COSM1674892 c.1306C>T p.R436W Substitution - Missense 9:129869339-129869339 + LP6005334-DNA_G03 COSM5036357 c.749C>T p.P250L Substitution - Missense 9:129868063-129868063 + TCGA-BS-A0UF-01 COSM1105909 c.1638C>A p.F546L Substitution - Missense 9:129870525-129870525 + sysucc-1397T COSM5475231 c.2665C>T p.R889C Substitution - Missense 9:129880193-129880193 + SNUH_G16_S1 COSM3982751 c.2172G>A p.A724A Substitution - coding silent 9:129875433-129875433 + ESCC-248T COSM3942913 c.1263C>T p.Y421Y Substitution - coding silent 9:129868989-129868989 + CSCC-31-T COSM4529988 c.1659G>A p.K553K Substitution - coding silent 9:129870546-129870546 + PTC-14C COSM4163420 c.2093C>G p.S698C Substitution - Missense 9:129875354-129875354 + LS174T COSM3328715 c.1814_1815insC p.L607fs*54 Insertion - Frameshift 9:129874649-129874650 + sysucc-773T COSM5460377 c.1075G>C p.D359H Substitution - Missense 9:129868389-129868389 + Pat_53_B COSM5487228 c.826C>T p.R276W Substitution - Missense 9:129868140-129868140 + BD19T COSM5499738 c.368C>T p.P123L Substitution - Missense 9:129860974-129860974 + TCGA-D1-A17R-01 COSM1105893 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + LN18 COSM1105896 c.1072_1074delGAC p.D359delD Deletion - In frame 9:129868386-129868388 + C99 COSM4620543 c.1710G>A p.V570V Substitution - coding silent 9:129873714-129873714 + AOCS-155-3-5 COSM4152097 c.1738G>A p.E580K Substitution - Missense 9:129873742-129873742 + I2L-P28-Tumor-Organoid COSM5359503 c.2278G>A p.V760I Substitution - Missense 9:129875619-129875619 + PT49 COSM5935526 c.1822G>A p.E608K Substitution - Missense 9:129874657-129874657 + tumor_4182393 COSM1161776 c.503C>A p.P168Q Substitution - Missense 9:129863191-129863191 + GHE0436 COSM5713766 c.2720T>A p.I907N Substitution - Missense 9:129880248-129880248 + PTC-7C COSM4163410 c.171T>C p.F57F Substitution - coding silent 9:129858085-129858085 + PTC-28C COSM4163413 c.575A>T p.Y192F Substitution - Missense 9:129863263-129863263 + TCGA-EK-A2PM-01 COSM3328745 c.2431G>A p.E811K Substitution - Missense 9:129878359-129878359 + C709 COSM4444160 c.1490C>T p.P497L Substitution - Missense 9:129869769-129869769 + TCGA-AY-6197-01 COSM1460442 c.232A>C p.T78P Substitution - Missense 9:129858500-129858500 + LUAD-S00484 COSM343155 c.2107C>T p.R703W Substitution - Missense 9:129875368-129875368 + CSCC-40-T COSM4472975 c.1819C>T p.L607F Substitution - Missense 9:129874654-129874654 + T3024 COSM4739712 c.2652C>T p.P884P Substitution - coding silent 9:129880180-129880180 + T3064 COSM4739703 c.1150G>A p.A384T Substitution - Missense 9:129868876-129868876 + 587224 COSM1231993 c.2108G>A p.R703Q Substitution - Missense 9:129875369-129875369 + SNU-175 COSM1231990 c.1837C>T p.R613C Substitution - Missense 9:129874672-129874672 + LP6005334-DNA_G03 COSM5036355 c.749C>T p.P250L Substitution - Missense 9:129868063-129868063 + 61 COSM5738758 c.532G>A p.G178S Substitution - Missense 9:129863220-129863220 + TCGA-AX-A05S-01 COSM1105919 c.1834C>A p.L612M Substitution - Missense 9:129874669-129874669 + YULOCUS COSM5410531 c.2701C>T p.L901L Substitution - coding silent 9:129880229-129880229 + HCC16 COSM1624621 c.686A>T p.Q229L Substitution - Missense 9:129865377-129865377 + TCGA-BS-A0TA-01 COSM1105897 c.1369G>A p.V457M Substitution - Missense 9:129869402-129869402 + CSCC-40-T COSM4455207 c.698A>G p.Q233R Substitution - Missense 9:129868012-129868012 + 753-01-5TD COSM5419023 c.2482T>C p.W828R Substitution - Missense 9:129878410-129878410 + LS180 COSM3328713 c.1814_1815insC p.L607fs*54 Insertion - Frameshift 9:129874649-129874650 + Pat_73_B COSM5875673 c.2567A>G p.H856R Substitution - Missense 9:129879627-129879627 + 1N40-VS-1T40 COSM3654854 c.2493C>T p.F831F Substitution - coding silent 9:129878421-129878421 + T2197 COSM4739709 c.2514_2515insC p.G841fs*4 Insertion - Frameshift 9:129879574-129879575 + HCC16T COSM1624621 c.686A>T p.Q229L Substitution - Missense 9:129865377-129865377 + HCT15 COSM1674890 c.1306C>T p.R436W Substitution - Missense 9:129869339-129869339 + I2L-P28-Tumor-Biopsy COSM5359503 c.2278G>A p.V760I Substitution - Missense 9:129875619-129875619 + KM12 COSM3328599 c.769C>T p.L257L Substitution - coding silent 9:129868083-129868083 + sysucc-311T COSM5467624 c.1774G>A p.E592K Substitution - Missense 9:129874609-129874609 + CSCC-31-T COSM4152095 c.1738G>A p.E580K Substitution - Missense 9:129873742-129873742 + BN38 COSM3664145 c.1608C>T p.V536V Substitution - coding silent 9:129870495-129870495 + 1265T COSM5762577 c.2524C>G p.P842A Substitution - Missense 9:129879584-129879584 + Pat_06_B COSM5875668 c.2266C>A p.L756M Substitution - Missense 9:129875607-129875607 + T3174 COSM4739690 c.102G>A p.G34G Substitution - coding silent 9:129856327-129856327 + SK-OV-3 COSM1674898 c.2235A>T p.K745N Substitution - Missense 9:129875576-129875576 + TCGA-FS-A4FC-06 COSM3654847 c.2256G>A p.L752L Substitution - coding silent 9:129875597-129875597 + CSCC-41-T COSM4461903 c.1225C>T p.P409S Substitution - Missense 9:129868951-129868951 + TCGA-BR-8680-01 COSM3328551 c.95C>T p.S32L Substitution - Missense 9:129856320-129856320 + RK021_C01 COSM1636059 c.1565+10C>G p.? Unknown 9:129869854-129869854 + MOLT-4 COSM1674893 c.2041T>C p.F681L Substitution - Missense 9:129874948-129874948 + TCGA-E9-A2JS-01 COSM3847842 c.2031C>A p.G677G Substitution - coding silent 9:129874938-129874938 + 587228 COSM1231991 c.2732C>T p.T911M Substitution - Missense 9:129880260-129880260 + LS180 COSM3328715 c.1814_1815insC p.L607fs*54 Insertion - Frameshift 9:129874649-129874650 + TCGA-HT-8564-01 COSM3328653 c.1186G>A p.V396I Substitution - Missense 9:129868912-129868912 + 587224 COSM1231995 c.2426A>G p.Q809R Substitution - Missense 9:129878354-129878354 + TCGA-D1-A103-01 COSM1105927 c.2523G>A p.G841G Substitution - coding silent 9:129879583-129879583 + TCGA-FY-A3R6-01 COSM3375126 c.1391G>A p.R464Q Substitution - Missense 9:129869424-129869424 + T3266 COSM4739696 c.827G>A p.R276Q Substitution - Missense 9:129868141-129868141 + CSCC-41-T COSM4538019 c.2494G>C p.V832L Substitution - Missense 9:129878422-129878422 + TCGA-CG-5723-01 COSM3904750 c.2022C>T p.N674N Substitution - coding silent 9:129874929-129874929 + 461 COSM1314560 c.172G>A p.A58T Substitution - Missense 9:129858086-129858086 + BN38T COSM3664145 c.1608C>T p.V536V Substitution - coding silent 9:129870495-129870495 + pfg122T COSM4761498 c.46G>T p.E16* Substitution - Nonsense 9:129852601-129852601 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.5452 9q34.11

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.Q161P c.482A>C 9 132623876 LUSC A G Missense p.D484G c.1451A>G 9 132632009 CM C A Missense p.L576M c.1726C>A 9 132636009 STAD C A Missense p.L612M c.1834C>A 9 132636948 UCEC C A Missense p.P168Q c.503C>A 9 132625470 DLBCL CC - Frameshift p.P123Yfs*5 c.367_368delCC 9 132623252 BRCA CC TT Missense p.P374F c.1120_1121delinsTT 9 132630713 CM C G IntronicSNV . c.1565+10C>G 9 132632133 HC C G Missense p.L460V c.1378C>G 9 132631690 PAAD C T Missense p.A724V c.2171C>T 9 132637711 STAD C T Missense p.A791V c.2372C>T 9 132638480 GBM C T Missense p.H856Y c.2566C>T 9 132641905 CM C T Missense p.P500S c.1498C>T 9 132632056 OV C T Missense p.S631L c.1892C>T 9 132637006 BLCA C T Synonymous p.F235F c.705C>T 9 132630298 CM C T Synonymous p.L40L c.118C>T 9 132618622 NB C T Synonymous p.P579P c.1737C>T 9 132636020 ESCA C T Synonymous p.P743P c.2229C>T 9 132637849 LUAD C T Synonymous p.S698S c.2094C>T 9 132637634 LUAD C T Synonymous p.T29T c.87C>T 9 132618591 CM C T Synonymous p.V754V c.2262C>T 9 132637882 HNSC C T Synonymous p.V851V c.2553C>T 9 132641892 CM G A Missense p.A58T c.172G>A 9 132620365 BLCA G A Missense p.E346K c.1036G>A 9 132630629 BLCA G A Missense p.E346K c.1036G>A 9 132630629 STAD G A Missense p.R464Q c.1391G>A 9 132631703 THCA G A Missense p.V457M c.1369G>A 9 132631681 UCEC G A Missense p.V914M c.2740G>A 9 132642547 COREAD G A Synonymous p.P167P c.501G>A 9 132625468 UCEC G A Synonymous p.R416R c.1248G>A 9 132631253 CM G A Synonymous p.T258T c.774G>A 9 132630367 CM G C Missense p.G881A c.2642G>C 9 132642449 LUSC G C Synonymous p.R276R c.828G>C 9 132630421 BLCA G T Missense p.R521L c.1562G>T 9 132632120 CM G T Missense p.R590L c.1769G>T 9 132636883 RCCC G T Missense p.R714L c.2141G>T 9 132637681 HC G T Synonymous p.A362A c.1086G>T 9 132630679 LUAD TC - Frameshift p.S197*fs*1 c.590_591delCT 9 132625554 GBM - T Frameshift p.H591Afs*70 c.1769_1770insT 9 132636883 RCCC - TG Frameshift p.M594Ifs*59 c.1781_1782insTG 9 132636895 ESCA T G Missense p.I14R c.41T>G 9 132614875 BLCA