Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 3 32860419 32860419 + Missense_Mutation SNP G G C TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr3:32860419G>C c.847G>C c.(847-849)Gac>Cac p.D283H BLCA 3 32915444 32915444 + Silent SNP G G A TCGA-R3-A69X-01A-22D-A30E-08 TCGA-R3-A69X-10A-01D-A30H-08 g.chr3:32915444G>A c.987G>A c.(985-987)ctG>ctA p.L329L BLCA 3 32927521 32927521 + Silent SNP G G A TCGA-BT-A20O-01A-21D-A14W-08 TCGA-BT-A20O-11A-11D-A14W-08 g.chr3:32927521G>A c.1116G>A c.(1114-1116)aaG>aaA p.K372K BLCA 3 32932040 32932040 + Silent SNP G G A TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr3:32932040G>A c.1344G>A c.(1342-1344)cgG>cgA p.R448R BLCA 3 32932056 32932056 + Nonsense_Mutation SNP C C T TCGA-DK-A6AV-01A-12D-A30E-08 TCGA-DK-A6AV-10A-01D-A30H-08 g.chr3:32932056C>T c.1360C>T c.(1360-1362)Cag>Tag p.Q454* BLCA 3 32932092 32932092 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr3:32932092C>G c.1396C>G c.(1396-1398)Cag>Gag p.Q466E BLCA 3 32932217 32932217 + Silent SNP C C A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr3:32932217C>A c.1521C>A c.(1519-1521)gtC>gtA p.V507V BLCA 3 32932318 32932318 + Missense_Mutation SNP G G C TCGA-FD-A3B4-01A-12D-A202-08 TCGA-FD-A3B4-10A-01D-A202-08 g.chr3:32932318G>C c.1622G>C c.(1621-1623)aGt>aCt p.S541T BLCA 3 32932410 32932410 + Missense_Mutation SNP G G C TCGA-CF-A3MG-01A-11D-A20D-08 TCGA-CF-A3MG-10A-01D-A20D-08 g.chr3:32932410G>C c.1714G>C c.(1714-1716)Gag>Cag p.E572Q BLCA 3 32932639 32932639 + Missense_Mutation SNP C C T TCGA-XF-A9SM-01A-11D-A42E-08 TCGA-XF-A9SM-10A-01D-A42H-08 g.chr3:32932639C>T c.1943C>T c.(1942-1944)tCc>tTc p.S648F BLCA 3 32932659 32932659 + Nonsense_Mutation SNP C C T TCGA-ZF-AA54-01A-11D-A391-08 TCGA-ZF-AA54-10A-01D-A394-08 g.chr3:32932659C>T c.1963C>T c.(1963-1965)Cga>Tga p.R655* BLCA 3 32932722 32932722 + Missense_Mutation SNP C C T TCGA-FD-A6TF-01A-52D-A32B-08 TCGA-FD-A6TF-10A-21D-A329-08 g.chr3:32932722C>T c.2026C>T c.(2026-2028)Cgc>Tgc p.R676C BLCA 3 32932942 32932942 + Missense_Mutation SNP C C A TCGA-E7-A97Q-01A-11D-A38G-08 TCGA-E7-A97Q-10A-01D-A38J-08 g.chr3:32932942C>A c.2246C>A c.(2245-2247)tCc>tAc p.S749Y BLCA 3 32933231 32933231 + Silent SNP C C T TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr3:32933231C>T c.2535C>T c.(2533-2535)tcC>tcT p.S845S BRCA 3 32932211 32932211 + Missense_Mutation SNP C C A TCGA-A8-A06Q-01A-11W-A050-09 TCGA-A8-A06Q-10A-01W-A055-09 g.chr3:32932211C>A c.1515C>A c.(1513-1515)ttC>ttA p.F505L BRCA 3 32933156 32933156 + Missense_Mutation SNP G G T TCGA-B6-A0IM-01A-11W-A050-09 TCGA-B6-A0IM-10A-01W-A055-09 g.chr3:32933156G>T c.2460G>T c.(2458-2460)atG>atT p.M820I BRCA 3 32933232 32933232 + Missense_Mutation SNP G G A TCGA-E2-A156-01A-11D-A12B-09 TCGA-E2-A156-10A-01D-A12B-09 g.chr3:32933232G>A c.2536G>A c.(2536-2538)Ggc>Agc p.G846S CESC 3 32915396 32915396 + Silent SNP C C T TCGA-FU-A3TX-01A-11D-A22X-09 TCGA-FU-A3TX-10A-01D-A22X-09 g.chr3:32915396C>T c.939C>T c.(937-939)taC>taT p.Y313Y COAD 3 32859629 32859629 + Silent SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr3:32859629C>T c.57C>T c.(55-57)tgC>tgT p.C19C COAD 3 32859658 32859658 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr3:32859658C>T c.86C>T c.(85-87)tCg>tTg p.S29L COAD 3 32927475 32927475 + Missense_Mutation SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr3:32927475C>T c.1070C>T c.(1069-1071)gCg>gTg p.A357V COAD 3 32927475 32927475 + Missense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:32927475C>T c.1070C>T c.(1069-1071)gCg>gTg p.A357V COAD 3 32931948 32931948 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr3:32931948G>A c.1252G>A c.(1252-1254)Gtg>Atg p.V418M COAD 3 32932074 32932074 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr3:32932074A>G c.1378A>G c.(1378-1380)Atg>Gtg p.M460V COAD 3 32932353 32932353 + Nonsense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr3:32932353C>T c.1657C>T c.(1657-1659)Cga>Tga p.R553* COAD 3 32932642 32932642 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr3:32932642G>A c.1946G>A c.(1945-1947)cGg>cAg p.R649Q COAD 3 32932939 32932939 + Missense_Mutation SNP A A T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr3:32932939A>T c.2243A>T c.(2242-2244)gAc>gTc p.D748V COAD 3 32932999 32932999 + Missense_Mutation SNP A A G TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr3:32932999A>G c.2303A>G c.(2302-2304)aAc>aGc p.N768S COAD 3 32933066 32933066 + Silent SNP C C A TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr3:32933066C>A c.2370C>A c.(2368-2370)ggC>ggA p.G790G COAD 3 32933116 32933116 + Missense_Mutation SNP G G A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr3:32933116G>A c.2420G>A c.(2419-2421)cGc>cAc p.R807H COAD 3 32933286 32933286 + Nonsense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:32933286C>T c.2590C>T c.(2590-2592)Cga>Tga p.R864* COADREAD 3 32859629 32859629 + Silent SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr3:32859629C>T c.57C>T c.(55-57)tgC>tgT p.C19C COADREAD 3 32859658 32859658 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr3:32859658C>T c.86C>T c.(85-87)tCg>tTg p.S29L COADREAD 3 32927475 32927475 + Missense_Mutation SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr3:32927475C>T c.1070C>T c.(1069-1071)gCg>gTg p.A357V COADREAD 3 32927475 32927475 + Missense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:32927475C>T c.1070C>T c.(1069-1071)gCg>gTg p.A357V COADREAD 3 32931948 32931948 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr3:32931948G>A c.1252G>A c.(1252-1254)Gtg>Atg p.V418M COADREAD 3 32932074 32932074 + Missense_Mutation SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr3:32932074A>G c.1378A>G c.(1378-1380)Atg>Gtg p.M460V COADREAD 3 32932173 32932173 + Missense_Mutation SNP G G T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr3:32932173G>T c.1477G>T c.(1477-1479)Ggc>Tgc p.G493C COADREAD 3 32932353 32932353 + Nonsense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr3:32932353C>T c.1657C>T c.(1657-1659)Cga>Tga p.R553* COADREAD 3 32932642 32932642 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr3:32932642G>A c.1946G>A c.(1945-1947)cGg>cAg p.R649Q COADREAD 3 32932939 32932939 + Missense_Mutation SNP A A T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr3:32932939A>T c.2243A>T c.(2242-2244)gAc>gTc p.D748V COADREAD 3 32932999 32932999 + Missense_Mutation SNP A A G TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr3:32932999A>G c.2303A>G c.(2302-2304)aAc>aGc p.N768S COADREAD 3 32933066 32933066 + Silent SNP C C A TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr3:32933066C>A c.2370C>A c.(2368-2370)ggC>ggA p.G790G COADREAD 3 32933116 32933116 + Missense_Mutation SNP G G A TCGA-D5-6927-01A-21D-1924-10 TCGA-D5-6927-10A-01D-1924-10 g.chr3:32933116G>A c.2420G>A c.(2419-2421)cGc>cAc p.R807H COADREAD 3 32933286 32933286 + Nonsense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr3:32933286C>T c.2590C>T c.(2590-2592)Cga>Tga p.R864* COADREAD 3 32933287 32933287 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:32933287G>A c.2591G>A c.(2590-2592)cGa>cAa p.R864Q ESCA 3 32859629 32859629 + Silent SNP C C T TCGA-L5-A88S-01A-11D-A36J-09 TCGA-L5-A88S-11A-21D-A36M-09 g.chr3:32859629C>T c.57C>T c.(55-57)tgC>tgT p.C19C ESCA 3 32931919 32931919 + Missense_Mutation SNP T T C TCGA-L5-A4ON-01A-11D-A27G-09 TCGA-L5-A4ON-11A-21D-A27G-09 g.chr3:32931919T>C c.1223T>C c.(1222-1224)cTc>cCc p.L408P ESCA 3 32932232 32932232 + Silent SNP C C T TCGA-LN-A7HZ-01A-31D-A351-09 TCGA-LN-A7HZ-10A-01D-A351-09 g.chr3:32932232C>T c.1536C>T c.(1534-1536)caC>caT p.H512H ESCA 3 32932582 32932582 + Missense_Mutation SNP G G C TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr3:32932582G>C c.1886G>C c.(1885-1887)cGc>cCc p.R629P GBM 3 32859692 32859692 + Silent SNP G G A TCGA-06-0195-01B-01D-1491-08 TCGA-06-0195-10A-01D-1491-08 g.chr3:32859692G>A c.120G>A c.(118-120)acG>acA p.T40T GBM 3 32859711 32859711 + Missense_Mutation SNP G G A TCGA-76-6280-01A-21D-1845-08 TCGA-76-6280-10A-01D-1845-08 g.chr3:32859711G>A c.139G>A c.(139-141)Ggg>Agg p.G47R GBM 3 32915463 32915463 + Nonsense_Mutation SNP C C T TCGA-19-5954-01A-11D-1696-08 TCGA-19-5954-11A-01D-1696-08 g.chr3:32915463C>T c.1006C>T c.(1006-1008)Cga>Tga p.R336* GBM 3 32932739 32932739 + Silent SNP G G A TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chr3:32932739G>A c.2043G>A c.(2041-2043)acG>acA p.T681T GBM 3 32933041 32933041 + Missense_Mutation SNP G G A TCGA-06-0174-01A-01D-1491-08 TCGA-06-0174-10B-01D-1491-08 g.chr3:32933041G>A c.2345G>A c.(2344-2346)cGc>cAc p.R782H GBM 3 32933302 32933302 + Silent SNP A A G TCGA-28-5215-01A-01D-1486-08 TCGA-28-5215-10A-01D-1486-08 g.chr3:32933302A>G c.2606A>G c.(2605-2607)tAa>tGa p.*869* GBMLGG 3 32859692 32859692 + Silent SNP G G A TCGA-06-0195-01B-01D-1491-08 TCGA-06-0195-10A-01D-1491-08 g.chr3:32859692G>A c.120G>A c.(118-120)acG>acA p.T40T GBMLGG 3 32859711 32859711 + Missense_Mutation SNP G G A TCGA-76-6280-01A-21D-1845-08 TCGA-76-6280-10A-01D-1845-08 g.chr3:32859711G>A c.139G>A c.(139-141)Ggg>Agg p.G47R GBMLGG 3 32915463 32915463 + Nonsense_Mutation SNP C C T TCGA-19-5954-01A-11D-1696-08 TCGA-19-5954-11A-01D-1696-08 g.chr3:32915463C>T c.1006C>T c.(1006-1008)Cga>Tga p.R336* GBMLGG 3 32927435 32927435 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:32927435G>A c.1030G>A c.(1030-1032)Gag>Aag p.E344K GBMLGG 3 32932670 32932670 + Silent SNP C C T TCGA-DB-A64L-01A-11D-A29Q-08 TCGA-DB-A64L-10A-01D-A29Q-08 g.chr3:32932670C>T c.1974C>T c.(1972-1974)ggC>ggT p.G658G GBMLGG 3 32932723 32932723 + Missense_Mutation SNP G G A TCGA-FG-A6IZ-01A-11D-A31L-08 TCGA-FG-A6IZ-10A-01D-A31J-08 g.chr3:32932723G>A c.2027G>A c.(2026-2028)cGc>cAc p.R676H GBMLGG 3 32932739 32932739 + Silent SNP G G A TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chr3:32932739G>A c.2043G>A c.(2041-2043)acG>acA p.T681T GBMLGG 3 32932914 32932914 + Missense_Mutation SNP G G A TCGA-DU-A6S6-01A-21D-A32B-08 TCGA-DU-A6S6-10A-01D-A329-08 g.chr3:32932914G>A c.2218G>A c.(2218-2220)Gag>Aag p.E740K GBMLGG 3 32933041 32933041 + Missense_Mutation SNP G G A TCGA-06-0174-01A-01D-1491-08 TCGA-06-0174-10B-01D-1491-08 g.chr3:32933041G>A c.2345G>A c.(2344-2346)cGc>cAc p.R782H GBMLGG 3 32933302 32933302 + Silent SNP A A G TCGA-28-5215-01A-01D-1486-08 TCGA-28-5215-10A-01D-1486-08 g.chr3:32933302A>G c.2606A>G c.(2605-2607)tAa>tGa p.*869* HNSC 3 32931915 32931915 + Missense_Mutation SNP A A C TCGA-CR-6471-01A-11D-1870-08 TCGA-CR-6471-10A-01D-1870-08 g.chr3:32931915A>C c.1219A>C c.(1219-1221)Aac>Cac p.N407H HNSC 3 32931948 32931948 + Missense_Mutation SNP G G A TCGA-CV-7422-01A-21D-2078-08 TCGA-CV-7422-10A-01D-2078-08 g.chr3:32931948G>A c.1252G>A c.(1252-1254)Gtg>Atg p.V418M HNSC 3 32932010 32932010 + Silent SNP G G T TCGA-CV-7245-01A-11D-2012-08 TCGA-CV-7245-10A-01D-2013-08 g.chr3:32932010G>T c.1314G>T c.(1312-1314)ctG>ctT p.L438L HNSC 3 32932864 32932864 + Missense_Mutation SNP G G A TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr3:32932864G>A c.2168G>A c.(2167-2169)cGg>cAg p.R723Q HNSC 3 32933083 32933083 + Missense_Mutation SNP G G A TCGA-CR-7382-01A-11D-2129-08 TCGA-CR-7382-10A-01D-2129-08 g.chr3:32933083G>A c.2387G>A c.(2386-2388)cGc>cAc p.R796H HNSC 3 32933123 32933123 + Silent SNP T T C TCGA-BB-A5HY-01A-11D-A28R-08 TCGA-BB-A5HY-10A-01D-A28U-08 g.chr3:32933123T>C c.2427T>C c.(2425-2427)atT>atC p.I809I HNSC 3 32933213 32933213 + Silent SNP G G A TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr3:32933213G>A c.2517G>A c.(2515-2517)ggG>ggA p.G839G KIPAN 3 32859580 32859581 + Missense_Mutation DNP CG CG TT TCGA-WN-A9G9-01A-12D-A36X-10 TCGA-WN-A9G9-10A-01D-A370-10 g.chr3:32859580_32859581CG>TT c.8_9CG>TT c.(7-9)tCG>tTT p.S3F KIPAN 3 32927537 32927537 + Missense_Mutation SNP C C A TCGA-BQ-5883-01A-11D-1589-08 TCGA-BQ-5883-11A-01D-1589-08 g.chr3:32927537C>A c.1132C>A c.(1132-1134)Cgc>Agc p.R378S KIPAN 3 32932071 32932071 + Missense_Mutation SNP G G C TCGA-B8-5159-01A-01D-1421-08 TCGA-B8-5159-10A-01D-1421-08 g.chr3:32932071G>C c.1375G>C c.(1375-1377)Gtc>Ctc p.V459L KIRC 3 32932071 32932071 + Missense_Mutation SNP G G C TCGA-B8-5159-01A-01D-1421-08 TCGA-B8-5159-10A-01D-1421-08 g.chr3:32932071G>C c.1375G>C c.(1375-1377)Gtc>Ctc p.V459L KIRP 3 32859580 32859581 + Missense_Mutation DNP CG CG TT TCGA-WN-A9G9-01A-12D-A36X-10 TCGA-WN-A9G9-10A-01D-A370-10 g.chr3:32859580_32859581CG>TT c.8_9CG>TT c.(7-9)tCG>tTT p.S3F KIRP 3 32927537 32927537 + Missense_Mutation SNP C C A TCGA-BQ-5883-01A-11D-1589-08 TCGA-BQ-5883-11A-01D-1589-08 g.chr3:32927537C>A c.1132C>A c.(1132-1134)Cgc>Agc p.R378S LGG 3 32927435 32927435 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:32927435G>A c.1030G>A c.(1030-1032)Gag>Aag p.E344K LGG 3 32932670 32932670 + Silent SNP C C T TCGA-DB-A64L-01A-11D-A29Q-08 TCGA-DB-A64L-10A-01D-A29Q-08 g.chr3:32932670C>T c.1974C>T c.(1972-1974)ggC>ggT p.G658G LGG 3 32932723 32932723 + Missense_Mutation SNP G G A TCGA-FG-A6IZ-01A-11D-A31L-08 TCGA-FG-A6IZ-10A-01D-A31J-08 g.chr3:32932723G>A c.2027G>A c.(2026-2028)cGc>cAc p.R676H LGG 3 32932914 32932914 + Missense_Mutation SNP G G A TCGA-DU-A6S6-01A-21D-A32B-08 TCGA-DU-A6S6-10A-01D-A329-08 g.chr3:32932914G>A c.2218G>A c.(2218-2220)Gag>Aag p.E740K LIHC 3 32915309 32915309 + Splice_Site SNP G G A TCGA-DD-A115-01A-11D-A12Z-10 TCGA-DD-A115-10A-01D-A12Z-10 g.chr3:32915309G>A c.e2-1 LIHC 3 32915309 32915309 + Splice_Site SNP G G A TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr3:32915309G>A c.e2-1 LIHC 3 32932669 32932669 + Missense_Mutation SNP G G A TCGA-T1-A6J8-01A-11D-A32G-10 TCGA-T1-A6J8-10A-01D-A32G-10 g.chr3:32932669G>A c.1973G>A c.(1972-1974)gGc>gAc p.G658D LUAD 3 32859640 32859640 + Missense_Mutation SNP C C G TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr3:32859640C>G c.68C>G c.(67-69)gCg>gGg p.A23G LUAD 3 32860298 32860298 + Silent SNP G G T TCGA-05-4418-01A-01D-1265-08 TCGA-05-4418-10A-01D-1265-08 g.chr3:32860298G>T c.726G>T c.(724-726)ccG>ccT p.P242P LUAD 3 32860366 32860366 + Missense_Mutation SNP T T A TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr3:32860366T>A c.794T>A c.(793-795)tTc>tAc p.F265Y LUAD 3 32932170 32932170 + Missense_Mutation SNP G G A TCGA-05-4422-01A-01D-1265-08 TCGA-05-4422-10A-01D-1265-08 g.chr3:32932170G>A c.1474G>A c.(1474-1476)Gat>Aat p.D492N LUAD 3 32932777 32932777 + Missense_Mutation SNP G G A TCGA-55-7727-01A-11D-2167-08 TCGA-55-7727-10A-01D-2167-08 g.chr3:32932777G>A c.2081G>A c.(2080-2082)gGa>gAa p.G694E LUAD 3 32933097 32933097 + Missense_Mutation SNP G G T TCGA-05-4244-01A-01D-1105-08 TCGA-05-4244-10A-01D-1105-08 g.chr3:32933097G>T c.2401G>T c.(2401-2403)Gct>Tct p.A801S LUAD 3 32933145 32933145 + Missense_Mutation SNP C C T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr3:32933145C>T c.2449C>T c.(2449-2451)Cgg>Tgg p.R817W LUAD 3 32933216 32933216 + Silent SNP G G A TCGA-95-7944-01A-11D-2184-08 TCGA-95-7944-10A-01D-2184-08 g.chr3:32933216G>A c.2520G>A c.(2518-2520)caG>caA p.Q840Q LUAD 3 32933250 32933250 + Missense_Mutation SNP G G T TCGA-55-8094-01A-11D-2238-08 TCGA-55-8094-10A-01D-2238-08 g.chr3:32933250G>T c.2554G>T c.(2554-2556)Gac>Tac p.D852Y LUAD 3 32933252 32933252 + Missense_Mutation SNP C C A TCGA-17-Z051-01A-01W-0747-08 TCGA-17-Z051-11A-01W-0747-08 g.chr3:32933252C>A c.2556C>A c.(2554-2556)gaC>gaA p.D852E LUSC 3 32933223 32933223 + Missense_Mutation SNP C C T TCGA-37-4141-01A-02D-1352-08 TCGA-37-4141-10A-01D-1352-08 g.chr3:32933223C>T c.2527C>T c.(2527-2529)Cgc>Tgc p.R843C OV 3 32915464 32915464 + Frame_Shift_Del DEL G G - TCGA-10-0938-01A-02W-0419-10 TCGA-10-0938-11A-01W-0419-10 g.chr3:32915464delG c.1007delG c.(1006-1008)cgafs p.R336fs OV 3 32932169 32932169 + Silent SNP C C T TCGA-13-0793-01A-01W-0370-10 TCGA-13-0793-10A-01W-0370-10 g.chr3:32932169C>T c.1473C>T c.(1471-1473)ggC>ggT p.G491G PAAD 3 32860298 32860298 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:32860298G>A c.726G>A c.(724-726)ccG>ccA p.P242P PCPG 3 32932862 32932862 + Silent SNP C C T TCGA-WB-A80V-01A-12D-A35I-08 TCGA-WB-A80V-10A-01D-A35G-08 g.chr3:32932862C>T c.2166C>T c.(2164-2166)caC>caT p.H722H PRAD 3 32932438 32932438 + Missense_Mutation SNP A A T TCGA-XQ-A8TA-01A-11D-A364-08 TCGA-XQ-A8TA-10A-01D-A362-08 g.chr3:32932438A>T c.1742A>T c.(1741-1743)aAg>aTg p.K581M PRAD 3 32932570 32932570 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:32932570G>A c.1874G>A c.(1873-1875)cGc>cAc p.R625H PRAD 3 32933082 32933082 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr3:32933082C>T c.2386C>T c.(2386-2388)Cgc>Tgc p.R796C READ 3 32932173 32932173 + Missense_Mutation SNP G G T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr3:32932173G>T c.1477G>T c.(1477-1479)Ggc>Tgc p.G493C READ 3 32933287 32933287 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:32933287G>A c.2591G>A c.(2590-2592)cGa>cAa p.R864Q SARC 3 32932838 32932838 + Silent SNP C C T TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr3:32932838C>T c.2142C>T c.(2140-2142)atC>atT p.I714I SARC 3 32933059 32933059 + Missense_Mutation SNP G G A TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr3:32933059G>A c.2363G>A c.(2362-2364)gGc>gAc p.G788D SKCM 3 32859584 32859584 + Silent SNP C C T TCGA-DA-A1HW-06A-11D-A19A-08 TCGA-DA-A1HW-10A-01D-A19A-08 g.chr3:32859584C>T c.12C>T c.(10-12)ttC>ttT p.F4F SKCM 3 32860396 32860396 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr3:32860396T>C c.824T>C c.(823-825)cTc>cCc p.L275P SKCM 3 32915324 32915324 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr3:32915324C>T c.867C>T c.(865-867)taC>taT p.Y289Y SKCM 3 32915400 32915400 + Nonsense_Mutation SNP C C T TCGA-FS-A4F9-06A-11D-A24R-08 TCGA-FS-A4F9-10A-01D-A24R-08 g.chr3:32915400C>T c.943C>T c.(943-945)Cag>Tag p.Q315* SKCM 3 32915464 32915464 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr3:32915464G>A c.1007G>A c.(1006-1008)cGa>cAa p.R336Q SKCM 3 32927434 32927434 + Silent SNP C C T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr3:32927434C>T c.1029C>T c.(1027-1029)atC>atT p.I343I SKCM 3 32927435 32927435 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr3:32927435G>A c.1030G>A c.(1030-1032)Gag>Aag p.E344K SKCM 3 32927476 32927476 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:32927476G>A c.1071G>A c.(1069-1071)gcG>gcA p.A357A SKCM 3 32931959 32931959 + Silent SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr3:32931959C>T c.1263C>T c.(1261-1263)gtC>gtT p.V421V SKCM 3 32931962 32931962 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr3:32931962G>A c.1266G>A c.(1264-1266)ctG>ctA p.L422L SKCM 3 32932199 32932199 + Silent SNP G G A TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr3:32932199G>A c.1503G>A c.(1501-1503)aaG>aaA p.K501K SKCM 3 32932226 32932226 + Nonsense_Mutation SNP T T G TCGA-D3-A51N-06A-11D-A25O-08 TCGA-D3-A51N-10A-01D-A25O-08 g.chr3:32932226T>G c.1530T>G c.(1528-1530)taT>taG p.Y510* SKCM 3 32932556 32932556 + Silent SNP C C T TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr3:32932556C>T c.1860C>T c.(1858-1860)atC>atT p.I620I SKCM 3 32932587 32932587 + Nonsense_Mutation SNP C C T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr3:32932587C>T c.1891C>T c.(1891-1893)Cag>Tag p.Q631* SKCM 3 32932625 32932625 + Silent SNP C C T TCGA-FR-A3YO-06A-11D-A23B-08 TCGA-FR-A3YO-10A-01D-A23B-08 g.chr3:32932625C>T c.1929C>T c.(1927-1929)ttC>ttT p.F643F SKCM 3 32932655 32932655 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr3:32932655C>T c.1959C>T c.(1957-1959)ttC>ttT p.F653F SKCM 3 32932655 32932655 + Silent SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr3:32932655C>T c.1959C>T c.(1957-1959)ttC>ttT p.F653F SKCM 3 32932694 32932694 + Silent SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr3:32932694G>A c.1998G>A c.(1996-1998)agG>agA p.R666R SKCM 3 32932742 32932742 + Silent SNP C C T TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr3:32932742C>T c.2046C>T c.(2044-2046)ttC>ttT p.F682F SKCM 3 32932742 32932742 + Silent SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr3:32932742C>T c.2046C>T c.(2044-2046)ttC>ttT p.F682F SKCM 3 32932809 32932809 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr3:32932809G>A c.2113G>A c.(2113-2115)Gat>Aat p.D705N SKCM 3 32932856 32932856 + Silent SNP G G A TCGA-D3-A5GL-06A-11D-A27K-08 TCGA-D3-A5GL-10A-01D-A27N-08 g.chr3:32932856G>A c.2160G>A c.(2158-2160)agG>agA p.R720R SKCM 3 32932942 32932942 + Missense_Mutation SNP C C T TCGA-EE-A2M6-06A-12D-A197-08 TCGA-EE-A2M6-10A-01D-A199-08 g.chr3:32932942C>T c.2246C>T c.(2245-2247)tCc>tTc p.S749F SKCM 3 32932942 32932942 + Missense_Mutation SNP C C T TCGA-EE-A2ML-06A-11D-A197-08 TCGA-EE-A2ML-10A-01D-A199-08 g.chr3:32932942C>T c.2246C>T c.(2245-2247)tCc>tTc p.S749F SKCM 3 32932943 32932943 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:32932943C>T c.2247C>T c.(2245-2247)tcC>tcT p.S749S SKCM 3 32933161 32933161 + Missense_Mutation SNP A A T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr3:32933161A>T c.2465A>T c.(2464-2466)gAa>gTa p.E822V SKCM 3 32933207 32933207 + Silent SNP C C G TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr3:32933207C>G c.2511C>G c.(2509-2511)ggC>ggG p.G837G SKCM 3 32933286 32933286 + Nonsense_Mutation SNP C C T TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr3:32933286C>T c.2590C>T c.(2590-2592)Cga>Tga p.R864* SKCM 3 32933287 32933287 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:32933287G>A c.2591G>A c.(2590-2592)cGa>cAa p.R864Q

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 3 32932230 32932230 single base substitution C T missense_variant H512Y 1534C>T BLCA-US 3 32927521 32927521 single base substitution G A synonymous_variant K372K 1116G>A BLCA-US 3 32932040 32932040 single base substitution G A synonymous_variant R448R 1344G>A BLCA-US 3 32932410 32932410 single base substitution G C missense_variant E572Q 1714G>C BLCA-US 3 32933231 32933231 single base substitution C T synonymous_variant S845S 2535C>T BOCA-FR 3 32862177 32862177 single base substitution G A intron_variant BOCA-FR 3 32878642 32878642 single base substitution G A intron_variant BOCA-FR 3 32910318 32910318 single base substitution C G intron_variant BRCA-EU 3 32854866 32854866 single base substitution G A upstream_gene_variant BRCA-EU 3 32855920 32855920 single base substitution C G upstream_gene_variant BRCA-EU 3 32855954 32855954 single base substitution C T upstream_gene_variant BRCA-EU 3 32857411 32857411 single base substitution C T upstream_gene_variant BRCA-EU 3 32858782 32858782 single base substitution G A upstream_gene_variant BRCA-EU 3 32858945 32858945 single base substitution C A upstream_gene_variant BRCA-EU 3 32860615 32860615 single base substitution G T intron_variant BRCA-EU 3 32860949 32860949 single base substitution C T intron_variant BRCA-EU 3 32861911 32861911 single base substitution G A intron_variant BRCA-EU 3 32862333 32862333 single base substitution G C intron_variant BRCA-EU 3 32862730 32862730 single base substitution A G intron_variant BRCA-EU 3 32862881 32862881 single base substitution G A intron_variant BRCA-EU 3 32863048 32863048 single base substitution C A intron_variant BRCA-EU 3 32865340 32865340 single base substitution C T intron_variant BRCA-EU 3 32866232 32866232 single base substitution T A intron_variant BRCA-EU 3 32869807 32869807 single base substitution G C intron_variant BRCA-EU 3 32870613 32870613 single base substitution G A intron_variant BRCA-EU 3 32870975 32870975 single base substitution A G intron_variant BRCA-EU 3 32871065 32871065 single base substitution G C intron_variant BRCA-EU 3 32871234 32871234 single base substitution C T intron_variant BRCA-EU 3 32871606 32871606 single base substitution G T intron_variant BRCA-EU 3 32873130 32873130 single base substitution G C intron_variant BRCA-EU 3 32873249 32873249 single base substitution G C intron_variant BRCA-EU 3 32873550 32873550 single base substitution T G intron_variant BRCA-EU 3 32875668 32875668 single base substitution C A intron_variant BRCA-EU 3 32875807 32875807 single base substitution G C intron_variant BRCA-EU 3 32876333 32876333 deletion of <=200bp A - intron_variant BRCA-EU 3 32876612 32876612 single base substitution G C intron_variant BRCA-EU 3 32880699 32880699 single base substitution G C intron_variant BRCA-EU 3 32880731 32880731 deletion of <=200bp T - intron_variant BRCA-EU 3 32881919 32881919 single base substitution A T intron_variant BRCA-EU 3 32882601 32882601 single base substitution G A intron_variant BRCA-EU 3 32882696 32882696 single base substitution C G intron_variant BRCA-EU 3 32882868 32882868 single base substitution T G intron_variant BRCA-EU 3 32886377 32886377 single base substitution G A intron_variant BRCA-EU 3 32888929 32888929 single base substitution C T intron_variant BRCA-EU 3 32891367 32891367 single base substitution G C intron_variant BRCA-EU 3 32893198 32893198 single base substitution T A intron_variant BRCA-EU 3 32893646 32893646 single base substitution C A intron_variant BRCA-EU 3 32895927 32895927 single base substitution G A intron_variant BRCA-EU 3 32896362 32896362 single base substitution G A intron_variant BRCA-EU 3 32896924 32896924 single base substitution C T intron_variant BRCA-EU 3 32901030 32901030 single base substitution G C intron_variant BRCA-EU 3 32902217 32902217 single base substitution T G intron_variant BRCA-EU 3 32902940 32902940 single base substitution G T intron_variant BRCA-EU 3 32904099 32904099 single base substitution C T intron_variant BRCA-EU 3 32904306 32904306 single base substitution T G intron_variant BRCA-EU 3 32905186 32905186 deletion of <=200bp T - intron_variant BRCA-EU 3 32908534 32908534 single base substitution G A intron_variant BRCA-EU 3 32909033 32909033 single base substitution C G intron_variant BRCA-EU 3 32909040 32909040 single base substitution G C intron_variant BRCA-EU 3 32909303 32909303 single base substitution C A intron_variant BRCA-EU 3 32910031 32910031 single base substitution C G intron_variant BRCA-EU 3 32910041 32910041 single base substitution C T intron_variant BRCA-EU 3 32910160 32910160 single base substitution A T intron_variant BRCA-EU 3 32910451 32910451 single base substitution G T intron_variant BRCA-EU 3 32910541 32910541 single base substitution A T intron_variant BRCA-EU 3 32911299 32911299 single base substitution G C intron_variant BRCA-EU 3 32912331 32912331 single base substitution T C intron_variant BRCA-EU 3 32912715 32912715 single base substitution C T intron_variant BRCA-EU 3 32914382 32914382 single base substitution T G intron_variant BRCA-EU 3 32916033 32916033 single base substitution G C intron_variant BRCA-EU 3 32916799 32916799 single base substitution G C intron_variant BRCA-EU 3 32917875 32917875 single base substitution A T intron_variant BRCA-EU 3 32920271 32920271 single base substitution C T intron_variant BRCA-EU 3 32920545 32920545 single base substitution C T intron_variant BRCA-EU 3 32920664 32920664 single base substitution G C intron_variant BRCA-EU 3 32921826 32921826 single base substitution C A intron_variant BRCA-EU 3 32921844 32921844 single base substitution G A intron_variant BRCA-EU 3 32921921 32921921 single base substitution A G intron_variant BRCA-EU 3 32924630 32924630 single base substitution C G intron_variant BRCA-EU 3 32926358 32926358 single base substitution G A intron_variant BRCA-EU 3 32926618 32926618 single base substitution C T intron_variant BRCA-EU 3 32928462 32928462 single base substitution G T intron_variant BRCA-EU 3 32928670 32928670 deletion of <=200bp A - intron_variant BRCA-EU 3 32930285 32930285 single base substitution G T intron_variant BRCA-EU 3 32930636 32930636 single base substitution T A intron_variant BRCA-EU 3 32931308 32931308 single base substitution C G intron_variant BRCA-EU 3 32931920 32931920 single base substitution C G synonymous_variant L408L 1224C>G BRCA-EU 3 32933249 32933249 single base substitution C T synonymous_variant P851P 2553C>T BRCA-EU 3 32933777 32933777 single base substitution T C 3_prime_UTR_variant BRCA-EU 3 32934167 32934167 single base substitution C T 3_prime_UTR_variant BRCA-EU 3 32937903 32937903 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 3 32939071 32939071 single base substitution C G 3_prime_UTR_variant BRCA-EU 3 32941056 32941056 single base substitution T C downstream_gene_variant BRCA-EU 3 32941063 32941063 single base substitution G A downstream_gene_variant BRCA-EU 3 32941567 32941567 single base substitution G C downstream_gene_variant BRCA-EU 3 32942937 32942937 single base substitution C A downstream_gene_variant BRCA-EU 3 32943631 32943631 single base substitution A G downstream_gene_variant BRCA-FR 3 32860045 32860045 single base substitution C G missense_variant P158R 473C>G BRCA-FR 3 32865836 32865836 single base substitution A T intron_variant BRCA-FR 3 32866811 32866811 single base substitution T G intron_variant BRCA-FR 3 32869807 32869807 single base substitution G C intron_variant BRCA-FR 3 32881757 32881757 single base substitution C G intron_variant BRCA-FR 3 32892818 32892818 single base substitution G A intron_variant BRCA-FR 3 32901030 32901030 single base substitution G C intron_variant BRCA-FR 3 32911299 32911299 single base substitution G C intron_variant BRCA-FR 3 32926814 32926814 single base substitution C T intron_variant BRCA-FR 3 32928462 32928462 single base substitution G T intron_variant BRCA-FR 3 32928987 32928987 single base substitution T A intron_variant BRCA-FR 3 32941488 32941488 single base substitution C T downstream_gene_variant BRCA-UK 3 32880699 32880699 single base substitution G C intron_variant BRCA-UK 3 32893646 32893646 single base substitution C A intron_variant BRCA-UK 3 32895927 32895927 single base substitution G A intron_variant BRCA-UK 3 32898961 32898961 single base substitution G C intron_variant BRCA-UK 3 32907775 32907775 single base substitution C G intron_variant BRCA-US 3 32932211 32932211 single base substitution C A missense_variant F505L 1515C>A BRCA-US 3 32933156 32933156 single base substitution G T missense_variant M820I 2460G>T BRCA-US 3 32933232 32933232 single base substitution G A missense_variant G846S 2536G>A BTCA-JP 3 32860056 32860056 single base substitution G A missense_variant A162T 484G>A BTCA-JP 3 32860392 32860392 single base substitution C T missense_variant R274C 820C>T BTCA-JP 3 32932183 32932183 single base substitution G A missense_variant R496H 1487G>A BTCA-JP 3 32932527 32932527 single base substitution G T missense_variant G611C 1831G>T CESC-US 3 32915396 32915396 single base substitution C T synonymous_variant Y313Y 939C>T CLLE-ES 3 32855435 32855435 single base substitution A G upstream_gene_variant CLLE-ES 3 32873182 32873182 single base substitution C T intron_variant CLLE-ES 3 32879382 32879382 single base substitution T G intron_variant CLLE-ES 3 32902180 32902180 single base substitution C T intron_variant CLLE-ES 3 32913364 32913364 single base substitution G A intron_variant CLLE-ES 3 32916593 32916593 single base substitution G A intron_variant CLLE-ES 3 32926821 32926821 single base substitution T G intron_variant COAD-US 3 32859629 32859629 single base substitution C T synonymous_variant C19C 57C>T COAD-US 3 32927475 32927475 single base substitution C T missense_variant A357V 1070C>T COAD-US 3 32927553 32927553 single base substitution T G missense_variant L383R 1148T>G COAD-US 3 32931948 32931948 single base substitution G A missense_variant V418M 1252G>A COAD-US 3 32932074 32932074 single base substitution A G missense_variant M460V 1378A>G COAD-US 3 32932353 32932353 single base substitution C T stop_gained R553* 1657C>T COAD-US 3 32932642 32932642 single base substitution G A missense_variant R649Q 1946G>A COAD-US 3 32932939 32932939 single base substitution A T missense_variant D748V 2243A>T COAD-US 3 32933066 32933066 single base substitution C A synonymous_variant G790G 2370C>A COAD-US 3 32933116 32933116 single base substitution G A missense_variant R807H 2420G>A COAD-US 3 32933286 32933286 single base substitution C T stop_gained R864* 2590C>T COCA-CN 3 32893536 32893536 single base substitution G T intron_variant COCA-CN 3 32932151 32932151 single base substitution A G synonymous_variant P485P 1455A>G COCA-CN 3 32932168 32932168 single base substitution G A missense_variant G491D 1472G>A COCA-CN 3 32932472 32932472 single base substitution G A synonymous_variant P592P 1776G>A COCA-CN 3 32932625 32932625 single base substitution C T synonymous_variant F643F 1929C>T COCA-CN 3 32932742 32932742 single base substitution C T synonymous_variant F682F 2046C>T COCA-CN 3 32932816 32932816 single base substitution C A missense_variant A707E 2120C>A COCA-CN 3 32933286 32933286 single base substitution C T stop_gained R864* 2590C>T COCA-CN 3 32933362 32933362 single base substitution C T 3_prime_UTR_variant EOPC-DE 3 32860768 32860768 single base substitution C T intron_variant EOPC-DE 3 32882571 32882571 single base substitution T C intron_variant ESAD-UK 3 32855263 32855263 single base substitution T C upstream_gene_variant ESAD-UK 3 32857412 32857412 single base substitution G A upstream_gene_variant ESAD-UK 3 32857641 32857641 single base substitution C T upstream_gene_variant ESAD-UK 3 32858261 32858261 single base substitution G A upstream_gene_variant ESAD-UK 3 32858655 32858655 single base substitution C T upstream_gene_variant ESAD-UK 3 32858828 32858828 single base substitution C T upstream_gene_variant ESAD-UK 3 32859343 32859343 single base substitution G A upstream_gene_variant ESAD-UK 3 32859521 32859521 single base substitution C A 5_prime_UTR_variant ESAD-UK 3 32859802 32859802 single base substitution C T missense_variant A77V 230C>T ESAD-UK 3 32860827 32860827 single base substitution C G intron_variant ESAD-UK 3 32861206 32861206 single base substitution G A intron_variant ESAD-UK 3 32865943 32865943 single base substitution C T intron_variant ESAD-UK 3 32866349 32866349 single base substitution C T intron_variant ESAD-UK 3 32866437 32866437 single base substitution C G intron_variant ESAD-UK 3 32866447 32866447 single base substitution T C intron_variant ESAD-UK 3 32869300 32869300 single base substitution T C intron_variant ESAD-UK 3 32869480 32869480 single base substitution G A intron_variant ESAD-UK 3 32872007 32872007 single base substitution G T intron_variant ESAD-UK 3 32872312 32872312 single base substitution T A intron_variant ESAD-UK 3 32873593 32873593 deletion of <=200bp G - intron_variant ESAD-UK 3 32874225 32874225 single base substitution A T intron_variant ESAD-UK 3 32875284 32875284 single base substitution G T intron_variant ESAD-UK 3 32878573 32878573 single base substitution T G intron_variant ESAD-UK 3 32879675 32879675 single base substitution A C intron_variant ESAD-UK 3 32881008 32881008 single base substitution A C intron_variant ESAD-UK 3 32881009 32881011 deletion of <=200bp CAG - intron_variant ESAD-UK 3 32883091 32883091 single base substitution C G intron_variant ESAD-UK 3 32883265 32883265 single base substitution A C intron_variant ESAD-UK 3 32883464 32883464 single base substitution G A intron_variant ESAD-UK 3 32885588 32885588 single base substitution C T intron_variant ESAD-UK 3 32886097 32886097 single base substitution C T intron_variant ESAD-UK 3 32887527 32887527 single base substitution A G intron_variant ESAD-UK 3 32890364 32890364 single base substitution T C intron_variant ESAD-UK 3 32890853 32890853 single base substitution G T intron_variant ESAD-UK 3 32891765 32891765 single base substitution T G intron_variant ESAD-UK 3 32892982 32892982 insertion of <=200bp - T intron_variant ESAD-UK 3 32893221 32893221 single base substitution T G intron_variant ESAD-UK 3 32893575 32893575 single base substitution G A intron_variant ESAD-UK 3 32893731 32893731 single base substitution G A intron_variant ESAD-UK 3 32894261 32894261 single base substitution A C intron_variant ESAD-UK 3 32895778 32895778 single base substitution G A intron_variant ESAD-UK 3 32895796 32895796 single base substitution C T intron_variant ESAD-UK 3 32898425 32898425 single base substitution G A intron_variant ESAD-UK 3 32898717 32898717 single base substitution C A intron_variant ESAD-UK 3 32899705 32899705 single base substitution T G intron_variant ESAD-UK 3 32900226 32900226 single base substitution T C intron_variant ESAD-UK 3 32900924 32900924 insertion of <=200bp - T intron_variant ESAD-UK 3 32902020 32902020 single base substitution A G intron_variant ESAD-UK 3 32902922 32902922 single base substitution C A intron_variant ESAD-UK 3 32905154 32905154 single base substitution T C intron_variant ESAD-UK 3 32905186 32905186 insertion of <=200bp - T intron_variant ESAD-UK 3 32911497 32911497 single base substitution C G intron_variant ESAD-UK 3 32915267 32915267 single base substitution G A intron_variant ESAD-UK 3 32920728 32920728 single base substitution C G intron_variant ESAD-UK 3 32920876 32920876 single base substitution C T intron_variant ESAD-UK 3 32921302 32921302 insertion of <=200bp - A intron_variant ESAD-UK 3 32922521 32922521 single base substitution A T intron_variant ESAD-UK 3 32924062 32924062 single base substitution G A intron_variant ESAD-UK 3 32924621 32924621 single base substitution G A intron_variant ESAD-UK 3 32926123 32926123 single base substitution G A intron_variant ESAD-UK 3 32926273 32926273 single base substitution C G intron_variant ESAD-UK 3 32926492 32926492 single base substitution T G intron_variant ESAD-UK 3 32927206 32927206 single base substitution A G intron_variant ESAD-UK 3 32927321 32927321 single base substitution C G intron_variant ESAD-UK 3 32929341 32929341 single base substitution C T intron_variant ESAD-UK 3 32930063 32930063 single base substitution G A intron_variant ESAD-UK 3 32932472 32932472 single base substitution G A synonymous_variant P592P 1776G>A ESAD-UK 3 32933008 32933008 single base substitution T A missense_variant L771H 2312T>A ESAD-UK 3 32933220 32933220 single base substitution G A missense_variant D842N 2524G>A ESAD-UK 3 32933341 32933341 single base substitution C T 3_prime_UTR_variant ESAD-UK 3 32933434 32933434 single base substitution T G 3_prime_UTR_variant ESAD-UK 3 32935672 32935672 single base substitution C A 3_prime_UTR_variant ESAD-UK 3 32936805 32936805 single base substitution G A 3_prime_UTR_variant ESAD-UK 3 32938062 32938062 single base substitution A G 3_prime_UTR_variant ESAD-UK 3 32939007 32939007 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 3 32942405 32942405 single base substitution G C downstream_gene_variant GBM-US 3 32859692 32859692 single base substitution G A synonymous_variant T40T 120G>A GBM-US 3 32859711 32859711 single base substitution G A missense_variant G47R 139G>A GBM-US 3 32932739 32932739 single base substitution G A synonymous_variant T681T 2043G>A GBM-US 3 32933041 32933041 single base substitution G A missense_variant R782H 2345G>A GBM-US 3 32933302 32933302 single base substitution A G stop_retained_variant *869* 2606A>G KIRC-US 3 32932071 32932071 single base substitution G C missense_variant V459L 1375G>C KIRP-US 3 32915387 32915387 single base substitution C A missense_variant S310R 930C>A KIRP-US 3 32932124 32932124 single base substitution C T synonymous_variant G476G 1428C>T LGG-US 3 32932670 32932670 single base substitution C T synonymous_variant G658G 1974C>T LICA-CN 3 32932663 32932663 single base substitution C T missense_variant P656L 1967C>T LICA-FR 3 32859585 32859585 single base substitution C A missense_variant P5T 13C>A LICA-FR 3 32859649 32859649 single base substitution C A missense_variant S26Y 77C>A LICA-FR 3 32859881 32859881 single base substitution G A synonymous_variant A103A 309G>A LICA-FR 3 32895223 32895223 single base substitution G A intron_variant LICA-FR 3 32927534 32927534 single base substitution G A missense_variant E377K 1129G>A LICA-FR 3 32932502 32932502 single base substitution C T synonymous_variant S602S 1806C>T LICA-FR 3 32932659 32932659 single base substitution C A synonymous_variant R655R 1963C>A LICA-FR 3 32933015 32933015 single base substitution T A synonymous_variant V773V 2319T>A LICA-FR 3 32933129 32933129 single base substitution G A synonymous_variant A811A 2433G>A LICA-FR 3 32933194 32933194 single base substitution C T missense_variant A833V 2498C>T LICA-FR 3 32944094 32944094 single base substitution C A downstream_gene_variant LIHC-US 3 32915309 32915309 single base substitution G A splice_acceptor_variant LIHC-US 3 32932714 32932714 single base substitution A G missense_variant D673G 2018A>G LINC-JP 3 32857524 32857524 single base substitution G A upstream_gene_variant LINC-JP 3 32857525 32857525 single base substitution C A upstream_gene_variant LINC-JP 3 32859011 32859011 single base substitution G T upstream_gene_variant LINC-JP 3 32860114 32860114 single base substitution C A missense_variant P181H 542C>A LINC-JP 3 32863322 32863322 single base substitution C T intron_variant LINC-JP 3 32867440 32867440 single base substitution A G intron_variant LINC-JP 3 32874705 32874705 single base substitution G A intron_variant LINC-JP 3 32880879 32880879 single base substitution C G intron_variant LINC-JP 3 32890145 32890145 single base substitution C A intron_variant LINC-JP 3 32901173 32901173 single base substitution G A intron_variant LINC-JP 3 32910157 32910157 single base substitution A G intron_variant LINC-JP 3 32933457 32933457 single base substitution T C 3_prime_UTR_variant LINC-JP 3 32935485 32935485 single base substitution A G 3_prime_UTR_variant LINC-JP 3 32941282 32941282 single base substitution T G downstream_gene_variant LINC-JP 3 32943018 32943018 single base substitution G A downstream_gene_variant LIRI-JP 3 32855791 32855791 single base substitution T C upstream_gene_variant LIRI-JP 3 32857567 32857567 single base substitution G A upstream_gene_variant LIRI-JP 3 32861384 32861384 single base substitution G C intron_variant LIRI-JP 3 32865232 32865232 single base substitution G T intron_variant LIRI-JP 3 32867408 32867408 single base substitution G A intron_variant LIRI-JP 3 32869016 32869016 single base substitution G A intron_variant LIRI-JP 3 32871405 32871405 single base substitution A T intron_variant LIRI-JP 3 32871638 32871638 single base substitution C T intron_variant LIRI-JP 3 32871957 32871957 single base substitution C A intron_variant LIRI-JP 3 32872176 32872176 single base substitution A C intron_variant LIRI-JP 3 32875176 32875178 deletion of <=200bp TGG - intron_variant LIRI-JP 3 32876286 32876286 single base substitution A G intron_variant LIRI-JP 3 32878224 32878224 single base substitution C T intron_variant LIRI-JP 3 32879620 32879620 single base substitution G A intron_variant LIRI-JP 3 32880726 32880726 single base substitution A G intron_variant LIRI-JP 3 32882839 32882839 single base substitution G C intron_variant LIRI-JP 3 32884569 32884569 single base substitution T A intron_variant LIRI-JP 3 32884709 32884709 single base substitution A G intron_variant LIRI-JP 3 32885291 32885291 single base substitution G A intron_variant LIRI-JP 3 32886185 32886185 single base substitution C A intron_variant LIRI-JP 3 32887986 32887986 single base substitution T C intron_variant LIRI-JP 3 32889484 32889484 single base substitution T A intron_variant LIRI-JP 3 32889522 32889522 single base substitution A C intron_variant LIRI-JP 3 32889542 32889542 single base substitution G T intron_variant LIRI-JP 3 32893786 32893786 single base substitution G A intron_variant LIRI-JP 3 32896784 32896784 single base substitution G T intron_variant LIRI-JP 3 32897090 32897090 single base substitution C T intron_variant LIRI-JP 3 32898213 32898213 single base substitution A G intron_variant LIRI-JP 3 32898606 32898606 single base substitution T C intron_variant LIRI-JP 3 32900518 32900518 single base substitution G T intron_variant LIRI-JP 3 32900519 32900519 single base substitution G T intron_variant LIRI-JP 3 32900774 32900774 single base substitution A G intron_variant LIRI-JP 3 32903954 32903954 deletion of <=200bp A - intron_variant LIRI-JP 3 32904097 32904097 single base substitution T A intron_variant LIRI-JP 3 32904926 32904926 single base substitution A C intron_variant LIRI-JP 3 32909612 32909612 single base substitution C G intron_variant LIRI-JP 3 32912532 32912532 single base substitution A G intron_variant LIRI-JP 3 32914872 32914872 single base substitution C G intron_variant LIRI-JP 3 32915203 32915203 single base substitution G A intron_variant LIRI-JP 3 32916213 32916213 single base substitution A G intron_variant LIRI-JP 3 32919213 32919213 single base substitution A T intron_variant LIRI-JP 3 32920384 32920384 single base substitution G A intron_variant LIRI-JP 3 32922508 32922509 deletion of <=200bp TG - intron_variant LIRI-JP 3 32923495 32923495 single base substitution A C intron_variant LIRI-JP 3 32924017 32924017 single base substitution T C intron_variant LIRI-JP 3 32924067 32924067 single base substitution G A intron_variant LIRI-JP 3 32924668 32924668 single base substitution A G intron_variant LIRI-JP 3 32925288 32925288 single base substitution A T intron_variant LIRI-JP 3 32925633 32925633 single base substitution A G intron_variant LIRI-JP 3 32925749 32925749 single base substitution G A intron_variant LIRI-JP 3 32927314 32927314 single base substitution C T intron_variant LIRI-JP 3 32931097 32931097 single base substitution T A intron_variant LIRI-JP 3 32931786 32931786 single base substitution A G intron_variant LIRI-JP 3 32931976 32931976 single base substitution C T missense_variant A427V 1280C>T LIRI-JP 3 32933792 32933792 single base substitution T C 3_prime_UTR_variant LIRI-JP 3 32933863 32933863 single base substitution T C 3_prime_UTR_variant LIRI-JP 3 32935908 32935908 single base substitution C A 3_prime_UTR_variant LIRI-JP 3 32936690 32936690 single base substitution C A 3_prime_UTR_variant LIRI-JP 3 32936848 32936848 single base substitution G T 3_prime_UTR_variant LIRI-JP 3 32938752 32938752 single base substitution T G 3_prime_UTR_variant LIRI-JP 3 32939028 32939028 single base substitution T C 3_prime_UTR_variant LIRI-JP 3 32939149 32939149 single base substitution G T 3_prime_UTR_variant LIRI-JP 3 32940851 32940851 single base substitution A C downstream_gene_variant LIRI-JP 3 32942184 32942184 single base substitution C T downstream_gene_variant LIRI-JP 3 32942763 32942763 single base substitution G A downstream_gene_variant LIRI-JP 3 32943836 32943836 single base substitution A T downstream_gene_variant LUSC-KR 3 32855404 32855404 single base substitution G A upstream_gene_variant LUSC-KR 3 32858803 32858803 single base substitution G A upstream_gene_variant LUSC-KR 3 32861705 32861705 single base substitution G A intron_variant LUSC-KR 3 32866209 32866209 single base substitution C G intron_variant LUSC-KR 3 32867041 32867041 single base substitution A C intron_variant LUSC-KR 3 32867563 32867563 single base substitution T A intron_variant LUSC-KR 3 32872452 32872452 single base substitution G A intron_variant LUSC-KR 3 32880818 32880818 single base substitution G A intron_variant LUSC-KR 3 32882188 32882188 single base substitution C G intron_variant LUSC-KR 3 32886319 32886319 single base substitution T G intron_variant LUSC-KR 3 32895816 32895816 single base substitution C G intron_variant LUSC-KR 3 32899595 32899595 single base substitution T C intron_variant LUSC-KR 3 32902983 32902983 single base substitution G A intron_variant LUSC-KR 3 32913125 32913125 single base substitution C T intron_variant LUSC-KR 3 32915296 32915296 single base substitution T G intron_variant LUSC-KR 3 32915819 32915819 single base substitution C T intron_variant LUSC-KR 3 32915822 32915822 single base substitution C T intron_variant LUSC-KR 3 32915859 32915859 single base substitution T A intron_variant LUSC-KR 3 32917211 32917211 single base substitution C T intron_variant LUSC-KR 3 32929717 32929717 single base substitution C T intron_variant LUSC-KR 3 32933078 32933078 single base substitution C T synonymous_variant F794F 2382C>T LUSC-US 3 32933223 32933223 single base substitution C T missense_variant R843C 2527C>T MALY-DE 3 32856014 32856014 single base substitution T C upstream_gene_variant MALY-DE 3 32859587 32859587 single base substitution C T synonymous_variant P5P 15C>T MALY-DE 3 32864430 32864430 single base substitution T A intron_variant MALY-DE 3 32864883 32864883 single base substitution G A intron_variant MALY-DE 3 32866079 32866079 single base substitution G T intron_variant MALY-DE 3 32873593 32873593 insertion of <=200bp - G intron_variant MALY-DE 3 32874588 32874588 single base substitution A C intron_variant MALY-DE 3 32877937 32877937 single base substitution T G intron_variant MALY-DE 3 32888620 32888620 single base substitution G A intron_variant MALY-DE 3 32896973 32896973 single base substitution G A intron_variant MALY-DE 3 32904410 32904410 single base substitution C T intron_variant MALY-DE 3 32910192 32910192 single base substitution T A intron_variant MALY-DE 3 32910363 32910363 single base substitution G A intron_variant MALY-DE 3 32925634 32925634 single base substitution G A intron_variant MALY-DE 3 32928666 32928666 single base substitution G A intron_variant MALY-DE 3 32928970 32928970 single base substitution T C intron_variant MALY-DE 3 32934067 32934067 single base substitution G T 3_prime_UTR_variant MALY-DE 3 32939007 32939007 deletion of <=200bp T - 3_prime_UTR_variant MALY-DE 3 32939486 32939486 single base substitution T A downstream_gene_variant MALY-DE 3 32943756 32943763 deletion of <=200bp AAAAAAAG - downstream_gene_variant MELA-AU 3 32854836 32854836 single base substitution A T upstream_gene_variant MELA-AU 3 32855138 32855138 single base substitution C T upstream_gene_variant MELA-AU 3 32855178 32855178 single base substitution C T upstream_gene_variant MELA-AU 3 32855551 32855551 single base substitution C A upstream_gene_variant MELA-AU 3 32855742 32855742 single base substitution C T upstream_gene_variant MELA-AU 3 32855758 32855758 single base substitution C T upstream_gene_variant MELA-AU 3 32855807 32855807 single base substitution G A upstream_gene_variant MELA-AU 3 32855823 32855823 single base substitution C T upstream_gene_variant MELA-AU 3 32855886 32855886 single base substitution T A upstream_gene_variant MELA-AU 3 32856179 32856179 single base substitution G A upstream_gene_variant MELA-AU 3 32856311 32856311 single base substitution C T upstream_gene_variant MELA-AU 3 32856663 32856663 single base substitution C T upstream_gene_variant MELA-AU 3 32856745 32856745 single base substitution G A upstream_gene_variant MELA-AU 3 32856801 32856801 single base substitution C T upstream_gene_variant MELA-AU 3 32857209 32857209 single base substitution C T upstream_gene_variant MELA-AU 3 32857342 32857342 single base substitution T G upstream_gene_variant MELA-AU 3 32857397 32857397 single base substitution G A upstream_gene_variant MELA-AU 3 32857552 32857552 single base substitution G A upstream_gene_variant MELA-AU 3 32858321 32858321 single base substitution C T upstream_gene_variant MELA-AU 3 32859440 32859440 single base substitution G A upstream_gene_variant MELA-AU 3 32860454 32860454 single base substitution C T intron_variant MELA-AU 3 32860488 32860488 single base substitution C T intron_variant MELA-AU 3 32860855 32860855 single base substitution T C intron_variant MELA-AU 3 32861288 32861288 single base substitution G A intron_variant MELA-AU 3 32861504 32861504 single base substitution C T intron_variant MELA-AU 3 32861505 32861505 single base substitution C T intron_variant MELA-AU 3 32861548 32861548 single base substitution C T intron_variant MELA-AU 3 32861577 32861577 single base substitution G A intron_variant MELA-AU 3 32861787 32861787 single base substitution G A intron_variant MELA-AU 3 32861942 32861942 single base substitution A G intron_variant MELA-AU 3 32862090 32862090 single base substitution C T intron_variant MELA-AU 3 32862143 32862143 single base substitution C T intron_variant MELA-AU 3 32862295 32862295 single base substitution C T intron_variant MELA-AU 3 32862416 32862416 single base substitution T C intron_variant MELA-AU 3 32862425 32862425 single base substitution C T intron_variant MELA-AU 3 32862658 32862658 single base substitution C T intron_variant MELA-AU 3 32862747 32862747 single base substitution C T intron_variant MELA-AU 3 32862748 32862748 single base substitution C T intron_variant MELA-AU 3 32862949 32862949 single base substitution C T intron_variant MELA-AU 3 32863133 32863133 single base substitution C T intron_variant MELA-AU 3 32863237 32863237 single base substitution G A intron_variant MELA-AU 3 32863300 32863300 single base substitution C T intron_variant MELA-AU 3 32863794 32863794 single base substitution G A intron_variant MELA-AU 3 32863868 32863868 single base substitution C T intron_variant MELA-AU 3 32863869 32863869 single base substitution C T intron_variant MELA-AU 3 32864222 32864222 single base substitution C T intron_variant MELA-AU 3 32864656 32864656 single base substitution A C intron_variant MELA-AU 3 32864880 32864880 single base substitution G A intron_variant MELA-AU 3 32865056 32865056 single base substitution G A intron_variant MELA-AU 3 32865086 32865086 single base substitution G A intron_variant MELA-AU 3 32865163 32865163 single base substitution G A intron_variant MELA-AU 3 32865521 32865521 single base substitution C T intron_variant MELA-AU 3 32865536 32865536 single base substitution C T intron_variant MELA-AU 3 32865626 32865626 single base substitution C T intron_variant MELA-AU 3 32865764 32865764 single base substitution G A intron_variant MELA-AU 3 32865883 32865883 single base substitution C T intron_variant MELA-AU 3 32865907 32865907 single base substitution A G intron_variant MELA-AU 3 32865936 32865936 single base substitution C T intron_variant MELA-AU 3 32865966 32865966 single base substitution G A intron_variant MELA-AU 3 32865973 32865973 single base substitution G A intron_variant MELA-AU 3 32866317 32866317 single base substitution C T intron_variant MELA-AU 3 32866501 32866501 single base substitution G A intron_variant MELA-AU 3 32866600 32866600 single base substitution T A intron_variant MELA-AU 3 32866610 32866610 single base substitution G A intron_variant MELA-AU 3 32866739 32866739 single base substitution C T intron_variant MELA-AU 3 32867054 32867054 single base substitution G A intron_variant MELA-AU 3 32867064 32867064 single base substitution C T intron_variant MELA-AU 3 32867129 32867129 single base substitution G A intron_variant MELA-AU 3 32867370 32867370 single base substitution C T intron_variant MELA-AU 3 32867642 32867642 single base substitution G A intron_variant MELA-AU 3 32867650 32867650 single base substitution C T intron_variant MELA-AU 3 32867856 32867856 single base substitution G A intron_variant MELA-AU 3 32868069 32868069 single base substitution G A intron_variant MELA-AU 3 32868114 32868114 single base substitution C T intron_variant MELA-AU 3 32868343 32868343 single base substitution C T intron_variant MELA-AU 3 32868452 32868452 single base substitution T C intron_variant MELA-AU 3 32868563 32868563 single base substitution T C intron_variant MELA-AU 3 32868568 32868568 single base substitution T A intron_variant MELA-AU 3 32868642 32868642 single base substitution C T intron_variant MELA-AU 3 32868749 32868749 single base substitution G A intron_variant MELA-AU 3 32868797 32868797 single base substitution C T intron_variant MELA-AU 3 32868880 32868880 single base substitution G C intron_variant MELA-AU 3 32868998 32868998 single base substitution C T intron_variant MELA-AU 3 32870001 32870001 single base substitution T A intron_variant MELA-AU 3 32870033 32870033 single base substitution T A intron_variant MELA-AU 3 32870141 32870141 single base substitution C G intron_variant MELA-AU 3 32870217 32870217 single base substitution C T intron_variant MELA-AU 3 32870389 32870389 single base substitution C T intron_variant MELA-AU 3 32870958 32870958 single base substitution G A intron_variant MELA-AU 3 32870973 32870973 single base substitution C T intron_variant MELA-AU 3 32870989 32870989 single base substitution C T intron_variant MELA-AU 3 32871294 32871294 single base substitution C G intron_variant MELA-AU 3 32871872 32871872 single base substitution A G intron_variant MELA-AU 3 32872123 32872123 single base substitution G C intron_variant MELA-AU 3 32872412 32872412 single base substitution C T intron_variant MELA-AU 3 32873061 32873061 single base substitution C T intron_variant MELA-AU 3 32873080 32873080 single base substitution G A intron_variant MELA-AU 3 32873094 32873094 single base substitution G A intron_variant MELA-AU 3 32873164 32873164 single base substitution G C intron_variant MELA-AU 3 32873575 32873575 single base substitution G A intron_variant MELA-AU 3 32873751 32873751 single base substitution G A intron_variant MELA-AU 3 32873824 32873824 single base substitution C T intron_variant MELA-AU 3 32873833 32873833 single base substitution C T intron_variant MELA-AU 3 32873859 32873859 single base substitution C T intron_variant MELA-AU 3 32874067 32874067 single base substitution C T intron_variant MELA-AU 3 32874171 32874171 single base substitution C T intron_variant MELA-AU 3 32874707 32874707 single base substitution G A intron_variant MELA-AU 3 32874725 32874725 single base substitution C T intron_variant MELA-AU 3 32874785 32874785 single base substitution C T intron_variant MELA-AU 3 32874908 32874908 single base substitution G A intron_variant MELA-AU 3 32874924 32874924 single base substitution C T intron_variant MELA-AU 3 32875005 32875005 single base substitution C A intron_variant MELA-AU 3 32875275 32875275 single base substitution A T intron_variant MELA-AU 3 32875503 32875503 single base substitution G A intron_variant MELA-AU 3 32875590 32875590 single base substitution G A intron_variant MELA-AU 3 32876153 32876153 single base substitution G A intron_variant MELA-AU 3 32876197 32876197 single base substitution G A intron_variant MELA-AU 3 32876603 32876603 single base substitution G A intron_variant MELA-AU 3 32876808 32876808 single base substitution T C intron_variant MELA-AU 3 32876915 32876915 single base substitution C T intron_variant MELA-AU 3 32877163 32877163 single base substitution C T intron_variant MELA-AU 3 32877255 32877255 single base substitution A G intron_variant MELA-AU 3 32877288 32877288 single base substitution G A intron_variant MELA-AU 3 32877332 32877332 single base substitution C T intron_variant MELA-AU 3 32878177 32878177 single base substitution C A intron_variant MELA-AU 3 32878523 32878523 single base substitution G A intron_variant MELA-AU 3 32879287 32879287 single base substitution G A intron_variant MELA-AU 3 32879366 32879366 single base substitution C T intron_variant MELA-AU 3 32879375 32879375 single base substitution C T intron_variant MELA-AU 3 32879436 32879436 single base substitution C T intron_variant MELA-AU 3 32879566 32879566 single base substitution G A intron_variant MELA-AU 3 32879603 32879603 single base substitution C T intron_variant MELA-AU 3 32879636 32879637 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 32879739 32879739 single base substitution G A intron_variant MELA-AU 3 32880366 32880366 single base substitution C A intron_variant MELA-AU 3 32880426 32880426 single base substitution G A intron_variant MELA-AU 3 32880474 32880474 single base substitution A T intron_variant MELA-AU 3 32880702 32880702 single base substitution G A intron_variant MELA-AU 3 32880789 32880789 single base substitution C T intron_variant MELA-AU 3 32880840 32880840 single base substitution A G intron_variant MELA-AU 3 32880967 32880968 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 32881038 32881038 single base substitution G A intron_variant MELA-AU 3 32881157 32881158 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 32881192 32881192 single base substitution C T intron_variant MELA-AU 3 32881433 32881433 single base substitution G A intron_variant MELA-AU 3 32881713 32881713 single base substitution C T intron_variant MELA-AU 3 32881721 32881721 single base substitution C T intron_variant MELA-AU 3 32881731 32881731 single base substitution C T intron_variant MELA-AU 3 32881922 32881922 single base substitution G A intron_variant MELA-AU 3 32881958 32881958 single base substitution G A intron_variant MELA-AU 3 32882344 32882344 single base substitution C T intron_variant MELA-AU 3 32882350 32882350 single base substitution C T intron_variant MELA-AU 3 32882365 32882365 single base substitution C T intron_variant MELA-AU 3 32882497 32882497 single base substitution G A intron_variant MELA-AU 3 32882632 32882632 single base substitution G A intron_variant MELA-AU 3 32882662 32882663 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 32883088 32883089 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 32883101 32883101 single base substitution C T intron_variant MELA-AU 3 32883297 32883297 single base substitution C T intron_variant MELA-AU 3 32883543 32883543 single base substitution C T intron_variant MELA-AU 3 32883870 32883870 single base substitution T C intron_variant MELA-AU 3 32884140 32884140 single base substitution G A intron_variant MELA-AU 3 32884354 32884355 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 32884766 32884766 single base substitution G A intron_variant MELA-AU 3 32884837 32884837 single base substitution C T intron_variant MELA-AU 3 32885139 32885139 single base substitution C T intron_variant MELA-AU 3 32885140 32885140 single base substitution C T intron_variant MELA-AU 3 32885285 32885285 single base substitution C T intron_variant MELA-AU 3 32885375 32885375 single base substitution C T intron_variant MELA-AU 3 32885648 32885648 single base substitution G A intron_variant MELA-AU 3 32885683 32885683 single base substitution G A intron_variant MELA-AU 3 32885806 32885806 single base substitution G A intron_variant MELA-AU 3 32886127 32886127 single base substitution C T intron_variant MELA-AU 3 32886405 32886405 single base substitution G A intron_variant MELA-AU 3 32886430 32886430 single base substitution G A intron_variant MELA-AU 3 32886736 32886736 single base substitution C T intron_variant MELA-AU 3 32886836 32886836 single base substitution C T intron_variant MELA-AU 3 32887293 32887293 single base substitution A G intron_variant MELA-AU 3 32887443 32887443 single base substitution C G intron_variant MELA-AU 3 32887488 32887488 single base substitution G A intron_variant MELA-AU 3 32887572 32887572 single base substitution T A intron_variant MELA-AU 3 32887598 32887598 single base substitution C T intron_variant MELA-AU 3 32887662 32887662 single base substitution G A intron_variant MELA-AU 3 32888148 32888148 single base substitution C T intron_variant MELA-AU 3 32888626 32888626 single base substitution C T intron_variant MELA-AU 3 32889152 32889152 single base substitution C T intron_variant MELA-AU 3 32889721 32889721 single base substitution A T intron_variant MELA-AU 3 32890425 32890425 single base substitution C T intron_variant MELA-AU 3 32890531 32890531 single base substitution G A intron_variant MELA-AU 3 32890581 32890581 single base substitution G A intron_variant MELA-AU 3 32890638 32890638 single base substitution G A intron_variant MELA-AU 3 32890878 32890878 single base substitution C T intron_variant MELA-AU 3 32891563 32891564 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 32891583 32891583 single base substitution C T intron_variant MELA-AU 3 32891603 32891603 single base substitution C T intron_variant MELA-AU 3 32891708 32891708 single base substitution G A intron_variant MELA-AU 3 32892184 32892185 multiple base substitution (>=2bp and <=200bp) TG AT intron_variant MELA-AU 3 32892314 32892314 single base substitution C T intron_variant MELA-AU 3 32892363 32892363 single base substitution G A intron_variant MELA-AU 3 32892437 32892437 single base substitution G A intron_variant MELA-AU 3 32893074 32893074 single base substitution G A intron_variant MELA-AU 3 32893466 32893466 single base substitution G A intron_variant MELA-AU 3 32893684 32893684 single base substitution G A intron_variant MELA-AU 3 32893795 32893795 single base substitution T C intron_variant MELA-AU 3 32894046 32894046 single base substitution G A intron_variant MELA-AU 3 32894524 32894524 single base substitution C T intron_variant MELA-AU 3 32894834 32894834 single base substitution C A intron_variant MELA-AU 3 32894836 32894836 single base substitution C T intron_variant MELA-AU 3 32894909 32894909 single base substitution A C intron_variant MELA-AU 3 32895056 32895056 single base substitution C T intron_variant MELA-AU 3 32895370 32895370 single base substitution C T intron_variant MELA-AU 3 32896198 32896198 single base substitution C T intron_variant MELA-AU 3 32896204 32896204 single base substitution C T intron_variant MELA-AU 3 32896363 32896363 single base substitution G A intron_variant MELA-AU 3 32896551 32896551 single base substitution C T intron_variant MELA-AU 3 32896692 32896692 single base substitution G A intron_variant MELA-AU 3 32896877 32896877 single base substitution C T intron_variant MELA-AU 3 32896891 32896891 single base substitution G A intron_variant MELA-AU 3 32896908 32896908 single base substitution G A intron_variant MELA-AU 3 32897558 32897558 single base substitution G A intron_variant MELA-AU 3 32897644 32897644 single base substitution G A intron_variant MELA-AU 3 32897890 32897890 single base substitution C T intron_variant MELA-AU 3 32897896 32897896 single base substitution C T intron_variant MELA-AU 3 32897905 32897905 single base substitution C T intron_variant MELA-AU 3 32897993 32897993 single base substitution G A intron_variant MELA-AU 3 32898012 32898012 single base substitution T G intron_variant MELA-AU 3 32898145 32898145 single base substitution C T intron_variant MELA-AU 3 32898583 32898583 single base substitution C T intron_variant MELA-AU 3 32898662 32898662 single base substitution C T intron_variant MELA-AU 3 32898785 32898785 single base substitution C T intron_variant MELA-AU 3 32898850 32898850 single base substitution C T intron_variant MELA-AU 3 32899235 32899235 single base substitution G A intron_variant MELA-AU 3 32899284 32899284 single base substitution G A intron_variant MELA-AU 3 32899377 32899377 single base substitution C T intron_variant MELA-AU 3 32900092 32900092 single base substitution G A intron_variant MELA-AU 3 32900358 32900358 single base substitution C T intron_variant MELA-AU 3 32900464 32900464 single base substitution C T intron_variant MELA-AU 3 32900484 32900484 single base substitution G A intron_variant MELA-AU 3 32900584 32900584 single base substitution C T intron_variant MELA-AU 3 32900633 32900633 single base substitution C T intron_variant MELA-AU 3 32900642 32900642 single base substitution G A intron_variant MELA-AU 3 32900643 32900643 single base substitution A T intron_variant MELA-AU 3 32900753 32900753 single base substitution G A intron_variant MELA-AU 3 32901563 32901563 single base substitution C T intron_variant MELA-AU 3 32901642 32901642 single base substitution C T intron_variant MELA-AU 3 32901656 32901656 single base substitution C T intron_variant MELA-AU 3 32901867 32901867 single base substitution C T intron_variant MELA-AU 3 32902135 32902135 single base substitution C T intron_variant MELA-AU 3 32902177 32902177 single base substitution C T intron_variant MELA-AU 3 32902189 32902189 single base substitution C T intron_variant MELA-AU 3 32902219 32902219 single base substitution C T intron_variant MELA-AU 3 32902247 32902247 single base substitution C T intron_variant MELA-AU 3 32902363 32902363 single base substitution G A intron_variant MELA-AU 3 32902429 32902429 single base substitution G A intron_variant MELA-AU 3 32902512 32902512 single base substitution C T intron_variant MELA-AU 3 32902750 32902750 single base substitution A G intron_variant MELA-AU 3 32903070 32903070 single base substitution C T intron_variant MELA-AU 3 32903465 32903465 single base substitution C T intron_variant MELA-AU 3 32903618 32903618 single base substitution G A intron_variant MELA-AU 3 32903653 32903653 single base substitution C T intron_variant MELA-AU 3 32904391 32904391 single base substitution C T intron_variant MELA-AU 3 32905444 32905444 single base substitution G A intron_variant MELA-AU 3 32905839 32905839 single base substitution G A intron_variant MELA-AU 3 32905879 32905879 single base substitution G A intron_variant MELA-AU 3 32906287 32906287 single base substitution C T intron_variant MELA-AU 3 32906444 32906444 single base substitution C T intron_variant MELA-AU 3 32906445 32906445 single base substitution C T intron_variant MELA-AU 3 32907830 32907830 single base substitution C T intron_variant MELA-AU 3 32908013 32908013 single base substitution C T intron_variant MELA-AU 3 32908126 32908126 single base substitution G A intron_variant MELA-AU 3 32908540 32908540 single base substitution C T intron_variant MELA-AU 3 32908678 32908678 single base substitution C T intron_variant MELA-AU 3 32908920 32908921 deletion of <=200bp TG - intron_variant MELA-AU 3 32908985 32908986 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 32909177 32909177 single base substitution G A intron_variant MELA-AU 3 32909369 32909369 single base substitution G A intron_variant MELA-AU 3 32909691 32909691 single base substitution C T intron_variant MELA-AU 3 32909785 32909785 single base substitution G A intron_variant MELA-AU 3 32909819 32909819 single base substitution C T intron_variant MELA-AU 3 32909822 32909822 single base substitution C T intron_variant MELA-AU 3 32910550 32910550 single base substitution C T intron_variant MELA-AU 3 32910690 32910690 single base substitution G A intron_variant MELA-AU 3 32910814 32910814 single base substitution A T intron_variant MELA-AU 3 32911296 32911296 single base substitution G A intron_variant MELA-AU 3 32911325 32911325 single base substitution G A intron_variant MELA-AU 3 32911461 32911461 single base substitution C T intron_variant MELA-AU 3 32911542 32911542 single base substitution C T intron_variant MELA-AU 3 32911722 32911722 single base substitution G A intron_variant MELA-AU 3 32911931 32911932 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 3 32912659 32912660 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 32913332 32913332 single base substitution C T intron_variant MELA-AU 3 32913451 32913451 single base substitution G A intron_variant MELA-AU 3 32913528 32913528 single base substitution C T intron_variant MELA-AU 3 32913980 32913980 single base substitution C T intron_variant MELA-AU 3 32914033 32914033 single base substitution C T intron_variant MELA-AU 3 32914511 32914511 single base substitution C T intron_variant MELA-AU 3 32915080 32915080 single base substitution C T intron_variant MELA-AU 3 32915179 32915179 single base substitution C T intron_variant MELA-AU 3 32915279 32915279 single base substitution C T intron_variant MELA-AU 3 32915293 32915293 single base substitution C T intron_variant MELA-AU 3 32915299 32915299 single base substitution C T intron_variant MELA-AU 3 32915305 32915305 single base substitution C T splice_region_variant MELA-AU 3 32915377 32915377 single base substitution G T missense_variant G307V 920G>T MELA-AU 3 32915403 32915403 single base substitution G A missense_variant E316K 946G>A MELA-AU 3 32915460 32915460 single base substitution G A missense_variant G335R 1003G>A MELA-AU 3 32915548 32915548 single base substitution G A intron_variant MELA-AU 3 32915626 32915626 single base substitution C T intron_variant MELA-AU 3 32915946 32915946 single base substitution C T intron_variant MELA-AU 3 32916088 32916088 single base substitution C T intron_variant MELA-AU 3 32916165 32916165 single base substitution C T intron_variant MELA-AU 3 32916376 32916376 single base substitution G A intron_variant MELA-AU 3 32916497 32916497 single base substitution G A intron_variant MELA-AU 3 32916907 32916907 single base substitution C T intron_variant MELA-AU 3 32917099 32917099 single base substitution G A intron_variant MELA-AU 3 32917336 32917336 single base substitution C T intron_variant MELA-AU 3 32917592 32917592 single base substitution C T intron_variant MELA-AU 3 32917775 32917775 single base substitution G A intron_variant MELA-AU 3 32917834 32917834 single base substitution G A intron_variant MELA-AU 3 32918186 32918186 single base substitution G A intron_variant MELA-AU 3 32918439 32918439 single base substitution G A intron_variant MELA-AU 3 32918572 32918572 single base substitution C T intron_variant MELA-AU 3 32918910 32918910 single base substitution G C intron_variant MELA-AU 3 32918956 32918956 single base substitution C T intron_variant MELA-AU 3 32918970 32918970 single base substitution C T intron_variant MELA-AU 3 32919089 32919089 single base substitution G A intron_variant MELA-AU 3 32919185 32919185 single base substitution C T intron_variant MELA-AU 3 32919231 32919231 single base substitution A C intron_variant MELA-AU 3 32919313 32919313 single base substitution A G intron_variant MELA-AU 3 32919422 32919422 single base substitution G A intron_variant MELA-AU 3 32919762 32919762 single base substitution G A intron_variant MELA-AU 3 32919849 32919849 single base substitution C T intron_variant MELA-AU 3 32919895 32919895 single base substitution A T intron_variant MELA-AU 3 32919936 32919936 single base substitution C T intron_variant MELA-AU 3 32920384 32920384 single base substitution G A intron_variant MELA-AU 3 32921090 32921090 single base substitution G A intron_variant MELA-AU 3 32922521 32922521 single base substitution A T intron_variant MELA-AU 3 32922752 32922752 single base substitution C T intron_variant MELA-AU 3 32922793 32922793 single base substitution G A intron_variant MELA-AU 3 32923100 32923100 single base substitution C T intron_variant MELA-AU 3 32923523 32923523 single base substitution C T intron_variant MELA-AU 3 32923687 32923687 single base substitution A G intron_variant MELA-AU 3 32924015 32924015 single base substitution C T intron_variant MELA-AU 3 32924150 32924150 single base substitution C T intron_variant MELA-AU 3 32924162 32924162 single base substitution C T intron_variant MELA-AU 3 32924276 32924276 single base substitution C T intron_variant MELA-AU 3 32924383 32924383 single base substitution C T intron_variant MELA-AU 3 32924802 32924802 single base substitution C T intron_variant MELA-AU 3 32924825 32924826 deletion of <=200bp AT - intron_variant MELA-AU 3 32924927 32924927 single base substitution C T intron_variant MELA-AU 3 32924986 32924986 single base substitution C A intron_variant MELA-AU 3 32925124 32925124 single base substitution C T intron_variant MELA-AU 3 32925125 32925125 single base substitution C T intron_variant MELA-AU 3 32925475 32925475 single base substitution C T intron_variant MELA-AU 3 32925883 32925883 single base substitution C T intron_variant MELA-AU 3 32926625 32926625 single base substitution C T intron_variant MELA-AU 3 32926638 32926638 single base substitution C T intron_variant MELA-AU 3 32926893 32926893 single base substitution G A intron_variant MELA-AU 3 32926899 32926899 single base substitution C T intron_variant MELA-AU 3 32926919 32926919 single base substitution C T intron_variant MELA-AU 3 32927030 32927030 single base substitution C T intron_variant MELA-AU 3 32927434 32927434 single base substitution C T synonymous_variant I343I 1029C>T MELA-AU 3 32927645 32927645 single base substitution C T intron_variant MELA-AU 3 32927949 32927949 single base substitution G T intron_variant MELA-AU 3 32928099 32928099 single base substitution G A intron_variant MELA-AU 3 32928198 32928198 single base substitution G A intron_variant MELA-AU 3 32928350 32928350 single base substitution G A intron_variant MELA-AU 3 32928739 32928740 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 32929341 32929341 single base substitution C T intron_variant MELA-AU 3 32929707 32929707 single base substitution A T intron_variant MELA-AU 3 32929987 32929987 single base substitution C T intron_variant MELA-AU 3 32930143 32930143 single base substitution C T intron_variant MELA-AU 3 32930290 32930290 single base substitution C T intron_variant MELA-AU 3 32930497 32930497 single base substitution C T intron_variant MELA-AU 3 32930895 32930895 single base substitution G A intron_variant MELA-AU 3 32931115 32931115 single base substitution C T intron_variant MELA-AU 3 32931844 32931844 single base substitution C T intron_variant MELA-AU 3 32931872 32931872 single base substitution G A synonymous_variant V392V 1176G>A MELA-AU 3 32932244 32932244 single base substitution C T synonymous_variant P516P 1548C>T MELA-AU 3 32932252 32932252 single base substitution C G stop_gained S519* 1556C>G MELA-AU 3 32932544 32932544 single base substitution G A synonymous_variant K616K 1848G>A MELA-AU 3 32932655 32932655 single base substitution C T synonymous_variant F653F 1959C>T MELA-AU 3 32932694 32932694 single base substitution G A synonymous_variant R666R 1998G>A MELA-AU 3 32932742 32932742 single base substitution C T synonymous_variant F682F 2046C>T MELA-AU 3 32932942 32932942 single base substitution C T missense_variant S749F 2246C>T MELA-AU 3 32933036 32933036 single base substitution G A synonymous_variant S780S 2340G>A MELA-AU 3 32933042 32933042 single base substitution C T synonymous_variant R782R 2346C>T MELA-AU 3 32933219 32933219 single base substitution G A missense_variant M841I 2523G>A MELA-AU 3 32933230 32933230 single base substitution C T missense_variant S845F 2534C>T MELA-AU 3 32933286 32933286 single base substitution C T stop_gained R864* 2590C>T MELA-AU 3 32933294 32933294 single base substitution C T synonymous_variant L866L 2598C>T MELA-AU 3 32933413 32933413 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32933534 32933534 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32933570 32933570 single base substitution T A 3_prime_UTR_variant MELA-AU 3 32933599 32933599 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32933631 32933631 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32934011 32934011 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32934412 32934412 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32934533 32934533 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32934677 32934677 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32934692 32934692 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32934888 32934888 single base substitution T G 3_prime_UTR_variant MELA-AU 3 32935469 32935469 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32935641 32935641 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32935650 32935650 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32935764 32935764 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32935801 32935801 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32936043 32936043 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32936103 32936103 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32936138 32936138 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32936210 32936210 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32936267 32936267 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32936349 32936349 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32936544 32936544 single base substitution T C 3_prime_UTR_variant MELA-AU 3 32936921 32936921 single base substitution T C 3_prime_UTR_variant MELA-AU 3 32937161 32937162 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 3 32937447 32937447 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32937706 32937706 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32937727 32937727 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32937844 32937844 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32938476 32938476 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32938678 32938678 single base substitution C A 3_prime_UTR_variant MELA-AU 3 32938958 32938958 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32939284 32939284 single base substitution G A 3_prime_UTR_variant MELA-AU 3 32939310 32939310 single base substitution C T 3_prime_UTR_variant MELA-AU 3 32939463 32939463 deletion of <=200bp G - downstream_gene_variant MELA-AU 3 32939646 32939646 single base substitution C T downstream_gene_variant MELA-AU 3 32939660 32939660 single base substitution C T downstream_gene_variant MELA-AU 3 32939763 32939763 single base substitution G A downstream_gene_variant MELA-AU 3 32939890 32939890 single base substitution C T downstream_gene_variant MELA-AU 3 32939970 32939970 single base substitution C T downstream_gene_variant MELA-AU 3 32939983 32939983 single base substitution C T downstream_gene_variant MELA-AU 3 32940665 32940665 single base substitution G A downstream_gene_variant MELA-AU 3 32941069 32941069 single base substitution C T downstream_gene_variant MELA-AU 3 32941258 32941258 single base substitution G A downstream_gene_variant MELA-AU 3 32941446 32941446 single base substitution A G downstream_gene_variant MELA-AU 3 32941451 32941451 single base substitution G A downstream_gene_variant MELA-AU 3 32941513 32941513 single base substitution G A downstream_gene_variant MELA-AU 3 32941547 32941547 single base substitution T C downstream_gene_variant MELA-AU 3 32941548 32941548 single base substitution C T downstream_gene_variant MELA-AU 3 32941559 32941560 multiple base substitution (>=2bp and <=200bp) AG GA downstream_gene_variant MELA-AU 3 32941625 32941625 single base substitution A T downstream_gene_variant MELA-AU 3 32941673 32941673 single base substitution G A downstream_gene_variant MELA-AU 3 32941769 32941769 single base substitution G A downstream_gene_variant MELA-AU 3 32941789 32941789 single base substitution G A downstream_gene_variant MELA-AU 3 32941891 32941891 single base substitution G A downstream_gene_variant MELA-AU 3 32941978 32941978 single base substitution G A downstream_gene_variant MELA-AU 3 32942015 32942015 single base substitution G A downstream_gene_variant MELA-AU 3 32942305 32942305 single base substitution A T downstream_gene_variant MELA-AU 3 32942406 32942406 single base substitution G A downstream_gene_variant MELA-AU 3 32942441 32942441 single base substitution G A downstream_gene_variant MELA-AU 3 32942638 32942638 single base substitution G A downstream_gene_variant MELA-AU 3 32942901 32942902 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 3 32943337 32943337 single base substitution C T downstream_gene_variant MELA-AU 3 32943672 32943672 single base substitution T C downstream_gene_variant MELA-AU 3 32943925 32943925 single base substitution C T downstream_gene_variant MELA-AU 3 32944198 32944198 single base substitution C T downstream_gene_variant ORCA-IN 3 32879439 32879439 single base substitution C T intron_variant ORCA-IN 3 32891608 32891608 single base substitution C A intron_variant OV-AU 3 32863912 32863912 single base substitution A T intron_variant OV-AU 3 32867102 32867102 single base substitution C A intron_variant OV-AU 3 32868801 32868801 single base substitution G T intron_variant OV-AU 3 32870243 32870243 single base substitution G C intron_variant OV-AU 3 32870365 32870365 single base substitution C G intron_variant OV-AU 3 32871033 32871033 single base substitution C T intron_variant OV-AU 3 32875051 32875051 single base substitution C G intron_variant OV-AU 3 32877515 32877515 single base substitution C G intron_variant OV-AU 3 32884553 32884553 single base substitution C G intron_variant OV-AU 3 32887347 32887347 single base substitution G A intron_variant OV-AU 3 32887854 32887854 single base substitution A G intron_variant OV-AU 3 32894154 32894154 single base substitution T C intron_variant OV-AU 3 32899733 32899733 single base substitution G T intron_variant OV-AU 3 32903029 32903029 single base substitution G T intron_variant OV-AU 3 32907054 32907054 single base substitution C G intron_variant OV-AU 3 32912696 32912696 single base substitution G T intron_variant OV-AU 3 32932739 32932739 single base substitution G A synonymous_variant T681T 2043G>A OV-AU 3 32933145 32933145 single base substitution C T missense_variant R817W 2449C>T OV-AU 3 32933438 32933438 single base substitution T C 3_prime_UTR_variant PACA-AU 3 32860346 32860346 single base substitution G A synonymous_variant P258P 774G>A PACA-AU 3 32867492 32867492 single base substitution G C intron_variant PACA-AU 3 32872013 32872013 single base substitution G T intron_variant PACA-AU 3 32876106 32876106 single base substitution C A intron_variant PACA-AU 3 32876341 32876341 single base substitution A G intron_variant PACA-AU 3 32877471 32877471 single base substitution A C intron_variant PACA-AU 3 32878484 32878484 single base substitution T A intron_variant PACA-AU 3 32879284 32879284 single base substitution C T intron_variant PACA-AU 3 32882575 32882575 insertion of <=200bp - A intron_variant PACA-AU 3 32885030 32885030 single base substitution A G intron_variant PACA-AU 3 32886152 32886152 single base substitution G T intron_variant PACA-AU 3 32888631 32888631 single base substitution C T intron_variant PACA-AU 3 32895761 32895761 single base substitution C A intron_variant PACA-AU 3 32896671 32896671 single base substitution G A intron_variant PACA-AU 3 32907567 32907567 single base substitution C G intron_variant PACA-AU 3 32908968 32908968 single base substitution G T intron_variant PACA-AU 3 32910191 32910191 single base substitution T A intron_variant PACA-AU 3 32910192 32910192 single base substitution T A intron_variant PACA-AU 3 32911150 32911150 single base substitution C T intron_variant PACA-AU 3 32913063 32913063 single base substitution T C intron_variant PACA-AU 3 32915227 32915227 single base substitution G A intron_variant PACA-AU 3 32917309 32917309 single base substitution C G intron_variant PACA-AU 3 32918689 32918689 single base substitution A C intron_variant PACA-AU 3 32920124 32920124 single base substitution A G intron_variant PACA-AU 3 32923427 32923427 single base substitution G A intron_variant PACA-AU 3 32925861 32925861 single base substitution G T intron_variant PACA-AU 3 32926988 32926988 single base substitution C T intron_variant PACA-AU 3 32933287 32933287 single base substitution G A missense_variant R864Q 2591G>A PACA-AU 3 32933360 32933360 single base substitution C T 3_prime_UTR_variant PACA-AU 3 32939075 32939075 single base substitution C T 3_prime_UTR_variant PACA-AU 3 32943438 32943438 single base substitution C T downstream_gene_variant PACA-CA 3 32857495 32857495 single base substitution C A upstream_gene_variant PACA-CA 3 32858855 32858855 single base substitution G A upstream_gene_variant PACA-CA 3 32860047 32860047 single base substitution C T missense_variant R159C 475C>T PACA-CA 3 32860259 32860259 single base substitution C T synonymous_variant R229R 687C>T PACA-CA 3 32863232 32863232 single base substitution C A intron_variant PACA-CA 3 32863424 32863424 single base substitution A C intron_variant PACA-CA 3 32864439 32864439 single base substitution T A intron_variant PACA-CA 3 32866804 32866804 insertion of <=200bp - T intron_variant PACA-CA 3 32868546 32868546 single base substitution C T intron_variant PACA-CA 3 32871667 32871667 deletion of <=200bp G - intron_variant PACA-CA 3 32873592 32873592 insertion of <=200bp - G intron_variant PACA-CA 3 32874172 32874172 single base substitution C T intron_variant PACA-CA 3 32877145 32877145 single base substitution T C intron_variant PACA-CA 3 32880870 32880870 single base substitution G A intron_variant PACA-CA 3 32886272 32886272 single base substitution C T intron_variant PACA-CA 3 32888302 32888302 single base substitution T C intron_variant PACA-CA 3 32889083 32889083 single base substitution T C intron_variant PACA-CA 3 32890089 32890089 single base substitution C T intron_variant PACA-CA 3 32890913 32890913 single base substitution C T intron_variant PACA-CA 3 32894852 32894852 single base substitution G A intron_variant PACA-CA 3 32896926 32896926 single base substitution C T intron_variant PACA-CA 3 32896993 32896993 single base substitution C T intron_variant PACA-CA 3 32897701 32897701 single base substitution G C intron_variant PACA-CA 3 32903406 32903406 single base substitution G A intron_variant PACA-CA 3 32906297 32906297 single base substitution G C intron_variant PACA-CA 3 32906560 32906560 single base substitution G A intron_variant PACA-CA 3 32906637 32906637 single base substitution C T intron_variant PACA-CA 3 32908284 32908284 single base substitution A G intron_variant PACA-CA 3 32910192 32910192 single base substitution T A intron_variant PACA-CA 3 32911256 32911256 single base substitution G A intron_variant PACA-CA 3 32912328 32912328 single base substitution C T intron_variant PACA-CA 3 32914911 32914911 single base substitution C G intron_variant PACA-CA 3 32916679 32916679 single base substitution C A intron_variant PACA-CA 3 32919867 32919867 single base substitution C T intron_variant PACA-CA 3 32920214 32920214 single base substitution G A intron_variant PACA-CA 3 32921399 32921399 single base substitution G A intron_variant PACA-CA 3 32922830 32922845 deletion of <=200bp GCACCACAGTAGCTCC - intron_variant PACA-CA 3 32922909 32922909 single base substitution G T intron_variant PACA-CA 3 32924324 32924324 single base substitution G A intron_variant PACA-CA 3 32924375 32924375 single base substitution G A intron_variant PACA-CA 3 32926926 32926926 single base substitution G C intron_variant PACA-CA 3 32927504 32927504 single base substitution G A missense_variant V367M 1099G>A PACA-CA 3 32928524 32928525 deletion of <=200bp CA - intron_variant PACA-CA 3 32936830 32936830 single base substitution A C 3_prime_UTR_variant PACA-CA 3 32938098 32938098 single base substitution C T 3_prime_UTR_variant PACA-CA 3 32939892 32939892 single base substitution A G downstream_gene_variant PACA-CA 3 32940184 32940184 single base substitution C G downstream_gene_variant PACA-CA 3 32940302 32940302 single base substitution A T downstream_gene_variant PACA-CA 3 32941630 32941630 single base substitution C T downstream_gene_variant PAEN-AU 3 32860651 32860651 single base substitution G A intron_variant PAEN-AU 3 32881147 32881147 deletion of <=200bp T - intron_variant PAEN-AU 3 32887661 32887661 single base substitution G A intron_variant PAEN-IT 3 32902432 32902432 single base substitution C T intron_variant PAEN-IT 3 32902756 32902756 single base substitution G A intron_variant PAEN-IT 3 32925915 32925915 single base substitution C T intron_variant PAEN-IT 3 32941237 32941237 single base substitution T A downstream_gene_variant PBCA-DE 3 32865057 32865057 insertion of <=200bp - A intron_variant PBCA-DE 3 32870157 32870157 insertion of <=200bp - A intron_variant PBCA-DE 3 32873320 32873320 single base substitution G T intron_variant PBCA-DE 3 32875635 32875635 single base substitution A G intron_variant PBCA-DE 3 32878712 32878712 single base substitution C T intron_variant PBCA-DE 3 32894267 32894267 single base substitution C A intron_variant PBCA-DE 3 32896639 32896639 single base substitution G A intron_variant PBCA-DE 3 32909515 32909515 single base substitution G T intron_variant PBCA-DE 3 32910115 32910115 single base substitution G A intron_variant PBCA-DE 3 32927503 32927503 single base substitution C T synonymous_variant A366A 1098C>T PBCA-DE 3 32930281 32930281 single base substitution C G intron_variant PBCA-DE 3 32932739 32932739 single base substitution G A synonymous_variant T681T 2043G>A PBCA-DE 3 32936812 32936812 single base substitution A T 3_prime_UTR_variant PBCA-DE 3 32941756 32941756 single base substitution C T downstream_gene_variant PRAD-CA 3 32862196 32862196 single base substitution G A intron_variant PRAD-CA 3 32865937 32865937 single base substitution G A intron_variant PRAD-CA 3 32875130 32875130 single base substitution A T intron_variant PRAD-CA 3 32897227 32897227 single base substitution A G intron_variant PRAD-CA 3 32902592 32902592 single base substitution G A intron_variant PRAD-UK 3 32884064 32884064 single base substitution G C intron_variant PRAD-UK 3 32894712 32894712 single base substitution G A intron_variant PRAD-UK 3 32895333 32895333 single base substitution G A intron_variant PRAD-UK 3 32896328 32896328 single base substitution A G intron_variant PRAD-UK 3 32898313 32898313 single base substitution T G intron_variant PRAD-UK 3 32902284 32902284 single base substitution C A intron_variant PRAD-UK 3 32903046 32903046 single base substitution C T intron_variant PRAD-UK 3 32904279 32904279 single base substitution T C intron_variant PRAD-UK 3 32936962 32936962 deletion of <=200bp A - 3_prime_UTR_variant PRAD-UK 3 32937280 32937280 single base substitution T C 3_prime_UTR_variant PRAD-UK 3 32937900 32937900 single base substitution T G 3_prime_UTR_variant READ-US 3 32932173 32932173 single base substitution G T missense_variant G493C 1477G>T READ-US 3 32932655 32932655 single base substitution C T synonymous_variant F653F 1959C>T READ-US 3 32932913 32932913 single base substitution C T synonymous_variant F739F 2217C>T RECA-EU 3 32857505 32857505 single base substitution T C upstream_gene_variant RECA-EU 3 32866022 32866022 single base substitution C A intron_variant RECA-EU 3 32873103 32873103 single base substitution T C intron_variant RECA-EU 3 32885216 32885216 single base substitution G T intron_variant RECA-EU 3 32887306 32887306 single base substitution G A intron_variant RECA-EU 3 32898665 32898665 single base substitution T C intron_variant RECA-EU 3 32922176 32922176 single base substitution G C intron_variant RECA-EU 3 32922307 32922307 single base substitution T C intron_variant RECA-EU 3 32928176 32928176 single base substitution T C intron_variant SKCA-BR 3 32856612 32856612 single base substitution C T upstream_gene_variant SKCA-BR 3 32857962 32857962 single base substitution G A upstream_gene_variant SKCA-BR 3 32860635 32860635 single base substitution C T intron_variant SKCA-BR 3 32862308 32862308 single base substitution G A intron_variant SKCA-BR 3 32863439 32863439 single base substitution C T intron_variant SKCA-BR 3 32863700 32863700 single base substitution T G intron_variant SKCA-BR 3 32864938 32864938 single base substitution C T intron_variant SKCA-BR 3 32865215 32865215 single base substitution C T intron_variant SKCA-BR 3 32868364 32868364 single base substitution C T intron_variant SKCA-BR 3 32869983 32869983 single base substitution G A intron_variant SKCA-BR 3 32870518 32870518 single base substitution C T intron_variant SKCA-BR 3 32871036 32871036 single base substitution A G intron_variant SKCA-BR 3 32872249 32872249 single base substitution G A intron_variant SKCA-BR 3 32873094 32873094 single base substitution G A intron_variant SKCA-BR 3 32874286 32874295 deletion of <=200bp TTCCTAGGGG - intron_variant SKCA-BR 3 32876113 32876113 single base substitution A G intron_variant SKCA-BR 3 32876248 32876248 single base substitution C T intron_variant SKCA-BR 3 32876778 32876778 single base substitution C T intron_variant SKCA-BR 3 32877509 32877509 single base substitution C T intron_variant SKCA-BR 3 32877770 32877770 single base substitution T G intron_variant SKCA-BR 3 32879305 32879306 deletion of <=200bp GA - intron_variant SKCA-BR 3 32879804 32879804 single base substitution C T intron_variant SKCA-BR 3 32879909 32879909 single base substitution T G intron_variant SKCA-BR 3 32881323 32881323 single base substitution G T intron_variant SKCA-BR 3 32882159 32882159 single base substitution G A intron_variant SKCA-BR 3 32885576 32885576 single base substitution C T intron_variant SKCA-BR 3 32887139 32887139 single base substitution A T intron_variant SKCA-BR 3 32888682 32888683 deletion of <=200bp AT - intron_variant SKCA-BR 3 32893684 32893684 single base substitution G A intron_variant SKCA-BR 3 32894267 32894267 single base substitution C A intron_variant SKCA-BR 3 32894610 32894613 deletion of <=200bp CTCT - intron_variant SKCA-BR 3 32895515 32895515 single base substitution G A intron_variant SKCA-BR 3 32895563 32895563 single base substitution C T intron_variant SKCA-BR 3 32896716 32896716 single base substitution G A intron_variant SKCA-BR 3 32899632 32899632 single base substitution C T intron_variant SKCA-BR 3 32900696 32900696 single base substitution C T intron_variant SKCA-BR 3 32902022 32902025 deletion of <=200bp TCTC - intron_variant SKCA-BR 3 32902042 32902042 single base substitution G A intron_variant SKCA-BR 3 32902174 32902174 single base substitution C T intron_variant SKCA-BR 3 32902884 32902884 single base substitution A C intron_variant SKCA-BR 3 32903716 32903716 single base substitution G A intron_variant SKCA-BR 3 32905348 32905348 single base substitution A T intron_variant SKCA-BR 3 32906076 32906076 single base substitution G A intron_variant SKCA-BR 3 32909368 32909368 single base substitution G A intron_variant SKCA-BR 3 32909754 32909754 single base substitution G A intron_variant SKCA-BR 3 32910722 32910722 single base substitution G A intron_variant SKCA-BR 3 32911470 32911470 single base substitution C T intron_variant SKCA-BR 3 32911584 32911584 single base substitution C T intron_variant SKCA-BR 3 32911691 32911691 single base substitution C T intron_variant SKCA-BR 3 32912609 32912609 single base substitution G C intron_variant SKCA-BR 3 32912761 32912761 single base substitution G A intron_variant SKCA-BR 3 32913824 32913824 single base substitution C T intron_variant SKCA-BR 3 32914123 32914123 single base substitution C T intron_variant SKCA-BR 3 32914555 32914555 single base substitution T C intron_variant SKCA-BR 3 32914775 32914775 single base substitution T G intron_variant SKCA-BR 3 32915751 32915751 single base substitution G A intron_variant SKCA-BR 3 32916259 32916259 single base substitution A C intron_variant SKCA-BR 3 32917365 32917365 single base substitution C T intron_variant SKCA-BR 3 32917858 32917858 single base substitution C T intron_variant SKCA-BR 3 32918956 32918956 single base substitution C T intron_variant SKCA-BR 3 32920715 32920715 single base substitution T G intron_variant SKCA-BR 3 32923111 32923111 single base substitution C T intron_variant SKCA-BR 3 32923363 32923363 single base substitution C T intron_variant SKCA-BR 3 32925938 32925938 single base substitution C T intron_variant SKCA-BR 3 32926821 32926821 single base substitution T G intron_variant SKCA-BR 3 32926828 32926828 single base substitution T G intron_variant SKCA-BR 3 32927267 32927267 single base substitution C T intron_variant SKCA-BR 3 32927685 32927685 single base substitution C T intron_variant SKCA-BR 3 32929514 32929514 single base substitution G A intron_variant SKCA-BR 3 32930698 32930698 single base substitution G A intron_variant SKCA-BR 3 32931051 32931051 insertion of <=200bp - AATT intron_variant SKCA-BR 3 32931335 32931335 single base substitution A G intron_variant SKCA-BR 3 32932943 32932943 single base substitution C T synonymous_variant S749S 2247C>T SKCA-BR 3 32933255 32933255 single base substitution A T synonymous_variant G853G 2559A>T SKCA-BR 3 32933344 32933344 insertion of <=200bp - GTC 3_prime_UTR_variant SKCA-BR 3 32936983 32936983 single base substitution T C 3_prime_UTR_variant SKCA-BR 3 32938044 32938044 single base substitution G A 3_prime_UTR_variant SKCA-BR 3 32939233 32939233 single base substitution T A 3_prime_UTR_variant SKCA-BR 3 32940666 32940666 single base substitution A G downstream_gene_variant SKCA-BR 3 32941527 32941527 single base substitution G A downstream_gene_variant SKCA-BR 3 32942638 32942638 single base substitution G A downstream_gene_variant SKCA-BR 3 32942830 32942830 single base substitution G A downstream_gene_variant SKCA-BR 3 32944029 32944029 single base substitution G A downstream_gene_variant SKCM-US 3 32859511 32859511 single base substitution C T 5_prime_UTR_variant SKCM-US 3 32859584 32859584 single base substitution C T synonymous_variant F4F 12C>T SKCM-US 3 32860396 32860396 single base substitution T C missense_variant L275P 824T>C SKCM-US 3 32915324 32915324 single base substitution C T synonymous_variant Y289Y 867C>T SKCM-US 3 32915400 32915400 single base substitution C T stop_gained Q315* 943C>T SKCM-US 3 32915464 32915464 single base substitution G A missense_variant R336Q 1007G>A SKCM-US 3 32927434 32927434 single base substitution C T synonymous_variant I343I 1029C>T SKCM-US 3 32927435 32927435 single base substitution G A missense_variant E344K 1030G>A SKCM-US 3 32927476 32927476 single base substitution G A synonymous_variant A357A 1071G>A SKCM-US 3 32931959 32931959 single base substitution C T synonymous_variant V421V 1263C>T SKCM-US 3 32931962 32931962 single base substitution G A synonymous_variant L422L 1266G>A SKCM-US 3 32932199 32932199 single base substitution G A synonymous_variant K501K 1503G>A SKCM-US 3 32932226 32932226 single base substitution T G stop_gained Y510* 1530T>G SKCM-US 3 32932358 32932358 single base substitution C T synonymous_variant P554P 1662C>T SKCM-US 3 32932556 32932556 single base substitution C T synonymous_variant I620I 1860C>T SKCM-US 3 32932625 32932625 single base substitution C T synonymous_variant F643F 1929C>T SKCM-US 3 32932655 32932655 single base substitution C T synonymous_variant F653F 1959C>T SKCM-US 3 32932694 32932694 single base substitution G A synonymous_variant R666R 1998G>A SKCM-US 3 32932742 32932742 single base substitution C T synonymous_variant F682F 2046C>T SKCM-US 3 32932809 32932809 single base substitution G A missense_variant D705N 2113G>A SKCM-US 3 32932868 32932868 single base substitution C T synonymous_variant I724I 2172C>T SKCM-US 3 32932869 32932869 single base substitution C T stop_gained Q725* 2173C>T SKCM-US 3 32932942 32932942 single base substitution C T missense_variant S749F 2246C>T SKCM-US 3 32932943 32932943 single base substitution C T synonymous_variant S749S 2247C>T SKCM-US 3 32933161 32933161 single base substitution A T missense_variant E822V 2465A>T SKCM-US 3 32933207 32933207 single base substitution C G synonymous_variant G837G 2511C>G SKCM-US 3 32933286 32933286 single base substitution C T stop_gained R864* 2590C>T SKCM-US 3 32933287 32933287 single base substitution G A missense_variant R864Q 2591G>A STAD-US 3 32859644 32859644 single base substitution G A synonymous_variant P24P 72G>A STAD-US 3 32859669 32859669 single base substitution T C missense_variant S33P 97T>C STAD-US 3 32859684 32859684 single base substitution A T missense_variant T38S 112A>T STAD-US 3 32859686 32859686 single base substitution G A synonymous_variant T38T 114G>A STAD-US 3 32859698 32859698 deletion of <=200bp G - frameshift_variant S42 STAD-US 3 32859727 32859727 single base substitution C T missense_variant A52V 155C>T STAD-US 3 32859730 32859730 single base substitution C G missense_variant A53G 158C>G STAD-US 3 32860312 32860312 single base substitution C T missense_variant A247V 740C>T STAD-US 3 32860324 32860324 single base substitution C T missense_variant A251V 752C>T STAD-US 3 32860341 32860341 single base substitution G A missense_variant G257R 769G>A STAD-US 3 32860361 32860361 single base substitution G A synonymous_variant P263P 789G>A STAD-US 3 32860404 32860404 single base substitution T A missense_variant C278S 832T>A STAD-US 3 32915308 32915308 single base substitution A G splice_acceptor_variant STAD-US 3 32932065 32932065 single base substitution G A missense_variant D457N 1369G>A STAD-US 3 32932136 32932136 single base substitution C T synonymous_variant S480S 1440C>T STAD-US 3 32932421 32932421 insertion of <=200bp - A frameshift_variant P575P? STAD-US 3 32932496 32932496 single base substitution T C synonymous_variant G600G 1800T>C STAD-US 3 32932581 32932581 single base substitution C T missense_variant R629C 1885C>T STAD-US 3 32932608 32932608 single base substitution G A missense_variant A638T 1912G>A STAD-US 3 32932739 32932739 single base substitution G A synonymous_variant T681T 2043G>A STAD-US 3 32932817 32932817 single base substitution G A synonymous_variant A707A 2121G>A STAD-US 3 32932852 32932852 single base substitution C T missense_variant T719M 2156C>T STAD-US 3 32933115 32933115 single base substitution C T missense_variant R807C 2419C>T THCA-SA 3 32860060 32860060 single base substitution C G missense_variant S163C 488C>G THCA-SA 3 32932841 32932841 single base substitution G A synonymous_variant L715L 2145G>A UCEC-US 3 32915329 32915329 single base substitution A G missense_variant D291G 872A>G UCEC-US 3 32915422 32915422 single base substitution G A missense_variant R322Q 965G>A UCEC-US 3 32927530 32927530 deletion of <=200bp G - frameshift_variant L375 UCEC-US 3 32927537 32927537 single base substitution C T missense_variant R378C 1132C>T UCEC-US 3 32932414 32932414 single base substitution A G missense_variant N573S 1718A>G UCEC-US 3 32932439 32932439 single base substitution G T missense_variant K581N 1743G>T UCEC-US 3 32932570 32932570 single base substitution G A missense_variant R625H 1874G>A UCEC-US 3 32932742 32932742 single base substitution C T synonymous_variant F682F 2046C>T UCEC-US 3 32933115 32933115 single base substitution C T missense_variant R807C 2419C>T UCEC-US 3 32933128 32933128 single base substitution C T missense_variant A811V 2432C>T UCEC-US 3 32933261 32933261 single base substitution C T synonymous_variant I855I 2565C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-24-2289-01 COSM118313 c.1512C>A p.S504S Substitution - coding silent 3:32890716-32890716 + TCGA-D1-A103-01 COSM1043676 c.2432C>T p.A811V Substitution - Missense 3:32891636-32891636 + TCGA-13-0793-01 COSM82429 c.1473C>T p.G491G Substitution - coding silent 3:32890677-32890677 + 57 COSM5011076 c.1121C>T p.A374V Substitution - Missense 3:32886034-32886034 + LUAD-NYU1026 COSM368321 c.2283G>A p.L761L Substitution - coding silent 3:32891487-32891487 + CHC892T COSM4961121 c.309G>A p.A103A Substitution - coding silent 3:32818389-32818389 + TCGA-GN-A266-06 COSM1230415 c.1030G>A p.E344K Substitution - Missense 3:32885943-32885943 + TCGA-EE-A3JD-06 COSM4397681 c.1266G>A p.L422L Substitution - coding silent 3:32890470-32890470 + Pat_50_A COSM5864318 c.1658G>A p.R553Q Substitution - Missense 3:32890862-32890862 + 8058333 COSM264198 c.2591G>A p.R864Q Substitution - Missense 3:32891795-32891795 + TCGA-BR-4361-01 COSM4116914 c.740C>T p.A247V Substitution - Missense 3:32818820-32818820 + TCGA-AP-A051-01 COSM1043671 c.1132C>T p.R378C Substitution - Missense 3:32886045-32886045 + TCGA-F1-6177-01 COSM4116924 c.1912G>A p.A638T Substitution - Missense 3:32891116-32891116 + 49M COSM5593590 c.1868C>T p.A623V Substitution - Missense 3:32891072-32891072 + QC2-03-T2 COSM4956443 c.1806C>T p.S602S Substitution - coding silent 3:32891010-32891010 + TCGA-D3-A5GO-06 COSM3592480 c.2511C>G p.G837G Substitution - coding silent 3:32891715-32891715 + CSCC-32-T COSM4535786 c.2232G>A p.W744* Substitution - Nonsense 3:32891436-32891436 + PD18748a COSM5771010 c.2553C>T p.P851P Substitution - coding silent 3:32891757-32891757 + S0078 COSM5883814 c.612delG p.G205fs*137 Deletion - Frameshift 3:32818692-32818692 + T2225 COSM4736223 c.123G>A p.S41S Substitution - coding silent 3:32818203-32818203 + TCGA-AZ-5407-01 COSM1422420 c.2370C>A p.G790G Substitution - coding silent 3:32891574-32891574 + TCGA-EE-A2MI-06 COSM3592470 c.1263C>T p.V421V Substitution - coding silent 3:32890467-32890467 + TCGA-AA-3713-01 COSM1422413 c.57C>T p.C19C Substitution - coding silent 3:32818137-32818137 + AOCS-130-1-0 COSM3408599 c.2043G>A p.T681T Substitution - coding silent 3:32891247-32891247 + TCGA-EE-A2MR-06 COSM359785 c.1959C>T p.F653F Substitution - coding silent 3:32891163-32891163 + TCGA-A8-A06Q-01 COSM446365 c.1515C>A p.F505L Substitution - Missense 3:32890719-32890719 + TCGA-FU-A3TX-01 COSM4849339 c.939C>T p.Y313Y Substitution - coding silent 3:32873904-32873904 + SCC-15 COSM4597198 c.1141G>A p.E381K Substitution - Missense 3:32886054-32886054 + 61 COSM5736549 c.48G>T p.K16N Substitution - Missense 3:32818128-32818128 + PTC-7C COSM4157972 c.2340G>A p.S780S Substitution - coding silent 3:32891544-32891544 + TCGA-FW-A3R5-06 COSM3915758 c.2247C>T p.S749S Substitution - coding silent 3:32891451-32891451 + SNUH_G76_S1 COSM4157972 c.2340G>A p.S780S Substitution - coding silent 3:32891544-32891544 + TCGA-B5-A0JN-01 COSM1043669 c.965G>A p.R322Q Substitution - Missense 3:32873930-32873930 + ESO-864 COSM1268579 c.1107G>A p.A369A Substitution - coding silent 3:32886020-32886020 + TCGA-G2-A3VY-01 COSM3774914 c.1344G>A p.R448R Substitution - coding silent 3:32890548-32890548 + CSCC-27-T COSM4531607 c.1807G>A p.D603N Substitution - Missense 3:32891011-32891011 + 45 COSM5734234 c.1972G>A p.G658S Substitution - Missense 3:32891176-32891176 + TCGA-CF-A3MG-01 COSM1309036 c.1714G>C p.E572Q Substitution - Missense 3:32890918-32890918 + LUAD-NYU847 COSM376794 c.1277G>A p.R426K Substitution - Missense 3:32890481-32890481 + Gp2D COSM2984142 c.742G>A p.A248T Substitution - Missense 3:32818822-32818822 + TCGA-10-0938-01 COSM69110 c.1007delG p.R336fs*6 Deletion - Frameshift 3:32873972-32873972 + TCGA-G4-6588-01 COSM1422414 c.1070C>T p.A357V Substitution - Missense 3:32885983-32885983 + CSCC-17-T COSM4525091 c.1308G>A p.R436R Substitution - coding silent 3:32890512-32890512 + ESO-640 COSM1268578 c.991G>A p.D331N Substitution - Missense 3:32873956-32873956 + LS174T COSM4646085 c.1213C>T p.R405W Substitution - Missense 3:32890417-32890417 + sysucc-1339T COSM5483244 c.2120C>A p.A707E Substitution - Missense 3:32891324-32891324 + 66 COSM5742934 c.323C>T p.A108V Substitution - Missense 3:32818403-32818403 + TCGA-BR-8589-01 COSM4116918 c.832T>A p.C278S Substitution - Missense 3:32818912-32818912 + BD57T COSM1230411 c.1487G>A p.R496H Substitution - Missense 3:32890691-32890691 + A3 COSM5350967 c.2391A>G p.P797P Substitution - coding silent 3:32891595-32891595 + CHC892T COSM4961121 c.309G>A p.A103A Substitution - coding silent 3:32818389-32818389 + TCGA-CG-4306-01 COSM4116909 c.97T>C p.S33P Substitution - Missense 3:32818177-32818177 + BCM723T COSM4956206 c.2433G>A p.A811A Substitution - coding silent 3:32891637-32891637 + TCGA-AD-6895-01 COSM1422417 c.1657C>T p.R553* Substitution - Nonsense 3:32890861-32890861 + PT36 COSM5915247 c.2327C>T p.P776L Substitution - Missense 3:32891531-32891531 + 66 COSM5742935 c.419C>T p.P140L Substitution - Missense 3:32818499-32818499 + 2492708 COSM5717106 c.2398G>A p.V800I Substitution - Missense 3:32891602-32891602 + TCGA-CG-5723-01 COSM4116923 c.1885C>T p.R629C Substitution - Missense 3:32891089-32891089 + TCGA-GN-A26C-01 COSM3592472 c.1662C>T p.P554P Substitution - coding silent 3:32890866-32890866 + TCGA-HE-A5NI-01 COSM4414264 c.930C>A p.S310R Substitution - Missense 3:32873895-32873895 + pfg272T COSM4752362 c.1163A>G p.K388R Substitution - Missense 3:32890367-32890367 + CHC465T COSM3669134 c.1129G>A p.E377K Substitution - Missense 3:32886042-32886042 + TCGA-HU-A4H8-01 COSM4116917 c.789G>A p.P263P Substitution - coding silent 3:32818869-32818869 + 2492705 COSM5716708 c.2395G>A p.G799R Substitution - Missense 3:32891599-32891599 + HCC89T COSM1617486 c.542C>A p.P181H Substitution - Missense 3:32818622-32818622 + TCGA-CU-A3YL-01 COSM3774915 c.2535C>T p.S845S Substitution - coding silent 3:32891739-32891739 + sysucc-325T COSM5461264 c.1472G>A p.G491D Substitution - Missense 3:32890676-32890676 + PCSI_0492_Pa_P_526 COSM4964837 c.687C>T p.R229R Substitution - coding silent 3:32818767-32818767 + TCGA-19-5954-01 COSM2156762 c.1006C>T p.R336* Substitution - Nonsense 3:32873971-32873971 + TCGA-EE-A2MR-06 COSM3592469 c.1007G>A p.R336Q Substitution - Missense 3:32873972-32873972 + TCGA-EE-A29L-06 COSM1422422 c.2590C>T p.R864* Substitution - Nonsense 3:32891794-32891794 + TCGA-DA-A1HW-06 COSM3592466 c.12C>T p.F4F Substitution - coding silent 3:32818092-32818092 + TCGA-CG-5728-01 COSM4116925 c.2121G>A p.A707A Substitution - coding silent 3:32891325-32891325 + I2L-P19Ta-Tumor-Biopsy COSM247996 c.2419C>T p.R807C Substitution - Missense 3:32891623-32891623 + CSCC-27-T COSM4528508 c.1540G>A p.G514S Substitution - Missense 3:32890744-32890744 + TCGA-BR-4362-01 COSM4116919 c.853-2A>G p.? Unknown 3:32873816-32873816 + TCGA-AZ-4615-01 COSM3696034 c.1148T>G p.L383R Substitution - Missense 3:32886061-32886061 + TCGA-AA-3663-01 COSM1422416 c.1378A>G p.M460V Substitution - Missense 3:32890582-32890582 + TCGA-06-0195-01 COSM3408597 c.120G>A p.T40T Substitution - coding silent 3:32818200-32818200 + RK090_C01 COSM3702411 c.1280C>T p.A427V Substitution - Missense 3:32890484-32890484 + CHC1754T COSM4792908 c.13C>A p.P5T Substitution - Missense 3:32818093-32818093 + TCGA-27-1838-01 COSM3408599 c.2043G>A p.T681T Substitution - coding silent 3:32891247-32891247 + CRC-02T COSM1043675 c.2046C>T p.F682F Substitution - coding silent 3:32891250-32891250 + TCGA-F4-6570-01 COSM1422414 c.1070C>T p.A357V Substitution - Missense 3:32885983-32885983 + HCT15 COSM4632925 c.298C>T p.L100L Substitution - coding silent 3:32818378-32818378 + TCGA-FW-A3R5-06 COSM3915756 c.1071G>A p.A357A Substitution - coding silent 3:32885984-32885984 + TCGA-FS-A4F9-06 COSM3592468 c.943C>T p.Q315* Substitution - Nonsense 3:32873908-32873908 + CSCC-27-T COSM4480492 c.2424C>T p.I808I Substitution - coding silent 3:32891628-32891628 + TCGA-EE-A3AG-06 COSM3592471 c.1503G>A p.K501K Substitution - coding silent 3:32890707-32890707 + HCC2998 COSM583472 c.1474G>A p.D492N Substitution - Missense 3:32890678-32890678 + CSCC-27-T COSM4525921 c.1362G>A p.Q454Q Substitution - coding silent 3:32890566-32890566 + J83_T COSM3945391 c.2382C>A p.F794L Substitution - Missense 3:32891586-32891586 + LUAD-S01356 COSM398230 c.55T>A p.C19S Substitution - Missense 3:32818135-32818135 + BD49T COSM5497705 c.484G>A p.A162T Substitution - Missense 3:32818564-32818564 + CHC1629T COSM4791897 c.2319T>A p.V773V Substitution - coding silent 3:32891523-32891523 + TCGA-E2-A156-01 COSM446367 c.2536G>A p.G846S Substitution - Missense 3:32891740-32891740 + ICGC_MB53 COSM3408599 c.2043G>A p.T681T Substitution - coding silent 3:32891247-32891247 + TCGA-A5-A0GJ-01 COSM1043673 c.1743G>T p.K581N Substitution - Missense 3:32890947-32890947 + HCT15 COSM4632926 c.315T>A p.G105G Substitution - coding silent 3:32818395-32818395 + TCGA-F4-6570-01 COSM1422415 c.1252G>A p.V418M Substitution - Missense 3:32890456-32890456 + HCC2998 COSM583472 c.1474G>A p.D492N Substitution - Missense 3:32890678-32890678 + MI1 COSM1165152 c.1306C>T p.R436W Substitution - Missense 3:32890510-32890510 + B105-1 COSM1753163 c.1534C>T p.H512Y Substitution - Missense 3:32890738-32890738 + 19 COSM5746094 c.1649T>C p.V550A Substitution - Missense 3:32890853-32890853 + TCGA-AP-A056-01 COSM1043668 c.872A>G p.D291G Substitution - Missense 3:32873837-32873837 + PR-00-1165 COSM247996 c.2419C>T p.R807C Substitution - Missense 3:32891623-32891623 + TCGA-CA-6717-01 COSM1422422 c.2590C>T p.R864* Substitution - Nonsense 3:32891794-32891794 + 587276 COSM1230411 c.1487G>A p.R496H Substitution - Missense 3:32890691-32890691 + TCGA-B8-5159-01 COSM480025 c.1375G>C p.V459L Substitution - Missense 3:32890579-32890579 + 61 COSM5736550 c.2221G>T p.G741W Substitution - Missense 3:32891425-32891425 + TCGA-G4-6309-01 COSM1422418 c.1946G>A p.R649Q Substitution - Missense 3:32891150-32891150 + TCGA-BR-7851-01 COSM4116916 c.769G>A p.G257R Substitution - Missense 3:32818849-32818849 + CSCC-49-T COSM4537876 c.2474G>A p.G825D Substitution - Missense 3:32891678-32891678 + 2492720 COSM5719978 c.2199C>T p.F733F Substitution - coding silent 3:32891403-32891403 + LUAD-YINHD COSM350862 c.1537G>A p.D513N Substitution - Missense 3:32890741-32890741 + TCGA-D5-6927-01 COSM1422421 c.2420G>A p.R807H Substitution - Missense 3:32891624-32891624 + Gp5D COSM2984142 c.742G>A p.A248T Substitution - Missense 3:32818822-32818822 + 2492723 COSM5719978 c.2199C>T p.F733F Substitution - coding silent 3:32891403-32891403 + 13280 COSM5615261 c.1630C>G p.Q544E Substitution - Missense 3:32890834-32890834 + 587222 COSM1230412 c.1688C>A p.S563Y Substitution - Missense 3:32890892-32890892 + 8065650 COSM3392351 c.774G>A p.P258P Substitution - coding silent 3:32818854-32818854 + CSCC-27-T COSM4323637 c.2001C>T p.I667I Substitution - coding silent 3:32891205-32891205 + CHEWS029 COSM4584253 c.2344C>T p.R782C Substitution - Missense 3:32891548-32891548 + CSCC-49-T COSM4535214 c.2168G>A p.R723Q Substitution - Missense 3:32891372-32891372 + S00050 COSM318178 c.1315G>T p.A439S Substitution - Missense 3:32890519-32890519 + CSCC-7-T COSM4464901 c.1358C>T p.P453L Substitution - Missense 3:32890562-32890562 + CSCC-7-T COSM3774914 c.1344G>A p.R448R Substitution - coding silent 3:32890548-32890548 + GBM_IV-19 COSM4966955 c.15C>T p.P5P Substitution - coding silent 3:32818095-32818095 + DLD1 COSM3993031 c.1428C>T p.G476G Substitution - coding silent 3:32890632-32890632 + TCGA-BR-7851-01 COSM3408599 c.2043G>A p.T681T Substitution - coding silent 3:32891247-32891247 + I2L-P6-Tumor-Biopsy COSM5355516 c.1044G>A p.T348T Substitution - coding silent 3:32885957-32885957 + TCGA-AA-3672-01 COSM267639 c.2303A>G p.N768S Substitution - Missense 3:32891507-32891507 + B80 COSM1753162 c.660C>A p.C220* Substitution - Nonsense 3:32818740-32818740 + T3152 COSM4736230 c.2556C>A p.D852E Substitution - Missense 3:32891760-32891760 + CSB10 COSM5025915 c.22G>A p.D8N Substitution - Missense 3:32818102-32818102 + TCGA-BR-6452-01 COSM4116911 c.114G>A p.T38T Substitution - coding silent 3:32818194-32818194 + BD114T COSM5502676 c.1831G>T p.G611C Substitution - Missense 3:32891035-32891035 + T263 COSM4736228 c.1484A>C p.K495T Substitution - Missense 3:32890688-32890688 + M006 COSM1738841 c.1661C>A p.P554H Substitution - Missense 3:32890865-32890865 + sysucc-311T COSM3592474 c.1929C>T p.F643F Substitution - coding silent 3:32891133-32891133 + TCGA-CD-A4MG-01 COSM4116908 c.72G>A p.P24P Substitution - coding silent 3:32818152-32818152 + TCGA-F1-6177-01 COSM4116913 c.158C>G p.A53G Substitution - Missense 3:32818238-32818238 + BCM723T COSM4956443 c.1806C>T p.S602S Substitution - coding silent 3:32891010-32891010 + LS174T COSM2984154 c.1389C>T p.P463P Substitution - coding silent 3:32890593-32890593 + 2_RESISTANT COSM1723326 c.924_925insT p.H309fs*64 Insertion - Frameshift 3:32873889-32873890 + CSCC-38-T COSM4535445 c.2192G>A p.G731D Substitution - Missense 3:32891396-32891396 + 2492710 COSM5717106 c.2398G>A p.V800I Substitution - Missense 3:32891602-32891602 + PT50 COSM5937119 c.1160A>C p.E387A Substitution - Missense 3:32890364-32890364 + LUAD-YINHD COSM350861 c.662A>T p.D221V Substitution - Missense 3:32818742-32818742 + CHC1754T COSM4792908 c.13C>A p.P5T Substitution - Missense 3:32818093-32818093 + CHC1211T COSM4954900 c.77C>A p.S26Y Substitution - Missense 3:32818157-32818157 + CSCC-62-T COSM4481775 c.2541C>T p.I847I Substitution - coding silent 3:32891745-32891745 + TCGA-AP-A056-01 COSM1043672 c.1718A>G p.N573S Substitution - Missense 3:32890922-32890922 + TCGA-EE-A2M6-06 COSM3592478 c.2246C>T p.S749F Substitution - Missense 3:32891450-32891450 + Mx43 COSM51064 c.258G>T p.P86P Substitution - coding silent 3:32818338-32818338 + TCGA-HU-A4GH-01 COSM4116915 c.752C>T p.A251V Substitution - Missense 3:32818832-32818832 + TP_2020 COSM5556092 c.252A>G p.G84G Substitution - coding silent 3:32818332-32818332 + TCGA-BR-6452-01 COSM4116910 c.112A>T p.T38S Substitution - Missense 3:32818192-32818192 + TCGA-EI-6507-01 COSM1566814 c.1477G>T p.G493C Substitution - Missense 3:32890681-32890681 + I2L-P6-Tumor-Organoid COSM5355516 c.1044G>A p.T348T Substitution - coding silent 3:32885957-32885957 + HCC094T COSM5806594 c.1967C>T p.P656L Substitution - Missense 3:32891171-32891171 + TCGA-G3-A3CK-01 COSM4922311 c.2018A>G p.D673G Substitution - Missense 3:32891222-32891222 + TCGA-B9-A5W9-01 COSM3993031 c.1428C>T p.G476G Substitution - coding silent 3:32890632-32890632 + 2492709 COSM5717106 c.2398G>A p.V800I Substitution - Missense 3:32891602-32891602 + TCGA-FD-A3B4-01 COSM1309035 c.1622G>C p.S541T Substitution - Missense 3:32890826-32890826 + 587376 COSM1230415 c.1030G>A p.E344K Substitution - Missense 3:32885943-32885943 + CHC465T COSM3669134 c.1129G>A p.E377K Substitution - Missense 3:32886042-32886042 + T3503 COSM4116920 c.1369G>A p.D457N Substitution - Missense 3:32890573-32890573 + TCGA-BR-8680-01 COSM4116920 c.1369G>A p.D457N Substitution - Missense 3:32890573-32890573 + 6115237 COSM5562605 c.1547C>A p.P516H Substitution - Missense 3:32890751-32890751 + TCGA-EE-A3J5-06 COSM3592479 c.2465A>T p.E822V Substitution - Missense 3:32891669-32891669 + pfg029T COSM1642235 c.2358G>A p.S786S Substitution - coding silent 3:32891562-32891562 + CHC432T COSM4953866 c.1963C>A p.R655R Substitution - coding silent 3:32891167-32891167 + TCGA-FR-A3YO-06 COSM3592474 c.1929C>T p.F643F Substitution - coding silent 3:32891133-32891133 + LUAD-RT-S01487 COSM377925 c.1749C>T p.G583G Substitution - coding silent 3:32890953-32890953 + T3091 COSM4736227 c.1387delC p.D465fs*59 Deletion - Frameshift 3:32890591-32890591 + TCGA-EI-6917-01 COSM3749832 c.2217C>T p.F739F Substitution - coding silent 3:32891421-32891421 + CHC892T COSM4798017 c.2498C>T p.A833V Substitution - Missense 3:32891702-32891702 + RKO COSM2984169 c.2136C>T p.G712G Substitution - coding silent 3:32891340-32891340 + 587234 COSM1230414 c.1075G>T p.V359F Substitution - Missense 3:32885988-32885988 + TCGA-EE-A20C-06 COSM3592475 c.1998G>A p.R666R Substitution - coding silent 3:32891202-32891202 + T3174 COSM4736229 c.2528G>A p.R843H Substitution - Missense 3:32891732-32891732 + 6115219 COSM5549511 c.92C>T p.A31V Substitution - Missense 3:32818172-32818172 + HCT15 COSM4632924 c.258G>A p.P86P Substitution - coding silent 3:32818338-32818338 + TCGA-76-6280-01 COSM3408598 c.139G>A p.G47R Substitution - Missense 3:32818219-32818219 + 002 COSM1162093 c.2172C>G p.I724M Substitution - Missense 3:32891376-32891376 + BCM723T COSM4956443 c.1806C>T p.S602S Substitution - coding silent 3:32891010-32891010 + YUKAT COSM5399060 c.1512C>T p.S504S Substitution - coding silent 3:32890716-32890716 + 2492704 COSM5716708 c.2395G>A p.G799R Substitution - Missense 3:32891599-32891599 + I2L-P19Ta-Tumor-Organoid COSM247996 c.2419C>T p.R807C Substitution - Missense 3:32891623-32891623 + TCGA-EB-A3Y7-01 COSM2984172 c.2173C>T p.Q725* Substitution - Nonsense 3:32891377-32891377 + TCGA-B5-A11E-01 COSM1043677 c.2565C>T p.I855I Substitution - coding silent 3:32891769-32891769 + CHC432T COSM4953866 c.1963C>A p.R655R Substitution - coding silent 3:32891167-32891167 + TCGA-AG-A002-01 COSM264198 c.2591G>A p.R864Q Substitution - Missense 3:32891795-32891795 + TCGA-EE-A29E-06 COSM3592476 c.2113G>A p.D705N Substitution - Missense 3:32891317-32891317 + TCGA-D5-6540-01 COSM1422419 c.2243A>T p.D748V Substitution - Missense 3:32891447-32891447 + 2492721 COSM5719978 c.2199C>T p.F733F Substitution - coding silent 3:32891403-32891403 + TCGA-D7-5579-01 COSM4116921 c.1440C>T p.S480S Substitution - coding silent 3:32890644-32890644 + 49M COSM5593591 c.929G>A p.S310N Substitution - Missense 3:32873894-32873894 + TCGA-ER-A198-06 COSM3592473 c.1860C>T p.I620I Substitution - coding silent 3:32891064-32891064 + TCGA-F5-6814-01 COSM359785 c.1959C>T p.F653F Substitution - coding silent 3:32891163-32891163 + TCGA-D1-A16Y-01 COSM1043675 c.2046C>T p.F682F Substitution - coding silent 3:32891250-32891250 + CHC892T COSM4798017 c.2498C>T p.A833V Substitution - Missense 3:32891702-32891702 + T2269 COSM4736224 c.661G>A p.D221N Substitution - Missense 3:32818741-32818741 + TCGA-28-5215-01 COSM3408601 c.2606A>G p.*869* Substitution - coding silent 3:32891810-32891810 + TCGA-AX-A0J1-01 COSM1043670 c.1125delG p.E376fs*11 Deletion - Frameshift 3:32886038-32886038 + TCGA-37-4141-01 COSM730317 c.2527C>T p.R843C Substitution - Missense 3:32891731-32891731 + T3262 COSM4736226 c.1133G>A p.R378H Substitution - Missense 3:32886046-32886046 + TCGA-EE-A2MD-06 COSM1043675 c.2046C>T p.F682F Substitution - coding silent 3:32891250-32891250 + CSCC-27-T COSM4522242 c.1152G>A p.W384* Substitution - Nonsense 3:32886065-32886065 + TCGA-DB-A64L-01 COSM3974377 c.1974C>T p.G658G Substitution - coding silent 3:32891178-32891178 + LUAD-B01970 COSM356132 c.2022T>A p.N674K Substitution - Missense 3:32891226-32891226 + BK0052 COSM4188071 c.705_706delCC p.D235fs*56 Deletion - Frameshift 3:32818785-32818786 + TCGA-D1-A17B-01 COSM247996 c.2419C>T p.R807C Substitution - Missense 3:32891623-32891623 + TCGA-D3-A51T-06 COSM2984146 c.1029C>T p.I343I Substitution - coding silent 3:32885942-32885942 + TCGA-BR-8369-01 COSM247996 c.2419C>T p.R807C Substitution - Missense 3:32891623-32891623 + TCGA-EI-6507-01 COSM5078230 c.2009C>A p.A670D Substitution - Missense 3:32891213-32891213 + TCGA-DD-A115-01 COSM4919668 c.853-1G>A p.? Unknown 3:32873817-32873817 + HT115 COSM2984170 c.2148C>T p.V716V Substitution - coding silent 3:32891352-32891352 + TCGA-BR-4361-01 COSM4116922 c.1800T>C p.G600G Substitution - coding silent 3:32891004-32891004 + TCGA-EE-A2MS-06 COSM1043675 c.2046C>T p.F682F Substitution - coding silent 3:32891250-32891250 + TCGA-A5-A0VP-01 COSM1043674 c.1874G>A p.R625H Substitution - Missense 3:32891078-32891078 + HN_62417 COSM129909 c.1179A>T p.K393N Substitution - Missense 3:32890383-32890383 + CSCC-31-T COSM4564801 c.1464_1465GG>AA p.A489T Substitution - Missense 3:32890668-32890669 + TCGA-FW-A3R5-06 COSM264198 c.2591G>A p.R864Q Substitution - Missense 3:32891795-32891795 + 587342 COSM1230413 c.2301C>A p.N767K Substitution - Missense 3:32891505-32891505 + 2492706 COSM5716708 c.2395G>A p.G799R Substitution - Missense 3:32891599-32891599 + S17_pre COSM5575049 c.2557G>A p.G853R Substitution - Missense 3:32891761-32891761 + SA071 COSM213284 c.922G>T p.G308C Substitution - Missense 3:32873887-32873887 + CHC1211T COSM4954900 c.77C>A p.S26Y Substitution - Missense 3:32818157-32818157 + EV002-R4 COSM1162093 c.2172C>G p.I724M Substitution - Missense 3:32891376-32891376 + TCGA-EE-A2ML-06 COSM3592478 c.2246C>T p.S749F Substitution - Missense 3:32891450-32891450 + LUAD-CHTN-MAD06-00668 COSM359785 c.1959C>T p.F653F Substitution - coding silent 3:32891163-32891163 + CSCC-27-T COSM3774914 c.1344G>A p.R448R Substitution - coding silent 3:32890548-32890548 + 66 COSM5742936 c.1750C>T p.R584C Substitution - Missense 3:32890954-32890954 + SC_9103 COSM5561698 c.495G>A p.P165P Substitution - coding silent 3:32818575-32818575 + TCGA-BT-A20O-01 COSM420046 c.1116G>A p.K372K Substitution - coding silent 3:32886029-32886029 + B105-1-Tumor COSM1753163 c.1534C>T p.H512Y Substitution - Missense 3:32890738-32890738 + TCGA-EB-A44O-01 COSM3592477 c.2172C>T p.I724I Substitution - coding silent 3:32891376-32891376 + TCGA-19-5954 COSM2156762 c.1006C>T p.R336* Substitution - Nonsense 3:32873971-32873971 + LUAD-RT-S01721 COSM380549 c.759G>T p.Q253H Substitution - Missense 3:32818839-32818839 + AOCS-161-1-9 COSM1537632 c.2449C>T p.R817W Substitution - Missense 3:32891653-32891653 + TCGA-EE-A29D-06 COSM3592467 c.867C>T p.Y289Y Substitution - coding silent 3:32873832-32873832 + YURAY COSM5399061 c.1943C>T p.S648F Substitution - Missense 3:32891147-32891147 + TCGA-BR-8591-01 COSM4116912 c.155C>T p.A52V Substitution - Missense 3:32818235-32818235 + S00050 COSM318178 c.1315G>T p.A439S Substitution - Missense 3:32890519-32890519 + LOVO COSM2984136 c.125C>A p.S42* Substitution - Nonsense 3:32818205-32818205 + TCGA-B6-A0IM-01 COSM446366 c.2460G>T p.M820I Substitution - Missense 3:32891664-32891664 + TCGA-CD-8536-01 COSM2984171 c.2156C>T p.T719M Substitution - Missense 3:32891360-32891360 + CHC1629T COSM4791897 c.2319T>A p.V773V Substitution - coding silent 3:32891523-32891523 + pfg068T COSM4752363 c.1993C>T p.R665C Substitution - Missense 3:32891197-32891197 + sysucc-311T COSM1422422 c.2590C>T p.R864* Substitution - Nonsense 3:32891794-32891794 + 134398 COSM323999 c.1135G>T p.E379* Substitution - Nonsense 3:32886048-32886048 + MO_1219 COSM5557461 c.2142C>A p.I714I Substitution - coding silent 3:32891346-32891346 + 1N05-VS-1T05 COSM4323637 c.2001C>T p.I667I Substitution - coding silent 3:32891205-32891205 + 2492722 COSM5719978 c.2199C>T p.F733F Substitution - coding silent 3:32891403-32891403 + TCGA-D9-A6EC-06 COSM4402060 c.824T>C p.L275P Substitution - Missense 3:32818904-32818904 + 325 COSM3723974 c.1668G>A p.L556L Substitution - coding silent 3:32890872-32890872 + BCM723T COSM4956206 c.2433G>A p.A811A Substitution - coding silent 3:32891637-32891637 + T36 COSM4736225 c.914G>A p.R305Q Substitution - Missense 3:32873879-32873879 + HCC89 COSM1617486 c.542C>A p.P181H Substitution - Missense 3:32818622-32818622 + 66 COSM1422421 c.2420G>A p.R807H Substitution - Missense 3:32891624-32891624 + TCGA-D3-A51N-06 COSM3915757 c.1530T>G p.Y510* Substitution - Nonsense 3:32890734-32890734 + MN-26 COSM1578574 c.2339C>T p.S780L Substitution - Missense 3:32891543-32891543 + TCGA-06-0174-01 COSM3408600 c.2345G>A p.R782H Substitution - Missense 3:32891549-32891549 + CSCC-27-T COSM4537380 c.2412G>A p.Q804Q Substitution - coding silent 3:32891616-32891616 + TCGA-BR-4361-01 COSM4116910 c.112A>T p.T38S Substitution - Missense 3:32818192-32818192 + LS180 COSM2984154 c.1389C>T p.P463P Substitution - coding silent 3:32890593-32890593 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.567678 3p22.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.N407H c.1219A>C 3 32931915 HNSC A G 3-UTRSNV . c.2604+2A>G 3 32933302 GBM A T Missense p.E822V c.2465A>T 3 32933161 CM A T Missense p.K393N c.1179A>T 3 32931875 HNSC C A Missense p.D852E c.2556C>A 3 32933252 LUAD C A Missense p.F505L c.1515C>A 3 32932211 BRCA C A Synonymous p.P296P c.888C>A 3 32915345 STAD C A Synonymous p.S504S c.1512C>A 3 32932208 OV C G Missense p.Q544E c.1630C>G 3 32932326 NSCLC C T Missense p.L687F c.2059C>T 3 32932755 CM C T Missense p.P463L c.1388C>T 3 32932084 CM C T Missense p.R807C c.2419C>T 3 32933115 UCEC C T Missense p.R843C c.2527C>T 3 32933223 LUSC C T Missense p.S749F c.2246C>T 3 32932942 CM C T Nonsense p.R336* c.1006C>T 3 32915463 GBM C T Nonsense p.R864* c.2590C>T 3 32933286 CM C T Synonymous p.D765D c.2295C>T 3 32932991 CM C T Synonymous p.F4F c.12C>T 3 32859584 CM C T Synonymous p.F633F c.1899C>T 3 32932595 CM C T Synonymous p.F682F c.2046C>T 3 32932742 CM C T Synonymous p.F682F c.2046C>T 3 32932742 UCEC C T Synonymous p.F794F c.2382C>T 3 32933078 CM C T Synonymous p.G491G c.1473C>T 3 32932169 OV C T Synonymous p.I267I c.801C>T 3 32860373 CM C T Synonymous p.I620I c.1860C>T 3 32932556 CM C T Synonymous p.P554P c.1662C>T 3 32932358 CM C T Synonymous p.S480S c.1440C>T 3 32932136 STAD C T Synonymous p.V421V c.1263C>T 3 32931959 CM G A Missense p.A638T c.1912G>A 3 32932608 STAD G A Missense p.D331N c.991G>A 3 32915448 ESCA G A Missense p.D492N c.1474G>A 3 32932170 LUAD G A Missense p.D8N c.22G>A 3 32859594 BRCA G A Missense p.G47R c.139G>A 3 32859711 GBM G A Missense p.G846S c.2536G>A 3 32933232 BRCA G A Missense p.R322Q c.965G>A 3 32915422 UCEC G A Missense p.R625H c.1874G>A 3 32932570 UCEC G A Missense p.R782H c.2345G>A 3 32933041 GBM G A Missense p.R796H c.2387G>A 3 32933083 HNSC G A Missense p.V418M c.1252G>A 3 32931948 HNSC G A Synonymous p.A369A c.1107G>A 3 32927512 ESCA G A Synonymous p.A707A c.2121G>A 3 32932817 STAD G A Synonymous p.G839G c.2517G>A 3 32933213 HNSC G A Synonymous p.K372K c.1116G>A 3 32927521 BLCA G A Synonymous p.K501K c.1503G>A 3 32932199 CM G A Synonymous p.L422L c.1266G>A 3 32931962 CM G A Synonymous p.R666R c.1998G>A 3 32932694 CM G A Synonymous p.S786S c.2358G>A 3 32933054 STAD G A Synonymous p.T40T c.120G>A 3 32859692 GBM G A Synonymous p.T681T c.2043G>A 3 32932739 GBM G A Synonymous p.T681T c.2043G>A 3 32932739 MB G C Missense p.E572Q c.1714G>C 3 32932410 BLCA G C Missense p.S541T c.1622G>C 3 32932318 BLCA G C Missense p.V459L c.1375G>C 3 32932071 RCCC G - Frameshift p.R336Hfs*6 c.1007delG 3 32915464 OV G T Missense p.A439S c.1315G>T 3 32932011 SCLC G T Missense p.A801S c.2401G>T 3 32933097 LUAD G T Missense p.G308C c.922G>T 3 32915379 BRCA G T Missense p.K581N c.1743G>T 3 32932439 UCEC G T Missense p.M820I c.2460G>T 3 32933156 BRCA G T Nonsense p.E379* c.1135G>T 3 32927540 SCLC G T Synonymous p.L438L c.1314G>T 3 32932010 HNSC G T Synonymous p.P242P c.726G>T 3 32860298 LUAD T C Missense p.S33P c.97T>C 3 32859669 STAD