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 20 33591402 33591402 + Silent SNP G G C TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr20:33591402G>C c.2067C>G c.(2065-2067)ctC>ctG p.L689L BLCA 20 33593524 33593524 + Missense_Mutation SNP C C T TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr20:33593524C>T c.1910G>A c.(1909-1911)cGa>cAa p.R637Q BLCA 20 33595366 33595366 + Missense_Mutation SNP C C T TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr20:33595366C>T c.1673G>A c.(1672-1674)cGa>cAa p.R558Q BLCA 20 33596493 33596493 + Silent SNP C C T TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr20:33596493C>T c.1569G>A c.(1567-1569)aaG>aaA p.K523K BLCA 20 33596513 33596513 + Missense_Mutation SNP G G A TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr20:33596513G>A c.1549C>T c.(1549-1551)Cgt>Tgt p.R517C BLCA 20 33609026 33609026 + Silent SNP G G C TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr20:33609026G>C c.1185C>G c.(1183-1185)ctC>ctG p.L395L BLCA 20 33632447 33632447 + Silent SNP G G A TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr20:33632447G>A c.726C>T c.(724-726)ctC>ctT p.L242L BLCA 20 33637720 33637720 + Silent SNP C C T TCGA-CF-A9FF-01A-11D-A38G-08 TCGA-CF-A9FF-10A-01D-A38J-08 g.chr20:33637720C>T c.606G>A c.(604-606)aaG>aaA p.K202K BLCA 20 33637735 33637735 + Missense_Mutation SNP C C G TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr20:33637735C>G c.591G>C c.(589-591)ttG>ttC p.L197F BLCA 20 33680544 33680544 + Missense_Mutation SNP C C A TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr20:33680544C>A c.41G>T c.(40-42)cGa>cTa p.R14L BRCA 20 33591329 33591329 + Missense_Mutation SNP G G A TCGA-C8-A3M7-01A-12D-A21Q-09 TCGA-C8-A3M7-10A-01D-A21Q-09 g.chr20:33591329G>A c.2140C>T c.(2140-2142)Cgg>Tgg p.R714W BRCA 20 33591392 33591392 + Silent SNP G G A TCGA-C8-A133-01A-32D-A12B-09 TCGA-C8-A133-10A-01D-A12B-09 g.chr20:33591392G>A c.2077C>T c.(2077-2079)Ctg>Ttg p.L693L BRCA 20 33598008 33598010 + In_Frame_Del DEL GCT GCT - TCGA-BH-A0GY-01A-11W-A071-09 TCGA-BH-A0GY-10A-01W-A071-09 g.chr20:33598008_33598010delGCT c.1491_1493delAGC c.(1489-1494)gaagct>gat p.497_498EA>D BRCA 20 33600860 33600860 + Missense_Mutation SNP A A T TCGA-BH-A0C0-01A-21W-A071-09 TCGA-BH-A0C0-11A-21W-A100-09 g.chr20:33600860A>T c.1360T>A c.(1360-1362)Ttg>Atg p.L454M BRCA 20 33603886 33603886 + Missense_Mutation SNP G G T TCGA-AC-A23G-01A-11D-A20S-09 TCGA-AC-A23G-11A-12D-A20S-09 g.chr20:33603886G>T c.1275C>A c.(1273-1275)gaC>gaA p.D425E BRCA 20 33609154 33609154 + Missense_Mutation SNP T T C TCGA-AO-A0J9-01A-11W-A050-09 TCGA-AO-A0J9-10A-01W-A055-09 g.chr20:33609154T>C c.1057A>G c.(1057-1059)Att>Gtt p.I353V BRCA 20 33623023 33623023 + Silent SNP G G A TCGA-AQ-A04J-01A-02W-A050-09 TCGA-AQ-A04J-10A-01W-A055-09 g.chr20:33623023G>A c.954C>T c.(952-954)ttC>ttT p.F318F BRCA 20 33645320 33645320 + Missense_Mutation SNP T T C TCGA-E9-A3HO-01A-11D-A20S-09 TCGA-E9-A3HO-10A-02D-A20S-09 g.chr20:33645320T>C c.469A>G c.(469-471)Aaa>Gaa p.K157E CESC 20 33591061 33591061 + Nonsense_Mutation SNP C C T TCGA-EK-A2H0-01A-11D-A17W-09 TCGA-EK-A2H0-10A-01D-A17W-09 g.chr20:33591061C>T c.2282G>A c.(2281-2283)tGg>tAg p.W761* CESC 20 33594341 33594341 + Missense_Mutation SNP G G A TCGA-C5-A1MJ-01A-11D-A14W-08 TCGA-C5-A1MJ-10A-01D-A14W-08 g.chr20:33594341G>A c.1724C>T c.(1723-1725)tCa>tTa p.S575L CESC 20 33603935 33603935 + Missense_Mutation SNP C C T TCGA-EK-A2RA-01A-11D-A18J-09 TCGA-EK-A2RA-10A-01D-A18J-09 g.chr20:33603935C>T c.1226G>A c.(1225-1227)aGa>aAa p.R409K CHOL 20 33632325 33632325 + Missense_Mutation SNP G G A TCGA-ZH-A8Y8-01A-51D-A417-09 TCGA-ZH-A8Y8-10A-01D-A41A-09 g.chr20:33632325G>A c.848C>T c.(847-849)gCa>gTa p.A283V COAD 20 33591308 33591308 + Missense_Mutation SNP A A G TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr20:33591308A>G c.2161T>C c.(2161-2163)Tac>Cac p.Y721H COAD 20 33591340 33591340 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr20:33591340C>T c.2129G>A c.(2128-2130)cGg>cAg p.R710Q COAD 20 33592270 33592270 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr20:33592270C>T c.2040G>A c.(2038-2040)acG>acA p.T680T COAD 20 33593572 33593572 + Missense_Mutation SNP A A G TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr20:33593572A>G c.1862T>C c.(1861-1863)cTg>cCg p.L621P COAD 20 33596482 33596482 + Missense_Mutation SNP G G A TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr20:33596482G>A c.1580C>T c.(1579-1581)gCa>gTa p.A527V COAD 20 33609028 33609028 + Missense_Mutation SNP G G T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr20:33609028G>T c.1183C>A c.(1183-1185)Ctc>Atc p.L395I COAD 20 33632316 33632316 + Missense_Mutation SNP A A G TCGA-CA-6716-01A-11D-1835-10 TCGA-CA-6716-10A-01D-1835-10 g.chr20:33632316A>G c.857T>C c.(856-858)aTc>aCc p.I286T COAD 20 33632433 33632433 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr20:33632433C>T c.740G>A c.(739-741)cGg>cAg p.R247Q COAD 20 33637714 33637714 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr20:33637714G>T c.612C>A c.(610-612)ttC>ttA p.F204L COADREAD 20 33591308 33591308 + Missense_Mutation SNP A A G TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr20:33591308A>G c.2161T>C c.(2161-2163)Tac>Cac p.Y721H COADREAD 20 33591340 33591340 + Missense_Mutation SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr20:33591340C>T c.2129G>A c.(2128-2130)cGg>cAg p.R710Q COADREAD 20 33592270 33592270 + Silent SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr20:33592270C>T c.2040G>A c.(2038-2040)acG>acA p.T680T COADREAD 20 33593572 33593572 + Missense_Mutation SNP A A G TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr20:33593572A>G c.1862T>C c.(1861-1863)cTg>cCg p.L621P COADREAD 20 33596482 33596482 + Missense_Mutation SNP G G A TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr20:33596482G>A c.1580C>T c.(1579-1581)gCa>gTa p.A527V COADREAD 20 33609028 33609028 + Missense_Mutation SNP G G T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr20:33609028G>T c.1183C>A c.(1183-1185)Ctc>Atc p.L395I COADREAD 20 33609059 33609059 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr20:33609059C>T c.1152G>A c.(1150-1152)gaG>gaA p.E384E COADREAD 20 33632316 33632316 + Missense_Mutation SNP A A G TCGA-CA-6716-01A-11D-1835-10 TCGA-CA-6716-10A-01D-1835-10 g.chr20:33632316A>G c.857T>C c.(856-858)aTc>aCc p.I286T COADREAD 20 33632316 33632316 + Missense_Mutation SNP A A G TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr20:33632316A>G c.857T>C c.(856-858)aTc>aCc p.I286T COADREAD 20 33632433 33632433 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr20:33632433C>T c.740G>A c.(739-741)cGg>cAg p.R247Q COADREAD 20 33637714 33637714 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr20:33637714G>T c.612C>A c.(610-612)ttC>ttA p.F204L COADREAD 20 33657149 33657149 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr20:33657149C>A c.364G>T c.(364-366)Gaa>Taa p.E122* DLBC 20 33665969 33665969 + Silent SNP C C T TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr20:33665969C>T c.177G>A c.(175-177)gaG>gaA p.E59E ESCA 20 33632411 33632411 + Silent SNP T T C TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr20:33632411T>C c.762A>G c.(760-762)tcA>tcG p.S254S GBM 20 33591328 33591328 + Missense_Mutation SNP C C T TCGA-14-1825-01A-01W-0643-08 TCGA-14-1825-10A-01W-0644-08 g.chr20:33591328C>T c.2141G>A c.(2140-2142)cGg>cAg p.R714Q GBMLGG 20 33591328 33591328 + Missense_Mutation SNP C C T TCGA-14-1825-01A-01W-0643-08 TCGA-14-1825-10A-01W-0644-08 g.chr20:33591328C>T c.2141G>A c.(2140-2142)cGg>cAg p.R714Q GBMLGG 20 33632378 33632378 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:33632378C>T c.795G>A c.(793-795)acG>acA p.T265T GBMLGG 20 33637791 33637791 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:33637791C>A c.535G>T c.(535-537)Gga>Tga p.G179* GBMLGG 20 33657162 33657162 + Missense_Mutation SNP C C A TCGA-CS-5397-01A-01D-1893-08 TCGA-CS-5397-10A-03D-1893-08 g.chr20:33657162C>A c.351G>T c.(349-351)agG>agT p.R117S HNSC 20 33593578 33593578 + Missense_Mutation SNP C C T TCGA-BA-5557-01A-01D-1512-08 TCGA-BA-5557-10A-01D-1512-08 g.chr20:33593578C>T c.1856G>A c.(1855-1857)aGc>aAc p.S619N HNSC 20 33596524 33596524 + Missense_Mutation SNP C C A TCGA-CQ-A4C9-01A-11D-A25D-08 TCGA-CQ-A4C9-10A-01D-A25E-08 g.chr20:33596524C>A c.1538G>T c.(1537-1539)gGc>gTc p.G513V HNSC 20 33609096 33609096 + Missense_Mutation SNP C C T TCGA-CV-5432-01A-02D-1683-08 TCGA-CV-5432-10A-01D-1870-08 g.chr20:33609096C>T c.1115G>A c.(1114-1116)aGa>aAa p.R372K HNSC 20 33632354 33632354 + Silent SNP C C T TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr20:33632354C>T c.819G>A c.(817-819)caG>caA p.Q273Q HNSC 20 33680571 33680571 + Missense_Mutation SNP G G A TCGA-UF-A7JK-01A-11D-A34J-08 TCGA-UF-A7JK-10A-01D-A34M-08 g.chr20:33680571G>A c.14C>T c.(13-15)cCg>cTg p.P5L KIPAN 20 33591257 33591257 + Missense_Mutation SNP G G T TCGA-DW-7837-01A-11D-2136-08 TCGA-DW-7837-10A-01D-2136-08 g.chr20:33591257G>T c.2212C>A c.(2212-2214)Cag>Aag p.Q738K KIPAN 20 33595391 33595391 + Missense_Mutation SNP C C T TCGA-CZ-5467-01A-01D-1501-10 TCGA-CZ-5467-11A-01D-1501-10 g.chr20:33595391C>T c.1648G>A c.(1648-1650)Gca>Aca p.A550T KIPAN 20 33596526 33596526 + Missense_Mutation SNP C C G TCGA-B0-4700-01A-02D-1534-10 TCGA-B0-4700-11A-01D-1534-10 g.chr20:33596526C>G c.1536G>C c.(1534-1536)agG>agC p.R512S KIPAN 20 33603843 33603844 + Frame_Shift_Ins INS - - AA TCGA-PJ-A5Z8-01A-11D-A28G-10 TCGA-PJ-A5Z8-10A-01D-A28G-10 g.chr20:33603843_33603844insAA c.1317_1318insTT c.(1315-1320)ctccatfs p.H440fs KIPAN 20 33603887 33603887 + Missense_Mutation SNP T T A TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr20:33603887T>A c.1274A>T c.(1273-1275)gAc>gTc p.D425V KIPAN 20 33623074 33623074 + Silent SNP A A C TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr20:33623074A>C c.903T>G c.(901-903)ctT>ctG p.L301L KIPAN 20 33623099 33623099 + Missense_Mutation SNP C C A TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr20:33623099C>A c.878G>T c.(877-879)aGc>aTc p.S293I KIRC 20 33595391 33595391 + Missense_Mutation SNP C C T TCGA-CZ-5467-01A-01D-1501-10 TCGA-CZ-5467-11A-01D-1501-10 g.chr20:33595391C>T c.1648G>A c.(1648-1650)Gca>Aca p.A550T KIRC 20 33596526 33596526 + Missense_Mutation SNP C C G TCGA-B0-4700-01A-02D-1534-10 TCGA-B0-4700-11A-01D-1534-10 g.chr20:33596526C>G c.1536G>C c.(1534-1536)agG>agC p.R512S KIRC 20 33603887 33603887 + Missense_Mutation SNP T T A TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr20:33603887T>A c.1274A>T c.(1273-1275)gAc>gTc p.D425V KIRP 20 33591257 33591257 + Missense_Mutation SNP G G T TCGA-DW-7837-01A-11D-2136-08 TCGA-DW-7837-10A-01D-2136-08 g.chr20:33591257G>T c.2212C>A c.(2212-2214)Cag>Aag p.Q738K KIRP 20 33603843 33603844 + Frame_Shift_Ins INS - - AA TCGA-PJ-A5Z8-01A-11D-A28G-10 TCGA-PJ-A5Z8-10A-01D-A28G-10 g.chr20:33603843_33603844insAA c.1317_1318insTT c.(1315-1320)ctccatfs p.H440fs KIRP 20 33623074 33623074 + Silent SNP A A C TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr20:33623074A>C c.903T>G c.(901-903)ctT>ctG p.L301L KIRP 20 33623099 33623099 + Missense_Mutation SNP C C A TCGA-HE-A5NL-01A-11D-A26P-10 TCGA-HE-A5NL-10A-01D-A26P-10 g.chr20:33623099C>A c.878G>T c.(877-879)aGc>aTc p.S293I LAML 20 33680571 33680571 + Missense_Mutation SNP G G A TCGA-AB-2989-03A-01D-0739-09 TCGA-AB-2989-11A-01D-0739-09 g.chr20:33680571G>A c.14C>T c.(13-15)cCg>cTg p.P5L LGG 20 33632378 33632378 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:33632378C>T c.795G>A c.(793-795)acG>acA p.T265T LGG 20 33637791 33637791 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:33637791C>A c.535G>T c.(535-537)Gga>Tga p.G179* LGG 20 33657162 33657162 + Missense_Mutation SNP C C A TCGA-CS-5397-01A-01D-1893-08 TCGA-CS-5397-10A-03D-1893-08 g.chr20:33657162C>A c.351G>T c.(349-351)agG>agT p.R117S LIHC 20 33598060 33598060 + Missense_Mutation SNP G G C TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr20:33598060G>C c.1441C>G c.(1441-1443)Ctg>Gtg p.L481V LIHC 20 33598060 33598060 + Missense_Mutation SNP G G C TCGA-EP-A12J-01A-11D-A12Z-10 TCGA-EP-A12J-10A-01D-A12Z-10 g.chr20:33598060G>C c.1441C>G c.(1441-1443)Ctg>Gtg p.L481V LIHC 20 33657145 33657145 + Missense_Mutation SNP G G C TCGA-DD-AADA-01A-11D-A40R-10 TCGA-DD-AADA-10A-01D-A40U-10 g.chr20:33657145G>C c.368C>G c.(367-369)aCc>aGc p.T123S LUAD 20 33591358 33591358 + Missense_Mutation SNP C C T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr20:33591358C>T c.2111G>A c.(2110-2112)cGg>cAg p.R704Q LUAD 20 33592273 33592273 + Silent SNP C C T TCGA-L4-A4E5-01A-11D-A24P-08 TCGA-L4-A4E5-10A-01D-A24P-08 g.chr20:33592273C>T c.2037G>A c.(2035-2037)caG>caA p.Q679Q LUAD 20 33603840 33603840 + Missense_Mutation SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr20:33603840C>A c.1321G>T c.(1321-1323)Ggt>Tgt p.G441C LUAD 20 33608995 33608995 + Nonsense_Mutation SNP G G A TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr20:33608995G>A c.1216C>T c.(1216-1218)Cag>Tag p.Q406* LUAD 20 33609050 33609050 + Silent SNP G G A TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chr20:33609050G>A c.1161C>T c.(1159-1161)taC>taT p.Y387Y LUAD 20 33609144 33609144 + Missense_Mutation SNP G G A TCGA-95-A4VN-01A-11D-A25L-08 TCGA-95-A4VN-10A-01D-A25L-08 g.chr20:33609144G>A c.1067C>T c.(1066-1068)cCt>cTt p.P356L LUAD 20 33623090 33623090 + Missense_Mutation SNP C C A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr20:33623090C>A c.887G>T c.(886-888)gGc>gTc p.G296V LUAD 20 33665863 33665863 + Missense_Mutation SNP G G C TCGA-73-4658-01A-01D-1753-08 TCGA-73-4658-11A-01D-1753-08 g.chr20:33665863G>C c.283C>G c.(283-285)Caa>Gaa p.Q95E LUAD 20 33665865 33665865 + Missense_Mutation SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr20:33665865C>A c.281G>T c.(280-282)tGt>tTt p.C94F LUAD 20 33665942 33665942 + Silent SNP T T C TCGA-86-8671-01A-11D-2393-08 TCGA-86-8671-10A-01D-2393-08 g.chr20:33665942T>C c.204A>G c.(202-204)caA>caG p.Q68Q LUSC 20 33591291 33591291 + Silent SNP G G C TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr20:33591291G>C c.2178C>G c.(2176-2178)ctC>ctG p.L726L LUSC 20 33593507 33593507 + Missense_Mutation SNP C C G TCGA-33-6737-01A-11D-1817-08 TCGA-33-6737-11A-01D-1817-08 g.chr20:33593507C>G c.1927G>C c.(1927-1929)Gat>Cat p.D643H LUSC 20 33593519 33593519 + Missense_Mutation SNP C C G TCGA-18-3410-01A-01D-0983-08 TCGA-18-3410-11A-01D-0983-08 g.chr20:33593519C>G c.1915G>C c.(1915-1917)Gaa>Caa p.E639Q LUSC 20 33593586 33593586 + Missense_Mutation SNP C C G TCGA-18-3410-01A-01D-0983-08 TCGA-18-3410-11A-01D-0983-08 g.chr20:33593586C>G c.1848G>C c.(1846-1848)caG>caC p.Q616H LUSC 20 33595396 33595396 + Missense_Mutation SNP G G A TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr20:33595396G>A c.1643C>T c.(1642-1644)tCc>tTc p.S548F LUSC 20 33596469 33596469 + Silent SNP G G A TCGA-39-5022-01A-21D-1817-08 TCGA-39-5022-11A-01D-1817-08 g.chr20:33596469G>A c.1593C>T c.(1591-1593)ttC>ttT p.F531F LUSC 20 33623037 33623037 + Missense_Mutation SNP C C A TCGA-22-4595-01A-01D-1267-08 TCGA-22-4595-11A-01D-1267-08 g.chr20:33623037C>A c.940G>T c.(940-942)Ggc>Tgc p.G314C LUSC 20 33623108 33623108 + Missense_Mutation SNP G G T TCGA-46-3765-01A-01D-0983-08 TCGA-46-3765-10A-01D-0983-08 g.chr20:33623108G>T c.869C>A c.(868-870)gCc>gAc p.A290D LUSC 20 33637788 33637788 + Missense_Mutation SNP C C A TCGA-66-2757-01A-01D-1522-08 TCGA-66-2757-11A-01D-1522-08 g.chr20:33637788C>A c.538G>T c.(538-540)Gtt>Ttt p.V180F LUSC 20 33657206 33657206 + Missense_Mutation SNP G G A TCGA-22-5480-01A-01D-1632-08 TCGA-22-5480-11A-01D-1632-08 g.chr20:33657206G>A c.307C>T c.(307-309)Cct>Tct p.P103S PAAD 20 33591414 33591414 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:33591414G>A c.2055C>T c.(2053-2055)aaC>aaT p.N685N PRAD 20 33665958 33665958 + Missense_Mutation SNP G G A TCGA-MG-AAMC-01A-11D-A41K-08 TCGA-MG-AAMC-10A-01D-A41N-08 g.chr20:33665958G>A c.188C>T c.(187-189)aCg>aTg p.T63M READ 20 33609059 33609059 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr20:33609059C>T c.1152G>A c.(1150-1152)gaG>gaA p.E384E READ 20 33632316 33632316 + Missense_Mutation SNP A A G TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr20:33632316A>G c.857T>C c.(856-858)aTc>aCc p.I286T READ 20 33657149 33657149 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr20:33657149C>A c.364G>T c.(364-366)Gaa>Taa p.E122* SARC 20 33632313 33632313 + Missense_Mutation SNP T T G TCGA-QQ-A8VG-01A-11D-A37C-09 TCGA-QQ-A8VG-10A-01D-A37F-09 g.chr20:33632313T>G c.860A>C c.(859-861)aAt>aCt p.N287T SKCM 20 33592285 33592285 + Silent SNP G G A TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr20:33592285G>A c.2025C>T c.(2023-2025)atC>atT p.I675I SKCM 20 33593574 33593574 + Silent SNP G G A TCGA-ER-A195-06A-11D-A196-08 TCGA-ER-A195-10A-01D-A198-08 g.chr20:33593574G>A c.1860C>T c.(1858-1860)tcC>tcT p.S620S SKCM 20 33596537 33596537 + Missense_Mutation SNP C C A TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr20:33596537C>A c.1525G>T c.(1525-1527)Gat>Tat p.D509Y SKCM 20 33596548 33596548 + Missense_Mutation SNP C C A TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr20:33596548C>A c.1514G>T c.(1513-1515)aGt>aTt p.S505I SKCM 20 33623094 33623094 + Missense_Mutation SNP G G A TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr20:33623094G>A c.883C>T c.(883-885)Cct>Tct p.P295S SKCM 20 33680544 33680544 + Missense_Mutation SNP C C T TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr20:33680544C>T c.41G>A c.(40-42)cGa>cAa p.R14Q

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 20 33585437 33585437 single base substitution C T downstream_gene_variant BLCA-CN 20 33587410 33587410 single base substitution G A downstream_gene_variant BLCA-CN 20 33588934 33588934 single base substitution G A downstream_gene_variant BLCA-US 20 33586326 33586326 single base substitution G C downstream_gene_variant BLCA-US 20 33588881 33588881 single base substitution G A downstream_gene_variant BLCA-US 20 33591402 33591402 single base substitution G C synonymous_variant L291L 873C>G BLCA-US 20 33591402 33591402 single base substitution G C synonymous_variant L650L 1950C>G BLCA-US 20 33591402 33591402 single base substitution G C synonymous_variant L681L 2043C>G BLCA-US 20 33591402 33591402 single base substitution G C synonymous_variant L689L 2067C>G BLCA-US 20 33593524 33593524 single base substitution C T missense_variant R239Q 716G>A BLCA-US 20 33593524 33593524 single base substitution C T missense_variant R598Q 1793G>A BLCA-US 20 33593524 33593524 single base substitution C T missense_variant R629Q 1886G>A BLCA-US 20 33593524 33593524 single base substitution C T missense_variant R637Q 1910G>A BLCA-US 20 33596493 33596493 single base substitution C T synonymous_variant K125K 375G>A BLCA-US 20 33596493 33596493 single base substitution C T synonymous_variant K484K 1452G>A BLCA-US 20 33596493 33596493 single base substitution C T synonymous_variant K515K 1545G>A BLCA-US 20 33596493 33596493 single base substitution C T synonymous_variant K523K 1569G>A BLCA-US 20 33632447 33632447 single base substitution G A synonymous_variant L203L 609C>T BLCA-US 20 33632447 33632447 single base substitution G A synonymous_variant L242L 726C>T BLCA-US 20 33680620 33680620 single base substitution C T 5_prime_UTR_variant BLCA-US 20 33680620 33680620 single base substitution C T upstream_gene_variant BOCA-FR 20 33590565 33590565 single base substitution T G 3_prime_UTR_variant BOCA-FR 20 33590565 33590565 single base substitution T G downstream_gene_variant BOCA-FR 20 33665767 33665767 single base substitution A C intron_variant BRCA-EU 20 33585711 33585711 single base substitution T G downstream_gene_variant BRCA-EU 20 33587320 33587320 single base substitution C G downstream_gene_variant BRCA-EU 20 33587593 33587593 single base substitution G A downstream_gene_variant BRCA-EU 20 33588118 33588118 single base substitution G A downstream_gene_variant BRCA-EU 20 33588881 33588881 single base substitution G A downstream_gene_variant BRCA-EU 20 33589625 33589625 single base substitution T C downstream_gene_variant BRCA-EU 20 33590208 33590208 single base substitution C A 3_prime_UTR_variant BRCA-EU 20 33590208 33590208 single base substitution C A downstream_gene_variant BRCA-EU 20 33592319 33592319 single base substitution G A missense_variant T266M 797C>T BRCA-EU 20 33592319 33592319 single base substitution G A missense_variant T625M 1874C>T BRCA-EU 20 33592319 33592319 single base substitution G A missense_variant T656M 1967C>T BRCA-EU 20 33592319 33592319 single base substitution G A missense_variant T664M 1991C>T BRCA-EU 20 33592546 33592546 deletion of <=200bp A - intron_variant BRCA-EU 20 33593048 33593048 deletion of <=200bp G - intron_variant BRCA-EU 20 33593066 33593066 single base substitution C G intron_variant BRCA-EU 20 33593282 33593282 single base substitution C A intron_variant BRCA-EU 20 33593402 33593402 single base substitution C T intron_variant BRCA-EU 20 33593491 33593491 single base substitution C T splice_region_variant BRCA-EU 20 33593502 33593502 single base substitution C T missense_variant M246I 738G>A BRCA-EU 20 33593502 33593502 single base substitution C T missense_variant M605I 1815G>A BRCA-EU 20 33593502 33593502 single base substitution C T missense_variant M636I 1908G>A BRCA-EU 20 33593502 33593502 single base substitution C T missense_variant M644I 1932G>A BRCA-EU 20 33593845 33593845 single base substitution C T intron_variant BRCA-EU 20 33594067 33594067 single base substitution G C intron_variant BRCA-EU 20 33594475 33594475 single base substitution C A intron_variant BRCA-EU 20 33598313 33598313 single base substitution C T intron_variant BRCA-EU 20 33600074 33600074 single base substitution T G intron_variant BRCA-EU 20 33601719 33601719 single base substitution G C intron_variant BRCA-EU 20 33602419 33602419 single base substitution G C intron_variant BRCA-EU 20 33602619 33602619 single base substitution A G intron_variant BRCA-EU 20 33604434 33604434 single base substitution G C intron_variant BRCA-EU 20 33607028 33607028 single base substitution G A intron_variant BRCA-EU 20 33607846 33607846 single base substitution C T intron_variant BRCA-EU 20 33610664 33610664 single base substitution A C intron_variant BRCA-EU 20 33611409 33611409 single base substitution C T intron_variant BRCA-EU 20 33611854 33611854 single base substitution C G intron_variant BRCA-EU 20 33611855 33611855 single base substitution T G intron_variant BRCA-EU 20 33612693 33612693 single base substitution G C intron_variant BRCA-EU 20 33612785 33612785 single base substitution T C intron_variant BRCA-EU 20 33612814 33612814 single base substitution C G intron_variant BRCA-EU 20 33613510 33613510 single base substitution A C intron_variant BRCA-EU 20 33613755 33613755 single base substitution G C intron_variant BRCA-EU 20 33614600 33614600 single base substitution T A intron_variant BRCA-EU 20 33614670 33614670 single base substitution A G intron_variant BRCA-EU 20 33614876 33614876 single base substitution A G intron_variant BRCA-EU 20 33614935 33614935 single base substitution C G intron_variant BRCA-EU 20 33615201 33615201 single base substitution A G intron_variant BRCA-EU 20 33617373 33617373 single base substitution C G intron_variant BRCA-EU 20 33618295 33618295 single base substitution T A intron_variant BRCA-EU 20 33618473 33618473 single base substitution G C intron_variant BRCA-EU 20 33618481 33618481 single base substitution G A intron_variant BRCA-EU 20 33620475 33620475 single base substitution C G intron_variant BRCA-EU 20 33621025 33621025 single base substitution C A intron_variant BRCA-EU 20 33622479 33622479 single base substitution C G intron_variant BRCA-EU 20 33623653 33623653 single base substitution G C intron_variant BRCA-EU 20 33623653 33623653 single base substitution G C upstream_gene_variant BRCA-EU 20 33625780 33625780 single base substitution T A intron_variant BRCA-EU 20 33625780 33625780 single base substitution T A upstream_gene_variant BRCA-EU 20 33627409 33627409 single base substitution C A intron_variant BRCA-EU 20 33627409 33627409 single base substitution C A upstream_gene_variant BRCA-EU 20 33628118 33628118 single base substitution C T intron_variant BRCA-EU 20 33628468 33628468 single base substitution A G intron_variant BRCA-EU 20 33629304 33629304 single base substitution T G intron_variant BRCA-EU 20 33631044 33631044 single base substitution T C intron_variant BRCA-EU 20 33632284 33632284 single base substitution A T intron_variant BRCA-EU 20 33634240 33634240 single base substitution T C intron_variant BRCA-EU 20 33634478 33634478 single base substitution G A intron_variant BRCA-EU 20 33634652 33634652 insertion of <=200bp - T intron_variant BRCA-EU 20 33635011 33635011 single base substitution G A intron_variant BRCA-EU 20 33635753 33635753 deletion of <=200bp A - intron_variant BRCA-EU 20 33638176 33638176 single base substitution T A intron_variant BRCA-EU 20 33638922 33638922 single base substitution T C intron_variant BRCA-EU 20 33638931 33638931 deletion of <=200bp T - intron_variant BRCA-EU 20 33638931 33638931 insertion of <=200bp - T intron_variant BRCA-EU 20 33639227 33639227 single base substitution C T intron_variant BRCA-EU 20 33640367 33640367 single base substitution C G intron_variant BRCA-EU 20 33640526 33640526 single base substitution C T intron_variant BRCA-EU 20 33640674 33640674 single base substitution G T intron_variant BRCA-EU 20 33641474 33641474 insertion of <=200bp - AC intron_variant BRCA-EU 20 33642160 33642160 single base substitution T C intron_variant BRCA-EU 20 33643444 33643444 single base substitution A T intron_variant BRCA-EU 20 33643585 33643585 single base substitution C G intron_variant BRCA-EU 20 33643948 33643948 single base substitution C G intron_variant BRCA-EU 20 33645991 33645991 single base substitution G A intron_variant BRCA-EU 20 33646073 33646073 single base substitution A C intron_variant BRCA-EU 20 33647333 33647333 single base substitution C T intron_variant BRCA-EU 20 33647543 33647543 single base substitution G A intron_variant BRCA-EU 20 33648146 33648146 single base substitution T A intron_variant BRCA-EU 20 33649496 33649496 single base substitution T C intron_variant BRCA-EU 20 33649915 33649915 single base substitution T A intron_variant BRCA-EU 20 33651556 33651556 single base substitution C T intron_variant BRCA-EU 20 33654359 33654359 single base substitution G A intron_variant BRCA-EU 20 33655077 33655077 single base substitution C T intron_variant BRCA-EU 20 33656344 33656344 insertion of <=200bp - T intron_variant BRCA-EU 20 33657227 33657227 deletion of <=200bp A - intron_variant BRCA-EU 20 33657227 33657227 single base substitution A T intron_variant BRCA-EU 20 33657511 33657511 single base substitution A C intron_variant BRCA-EU 20 33658071 33658071 single base substitution A G intron_variant BRCA-EU 20 33660403 33660403 single base substitution G A intron_variant BRCA-EU 20 33660555 33660555 single base substitution T A intron_variant BRCA-EU 20 33660812 33660812 single base substitution A T intron_variant BRCA-EU 20 33662203 33662203 single base substitution T G intron_variant BRCA-EU 20 33662365 33662365 single base substitution C G intron_variant BRCA-EU 20 33662366 33662366 single base substitution C A intron_variant BRCA-EU 20 33664297 33664297 single base substitution C T intron_variant BRCA-EU 20 33664715 33664715 single base substitution T A intron_variant BRCA-EU 20 33669771 33669771 single base substitution G C intron_variant BRCA-EU 20 33670307 33670307 single base substitution G A intron_variant BRCA-EU 20 33670322 33670322 single base substitution G C intron_variant BRCA-EU 20 33670698 33670698 single base substitution G A intron_variant BRCA-EU 20 33671774 33671774 single base substitution A C intron_variant BRCA-EU 20 33674544 33674544 single base substitution G C intron_variant BRCA-EU 20 33674552 33674552 single base substitution A T intron_variant BRCA-EU 20 33676579 33676579 single base substitution C T intron_variant BRCA-EU 20 33677019 33677020 deletion of <=200bp AT - intron_variant BRCA-EU 20 33679195 33679195 single base substitution G C intron_variant BRCA-EU 20 33679222 33679222 single base substitution C G intron_variant BRCA-EU 20 33679429 33679429 single base substitution C T intron_variant BRCA-EU 20 33681065 33681065 single base substitution T C upstream_gene_variant BRCA-EU 20 33681167 33681167 single base substitution C T upstream_gene_variant BRCA-EU 20 33682560 33682560 single base substitution A T upstream_gene_variant BRCA-EU 20 33683385 33683385 single base substitution G C upstream_gene_variant BRCA-EU 20 33683630 33683630 single base substitution C A upstream_gene_variant BRCA-FR 20 33593491 33593491 single base substitution C T splice_region_variant BRCA-FR 20 33593502 33593502 single base substitution C T missense_variant M246I 738G>A BRCA-FR 20 33593502 33593502 single base substitution C T missense_variant M605I 1815G>A BRCA-FR 20 33593502 33593502 single base substitution C T missense_variant M636I 1908G>A BRCA-FR 20 33593502 33593502 single base substitution C T missense_variant M644I 1932G>A BRCA-FR 20 33617373 33617373 single base substitution C G intron_variant BRCA-FR 20 33618068 33618068 single base substitution T C intron_variant BRCA-FR 20 33618481 33618481 single base substitution G A intron_variant BRCA-FR 20 33628118 33628118 single base substitution C T intron_variant BRCA-FR 20 33632284 33632284 single base substitution A T intron_variant BRCA-FR 20 33634478 33634478 single base substitution G A intron_variant BRCA-FR 20 33638784 33638784 single base substitution C G intron_variant BRCA-FR 20 33645991 33645991 single base substitution G A intron_variant BRCA-FR 20 33657227 33657227 single base substitution A T intron_variant BRCA-FR 20 33660403 33660403 single base substitution G A intron_variant BRCA-FR 20 33664261 33664261 single base substitution C A intron_variant BRCA-FR 20 33669771 33669771 single base substitution G C intron_variant BRCA-FR 20 33670307 33670307 single base substitution G A intron_variant BRCA-FR 20 33670322 33670322 single base substitution G C intron_variant BRCA-FR 20 33677317 33677317 single base substitution G C intron_variant BRCA-FR 20 33679429 33679429 single base substitution C T intron_variant BRCA-FR 20 33683385 33683385 single base substitution G C upstream_gene_variant BRCA-UK 20 33589894 33589894 single base substitution G C downstream_gene_variant BRCA-UK 20 33596406 33596406 single base substitution C G intron_variant BRCA-UK 20 33628468 33628468 single base substitution A G intron_variant BRCA-UK 20 33632315 33632315 single base substitution G A synonymous_variant I247I 741C>T BRCA-UK 20 33632315 33632315 single base substitution G A synonymous_variant I286I 858C>T BRCA-UK 20 33638922 33638922 single base substitution T C intron_variant BRCA-UK 20 33640367 33640367 single base substitution C G intron_variant BRCA-UK 20 33640674 33640674 single base substitution G T intron_variant BRCA-UK 20 33652855 33652855 single base substitution G C intron_variant BRCA-UK 20 33662365 33662365 single base substitution C G intron_variant BRCA-UK 20 33662366 33662366 single base substitution C A intron_variant BRCA-US 20 33585277 33585277 single base substitution C A downstream_gene_variant BRCA-US 20 33586315 33586315 single base substitution G A downstream_gene_variant BRCA-US 20 33586607 33586607 single base substitution C A downstream_gene_variant BRCA-US 20 33587190 33587190 single base substitution G A downstream_gene_variant BRCA-US 20 33587427 33587427 single base substitution G A downstream_gene_variant BRCA-US 20 33591329 33591329 single base substitution G A missense_variant R316W 946C>T BRCA-US 20 33591329 33591329 single base substitution G A missense_variant R675W 2023C>T BRCA-US 20 33591329 33591329 single base substitution G A missense_variant R706W 2116C>T BRCA-US 20 33591329 33591329 single base substitution G A missense_variant R714W 2140C>T BRCA-US 20 33591353 33591353 single base substitution G C missense_variant P308A 922C>G BRCA-US 20 33591353 33591353 single base substitution G C missense_variant P667A 1999C>G BRCA-US 20 33591353 33591353 single base substitution G C missense_variant P698A 2092C>G BRCA-US 20 33591353 33591353 single base substitution G C missense_variant P706A 2116C>G BRCA-US 20 33591392 33591392 single base substitution G A synonymous_variant L295L 883C>T BRCA-US 20 33591392 33591392 single base substitution G A synonymous_variant L654L 1960C>T BRCA-US 20 33591392 33591392 single base substitution G A synonymous_variant L685L 2053C>T BRCA-US 20 33591392 33591392 single base substitution G A synonymous_variant L693L 2077C>T BRCA-US 20 33598008 33598010 deletion of <=200bp GCT - disruptive_inframe_deletion EA458D BRCA-US 20 33598008 33598010 deletion of <=200bp GCT - disruptive_inframe_deletion EA489D BRCA-US 20 33598008 33598010 deletion of <=200bp GCT - disruptive_inframe_deletion EA497D BRCA-US 20 33598008 33598010 deletion of <=200bp GCT - disruptive_inframe_deletion EA99D BRCA-US 20 33600860 33600860 single base substitution A T missense_variant L415M 1243T>A BRCA-US 20 33600860 33600860 single base substitution A T missense_variant L446M 1336T>A BRCA-US 20 33600860 33600860 single base substitution A T missense_variant L454M 1360T>A BRCA-US 20 33600860 33600860 single base substitution A T missense_variant L56M 166T>A BRCA-US 20 33603886 33603886 single base substitution G T missense_variant D27E 81C>A BRCA-US 20 33603886 33603886 single base substitution G T missense_variant D386E 1158C>A BRCA-US 20 33603886 33603886 single base substitution G T missense_variant D417E 1251C>A BRCA-US 20 33603886 33603886 single base substitution G T missense_variant D425E 1275C>A BRCA-US 20 33609154 33609154 single base substitution T C intron_variant BRCA-US 20 33609154 33609154 single base substitution T C missense_variant I314V 940A>G BRCA-US 20 33609154 33609154 single base substitution T C missense_variant I353V 1057A>G BRCA-US 20 33623023 33623023 single base substitution G A 5_prime_UTR_variant BRCA-US 20 33623023 33623023 single base substitution G A synonymous_variant F279F 837C>T BRCA-US 20 33623023 33623023 single base substitution G A synonymous_variant F318F 954C>T BRCA-US 20 33645320 33645320 single base substitution T C missense_variant K118E 352A>G BRCA-US 20 33645320 33645320 single base substitution T C missense_variant K157E 469A>G BTCA-JP 20 33586143 33586143 single base substitution G A downstream_gene_variant BTCA-JP 20 33586993 33586993 single base substitution C T downstream_gene_variant BTCA-JP 20 33587565 33587565 single base substitution A C downstream_gene_variant BTCA-JP 20 33589107 33589107 single base substitution G A downstream_gene_variant BTCA-JP 20 33591339 33591339 single base substitution C A synonymous_variant R312R 936G>T BTCA-JP 20 33591339 33591339 single base substitution C A synonymous_variant R671R 2013G>T BTCA-JP 20 33591339 33591339 single base substitution C A synonymous_variant R702R 2106G>T BTCA-JP 20 33591339 33591339 single base substitution C A synonymous_variant R710R 2130G>T BTCA-JP 20 33598008 33598008 single base substitution G A missense_variant A100V 299C>T BTCA-JP 20 33598008 33598008 single base substitution G A missense_variant A459V 1376C>T BTCA-JP 20 33598008 33598008 single base substitution G A missense_variant A490V 1469C>T BTCA-JP 20 33598008 33598008 single base substitution G A missense_variant A498V 1493C>T BTCA-JP 20 33600840 33600840 single base substitution C T synonymous_variant R421R 1263G>A BTCA-JP 20 33600840 33600840 single base substitution C T synonymous_variant R452R 1356G>A BTCA-JP 20 33600840 33600840 single base substitution C T synonymous_variant R460R 1380G>A BTCA-JP 20 33600840 33600840 single base substitution C T synonymous_variant R62R 186G>A BTCA-JP 20 33623090 33623090 single base substitution C T 5_prime_UTR_variant BTCA-JP 20 33623090 33623090 single base substitution C T missense_variant G257D 770G>A BTCA-JP 20 33623090 33623090 single base substitution C T missense_variant G296D 887G>A BTCA-JP 20 33657227 33657227 single base substitution A T intron_variant BTCA-JP 20 33665776 33665776 deletion of <=200bp A - intron_variant BTCA-JP 20 33680682 33680682 single base substitution C A upstream_gene_variant CESC-US 20 33587058 33587058 single base substitution C T downstream_gene_variant CESC-US 20 33588263 33588263 single base substitution C T downstream_gene_variant CESC-US 20 33591061 33591061 single base substitution C T stop_gained W363* 1088G>A CESC-US 20 33591061 33591061 single base substitution C T stop_gained W722* 2165G>A CESC-US 20 33591061 33591061 single base substitution C T stop_gained W753* 2258G>A CESC-US 20 33591061 33591061 single base substitution C T stop_gained W761* 2282G>A CESC-US 20 33594341 33594341 single base substitution G A missense_variant S177L 530C>T CESC-US 20 33594341 33594341 single base substitution G A missense_variant S536L 1607C>T CESC-US 20 33594341 33594341 single base substitution G A missense_variant S567L 1700C>T CESC-US 20 33594341 33594341 single base substitution G A missense_variant S575L 1724C>T CESC-US 20 33603935 33603935 single base substitution C T missense_variant R11K 32G>A CESC-US 20 33603935 33603935 single base substitution C T missense_variant R370K 1109G>A CESC-US 20 33603935 33603935 single base substitution C T missense_variant R401K 1202G>A CESC-US 20 33603935 33603935 single base substitution C T missense_variant R409K 1226G>A CLLE-ES 20 33631624 33631624 single base substitution A C intron_variant CLLE-ES 20 33637453 33637453 single base substitution G C intron_variant CLLE-ES 20 33642977 33642977 single base substitution T C intron_variant CLLE-ES 20 33651221 33651221 single base substitution C G intron_variant COAD-US 20 33585345 33585345 single base substitution C G downstream_gene_variant COAD-US 20 33586193 33586193 single base substitution C T downstream_gene_variant COAD-US 20 33586196 33586196 single base substitution G A downstream_gene_variant COAD-US 20 33586407 33586407 single base substitution G A downstream_gene_variant COAD-US 20 33586679 33586679 single base substitution C A downstream_gene_variant COAD-US 20 33587011 33587011 single base substitution C T downstream_gene_variant COAD-US 20 33587198 33587198 single base substitution G C downstream_gene_variant COAD-US 20 33588395 33588395 single base substitution A T downstream_gene_variant COAD-US 20 33588699 33588720 deletion of <=200bp GAGGCTGGGCAAGGGCTGTGGG - downstream_gene_variant COAD-US 20 33589107 33589107 single base substitution G A downstream_gene_variant COAD-US 20 33591308 33591308 single base substitution A G missense_variant Y323H 967T>C COAD-US 20 33591308 33591308 single base substitution A G missense_variant Y682H 2044T>C COAD-US 20 33591308 33591308 single base substitution A G missense_variant Y713H 2137T>C COAD-US 20 33591308 33591308 single base substitution A G missense_variant Y721H 2161T>C COAD-US 20 33591340 33591340 single base substitution C T missense_variant R312Q 935G>A COAD-US 20 33591340 33591340 single base substitution C T missense_variant R671Q 2012G>A COAD-US 20 33591340 33591340 single base substitution C T missense_variant R702Q 2105G>A COAD-US 20 33591340 33591340 single base substitution C T missense_variant R710Q 2129G>A COAD-US 20 33592270 33592270 single base substitution C T synonymous_variant T282T 846G>A COAD-US 20 33592270 33592270 single base substitution C T synonymous_variant T641T 1923G>A COAD-US 20 33592270 33592270 single base substitution C T synonymous_variant T672T 2016G>A COAD-US 20 33592270 33592270 single base substitution C T synonymous_variant T680T 2040G>A COAD-US 20 33637714 33637714 single base substitution G T missense_variant F165L 495C>A COAD-US 20 33637714 33637714 single base substitution G T missense_variant F204L 612C>A COCA-CN 20 33586295 33586295 single base substitution C T downstream_gene_variant COCA-CN 20 33586801 33586801 single base substitution T G downstream_gene_variant COCA-CN 20 33587557 33587557 single base substitution C T downstream_gene_variant COCA-CN 20 33587596 33587596 single base substitution G A downstream_gene_variant COCA-CN 20 33587689 33587689 single base substitution C G downstream_gene_variant COCA-CN 20 33588401 33588401 single base substitution G T downstream_gene_variant COCA-CN 20 33588924 33588924 single base substitution G C downstream_gene_variant COCA-CN 20 33590034 33590034 single base substitution C T downstream_gene_variant COCA-CN 20 33590096 33590096 single base substitution A G downstream_gene_variant COCA-CN 20 33592318 33592318 single base substitution C T synonymous_variant T266T 798G>A COCA-CN 20 33592318 33592318 single base substitution C T synonymous_variant T625T 1875G>A COCA-CN 20 33592318 33592318 single base substitution C T synonymous_variant T656T 1968G>A COCA-CN 20 33592318 33592318 single base substitution C T synonymous_variant T664T 1992G>A COCA-CN 20 33595300 33595300 single base substitution C T intron_variant COCA-CN 20 33600827 33600827 single base substitution A C missense_variant F426V 1276T>G COCA-CN 20 33600827 33600827 single base substitution A C missense_variant F457V 1369T>G COCA-CN 20 33600827 33600827 single base substitution A C missense_variant F465V 1393T>G COCA-CN 20 33600827 33600827 single base substitution A C missense_variant F67V 199T>G COCA-CN 20 33632224 33632224 single base substitution G A intron_variant COCA-CN 20 33637857 33637857 single base substitution A C intron_variant COCA-CN 20 33657227 33657227 single base substitution A T intron_variant EOPC-DE 20 33611489 33611489 single base substitution G A intron_variant EOPC-DE 20 33627686 33627686 single base substitution G A intron_variant EOPC-DE 20 33627686 33627686 single base substitution G A upstream_gene_variant EOPC-DE 20 33645578 33645578 single base substitution G A intron_variant ESAD-UK 20 33585540 33585540 single base substitution C T downstream_gene_variant ESAD-UK 20 33587819 33587819 single base substitution G T downstream_gene_variant ESAD-UK 20 33588850 33588850 single base substitution G C downstream_gene_variant ESAD-UK 20 33590886 33590886 single base substitution G A 3_prime_UTR_variant ESAD-UK 20 33591026 33591026 single base substitution G A missense_variant R375W 1123C>T ESAD-UK 20 33591026 33591026 single base substitution G A missense_variant R734W 2200C>T ESAD-UK 20 33591026 33591026 single base substitution G A missense_variant R765W 2293C>T ESAD-UK 20 33591026 33591026 single base substitution G A missense_variant R773W 2317C>T ESAD-UK 20 33591781 33591781 single base substitution C T intron_variant ESAD-UK 20 33594990 33594993 deletion of <=200bp GAAA - intron_variant ESAD-UK 20 33597561 33597561 single base substitution G C intron_variant ESAD-UK 20 33601104 33601104 single base substitution C A intron_variant ESAD-UK 20 33602573 33602573 single base substitution T G intron_variant ESAD-UK 20 33604046 33604046 single base substitution A C intron_variant ESAD-UK 20 33605910 33605910 single base substitution A C intron_variant ESAD-UK 20 33606774 33606774 deletion of <=200bp A - intron_variant ESAD-UK 20 33607969 33607969 single base substitution C G intron_variant ESAD-UK 20 33608171 33608171 single base substitution C T intron_variant ESAD-UK 20 33609587 33609587 single base substitution G A intron_variant ESAD-UK 20 33609910 33609910 single base substitution C T intron_variant ESAD-UK 20 33610125 33610125 single base substitution A C intron_variant ESAD-UK 20 33613779 33613779 single base substitution C A intron_variant ESAD-UK 20 33614044 33614044 single base substitution G C intron_variant ESAD-UK 20 33614838 33614838 single base substitution C A intron_variant ESAD-UK 20 33616008 33616008 single base substitution T A intron_variant ESAD-UK 20 33616189 33616189 single base substitution C T intron_variant ESAD-UK 20 33617116 33617116 single base substitution T C intron_variant ESAD-UK 20 33622978 33622982 deletion of <=200bp CAAAG - 5_prime_UTR_variant ESAD-UK 20 33622978 33622982 deletion of <=200bp CAAAG - frameshift_variant AL293 ESAD-UK 20 33622978 33622982 deletion of <=200bp CAAAG - frameshift_variant AL332 ESAD-UK 20 33622986 33622987 deletion of <=200bp TG - 5_prime_UTR_variant ESAD-UK 20 33622986 33622987 deletion of <=200bp TG - frameshift_variant DN291 ESAD-UK 20 33622986 33622987 deletion of <=200bp TG - frameshift_variant DN330 ESAD-UK 20 33623903 33623903 single base substitution T G intron_variant ESAD-UK 20 33623903 33623903 single base substitution T G upstream_gene_variant ESAD-UK 20 33627969 33627969 single base substitution G A intron_variant ESAD-UK 20 33627969 33627969 single base substitution G A upstream_gene_variant ESAD-UK 20 33628163 33628163 single base substitution C T intron_variant ESAD-UK 20 33630954 33630954 single base substitution T C intron_variant ESAD-UK 20 33633288 33633288 single base substitution C A intron_variant ESAD-UK 20 33636172 33636172 single base substitution G A intron_variant ESAD-UK 20 33637582 33637582 insertion of <=200bp - A intron_variant ESAD-UK 20 33639575 33639575 single base substitution C A intron_variant ESAD-UK 20 33640723 33640723 single base substitution A T intron_variant ESAD-UK 20 33641526 33641526 single base substitution C A intron_variant ESAD-UK 20 33642243 33642243 single base substitution G A intron_variant ESAD-UK 20 33645379 33645379 deletion of <=200bp A - splice_region_variant ESAD-UK 20 33647440 33647443 deletion of <=200bp GGCA - intron_variant ESAD-UK 20 33648087 33648088 deletion of <=200bp AC - intron_variant ESAD-UK 20 33648142 33648142 single base substitution C T intron_variant ESAD-UK 20 33648257 33648260 deletion of <=200bp GGTA - intron_variant ESAD-UK 20 33649295 33649295 single base substitution C G intron_variant ESAD-UK 20 33650040 33650040 single base substitution T C intron_variant ESAD-UK 20 33650379 33650379 single base substitution C A intron_variant ESAD-UK 20 33650902 33650902 single base substitution C T intron_variant ESAD-UK 20 33655519 33655519 single base substitution C G intron_variant ESAD-UK 20 33656053 33656053 single base substitution T A intron_variant ESAD-UK 20 33657227 33657227 single base substitution A T intron_variant ESAD-UK 20 33657680 33657680 single base substitution G A intron_variant ESAD-UK 20 33661955 33661955 single base substitution A G intron_variant ESAD-UK 20 33662046 33662046 single base substitution G C intron_variant ESAD-UK 20 33665912 33665912 single base substitution G A synonymous_variant L78L 234C>T ESAD-UK 20 33666469 33666469 single base substitution T C intron_variant ESAD-UK 20 33666842 33666842 single base substitution C T intron_variant ESAD-UK 20 33668611 33668611 insertion of <=200bp - TG intron_variant ESAD-UK 20 33669343 33669343 single base substitution T A intron_variant ESAD-UK 20 33669344 33669344 single base substitution A T intron_variant ESAD-UK 20 33669555 33669555 single base substitution C T intron_variant ESAD-UK 20 33677740 33677740 single base substitution G C intron_variant ESAD-UK 20 33680378 33680378 single base substitution G C intron_variant ESAD-UK 20 33684687 33684687 single base substitution C T upstream_gene_variant ESAD-UK 20 33684943 33684943 single base substitution T C upstream_gene_variant ESCA-CN 20 33587250 33587250 single base substitution G A downstream_gene_variant ESCA-CN 20 33591013 33591013 single base substitution G C missense_variant S379C 1136C>G ESCA-CN 20 33591013 33591013 single base substitution G C missense_variant S738C 2213C>G ESCA-CN 20 33591013 33591013 single base substitution G C missense_variant S769C 2306C>G ESCA-CN 20 33591013 33591013 single base substitution G C missense_variant S777C 2330C>G ESCA-CN 20 33592231 33592231 single base substitution C T intron_variant ESCA-CN 20 33592474 33592474 single base substitution A G intron_variant ESCA-CN 20 33665971 33665971 single base substitution C G missense_variant E59Q 175G>C GBM-US 20 33586908 33586908 single base substitution G A downstream_gene_variant GBM-US 20 33591328 33591328 single base substitution C T missense_variant R316Q 947G>A GBM-US 20 33591328 33591328 single base substitution C T missense_variant R675Q 2024G>A GBM-US 20 33591328 33591328 single base substitution C T missense_variant R706Q 2117G>A GBM-US 20 33591328 33591328 single base substitution C T missense_variant R714Q 2141G>A KIRC-US 20 33585398 33585398 single base substitution G C downstream_gene_variant KIRC-US 20 33587596 33587596 single base substitution G A downstream_gene_variant KIRC-US 20 33587603 33587603 single base substitution G T downstream_gene_variant KIRC-US 20 33589107 33589107 single base substitution G A downstream_gene_variant KIRC-US 20 33595391 33595391 single base substitution C T missense_variant A152T 454G>A KIRC-US 20 33595391 33595391 single base substitution C T missense_variant A511T 1531G>A KIRC-US 20 33595391 33595391 single base substitution C T missense_variant A542T 1624G>A KIRC-US 20 33595391 33595391 single base substitution C T missense_variant A550T 1648G>A KIRC-US 20 33596526 33596526 single base substitution C G missense_variant R114S 342G>C KIRC-US 20 33596526 33596526 single base substitution C G missense_variant R473S 1419G>C KIRC-US 20 33596526 33596526 single base substitution C G missense_variant R504S 1512G>C KIRC-US 20 33596526 33596526 single base substitution C G missense_variant R512S 1536G>C KIRP-US 20 33591257 33591257 single base substitution G T missense_variant Q340K 1018C>A KIRP-US 20 33591257 33591257 single base substitution G T missense_variant Q699K 2095C>A KIRP-US 20 33591257 33591257 single base substitution G T missense_variant Q730K 2188C>A KIRP-US 20 33591257 33591257 single base substitution G T missense_variant Q738K 2212C>A KIRP-US 20 33603843 33603843 insertion of <=200bp - AA frameshift_variant H401L? KIRP-US 20 33603843 33603843 insertion of <=200bp - AA frameshift_variant H42L? KIRP-US 20 33603843 33603843 insertion of <=200bp - AA frameshift_variant H432L? KIRP-US 20 33603843 33603843 insertion of <=200bp - AA frameshift_variant H440L? KIRP-US 20 33622951 33622951 single base substitution G T 5_prime_UTR_variant KIRP-US 20 33622951 33622951 single base substitution G T synonymous_variant A303A 909C>A KIRP-US 20 33622951 33622951 single base substitution G T synonymous_variant A342A 1026C>A KIRP-US 20 33623074 33623074 single base substitution A C 5_prime_UTR_premature_start_codon_gain_variant KIRP-US 20 33623074 33623074 single base substitution A C synonymous_variant L262L 786T>G KIRP-US 20 33623074 33623074 single base substitution A C synonymous_variant L301L 903T>G KIRP-US 20 33623099 33623099 single base substitution C A missense_variant S254I 761G>T KIRP-US 20 33623099 33623099 single base substitution C A missense_variant S293I 878G>T KIRP-US 20 33623099 33623099 single base substitution C A upstream_gene_variant LAML-KR 20 33586193 33586193 single base substitution C T downstream_gene_variant LAML-KR 20 33604042 33604042 single base substitution T C intron_variant LAML-KR 20 33623196 33623196 single base substitution A C intron_variant LAML-KR 20 33623196 33623196 single base substitution A C upstream_gene_variant LAML-KR 20 33632600 33632600 single base substitution C T intron_variant LGG-US 20 33657162 33657162 single base substitution C A intron_variant LGG-US 20 33657162 33657162 single base substitution C A missense_variant R117S 351G>T LICA-CN 20 33592328 33592328 single base substitution T A missense_variant Q263L 788A>T LICA-CN 20 33592328 33592328 single base substitution T A missense_variant Q622L 1865A>T LICA-CN 20 33592328 33592328 single base substitution T A missense_variant Q653L 1958A>T LICA-CN 20 33592328 33592328 single base substitution T A missense_variant Q661L 1982A>T LICA-CN 20 33608993 33608993 single base substitution C G intron_variant LICA-CN 20 33608993 33608993 single base substitution C G missense_variant Q367H 1101G>C LICA-CN 20 33608993 33608993 single base substitution C G missense_variant Q398H 1194G>C LICA-CN 20 33608993 33608993 single base substitution C G missense_variant Q406H 1218G>C LICA-FR 20 33587701 33587701 deletion of <=200bp T - downstream_gene_variant LICA-FR 20 33595590 33595590 single base substitution C T intron_variant LICA-FR 20 33616015 33616015 insertion of <=200bp - TT intron_variant LICA-FR 20 33617879 33617879 single base substitution T C intron_variant LICA-FR 20 33630259 33630259 single base substitution A C intron_variant LICA-FR 20 33684157 33684157 deletion of <=200bp A - upstream_gene_variant LIHC-US 20 33598060 33598060 single base substitution G C missense_variant L442V 1324C>G LIHC-US 20 33598060 33598060 single base substitution G C missense_variant L473V 1417C>G LIHC-US 20 33598060 33598060 single base substitution G C missense_variant L481V 1441C>G LIHC-US 20 33598060 33598060 single base substitution G C missense_variant L83V 247C>G LINC-JP 20 33585534 33585534 single base substitution C T downstream_gene_variant LINC-JP 20 33588281 33588281 single base substitution A G downstream_gene_variant LINC-JP 20 33590201 33590201 single base substitution C T downstream_gene_variant LINC-JP 20 33591159 33591159 single base substitution A C intron_variant LINC-JP 20 33591709 33591709 single base substitution G A intron_variant LINC-JP 20 33596700 33596700 single base substitution C T intron_variant LINC-JP 20 33604797 33604797 single base substitution T C intron_variant LINC-JP 20 33609289 33609289 single base substitution T C intron_variant LINC-JP 20 33627330 33627330 single base substitution A G intron_variant LINC-JP 20 33627330 33627330 single base substitution A G upstream_gene_variant LINC-JP 20 33630843 33630843 single base substitution A C intron_variant LINC-JP 20 33635217 33635217 single base substitution T G intron_variant LINC-JP 20 33637680 33637680 single base substitution C T missense_variant G177S 529G>A LINC-JP 20 33637680 33637680 single base substitution C T missense_variant G216S 646G>A LINC-JP 20 33664061 33664061 single base substitution T C intron_variant LINC-JP 20 33669986 33669986 single base substitution A C intron_variant LINC-JP 20 33685153 33685153 single base substitution C T upstream_gene_variant LINC-JP 20 33685258 33685258 single base substitution G A upstream_gene_variant LINC-JP 20 33685265 33685265 single base substitution C T upstream_gene_variant LIRI-JP 20 33586973 33586973 single base substitution A G downstream_gene_variant LIRI-JP 20 33588187 33588187 single base substitution A G downstream_gene_variant LIRI-JP 20 33588699 33588720 deletion of <=200bp GAGGCTGGGCAAGGGCTGTGGG - downstream_gene_variant LIRI-JP 20 33594832 33594832 single base substitution T G intron_variant LIRI-JP 20 33595327 33595327 single base substitution A T intron_variant LIRI-JP 20 33596557 33596557 single base substitution T C splice_region_variant LIRI-JP 20 33597003 33597003 single base substitution T C intron_variant LIRI-JP 20 33600530 33600530 single base substitution T C intron_variant LIRI-JP 20 33604038 33604038 single base substitution C T intron_variant LIRI-JP 20 33606625 33606625 single base substitution A T intron_variant LIRI-JP 20 33607041 33607041 single base substitution T A intron_variant LIRI-JP 20 33610965 33610965 single base substitution G A intron_variant LIRI-JP 20 33611606 33611606 single base substitution G T intron_variant LIRI-JP 20 33612725 33612725 single base substitution T C intron_variant LIRI-JP 20 33614574 33614574 single base substitution A G intron_variant LIRI-JP 20 33616191 33616191 single base substitution G T intron_variant LIRI-JP 20 33618245 33618245 single base substitution G C intron_variant LIRI-JP 20 33618772 33618772 single base substitution C T intron_variant LIRI-JP 20 33622947 33622947 deletion of <=200bp C - frameshift_variant E305 LIRI-JP 20 33622947 33622947 deletion of <=200bp C - frameshift_variant E344 LIRI-JP 20 33622947 33622947 deletion of <=200bp C - frameshift_variant M1 LIRI-JP 20 33625898 33625898 single base substitution A G intron_variant LIRI-JP 20 33625898 33625898 single base substitution A G upstream_gene_variant LIRI-JP 20 33627581 33627581 single base substitution C G intron_variant LIRI-JP 20 33627581 33627581 single base substitution C G upstream_gene_variant LIRI-JP 20 33628147 33628147 single base substitution G T intron_variant LIRI-JP 20 33629200 33629200 single base substitution C T intron_variant LIRI-JP 20 33632624 33632624 single base substitution A T intron_variant LIRI-JP 20 33636789 33636789 single base substitution G C intron_variant LIRI-JP 20 33637319 33637328 deletion of <=200bp ATAGCATACA - intron_variant LIRI-JP 20 33637563 33637563 single base substitution T C intron_variant LIRI-JP 20 33638914 33638914 single base substitution A T intron_variant LIRI-JP 20 33640445 33640445 single base substitution C T intron_variant LIRI-JP 20 33640481 33640481 single base substitution G T intron_variant LIRI-JP 20 33641417 33641417 single base substitution G T intron_variant LIRI-JP 20 33642696 33642696 single base substitution C T intron_variant LIRI-JP 20 33644385 33644385 single base substitution A C intron_variant LIRI-JP 20 33645123 33645137 deletion of <=200bp TCTGAATTTCTACGC - intron_variant LIRI-JP 20 33645911 33645911 single base substitution T C intron_variant LIRI-JP 20 33646133 33646133 single base substitution T C intron_variant LIRI-JP 20 33647975 33647975 single base substitution C T intron_variant LIRI-JP 20 33650364 33650364 single base substitution G C intron_variant LIRI-JP 20 33651548 33651548 single base substitution C T intron_variant LIRI-JP 20 33652068 33652068 single base substitution T C intron_variant LIRI-JP 20 33652568 33652568 single base substitution A G intron_variant LIRI-JP 20 33652907 33652907 single base substitution T C intron_variant LIRI-JP 20 33653237 33653237 single base substitution T C intron_variant LIRI-JP 20 33659788 33659788 single base substitution T C intron_variant LIRI-JP 20 33661502 33661502 single base substitution T G intron_variant LIRI-JP 20 33661862 33661862 single base substitution G A intron_variant LIRI-JP 20 33663772 33663772 single base substitution T G intron_variant LIRI-JP 20 33663802 33663802 single base substitution T A intron_variant LIRI-JP 20 33665817 33665817 single base substitution G A intron_variant LIRI-JP 20 33666449 33666449 single base substitution T C intron_variant LIRI-JP 20 33666929 33666929 single base substitution T C intron_variant LIRI-JP 20 33667980 33667980 single base substitution C A intron_variant LIRI-JP 20 33668156 33668156 single base substitution T C intron_variant LIRI-JP 20 33669303 33669303 single base substitution G A intron_variant LIRI-JP 20 33669304 33669304 single base substitution C A intron_variant LIRI-JP 20 33672966 33672966 single base substitution T C intron_variant LIRI-JP 20 33681679 33681679 single base substitution A G upstream_gene_variant LIRI-JP 20 33681715 33681715 single base substitution A G upstream_gene_variant LIRI-JP 20 33681748 33681748 single base substitution A C upstream_gene_variant LIRI-JP 20 33682141 33682141 single base substitution C T upstream_gene_variant LUSC-KR 20 33587508 33587508 single base substitution T A downstream_gene_variant LUSC-KR 20 33593457 33593457 single base substitution T C intron_variant LUSC-KR 20 33594809 33594809 single base substitution G A intron_variant LUSC-KR 20 33594847 33594847 single base substitution G T intron_variant LUSC-KR 20 33602001 33602001 single base substitution A G intron_variant LUSC-KR 20 33602518 33602518 single base substitution T A intron_variant LUSC-KR 20 33603284 33603284 single base substitution G T intron_variant LUSC-KR 20 33604042 33604042 single base substitution T C intron_variant LUSC-KR 20 33610912 33610912 single base substitution C T intron_variant LUSC-KR 20 33612629 33612629 single base substitution A C intron_variant LUSC-KR 20 33622981 33622981 single base substitution A C 5_prime_UTR_variant LUSC-KR 20 33622981 33622981 single base substitution A C synonymous_variant A293A 879T>G LUSC-KR 20 33622981 33622981 single base substitution A C synonymous_variant A332A 996T>G LUSC-KR 20 33627893 33627893 single base substitution C T intron_variant LUSC-KR 20 33627893 33627893 single base substitution C T upstream_gene_variant LUSC-KR 20 33636124 33636124 single base substitution C T intron_variant LUSC-KR 20 33637313 33637313 single base substitution C T intron_variant LUSC-KR 20 33637515 33637515 single base substitution T C intron_variant LUSC-KR 20 33639310 33639310 single base substitution T A intron_variant LUSC-KR 20 33639870 33639870 single base substitution C T intron_variant LUSC-KR 20 33644641 33644641 single base substitution T C intron_variant LUSC-KR 20 33646658 33646658 single base substitution C T intron_variant LUSC-KR 20 33647736 33647736 single base substitution G A intron_variant LUSC-KR 20 33647964 33647964 single base substitution A T intron_variant LUSC-KR 20 33650142 33650142 single base substitution C A intron_variant LUSC-KR 20 33650320 33650320 single base substitution G T intron_variant LUSC-KR 20 33659736 33659736 single base substitution C A intron_variant LUSC-KR 20 33667409 33667409 single base substitution G C intron_variant LUSC-KR 20 33669218 33669218 single base substitution G A intron_variant LUSC-KR 20 33672753 33672753 single base substitution C A intron_variant LUSC-KR 20 33677014 33677014 single base substitution T C intron_variant LUSC-US 20 33585348 33585348 single base substitution C A downstream_gene_variant LUSC-US 20 33586326 33586326 single base substitution G A downstream_gene_variant LUSC-US 20 33589814 33589814 single base substitution G C downstream_gene_variant LUSC-US 20 33591291 33591291 single base substitution G C synonymous_variant L328L 984C>G LUSC-US 20 33591291 33591291 single base substitution G C synonymous_variant L687L 2061C>G LUSC-US 20 33591291 33591291 single base substitution G C synonymous_variant L718L 2154C>G LUSC-US 20 33591291 33591291 single base substitution G C synonymous_variant L726L 2178C>G LUSC-US 20 33593507 33593507 single base substitution C G missense_variant D245H 733G>C LUSC-US 20 33593507 33593507 single base substitution C G missense_variant D604H 1810G>C LUSC-US 20 33593507 33593507 single base substitution C G missense_variant D635H 1903G>C LUSC-US 20 33593507 33593507 single base substitution C G missense_variant D643H 1927G>C LUSC-US 20 33593519 33593519 single base substitution C G missense_variant E241Q 721G>C LUSC-US 20 33593519 33593519 single base substitution C G missense_variant E600Q 1798G>C LUSC-US 20 33593519 33593519 single base substitution C G missense_variant E631Q 1891G>C LUSC-US 20 33593519 33593519 single base substitution C G missense_variant E639Q 1915G>C LUSC-US 20 33593586 33593586 single base substitution C G missense_variant Q218H 654G>C LUSC-US 20 33593586 33593586 single base substitution C G missense_variant Q577H 1731G>C LUSC-US 20 33593586 33593586 single base substitution C G missense_variant Q608H 1824G>C LUSC-US 20 33593586 33593586 single base substitution C G missense_variant Q616H 1848G>C LUSC-US 20 33595396 33595396 single base substitution G A missense_variant S150F 449C>T LUSC-US 20 33595396 33595396 single base substitution G A missense_variant S509F 1526C>T LUSC-US 20 33595396 33595396 single base substitution G A missense_variant S540F 1619C>T LUSC-US 20 33595396 33595396 single base substitution G A missense_variant S548F 1643C>T LUSC-US 20 33596469 33596469 single base substitution G A splice_region_variant LUSC-US 20 33623037 33623037 single base substitution C A 5_prime_UTR_variant LUSC-US 20 33623037 33623037 single base substitution C A missense_variant G275C 823G>T LUSC-US 20 33623037 33623037 single base substitution C A missense_variant G314C 940G>T LUSC-US 20 33623108 33623108 single base substitution G T missense_variant A251D 752C>A LUSC-US 20 33623108 33623108 single base substitution G T missense_variant A290D 869C>A LUSC-US 20 33623108 33623108 single base substitution G T upstream_gene_variant LUSC-US 20 33637788 33637788 single base substitution C A missense_variant V141F 421G>T LUSC-US 20 33637788 33637788 single base substitution C A missense_variant V180F 538G>T LUSC-US 20 33657206 33657206 single base substitution G A intron_variant LUSC-US 20 33657206 33657206 single base substitution G A missense_variant P103S 307C>T MALY-DE 20 33591270 33591270 single base substitution C T synonymous_variant L335L 1005G>A MALY-DE 20 33591270 33591270 single base substitution C T synonymous_variant L694L 2082G>A MALY-DE 20 33591270 33591270 single base substitution C T synonymous_variant L725L 2175G>A MALY-DE 20 33591270 33591270 single base substitution C T synonymous_variant L733L 2199G>A MALY-DE 20 33597419 33597419 single base substitution C T intron_variant MALY-DE 20 33600990 33600990 single base substitution T G intron_variant MALY-DE 20 33601254 33601254 single base substitution G A intron_variant MALY-DE 20 33605230 33605230 single base substitution C A intron_variant MALY-DE 20 33608946 33608946 single base substitution G A intron_variant MALY-DE 20 33609116 33609116 single base substitution G T intron_variant MALY-DE 20 33609116 33609116 single base substitution G T synonymous_variant G326G 978C>A MALY-DE 20 33609116 33609116 single base substitution G T synonymous_variant G357G 1071C>A MALY-DE 20 33609116 33609116 single base substitution G T synonymous_variant G365G 1095C>A MALY-DE 20 33619481 33619481 single base substitution C T intron_variant MALY-DE 20 33625173 33625174 deletion of <=200bp GT - intron_variant MALY-DE 20 33625173 33625174 deletion of <=200bp GT - upstream_gene_variant MALY-DE 20 33635683 33635683 single base substitution G A intron_variant MALY-DE 20 33645472 33645472 single base substitution G A intron_variant MALY-DE 20 33652822 33652822 single base substitution C T intron_variant MALY-DE 20 33666385 33666385 single base substitution A C intron_variant MALY-DE 20 33668099 33668099 single base substitution T C intron_variant MALY-DE 20 33670968 33670968 single base substitution T A intron_variant MALY-DE 20 33671475 33671475 single base substitution A C intron_variant MALY-DE 20 33671632 33671632 single base substitution A G intron_variant MALY-DE 20 33680825 33680825 single base substitution A G upstream_gene_variant MELA-AU 20 33585396 33585396 single base substitution G A downstream_gene_variant MELA-AU 20 33585844 33585844 single base substitution G A downstream_gene_variant MELA-AU 20 33586455 33586455 single base substitution G A downstream_gene_variant MELA-AU 20 33586690 33586690 single base substitution C T downstream_gene_variant MELA-AU 20 33586760 33586760 single base substitution A G downstream_gene_variant MELA-AU 20 33587271 33587271 single base substitution G A downstream_gene_variant MELA-AU 20 33587465 33587465 single base substitution G A downstream_gene_variant MELA-AU 20 33587597 33587597 single base substitution G A downstream_gene_variant MELA-AU 20 33587757 33587758 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 20 33587800 33587800 single base substitution G A downstream_gene_variant MELA-AU 20 33588570 33588570 single base substitution G A downstream_gene_variant MELA-AU 20 33588850 33588850 single base substitution G A downstream_gene_variant MELA-AU 20 33589054 33589054 single base substitution G A downstream_gene_variant MELA-AU 20 33589356 33589356 single base substitution G A downstream_gene_variant MELA-AU 20 33589626 33589626 single base substitution G A downstream_gene_variant MELA-AU 20 33589744 33589744 single base substitution C T downstream_gene_variant MELA-AU 20 33589751 33589751 single base substitution G A downstream_gene_variant MELA-AU 20 33590497 33590497 single base substitution G A 3_prime_UTR_variant MELA-AU 20 33590497 33590497 single base substitution G A downstream_gene_variant MELA-AU 20 33591100 33591100 single base substitution G A intron_variant MELA-AU 20 33591563 33591563 single base substitution G A intron_variant MELA-AU 20 33591721 33591721 single base substitution G A intron_variant MELA-AU 20 33591737 33591737 single base substitution G A intron_variant MELA-AU 20 33593239 33593239 single base substitution C T intron_variant MELA-AU 20 33593276 33593276 single base substitution G A intron_variant MELA-AU 20 33594039 33594039 single base substitution G A intron_variant MELA-AU 20 33594082 33594082 single base substitution C A intron_variant MELA-AU 20 33594373 33594373 single base substitution G A synonymous_variant I166I 498C>T MELA-AU 20 33594373 33594373 single base substitution G A synonymous_variant I525I 1575C>T MELA-AU 20 33594373 33594373 single base substitution G A synonymous_variant I556I 1668C>T MELA-AU 20 33594373 33594373 single base substitution G A synonymous_variant I564I 1692C>T MELA-AU 20 33594756 33594756 single base substitution G A intron_variant MELA-AU 20 33594813 33594813 single base substitution G A intron_variant MELA-AU 20 33595511 33595511 single base substitution G A intron_variant MELA-AU 20 33595595 33595595 single base substitution G A intron_variant MELA-AU 20 33595998 33595998 single base substitution G A intron_variant MELA-AU 20 33596098 33596098 single base substitution G A intron_variant MELA-AU 20 33596336 33596336 single base substitution A G intron_variant MELA-AU 20 33597033 33597033 single base substitution G A intron_variant MELA-AU 20 33597690 33597690 single base substitution G A intron_variant MELA-AU 20 33597782 33597783 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 33598164 33598164 single base substitution G A intron_variant MELA-AU 20 33598286 33598286 single base substitution C T intron_variant MELA-AU 20 33598739 33598739 single base substitution A G intron_variant MELA-AU 20 33599167 33599167 single base substitution A T intron_variant MELA-AU 20 33599520 33599520 single base substitution T G intron_variant MELA-AU 20 33599893 33599893 single base substitution G A intron_variant MELA-AU 20 33600465 33600465 single base substitution C T intron_variant MELA-AU 20 33600648 33600648 single base substitution G A intron_variant MELA-AU 20 33601579 33601579 single base substitution A C intron_variant MELA-AU 20 33601792 33601792 single base substitution G A intron_variant MELA-AU 20 33602104 33602104 single base substitution G A intron_variant MELA-AU 20 33602414 33602414 single base substitution G A intron_variant MELA-AU 20 33602906 33602906 single base substitution G A intron_variant MELA-AU 20 33603249 33603249 single base substitution G A intron_variant MELA-AU 20 33603389 33603390 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 20 33603499 33603499 single base substitution G A intron_variant MELA-AU 20 33603688 33603688 single base substitution A G intron_variant MELA-AU 20 33603722 33603722 single base substitution G A intron_variant MELA-AU 20 33604434 33604434 single base substitution G T intron_variant MELA-AU 20 33605787 33605787 single base substitution G A intron_variant MELA-AU 20 33606021 33606021 single base substitution G A intron_variant MELA-AU 20 33606326 33606326 single base substitution G A intron_variant MELA-AU 20 33606813 33606813 single base substitution G A intron_variant MELA-AU 20 33606872 33606872 single base substitution G A intron_variant MELA-AU 20 33606925 33606925 single base substitution G A intron_variant MELA-AU 20 33607406 33607406 single base substitution G A intron_variant MELA-AU 20 33608317 33608317 single base substitution G A intron_variant MELA-AU 20 33609600 33609600 single base substitution G A intron_variant MELA-AU 20 33609620 33609620 single base substitution C T intron_variant MELA-AU 20 33609926 33609926 single base substitution C G intron_variant MELA-AU 20 33610751 33610751 single base substitution G A intron_variant MELA-AU 20 33610818 33610818 single base substitution G A intron_variant MELA-AU 20 33611377 33611377 single base substitution A C intron_variant MELA-AU 20 33611581 33611581 single base substitution G A intron_variant MELA-AU 20 33611658 33611658 single base substitution G A intron_variant MELA-AU 20 33612429 33612429 single base substitution C T intron_variant MELA-AU 20 33612639 33612639 single base substitution A C intron_variant MELA-AU 20 33612762 33612762 single base substitution C T intron_variant MELA-AU 20 33612967 33612967 single base substitution A G intron_variant MELA-AU 20 33613363 33613363 single base substitution G A intron_variant MELA-AU 20 33613767 33613767 single base substitution G A intron_variant MELA-AU 20 33614511 33614511 single base substitution G A intron_variant MELA-AU 20 33614561 33614561 single base substitution G A intron_variant MELA-AU 20 33614694 33614694 insertion of <=200bp - T intron_variant MELA-AU 20 33615063 33615063 single base substitution G A intron_variant MELA-AU 20 33615106 33615106 single base substitution G A intron_variant MELA-AU 20 33616116 33616116 single base substitution G A intron_variant MELA-AU 20 33616173 33616173 single base substitution G A intron_variant MELA-AU 20 33617138 33617138 single base substitution T A intron_variant MELA-AU 20 33617143 33617143 single base substitution T A intron_variant MELA-AU 20 33617661 33617661 single base substitution G A intron_variant MELA-AU 20 33617744 33617744 single base substitution T C intron_variant MELA-AU 20 33617869 33617869 single base substitution A G intron_variant MELA-AU 20 33618010 33618010 single base substitution C T intron_variant MELA-AU 20 33618129 33618129 single base substitution G A intron_variant MELA-AU 20 33619827 33619827 single base substitution G A intron_variant MELA-AU 20 33620186 33620186 single base substitution C T intron_variant MELA-AU 20 33620411 33620411 single base substitution G A intron_variant MELA-AU 20 33620631 33620631 single base substitution G A intron_variant MELA-AU 20 33620983 33620983 single base substitution G A intron_variant MELA-AU 20 33621636 33621636 insertion of <=200bp - T intron_variant MELA-AU 20 33622709 33622709 single base substitution G A intron_variant MELA-AU 20 33624123 33624123 single base substitution G A intron_variant MELA-AU 20 33624123 33624123 single base substitution G A upstream_gene_variant MELA-AU 20 33624363 33624363 single base substitution G A intron_variant MELA-AU 20 33624363 33624363 single base substitution G A upstream_gene_variant MELA-AU 20 33624429 33624429 single base substitution G A intron_variant MELA-AU 20 33624429 33624429 single base substitution G A upstream_gene_variant MELA-AU 20 33624477 33624477 single base substitution C T intron_variant MELA-AU 20 33624477 33624477 single base substitution C T upstream_gene_variant MELA-AU 20 33624836 33624836 single base substitution A G intron_variant MELA-AU 20 33624836 33624836 single base substitution A G upstream_gene_variant MELA-AU 20 33625012 33625012 single base substitution C G intron_variant MELA-AU 20 33625012 33625012 single base substitution C G upstream_gene_variant MELA-AU 20 33625667 33625667 single base substitution G A intron_variant MELA-AU 20 33625667 33625667 single base substitution G A upstream_gene_variant MELA-AU 20 33626288 33626288 single base substitution G A intron_variant MELA-AU 20 33626288 33626288 single base substitution G A upstream_gene_variant MELA-AU 20 33627017 33627018 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 33627017 33627018 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 20 33627592 33627592 single base substitution C T intron_variant MELA-AU 20 33627592 33627592 single base substitution C T upstream_gene_variant MELA-AU 20 33627823 33627823 single base substitution G A intron_variant MELA-AU 20 33627823 33627823 single base substitution G A upstream_gene_variant MELA-AU 20 33628105 33628105 single base substitution G A intron_variant MELA-AU 20 33628164 33628164 single base substitution G A intron_variant MELA-AU 20 33628348 33628348 single base substitution G A intron_variant MELA-AU 20 33628383 33628383 single base substitution A T intron_variant MELA-AU 20 33628434 33628434 single base substitution G A intron_variant MELA-AU 20 33628553 33628553 single base substitution T A intron_variant MELA-AU 20 33628912 33628912 single base substitution G A intron_variant MELA-AU 20 33630054 33630054 single base substitution G A intron_variant MELA-AU 20 33631197 33631197 single base substitution G A intron_variant MELA-AU 20 33631706 33631707 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 33631816 33631816 single base substitution G A intron_variant MELA-AU 20 33631895 33631895 single base substitution G A intron_variant MELA-AU 20 33632716 33632716 single base substitution G A intron_variant MELA-AU 20 33638447 33638447 single base substitution T C intron_variant MELA-AU 20 33638589 33638589 single base substitution G A intron_variant MELA-AU 20 33638721 33638722 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 33638744 33638744 single base substitution G A intron_variant MELA-AU 20 33640898 33640898 single base substitution G A intron_variant MELA-AU 20 33641079 33641079 single base substitution C G intron_variant MELA-AU 20 33641303 33641303 single base substitution G A intron_variant MELA-AU 20 33641603 33641603 single base substitution A G intron_variant MELA-AU 20 33641773 33641773 single base substitution A C intron_variant MELA-AU 20 33641977 33641977 single base substitution G A intron_variant MELA-AU 20 33642244 33642244 single base substitution G A intron_variant MELA-AU 20 33642439 33642439 single base substitution A G intron_variant MELA-AU 20 33643130 33643130 single base substitution T C intron_variant MELA-AU 20 33643155 33643155 single base substitution G A intron_variant MELA-AU 20 33643406 33643406 single base substitution G C intron_variant MELA-AU 20 33643704 33643704 single base substitution G A intron_variant MELA-AU 20 33643847 33643848 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 33644139 33644139 single base substitution G A intron_variant MELA-AU 20 33645233 33645233 single base substitution G A intron_variant MELA-AU 20 33645256 33645256 single base substitution G A intron_variant MELA-AU 20 33645511 33645511 single base substitution T C intron_variant MELA-AU 20 33646654 33646654 single base substitution G A intron_variant MELA-AU 20 33646880 33646880 single base substitution G A intron_variant MELA-AU 20 33647487 33647487 single base substitution A G intron_variant MELA-AU 20 33647489 33647489 single base substitution G A intron_variant MELA-AU 20 33647600 33647600 single base substitution G A intron_variant MELA-AU 20 33647730 33647730 single base substitution G A intron_variant MELA-AU 20 33647947 33647947 single base substitution G A intron_variant MELA-AU 20 33648330 33648330 single base substitution C T intron_variant MELA-AU 20 33649080 33649080 single base substitution A G intron_variant MELA-AU 20 33649808 33649808 single base substitution G A intron_variant MELA-AU 20 33650088 33650089 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 33650435 33650435 single base substitution A T intron_variant MELA-AU 20 33652335 33652335 single base substitution T A intron_variant MELA-AU 20 33652843 33652845 deletion of <=200bp TTC - intron_variant MELA-AU 20 33653452 33653452 single base substitution G A intron_variant MELA-AU 20 33654070 33654070 single base substitution G A intron_variant MELA-AU 20 33654629 33654629 single base substitution A G intron_variant MELA-AU 20 33656088 33656088 single base substitution G A intron_variant MELA-AU 20 33656783 33656783 single base substitution A C intron_variant MELA-AU 20 33656788 33656788 insertion of <=200bp - AAAAC intron_variant MELA-AU 20 33657083 33657083 single base substitution A T intron_variant MELA-AU 20 33657338 33657338 single base substitution G A intron_variant MELA-AU 20 33657730 33657730 single base substitution G A intron_variant MELA-AU 20 33657773 33657773 single base substitution C T intron_variant MELA-AU 20 33658244 33658244 single base substitution C T intron_variant MELA-AU 20 33658439 33658439 single base substitution G A intron_variant MELA-AU 20 33658503 33658503 single base substitution A G intron_variant MELA-AU 20 33659217 33659217 single base substitution A T intron_variant MELA-AU 20 33659405 33659405 single base substitution G T intron_variant MELA-AU 20 33660403 33660403 single base substitution G A intron_variant MELA-AU 20 33660816 33660816 single base substitution G A intron_variant MELA-AU 20 33661606 33661606 single base substitution T C intron_variant MELA-AU 20 33661888 33661888 single base substitution T C intron_variant MELA-AU 20 33662030 33662030 single base substitution G A intron_variant MELA-AU 20 33662049 33662049 single base substitution G C intron_variant MELA-AU 20 33662718 33662718 single base substitution G A intron_variant MELA-AU 20 33662948 33662948 single base substitution A G intron_variant MELA-AU 20 33663294 33663294 single base substitution G A intron_variant MELA-AU 20 33663541 33663541 single base substitution G A intron_variant MELA-AU 20 33664130 33664130 single base substitution G A intron_variant MELA-AU 20 33664238 33664238 single base substitution G A intron_variant MELA-AU 20 33664569 33664569 single base substitution G A intron_variant MELA-AU 20 33664769 33664769 single base substitution G A intron_variant MELA-AU 20 33665285 33665287 multiple base substitution (>=2bp and <=200bp) TCC ATA intron_variant MELA-AU 20 33665669 33665669 single base substitution G A intron_variant MELA-AU 20 33666170 33666170 single base substitution G A intron_variant MELA-AU 20 33666374 33666374 single base substitution G A intron_variant MELA-AU 20 33666884 33666884 single base substitution G A intron_variant MELA-AU 20 33666895 33666895 single base substitution G A intron_variant MELA-AU 20 33666919 33666919 single base substitution G A intron_variant MELA-AU 20 33667002 33667002 single base substitution G A intron_variant MELA-AU 20 33667176 33667177 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 33667648 33667648 single base substitution C T intron_variant MELA-AU 20 33668347 33668347 single base substitution A C intron_variant MELA-AU 20 33668610 33668610 insertion of <=200bp - TTG intron_variant MELA-AU 20 33668612 33668612 single base substitution T G intron_variant MELA-AU 20 33669158 33669158 single base substitution G A intron_variant MELA-AU 20 33669806 33669806 single base substitution A C intron_variant MELA-AU 20 33669884 33669884 single base substitution G A intron_variant MELA-AU 20 33670307 33670307 single base substitution G A intron_variant MELA-AU 20 33670449 33670449 single base substitution A G intron_variant MELA-AU 20 33670453 33670453 single base substitution G A intron_variant MELA-AU 20 33670702 33670703 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 20 33670992 33670992 single base substitution T C intron_variant MELA-AU 20 33672852 33672852 single base substitution G A intron_variant MELA-AU 20 33672894 33672894 single base substitution C T intron_variant MELA-AU 20 33673187 33673187 single base substitution G A intron_variant MELA-AU 20 33674270 33674270 single base substitution G A intron_variant MELA-AU 20 33674380 33674380 single base substitution A G intron_variant MELA-AU 20 33674745 33674745 single base substitution G A intron_variant MELA-AU 20 33675125 33675125 single base substitution G A intron_variant MELA-AU 20 33675304 33675304 single base substitution G A intron_variant MELA-AU 20 33675313 33675314 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 33675489 33675489 single base substitution G A intron_variant MELA-AU 20 33676120 33676120 single base substitution T A intron_variant MELA-AU 20 33676610 33676610 single base substitution C T intron_variant MELA-AU 20 33676749 33676749 single base substitution T C intron_variant MELA-AU 20 33677361 33677361 single base substitution G A intron_variant MELA-AU 20 33677598 33677598 single base substitution G A intron_variant MELA-AU 20 33677661 33677661 single base substitution T A intron_variant MELA-AU 20 33680643 33680644 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 20 33680643 33680644 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 20 33680841 33680841 single base substitution C T upstream_gene_variant MELA-AU 20 33681864 33681864 single base substitution G A upstream_gene_variant MELA-AU 20 33681892 33681892 single base substitution G A upstream_gene_variant MELA-AU 20 33682158 33682158 single base substitution G A upstream_gene_variant MELA-AU 20 33682256 33682256 single base substitution C T upstream_gene_variant MELA-AU 20 33682487 33682487 single base substitution G A upstream_gene_variant MELA-AU 20 33682502 33682502 single base substitution G A upstream_gene_variant MELA-AU 20 33682587 33682587 single base substitution G A upstream_gene_variant MELA-AU 20 33682731 33682731 single base substitution C T upstream_gene_variant MELA-AU 20 33682844 33682844 single base substitution C T upstream_gene_variant MELA-AU 20 33683030 33683030 single base substitution A G upstream_gene_variant MELA-AU 20 33683376 33683376 single base substitution C T upstream_gene_variant MELA-AU 20 33683614 33683615 multiple base substitution (>=2bp and <=200bp) GG AT upstream_gene_variant MELA-AU 20 33683908 33683908 single base substitution C T upstream_gene_variant MELA-AU 20 33684755 33684755 single base substitution G A upstream_gene_variant MELA-AU 20 33685526 33685526 single base substitution A G upstream_gene_variant ORCA-IN 20 33591268 33591268 single base substitution C A missense_variant R336L 1007G>T ORCA-IN 20 33591268 33591268 single base substitution C A missense_variant R695L 2084G>T ORCA-IN 20 33591268 33591268 single base substitution C A missense_variant R726L 2177G>T ORCA-IN 20 33591268 33591268 single base substitution C A missense_variant R734L 2201G>T ORCA-IN 20 33602682 33602682 single base substitution G C intron_variant ORCA-IN 20 33619220 33619220 single base substitution A T intron_variant ORCA-IN 20 33624291 33624291 single base substitution C G intron_variant ORCA-IN 20 33624291 33624291 single base substitution C G upstream_gene_variant ORCA-IN 20 33626927 33626927 single base substitution C G intron_variant ORCA-IN 20 33626927 33626927 single base substitution C G upstream_gene_variant ORCA-IN 20 33637206 33637206 single base substitution C T intron_variant ORCA-IN 20 33640581 33640581 single base substitution C T intron_variant ORCA-IN 20 33646038 33646038 single base substitution C G intron_variant OV-AU 20 33590853 33590853 single base substitution G C 3_prime_UTR_variant OV-AU 20 33591783 33591783 single base substitution C T intron_variant OV-AU 20 33598877 33598877 single base substitution C T intron_variant OV-AU 20 33612398 33612398 single base substitution G A intron_variant OV-AU 20 33614486 33614486 single base substitution T C intron_variant OV-AU 20 33617345 33617345 single base substitution C T intron_variant OV-AU 20 33618410 33618410 single base substitution A G intron_variant OV-AU 20 33624221 33624221 single base substitution A G intron_variant OV-AU 20 33624221 33624221 single base substitution A G upstream_gene_variant OV-AU 20 33624341 33624341 single base substitution G A intron_variant OV-AU 20 33624341 33624341 single base substitution G A upstream_gene_variant OV-AU 20 33631176 33631176 single base substitution A T intron_variant OV-AU 20 33632172 33632172 single base substitution G A intron_variant OV-AU 20 33633290 33633290 single base substitution C G intron_variant OV-AU 20 33633725 33633725 single base substitution G T intron_variant OV-AU 20 33643585 33643585 single base substitution C G intron_variant OV-AU 20 33644538 33644538 single base substitution C G intron_variant OV-AU 20 33648876 33648876 single base substitution C G intron_variant OV-AU 20 33663868 33663868 single base substitution G C intron_variant OV-AU 20 33665205 33665205 single base substitution A C intron_variant OV-AU 20 33677818 33677818 single base substitution G A intron_variant OV-AU 20 33681664 33681664 single base substitution C A upstream_gene_variant OV-AU 20 33681969 33681969 single base substitution G T upstream_gene_variant OV-AU 20 33682983 33682983 single base substitution C A upstream_gene_variant PACA-AU 20 33589375 33589396 deletion of <=200bp TGCCCCAGGGTCTGTGGCCAGG - downstream_gene_variant PACA-AU 20 33590080 33590080 single base substitution G A downstream_gene_variant PACA-AU 20 33593738 33593738 single base substitution C T intron_variant PACA-AU 20 33593740 33593740 single base substitution C T intron_variant PACA-AU 20 33597393 33597393 single base substitution G A intron_variant PACA-AU 20 33601312 33601312 single base substitution C T intron_variant PACA-AU 20 33605472 33605472 single base substitution G A intron_variant PACA-AU 20 33608256 33608256 single base substitution C T intron_variant PACA-AU 20 33609334 33609334 single base substitution G A intron_variant PACA-AU 20 33612640 33612640 single base substitution A C intron_variant PACA-AU 20 33612646 33612646 single base substitution A C intron_variant PACA-AU 20 33613535 33613535 insertion of <=200bp - T intron_variant PACA-AU 20 33617108 33617108 single base substitution T C intron_variant PACA-AU 20 33618241 33618241 single base substitution C T intron_variant PACA-AU 20 33620541 33620541 single base substitution C T intron_variant PACA-AU 20 33631502 33631502 single base substitution A G intron_variant PACA-AU 20 33638870 33638870 single base substitution C T intron_variant PACA-AU 20 33641384 33641393 deletion of <=200bp TGGCTATACA - intron_variant PACA-AU 20 33643300 33643300 single base substitution A T intron_variant PACA-AU 20 33646036 33646036 single base substitution C T intron_variant PACA-AU 20 33647524 33647524 single base substitution A G intron_variant PACA-AU 20 33649239 33649239 single base substitution A G intron_variant PACA-AU 20 33649408 33649408 single base substitution A C intron_variant PACA-AU 20 33657092 33657092 single base substitution T G intron_variant PACA-AU 20 33657092 33657092 single base substitution T G splice_region_variant PACA-AU 20 33657227 33657227 single base substitution A T intron_variant PACA-AU 20 33668610 33668610 insertion of <=200bp - TTG intron_variant PACA-AU 20 33675135 33675135 single base substitution C T intron_variant PACA-AU 20 33677464 33677464 single base substitution C T intron_variant PACA-AU 20 33681282 33681282 single base substitution G T upstream_gene_variant PACA-AU 20 33681954 33681954 single base substitution A C upstream_gene_variant PACA-AU 20 33685245 33685245 single base substitution T C upstream_gene_variant PACA-CA 20 33589011 33589011 single base substitution G A downstream_gene_variant PACA-CA 20 33593048 33593048 deletion of <=200bp G - intron_variant PACA-CA 20 33593116 33593116 single base substitution C T intron_variant PACA-CA 20 33594070 33594070 single base substitution C T intron_variant PACA-CA 20 33600571 33600571 single base substitution A G intron_variant PACA-CA 20 33602181 33602181 single base substitution C T intron_variant PACA-CA 20 33607656 33607656 single base substitution T C intron_variant PACA-CA 20 33611618 33611618 single base substitution G A intron_variant PACA-CA 20 33611666 33611666 single base substitution G A intron_variant PACA-CA 20 33618201 33618202 deletion of <=200bp AT - intron_variant PACA-CA 20 33620138 33620138 single base substitution A G intron_variant PACA-CA 20 33620568 33620568 single base substitution C T intron_variant PACA-CA 20 33626600 33626600 single base substitution G A intron_variant PACA-CA 20 33626600 33626600 single base substitution G A upstream_gene_variant PACA-CA 20 33628246 33628246 single base substitution A G intron_variant PACA-CA 20 33631367 33631367 single base substitution T C intron_variant PACA-CA 20 33631377 33631377 single base substitution C T intron_variant PACA-CA 20 33638872 33638872 insertion of <=200bp - ACACAT intron_variant PACA-CA 20 33638931 33638931 deletion of <=200bp T - intron_variant PACA-CA 20 33639522 33639522 single base substitution A T intron_variant PACA-CA 20 33642734 33642734 single base substitution C T intron_variant PACA-CA 20 33646015 33646015 single base substitution A G intron_variant PACA-CA 20 33647803 33647803 single base substitution T A intron_variant PACA-CA 20 33648805 33648805 insertion of <=200bp - A intron_variant PACA-CA 20 33649470 33649470 single base substitution G A intron_variant PACA-CA 20 33651432 33651432 single base substitution C G intron_variant PACA-CA 20 33651974 33651974 single base substitution C T intron_variant PACA-CA 20 33660160 33660160 single base substitution G A intron_variant PACA-CA 20 33664269 33664269 single base substitution T G intron_variant PACA-CA 20 33665022 33665022 single base substitution A G intron_variant PACA-CA 20 33667447 33667447 insertion of <=200bp - A intron_variant PACA-CA 20 33667629 33667629 single base substitution G C intron_variant PACA-CA 20 33671284 33671284 single base substitution C T intron_variant PACA-CA 20 33672403 33672403 single base substitution G A intron_variant PACA-CA 20 33672872 33672872 single base substitution C G intron_variant PACA-CA 20 33673002 33673002 insertion of <=200bp - T intron_variant PACA-CA 20 33674023 33674023 single base substitution A G intron_variant PACA-CA 20 33677749 33677749 single base substitution C T intron_variant PACA-CA 20 33678896 33678896 single base substitution C T intron_variant PACA-CA 20 33678982 33678982 single base substitution A C intron_variant PACA-CA 20 33683576 33683576 single base substitution A G upstream_gene_variant PAEN-AU 20 33595492 33595492 single base substitution C T intron_variant PAEN-AU 20 33621417 33621417 single base substitution C A intron_variant PAEN-AU 20 33677086 33677086 single base substitution A T intron_variant PAEN-AU 20 33683135 33683135 single base substitution G T upstream_gene_variant PAEN-IT 20 33596614 33596614 single base substitution C A intron_variant PAEN-IT 20 33639546 33639546 single base substitution G T intron_variant PAEN-IT 20 33665566 33665566 single base substitution G A intron_variant PBCA-DE 20 33594881 33594881 single base substitution C A intron_variant PBCA-DE 20 33594903 33594903 single base substitution T A intron_variant PBCA-DE 20 33596697 33596697 deletion of <=200bp C - intron_variant PBCA-DE 20 33599419 33599441 deletion of <=200bp CCTGTGACTGTGACCCACAACAC - intron_variant PBCA-DE 20 33606695 33606695 single base substitution G T intron_variant PBCA-DE 20 33608442 33608442 single base substitution G A intron_variant PBCA-DE 20 33622296 33622296 single base substitution C T intron_variant PBCA-DE 20 33624764 33624765 deletion of <=200bp AC - intron_variant PBCA-DE 20 33624764 33624765 deletion of <=200bp AC - upstream_gene_variant PBCA-DE 20 33629184 33629184 single base substitution C G intron_variant PBCA-DE 20 33630656 33630673 deletion of <=200bp GTTCTAAAATCAAACAAT - intron_variant PBCA-DE 20 33633622 33633622 single base substitution C T intron_variant PBCA-DE 20 33653382 33653382 single base substitution G C intron_variant PBCA-DE 20 33656170 33656170 single base substitution C T intron_variant PBCA-DE 20 33660021 33660021 single base substitution C A intron_variant PBCA-DE 20 33685073 33685073 single base substitution T C upstream_gene_variant PBCA-DE 20 33685461 33685461 single base substitution C T upstream_gene_variant PBCA-DE 20 33685507 33685507 single base substitution T C upstream_gene_variant PRAD-CA 20 33635099 33635099 single base substitution T G intron_variant PRAD-CA 20 33650771 33650771 single base substitution G A intron_variant PRAD-CA 20 33657227 33657227 single base substitution A T intron_variant PRAD-CA 20 33667395 33667395 single base substitution T C intron_variant PRAD-CA 20 33674330 33674330 single base substitution G A intron_variant PRAD-CA 20 33685437 33685437 single base substitution C T upstream_gene_variant PRAD-UK 20 33591493 33591493 single base substitution T A intron_variant PRAD-UK 20 33593116 33593116 single base substitution C T intron_variant PRAD-UK 20 33614272 33614272 single base substitution G A intron_variant PRAD-UK 20 33625999 33625999 single base substitution C A intron_variant PRAD-UK 20 33625999 33625999 single base substitution C A upstream_gene_variant PRAD-UK 20 33646911 33646911 single base substitution T C intron_variant PRAD-UK 20 33647804 33647804 single base substitution A T intron_variant PRAD-UK 20 33648025 33648025 single base substitution C T intron_variant PRAD-UK 20 33653546 33653546 single base substitution C A intron_variant PRAD-UK 20 33664883 33664883 single base substitution C G intron_variant PRAD-UK 20 33665146 33665146 single base substitution C T intron_variant PRAD-UK 20 33665259 33665259 single base substitution C A intron_variant PRAD-UK 20 33665321 33665321 single base substitution C T intron_variant PRAD-UK 20 33684109 33684109 single base substitution A T upstream_gene_variant PRAD-US 20 33589834 33589834 single base substitution G A downstream_gene_variant READ-US 20 33587055 33587055 single base substitution C T downstream_gene_variant READ-US 20 33589110 33589110 single base substitution C T downstream_gene_variant READ-US 20 33592305 33592305 single base substitution G T missense_variant L271I 811C>A READ-US 20 33592305 33592305 single base substitution G T missense_variant L630I 1888C>A READ-US 20 33592305 33592305 single base substitution G T missense_variant L661I 1981C>A READ-US 20 33592305 33592305 single base substitution G T missense_variant L669I 2005C>A RECA-EU 20 33586544 33586544 single base substitution C A downstream_gene_variant RECA-EU 20 33590612 33590612 single base substitution T A 3_prime_UTR_variant RECA-EU 20 33590612 33590612 single base substitution T A downstream_gene_variant RECA-EU 20 33596555 33596555 single base substitution A T splice_region_variant RECA-EU 20 33603543 33603543 single base substitution C T intron_variant RECA-EU 20 33605443 33605443 single base substitution C T intron_variant RECA-EU 20 33608470 33608470 single base substitution A T intron_variant RECA-EU 20 33611525 33611525 single base substitution C A intron_variant RECA-EU 20 33611539 33611539 single base substitution A T intron_variant RECA-EU 20 33622282 33622282 single base substitution T G intron_variant RECA-EU 20 33637733 33637733 single base substitution A T missense_variant M159K 476T>A RECA-EU 20 33637733 33637733 single base substitution A T missense_variant M198K 593T>A RECA-EU 20 33645975 33645975 single base substitution A T intron_variant RECA-EU 20 33645978 33645978 single base substitution A G intron_variant RECA-EU 20 33646012 33646012 single base substitution A G intron_variant RECA-EU 20 33650952 33650952 single base substitution C G intron_variant RECA-EU 20 33654827 33654827 single base substitution T G intron_variant RECA-EU 20 33655696 33655696 single base substitution T A intron_variant RECA-EU 20 33657227 33657227 single base substitution A T intron_variant RECA-EU 20 33661365 33661365 single base substitution G A intron_variant RECA-EU 20 33664086 33664086 single base substitution C T intron_variant RECA-EU 20 33668347 33668347 single base substitution A C intron_variant RECA-EU 20 33672288 33672288 single base substitution T C intron_variant RECA-EU 20 33685051 33685051 single base substitution T C upstream_gene_variant SKCA-BR 20 33587553 33587555 deletion of <=200bp TCC - downstream_gene_variant SKCA-BR 20 33587564 33587565 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 20 33592031 33592031 single base substitution A G intron_variant SKCA-BR 20 33592426 33592426 single base substitution T G intron_variant SKCA-BR 20 33595061 33595061 single base substitution G A intron_variant SKCA-BR 20 33600069 33600069 single base substitution G A intron_variant SKCA-BR 20 33600560 33600560 single base substitution A G intron_variant SKCA-BR 20 33605087 33605087 single base substitution G A intron_variant SKCA-BR 20 33605375 33605375 single base substitution A G intron_variant SKCA-BR 20 33606381 33606381 single base substitution G A intron_variant SKCA-BR 20 33606406 33606407 deletion of <=200bp AG - intron_variant SKCA-BR 20 33606430 33606430 single base substitution G A intron_variant SKCA-BR 20 33606695 33606695 single base substitution G A intron_variant SKCA-BR 20 33609203 33609203 single base substitution G A intron_variant SKCA-BR 20 33610827 33610828 deletion of <=200bp CA - intron_variant SKCA-BR 20 33611582 33611582 single base substitution G A intron_variant SKCA-BR 20 33612629 33612629 single base substitution A C intron_variant SKCA-BR 20 33612638 33612638 insertion of <=200bp - AC intron_variant SKCA-BR 20 33614732 33614732 single base substitution A T intron_variant SKCA-BR 20 33615020 33615020 single base substitution G A intron_variant SKCA-BR 20 33619218 33619218 insertion of <=200bp - TC intron_variant SKCA-BR 20 33619291 33619291 single base substitution G A intron_variant SKCA-BR 20 33628183 33628183 single base substitution G A intron_variant SKCA-BR 20 33628930 33628931 deletion of <=200bp CT - intron_variant SKCA-BR 20 33632775 33632775 single base substitution T C intron_variant SKCA-BR 20 33633292 33633292 single base substitution G T intron_variant SKCA-BR 20 33636015 33636015 single base substitution G T intron_variant SKCA-BR 20 33639418 33639419 deletion of <=200bp TA - intron_variant SKCA-BR 20 33639901 33639902 deletion of <=200bp GT - intron_variant SKCA-BR 20 33640585 33640585 single base substitution G A intron_variant SKCA-BR 20 33640586 33640586 single base substitution T A intron_variant SKCA-BR 20 33642325 33642325 single base substitution G A intron_variant SKCA-BR 20 33642430 33642430 single base substitution G A intron_variant SKCA-BR 20 33642772 33642772 single base substitution T G splice_region_variant SKCA-BR 20 33645112 33645112 single base substitution C T intron_variant SKCA-BR 20 33645279 33645279 single base substitution T G intron_variant SKCA-BR 20 33645878 33645878 single base substitution G A intron_variant SKCA-BR 20 33647709 33647709 single base substitution G A intron_variant SKCA-BR 20 33647738 33647741 deletion of <=200bp CGAA - intron_variant SKCA-BR 20 33651137 33651137 single base substitution A G intron_variant SKCA-BR 20 33656749 33656749 insertion of <=200bp - TAC intron_variant SKCA-BR 20 33659235 33659235 single base substitution T C intron_variant SKCA-BR 20 33660273 33660273 single base substitution G A intron_variant SKCA-BR 20 33660989 33660989 single base substitution G A intron_variant SKCA-BR 20 33663889 33663889 single base substitution C G intron_variant SKCA-BR 20 33664195 33664195 single base substitution G A intron_variant SKCA-BR 20 33667663 33667663 insertion of <=200bp - TA intron_variant SKCA-BR 20 33668337 33668337 insertion of <=200bp - TA intron_variant SKCA-BR 20 33669764 33669764 single base substitution G A intron_variant SKCA-BR 20 33669963 33669963 single base substitution G A intron_variant SKCA-BR 20 33670300 33670300 single base substitution G A intron_variant SKCA-BR 20 33671564 33671564 single base substitution T A intron_variant SKCA-BR 20 33671591 33671591 single base substitution G A intron_variant SKCA-BR 20 33674310 33674312 deletion of <=200bp ATG - intron_variant SKCA-BR 20 33674324 33674324 single base substitution A G intron_variant SKCA-BR 20 33674330 33674330 single base substitution G A intron_variant SKCA-BR 20 33674374 33674374 single base substitution G A intron_variant SKCA-BR 20 33675141 33675141 insertion of <=200bp - CA intron_variant SKCA-BR 20 33677201 33677201 single base substitution T G intron_variant SKCA-BR 20 33677904 33677905 deletion of <=200bp CA - intron_variant SKCA-BR 20 33680351 33680351 single base substitution T C intron_variant SKCA-BR 20 33680557 33680557 single base substitution A C missense_variant S10A 28T>G SKCA-BR 20 33682374 33682374 insertion of <=200bp - GA upstream_gene_variant SKCA-BR 20 33685265 33685265 single base substitution C T upstream_gene_variant SKCA-BR 20 33685317 33685317 single base substitution C T upstream_gene_variant SKCA-BR 20 33685373 33685373 single base substitution T C upstream_gene_variant SKCA-BR 20 33685398 33685400 deletion of <=200bp GTA - upstream_gene_variant SKCA-BR 20 33685424 33685424 single base substitution A G upstream_gene_variant SKCA-BR 20 33685444 33685444 insertion of <=200bp - GTGTGTATA upstream_gene_variant SKCA-BR 20 33685451 33685451 single base substitution T C upstream_gene_variant SKCA-BR 20 33685465 33685465 single base substitution C T upstream_gene_variant SKCA-BR 20 33685470 33685472 deletion of <=200bp GTA - upstream_gene_variant SKCA-BR 20 33685472 33685472 single base substitution A G upstream_gene_variant SKCA-BR 20 33685477 33685477 single base substitution T C upstream_gene_variant SKCA-BR 20 33685485 33685485 insertion of <=200bp - TATATACAC upstream_gene_variant SKCA-BR 20 33685489 33685489 single base substitution C T upstream_gene_variant SKCA-BR 20 33685495 33685495 single base substitution C T upstream_gene_variant SKCA-BR 20 33685666 33685666 insertion of <=200bp - ATG upstream_gene_variant SKCM-US 20 33585423 33585423 single base substitution G A downstream_gene_variant SKCM-US 20 33586218 33586218 single base substitution G A downstream_gene_variant SKCM-US 20 33586397 33586397 single base substitution G A downstream_gene_variant SKCM-US 20 33586421 33586421 single base substitution G A downstream_gene_variant SKCM-US 20 33586667 33586667 single base substitution G A downstream_gene_variant SKCM-US 20 33586675 33586675 single base substitution G A downstream_gene_variant SKCM-US 20 33586685 33586685 single base substitution C T downstream_gene_variant SKCM-US 20 33586701 33586701 single base substitution G A downstream_gene_variant SKCM-US 20 33587427 33587427 single base substitution G A downstream_gene_variant SKCM-US 20 33587611 33587611 single base substitution G A downstream_gene_variant SKCM-US 20 33588110 33588110 single base substitution G A downstream_gene_variant SKCM-US 20 33588192 33588192 single base substitution G A downstream_gene_variant SKCM-US 20 33588607 33588607 single base substitution G A downstream_gene_variant SKCM-US 20 33589068 33589068 single base substitution G A downstream_gene_variant SKCM-US 20 33589751 33589751 single base substitution G A downstream_gene_variant SKCM-US 20 33589805 33589805 single base substitution G A downstream_gene_variant SKCM-US 20 33589863 33589863 single base substitution G A downstream_gene_variant SKCM-US 20 33592285 33592285 single base substitution G A synonymous_variant I277I 831C>T SKCM-US 20 33592285 33592285 single base substitution G A synonymous_variant I636I 1908C>T SKCM-US 20 33592285 33592285 single base substitution G A synonymous_variant I667I 2001C>T SKCM-US 20 33592285 33592285 single base substitution G A synonymous_variant I675I 2025C>T SKCM-US 20 33593574 33593574 single base substitution G A synonymous_variant S222S 666C>T SKCM-US 20 33593574 33593574 single base substitution G A synonymous_variant S581S 1743C>T SKCM-US 20 33593574 33593574 single base substitution G A synonymous_variant S612S 1836C>T SKCM-US 20 33593574 33593574 single base substitution G A synonymous_variant S620S 1860C>T SKCM-US 20 33596537 33596537 single base substitution C A missense_variant D111Y 331G>T SKCM-US 20 33596537 33596537 single base substitution C A missense_variant D470Y 1408G>T SKCM-US 20 33596537 33596537 single base substitution C A missense_variant D501Y 1501G>T SKCM-US 20 33596537 33596537 single base substitution C A missense_variant D509Y 1525G>T SKCM-US 20 33596548 33596548 single base substitution C A missense_variant S107I 320G>T SKCM-US 20 33596548 33596548 single base substitution C A missense_variant S466I 1397G>T SKCM-US 20 33596548 33596548 single base substitution C A missense_variant S497I 1490G>T SKCM-US 20 33596548 33596548 single base substitution C A missense_variant S505I 1514G>T SKCM-US 20 33623094 33623094 single base substitution G A 5_prime_UTR_variant SKCM-US 20 33623094 33623094 single base substitution G A missense_variant P256S 766C>T SKCM-US 20 33623094 33623094 single base substitution G A missense_variant P295S 883C>T SKCM-US 20 33632470 33632470 single base substitution A T missense_variant S196T 586T>A SKCM-US 20 33632470 33632470 single base substitution A T missense_variant S235T 703T>A SKCM-US 20 33680544 33680544 single base substitution C T missense_variant R14Q 41G>A STAD-US 20 33585431 33585431 single base substitution G C downstream_gene_variant STAD-US 20 33588098 33588098 single base substitution G A downstream_gene_variant STAD-US 20 33588235 33588235 single base substitution C T downstream_gene_variant STAD-US 20 33588873 33588873 single base substitution C T downstream_gene_variant STAD-US 20 33589114 33589114 single base substitution C T downstream_gene_variant STAD-US 20 33589767 33589767 single base substitution C A downstream_gene_variant STAD-US 20 33591321 33591321 single base substitution C T synonymous_variant E318E 954G>A STAD-US 20 33591321 33591321 single base substitution C T synonymous_variant E677E 2031G>A STAD-US 20 33591321 33591321 single base substitution C T synonymous_variant E708E 2124G>A STAD-US 20 33591321 33591321 single base substitution C T synonymous_variant E716E 2148G>A STAD-US 20 33591350 33591350 deletion of <=200bp G - frameshift_variant L309 STAD-US 20 33591350 33591350 deletion of <=200bp G - frameshift_variant L668 STAD-US 20 33591350 33591350 deletion of <=200bp G - frameshift_variant L699 STAD-US 20 33591350 33591350 deletion of <=200bp G - frameshift_variant L707 STAD-US 20 33592318 33592318 single base substitution C T synonymous_variant T266T 798G>A STAD-US 20 33592318 33592318 single base substitution C T synonymous_variant T625T 1875G>A STAD-US 20 33592318 33592318 single base substitution C T synonymous_variant T656T 1968G>A STAD-US 20 33592318 33592318 single base substitution C T synonymous_variant T664T 1992G>A STAD-US 20 33593526 33593526 single base substitution G A synonymous_variant D238D 714C>T STAD-US 20 33593526 33593526 single base substitution G A synonymous_variant D597D 1791C>T STAD-US 20 33593526 33593526 single base substitution G A synonymous_variant D628D 1884C>T STAD-US 20 33593526 33593526 single base substitution G A synonymous_variant D636D 1908C>T STAD-US 20 33632505 33632505 single base substitution C T missense_variant R184Q 551G>A STAD-US 20 33632505 33632505 single base substitution C T missense_variant R223Q 668G>A STAD-US 20 33657209 33657209 single base substitution A T intron_variant STAD-US 20 33657209 33657209 single base substitution A T missense_variant S102T 304T>A THCA-SA 20 33588266 33588266 single base substitution G A downstream_gene_variant THCA-SA 20 33590358 33590358 single base substitution C T 3_prime_UTR_variant THCA-SA 20 33590358 33590358 single base substitution C T downstream_gene_variant THCA-SA 20 33665957 33665957 single base substitution C T synonymous_variant T63T 189G>A UCEC-US 20 33586109 33586109 single base substitution G A downstream_gene_variant UCEC-US 20 33586130 33586130 single base substitution G T downstream_gene_variant UCEC-US 20 33586552 33586552 single base substitution G A downstream_gene_variant UCEC-US 20 33586667 33586667 single base substitution G T downstream_gene_variant UCEC-US 20 33587061 33587061 single base substitution C T downstream_gene_variant UCEC-US 20 33587422 33587422 single base substitution T C downstream_gene_variant UCEC-US 20 33588658 33588658 single base substitution C T downstream_gene_variant UCEC-US 20 33591288 33591288 single base substitution G A synonymous_variant N329N 987C>T UCEC-US 20 33591288 33591288 single base substitution G A synonymous_variant N688N 2064C>T UCEC-US 20 33591288 33591288 single base substitution G A synonymous_variant N719N 2157C>T UCEC-US 20 33591288 33591288 single base substitution G A synonymous_variant N727N 2181C>T UCEC-US 20 33592341 33592341 single base substitution C T missense_variant A259T 775G>A UCEC-US 20 33592341 33592341 single base substitution C T missense_variant A618T 1852G>A UCEC-US 20 33592341 33592341 single base substitution C T missense_variant A649T 1945G>A UCEC-US 20 33592341 33592341 single base substitution C T missense_variant A657T 1969G>A UCEC-US 20 33594249 33594249 single base substitution T C missense_variant T208A 622A>G UCEC-US 20 33594249 33594249 single base substitution T C missense_variant T567A 1699A>G UCEC-US 20 33594249 33594249 single base substitution T C missense_variant T598A 1792A>G UCEC-US 20 33594249 33594249 single base substitution T C missense_variant T606A 1816A>G UCEC-US 20 33594318 33594318 single base substitution A C missense_variant F185V 553T>G UCEC-US 20 33594318 33594318 single base substitution A C missense_variant F544V 1630T>G UCEC-US 20 33594318 33594318 single base substitution A C missense_variant F575V 1723T>G UCEC-US 20 33594318 33594318 single base substitution A C missense_variant F583V 1747T>G UCEC-US 20 33595429 33595429 single base substitution C T missense_variant R139Q 416G>A UCEC-US 20 33595429 33595429 single base substitution C T missense_variant R498Q 1493G>A UCEC-US 20 33595429 33595429 single base substitution C T missense_variant R529Q 1586G>A UCEC-US 20 33595429 33595429 single base substitution C T missense_variant R537Q 1610G>A UCEC-US 20 33603857 33603857 single base substitution G C missense_variant S37C 110C>G UCEC-US 20 33603857 33603857 single base substitution G C missense_variant S396C 1187C>G UCEC-US 20 33603857 33603857 single base substitution G C missense_variant S427C 1280C>G UCEC-US 20 33603857 33603857 single base substitution G C missense_variant S435C 1304C>G UCEC-US 20 33603862 33603862 single base substitution T C synonymous_variant S35S 105A>G UCEC-US 20 33603862 33603862 single base substitution T C synonymous_variant S394S 1182A>G UCEC-US 20 33603862 33603862 single base substitution T C synonymous_variant S425S 1275A>G UCEC-US 20 33603862 33603862 single base substitution T C synonymous_variant S433S 1299A>G UCEC-US 20 33609001 33609001 single base substitution G A intron_variant UCEC-US 20 33609001 33609001 single base substitution G A stop_gained R365* 1093C>T UCEC-US 20 33609001 33609001 single base substitution G A stop_gained R396* 1186C>T UCEC-US 20 33609001 33609001 single base substitution G A stop_gained R404* 1210C>T UCEC-US 20 33645345 33645345 single base substitution C T synonymous_variant T109T 327G>A UCEC-US 20 33645345 33645345 single base substitution C T synonymous_variant T148T 444G>A UCEC-US 20 33665958 33665958 single base substitution G A missense_variant T63M 188C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T3064 COSM4736480 c.1631G>A p.R544Q Substitution - Missense 20:35007605-35007605 - TCGA-DK-A1AC-01 COSM1307314 c.2067C>G p.L689L Substitution - coding silent 20:35003599-35003599 - TCGA-B0-5098-01 COSM1495021 c.1274A>T p.D425V Substitution - Missense 20:35016084-35016084 - TCGA-DW-7837-01 COSM3991658 c.2212C>A p.Q738K Substitution - Missense 20:35003454-35003454 - TCGA-CD-8529-01 COSM4097872 c.304T>A p.S102T Substitution - Missense 20:35069406-35069406 - TCGA-EK-A2H0-01 COSM4818897 c.2282G>A p.W761* Substitution - Nonsense 20:35003258-35003258 - TCGA-22-5480-01 COSM723933 c.307C>T p.P103S Substitution - Missense 20:35069403-35069403 - CCK81 COSM2758574 c.1646A>G p.Y549C Substitution - Missense 20:35007590-35007590 - LUAD-CHTN-3090415 COSM357319 c.730A>G p.N244D Substitution - Missense 20:35044640-35044640 - TCGA-46-3765-01 COSM723935 c.869C>A p.A290D Substitution - Missense 20:35035305-35035305 - PT48 COSM4487378 c.317C>T p.S106F Substitution - Missense 20:35069393-35069393 - TCGA-ER-A2NC-06 COSM3545639 c.1514G>T p.S505I Substitution - Missense 20:35008745-35008745 - TCGA-BT-A20J-01 COSM419429 c.726C>T p.L242L Substitution - coding silent 20:35044644-35044644 - TCGA-BH-A0GY-01 COSM443703 c.1491_1493delAGC p.E497_A498>D Complex - deletion inframe 20:35010205-35010207 - TCGA-B5-A0JY-01 COSM1026182 c.188C>T p.T63M Substitution - Missense 20:35078155-35078155 - TCGA-BS-A0UJ-01 COSM1026175 c.1299A>G p.S433S Substitution - coding silent 20:35016059-35016059 - CSCC-15-T COSM4535954 c.2253G>A p.E751E Substitution - coding silent 20:35003413-35003413 - TCGA-CS-5397-01 COSM3972528 c.351G>T p.R117S Substitution - Missense 20:35069359-35069359 - TCGA-P4-A5E7-01 COSM3991659 c.1026C>A p.A342A Substitution - coding silent 20:35035148-35035148 - sysucc-1397T COSM4097868 c.1992G>A p.T664T Substitution - coding silent 20:35004515-35004515 - YUKAT COSM5391897 c.1612G>A p.A538T Substitution - Missense 20:35007624-35007624 - YULAN COSM1713388 c.2005C>T p.L669F Substitution - Missense 20:35004502-35004502 - HCT15 COSM2758579 c.1389G>T p.Q463H Substitution - Missense 20:35013028-35013028 - 8031681 COSM3389702 c.414+7A>C p.? Unknown 20:35069289-35069289 - 19 COSM5748160 c.980C>T p.T327I Substitution - Missense 20:35035194-35035194 - 08-129 COSM305423 c.914C>T p.A305V Substitution - Missense 20:35035260-35035260 - TCGA-14-1825-01 COSM2758565 c.2141G>A p.R714Q Substitution - Missense 20:35003525-35003525 - TCGA-AO-A0J9-01 COSM443705 c.1057A>G p.I353V Substitution - Missense 20:35021351-35021351 - TCGA-B0-4700-01 COSM478066 c.1536G>C p.R512S Substitution - Missense 20:35008723-35008723 - HCC079T COSM5808102 c.1218G>C p.Q406H Substitution - Missense 20:35021190-35021190 - 587376 COSM1230506 c.991A>C p.N331H Substitution - Missense 20:35035183-35035183 - TCGA-A6-5665-01 COSM1411373 c.2040G>A p.T680T Substitution - coding silent 20:35004467-35004467 - PARPNM COSM4429209 c.630C>T p.L210L Substitution - coding silent 20:35049893-35049893 - GC8_T COSM149164 c.2330C>G p.S777C Substitution - Missense 20:35003210-35003210 - C0029T COSM4164688 c.1512-5T>A p.? Unknown 20:35008752-35008752 - TCGA-22-4595-01 COSM723936 c.940G>T p.G314C Substitution - Missense 20:35035234-35035234 - TCGA-EK-A2RA-01 COSM4848133 c.1226G>A p.R409K Substitution - Missense 20:35016132-35016132 - TCGA-AC-A23G-01 COSM3840836 c.1275C>A p.D425E Substitution - Missense 20:35016083-35016083 - SNUH_G37_S1 COSM3681178 c.1946T>G p.V649G Substitution - Missense 20:35004561-35004561 - TCGA-EP-A12J-01 COSM4926632 c.1441C>G p.L481V Substitution - Missense 20:35010257-35010257 - BD114T COSM5504657 c.887G>A p.G296D Substitution - Missense 20:35035287-35035287 - RK223_C01 COSM4779157 c.1512-7A>G p.? Unknown 20:35008754-35008754 - DN1122F COSM5782868 c.1932G>A p.M644I Substitution - Missense 20:35005699-35005699 - C008 COSM109284 c.190G>A p.E64K Substitution - Missense 20:35078153-35078153 - 3N40-VS-3T40 COSM4981671 c.2274C>T p.F758F Substitution - coding silent 20:35003266-35003266 - TCGA-C5-A1MJ-01 COSM4842761 c.1724C>T p.S575L Substitution - Missense 20:35006538-35006538 - TCGA-E2-A15I-01 COSM3840835 c.2116C>G p.P706A Substitution - Missense 20:35003550-35003550 - T1154 COSM4736479 c.2048A>C p.Q683P Substitution - Missense 20:35004459-35004459 - PT44 COSM5391898 c.695C>T p.S232F Substitution - Missense 20:35044675-35044675 - I2L-P24Tb-Tumor-Organoid COSM5365985 c.177G>A p.E59E Substitution - coding silent 20:35078166-35078166 - TCGA-C8-A133-01 COSM443702 c.2077C>T p.L693L Substitution - coding silent 20:35003589-35003589 - TCGA-D1-A17F-01 COSM1026173 c.1610G>A p.R537Q Substitution - Missense 20:35007626-35007626 - RMS112_ COSM4987781 c.920G>A p.R307Q Substitution - Missense 20:35035254-35035254 - TCGA-18-3410-01 COSM723939 c.1848G>C p.Q616H Substitution - Missense 20:35005783-35005783 - T3021 COSM4736478 c.2390A>C p.E797A Substitution - Missense 20:35003150-35003150 - HCC74T COSM1615497 c.646G>A p.G216S Substitution - Missense 20:35049877-35049877 - PD11344a COSM5782868 c.1932G>A p.M644I Substitution - Missense 20:35005699-35005699 - I2L-P24Ta-Tumor-Organoid COSM5365985 c.177G>A p.E59E Substitution - coding silent 20:35078166-35078166 - TCGA-C8-A3M7-01 COSM3840834 c.2140C>T p.R714W Substitution - Missense 20:35003526-35003526 - CLL101 COSM1291102 c.1846C>G p.Q616E Substitution - Missense 20:35005785-35005785 - TCGA-BH-A0C0-01 COSM443704 c.1360T>A p.L454M Substitution - Missense 20:35013057-35013057 - TCGA-B5-A11E-01 COSM1026176 c.1210C>T p.R404* Substitution - Nonsense 20:35021198-35021198 - HCC074T COSM5810050 c.1982A>T p.Q661L Substitution - Missense 20:35004525-35004525 - TCGA-A5-A0G9-01 COSM1026181 c.232C>G p.L78V Substitution - Missense 20:35078111-35078111 - TCGA-39-5022-01 COSM723937 c.1593C>T p.F531F Substitution - coding silent 20:35008666-35008666 - TCGA-60-2698-01 COSM723938 c.1643C>T p.S548F Substitution - Missense 20:35007593-35007593 - TCGA-BS-A0UV-01 COSM1026171 c.1816A>G p.T606A Substitution - Missense 20:35006446-35006446 - OSCC-GB_01290111 COSM5955237 c.2201G>T p.R734L Substitution - Missense 20:35003465-35003465 - TCGA-BS-A0UV-01 COSM1026180 c.444G>A p.T148T Substitution - coding silent 20:35057542-35057542 - tumor_4139696 COSM3357245 c.2199G>A p.L733L Substitution - coding silent 20:35003467-35003467 - 587228 COSM1026170 c.1969G>A p.A657T Substitution - Missense 20:35004538-35004538 - S00933 COSM316199 c.1309C>T p.L437F Substitution - Missense 20:35016049-35016049 - RMS231 COSM5881262 c.1979C>T p.S660F Substitution - Missense 20:35004528-35004528 - TCGA-CZ-5467-01 COSM478065 c.1648G>A p.A550T Substitution - Missense 20:35007588-35007588 - SNUH_G40_S1 COSM4001889 c.528+7A>C p.? Unknown 20:35054969-35054969 - PT37 COSM5921770 c.487T>A p.S163T Substitution - Missense 20:35055017-35055017 - ZZUFHECRKL-G075T COSM149164 c.2330C>G p.S777C Substitution - Missense 20:35003210-35003210 - tumor_4128852 COSM5948336 c.1095C>A p.G365G Substitution - coding silent 20:35021313-35021313 - RMS217 COSM5881180 c.1963C>A p.L655M Substitution - Missense 20:35004544-35004544 - LC_C13 COSM1190246 c.398T>C p.L133S Substitution - Missense 20:35069312-35069312 - 399 COSM4429209 c.630C>T p.L210L Substitution - coding silent 20:35049893-35049893 - PTC-14C COSM4134475 c.814C>A p.Q272K Substitution - Missense 20:35044556-35044556 - TCGA-EB-A5UM-01 COSM3545641 c.703T>A p.S235T Substitution - Missense 20:35044667-35044667 - 250LT COSM149164 c.2330C>G p.S777C Substitution - Missense 20:35003210-35003210 - TCGA-AQ-A04J-01 COSM443706 c.954C>T p.F318F Substitution - coding silent 20:35035220-35035220 - TCGA-D1-A103-01 COSM1026172 c.1747T>G p.F583V Substitution - Missense 20:35006515-35006515 - BD72T COSM5513612 c.1493C>T p.A498V Substitution - Missense 20:35010205-35010205 - TCGA-A3-3374-01 COSM1495022 c.2370A>G p.I790M Substitution - Missense 20:35003170-35003170 - QC2-32-T2 COSM5654396 c.1779C>T p.N593N Substitution - coding silent 20:35006483-35006483 - Pat_45_B COSM5857740 c.2357C>T p.P786L Substitution - Missense 20:35003183-35003183 - TCGA-D3-A3C8-06 COSM3545640 c.883C>T p.P295S Substitution - Missense 20:35035291-35035291 - 12T COSM109284 c.190G>A p.E64K Substitution - Missense 20:35078153-35078153 - TCGA-33-6737-01 COSM723941 c.1927G>C p.D643H Substitution - Missense 20:35005704-35005704 - 46M COSM5589212 c.1032G>A p.E344E Substitution - coding silent 20:35035142-35035142 - TC71 COSM2758558 c.2389G>T p.E797* Substitution - Nonsense 20:35003151-35003151 - TCGA-ER-A195-06 COSM3545637 c.1860C>T p.S620S Substitution - coding silent 20:35005771-35005771 - TCGA-AB-2989-03 COSM166854 c.14C>T p.P5L Substitution - Missense 20:35092768-35092768 - Gp2D COSM4627805 c.2242A>G p.T748A Substitution - Missense 20:35003424-35003424 - LUAD_E00623 COSM354158 c.252C>T p.T84T Substitution - coding silent 20:35078091-35078091 - YUWAND COSM1713389 c.1960C>T p.R654C Substitution - Missense 20:35004547-35004547 - Br27P COSM40720 c.858C>A p.I286I Substitution - coding silent 20:35044512-35044512 - BD186T COSM5501258 c.2130G>T p.R710R Substitution - coding silent 20:35003536-35003536 - PD11344a COSM5798725 c.1936+7G>A p.? Unknown 20:35005688-35005688 - HT115 COSM2758595 c.305C>A p.S102Y Substitution - Missense 20:35069405-35069405 - YUTRAIN COSM5391898 c.695C>T p.S232F Substitution - Missense 20:35044675-35044675 - TCGA-HU-A4GQ-01 COSM4097868 c.1992G>A p.T664T Substitution - coding silent 20:35004515-35004515 - TCGA-CA-6717-01 COSM1411376 c.612C>A p.F204L Substitution - Missense 20:35049911-35049911 - ESCC-129T COSM3939316 c.175G>C p.E59Q Substitution - Missense 20:35078168-35078168 - PD4847a COSM5795037 c.1991C>T p.T664M Substitution - Missense 20:35004516-35004516 - U343 COSM5712941 c.354A>G p.K118K Substitution - coding silent 20:35069356-35069356 - TCGA-AA-3492-01 COSM1411372 c.2129G>A p.R710Q Substitution - Missense 20:35003537-35003537 - DN1122F COSM5798725 c.1936+7G>A p.? Unknown 20:35005688-35005688 - S00829 COSM5660054 c.2356C>G p.P786A Substitution - Missense 20:35003184-35003184 - TCGA-60-2698-01 COSM723942 c.2178C>G p.L726L Substitution - coding silent 20:35003488-35003488 - LP6005690-DNA_D01 COSM4966235 c.2317C>T p.R773W Substitution - Missense 20:35003223-35003223 - PD4937a COSM165172 c.858C>T p.I286I Substitution - coding silent 20:35044512-35044512 - E18 COSM1666520 c.298-5_298-4insAC p.? Unknown 20:35069416-35069417 - TCGA-HF-7132-01 COSM4097869 c.1908C>T p.D636D Substitution - coding silent 20:35005723-35005723 - TCGA-CM-5861-01 COSM1411371 c.2161T>C p.Y721H Substitution - Missense 20:35003505-35003505 - TCGA-BT-A3PK-01 COSM3799469 c.1910G>A p.R637Q Substitution - Missense 20:35005721-35005721 - TCGA-RP-A694-06 COSM4894161 c.41G>A p.R14Q Substitution - Missense 20:35092741-35092741 - TCGA-AP-A059-01 COSM1026169 c.2181C>T p.N727N Substitution - coding silent 20:35003485-35003485 - YURTHE COSM1713390 c.1831C>T p.Q611* Substitution - Nonsense 20:35005800-35005800 - TCGA-E9-A3HO-01 COSM3840837 c.469A>G p.K157E Substitution - Missense 20:35057517-35057517 - BD114T COSM5504656 c.1380G>A p.R460R Substitution - coding silent 20:35013037-35013037 - TCGA-EE-A2A0-06 COSM3545638 c.1525G>T p.D509Y Substitution - Missense 20:35008734-35008734 - L10 COSM5368974 c.488C>G p.S163C Substitution - Missense 20:35055016-35055016 - 6115114 COSM5547373 c.801_825del25 p.K269fs*1 Deletion - Frameshift 20:35044545-35044569 - TCGA-BR-8361-01 COSM4097871 c.668G>A p.R223Q Substitution - Missense 20:35044702-35044702 - SNUH_G37_S1 COSM4001889 c.528+7A>C p.? Unknown 20:35054969-35054969 - HB9 COSM5346137 c.1942G>A p.E648K Substitution - Missense 20:35004565-35004565 - TCGA-B5-A0JN-01 COSM1026174 c.1304C>G p.S435C Substitution - Missense 20:35016054-35016054 - TCGA-F5-6814-01 COSM3423602 c.2005C>A p.L669I Substitution - Missense 20:35004502-35004502 - DLD1 COSM2758579 c.1389G>T p.Q463H Substitution - Missense 20:35013028-35013028 - TCGA-18-3410-01 COSM723940 c.1915G>C p.E639Q Substitution - Missense 20:35005716-35005716 - TCGA-HE-A5NL-01 COSM3991660 c.903T>G p.L301L Substitution - coding silent 20:35035271-35035271 - CCK81 COSM2758573 c.1666C>T p.L556L Substitution - coding silent 20:35007570-35007570 - TCGA-H4-A2HQ-01 COSM1307315 c.1569G>A p.K523K Substitution - coding silent 20:35008690-35008690 - CSCC-27-T COSM4487378 c.317C>T p.S106F Substitution - Missense 20:35069393-35069393 - sysucc-311T COSM5464906 c.1393T>G p.F465V Substitution - Missense 20:35013024-35013024 - TCGA-B5-A11E-01 COSM1026170 c.1969G>A p.A657T Substitution - Missense 20:35004538-35004538 - C0086T COSM4164690 c.593T>A p.M198K Substitution - Missense 20:35049930-35049930 - S02384 COSM5698404 c.713A>T p.D238V Substitution - Missense 20:35044657-35044657 - T3021 COSM4736481 c.1343G>A p.C448Y Substitution - Missense 20:35016015-35016015 - TCGA-66-2757-01 COSM723934 c.538G>T p.V180F Substitution - Missense 20:35049985-35049985 - TCGA-EE-A3AC-06 COSM3545636 c.2025C>T p.I675I Substitution - coding silent 20:35004482-35004482 - NCI-H747 COSM4647084 c.2232C>T p.D744D Substitution - coding silent 20:35003434-35003434 - TCGA-EQ-A4SO-01 COSM4097867 c.2148G>A p.E716E Substitution - coding silent 20:35003518-35003518 - ESCC_114 COSM5639679 c.1072C>T p.P358S Substitution - Missense 20:35021336-35021336 - TCGA-HE-A5NL-01 COSM3991661 c.878G>T p.S293I Substitution - Missense 20:35035296-35035296 - HCC74 COSM1615497 c.646G>A p.G216S Substitution - Missense 20:35049877-35049877 - I2L-P24Ta-Tumor-Biopsy COSM5365985 c.177G>A p.E59E Substitution - coding silent 20:35078166-35078166 - I2L-P24Tb-Tumor-Biopsy COSM5365985 c.177G>A p.E59E Substitution - coding silent 20:35078166-35078166 - S00933 COSM316199 c.1309C>T p.L437F Substitution - Missense 20:35016049-35016049 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.167805;Hs.168073 20q11.22 608430

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A T IntronicSNV . c.298-12T>A 20 33657227 STAD A T Missense p.L454M c.1360T>A 20 33600860 BRCA C A Missense p.D509Y c.1525G>T 20 33596537 CM C A Missense p.G314C c.940G>T 20 33623037 LUSC C A Missense p.R117S c.351G>T 20 33657162 LGG C A Missense p.S505I c.1514G>T 20 33596548 CM C A Missense p.V180F c.538G>T 20 33637788 LUSC C A Synonymous p.I286I c.858C>A 20 33632315 GBM C G Missense p.D643H c.1927G>C 20 33593507 LUSC C G Missense p.E639Q c.1915G>C 20 33593519 LUSC C G Missense p.Q616H c.1848G>C 20 33593586 LUSC C G Missense p.R512S c.1536G>C 20 33596526 RCCC C T Missense p.A550T c.1648G>A 20 33595391 RCCC C T Missense p.G9R c.25G>A 20 33680560 CM C T Missense p.R372K c.1115G>A 20 33609096 HNSC C T Missense p.R537Q c.1610G>A 20 33595429 UCEC C T Missense p.R637Q c.1910G>A 20 33593524 BLCA C T Missense p.R714Q c.2141G>A 20 33591328 GBM C T Synonymous p.K523K c.1569G>A 20 33596493 BLCA G A 3-UTRSNV . c.2391+164C>T 20 33590788 CM G A Missense p.L437F c.1309C>T 20 33603852 SCLC G A Missense p.P103S c.307C>T 20 33657206 LUSC G A Missense p.P295S c.883C>T 20 33623094 CM G A Missense p.P5L c.14C>T 20 33680571 AML G A Synonymous p.F318F c.954C>T 20 33623023 BRCA G A Synonymous p.F531F c.1593C>T 20 33596469 LUSC G A Synonymous p.I286I c.858C>T 20 33632315 BRCA G A Synonymous p.I675I c.2025C>T 20 33592285 CM G A Synonymous p.L242L c.726C>T 20 33632447 BLCA G A Synonymous p.L693L c.2077C>T 20 33591392 BRCA G A Synonymous p.S620S c.1860C>T 20 33593574 CM G C Missense p.Q616E c.1846C>G 20 33593588 CLL G C Missense p.Q95E c.283C>G 20 33665863 LUAD G C Missense p.S435C c.1304C>G 20 33603857 UCEC GCT - MultiAAMissense p.E497_A498delinsD c.1491_1493delAGC 20 33598008 BRCA G T Missense p.A290D c.869C>A 20 33623108 LUSC T C Missense p.I353V c.1057A>G 20 33609154 BRCA T C Missense p.K415R c.1244A>G 20 33603917 BRCA