Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 16 75269596 75269596 + Missense_Mutation SNP C C G TCGA-OR-A5K8-01A-11D-A29I-10 TCGA-OR-A5K8-10A-01D-A29L-10 g.chr16:75269596C>G c.1201G>C c.(1201-1203)Gat>Cat p.D401H BLCA 16 75263468 75263468 + Missense_Mutation SNP C C T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr16:75263468C>T c.2554G>A c.(2554-2556)Gag>Aag p.E852K BLCA 16 75269197 75269197 + Missense_Mutation SNP C C T TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr16:75269197C>T c.1600G>A c.(1600-1602)Gac>Aac p.D534N BLCA 16 75269218 75269218 + Missense_Mutation SNP C C G TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr16:75269218C>G c.1579G>C c.(1579-1581)Ggc>Cgc p.G527R BLCA 16 75269588 75269597 + Frame_Shift_Del DEL GCCACCATCA GCCACCATCA - TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr16:75269588_75269597delGCCACCATCA c.1200_1209delTGATGGTGGC c.(1198-1209)gctgatggtggcfs p.ADGG400fs BLCA 16 75269625 75269625 + Missense_Mutation SNP C C T TCGA-XF-A9SU-01A-31D-A391-08 TCGA-XF-A9SU-10A-01D-A394-08 g.chr16:75269625C>T c.1172G>A c.(1171-1173)cGt>cAt p.R391H BLCA 16 75276374 75276374 + Silent SNP C C T TCGA-FD-A3N6-01A-11D-A21A-08 TCGA-FD-A3N6-10A-01D-A21A-08 g.chr16:75276374C>T c.627G>A c.(625-627)ccG>ccA p.P209P BLCA 16 75276443 75276443 + Silent SNP C C G TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr16:75276443C>G c.558G>C c.(556-558)ggG>ggC p.G186G BLCA 16 75276448 75276448 + Missense_Mutation SNP C C A TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr16:75276448C>A c.553G>T c.(553-555)Gcc>Tcc p.A185S BLCA 16 75276878 75276878 + Silent SNP G G A TCGA-DK-A3IL-01A-11D-A20D-08 TCGA-DK-A3IL-10A-01D-A20D-08 g.chr16:75276878G>A c.123C>T c.(121-123)gaC>gaT p.D41D BRCA 16 75263772 75263773 + Frame_Shift_Ins INS - - T TCGA-BH-A0B1-01A-12W-A071-09 TCGA-BH-A0B1-10A-01W-A071-09 g.chr16:75263772_75263773insT c.2249_2250insA c.(2248-2250)cagfs p.Q750fs BRCA 16 75263776 75263776 + Frame_Shift_Del DEL T T - TCGA-BH-A0B1-01A-12W-A071-09 TCGA-BH-A0B1-10A-01W-A071-09 g.chr16:75263776delT c.2246delA c.(2245-2247)gagfs p.E749fs BRCA 16 75263783 75263783 + Missense_Mutation SNP A A G TCGA-A2-A3Y0-01A-11D-A23C-09 TCGA-A2-A3Y0-10A-01D-A23C-09 g.chr16:75263783A>G c.2239T>C c.(2239-2241)Tac>Cac p.Y747H BRCA 16 75267782 75267782 + Missense_Mutation SNP T T C TCGA-E9-A1RF-01A-11D-A159-09 TCGA-E9-A1RF-10A-01D-A159-09 g.chr16:75267782T>C c.2062A>G c.(2062-2064)Atc>Gtc p.I688V BRCA 16 75267803 75267803 + Nonsense_Mutation SNP C C A TCGA-D8-A1JD-01A-11D-A13L-09 TCGA-D8-A1JD-10A-01D-A13O-09 g.chr16:75267803C>A c.2041G>T c.(2041-2043)Gag>Tag p.E681* BRCA 16 75270832 75270832 + Missense_Mutation SNP T T C TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr16:75270832T>C c.860A>G c.(859-861)tAt>tGt p.Y287C BRCA 16 75271166 75271166 + Missense_Mutation SNP G G A TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr16:75271166G>A c.710C>T c.(709-711)cCg>cTg p.P237L CESC 16 75263742 75263742 + Silent SNP G G A TCGA-EK-A2GZ-01A-11D-A17W-09 TCGA-EK-A2GZ-10A-01D-A17W-09 g.chr16:75263742G>A c.2280C>T c.(2278-2280)aaC>aaT p.N760N CESC 16 75301816 75301816 + Silent SNP G G A TCGA-EA-A439-01A-11D-A243-09 TCGA-EA-A439-10A-01D-A243-09 g.chr16:75301816G>A c.63C>T c.(61-63)ctC>ctT p.L21L COAD 16 75263595 75263595 + Silent SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr16:75263595G>A c.2427C>T c.(2425-2427)cgC>cgT p.R809R COAD 16 75268928 75268928 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:75268928G>A c.1869C>T c.(1867-1869)ccC>ccT p.P623P COAD 16 75268995 75268995 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:75268995G>T c.1802C>A c.(1801-1803)gCc>gAc p.A601D COAD 16 75270802 75270802 + Missense_Mutation SNP A A C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:75270802A>C c.890T>G c.(889-891)cTg>cGg p.L297R COAD 16 75271113 75271113 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr16:75271113G>A c.763C>T c.(763-765)Cgg>Tgg p.R255W COAD 16 75276447 75276447 + Missense_Mutation SNP G G T TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr16:75276447G>T c.554C>A c.(553-555)gCc>gAc p.A185D COAD 16 75276825 75276825 + Missense_Mutation SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:75276825C>T c.176G>A c.(175-177)cGc>cAc p.R59H COADREAD 16 75263595 75263595 + Silent SNP G G A TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr16:75263595G>A c.2427C>T c.(2425-2427)cgC>cgT p.R809R COADREAD 16 75268928 75268928 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:75268928G>A c.1869C>T c.(1867-1869)ccC>ccT p.P623P COADREAD 16 75268995 75268995 + Missense_Mutation SNP G G T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:75268995G>T c.1802C>A c.(1801-1803)gCc>gAc p.A601D COADREAD 16 75270802 75270802 + Missense_Mutation SNP A A C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:75270802A>C c.890T>G c.(889-891)cTg>cGg p.L297R COADREAD 16 75271113 75271113 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr16:75271113G>A c.763C>T c.(763-765)Cgg>Tgg p.R255W COADREAD 16 75276447 75276447 + Missense_Mutation SNP G G T TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr16:75276447G>T c.554C>A c.(553-555)gCc>gAc p.A185D COADREAD 16 75276775 75276775 + Missense_Mutation SNP G G A TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr16:75276775G>A c.226C>T c.(226-228)Ccc>Tcc p.P76S COADREAD 16 75276825 75276825 + Missense_Mutation SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:75276825C>T c.176G>A c.(175-177)cGc>cAc p.R59H DLBC 16 75269730 75269730 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr16:75269730G>A c.1067C>T c.(1066-1068)cCg>cTg p.P356L ESCA 16 75263637 75263637 + Silent SNP G G A TCGA-L5-A4OJ-01A-11D-A27G-09 TCGA-L5-A4OJ-11A-12D-A27G-09 g.chr16:75263637G>A c.2385C>T c.(2383-2385)atC>atT p.I795I ESCA 16 75263768 75263768 + Missense_Mutation SNP C C T TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr16:75263768C>T c.2254G>A c.(2254-2256)Gag>Aag p.E752K ESCA 16 75263905 75263905 + Missense_Mutation SNP C C T TCGA-R6-A6DN-01B-11D-A31U-09 TCGA-R6-A6DN-10A-01D-A31U-09 g.chr16:75263905C>T c.2117G>A c.(2116-2118)cGa>cAa p.R706Q ESCA 16 75269147 75269147 + Missense_Mutation SNP G G T TCGA-2H-A9GR-01A-12D-A37C-09 TCGA-2H-A9GR-11A-11D-A37F-09 g.chr16:75269147G>T c.1650C>A c.(1648-1650)gaC>gaA p.D550E ESCA 16 75271130 75271130 + Missense_Mutation SNP T T C TCGA-LN-A49S-01A-11D-A247-09 TCGA-LN-A49S-10A-01D-A247-09 g.chr16:75271130T>C c.746A>G c.(745-747)tAt>tGt p.Y249C ESCA 16 75276907 75276907 + Missense_Mutation SNP C C T TCGA-JY-A6FD-01A-11D-A33E-09 TCGA-JY-A6FD-10A-01D-A33H-09 g.chr16:75276907C>T c.94G>A c.(94-96)Gtg>Atg p.V32M ESCA 16 75298373 75298373 + Missense_Mutation SNP G G C TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr16:75298373G>C c.26C>G c.(25-27)tCt>tGt p.S9C GBMLGG 16 75263741 75263741 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:75263741C>T c.2281G>A c.(2281-2283)Gcc>Acc p.A761T GBMLGG 16 75271148 75271148 + Frame_Shift_Del DEL G G - TCGA-HT-A74H-01A-11D-A32B-08 TCGA-HT-A74H-10A-01D-A329-08 g.chr16:75271148delG c.728delC c.(727-729)ccgfs p.P243fs GBMLGG 16 75276756 75276756 + Missense_Mutation SNP G G A TCGA-S9-A6U5-01A-12D-A33T-08 TCGA-S9-A6U5-10A-01D-A33W-08 g.chr16:75276756G>A c.245C>T c.(244-246)cCg>cTg p.P82L HNSC 16 75263550 75263550 + Silent SNP G G T TCGA-BA-A4IG-01A-11D-A25Y-08 TCGA-BA-A4IG-10A-01D-A25Y-08 g.chr16:75263550G>T c.2472C>A c.(2470-2472)cgC>cgA p.R824R HNSC 16 75268875 75268875 + Frame_Shift_Del DEL G G - TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr16:75268875delG c.1922delC c.(1921-1923)cctfs p.P641fs HNSC 16 75269450 75269450 + Silent SNP C C A TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr16:75269450C>A c.1347G>T c.(1345-1347)ccG>ccT p.P449P HNSC 16 75269680 75269680 + Missense_Mutation SNP C C T TCGA-CN-A640-01A-21D-A30E-08 TCGA-CN-A640-10A-01D-A30H-08 g.chr16:75269680C>T c.1117G>A c.(1117-1119)Gac>Aac p.D373N HNSC 16 75276926 75276926 + Silent SNP G G T TCGA-CV-7101-01A-11D-2012-08 TCGA-CV-7101-10A-01D-2013-08 g.chr16:75276926G>T c.75C>A c.(73-75)cgC>cgA p.R25R HNSC 16 75276935 75276935 + Silent SNP G G A TCGA-DQ-5629-01A-01D-1870-08 TCGA-DQ-5629-10A-01D-1870-08 g.chr16:75276935G>A c.66C>T c.(64-66)ctC>ctT p.L22L HNSC 16 75301841 75301841 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr16:75301841C>T c.38G>A c.(37-39)aGg>aAg p.R13K KICH 16 75263529 75263530 + Frame_Shift_Del DEL CT CT - TCGA-KM-8639-01A-11D-2397-10 TCGA-KM-8639-10A-01D-2397-10 g.chr16:75263529_75263530delCT c.2492_2493delAG c.(2491-2493)aagfs p.K831fs KICH 16 75263533 75263534 + Frame_Shift_Ins INS - - T TCGA-KM-8639-01A-11D-2397-10 TCGA-KM-8639-10A-01D-2397-10 g.chr16:75263533_75263534insT c.2488_2489insA c.(2488-2490)accfs p.T830fs KICH 16 75269477 75269477 + Silent SNP A A C TCGA-KO-8409-01A-11D-2310-10 TCGA-KO-8409-11A-01D-2311-10 g.chr16:75269477A>C c.1320T>G c.(1318-1320)tcT>tcG p.S440S KICH 16 75270827 75270827 + Missense_Mutation SNP C C T TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr16:75270827C>T c.865G>A c.(865-867)Gtg>Atg p.V289M KIPAN 16 75263502 75263502 + Silent SNP A A T TCGA-2Z-A9JM-01A-12D-A42J-10 TCGA-2Z-A9JM-10A-01D-A42M-10 g.chr16:75263502A>T c.2520T>A c.(2518-2520)ccT>ccA p.P840P KIPAN 16 75263529 75263530 + Frame_Shift_Del DEL CT CT - TCGA-KM-8639-01A-11D-2397-10 TCGA-KM-8639-10A-01D-2397-10 g.chr16:75263529_75263530delCT c.2492_2493delAG c.(2491-2493)aagfs p.K831fs KIPAN 16 75263533 75263534 + Frame_Shift_Ins INS - - T TCGA-KM-8639-01A-11D-2397-10 TCGA-KM-8639-10A-01D-2397-10 g.chr16:75263533_75263534insT c.2488_2489insA c.(2488-2490)accfs p.T830fs KIPAN 16 75269312 75269312 + Missense_Mutation SNP C C A TCGA-BP-5169-01A-01D-1429-08 TCGA-BP-5169-11A-01D-1429-08 g.chr16:75269312C>A c.1485G>T c.(1483-1485)gaG>gaT p.E495D KIPAN 16 75269477 75269477 + Silent SNP A A C TCGA-KO-8409-01A-11D-2310-10 TCGA-KO-8409-11A-01D-2311-10 g.chr16:75269477A>C c.1320T>G c.(1318-1320)tcT>tcG p.S440S KIPAN 16 75270827 75270827 + Missense_Mutation SNP C C T TCGA-KM-8443-01A-11D-2310-10 TCGA-KM-8443-10A-01D-2311-10 g.chr16:75270827C>T c.865G>A c.(865-867)Gtg>Atg p.V289M KIPAN 16 75276448 75276448 + Missense_Mutation SNP C C A TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chr16:75276448C>A c.553G>T c.(553-555)Gcc>Tcc p.A185S KIRC 16 75269312 75269312 + Missense_Mutation SNP C C A TCGA-BP-5169-01A-01D-1429-08 TCGA-BP-5169-11A-01D-1429-08 g.chr16:75269312C>A c.1485G>T c.(1483-1485)gaG>gaT p.E495D KIRC 16 75276448 75276448 + Missense_Mutation SNP C C A TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chr16:75276448C>A c.553G>T c.(553-555)Gcc>Tcc p.A185S KIRP 16 75263502 75263502 + Silent SNP A A T TCGA-2Z-A9JM-01A-12D-A42J-10 TCGA-2Z-A9JM-10A-01D-A42M-10 g.chr16:75263502A>T c.2520T>A c.(2518-2520)ccT>ccA p.P840P LGG 16 75263741 75263741 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:75263741C>T c.2281G>A c.(2281-2283)Gcc>Acc p.A761T LGG 16 75271148 75271148 + Frame_Shift_Del DEL G G - TCGA-HT-A74H-01A-11D-A32B-08 TCGA-HT-A74H-10A-01D-A329-08 g.chr16:75271148delG c.728delC c.(727-729)ccgfs p.P243fs LGG 16 75276756 75276756 + Missense_Mutation SNP G G A TCGA-S9-A6U5-01A-12D-A33T-08 TCGA-S9-A6U5-10A-01D-A33W-08 g.chr16:75276756G>A c.245C>T c.(244-246)cCg>cTg p.P82L LIHC 16 75263466 75263466 + Missense_Mutation SNP C C A TCGA-FV-A4ZQ-01A-11D-A25V-10 TCGA-FV-A4ZQ-10A-01D-A25V-10 g.chr16:75263466C>A c.2556G>T c.(2554-2556)gaG>gaT p.E852D LIHC 16 75269533 75269533 + Frame_Shift_Del DEL C C - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr16:75269533delC c.1264delG c.(1264-1266)gcafs p.A422fs LIHC 16 75269535 75269535 + Missense_Mutation SNP G G T TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr16:75269535G>T c.1262C>A c.(1261-1263)cCg>cAg p.P421Q LUAD 16 75263547 75263547 + Silent SNP G G A TCGA-95-A4VK-01A-11D-A25L-08 TCGA-95-A4VK-10A-01D-A25L-08 g.chr16:75263547G>A c.2475C>T c.(2473-2475)ggC>ggT p.G825G LUAD 16 75263684 75263684 + Missense_Mutation SNP C C A TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr16:75263684C>A c.2338G>T c.(2338-2340)Gcg>Tcg p.A780S LUAD 16 75263718 75263718 + Silent SNP G G A TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr16:75263718G>A c.2304C>T c.(2302-2304)gcC>gcT p.A768A LUAD 16 75268814 75268814 + Missense_Mutation SNP C C A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr16:75268814C>A c.1983G>T c.(1981-1983)atG>atT p.M661I LUAD 16 75269174 75269174 + Silent SNP A A T TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr16:75269174A>T c.1623T>A c.(1621-1623)ctT>ctA p.L541L LUAD 16 75269347 75269347 + Missense_Mutation SNP C C T TCGA-53-7624-01A-11D-2063-08 TCGA-53-7624-10A-01D-2063-08 g.chr16:75269347C>T c.1450G>A c.(1450-1452)Gcc>Acc p.A484T LUAD 16 75276842 75276842 + Silent SNP G G T TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr16:75276842G>T c.159C>A c.(157-159)ggC>ggA p.G53G LUSC 16 75263572 75263572 + Missense_Mutation SNP T T A TCGA-22-4599-01A-01D-1441-08 TCGA-22-4599-11A-01D-1441-08 g.chr16:75263572T>A c.2450A>T c.(2449-2451)aAc>aTc p.N817I LUSC 16 75263596 75263596 + Missense_Mutation SNP C C T TCGA-22-1012-01A-01D-1521-08 TCGA-22-1012-11A-01D-1521-08 g.chr16:75263596C>T c.2426G>A c.(2425-2427)cGc>cAc p.R809H LUSC 16 75263738 75263738 + Missense_Mutation SNP C C A TCGA-22-5478-01A-01D-1632-08 TCGA-22-5478-11A-11D-1632-08 g.chr16:75263738C>A c.2284G>T c.(2284-2286)Gtg>Ttg p.V762L LUSC 16 75263782 75263782 + Missense_Mutation SNP T T C TCGA-39-5021-01A-01D-1441-08 TCGA-39-5021-11A-01D-1441-08 g.chr16:75263782T>C c.2240A>G c.(2239-2241)tAc>tGc p.Y747C LUSC 16 75263896 75263896 + Missense_Mutation SNP T T A TCGA-18-3417-01A-01D-1441-08 TCGA-18-3417-11A-01D-1441-08 g.chr16:75263896T>A c.2126A>T c.(2125-2127)cAg>cTg p.Q709L LUSC 16 75268934 75268934 + Silent SNP C C G TCGA-37-4141-01A-02D-1352-08 TCGA-37-4141-10A-01D-1352-08 g.chr16:75268934C>G c.1863G>C c.(1861-1863)ctG>ctC p.L621L LUSC 16 75269714 75269714 + Silent SNP C C A TCGA-43-6143-01A-11D-1817-08 TCGA-43-6143-11A-01D-1817-08 g.chr16:75269714C>A c.1083G>T c.(1081-1083)gtG>gtT p.V361V LUSC 16 75276604 75276604 + Missense_Mutation SNP G G T TCGA-21-1077-01A-01D-1521-08 TCGA-21-1077-11A-01D-1521-08 g.chr16:75276604G>T c.397C>A c.(397-399)Ccc>Acc p.P133T PAAD 16 75263526 75263526 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:75263526G>A c.2496C>T c.(2494-2496)gcC>gcT p.A832A PAAD 16 75267776 75267776 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:75267776G>A c.2068C>T c.(2068-2070)Cgg>Tgg p.R690W PAAD 16 75276721 75276721 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:75276721G>A c.280C>T c.(280-282)Cct>Tct p.P94S PCPG 16 75263909 75263909 + Missense_Mutation SNP C C T TCGA-QR-A702-01A-11D-A35D-08 TCGA-QR-A702-10A-01D-A35B-08 g.chr16:75263909C>T c.2113G>A c.(2113-2115)Gaa>Aaa p.E705K PCPG 16 75263909 75263909 + Nonsense_Mutation SNP C C A TCGA-QR-A700-01A-11D-A35D-08 TCGA-QR-A700-10A-01D-A35B-08 g.chr16:75263909C>A c.2113G>T c.(2113-2115)Gaa>Taa p.E705* PRAD 16 75263755 75263755 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:75263755G>A c.2267C>T c.(2266-2268)aCc>aTc p.T756I PRAD 16 75268802 75268802 + Missense_Mutation SNP G G T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:75268802G>T c.1995C>A c.(1993-1995)gaC>gaA p.D665E PRAD 16 75271144 75271144 + Frame_Shift_Del DEL C C - TCGA-EJ-A65B-01A-12D-A30E-08 TCGA-EJ-A65B-10A-01D-A30H-08 g.chr16:75271144delC c.732delG c.(730-732)gggfs p.G244fs READ 16 75276775 75276775 + Missense_Mutation SNP G G A TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr16:75276775G>A c.226C>T c.(226-228)Ccc>Tcc p.P76S SARC 16 75269881 75269881 + Missense_Mutation SNP A A G TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr16:75269881A>G c.916T>C c.(916-918)Tac>Cac p.Y306H SKCM 16 75263556 75263556 + Silent SNP G G A TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr16:75263556G>A c.2466C>T c.(2464-2466)ctC>ctT p.L822L SKCM 16 75263823 75263823 + Silent SNP T T G TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr16:75263823T>G c.2199A>C c.(2197-2199)acA>acC p.T733T SKCM 16 75268868 75268868 + Silent SNP G G A TCGA-EE-A2GU-06A-11D-A196-08 TCGA-EE-A2GU-10A-01D-A198-08 g.chr16:75268868G>A c.1929C>T c.(1927-1929)ttC>ttT p.F643F SKCM 16 75268959 75268959 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr16:75268959G>A c.1838C>T c.(1837-1839)cCg>cTg p.P613L SKCM 16 75268985 75268985 + Silent SNP G G T TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr16:75268985G>T c.1812C>A c.(1810-1812)ctC>ctA p.L604L SKCM 16 75268999 75268999 + Missense_Mutation SNP T T A TCGA-EE-A20F-06A-21D-A196-08 TCGA-EE-A20F-10A-01D-A198-08 g.chr16:75268999T>A c.1798A>T c.(1798-1800)Aat>Tat p.N600Y SKCM 16 75269071 75269071 + Silent SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr16:75269071G>A c.1726C>T c.(1726-1728)Ctg>Ttg p.L576L SKCM 16 75276399 75276399 + Missense_Mutation SNP C C T TCGA-ER-A2NF-06A-11D-A19A-08 TCGA-ER-A2NF-10A-01D-A19A-08 g.chr16:75276399C>T c.602G>A c.(601-603)cGc>cAc p.R201H SKCM 16 75276498 75276498 + Missense_Mutation SNP G G A TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr16:75276498G>A c.503C>T c.(502-504)cCc>cTc p.P168L SKCM 16 75276760 75276760 + Missense_Mutation SNP T T C TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr16:75276760T>C c.241A>G c.(241-243)Acc>Gcc p.T81A

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 16 75276706 75276706 single base substitution A T 3_prime_UTR_variant BLCA-CN 16 75276706 75276706 single base substitution A T downstream_gene_variant BLCA-CN 16 75276706 75276706 single base substitution A T intron_variant BLCA-CN 16 75276706 75276706 single base substitution A T missense_variant Y117N 349T>A BLCA-CN 16 75276706 75276706 single base substitution A T missense_variant Y145N 433T>A BLCA-CN 16 75276706 75276706 single base substitution A T missense_variant Y70N 208T>A BLCA-CN 16 75276706 75276706 single base substitution A T missense_variant Y97N 289T>A BLCA-CN 16 75276706 75276706 single base substitution A T missense_variant Y99N 295T>A BLCA-CN 16 75276706 75276706 single base substitution A T upstream_gene_variant BOCA-UK 16 75263853 75263853 single base substitution C T 3_prime_UTR_variant BOCA-UK 16 75263853 75263853 single base substitution C T exon_variant BOCA-UK 16 75263853 75263853 single base substitution C T synonymous_variant T575T 1725G>A BOCA-UK 16 75263853 75263853 single base substitution C T synonymous_variant T694T 2082G>A BOCA-UK 16 75263853 75263853 single base substitution C T synonymous_variant T721T 2163G>A BOCA-UK 16 75263853 75263853 single base substitution C T synonymous_variant T723T 2169G>A BOCA-UK 16 75263853 75263853 single base substitution C T synonymous_variant T741T 2223G>A BOCA-UK 16 75263853 75263853 single base substitution C T synonymous_variant T769T 2307G>A BRCA-EU 16 75258785 75258785 single base substitution C T downstream_gene_variant BRCA-EU 16 75260216 75260216 single base substitution C G downstream_gene_variant BRCA-EU 16 75260247 75260247 single base substitution G A downstream_gene_variant BRCA-EU 16 75265022 75265022 single base substitution T A downstream_gene_variant BRCA-EU 16 75265022 75265022 single base substitution T A intron_variant BRCA-EU 16 75265102 75265102 single base substitution C T downstream_gene_variant BRCA-EU 16 75265102 75265102 single base substitution C T intron_variant BRCA-EU 16 75271012 75271012 single base substitution C T intron_variant BRCA-EU 16 75271012 75271012 single base substitution C T upstream_gene_variant BRCA-EU 16 75274575 75274575 single base substitution C T downstream_gene_variant BRCA-EU 16 75274575 75274575 single base substitution C T intron_variant BRCA-EU 16 75274575 75274575 single base substitution C T upstream_gene_variant BRCA-EU 16 75274632 75274632 single base substitution C G downstream_gene_variant BRCA-EU 16 75274632 75274632 single base substitution C G intron_variant BRCA-EU 16 75274632 75274632 single base substitution C G upstream_gene_variant BRCA-EU 16 75276374 75276374 single base substitution C T 3_prime_UTR_variant BRCA-EU 16 75276374 75276374 single base substitution C T downstream_gene_variant BRCA-EU 16 75276374 75276374 single base substitution C T intron_variant BRCA-EU 16 75276374 75276374 single base substitution C T synonymous_variant P180P 540G>A BRCA-EU 16 75276374 75276374 single base substitution C T synonymous_variant P207P 621G>A BRCA-EU 16 75276374 75276374 single base substitution C T synonymous_variant P209P 627G>A BRCA-EU 16 75276374 75276374 single base substitution C T synonymous_variant P227P 681G>A BRCA-EU 16 75276374 75276374 single base substitution C T synonymous_variant P255P 765G>A BRCA-EU 16 75276374 75276374 single base substitution C T synonymous_variant P75P 225G>A BRCA-EU 16 75276374 75276374 single base substitution C T upstream_gene_variant BRCA-EU 16 75281519 75281519 single base substitution C T intron_variant BRCA-EU 16 75281519 75281519 single base substitution C T upstream_gene_variant BRCA-EU 16 75283197 75283197 single base substitution C T intron_variant BRCA-EU 16 75283197 75283197 single base substitution C T upstream_gene_variant BRCA-EU 16 75284697 75284697 single base substitution C G 5_prime_UTR_variant BRCA-EU 16 75284697 75284697 single base substitution C G intron_variant BRCA-EU 16 75284697 75284697 single base substitution C G upstream_gene_variant BRCA-EU 16 75286430 75286430 single base substitution C T intron_variant BRCA-EU 16 75286430 75286430 single base substitution C T upstream_gene_variant BRCA-EU 16 75290519 75290519 single base substitution G A intron_variant BRCA-EU 16 75290519 75290519 single base substitution G A upstream_gene_variant BRCA-EU 16 75291164 75291164 single base substitution G C intron_variant BRCA-EU 16 75291164 75291164 single base substitution G C upstream_gene_variant BRCA-EU 16 75291893 75291893 single base substitution C A intron_variant BRCA-EU 16 75291893 75291893 single base substitution C A upstream_gene_variant BRCA-EU 16 75293057 75293057 single base substitution T G intron_variant BRCA-EU 16 75293057 75293057 single base substitution T G upstream_gene_variant BRCA-EU 16 75293310 75293310 single base substitution C T intron_variant BRCA-EU 16 75293310 75293310 single base substitution C T upstream_gene_variant BRCA-EU 16 75293815 75293815 single base substitution G T intron_variant BRCA-EU 16 75293815 75293815 single base substitution G T upstream_gene_variant BRCA-EU 16 75295101 75295101 single base substitution G A intron_variant BRCA-EU 16 75295101 75295101 single base substitution G A upstream_gene_variant BRCA-EU 16 75296128 75296128 single base substitution C T intron_variant BRCA-EU 16 75298038 75298038 single base substitution T C 3_prime_UTR_variant BRCA-EU 16 75298038 75298038 single base substitution T C 5_prime_UTR_variant BRCA-EU 16 75298038 75298038 single base substitution T C intron_variant BRCA-EU 16 75298040 75298040 single base substitution T C 3_prime_UTR_variant BRCA-EU 16 75298040 75298040 single base substitution T C 5_prime_UTR_variant BRCA-EU 16 75298040 75298040 single base substitution T C intron_variant BRCA-EU 16 75298703 75298703 single base substitution C G 5_prime_UTR_variant BRCA-EU 16 75298703 75298703 single base substitution C G intron_variant BRCA-EU 16 75298703 75298703 single base substitution C G upstream_gene_variant BRCA-EU 16 75298986 75298986 single base substitution G C 5_prime_UTR_variant BRCA-EU 16 75298986 75298986 single base substitution G C intron_variant BRCA-EU 16 75298986 75298986 single base substitution G C upstream_gene_variant BRCA-EU 16 75299897 75299897 single base substitution G C 5_prime_UTR_variant BRCA-EU 16 75299897 75299897 single base substitution G C intron_variant BRCA-EU 16 75299897 75299897 single base substitution G C upstream_gene_variant BRCA-EU 16 75300233 75300233 single base substitution G A 5_prime_UTR_variant BRCA-EU 16 75300233 75300233 single base substitution G A intron_variant BRCA-EU 16 75300233 75300233 single base substitution G A upstream_gene_variant BRCA-EU 16 75300862 75300862 single base substitution G C intron_variant BRCA-EU 16 75300862 75300862 single base substitution G C upstream_gene_variant BRCA-EU 16 75301218 75301218 single base substitution C T intron_variant BRCA-EU 16 75301218 75301218 single base substitution C T upstream_gene_variant BRCA-EU 16 75301303 75301303 deletion of <=200bp T - intron_variant BRCA-EU 16 75301303 75301303 deletion of <=200bp T - upstream_gene_variant BRCA-EU 16 75302016 75302016 single base substitution C T upstream_gene_variant BRCA-EU 16 75303245 75303245 single base substitution A C upstream_gene_variant BRCA-EU 16 75303699 75303699 single base substitution G T upstream_gene_variant BRCA-EU 16 75303916 75303916 single base substitution G A upstream_gene_variant BRCA-EU 16 75306287 75306287 single base substitution G C upstream_gene_variant BRCA-FR 16 75260247 75260247 single base substitution G A downstream_gene_variant BRCA-FR 16 75276374 75276374 single base substitution C T 3_prime_UTR_variant BRCA-FR 16 75276374 75276374 single base substitution C T downstream_gene_variant BRCA-FR 16 75276374 75276374 single base substitution C T intron_variant BRCA-FR 16 75276374 75276374 single base substitution C T synonymous_variant P180P 540G>A BRCA-FR 16 75276374 75276374 single base substitution C T synonymous_variant P207P 621G>A BRCA-FR 16 75276374 75276374 single base substitution C T synonymous_variant P209P 627G>A BRCA-FR 16 75276374 75276374 single base substitution C T synonymous_variant P227P 681G>A BRCA-FR 16 75276374 75276374 single base substitution C T synonymous_variant P255P 765G>A BRCA-FR 16 75276374 75276374 single base substitution C T synonymous_variant P75P 225G>A BRCA-FR 16 75276374 75276374 single base substitution C T upstream_gene_variant BRCA-FR 16 75293310 75293310 single base substitution C T intron_variant BRCA-FR 16 75293310 75293310 single base substitution C T upstream_gene_variant BRCA-UK 16 75270746 75270746 single base substitution G A exon_variant BRCA-UK 16 75270746 75270746 single base substitution G A intron_variant BRCA-UK 16 75270746 75270746 single base substitution G A synonymous_variant L316L 946C>T BRCA-UK 16 75270746 75270746 single base substitution G A upstream_gene_variant BRCA-UK 16 75303916 75303916 single base substitution G A upstream_gene_variant BRCA-US 16 75263772 75263772 insertion of <=200bp - T 3_prime_UTR_variant BRCA-US 16 75263772 75263772 insertion of <=200bp - T exon_variant BRCA-US 16 75263772 75263772 insertion of <=200bp - T frameshift_variant Q602Q? BRCA-US 16 75263772 75263772 insertion of <=200bp - T frameshift_variant Q721Q? BRCA-US 16 75263772 75263772 insertion of <=200bp - T frameshift_variant Q748Q? BRCA-US 16 75263772 75263772 insertion of <=200bp - T frameshift_variant Q750Q? BRCA-US 16 75263772 75263772 insertion of <=200bp - T frameshift_variant Q768Q? BRCA-US 16 75263772 75263772 insertion of <=200bp - T frameshift_variant Q796Q? BRCA-US 16 75263776 75263776 deletion of <=200bp T - 3_prime_UTR_variant BRCA-US 16 75263776 75263776 deletion of <=200bp T - exon_variant BRCA-US 16 75263776 75263776 deletion of <=200bp T - frameshift_variant E601 BRCA-US 16 75263776 75263776 deletion of <=200bp T - frameshift_variant E720 BRCA-US 16 75263776 75263776 deletion of <=200bp T - frameshift_variant E747 BRCA-US 16 75263776 75263776 deletion of <=200bp T - frameshift_variant E749 BRCA-US 16 75263776 75263776 deletion of <=200bp T - frameshift_variant E767 BRCA-US 16 75263776 75263776 deletion of <=200bp T - frameshift_variant E795 BRCA-US 16 75263783 75263783 single base substitution A G 3_prime_UTR_variant BRCA-US 16 75263783 75263783 single base substitution A G exon_variant BRCA-US 16 75263783 75263783 single base substitution A G missense_variant Y599H 1795T>C BRCA-US 16 75263783 75263783 single base substitution A G missense_variant Y718H 2152T>C BRCA-US 16 75263783 75263783 single base substitution A G missense_variant Y745H 2233T>C BRCA-US 16 75263783 75263783 single base substitution A G missense_variant Y747H 2239T>C BRCA-US 16 75263783 75263783 single base substitution A G missense_variant Y765H 2293T>C BRCA-US 16 75263783 75263783 single base substitution A G missense_variant Y793H 2377T>C BRCA-US 16 75267782 75267782 single base substitution T C 3_prime_UTR_variant BRCA-US 16 75267782 75267782 single base substitution T C downstream_gene_variant BRCA-US 16 75267782 75267782 single base substitution T C exon_variant BRCA-US 16 75267782 75267782 single base substitution T C missense_variant I540V 1618A>G BRCA-US 16 75267782 75267782 single base substitution T C missense_variant I659V 1975A>G BRCA-US 16 75267782 75267782 single base substitution T C missense_variant I686V 2056A>G BRCA-US 16 75267782 75267782 single base substitution T C missense_variant I688V 2062A>G BRCA-US 16 75267782 75267782 single base substitution T C missense_variant I706V 2116A>G BRCA-US 16 75267782 75267782 single base substitution T C missense_variant I734V 2200A>G BRCA-US 16 75267803 75267803 single base substitution C A 3_prime_UTR_variant BRCA-US 16 75267803 75267803 single base substitution C A downstream_gene_variant BRCA-US 16 75267803 75267803 single base substitution C A exon_variant BRCA-US 16 75267803 75267803 single base substitution C A stop_gained E533* 1597G>T BRCA-US 16 75267803 75267803 single base substitution C A stop_gained E652* 1954G>T BRCA-US 16 75267803 75267803 single base substitution C A stop_gained E679* 2035G>T BRCA-US 16 75267803 75267803 single base substitution C A stop_gained E681* 2041G>T BRCA-US 16 75267803 75267803 single base substitution C A stop_gained E699* 2095G>T BRCA-US 16 75267803 75267803 single base substitution C A stop_gained E727* 2179G>T BRCA-US 16 75270832 75270832 single base substitution T C 3_prime_UTR_variant BRCA-US 16 75270832 75270832 single base substitution T C exon_variant BRCA-US 16 75270832 75270832 single base substitution T C intron_variant BRCA-US 16 75270832 75270832 single base substitution T C missense_variant Y139C 416A>G BRCA-US 16 75270832 75270832 single base substitution T C missense_variant Y258C 773A>G BRCA-US 16 75270832 75270832 single base substitution T C missense_variant Y285C 854A>G BRCA-US 16 75270832 75270832 single base substitution T C missense_variant Y287C 860A>G BRCA-US 16 75270832 75270832 single base substitution T C missense_variant Y305C 914A>G BRCA-US 16 75270832 75270832 single base substitution T C missense_variant Y333C 998A>G BRCA-US 16 75270832 75270832 single base substitution T C upstream_gene_variant BRCA-US 16 75271166 75271166 single base substitution G A 3_prime_UTR_variant BRCA-US 16 75271166 75271166 single base substitution G A exon_variant BRCA-US 16 75271166 75271166 single base substitution G A missense_variant P103L 308C>T BRCA-US 16 75271166 75271166 single base substitution G A missense_variant P208L 623C>T BRCA-US 16 75271166 75271166 single base substitution G A missense_variant P235L 704C>T BRCA-US 16 75271166 75271166 single base substitution G A missense_variant P237L 710C>T BRCA-US 16 75271166 75271166 single base substitution G A missense_variant P255L 764C>T BRCA-US 16 75271166 75271166 single base substitution G A missense_variant P283L 848C>T BRCA-US 16 75271166 75271166 single base substitution G A missense_variant P89L 266C>T BRCA-US 16 75271166 75271166 single base substitution G A upstream_gene_variant BTCA-JP 16 75277392 75277392 single base substitution G A intron_variant BTCA-JP 16 75277392 75277392 single base substitution G A upstream_gene_variant CESC-US 16 75260568 75260568 single base substitution C T downstream_gene_variant CESC-US 16 75260587 75260587 single base substitution G A downstream_gene_variant CESC-US 16 75263742 75263742 single base substitution G A 3_prime_UTR_variant CESC-US 16 75263742 75263742 single base substitution G A exon_variant CESC-US 16 75263742 75263742 single base substitution G A synonymous_variant N612N 1836C>T CESC-US 16 75263742 75263742 single base substitution G A synonymous_variant N731N 2193C>T CESC-US 16 75263742 75263742 single base substitution G A synonymous_variant N758N 2274C>T CESC-US 16 75263742 75263742 single base substitution G A synonymous_variant N760N 2280C>T CESC-US 16 75263742 75263742 single base substitution G A synonymous_variant N778N 2334C>T CESC-US 16 75263742 75263742 single base substitution G A synonymous_variant N806N 2418C>T CESC-US 16 75301816 75301816 single base substitution G A synonymous_variant L21L 63C>T CESC-US 16 75301816 75301816 single base substitution G A upstream_gene_variant COAD-US 16 75258617 75258617 single base substitution C T downstream_gene_variant COAD-US 16 75258738 75258738 single base substitution G A downstream_gene_variant COAD-US 16 75263595 75263595 single base substitution G A 3_prime_UTR_variant COAD-US 16 75263595 75263595 single base substitution G A exon_variant COAD-US 16 75263595 75263595 single base substitution G A synonymous_variant R661R 1983C>T COAD-US 16 75263595 75263595 single base substitution G A synonymous_variant R780R 2340C>T COAD-US 16 75263595 75263595 single base substitution G A synonymous_variant R807R 2421C>T COAD-US 16 75263595 75263595 single base substitution G A synonymous_variant R809R 2427C>T COAD-US 16 75263595 75263595 single base substitution G A synonymous_variant R827R 2481C>T COAD-US 16 75263595 75263595 single base substitution G A synonymous_variant R855R 2565C>T COAD-US 16 75263661 75263661 single base substitution G A 3_prime_UTR_variant COAD-US 16 75263661 75263661 single base substitution G A exon_variant COAD-US 16 75263661 75263661 single base substitution G A synonymous_variant L639L 1917C>T COAD-US 16 75263661 75263661 single base substitution G A synonymous_variant L758L 2274C>T COAD-US 16 75263661 75263661 single base substitution G A synonymous_variant L785L 2355C>T COAD-US 16 75263661 75263661 single base substitution G A synonymous_variant L787L 2361C>T COAD-US 16 75263661 75263661 single base substitution G A synonymous_variant L805L 2415C>T COAD-US 16 75263661 75263661 single base substitution G A synonymous_variant L833L 2499C>T COAD-US 16 75268995 75268995 single base substitution G T 3_prime_UTR_variant COAD-US 16 75268995 75268995 single base substitution G T downstream_gene_variant COAD-US 16 75268995 75268995 single base substitution G T exon_variant COAD-US 16 75268995 75268995 single base substitution G T missense_variant A453D 1358C>A COAD-US 16 75268995 75268995 single base substitution G T missense_variant A572D 1715C>A COAD-US 16 75268995 75268995 single base substitution G T missense_variant A599D 1796C>A COAD-US 16 75268995 75268995 single base substitution G T missense_variant A601D 1802C>A COAD-US 16 75268995 75268995 single base substitution G T missense_variant A619D 1856C>A COAD-US 16 75268995 75268995 single base substitution G T missense_variant A647D 1940C>A COAD-US 16 75269267 75269267 single base substitution A G 3_prime_UTR_variant COAD-US 16 75269267 75269267 single base substitution A G downstream_gene_variant COAD-US 16 75269267 75269267 single base substitution A G exon_variant COAD-US 16 75269267 75269267 single base substitution A G synonymous_variant A362A 1086T>C COAD-US 16 75269267 75269267 single base substitution A G synonymous_variant A481A 1443T>C COAD-US 16 75269267 75269267 single base substitution A G synonymous_variant A508A 1524T>C COAD-US 16 75269267 75269267 single base substitution A G synonymous_variant A510A 1530T>C COAD-US 16 75269267 75269267 single base substitution A G synonymous_variant A528A 1584T>C COAD-US 16 75269267 75269267 single base substitution A G synonymous_variant A556A 1668T>C COAD-US 16 75269477 75269477 single base substitution A C 3_prime_UTR_variant COAD-US 16 75269477 75269477 single base substitution A C downstream_gene_variant COAD-US 16 75269477 75269477 single base substitution A C exon_variant COAD-US 16 75269477 75269477 single base substitution A C synonymous_variant S292S 876T>G COAD-US 16 75269477 75269477 single base substitution A C synonymous_variant S411S 1233T>G COAD-US 16 75269477 75269477 single base substitution A C synonymous_variant S438S 1314T>G COAD-US 16 75269477 75269477 single base substitution A C synonymous_variant S440S 1320T>G COAD-US 16 75269477 75269477 single base substitution A C synonymous_variant S458S 1374T>G COAD-US 16 75269477 75269477 single base substitution A C synonymous_variant S486S 1458T>G COAD-US 16 75270855 75270855 single base substitution G A 3_prime_UTR_variant COAD-US 16 75270855 75270855 single base substitution G A exon_variant COAD-US 16 75270855 75270855 single base substitution G A intron_variant COAD-US 16 75270855 75270855 single base substitution G A synonymous_variant G131G 393C>T COAD-US 16 75270855 75270855 single base substitution G A synonymous_variant G250G 750C>T COAD-US 16 75270855 75270855 single base substitution G A synonymous_variant G277G 831C>T COAD-US 16 75270855 75270855 single base substitution G A synonymous_variant G279G 837C>T COAD-US 16 75270855 75270855 single base substitution G A synonymous_variant G297G 891C>T COAD-US 16 75270855 75270855 single base substitution G A synonymous_variant G325G 975C>T COAD-US 16 75270855 75270855 single base substitution G A upstream_gene_variant COAD-US 16 75271113 75271113 single base substitution G A 3_prime_UTR_variant COAD-US 16 75271113 75271113 single base substitution G A exon_variant COAD-US 16 75271113 75271113 single base substitution G A missense_variant R107W 319C>T COAD-US 16 75271113 75271113 single base substitution G A missense_variant R121W 361C>T COAD-US 16 75271113 75271113 single base substitution G A missense_variant R226W 676C>T COAD-US 16 75271113 75271113 single base substitution G A missense_variant R253W 757C>T COAD-US 16 75271113 75271113 single base substitution G A missense_variant R255W 763C>T COAD-US 16 75271113 75271113 single base substitution G A missense_variant R273W 817C>T COAD-US 16 75271113 75271113 single base substitution G A missense_variant R301W 901C>T COAD-US 16 75271113 75271113 single base substitution G A upstream_gene_variant COAD-US 16 75276775 75276775 single base substitution G A 3_prime_UTR_variant COAD-US 16 75276775 75276775 single base substitution G A downstream_gene_variant COAD-US 16 75276775 75276775 single base substitution G A intron_variant COAD-US 16 75276775 75276775 single base substitution G A missense_variant P122S 364C>T COAD-US 16 75276775 75276775 single base substitution G A missense_variant P47S 139C>T COAD-US 16 75276775 75276775 single base substitution G A missense_variant P74S 220C>T COAD-US 16 75276775 75276775 single base substitution G A missense_variant P76S 226C>T COAD-US 16 75276775 75276775 single base substitution G A missense_variant P94S 280C>T COAD-US 16 75276775 75276775 single base substitution G A upstream_gene_variant COAD-US 16 75276825 75276825 single base substitution C T 3_prime_UTR_variant COAD-US 16 75276825 75276825 single base substitution C T downstream_gene_variant COAD-US 16 75276825 75276825 single base substitution C T missense_variant R105H 314G>A COAD-US 16 75276825 75276825 single base substitution C T missense_variant R30H 89G>A COAD-US 16 75276825 75276825 single base substitution C T missense_variant R57H 170G>A COAD-US 16 75276825 75276825 single base substitution C T missense_variant R59H 176G>A COAD-US 16 75276825 75276825 single base substitution C T missense_variant R77H 230G>A COAD-US 16 75276825 75276825 single base substitution C T upstream_gene_variant COAD-US 16 75301828 75301828 single base substitution C A missense_variant K17N 51G>T COAD-US 16 75301828 75301828 single base substitution C A upstream_gene_variant COCA-CN 16 75258565 75258565 single base substitution G A downstream_gene_variant COCA-CN 16 75263636 75263636 single base substitution C T 3_prime_UTR_variant COCA-CN 16 75263636 75263636 single base substitution C T exon_variant COCA-CN 16 75263636 75263636 single base substitution C T missense_variant G648R 1942G>A COCA-CN 16 75263636 75263636 single base substitution C T missense_variant G767R 2299G>A COCA-CN 16 75263636 75263636 single base substitution C T missense_variant G794R 2380G>A COCA-CN 16 75263636 75263636 single base substitution C T missense_variant G796R 2386G>A COCA-CN 16 75263636 75263636 single base substitution C T missense_variant G814R 2440G>A COCA-CN 16 75263636 75263636 single base substitution C T missense_variant G842R 2524G>A COCA-CN 16 75269432 75269432 single base substitution C T 3_prime_UTR_variant COCA-CN 16 75269432 75269432 single base substitution C T downstream_gene_variant COCA-CN 16 75269432 75269432 single base substitution C T exon_variant COCA-CN 16 75269432 75269432 single base substitution C T synonymous_variant E307E 921G>A COCA-CN 16 75269432 75269432 single base substitution C T synonymous_variant E426E 1278G>A COCA-CN 16 75269432 75269432 single base substitution C T synonymous_variant E453E 1359G>A COCA-CN 16 75269432 75269432 single base substitution C T synonymous_variant E455E 1365G>A COCA-CN 16 75269432 75269432 single base substitution C T synonymous_variant E473E 1419G>A COCA-CN 16 75269432 75269432 single base substitution C T synonymous_variant E501E 1503G>A COCA-CN 16 75269727 75269727 single base substitution G A 3_prime_UTR_variant COCA-CN 16 75269727 75269727 single base substitution G A downstream_gene_variant COCA-CN 16 75269727 75269727 single base substitution G A exon_variant COCA-CN 16 75269727 75269727 single base substitution G A missense_variant P184L 551C>T COCA-CN 16 75269727 75269727 single base substitution G A missense_variant P209L 626C>T COCA-CN 16 75269727 75269727 single base substitution G A missense_variant P328L 983C>T COCA-CN 16 75269727 75269727 single base substitution G A missense_variant P355L 1064C>T COCA-CN 16 75269727 75269727 single base substitution G A missense_variant P357L 1070C>T COCA-CN 16 75269727 75269727 single base substitution G A missense_variant P375L 1124C>T COCA-CN 16 75269727 75269727 single base substitution G A missense_variant P403L 1208C>T COCA-CN 16 75269748 75269748 single base substitution G A 3_prime_UTR_variant COCA-CN 16 75269748 75269748 single base substitution G A downstream_gene_variant COCA-CN 16 75269748 75269748 single base substitution G A exon_variant COCA-CN 16 75269748 75269748 single base substitution G A missense_variant A177V 530C>T COCA-CN 16 75269748 75269748 single base substitution G A missense_variant A202V 605C>T COCA-CN 16 75269748 75269748 single base substitution G A missense_variant A321V 962C>T COCA-CN 16 75269748 75269748 single base substitution G A missense_variant A348V 1043C>T COCA-CN 16 75269748 75269748 single base substitution G A missense_variant A350V 1049C>T COCA-CN 16 75269748 75269748 single base substitution G A missense_variant A368V 1103C>T COCA-CN 16 75269748 75269748 single base substitution G A missense_variant A396V 1187C>T COCA-CN 16 75269760 75269760 single base substitution A G 3_prime_UTR_variant COCA-CN 16 75269760 75269760 single base substitution A G downstream_gene_variant COCA-CN 16 75269760 75269760 single base substitution A G exon_variant COCA-CN 16 75269760 75269760 single base substitution A G missense_variant L173P 518T>C COCA-CN 16 75269760 75269760 single base substitution A G missense_variant L198P 593T>C COCA-CN 16 75269760 75269760 single base substitution A G missense_variant L317P 950T>C COCA-CN 16 75269760 75269760 single base substitution A G missense_variant L344P 1031T>C COCA-CN 16 75269760 75269760 single base substitution A G missense_variant L346P 1037T>C COCA-CN 16 75269760 75269760 single base substitution A G missense_variant L364P 1091T>C COCA-CN 16 75269760 75269760 single base substitution A G missense_variant L392P 1175T>C COCA-CN 16 75270853 75270853 single base substitution C T 3_prime_UTR_variant COCA-CN 16 75270853 75270853 single base substitution C T exon_variant COCA-CN 16 75270853 75270853 single base substitution C T intron_variant COCA-CN 16 75270853 75270853 single base substitution C T missense_variant R132Q 395G>A COCA-CN 16 75270853 75270853 single base substitution C T missense_variant R251Q 752G>A COCA-CN 16 75270853 75270853 single base substitution C T missense_variant R278Q 833G>A COCA-CN 16 75270853 75270853 single base substitution C T missense_variant R280Q 839G>A COCA-CN 16 75270853 75270853 single base substitution C T missense_variant R298Q 893G>A COCA-CN 16 75270853 75270853 single base substitution C T missense_variant R326Q 977G>A COCA-CN 16 75270853 75270853 single base substitution C T upstream_gene_variant COCA-CN 16 75270966 75270966 single base substitution G A intron_variant COCA-CN 16 75270966 75270966 single base substitution G A upstream_gene_variant COCA-CN 16 75276521 75276521 single base substitution C T 3_prime_UTR_variant COCA-CN 16 75276521 75276521 single base substitution C T downstream_gene_variant COCA-CN 16 75276521 75276521 single base substitution C T intron_variant COCA-CN 16 75276521 75276521 single base substitution C T synonymous_variant P131P 393G>A COCA-CN 16 75276521 75276521 single base substitution C T synonymous_variant P158P 474G>A COCA-CN 16 75276521 75276521 single base substitution C T synonymous_variant P160P 480G>A COCA-CN 16 75276521 75276521 single base substitution C T synonymous_variant P178P 534G>A COCA-CN 16 75276521 75276521 single base substitution C T synonymous_variant P206P 618G>A COCA-CN 16 75276521 75276521 single base substitution C T synonymous_variant P26P 78G>A COCA-CN 16 75276521 75276521 single base substitution C T upstream_gene_variant COCA-CN 16 75277424 75277424 single base substitution G T intron_variant COCA-CN 16 75277424 75277424 single base substitution G T upstream_gene_variant COCA-CN 16 75281979 75281979 single base substitution G T 5_prime_UTR_variant COCA-CN 16 75281979 75281979 single base substitution G T intron_variant ESAD-UK 16 75260914 75260914 single base substitution T C downstream_gene_variant ESAD-UK 16 75263165 75263165 single base substitution C T 3_prime_UTR_variant ESAD-UK 16 75263165 75263165 single base substitution C T downstream_gene_variant ESAD-UK 16 75263165 75263165 single base substitution C T exon_variant ESAD-UK 16 75263414 75263414 single base substitution C T 3_prime_UTR_variant ESAD-UK 16 75263414 75263414 single base substitution C T exon_variant ESAD-UK 16 75263414 75263414 single base substitution C T missense_variant A722T 2164G>A ESAD-UK 16 75263414 75263414 single base substitution C T missense_variant A841T 2521G>A ESAD-UK 16 75263414 75263414 single base substitution C T missense_variant A868T 2602G>A ESAD-UK 16 75263414 75263414 single base substitution C T missense_variant A870T 2608G>A ESAD-UK 16 75263414 75263414 single base substitution C T missense_variant A888T 2662G>A ESAD-UK 16 75263414 75263414 single base substitution C T missense_variant A916T 2746G>A ESAD-UK 16 75263551 75263551 single base substitution C T 3_prime_UTR_variant ESAD-UK 16 75263551 75263551 single base substitution C T exon_variant ESAD-UK 16 75263551 75263551 single base substitution C T missense_variant R676H 2027G>A ESAD-UK 16 75263551 75263551 single base substitution C T missense_variant R795H 2384G>A ESAD-UK 16 75263551 75263551 single base substitution C T missense_variant R822H 2465G>A ESAD-UK 16 75263551 75263551 single base substitution C T missense_variant R824H 2471G>A ESAD-UK 16 75263551 75263551 single base substitution C T missense_variant R842H 2525G>A ESAD-UK 16 75263551 75263551 single base substitution C T missense_variant R870H 2609G>A ESAD-UK 16 75265164 75265164 single base substitution G A downstream_gene_variant ESAD-UK 16 75265164 75265164 single base substitution G A intron_variant ESAD-UK 16 75267057 75267057 single base substitution C G downstream_gene_variant ESAD-UK 16 75267057 75267057 single base substitution C G intron_variant ESAD-UK 16 75268833 75268833 single base substitution T C 3_prime_UTR_variant ESAD-UK 16 75268833 75268833 single base substitution T C downstream_gene_variant ESAD-UK 16 75268833 75268833 single base substitution T C exon_variant ESAD-UK 16 75268833 75268833 single base substitution T C missense_variant N507S 1520A>G ESAD-UK 16 75268833 75268833 single base substitution T C missense_variant N626S 1877A>G ESAD-UK 16 75268833 75268833 single base substitution T C missense_variant N653S 1958A>G ESAD-UK 16 75268833 75268833 single base substitution T C missense_variant N655S 1964A>G ESAD-UK 16 75268833 75268833 single base substitution T C missense_variant N673S 2018A>G ESAD-UK 16 75268833 75268833 single base substitution T C missense_variant N701S 2102A>G ESAD-UK 16 75269223 75269223 single base substitution G A 3_prime_UTR_variant ESAD-UK 16 75269223 75269223 single base substitution G A downstream_gene_variant ESAD-UK 16 75269223 75269223 single base substitution G A exon_variant ESAD-UK 16 75269223 75269223 single base substitution G A missense_variant A377V 1130C>T ESAD-UK 16 75269223 75269223 single base substitution G A missense_variant A496V 1487C>T ESAD-UK 16 75269223 75269223 single base substitution G A missense_variant A523V 1568C>T ESAD-UK 16 75269223 75269223 single base substitution G A missense_variant A525V 1574C>T ESAD-UK 16 75269223 75269223 single base substitution G A missense_variant A543V 1628C>T ESAD-UK 16 75269223 75269223 single base substitution G A missense_variant A571V 1712C>T ESAD-UK 16 75269351 75269351 single base substitution G A 3_prime_UTR_variant ESAD-UK 16 75269351 75269351 single base substitution G A downstream_gene_variant ESAD-UK 16 75269351 75269351 single base substitution G A exon_variant ESAD-UK 16 75269351 75269351 single base substitution G A synonymous_variant G334G 1002C>T ESAD-UK 16 75269351 75269351 single base substitution G A synonymous_variant G453G 1359C>T ESAD-UK 16 75269351 75269351 single base substitution G A synonymous_variant G480G 1440C>T ESAD-UK 16 75269351 75269351 single base substitution G A synonymous_variant G482G 1446C>T ESAD-UK 16 75269351 75269351 single base substitution G A synonymous_variant G500G 1500C>T ESAD-UK 16 75269351 75269351 single base substitution G A synonymous_variant G528G 1584C>T ESAD-UK 16 75272658 75272658 single base substitution T A downstream_gene_variant ESAD-UK 16 75272658 75272658 single base substitution T A intron_variant ESAD-UK 16 75272658 75272658 single base substitution T A upstream_gene_variant ESAD-UK 16 75276105 75276105 single base substitution C A downstream_gene_variant ESAD-UK 16 75276105 75276105 single base substitution C A intron_variant ESAD-UK 16 75276105 75276105 single base substitution C A upstream_gene_variant ESAD-UK 16 75277102 75277102 single base substitution C A intron_variant ESAD-UK 16 75277102 75277102 single base substitution C A upstream_gene_variant ESAD-UK 16 75279368 75279368 single base substitution A G intron_variant ESAD-UK 16 75279368 75279368 single base substitution A G upstream_gene_variant ESAD-UK 16 75285610 75285610 single base substitution C G intron_variant ESAD-UK 16 75285610 75285610 single base substitution C G upstream_gene_variant ESAD-UK 16 75287312 75287312 single base substitution C T intron_variant ESAD-UK 16 75287312 75287312 single base substitution C T upstream_gene_variant ESAD-UK 16 75289660 75289660 single base substitution C T intron_variant ESAD-UK 16 75289660 75289660 single base substitution C T upstream_gene_variant ESAD-UK 16 75293197 75293197 insertion of <=200bp - T intron_variant ESAD-UK 16 75293197 75293197 insertion of <=200bp - T upstream_gene_variant ESAD-UK 16 75293459 75293459 single base substitution A T intron_variant ESAD-UK 16 75293459 75293459 single base substitution A T upstream_gene_variant ESAD-UK 16 75293527 75293527 single base substitution G C intron_variant ESAD-UK 16 75293527 75293527 single base substitution G C upstream_gene_variant ESAD-UK 16 75294234 75294234 single base substitution A G intron_variant ESAD-UK 16 75294234 75294234 single base substitution A G upstream_gene_variant ESAD-UK 16 75297944 75297944 single base substitution G A 3_prime_UTR_variant ESAD-UK 16 75297944 75297944 single base substitution G A 5_prime_UTR_variant ESAD-UK 16 75297944 75297944 single base substitution G A intron_variant ESAD-UK 16 75299921 75299921 insertion of <=200bp - C intron_variant ESAD-UK 16 75299921 75299921 insertion of <=200bp - C upstream_gene_variant ESAD-UK 16 75303202 75303202 single base substitution C T upstream_gene_variant ESAD-UK 16 75303672 75303672 single base substitution T A upstream_gene_variant ESAD-UK 16 75304465 75304465 single base substitution G T upstream_gene_variant ESAD-UK 16 75304983 75304983 single base substitution A G upstream_gene_variant KIRC-US 16 75269312 75269312 single base substitution C A 3_prime_UTR_variant KIRC-US 16 75269312 75269312 single base substitution C A downstream_gene_variant KIRC-US 16 75269312 75269312 single base substitution C A exon_variant KIRC-US 16 75269312 75269312 single base substitution C A missense_variant E347D 1041G>T KIRC-US 16 75269312 75269312 single base substitution C A missense_variant E466D 1398G>T KIRC-US 16 75269312 75269312 single base substitution C A missense_variant E493D 1479G>T KIRC-US 16 75269312 75269312 single base substitution C A missense_variant E495D 1485G>T KIRC-US 16 75269312 75269312 single base substitution C A missense_variant E513D 1539G>T KIRC-US 16 75269312 75269312 single base substitution C A missense_variant E541D 1623G>T KIRC-US 16 75276448 75276448 single base substitution C A 3_prime_UTR_variant KIRC-US 16 75276448 75276448 single base substitution C A downstream_gene_variant KIRC-US 16 75276448 75276448 single base substitution C A intron_variant KIRC-US 16 75276448 75276448 single base substitution C A missense_variant A156S 466G>T KIRC-US 16 75276448 75276448 single base substitution C A missense_variant A183S 547G>T KIRC-US 16 75276448 75276448 single base substitution C A missense_variant A185S 553G>T KIRC-US 16 75276448 75276448 single base substitution C A missense_variant A203S 607G>T KIRC-US 16 75276448 75276448 single base substitution C A missense_variant A231S 691G>T KIRC-US 16 75276448 75276448 single base substitution C A missense_variant A51S 151G>T KIRC-US 16 75276448 75276448 single base substitution C A upstream_gene_variant KIRP-US 16 75276534 75276534 single base substitution G C 3_prime_UTR_variant KIRP-US 16 75276534 75276534 single base substitution G C downstream_gene_variant KIRP-US 16 75276534 75276534 single base substitution G C intron_variant KIRP-US 16 75276534 75276534 single base substitution G C missense_variant P127R 380C>G KIRP-US 16 75276534 75276534 single base substitution G C missense_variant P154R 461C>G KIRP-US 16 75276534 75276534 single base substitution G C missense_variant P156R 467C>G KIRP-US 16 75276534 75276534 single base substitution G C missense_variant P174R 521C>G KIRP-US 16 75276534 75276534 single base substitution G C missense_variant P202R 605C>G KIRP-US 16 75276534 75276534 single base substitution G C missense_variant P22R 65C>G KIRP-US 16 75276534 75276534 single base substitution G C upstream_gene_variant LAML-KR 16 75266119 75266119 single base substitution C T downstream_gene_variant LAML-KR 16 75266119 75266119 single base substitution C T intron_variant LAML-KR 16 75276775 75276775 single base substitution G A 3_prime_UTR_variant LAML-KR 16 75276775 75276775 single base substitution G A downstream_gene_variant LAML-KR 16 75276775 75276775 single base substitution G A intron_variant LAML-KR 16 75276775 75276775 single base substitution G A missense_variant P122S 364C>T LAML-KR 16 75276775 75276775 single base substitution G A missense_variant P47S 139C>T LAML-KR 16 75276775 75276775 single base substitution G A missense_variant P74S 220C>T LAML-KR 16 75276775 75276775 single base substitution G A missense_variant P76S 226C>T LAML-KR 16 75276775 75276775 single base substitution G A missense_variant P94S 280C>T LAML-KR 16 75276775 75276775 single base substitution G A upstream_gene_variant LICA-CN 16 75269657 75269657 single base substitution C A 3_prime_UTR_variant LICA-CN 16 75269657 75269657 single base substitution C A downstream_gene_variant LICA-CN 16 75269657 75269657 single base substitution C A exon_variant LICA-CN 16 75269657 75269657 single base substitution C A synonymous_variant R207R 621G>T LICA-CN 16 75269657 75269657 single base substitution C A synonymous_variant R232R 696G>T LICA-CN 16 75269657 75269657 single base substitution C A synonymous_variant R351R 1053G>T LICA-CN 16 75269657 75269657 single base substitution C A synonymous_variant R378R 1134G>T LICA-CN 16 75269657 75269657 single base substitution C A synonymous_variant R380R 1140G>T LICA-CN 16 75269657 75269657 single base substitution C A synonymous_variant R398R 1194G>T LICA-CN 16 75269657 75269657 single base substitution C A synonymous_variant R426R 1278G>T LICA-FR 16 75258686 75258686 single base substitution C T downstream_gene_variant LICA-FR 16 75268806 75268806 single base substitution T C 3_prime_UTR_variant LICA-FR 16 75268806 75268806 single base substitution T C downstream_gene_variant LICA-FR 16 75268806 75268806 single base substitution T C exon_variant LICA-FR 16 75268806 75268806 single base substitution T C missense_variant Y516C 1547A>G LICA-FR 16 75268806 75268806 single base substitution T C missense_variant Y635C 1904A>G LICA-FR 16 75268806 75268806 single base substitution T C missense_variant Y662C 1985A>G LICA-FR 16 75268806 75268806 single base substitution T C missense_variant Y664C 1991A>G LICA-FR 16 75268806 75268806 single base substitution T C missense_variant Y682C 2045A>G LICA-FR 16 75268806 75268806 single base substitution T C missense_variant Y710C 2129A>G LICA-FR 16 75269075 75269075 single base substitution C T 3_prime_UTR_variant LICA-FR 16 75269075 75269075 single base substitution C T downstream_gene_variant LICA-FR 16 75269075 75269075 single base substitution C T exon_variant LICA-FR 16 75269075 75269075 single base substitution C T synonymous_variant E426E 1278G>A LICA-FR 16 75269075 75269075 single base substitution C T synonymous_variant E545E 1635G>A LICA-FR 16 75269075 75269075 single base substitution C T synonymous_variant E572E 1716G>A LICA-FR 16 75269075 75269075 single base substitution C T synonymous_variant E574E 1722G>A LICA-FR 16 75269075 75269075 single base substitution C T synonymous_variant E592E 1776G>A LICA-FR 16 75269075 75269075 single base substitution C T synonymous_variant E620E 1860G>A LICA-FR 16 75282300 75282301 deletion of <=200bp AG - intron_variant LICA-FR 16 75282300 75282301 deletion of <=200bp AG - upstream_gene_variant LICA-FR 16 75291791 75291791 single base substitution G A intron_variant LICA-FR 16 75291791 75291791 single base substitution G A upstream_gene_variant LICA-FR 16 75294334 75294334 single base substitution C A intron_variant LICA-FR 16 75294334 75294334 single base substitution C A upstream_gene_variant LIHC-US 16 75263466 75263466 single base substitution C A 3_prime_UTR_variant LIHC-US 16 75263466 75263466 single base substitution C A exon_variant LIHC-US 16 75263466 75263466 single base substitution C A missense_variant E704D 2112G>T LIHC-US 16 75263466 75263466 single base substitution C A missense_variant E823D 2469G>T LIHC-US 16 75263466 75263466 single base substitution C A missense_variant E850D 2550G>T LIHC-US 16 75263466 75263466 single base substitution C A missense_variant E852D 2556G>T LIHC-US 16 75263466 75263466 single base substitution C A missense_variant E870D 2610G>T LIHC-US 16 75263466 75263466 single base substitution C A missense_variant E898D 2694G>T LIHC-US 16 75269535 75269535 single base substitution G T 3_prime_UTR_variant LIHC-US 16 75269535 75269535 single base substitution G T downstream_gene_variant LIHC-US 16 75269535 75269535 single base substitution G T exon_variant LIHC-US 16 75269535 75269535 single base substitution G T missense_variant P273Q 818C>A LIHC-US 16 75269535 75269535 single base substitution G T missense_variant P392Q 1175C>A LIHC-US 16 75269535 75269535 single base substitution G T missense_variant P419Q 1256C>A LIHC-US 16 75269535 75269535 single base substitution G T missense_variant P421Q 1262C>A LIHC-US 16 75269535 75269535 single base substitution G T missense_variant P439Q 1316C>A LIHC-US 16 75269535 75269535 single base substitution G T missense_variant P467Q 1400C>A LINC-JP 16 75263293 75263293 single base substitution C A 3_prime_UTR_variant LINC-JP 16 75263293 75263293 single base substitution C A downstream_gene_variant LINC-JP 16 75263293 75263293 single base substitution C A exon_variant LINC-JP 16 75263559 75263559 single base substitution G A 3_prime_UTR_variant LINC-JP 16 75263559 75263559 single base substitution G A exon_variant LINC-JP 16 75263559 75263559 single base substitution G A synonymous_variant D673D 2019C>T LINC-JP 16 75263559 75263559 single base substitution G A synonymous_variant D792D 2376C>T LINC-JP 16 75263559 75263559 single base substitution G A synonymous_variant D819D 2457C>T LINC-JP 16 75263559 75263559 single base substitution G A synonymous_variant D821D 2463C>T LINC-JP 16 75263559 75263559 single base substitution G A synonymous_variant D839D 2517C>T LINC-JP 16 75263559 75263559 single base substitution G A synonymous_variant D867D 2601C>T LINC-JP 16 75263649 75263649 single base substitution C T 3_prime_UTR_variant LINC-JP 16 75263649 75263649 single base substitution C T exon_variant LINC-JP 16 75263649 75263649 single base substitution C T synonymous_variant K643K 1929G>A LINC-JP 16 75263649 75263649 single base substitution C T synonymous_variant K762K 2286G>A LINC-JP 16 75263649 75263649 single base substitution C T synonymous_variant K789K 2367G>A LINC-JP 16 75263649 75263649 single base substitution C T synonymous_variant K791K 2373G>A LINC-JP 16 75263649 75263649 single base substitution C T synonymous_variant K809K 2427G>A LINC-JP 16 75263649 75263649 single base substitution C T synonymous_variant K837K 2511G>A LINC-JP 16 75276952 75276952 single base substitution C T 3_prime_UTR_variant LINC-JP 16 75276952 75276952 single base substitution C T 5_prime_UTR_variant LINC-JP 16 75276952 75276952 single base substitution C T downstream_gene_variant LINC-JP 16 75276952 75276952 single base substitution C T missense_variant E15K 43G>A LINC-JP 16 75276952 75276952 single base substitution C T missense_variant E17K 49G>A LINC-JP 16 75276952 75276952 single base substitution C T missense_variant E35K 103G>A LINC-JP 16 75276952 75276952 single base substitution C T missense_variant E63K 187G>A LINC-JP 16 75276952 75276952 single base substitution C T upstream_gene_variant LINC-JP 16 75277382 75277382 single base substitution C A intron_variant LINC-JP 16 75277382 75277382 single base substitution C A upstream_gene_variant LINC-JP 16 75288072 75288072 single base substitution A T intron_variant LINC-JP 16 75288072 75288072 single base substitution A T upstream_gene_variant LIRI-JP 16 75258568 75258568 single base substitution T A downstream_gene_variant LIRI-JP 16 75262513 75262513 single base substitution C T downstream_gene_variant LIRI-JP 16 75263823 75263823 single base substitution T C 3_prime_UTR_variant LIRI-JP 16 75263823 75263823 single base substitution T C exon_variant LIRI-JP 16 75263823 75263823 single base substitution T C synonymous_variant T585T 1755A>G LIRI-JP 16 75263823 75263823 single base substitution T C synonymous_variant T704T 2112A>G LIRI-JP 16 75263823 75263823 single base substitution T C synonymous_variant T731T 2193A>G LIRI-JP 16 75263823 75263823 single base substitution T C synonymous_variant T733T 2199A>G LIRI-JP 16 75263823 75263823 single base substitution T C synonymous_variant T751T 2253A>G LIRI-JP 16 75263823 75263823 single base substitution T C synonymous_variant T779T 2337A>G LIRI-JP 16 75266098 75266098 single base substitution G A downstream_gene_variant LIRI-JP 16 75266098 75266098 single base substitution G A intron_variant LIRI-JP 16 75266856 75266856 single base substitution T C downstream_gene_variant LIRI-JP 16 75266856 75266856 single base substitution T C intron_variant LIRI-JP 16 75274136 75274136 single base substitution C G downstream_gene_variant LIRI-JP 16 75274136 75274136 single base substitution C G intron_variant LIRI-JP 16 75274136 75274136 single base substitution C G upstream_gene_variant LIRI-JP 16 75278125 75278125 single base substitution G A intron_variant LIRI-JP 16 75278125 75278125 single base substitution G A upstream_gene_variant LIRI-JP 16 75281297 75281297 single base substitution C T intron_variant LIRI-JP 16 75281297 75281297 single base substitution C T upstream_gene_variant LIRI-JP 16 75282784 75282784 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LIRI-JP 16 75282784 75282784 single base substitution G A intron_variant LIRI-JP 16 75282784 75282784 single base substitution G A upstream_gene_variant LIRI-JP 16 75283071 75283071 single base substitution G A intron_variant LIRI-JP 16 75283071 75283071 single base substitution G A upstream_gene_variant LIRI-JP 16 75286799 75286799 single base substitution G C intron_variant LIRI-JP 16 75286799 75286799 single base substitution G C upstream_gene_variant LIRI-JP 16 75287590 75287590 single base substitution G T intron_variant LIRI-JP 16 75287590 75287590 single base substitution G T upstream_gene_variant LIRI-JP 16 75287676 75287680 deletion of <=200bp GGCCG - intron_variant LIRI-JP 16 75287676 75287680 deletion of <=200bp GGCCG - upstream_gene_variant LIRI-JP 16 75292781 75292781 single base substitution G A intron_variant LIRI-JP 16 75292781 75292781 single base substitution G A upstream_gene_variant LIRI-JP 16 75302994 75302994 single base substitution G A upstream_gene_variant LIRI-JP 16 75306258 75306258 single base substitution G T upstream_gene_variant LUSC-KR 16 75259071 75259071 single base substitution C A downstream_gene_variant LUSC-KR 16 75263024 75263024 single base substitution T A 3_prime_UTR_variant LUSC-KR 16 75263024 75263024 single base substitution T A downstream_gene_variant LUSC-KR 16 75263024 75263024 single base substitution T A exon_variant LUSC-KR 16 75269534 75269534 single base substitution C T 3_prime_UTR_variant LUSC-KR 16 75269534 75269534 single base substitution C T downstream_gene_variant LUSC-KR 16 75269534 75269534 single base substitution C T exon_variant LUSC-KR 16 75269534 75269534 single base substitution C T synonymous_variant P273P 819G>A LUSC-KR 16 75269534 75269534 single base substitution C T synonymous_variant P392P 1176G>A LUSC-KR 16 75269534 75269534 single base substitution C T synonymous_variant P419P 1257G>A LUSC-KR 16 75269534 75269534 single base substitution C T synonymous_variant P421P 1263G>A LUSC-KR 16 75269534 75269534 single base substitution C T synonymous_variant P439P 1317G>A LUSC-KR 16 75269534 75269534 single base substitution C T synonymous_variant P467P 1401G>A LUSC-KR 16 75271022 75271022 single base substitution C A intron_variant LUSC-KR 16 75271022 75271022 single base substitution C A upstream_gene_variant LUSC-KR 16 75275657 75275657 single base substitution C T downstream_gene_variant LUSC-KR 16 75275657 75275657 single base substitution C T intron_variant LUSC-KR 16 75275657 75275657 single base substitution C T upstream_gene_variant LUSC-KR 16 75276173 75276173 single base substitution C G downstream_gene_variant LUSC-KR 16 75276173 75276173 single base substitution C G intron_variant LUSC-KR 16 75276173 75276173 single base substitution C G upstream_gene_variant LUSC-KR 16 75289165 75289165 single base substitution G A intron_variant LUSC-KR 16 75289165 75289165 single base substitution G A upstream_gene_variant LUSC-KR 16 75304725 75304725 single base substitution G A upstream_gene_variant LUSC-US 16 75263572 75263572 single base substitution T A 3_prime_UTR_variant LUSC-US 16 75263572 75263572 single base substitution T A exon_variant LUSC-US 16 75263572 75263572 single base substitution T A missense_variant N669I 2006A>T LUSC-US 16 75263572 75263572 single base substitution T A missense_variant N788I 2363A>T LUSC-US 16 75263572 75263572 single base substitution T A missense_variant N815I 2444A>T LUSC-US 16 75263572 75263572 single base substitution T A missense_variant N817I 2450A>T LUSC-US 16 75263572 75263572 single base substitution T A missense_variant N835I 2504A>T LUSC-US 16 75263572 75263572 single base substitution T A missense_variant N863I 2588A>T LUSC-US 16 75263596 75263596 single base substitution C T 3_prime_UTR_variant LUSC-US 16 75263596 75263596 single base substitution C T exon_variant LUSC-US 16 75263596 75263596 single base substitution C T missense_variant R661H 1982G>A LUSC-US 16 75263596 75263596 single base substitution C T missense_variant R780H 2339G>A LUSC-US 16 75263596 75263596 single base substitution C T missense_variant R807H 2420G>A LUSC-US 16 75263596 75263596 single base substitution C T missense_variant R809H 2426G>A LUSC-US 16 75263596 75263596 single base substitution C T missense_variant R827H 2480G>A LUSC-US 16 75263596 75263596 single base substitution C T missense_variant R855H 2564G>A LUSC-US 16 75263738 75263738 single base substitution C A 3_prime_UTR_variant LUSC-US 16 75263738 75263738 single base substitution C A exon_variant LUSC-US 16 75263738 75263738 single base substitution C A missense_variant V614L 1840G>T LUSC-US 16 75263738 75263738 single base substitution C A missense_variant V733L 2197G>T LUSC-US 16 75263738 75263738 single base substitution C A missense_variant V760L 2278G>T LUSC-US 16 75263738 75263738 single base substitution C A missense_variant V762L 2284G>T LUSC-US 16 75263738 75263738 single base substitution C A missense_variant V780L 2338G>T LUSC-US 16 75263738 75263738 single base substitution C A missense_variant V808L 2422G>T LUSC-US 16 75263782 75263782 single base substitution T C 3_prime_UTR_variant LUSC-US 16 75263782 75263782 single base substitution T C exon_variant LUSC-US 16 75263782 75263782 single base substitution T C missense_variant Y599C 1796A>G LUSC-US 16 75263782 75263782 single base substitution T C missense_variant Y718C 2153A>G LUSC-US 16 75263782 75263782 single base substitution T C missense_variant Y745C 2234A>G LUSC-US 16 75263782 75263782 single base substitution T C missense_variant Y747C 2240A>G LUSC-US 16 75263782 75263782 single base substitution T C missense_variant Y765C 2294A>G LUSC-US 16 75263782 75263782 single base substitution T C missense_variant Y793C 2378A>G LUSC-US 16 75263896 75263896 single base substitution T A 3_prime_UTR_variant LUSC-US 16 75263896 75263896 single base substitution T A exon_variant LUSC-US 16 75263896 75263896 single base substitution T A missense_variant Q561L 1682A>T LUSC-US 16 75263896 75263896 single base substitution T A missense_variant Q680L 2039A>T LUSC-US 16 75263896 75263896 single base substitution T A missense_variant Q707L 2120A>T LUSC-US 16 75263896 75263896 single base substitution T A missense_variant Q709L 2126A>T LUSC-US 16 75263896 75263896 single base substitution T A missense_variant Q727L 2180A>T LUSC-US 16 75263896 75263896 single base substitution T A missense_variant Q755L 2264A>T LUSC-US 16 75268934 75268934 single base substitution C G 3_prime_UTR_variant LUSC-US 16 75268934 75268934 single base substitution C G downstream_gene_variant LUSC-US 16 75268934 75268934 single base substitution C G exon_variant LUSC-US 16 75268934 75268934 single base substitution C G synonymous_variant L473L 1419G>C LUSC-US 16 75268934 75268934 single base substitution C G synonymous_variant L592L 1776G>C LUSC-US 16 75268934 75268934 single base substitution C G synonymous_variant L619L 1857G>C LUSC-US 16 75268934 75268934 single base substitution C G synonymous_variant L621L 1863G>C LUSC-US 16 75268934 75268934 single base substitution C G synonymous_variant L639L 1917G>C LUSC-US 16 75268934 75268934 single base substitution C G synonymous_variant L667L 2001G>C LUSC-US 16 75269714 75269714 single base substitution C A 3_prime_UTR_variant LUSC-US 16 75269714 75269714 single base substitution C A downstream_gene_variant LUSC-US 16 75269714 75269714 single base substitution C A exon_variant LUSC-US 16 75269714 75269714 single base substitution C A synonymous_variant V188V 564G>T LUSC-US 16 75269714 75269714 single base substitution C A synonymous_variant V213V 639G>T LUSC-US 16 75269714 75269714 single base substitution C A synonymous_variant V332V 996G>T LUSC-US 16 75269714 75269714 single base substitution C A synonymous_variant V359V 1077G>T LUSC-US 16 75269714 75269714 single base substitution C A synonymous_variant V361V 1083G>T LUSC-US 16 75269714 75269714 single base substitution C A synonymous_variant V379V 1137G>T LUSC-US 16 75269714 75269714 single base substitution C A synonymous_variant V407V 1221G>T LUSC-US 16 75276604 75276604 single base substitution G T 3_prime_UTR_variant LUSC-US 16 75276604 75276604 single base substitution G T downstream_gene_variant LUSC-US 16 75276604 75276604 single base substitution G T intron_variant LUSC-US 16 75276604 75276604 single base substitution G T missense_variant P104T 310C>A LUSC-US 16 75276604 75276604 single base substitution G T missense_variant P131T 391C>A LUSC-US 16 75276604 75276604 single base substitution G T missense_variant P133T 397C>A LUSC-US 16 75276604 75276604 single base substitution G T missense_variant P151T 451C>A LUSC-US 16 75276604 75276604 single base substitution G T missense_variant P179T 535C>A LUSC-US 16 75276604 75276604 single base substitution G T upstream_gene_variant MALY-DE 16 75261370 75261370 single base substitution T C downstream_gene_variant MALY-DE 16 75262325 75262325 single base substitution C T downstream_gene_variant MALY-DE 16 75262494 75262494 single base substitution A G downstream_gene_variant MALY-DE 16 75264928 75264928 single base substitution G T downstream_gene_variant MALY-DE 16 75264928 75264928 single base substitution G T intron_variant MALY-DE 16 75267995 75267996 deletion of <=200bp AC - downstream_gene_variant MALY-DE 16 75267995 75267996 deletion of <=200bp AC - intron_variant MALY-DE 16 75274261 75274261 single base substitution C T downstream_gene_variant MALY-DE 16 75274261 75274261 single base substitution C T intron_variant MALY-DE 16 75274261 75274261 single base substitution C T upstream_gene_variant MALY-DE 16 75288178 75288178 single base substitution G T intron_variant MALY-DE 16 75288178 75288178 single base substitution G T upstream_gene_variant MALY-DE 16 75290218 75290218 insertion of <=200bp - CCTGCTCTCGAGGGTGGAGTG intron_variant MALY-DE 16 75290218 75290218 insertion of <=200bp - CCTGCTCTCGAGGGTGGAGTG upstream_gene_variant MALY-DE 16 75295369 75295369 single base substitution C T intron_variant MALY-DE 16 75298276 75298276 single base substitution G A 5_prime_UTR_variant MALY-DE 16 75298276 75298276 single base substitution G A exon_variant MALY-DE 16 75298276 75298276 single base substitution G A intron_variant MALY-DE 16 75298276 75298276 single base substitution G A synonymous_variant G41G 123C>T MALY-DE 16 75305253 75305253 single base substitution A T upstream_gene_variant MELA-AU 16 75259051 75259051 single base substitution G A downstream_gene_variant MELA-AU 16 75260749 75260749 single base substitution G A downstream_gene_variant MELA-AU 16 75261025 75261025 single base substitution A T downstream_gene_variant MELA-AU 16 75261659 75261659 single base substitution G A downstream_gene_variant MELA-AU 16 75261770 75261770 single base substitution A G downstream_gene_variant MELA-AU 16 75261772 75261772 single base substitution C A downstream_gene_variant MELA-AU 16 75261926 75261926 single base substitution G A downstream_gene_variant MELA-AU 16 75262835 75262835 single base substitution C T downstream_gene_variant MELA-AU 16 75262994 75262994 single base substitution G A 3_prime_UTR_variant MELA-AU 16 75262994 75262994 single base substitution G A downstream_gene_variant MELA-AU 16 75262994 75262994 single base substitution G A exon_variant MELA-AU 16 75263225 75263225 single base substitution G A 3_prime_UTR_variant MELA-AU 16 75263225 75263225 single base substitution G A downstream_gene_variant MELA-AU 16 75263225 75263225 single base substitution G A exon_variant MELA-AU 16 75264219 75264219 single base substitution C T intron_variant MELA-AU 16 75265241 75265242 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant MELA-AU 16 75265241 75265242 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 16 75266034 75266035 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 75266034 75266035 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 75268868 75268868 single base substitution G A 3_prime_UTR_variant MELA-AU 16 75268868 75268868 single base substitution G A downstream_gene_variant MELA-AU 16 75268868 75268868 single base substitution G A exon_variant MELA-AU 16 75268868 75268868 single base substitution G A synonymous_variant F495F 1485C>T MELA-AU 16 75268868 75268868 single base substitution G A synonymous_variant F614F 1842C>T MELA-AU 16 75268868 75268868 single base substitution G A synonymous_variant F641F 1923C>T MELA-AU 16 75268868 75268868 single base substitution G A synonymous_variant F643F 1929C>T MELA-AU 16 75268868 75268868 single base substitution G A synonymous_variant F661F 1983C>T MELA-AU 16 75268868 75268868 single base substitution G A synonymous_variant F689F 2067C>T MELA-AU 16 75269434 75269434 single base substitution C T 3_prime_UTR_variant MELA-AU 16 75269434 75269434 single base substitution C T downstream_gene_variant MELA-AU 16 75269434 75269434 single base substitution C T exon_variant MELA-AU 16 75269434 75269434 single base substitution C T missense_variant E307K 919G>A MELA-AU 16 75269434 75269434 single base substitution C T missense_variant E426K 1276G>A MELA-AU 16 75269434 75269434 single base substitution C T missense_variant E453K 1357G>A MELA-AU 16 75269434 75269434 single base substitution C T missense_variant E455K 1363G>A MELA-AU 16 75269434 75269434 single base substitution C T missense_variant E473K 1417G>A MELA-AU 16 75269434 75269434 single base substitution C T missense_variant E501K 1501G>A MELA-AU 16 75269790 75269790 single base substitution G A 3_prime_UTR_variant MELA-AU 16 75269790 75269790 single base substitution G A downstream_gene_variant MELA-AU 16 75269790 75269790 single base substitution G A exon_variant MELA-AU 16 75269790 75269790 single base substitution G A missense_variant A163V 488C>T MELA-AU 16 75269790 75269790 single base substitution G A missense_variant A188V 563C>T MELA-AU 16 75269790 75269790 single base substitution G A missense_variant A307V 920C>T MELA-AU 16 75269790 75269790 single base substitution G A missense_variant A334V 1001C>T MELA-AU 16 75269790 75269790 single base substitution G A missense_variant A336V 1007C>T MELA-AU 16 75269790 75269790 single base substitution G A missense_variant A354V 1061C>T MELA-AU 16 75269790 75269790 single base substitution G A missense_variant A382V 1145C>T MELA-AU 16 75270658 75270658 single base substitution G A exon_variant MELA-AU 16 75270658 75270658 single base substitution G A intron_variant MELA-AU 16 75270658 75270658 single base substitution G A upstream_gene_variant MELA-AU 16 75270958 75270958 single base substitution G A intron_variant MELA-AU 16 75270958 75270958 single base substitution G A upstream_gene_variant MELA-AU 16 75271132 75271132 single base substitution G A 3_prime_UTR_variant MELA-AU 16 75271132 75271132 single base substitution G A exon_variant MELA-AU 16 75271132 75271132 single base substitution G A synonymous_variant I100I 300C>T MELA-AU 16 75271132 75271132 single base substitution G A synonymous_variant I114I 342C>T MELA-AU 16 75271132 75271132 single base substitution G A synonymous_variant I219I 657C>T MELA-AU 16 75271132 75271132 single base substitution G A synonymous_variant I246I 738C>T MELA-AU 16 75271132 75271132 single base substitution G A synonymous_variant I248I 744C>T MELA-AU 16 75271132 75271132 single base substitution G A synonymous_variant I266I 798C>T MELA-AU 16 75271132 75271132 single base substitution G A synonymous_variant I294I 882C>T MELA-AU 16 75271132 75271132 single base substitution G A upstream_gene_variant MELA-AU 16 75271464 75271464 single base substitution G A intron_variant MELA-AU 16 75271464 75271464 single base substitution G A upstream_gene_variant MELA-AU 16 75271945 75271945 single base substitution G A downstream_gene_variant MELA-AU 16 75271945 75271945 single base substitution G A intron_variant MELA-AU 16 75271945 75271945 single base substitution G A upstream_gene_variant MELA-AU 16 75272313 75272313 single base substitution C G downstream_gene_variant MELA-AU 16 75272313 75272313 single base substitution C G exon_variant MELA-AU 16 75272313 75272313 single base substitution C G intron_variant MELA-AU 16 75272313 75272313 single base substitution C G upstream_gene_variant MELA-AU 16 75272887 75272888 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant MELA-AU 16 75272887 75272888 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 16 75272887 75272888 multiple base substitution (>=2bp and <=200bp) CC AT upstream_gene_variant MELA-AU 16 75273581 75273581 single base substitution C A downstream_gene_variant MELA-AU 16 75273581 75273581 single base substitution C A intron_variant MELA-AU 16 75273581 75273581 single base substitution C A upstream_gene_variant MELA-AU 16 75273931 75273931 single base substitution G A downstream_gene_variant MELA-AU 16 75273931 75273931 single base substitution G A intron_variant MELA-AU 16 75273931 75273931 single base substitution G A upstream_gene_variant MELA-AU 16 75274912 75274912 single base substitution G A downstream_gene_variant MELA-AU 16 75274912 75274912 single base substitution G A intron_variant MELA-AU 16 75274912 75274912 single base substitution G A upstream_gene_variant MELA-AU 16 75275596 75275596 single base substitution G A downstream_gene_variant MELA-AU 16 75275596 75275596 single base substitution G A intron_variant MELA-AU 16 75275596 75275596 single base substitution G A upstream_gene_variant MELA-AU 16 75275843 75275843 single base substitution G A downstream_gene_variant MELA-AU 16 75275843 75275843 single base substitution G A intron_variant MELA-AU 16 75275843 75275843 single base substitution G A upstream_gene_variant MELA-AU 16 75275921 75275921 single base substitution G A downstream_gene_variant MELA-AU 16 75275921 75275921 single base substitution G A intron_variant MELA-AU 16 75275921 75275921 single base substitution G A upstream_gene_variant MELA-AU 16 75275958 75275958 single base substitution C T downstream_gene_variant MELA-AU 16 75275958 75275958 single base substitution C T intron_variant MELA-AU 16 75275958 75275958 single base substitution C T upstream_gene_variant MELA-AU 16 75276947 75276948 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 16 75276947 75276948 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 16 75276947 75276948 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 75276947 75276948 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S16F 47CC>TT MELA-AU 16 75276947 75276948 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S18F 53CC>TT MELA-AU 16 75276947 75276948 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S36F 107CC>TT MELA-AU 16 75276947 75276948 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S64F 191CC>TT MELA-AU 16 75276947 75276948 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 75277189 75277189 single base substitution T C intron_variant MELA-AU 16 75277189 75277189 single base substitution T C upstream_gene_variant MELA-AU 16 75278272 75278272 single base substitution G A intron_variant MELA-AU 16 75278272 75278272 single base substitution G A upstream_gene_variant MELA-AU 16 75279073 75279073 single base substitution T A intron_variant MELA-AU 16 75279073 75279073 single base substitution T A upstream_gene_variant MELA-AU 16 75279681 75279681 single base substitution G A intron_variant MELA-AU 16 75279681 75279681 single base substitution G A upstream_gene_variant MELA-AU 16 75279853 75279853 single base substitution A G intron_variant MELA-AU 16 75279853 75279853 single base substitution A G upstream_gene_variant MELA-AU 16 75279855 75279855 single base substitution G A intron_variant MELA-AU 16 75279855 75279855 single base substitution G A upstream_gene_variant MELA-AU 16 75280152 75280152 single base substitution A G intron_variant MELA-AU 16 75280152 75280152 single base substitution A G upstream_gene_variant MELA-AU 16 75280316 75280316 single base substitution G A intron_variant MELA-AU 16 75280316 75280316 single base substitution G A upstream_gene_variant MELA-AU 16 75280455 75280455 single base substitution G A intron_variant MELA-AU 16 75280455 75280455 single base substitution G A upstream_gene_variant MELA-AU 16 75280689 75280689 single base substitution G A intron_variant MELA-AU 16 75280689 75280689 single base substitution G A upstream_gene_variant MELA-AU 16 75280794 75280794 single base substitution G A intron_variant MELA-AU 16 75280794 75280794 single base substitution G A upstream_gene_variant MELA-AU 16 75281510 75281510 single base substitution A G intron_variant MELA-AU 16 75281510 75281510 single base substitution A G upstream_gene_variant MELA-AU 16 75281810 75281810 single base substitution G A intron_variant MELA-AU 16 75283880 75283880 single base substitution G A exon_variant MELA-AU 16 75283880 75283880 single base substitution G A intron_variant MELA-AU 16 75283880 75283880 single base substitution G A upstream_gene_variant MELA-AU 16 75286230 75286231 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 16 75286230 75286231 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 75286230 75286231 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 75286309 75286309 single base substitution G A intron_variant MELA-AU 16 75286309 75286309 single base substitution G A upstream_gene_variant MELA-AU 16 75287386 75287386 single base substitution A C intron_variant MELA-AU 16 75287386 75287386 single base substitution A C upstream_gene_variant MELA-AU 16 75287455 75287455 single base substitution G A intron_variant MELA-AU 16 75287455 75287455 single base substitution G A upstream_gene_variant MELA-AU 16 75287500 75287501 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 75287500 75287501 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 75288091 75288091 single base substitution G A intron_variant MELA-AU 16 75288091 75288091 single base substitution G A upstream_gene_variant MELA-AU 16 75288970 75288970 single base substitution G A intron_variant MELA-AU 16 75288970 75288970 single base substitution G A upstream_gene_variant MELA-AU 16 75289876 75289876 single base substitution G A intron_variant MELA-AU 16 75289876 75289876 single base substitution G A upstream_gene_variant MELA-AU 16 75290425 75290425 single base substitution G A intron_variant MELA-AU 16 75290425 75290425 single base substitution G A upstream_gene_variant MELA-AU 16 75292826 75292826 single base substitution A C intron_variant MELA-AU 16 75292826 75292826 single base substitution A C upstream_gene_variant MELA-AU 16 75292858 75292858 single base substitution G A intron_variant MELA-AU 16 75292858 75292858 single base substitution G A upstream_gene_variant MELA-AU 16 75293165 75293165 single base substitution G A intron_variant MELA-AU 16 75293165 75293165 single base substitution G A upstream_gene_variant MELA-AU 16 75293372 75293372 single base substitution T C intron_variant MELA-AU 16 75293372 75293372 single base substitution T C upstream_gene_variant MELA-AU 16 75293568 75293568 single base substitution G A intron_variant MELA-AU 16 75293568 75293568 single base substitution G A upstream_gene_variant MELA-AU 16 75293677 75293677 single base substitution G A intron_variant MELA-AU 16 75293677 75293677 single base substitution G A upstream_gene_variant MELA-AU 16 75294018 75294019 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 75294018 75294019 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 16 75295672 75295672 single base substitution G A intron_variant MELA-AU 16 75295910 75295910 single base substitution C T intron_variant MELA-AU 16 75295929 75295929 single base substitution A G intron_variant MELA-AU 16 75296297 75296297 single base substitution C T intron_variant MELA-AU 16 75296418 75296418 single base substitution G A intron_variant MELA-AU 16 75297022 75297022 single base substitution G A intron_variant MELA-AU 16 75298170 75298170 single base substitution G A 3_prime_UTR_variant MELA-AU 16 75298170 75298170 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 16 75298170 75298170 single base substitution G A intron_variant MELA-AU 16 75298413 75298413 single base substitution C T 5_prime_UTR_variant MELA-AU 16 75298413 75298413 single base substitution C T intron_variant MELA-AU 16 75298413 75298413 single base substitution C T upstream_gene_variant MELA-AU 16 75299083 75299083 single base substitution C T 5_prime_UTR_variant MELA-AU 16 75299083 75299083 single base substitution C T intron_variant MELA-AU 16 75299083 75299083 single base substitution C T upstream_gene_variant MELA-AU 16 75300321 75300321 single base substitution C T intron_variant MELA-AU 16 75300321 75300321 single base substitution C T upstream_gene_variant MELA-AU 16 75300351 75300351 single base substitution C T intron_variant MELA-AU 16 75300351 75300351 single base substitution C T upstream_gene_variant MELA-AU 16 75301118 75301119 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 75301118 75301119 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 75301446 75301446 single base substitution G A intron_variant MELA-AU 16 75301446 75301446 single base substitution G A upstream_gene_variant MELA-AU 16 75301540 75301540 single base substitution C T intron_variant MELA-AU 16 75301540 75301540 single base substitution C T upstream_gene_variant MELA-AU 16 75301619 75301619 single base substitution G T intron_variant MELA-AU 16 75301619 75301619 single base substitution G T upstream_gene_variant MELA-AU 16 75302275 75302275 single base substitution C T upstream_gene_variant MELA-AU 16 75302613 75302613 single base substitution C T upstream_gene_variant MELA-AU 16 75302754 75302754 single base substitution C T upstream_gene_variant MELA-AU 16 75303158 75303158 single base substitution T C upstream_gene_variant MELA-AU 16 75303872 75303872 single base substitution C T upstream_gene_variant MELA-AU 16 75303907 75303907 single base substitution C T upstream_gene_variant MELA-AU 16 75305128 75305128 single base substitution C T upstream_gene_variant MELA-AU 16 75305328 75305328 single base substitution G A upstream_gene_variant MELA-AU 16 75305737 75305738 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 16 75306526 75306526 single base substitution G A upstream_gene_variant ORCA-IN 16 75258726 75258726 single base substitution C T downstream_gene_variant ORCA-IN 16 75261670 75261670 single base substitution G A downstream_gene_variant ORCA-IN 16 75269128 75269128 single base substitution C A 3_prime_UTR_variant ORCA-IN 16 75269128 75269128 single base substitution C A downstream_gene_variant ORCA-IN 16 75269128 75269128 single base substitution C A exon_variant ORCA-IN 16 75269128 75269128 single base substitution C A missense_variant A409S 1225G>T ORCA-IN 16 75269128 75269128 single base substitution C A missense_variant A528S 1582G>T ORCA-IN 16 75269128 75269128 single base substitution C A missense_variant A555S 1663G>T ORCA-IN 16 75269128 75269128 single base substitution C A missense_variant A557S 1669G>T ORCA-IN 16 75269128 75269128 single base substitution C A missense_variant A575S 1723G>T ORCA-IN 16 75269128 75269128 single base substitution C A missense_variant A603S 1807G>T ORCA-IN 16 75269343 75269343 single base substitution C A 3_prime_UTR_variant ORCA-IN 16 75269343 75269343 single base substitution C A downstream_gene_variant ORCA-IN 16 75269343 75269343 single base substitution C A exon_variant ORCA-IN 16 75269343 75269343 single base substitution C A missense_variant G337V 1010G>T ORCA-IN 16 75269343 75269343 single base substitution C A missense_variant G456V 1367G>T ORCA-IN 16 75269343 75269343 single base substitution C A missense_variant G483V 1448G>T ORCA-IN 16 75269343 75269343 single base substitution C A missense_variant G485V 1454G>T ORCA-IN 16 75269343 75269343 single base substitution C A missense_variant G503V 1508G>T ORCA-IN 16 75269343 75269343 single base substitution C A missense_variant G531V 1592G>T ORCA-IN 16 75290408 75290408 single base substitution C A intron_variant ORCA-IN 16 75290408 75290408 single base substitution C A upstream_gene_variant OV-AU 16 75265620 75265620 single base substitution C T downstream_gene_variant OV-AU 16 75265620 75265620 single base substitution C T intron_variant OV-AU 16 75271051 75271051 single base substitution C A intron_variant OV-AU 16 75271051 75271051 single base substitution C A upstream_gene_variant OV-AU 16 75271052 75271052 single base substitution C A intron_variant OV-AU 16 75271052 75271052 single base substitution C A upstream_gene_variant OV-AU 16 75285412 75285412 single base substitution G C 5_prime_UTR_variant OV-AU 16 75285412 75285412 single base substitution G C intron_variant OV-AU 16 75285412 75285412 single base substitution G C upstream_gene_variant OV-AU 16 75289133 75289133 single base substitution C A intron_variant OV-AU 16 75289133 75289133 single base substitution C A upstream_gene_variant OV-AU 16 75295533 75295533 single base substitution C G intron_variant OV-AU 16 75298736 75298736 single base substitution A G 5_prime_UTR_variant OV-AU 16 75298736 75298736 single base substitution A G intron_variant OV-AU 16 75298736 75298736 single base substitution A G upstream_gene_variant OV-AU 16 75302191 75302191 single base substitution C G upstream_gene_variant PACA-AU 16 75260770 75260770 single base substitution G A downstream_gene_variant PACA-AU 16 75262529 75262529 single base substitution C A downstream_gene_variant PACA-AU 16 75263423 75263423 single base substitution G A 3_prime_UTR_variant PACA-AU 16 75263423 75263423 single base substitution G A exon_variant PACA-AU 16 75263423 75263423 single base substitution G A synonymous_variant L719L 2155C>T PACA-AU 16 75263423 75263423 single base substitution G A synonymous_variant L838L 2512C>T PACA-AU 16 75263423 75263423 single base substitution G A synonymous_variant L865L 2593C>T PACA-AU 16 75263423 75263423 single base substitution G A synonymous_variant L867L 2599C>T PACA-AU 16 75263423 75263423 single base substitution G A synonymous_variant L885L 2653C>T PACA-AU 16 75263423 75263423 single base substitution G A synonymous_variant L913L 2737C>T PACA-AU 16 75264022 75264022 single base substitution G A intron_variant PACA-AU 16 75264929 75264929 single base substitution T G downstream_gene_variant PACA-AU 16 75264929 75264929 single base substitution T G intron_variant PACA-AU 16 75267266 75267266 single base substitution G C downstream_gene_variant PACA-AU 16 75267266 75267266 single base substitution G C intron_variant PACA-AU 16 75268542 75268542 single base substitution C T downstream_gene_variant PACA-AU 16 75268542 75268542 single base substitution C T intron_variant PACA-AU 16 75272349 75272349 single base substitution G A downstream_gene_variant PACA-AU 16 75272349 75272349 single base substitution G A exon_variant PACA-AU 16 75272349 75272349 single base substitution G A intron_variant PACA-AU 16 75272349 75272349 single base substitution G A upstream_gene_variant PACA-AU 16 75273520 75273520 insertion of <=200bp - C downstream_gene_variant PACA-AU 16 75273520 75273520 insertion of <=200bp - C intron_variant PACA-AU 16 75273520 75273520 insertion of <=200bp - C upstream_gene_variant PACA-AU 16 75276821 75276821 single base substitution G A 3_prime_UTR_variant PACA-AU 16 75276821 75276821 single base substitution G A downstream_gene_variant PACA-AU 16 75276821 75276821 single base substitution G A synonymous_variant L106L 318C>T PACA-AU 16 75276821 75276821 single base substitution G A synonymous_variant L31L 93C>T PACA-AU 16 75276821 75276821 single base substitution G A synonymous_variant L58L 174C>T PACA-AU 16 75276821 75276821 single base substitution G A synonymous_variant L60L 180C>T PACA-AU 16 75276821 75276821 single base substitution G A synonymous_variant L78L 234C>T PACA-AU 16 75276821 75276821 single base substitution G A upstream_gene_variant PACA-AU 16 75278413 75278413 single base substitution C T intron_variant PACA-AU 16 75278413 75278413 single base substitution C T upstream_gene_variant PACA-AU 16 75280717 75280717 single base substitution C G intron_variant PACA-AU 16 75280717 75280717 single base substitution C G upstream_gene_variant PACA-AU 16 75282217 75282217 single base substitution G A intron_variant PACA-AU 16 75282217 75282217 single base substitution G A upstream_gene_variant PACA-AU 16 75284850 75284850 single base substitution G A intron_variant PACA-AU 16 75284850 75284850 single base substitution G A upstream_gene_variant PACA-AU 16 75292125 75292125 single base substitution C T intron_variant PACA-AU 16 75292125 75292125 single base substitution C T upstream_gene_variant PACA-AU 16 75293830 75293830 single base substitution G A intron_variant PACA-AU 16 75293830 75293830 single base substitution G A upstream_gene_variant PACA-AU 16 75296466 75296466 single base substitution C T intron_variant PACA-AU 16 75301729 75301729 single base substitution C T intron_variant PACA-AU 16 75301729 75301729 single base substitution C T upstream_gene_variant PACA-AU 16 75302731 75302731 single base substitution G A upstream_gene_variant PACA-CA 16 75258190 75258190 single base substitution G C downstream_gene_variant PACA-CA 16 75262061 75262061 single base substitution A G downstream_gene_variant PACA-CA 16 75262675 75262675 single base substitution G A downstream_gene_variant PACA-CA 16 75262806 75262806 single base substitution C G downstream_gene_variant PACA-CA 16 75266058 75266062 deletion of <=200bp ATTTT - downstream_gene_variant PACA-CA 16 75266058 75266062 deletion of <=200bp ATTTT - intron_variant PACA-CA 16 75267143 75267143 single base substitution C T downstream_gene_variant PACA-CA 16 75267143 75267143 single base substitution C T intron_variant PACA-CA 16 75267888 75267888 single base substitution A G downstream_gene_variant PACA-CA 16 75267888 75267888 single base substitution A G intron_variant PACA-CA 16 75269564 75269564 single base substitution C T 3_prime_UTR_variant PACA-CA 16 75269564 75269564 single base substitution C T downstream_gene_variant PACA-CA 16 75269564 75269564 single base substitution C T exon_variant PACA-CA 16 75269564 75269564 single base substitution C T synonymous_variant A263A 789G>A PACA-CA 16 75269564 75269564 single base substitution C T synonymous_variant A382A 1146G>A PACA-CA 16 75269564 75269564 single base substitution C T synonymous_variant A409A 1227G>A PACA-CA 16 75269564 75269564 single base substitution C T synonymous_variant A411A 1233G>A PACA-CA 16 75269564 75269564 single base substitution C T synonymous_variant A429A 1287G>A PACA-CA 16 75269564 75269564 single base substitution C T synonymous_variant A457A 1371G>A PACA-CA 16 75273163 75273163 single base substitution G A downstream_gene_variant PACA-CA 16 75273163 75273163 single base substitution G A intron_variant PACA-CA 16 75273163 75273163 single base substitution G A upstream_gene_variant PACA-CA 16 75275018 75275018 single base substitution C T downstream_gene_variant PACA-CA 16 75275018 75275018 single base substitution C T intron_variant PACA-CA 16 75275018 75275018 single base substitution C T upstream_gene_variant PACA-CA 16 75276078 75276078 single base substitution G A downstream_gene_variant PACA-CA 16 75276078 75276078 single base substitution G A intron_variant PACA-CA 16 75276078 75276078 single base substitution G A upstream_gene_variant PACA-CA 16 75278253 75278253 single base substitution G A intron_variant PACA-CA 16 75278253 75278253 single base substitution G A upstream_gene_variant PACA-CA 16 75280794 75280794 single base substitution G C intron_variant PACA-CA 16 75280794 75280794 single base substitution G C upstream_gene_variant PACA-CA 16 75283893 75283893 single base substitution A C exon_variant PACA-CA 16 75283893 75283893 single base substitution A C intron_variant PACA-CA 16 75283893 75283893 single base substitution A C upstream_gene_variant PACA-CA 16 75284786 75284786 single base substitution G A 5_prime_UTR_variant PACA-CA 16 75284786 75284786 single base substitution G A intron_variant PACA-CA 16 75284786 75284786 single base substitution G A upstream_gene_variant PACA-CA 16 75286626 75286626 single base substitution C T intron_variant PACA-CA 16 75286626 75286626 single base substitution C T upstream_gene_variant PACA-CA 16 75287979 75287979 single base substitution G A intron_variant PACA-CA 16 75287979 75287979 single base substitution G A upstream_gene_variant PACA-CA 16 75296087 75296099 deletion of <=200bp GGCTGAGATCCCA - intron_variant PACA-CA 16 75296212 75296212 insertion of <=200bp - G intron_variant PACA-CA 16 75297029 75297029 single base substitution C T intron_variant PACA-CA 16 75299508 75299508 single base substitution C G intron_variant PACA-CA 16 75299508 75299508 single base substitution C G upstream_gene_variant PACA-CA 16 75304234 75304234 single base substitution C T upstream_gene_variant PACA-CA 16 75305446 75305446 single base substitution C G upstream_gene_variant PAEN-AU 16 75263898 75263898 single base substitution T C 3_prime_UTR_variant PAEN-AU 16 75263898 75263898 single base substitution T C exon_variant PAEN-AU 16 75263898 75263898 single base substitution T C synonymous_variant E560E 1680A>G PAEN-AU 16 75263898 75263898 single base substitution T C synonymous_variant E679E 2037A>G PAEN-AU 16 75263898 75263898 single base substitution T C synonymous_variant E706E 2118A>G PAEN-AU 16 75263898 75263898 single base substitution T C synonymous_variant E708E 2124A>G PAEN-AU 16 75263898 75263898 single base substitution T C synonymous_variant E726E 2178A>G PAEN-AU 16 75263898 75263898 single base substitution T C synonymous_variant E754E 2262A>G PAEN-AU 16 75289168 75289168 single base substitution T G intron_variant PAEN-AU 16 75289168 75289168 single base substitution T G upstream_gene_variant PAEN-AU 16 75299826 75299826 single base substitution T G 5_prime_UTR_variant PAEN-AU 16 75299826 75299826 single base substitution T G intron_variant PAEN-AU 16 75299826 75299826 single base substitution T G upstream_gene_variant PBCA-DE 16 75267664 75267664 single base substitution G A downstream_gene_variant PBCA-DE 16 75267664 75267664 single base substitution G A intron_variant PBCA-DE 16 75298597 75298597 single base substitution T G 5_prime_UTR_variant PBCA-DE 16 75298597 75298597 single base substitution T G intron_variant PBCA-DE 16 75298597 75298597 single base substitution T G upstream_gene_variant PBCA-DE 16 75302365 75302365 single base substitution C A upstream_gene_variant PBCA-DE 16 75305938 75305938 single base substitution C G upstream_gene_variant PRAD-CA 16 75262031 75262031 single base substitution G T downstream_gene_variant PRAD-CA 16 75277448 75277448 single base substitution G A intron_variant PRAD-CA 16 75277448 75277448 single base substitution G A upstream_gene_variant PRAD-CA 16 75280943 75280943 single base substitution G A intron_variant PRAD-CA 16 75280943 75280943 single base substitution G A upstream_gene_variant PRAD-CA 16 75293711 75293711 single base substitution C T intron_variant PRAD-CA 16 75293711 75293711 single base substitution C T upstream_gene_variant PRAD-UK 16 75259568 75259568 single base substitution C A downstream_gene_variant PRAD-UK 16 75259758 75259758 single base substitution G A downstream_gene_variant PRAD-UK 16 75272256 75272256 single base substitution G C downstream_gene_variant PRAD-UK 16 75272256 75272256 single base substitution G C exon_variant PRAD-UK 16 75272256 75272256 single base substitution G C intron_variant PRAD-UK 16 75272256 75272256 single base substitution G C upstream_gene_variant PRAD-UK 16 75272646 75272646 insertion of <=200bp - A downstream_gene_variant PRAD-UK 16 75272646 75272646 insertion of <=200bp - A intron_variant PRAD-UK 16 75272646 75272646 insertion of <=200bp - A upstream_gene_variant PRAD-UK 16 75286236 75286236 single base substitution G A 5_prime_UTR_variant PRAD-UK 16 75286236 75286236 single base substitution G A intron_variant PRAD-UK 16 75286236 75286236 single base substitution G A upstream_gene_variant PRAD-UK 16 75293561 75293561 single base substitution T C intron_variant PRAD-UK 16 75293561 75293561 single base substitution T C upstream_gene_variant PRAD-US 16 75271144 75271144 deletion of <=200bp C - 3_prime_UTR_variant PRAD-US 16 75271144 75271144 deletion of <=200bp C - exon_variant PRAD-US 16 75271144 75271144 deletion of <=200bp C - frameshift_variant G110 PRAD-US 16 75271144 75271144 deletion of <=200bp C - frameshift_variant G215 PRAD-US 16 75271144 75271144 deletion of <=200bp C - frameshift_variant G242 PRAD-US 16 75271144 75271144 deletion of <=200bp C - frameshift_variant G244 PRAD-US 16 75271144 75271144 deletion of <=200bp C - frameshift_variant G262 PRAD-US 16 75271144 75271144 deletion of <=200bp C - frameshift_variant G290 PRAD-US 16 75271144 75271144 deletion of <=200bp C - frameshift_variant G96 PRAD-US 16 75271144 75271144 deletion of <=200bp C - upstream_gene_variant READ-US 16 75269223 75269223 single base substitution G A 3_prime_UTR_variant READ-US 16 75269223 75269223 single base substitution G A downstream_gene_variant READ-US 16 75269223 75269223 single base substitution G A exon_variant READ-US 16 75269223 75269223 single base substitution G A missense_variant A377V 1130C>T READ-US 16 75269223 75269223 single base substitution G A missense_variant A496V 1487C>T READ-US 16 75269223 75269223 single base substitution G A missense_variant A523V 1568C>T READ-US 16 75269223 75269223 single base substitution G A missense_variant A525V 1574C>T READ-US 16 75269223 75269223 single base substitution G A missense_variant A543V 1628C>T READ-US 16 75269223 75269223 single base substitution G A missense_variant A571V 1712C>T RECA-EU 16 75275210 75275210 single base substitution G A downstream_gene_variant RECA-EU 16 75275210 75275210 single base substitution G A intron_variant RECA-EU 16 75275210 75275210 single base substitution G A upstream_gene_variant RECA-EU 16 75279926 75279926 single base substitution A G intron_variant RECA-EU 16 75279926 75279926 single base substitution A G upstream_gene_variant RECA-EU 16 75280891 75280891 single base substitution C A intron_variant RECA-EU 16 75280891 75280891 single base substitution C A upstream_gene_variant RECA-EU 16 75283066 75283066 single base substitution G C intron_variant RECA-EU 16 75283066 75283066 single base substitution G C upstream_gene_variant RECA-EU 16 75287817 75287817 single base substitution T A intron_variant RECA-EU 16 75287817 75287817 single base substitution T A upstream_gene_variant RECA-EU 16 75295187 75295187 single base substitution A G intron_variant RECA-EU 16 75295194 75295194 single base substitution C G intron_variant RECA-EU 16 75295341 75295341 single base substitution C T intron_variant RECA-EU 16 75305553 75305553 single base substitution T C upstream_gene_variant SKCA-BR 16 75259404 75259404 insertion of <=200bp - CT downstream_gene_variant SKCA-BR 16 75262759 75262759 single base substitution A C downstream_gene_variant SKCA-BR 16 75262994 75262994 single base substitution G A 3_prime_UTR_variant SKCA-BR 16 75262994 75262994 single base substitution G A downstream_gene_variant SKCA-BR 16 75262994 75262994 single base substitution G A exon_variant SKCA-BR 16 75266097 75266097 single base substitution C T downstream_gene_variant SKCA-BR 16 75266097 75266097 single base substitution C T intron_variant SKCA-BR 16 75267956 75267956 single base substitution C A downstream_gene_variant SKCA-BR 16 75267956 75267956 single base substitution C A intron_variant SKCA-BR 16 75268117 75268117 single base substitution A T downstream_gene_variant SKCA-BR 16 75268117 75268117 single base substitution A T intron_variant SKCA-BR 16 75271150 75271150 single base substitution G A 3_prime_UTR_variant SKCA-BR 16 75271150 75271150 single base substitution G A exon_variant SKCA-BR 16 75271150 75271150 single base substitution G A synonymous_variant A108A 324C>T SKCA-BR 16 75271150 75271150 single base substitution G A synonymous_variant A213A 639C>T SKCA-BR 16 75271150 75271150 single base substitution G A synonymous_variant A240A 720C>T SKCA-BR 16 75271150 75271150 single base substitution G A synonymous_variant A242A 726C>T SKCA-BR 16 75271150 75271150 single base substitution G A synonymous_variant A260A 780C>T SKCA-BR 16 75271150 75271150 single base substitution G A synonymous_variant A288A 864C>T SKCA-BR 16 75271150 75271150 single base substitution G A synonymous_variant A94A 282C>T SKCA-BR 16 75271150 75271150 single base substitution G A upstream_gene_variant SKCA-BR 16 75271833 75271833 single base substitution T G downstream_gene_variant SKCA-BR 16 75271833 75271833 single base substitution T G intron_variant SKCA-BR 16 75271833 75271833 single base substitution T G upstream_gene_variant SKCA-BR 16 75274252 75274252 single base substitution A G downstream_gene_variant SKCA-BR 16 75274252 75274252 single base substitution A G intron_variant SKCA-BR 16 75274252 75274252 single base substitution A G upstream_gene_variant SKCA-BR 16 75278570 75278570 single base substitution A C intron_variant SKCA-BR 16 75278570 75278570 single base substitution A C upstream_gene_variant SKCA-BR 16 75281739 75281739 single base substitution A C intron_variant SKCA-BR 16 75284172 75284172 single base substitution T C intron_variant SKCA-BR 16 75284172 75284172 single base substitution T C upstream_gene_variant SKCA-BR 16 75284398 75284398 single base substitution G C intron_variant SKCA-BR 16 75284398 75284398 single base substitution G C upstream_gene_variant SKCA-BR 16 75284406 75284406 single base substitution T G intron_variant SKCA-BR 16 75284406 75284406 single base substitution T G upstream_gene_variant SKCA-BR 16 75284412 75284412 single base substitution A G intron_variant SKCA-BR 16 75284412 75284412 single base substitution A G upstream_gene_variant SKCA-BR 16 75285119 75285119 single base substitution A C intron_variant SKCA-BR 16 75285119 75285119 single base substitution A C upstream_gene_variant SKCA-BR 16 75285669 75285669 single base substitution A G intron_variant SKCA-BR 16 75285669 75285669 single base substitution A G upstream_gene_variant SKCA-BR 16 75286916 75286916 single base substitution G T intron_variant SKCA-BR 16 75286916 75286916 single base substitution G T upstream_gene_variant SKCA-BR 16 75290662 75290662 single base substitution T C intron_variant SKCA-BR 16 75290662 75290662 single base substitution T C upstream_gene_variant SKCA-BR 16 75293775 75293775 single base substitution T A intron_variant SKCA-BR 16 75293775 75293775 single base substitution T A upstream_gene_variant SKCA-BR 16 75295235 75295235 single base substitution G A intron_variant SKCA-BR 16 75296247 75296247 single base substitution G A intron_variant SKCA-BR 16 75303336 75303336 single base substitution A C upstream_gene_variant SKCA-BR 16 75303378 75303378 single base substitution C T upstream_gene_variant SKCA-BR 16 75303987 75303987 insertion of <=200bp - TTTTTA upstream_gene_variant SKCA-BR 16 75303987 75303992 deletion of <=200bp TTTTTA - upstream_gene_variant SKCA-BR 16 75303987 75303997 deletion of <=200bp TTTTTATTTTA - upstream_gene_variant SKCM-US 16 75258657 75258657 single base substitution G A downstream_gene_variant SKCM-US 16 75263520 75263520 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75263520 75263520 single base substitution G A exon_variant SKCM-US 16 75263520 75263520 single base substitution G A synonymous_variant A686A 2058C>T SKCM-US 16 75263520 75263520 single base substitution G A synonymous_variant A805A 2415C>T SKCM-US 16 75263520 75263520 single base substitution G A synonymous_variant A832A 2496C>T SKCM-US 16 75263520 75263520 single base substitution G A synonymous_variant A834A 2502C>T SKCM-US 16 75263520 75263520 single base substitution G A synonymous_variant A852A 2556C>T SKCM-US 16 75263520 75263520 single base substitution G A synonymous_variant A880A 2640C>T SKCM-US 16 75263556 75263556 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75263556 75263556 single base substitution G A exon_variant SKCM-US 16 75263556 75263556 single base substitution G A synonymous_variant L674L 2022C>T SKCM-US 16 75263556 75263556 single base substitution G A synonymous_variant L793L 2379C>T SKCM-US 16 75263556 75263556 single base substitution G A synonymous_variant L820L 2460C>T SKCM-US 16 75263556 75263556 single base substitution G A synonymous_variant L822L 2466C>T SKCM-US 16 75263556 75263556 single base substitution G A synonymous_variant L840L 2520C>T SKCM-US 16 75263556 75263556 single base substitution G A synonymous_variant L868L 2604C>T SKCM-US 16 75263721 75263721 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75263721 75263721 single base substitution G A exon_variant SKCM-US 16 75263721 75263721 single base substitution G A synonymous_variant T619T 1857C>T SKCM-US 16 75263721 75263721 single base substitution G A synonymous_variant T738T 2214C>T SKCM-US 16 75263721 75263721 single base substitution G A synonymous_variant T765T 2295C>T SKCM-US 16 75263721 75263721 single base substitution G A synonymous_variant T767T 2301C>T SKCM-US 16 75263721 75263721 single base substitution G A synonymous_variant T785T 2355C>T SKCM-US 16 75263721 75263721 single base substitution G A synonymous_variant T813T 2439C>T SKCM-US 16 75263823 75263823 single base substitution T G 3_prime_UTR_variant SKCM-US 16 75263823 75263823 single base substitution T G exon_variant SKCM-US 16 75263823 75263823 single base substitution T G synonymous_variant T585T 1755A>C SKCM-US 16 75263823 75263823 single base substitution T G synonymous_variant T704T 2112A>C SKCM-US 16 75263823 75263823 single base substitution T G synonymous_variant T731T 2193A>C SKCM-US 16 75263823 75263823 single base substitution T G synonymous_variant T733T 2199A>C SKCM-US 16 75263823 75263823 single base substitution T G synonymous_variant T751T 2253A>C SKCM-US 16 75263823 75263823 single base substitution T G synonymous_variant T779T 2337A>C SKCM-US 16 75268868 75268868 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75268868 75268868 single base substitution G A downstream_gene_variant SKCM-US 16 75268868 75268868 single base substitution G A exon_variant SKCM-US 16 75268868 75268868 single base substitution G A synonymous_variant F495F 1485C>T SKCM-US 16 75268868 75268868 single base substitution G A synonymous_variant F614F 1842C>T SKCM-US 16 75268868 75268868 single base substitution G A synonymous_variant F641F 1923C>T SKCM-US 16 75268868 75268868 single base substitution G A synonymous_variant F643F 1929C>T SKCM-US 16 75268868 75268868 single base substitution G A synonymous_variant F661F 1983C>T SKCM-US 16 75268868 75268868 single base substitution G A synonymous_variant F689F 2067C>T SKCM-US 16 75268959 75268959 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75268959 75268959 single base substitution G A downstream_gene_variant SKCM-US 16 75268959 75268959 single base substitution G A exon_variant SKCM-US 16 75268959 75268959 single base substitution G A missense_variant P465L 1394C>T SKCM-US 16 75268959 75268959 single base substitution G A missense_variant P584L 1751C>T SKCM-US 16 75268959 75268959 single base substitution G A missense_variant P611L 1832C>T SKCM-US 16 75268959 75268959 single base substitution G A missense_variant P613L 1838C>T SKCM-US 16 75268959 75268959 single base substitution G A missense_variant P631L 1892C>T SKCM-US 16 75268959 75268959 single base substitution G A missense_variant P659L 1976C>T SKCM-US 16 75268985 75268985 single base substitution G T 3_prime_UTR_variant SKCM-US 16 75268985 75268985 single base substitution G T downstream_gene_variant SKCM-US 16 75268985 75268985 single base substitution G T exon_variant SKCM-US 16 75268985 75268985 single base substitution G T synonymous_variant L456L 1368C>A SKCM-US 16 75268985 75268985 single base substitution G T synonymous_variant L575L 1725C>A SKCM-US 16 75268985 75268985 single base substitution G T synonymous_variant L602L 1806C>A SKCM-US 16 75268985 75268985 single base substitution G T synonymous_variant L604L 1812C>A SKCM-US 16 75268985 75268985 single base substitution G T synonymous_variant L622L 1866C>A SKCM-US 16 75268985 75268985 single base substitution G T synonymous_variant L650L 1950C>A SKCM-US 16 75268999 75268999 single base substitution T A 3_prime_UTR_variant SKCM-US 16 75268999 75268999 single base substitution T A downstream_gene_variant SKCM-US 16 75268999 75268999 single base substitution T A exon_variant SKCM-US 16 75268999 75268999 single base substitution T A missense_variant N452Y 1354A>T SKCM-US 16 75268999 75268999 single base substitution T A missense_variant N571Y 1711A>T SKCM-US 16 75268999 75268999 single base substitution T A missense_variant N598Y 1792A>T SKCM-US 16 75268999 75268999 single base substitution T A missense_variant N600Y 1798A>T SKCM-US 16 75268999 75268999 single base substitution T A missense_variant N618Y 1852A>T SKCM-US 16 75268999 75268999 single base substitution T A missense_variant N646Y 1936A>T SKCM-US 16 75269071 75269071 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75269071 75269071 single base substitution G A downstream_gene_variant SKCM-US 16 75269071 75269071 single base substitution G A exon_variant SKCM-US 16 75269071 75269071 single base substitution G A synonymous_variant L428L 1282C>T SKCM-US 16 75269071 75269071 single base substitution G A synonymous_variant L547L 1639C>T SKCM-US 16 75269071 75269071 single base substitution G A synonymous_variant L574L 1720C>T SKCM-US 16 75269071 75269071 single base substitution G A synonymous_variant L576L 1726C>T SKCM-US 16 75269071 75269071 single base substitution G A synonymous_variant L594L 1780C>T SKCM-US 16 75269071 75269071 single base substitution G A synonymous_variant L622L 1864C>T SKCM-US 16 75269650 75269650 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75269650 75269650 single base substitution G A downstream_gene_variant SKCM-US 16 75269650 75269650 single base substitution G A exon_variant SKCM-US 16 75269650 75269650 single base substitution G A missense_variant P210S 628C>T SKCM-US 16 75269650 75269650 single base substitution G A missense_variant P235S 703C>T SKCM-US 16 75269650 75269650 single base substitution G A missense_variant P354S 1060C>T SKCM-US 16 75269650 75269650 single base substitution G A missense_variant P381S 1141C>T SKCM-US 16 75269650 75269650 single base substitution G A missense_variant P383S 1147C>T SKCM-US 16 75269650 75269650 single base substitution G A missense_variant P401S 1201C>T SKCM-US 16 75269650 75269650 single base substitution G A missense_variant P429S 1285C>T SKCM-US 16 75276399 75276399 single base substitution C T 3_prime_UTR_variant SKCM-US 16 75276399 75276399 single base substitution C T downstream_gene_variant SKCM-US 16 75276399 75276399 single base substitution C T intron_variant SKCM-US 16 75276399 75276399 single base substitution C T missense_variant R172H 515G>A SKCM-US 16 75276399 75276399 single base substitution C T missense_variant R199H 596G>A SKCM-US 16 75276399 75276399 single base substitution C T missense_variant R201H 602G>A SKCM-US 16 75276399 75276399 single base substitution C T missense_variant R219H 656G>A SKCM-US 16 75276399 75276399 single base substitution C T missense_variant R247H 740G>A SKCM-US 16 75276399 75276399 single base substitution C T missense_variant R67H 200G>A SKCM-US 16 75276399 75276399 single base substitution C T upstream_gene_variant SKCM-US 16 75276498 75276498 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75276498 75276498 single base substitution G A downstream_gene_variant SKCM-US 16 75276498 75276498 single base substitution G A intron_variant SKCM-US 16 75276498 75276498 single base substitution G A missense_variant P139L 416C>T SKCM-US 16 75276498 75276498 single base substitution G A missense_variant P166L 497C>T SKCM-US 16 75276498 75276498 single base substitution G A missense_variant P168L 503C>T SKCM-US 16 75276498 75276498 single base substitution G A missense_variant P186L 557C>T SKCM-US 16 75276498 75276498 single base substitution G A missense_variant P214L 641C>T SKCM-US 16 75276498 75276498 single base substitution G A missense_variant P34L 101C>T SKCM-US 16 75276498 75276498 single base substitution G A upstream_gene_variant SKCM-US 16 75276718 75276718 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75276718 75276718 single base substitution G A downstream_gene_variant SKCM-US 16 75276718 75276718 single base substitution G A intron_variant SKCM-US 16 75276718 75276718 single base substitution G A missense_variant P113S 337C>T SKCM-US 16 75276718 75276718 single base substitution G A missense_variant P141S 421C>T SKCM-US 16 75276718 75276718 single base substitution G A missense_variant P66S 196C>T SKCM-US 16 75276718 75276718 single base substitution G A missense_variant P93S 277C>T SKCM-US 16 75276718 75276718 single base substitution G A missense_variant P95S 283C>T SKCM-US 16 75276718 75276718 single base substitution G A upstream_gene_variant SKCM-US 16 75276752 75276752 single base substitution G A 3_prime_UTR_variant SKCM-US 16 75276752 75276752 single base substitution G A downstream_gene_variant SKCM-US 16 75276752 75276752 single base substitution G A intron_variant SKCM-US 16 75276752 75276752 single base substitution G A synonymous_variant A101A 303C>T SKCM-US 16 75276752 75276752 single base substitution G A synonymous_variant A129A 387C>T SKCM-US 16 75276752 75276752 single base substitution G A synonymous_variant A54A 162C>T SKCM-US 16 75276752 75276752 single base substitution G A synonymous_variant A81A 243C>T SKCM-US 16 75276752 75276752 single base substitution G A synonymous_variant A83A 249C>T SKCM-US 16 75276752 75276752 single base substitution G A upstream_gene_variant SKCM-US 16 75276760 75276760 single base substitution T C 3_prime_UTR_variant SKCM-US 16 75276760 75276760 single base substitution T C downstream_gene_variant SKCM-US 16 75276760 75276760 single base substitution T C intron_variant SKCM-US 16 75276760 75276760 single base substitution T C missense_variant T127A 379A>G SKCM-US 16 75276760 75276760 single base substitution T C missense_variant T52A 154A>G SKCM-US 16 75276760 75276760 single base substitution T C missense_variant T79A 235A>G SKCM-US 16 75276760 75276760 single base substitution T C missense_variant T81A 241A>G SKCM-US 16 75276760 75276760 single base substitution T C missense_variant T99A 295A>G SKCM-US 16 75276760 75276760 single base substitution T C upstream_gene_variant STAD-US 16 75263554 75263556 deletion of <=200bp AGG - 3_prime_UTR_variant STAD-US 16 75263554 75263556 deletion of <=200bp AGG - disruptive_inframe_deletion LL674L STAD-US 16 75263554 75263556 deletion of <=200bp AGG - disruptive_inframe_deletion LL793L STAD-US 16 75263554 75263556 deletion of <=200bp AGG - disruptive_inframe_deletion LL820L STAD-US 16 75263554 75263556 deletion of <=200bp AGG - disruptive_inframe_deletion LL822L STAD-US 16 75263554 75263556 deletion of <=200bp AGG - disruptive_inframe_deletion LL840L STAD-US 16 75263554 75263556 deletion of <=200bp AGG - disruptive_inframe_deletion LL868L STAD-US 16 75263554 75263556 deletion of <=200bp AGG - exon_variant STAD-US 16 75263597 75263597 single base substitution G A 3_prime_UTR_variant STAD-US 16 75263597 75263597 single base substitution G A exon_variant STAD-US 16 75263597 75263597 single base substitution G A missense_variant R661C 1981C>T STAD-US 16 75263597 75263597 single base substitution G A missense_variant R780C 2338C>T STAD-US 16 75263597 75263597 single base substitution G A missense_variant R807C 2419C>T STAD-US 16 75263597 75263597 single base substitution G A missense_variant R809C 2425C>T STAD-US 16 75263597 75263597 single base substitution G A missense_variant R827C 2479C>T STAD-US 16 75263597 75263597 single base substitution G A missense_variant R855C 2563C>T STAD-US 16 75263732 75263732 single base substitution C T 3_prime_UTR_variant STAD-US 16 75263732 75263732 single base substitution C T exon_variant STAD-US 16 75263732 75263732 single base substitution C T missense_variant A616T 1846G>A STAD-US 16 75263732 75263732 single base substitution C T missense_variant A735T 2203G>A STAD-US 16 75263732 75263732 single base substitution C T missense_variant A762T 2284G>A STAD-US 16 75263732 75263732 single base substitution C T missense_variant A764T 2290G>A STAD-US 16 75263732 75263732 single base substitution C T missense_variant A782T 2344G>A STAD-US 16 75263732 75263732 single base substitution C T missense_variant A810T 2428G>A STAD-US 16 75263765 75263765 single base substitution C T 3_prime_UTR_variant STAD-US 16 75263765 75263765 single base substitution C T exon_variant STAD-US 16 75263765 75263765 single base substitution C T missense_variant A605T 1813G>A STAD-US 16 75263765 75263765 single base substitution C T missense_variant A724T 2170G>A STAD-US 16 75263765 75263765 single base substitution C T missense_variant A751T 2251G>A STAD-US 16 75263765 75263765 single base substitution C T missense_variant A753T 2257G>A STAD-US 16 75263765 75263765 single base substitution C T missense_variant A771T 2311G>A STAD-US 16 75263765 75263765 single base substitution C T missense_variant A799T 2395G>A STAD-US 16 75269317 75269317 insertion of <=200bp - G 3_prime_UTR_variant STAD-US 16 75269317 75269317 insertion of <=200bp - G downstream_gene_variant STAD-US 16 75269317 75269317 insertion of <=200bp - G exon_variant STAD-US 16 75269317 75269317 insertion of <=200bp - G frameshift_variant S346S? STAD-US 16 75269317 75269317 insertion of <=200bp - G frameshift_variant S465S? STAD-US 16 75269317 75269317 insertion of <=200bp - G frameshift_variant S492S? STAD-US 16 75269317 75269317 insertion of <=200bp - G frameshift_variant S494S? STAD-US 16 75269317 75269317 insertion of <=200bp - G frameshift_variant S512S? STAD-US 16 75269317 75269317 insertion of <=200bp - G frameshift_variant S540S? STAD-US 16 75269703 75269703 single base substitution G A 3_prime_UTR_variant STAD-US 16 75269703 75269703 single base substitution G A downstream_gene_variant STAD-US 16 75269703 75269703 single base substitution G A exon_variant STAD-US 16 75269703 75269703 single base substitution G A missense_variant P192L 575C>T STAD-US 16 75269703 75269703 single base substitution G A missense_variant P217L 650C>T STAD-US 16 75269703 75269703 single base substitution G A missense_variant P336L 1007C>T STAD-US 16 75269703 75269703 single base substitution G A missense_variant P363L 1088C>T STAD-US 16 75269703 75269703 single base substitution G A missense_variant P365L 1094C>T STAD-US 16 75269703 75269703 single base substitution G A missense_variant P383L 1148C>T STAD-US 16 75269703 75269703 single base substitution G A missense_variant P411L 1232C>T STAD-US 16 75271108 75271108 deletion of <=200bp C - 3_prime_UTR_variant STAD-US 16 75271108 75271108 deletion of <=200bp C - exon_variant STAD-US 16 75271108 75271108 deletion of <=200bp C - frameshift_variant G108 STAD-US 16 75271108 75271108 deletion of <=200bp C - frameshift_variant G122 STAD-US 16 75271108 75271108 deletion of <=200bp C - frameshift_variant G227 STAD-US 16 75271108 75271108 deletion of <=200bp C - frameshift_variant G254 STAD-US 16 75271108 75271108 deletion of <=200bp C - frameshift_variant G256 STAD-US 16 75271108 75271108 deletion of <=200bp C - frameshift_variant G274 STAD-US 16 75271108 75271108 deletion of <=200bp C - frameshift_variant G302 STAD-US 16 75271108 75271108 deletion of <=200bp C - upstream_gene_variant STAD-US 16 75276437 75276437 single base substitution C T 3_prime_UTR_variant STAD-US 16 75276437 75276437 single base substitution C T downstream_gene_variant STAD-US 16 75276437 75276437 single base substitution C T intron_variant STAD-US 16 75276437 75276437 single base substitution C T synonymous_variant G159G 477G>A STAD-US 16 75276437 75276437 single base substitution C T synonymous_variant G186G 558G>A STAD-US 16 75276437 75276437 single base substitution C T synonymous_variant G188G 564G>A STAD-US 16 75276437 75276437 single base substitution C T synonymous_variant G206G 618G>A STAD-US 16 75276437 75276437 single base substitution C T synonymous_variant G234G 702G>A STAD-US 16 75276437 75276437 single base substitution C T synonymous_variant G54G 162G>A STAD-US 16 75276437 75276437 single base substitution C T upstream_gene_variant STAD-US 16 75276727 75276727 single base substitution G T 3_prime_UTR_variant STAD-US 16 75276727 75276727 single base substitution G T downstream_gene_variant STAD-US 16 75276727 75276727 single base substitution G T intron_variant STAD-US 16 75276727 75276727 single base substitution G T missense_variant P110T 328C>A STAD-US 16 75276727 75276727 single base substitution G T missense_variant P138T 412C>A STAD-US 16 75276727 75276727 single base substitution G T missense_variant P63T 187C>A STAD-US 16 75276727 75276727 single base substitution G T missense_variant P90T 268C>A STAD-US 16 75276727 75276727 single base substitution G T missense_variant P92T 274C>A STAD-US 16 75276727 75276727 single base substitution G T upstream_gene_variant THCA-SA 16 75269477 75269477 single base substitution A C 3_prime_UTR_variant THCA-SA 16 75269477 75269477 single base substitution A C downstream_gene_variant THCA-SA 16 75269477 75269477 single base substitution A C exon_variant THCA-SA 16 75269477 75269477 single base substitution A C synonymous_variant S292S 876T>G THCA-SA 16 75269477 75269477 single base substitution A C synonymous_variant S411S 1233T>G THCA-SA 16 75269477 75269477 single base substitution A C synonymous_variant S438S 1314T>G THCA-SA 16 75269477 75269477 single base substitution A C synonymous_variant S440S 1320T>G THCA-SA 16 75269477 75269477 single base substitution A C synonymous_variant S458S 1374T>G THCA-SA 16 75269477 75269477 single base substitution A C synonymous_variant S486S 1458T>G UCEC-US 16 75267742 75267742 single base substitution A G downstream_gene_variant UCEC-US 16 75267742 75267742 single base substitution A G splice_donor_variant UCEC-US 16 75269100 75269100 single base substitution C T 3_prime_UTR_variant UCEC-US 16 75269100 75269100 single base substitution C T downstream_gene_variant UCEC-US 16 75269100 75269100 single base substitution C T exon_variant UCEC-US 16 75269100 75269100 single base substitution C T missense_variant R418Q 1253G>A UCEC-US 16 75269100 75269100 single base substitution C T missense_variant R537Q 1610G>A UCEC-US 16 75269100 75269100 single base substitution C T missense_variant R564Q 1691G>A UCEC-US 16 75269100 75269100 single base substitution C T missense_variant R566Q 1697G>A UCEC-US 16 75269100 75269100 single base substitution C T missense_variant R584Q 1751G>A UCEC-US 16 75269100 75269100 single base substitution C T missense_variant R612Q 1835G>A UCEC-US 16 75271174 75271174 single base substitution G A 3_prime_UTR_variant UCEC-US 16 75271174 75271174 single base substitution G A exon_variant UCEC-US 16 75271174 75271174 single base substitution G A synonymous_variant Y100Y 300C>T UCEC-US 16 75271174 75271174 single base substitution G A synonymous_variant Y205Y 615C>T UCEC-US 16 75271174 75271174 single base substitution G A synonymous_variant Y232Y 696C>T UCEC-US 16 75271174 75271174 single base substitution G A synonymous_variant Y234Y 702C>T UCEC-US 16 75271174 75271174 single base substitution G A synonymous_variant Y252Y 756C>T UCEC-US 16 75271174 75271174 single base substitution G A synonymous_variant Y280Y 840C>T UCEC-US 16 75271174 75271174 single base substitution G A synonymous_variant Y86Y 258C>T UCEC-US 16 75271174 75271174 single base substitution G A upstream_gene_variant UCEC-US 16 75276447 75276447 single base substitution G A 3_prime_UTR_variant UCEC-US 16 75276447 75276447 single base substitution G A downstream_gene_variant UCEC-US 16 75276447 75276447 single base substitution G A intron_variant UCEC-US 16 75276447 75276447 single base substitution G A missense_variant A156V 467C>T UCEC-US 16 75276447 75276447 single base substitution G A missense_variant A183V 548C>T UCEC-US 16 75276447 75276447 single base substitution G A missense_variant A185V 554C>T UCEC-US 16 75276447 75276447 single base substitution G A missense_variant A203V 608C>T UCEC-US 16 75276447 75276447 single base substitution G A missense_variant A231V 692C>T UCEC-US 16 75276447 75276447 single base substitution G A missense_variant A51V 152C>T UCEC-US 16 75276447 75276447 single base substitution G A upstream_gene_variant UCEC-US 16 75276529 75276529 single base substitution G A 3_prime_UTR_variant UCEC-US 16 75276529 75276529 single base substitution G A downstream_gene_variant UCEC-US 16 75276529 75276529 single base substitution G A intron_variant UCEC-US 16 75276529 75276529 single base substitution G A missense_variant P129S 385C>T UCEC-US 16 75276529 75276529 single base substitution G A missense_variant P156S 466C>T UCEC-US 16 75276529 75276529 single base substitution G A missense_variant P158S 472C>T UCEC-US 16 75276529 75276529 single base substitution G A missense_variant P176S 526C>T UCEC-US 16 75276529 75276529 single base substitution G A missense_variant P204S 610C>T UCEC-US 16 75276529 75276529 single base substitution G A missense_variant P24S 70C>T UCEC-US 16 75276529 75276529 single base substitution G A upstream_gene_variant UCEC-US 16 75276618 75276618 single base substitution T C 3_prime_UTR_variant UCEC-US 16 75276618 75276618 single base substitution T C downstream_gene_variant UCEC-US 16 75276618 75276618 single base substitution T C intron_variant UCEC-US 16 75276618 75276618 single base substitution T C missense_variant Y126C 377A>G UCEC-US 16 75276618 75276618 single base substitution T C missense_variant Y128C 383A>G UCEC-US 16 75276618 75276618 single base substitution T C missense_variant Y146C 437A>G UCEC-US 16 75276618 75276618 single base substitution T C missense_variant Y174C 521A>G UCEC-US 16 75276618 75276618 single base substitution T C missense_variant Y99C 296A>G UCEC-US 16 75276618 75276618 single base substitution T C upstream_gene_variant UCEC-US 16 75276891 75276891 single base substitution G A 3_prime_UTR_variant UCEC-US 16 75276891 75276891 single base substitution G A downstream_gene_variant UCEC-US 16 75276891 75276891 single base substitution G A missense_variant T35M 104C>T UCEC-US 16 75276891 75276891 single base substitution G A missense_variant T37M 110C>T UCEC-US 16 75276891 75276891 single base substitution G A missense_variant T55M 164C>T UCEC-US 16 75276891 75276891 single base substitution G A missense_variant T83M 248C>T UCEC-US 16 75276891 75276891 single base substitution G A missense_variant T8M 23C>T UCEC-US 16 75276891 75276891 single base substitution G A upstream_gene_variant UCEC-US 16 75276913 75276913 single base substitution T C 3_prime_UTR_variant UCEC-US 16 75276913 75276913 single base substitution T C downstream_gene_variant UCEC-US 16 75276913 75276913 single base substitution T C missense_variant M28V 82A>G UCEC-US 16 75276913 75276913 single base substitution T C missense_variant M30V 88A>G UCEC-US 16 75276913 75276913 single base substitution T C missense_variant M48V 142A>G UCEC-US 16 75276913 75276913 single base substitution T C missense_variant M76V 226A>G UCEC-US 16 75276913 75276913 single base substitution T C start_lost M1V 1A>G UCEC-US 16 75276913 75276913 single base substitution T C upstream_gene_variant UCEC-US 16 75298392 75298392 single base substitution C A 5_prime_UTR_variant UCEC-US 16 75298392 75298392 single base substitution C A exon_variant UCEC-US 16 75298392 75298392 single base substitution C A intron_variant UCEC-US 16 75298392 75298392 single base substitution C A missense_variant A3S 7G>T UCEC-US 16 75298392 75298392 single base substitution C A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PD6361a COSM1637163 c.2169G>A p.T723T Substitution - coding silent 16:75229955-75229955 - 545 COSM5612630 c.1207C>T p.P403S Substitution - Missense 16:75235830-75235830 - T3118 COSM4665320 c.2584C>T p.R862C Substitution - Missense 16:75229540-75229540 - CCC4T COSM3717084 c.49G>A p.E17K Substitution - Missense 16:75243054-75243054 - TCGA-A3-3320-01 COSM1135840 c.100G>T p.E34* Substitution - Nonsense 16:75243003-75243003 - PT19_2 COSM5900322 c.633G>C p.K211N Substitution - Missense 16:75242470-75242470 - KYSE-140 COSM2691275 c.377G>C p.G126A Substitution - Missense 16:75242726-75242726 - TCGA-EE-A29M-06 COSM3512244 c.1864C>T p.L622L Substitution - coding silent 16:75235173-75235173 - TCGA-BH-A18G-01 COSM3818563 c.848C>T p.P283L Substitution - Missense 16:75237268-75237268 - BN42T COSM1609667 c.955G>T p.G319C Substitution - Missense 16:75235944-75235944 - TCGA-22-5478-01 COSM1147703 c.2422G>T p.V808L Substitution - Missense 16:75229840-75229840 - TCGA-G4-6298-01 COSM3755077 c.1668T>C p.A556A Substitution - coding silent 16:75235369-75235369 - Detroit_562 COSM2691176 c.2108A>G p.Q703R Substitution - Missense 16:75230016-75230016 - TCGA-09-0364-01 COSM1324262 c.1286C>T p.P429L Substitution - Missense 16:75235751-75235751 - CSCC-55-T COSM4514231 c.830C>T p.P277L Substitution - Missense 16:75236964-75236964 - STC252 COSM5055098 c.1788C>T p.D596D Substitution - coding silent 16:75235249-75235249 - TCGA-A3-3320-01 COSM1135841 c.237_238GG>TT p.E80* Substitution - Nonsense 16:75243003-75243004 - HCC13 COSM1609664 c.2373G>A p.K791K Substitution - coding silent 16:75229751-75229751 - CHC1044T COSM4790955 c.1991A>G p.Y664C Substitution - Missense 16:75234908-75234908 - TCGA-FD-A3N6-01 COSM1302247 c.765G>A p.P255P Substitution - coding silent 16:75242476-75242476 - 1517_CLM COSM5754911 c.1021C>A p.P341T Substitution - Missense 16:75235878-75235878 - TCGA-A2-A3Y0-01 COSM3818555 c.2377T>C p.Y793H Substitution - Missense 16:75229885-75229885 - TCGA-EE-A17X-06 COSM3512255 c.503C>T p.P168L Substitution - Missense 16:75242600-75242600 - TCGA-AA-3712-01 COSM3755080 c.1530T>C p.A510A Substitution - coding silent 16:75235369-75235369 - TCGA-B1-A656-01 COSM4413995 c.467C>G p.P156R Substitution - Missense 16:75242636-75242636 - SNUH_G46_S1 COSM3680021 c.246G>A p.P82P Substitution - coding silent 16:75242857-75242857 - TCGA-EE-A184-06 COSM3512240 c.1812C>A p.L604L Substitution - coding silent 16:75235087-75235087 - B96-Tumor COSM1749780 c.433T>A p.Y145N Substitution - Missense 16:75242808-75242808 - HN_62505 COSM127427 c.1290C>A p.S430S Substitution - coding silent 16:75235609-75235609 - 587316 COSM1184528 c.1834C>T p.R612W Substitution - Missense 16:75235203-75235203 - ACINAR01 COSM1735341 c.1162G>A p.D388N Substitution - Missense 16:75235737-75235737 - PT19_2 COSM5900318 c.771G>C p.K257N Substitution - Missense 16:75242470-75242470 - ACINAR01 COSM1735339 c.1300G>A p.D434N Substitution - Missense 16:75235737-75235737 - TCGA-B1-A656-01 COSM4413992 c.605C>G p.P202R Substitution - Missense 16:75242636-75242636 - TCGA-FV-A4ZQ-01 COSM4922003 c.2694G>T p.E898D Substitution - Missense 16:75229568-75229568 - TCGA-43-6143-01 COSM704110 c.1083G>T p.V361V Substitution - coding silent 16:75235816-75235816 - 49M COSM5589802 c.972G>A p.E324E Substitution - coding silent 16:75235927-75235927 - CHC892T COSM4795623 c.1722G>A p.E574E Substitution - coding silent 16:75235177-75235177 - CSCC-20-T COSM4564896 c.1385_1386CC>TT p.A462V Substitution - Missense 16:75235513-75235514 - C086 COSM5527288 c.1296C>T p.T432T Substitution - coding silent 16:75235603-75235603 - TCGA-BR-8487-01 COSM4062826 c.412C>A p.P138T Substitution - Missense 16:75242829-75242829 - TCGA-AA-3712-01 COSM1563497 c.364C>T p.P122S Substitution - Missense 16:75242877-75242877 - ESCC_118 COSM5640196 c.74G>A p.R25H Substitution - Missense 16:75243029-75243029 - YUGATOR COSM973710 c.472C>T p.P158S Substitution - Missense 16:75242631-75242631 - TCGA-BS-A0UJ-01 COSM1588542 c.226A>G p.M76V Substitution - Missense 16:75243015-75243015 - pfg016T COSM1640557 c.2168C>T p.T723M Substitution - Missense 16:75229956-75229956 - 545 COSM5612634 c.1069C>T p.P357S Substitution - Missense 16:75235830-75235830 - LUAD-NYU947 COSM377049 c.2206C>T p.L736L Substitution - coding silent 16:75229918-75229918 - 19M COSM5578102 c.1782G>A p.M594I Substitution - Missense 16:75235255-75235255 - RMS105_ COSM4986057 c.680C>G p.A227G Substitution - Missense 16:75237298-75237298 - B96-Tumor COSM1749782 c.295T>A p.Y99N Substitution - Missense 16:75242808-75242808 - TCGA-E9-A1RF-01 COSM1479101 c.2062A>G p.I688V Substitution - Missense 16:75233884-75233884 - TCGA-A6-5665-01 COSM1379800 c.314G>A p.R105H Substitution - Missense 16:75242927-75242927 - WSU-HN30 COSM4600912 c.1472G>T p.R491L Substitution - Missense 16:75235427-75235427 - PTC-70C COSM4129363 c.1263G>A p.P421P Substitution - coding silent 16:75235636-75235636 - PR-2858 COSM243179 c.1568G>A p.R523H Substitution - Missense 16:75235331-75235331 - TCGA-DD-A39Y-01 COSM4934474 c.1400C>A p.P467Q Substitution - Missense 16:75235637-75235637 - 66 COSM5743782 c.680C>T p.A227V Substitution - Missense 16:75237298-75237298 - SNUH_G16_S1 COSM3680016 c.1711G>A p.A571T Substitution - Missense 16:75235326-75235326 - TCGA-21-1077-01 COSM704108 c.397C>A p.P133T Substitution - Missense 16:75242706-75242706 - 1266T COSM5762775 c.2124A>G p.E708E Substitution - coding silent 16:75230000-75230000 - TCGA-AM-5821-01 COSM1563499 c.226C>T p.P76S Substitution - Missense 16:75242877-75242877 - TCGA-G4-6298-01 COSM3755080 c.1530T>C p.A510A Substitution - coding silent 16:75235369-75235369 - YUROL COSM5385387 c.1218C>T p.D406D Substitution - coding silent 16:75235819-75235819 - LIM1215 COSM4262573 c.2189C>T p.P730L Substitution - Missense 16:75229935-75229935 - Pat_41_B COSM5851485 c.1876G>A p.V626M Substitution - Missense 16:75235161-75235161 - TCGA-EB-A3Y6-01 COSM3512261 c.249C>T p.A83A Substitution - coding silent 16:75242854-75242854 - TCGA-BG-A0LX-01 COSM973708 c.554C>T p.A185V Substitution - Missense 16:75242549-75242549 - I2L-P19Ta-Tumor-Organoid COSM5363356 c.2322G>A p.P774P Substitution - coding silent 16:75229802-75229802 - HCC172 COSM3717081 c.2463C>T p.D821D Substitution - coding silent 16:75229661-75229661 - pfg092T COSM4757628 c.1106G>T p.R369L Substitution - Missense 16:75235931-75235931 - YUROS COSM5385392 c.915C>T p.P305P Substitution - coding silent 16:75237201-75237201 - C086 COSM5527278 c.1295C>T p.T432I Substitution - Missense 16:75235604-75235604 - TCGA-EI-6882-01 COSM3421161 c.1574C>T p.A525V Substitution - Missense 16:75235325-75235325 - TCGA-G9-6364-01 COSM1128876 c.1320T>G p.S440S Substitution - coding silent 16:75235579-75235579 - TCGA-AA-3712-01 COSM1563499 c.226C>T p.P76S Substitution - Missense 16:75242877-75242877 - TCGA-EB-A57M-01 COSM3512228 c.2301C>T p.T767T Substitution - coding silent 16:75229823-75229823 - TCGA-EB-A4P0-01 COSM3512222 c.2502C>T p.A834A Substitution - coding silent 16:75229622-75229622 - HCC113T COSM1609670 c.226C>G p.P76A Substitution - Missense 16:75242877-75242877 - TCGA-09-0364-01 COSM1324264 c.1148C>T p.P383L Substitution - Missense 16:75235751-75235751 - TCGA-A3-3320-01 COSM1135844 c.237G>T p.L79L Substitution - coding silent 16:75243004-75243004 - TCGA-BS-A0UV-01 COSM973714 c.110C>T p.T37M Substitution - Missense 16:75242993-75242993 - CCC4 COSM3717082 c.187G>A p.E63K Substitution - Missense 16:75243054-75243054 - T191 COSM4665333 c.764C>T p.P255L Substitution - Missense 16:75242477-75242477 - TCGA-AM-5820-01 COSM3755076 c.2361C>T p.L787L Substitution - coding silent 16:75229763-75229763 - CHC892T COSM4795620 c.1860G>A p.E620E Substitution - coding silent 16:75235177-75235177 - 8060086 COSM4389178 c.318C>T p.L106L Substitution - coding silent 16:75242923-75242923 - sysucc-774T COSM5461575 c.977G>A p.R326Q Substitution - Missense 16:75236955-75236955 - TCGA-BG-A0LX-01 COSM1588546 c.692C>T p.A231V Substitution - Missense 16:75242549-75242549 - PTC-50C COSM4129363 c.1263G>A p.P421P Substitution - coding silent 16:75235636-75235636 - I2L-P19Tb-Tumor-Organoid COSM5363489 c.2205G>A p.T735T Substitution - coding silent 16:75233879-75233879 - CN-AML-CR-21-Dx COSM1563497 c.364C>T p.P122S Substitution - Missense 16:75242877-75242877 - T2269 COSM4665337 c.536C>T p.P179L Substitution - Missense 16:75242705-75242705 - TCGA-CM-6674-01 COSM3691315 c.837C>T p.G279G Substitution - coding silent 16:75236957-75236957 - TCGA-A3-3320-01 COSM1135843 c.99_100GG>TT p.E34* Substitution - Nonsense 16:75243003-75243004 - TCGA-22-4599-01 COSM1147701 c.2588A>T p.N863I Substitution - Missense 16:75229674-75229674 - TCGA-43-6143-01 COSM1147707 c.1221G>T p.V407V Substitution - coding silent 16:75235816-75235816 - TCGA-AP-A059-01 COSM1588544 c.521A>G p.Y174C Substitution - Missense 16:75242720-75242720 - TCGA-D8-A1JD-01 COSM1479104 c.2041G>T p.E681* Substitution - Nonsense 16:75233905-75233905 - TCGA-EE-A29D-06 COSM3512231 c.2199A>C p.T733T Substitution - coding silent 16:75229925-75229925 - CCC4T COSM3717082 c.187G>A p.E63K Substitution - Missense 16:75243054-75243054 - sysucc-774T COSM5461579 c.839G>A p.R280Q Substitution - Missense 16:75236955-75236955 - T3204 COSM4665329 c.1609C>T p.R537C Substitution - Missense 16:75235428-75235428 - TCGA-BP-4167-01 COSM1135834 c.1008C>T p.P336P Substitution - coding silent 16:75236924-75236924 - 1517_PT COSM5754907 c.1159C>A p.P387T Substitution - Missense 16:75235878-75235878 - HCC1395 COSM24662 c.1220G>C p.S407T Substitution - Missense 16:75235679-75235679 - TCGA-D3-A51G-06 COSM3512262 c.379A>G p.T127A Substitution - Missense 16:75242862-75242862 - 49M COSM5589798 c.1110G>A p.E370E Substitution - coding silent 16:75235927-75235927 - TCGA-BS-A0UV-01 COSM1588548 c.1835G>A p.R612Q Substitution - Missense 16:75235202-75235202 - CHEWS024 COSM4579265 c.596C>A p.P199H Substitution - Missense 16:75242645-75242645 - T3498 COSM4665324 c.2402G>T p.R801L Substitution - Missense 16:75229722-75229722 - 19M COSM5578106 c.1644G>A p.M548I Substitution - Missense 16:75235255-75235255 - TCGA-EE-A184-06 COSM3512238 c.1950C>A p.L650L Substitution - coding silent 16:75235087-75235087 - HCC1395 COSM24662 c.1220G>C p.S407T Substitution - Missense 16:75235679-75235679 - TCGA-AD-6895-01 COSM1379785 c.2565C>T p.R855R Substitution - coding silent 16:75229697-75229697 - PTC-28C COSM4129356 c.1932C>T p.H644H Substitution - coding silent 16:75235105-75235105 - TCGA-BS-A0UJ-01 COSM973700 c.2100+2T>C p.? Unknown 16:75233844-75233844 - I2L-P19Tb-Tumor-Organoid COSM5363434 c.1977G>A p.P659P Substitution - coding silent 16:75235060-75235060 - ESCC_118 COSM5640192 c.212G>A p.R71H Substitution - Missense 16:75243029-75243029 - OV207 COSM252375 c.2470C>T p.R824C Substitution - Missense 16:75229654-75229654 - TCGA-ER-A2NF-06 COSM3512252 c.602G>A p.R201H Substitution - Missense 16:75242501-75242501 - TCGA-CA-6718-01 COSM1379796 c.763C>T p.R255W Substitution - Missense 16:75237215-75237215 - SNUH_G46_S1 COSM3680019 c.384G>A p.P128P Substitution - coding silent 16:75242857-75242857 - 2521262 COSM5892274 c.1870C>T p.R624W Substitution - Missense 16:75235167-75235167 - TCGA-EK-A2GZ-01 COSM2691161 c.2280C>T p.N760N Substitution - coding silent 16:75229844-75229844 - YUROL COSM5385398 c.206C>T p.S69F Substitution - Missense 16:75243035-75243035 - sysucc-1317T COSM5448903 c.1187C>T p.A396V Substitution - Missense 16:75235850-75235850 - TCGA-F1-A448-01 COSM4062812 c.2425C>T p.R809C Substitution - Missense 16:75229699-75229699 - RK141_C01 COSM1629988 c.2337A>G p.T779T Substitution - coding silent 16:75229925-75229925 - pfg016T COSM1640555 c.2306C>T p.T769M Substitution - Missense 16:75229956-75229956 - sysucc-1370T COSM4665328 c.2386G>A p.G796R Substitution - Missense 16:75229738-75229738 - TCGA-G4-6588-01 COSM1379788 c.1940C>A p.A647D Substitution - Missense 16:75235097-75235097 - TCGA-18-3417-01 COSM704114 c.2126A>T p.Q709L Substitution - Missense 16:75229998-75229998 - TCGA-CJ-4881-01 COSM3361896 c.691G>T p.A231S Substitution - Missense 16:75242550-75242550 - 2521262 COSM5892278 c.1732C>T p.R578W Substitution - Missense 16:75235167-75235167 - TCGA-A6-5665-01 COSM1379802 c.176G>A p.R59H Substitution - Missense 16:75242927-75242927 - CCK81 COSM2691219 c.1389A>G p.E463E Substitution - coding silent 16:75235648-75235648 - TCGA-D1-A16X-01 COSM1588545 c.610C>T p.P204S Substitution - Missense 16:75242631-75242631 - T613 COSM4665325 c.2524G>A p.G842R Substitution - Missense 16:75229738-75229738 - S02285 COSM5684599 c.1933G>T p.G645C Substitution - Missense 16:75235104-75235104 - TCGA-D1-A17H-01 COSM1153009 c.739C>T p.R247C Substitution - Missense 16:75242502-75242502 - 66 COSM5743778 c.818C>T p.A273V Substitution - Missense 16:75237298-75237298 - HN_62863 COSM127426 c.2385C>T p.I795I Substitution - coding silent 16:75229739-75229739 - TCGA-EE-A29M-06 COSM3512246 c.1726C>T p.L576L Substitution - coding silent 16:75235173-75235173 - RMS105_ COSM4986054 c.818C>G p.A273G Substitution - Missense 16:75237298-75237298 - HCC113T COSM1609668 c.364C>G p.P122A Substitution - Missense 16:75242877-75242877 - YUROL COSM5385391 c.1080C>T p.D360D Substitution - coding silent 16:75235819-75235819 - C086 COSM5527279 c.2060C>T p.P687L Substitution - Missense 16:75234977-75234977 - CHC892T COSM4795623 c.1722G>A p.E574E Substitution - coding silent 16:75235177-75235177 - TCGA-CA-6718-01 COSM1379794 c.901C>T p.R301W Substitution - Missense 16:75237215-75237215 - 6 COSM4166699 c.375C>T p.P125P Substitution - coding silent 16:75242866-75242866 - TCGA-FV-A4ZQ-01 COSM4922006 c.2556G>T p.E852D Substitution - Missense 16:75229568-75229568 - Pat_41_B COSM5851489 c.1738G>A p.V580M Substitution - Missense 16:75235161-75235161 - TCGA-37-4141-01 COSM1147706 c.2001G>C p.L667L Substitution - coding silent 16:75235036-75235036 - TCGA-AM-5821-01 COSM1563497 c.364C>T p.P122S Substitution - Missense 16:75242877-75242877 - 9210_T COSM5042204 c.748G>A p.E250K Substitution - Missense 16:75242493-75242493 - TCGA-BP-5169-01 COSM472108 c.1485G>T p.E495D Substitution - Missense 16:75235414-75235414 - T3498 COSM4665321 c.2540G>T p.R847L Substitution - Missense 16:75229722-75229722 - OSCC-GB_00700111 COSM4890600 c.1592G>T p.G531V Substitution - Missense 16:75235445-75235445 - TCGA-DD-A39Y-01 COSM4934477 c.1262C>A p.P421Q Substitution - Missense 16:75235637-75235637 - PT42 COSM5925849 c.2326C>T p.P776S Substitution - Missense 16:75229936-75229936 - ESO-859 COSM1238291 c.1117G>A p.D373N Substitution - Missense 16:75235782-75235782 - TCGA-D1-A16X-01 COSM973710 c.472C>T p.P158S Substitution - Missense 16:75242631-75242631 - TCGA-22-4599-01 COSM704122 c.2450A>T p.N817I Substitution - Missense 16:75229674-75229674 - TCGA-EB-A4P0-01 COSM3512220 c.2640C>T p.A880A Substitution - coding silent 16:75229622-75229622 - TCGA-BH-A0B1-01 COSM5833173 c.2249_2250insA p.C751fs*2 Insertion - Frameshift 16:75229874-75229875 - 66 COSM5743777 c.1339G>A p.A447T Substitution - Missense 16:75235560-75235560 - OSCC-GB_01060111 COSM4883098 c.1807G>T p.A603S Substitution - Missense 16:75235230-75235230 - CSCC-55-T COSM4514228 c.968C>T p.P323L Substitution - Missense 16:75236964-75236964 - TCGA-EE-A29D-06 COSM3512229 c.2337A>C p.T779T Substitution - coding silent 16:75229925-75229925 - YUROL COSM5385402 c.68C>T p.S23F Substitution - Missense 16:75243035-75243035 - TCGA-A3-3320-01 COSM1135838 c.238G>T p.E80* Substitution - Nonsense 16:75243003-75243003 - TCGA-39-5021-01 COSM704116 c.2240A>G p.Y747C Substitution - Missense 16:75229884-75229884 - TCGA-37-4141-01 COSM704112 c.1863G>C p.L621L Substitution - coding silent 16:75235036-75235036 - 2249677 COSM4413304 c.1472G>A p.R491H Substitution - Missense 16:75235427-75235427 - TCGA-D1-A167-01 COSM1588547 c.840C>T p.Y280Y Substitution - coding silent 16:75237276-75237276 - TCGA-AO-A128-01 COSM3818559 c.998A>G p.Y333C Substitution - Missense 16:75236934-75236934 - I2L-P19Tb-Tumor-Biopsy COSM5363434 c.1977G>A p.P659P Substitution - coding silent 16:75235060-75235060 - C086 COSM5527293 c.582C>T p.V194V Substitution - coding silent 16:75242521-75242521 - 587316 COSM1184536 c.826G>T p.G276C Substitution - Missense 16:75236968-75236968 - CHC1044T COSM4790952 c.2129A>G p.Y710C Substitution - Missense 16:75234908-75234908 - TCGA-BR-8487-01 COSM4062829 c.274C>A p.P92T Substitution - Missense 16:75242829-75242829 - pfg092T COSM4757631 c.968G>T p.R323L Substitution - Missense 16:75235931-75235931 - S02290 COSM5686517 c.1445G>T p.R482L Substitution - Missense 16:75235592-75235592 - 587332 COSM1184539 c.908A>G p.H303R Substitution - Missense 16:75236886-75236886 - TCGA-IH-A3EA-01 COSM3512256 c.421C>T p.P141S Substitution - Missense 16:75242820-75242820 - B96 COSM1749780 c.433T>A p.Y145N Substitution - Missense 16:75242808-75242808 - ESO-859 COSM1238289 c.1255G>A p.D419N Substitution - Missense 16:75235782-75235782 - T3118 COSM4665317 c.2722C>T p.R908C Substitution - Missense 16:75229540-75229540 - 66 COSM5743773 c.1477G>A p.A493T Substitution - Missense 16:75235560-75235560 - T3204 COSM4665332 c.1471C>T p.R491C Substitution - Missense 16:75235428-75235428 - CN-AML-CR-21-Dx COSM1563499 c.226C>T p.P76S Substitution - Missense 16:75242877-75242877 - CCC4 COSM3717084 c.49G>A p.E17K Substitution - Missense 16:75243054-75243054 - TCGA-ER-A2NF-06 COSM3512250 c.740G>A p.R247H Substitution - Missense 16:75242501-75242501 - C086 COSM5527274 c.1433C>T p.T478I Substitution - Missense 16:75235604-75235604 - I2L-P19Tb-Tumor-Organoid COSM5363438 c.1839G>A p.P613P Substitution - coding silent 16:75235060-75235060 - TCGA-HU-A4GQ-01 COSM4062824 c.1094C>T p.P365L Substitution - Missense 16:75235805-75235805 - TCGA-EE-A2GM-06 COSM3512223 c.2604C>T p.L868L Substitution - coding silent 16:75229658-75229658 - TCGA-IH-A3EA-01 COSM3512258 c.283C>T p.P95S Substitution - Missense 16:75242820-75242820 - LP6005690-DNA_C01 COSM4409439 c.2746G>A p.A916T Substitution - Missense 16:75229516-75229516 - HCC172 COSM3717079 c.2601C>T p.D867D Substitution - coding silent 16:75229661-75229661 - 587332 COSM1184537 c.1046A>G p.H349R Substitution - Missense 16:75236886-75236886 - TCGA-AD-6895-01 COSM1379787 c.2427C>T p.R809R Substitution - coding silent 16:75229697-75229697 - sysucc-1317T COSM5448907 c.1049C>T p.A350V Substitution - Missense 16:75235850-75235850 - C086 COSM5527289 c.720C>T p.V240V Substitution - coding silent 16:75242521-75242521 - TCGA-EK-A2GZ-01 COSM2691159 c.2418C>T p.N806N Substitution - coding silent 16:75229844-75229844 - tumor_4177987 COSM3356860 c.123C>T p.G41G Substitution - coding silent 16:75264378-75264378 - OSCC-GB_01060111 COSM4883101 c.1669G>T p.A557S Substitution - Missense 16:75235230-75235230 - TCGA-21-1077-01 COSM1147708 c.535C>A p.P179T Substitution - Missense 16:75242706-75242706 - PTC-54C COSM1128876 c.1320T>G p.S440S Substitution - coding silent 16:75235579-75235579 - BN42T COSM1609665 c.1093G>T p.G365C Substitution - Missense 16:75235944-75235944 - TCGA-D1-A167-01 COSM973704 c.702C>T p.Y234Y Substitution - coding silent 16:75237276-75237276 - HCC13 COSM1609662 c.2511G>A p.K837K Substitution - coding silent 16:75229751-75229751 - C086 COSM5527283 c.1922C>T p.P641L Substitution - Missense 16:75234977-75234977 - PTC-54C COSM3755081 c.1458T>G p.S486S Substitution - coding silent 16:75235579-75235579 - HCC093T COSM5810979 c.1140G>T p.R380R Substitution - coding silent 16:75235759-75235759 - S02285 COSM5684603 c.1795G>T p.G599C Substitution - Missense 16:75235104-75235104 - T2979 COSM2691156 c.2502C>T p.S834S Substitution - coding silent 16:75229760-75229760 - PTC-28C COSM4129359 c.1794C>T p.H598H Substitution - coding silent 16:75235105-75235105 - I2L-P19Ta-Tumor-Biopsy COSM5363352 c.2460G>A p.P820P Substitution - coding silent 16:75229802-75229802 - LOVO COSM2691143 c.2606C>T p.A869V Substitution - Missense 16:75229518-75229518 - TCGA-EE-A2MS-06 COSM3512235 c.1976C>T p.P659L Substitution - Missense 16:75235061-75235061 - TCGA-A2-A3Y0-01 COSM3818558 c.2239T>C p.Y747H Substitution - Missense 16:75229885-75229885 - HCC13T COSM1609662 c.2511G>A p.K837K Substitution - coding silent 16:75229751-75229751 - ACINAR29 COSM1735342 c.767C>T p.A256V Substitution - Missense 16:75242474-75242474 - TCGA-BP-4968-01 COSM472110 c.564G>A p.G188G Substitution - coding silent 16:75242539-75242539 - T613 COSM4665328 c.2386G>A p.G796R Substitution - Missense 16:75229738-75229738 - TCGA-FD-A3N6-01 COSM1302249 c.627G>A p.P209P Substitution - coding silent 16:75242476-75242476 - LP6005409-DNA_G03 COSM4409185 c.1964A>G p.N655S Substitution - Missense 16:75234935-75234935 - TCGA-D8-A1JD-01 COSM1479102 c.2179G>T p.E727* Substitution - Nonsense 16:75233905-75233905 - PCSI_0090_Pa_X COSM3377982 c.1233G>A p.A411A Substitution - coding silent 16:75235666-75235666 - 9210_T COSM5042207 c.610G>A p.E204K Substitution - Missense 16:75242493-75242493 - ACINAR29 COSM1735344 c.629C>T p.A210V Substitution - Missense 16:75242474-75242474 - HCC093T COSM5810975 c.1278G>T p.R426R Substitution - coding silent 16:75235759-75235759 - TCGA-AP-A059-01 COSM973712 c.383A>G p.Y128C Substitution - Missense 16:75242720-75242720 - PTC-50C COSM4129360 c.1401G>A p.P467P Substitution - coding silent 16:75235636-75235636 - T2979 COSM2691158 c.2364C>T p.S788S Substitution - coding silent 16:75229760-75229760 - I2L-P19Tb-Tumor-Organoid COSM5363493 c.2067G>A p.T689T Substitution - coding silent 16:75233879-75233879 - I2L-P19Ta-Tumor-Organoid COSM5363352 c.2460G>A p.P820P Substitution - coding silent 16:75229802-75229802 - OSCC-GB_00700111 COSM4890603 c.1454G>T p.G485V Substitution - Missense 16:75235445-75235445 - TCGA-BS-A0WQ-01 COSM973717 c.7G>T p.A3S Substitution - Missense 16:75264494-75264494 - SJBALL020649_D1 COSM4993818 c.290G>A p.R97H Substitution - Missense 16:75242951-75242951 - TCGA-EE-A2GU-06 COSM3512234 c.1929C>T p.F643F Substitution - coding silent 16:75234970-75234970 - TCGA-D1-A17H-01 COSM973706 c.601C>T p.R201C Substitution - Missense 16:75242502-75242502 - TCGA-EE-A2MS-06 COSM3512237 c.1838C>T p.P613L Substitution - Missense 16:75235061-75235061 - 8060086 COSM4389181 c.180C>T p.L60L Substitution - coding silent 16:75242923-75242923 - TCGA-A3-3320-01 COSM1135846 c.99G>T p.L33L Substitution - coding silent 16:75243004-75243004 - CSCC-20-T COSM4564893 c.1523_1524CC>TT p.A508V Substitution - Missense 16:75235513-75235514 - T191 COSM4665336 c.626C>T p.P209L Substitution - Missense 16:75242477-75242477 - YUKLAB COSM1709398 c.2477C>T p.A826V Substitution - Missense 16:75229785-75229785 - PTC-77C COSM1563499 c.226C>T p.P76S Substitution - Missense 16:75242877-75242877 - 2334195 COSM318900 c.2326A>G p.K776E Substitution - Missense 16:75229798-75229798 - STC252 COSM5055101 c.1650C>T p.D550D Substitution - coding silent 16:75235249-75235249 - T2269 COSM4665340 c.398C>T p.P133L Substitution - Missense 16:75242705-75242705 - 8030032 COSM3387601 c.2599C>T p.L867L Substitution - coding silent 16:75229525-75229525 - TCGA-EE-A20F-06 COSM3512241 c.1936A>T p.N646Y Substitution - Missense 16:75235101-75235101 - TCGA-BS-A0UJ-01 COSM1588549 c.2238+2T>C p.? Unknown 16:75233844-75233844 - CCK81 COSM2691221 c.1251A>G p.E417E Substitution - coding silent 16:75235648-75235648 - TCGA-CG-5723-01 COSM4062820 c.2257G>A p.A753T Substitution - Missense 16:75229867-75229867 - CHEWS024 COSM4579268 c.458C>A p.P153H Substitution - Missense 16:75242645-75242645 - 6 COSM4166702 c.237C>T p.P79P Substitution - coding silent 16:75242866-75242866 - TCGA-CJ-4881-01 COSM3361898 c.553G>T p.A185S Substitution - Missense 16:75242550-75242550 - 587316 COSM1184534 c.964G>T p.G322C Substitution - Missense 16:75236968-75236968 - 1266T COSM5762771 c.2262A>G p.E754E Substitution - coding silent 16:75230000-75230000 - CSCC-27-T COSM4480030 c.2380C>T p.L794L Substitution - coding silent 16:75229882-75229882 - ATL052 COSM5706222 c.124G>A p.G42R Substitution - Missense 16:75264377-75264377 - S02290 COSM5686521 c.1307G>T p.R436L Substitution - Missense 16:75235592-75235592 - SNUH_G16_S1 COSM3680018 c.1573G>A p.A525T Substitution - Missense 16:75235326-75235326 - TCGA-BR-8487-01 COSM1135837 c.702G>A p.G234G Substitution - coding silent 16:75242539-75242539 - TCGA-EB-A3Y6-01 COSM3512259 c.387C>T p.A129A Substitution - coding silent 16:75242854-75242854 - 1517_PT COSM5754911 c.1021C>A p.P341T Substitution - Missense 16:75235878-75235878 - 112038 COSM95778 c.1749G>A p.S583S Substitution - coding silent 16:75235150-75235150 - TCGA-BS-A0UJ-01 COSM973716 c.88A>G p.M30V Substitution - Missense 16:75243015-75243015 - TCGA-E9-A1RF-01 COSM1479099 c.2200A>G p.I734V Substitution - Missense 16:75233884-75233884 - YUGATOR COSM1588545 c.610C>T p.P204S Substitution - Missense 16:75242631-75242631 - TCGA-EB-A431-01 COSM3512247 c.1285C>T p.P429S Substitution - Missense 16:75235752-75235752 - TCGA-BR-8487-01 COSM472110 c.564G>A p.G188G Substitution - coding silent 16:75242539-75242539 - PD6361a COSM1637161 c.2307G>A p.T769T Substitution - coding silent 16:75229955-75229955 - TCGA-BP-4167-01 COSM1135836 c.870C>T p.P290P Substitution - coding silent 16:75236924-75236924 - LP6005690-DNA_C01 COSM4409442 c.2608G>A p.A870T Substitution - Missense 16:75229516-75229516 - 587316 COSM1184531 c.1669G>A p.V557I Substitution - Missense 16:75235368-75235368 - TCGA-G4-6588-01 COSM1379790 c.1802C>A p.A601D Substitution - Missense 16:75235097-75235097 - TCGA-EB-A57M-01 COSM3512226 c.2439C>T p.T813T Substitution - coding silent 16:75229823-75229823 - TCGA-39-5021-01 COSM1147704 c.2378A>G p.Y793C Substitution - Missense 16:75229884-75229884 - TCGA-EB-A431-01 COSM3512249 c.1147C>T p.P383S Substitution - Missense 16:75235752-75235752 - HCT116 COSM2691249 c.951_952insC p.M318fs*17 Insertion - Frameshift 16:75236980-75236981 - PT42 COSM5925853 c.2188C>T p.P730S Substitution - Missense 16:75229936-75229936 - CSCC-27-T COSM4480033 c.2242C>T p.L748L Substitution - coding silent 16:75229882-75229882 - CHC892T COSM4795620 c.1860G>A p.E620E Substitution - coding silent 16:75235177-75235177 - WSU-HN30 COSM4600909 c.1610G>T p.R537L Substitution - Missense 16:75235427-75235427 - TCGA-22-1012-01 COSM704120 c.2426G>A p.R809H Substitution - Missense 16:75229698-75229698 - 8030032 COSM3387599 c.2737C>T p.L913L Substitution - coding silent 16:75229525-75229525 - sysucc-1370T COSM4665325 c.2524G>A p.G842R Substitution - Missense 16:75229738-75229738 - 75 COSM5015407 c.1535A>T p.Q512L Substitution - Missense 16:75235364-75235364 - Detroit_562 COSM2691174 c.2246A>G p.Q749R Substitution - Missense 16:75230016-75230016 - 2249677 COSM4413301 c.1610G>A p.R537H Substitution - Missense 16:75235427-75235427 - 75 COSM5015404 c.1673A>T p.Q558L Substitution - Missense 16:75235364-75235364 - TCGA-BH-A18G-01 COSM3818566 c.710C>T p.P237L Substitution - Missense 16:75237268-75237268 - STC252 COSM5055102 c.620C>T p.A207V Substitution - Missense 16:75242621-75242621 - TCGA-CD-A4MI-01 COSM4062813 c.2428G>A p.A810T Substitution - Missense 16:75229834-75229834 - TCGA-22-5478-01 COSM704118 c.2284G>T p.V762L Substitution - Missense 16:75229840-75229840 - TCGA-AA-3712-01 COSM3755081 c.1458T>G p.S486S Substitution - coding silent 16:75235579-75235579 - 587316 COSM1184530 c.1696C>T p.R566W Substitution - Missense 16:75235203-75235203 - TCGA-BS-A0UV-01 COSM1588543 c.248C>T p.T83M Substitution - Missense 16:75242993-75242993 - TCGA-CM-6674-01 COSM3691313 c.975C>T p.G325G Substitution - coding silent 16:75236957-75236957 - SJBALL020649_D1 COSM4993821 c.152G>A p.R51H Substitution - Missense 16:75242951-75242951 - TCGA-AO-A128-01 COSM3818562 c.860A>G p.Y287C Substitution - Missense 16:75236934-75236934 - TCGA-BP-4968-01 COSM1135837 c.702G>A p.G234G Substitution - coding silent 16:75242539-75242539 - C086 COSM5527284 c.1434C>T p.T478T Substitution - coding silent 16:75235603-75235603 - KYSE-140 COSM2691273 c.515G>C p.G172A Substitution - Missense 16:75242726-75242726 - TCGA-BH-A0B1-01 COSM5833178 c.2246delA p.E749fs*7 Deletion - Frameshift 16:75229878-75229878 - TCGA-BP-5169-01 COSM1135833 c.1623G>T p.E541D Substitution - Missense 16:75235414-75235414 - HCC172T COSM3717081 c.2463C>T p.D821D Substitution - coding silent 16:75229661-75229661 - YUKLAB COSM35325 c.2339C>T p.A780V Substitution - Missense 16:75229785-75229785 - PCSI_0090_Pa_X COSM3377980 c.1371G>A p.A457A Substitution - coding silent 16:75235666-75235666 - TCGA-EE-A17X-06 COSM3512253 c.641C>T p.P214L Substitution - Missense 16:75242600-75242600 - TCGA-EI-6882-01 COSM3421159 c.1712C>T p.A571V Substitution - Missense 16:75235325-75235325 - LOVO COSM2691141 c.2744C>T p.A915V Substitution - Missense 16:75229518-75229518 - CHC1044T COSM4790955 c.1991A>G p.Y664C Substitution - Missense 16:75234908-75234908 - HCC13T COSM1609664 c.2373G>A p.K791K Substitution - coding silent 16:75229751-75229751 - RK141_C01 COSM1629990 c.2199A>G p.T733T Substitution - coding silent 16:75229925-75229925 - PTC-7C COSM3755080 c.1530T>C p.A510A Substitution - coding silent 16:75235369-75235369 - TCGA-D3-A51G-06 COSM3512264 c.241A>G p.T81A Substitution - Missense 16:75242862-75242862 - HCC172T COSM3717079 c.2601C>T p.D867D Substitution - coding silent 16:75229661-75229661 - sysucc-783T COSM5484050 c.1208C>T p.P403L Substitution - Missense 16:75235829-75235829 - TCGA-EE-A2GM-06 COSM3512225 c.2466C>T p.L822L Substitution - coding silent 16:75229658-75229658 - TCGA-BH-A0B1-01 COSM5833169 c.2387_2388insA p.C797fs*2 Insertion - Frameshift 16:75229874-75229875 - TCGA-CG-5723-01 COSM4062817 c.2395G>A p.A799T Substitution - Missense 16:75229867-75229867 - HCT116 COSM2691251 c.813_814insC p.M272fs*17 Insertion - Frameshift 16:75236980-75236981 - B96 COSM1749782 c.295T>A p.Y99N Substitution - Missense 16:75242808-75242808 - I2L-P19Ta-Tumor-Biopsy COSM5363356 c.2322G>A p.P774P Substitution - coding silent 16:75229802-75229802 - PTC-7C COSM3755077 c.1668T>C p.A556A Substitution - coding silent 16:75235369-75235369 - STC252 COSM5055105 c.482C>T p.A161V Substitution - Missense 16:75242621-75242621 - TCGA-CD-A4MI-01 COSM4062816 c.2290G>A p.A764T Substitution - Missense 16:75229834-75229834 - HCC13T COSM131194 c.1776G>T p.Q592H Substitution - Missense 16:75235123-75235123 - TCGA-18-3417-01 COSM1147705 c.2264A>T p.Q755L Substitution - Missense 16:75229998-75229998 - TCGA-F1-A448-01 COSM4062809 c.2563C>T p.R855C Substitution - Missense 16:75229699-75229699 - LP6005409-DNA_G03 COSM4409182 c.2102A>G p.N701S Substitution - Missense 16:75234935-75234935 - TCGA-22-1012-01 COSM1147702 c.2564G>A p.R855H Substitution - Missense 16:75229698-75229698 - sysucc-783T COSM5484054 c.1070C>T p.P357L Substitution - Missense 16:75235829-75235829 - 1517_CLM COSM5754907 c.1159C>A p.P387T Substitution - Missense 16:75235878-75235878 - TCGA-AA-3712-01 COSM1128876 c.1320T>G p.S440S Substitution - coding silent 16:75235579-75235579 - 587316 COSM1184533 c.1531G>A p.V511I Substitution - Missense 16:75235368-75235368 - TCGA-EE-A20F-06 COSM3512243 c.1798A>T p.N600Y Substitution - Missense 16:75235101-75235101 - TCGA-EE-A2GU-06 COSM3512232 c.2067C>T p.F689F Substitution - coding silent 16:75234970-75234970 - CHC1044T COSM4790952 c.2129A>G p.Y710C Substitution - Missense 16:75234908-75234908 - TCGA-BS-A0UV-01 COSM973702 c.1697G>A p.R566Q Substitution - Missense 16:75235202-75235202 - PTC-77C COSM1563497 c.364C>T p.P122S Substitution - Missense 16:75242877-75242877 - TCGA-AA-3712-01 COSM3755077 c.1668T>C p.A556A Substitution - coding silent 16:75235369-75235369 - TCGA-AM-5820-01 COSM3755073 c.2499C>T p.L833L Substitution - coding silent 16:75229763-75229763 - LIM1215 COSM4262570 c.2327C>T p.P776L Substitution - Missense 16:75229935-75229935 - TCGA-HU-A4GQ-01 COSM4062821 c.1232C>T p.P411L Substitution - Missense 16:75235805-75235805 - PTC-70C COSM4129360 c.1401G>A p.P467P Substitution - coding silent 16:75235636-75235636 - YUROS COSM5385396 c.777C>T p.P259P Substitution - coding silent 16:75237201-75237201 - TCGA-BH-A0B1-01 COSM5833174 c.2384delA p.E795fs*7 Deletion - Frameshift 16:75229878-75229878 - I2L-P19Tb-Tumor-Biopsy COSM5363438 c.1839G>A p.P613P Substitution - coding silent 16:75235060-75235060 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.479728;Hs.479744;Hs.479747 16q23.1 602941 2466988|CGAP|BC062556|A/T|non-coding||2998|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.V260G c.779T>G 16 75271235 BRCA A T Missense p.V420E c.1259T>A 16 75269676 CM A T Synonymous p.L587L c.1761T>A 16 75269174 LUAD C A Missense p.A231S c.691G>T 16 75276448 RCCC C A Missense p.A3S c.7G>T 16 75298392 UCEC C A Missense p.E541D c.1623G>T 16 75269312 RCCC C A Missense p.K723N c.2169G>T 16 75267813 STAD C A Missense p.M707I c.2121G>T 16 75268814 LUAD C A Missense p.V808L c.2422G>T 16 75263738 LUSC C A Nonsense p.E727* c.2179G>T 16 75267803 BRCA C A Nonsense p.E80* c.238G>T 16 75276901 RCCC C A Synonymous p.L79L c.237G>T 16 75276902 RCCC C A Synonymous p.P495P c.1485G>T 16 75269450 HNSC C A Synonymous p.V407V c.1221G>T 16 75269714 LUSC C - Frameshift p.P291Hfs*68 c.870delG 16 75271144 PRAD C G Synonymous p.L667L c.2001G>C 16 75268934 LUSC C T Missense p.D419N c.1255G>A 16 75269680 ESCA C T Missense p.R855H c.2564G>A 16 75263596 LUSC C T Synonymous p.P255P c.765G>A 16 75276374 BLCA G A IntronicSNV . c.1050+34C>T 16 75270746 BRCA G A IntronicSNV . c.151-5796C>T 16 75282784 HC G A Missense p.A231V c.692C>T 16 75276447 UCEC G A Missense p.P141S c.421C>T 16 75276718 CM G A Missense p.P214L c.641C>T 16 75276498 CM G A Missense p.P659L c.1976C>T 16 75268959 CM G A Missense p.T769M c.2306C>T 16 75263854 STAD G A Synonymous p.F689F c.2067C>T 16 75268868 CM G A Synonymous p.F792F c.2376C>T 16 75263784 LUAD G A Synonymous p.I841I c.2523C>T 16 75263637 HNSC G A Synonymous p.L622L c.1864C>T 16 75269071 CM G A Synonymous p.L68L c.204C>T 16 75276935 HNSC G A Synonymous p.L868L c.2604C>T 16 75263556 CM G A Synonymous p.P166P c.498C>T 16 75276641 CM G C Missense p.S453T c.1358G>C 16 75269577 BRCA G - Frameshift p.P687Lfs*61 c.2060delC 16 75268875 HNSC G T Missense p.P179T c.535C>A 16 75276604 LUSC G T Missense p.R71S c.211C>A 16 75276928 CM G T Synonymous p.L650L c.1950C>A 16 75268985 CM G T Synonymous p.R71R c.213C>A 16 75276926 HNSC G T Synonymous p.S476S c.1428C>A 16 75269507 HNSC T A Missense p.N646Y c.1936A>T 16 75268999 CM T A Missense p.N863I c.2588A>T 16 75263572 LUSC T A Missense p.Q755L c.2264A>T 16 75263896 LUSC T C Missense p.I734V c.2200A>G 16 75267782 BRCA T C Missense p.K822E c.2464A>G 16 75263696 SCLC T C Missense p.Y793C c.2378A>G 16 75263782 LUSC T C Synonymous p.T779T c.2337A>G 16 75263823 HC