PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.4186G>A; p.A1396T;

c.2080C>T; p.R694C;

c.4202delA; p.K1401fs*29;

c.2540C>A; p.S847*;

c.5085G>C; p.E1695D;

c.2486C>T; p.A829V;

c.4394G>A; p.G1465D;

c.4810G>A; p.A1604T;

c.197G>A; p.R66H;

c.3119C>T; p.A1040V;

c.731G>A; p.R244H;

c.1589G>A; p.S530N;

c.1366G>A; p.A456T;

c.3328G>A; p.V1110M;

c.1460G>A; p.R487H;

c.4201A>C; p.K1401Q;

c.1938G>T; p.K646N;

c.829C>T; p.R277W;

c.5177C>T; p.A1726V;

c.2420G>T; p.G807V;

c.1460G>A; p.R487H;

c.5133_5138delCGACGA; p.D1711_D1712delDD;

c.1840C>T; p.R614C;

c.1840C>T; p.R614C;

c.1840C>T; p.R614C;

c.4734C>T; p.C1578C;

c.1968C>T; p.Y656Y;

c.2162G>T; p.S721I;

c.2179G>C; p.D727H;

c.1268A>C; p.N423T;

c.312C>T; p.P104P;

c.3276C>T; p.V1092V;

c.1136G>A; p.R379Q;

c.990G>C; p.G330G;

c.1353C>T; p.P451P;

c.3287C>T; p.T1096M;

c.3263C>T; p.P1088L;

c.80G>T; p.G27V;

c.1508C>T; p.T503M;

c.4655G>T; p.S1552I;

c.64delG; p.A22fs*8;

c.754C>G; p.L252V;

c.683A>T; p.D228V;

c.366C>T; p.Y122Y;

c.1866G>C; p.K622N;

c.3817_3818insC; p.A1274fs*76;

c.3137_3145delACGGGGCCA; p.D1046_I1049>V;

c.891C>T; p.H297H;

c.1508C>T; p.T503M;

c.3840C>T; p.F1280F;

c.2064C>G; p.H688Q;

c.3976C>T; p.R1326W;

c.4138G>T; p.V1380L;

c.2589G>A; p.M863I;

c.4099G>C; p.E1367Q;

c.1923C>T; p.A641A;

c.4111A>T; p.M1371L;

c.2659C>G; p.P887A;

c.80G>A; p.G27D;

c.1582C>T; p.R528C;

c.1410-1G>C; p.?;

c.4635C>T; p.A1545A;

c.964G>A; p.G322S;

c.2193G>T; p.L731L;

c.5100C>G; p.D1700E;

c.2733G>T; p.P911P;

c.2044A>C; p.T682P;

c.1555G>A; p.D519N;

c.1582C>T; p.R528C;

c.4022G>C; p.G1341A;

c.3684_3685delCT; p.C1229fs*38;

c.4382G>A; p.R1461H;

c.3427C>T; p.P1143S;

c.1114C>T; p.R372C;

c.3555C>T; p.L1185L;

c.2266G>A; p.A756T;

c.3644A>G; p.N1215S;

c.633G>A; p.A211A;

c.233G>A; p.R78H;

c.1084G>A; p.A362T;

c.5133_5138delCGACGA; p.D1711_D1712delDD;

c.254G>A; p.R85Q;

c.1608C>T; p.S536S;

c.3310G>A; p.A1104T;

c.4402T>C; p.F1468L;

c.966C>T; p.G322G;

c.1762C>T; p.R588C;

c.2025C>T; p.C675C;

c.1795G>A; p.D599N;

c.3229G>A; p.E1077K;

c.3154G>A; p.A1052T;

c.555C>T; p.F185F;

c.3709C>T; p.R1237*;

c.3598G>A; p.E1200K;

c.1528C>T; p.R510C;

c.1547A>G; p.K516R;

c.455A>T; p.D152V;

c.549C>T; p.T183T;

c.3911G>A; p.R1304Q;

c.2167G>A; p.D723N;

c.2221T>C; p.S741P;

c.2934G>A; p.A978A;

c.1946A>G; p.Y649C;

c.2099C>T; p.S700L;

c.2844G>A; p.P948P;

c.1688C>A; p.T563K;

c.4672G>A; p.A1558T;

c.4401G>A; p.K1467K;

c.3351C>T; p.L1117L;

c.301G>A; p.A101T;

c.412G>C; p.E138Q;

c.4707G>A; p.S1569S;

c.5173G>A; p.E1725K;

c.2080C>T; p.R694C;

c.4203G>A; p.K1401K;

c.747C>T; p.G249G;

c.4347G>A; p.Q1449Q;

c.254G>A; p.R85Q;

c.2835C>T; p.H945H;

c.5044_5064del21; p.L1682_E1688delLELPEEE;

c.4612G>A; p.G1538S;

c.5128_5142del15; p.D1710_D1714delDDDED;

c.5034G>C; p.E1678D;

c.2754C>T; p.G918G;

c.531C>T; p.Y177Y;

c.2951C>T; p.A984V;

c.2123C>T; p.S708L;

c.817C>T; p.L273L;

c.3032G>A; p.R1011H;

c.5103C>G; p.D1701E;

c.3117C>T; p.G1039G;

c.1217C>T; p.A406V;

c.4743G>A; p.T1581T;

c.532G>A; p.A178T;

c.3917G>A; p.G1306D;

c.3244A>G; p.M1082V;

c.2118G>A; p.P706P;

c.701C>T; p.A234V;

c.2349A>G; p.S783S;

c.1599C>T; p.D533D;

c.3806C>T; p.A1269V;

c.1954G>A; p.E652K;

c.3326C>T; p.S1109F;

c.454G>A; p.D152N;

c.3352G>C; p.A1118P;

c.1477C>G; p.L493V;

c.1792G>A; p.A598T;

c.3257C>T; p.S1086F;

c.352C>T; p.P118S;

c.3118G>A; p.A1040T;