PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.958A>T; p.M320L;

c.877A>T; p.S293C;

c.1738G>C; p.D580H; 9:92690702-92690702

c.810T>G; p.F270L;

c.810T>G; p.F270L;

c.1625C>T; p.A542V;

c.1625C>T; p.A542V;

c.254C>T; p.P85L;

c.1828G>A; p.V610M;

c.154G>A; p.A52T;

c.1213G>A; p.D405N;

c.176G>A; p.R59K;

c.1796T>C; p.V599A;

c.851C>T; p.S284F;

c.259G>T; p.D87Y;

c.1428T>C; p.N476N;

c.1097A>G; p.Y366C;

c.1105A>C; p.M369L;

c.1432T>C; p.L478L;

c.76G>A; p.E26K;

c.988G>A; p.A330T;

c.685C>T; p.P229S;

c.854C>A; p.P285H;

c.647A>G; p.Y216C;

c.311A>G; p.K104R;

c.922G>T; p.A308S;

c.1635T>G; p.Y545*;

c.583C>T; p.R195*;

c.313A>G; p.K105E;

c.315G>T; p.K105N;

c.1368C>T; p.S456S; 9:92680912-92680912

c.1799A>G; p.E600G;

c.702C>A; p.F234L;

c.988G>A; p.A330T;

c.131G>T; p.S44I;

c.1048G>T; p.E350*;

c.1809G>A; p.L603L;

c.1014G>T; p.K338N;

c.1548C>T; p.Y516Y;

c.1548C>T; p.Y516Y;

c.1637G>T; p.G546V;

c.1113-1G>C; p.?;

c.936C>A; p.G312G;

c.1635T>G; p.Y545*;

c.1239C>T; p.I413I;

c.437C>G; p.A146G;

c.534T>C; p.S178S;

c.1772A>G; p.E591G;

c.1092G>T; p.K364N;

c.1651C>T; p.R551*;

c.490_491insA; p.M166fs*14;

c.272A>G; p.Y91C;

c.702C>T; p.F234F;

c.717+1G>A; p.?;

c.702C>T; p.F234F;

c.1206G>T; p.Q402H;

c.1043C>T; p.T348M;

c.108T>C; p.D36D;

c.897G>A; p.P299P;

c.1811G>A; p.R604H;

c.897G>A; p.P299P;

c.1706G>T; p.G569V;

c.1512G>T; p.K504N;

c.988G>A; p.A330T;

c.125G>A; p.R42H;

c.1367C>T; p.S456F;

c.965C>G; p.T322R;

c.737A>G; p.Y246C;

c.1465G>A; p.D489N;

c.1664G>A; p.G555E;

c.1700_1701GG>AC; p.R567H;

c.215G>A; p.G72D;

c.1142T>C; p.L381P;

c.1213G>A; p.D405N;

c.1372G>A; p.G458S;