PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.846G>A; p.K282K;

c.206G>A; p.R69H;

c.656C>T; p.S219L;

c.624C>T; p.L208L;

c.438C>A; p.F146L;

c.618G>T; p.S206S;

c.1065C>A; p.A355A;

c.1130C>A; p.A377D;

c.453C>A; p.Y151*;

c.437T>C; p.F146S;

c.1150_1151CA>AG; p.H384S;

c.933_934insA; p.A312fs*20;

c.1118C>A; p.A373D;

c.483C>A; p.S161S;

c.1152C>T; p.H384H;

c.584A>G; p.Y195C;

c.852G>A; p.T284T;

c.523C>T; p.R175W;

c.799C>A; p.R267R;

c.865C>G; p.R289G;

c.941G>A; p.R314Q;

c.603C>T; p.H201H;

c.580G>T; p.V194F;

c.1175C>G; p.P392R;

c.875G>A; p.R292Q;

c.524G>A; p.R175Q;

c.449G>A; p.R150H;

c.1142C>T; p.T381M;

c.876G>A; p.R292R;

c.517G>A; p.E173K;

c.391G>A; p.D131N;

c.556G>A; p.D186N;

c.1286G>A; p.G429D;

c.895C>T; p.R299C;

c.1130C>T; p.A377V;

c.544C>T; p.R182W;

c.1066G>A; p.A356T;

c.372C>A; p.S124R;

c.517G>A; p.E173K;

c.1062C>T; p.Y354Y;

c.1254G>T; p.K418N;

c.418G>A; p.V140M;

c.461G>T; p.R154L;

c.1050G>A; p.A350A;

c.1169C>T; p.T390M;

c.160A>G; p.M54V;

c.1049C>T; p.A350V;

c.881C>T; p.T294M;

c.1216G>A; p.V406I;

c.875G>A; p.R292Q;

c.744G>A; p.S248S;

c.517G>A; p.E173K;

c.907C>T; p.R303C;

c.265G>A; p.A89T;

c.1169C>T; p.T390M;

c.134G>A; p.R45H;

c.801G>A; p.R267R;

c.848C>G; p.A283G;

c.973G>A; p.D325N;

c.343G>A; p.G115S;