PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.759T>G; p.I253M;

c.205A>G; p.S69G;

c.319A>G; p.N107D;

c.1070G>A; p.R357Q;

c.762C>A; p.S254S;

c.85G>T; p.G29W;

c.1005A>T; p.G335G;

c.688T>C; p.S230P;

c.499A>G; p.I167V;

c.951G>C; p.W317C; 1:206128671-206128671

c.18C>T; p.G6G;

c.86G>A; p.G29E;

c.567C>T; p.I189I;

c.754G>T; p.E252*;

c.292G>T; p.V98L;

c.292G>T; p.V98L;

c.717G>T; p.R239S;

c.370C>A; p.P124T;

c.136C>A; p.Q46K;

c.1004G>T; p.G335V;

c.1025G>T; p.G342V;

c.114T>A; p.T38T;

c.406C>T; p.P136S;

c.1100C>A; p.A367D;

c.42G>A; p.P14P;

c.949T>C; p.W317R;

c.950G>A; p.W317*;

c.765C>T; p.S255S;

c.138G>T; p.Q46H;

c.544G>A; p.E182K;

c.890C>T; p.S297L;

c.488C>A; p.S163*;

c.470C>A; p.P157H;

c.904G>T; p.A302S;

c.378C>T; p.N126N;

c.950G>A; p.W317*;

c.867G>T; p.K289N;

c.684A>C; p.V228V;

c.1040C>T; p.P347L;

c.1092C>T; p.T364T;

c.752C>A; p.T251K;

c.302C>G; p.S101*;