PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.522C>T; p.V174V;

c.1147C>T; p.H383Y;

c.296T>G; p.V99G;

c.1915A>C; p.K639Q;

c.989C>T; p.S330L;

c.550C>A; p.L184M;

c.323G>T; p.R108L;

c.930C>G; p.A310A;

c.1026G>A; p.A342A;

c.1934C>T; p.P645L;

c.333C>A; p.A111A;

c.1087A>G; p.I363V; 23:47320545-47320545

c.724G>A; p.E242K;

c.981G>A; p.M327I;

c.399A>T; p.K133N;

c.98C>A; p.P33Q;

c.821A>G; p.H274R;

c.406C>A; p.H136N;

c.1298A>T; p.H433L;

c.1122G>A; p.A374A;

c.483C>A; p.F161L;

c.977A>G; p.Y326C;

c.943C>T; p.R315C;

c.732C>A; p.F244L;

c.817G>A; p.A273T;

c.740T>C; p.I247T;

c.1111G>A; p.A371T;

c.444C>A; p.F148L;

c.1026G>A; p.A342A;

c.623C>A; p.A208D;

c.892A>G; p.T298A;

c.530C>A; p.S177Y;

c.390C>A; p.F130L;

c.1337G>A; p.R446H;

c.754T>C; p.Y252H;

c.1227C>T; p.L409L;

c.464C>A; p.A155D;

c.1138G>A; p.G380R;

c.700C>T; p.R234*;

c.39T>G; p.F13L;

c.1076C>T; p.T359M;

c.985A>G; p.T329A;

c.444C>A; p.F148L;

c.1368G>A; p.P456P;

c.882C>T; p.V294V;

c.727G>A; p.E243K;

c.1005G>A; p.W335*;

c.1968G>A; p.P656P;

c.398A>T; p.K133I;