PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.859A>T; p.I287F;

c.707C>T; p.S236L;

c.387G>T; p.E129D;

c.404C>T; p.A135V;

c.84A>C; p.K28N;

c.784G>A; p.G262R;

c.528G>C; p.G176G;

c.609C>T; p.Y203Y;

c.795G>A; p.A265A;

c.221A>T; p.K74M;

c.394G>T; p.D132Y;

c.264delC; p.H90fs*2;

c.760G>T; p.G254C;

c.29T>G; p.L10*;

c.373G>A; p.A125T;

c.860T>A; p.I287N;

c.205C>T; p.R69C;

c.866A>T; p.K289M;

c.771A>T; p.P257P;

c.856A>G; p.K286E;

c.639G>T; p.R213R;

c.206G>A; p.R69H;

c.609C>T; p.Y203Y;

c.835G>A; p.D279N;

c.555G>A; p.A185A;

c.717+2T>C; p.?;

c.404C>T; p.A135V;

c.213G>T; p.A71A;

c.86delA; p.K29fs*36;

c.809C>T; p.S270L;

c.783C>T; p.Y261Y;

c.835G>A; p.D279N;

c.109C>T; p.R37W;

c.512T>C; p.I171T;

c.122A>T; p.E41V;

c.883A>G; p.S295G;

c.139G>A; p.G47R;

c.34G>T; p.A12S;

c.23G>A; p.R8Q;

c.86delA; p.K29fs*36;

c.86delA; p.K29fs*36;

c.637C>T; p.R213W;

c.757G>A; p.E253K;

c.713G>A; p.G238E;

c.23G>T; p.R8L;