PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.592A>T; p.I198F;

c.793G>A; p.A265T;

c.1115C>T; p.A372V;

c.347C>T; p.S116L;

c.620C>T; p.S207L;

c.811G>T; p.V271F;

c.1167G>A; p.P389P;

c.215C>A; p.P72H;

c.1084C>T; p.Q362*;

c.910A>C; p.N304H;

c.134C>T; p.S45L;

c.196C>A; p.Q66K;

c.1145G>A; p.R382Q;

c.1178G>A; p.S393N;

c.873C>A; p.I291I;

c.663C>T; p.G221G;

c.888C>A; p.P296P;

c.626C>T; p.T209I;

c.1094A>G; p.K365R;

c.226C>A; p.P76T;

c.1352C>T; p.T451I;

c.1317C>A; p.N439K;

c.684G>C; p.E228D;

c.1103C>T; p.T368M;

c.113C>A; p.S38*;

c.1376G>A; p.R459K;

c.212C>A; p.P71Q;

c.697G>T; p.V233F;

c.990G>T; p.E330D;

c.813C>T; p.V271V;

c.813C>T; p.V271V;

c.1123C>A; p.R375R;

c.3G>T; p.M1I;

c.430G>A; p.V144I;

c.429G>C; p.S143S;

c.766C>G; p.R256G;

c.1135G>A; p.G379R;

c.888C>T; p.P296P;

c.292C>T; p.L98L;

c.157A>T; p.S53C;

c.1200C>T; p.L400L;

c.993T>G; p.F331L;

c.534C>T; p.D178D;

c.428C>T; p.S143L;

c.937G>A; p.E313K;

c.640A>G; p.N214D;

c.214delC; p.Y74fs*22;

c.918G>A; p.T306T;

c.91G>A; p.D31N;

c.1271C>T; p.A424V;

c.252delC; p.Y86fs*10;

c.1212C>T; p.G404G;

c.899G>A; p.R300H;

c.601G>T; p.V201F;

c.853C>T; p.R285*;

c.1062G>T; p.K354N;

c.81+7C>T; p.?;

c.430G>C; p.V144L;

c.1083G>A; p.K361K;

c.548A>T; p.E183V;

c.428C>T; p.S143L;

c.731C>T; p.S244L;

c.1057C>T; p.R353*;

c.1069C>A; p.L357M;

c.1211G>A; p.G404D;

c.899delG; p.R300fs*20;

c.797C>A; p.S266Y;

c.1236C>T; p.A412A;

c.585G>C; p.Q195H;

c.629C>T; p.S210F;

c.320G>A; p.G107E;

c.731C>T; p.S244L;

c.1245G>A; p.T415T;

c.1237G>A; p.A413T;

c.986C>T; p.T329M;

c.332G>A; p.R111Q;

c.731C>T; p.S244L;

c.54G>T; p.E18D;

c.982G>A; p.E328K;

c.1215C>T; p.F405F;

c.1375A>G; p.R459G;

c.995C>A; p.P332H;

c.1206G>A; p.T402T;

c.135G>A; p.S45S;

c.1187C>T; p.T396M;

c.347C>T; p.S116L;

c.270C>T; p.N90N;

c.160G>A; p.A54T;

c.693C>T; p.C231C;

c.160G>A; p.A54T;

c.1335A>G; p.E445E;