PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.1537G>A; p.D513N;

c.1537G>A; p.D513N;

c.1798C>T; p.P600S;

c.538T>G; p.F180V;

c.766C>T; p.P256S;

c.1164C>T; p.F388F;

c.766C>T; p.P256S;

c.1164C>T; p.F388F;

c.262_268delGGGCGCC; p.G88fs*46;

c.24_26delGCT; p.L12delL;

c.1730G>A; p.G577E;

c.1049G>T; p.R350I;

c.1663G>C; p.G555R;

c.1612G>A; p.G538S;

c.862G>A; p.A288T;

c.1537G>A; p.D513N;

c.534G>T; p.L178F;

c.1894G>A; p.D632N;

c.566G>A; p.R189K;

c.1801delG; p.A601fs*4; 4:145875383-145875383

c.1267G>A; p.E423K;

c.190G>A; p.G64R;

c.190G>A; p.G64R;

c.1287C>T; p.L429L;

c.493G>T; p.D165Y;

c.13C>T; p.L5F;

c.255G>A; p.P85P;

c.758T>G; p.I253R;

c.287C>A; p.S96Y;

c.1490A>C; p.Y497S;

c.1719G>T; p.Q573H;

c.1684G>T; p.V562F;

c.1703G>A; p.S568N;

c.955C>T; p.L319F;

c.1209C>A; p.N403K;

c.803T>G; p.I268S;

c.1931G>A; p.R644H;

c.755A>C; p.K252T;

c.1891G>T; p.G631W;

c.642C>A; p.H214Q;

c.1413G>A; p.G471G;

c.116G>A; p.C39Y;

c.1226C>A; p.P409Q; 4:145848838-145848838

c.1423+2T>C; p.?; 4:145852675-145852675

c.1164C>T; p.F388F;

c.1700G>C; p.S567T;

c.1830G>T; p.R610S;

c.137A>G; p.K46R;

c.134C>T; p.P45L;

c.862G>A; p.A288T;

c.139C>T; p.R47C;

c.1526A>G; p.Y509C;

c.1745T>G; p.I582S;

c.734T>C; p.L245P;

c.284T>G; p.F95C;

c.1745T>G; p.I582S;

c.1540C>T; p.R514C;

c.1815T>G; p.T605T;

c.1612G>A; p.G538S;

c.97G>A; p.G33R;

c.1574C>A; p.P525H;

c.261A>C; p.L87L;

c.1097A>G; p.Y366C;

c.142C>A; p.L48M;

c.139C>T; p.R47C;

c.1421A>G; p.Y474C;

c.775G>T; p.E259*;

c.444C>A; p.F148L;

c.1672G>A; p.E558K;

c.1758A>G; p.K586K;

c.444C>A; p.F148L;

c.518G>T; p.R173I;

c.1461T>C; p.S487S;

c.1227A>G; p.P409P;

c.1740C>A; p.Y580*;

c.722G>A; p.R241H;

c.1085A>G; p.D362G;

c.1743A>C; p.K581N;

c.1524C>G; p.S508R;

c.54C>A; p.F18L;

c.1910-2A>G; p.?;

c.105G>T; p.R35S;

c.223C>T; p.R75W;

c.1291G>A; p.D431N;

c.350C>T; p.P117L;

c.1291G>A; p.D431N;

c.88G>A; p.E30K;

c.1594G>A; p.E532K;

c.1547G>A; p.G516E;