PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.101A>C; p.K34T;

c.908C>T; p.S303L;

c.3G>T; p.M1I;

c.2051A>C; p.H684P;

c.2055T>G; p.T685T;

c.2660T>C; p.L887P;

c.64T>C; p.F22L;

c.2402T>G; p.F801C;

c.1204C>T; p.R402*;

c.2480delG; p.S827fs*18;

c.1042G>C; p.V348L;

c.1342A>T; p.R448*;

c.1894_1895insT; p.V633fs*12;

c.1710C>A; p.F570L;

c.111C>A; p.C37*;

c.776G>T; p.S259I;

c.958A>G; p.S320G;

c.1129C>T; p.P377S;

c.2601G>T; p.M867I;

c.2016A>G; p.S672S;

c.655G>T; p.G219*;

c.2030A>T; p.Q677L;

c.1033G>T; p.G345W;

c.1389A>T; p.Q463H;

c.1270G>T; p.E424*;

c.790C>T; p.P264S;

c.254C>T; p.T85I;

c.195G>C; p.E65D;

c.1951G>C; p.G651R;

c.2578T>A; p.L860I;

c.191A>T; p.Y64F;

c.2673G>T; p.K891N;

c.1889A>T; p.Y630F;

c.1542G>T; p.R514S;

c.276G>T; p.R92R;

c.464A>T; p.Y155F;

c.1804G>T; p.D602Y;

c.1390T>A; p.L464M;

c.1024A>G; p.T342A;

c.179C>T; p.S60L;

c.2273G>A; p.W758*;

c.72G>T; p.L24F;

c.909G>T; p.S303S;

c.1034G>T; p.G345V;

c.152C>A; p.A51D;

c.1296C>T; p.I432I;

c.2223G>T; p.V741V;

c.546G>A; p.Q182Q;

c.2059T>G; p.C687G;

c.2374G>C; p.V792L;

c.1798G>T; p.V600F;

c.553C>T; p.H185Y;

c.370G>T; p.D124Y;

c.767C>A; p.S256Y;

c.1674G>A; p.W558*;

c.2440A>C; p.I814L;

c.41-1G>T; p.?;

c.370+5G>A; p.?;

c.2538G>A; p.V846V;

c.580T>G; p.C194G;

c.290G>T; p.R97I;

c.343G>A; p.V115I;

c.736G>A; p.E246K;

c.2678C>T; p.T893M;

c.2484C>T; p.F828F;

c.1628T>C; p.V543A;

c.1818C>T; p.V606V;

c.593T>C; p.V198A;

c.227G>A; p.G76D;

c.1761G>A; p.E587E;

c.2284delC; p.S763fs*5;

c.866C>G; p.S289*;

c.1258C>T; p.H420Y;

c.1448C>A; p.S483Y;

c.95G>T; p.R32I;

c.180G>A; p.S60S;

c.767C>A; p.S256Y;

c.2656G>T; p.G886*;

c.2534T>C; p.I845T;

c.1286-1G>T; p.?;

c.1340G>A; p.C447Y;

c.2175A>G; p.A725A;

c.2608C>T; p.L870L;

c.1785T>G; p.S595S;

c.1834C>T; p.R612C;

c.866C>T; p.S289L;

c.2149A>T; p.I717F;

c.2171T>C; p.V724A;

c.976C>T; p.R326C;

c.1129C>T; p.P377S;

c.475G>A; p.V159I;

c.898C>T; p.P300S;

c.950G>A; p.G317E;