PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.1105A>G; p.N369D;

c.410G>T; p.R137M;

c.531G>T; p.K177N;

c.16G>A; p.D6N;

c.659+1G>T; p.?;

c.874A>G; p.K292E;

c.1039C>G; p.L347V;

c.15C>T; p.G5G;

c.874A>G; p.K292E;

c.791+1G>A; p.?;

c.748C>G; p.L250V;

c.1478A>T; p.H493L;

c.1015A>T; p.I339L;

c.338_341delAGAA; p.K114fs*98; 14:89499549-89499552

c.95C>T; p.S32F;

c.1187_1193delGTCAGTT; p.G396fs*24; 14:89525057-89525063

c.1703C>G; p.A568G;

c.1444G>T; p.A482S;

c.675G>T; p.L225L;

c.675G>T; p.L225L;

c.483_484GA>TT; p.N162Y;

c.1180G>T; p.V394F;

c.553A>G; p.I185V;

c.843C>T; p.T281T;

c.1177C>T; p.P393S;

c.147C>T; p.S49S;

c.513C>A; p.V171V;

c.911G>A; p.R304Q;

c.1027C>A; p.H343N;

c.1084T>C; p.F362L;

c.556A>G; p.K186E;

c.519A>G; p.G173G;

c.444A>G; p.S148S;

c.963T>C; p.A321A;

c.774G>A; p.A258A;

c.1243G>C; p.E415Q;

c.688G>A; p.D230N;

c.1270G>T; p.G424W;

c.1147G>A; p.A383T;

c.1686C>T; p.G562G;

c.16G>A; p.D6N;

c.750C>T; p.L250L;

c.330C>G; p.I110M;

c.945G>A; p.S315S;

c.944C>T; p.S315L;

c.1777C>T; p.P593S;

c.1154C>T; p.S385F;