PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.82A>G; p.I28V; 17:37695037-37695037

c.1905C>T; p.S635S;

c.1905C>T; p.S635S;

c.1151A>G; p.K384R;

c.2018G>A; p.R673H;

c.1906C>T; p.P636S;

c.1363C>T; p.L455F;

c.2305C>T; p.R769C;

c.2271C>T; p.T757T;

c.152C>T; p.P51L;

c.996C>T; p.F332F;

c.2384G>C; p.*795S;

c.1887C>T; p.I629I;

c.834G>A; p.W278*;

c.1681G>T; p.E561*;

c.1071C>T; p.G357G;

c.1099C>T; p.P367S;

c.464C>T; p.T155M;

c.1974C>G; p.D658E;

c.98A>T; p.Y33F;

c.2034C>T; p.V678V;

c.1054G>A; p.V352I;

c.562C>T; p.Q188*;

c.1651C>T; p.L551L;

c.320G>A; p.R107H;

c.1126G>T; p.E376*;

c.1888G>A; p.A630T;

c.489G>T; p.K163N;

c.1096delC; p.Q368fs*2;

c.850G>A; p.E284K;

c.118A>T; p.S40C;

c.82A>G; p.I28V; 17:37695037-37695037

c.1565A>G; p.N522S;

c.1303G>A; p.V435M;

c.1007A>G; p.K336R;

c.819C>T; p.D273D;

c.990-1G>A; p.?;

c.1447C>T; p.L483L;

c.559G>T; p.A187S;

c.1096delC; p.Q368fs*2;

c.1058G>A; p.R353H;

c.1946G>A; p.R649Q;

c.1203C>T; p.C401C;

c.2018G>A; p.R673H;

c.534G>C; p.E178D;

c.1170C>T; p.N390N;

c.1064T>C; p.L355P;

c.1064T>C; p.L355P;

c.1096C>T; p.P366S;