PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.995G>C; p.R332T;

c.1010G>T; p.R337I;

c.178T>G; p.Y60D;

c.535C>A; p.L179I;

c.628A>G; p.T210A;

c.950C>T; p.A317V;

c.1016T>G; p.F339C;

c.543G>A; p.W181*;

c.931G>T; p.G311C;

c.545C>G; p.A182G;

c.1567C>T; p.P523S;

c.770A>G; p.K257R;

c.1192-1G>A; p.?;

c.1169C>A; p.P390H;

c.1022A>G; p.Q341R;

c.1344G>A; p.M448I;

c.418C>G; p.Q140E;

c.765C>T; p.I255I; 4:74529625-74529625

c.722C>A; p.T241N;

c.53C>G; p.S18C;

c.17C>T; p.S6L;

c.545C>G; p.A182G;

c.318G>T; p.E106D;

c.989T>A; p.L330Q;

c.1465G>A; p.E489K;

c.551G>A; p.R184H;

c.1260G>T; p.Q420H;

c.1036_1037insA; p.N348fs*10;

c.1494C>T; p.G498G;

c.148T>G; p.F50V;

c.1088C>T; p.P363L;

c.671G>A; p.C224Y;

c.1593C>A; p.F531L;

c.1578C>A; p.F526L;

c.1747T>A; p.C583S;

c.1427C>T; p.A476V;

c.697C>T; p.R233*;

c.855G>A; p.M285I;

c.1631C>T; p.A544V;

c.368A>C; p.N123T;

c.725A>G; p.K242R;

c.965A>C; p.K322T;

c.746A>G; p.K249R;

c.1111C>A; p.L371I;

c.64C>T; p.H22Y;

c.312T>G; p.I104M;

c.538C>A; p.L180I;

c.1823G>T; p.G608V;

c.1443C>T; p.I481I;

c.68G>T; p.R23I;

c.764T>C; p.I255T;

c.647G>T; p.S216I;

c.1061T>G; p.F354C;

c.1466A>G; p.E489G;

c.101C>A; p.S34Y;

c.404C>T; p.S135L;

c.424C>T; p.P142S;

c.409C>T; p.P137S;

c.1118T>C; p.V373A;

c.1447C>T; p.H483Y;