PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.773C>A; p.A258E;

c.547C>T; p.R183W;

c.21A>C; p.E7D;

c.57T>C; p.T19T;

c.460C>T; p.R154W;

c.1231G>A; p.G411R;

c.1231G>A; p.G411R;

c.1276C>T; p.P426S;

c.811A>G; p.I271V;

c.826G>A; p.G276S;

c.1367C>T; p.S456L;

c.382G>T; p.V128F;

c.1186A>G; p.T396A;

c.1186A>G; p.T396A;

c.21A>C; p.E7D;

c.270T>G; p.A90A;

c.29A>G; p.D10G; 2:10502581-10502581

c.774G>T; p.A258A;

c.493C>T; p.R165C;

c.1319C>A; p.S440Y;

c.159G>A; p.L53L;

c.568G>A; p.D190N;

c.108T>C; p.D36D;

c.199G>A; p.A67T;

c.654T>A; p.V218V;

c.295C>T; p.Q99*;

c.1023A>G; p.Q341Q;

c.1367C>T; p.S456L;

c.390G>T; p.M130I;

c.791C>T; p.P264L;

c.510C>T; p.F170F;

c.20A>G; p.E7G;

c.705C>T; p.G235G;

c.1282G>A; p.E428K;

c.417G>A; p.L139L;

c.316G>T; p.E106*;

c.29A>G; p.D10G; 2:10502581-10502581

c.889T>C; p.L297L;

c.29A>G; p.D10G; 2:10502581-10502581

c.1142T>C; p.M381T;