PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.1427G>A; p.R476H;

c.2935A>G; p.T979A;

c.3330-2A>G; p.?;

c.2947T>G; p.F983V;

c.1448C>T; p.T483M;

c.3263C>T; p.A1088V;

c.1074C>T; p.P358P;

c.2093G>A; p.C698Y;

c.1328C>T; p.S443F;

c.850C>A; p.R284S;

c.3183G>A; p.V1061V;

c.1717_1718insC; p.R573fs*8;

c.1013T>A; p.V338D;

c.2306-1G>A; p.?;

c.918G>T; p.G306G;

c.51G>A; p.L17L;

c.2161A>G; p.T721A;

c.1747C>G; p.Q583E; 17:39520443-39520443

c.1322A>T; p.H441L;

c.846G>A; p.L282L;

c.1038C>T; p.L346L;

c.1038C>T; p.L346L;

c.2220C>G; p.I740M;

c.2234C>G; p.S745C;

c.622C>T; p.P208S;

c.2594T>C; p.L865P;

c.1722G>T; p.E574D;

c.2079G>A; p.K693K;

c.3127G>A; p.A1043T;

c.924G>A; p.S308S;

c.1140C>A; p.V380V;

c.3127G>A; p.A1043T;

c.3028G>A; p.A1010T;

c.2501C>T; p.A834V;

c.2142C>A; p.I714I;

c.588G>T; p.K196N;

c.178C>T; p.R60W;

c.2727+1G>A; p.?;

c.2639C>T; p.A880V;

c.370C>T; p.L124L;

c.1748A>G; p.Q583R;

c.1871C>A; p.A624D;

c.2793delC; p.I932fs*14;

c.1749G>T; p.Q583H;

c.2330C>T; p.A777V;

c.420G>A; p.E140E;

c.1700G>A; p.G567E;

c.2796T>C; p.I932I;

c.604G>A; p.G202S;

c.3154G>A; p.E1052K;

c.1181C>T; p.S394L;

c.1402C>T; p.Q468*;

c.1696_1697insG; p.E566fs*15;

c.1748A>G; p.Q583R;

c.1444C>T; p.R482W;

c.927C>T; p.S309S;

c.2129G>A; p.R710Q;

c.1686C>A; p.V562V;

c.1748A>G; p.Q583R;

c.1265C>T; p.S422F;

c.1479G>A; p.L493L;

c.1838C>T; p.A613V;

c.2763C>T; p.N921N;

c.923C>T; p.S308L;

c.3132G>A; p.V1044V;

c.1748A>G; p.Q583R;

c.1789G>A; p.E597K;