PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.652C>T; p.L218L;

c.652C>T; p.L218L;

c.716G>A; p.S239N;

c.1226G>A; p.R409H;

c.404T>C; p.F135S;

c.1272T>C; p.S424S;

c.1352A>C; p.Q451P;

c.963C>G; p.L321L;

c.1009C>T; p.L337L;

c.1204G>A; p.D402N;

c.1022G>C; p.R341P;

c.777G>C; p.S259S; 17:38071305-38071305

c.1111C>A; p.H371N;

c.1098C>T; p.Y366Y;

c.1069C>T; p.Q357*;

c.314C>A; p.A105D;

c.675C>T; p.F225F;

c.127G>A; p.E43K;

c.406G>A; p.V136M;

c.1060G>A; p.A354T;

c.466C>T; p.R156*;

c.1049C>T; p.P350L;

c.717C>T; p.S239S;

c.436G>A; p.G146S;

c.1268G>T; p.R423M;

c.526G>A; p.D176N;

c.928G>A; p.D310N;

c.777G>T; p.S259S;

c.421A>T; p.I141F;

c.120C>T; p.F40F;

c.650G>A; p.R217H;

c.126C>T; p.T42T;

c.735delC; p.G247fs*3;

c.926G>A; p.R309Q;

c.772G>A; p.A258T;

c.814G>A; p.G272S;

c.775T>C; p.S259P;

c.100G>T; p.E34*;

c.576C>G; p.L192L;

c.1106C>T; p.S369L;

c.775T>C; p.S259P;

c.731G>A; p.R244H;

c.419_420CC>TT; p.S140F;