PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.1108G>A; p.D370N;

c.704C>T; p.A235V;

c.1694T>G; p.F565C;

c.194C>T; p.S65F; 13:112931816-112931816

c.112T>G; p.C38G;

c.1422A>G; p.G474G;

c.169G>A; p.D57N;

c.1446_1447insT; p.K483fs*1;

c.1029C>G; p.I343M;

c.1452+1G>C; p.?;

c.376-2A>C; p.?;

c.955G>A; p.A319T;

c.1591C>T; p.L531L;

c.1074delA; p.R360fs*62;

c.297G>T; p.L99L;

c.1470G>A; p.Q490Q; 13:112957025-112957025

c.823G>A; p.V275M;

c.300C>T; p.I100I;

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

c.906C>T; p.P302P;

c.139-1G>C; p.?;

c.658G>T; p.A220S;

c.872A>G; p.K291R;

c.520G>A; p.V174I;

c.1726G>A; p.E576K;

c.693C>T; p.G231G;

c.1971C>T; p.Y657Y;

c.1093_1094delAA; p.S366fs*6;

c.748G>A; p.A250T;

c.753C>T; p.I251I;

c.579G>T; p.Q193H;

c.724G>A; p.E242K;

c.604A>G; p.I202V;

c.967G>T; p.E323*;

c.1550C>T; p.T517M;

c.1511A>C; p.E504A;

c.903A>G; p.R301R;

c.1373A>G; p.Y458C;

c.1470G>T; p.Q490H;

c.1469A>G; p.Q490R;

c.324C>T; p.A108A;

c.995C>T; p.T332M;

c.385G>T; p.D129Y;

c.1468C>T; p.Q490*;

c.1005G>C; p.K335N;

c.846G>A; p.K282K;

c.1717C>G; p.Q573E;

c.790G>C; p.D264H;

c.1030C>T; p.H344Y;

c.755T>C; p.V252A;