PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

DOCK5_intron; chr8; 25182874

DOCK5_intron; chr8; 25182874

COSMIC somatic mutation   [Top]

c.4138A>G; p.I1380V;

c.2851-2_2851-1insG; p.?;

c.904C>T; p.R302C;

c.904C>T; p.R302C;

c.4417A>G; p.K1473E;

c.2108T>C; p.L703P;

c.2425G>A; p.A809T;

c.4958G>A; p.R1653H;

c.992A>T; p.D331V;

c.4036G>A; p.A1346T;

c.4372G>T; p.E1458*;

c.1257C>T; p.H419H;

c.4927C>T; p.P1643S;

c.3042C>T; p.N1014N;

c.4669C>G; p.P1557A;

c.1660C>G; p.L554V;

c.2709G>A; p.S903S;

c.3068A>G; p.Q1023R;

c.3618C>T; p.D1206D;

c.1827C>T; p.F609F;

c.1994T>C; p.I665T;

c.2959A>T; p.M987L;

c.2132A>G; p.H711R;

c.2137A>T; p.N713Y;

c.3214_3215insA; p.I1072fs*3;

c.680A>C; p.N227T;

c.2886G>T; p.Q962H;

c.2083G>C; p.D695H;

c.4221G>A; p.K1407K;

c.1684C>G; p.L562V;

c.4405C>A; p.R1469R;

c.4130G>A; p.R1377Q;

c.275C>T; p.T92M;

c.1856G>A; p.S619N;

c.3525G>T; p.L1175L;

c.4037C>A; p.A1346D;

c.4339C>G; p.P1447A;

c.4339C>G; p.P1447A;

c.225-1G>A; p.?;

c.2097T>C; p.F699F;

c.3709G>A; p.E1237K;

c.3627C>A; p.T1209T;

c.5082G>T; p.P1694P;

c.2400G>T; p.M800I; 8:25254382-25254382

c.1747A>G; p.K583E;

c.3122A>T; p.Q1041L;

c.238G>T; p.V80L;

c.2549A>G; p.N850S; 8:25255872-25255872

c.242T>C; p.I81T; 8:25192019-25192019

c.4246G>A; p.E1416K;

c.3917C>T; p.S1306L;

c.136A>G; p.R46G;

c.5002C>T; p.R1668W;

c.2627A>T; p.E876V;

c.3061A>G; p.I1021V;

c.4942G>T; p.E1648*;

c.3902A>G; p.Y1301C;

c.3337A>T; p.T1113S;

c.5096C>T; p.S1699L;

c.3184G>C; p.E1062Q;

c.4500G>A; p.K1500K;

c.4859A>T; p.E1620V;

c.3778G>T; p.A1260S;

c.1190A>C; p.Q397P;

c.126_127GG>AT; p.G43C;

c.2792G>T; p.R931L;

c.2879T>G; p.L960R;

c.2193G>A; p.V731V;

c.501T>C; p.D167D;

c.4313C>T; p.P1438L;

c.4707delT; p.F1571fs*19;

c.3807G>A; p.E1269E;

c.1543G>A; p.V515I;

c.1828_1829insC; p.S612fs*4;

c.3580G>A; p.A1194T;

c.4633C>T; p.H1545Y;

c.877C>T; p.R293C;

c.5137G>A; p.A1713T;

c.751T>C; p.S251P;

c.4706_4707insT; p.T1572fs*10;

c.3003C>A; p.V1001V;

c.2375G>A; p.R792H;

c.100A>G; p.T34A;

c.529G>A; p.E177K;

c.2609G>A; p.R870Q;

c.529G>A; p.E177K;

c.250G>A; p.E84K;

c.4707delT; p.F1571fs*19;

c.1931G>A; p.R644H;

c.4272G>T; p.Q1424H;

c.3581C>T; p.A1194V;

c.5183G>A; p.R1728Q;

c.5007G>T; p.R1669S;

c.2709G>A; p.S903S;

c.3213A>C; p.K1071N;

c.1031A>G; p.H344R;

c.1901A>G; p.N634S;

c.5100C>A; p.I1700I;

c.2353G>T; p.D785Y;

c.3863A>G; p.Y1288C;

c.4850C>T; p.P1617L;

c.2001+2T>C; p.?;

c.132G>A; p.W44*;

c.2166G>T; p.K722N;

c.3294A>C; p.K1098N;

c.3363G>A; p.R1121R;

c.3883G>T; p.E1295*;

c.4259C>T; p.S1420L;

c.4037C>G; p.A1346G;

c.529G>A; p.E177K;

c.2331T>G; p.F777L;

c.4398G>A; p.R1466R;

c.241A>G; p.I81V;

c.2399T>C; p.M800T;

c.2548A>G; p.N850D;

c.71A>G; p.D24G;

c.5281G>T; p.A1761S;

c.625G>A; p.D209N;

c.3678C>T; p.N1226N;

c.796G>A; p.G266R;

c.1097C>T; p.P366L;

c.4344G>T; p.E1448D;

c.360G>A; p.M120I;

c.5130G>C; p.S1710S;

c.5505T>C; p.T1835T;

c.808G>T; p.E270*;

c.1215C>G; p.L405L;

c.1118T>C; p.I373T;

c.1113C>T; p.H371H;

c.4904A>T; p.K1635M;

c.3206G>A; p.R1069H;

c.3907G>A; p.E1303K;

c.1852G>A; p.D618N;

c.2236G>T; p.D746Y;

c.1924A>T; p.N642Y;

c.2563C>T; p.Q855*;

c.1729delA; p.M579fs*8;

c.2549A>G; p.N850S; 8:25255872-25255872

c.2766G>A; p.A922A;

c.3817-2A>G; p.?;

c.1228C>A; p.L410I;

c.2117A>G; p.D706G;

c.3250G>A; p.G1084S;

c.452A>C; p.K151T;

c.4558G>A; p.E1520K;

c.976+2T>G; p.?;

c.4043_4057del15; p.Y1349_I1353delYENII;

c.250G>A; p.E84K;

c.1353C>G; p.I451M;

c.241A>G; p.I81V;

c.1960C>A; p.L654I;

c.831C>G; p.L277L;

c.3928A>T; p.K1310*;

c.1374_1376delGAA; p.K461delK;

c.5091T>C; p.D1697D;

c.1162G>A; p.A388T;

c.127+1G>A; p.?;

c.4486C>T; p.P1496S;

c.4371T>C; p.N1457N;

c.397T>C; p.S133P;

c.871C>T; p.R291W;

c.1165G>A; p.A389T;

c.1072C>T; p.R358C;

c.242T>C; p.I81T; 8:25192019-25192019

c.2201C>T; p.S734F;

c.2867G>T; p.C956F;

c.2534A>C; p.Q845P;