
| 基因名 | 突变 |
|---|---|
| EVA1C(NM_058187,eva-1 homolog C (C. elegans),441aa) | g.21:33876260C>T,c.884C>T,p.S295L |
| EVA1C(NM_058187,eva-1 homolog C (C. elegans),441aa) | g.21:33829993G>A,c.446G>A,p.S149N |
| EVA1B(NM_018166,eva-1 homolog B (C. elegans),165aa) | g.1:36787970C>G,c.424G>C,p.D142H |
| EVA1A(NM_001135032,eva-1 homolog A (C. elegans),152aa) | g.2:75720637C>T,c.184G>A,p.D62N |
| EVA1A(NM_001135032,eva-1 homolog A (C. elegans),152aa) | g.2:75720569_75720577del,c.244_252del,p.82_84del |
| EVA1A(NM_001135032,eva-1 homolog A (C. elegans),152aa) | g.2:75720372C>T,c.449G>A,p.R150H |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343727C>T,c.10G>A,p.G4R |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343721G>A,c.16C>T,p.R6W |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343720C>T,c.17G>A,p.R6Q |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343714C>T,c.23G>A,p.R8Q |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343699C>T,c.38G>A,p.R13H |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343673G>A,c.64C>T,p.L22F |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343658C>T,c.79G>A,p.A27T |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343639T>C,c.98A>G,p.K33R |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36343616C>T,c.121G>A,p.G41R |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36341251G>A,c.235C>T,p.H79Y |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36339176C>T,c.418G>A,p.G140S |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36339143C>T,c.451G>A,p.A151T |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36339136G>A,c.458C>T,p.P153L |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36336803G>A,c.533C>T,p.T178I |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36336764G>A,c.572C>T,p.A191V |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36334749G>A,c.634C>T,p.R212W |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36334748C>T,c.635G>A,p.R212Q |
| ETV7(NM_001207037,ets variant 7,282aa) | g.6:36334731C>T,c.652G>A,p.E218K |
| ETV6(NM_001987,ets variant 6,452aa) | g.12:12022766G>A,c.872G>A,p.R291K |
| ETV6(NM_001987,ets variant 6,452aa) | g.12:12022499G>A,c.605G>A,p.R202Q |
| ETV6(NM_001987,ets variant 6,452aa) | g.12:12022496T>C,c.602T>C,p.L201P |
| ETV6(NM_001987,ets variant 6,452aa) | g.12:12022390G>A,c.496G>A,p.V166M |