
| 基因名 | 突变 |
|---|---|
| FMN2(NM_020066,formin 2,1722aa) | g.1:240370354C>T,c.2242C>T,p.P748S |
| FMN2(NM_020066,formin 2,1722aa) | g.1:240351543G>A,c.1967G>A,p.R656H |
| FMN2(NM_020066,formin 2,1722aa) | g.1:240351542C>T,c.1966C>T,p.R656C |
| FMN2(NM_020066,formin 2,1722aa) | g.1:240351534C>T,c.1958C>T,p.P653L |
| FMN2(NM_020066,formin 2,1722aa) | g.1:240256668A>C,c.1259A>C,p.K420T |
| FMN2(NM_020066,formin 2,1722aa) | g.1:240256112C>T,c.703C>T,p.P235S |
| FMN2(NM_020066,formin 2,1722aa) | g.1:240255571_240255573del,c.162_164del,p.54_55del |
| FMN2(NM_020066,formin 2,1722aa) | g.1:240255570_240255572del,c.161_163del,p.54_55del |
| FMN2(NM_020066,formin 2,1722aa) | g.1:240255569_240255571del,c.160_162del,p.54del |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33447024C>G,c.92G>C,p.G31A |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446971T>C,c.145A>G,p.N49D |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446947A>C,c.169T>G,p.S57A |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446919G>A,c.197C>T,p.P66L |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446748G>A,c.368C>T,p.S123F |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446610A>G,c.506T>C,p.F169S |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446388G>A,c.728C>T,p.T243M |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446344T>C,c.772A>G,p.K258E |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446311G>C,c.805C>G,p.P269A |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446301C>G,c.815G>C,p.S272T |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33446160C>T,c.956G>A,p.R319Q |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33445999G>C,c.1117C>G,p.L373V |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33445983G>A,c.1133C>T,p.A378V |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33445551G>A,c.1565C>T,p.S522L |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33445450A>C,c.1666T>G,p.C556G |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33445438G>A,c.1678C>T,p.R560C |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33445338C>T,c.1778G>A,p.G593D |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33381139T>C,c.1904A>G,p.N635S |
| FMN1(NM_001277313,formin 1,1419aa) | g.15:33381040C>G,c.2003G>C,p.R668T |