| 基因名 | 突变 |
|---|---|
| IPO8(NM_006390,importin 8,1037aa) | g.12:30818691A>G,c.1310T>C,p.I437T |
| IPO8(NM_006390,importin 8,1037aa) | g.12:30809648T>C,c.1918A>G,p.I640V |
| IPO8(NM_006390,importin 8,1037aa) | g.12:30802105A>G,c.2234T>C,p.I745T |
| IPO8(NM_006390,importin 8,1037aa) | g.12:30789975C>T,c.2636G>A,p.R879K |
| IPO8(NM_006390,importin 8,1037aa) | g.12:30787059T>C,c.2857A>G,p.N953D |
| IPO5(NM_002271,importin 5,1115aa) | g.13:98672038A>C,c.3094A>C,p.N1032H |
| IPO5(NM_002271,importin 5,1115aa) | g.13:98671883C>T,c.2939C>T,p.T980I |
| IPO5(NM_002271,importin 5,1115aa) | g.13:98669078G>T,c.2643G>T,p.Q881H |
| IPO5(NM_002271,importin 5,1115aa) | g.13:98645416G>A,c.904G>A,p.V302I |
| IPO5(NM_002271,importin 5,1115aa) | g.13:98642472C>T,c.614C>T,p.P205L |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24657936G>A,c.58C>T,p.R20C |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24656739G>A,c.455C>T,p.A152V |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24655174C>T,c.1062G>A,p.M354I |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24655130C>T,c.1106G>A,p.R369H |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24654455G>C,c.1342C>G,p.P448A |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24653957T>C,c.1535A>G,p.Q512R |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24653954G>A,c.1538C>T,p.A513V |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24653523G>C,c.1738C>G,p.P580A |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24652331C>T,c.2272G>A,p.A758T |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24652315C>T,c.2288G>A,p.R763Q |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24651492A>G,c.2590T>C,p.C864R |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24649946C>G,c.3064G>C,p.E1022Q |
| IPO4(NM_024658,importin 4,1081aa) | g.14:24649937G>T,c.3073C>A,p.R1025S |
| IPO13(NM_014652,importin 13,963aa) | g.1:44426880A>T,c.2290A>T,p.I764F |
| IPO13(NM_014652,importin 13,963aa) | g.1:44425999G>A,c.2107G>A,p.E703K |
| IPO13(NM_014652,importin 13,963aa) | g.1:44422051G>A,c.881G>A,p.R294Q |
| IPO13(NM_014652,importin 13,963aa) | g.1:44415735A>T,c.731A>T,p.Q244L |
| IPO13(NM_014652,importin 13,963aa) | g.1:44415659C>T,c.655C>T,p.R219C |