| 基因名 | 突变 |
|---|---|
| HOXC11(NM_014212,homeobox C11,304aa) | g.12:54367216C>T,c.191C>T,p.S64L |
| HOXC10(NM_017409,homeobox C10,342aa) | g.12:54383021C>T,c.820C>T,p.P274S |
| HOXC10(NM_017409,homeobox C10,342aa) | g.12:54379780A>C,c.737A>C,p.D246A |
| HOXC10(NM_017409,homeobox C10,342aa) | g.12:54379335T>G,c.292T>G,p.S98A |
| HOXC10(NM_017409,homeobox C10,342aa) | g.12:54379117A>G,c.74A>G,p.Y25C |
| HOXB9(NM_024017,homeobox B9,250aa) | g.17:46703403C>A,c.229G>T,p.V77F |
| HOXB9(NM_024017,homeobox B9,250aa) | g.17:46703400A>G,c.232T>C,p.Y78H |
| HOXB9(NM_024017,homeobox B9,250aa) | g.17:46700486C>T,c.529G>A,p.A177T |
| HOXB9(NM_024017,homeobox B9,250aa) | g.17:46700467C>T,c.548G>A,p.R183H |
| HOXB7(NM_004502,homeobox B7,217aa) | g.17:46688256T>C,c.25A>G,p.T9A |
| HOXB7(NM_004502,homeobox B7,217aa) | g.17:46688135G>A,c.146C>T,p.A49V |
| HOXB7(NM_004502,homeobox B7,217aa) | g.17:46688096C>G,c.185G>C,p.G62A |
| HOXB7(NM_004502,homeobox B7,217aa) | g.17:46688048T>C,c.233A>G,p.Y78C |
| HOXB7(NM_004502,homeobox B7,217aa) | g.17:46685227C>T,c.631G>A,p.A211T |
| HOXB5(NM_002147,homeobox B5,269aa) | g.17:46670974T>C,c.71A>G,p.Y24C |
| HOXB4(NM_024015,homeobox B4,251aa) | g.17:46655411G>A,c.271C>T,p.P91S |
| HOXB4(NM_024015,homeobox B4,251aa) | g.17:46655230C>G,c.452G>C,p.S151T |
| HOXB4(NM_024015,homeobox B4,251aa) | g.17:46654112C>G,c.728G>C,p.R243P |
| HOXB3(NM_002146,homeobox B3,431aa) | g.17:46629746C>A,c.91G>T,p.V31F |
| HOXB3(NM_002146,homeobox B3,431aa) | g.17:46629593G>T,c.244C>A,p.P82T |
| HOXB3(NM_002146,homeobox B3,431aa) | g.17:46629464G>A,c.373C>T,p.L125F |
| HOXB3(NM_002146,homeobox B3,431aa) | g.17:46628510C>T,c.482G>A,p.G161D |
| HOXB3(NM_002146,homeobox B3,431aa) | g.17:46628228G>A,c.764C>T,p.S255L |
| HOXB3(NM_002146,homeobox B3,431aa) | g.17:46628177G>A,c.815C>T,p.T272M |
| HOXB3(NM_002146,homeobox B3,431aa) | g.17:46628142G>A,c.850C>T,p.P284S |
| HOXB3(NM_002146,homeobox B3,431aa) | g.17:46627916G>A,c.1076C>T,p.A359V |
| HOXB2(NM_002145,homeobox B2,356aa) | g.17:46621954G>A,c.320C>T,p.P107L |
| HOXB2(NM_002145,homeobox B2,356aa) | g.17:46620725T>A,c.776A>T,p.D259V |