| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139561941T>G | CA414446889 | F9 | c.1256T>G (p.Val419Gly) n.1723+200T>G c.1142T>G (p.Val381Gly) c.1127T>G (p.Val376Gly) | ClinVar dbSNP |
| X | g.139561941T>A | CA255452 | F9 | c.1256T>A (p.Val419Glu) n.1723+200T>A c.1142T>A (p.Val381Glu) c.1127T>A (p.Val376Glu) | ClinVar dbSNP |
| X | g.139561941T= | CA2461412258 | F9 | c.1256T= (p.Val419=) n.1723+200T= c.1142T= (p.Val381=) c.1127T= (p.Val376=) | dbSNP |