| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139561754G>A | CA255389 | F9 | c.1069G>A (p.Gly357Arg) n.1723+13G>A c.955G>A (p.Gly319Arg) c.940G>A (p.Gly314Arg) | ClinVar dbSNP |
| X | g.139561754G= | CA2461412162 | F9 | c.1069G= (p.Gly357=) n.1723+13G= c.955G= (p.Gly319=) c.940G= (p.Gly314=) | dbSNP |