| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139561602A>C | CA414444777 | F9 | c.917A>C (p.Asn306Thr) n.1584A>C c.803A>C (p.Asn268Thr) c.788A>C (p.Asn263Thr) | dbSNP |
| X | g.139561602A>G | CA255373 | F9 | c.917A>G (p.Asn306Ser) n.1584A>G c.803A>G (p.Asn268Ser) c.788A>G (p.Asn263Ser) | ClinVar dbSNP |