| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139561992C>A | CA255413 | F9 | c.1307C>A (p.Ala436Glu) n.1723+251C>A c.1193C>A (p.Ala398Glu) c.1178C>A (p.Ala393Glu) | ClinVar dbSNP |
| X | g.139561992C>T | CA255416 | F9 | c.1307C>T (p.Ala436Val) n.1723+251C>T c.1193C>T (p.Ala398Val) c.1178C>T (p.Ala393Val) | ClinVar dbSNP |
| X | g.139561992C= | CA2461412286 | F9 | c.1307C= (p.Ala436=) n.1723+251C= c.1193C= (p.Ala398=) c.1178C= (p.Ala393=) | dbSNP |