| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139551251A>T | CA255360 | F9 | c.710A>T (p.Gln237Leu) n.1377A>T c.596A>T (p.Gln199Leu) c.581A>T (p.Gln194Leu) | ClinVar dbSNP |
| X | g.139551251A= | CA2461408649 | F9 | c.710A= (p.Gln237=) n.1377A= c.596A= (p.Gln199=) c.581A= (p.Gln194=) | dbSNP |