| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139551250C>T | CA255357 | F9 | c.709C>T (p.Gln237Ter) n.1376C>T c.595C>T (p.Gln199Ter) c.580C>T (p.Gln194Ter) | ClinVar dbSNP |
| X | g.139551250C>G | CA414441325 | F9 | c.709C>G (p.Gln237Glu) n.1376C>G c.595C>G (p.Gln199Glu) c.580C>G (p.Gln194Glu) | dbSNP |