| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.139551196C>T | CA255347 | F9 | c.655C>T (p.Gln219Ter) n.1322C>T c.541C>T (p.Gln181Ter) c.526C>T (p.Gln176Ter) | ClinVar dbSNP |
| X | g.139551196C= | CA2461408629 | F9 | c.655C= (p.Gln219=) n.1322C= c.541C= (p.Gln181=) c.526C= (p.Gln176=) | dbSNP |