| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154904839G>T | CA414908483 | F8 | c.5558C>A (p.Ala1853Asp) c.5453C>A (p.Ala1818Asp) | dbSNP |
| X | g.154904839G>A | CA255174 | F8 | c.5558C>T (p.Ala1853Val) c.5453C>T (p.Ala1818Val) | ClinVar dbSNP |
| X | g.154904839G= | CA2466828423 | F8 | c.5558C= (p.Ala1853=) c.5453C= (p.Ala1818=) | dbSNP |