| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154896228T>C | CA255201 | F8 | c.6278A>G (p.Asp2093Gly) c.6173A>G (p.Asp2058Gly) | ClinVar dbSNP |
| X | g.154896228T>A | CA414900400 | F8 | c.6278A>T (p.Asp2093Val) c.6173A>T (p.Asp2058Val) | ClinVar dbSNP |
| X | g.154896228T= | CA2466826050 | F8 | c.6278A= (p.Asp2093=) c.6173A= (p.Asp2058=) | dbSNP |