| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154993127G>A | CA255063 | F8 | c.410C>T (p.Thr137Ile) c.*196C>T (n.*196C>T) c.305C>T (p.Thr102Ile) c.392C>T (p.Thr131Ile) | ClinVar dbSNP |
| X | g.154993127G= | CA2466856569 | F8 | c.410C= (p.Thr137=) c.*196C= (n.*196C=) c.305C= (p.Thr102=) c.392C= (p.Thr131=) | dbSNP |