| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154969459G>A | CA255077 | F8 | c.881C>T (p.Thr294Ile) c.*757C>T (n.*757C>T) c.776C>T (p.Thr259Ile) | ClinVar dbSNP |
| X | g.154969459G= | CA2466849022 | F8 | c.881C= (p.Thr294=) c.*757C= (n.*757C=) c.776C= (p.Thr259=) | dbSNP |
| X | g.154969459G>C | CA414918087 | F8 | c.881C>G (p.Thr294Arg) c.*757C>G (n.*757C>G) c.776C>G (p.Thr259Arg) | ClinVar dbSNP |