| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154837685C>T | CA255226 | F8 | c.6968G>A (p.Arg2323His) c.701G>A (p.Arg234His) c.563G>A (p.Arg188His) c.6863G>A (p.Arg2288His) | ClinVar dbSNP |
| X | g.154837685C>G | CA414897240 | F8 | c.6968G>C (p.Arg2323Pro) c.701G>C (p.Arg234Pro) c.563G>C (p.Arg188Pro) c.6863G>C (p.Arg2288Pro) | ClinVar dbSNP |