| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154928668G>A | CA120919 | F8 | c.5122C>T (p.Arg1708Cys) c.5017C>T (p.Arg1673Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| X | g.154928668G>T | CA414913844 | F8 | c.5122C>A (p.Arg1708Ser) c.5017C>A (p.Arg1673Ser) | dbSNP |
| X | g.154928668G= | CA2466835762 | F8 | c.5122C= (p.Arg1708=) c.5017C= (p.Arg1673=) | dbSNP |