| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154904026G>A | CA255024 | F8 | c.5878C>T (p.Arg1960Ter) c.5773C>T (p.Arg1925Ter) | ClinVar dbSNP |
| X | g.154904026G>T | CA10567927 | F8 | c.5878C>A (p.Arg1960=) c.5773C>A (p.Arg1925=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.154904026G= | CA2466828176 | F8 | c.5878C= (p.Arg1960=) c.5773C= (p.Arg1925=) | dbSNP |