| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154837698G>A | CA255041 | F8 | c.6955C>T (p.Pro2319Ser) c.688C>T (p.Pro230Ser) c.550C>T (p.Pro184Ser) c.6850C>T (p.Pro2284Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.154837698G= | CA2466807447 | F8 | c.6955C= (p.Pro2319=) c.688C= (p.Pro230=) c.550C= (p.Pro184=) c.6850C= (p.Pro2284=) | dbSNP |