| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154997011A>C | CA255058 | F8 | c.350T>G (p.Leu117Arg) c.*136T>G (n.*136T>G) c.245T>G (p.Leu82Arg) c.332T>G (p.Leu111Arg) | ClinVar dbSNP |
| X | g.154997011A= | CA2466857767 | F8 | c.350T= (p.Leu117=) c.*136T= (n.*136T=) c.245T= (p.Leu82=) c.332T= (p.Leu111=) | dbSNP |