| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154993133T>C | CA255062 | F8 | c.404A>G (p.Asp135Gly) c.*190A>G (n.*190A>G) c.299A>G (p.Asp100Gly) c.386A>G (p.Asp129Gly) | ClinVar dbSNP |
| X | g.154993133T= | CA2466856570 | F8 | c.404A= (p.Asp135=) c.*190A= (n.*190A=) c.299A= (p.Asp100=) c.386A= (p.Asp129=) | dbSNP |