| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154966471T>C | CA255099 | F8 | c.1226A>G (p.Glu409Gly) c.*1102A>G (n.*1102A>G) n.46A>G c.1121A>G (p.Glu374Gly) | ClinVar dbSNP |
| X | g.154966471T= | CA2466848104 | F8 | c.1226A= (p.Glu409=) c.*1102A= (n.*1102A=) n.46A= c.1121A= (p.Glu374=) | dbSNP |