| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154961138A>G | CA337334229 | F8 | c.1474T>C (p.Tyr492His) c.*1350T>C (n.*1350T>C) c.1369T>C (p.Tyr457His) | ClinVar dbSNP |
| X | g.154961138A= | CA2466846501 | F8 | c.1474T= (p.Tyr492=) c.*1350T= (n.*1350T=) c.1369T= (p.Tyr457=) | dbSNP |