| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154969438C>T | CA255079 | F8 | c.902G>A (p.Arg301His) c.*778G>A (n.*778G>A) c.797G>A (p.Arg266His) | ClinVar dbSNP |
| X | g.154969438C>A | CA255080 | F8 | c.902G>T (p.Arg301Leu) c.*778G>T (n.*778G>T) c.797G>T (p.Arg266Leu) | ClinVar dbSNP |
| X | g.154969438C= | CA2466849013 | F8 | c.902G= (p.Arg301=) c.*778G= (n.*778G=) c.797G= (p.Arg266=) | dbSNP |