| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154961120C>T | CA255109 | F8 | c.1492G>A (p.Gly498Arg) c.*1368G>A (n.*1368G>A) c.1387G>A (p.Gly463Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| X | g.154961120C>A | CA414912740 | F8 | c.1492G>T (p.Gly498Ter) c.*1368G>T (n.*1368G>T) c.1387G>T (p.Gly463Ter) | dbSNP |
| X | g.154961120C>G | CA414912741 | F8 | c.1492G>C (p.Gly498Arg) c.*1368G>C (n.*1368G>C) c.1387G>C (p.Gly463Arg) | dbSNP |