| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154997095C>T | CA255052 | F8 | c.266G>A (p.Gly89Asp) c.*52G>A (n.*52G>A) c.161G>A (p.Gly54Asp) c.248G>A (p.Gly83Asp) | ClinVar dbSNP |
| X | g.154997095C>A | CA414920126 | F8 | c.266G>T (p.Gly89Val) c.*52G>T (n.*52G>T) c.161G>T (p.Gly54Val) c.248G>T (p.Gly83Val) | dbSNP |