| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154904989G>A | CA414908976 | F8 | c.5408C>T (p.Ser1803Phe) c.5303C>T (p.Ser1768Phe) | dbSNP |
| X | g.154904989G>T | CA255165 | F8 | c.5408C>A (p.Ser1803Tyr) c.5303C>A (p.Ser1768Tyr) | ClinVar dbSNP |
| X | g.154904989G= | CA2466828474 | F8 | c.5408C= (p.Ser1803=) c.5303C= (p.Ser1768=) | dbSNP |