| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154860538T>C | CA255219 | F8 | c.6794A>G (p.Gln2265Arg) c.527A>G (p.Gln176Arg) c.389A>G (p.Gln130Arg) c.6689A>G (p.Gln2230Arg) | ClinVar dbSNP gnomAD v4 |
| X | g.154860538T= | CA2466815013 | F8 | c.6794A= (p.Gln2265=) c.527A= (p.Gln176=) c.389A= (p.Gln130=) c.6689A= (p.Gln2230=) | dbSNP |