| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.169529635C>T | CA215971 | F5 | c.5392G>A (p.Glu1798Lys) c.5407G>A (p.Glu1803Lys) c.4981G>A (p.Glu1661Lys) | ClinVar dbSNP |
| 1 | g.169529635C= | CA1144229041 | F5 | c.5392G= (p.Glu1798=) c.5407G= (p.Glu1803=) c.4981G= (p.Glu1661=) | dbSNP |
| 1 | g.169529635C>G | CA343129438 | F5 | c.5392G>C (p.Glu1798Gln) c.5407G>C (p.Glu1803Gln) c.4981G>C (p.Glu1661Gln) | dbSNP gnomAD v4 |