| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.186209263A>G | CA276932 | CYP4V2,KLKB1 | c.1396A>G (p.Asn466Asp) n.631A>G n.6094A>G c.192A>G n.486A>G c.1393A>G (p.Asn465Asp) c.1000A>G (p.Asn334Asp) | ClinVar dbSNP |
| 4 | g.186209263A= | CA1519891500 | CYP4V2,KLKB1 | c.1396A= (p.Asn466=) n.631A= n.6094A= c.192A= n.486A= c.1393A= (p.Asn465=) c.1000A= (p.Asn334=) | dbSNP |