| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.7809900A>G | CA355000 | PER3 | c.1250A>G (p.His417Arg) c.1247A>G (p.His416Arg) n.268A>G c.293A>G (p.His98Arg) c.725A>G (p.His242Arg) c.1082A>G (p.His361Arg) c.902A>G (p.His301Arg) c.887A>G (p.His296Arg) c.-122A>G (n.-122A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.7809900A= | CA1141671906 | PER3 | c.1250A= (p.His417=) c.1247A= (p.His416=) n.268A= c.293A= (p.His98=) c.725A= (p.His242=) c.1082A= (p.His361=) c.902A= (p.His301=) c.887A= (p.His296=) c.-122A= (n.-122A=) | dbSNP |