Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.55039974G>A | CA22792102 | PCSK9 | c.137G>A (p.Arg46His) c.494G>A (p.Arg165His) | dbSNP gnomAD v4 COSMIC COSMIC |
1 | g.55039974G>T | CA023110 | PCSK9 | c.137G>T (p.Arg46Leu) c.494G>T (p.Arg165Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.55039974G= | CA1140280946 | PCSK9 | c.137G= (p.Arg46=) c.494G= (p.Arg165=) | dbSNP |