Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.186191953T>A | CA339954 | CYP4V2 | c.130T>A (p.Trp44Arg) c.-181T>A (n.-181T>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186191953T>C | CA3162423 | CYP4V2 | c.130T>C (p.Trp44Arg) c.-181T>C (n.-181T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.186191953T= | CA1519910962 | CYP4V2 | c.130T= (p.Trp44=) c.-181T= (n.-181T=) | dbSNP |