| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.186199057C>A | CA3162645 | CYP4V2 | c.775C>A (p.Gln259Lys) n.1616C>A c.379C>A (p.Gln127Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186199057C>T | CA358948100 | CYP4V2 | c.775C>T (p.Gln259Ter) n.1616C>T c.379C>T (p.Gln127Ter) | dbSNP |
| 4 | g.186199057C= | CA1519920467 | CYP4V2 | c.775C= (p.Gln259=) n.1616C= c.379C= (p.Gln127=) | dbSNP |