Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44908751G>A | CA127517 | APOE | c.455G>A (p.Arg152Gln) c.533G>A (p.Arg178Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44908751G>T | CA406304060 | APOE | c.455G>T (p.Arg152Leu) c.533G>T (p.Arg178Leu) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.44908751G>C | CA308885664 | APOE | c.455G>C (p.Arg152Pro) c.533G>C (p.Arg178Pro) | dbSNP |