Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44908757G>C | CA308885705 | APOE | c.461G>C (p.Arg154Pro) c.539G>C (p.Arg180Pro) | dbSNP |
19 | g.44908757G>A | CA406304067 | APOE | c.461G>A (p.Arg154His) c.539G>A (p.Arg180His) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.44908757G>T | CA16044403 | APOE | c.461G>T (p.Arg154Leu) c.539G>T (p.Arg180Leu) | ClinVar dbSNP gnomAD v4 |