Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44909020C>T | CA406304858 | APOE | c.724C>T (p.Arg242Trp) c.802C>T (p.Arg268Trp) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.44909020C>G | CA308885969 | APOE | c.724C>G (p.Arg242Gly) c.802C>G (p.Arg268Gly) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.44909020C>A | CA507947695 | APOE | c.724C>A (p.Arg242=) c.802C>A (p.Arg268=) | dbSNP gnomAD v4 |