| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44908774C>G | CA406304095 | APOE | c.478C>G (p.Arg160Gly) c.556C>G (p.Arg186Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.44908774C>T | CA041132 | APOE | c.478C>T (p.Arg160Cys) c.556C>T (p.Arg186Cys) | ClinVar dbSNP gnomAD v4 |
| 19 | g.44908774C= | CA2338167868 | APOE | c.478C= (p.Arg160=) c.556C= (p.Arg186=) | dbSNP |
| 19 | g.44908774C>A | CA406304094 | APOE | c.478C>A (p.Arg160Ser) c.556C>A (p.Arg186Ser) | dbSNP gnomAD v4 |