| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44909080G>A | CA040712 | APOE | c.784G>A (p.Glu262Lys) c.862G>A (p.Glu288Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.44909080G>T | CA406305221 | APOE | c.784G>T (p.Glu262Ter) c.862G>T (p.Glu288Ter) | dbSNP gnomAD v4 |
| 19 | g.44909080G= | CA2338168051 | APOE | c.784G= (p.Glu262=) c.862G= (p.Glu288=) | dbSNP |