| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44908730G>C | CA406304018 | APOE | c.434G>C (p.Gly145Ala) c.512G>C (p.Gly171Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.44908730G>A | CA041273 | APOE | c.434G>A (p.Gly145Asp) c.512G>A (p.Gly171Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.44908730G>T | CA406304019 | APOE | c.434G>T (p.Gly145Val) c.512G>T (p.Gly171Val) | dbSNP gnomAD v4 |
| 19 | g.44908730G= | CA2338167652 | APOE | c.434G= (p.Gly145=) c.512G= (p.Gly171=) | dbSNP |