| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44908786A>G | CA127506 | APOE | c.490A>G (p.Lys164Glu) c.568A>G (p.Lys190Glu) | ClinVar dbSNP gnomAD v4 |
| 19 | g.44908786A>C | CA127507 | APOE | c.490A>C (p.Lys164Gln) c.568A>C (p.Lys190Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.44908786A= | CA2338167878 | APOE | c.490A= (p.Lys164=) c.568A= (p.Lys190=) | dbSNP |