| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44909171G>A | CA127519 | APOE | c.875G>A (p.Arg292His) c.953G>A (p.Arg318His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.44909171G>T | CA406305731 | APOE | c.875G>T (p.Arg292Leu) c.953G>T (p.Arg318Leu) | dbSNP gnomAD v4 COSMIC |
| 19 | g.44909171G= | CA2338168109 | APOE | c.875G= (p.Arg292=) c.953G= (p.Arg318=) | dbSNP |