Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44908784G>T | CA406304113 | APOE | c.488G>T (p.Arg163Leu) c.566G>T (p.Arg189Leu) | ClinVar dbSNP |
19 | g.44908784G>C | CA127524 | APOE | c.488G>C (p.Arg163Pro) c.566G>C (p.Arg189Pro) | ClinVar dbSNP gnomAD v4 |
19 | g.44908784G>A | CA127513 | APOE | c.488G>A (p.Arg163His) c.566G>A (p.Arg189His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |