Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44909101C>T | CA9506100 | APOE | c.805C>T (p.Arg269Cys) c.883C>T (p.Arg295Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.44909101C>G | CA041514 | APOE | c.805C>G (p.Arg269Gly) c.883C>G (p.Arg295Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44909101C= | CA2338168065 | APOE | c.805C= (p.Arg269=) c.883C= (p.Arg295=) | dbSNP |