Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44907853T>C | CA041808 | APOE | c.137T>C (p.Leu46Pro) c.215T>C (p.Leu72Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44907853T>A | CA406303362 | APOE | c.137T>A (p.Leu46Gln) c.215T>A (p.Leu72Gln) | dbSNP |
19 | g.44907853T= | CA2338167357 | APOE | c.137T= (p.Leu46=) c.215T= (p.Leu72=) | dbSNP |