| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.56962023C>G | CA8070732 | CETP | c.44C>G (p.Ala15Gly) n.42C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.56962023C>A | CA8070733 | CETP | c.44C>A (p.Ala15Asp) n.42C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.56962023C= | CA2224392351 | CETP | c.44C= (p.Ala15=) n.42C= | dbSNP |
| 16 | g.56962023C>T | CA395995695 | CETP | c.44C>T (p.Ala15Val) n.42C>T | ClinVar dbSNP |