| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.73416262G>A | CA127908 | ALB | c.1198G>A (p.Glu400Lys) c.853G>A (p.Glu285Lys) c.622G>A (p.Glu208Lys) c.*477G>A (n.*477G>A) n.518G>A c.748G>A (p.Glu250Lys) n.884G>A c.731G>A c.559G>A (p.Glu187Lys) | ClinVar dbSNP |
| 4 | g.73416262G>C | CA127970 | ALB | c.1198G>C (p.Glu400Gln) c.853G>C (p.Glu285Gln) c.622G>C (p.Glu208Gln) c.*477G>C (n.*477G>C) n.518G>C c.748G>C (p.Glu250Gln) n.884G>C c.731G>C c.559G>C (p.Glu187Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |