| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.44419813C>T | CA120182 | HNF4A | c.763C>T (p.Gln255Ter) c.829C>T (p.Gln277Ter) c.803C>T n.805C>T n.1953C>T c.*596C>T (n.*596C>T) c.754C>T (p.Gln252Ter) c.808C>T (p.Gln270Ter) c.946C>T (p.Gln316Ter) c.877C>T (p.Gln293Ter) | ClinVar dbSNP |
| 20 | g.44419813C>G | CA409107507 | HNF4A | c.763C>G (p.Gln255Glu) c.829C>G (p.Gln277Glu) c.803C>G n.805C>G n.1953C>G c.*596C>G (n.*596C>G) c.754C>G (p.Gln252Glu) c.808C>G (p.Gln270Glu) c.946C>G (p.Gln316Glu) c.877C>G (p.Gln293Glu) | ClinVar dbSNP |