| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.44424243T>G | CA120226 | HNF4A | c.1052T>G (p.Met351Arg) c.1118T>G (p.Met373Arg) c.1092T>G c.*885T>G (n.*885T>G) c.1043T>G (p.Met348Arg) c.1097T>G (p.Met366Arg) c.1235T>G (p.Met412Arg) c.1166T>G (p.Met389Arg) | ClinVar dbSNP |
| 20 | g.44424243T= | CA2365765888 | HNF4A | c.1052T= (p.Met351=) c.1118T= (p.Met373=) c.1092T= c.*885T= (n.*885T=) c.1043T= (p.Met348=) c.1097T= (p.Met366=) c.1235T= (p.Met412=) c.1166T= (p.Met389=) | dbSNP |