| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37739473A>G | CA214361 | HNF1B | c.511T>C (p.Trp171Arg) | ClinVar dbSNP |
| 17 | g.37739473A>T | CA398751173 | HNF1B | c.511T>A (p.Trp171Arg) | ClinVar dbSNP |
| 17 | g.37739473A= | CA3223295346 | HNF1B | c.511T= (p.Trp171=) | dbSNP |