| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37739455G>A | CA122597 | HNF1B | c.529C>T (p.Arg177Ter) | ClinVar dbSNP |
| 17 | g.37739455G>T | CA499603852 | HNF1B | c.529C>A (p.Arg177=) | dbSNP |
| 17 | g.37739455G= | CA3223262508 | HNF1B | c.529C= (p.Arg177=) | dbSNP |
| 17 | g.37739455G>C | CA398751075 | HNF1B | c.529C>G (p.Arg177Gly) | dbSNP gnomAD v4 |