| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37739490C>T | CA122605 | HNF1B | c.494G>A (p.Arg165His) | ClinVar dbSNP |
| 17 | g.37739490C>G | CA398751241 | HNF1B | c.494G>C (p.Arg165Pro) | ClinVar dbSNP |
| 17 | g.37739490C= | CA2838147743 | HNF1B | c.494G= (p.Arg165=) | dbSNP |