| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37739541G>C | CA122604 | HNF1B | c.443C>G (p.Ser148Trp) | ClinVar dbSNP |
| 17 | g.37739541G>A | CA398751429 | HNF1B | c.443C>T (p.Ser148Leu) | ClinVar dbSNP gnomAD v4 |
| 17 | g.37739541G= | CA2844644711 | HNF1B | c.443C= (p.Ser148=) | dbSNP |
| 17 | g.37739541G>T | CA398751431 | HNF1B | c.443C>A (p.Ser148Ter) | ClinVar dbSNP |