| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37743574A>C | CA983447196 | HNF1B | c.344+967T>G (n.344+967T>G) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.37743574A>G | CA290292151 | HNF1B | c.344+967T>C (n.344+967T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.37743574A= | CA14474833 | HNF1B | c.344+967T= (n.344+967T=) | ClinVar dbSNP |