| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37739640C>A | CA214359 | HNF1B | c.345-1G>T (n.345-1G>T) | ClinVar dbSNP |
| 17 | g.37739640C>T | CA398751764 | HNF1B | c.345-1G>A (n.345-1G>A) | ClinVar dbSNP |
| 17 | g.37739640C>G | CA398751763 | HNF1B | c.345-1G>C (n.345-1G>C) | ClinVar dbSNP |
| 17 | g.37739640C= | CA3223295348 | HNF1B | c.345-1G= (n.345-1G=) | dbSNP |