| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37741165C>G | CA2580582068 | HNF1B | c.345-1526G>C (n.345-1526G>C) | dbSNP |
| 17 | g.37741165C>T | CA290290149 | HNF1B | c.345-1526G>A (n.345-1526G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.37741165C= | CA16538933 | HNF1B | c.345-1526G= (n.345-1526G=) | dbSNP |