| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37744745G>A | CA214348 | HNF1B | c.140C>T (p.Pro47Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.37744745G>C | CA398754294 | HNF1B | c.140C>G (p.Pro47Arg) | dbSNP |
| 17 | g.37744745G= | CA3223295353 | HNF1B | c.140C= (p.Pro47=) | dbSNP |
| 17 | g.37744745G>T | CA398754288 | HNF1B | c.140C>A (p.Pro47His) | dbSNP gnomAD v4 |