Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.37736525C>T | CA290286132 | HNF1B | c.545-2704G>A (n.545-2704G>A) c.545-2782G>A (n.545-2782G>A) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37736525C>G | CA290286130 | HNF1B | c.545-2704G>C (n.545-2704G>C) c.545-2782G>C (n.545-2782G>C) | dbSNP gnomAD v3 gnomAD v4 |