Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.37736310G>T | CA2580606435 | HNF1B | c.545-2489C>A (n.545-2489C>A) c.545-2567C>A (n.545-2567C>A) | dbSNP |
17 | g.37736310G>A | CA290285943 | HNF1B | c.545-2489C>T (n.545-2489C>T) c.545-2567C>T (n.545-2567C>T) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37736310G>C | CA2580606436 | HNF1B | c.545-2489C>G (n.545-2489C>G) c.545-2567C>G (n.545-2567C>G) | dbSNP |