Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.17269655C>G | CA1691290884 | AHR | c.-203+21929C>G (n.-203+21929C>G) n.785-10327G>C | dbSNP gnomAD v4 |
7 | g.17269655C>A | CA12458239 | AHR | c.-203+21929C>A (n.-203+21929C>A) n.785-10327G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17269655C>T | CA1691290886 | AHR | c.-203+21929C>T (n.-203+21929C>T) n.785-10327G>A | dbSNP |