Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.99412399G>T | CA1479986654 | ADH7 | c.*749C>A (n.*749C>A) | dbSNP |
4 | g.99412399G>A | CA15355691 | ADH7 | c.*749C>T (n.*749C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.99412399G>C | CA1479986653 | ADH7 | c.*749C>G (n.*749C>G) | dbSNP |