Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.279705C>A | CA1232989894 | ALKAL2 | c.*442G>T (n.*442G>T) | dbSNP gnomAD v4 |
2 | g.279705C>G | CA1232989895 | ALKAL2 | c.*442G>C (n.*442G>C) | dbSNP |
2 | g.279705C>T | CA10995152 | ALKAL2 | c.*442G>A (n.*442G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |