Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.75921721G>A | CA1469330269 | NAAA | c.667-598C>T (n.667-598C>T) c.78-598C>T c.364-598C>T (n.364-598C>T) c.80-598C>T c.291-598C>T n.713-598C>T | dbSNP |
4 | g.75921721G>T | CA11691279 | NAAA | c.667-598C>A (n.667-598C>A) c.78-598C>A c.364-598C>A (n.364-598C>A) c.80-598C>A c.291-598C>A n.713-598C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |