Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.72933566C>T | CA1637932975 | KCNQ5 | c.399-70342C>T (n.399-70342C>T) c.408-70351C>T (n.408-70351C>T) | dbSNP |
6 | g.72933566C>G | CA1637932974 | KCNQ5 | c.399-70342C>G (n.399-70342C>G) c.408-70351C>G (n.408-70351C>G) | dbSNP |
6 | g.72933566C>A | CA12240114 | KCNQ5 | c.399-70342C>A (n.399-70342C>A) c.408-70351C>A (n.408-70351C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |