Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.117592325C>T | CA326756 | CFTR | c.2158C>T (p.Gln720Ter) c.*1872C>T (n.*1872C>T) c.1975C>T (p.Gln659Ter) c.*458C>T (n.*458C>T) c.*1982C>T (n.*1982C>T) c.1732C>T (p.Gln578Ter) c.1402-10501C>T (n.1402-10501C>T) c.2068C>T (p.Gln690Ter) c.2248C>T (p.Gln750Ter) c.1915C>T (p.Gln639Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.117592325C= | CA1737394909 | CFTR | c.2158C= (p.Gln720=) c.*1872C= (n.*1872C=) c.1975C= (p.Gln659=) c.*458C= (n.*458C=) c.*1982C= (n.*1982C=) c.1732C= (p.Gln578=) c.1402-10501C= (n.1402-10501C=) c.2068C= (p.Gln690=) c.2248C= (p.Gln750=) c.1915C= (p.Gln639=) | dbSNP |