Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.117603542C>T | CA325590 | CFTR | c.2668C>T (p.Gln890Ter) c.*2382C>T (n.*2382C>T) c.2485C>T (p.Gln829Ter) c.*968C>T (n.*968C>T) c.*2492C>T (n.*2492C>T) c.2242C>T (p.Gln748Ter) c.259C>T (p.Gln87Ter) c.318C>T c.1450C>T (p.Gln484Ter) c.2578C>T (p.Gln860Ter) c.2758C>T (p.Gln920Ter) c.2425C>T (p.Gln809Ter) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.117603542C= | CA1737374421 | CFTR | c.2668C= (p.Gln890=) c.*2382C= (n.*2382C=) c.2485C= (p.Gln829=) c.*968C= (n.*968C=) c.*2492C= (n.*2492C=) c.2242C= (p.Gln748=) c.259C= (p.Gln87=) c.318C= c.1450C= (p.Gln484=) c.2578C= (p.Gln860=) c.2758C= (p.Gln920=) c.2425C= (p.Gln809=) | dbSNP |