Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.117603542C>TCA325590CFTRc.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
7g.117603542C=CA1737374421CFTRc.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

Number of alleles fetched