Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.117530952T>GCA368974384CFTRc.327T>G (p.Tyr109Ter)
c.*224T>G (n.*224T>G)
c.*151T>G (n.*151T>G)
c.84T>G (p.Tyr28Ter)
c.417T>G (p.Tyr139Ter)
ClinVar dbSNP
7g.117530952T>CCA457448601CFTRc.327T>C (p.Tyr109=)
c.*224T>C (n.*224T>C)
c.*151T>C (n.*151T>C)
c.84T>C (p.Tyr28=)
c.417T>C (p.Tyr139=)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.117530952T>ACA327123CFTRc.327T>A (p.Tyr109Ter)
c.*224T>A (n.*224T>A)
c.*151T>A (n.*151T>A)
c.84T>A (p.Tyr28Ter)
c.417T>A (p.Tyr139Ter)
ClinVar dbSNP

Number of alleles fetched