Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.117665565G>ACA327465CFTRc.4242+1G>A (p.=)
c.4332+1G>A (p.=)
c.3999+1G>A (p.=)
n.4152+1G>A (p.=)
n.368+1G>A
ClinVar dbSNP
7g.117665565G>TCA327466CFTRc.4242+1G>T (p.=)
c.4332+1G>T (p.=)
c.3999+1G>T (p.=)
n.4152+1G>T (p.=)
n.368+1G>T
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched