Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.117504364G>CCA326563CFTRc.164+1G>C (p.=)
c.254+1G>C (p.=)
c.-80+1G>C (p.=)
c.-154+1G>C (p.=)
n.164+1G>C (p.=)
ClinVar dbSNP
7g.117504364G>TCA326564CFTRc.164+1G>T (p.=)
c.254+1G>T (p.=)
c.-80+1G>T (p.=)
c.-154+1G>T (p.=)
n.164+1G>T (p.=)
ClinVar dbSNP
7g.117504364G>ACA326562CFTRc.164+1G>A (p.=)
c.254+1G>A (p.=)
c.-80+1G>A (p.=)
c.-154+1G>A (p.=)
n.164+1G>A (p.=)
ClinVar dbSNP

Number of alleles fetched