Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.117590440G>ACA340648CFTRc.1766+1G>A (p.=)
c.*1480+1G>A (p.=)
c.1402-12386G>A (p.=)
c.1583+1G>A (p.=)
n.1583+1G>A (p.=)
n.1676+1G>A (p.=)
c.1856+1G>A (p.=)
c.1523+1G>A (p.=)
ClinVar dbSNP ExAC gnomAD
7g.117590440G>TCA326660CFTRc.1766+1G>T (p.=)
c.*1480+1G>T (p.=)
c.1402-12386G>T (p.=)
c.1583+1G>T (p.=)
n.1583+1G>T (p.=)
n.1676+1G>T (p.=)
c.1856+1G>T (p.=)
c.1523+1G>T (p.=)
ClinVar dbSNP
7g.117590440G>CCA326659CFTRc.1766+1G>C (p.=)
c.*1480+1G>C (p.=)
c.1402-12386G>C (p.=)
c.1583+1G>C (p.=)
n.1583+1G>C (p.=)
n.1676+1G>C (p.=)
c.1856+1G>C (p.=)
c.1523+1G>C (p.=)
ClinVar dbSNP gnomAD

Number of alleles fetched