Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.218809730C>ACA65830477CYP27A1c.409C>A (p.Arg137=)
c.127C>A (p.Arg43=)
c.256-2492C>A (n.256-2492C>A)
n.265-2492C>A
n.843C>A
c.27-2492C>A (n.27-2492C>A)
ClinVar dbSNP
2g.218809730C>TCA345197CYP27A1c.409C>T (p.Arg137Trp)
c.127C>T (p.Arg43Trp)
c.256-2492C>T (n.256-2492C>T)
n.265-2492C>T
n.843C>T
c.27-2492C>T (n.27-2492C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218809730C=CA1328927551CYP27A1c.409C= (p.Arg137=)
c.127C= (p.Arg43=)
c.256-2492C= (n.256-2492C=)
n.265-2492C=
n.843C=
c.27-2492C= (n.27-2492C=)
dbSNP

Number of alleles fetched