Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.45950453C>ACA358018ZNF335c.3332G>T (p.Arg1111Leu)
c.3329G>T (p.Arg1110Leu)
c.2804G>T (p.Arg935Leu)
n.5279G>T
n.3728G>T
n.3843G>T
ClinVar dbSNP gnomAD v4
20g.45950453C>TCA210874ZNF335c.3332G>A (p.Arg1111His)
c.3329G>A (p.Arg1110His)
c.2804G>A (p.Arg935His)
n.5279G>A
n.3728G>A
n.3843G>A
ClinVar dbSNP gnomAD v3 gnomAD v4
20g.45950453C=CA2366449599ZNF335c.3332G= (p.Arg1111=)
c.3329G= (p.Arg1110=)
c.2804G= (p.Arg935=)
n.5279G=
n.3728G=
n.3843G=
dbSNP

Number of alleles fetched