Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.88433649C>ACA151295ZNF469c.6179C>A (p.Ser2060Tyr)
c.6095C>A (p.Ser2032Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88433649C>TCA397104499ZNF469c.6179C>T (p.Ser2060Phe)
c.6095C>T (p.Ser2032Phe)
 dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched