Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.73323289G>TCA7648952HCN4c.2804C>A (p.Ser935Tyr)
c.1586C>A (p.Ser529Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323289G>ACA301966HCN4c.2804C>T (p.Ser935Phe)
c.1586C>T (p.Ser529Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323289G>CCA393087921HCN4c.2804C>G (p.Ser935Cys)
c.1586C>G (p.Ser529Cys)
ClinVar dbSNP
15g.73323289G=CA2187187930HCN4c.2804C= (p.Ser935=)
c.1586C= (p.Ser529=)
dbSNP

Number of alleles fetched