Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119676479C>TCA10576779BAG3c.925C>T (p.Arg309Ter)
c.748C>T (p.Arg250Ter)
c.922C>T (p.Arg308Ter)
ClinVar dbSNP gnomAD v4
10g.119676479C>GCA378296277BAG3c.925C>G (p.Arg309Gly)
c.748C>G (p.Arg250Gly)
c.922C>G (p.Arg308Gly)
ClinVar dbSNP
10g.119676479C>ACA471634776BAG3c.925C>A (p.Arg309=)
c.748C>A (p.Arg250=)
c.922C>A (p.Arg308=)
dbSNP gnomAD v4

Number of alleles fetched