Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119672373C>ACA170913BAG3c.626C>A (p.Pro209Gln)
c.452C>A (p.Pro151Gln)
ClinVar dbSNP
10g.119672373C>TCA308228BAG3c.626C>T (p.Pro209Leu)
c.452C>T (p.Pro151Leu)
ClinVar dbSNP COSMIC

Number of alleles fetched