Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32362691C>GCA025361BRCA2c.7974C>G (p.Tyr2658Ter)
c.7605C>G (p.Tyr2535Ter)
c.441C>G (p.Tyr147Ter)
c.7982C>G (n.7982C>G)
c.539C>G
c.7878C>G (p.Tyr2626Ter)
ClinVar dbSNP
13g.32362691C>TCA483261063BRCA2c.7974C>T (p.Tyr2658=)
c.7605C>T (p.Tyr2535=)
c.441C>T (p.Tyr147=)
c.7982C>T (n.7982C>T)
c.539C>T
c.7878C>T (p.Tyr2626=)
ClinVar dbSNP
13g.32362691C>ACA10589460BRCA2c.7974C>A (p.Tyr2658Ter)
c.7605C>A (p.Tyr2535Ter)
c.441C>A (p.Tyr147Ter)
c.7982C>A (n.7982C>A)
c.539C>A
c.7878C>A (p.Tyr2626Ter)
ClinVar dbSNP

Number of alleles fetched