Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32363370A>TCA025485BRCA2c.8168A>T (p.Asp2723Val)
c.7799A>T (p.Asp2600Val)
c.635A>T (p.Asp212Val)
c.8176A>T (n.8176A>T)
c.733A>T
c.8072A>T (p.Asp2691Val)
ClinVar dbSNP gnomAD v4
13g.32363370A>GCA025484BRCA2c.8168A>G (p.Asp2723Gly)
c.7799A>G (p.Asp2600Gly)
c.635A>G (p.Asp212Gly)
c.8176A>G (n.8176A>G)
c.733A>G
c.8072A>G (p.Asp2691Gly)
ClinVar dbSNP gnomAD v4
13g.32363370A>CCA025483BRCA2c.8168A>C (p.Asp2723Ala)
c.7799A>C (p.Asp2600Ala)
c.635A>C (p.Asp212Ala)
c.8176A>C (n.8176A>C)
c.733A>C
c.8072A>C (p.Asp2691Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched