Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32338162T>CCA018842BRCA2c.3807T>C (p.Val1269=)
c.3438T>C (p.Val1146=)
n.3807T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32338162T>GCA018847BRCA2c.3807T>G (p.Val1269=)
c.3438T>G (p.Val1146=)
n.3807T>G
 ClinVar dbSNP

Number of alleles fetched