Log in
HomeVariants

chr13:32921034 G>A

Annotations

GeneBRCA2
TranscriptNM_000059.3
cDNAc.7007+1G>A
Protein
Functionsplicing
Localizationsplice site
hg19chr13:32921034 G>A

Frequency in gnomAD

GenomeExome
MAX
AFR
AMR
ASJ
EAS
FIN
NFE
SAS

ClinVar

IDPhenotypeEffect
RCV000232637.1Hereditary breast and ovarian cancer syndromePathogenic