All variants in the BRCA2 gene

All records describing functional studies of specific variants.
BRCA2 variants classified by the ENIGMA consortium.
Variants associated with Fanconi anemia
A Fanconi anemia mutation database.
Information The variants shown are described using the NM_000059.3 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Haplotype     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. 1 c.-82G>C r.(?) p.(=) - - VUS g.32889762G>C g.32315625G>C - - BRCA2_005829 - - - - Germline - - - 0 - Rien Blok
?/. 1 c.-82G>C r.(?) p.(=) - - VUS g.32889762G>C g.32315625G>C - - BRCA2_005829 - - - - Germline - - - 0 - Rien Blok
?/. 1 c.-82G>C r.(?) p.(=) - - VUS g.32889762G>C g.32315625G>C - - BRCA2_005829 not in 442 controls PubMed: Burke 2018, Journal: Burke 2018 - - Germline - 1/6603 cases - 0 - Lez J Burke
?/. 1 c.-82G>C r.= p.= - - NA g.32889762G>C g.32315625G>C - - BRCA2_005829 expression cloning luciferase assay no effect PubMed: Burke 2018, Journal: Burke 2018 - - In vitro (cloned) - - - 0 - Lez J Burke
-?/. - c.-82G>C r.(?) p.(=) - - likely benign g.32889762G>C g.32315625G>C - - BRCA2_005829 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Nijmegen
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