×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
The functional impact of variants of uncertain significance in BRCA2.
29988080
2019
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
BRCA Reversion Mutations in Circulating Tumor DNA Predict Primary and Acquired Resistance to the PARP Inhibitor Rucaparib in High-Grade Ovarian Carcinoma.
30425037
2019
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
GeneticVariation
disease
CLINVAR
Impact of amino acid substitutions at secondary structures in the BRCT domains of the tumor suppressor BRCA1: Implications for clinical annotation.
30765603
2019
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
GeneticVariation
disease
CLINVAR
Quantifying BRCA1 and BRCA2 mRNA Isoform Expression Levels in Single Cells.
30736279
2019
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
CausalMutation
disease
CLINVAR
Impact of amino acid substitutions at secondary structures in the BRCT domains of the tumor suppressor BRCA1: Implications for clinical annotation.
30765603
2019
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
CausalMutation
disease
CLINVAR
Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls.
31341520
2019
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
CausalMutation
disease
CLINVAR
Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia-like phenotype, and no chromosome fragility.
31347298
2019
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
Mis-splicing in breast cancer: identification of pathogenic BRCA2 variants by systematic minigene assays.
30883759
2019
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
Population and breast cancer patients' analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population.
30630528
2019
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
CausalMutation
disease
CLINVAR
Combining Homologous Recombination and Phosphopeptide-binding Data to Predict the Impact of BRCA1 BRCT Variants on Cancer Risk.
30257991
2019
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
BRCA1 and BRCA2 mutations and clinical interpretation in 398 ovarian cancer patients: comparison with breast cancer variants in a similar population.
30103829
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
CausalMutation
disease
CLINVAR
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1 .
29712865
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
GeneticVariation
disease
CLINVAR
Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer.
29368341
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
Characterization of spliceogenic variants located in regions linked to high levels of alternative splicing: BRCA2 c.7976+5G > T as a case study.
29969168
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
Inherited mutations in BRCA1 and BRCA2 in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia.
28993434
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
Full in-frame exon 3 skipping of BRCA2 confers high risk of breast and/or ovarian cancer.
29707112
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
Mutation analysis of BRCA1/2 mutations with special reference to polymorphic SNPs in Indian breast cancer patients.
29785135
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
CausalMutation
disease
CLINVAR
Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?
30254663
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
GeneticVariation
disease
CLINVAR
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
29394989
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
CausalMutation
disease
CLINVAR
BRCA germline mutations in an unselected nationwide cohort of Chinese patients with ovarian cancer and healthy controls.
30078507
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
CausalMutation
disease
CLINVAR
Clinical genetic testing outcome with multi-gene panel in Asian patients with multiple primary cancers.
30093976
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR).
28726806
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
GeneticVariation
disease
CLINVAR
Ipilimumab plus nivolumab and DNA-repair defects in AR-V7-expressing metastatic prostate cancer.
29983880
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
0.800
GeneticVariation
disease
CLINVAR
Validation and Implementation of BRCA1/2 Variant Screening in Ovarian Tumor Tissue.
29936257
2018
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.800
CausalMutation
disease
CLINVAR
Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer.
29368341
2018