×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Mutation detection rates associated with specific selection criteria for BRCA1/2 testing in 1854 high-risk families: A monocentric Italian study.
27062684
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
GeneticVariation
disease
CLINVAR
Adding In Silico Assessment of Potential Splice Aberration to the Integrated Evaluation of BRCA Gene Unclassified Variants.
26913838
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Genetic testing in a cohort of young patients with HER2-amplified breast cancer.
26681682
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Exonic Splicing Mutations Are More Prevalent than Currently Estimated and Can Be Predicted by Using In Silico Tools.
26761715
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.
26586665
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
In silico, in vitro and case-control analyses as an effective combination for analyzing BRCA1 and BRCA2 unclassified variants in a population-based sample.
27886673
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
GeneticVariation
disease
CLINVAR
Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries.
26187060
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Improving performance of multigene panels for genomic analysis of cancer predisposition.
26845104
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
BRCA1 and BRCA2 mutations in Japanese patients with ovarian, fallopian tube, and primary peritoneal cancer.
26439132
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
GeneticVariation
disease
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients.
26483394
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
26787237
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Identification of germline alterations in breast cancer predisposition genes among Malaysian breast cancer patients using panel testing.
26757417
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
GeneticVariation
disease
CLINVAR
Improving performance of multigene panels for genomic analysis of cancer predisposition.
26845104
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries.
26187060
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Multidisciplinary team for elucidation of any new mutation and how this approach can be useful to individualize any genetic result: the case of BRCA2 c.631G>A/c.7008-2A>T genotype Response to: Nagy PL, Mansukhani M. The role of clinical genomic testing in diagnosis and discovery of pathogenic mutations. Expert Rev Mol Diagn 2015;15(9):1101-5.
27125725
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Prevalence of Hispanic BRCA1 and BRCA2 mutations among hereditary breast and ovarian cancer patients from Brazil reveals differences among Latin American populations.
27425403
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
GeneticVariation
disease
CLINVAR
Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.
26556299
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
27153395
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
A Survey of BRCA1, BRCA2, and PALB2 mutations in women with breast cancer in Trinidad and Tobago.
27469594
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Evaluation of germline BRCA1 and BRCA2 mutations in a multi-ethnic Asian cohort of ovarian cancer patients.
26541979
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients.
27406733
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Adding In Silico Assessment of Potential Splice Aberration to the Integrated Evaluation of BRCA Gene Unclassified Variants.
26913838
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Detection of Germline Mutation in Hereditary Breast and/or Ovarian Cancers by Next-Generation Sequencing on a Four-Gene Panel.
27157322
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.700
CausalMutation
disease
CLINVAR
Increased risk of male cancer and identification of a potential prostate cancer cluster region in BRCA2.
26360800
2016