×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population?
29161300 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
28423363 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
The Clinical Utility of Next Generation Sequencing Results in a Community-Based Hereditary Cancer Risk Program.
27276934 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.
28008555 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Molecular characterization and clinical interpretation of BRCA1/BRCA2 variants in families from Murcia (south-eastern Spain) with hereditary breast and ovarian cancer: clinical-pathological features in BRCA carriers and non-carriers.
28477318 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.
28008555 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Prevalence and spectrum of germline rare variants in BRCA1/2 and PALB2 among breast cancer cases in Sarawak, Malaysia.
28664506 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.
28324225 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.
28127413 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Biological and clinical evidence for somatic mutations in BRCA1 and BRCA2 as predictive markers for olaparib response in high-grade serous ovarian cancers in the maintenance setting.
28525389 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.
28102861 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Revisiting breast cancer patients who previously tested negative for BRCA mutations using a 12-gene panel.
27798748 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Multigene panels in Ashkenazi Jewish patients yield high rates of actionable mutations in multiple non-BRCA cancer-associated genes.
28495237 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast-ovarian cancer prevention and control.
28577564 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Characteristics of BRCA1/2 mutations carriers including large genomic rearrangements in high risk breast cancer patients.
28205045 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50.
28678401 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Germline and somatic mutations in homologous recombination genes among Chinese ovarian cancer patients detected using next-generation sequencing.
28541631 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
28152038 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
BRCA1 and BRCA2 founder mutations account for 78% of germline carriers among hereditary breast cancer families in Chile.29088781 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Analysis of BRCA1/2 mutation spectrum and prevalence in unselected Chinese breast cancer patients by next-generation sequencing.
28664449 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Prostate Cancer in a Patient with a Family History of BRCA Mutation: a Case Report and Literature Review.
28049253 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
27978560 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
BRCA1 and BRCA2 mutation testing in Cyprus; a population based study.
27882536 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.
28281021 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Simultaneous detection of genetic and copy number alterations in BRCA1/2 genes.
29383094 2017