×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
BRCA1-2 mutations in breast cancer: identification of nine new variants of BRCA1-2 genes in a population from central Western Spain.
15876480 2006
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
25980754 2015
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Peru.
25256238 2015
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
A comprehensive focus on global spectrum of BRCA1 and BRCA2 mutations in breast cancer.
24312913 2013
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Functional assays for classification of BRCA2 variants of uncertain significance.
18451181 2008
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
An efficient pipeline for the generation and functional analysis of human BRCA2 variants of uncertain significance.
25146914 2014
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
A high frequency of PALB2 mutations in Jamaican patients with breast cancer.
28194609 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
BRCA2 mutations and androgen receptor expression as independent predictors of outcome of male breast cancer patients.
14555518 2003
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
The role of BRCA1 and BRCA2 in prostate cancer.
23747895 2013
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil.
23469205 2013
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Structure-based assessment of BRCA1 and BRCA2 mutations in a small Spanish population.
15944772 2005
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Exceptions to the rule: case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genes.
25639900 2015
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling.
21520273 2011
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Prostate cancer in BRCA2 germline mutation carriers is associated with poorer prognosis.
20736950 2010
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women.
27836010 2016
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Mutational analysis of BRCA1 and BRCA2 in hereditary breast and ovarian cancer families from Asturias (Northern Spain).
23683081 2013
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
The prevalence and spectrum of BRCA1 and BRCA2 mutations in Korean population: recent update of the Korean Hereditary Breast Cancer (KOHBRA) study.
25863477 2015
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
New recurrent BRCA1/2 mutations in Polish patients with familial breast/ovarian cancer detected by next generation sequencing.
25948282 2015
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Low frequency of recurrent BRCA1 and BRCA2 mutations in Spain.
11857748 2002
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).
21990134 2012
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
High prevalence of BRCA1 and BRCA2 germline mutations with loss of heterozygosity in a series of resected pancreatic adenocarcinoma and other neoplastic lesions.
23658460 2013
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Screening BRCA1 and BRCA2 unclassified variants for splicing mutations using reverse transcription PCR on patient RNA and an ex vivo assay based on a splicing reporter minigene.
18424508 2008
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
BRCAPAP: feasibility of clinical BRCA testing on liquid-based cervical cytology: implications for biomarker development.
15342457 2004
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Functional classification of BRCA2 DNA variants by splicing assays in a large minigene with 9 exons.
25382762 2015