Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
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
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer.
|
20694749 |
2010 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
BRCA1/BRCA2 gene mutations/SNPs and BRCA1 haplotypes in early-onset breast cancer patients of Indian ethnicity.
|
22752604 |
2012 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Genetic diagnosis of familial breast cancer using clonal sequencing.
|
20127978 |
2010 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer.
|
19241424 |
2009 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Contribution of BRCA2 germline mutations to hereditary breast/ovarian cancer in Germany.
|
11897832 |
2002 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Founder mutations account for the majority of BRCA1-attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central Italy.
|
18821011 |
2009 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
|
16683254 |
2006 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.
|
16489001 |
2006 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Clinical and molecular characterization of the BRCA2 p.Asn3124Ile variant reveals substantial evidence for pathogenic significance.
|
24728577 |
2014 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
BRCA1 and BRCA2 mutations in breast cancer patients from Venezuela.
|
23096355 |
2012 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
The relative contribution of point mutations and genomic rearrangements in BRCA1 and BRCA2 in high-risk breast cancer families.
|
18703817 |
2008 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer.
|
11504767 |
2001 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
BRCA2 mutations in hereditary breast and ovarian cancer in France.
|
9150172 |
1997 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
BRCA2 splice site mutations in an Italian breast/ovarian cancer family.
|
19542536 |
2009 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer.
|
25682074 |
2015 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Recurrent germline mutations in BRCA1 and BRCA2 genes in high risk families in Israel.
|
22399190 |
2012 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Comprehensive splicing functional analysis of DNA variants of the BRCA2 gene by hybrid minigenes.
|
22632462 |
2012 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.
|
9585613 |
1998 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
|
23613520 |
2013 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
BRCA-associated pancreatico-biliary neoplasms: Four cases illustrating the emerging clinical impact of genotyping.
|
26004055 |
2016 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer.
|
23569316 |
2013 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Computational and structural investigation of deleterious functional SNPs in breast cancer BRCA2 gene.
|
18724707 |
2008 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Classifying Variants of Undetermined Significance in BRCA2 with protein likelihood ratios.
|
19043619 |
2008 |
Entrez Id: |
675 |
Gene Symbol: |
BRCA2 |
BRCA2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer.
|
16168123 |
2005 |