|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Investigating the effect of 28 BRCA1 and BRCA2 mutations on their related transcribed mRNA.
|
26780556 |
2016 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making.
|
27272900 |
2016 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Germline missense pathogenic variants in the BRCA1 BRCT domain, p.Gly1706Glu and p.Ala1708Glu, increase cellular sensitivity to PARP inhibitor olaparib by a dominant negative effect.
|
27742776 |
2016 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
DNA repair capacity is impaired in healthy BRCA1 heterozygous mutation carriers.
|
26071757 |
2015 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A high-throughput functional complementation assay for classification of BRCA1 missense variants.
|
23867111 |
2013 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).
|
21990134 |
2012 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A computational method to classify variants of uncertain significance using functional assay data with application to BRCA1.
|
21447777 |
2011 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Comprehensive analysis of missense variations in the BRCT domain of BRCA1 by structural and functional assays.
|
20516115 |
2010 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.
|
23199084 |
2010 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Non-founder BRCA1 mutations in Russian breast cancer patients.
|
20727672 |
2010 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Nbs1 flexibly tethers Ctp1 and Mre11-Rad50 to coordinate DNA double-strand break processing and repair.
|
19804755 |
2009 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis.
|
17308087 |
2007 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Crystal structure of the BARD1 BRCT domains.
|
17550235 |
2007 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
|
17924331 |
2007 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Functional impact of missense variants in BRCA1 predicted by supervised learning.
|
17305420 |
2007 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Structure-based assessment of missense mutations in human BRCA1: implications for breast and ovarian cancer predisposition.
|
15172985 |
2004 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation.
|
15235020 |
2004 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects.
|
12955716 |
2003 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Loss of heterozygosity analysis at the BRCA loci in tumor samples from patients with familial breast cancer.
|
11979449 |
2002 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Crystal structure of the BRCT repeat region from the breast cancer-associated protein BRCA1.
|
11573086 |
2001 |
|
rs80356860
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Molecular analysis of the BRCA1 and BRCA2 genes in 32 breast and/or ovarian cancer Spanish families.
|
10755399 |
2000 |