rs41293511
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Classifying Variants of Undetermined Significance in BRCA2 with protein likelihood ratios.
|
19043619 |
2008 |
rs41293511
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure.
|
12228710 |
2002 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Functional assays for analysis of variants of uncertain significance in BRCA2.
|
24323938 |
2014 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population.
|
24728189 |
2014 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
An efficient pipeline for the generation and functional analysis of human BRCA2 variants of uncertain significance.
|
25146914 |
2014 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Comparison of locus-specific databases for BRCA1 and BRCA2 variants reveals disparity in variant classification within and among databases.
|
25782689 |
2015 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer.
|
28283652 |
2017 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Functional assays for classification of BRCA2 variants of uncertain significance.
|
18451181 |
2008 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Functional evaluation and cancer risk assessment of BRCA2 unclassified variants.
|
15695382 |
2005 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.
|
28324225 |
2017 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A cancer-associated BRCA2 mutation reveals masked nuclear export signals controlling localization.
|
24013206 |
2013 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2.
|
15290653 |
2004 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes.
|
21702907 |
2011 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Classifying Variants of Undetermined Significance in BRCA2 with protein likelihood ratios.
|
19043619 |
2008 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications.
|
18951461 |
2008 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Screening of male breast cancer and of breast-ovarian cancer families for BRCA2 mutations using large bifluorescent amplicons.
|
11207042 |
2001 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity.
|
23108138 |
2013 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).
|
21990134 |
2012 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mouse embryonic stem cell-based functional assay to evaluate mutations in BRCA2.
|
18607349 |
2008 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.
|
16489001 |
2006 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Development and validation of a new algorithm for the reclassification of genetic variants identified in the BRCA1 and BRCA2 genes.
|
25085752 |
2014 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 And BRCA2 analysis of Argentinean breastovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin.
|
23961350 |
2012 |