rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer.
|
28283652 |
2017 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
|
16683254 |
2006 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A high-throughput functional complementation assay for classification of BRCA1 missense variants.
|
23867111 |
2013 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history.
|
19200354 |
2009 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A mutation analysis of the BRCA1 gene in 140 families from southeast France with a history of breast and/or ovarian cancer.
|
12827452 |
2003 |
rs41293459
|
|
T |
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 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example.
|
19563646 |
2009 |
rs41293459
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk.
|
22889855 |
2012 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk.
|
22889855 |
2012 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort.
|
27495310 |
2017 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status.
|
24504028 |
2014 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Combining Homologous Recombination and Phosphopeptide-binding Data to Predict the Impact of BRCA1 BRCT Variants on Cancer Risk.
|
30257991 |
2019 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Comprehensive analysis of missense variations in the BRCT domain of BRCA1 by structural and functional assays.
|
20516115 |
2010 |
rs41293459
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Detection of protein folding defects caused by BRCA1-BRCT truncation and missense mutations.
|
14534301 |
2003 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Detection of protein folding defects caused by BRCA1-BRCT truncation and missense mutations.
|
14534301 |
2003 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis.
|
17308087 |
2007 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Diagnostic strategy for analytical scanning of BRCA1 gene by fluorescence-assisted mismatch analysis using large, bifluorescently labeled amplicons.
|
11410501 |
2001 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
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 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families.
|
11157798 |
2001 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.
|
16489001 |
2006 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants.
|
22505045 |
2012 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations.
|
20455026 |
2010 |
rs41293459
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?
|
18036263 |
2007 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?
|
18036263 |
2007 |
rs41293459
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Impact of BRCA1 BRCT domain missense substitutions on phosphopeptide recognition.
|
21473589 |
2011 |