rs41293463
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A guide for functional analysis of BRCA1 variants of uncertain significance.
|
22753008 |
2012 |
rs41293463
|
|
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 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
|
7545954 |
1994 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Analysis of BRCA1 variants in double-strand break repair by homologous recombination and single-strand annealing.
|
23161852 |
2013 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation.
|
15235020 |
2004 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.
|
16267036 |
2005 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling.
|
21520273 |
2011 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
ATM activation by ionizing radiation requires BRCA1-associated BAAT1.
|
16452482 |
2006 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 mutations in primary breast and ovarian carcinomas.
|
7939630 |
1994 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
BRCT repeats as phosphopeptide-binding modules involved in protein targeting.
|
14576432 |
2003 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Breast cancer in young women (YBC): prevalence of BRCA1/2 mutations and risk of secondary malignancies across diverse racial groups.
|
19491284 |
2009 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Characterisation of gene expression profiles of yeast cells expressing BRCA1 missense variants.
|
19493677 |
2009 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Characteristics of triple-negative breast cancer in patients with a BRCA1 mutation: results from a population-based study of young women.
|
22010008 |
2011 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.
|
20104584 |
2010 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Classification of BRCA1 missense variants of unknown clinical significance.
|
15689452 |
2005 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Comprehensive analysis of missense variations in the BRCT domain of BRCA1 by structural and functional assays.
|
20516115 |
2010 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Crystal structure of the BRCT repeat region from the breast cancer-associated protein BRCA1.
|
11573086 |
2001 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases.
|
22144684 |
2012 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Detection of protein folding defects caused by BRCA1-BRCT truncation and missense mutations.
|
14534301 |
2003 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis.
|
17308087 |
2007 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Direct interaction between BRCA1 and the estrogen receptor regulates vascular endothelial growth factor (VEGF) transcription and secretion in breast cancer cells.
|
12400015 |
2002 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Evidence for a transcriptional activation function of BRCA1 C-terminal region.
|
8942979 |
1996 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas.
|
24240112 |
2014 |
rs41293463
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of BRCA1 and BRCA2 mutations in unselected Nigerian breast cancer patients.
|
22034289 |
2012 |