rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Frequency of germline and somatic BRCA1 mutations in ovarian cancer.
|
9796975 |
1998 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Molecular evidence for putative tumour suppressor genes on chromosome 13q specific to BRCA1 related ovarian and fallopian tube cancer.
|
12354934 |
2002 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Detection of protein folding defects caused by BRCA1-BRCT truncation and missense mutations.
|
14534301 |
2003 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Functional characterization of BRCA1 sequence variants using a yeast small colony phenotype assay.
|
15004537 |
2004 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Structure-based assessment of missense mutations in human BRCA1: implications for breast and ovarian cancer predisposition.
|
15172985 |
2004 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation.
|
15235020 |
2004 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Classification of BRCA1 missense variants of unknown clinical significance.
|
15689452 |
2005 |
rs80357069
|
|
A |
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 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis.
|
17308087 |
2007 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
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 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Classification of Missense Mutations of Disease Genes.
|
18418466 |
2005 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 germline mutations and tumor characteristics in Chinese women with familial or early-onset breast cancer.
|
18512148 |
2009 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1.
|
18992264 |
2009 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Toward classification of BRCA1 missense variants using a biophysical approach.
|
20378548 |
2010 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Comprehensive analysis of missense variations in the BRCT domain of BRCA1 by structural and functional assays.
|
20516115 |
2010 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prevalence and characterization of BRCA1 and BRCA2 germline mutations in Chinese women with familial breast cancer.
|
21614564 |
2012 |
rs80357069
|
|
A |
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 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Hereditary breast cancer in the Han Chinese population.
|
23318652 |
2013 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Patterns and functional implications of rare germline variants across 12 cancer types.
|
26689913 |
2015 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making.
|
27272900 |
2016 |