rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
|
26787237 |
2016 |
rs80357069
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Addressing health disparities in Hispanic breast cancer: accurate and inexpensive sequencing of BRCA1 and BRCA2.
|
26543556 |
2015 |
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 |
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 |
A computational method to classify variants of uncertain significance using functional assay data with application to BRCA1.
|
21447777 |
2011 |
rs80357069
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A computational method to classify variants of uncertain significance using functional assay data with application to BRCA1.
|
21447777 |
2011 |
rs80357069
|
|
T |
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 |
Comprehensive analysis of missense variations in the BRCT domain of BRCA1 by structural and functional assays.
|
20516115 |
2010 |
rs80357069
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Functional impact of missense variants in BRCA1 predicted by supervised learning.
|
17305420 |
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 BRCA1 missense variants of unknown clinical significance.
|
15689452 |
2005 |
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 |
Structure and mechanism of BRCA1 BRCT domain recognition of phosphorylated BACH1 with implications for cancer.
|
15133502 |
2004 |
rs80357069
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Structure and mechanism of BRCA1 BRCT domain recognition of phosphorylated BACH1 with implications for cancer.
|
15133502 |
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
|
|
T |
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 |
Frequency of germline and somatic BRCA1 mutations in ovarian cancer.
|
9796975 |
1998 |