|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
The spectrum of BRCA mutations and characteristics of BRCA-associated breast cancers in China: Screening of 2,991 patients and 1,043 controls by next-generation sequencing.
|
28294317 |
2017 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
BRCA1 and BRCA2 mutations in ovarian cancer patients from China: ethnic-related mutations in BRCA1 associated with an increased risk of ovarian cancer.
|
28176296 |
2017 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Functional classification of DNA variants by hybrid minigenes: Identification of 30 spliceogenic variants of BRCA2 exons 17 and 18.
|
28339459 |
2017 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries.
|
26187060 |
2016 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence and differentiation of hereditary breast and ovarian cancers in Japan.
|
24249303 |
2015 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A high frequency of BRCA mutations in young black women with breast cancer residing in Florida.
|
26287763 |
2015 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Exceptions to the rule: case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genes.
|
25639900 |
2015 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Deleterious BRCA1/2 mutations in an urban population of Black women.
|
26250392 |
2015 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Clear cell sarcoma of the kidney in a child with Fanconi anemia.
|
24735155 |
2014 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
BRCA1 and BRCA2 mutations in breast cancer patients from Venezuela.
|
23096355 |
2012 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Hereditary inflammatory breast cancer associated with BRCA2 mutation: a rare disease presentation in mother and daughter.
|
22895246 |
2012 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes.
|
21702907 |
2011 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Classifying Variants of Undetermined Significance in BRCA2 with protein likelihood ratios.
|
19043619 |
2008 |
|
rs80359035
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Does nonsense-mediated mRNA decay explain the ovarian cancer cluster region of the BRCA2 gene?
|
16170354 |
2006 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.
|
16489001 |
2006 |
|
rs80359035
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk families.
|
16528604 |
2006 |
|
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Cancer variation associated with the position of the mutation in the BRCA2 gene.
|
15131399 |
2004 |