rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A high proportion of mutations in the BRCA1 gene in German breast/ovarian cancer families with clustering of mutations in the 3' third of the gene.
|
9760198 |
1998 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population.
|
11802209 |
2002 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Assessing the RNA effect of 26 DNA variants in the BRCA1 and BRCA2 genes.
|
21735045 |
2012 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
The prevalence and spectrum of BRCA1 and BRCA2 mutations in Korean population: recent update of the Korean Hereditary Breast Cancer (KOHBRA) study.
|
25863477 |
2015 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Evaluation of BRCA1 and BRCA2 mutations and risk-prediction models in a typical Asian country (Malaysia) with a relatively low incidence of breast cancer.
|
18627636 |
2008 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations.
|
24285858 |
2014 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence.
|
23479189 |
2013 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Implications of a novel cryptic splice site in the BRCA1 gene.
|
9805131 |
1998 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Functional characterization of BRCA1 gene variants by mini-gene splicing assay.
|
24667779 |
2014 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
|
16683254 |
2006 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Genetic testing and prevention of hereditary cancer at the MMCI--over 10 years of experience.
|
21348412 |
2010 |
rs80358163
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Germline truncating-mutations in BRCA1 and MSH6 in a patient with early onset endometrial cancer.
|
23164213 |
2012 |
rs80358163
|
|
C |
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 |