×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
The yield of targeted genotyping for the recurring mutations in BRCA1/2 in Israel.
29086229
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium.
28490613
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication.
28802053
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
29446198
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia.
29335924
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Is there a genetic anticipation in breast and/or ovarian cancer families with the germline c.3481_3491del11 mutation?
28493033
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
GeneticVariation
CLINVAR
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.
29339979
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Mutations in context: implications of BRCA testing in diverse populations.
28918466
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Germline BRCA mutation and outcome in young-onset breast cancer (POSH): a prospective cohort study.
29337092
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.
29339979
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: first report after establishment of HBOC registration system in Japan.
29176636
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Characterization of mutations in BRCA1/2 and the relationship with clinic-pathological features of breast cancer in a hereditarily high-risk sample of chinese population.
29435039
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
High prevalence of deleterious BRCA1 and BRCA2 germline mutations in arab breast and ovarian cancer patients.
29297111
2018
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
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
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
"A new case of ""de novo"" BRCA1 mutation in a patient with early-onset breast cancer."
28265380
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
A case series of three Sri Lankan families with hereditary breast and ovarian cancer syndrome due to pathogenic germline mutations in the BRCA1 gene
28390335
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
GeneticVariation
CLINVAR
Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory.
28408614
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
GeneticVariation
CLINVAR
Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.
28324225
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.
28324225
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Molecular characterization and clinical interpretation of BRCA1/BRCA2 variants in families from Murcia (south-eastern Spain) with hereditary breast and ovarian cancer: clinical-pathological features in BRCA carriers and non-carriers.
28477318
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Lost in translation: returning germline genetic results in genome-scale cancer research.
28454591
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Contribution of germline mutations in cancer predisposition genes to tumor etiology in young women diagnosed with invasive breast cancer.
28503720
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
A high frequency of PALB2 mutations in Jamaican patients with breast cancer.
28194609
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
Next-generation sequencing in familial breast cancer patients from Lebanon.
28202063
2017
×
Entrez Id:
672
Gene Symbol:
BRCA1
BRCA1
Neoplastic Syndromes, Hereditary
0.150
CausalMutation
CLINVAR
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer.
28283652
2017