×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
28152038 2017
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Multigene panels in Ashkenazi Jewish patients yield high rates of actionable mutations in multiple non-BRCA cancer-associated genes.
28495237 2017
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Pathologic findings in breast, fallopian tube, and ovary specimens in non-BRCA hereditary breast and/or ovarian cancer syndromes: a study of 18 patients with deleterious germline mutations in RAD51C, BARD1, BRIP1, PALB2, MUTYH, or CHEK2.
28709830 2017
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
28423363 2017
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Near-atomic resolution visualization of human transcription promoter opening.
27193682 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer.
27165003 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Germline Variants of Prostate Cancer in Japanese Families.
27701467 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer.
26824983 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Analysis of BRIP1 Variants among Korean Patients with BRCA1/2 Mutation-Negative High-Risk Breast Cancer.
26790966 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.
27433846 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India.
26911350 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Inherited Mutations in Women With Ovarian Carcinoma.
26720728 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
26786923 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Understanding the Significance of Mutations in Tumor Suppressor Genes Identified Using Next-Generation Sequencing: A Case Report.
27462233 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Inherited Mutations in Women With Ovarian Carcinoma.
26720728 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Mutational analysis of FANCJ helicase.
27107905 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Fanconi anemia in 55-year-old identical twins first presenting as fatal post-chemotherapy pancytopenia.
27427815 2016
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
25980754 2015
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
26315354 2015
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159 2015
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Biogenesis of cytosolic and nuclear iron-sulfur proteins and their role in genome stability.
25583461 2015
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Mutations predisposing to breast cancer in 12 candidate genes in breast cancer patients from Poland.
25330149 2015
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Rescreening for genetic mutations using multi-gene panel testing in patients who previously underwent non-informative genetic screening.
26296696 2015