×
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
Hereditary breast cancer and the BRCA1-associated FANCJ/BACH1/BRIP1.
21345144 2011
×
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
GeneticVariation
CLINVAR
Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
23613520 2013
×
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
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
22006311 2011
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease.
24556621 2014
×
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
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer.
25452441 2015
×
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
The DNA repair helicases XPD and FancJ have essential iron-sulfur domains.
16973432 2006
×
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
CausalMutation
CLINVAR
Integrated analysis of germline and somatic variants in ovarian cancer.
24448499 2014
×
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
GeneticVariation
CLINVAR
Structural basis for the function of DEAH helicases.
20168331 2010
×
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
CausalMutation
CLINVAR
BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer.
21409391 2011
×
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
GeneticVariation
CLINVAR
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing.
20616022 2010
×
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
GeneticVariation
CLINVAR
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.
16116424 2005
×
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
Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
28423363 2017