×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
28152038 2017
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
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: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics.
15040442 2004
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Frequent incidence of BARD1-truncating mutations in germline DNA from triple-negative breast cancer patients.
26010302 2016
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Crystal structure of the BARD1 BRCT domains.
17550235 2007
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
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: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
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: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Cancer predisposing BARD1 mutations in breast-ovarian cancer families.
21344236 2012
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
28724667 2017
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families.
20077502 2010
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example.
25994375 2015
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.
28008555 2017
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Crystal structure of the BARD1 ankyrin repeat domain and its functional consequences.
18480049 2008
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
26315354 2015
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
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: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
BARD1 nonsense variant c.1921C>T in a patient with recurrent breast cancer.28174632 2017
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
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: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Phosphopeptide binding specificities of BRCA1 COOH-terminal (BRCT) domains.
14578343 2003
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
25503501 2015
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
The BARD1 C-terminal domain structure and interactions with polyadenylation factor CstF-50.
18842000 2008
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
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: 580
Gene Symbol: BARD1
BARD1
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: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
BARD1 induces apoptosis by catalysing phosphorylation of p53 by DNA-damage response kinase.
15782130 2005
×
Entrez Id: 580
Gene Symbol: BARD1
BARD1
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: 580
Gene Symbol: BARD1
BARD1
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes.
24549055 2014