×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.
28281021 2017
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer.
28905878 2017
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes.
28829762 2017
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
The RAD51C exonic splice-site mutations c.404G>C and c.404G>T are associated with familial breast and ovarian cancer.
27622768 2017
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Genetic epidemiology of ovarian cancer and prospects for polygenic risk prediction.
29054568 2017
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Secondary Somatic Mutations Restoring RAD51C and RAD51D Associated with Acquired Resistance to the PARP Inhibitor Rucaparib in High-Grade Ovarian Carcinoma.
28588062 2017
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2.
27616075 2017
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer.
28024868 2017
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients.
26822949 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing.
27621404 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.
27433846 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Inherited Mutations in Women With Ovarian Carcinoma.
26720728 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Trans-dichlorooxovandium (IV) complex as a novel photoinducible DNA interstrand crosslinker for cancer therapy.
26678223 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Veliparib Alone or in Combination with Mitomycin C in Patients with Solid Tumors With Functional Deficiency in Homologous Recombination Repair.
26848151 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Identification of six pathogenic RAD51C mutations via mutational screening of 1228 Danish individuals with increased risk of hereditary breast and/or ovarian cancer.
26740214 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Inherited Mutations in Women With Ovarian Carcinoma.
26720728 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer.
26824983 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Identification of six pathogenic RAD51C mutations via mutational screening of 1228 Danish individuals with increased risk of hereditary breast and/or ovarian cancer.
26740214 2016
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
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: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159 2015
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations.
25154786 2015
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic.
26057125 2015
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population.
26261251 2015
×
Entrez Id: 5889
Gene Symbol: RAD51C
RAD51C
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: 5889
Gene Symbol: RAD51C
RAD51C
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Genetic testing for RAD51C mutations: in the clinic and community.
25470109 2015