|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.
|
26270727 |
2015 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
Patterns and functional implications of rare germline variants across 12 cancer types.
|
26689913 |
2015 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Mammalian RAD51 paralogs protect nascent DNA at stalled forks and mediate replication restart.
|
26354865 |
2015 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
UNIPROT |
Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair.
|
24141787 |
2014 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
RAD51C--a new human cancer susceptibility gene for sporadic squamous cell carcinoma of the head and neck (HNSCC).
|
24315737 |
2014 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair.
|
24141787 |
2014 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families.
|
25086635 |
2014 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Pathological features of breast and ovarian cancers in RAD51C germline mutation carriers.
|
24993905 |
2014 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan.
|
24800917 |
2014 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan.
|
24800917 |
2014 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes.
|
24549055 |
2014 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Germline mutation in the RAD51B gene confers predisposition to breast cancer.
|
24139550 |
2013 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
Germline mutation in the RAD51B gene confers predisposition to breast cancer.
|
24139550 |
2013 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
Germline RAD51C mutations in ovarian cancer susceptibility.
|
22725699 |
2013 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility.
|
22167183 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Germline RAD51C mutations confer susceptibility to ovarian cancer.
|
22538716 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
Biomarker
|
disease |
CLINGEN |
Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility.
|
22167183 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families.
|
22451500 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility.
|
22167183 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients.
|
21990120 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation.
|
22232082 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
GeneticVariation
|
disease |
CLINVAR |
Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients.
|
21990120 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
Germline RAD51C mutations confer susceptibility to ovarian cancer.
|
22538716 |
2012 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
RAD51C is a susceptibility gene for ovarian cancer.
|
21616938 |
2011 |
|
| Entrez Id: |
5889 |
| Gene Symbol: |
RAD51C |
RAD51C
|
0.710 |
CausalMutation
|
disease |
CLINVAR |
A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families.
|
21537932 |
2011 |