Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes. 28829762

2017

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Trans-dichlorooxovandium (IV) complex as a novel photoinducible DNA interstrand crosslinker for cancer therapy. 26678223

2016

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Mammalian RAD51 paralogs protect nascent DNA at stalled forks and mediate replication restart. 26354865

2015

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Genetic testing for RAD51C mutations: in the clinic and community. 25470109

2015

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Enhanced non-homologous end joining contributes toward synthetic lethality of pathological RAD51C mutants with poly (ADP-ribose) polymerase. 25292178

2015

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair. 24141787

2014

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Pathological features of breast and ovarian cancers in RAD51C germline mutation carriers. 24993905

2014

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR ATM- and ATR-mediated phosphorylation of XRCC3 regulates DNA double-strand break-induced checkpoint activation and repair. 23438602

2013

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility. 22167183

2012

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. 22451500

2012

dbSNP: rs267606999
rs267606999
C 0.700 GeneticVariation CLINVAR Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. 20400964

2010