ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.860del (p.Thr287fs)

dbSNP: rs2143930383
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001920731 SCV002186554 pathogenic Fanconi anemia complementation group O 2023-10-16 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Thr287Lysfs*15) in the RAD51C gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in RAD51C are known to be pathogenic (PMID: 20400964, 21990120, 24800917, 29278735). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with RAD51C-related conditions. ClinVar contains an entry for this variant (Variation ID: 1411600). For these reasons, this variant has been classified as Pathogenic.
Baylor Genetics RCV003464227 SCV004208020 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 3 2023-02-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV003464227 SCV004932633 pathogenic Breast-ovarian cancer, familial, susceptibility to, 3 2024-01-03 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.