ClinVar Miner

Submissions for variant NM_005732.4(RAD50):c.757-4T>C (rs1554098154)

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
Ambry Genetics RCV000564604 SCV000674663 uncertain significance Hereditary cancer-predisposing syndrome 2017-04-03 criteria provided, single submitter clinical testing The c.757-4T>C intronic variant results from a T to C substitution 4 nucleotides upstream from coding exon 6 in the RAD50 gene. This nucleotide position is well conserved in available vertebrate species. Using the BDGP and ESEfinder splice site prediction tools, this alteration is not predicted to have any significant effect on this splice acceptor site; however, direct evidence is unavailable. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.
Invitae RCV000982983 SCV001131002 likely benign not provided 2018-12-27 criteria provided, single submitter clinical testing
Invitae RCV000564604 SCV001701928 likely benign Hereditary cancer-predisposing syndrome 2018-12-27 criteria provided, single submitter clinical testing

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.