ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2302G>T (p.Gly768Cys)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002446349 SCV002734872 uncertain significance Hereditary cancer-predisposing syndrome 2022-05-15 criteria provided, single submitter clinical testing The p.G768C variant (also known as c.2302G>T), located in coding exon 15 of the BRIP1 gene, results from a G to T substitution at nucleotide position 2302. The glycine at codon 768 is replaced by cysteine, an amino acid with highly dissimilar properties. This amino acid position is conserved. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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.