ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.848_849del (p.Arg283fs)

dbSNP: rs2073188904
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Biochemistry, Molecular Biology and Biotechnology, University of Colombo RCV001265628 SCV001443791 pathogenic Familial cancer of breast criteria provided, single submitter case-control
Ambry Genetics RCV004951438 SCV005522140 pathogenic Hereditary cancer-predisposing syndrome 2024-11-08 criteria provided, single submitter clinical testing The c.848_849delGC pathogenic mutation, located in coding exon 7 of the TP53 gene, results from a deletion of two nucleotides at nucleotide positions 848 to 849, causing a translational frameshift with a predicted alternate stop codon (p.R283Hfs*22). This variant is considered to be rare based on population cohorts in the Genome Aggregation Database (gnomAD). This alteration is expected to result in loss of function by premature protein truncation or nonsense-mediated mRNA decay. As such, this alteration is interpreted as a disease-causing mutation.

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.