ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.2712del (p.Trp904fs)

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
Ambry Genetics RCV002431204 SCV002743543 pathogenic Hereditary cancer-predisposing syndrome 2022-06-03 criteria provided, single submitter clinical testing The c.2712delG pathogenic mutation, located in coding exon 7 of the PALB2 gene, results from a deletion of one nucleotide at nucleotide position 2712, causing a translational frameshift with a predicted alternate stop codon (p.W904Cfs*19). 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.
Myriad Genetics, Inc. RCV003455493 SCV004187441 pathogenic Familial cancer of breast 2023-09-13 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.