ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.5087del (p.Leu1696fs)

dbSNP: rs1555533368
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 RCV002341492 SCV002641513 pathogenic Hereditary cancer-predisposing syndrome; Cardiovascular phenotype 2020-05-05 criteria provided, single submitter clinical testing The c.5024delT variant, located in coding exon 36 of the NF1 gene, results from a deletion of one nucleotide at nucleotide position 5024, causing a translational frameshift with a predicted alternate stop codon (p.L1675Rfs*2). 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.
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals RCV000578376 SCV000680118 pathogenic Neurofibromatosis, type 1 2017-06-26 no assertion criteria provided 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.