ClinVar Miner

Submissions for variant NM_000267.3(NF1):c.3484A>G (p.Met1162Val) (rs773968270)

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 RCV000492521 SCV000581281 uncertain significance Hereditary cancer-predisposing syndrome 2015-06-25 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Co-occurence with mutation in same gene (phase unknown),Rarity in general population databases (dbsnp, esp, 1000 genomes),In silico models in agreement (benign),In silico models in agreement (deleterious) and/or completely conserved position in appropriate species,Insufficient or conflicting evidence
Invitae RCV000206616 SCV000259797 likely benign Neurofibromatosis, type 1 2018-01-08 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.