ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.1702dup (p.Leu568fs)

dbSNP: rs772716663
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001919364 SCV002189943 pathogenic Acrocallosal syndrome 2022-06-05 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 1422094). This premature translational stop signal has been observed in individual(s) with acrocallosal syndrome (PMID: 26349186). This variant is present in population databases (rs772716663, gnomAD 0.003%). This sequence change creates a premature translational stop signal (p.Leu568Profs*21) in the KIF7 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in KIF7 are known to be pathogenic (PMID: 19666503, 21552264, 21633164, 26648833).

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.