ClinVar Miner

Submissions for variant NM_153704.6(TMEM67):c.982A>T (p.Thr328Ser)

dbSNP: rs2130668443
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 RCV001930879 SCV002191956 uncertain significance Familial aplasia of the vermis; Meckel-Gruber syndrome 2021-09-26 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt TMEM67 protein function. This variant has not been reported in the literature in individuals affected with TMEM67-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces threonine with serine at codon 328 of the TMEM67 protein (p.Thr328Ser). The threonine residue is weakly conserved and there is a small physicochemical difference between threonine and serine.

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.