ClinVar Miner

Submissions for variant NM_024809.5(TCTN2):c.1958_1963del (p.Leu653_Tyr654del)

dbSNP: rs377628976
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001921015 SCV002196935 uncertain significance Familial aplasia of the vermis; Meckel-Gruber syndrome 2023-07-14 criteria provided, single submitter clinical testing This variant, c.1958_1963del, results in the deletion of 2 amino acid(s) of the TCTN2 protein (p.Leu653_Tyr654del), but otherwise preserves the integrity of the reading frame. This variant is present in population databases (rs377628976, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with TCTN2-related conditions. ClinVar contains an entry for this variant (Variation ID: 1415552). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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.
Fulgent Genetics, Fulgent Genetics RCV005006224 SCV005634164 uncertain significance Meckel syndrome, type 8; Joubert syndrome 24 2024-03-02 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.