ClinVar Miner

Submissions for variant NM_198994.3(TGM6):c.1882G>T (p.Val628Leu)

dbSNP: rs1162119013
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
Athena Diagnostics RCV000713835 SCV000844472 uncertain significance not provided 2018-05-14 criteria provided, single submitter clinical testing
Ambry Genetics RCV003258947 SCV003969784 uncertain significance Inborn genetic diseases 2023-04-18 criteria provided, single submitter clinical testing The c.1882G>T (p.V628L) alteration is located in exon 12 (coding exon 12) of the TGM6 gene. This alteration results from a G to T substitution at nucleotide position 1882, causing the valine (V) at amino acid position 628 to be replaced by a leucine (L). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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.