ClinVar Miner

Submissions for variant NM_005908.4(MANBA):c.1162C>T (p.Arg388Trp)

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
Center of Genomic medicine, Geneva, University Hospital of Geneva RCV003387495 SCV004098985 likely pathogenic Beta-D-mannosidosis 2023-01-26 criteria provided, single submitter clinical testing This variant is present in compound heterozygosity with another variant in the same gene
Ambry Genetics RCV004985339 SCV005616275 uncertain significance Inborn genetic diseases 2024-11-15 criteria provided, single submitter clinical testing The c.1162C>T (p.R388W) alteration is located in exon 9 (coding exon 9) of the MANBA gene. This alteration results from a C to T substitution at nucleotide position 1162, causing the arginine (R) at amino acid position 388 to be replaced by a tryptophan (W). 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.