ClinVar Miner

Submissions for variant NM_000528.4(MAN2B1):c.1383C>T (p.Tyr461=)

dbSNP: rs775200333
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000963526 SCV001110690 likely benign Deficiency of alpha-mannosidase 2024-01-09 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000963526 SCV001287799 uncertain significance Deficiency of alpha-mannosidase 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Genome-Nilou Lab RCV000963526 SCV002014542 likely benign Deficiency of alpha-mannosidase 2021-09-05 criteria provided, single submitter clinical testing
Natera, Inc. RCV000963526 SCV002086928 likely benign Deficiency of alpha-mannosidase 2020-01-20 no assertion criteria provided 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.