ClinVar Miner

Submissions for variant NM_015506.3(MMACHC):c.477C>T (p.Ala159=)

gnomAD frequency: 0.00001  dbSNP: rs747698015
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
GeneDx RCV000608706 SCV000722851 likely benign not specified 2017-09-13 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV001496602 SCV001701302 likely benign Cobalamin C disease 2023-12-13 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001496602 SCV004178183 likely benign Cobalamin C disease 2023-04-11 criteria provided, single submitter clinical testing
Natera, Inc. RCV001273227 SCV001456019 likely benign Methylmalonic acidemia with homocystinuria cblC 2020-09-16 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.