ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.1098C>T (p.Asn366=)

gnomAD frequency: 0.00001  dbSNP: rs749902808
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000205799 SCV000259574 likely benign Familial adenomatous polyposis 2 2025-01-08 criteria provided, single submitter clinical testing
Ambry Genetics RCV000222680 SCV000274113 likely benign Hereditary cancer-predisposing syndrome 2015-02-25 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Color Diagnostics, LLC DBA Color Health RCV000222680 SCV000907353 likely benign Hereditary cancer-predisposing syndrome 2017-11-20 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000205799 SCV004841838 likely benign Familial adenomatous polyposis 2 2023-08-15 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.