ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.31C>T (p.Leu11=)

dbSNP: rs864622596
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000429872 SCV000533988 likely benign not specified 2016-11-15 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV002063573 SCV002347544 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-12-10 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247017 SCV005898834 benign Colorectal cancer, hereditary nonpolyposis, type 2 2024-11-15 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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.