ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.388C>T (p.Leu130=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV004050338 SCV002624299 likely benign not specified 2021-01-23 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV003505220 SCV004283997 likely benign Colorectal cancer, hereditary nonpolyposis, type 7 2023-08-24 criteria provided, single submitter clinical testing

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