ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.714A>G (p.Leu238=)

dbSNP: rs1575480529
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001429656 SCV001632373 likely benign Hereditary nonpolyposis colorectal neoplasms 2021-07-06 criteria provided, single submitter clinical testing
Ambry Genetics RCV002363421 SCV002662322 likely benign Hereditary cancer-predisposing syndrome 2021-07-30 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.
All of Us Research Program, National Institutes of Health RCV004003288 SCV004828938 likely benign Lynch syndrome 2023-06-08 criteria provided, single submitter clinical testing

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