ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.1495A>C (p.Met499Leu)

dbSNP: rs1114167745
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001948888 SCV002211069 uncertain significance Hereditary nonpolyposis colorectal neoplasms 2022-02-24 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with MSH6-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt MSH6 protein function. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces methionine, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 499 of the MSH6 protein (p.Met499Leu).
All of Us Research Program, National Institutes of Health RCV004010948 SCV004827159 uncertain significance Lynch syndrome 2023-06-28 criteria provided, single submitter clinical testing

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