ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3555A>C (p.Ser1185=)

dbSNP: rs1669881416
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001203597 SCV001374770 uncertain significance Hereditary nonpolyposis colorectal neoplasms 2020-06-07 criteria provided, single submitter clinical testing 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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing, but this prediction has not been confirmed by published transcriptional studies. This variant has not been reported in the literature in individuals with MSH6-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change affects codon 1185 of the MSH6 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the MSH6 protein.
All of Us Research Program, National Institutes of Health RCV004010629 SCV004824634 likely benign Lynch syndrome 2023-05-04 criteria provided, single submitter clinical testing

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