ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.2238T>C (p.Phe746=)

dbSNP: rs1384756767
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001188998 SCV001356191 likely benign Hereditary cancer-predisposing syndrome 2018-12-03 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001356987 SCV005429322 likely benign Lynch syndrome 2024-09-23 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV001356987 SCV001552298 likely benign Lynch syndrome no assertion criteria provided clinical testing The MSH6 p.Phe746= variant was not identified in the literature nor was it identified in the dbSNP, ClinVar, or UMD-LSDB databases. The variant was identified in control databases in 1 of 245650 chromosomes at a frequency of 0.000004 (Genome Aggregation Database Feb 27, 2017). The variant was observed in the Latino population in 1 of 33568 chromosomes (freq: 0.00003), while the variant was not observed in the African, Other, European, Ashkenazi Jewish, East Asian, Finnish, or South Asian populations. The p.Phe746= variant is not expected to have clinical significance because it does not result in a change of amino acid and is not located in a known consensus splice site. In addition, in silico or computational prediction software programs (SpliceSiteFinder, MaxEntScan, NNSPLICE, GeneSplicer) do not predict a difference in splicing. In summary, based on the above information, the clinical significance of this variant cannot be determined with certainty at this time although we would lean towards a more benign role for this variant. This variant is classified as likely benign.

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