ClinVar Miner

Submissions for variant NM_001048174.2(MUTYH):c.811C>T (p.Gln271Ter)

dbSNP: rs2149137694
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001380116 SCV001578062 pathogenic Familial adenomatous polyposis 2 2021-08-03 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 1068517). This variant has not been reported in the literature in individuals affected with MUTYH-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Gln299*) in the MUTYH gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in MUTYH are known to be pathogenic (PMID: 18534194, 20663686). For these reasons, this variant has been classified as Pathogenic.

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