ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1179dup (p.Gln394fs)

dbSNP: rs2149782151
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003337378 SCV002201199 pathogenic Familial adenomatous polyposis 1 2020-11-15 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln394Thrfs*3) in the APC gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in APC are known to be pathogenic (PMID: 17963004, 20685668). This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with APC-related conditions. For these reasons, this variant has been classified as Pathogenic.
Myriad Genetics, Inc. RCV003337378 SCV004043630 pathogenic Familial adenomatous polyposis 1 2023-04-28 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

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