ClinVar Miner

Submissions for variant NM_013254.4(TBK1):c.1956del (p.Asn652fs)

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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 RCV003754706 SCV004451041 pathogenic Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 2023-04-07 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Asn652Lysfs*22) in the TBK1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in TBK1 are known to be pathogenic (PMID: 25803835, 26476236, 26581300). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with TBK1-related conditions. For these reasons, this variant has been classified as Pathogenic.

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