ClinVar Miner

Submissions for variant NM_153033.5(KCTD7):c.367C>T (p.Arg123Ter)

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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 RCV003088277 SCV003479025 pathogenic Progressive myoclonic epilepsy type 3 2024-06-09 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Arg123*) in the KCTD7 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in KCTD7 are known to be pathogenic (PMID: 22693283). This variant is present in population databases (rs367608044, gnomAD 0.003%). This variant has not been reported in the literature in individuals affected with KCTD7-related conditions. ClinVar contains an entry for this variant (Variation ID: 2164909). For these reasons, this variant has been classified as Pathogenic.

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