ClinVar Miner

Submissions for variant NC_000008.11:g.(?_99096302)_(99136762_?)del

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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 RCV001032868 SCV001196175 pathogenic Cohen syndrome 2019-04-17 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with VPS13B-related conditions. This variant is an out-of-frame deletion of the genomic region encompassing exons 4-12 of the VPS13B gene. This is expected to create a premature translational stop signal and result in an absent or disrupted protein product. Loss-of-function variants in VPS13B are known to be pathogenic (PMID: 15141358, 16648375, 20461111). For these reasons, this variant has been classified as Pathogenic.

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