ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.11809_11810dup (p.Thr3938fs)

dbSNP: rs1371736348
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001784018 SCV002024790 likely pathogenic Cohen syndrome 2021-06-24 criteria provided, single submitter clinical testing
Invitae RCV001784018 SCV003034430 pathogenic Cohen syndrome 2023-12-12 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Thr3963Argfs*51) in the VPS13B gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 60 amino acid(s) of the VPS13B protein. This variant is present in population databases (no rsID available, gnomAD 0.007%). This variant has not been reported in the literature in individuals affected with VPS13B-related conditions. ClinVar contains an entry for this variant (Variation ID: 1325343). This variant disrupts a region of the VPS13B protein in which other variant(s) (p.Pro3969Leufs*41) have been determined to be pathogenic (Invitae). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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