ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.3782del (p.Pro1261fs)

dbSNP: rs753645306
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000671779 SCV000796798 likely pathogenic Cohen syndrome 2017-12-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000671779 SCV002118635 pathogenic Cohen syndrome 2022-10-17 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 555869). This variant has not been reported in the literature in individuals affected with VPS13B-related conditions. This variant is present in population databases (rs753645306, gnomAD 0.01%). This sequence change creates a premature translational stop signal (p.Pro1261Leufs*9) in the VPS13B gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in VPS13B are known to be pathogenic (PMID: 15141358, 16648375, 20461111).

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