ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.11040C>T (p.Ser3680=)

gnomAD frequency: 0.00001  dbSNP: rs199748413
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000946372 SCV001092501 likely benign Cohen syndrome 2024-01-19 criteria provided, single submitter clinical testing
Ambry Genetics RCV002427377 SCV002741456 likely benign Inborn genetic diseases 2017-09-21 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
PreventionGenetics, part of Exact Sciences RCV003942997 SCV004759416 likely benign VPS13B-related disorder 2021-06-02 criteria provided, single submitter clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).
Natera, Inc. RCV000946372 SCV001454474 uncertain significance Cohen syndrome 2020-01-24 no assertion criteria provided clinical testing

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