ClinVar Miner

Submissions for variant NM_001205293.3(CACNA1E):c.50G>A (p.Gly17Glu)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002288141 SCV002578724 uncertain significance not provided 2022-04-04 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV002288141 SCV003007527 benign not provided 2022-09-07 criteria provided, single submitter clinical testing
Ambry Genetics RCV003355846 SCV004054336 likely benign Inborn genetic diseases 2023-08-08 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.

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