ClinVar Miner

Submissions for variant NM_002230.4(JUP):c.510G>A (p.Ser170=)

gnomAD frequency: 0.00041  dbSNP: rs140539043
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000232719 SCV000287313 benign Naxos disease; Arrhythmogenic right ventricular dysplasia 12 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000439668 SCV000513310 benign not specified 2015-05-29 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Ambry Genetics RCV000618402 SCV000734876 likely benign Cardiovascular phenotype 2016-01-12 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.
Fulgent Genetics, Fulgent Genetics RCV000232719 SCV002802256 likely benign Naxos disease; Arrhythmogenic right ventricular dysplasia 12 2021-08-10 criteria provided, single submitter clinical testing

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