ClinVar Miner

Submissions for variant NM_174934.4(SCN4B):c.480C>T (p.Asn160=)

gnomAD frequency: 0.00083  dbSNP: rs72546675
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000434021 SCV000514531 benign not specified 2016-06-23 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.
Invitae RCV000541553 SCV000647073 benign Long QT syndrome 10 2024-01-26 criteria provided, single submitter clinical testing
Ambry Genetics RCV002338990 SCV002639603 likely benign Cardiovascular phenotype 2018-10-17 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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