ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.3887G>T (p.Ser1296Ile)

dbSNP: rs779527264
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000865260 SCV001006197 likely benign Brugada syndrome 2024-01-04 criteria provided, single submitter clinical testing
Ambry Genetics RCV002352528 SCV002620580 likely benign Cardiovascular phenotype 2020-01-30 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 RCV004540187 SCV004777373 likely benign SCN10A-related disorder 2022-05-10 no assertion criteria provided 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).

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