ClinVar Miner

Submissions for variant NM_001458.5(FLNC):c.6774G>A (p.Ser2258=)

gnomAD frequency: 0.00002  dbSNP: rs767691386
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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 RCV001500501 SCV001705291 likely benign Myofibrillar myopathy 5; Distal myopathy with posterior leg and anterior hand involvement; Hypertrophic cardiomyopathy 26; Dilated Cardiomyopathy, Dominant 2024-12-04 criteria provided, single submitter clinical testing
GeneDx RCV001581161 SCV001812965 likely benign not provided 2019-09-04 criteria provided, single submitter clinical testing
Ambry Genetics RCV003365417 SCV004054504 likely benign Cardiovascular phenotype 2023-07-15 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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