ClinVar Miner

Submissions for variant NM_001130987.2(DYSF):c.3687del (p.Phe1229fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003230988 SCV003929327 likely pathogenic Autosomal recessive limb-girdle muscular dystrophy 2023-04-13 criteria provided, single submitter clinical testing Variant summary: DYSF c.3633delT (p.Phe1211LeufsX50) results in a premature termination codon, predicted to cause a truncation of the encoded protein or absence of the protein due to nonsense mediated decay, which are commonly known mechanisms for disease. Truncations downstream of this position have been classified as pathogenic by our laboratory. The variant was absent in 251298 control chromosomes (gnomAD). To our knowledge, no occurrence of c.3633delT in individuals affected with Limb-Girdle Muscular Dystrophy, Autosomal Recessive and no experimental evidence demonstrating its impact on protein function have been reported. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014. Based on the evidence outlined above, the variant was classified as likely pathogenic.

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