ClinVar Miner

Submissions for variant NM_001130987.2(DYSF):c.3333_3335del (p.Trp1112del)

dbSNP: rs1553361884
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000671002 SCV000795937 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2B 2017-11-29 criteria provided, single submitter clinical testing
Invitae RCV003574800 SCV004334213 pathogenic Qualitative or quantitative defects of dysferlin 2023-10-27 criteria provided, single submitter clinical testing This variant, c.3279_3281del, results in the deletion of 1 amino acid(s) of the DYSF protein (p.Trp1094del), but otherwise preserves the integrity of the reading frame. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with DYSF-related conditions. ClinVar contains an entry for this variant (Variation ID: 555223). This variant disrupts a region of the DYSF protein in which other variant(s) (p.Trp1094Arg) have been determined to be pathogenic (PMID: 31268554, 33250842). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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