ClinVar Miner

Submissions for variant NM_004370.6(COL12A1):c.5940AGT[1] (p.Val1982del)

dbSNP: rs1766274789
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001061284 SCV001226022 uncertain significance Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 2019-03-07 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with COL12A1-related conditions. This variant is not present in population databases (ExAC no frequency). This variant, c.5943_5945del, results in the deletion of 1 amino acid(s) of the COL12A1 protein (p.Val1982del), but otherwise preserves the integrity of the reading frame. Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the affected amino acid(s) is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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