ClinVar Miner

Submissions for variant NC_000002.12:g.(?_237333450)_(237334889_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000539865 SCV000656966 uncertain significance Bethlem myopathy 1 2016-10-09 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exons 41-42 of the COL6A3 gene. This leads to an in-frame deletion, preserving the integrity of the reading frame. This variant has not been reported in the literature in an individual with a COL6A3-related disease. Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the deleted amino acids is currently unknown. In summary, the impact of this deletion on COL6A3 protein function has not been established. Therefore, it has been classified as a Variant of Unknown Significance.

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