ClinVar Miner

Submissions for variant NC_000016.9:g.(?_2105383)_(2124410_?)del

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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 RCV003111434 SCV003794251 pathogenic Tuberous sclerosis 2 2022-07-14 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant disrupts a region of the TSC2 protein in which other variant(s) (p.Leu219Pro) have been determined to be pathogenic (PMID: 21309039, 32211034). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. This variant has not been reported in the literature in individuals affected with TSC2-related conditions. This variant is a gross deletion of the genomic region encompassing exon(s) 6-22 of the TSC2 gene. This variant would be expected to be in-frame, preserving the integrity of the reading frame.

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