ClinVar Miner

Submissions for variant NC_000010.10:g.(?_14974833)_(14981888_?)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 RCV004580460 SCV005065744 pathogenic Severe combined immunodeficiency due to DCLRE1C deficiency 2023-11-10 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exon(s) 4-9 of the DCLRE1C gene. This variant would be expected to be in-frame, preserving the integrity of the reading frame. This variant has not been reported in the literature in individuals affected with DCLRE1C-related conditions. This variant disrupts a region of the DCLRE1C protein in which other variant(s) (p.Thr167_Phe168delinsMetLeu) have been determined to be pathogenic (Invitae). 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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