ClinVar Miner

Submissions for variant NC_000010.11:g.14935443_14954030del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001215031 SCV001386750 pathogenic Severe combined immunodeficiency due to DCLRE1C deficiency 2019-07-28 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exons 1-6 of the DCLRE1C gene, which includes the initiator codon. The 5' end of this event is unknown as it extends beyond the assayed region for this gene and therefore may encompass additional genes. The 3' boundary is likely confined to intron 6 of the DCLRE1C gene. This is expected to result in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with DCLRE1C-related conditions. Loss-of-function variants in DCLRE1C are known to be pathogenic (PMID: 21664875, 26123418). For these reasons, this variant has been classified as Pathogenic.

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