ClinVar Miner

Submissions for variant NC_000016.10:g.(?_88646106)_(88647185_?)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 RCV001031626 SCV001194932 pathogenic Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative 2021-12-02 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exon(s) 3-5 of the CYBA gene. While this deletion is not anticipated to lead to nonsense mediated decay, it is expected to disrupt the C-terminus of the protein. A similar copy number variant has been observed in individual(s) with chronic granulomatous disease (PMID: 18422995). This variant disrupts a region of the CYBA protein in which other variant(s) (p.Arg90Trp) have been determined to be pathogenic (PMID: 10910929, 20167518; 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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