ClinVar Miner

Submissions for variant NC_000009.12:g.(?_286441)_(289601_?)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 RCV000553243 SCV000645680 likely pathogenic Combined immunodeficiency due to DOCK8 deficiency 2017-11-06 criteria provided, single submitter clinical testing This variant is an in-frame deletion of the genomic region encompassing exons 3-4 of the DOCK8 gene. It preserves the integrity of the reading frame. Deletions of exons 3-4 have not been reported in the literature in individuals with DOCK8-related disease. This variant has been observed on the opposite chromosome (in trans) from a pathogenic variant in an individual with symptoms consistent with hyper-IgE syndrome (Invitae). This finding is consistent with autosomal recessive inheritance, and suggests that this variant contributes to disease. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.

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