ClinVar Miner

Submissions for variant NM_004946.3(DOCK2):c.3967-3T>C

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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 RCV002671690 SCV002997890 uncertain significance DOCK2 deficiency 2022-02-05 criteria provided, single submitter clinical testing This variant is present in population databases (rs773407433, gnomAD 0.0009%). This sequence change falls in intron 39 of the DOCK2 gene. It does not directly change the encoded amino acid sequence of the DOCK2 protein. It affects a nucleotide within the consensus splice site. This variant has not been reported in the literature in individuals affected with DOCK2-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing.

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