ClinVar Miner

Submissions for variant NM_004946.3(DOCK2):c.2789A>G (p.His930Arg)

gnomAD frequency: 0.00002  dbSNP: rs1209214064
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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 RCV001346999 SCV001541238 uncertain significance DOCK2 deficiency 2020-10-09 criteria provided, single submitter clinical testing This variant is not present in population databases (ExAC no frequency). 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. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with DOCK2-related conditions. This sequence change replaces histidine with arginine at codon 930 of the DOCK2 protein (p.His930Arg). The histidine residue is weakly conserved and there is a small physicochemical difference between histidine and arginine.

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