ClinVar Miner

Submissions for variant NM_006904.7(PRKDC):c.2887A>G (p.Lys963Glu)

gnomAD frequency: 0.00001  dbSNP: rs764099792
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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 RCV003081486 SCV003461549 uncertain significance Severe combined immunodeficiency due to DNA-PKcs deficiency 2022-07-19 criteria provided, single submitter clinical testing This sequence change replaces lysine, which is basic and polar, with glutamic acid, which is acidic and polar, at codon 963 of the PRKDC protein (p.Lys963Glu). This variant is present in population databases (rs764099792, gnomAD 0.003%). This variant has not been reported in the literature in individuals affected with PRKDC-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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.

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