ClinVar Miner

Submissions for variant NM_006904.6(PRKDC):c.4059G>A (p.Pro1353=) (rs762998738)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000652360 SCV000774230 uncertain significance Immunodeficiency 26 with or without neurologic abnormalities 2017-12-08 criteria provided, single submitter clinical testing This sequence change affects codon 1353 of the PRKDC mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the PRKDC protein. This variant is present in population databases (rs762998738, ExAC 0.04%). This variant has not been reported in the literature in individuals with PRKDC-related disease. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. 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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