ClinVar Miner

Submissions for variant NM_012463.4(ATP6V0A2):c.2376G>A (p.Pro792=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001322817 SCV001513706 uncertain significance ALG9 congenital disorder of glycosylation 2020-06-12 criteria provided, single submitter clinical testing This sequence change affects codon 792 of the ATP6V0A2 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the ATP6V0A2 protein. This variant is present in population databases (rs571286312, ExAC 0.003%). This variant has not been reported in the literature in individuals with ATP6V0A2-related conditions. 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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