ClinVar Miner

Submissions for variant NM_032776.3(JMJD1C):c.2298C>A (p.Ala766=)

dbSNP: rs569430257
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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 RCV001367054 SCV001563388 uncertain significance Early myoclonic encephalopathy 2020-10-03 criteria provided, single submitter clinical testing This variant is present in population databases (rs569430257, ExAC 0.02%). 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 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. This variant has not been reported in the literature in individuals with JMJD1C-related conditions. This sequence change affects codon 766 of the JMJD1C mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the JMJD1C protein.

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