ClinVar Miner

Submissions for variant NM_032776.3(JMJD1C):c.2300G>C (p.Gly767Ala)

gnomAD frequency: 0.00001  dbSNP: rs746786140
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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 RCV000707220 SCV000836308 uncertain significance Early myoclonic encephalopathy 2021-03-05 criteria provided, single submitter clinical testing 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with JMJD1C-related disease. This variant is present in population databases (rs746786140, ExAC 0.009%). This sequence change replaces glycine with alanine at codon 767 of the JMJD1C protein (p.Gly767Ala). The glycine residue is moderately conserved and there is a small physicochemical difference between glycine and alanine.

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