ClinVar Miner

Submissions for variant NM_003647.3(DGKE):c.531T>G (p.Cys177Trp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV003338052 SCV004046930 uncertain significance Immunoglobulin-mediated membranoproliferative glomerulonephritis criteria provided, single submitter clinical testing The missense variant in c.531T>G (p.Cys177Trp) in DGKE gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Cys177Trp variant is novel (not in any individuals) in gnomAD Exomes and 1000 Genomes. The amino acid Cys at position 177 is changed to a Trp changing protein sequence and it might alter its composition and physico-chemical properties. The variant is predicted to be damaging by both SIFT and PolyPhen2. The residue is conserved across species. The amino acid change p.Cys177Trp in DGKE is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. For these reasons, this variant has been classified as Uncertain Significance.

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