ClinVar Miner

Submissions for variant NM_001005273.3(CHD3):c.2960A>C (p.Glu987Ala)

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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 RCV004764315 SCV005373594 uncertain significance Snijders Blok-Campeau syndrome 2023-06-02 criteria provided, single submitter clinical testing The missense variant c.2960A>C (p.Glu987Ala) in the CHD3 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. This variant is absent in the gnomAD Exomes. The amino acid Glu at position 987 is changed to a Ala changing protein sequence and it might alter its composition and physico-chemical properties. Multiple lines of computational evidence (Polyphen - Damaging, SIFT - Damaging and MutationTaster - Disease causing) predict a damaging effect on protein structure and function for this variant. The amino acid change p.Glu987Ala in CHD3 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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