ClinVar Miner

Submissions for variant NM_014000.2(VCL):c.379G>A (p.Asp127Asn) (rs1554816666)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000522532 SCV000619461 uncertain significance not provided 2017-07-31 criteria provided, single submitter clinical testing A variant of uncertain significance has been identified in the VCL gene. The D127N variant has not been published as pathogenic or been reported as benign to our knowledge. This variant is also not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The D127N variant is a semi-conservative amino acid substitution, which may impact secondary protein structure as these residues differ in some properties. Additionally, this substitution occurs at a position that is conserved across species and in silico analysis predicts this variant is probably damaging to the protein structure/function. However, D127N lacks observation in a significant number of affected individuals, segregation studies, and functional evidence, all of which would further clarify its role in disease.

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