ClinVar Miner

Submissions for variant NM_004415.4(DSP):c.6527T>G (p.Val2176Gly) (rs1257672827)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000497727 SCV000590296 uncertain significance not provided 2017-06-07 criteria provided, single submitter clinical testing The V2176G variant of uncertain significance in the DSP gene has not been published as pathogenic or been reported as benign to our knowledge. This variant was not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server), indicating it is not a common benign variant. However, the V2176G variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties and this substitution occurs at a position that is not conserved across species. Finally, two of three in silico analysis algorithms predict this variant likely does not alter the protein structure/function. Nonetheless, based on the currently available information, it is unclear whether this variant is pathogenic or rare benign.

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