ClinVar Miner

Submissions for variant NM_001367624.1(ZNF469):c.8762G>A (p.Cys2921Tyr) (rs1029645463)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000413415 SCV000491910 uncertain significance not specified 2016-11-18 criteria provided, single submitter clinical testing A variant of uncertain significance has been identified in the ZNF469 gene. The C2893Y variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. This variant was not observed in approximately 2,300 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project (average read depth 8.0). The C2893Y variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is not conserved across species. In silico analysis suggests this variant likely does not alter the protein structure/function.Therefore, based on the currently available information, it is unclear whether this variant is pathogenic or rare benign.

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