ClinVar Miner

Submissions for variant NM_001429.4(EP300):c.3649G>A (p.Asp1217Asn) (rs1085307911)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000489263 SCV000577651 likely pathogenic not provided 2015-08-10 criteria provided, single submitter clinical testing The D1217N variant in the EP300 gene has not been published as a pathogenic variant, nor has it been reported as a benign polymorphism to our knowledge. This variant was not observed in approximately 6500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The D1217N variant is a semi-conservative amino acid substitution, which may impact secondary protein structure as these residues differ in some properties. This substitution occurs at a position that is conserved across species. In silico analysis predicts this variant is probably damaging to the protein structure/function. The D1217N variant is a strong candidate for a disease-causing variant however, the possibility it may be a rare benign variant cannot be excluded.

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