ClinVar Miner

Submissions for variant NM_005763.4(AASS):c.191G>A (p.Arg64Gln)

gnomAD frequency: 0.00001  dbSNP: rs369365675
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000442322 SCV000532461 uncertain significance not provided 2016-10-10 criteria provided, single submitter clinical testing The R64Q variant in the AASS gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. The R64Q variant was not observed with any significant frequency 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 R64Q 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. We interpret R64Q as a variant of uncertain significance.

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