ClinVar Miner

Submissions for variant NM_001130438.3(SPTAN1):c.6610C>T (p.Arg2204Trp) (rs1057524104)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000437135 SCV000534570 uncertain significance not provided 2016-12-20 criteria provided, single submitter clinical testing The R2204W variant in the SPTAN1 gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. The R2204W variant was not observed in approximately 5,900 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 R2204W 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 conserved across species. In silico analysis predicts this variant is probably damaging to the protein structure/function. We interpret R2204W as a variant of uncertain significance.

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