ClinVar Miner

Submissions for variant NM_001369.2(DNAH5):c.5807C>T (p.Thr1936Ile) (rs779609286)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000425418 SCV000536226 uncertain significance not provided 2017-01-23 criteria provided, single submitter clinical testing The T1936I variant in the DNAH5 gene has not been reported previously as a pathogenic variant, nor as a benign variant, 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 T1936I 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, and in silico analysis predicts this variant is probably damaging to the protein structure/function. We interpret T1936I as a variant of uncertain significance.

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