ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.9563T>A (p.Val3188Glu)

dbSNP: rs761194521
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001341026 SCV001534865 uncertain significance Primary ciliary dyskinesia 2020-01-29 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with DNAH11-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces valine with glutamic acid at codon 3188 of the DNAH11 protein (p.Val3188Glu). The valine residue is moderately conserved and there is a moderate physicochemical difference between valine and glutamic acid. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C35"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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