ClinVar Miner

Submissions for variant NM_015512.5(DNAH1):c.7739G>T (p.Gly2580Val)

gnomAD frequency: 0.00001  dbSNP: rs1703856754
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001041674 SCV001205300 uncertain significance Spermatogenic failure 18; Ciliary dyskinesia, primary, 37 2019-04-18 criteria provided, single submitter clinical testing This sequence change replaces glycine with valine at codon 2580 of the DNAH1 protein (p.Gly2580Val). The glycine residue is highly conserved and there is a moderate physicochemical difference between glycine and valine. This variant is not present in population databases (ExAC no frequency). 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. 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: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with DNAH1-related conditions.

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