ClinVar Miner

Submissions for variant NM_001369.3(DNAH5):c.2753AAG[1] (p.Glu919del)

dbSNP: rs762827509
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000696189 SCV000824740 uncertain significance Primary ciliary dyskinesia 2021-09-01 criteria provided, single submitter clinical testing This variant, c.2756_2758del, results in the deletion of 1 amino acid(s) of the DNAH5 protein (p.Glu919del), but otherwise preserves the integrity of the reading frame. This variant is present in population databases (rs762827509, ExAC 0.005%). This variant has not been reported in the literature in individuals affected with DNAH5-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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.
Natera, Inc. RCV000696189 SCV002081772 uncertain significance Primary ciliary dyskinesia 2019-10-28 no assertion criteria provided clinical testing

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