ClinVar Miner

Submissions for variant NM_015512.5(DNAH1):c.2300+5G>A

gnomAD frequency: 0.00001  dbSNP: rs781060120
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000655808 SCV000777739 uncertain significance Spermatogenic failure 18; Ciliary dyskinesia, primary, 37 2017-10-31 criteria provided, single submitter clinical testing 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. Nucleotide substitutions within the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site, but this prediction has not been confirmed by published transcriptional studies. This variant has not been reported in the literature in individuals with DNAH1-related disease. This variant is present in population databases (rs781060120, ExAC 0.009%). This sequence change falls in intron 13 of the DNAH1 gene. It does not directly change the encoded amino acid sequence of the DNAH1 protein, but it affects a nucleotide within the consensus splice site of the intron.

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