ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.2440G>A (p.Glu814Lys)

gnomAD frequency: 0.00001  dbSNP: rs529566924
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000629493 SCV000750438 benign Primary ciliary dyskinesia 2023-12-25 criteria provided, single submitter clinical testing
Ambry Genetics RCV000629493 SCV002737952 uncertain significance Primary ciliary dyskinesia 2015-08-25 criteria provided, single submitter clinical testing The p.E814K variant (also known as c.2440G>A), located in coding exon 14 of the DNAH11 gene, results from a G to A substitution at nucleotide position 2440. The glutamic acid at codon 814 is replaced by lysine, an amino acid with similar properties. This variant was not reported in population based cohorts in the following databases: Database of Single Nucleotide Polymorphisms (dbSNP), NHLBI Exome Sequencing Project (ESP), and 1000 Genomes Project. In the ESP, this variant was not observed in 6309 samples (12618 alleles) with coverage at this position. This amino acid position is poorly conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this variant remains unclear.

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