ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.8821G>A (p.Asp2941Asn)

dbSNP: rs776368544
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001374227 SCV001571025 likely benign Primary ciliary dyskinesia 2023-12-06 criteria provided, single submitter clinical testing
Ambry Genetics RCV001374227 SCV002683896 uncertain significance Primary ciliary dyskinesia 2014-09-14 criteria provided, single submitter clinical testing The p.D2948N variant (also known as c.8842G>A), located in coding exon 54 of the DNAH11 gene, results from a G to A substitution at nucleotide position 8842. The aspartic acid at codon 2948 is replaced by asparagine, an amino acid with highly 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 5960 samples (11920 alleles) with coverage at this position. This amino acid position is well conserved in available vertebrate species. In addition, this alteration is predicted to be probably damaging but tolerated by PolyPhen and SIFT in silico analyses, respectively. Since supporting evidence is limited at this time, the clinical significance of this variant remains unclear.

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