ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.12869G>A (p.Gly4290Glu)

dbSNP: rs1555412242
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000555198 SCV000651609 likely benign Charcot-Marie-Tooth disease axonal type 2O 2023-10-05 criteria provided, single submitter clinical testing
GeneDx RCV002245008 SCV002513548 uncertain significance not provided 2022-04-21 criteria provided, single submitter clinical testing Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 25512093, 26100331, 25609763)
Ambry Genetics RCV002384226 SCV002691515 uncertain significance Inborn genetic diseases 2020-09-28 criteria provided, single submitter clinical testing The p.G4290E variant (also known as c.12869G>A), located in coding exon 71 of the DYNC1H1 gene, results from a G to A substitution at nucleotide position 12869. The glycine at codon 4290 is replaced by glutamic acid, an amino acid with similar properties. This amino acid position is highly 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 alteration remains unclear.

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