ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.9238G>A (p.Ala3080Thr) (rs369395479)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000223358 SCV000268857 benign not specified 2016-03-03 criteria provided, single submitter clinical testing c.9238G>A (p.Ala3080Thr) in exon 64 of CDH23: This variant is not expected to ha ve clinical significance because it has been identified in 1% (163/16512) of Sou th Asian chromosomes by the Exome Aggregation Consortium (ExAC, http://exac.broa dinstitute.org; dbSNP rs369395479).
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000223358 SCV000701664 benign not specified 2016-10-28 criteria provided, single submitter clinical testing
GeneDx RCV000223358 SCV000714453 likely benign not specified 2017-10-12 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000911027 SCV001056080 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV001103166 SCV001259887 uncertain significance Deafness, autosomal recessive 12 2017-07-20 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). Publications were found based on this search. However, the evidence from the literature, in combination with allele frequency data from public databases where available, was not sufficient to rule this variant in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Illumina Clinical Services Laboratory,Illumina RCV001103167 SCV001259888 benign Usher syndrome type 1D 2017-07-20 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases was too high to be consistent with this variant causing disease. Therefore, this variant is classified as benign.

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