ClinVar Miner

Submissions for variant NM_015697.8(COQ2):c.196G>T (p.Val66Leu) (rs6818847)

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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000116807 SCV000167974 benign not specified 2011-07-01 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.
PreventionGenetics,PreventionGenetics RCV000116807 SCV000312582 benign not specified criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000116807 SCV000344571 benign not specified 2016-08-23 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000297119 SCV000451439 benign Coenzyme Q10 deficiency, primary 2016-06-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000676768 SCV000885251 benign not provided 2017-05-02 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000116807 SCV000150881 likely benign not specified no assertion criteria provided clinical testing Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed.
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000613316 SCV000734367 benign Coenzyme Q10 deficiency, primary 1 no assertion criteria provided clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000676768 SCV000802569 benign not provided 2016-02-11 no assertion criteria provided clinical testing

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