ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.6289C>T (p.Arg2097Cys) (rs16868974)

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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 RCV000039606 SCV000063295 benign not specified 2012-05-14 criteria provided, single submitter clinical testing Arg2097Cys in exon 29 of GPR98: This variant is not expected to have clinical si gnificance because it is has been identified in 1.3% (89/6626) of European Ameri can chromosomes and 10.0% (305/3030) of African American chromosomes from a broa d population by the NHLBI Exome sequencing project ( /EVS/; dbSNP rs16868974).
GeneDx RCV000039606 SCV000168706 benign not specified 2013-05-02 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.
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000039606 SCV000338401 benign not specified 2015-12-16 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV001155312 SCV001316734 benign Usher syndrome, type 2C 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
Invitae RCV001509772 SCV001716643 benign not provided 2020-11-21 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000039606 SCV000193280 likely benign not specified no assertion criteria provided clinical testing

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