ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.9607T>A (p.Ser3203Thr) (rs116480183)

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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 RCV000150768 SCV000198255 benign not specified 2012-04-30 criteria provided, single submitter clinical testing Ser3203Thr in Exon 44 of GPR98: This variant is not expected to have clinical si gnificance because it has been identified in 1.5% (42/2890) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http: //evs.gs.washington.edu/EVS; dbSNP rs116480183).
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000515025 SCV000610805 likely benign not provided 2017-02-22 criteria provided, single submitter clinical testing
GeneDx RCV000150768 SCV000718746 likely benign not specified 2017-12-26 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.
Athena Diagnostics Inc RCV000515025 SCV000840697 benign not provided 2018-08-10 criteria provided, single submitter clinical testing
Invitae RCV000515025 SCV001093018 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV001151754 SCV001312919 likely benign Usher syndrome, type 2C 2018-01-12 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 likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease.

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