ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.12476A>C (p.His4159Pro)

gnomAD frequency: 0.00012  dbSNP: rs200805176
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000039516 SCV000063205 benign not specified 2016-06-07 criteria provided, single submitter clinical testing p.His4159Pro in exon 61 of GPR98: This variant is not expected to have clinical significance because it has been identified in 0.5% (76/16486) of South Asian ch romosomes by the Exome Aggregation Consortium (ExAC, http://exac.broadinstitute. org; dbSNP rs200805176).
Invitae RCV000888279 SCV001031907 likely benign not provided 2024-01-13 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001157416 SCV001318984 uncertain significance 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, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
PreventionGenetics, part of Exact Sciences RCV003904940 SCV004722853 likely benign ADGRV1-related condition 2019-10-11 criteria provided, single submitter clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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