ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.3018G>T (p.Val1006=) (rs41307518)

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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 RCV000039720 SCV000063409 benign not specified 2010-10-26 criteria provided, single submitter clinical testing Val1006Val in exon 23 of PCDH15: This variant is not expected to have clinical s ignificance because it does not alter an amino acid residue, is not located near a splice junction and is presnet in dbSNP (rs41307518 - 5 submissions).
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000039720 SCV000203208 benign not specified 2017-03-01 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000269711 SCV000363168 uncertain significance Nonsyndromic Hearing Loss, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000327217 SCV000363169 likely benign Usher syndrome type 1 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 likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease.
GeneDx RCV000840674 SCV000982603 likely benign not provided 2018-03-30 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 RCV000840674 SCV001034973 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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