ClinVar Miner

Submissions for variant NM_001199107.1(TBC1D24):c.1427C>A (p.Ala476Asp) (rs202216463)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000718636 SCV000849500 benign Seizures 2017-02-01 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: General population or sub-population frequency is too high to be a pathogenic mutation based on disease/syndrome prevalence and penetrance
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000514560 SCV000611010 likely benign not provided 2017-06-12 criteria provided, single submitter clinical testing
GeneDx RCV000441062 SCV000514858 likely benign not specified 2017-09-01 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.
Invitae RCV000457294 SCV000560539 benign Epileptic encephalopathy, early infantile, 1; Deafness, autosomal dominant 65; Caused by mutation in the TBC1 domain family, member 24 2017-02-14 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000441062 SCV000711548 benign not specified 2014-11-24 criteria provided, single submitter clinical testing Ala476Asp in exon 7 of TBC1D24: This variant is not expected to have clinical significance because it has been identified in 0.9% (38/4142) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http://evs.gs.washington.edu/EVS; dbSNP rs202216463).

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