ClinVar Miner

Submissions for variant NM_139343.3(BIN1):c.1595C>T (p.Thr532Met)

gnomAD frequency: 0.03069  dbSNP: rs112318500
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000145338 SCV000315932 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000404410 SCV000416287 likely benign Myopathy, centronuclear, 2 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 RCV000145338 SCV000525314 benign not specified 2016-05-19 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 RCV000404410 SCV000634509 benign Myopathy, centronuclear, 2 2024-01-29 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000145338 SCV000192417 likely benign not specified no assertion criteria provided clinical testing

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