ClinVar Miner

Submissions for variant NM_001077365.2(POMT1):c.891G>A (p.Leu297=) (rs76109289)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000081496 SCV000113427 benign not specified 2013-10-18 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000081496 SCV000152361 benign not specified 2013-05-10 criteria provided, single submitter clinical testing
GeneDx RCV000081496 SCV000196870 benign not specified 2014-07-31 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.
PreventionGenetics,PreventionGenetics RCV000081496 SCV000311764 likely benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000388392 SCV000477655 benign Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 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 benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
Invitae RCV001079487 SCV000649913 benign Limb-girdle muscular dystrophy-dystroglycanopathy, type C1; Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1; Walker-Warburg congenital muscular dystrophy 2020-11-26 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000712830 SCV000843365 benign not provided 2017-12-15 criteria provided, single submitter clinical testing

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