ClinVar Miner

Submissions for variant NM_005908.4(MANBA):c.693G>A (p.Trp231Ter) (rs763849774)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000780390 SCV000917603 pathogenic Beta-D-mannosidosis 2018-05-25 criteria provided, single submitter clinical testing Variant summary: MANBA c.693G>A (p.Trp231X) results in a premature termination codon, predicted to cause a truncation of the encoded protein or absence of the protein due to nonsense mediated decay, which are commonly known mechanisms for disease. The variant allele was found at a frequency of 2.3e-05 in 265406 control chromosomes. This frequency is lower than expected for a pathogenic variant in MANBA causing Beta-Mannosidosis (2.3e-05 vs 0.0011), allowing no conclusion about variant significance. c.693G>A has been reported in the literature in individuals affected with Beta-Mannosidosis. These data indicate that the variant may be associated with disease. At least one publication reports experimental evidence evaluating an impact on protein function. The most pronounced variant effect results in <10% of normal activity. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014. Based on the evidence outlined above, the variant was classified as pathogenic.

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