ClinVar Miner

Submissions for variant NM_013339.4(ALG6):c.1398A>T (p.Leu466=)

gnomAD frequency: 0.00167  dbSNP: rs140158304
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000424214 SCV000521842 likely benign not specified 2017-02-28 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.
Genetic Services Laboratory, University of Chicago RCV000424214 SCV000593107 likely benign not specified 2016-08-05 criteria provided, single submitter clinical testing
Invitae RCV000874946 SCV001017196 benign ALG6-congenital disorder of glycosylation 1C 2024-01-28 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000874946 SCV001253772 uncertain significance ALG6-congenital disorder of glycosylation 1C 2018-01-12 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, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
Natera, Inc. RCV000874946 SCV002092728 benign ALG6-congenital disorder of glycosylation 1C 2019-12-10 no assertion criteria provided clinical testing

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