ClinVar Miner

Submissions for variant NM_016013.4(NDUFAF1):c.558A>G (p.Ile186Met)

gnomAD frequency: 0.01822  dbSNP: rs34979001
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000127120 SCV000170674 benign not specified 2014-05-28 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.
Invitae RCV000676310 SCV001113256 benign not provided 2024-01-24 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001120993 SCV001279522 likely benign Mitochondrial complex I deficiency, nuclear type 1 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.
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003758692 SCV004562879 benign Mitochondrial complex 1 deficiency, nuclear type 11 2023-11-29 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676310 SCV000802068 benign not provided 2017-09-15 no assertion criteria provided clinical testing

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