Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Clin |
RCV001090167 | SCV005088554 | uncertain significance | Mitochondrial disease | 2024-04-23 | reviewed by expert panel | curation | The m.15958A>T variant in MT-TP has been reported in one individual from one family to date (PMID: 27816331), in a boy with myopathy and failure to thrive. Muscle biopsy showed ragged red fibers, COX-deficient fibers, mitochondrial proliferation, complex I deficiency, and complex IV deficiency. The variant was present at 94% heteroplasmy in muscle, 78% in urine, 48% in skin fibroblasts, 9% in blood, and was undetectable in buccal sample. The variant was undetectable in urine, blood, and buccal sample from his mother (PM6_supporting, PMID: 27816331). The computational predictor MitoTIP suggests this variant is pathogenic (93.8 percentile) and HmtVAR predicts it to be pathogenic score of 0.4 (PP3). This variant is absent in the GenBank dataset, Helix dataset, and gnomAD v3.1.2 (PM2_supporting). Single fiber testing showed higher levels of the variant in COX negative fibers (96.10% ± 1.66) than in COX positive fibers (68.78% ± 18.11), p=0.0002 (PS3_supporting, PMID: 32419253). In summary, this variant meets criteria to be classified as uncertain significance for primary mitochondrial disease inherited in a mitochondrial manner. This classification was approved by the NICHD/NINDS U24 ClinGen Mitochondrial Disease Variant Curation Expert Panel on April 23, 2024. Mitochondrial DNA-specific ACMG/AMP criteria applied (PMID: 32906214): PS3_supporting, PM6_supporting, PM2_supporting, PP3. |
Service de Génétique Médicale, |
RCV001090167 | SCV001244369 | pathogenic | Mitochondrial disease | 2019-10-01 | no assertion criteria provided | in vitro | Exercise intolerance, myalgia, amyotrophy and mild weakness in the lower limbs, intermittent unilateral ptosis, dysarthria, failure to thrive |