Annotation Detail
Information
- Associated Genes
- MT-TK
- Associated Variants
-
m.8356T>C
m.8356T>C - Associated Disease
- Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
- Source Database
- ClinVar
- Description
- m.8356T>C AND Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
- ClinVar Allele ID
- 24619
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-05-04
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000850957
- ClinVar Disease
- Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
- Observed Origin Sample
- germline
Drugs