ClinVar Miner

List of variants in gene MT-TF reported as benign for Juvenile myopathy, encephalopathy, lactic acidosis AND stroke

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NC_012920.1(MT-CYB):m.592C>T rs1603218450
NC_012920.1(MT-CYB):m.593T>C rs879123694
NC_012920.1(MT-CYB):m.595dup rs1603218451
NC_012920.1(MT-CYB):m.596T>C rs1556422474
NC_012920.1(MT-CYB):m.597C>T rs1603218453
NC_012920.1(MT-CYB):m.606A>G rs200056066
NC_012920.1(MT-CYB):m.619T>C rs1603218462
NC_012920.1(MT-CYB):m.629T>C rs201031012
NC_012920.1(MT-CYB):m.630C>T rs1603218468
NC_012920.1(MT-CYB):m.633A>G rs1603218469
NC_012920.1(MT-CYB):m.634T>A rs1603218470
NC_012920.1(MT-CYB):m.634T>C rs1603218470
NC_012920.1(MT-CYB):m.635C>T rs1603218471
NC_012920.1(MT-CYB):m.644A>G rs1556422475
NC_012920.1(MT-CYB):m.647A>G rs1569483788

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.