List of variants in gene MT-TG reported as uncertain significance for MELAS syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.10005A>T	rs1603222621
NC_012920.1(MT-CYB):m.10008A>G	rs1603222626
NC_012920.1(MT-CYB):m.10014G>A	rs1603222629
NC_012920.1(MT-CYB):m.10015T>C	rs28374827
NC_012920.1(MT-CYB):m.10020T>C	rs1603222636
NC_012920.1(MT-CYB):m.10027T>C	rs1603222638
NC_012920.1(MT-CYB):m.10043del	rs1603222645
NC_012920.1(MT-CYB):m.10048A>G	rs878957961
NC_012920.1(MT-CYB):m.10055A>G	rs1603222653
NC_012920.1(MT-CYB):m.9993T>C	rs1603222613
NC_012920.1(MT-CYB):m.9996T>C	rs1556423755

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.