List of variants in gene MT-TI reported as benign for congenital myopathy

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TI):m.4277T>C	rs876661358
NC_012920.1(MT-TI):m.4295A>G	rs121434467
NC_012920.1(MT-TI):m.4310A>G	rs1556422841
NC_012920.1(MT-TI):m.4312C>T	rs193303033
NC_012920.1(MT-TI):m.4313T>C	rs1603219398
NC_012920.1(MT-TI):m.4314T>A	rs1603219401
NC_012920.1(MT-TI):m.4314T>C	rs1603219401
NC_012920.1(MT-TI):m.4316A>G	rs876661360
NC_012920.1(MT-TI):m.4317A>G	rs121434465
NC_012920.1(MT-TI):m.4317del	rs876661361

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.