List of variants in gene MT-CO1 reported by Molecular Biology Laboratory, University of Basrah

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CO1):m.5954del	rs1569484042
NC_012920.1(MT-CO1):m.6608del	rs1569484091
NC_012920.1(MT-CO1):m.6674del	rs1569484096
NC_012920.1(MT-CO1):m.6698del	rs1569484100
NC_012920.1(MT-CO1):m.6750del	rs1569484108
NC_012920.1(MT-CO1):m.6817del	rs1569484115
NC_012920.1(MT-CO1):m.6860del	rs1569484116
NC_012920.1(MT-CO1):m.6902del	rs1569484122
NC_012920.1(MT-CO1):m.6927del	rs1569484124
NC_012920.1(MT-CO1):m.6936del	rs1569484125
NC_012920.1(MT-CO1):m.6941del	rs1569484126
NC_012920.1:m.6688_6689insACC	rs1569484098
NC_012920.1:m.6717_6718insGGG	rs1569484104
NC_012920.1:m.6743_6744insTGG	rs1569484107
NC_012920.1:m.6809_6810insAAG	rs1569484114
NC_012920.1:m.6887_6888insGGG	rs1569484120
NC_012920.1:m.6906_6907insCCT	rs1569484123

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.