List of variants in gene MT-ATP6 studied for Mitochondrial disease

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: 20

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ATP6):m.8803A>T	rs878853020
NC_012920.1(MT-ATP6):m.8839G>C	rs1556423547
NC_012920.1(MT-ATP6):m.8851T>C	rs199476136
NC_012920.1(MT-ATP6):m.8932C>T	rs878853013
NC_012920.1(MT-ATP6):m.8936T>A	rs1603221920
NC_012920.1(MT-ATP6):m.8993T>C	rs199476133
NC_012920.1(MT-ATP6):m.9026G>A	rs1603221987
NC_012920.1(MT-ATP6):m.9032T>C	rs1603221994
NC_012920.1(MT-ATP6):m.9035T>C	rs1603222000
NC_012920.1(MT-ATP6):m.9038T>C	rs1603222003
NC_012920.1(MT-ATP6):m.9055G>A	rs193303045
NC_012920.1(MT-ATP6):m.9091A>G	rs1057520079
NC_012920.1(MT-ATP6):m.9152T>C	rs878853096
NC_012920.1(MT-ATP6):m.9155A>G
NC_012920.1(MT-ATP6):m.9166T>C	rs1057516063
NC_012920.1(MT-ATP6):m.9176T>C	rs199476135
NC_012920.1(MT-ATP6):m.9176T>G	rs199476135
NC_012920.1(MT-ATP6):m.9185T>C	rs199476138
NC_012920.1(MT-ATP6):m.9191T>C	rs1556423632
NC_012920.1:m.8969G>A	rs794726857

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.