ClinVar Miner

List of variants in gene COX10 reported as benign for Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_001303.3(COX10):c.*1076T>C rs1050216
NM_001303.3(COX10):c.*151_*152delTT rs200239586
NM_001303.3(COX10):c.*322T>C rs11078233
NM_001303.3(COX10):c.*371A>G rs11078234
NM_001303.3(COX10):c.*646C>A rs7214082
NM_001303.3(COX10):c.*757T>C rs1802618
NM_001303.3(COX10):c.*833_*834delCT rs397763766
NM_001303.3(COX10):c.-112G>A rs6502330
NM_001303.3(COX10):c.476G>A (p.Arg159Gln) rs2072279
NM_001303.3(COX10):c.504G>A (p.Leu168=) rs2159132

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.