Gene entry
MT-CO1
No public annotation
- Chromosome
- —
- Cytoband
- —
- Variants (rsID)
- 107
MT-CO1 is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 107 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs199476128Benignsingle nucleotide variantCytochrome-c oxidase deficiency disease|Leigh syndrome
- rs201395766Benignsingle nucleotide variant
- rs28358874Benignsingle nucleotide variant
- rs28461189Benignsingle nucleotide variantCytochrome c oxidase i deficiency|Leigh syndrome
- rs41413745Benignsingle nucleotide variant
- rs28358872Likely benignsingle nucleotide variant
- rs199476127Pathogenicsingle nucleotide variantMyelodysplastic syndrome with ring sideroblasts
- rs267606883Pathogenicsingle nucleotide variantCytochrome c oxidase i deficiency
- rs28679680Pathogenicsingle nucleotide variantCytochrome-c oxidase deficiency disease
- rs267606882Uncertain significancesingle nucleotide variantFamilial colorectal cancer|Leigh syndrome
Other listed variants
- rs1029272
- rs1029293
- rs2854136
- rs2856983
- rs3020561
- rs3020601
- rs3020602
- rs3021086
- rs3021088
- rs3902405
- rs11510098
- rs11510099
- rs28357980
- rs28357981
- rs28357982
- rs28357986
- rs28357987
- rs28415376
- rs28429662
- rs28439827
- rs28456039
- rs28464073
- rs28464094
- rs28494478
- rs28542511
- rs28552781
- rs28570593
- rs28571027
- rs28575273
- rs28631235
- rs28647453
- rs28709555
- rs41333444
- rs41419549
- rs41504646
- rs41524046
- rs56133209
- rs118203891
- rs118203894
- rs121434465
- rs121434467
- rs121434468
- rs121434469
- rs121434470
- rs121434471
- rs193303033
- rs199474671
- rs199474673
- rs199474674
- rs199476123
- rs199794187
- rs200009705
- rs200077222
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.