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Gene entry

COX10

cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10

Chromosome
17
Cytoband
17p12
Variants (rsID)
36

COX10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p12). Its official name is “cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10”. The reference table lists 36 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs11078234Benignsingle nucleotide variantCytochrome-c oxidase deficiency disease|Leigh syndrome
  • rs2159132Benignsingle nucleotide variantLeigh syndrome|Cytochrome-c oxidase deficiency disease
  • rs77877576Benignsingle nucleotide variantLeigh syndrome|Cytochrome-c oxidase deficiency disease
  • rs113058506Conflicting interpretationssingle nucleotide variantLeigh syndrome|Cytochrome-c oxidase deficiency disease
  • rs114521946Conflicting interpretationssingle nucleotide variantLeigh syndrome|Cytochrome-c oxidase deficiency disease
  • rs146175179Conflicting interpretationssingle nucleotide variantCytochrome-c oxidase deficiency disease|Leigh syndrome
  • rs62052075Conflicting interpretationssingle nucleotide variantLeigh syndrome|Cytochrome-c oxidase deficiency disease

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.