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Gene entry

NDUFA10

NADH:ubiquinone oxidoreductase subunit A10

Chromosome
2
Cytoband
2q37.3
Variants (rsID)
49

NDUFA10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q37.3). Its official name is “NADH:ubiquinone oxidoreductase subunit A10”. The reference table lists 49 variants (rsID) for this gene.

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Clinically classified variants

10 reference-table entries with clinical significance.

  • rs10804402Benignsingle nucleotide variant
  • rs13424612Benignsingle nucleotide variantLeigh syndrome|Mitochondrial complex I deficiency, nuclear type 1
  • rs2083411Benignsingle nucleotide variantLeigh syndrome|Mitochondrial complex I deficiency, nuclear type 1|Mitochondrial complex 1 deficiency, nuclear type 22
  • rs35715497Benignsingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
  • rs74614612Benignsingle nucleotide variantLeigh syndrome|Mitochondrial complex I deficiency, nuclear type 1
  • rs77216981Benignsingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
  • rs140776586Conflicting interpretationssingle nucleotide variantLeigh syndrome|Mitochondrial complex I deficiency, nuclear type 1
  • rs147876332Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
  • rs199648872Conflicting interpretationssingle nucleotide variantMitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
  • rs200387097Uncertain significancesingle nucleotide variant

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.