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Gene entry

MT-CYB

No public annotation

Chromosome
—
Cytoband
—
Variants (rsID)
248

MT-CYB is a gene identifier without a current public annotation, located with no chromosome location recorded. The reference table lists 248 variants (rsID) for this gene.

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Clinically classified variants

23 reference-table entries with clinical significance.

  • rs199795644Benignsingle nucleotide variantLeber optic atrophy|Leigh syndrome
  • rs199999794Benignsingle nucleotide variantLeigh syndrome
  • rs207459996Benignsingle nucleotide variantFamilial colorectal cancer
  • rs2853508Benignsingle nucleotide variantFamilial cancer of breast|Leigh syndrome|Mitochondrial disease
  • rs386829260Benignsingle nucleotide variantLeigh syndrome
  • rs41518645Benignsingle nucleotide variantLeber optic atrophy|Leigh syndrome
  • rs527236176Benignsingle nucleotide variantNeoplasm of ovary|Leigh syndrome
  • rs527236193Benignsingle nucleotide variantFamilial cancer of breast|Leigh syndrome
  • rs879182710Benignsingle nucleotide variantLeigh syndrome
  • rs193302989Likely benignsingle nucleotide variant
  • rs28357370Likely benignsingle nucleotide variant
  • rs41504845Likely benignsingle nucleotide variant
  • rs878853086Likely benignsingle nucleotide variant
  • rs207459997Likely pathogenicsingle nucleotide variantExercise intolerance|Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
  • rs527236174Likely pathogenicsingle nucleotide variantFamilial cancer of breast
  • rs527236194Likely pathogenicsingle nucleotide variantFamilial cancer of breast
  • rs527236206Likely pathogenicsingle nucleotide variantNeoplasm of ovary
  • rs207459998Pathogenicsingle nucleotide variantExercise intolerance|Mitochondrial myopathy with reversible cytochrome C oxidase deficiency|MT-CYB associated Exercise intolerance|MT-CYB associated Mitochondrial myopathy
  • rs207459999Pathogenicsingle nucleotide variantMitochondrial encephalomyopathy|Leigh syndrome
  • rs207460001Pathogenicsingle nucleotide variantExercise intolerance
  • rs207460002Pathogenicsingle nucleotide variantMultisystem disorder|Mitochondrial myopathy with reversible cytochrome C oxidase deficiency|Leber optic atrophy
  • rs207459995Uncertain significancesingle nucleotide variantFamilial colorectal cancer|Leigh syndrome
  • rs207460004Uncertain significancesingle nucleotide variantExercise intolerance, cardiomyopathy, and septooptic dysplasia|Leigh syndrome|Mitochondrial 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.