Variant: rs207459997 

    present in Gene: ND6;CYTB
    present in Chromosome: MT
    Position on Chromosome: 15615
    Alleles of this Variant: G/A

rs207459997 in ND6;CYTB gene and MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT PMID 8988236 1996 Antimycin resistance and ubiquinol cytochrome c reductase instability associated with a human cytochrome b mutation.

PMID 8910895 1996 A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance.