Variant: rs1556424691 

    present in Gene: CYTB;ND6;TRNT
    present in Chromosome: MT
    Position on Chromosome: 15923
    Alleles of this Variant: A/G

rs1556424691 in CYTB;ND6;TRNT gene and Abnormal color vision PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

rs1556424691 in CYTB;ND6;TRNT gene and Abnormality of the cerebral cortex PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

rs1556424691 in CYTB;ND6;TRNT gene and Cerebral cortical atrophy PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

rs1556424691 in CYTB;ND6;TRNT gene and Hyperreflexia in upper limbs PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

rs1556424691 in CYTB;ND6;TRNT gene and Increased CSF lactate PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

rs1556424691 in CYTB;ND6;TRNT gene and Memory impairment PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

rs1556424691 in CYTB;ND6;TRNT gene and Mental deterioration PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

rs1556424691 in CYTB;ND6;TRNT gene and Mitochondrial Diseases PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

rs1556424691 in CYTB;ND6;TRNT gene and Muscle Weakness PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

rs1556424691 in CYTB;ND6;TRNT gene and Secondary physiologic amenorrhea PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

rs1556424691 in CYTB;ND6;TRNT gene and Seizures PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

rs1556424691 in CYTB;ND6;TRNT gene and Seizures, Focal PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.