present in Gene: TRNP;ND6;CYTB
present in Chromosome: MT
Position on Chromosome: 15967
Alleles of this Variant: G/A
rs199474701 in
TRNP;ND6;CYTB gene and
MELAS Syndrome
PMID 19273760 2009 A new mitochondrial transfer RNAPro gene mutation associated with myoclonic epilepsy with ragged-red fibers and other neurological features.
PMID 19718780 2009 Pathogenic mitochondrial tRNA mutations--which mutations are inherited and why?