Variant: rs199474701

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?