Sample Details for Hap5016755

Hg ID: Hap5016755
GenBank ID: GQ404809.1
Haplogroup: T2b17a

Published in: Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNAPhe gene
Publication Notes: 2
Details:
Sample source link: http://www.ncbi.nlm.nih.gov/nuccore/GQ404809.1

RSRS Haplotype: 1-12d, 146, 152, 195, 247, 310, 497N, 616G, 709, 769, 825T, 930, 1018, 1683N, 1888, 2758, 2885, 3574N, 3594, 4104, 4216, 4312, 4688, 4917, 5147, 6171N, 7146, 7256, 7469N, 7521, 7891, 8468, 8655, 8697, 8701, 9540, 10398, 10456N, 10459N, 10460N, 10463, 10664, 10688, 10810, 10873, 10915, 11251, 11812, 11914, 12110N, 12705, 13027N, 13059N, 13105, 13130N, 13276, 13368, 13506, 13650, 13685N, 13692, 14233, 14905, 15265N, 15452A, 15607, 15928, 16126, 16129, 16187, 16189, 16223, 16230, 16260N, 16278, 16291, 16294N, 16295N, 16296A, 16297G, 16298N, 16300N, 16302N, 16304, 16311, 16558-16569d

Missing Variants: T2b17a:16294, 16296

Additional Variants: T2b17a:1-12d, 310, 497N, 616G, 1683N, 3574N, 6171N, 7469N, 10456N, 10459N, 10460N, 12110N, 13027N, 13059N, 13130N, 13685N, 15265N, 16260N, 16291, 16294N, 16295N, 16296A, 16297G, 16298N, 16300N, 16302N, 16558-16569d


Last Updated: 2016/06/29 10:51:00 PM