Sample Details for Hap5016248

Hg ID: Hap5016248
GenBank ID: FJ198227.1
Haplogroup: M8a2

Published in: Mitochondrial DNA Haplogroups M7b1′2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G→A Mutation
Publication Notes: LHON family Le1031
Details:
Sample source link: http://www.ncbi.nlm.nih.gov/nuccore/FJ198227.1

RSRS Haplotype: 146, 152, 195, 247, 315.1C, 489, 769, 825T, 1018, 2758, 2835, 2885, 3594, 4104, 4312, 4715, 6179, 7146, 7196A, 7256, 7521, 8468, 8584, 8655, 8684, 10400, 10664, 10688, 10810, 10915, 11778, 11914, 12172, 13105, 13276, 13506, 13650, 14470, 14783, 15043, 15301, 15487T, 15530, 15734, 16129, 16184, 16187, 16189, 16230, 16278, 16298, 16311, 16319, 16519

Missing Variants: none

Additional Variants: M8a2:315.1C, 11778, 12172, 15530, 15734, 16519


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