Sample Details for Hap5019548

ID

Hg ID: Hap5019548, GenBank ID: JX462687.1

Haplogroup

Phylotree BLD 16: M5, Phylotree BLD 17: , YFull: M5*

Publication

Published in: Khan et al., 2013 | Khan, N.A., Govindaraj, P., Jyothi, V., Meena, A.K. and Thangaraj, K. (2013). Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy. Molecular vision, 19, 1282.

Sample source link: http://www.ncbi.nlm.nih.gov/nuccore/JX462687.1

Origin:

Publication Notes: P23

Results Profile

RSRS Haplotype:

146, 195, 247, 315.1C, 489, 494, 769, 825T, 1018, 1555, 1888, 2758, 2885, 3594, 4104, 4312, 6047, 7146, 7256, 7521, 8020, 8468, 8655, 10400, 10664, 10688, 10810, 10915, 11778, 11914, 13105, 13276, 13506, 13650, 14783, 15043, 15301, 16093, 16187, 16189, 16230, 16278, 16311

rCRS Haplotype:

Coming soon…

FASTA Profile:


Phylotree Build 17 Analysis

Missing Variants: M5:152

Additional Variants: M5:315.1C, 494, 1555, 6047, 8020, 11778, 16093


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

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