Sample Details for Hap5018333

ID

Hg ID: Hap5018333, GenBank ID: JN415471.1

Haplogroup

Phylotree BLD 16: H26a, Phylotree BLD 17: , YFull: -

Publication

Published in: Achilli et al., 2012 | Achilli, A., Iommarini, L., Olivieri, A., Pala, M., Kashani, B.H., Reynier, P., La Morgia, C., Valentino, M.L., Liguori, R., Pizza, F. and Barboni, P., (2012). Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber’s Hereditary Optic Neuropathy. PLoS ONE, 7(8), e42242.

Sample source link: http://www.ncbi.nlm.nih.gov/nuccore/JN415471.1

Origin: -

Publication Notes: 2_Tor526

Results Profile

RSRS Haplotype:

73, 146, 152, 195, 210, 247, 309.1CC, 315.1C, 523-524d, 769, 825T, 1018, 2706, 2758, 2885, 3594, 3700, 4104, 4312, 7028, 7146, 7256, 7521, 8468, 8655, 8701, 9540, 9545, 10398, 10664, 10688, 10810, 10873, 10915, 11152, 11719, 11914, 12705, 13105, 13276, 13506, 13650, 14766, 16129, 16187, 16189, 16223, 16230, 16278, 16311

rCRS Haplotype:

Coming soon…

FASTA Profile:


Phylotree Build 17 Analysis

Missing Variants: none

Additional Variants: H26a:210, 309.1CC, 315.1C, 523-524d, 3700


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

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