Sample Details for Hap5009394

ID

Hg ID: Hap5009394, GenBank ID: EU597580.1

Haplogroup

Phylotree BLD 16: B2, Phylotree BLD 17: , YFull: -

Publication

Published in: Hartmann et al., 2008 | Hartmann, A., Thieme, M., Nanduri, L.K., Stempfl, T., Moehle, C., Kivisild, T. and Oefner, P.J. (2008). Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes. Human mutation, 30(1), 115-122.

The human mitochondrial genome consists of a multicopy, circular dsDNA molecule of 16,569 base pairs. It encodes for 13 proteins, two ribosomal genes, and 22 tRNAs that are essential in the generation of cellular ATP by oxidative phosphorylation in eukaryotic cells. Germline mutations in mitochondrial DNA (mtDNA) are an important cause of maternally inherited diseases, while somatic mtDNA mutations may play important roles in aging and cancer.

Sample source link: http://www.ncbi.nlm.nih.gov/nuccore/EU597580.1

Origin: -

Publication Notes: HGDP00710

Results Profile

RSRS Haplotype:

146, 152, 195, 247, 309.1CC, 315.1C, 769, 825T, 827, 1018, 2758, 2885, 3547, 3594, 3760G, 4104, 4312, 4820, 4977, 5095, 6473, 7146, 7256, 7521, 7813, 8281-8289d, 8468, 8655, 8701, 9540, 9950, 10398, 10664, 10688, 10810, 10873, 10915, 11177, 11914, 12705, 13105, 13276, 13506, 13590, 13650, 15265, 15535, 16129, 16150, 16183C, 16187, 16217, 16223, 16230, 16278, 16311

rCRS Haplotype:

Coming soon…

FASTA Profile:


Phylotree Build 17 Analysis

Missing Variants: B2:499

Additional Variants: B2:309.1CC, 315.1C, 3760G, 5095, 7813, 15265, 16150, 16183C


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

you're currently offline