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One ancient individual carried the T2b subclade (1/9; 11%). [8] Additionally, haplogroup T has been observed among ancient Egyptian mummies excavated at the Abusir el-Meleq archaeological site in Middle Egypt, which date from the Pre-Ptolemaic/late New Kingdom (T1, T2), Ptolemaic (T1, T2), and Roman (undifferentiated T, T1) periods. [9]
The Y haplogroup of Richard III, last king of the House of York and last of the House of Plantagenet, was identified as Y-DNA G-P287, in contrast to the Y haplotypes of five of the putative modern relatives, descendants of Henry Somerset, 5th Duke of Beaufort, of whom four belong to haplogroup R1b-U152 (x L2, Z36, Z56, M160, M126 and Z192) and ...
The haplogroup is one of two primary branches of T (T-M184), the other subclade being T2 (T-PH110). T1 is the most common descendant of the T-M184 haplogroup, being the lineage of more than 95% of all T-M184 members in Africa and Eurasia (as well as countries to which those populations have migrated in the modern era, in the Americas and ...
In human genetics, a human mitochondrial DNA haplogroup is a haplogroup defined by differences in human mitochondrial DNA. Haplogroups are used to represent the major branch points on the mitochondrial phylogenetic tree.
This is a purported list of ancient humans remains, including mummies, that may have been DNA tested. Provided as evidence of the testing are links to the mitochondrial DNA sequences, and/or to the human haplogroups to which each case has been assigned.
As a primary branch of haplogroup LT (a.k.a. K1), the basal, undivergent haplogroup T* currently has the alternate phylogenetic name of K1b and is a sibling of haplogroup L* (a.k.a. K1a). (Before 2008, haplogroup T and its subclades were known as haplogroup K2. [5] The name K2 has since been reassigned to a primary subclade of haplogroup K.)
A haplotype is a group of alleles in an organism that are inherited together from a single parent, [1] [2] and a haplogroup (haploid from the Greek: ἁπλοῦς, haploûs, "onefold, simple" and English: group) is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. [3]
YCC shorthand nomenclature names Y-DNA haplogroups and their subclades with the first letter of the major Y-DNA haplogroup followed by a dash and the name of the defining terminal SNP. [6] Y-DNA haplogroup nomenclature is changing over time to accommodate the increasing number of SNPs being discovered and tested, and the resulting expansion of ...