Haplogroup A | |
---|---|
Possible time of origin | 40,000 ± 10,000 YBP |
Possible place of origin | Asia |
Ancestor | N |
Descendants | A3, A4, A5, A7, A8 |
Defining mutations | 152, 235, 523-524d, 663, 1736, 4248, 4824, 8794, 16290, 16319 |
In , Haplogroup A is a .
Haplogroup A is believed to have arisen in Asia some 30,000–50,000 years before present. Its ancestral haplogroup was Haplogroup N.
Its highest frequencies are among Indigenous peoples of the Americas, its largest overall population is in East Asia, and its greatest variety (which suggests its origin point) is in East Asia. Thus, it might have originated in and spread from the Far East.
Its subgroup A2 (actually a subclade of A4, which is widespread in Asia) is found in Chukotko–Kamchatka and is also one of five mtDNA haplogroups found in the indigenous peoples of the Americas, the others being B, C, D, and X.
Haplogroup A2 is the most common haplogroup among the Inuit, Na-Dene, and many Amerind ethnic groups of North and Central America. Lineages belonging to haplogroup A2 also comprise the majority of the mtDNA pool of the Inuit and their neighbors, the Chukchis, in northeasternmost Siberia.
Other branches of haplogroup A are less frequent but widespread among other populations of Asia. In particular, haplogroup A4(xA2) is ubiquitous in populations from Siberia in the north to Iran and Vietnam in the south. Haplogroup A5, on the other hand, is rather limited to populations from Korea and Japan southward, though it has been detected as singletons in a pair of large samples of Khamnigans (1/99 = 1.0%) and Buryats (1/295 = 0.3%) from the Buryat Republic.