See also
Y-DNA Q-M242 subclades
Y-DNA backbone tree
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Footnotes
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| Haplogroup Q-Z780 | |
|---|---|
| Possible place of origin | Eurasia |
| Ancestor | Q-L54 |
| Descendants | Q-L191 and Q-L400 |
| Defining mutations | Z780 |
Haplogroup Q-Z780 is a subclade of the Y-DNA Haplogroup Q-L54. Q-Z780 is defined by the presence of the Z780 Single Nucleotide Polymorphism (SNP).
Q-Z780 has descendants across much of the pre-Columbian Americas. It is the second most common branch of Q-M242 in the Americas. The Anzick child who lived 12,600 years ago and was found in the state of Montana, has a Y-chromosome that was initially determined to Q-L54*(xM3) [1] but is now assigned, along with modern Native American sample, to a subclade of Q-Z780, Q-FGC47532, or to Q1b-M971. [2] [3]
Q-Z780 is currently defined by the Z780 SNP.
This is Thomas Krahn at the Genomic Research Center's Draft tree Proposed Tree for haplogroup Q-Z780.
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Footnotes
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Haplogroup K or K-M9 is a human Y-chromosome DNA haplogroup. A sublineage of haplogroup IJK, K-M9, and its descendant clades represent a geographically widespread and diverse haplogroup. The lineages have long been found among males on every continent except Antarctica.
Haplogroup Q or Q-M242 is a Y-chromosome DNA haplogroup. It has one primary subclade, Haplogroup Q1 (L232/S432), which includes numerous subclades that have been sampled and identified in males among modern populations.
Haplogroup Q-M3 (Y-DNA) is a Y-chromosome DNA haplogroup. Haplogroup Q-M3 is a subclade of Haplogroup Q-L54. Haplogroup Q-M3 was previously known as Haplogroup Q3; currently Q-M3 is Q1b1a1a below Q1b-M346.
Haplogroup R1, or R-M173, is a Y-chromosome DNA haplogroup. A primary subclade of Haplogroup R (R-M207), it is defined by the SNP M173. The other primary subclade of Haplogroup R is Haplogroup R2 (R-M479).
In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by mutations in the non-recombining portions of DNA from the male-specific Y chromosome. Many people within a haplogroup share similar numbers of short tandem repeats (STRs) and types of mutations called single-nucleotide polymorphisms (SNPs).
In human population genetics, Y-Chromosome haplogroups define the major lineages of direct paternal (male) lines back to a shared common ancestor in Africa. Men in the same haplogroup share a set of differences, or markers, on their Y-Chromosome, which distinguish them from men in other haplogroups. These UEPs, or markers used to define haplogroups, are SNP mutations. Y-Chromosome Haplogroups all form "family trees" or "phylogenies", with both branches or sub-clades diverging from a common haplogroup ancestor, and also with all haplogroups themselves linked into one family tree which traces back ultimately to the most recent shared male line ancestor of all men alive today, called in popular science Y Chromosome Adam.
The genetic history of Indigenous peoples of the Americas is divided into two distinct episodes: the initial peopling of the Americas during about 20,000 to 14,000 years ago, and European contact, after about 500 years ago. The former is the determinant factor for the number of genetic lineages, zygosity mutations and founding haplotypes present in today's Indigenous Amerindian populations.
Haplogroup Q-M346 is a subclade of Y-DNA Haplogroup Q. Haplogroup Q-M346 is defined by the presence of the M346 Single Nucleotide Polymorphism (SNP).
Haplogroup Q-L54 is a subclade of Y-DNA haplogroup Q-L53. Q1a3a-L54 is defined by the presence of the L54 Single Nucleotide Polymorphism (SNP).
Haplogroup Q-L275 or Haplogroup Q2 is a human Y-chromosome DNA haplogroup believed to have originated in Eurasia. Haplogroup Q-L275 is defined by the presence of the L275 single-nucleotide polymorphism (SNP). Haplogroup Q-L275 can be identified through genealogical DNA testing.
Haplogroup Q-NWT01 is a subclade of Y-DNA Haplogroup Q-MEH2. Haplogroup Q-NWT01 is defined by the presence of the NWT01 Single Nucleotide Polymorphism (SNP).
Haplogroup Q-P89.1 is a subclade of Y-DNA Haplogroup Q-MEH2. Haplogroup Q-P89.1 is defined by the presence of the P89.1 Single Nucleotide Polymorphism (SNP). In 2010, Q-P89.1 was reclassified as "private" and removed from the haplotree.
Haplogroup Q-M25, also known as Q1a1b is a subclade or branch of human Y-DNA haplogroup Q-F1096 (Q1a1), which is, in turn, a subclade of Q-MEH2 (Q1a). In human genetics, each Y-DNA haplogroup constitutes a biological paternal lineages back to a shared common male ancestor.
Haplogroup Q-M120, also known as Q1a1a1, is a Y-DNA haplogroup. It is the only primary branch of haplogroup Q1a1a (F746/NWT01). The lineage is most common amongst modern populations in north-east Eurasia.
Q-L53 is a subclade of haplogroup Q-M346. Q-L53 is defined by the presence of the L53 Single Nucleotide Polymorphism (SNP).
Haplogroup Q-M323 is a subclade of Y-DNA Haplogroup Q-M346. Haplogroup Q-M323 is defined by the presence of the M323 Single Nucleotide Polymorphism (SNP).
Haplogroup K2b (P331), also known as MPS is a human y-chromosome haplogroup that is thought to be less than 3,000 years younger than K, and less than 10,000 years younger than F, meaning it probably is around 50,000 years old, according to the age estimates of Tatiana Karafet et al. 2014.
Anzick-1 is a Paleo-Indian male infant whose remains were found in south central Montana, United States, in 1968, and date to 13,000–12,850 years BP. The child was found with more than 115 tools made of stone and antlers and dusted with red ocher, suggesting an honorary burial. Anzick-1 is the only human who has been discovered from the Clovis Complex, and is the first ancient Native American genome to be fully sequenced.
Haplogroup P1, also known as P-M45 and K2b2a, is a Y-chromosome DNA haplogroup in human genetics. Defined by the SNPs M45 and PF5962, P1 is a primary branch (subclade) of P.
Haplogroup Q-L804 (Y-DNA) is a Y-chromosome DNA haplogroup. Haplogroup Q-L804 is a subclade of Haplogroup Q-L54. Currently Q-L804 is Q1b1a1b below Q1b-M346.
