See also
Y-DNA Q-M242 Subclades
Y-DNA Backbone Tree
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Footnotes
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| Haplogroup Q-M323 | |
|---|---|
| Possible place of origin | Eurasia |
| Ancestor | Q-M346 |
| Defining mutations | M323 |
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).
Q-M323 was discovered in the Yemeni Jewish population. [1] In the time since its discovery, it has not been detected in other populations. It could then be exclusive to this population.
Q-M323 is currently defined by the M323 SNP.
This is Thomas Krahn at the Genomic Research Center's Draft tree Proposed Tree for haplogroup Q-M323.
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Footnotes
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A haplotype is a group of alleles in an organism that are inherited together from a single parent, and a haplogroup is a group of similar haplotypes that share a common ancestor with a single-nucleotide polymorphism mutation. More specifically, a haplogroup is a combination of alleles at different chromosomal regions that are closely linked and that tend to be inherited together. As a haplogroup consists of similar haplotypes, it is usually possible to predict a haplogroup from haplotypes. Haplogroups pertain to a single line of descent. As such, membership of a haplogroup, by any individual, relies on a relatively small proportion of the genetic material possessed by that individual.
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.
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).
Haplogroup NO, also known as NO-M214 and NO1, is a human Y-chromosome DNA haplogroup. NO is the sole confirmed subclade of Haplogroup K2a1 (K-M2313), which is the sole subclade of Haplogroup K2a (K-M2308). NO is the dominant Y-DNA haplogroup in most parts of eastern and northern Eurasia, including East Asia, Siberia and northern Fennoscandia.
Haplogroup IJK is a human Y-chromosome DNA haplogroup. IJK is a primary branch of the macrohaplogroup HIJK. Its direct descendants are haplogroup IJ and haplogroup K.
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.
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-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).
HaplogroupGHIJK, defined by the SNPs M3658, F1329, PF2622, and YSC0001299, is a common Y-chromosome haplogroup. This macrohaplogroup and its subclades contain the vast majority of the world's existing male population.
Haplogroup HIJK, defined by the SNPs F929, M578, PF3494 and S6397, is a common Y-chromosome haplogroup. Like its parent macrohaplogroup GHIJK, Haplogroup HIJK and its subclades comprise the vast majority of the world's male population.
Haplogroup K2a is a human Y-chromosome DNA haplogroup. K2a is a primary subclade of haplogroup K2 (M526), which in turn is a primary descendant of haplogroup K (M9). Its sole primary descendant is haplogroup K-M2313.
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.
