fbpx
Wikipedia

Haplogroup G-M201

Haplogroup G (M201) is a human Y-chromosome haplogroup. It is one of two branches of the parent haplogroup GHIJK, the other being HIJK.

Haplogroup G
Possible time of origin48,500 years before present[1]
Coalescence age25,200 years before present[2]
Possible place of originWest Asia
AncestorHaplogroup GHIJK
Descendantsprimary: G1, G2
Defining mutationsM201, PF2957, L116, L154, L204, L240, L269, L402, L520, L521, L522, L523, L605, L769, L770, L836, L837, M201, P257/U6, Page94/U17, U2, U3, U7, U12, U20, U21, U23, U33

G-M201 is most commonly found among various ethnic groups of the Caucasus, but is also widely distributed at low frequencies among ethnic groups throughout Europe, South Asia, Central Asia, and North Africa.

The most commonly occurring subclades are G1* (M285) and many subclades of G2 (G-P287), especially: G2a (P15), G2a1 (G-FGC7535, formerly G-L293), G2a2b2a (G-P303) formerly G2a3b1); G2a2b1 (G-M406) formerly G2a3a; G2a2b2a1 (G-L140) formerly G2a3b1a; G2a2b2a1a1b (G-L497) formerly G2a3b1a2; G2a2b2a1a1a1 (G-L13) formerly G2a3b1a1a; G2a2b2a1a1c1a (G-CTS5990 or G-Z1903) formerly G2a3b1a3; G2b (G-M3115) and; G2b1 (G-M377), formerly G2b.

Origins edit

Various estimated dates and locations have been proposed for the origin of G-M201, most of them in Western Asia.[3]

In 2012, a paper by Siiri Rootsi et al. suggested that: "We estimate that the geographic origin of haplogroup G plausibly locates somewhere nearby eastern Anatolia, Armenia or western Iran."[4]

Previously the National Geographic Society placed its origins in the Middle East 30,000 years ago and presumes that people carrying the haplogroup took part in the spread of the Neolithic.[5]

Two scholarly papers have also suggested an origin in the Middle East, while differing on the date. Semino et al. (2000) suggested 17,000 years ago.[6] Cinnioglu et al. (2004) suggested the mutation took place only 9,500 years ago.[7]

A more eastern origin has also been mentioned, believed by some to originate in an area of the Middle East close to the Himalayan foothills.[8]

Structure edit

G* (M201)

  • G1 (M285, M342)
    • G1a (P20.1, P20.2, P20.3)
      • G1a1 (L201, L202, L203)
    • G1b (L830, L831, L832, L834, L835)
  • G2 (P287)
    • G2a (P15, U5, L31/S149, L149)
      • G2a1 (L293^)
        • G2a1a (P16.1, P16.2)
          • G2a1a1 (P18.1, P18.2, P18.3)
      • G2a2 (L223^)
        • G2a2a (M286)
        • G2a2b (L91)
          • G2a2b1 (L166, L167)
      • G2a3 (L30/S126, L32/S148, L190/M485)
        • G2a3a (M406)
          • G2a3a1 (L14/Page57/S130/U16, L90/S133)
          • G2a3a2 (L645)
        • G2a3b (L141.1)
          • G2a3b1 (P303/S135)
            • G2a3b1a (L140)
              • G2a3b1a1 (U1)
                • G2a3b1a1a (L13/S131/U13, L78/M527)
                  • G2a3b1a1a1 (L1263^)
                • G2a3b1a1b (L1266^)
                  • G2a3b1a1b1 (L1264^, L1265^, L1268^)
              • G2a3b1a2 (L497, L353.1^,L353.2^)
                • G2a3b1a2a (Z725^)
                  • G2a3b1a2a1 (L43/S147)
                    • G2a3b1a2a1a (L42/S146)
              • G2a3b1a3 (Z1903^)
                • G2a3b1a3a (Z724^)
                  • G2a3b1a3a1 (L640)
              • G2a3b1a4 (L660, L662)
            • G2a3b1b (L694)
          • G2a3b2 (L177.1, L177.2, L177.3)
    • G2b (M377, L72, L183)
      • G2b1 (M283)

(Subclades here conform to the Y-DNA SNP definitions used by ISOGG In 2012, several categories found only in one man in research studies were removed from the ISOGG tree causing some renaming.)

Geographic distribution edit

Prehistoric presence edit

Ancient G-M201s with sequencing[self-published source?] Haplogroup G2a (G-P15) has been identified in Neolithic human remains in Europe dating between 5000 and 3000 BC. These Neolithic Europeans were descendants of Neolithic farmers from Anatolia, among some of the earliest peoples in the world to practice agriculture. G-M201 has also been found in Neolithic Anatolian sites such as Boncuklu dating back to 8300-7600 BCE, and Barcin dating back to 6419-6238 BCE.[9][10]

Furthermore, the majority of all the male skeletons from the European Neolithic period have so far yielded Y-DNA belonging to this haplogroup. The oldest skeletons confirmed by ancient DNA testing as carrying haplogroup G2a were five found in the Avellaner cave burial site, near Les Planes d'Hostoles, in Catalonia, Spain and were dated by radiocarbon dating to about 5000 BCE.[11]

A skeleton found at the Neolithic cemetery known as Derenburg Meerenstieg II, in Saxony-Anhalt Germany, apparently belonged to G2a3 (G-S126) or a subclade. It was found with burial artifacts belonging to the Linearbandkeramische Kultur ("Linear Band Ceramic Culture"; LBK). This skeleton could not be dated by radiocarbon dating, but other skeletons there were dated to between 5,100 and 6,100 years old. The most detailed SNP mutation identified was S126 (L30), which defines G2a3.[12]

G2a was found also in 20 out of 22 samples of ancient Y-DNA from Treilles, the type-site of a Late Neolithic group of farmers in the South of France, dated to about 5000 years ago.[13] The fourth site also from the same period is the Ötztal of the Alps where the mummified remains of Ötzi the Iceman were discovered. The Iceman belongs to haplogroup G2a2b [14] (earlier called G2a4).

Haplogroup G2a2b is a rare group today in Europe. The authors of the Spanish study indicated that the Avellaner men had rare marker values in testing of their short tandem repeat (STR) markers.

Modern presence edit

In Russia, Ukraine and Central Asia, members of various ethnic minorities and/or residents in particular localities possess G-M201 at its highest levels in the world – even though the average rate at the national level is about 1% or less. The Madjar and Argyn tribes (or clans) of Kazakhstan were found to possess the highest levels of G-M201 among any modern ethnic group. Amongst the Madjars, G1 was found at a rate of 87%. A separate study on the Argyns found that 71% of males belong to G1. In the Russian North Caucasus the Kabardinian and Ossetian populations are also notable for high rates of G-M201. Digora, North Ossetia has the highest known concentration of G in a single city, as 74% of the tested men were G.[15] Haplogroup G is found as far east as northern China in small percentages where G can reach more substantial percentages in minority groups such as the Uyghurs.

In Turkey, the South Caucasus and Iran, haplogroup G reaches the highest percentage of national populations. Among Turkish males 11% of the population is G.[7] In Iran, Haplogroup G reaches 13 to 15% of the population in various parts of the country. While it is found in percentages higher than 10% among the Bakhtiari, Talysh people, Gilaki, Mazandarani and Iranian Azeris, it is closer to 5% among the Iranian Arabs and in some large cities.[16] Among the samples in the YHRD database from the southern Caucasus countries, 29% of the samples from Abazinia, 31% from Georgia, 18% from Azerbaijan and 11% from Armenia appear to be G samples.

In Europe west of the Black Sea, Haplogroup G is found at about 5% of the population on average throughout most of the continent.[17] The concentration of G falls below this average in Scandinavia, the westernmost former Soviet republics and Poland, as well as in Iceland and the British Isles. There are seeming pockets of unusual concentrations within Europe. In Wales, a distinctive G2a3b1 type (DYS388=13 and DYS594=11) dominates there and pushes the G percentage of the population higher than in England.

In the Tirol (Tyrol) of western Austria, the percentage of G-M201 can reach 40% or more; perhaps the most famous example is the ancient remains of the so-called "Iceman", Ötzi. In the northern and highland areas of the island of Sardinia off western Italy, G percentages reach 11% of the population in one study[18] and reached 21% in the town of Tempio in another study. In the Greek island of Crete, approximately 7%[19] to 11%[20] of males belong to haplogroup G. In north-eastern Croatia, in the town of Osijek, G was found in 14% of the males.[21] The city is on the banks of the river Drava, which notably begins in the Tirol/Tyrol region of the Alps, another haplogroup G focus area in Europe. Farther north, 8% of ethnic Hungarian males and 5.1% of ethnic Bohemian (Czech) males have been found to belong to Haplogroup G.

In South Asia, some ethnic minorities possess haplogroup G at concentrations of approximately 18%[22] to 20%[23] of Kalash, approximately 16% of Brahui,[23] and approximately 11.5% of sampled Pashtun,[22] but in only about 3% of the general Pakistani population.[22] In a study of 936 Indians, haplogroup G made up less than 1% of the sample and was completely absent in the tested Northwestern Indian population.[24] About 6% of the samples from Sri Lanka and Malaysia were reported as haplogroup G, but none were found in the other coastal lands of the Indian Ocean or Pacific Ocean in Asia.[25] Haplogroup G-M201 is believed to have been relatively absent during the Indian Neolithic period; the frequencies of the G2a-P15 subclade for example were negligible in indigenous Indian populations.[26]

In the Middle East, haplogroup G accounts for about 3% of the population in almost all areas.[27][28] Among the Druze mostly residents of Israel 10% were found to be haplogroup G.[29]

Around 10% of Jewish males are Haplogroup G.[citation needed]

In Africa, haplogroup G is rarely found in sub-Saharan Africa or south of the horn of Africa among native populations. In Egypt, studies have provided information that pegs the G percentage there to be between 2% and 9%.[30][31][32] 3% of North African Berbers were found to be haplogroup G.[33] 2% of Arab Moroccans and 0.8% of Berber Moroccans were likewise found to be G.[34]

In the Americas, the percentage of haplogroup G corresponds to the numbers of persons from Old World countries who emigrated. It is not found among Native Americans except where intermarriage with non-native persons has occurred. It has been found in Mexican mestizos.

G1 (M285 or M342) edit

Almost all haplogroup G1 persons have the value of 12 at short tandem repeat (STR) marker DYS392 and all will have the M285 or M342 SNP mutation which characterizes this group. This value of 12 is uncommon in other G categories other than G1.

subclades of G1a, G1a1, G1b exist.

The highest reported concentration of G1 and its subclades in a single country is in Iran, with next most frequent concentrations in neighboring countries to the west.

There are distinctive Ashkenazi Jewish and Kazakh subclades based on STR marker value combinations.

G2 (P287) edit

Men who belong to this group but are negative for all G2 subclades represent a small number of haplogroup G men. P287 was identified at the University of Arizona and became widely known in late 2007. Its identification caused considerable renaming of G categories.

G2a (P15) edit

Haplogroup G men who belong to this group, but are negative for all G2a subclades, are uncommon in Europe but may represent a sizeable group in so far poorly tested areas east of Turkey. P15 was identified at the University of Arizona and became widely known by 2002. Its chromosome location listed as 21653414. G2a was found in medieval remains in a 7th- century CE high-status tomb in Ergolding, Bavaria, Germany, but G2a subclades were not tested.[35]

There are multiple SNPs which so far have the same coverage as P15. They are—with accompanying Y-chromosome locations—U5 (rs2178500), L149 (8486380) and L31 (also called S149) (rs35617575..12538148). Should any man with the P15 mutation test negative (ancestral) for any of these or vice versa, that finding would be the basis of a new G2a category.

G2a1 (FGC7535) edit

Haplogroup G2a1 (also known as G-FGC753 and previously as G-L293) and its subclades represent the majority of haplogroup G samples in some parts of the Caucasus Mountains area. They are found only in tiny numbers elsewhere. So far all G2a1 persons have a value of 10 at STR marker DYS392. G2a1a persons also typically have higher values for DYS385b, such as 16, 17 or 18, than seen in most G persons.

The North Ossetians in the mid northern Caucasus area of Russia belong overwhelmingly to the G2a1 subclade based on available samples. The South Ossetians and Svans generally south of North Ossetia have significant number of G2a1 persons, but population percentages have not yet been provided.

The presence of the SNP P18 mutation characterizes G2a1a's only subclade, G2a1a. The reliability of both P16 and P18 in identifying everyone in each of these categories has been questioned and individual components of the SNP have to be examined.

Ashkenazi Jewish G2a1a men with northeastern European ancestry form a distinct cluster based on STR marker values. Men from the Caucasus and men from eastern Europe also form distinctive STR clusters.

G2a2a (PF3147) edit

G-PF3147 (previously G-L223 and G-PF3146) is characterized by having the L223 mutation. L223 is found on the Y chromosome at rs810801 and 6405148 with a mutation from C to G. L223 was first identified in samples at 23andMe in 2009 but proved problematic as an individual test, the first successful results being reported at Family Tree DNA in late 2011 under its assigned L223 label. It was then learned that several subclades belong under L223, including:

G-L91 was identified in 2009. Its members include "Ötzi", [36] the so-called Iceman, who died at least 5,000 years BP in the European Alps. G-L91 would seem to encompass a significant proportion of men belonging to G. L91 is found so far in scattered parts of Europe and North Africa and in Armenia. Included within G-L91 are some men with double values for STR marker DYS19, but there are also G2a2 men with this finding who are not L91+. The double 19 value situation is not seen in the G2a1 and G2a3 subclades. The L91 mutation is found at 21327383 and rs35474563 on the Y-chromosome. The forward primer is GTATTGAACTTACAATTCACGTCCC, and the reverse is CTCTCCAAATCGGGTTTCCT. The mutation involves a change from C to T.[37] L223 is found on the Y chromosome at rs13304806.

The G-M286 subclade (M286+) is small compared with G-L91. Samples have been identified in England, Germany, Montenegro (Bosniak), Spain, Cyprus (Greek), Turkey, Armenia, Georgia, Lebanon, Syria and Kuwait. The British samples have inconsistent double values for STR marker DYS19 in many cases. M286 was first identified at Stanford University at chromosome position 21151187, and is a mutation from G to A.

The L293 SNP that characterizes a third subclade was identified in June 2010 at Family Tree DNA. It encompasses a small group of Hispanic men who also so far all have the odd value of 13,21 at the YCA marker. The mutation is found on the Y chromosome at 10595022 and is a change from G to C.

G2a2b (L30, PF3267, S126, U8) edit

G-L30 (also G-PF3267, G-S126 or G-U8; G2a2b, previously G2a3) Men who belong to this group but are negative for all its subclades represent a small number today. This haplogroup was found in a Neolithic skeleton from around 5000 BC, in the cemetery of Derenburg Meerenstieg II, Germany, which forms part of the Linear Pottery culture, known in German as Linearbandkeramik (LBK),[12] but was not tested for G2a3 subclades.

G2a2b1 (M406) edit

G-M406* (G2a2b1*; previously G2a3a*) and its subclades seem most commonly found in Turkey and the coastal areas of the eastern Mediterranean where it can constitute up to 5% of all makes and 50% of haplogroup G samples. G2a2b1 is more common in southern Europe than northern Europe. In Europe—except in Italy – G2a2b1 constitutes less than 20% of G samples. G2a2b1 so far has seldom surfaced in northern Africa or southern Asia, but represents a small percentage of the G population in the Caucasus Mountains region and in Iran.

A relatively high percentage of G2a2b1 persons have a value of 21 at STR marker DYS390. The DYS391 marker has mostly a value of 10, but sometimes 11, in G2a2b1 persons, and DYS392 is almost always 11. If a sample meets the criteria indicated for these three markers, it is likely the sample is G2a2b1.

G2a2b2 (CTS2488) edit

G-CTS2488 or G2a2b2 (also known as G-L141.1; previously G-141 and G2a3b) was identified only in mid-2009 at Family Tree DNA. Almost all L141 men belong to L141 subclades. Samples from persons with British Isles, Sicilian and Turkish ancestry have been identified. L141 persons who do not belong to any L141 subclade so far have the value of 11 at STR marker DYS490 — a finding rare in other G categories. The L141 mutation is found on the Y chromosome at 2948607. The L141 mutation involves an insertion.[38]

G2a2b2a (G-P303) edit

G-P303*, also known as G2a2b2a* (previously G2a3b1*), and its subclades are now concentrated in southern Russia and the Caucasus, as well as, at lower levels, other parts of Europe and South West Asia, especially an area including Turkey, Iran and the Middle East where G2a2b2a may have originated. G2a2b2a is also found in India.

A majority of members of G-P303 belong to one of its subclades, rather than to G-P303*

The largest G-P303* subclade based on available samples is one in which almost all persons have the value of 13 at STR marker DYS388. The SNP L497 encompasses these men, but most G-L497 men belong to its subclade G-Z725, also known as G-DYS388=13. There are additional subclades of DYS388=13 men characterized by the presence of specific SNPs or uncommon STR marker oddities. Members of this group have been found in Europe and the Middle East.[4]

The next largest subclade of G-P303 is characterized by the presence of the U1 mutation. But a high percentage of U1 men belong to its two subclades, G-L13/S13 and Z1266 (G2a3b1a1b). The G-L13 subclade is most common in north central Europe, and G-Z1266 is most common in the western Caucasus Mountains.

The final major subclade is characterized by presence of the SNP Z1903 and by a value of 9 at marker DYS568. A high percentage of G-Z1903 men belong to its subclade, G-Z724.

The highest percentage of G-P303 persons in a discrete population so far described is on the island of Ibiza off the eastern Spanish coast. This group has been linked with the Crypto-Jewish population which fled to the island during the time of the Spanish Inquisition, of which a significant portion are identifiable as G-Z725 (DYS388=13).[39]

G2a2b2b (PF3359) edit

G-PF3359 (or G2a2b2b; previously G2a3b2) was known prior to 2013 as G-L177. The SNP L177 (a.k.a. L1771.1/ L177_1, L1771.2/L177_2, L177.3/L177_3) was withdrawn as an identifier by ISOGG in 2013, after it was "found to be an unreliable palindromic snp".[3][40]

Ancient DNA identified as G-PF3359 has been found at archaeological sites in: Hungary (the subclade G-F872*), dated at 7,500 years before present (BP); Hungary (subclade G-F1193*) 7,150 BP, and; Spain (G-PF3359*) 4,700 BP.[3]

The members of G-PF3359 are probably smaller in number than men included in G-P303, but only a small amount of testing has occurred for the relevant mutations. So far the men positive for this have had Irish, English, Dutch, Lebanese and/or Turkish (Armenian surname) ancestry. Several G-PF3359 subclades, based on shared STR markers, probably exist.

The number of STR marker values separating men in this group suggest G-PF3359 is a relatively old group despite the small number of men involved.[41][self-published source?] The mutations involved may be complicated and difficult to interpret.

G2b1 (M377) edit

G-M377, now also known as G2b1, has previously been designated G2b and G2c. A clade of closely related Ashkenazi Jews represent virtually all G2b persons, with just three other G2b haplotypes having been reported so far: one Turk from Kars in northeast Turkey near Armenia, one Pashtun, and one Burusho in Pakistan.

The extreme rarity of G-M377 in northern Pakistan could indicate that G2b in this area originates outside the region and was brought there in the historic period, perhaps from further west (Pakistan was part of both the Achaemenid Persian Empire, conquered by Alexander the Great, and then formed a part of the Greco-Bactrian Kingdom). These two reported Pakistani G-M377 haplotypes are quite divergent from the Ashkenazi Jewish clade, and therefore do not at all indicate a recent common origin. The Turkish G-M377 is somewhat closer, but not identical. It remains to be seen if testing will reveal G-M377 haplotypes in other populations — this is some indication that G-M377 occurs at low levels in the Near East.

All G-M377 men tested so far also have a rare null value for the DYS425 marker, (a missing "T" allele of the DYS371 palindromic STR), the result of a RecLOH event, a finding not yet seen among most other G haplotypes. Among Jews in Israel drawn from many areas of the world, G-M377 constituted 3.7% in one study.[42]

Haplogroup G-M377 has been found at a frequency of 60% out of a sample of five Pashtuns in the Wardak region of Afghanistan. This is likely due to a local founder effect.[43]

Defining SNPs edit

The International Society of Genetic Genealogy (ISOGG) maintains the most up-to-date consensus version of haplogroup categories.[44] These classifications are based on shared SNP mutations. The discovery of new SNPs can result in assignment of new names to haplogroup categories. There were only a few G categories until 2008 when major revisions to categories were made. Even more G SNPs were identified in 2009 to 2012 leading to more changes. Until 2008, new G SNPs were reported from labs at the University of Arizona (P designations), Stanford University (M designations) or the University of Central Florida (U designations). Beginning in 2008, additional G SNPs were identified at Family Tree DNA (L designations) and Ethnoancestry (S designations). These latter labs also made use of raw data results reported by individuals tested for about 2,000 SNPs at 23andMe to provide new L or S-designated SNP tests. In 2009-10, Family Tree DNA's Walk through the Y Project, sequencing certain Y-chromosome segments, provided a number of new G SNPs with the L designation. In 2012, SNPs with the Z designation as first identified by citizen researchers from 1000 Genomes Project data began to appear.

Because SNPs provide the most reliable method of categorization, each is allowed to represent an official G category. Categories have alternating letters and numbers. But unusual values or unusual value combinations found at short tandem repeat markers (STRs) can also provide the basis of additional taxonomisation. The identification of a new SNP can necessitate renaming of one or more categories.

The M201 SNP mutation that characterizes haplogroup G was identified at Stanford University and was first reported in 2001.[45] The technical specifications of M201 are given as: refSNPid is rs2032636.....Y chromosome location of 13536923....forward primer is tatgcatttgttgagtatatgtc.....reverse primer is gttctgaatgaaagttcaaacg.....the mutation involves a change from G to T.

A number of SNPs have been identified with seemingly the same coverage in the population as M201. Because M201 was identified first, it is the standard SNP test used when testing for G persons. In order to determine if one of these alternative SNPs represents a subclade of M201, the alternative SNPs must be tested in G persons who are negative for the known subclades of G. There are only a tiny number of persons in such a category, and only a tiny number of persons have been tested for G equivalent SNPs other than M201.

The following SNPs are so far identified as M201 equivalents: L116, L154, L269, L294, L240, P257, L402, L520, L521, L522, L523, L605, Page 94, U2, U3, U6, U7, U12, U17, U20, U21, U23 and U33. P257 was first reported in 2008.[46] L240 was identified in 2009.[47] The "U" SNPs were identified in 2006 but not published until 2009.[48]

In addition, there are multiple other SNPs thought to have the same coverage as M201. These are found at: rs9786910, rs9786537, rs2713254, rs35567891 and rs34621155 on the Y chromosome. No labs have yet assigned them shorthand names.

Prominent members of G edit

  • The man known as "Ötzi" – whose remains, dating from the 4th millennium BCE, were found on the modern border between Austria and Italy – is a member of G-L91 (G2a2b).
  • Many members of the so-called Bure kinship, a clan-like group that traces its descent from an individual born in Sweden in the late 14th or early 15th century, reportedly belong to G-Y12970 (also known as G-Y12971 and G-Z30735), also known as G2a2b2a1a1b1a1a2a1c2a~ (according to the 2017 ISOGG tree; previously G2a3b1a2).[3]
  • King Richard III of England, who was exhumed in 2012, was a member of G2 (G-P287).[49]
  • Joseph Stalin (born Ioseb Besarionis dzе Jugashvili) was, according to a genetic test on one of his grandsons (Alexander Burdonsky), a member of Y-DNA haplogroup G2a1a (FGC595/Z6553).[3][50]
  • Al Capone was an American gangster and businessman who, according to Geni.com, was a member of Y-DNA haplogroup G-P303.[51][self-published source?]
  • Yuya was Tutankhamun's great grandfather. Predicted haplotype G2a, based on ancient Y-STR profiles. Yuya served as a key adviser for Amenhotep III, and held posts such as "King’s Lieutenant" and "Master of the Horse"; his title "Father-of-the-god" possibly referred specifically to his being Amenhotep's father-in-law. In his native town of Akhmin, Yuya was a prophet of Min, the chief "god" of the area, and served as this deity's "Superintendent of Cattle".[52]
  • Larry Bird is an American professional basketball executive, former coach and former player for the Boston Celtics, has been shown to belong to haplogroup G-Z6748 based on the testing of several relatives descending from Thomas Bird at the Haplogroup G-L497 Y-DNA Project.[53]
  • Other males purported to be members of Haplogroup G include: German-American pioneer and soldier Phillip Hamman, Phillips's 5th great grandson Shane Hamman, a US Olympic weightlifter,[54] US politician Linn Banks, physicist John G. Cramer, American actors James Franciscus and Jake Gyllenhaal, American former professional basketball player Larry Bird, American businessman Najeeb Halaby, US lawyer and administrator Newton Minow, and US lawyer and signer of the Declaration of Independence Richard Stockton.[55][self-published source?]

See also edit

References edit

  1. ^ "G YTree".
  2. ^ "G YTree".
  3. ^ a b c d e ISOGG, 2017, Y-DNA Haplogroup G and its Subclades - 2017 (17 May 2017).
  4. ^ a b Rootsi, Siiri; Myres, Natalie M; Lin, Alice A; Järve, Mari; King, Roy J; Kutuev, Ildus; Cabrera, Vicente M; Khusnutdinova, Elza K; Varendi, Kärt; Sahakyan, Hovhannes; Behar, Doron M; Khusainova, Rita; Balanovsky, Oleg; Balanovska, Elena; Rudan, Pavao; Yepiskoposyan, Levon; Bahmanimehr, Ardeshir; Farjadian, Shirin; Kushniarevich, Alena; Herrera, Rene J; Grugni, Viola; Battaglia, Vincenza; Nici, Carmela; Crobu, Francesca; Karachanak, Sena; Kashani, Baharak Hooshiar; Houshmand, Massoud; Sanati, Mohammad H; Toncheva, Draga; Lisa, Antonella; Semino, Ornella; Chiaroni, Jacques; Cristofaro, Julie Di; Villems, Richard; Kivisild, Toomas; Underhill, Peter A (16 May 2012). "Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus". European Journal of Human Genetics. 20 (12): 1275–1282. doi:10.1038/ejhg.2012.86. PMC 3499744. PMID 22588667.
  5. ^ . Archived from the original on 5 February 2011. Retrieved 25 March 2023.
  6. ^ Semino O, Passarino G, Oefner PJ, Lin AA, Arbuzova S, Beckman LE, De Benedictis G, Francalacci P, Kouvatsi A, Limborska S, Marcikiae M, Mika A, Mika B, Primorac D, Santachiara-Benerecetti AS, Cavalli-Sforza LL, Underhill PA (November 2000). "The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective". Science. 290 (5494): 1155–9. Bibcode:2000Sci...290.1155S. doi:10.1126/science.290.5494.1155. PMID 11073453.
  7. ^ a b Cinnioğlu C, et al. (January 2004). "Excavating Y-chromosome haplotype strata in Anatolia". Human Genetics. 114 (2): 127–48. doi:10.1007/s00439-003-1031-4. PMID 14586639. S2CID 10763736.
  8. ^ Mahal, David G.; Matsoukas, Ianis G. (23 January 2018). "The Geographic Origins of Ethnic Groups in the Indian Subcontinent: Exploring Ancient Footprints with Y-DNA Haplogroups". Frontiers in Genetics. 9: 4. doi:10.3389/fgene.2018.00004. PMC 5787057. PMID 29410676.
  9. ^ Feldman, Michal; Fernández-Domínguez, Eva; Reynolds, Luke; Baird, Douglas; Pearson, Jessica; Hershkovitz, Israel; May, Hila; Goring-Morris, Nigel; Benz, Marion; Gresky, Julia; Bianco, Raffaela A.; Fairbairn, Andrew; Mustafaoğlu, Gökhan; Stockhammer, Philipp W.; Posth, Cosimo; Haak, Wolfgang; Jeong, Choongwon; Krause, Johannes (19 March 2019). "Late Pleistocene human genome suggests a local origin for the first farmers of central Anatolia". Nature Communications. 10 (1): 1218. Bibcode:2019NatCo..10.1218F. doi:10.1038/s41467-019-09209-7. PMC 6425003. PMID 30890703. S2CID 83464300.
  10. ^ Hofmanová, Zuzana; Kreutzer, Susanne; Hellenthal, Garrett; Sell, Christian; Diekmann, Yoan; Díez-del-Molino, David; Dorp, Lucy van; López, Saioa; Kousathanas, Athanasios; Link, Vivian; Kirsanow, Karola; Cassidy, Lara M.; Martiniano, Rui; Strobel, Melanie; Scheu, Amelie; Kotsakis, Kostas; Halstead, Paul; Triantaphyllou, Sevi; Kyparissi-Apostolika, Nina; Urem-Kotsou, Dushanka-Christina; Ziota, Christina; Adaktylou, Fotini; Gopalan, Shyamalika; Bobo, Dean M.; Winkelbach, Laura; Blöcher, Jens; Unterländer, Martina; Leuenberger, Christoph; Çilingiroğlu, Çiler; Horejs, Barbara; Gerritsen, Fokke; Shennan, Stephen; Bradley, Daniel G.; Currat, Mathias; Veeramah, Krishna R.; Wegmann, Daniel; Thomas, Mark G.; Papageorgopoulou, Christina; Burger, Joachim (25 November 2015). "Early farmers from across Europe directly descended from Neolithic Aegeans" (PDF). bioRxiv: 032763. doi:10.1101/032763. S2CID 196682085.
  11. ^ Lacan, Marie; Keyser, Christine; Ricaut, François-Xavier; Brucato, Nicolas; Tarrús, Josep; Bosch, Angel; Guilaine, Jean; Crubézy, Eric; Ludes, Bertrand (8 November 2011). "Ancient DNA suggests the leading role played by men in the Neolithic dissemination". Proceedings of the National Academy of Sciences of the United States of America. 108 (45): 18255–18259. Bibcode:2011PNAS..10818255L. doi:10.1073/pnas.1113061108. PMC 3215063. PMID 22042855.
  12. ^ a b Haak W, Balanovsky O, Sanchez JJ, Koshel S, Zaporozhchenko V, Adler CJ, Der Sarkissian CS, Brandt G, Schwarz C, Nicklisch N, Dresely V, Fritsch B, Balanovska E, Villems R, Meller H, Alt KW, Cooper A (2010). Penny D (ed.). "Ancient DNA from European Early Neolithic Farmers Reveals Their Near Eastern Affinities". PLOS Biology. 8 (11): e1000536. doi:10.1371/journal.pbio.1000536. PMC 2976717. PMID 21085689.
  13. ^ Marie Lacan, Christine Keyser, François-Xavier Ricaut, Nicolas Brucato, Francis Duranthon, Jean Guilaine, Eric Crubézy, and Bertrand Ludes, Ancient DNA reveals male diffusion through the Neolithic Mediterranean route, Proceedings of the National Academy of Sciences of the USA, online May 31, 2011 before print.
  14. ^ Interview Dr. Eduard Egarter-Vigl, Head of Conservation and Assistant to research projects of the Archaeological Museum in Bozen. From the Docu-Movie: "Ötzi, ein Archäologiekrimi" [Ötzi, a Archaeology Crime] by Christine Sprachmann. TV-Broadcast by 3sat 10 August 2011 and br-alpha 13 September 2011
  15. ^ Nasidze, Ivan; Sarkisian, Tamara; Kerimov, Azer; Stoneking, Mark (14 December 2002). "Testing hypotheses of language replacement in the Caucasus: evidence from the Y-chromosome". Human Genetics. 112 (3): 255–261. doi:10.1007/s00439-002-0874-4. PMID 12596050. S2CID 13232436.
  16. ^ Nasidze I, et al. (2008). "Close Genetic Relationship Between Semitic-speaking and Indo-European-speaking Groups in Iran". Annals of Human Genetics. 72 (Pt 2): 241–52. doi:10.1111/j.1469-1809.2007.00413.x. PMID 18205892. S2CID 5873833.
  17. ^ "G-Z7941 - Haplogroup G Project". google.com.
  18. ^ Zei G, et al. (2003). "From surnames to the history of Y chromosomes: the Sardinian population as a paradigm". European Journal of Human Genetics. 11 (10): 802–07. doi:10.1038/sj.ejhg.5201040. PMID 14512971.
  19. ^ Martinez L, et al. (April 2007). "Paleolithic Y-haplogroup heritage predominates in a Cretan highland plateau". European Journal of Human Genetics. 15 (4): 485–93. doi:10.1038/sj.ejhg.5201769. PMID 17264870.
  20. ^ King RJ, et al. (March 2008). "Differential Y-chromosome Anatolian influences on the Greek and Cretan Neolithic". Annals of Human Genetics. 72 (Pt 2): 205–14. doi:10.1111/j.1469-1809.2007.00414.x. PMID 18269686. S2CID 22406638.
  21. ^ Battaglia, Vincenza; Fornarino, Simona; Al-Zahery, Nadia; Olivieri, Anna; Pala, Maria; Myres, Natalie M; King, Roy J; Rootsi, Siiri; Marjanovic, Damir; Primorac, Dragan; Hadziselimovic, Rifat; Vidovic, Stojko; Drobnic, Katia; Durmishi, Naser; Torroni, Antonio; Santachiara-Benerecetti, A Silvana; Underhill, Peter A; Semino, Ornella (24 December 2008). "Y-chromosomal evidence of the cultural diffusion of agriculture in southeast Europe". European Journal of Human Genetics. 17 (6): 820–830. doi:10.1038/ejhg.2008.249. PMC 2947100. PMID 19107149.
  22. ^ a b c Firasat S, Khaliq S, Mohyuddin A, Papaioannou M, Tyler-Smith C, Underhill PA, Ayub Q (2006). "Y Chromosomal Evidence for a Limited Greek Contribution to the Pathan Population of Pakistan". European Journal of Human Genetics. 15 (1): 121–26. doi:10.1038/sj.ejhg.5201726. PMC 2588664. PMID 17047675.
  23. ^ a b Sengupta S, et al. (February 2006). "Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralists". American Journal of Human Genetics. 78 (2): 202–21. doi:10.1086/499411. PMC 1380230. PMID 16400607.
  24. ^ Sahoo, Sanghamitra; Singh, Anamika; Himabindu, G.; Banerjee, Jheelam; Sitalaximi, T.; Gaikwad, Sonali; Trivedi, R.; Endicott, Phillip; Kivisild, Toomas; Metspalu, Mait; Villems, Richard (2006-01-24). "A prehistory of Indian Y chromosomes: Evaluating demic diffusion scenarios". Proceedings of the National Academy of Sciences. 103 (4): 843–848. Bibcode:2006PNAS..103..843S. doi:10.1073/pnas.0507714103. ISSN 0027-8424. PMC 1347984. PMID 16415161.
  25. ^ Hammer MF, et al. (2006). "Dual Origins of the Japanese: Common Ground for Hunter-Gatherer and Farmer Y-Chromosomes". Journal of Human Genetics. 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082.
  26. ^ Singh, Sakshi; Singh, Ashish; Rajkumar, Raja; Sampath Kumar, Katakam; Kadarkarai Samy, Subburaj; Nizamuddin, Sheikh; Singh, Amita; Ahmed Sheikh, Shahnawaz; Peddada, Vidya; Khanna, Vinee; Veeraiah, Pandichelvam; Pandit, Aridaman; Chaubey, Gyaneshwer; Singh, Lalji; Thangaraj, Kumarasamy (2016). "Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup". Scientific Reports. 6: 19157. Bibcode:2016NatSR...619157S. doi:10.1038/srep19157. PMC 4709632. PMID 26754573.
  27. ^ In Lebanon, however, G accounts for 6.5% of the population and in Iran to around 10%. Flores C, et al. (2005). "Isolates in a corridor of migrations: a high-resolution analysis of Y-chromosome variation in Jordan". Journal of Human Genetics. 50 (9): 435–41. doi:10.1007/s10038-005-0274-4. PMID 16142507.
  28. ^ Cadenas AM, et al. (2008). "Chromosome Diversity Characterizes the Gulf of Oman". European Journal of Human Genetics. 16 (3): 374–86. doi:10.1038/sj.ejhg.5201934. PMID 17928816.
  29. ^ Shlush LI, et al. (2008). Gemmell NJ (ed.). "The Druze: A Population Genetic Refugium of the Near East". PLOS ONE. 3 (5): e2105. Bibcode:2008PLoSO...3.2105S. doi:10.1371/journal.pone.0002105. PMC 2324201. PMID 18461126.
  30. ^ Elizabeth T Wood, Daryn A Stover, Christopher Ehret et al., "Contrasting patterns of Y chromosome and mtDNA variation in Africa: evidence for sex-biased demographic processes," European Journal of Human Genetics (2005) 13, 867–876. (cf. Appendix A: Y Chromosome Haplotype Frequencies)
  31. ^ Luis JR, et al. (2004). "The Levant versus the Horn of Africa: Evidence for Bidirectional Corridors of Human Migrations". American Journal of Human Genetics. 74 (3): 532–44. doi:10.1086/382286. PMC 1182266. PMID 14973781.
  32. ^ El-Sibai M, Platt DE, Haber M, Xue Y, Youhanna SC, Wells RS, Izaabel H, Sanyoura MF, Harmanani H, Bonab MA, Behbehani J, Hashwa F, Tyler-Smith C, Zalloua PA (2009). "Geographical Structure of the Y-Chromosomal Genetic Landscape of the Levant: A Coastal-Inland Contrast". Annals of Human Genetics. 73 (Pt6): 561–81. doi:10.1111/j.1469-1809.2009.00538.x. PMC 3312577. PMID 19686289.
  33. ^ Alonso S, Flores C, Cabrera V, Alonso A, Martín P, Albarrán C, Izagirre N, de la Rúa C, García O (2005). "The place of the Basques in the European Y-chromosome diversity landscape". European Journal of Human Genetics. 13 (12): 1293–1302. doi:10.1038/sj.ejhg.5201482. PMID 16094307.
  34. ^ Cruciani F, et al. (2002). "A Back Migration from Asia to Sub-Saharan Africa Is Supported by High-Resolution Analysis of Human Y-Chromosome Haplotypes". American Journal of Human Genetics. 70 (5): 1197–1214. doi:10.1086/340257. PMC 447595. PMID 11910562.
  35. ^ Vanek D, Saskova L, Koch H (2009). "Kinship and Y-Chromosome Analysis of 7th Century Human Remains: Novel DNA Extraction and Typing Procedure for Ancient Material". Croatian Medical Journal. 50 (3): 286–95. doi:10.3325/cmj.2009.50.286. PMC 2702742. PMID 19480023.
  36. ^ . Premium. 2021-09-15. Archived from the original on May 27, 2023. Retrieved 2023-10-21.
  37. ^ "A point mutation which involves change A → G, C → T, C → G and T → A in DNA are". Toppr Ask. Retrieved 2023-10-21.
  38. ^ ymap.ftdna.com[permanent dead link]
  39. ^ Adams SM, Bosch E, Balaresque PL, Ballereau SJ, Lee AC, Arroyo E, López-Parra AM, Aler M, Grifo MS, Brion M, Carracedo A, Lavinha J, Martínez-Jarreta B, Quintana-Murci L, Picornell A, Ramon M, Skorecki K, Behar DM, Calafell F, Jobling MA (December 2008). "The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula". American Journal of Human Genetics. 83 (6): 725–36. doi:10.1016/j.ajhg.2008.11.007. PMC 2668061. PMID 19061982.
  40. ^ L177, later discarded in favour of PF3359 and equivalent SNPs, was first identified at Family Tree DNA in 2009. The L177.1 component is found at Y chromosome position 23397163; L177.2 at 25030912; L177.3 at 25750264. See: http://ytree.ftdna.com/index.php?name=Draft&parent=20173662 2010-10-18 at the Wayback Machine .
  41. ^ . google.com. Archived from the original on 2013-11-27. Retrieved 2011-12-09.
  42. ^ Hammer MF, et al. (2009). "Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthood". Human Genetics. 126 (5): 707–17. doi:10.1007/s00439-009-0727-5. PMC 2771134. PMID 19669163.
  43. ^ Habe, M; et al. (March 28, 2012). "Afghanistan's Ethnic Groups Share a Y-Chromosomal Heritage Structured by Historical Events". PLOS ONE. 7 (3): e34288. Bibcode:2012PLoSO...734288H. doi:10.1371/journal.pone.0034288. PMC 3314501. PMID 22470552.
  44. ^ Copyright 2015 ISOGG. "ISOGG 2015 Y-DNA Haplogroup Tree". isogg.org.{{cite web}}: CS1 maint: numeric names: authors list (link)
  45. ^ Underhill PA, Passarino G, Lin AA, Shen P, Mirazón Lahr M, Foley RA, Oefner PJ, Cavalli-Sforza LL (2001). "The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations". Annals of Human Genetics. 65 (Pt1): 43–62. doi:10.1046/j.1469-1809.2001.6510043.x. PMID 11415522. S2CID 9441236.
  46. ^ Karafet TM, Mendez FL, Meilerman MB, Underhill PA, Zegura SL, Hammer MF (2008). "New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree". Genome Research. 18 (5): 830–38. doi:10.1101/gr.7172008. PMC 2336805. PMID 18385274.
  47. ^ http://ymap.ftdna.com/cgi-bin/gbrowse_details/hs_chrY?name=L240;class=Sequence;ref=ChrY;start=3191153;end=3191153;feature_id=40369[permanent dead link]
  48. ^ Sims LM, et al. (2009). Batzer MA (ed.). "Improved Resolution Haplogroup G Phylogeny in the Y Chromosome, Revealed by a Set of Newly Characterized SNPs". PLOS ONE. 4 (6): 1–5. Bibcode:2009PLoSO...4.5792S. doi:10.1371/journal.pone.0005792. PMC 2686153. PMID 19495413.
  49. ^ King TE, Fortes GG, Balaresque P, Thomas MG, Balding D, Maisano Delser P, Neumann R, Parson W, Knapp M, Walsh S, Tonasso L, Holt J, Kayser M, Appleby J, Forster P, Ekserdjian D, Hofreiter M, Schürer K (2014). "Identification of the remains of King Richard III". Nat. Commun. 5: 5631. Bibcode:2014NatCo...5.5631K. doi:10.1038/ncomms6631. PMC 4268703. PMID 25463651.
  50. ^ "The Daily Beast".
  51. ^ "G-P303 (Y-DNA)".
  52. ^ Ancient DNA list
  53. ^ Maciamo. "Eupedia". Eupedia. Retrieved 2022-08-07.
  54. ^ "Results from the Hamman Family Y-Chromosome DNA Tests".
  55. ^ "Haplogroup G2a (Y-chromosomal DNA) - Eupedia".

External links edit

  • Haplogroup G Project Site
  • , from National Geographic
  • Y-DNA Haplogroup G and its subclades from the current year ISOGG haplotree
  • Y-Search Users with Haplogroup G[permanent dead link]
  • British Isles DNA Project
  • Haplogroup G Project in Family Tree DNA
  • G Arabia Project in Family Tree DNA

haplogroup, m201, this, article, about, human, haplogroup, human, mtdna, haplogroup, haplogroup, mtdna, haplogroup, m201, human, chromosome, haplogroup, branches, parent, haplogroup, ghijk, other, being, hijk, haplogroup, gpossible, time, origin48, years, befo. This article is about the human Y DNA haplogroup For the human mtDNA haplogroup see Haplogroup G mtDNA Haplogroup G M201 is a human Y chromosome haplogroup It is one of two branches of the parent haplogroup GHIJK the other being HIJK Haplogroup GPossible time of origin48 500 years before present 1 Coalescence age25 200 years before present 2 Possible place of originWest AsiaAncestorHaplogroup GHIJKDescendantsprimary G1 G2Defining mutationsM201 PF2957 L116 L154 L204 L240 L269 L402 L520 L521 L522 L523 L605 L769 L770 L836 L837 M201 P257 U6 Page94 U17 U2 U3 U7 U12 U20 U21 U23 U33G M201 is most commonly found among various ethnic groups of the Caucasus but is also widely distributed at low frequencies among ethnic groups throughout Europe South Asia Central Asia and North Africa The most commonly occurring subclades are G1 M285 and many subclades of G2 G P287 especially G2a P15 G2a1 G FGC7535 formerly G L293 G2a2b2a G P303 formerly G2a3b1 G2a2b1 G M406 formerly G2a3a G2a2b2a1 G L140 formerly G2a3b1a G2a2b2a1a1b G L497 formerly G2a3b1a2 G2a2b2a1a1a1 G L13 formerly G2a3b1a1a G2a2b2a1a1c1a G CTS5990 or G Z1903 formerly G2a3b1a3 G2b G M3115 and G2b1 G M377 formerly G2b Contents 1 Origins 2 Structure 3 Geographic distribution 3 1 Prehistoric presence 3 2 Modern presence 4 G1 M285 or M342 5 G2 P287 5 1 G2a P15 5 2 G2a1 FGC7535 5 3 G2a2a PF3147 5 4 G2a2b L30 PF3267 S126 U8 5 5 G2a2b1 M406 5 6 G2a2b2 CTS2488 5 7 G2a2b2a G P303 5 8 G2a2b2b PF3359 5 9 G2b1 M377 6 Defining SNPs 7 Prominent members of G 8 See also 9 References 10 External linksOrigins editVarious estimated dates and locations have been proposed for the origin of G M201 most of them in Western Asia 3 In 2012 a paper by Siiri Rootsi et al suggested that We estimate that the geographic origin of haplogroup G plausibly locates somewhere nearby eastern Anatolia Armenia or western Iran 4 Previously the National Geographic Society placed its origins in the Middle East 30 000 years ago and presumes that people carrying the haplogroup took part in the spread of the Neolithic 5 Two scholarly papers have also suggested an origin in the Middle East while differing on the date Semino et al 2000 suggested 17 000 years ago 6 Cinnioglu et al 2004 suggested the mutation took place only 9 500 years ago 7 A more eastern origin has also been mentioned believed by some to originate in an area of the Middle East close to the Himalayan foothills 8 Structure editG M201 G1 M285 M342 G1a P20 1 P20 2 P20 3 G1a1 L201 L202 L203 G1b L830 L831 L832 L834 L835 G2 P287 G2a P15 U5 L31 S149 L149 G2a1 L293 G2a1a P16 1 P16 2 G2a1a1 P18 1 P18 2 P18 3 G2a2 L223 G2a2a M286 G2a2b L91 G2a2b1 L166 L167 G2a3 L30 S126 L32 S148 L190 M485 G2a3a M406 G2a3a1 L14 Page57 S130 U16 L90 S133 G2a3a2 L645 G2a3b L141 1 G2a3b1 P303 S135 G2a3b1a L140 G2a3b1a1 U1 G2a3b1a1a L13 S131 U13 L78 M527 G2a3b1a1a1 L1263 G2a3b1a1b L1266 G2a3b1a1b1 L1264 L1265 L1268 G2a3b1a2 L497 L353 1 L353 2 G2a3b1a2a Z725 G2a3b1a2a1 L43 S147 G2a3b1a2a1a L42 S146 G2a3b1a3 Z1903 G2a3b1a3a Z724 G2a3b1a3a1 L640 G2a3b1a4 L660 L662 G2a3b1b L694 G2a3b2 L177 1 L177 2 L177 3 G2b M377 L72 L183 G2b1 M283 Subclades here conform to the Y DNA SNP definitions used by ISOGG In 2012 several categories found only in one man in research studies were removed from the ISOGG tree causing some renaming Geographic distribution editPrehistoric presence edit Ancient G M201s with sequencing self published source Haplogroup G2a G P15 has been identified in Neolithic human remains in Europe dating between 5000 and 3000 BC These Neolithic Europeans were descendants of Neolithic farmers from Anatolia among some of the earliest peoples in the world to practice agriculture G M201 has also been found in Neolithic Anatolian sites such as Boncuklu dating back to 8300 7600 BCE and Barcin dating back to 6419 6238 BCE 9 10 Furthermore the majority of all the male skeletons from the European Neolithic period have so far yielded Y DNA belonging to this haplogroup The oldest skeletons confirmed by ancient DNA testing as carrying haplogroup G2a were five found in the Avellaner cave burial site near Les Planes d Hostoles in Catalonia Spain and were dated by radiocarbon dating to about 5000 BCE 11 A skeleton found at the Neolithic cemetery known as Derenburg Meerenstieg II in Saxony Anhalt Germany apparently belonged to G2a3 G S126 or a subclade It was found with burial artifacts belonging to the Linearbandkeramische Kultur Linear Band Ceramic Culture LBK This skeleton could not be dated by radiocarbon dating but other skeletons there were dated to between 5 100 and 6 100 years old The most detailed SNP mutation identified was S126 L30 which defines G2a3 12 G2a was found also in 20 out of 22 samples of ancient Y DNA from Treilles the type site of a Late Neolithic group of farmers in the South of France dated to about 5000 years ago 13 The fourth site also from the same period is the Otztal of the Alps where the mummified remains of Otzi the Iceman were discovered The Iceman belongs to haplogroup G2a2b 14 earlier called G2a4 Haplogroup G2a2b is a rare group today in Europe The authors of the Spanish study indicated that the Avellaner men had rare marker values in testing of their short tandem repeat STR markers Modern presence edit Main article Haplogroup G Y DNA by country In Russia Ukraine and Central Asia members of various ethnic minorities and or residents in particular localities possess G M201 at its highest levels in the world even though the average rate at the national level is about 1 or less The Madjar and Argyn tribes or clans of Kazakhstan were found to possess the highest levels of G M201 among any modern ethnic group Amongst the Madjars G1 was found at a rate of 87 A separate study on the Argyns found that 71 of males belong to G1 In the Russian North Caucasus the Kabardinian and Ossetian populations are also notable for high rates of G M201 Digora North Ossetia has the highest known concentration of G in a single city as 74 of the tested men were G 15 Haplogroup G is found as far east as northern China in small percentages where G can reach more substantial percentages in minority groups such as the Uyghurs In Turkey the South Caucasus and Iran haplogroup G reaches the highest percentage of national populations Among Turkish males 11 of the population is G 7 In Iran Haplogroup G reaches 13 to 15 of the population in various parts of the country While it is found in percentages higher than 10 among the Bakhtiari Talysh people Gilaki Mazandarani and Iranian Azeris it is closer to 5 among the Iranian Arabs and in some large cities 16 Among the samples in the YHRD database from the southern Caucasus countries 29 of the samples from Abazinia 31 from Georgia 18 from Azerbaijan and 11 from Armenia appear to be G samples In Europe west of the Black Sea Haplogroup G is found at about 5 of the population on average throughout most of the continent 17 The concentration of G falls below this average in Scandinavia the westernmost former Soviet republics and Poland as well as in Iceland and the British Isles There are seeming pockets of unusual concentrations within Europe In Wales a distinctive G2a3b1 type DYS388 13 and DYS594 11 dominates there and pushes the G percentage of the population higher than in England In the Tirol Tyrol of western Austria the percentage of G M201 can reach 40 or more perhaps the most famous example is the ancient remains of the so called Iceman Otzi In the northern and highland areas of the island of Sardinia off western Italy G percentages reach 11 of the population in one study 18 and reached 21 in the town of Tempio in another study In the Greek island of Crete approximately 7 19 to 11 20 of males belong to haplogroup G In north eastern Croatia in the town of Osijek G was found in 14 of the males 21 The city is on the banks of the river Drava which notably begins in the Tirol Tyrol region of the Alps another haplogroup G focus area in Europe Farther north 8 of ethnic Hungarian males and 5 1 of ethnic Bohemian Czech males have been found to belong to Haplogroup G In South Asia some ethnic minorities possess haplogroup G at concentrations of approximately 18 22 to 20 23 of Kalash approximately 16 of Brahui 23 and approximately 11 5 of sampled Pashtun 22 but in only about 3 of the general Pakistani population 22 In a study of 936 Indians haplogroup G made up less than 1 of the sample and was completely absent in the tested Northwestern Indian population 24 About 6 of the samples from Sri Lanka and Malaysia were reported as haplogroup G but none were found in the other coastal lands of the Indian Ocean or Pacific Ocean in Asia 25 Haplogroup G M201 is believed to have been relatively absent during the Indian Neolithic period the frequencies of the G2a P15 subclade for example were negligible in indigenous Indian populations 26 In the Middle East haplogroup G accounts for about 3 of the population in almost all areas 27 28 Among the Druze mostly residents of Israel 10 were found to be haplogroup G 29 Around 10 of Jewish males are Haplogroup G citation needed In Africa haplogroup G is rarely found in sub Saharan Africa or south of the horn of Africa among native populations In Egypt studies have provided information that pegs the G percentage there to be between 2 and 9 30 31 32 3 of North African Berbers were found to be haplogroup G 33 2 of Arab Moroccans and 0 8 of Berber Moroccans were likewise found to be G 34 In the Americas the percentage of haplogroup G corresponds to the numbers of persons from Old World countries who emigrated It is not found among Native Americans except where intermarriage with non native persons has occurred It has been found in Mexican mestizos G1 M285 or M342 editMain article Haplogroup G1 Y DNA Almost all haplogroup G1 persons have the value of 12 at short tandem repeat STR marker DYS392 and all will have the M285 or M342 SNP mutation which characterizes this group This value of 12 is uncommon in other G categories other than G1 subclades of G1a G1a1 G1b exist The highest reported concentration of G1 and its subclades in a single country is in Iran with next most frequent concentrations in neighboring countries to the west There are distinctive Ashkenazi Jewish and Kazakh subclades based on STR marker value combinations G2 P287 editMen who belong to this group but are negative for all G2 subclades represent a small number of haplogroup G men P287 was identified at the University of Arizona and became widely known in late 2007 Its identification caused considerable renaming of G categories G2a P15 edit Haplogroup G men who belong to this group but are negative for all G2a subclades are uncommon in Europe but may represent a sizeable group in so far poorly tested areas east of Turkey P15 was identified at the University of Arizona and became widely known by 2002 Its chromosome location listed as 21653414 G2a was found in medieval remains in a 7th century CE high status tomb in Ergolding Bavaria Germany but G2a subclades were not tested 35 There are multiple SNPs which so far have the same coverage as P15 They are with accompanying Y chromosome locations U5 rs2178500 L149 8486380 and L31 also called S149 rs35617575 12538148 Should any man with the P15 mutation test negative ancestral for any of these or vice versa that finding would be the basis of a new G2a category G2a1 FGC7535 edit Main article Haplogroup G FGC7535 Haplogroup G2a1 also known as G FGC753 and previously as G L293 and its subclades represent the majority of haplogroup G samples in some parts of the Caucasus Mountains area They are found only in tiny numbers elsewhere So far all G2a1 persons have a value of 10 at STR marker DYS392 G2a1a persons also typically have higher values for DYS385b such as 16 17 or 18 than seen in most G persons The North Ossetians in the mid northern Caucasus area of Russia belong overwhelmingly to the G2a1 subclade based on available samples The South Ossetians and Svans generally south of North Ossetia have significant number of G2a1 persons but population percentages have not yet been provided The presence of the SNP P18 mutation characterizes G2a1a s only subclade G2a1a The reliability of both P16 and P18 in identifying everyone in each of these categories has been questioned and individual components of the SNP have to be examined Ashkenazi Jewish G2a1a men with northeastern European ancestry form a distinct cluster based on STR marker values Men from the Caucasus and men from eastern Europe also form distinctive STR clusters G2a2a PF3147 edit G PF3147 previously G L223 and G PF3146 is characterized by having the L223 mutation L223 is found on the Y chromosome at rs810801 and 6405148 with a mutation from C to G L223 was first identified in samples at 23andMe in 2009 but proved problematic as an individual test the first successful results being reported at Family Tree DNA in late 2011 under its assigned L223 label It was then learned that several subclades belong under L223 including G L91 was identified in 2009 Its members include Otzi 36 the so called Iceman who died at least 5 000 years BP in the European Alps G L91 would seem to encompass a significant proportion of men belonging to G L91 is found so far in scattered parts of Europe and North Africa and in Armenia Included within G L91 are some men with double values for STR marker DYS19 but there are also G2a2 men with this finding who are not L91 The double 19 value situation is not seen in the G2a1 and G2a3 subclades The L91 mutation is found at 21327383 and rs35474563 on the Y chromosome The forward primer is GTATTGAACTTACAATTCACGTCCC and the reverse is CTCTCCAAATCGGGTTTCCT The mutation involves a change from C to T 37 L223 is found on the Y chromosome at rs13304806 The G M286 subclade M286 is small compared with G L91 Samples have been identified in England Germany Montenegro Bosniak Spain Cyprus Greek Turkey Armenia Georgia Lebanon Syria and Kuwait The British samples have inconsistent double values for STR marker DYS19 in many cases M286 was first identified at Stanford University at chromosome position 21151187 and is a mutation from G to A The L293 SNP that characterizes a third subclade was identified in June 2010 at Family Tree DNA It encompasses a small group of Hispanic men who also so far all have the odd value of 13 21 at the YCA marker The mutation is found on the Y chromosome at 10595022 and is a change from G to C G2a2b L30 PF3267 S126 U8 edit G L30 also G PF3267 G S126 or G U8 G2a2b previously G2a3 Men who belong to this group but are negative for all its subclades represent a small number today This haplogroup was found in a Neolithic skeleton from around 5000 BC in the cemetery of Derenburg Meerenstieg II Germany which forms part of the Linear Pottery culture known in German as Linearbandkeramik LBK 12 but was not tested for G2a3 subclades G2a2b1 M406 edit Main article Haplogroup G M406 G M406 G2a2b1 previously G2a3a and its subclades seem most commonly found in Turkey and the coastal areas of the eastern Mediterranean where it can constitute up to 5 of all makes and 50 of haplogroup G samples G2a2b1 is more common in southern Europe than northern Europe In Europe except in Italy G2a2b1 constitutes less than 20 of G samples G2a2b1 so far has seldom surfaced in northern Africa or southern Asia but represents a small percentage of the G population in the Caucasus Mountains region and in Iran A relatively high percentage of G2a2b1 persons have a value of 21 at STR marker DYS390 The DYS391 marker has mostly a value of 10 but sometimes 11 in G2a2b1 persons and DYS392 is almost always 11 If a sample meets the criteria indicated for these three markers it is likely the sample is G2a2b1 G2a2b2 CTS2488 edit G CTS2488 or G2a2b2 also known as G L141 1 previously G 141 and G2a3b was identified only in mid 2009 at Family Tree DNA Almost all L141 men belong to L141 subclades Samples from persons with British Isles Sicilian and Turkish ancestry have been identified L141 persons who do not belong to any L141 subclade so far have the value of 11 at STR marker DYS490 a finding rare in other G categories The L141 mutation is found on the Y chromosome at 2948607 The L141 mutation involves an insertion 38 G2a2b2a G P303 edit Main article Haplogroup G P303 G P303 also known as G2a2b2a previously G2a3b1 and its subclades are now concentrated in southern Russia and the Caucasus as well as at lower levels other parts of Europe and South West Asia especially an area including Turkey Iran and the Middle East where G2a2b2a may have originated G2a2b2a is also found in India A majority of members of G P303 belong to one of its subclades rather than to G P303 The largest G P303 subclade based on available samples is one in which almost all persons have the value of 13 at STR marker DYS388 The SNP L497 encompasses these men but most G L497 men belong to its subclade G Z725 also known as G DYS388 13 There are additional subclades of DYS388 13 men characterized by the presence of specific SNPs or uncommon STR marker oddities Members of this group have been found in Europe and the Middle East 4 The next largest subclade of G P303 is characterized by the presence of the U1 mutation But a high percentage of U1 men belong to its two subclades G L13 S13 and Z1266 G2a3b1a1b The G L13 subclade is most common in north central Europe and G Z1266 is most common in the western Caucasus Mountains The final major subclade is characterized by presence of the SNP Z1903 and by a value of 9 at marker DYS568 A high percentage of G Z1903 men belong to its subclade G Z724 The highest percentage of G P303 persons in a discrete population so far described is on the island of Ibiza off the eastern Spanish coast This group has been linked with the Crypto Jewish population which fled to the island during the time of the Spanish Inquisition of which a significant portion are identifiable as G Z725 DYS388 13 39 G2a2b2b PF3359 edit G PF3359 or G2a2b2b previously G2a3b2 was known prior to 2013 as G L177 The SNP L177 a k a L1771 1 L177 1 L1771 2 L177 2 L177 3 L177 3 was withdrawn as an identifier by ISOGG in 2013 after it was found to be an unreliable palindromic snp 3 40 Ancient DNA identified as G PF3359 has been found at archaeological sites in Hungary the subclade G F872 dated at 7 500 years before present BP Hungary subclade G F1193 7 150 BP and Spain G PF3359 4 700 BP 3 The members of G PF3359 are probably smaller in number than men included in G P303 but only a small amount of testing has occurred for the relevant mutations So far the men positive for this have had Irish English Dutch Lebanese and or Turkish Armenian surname ancestry Several G PF3359 subclades based on shared STR markers probably exist The number of STR marker values separating men in this group suggest G PF3359 is a relatively old group despite the small number of men involved 41 self published source The mutations involved may be complicated and difficult to interpret G2b1 M377 edit Main article Haplogroup G M377 Y DNA G M377 now also known as G2b1 has previously been designated G2b and G2c A clade of closely related Ashkenazi Jews represent virtually all G2b persons with just three other G2b haplotypes having been reported so far one Turk from Kars in northeast Turkey near Armenia one Pashtun and one Burusho in Pakistan The extreme rarity of G M377 in northern Pakistan could indicate that G2b in this area originates outside the region and was brought there in the historic period perhaps from further west Pakistan was part of both the Achaemenid Persian Empire conquered by Alexander the Great and then formed a part of the Greco Bactrian Kingdom These two reported Pakistani G M377 haplotypes are quite divergent from the Ashkenazi Jewish clade and therefore do not at all indicate a recent common origin The Turkish G M377 is somewhat closer but not identical It remains to be seen if testing will reveal G M377 haplotypes in other populations this is some indication that G M377 occurs at low levels in the Near East All G M377 men tested so far also have a rare null value for the DYS425 marker a missing T allele of the DYS371 palindromic STR the result of a RecLOH event a finding not yet seen among most other G haplotypes Among Jews in Israel drawn from many areas of the world G M377 constituted 3 7 in one study 42 Haplogroup G M377 has been found at a frequency of 60 out of a sample of five Pashtuns in the Wardak region of Afghanistan This is likely due to a local founder effect 43 Defining SNPs editThe International Society of Genetic Genealogy ISOGG maintains the most up to date consensus version of haplogroup categories 44 These classifications are based on shared SNP mutations The discovery of new SNPs can result in assignment of new names to haplogroup categories There were only a few G categories until 2008 when major revisions to categories were made Even more G SNPs were identified in 2009 to 2012 leading to more changes Until 2008 new G SNPs were reported from labs at the University of Arizona P designations Stanford University M designations or the University of Central Florida U designations Beginning in 2008 additional G SNPs were identified at Family Tree DNA L designations and Ethnoancestry S designations These latter labs also made use of raw data results reported by individuals tested for about 2 000 SNPs at 23andMe to provide new L or S designated SNP tests In 2009 10 Family Tree DNA s Walk through the Y Project sequencing certain Y chromosome segments provided a number of new G SNPs with the L designation In 2012 SNPs with the Z designation as first identified by citizen researchers from 1000 Genomes Project data began to appear Because SNPs provide the most reliable method of categorization each is allowed to represent an official G category Categories have alternating letters and numbers But unusual values or unusual value combinations found at short tandem repeat markers STRs can also provide the basis of additional taxonomisation The identification of a new SNP can necessitate renaming of one or more categories The M201 SNP mutation that characterizes haplogroup G was identified at Stanford University and was first reported in 2001 45 The technical specifications of M201 are given as refSNPid is rs2032636 Y chromosome location of 13536923 forward primer is tatgcatttgttgagtatatgtc reverse primer is gttctgaatgaaagttcaaacg the mutation involves a change from G to T A number of SNPs have been identified with seemingly the same coverage in the population as M201 Because M201 was identified first it is the standard SNP test used when testing for G persons In order to determine if one of these alternative SNPs represents a subclade of M201 the alternative SNPs must be tested in G persons who are negative for the known subclades of G There are only a tiny number of persons in such a category and only a tiny number of persons have been tested for G equivalent SNPs other than M201 The following SNPs are so far identified as M201 equivalents L116 L154 L269 L294 L240 P257 L402 L520 L521 L522 L523 L605 Page 94 U2 U3 U6 U7 U12 U17 U20 U21 U23 and U33 P257 was first reported in 2008 46 L240 was identified in 2009 47 The U SNPs were identified in 2006 but not published until 2009 48 In addition there are multiple other SNPs thought to have the same coverage as M201 These are found at rs9786910 rs9786537 rs2713254 rs35567891 and rs34621155 on the Y chromosome No labs have yet assigned them shorthand names Prominent members of G editSee also List of genetic results derived from historical figures The man known as Otzi whose remains dating from the 4th millennium BCE were found on the modern border between Austria and Italy is a member of G L91 G2a2b Many members of the so called Bure kinship a clan like group that traces its descent from an individual born in Sweden in the late 14th or early 15th century reportedly belong to G Y12970 also known as G Y12971 and G Z30735 also known as G2a2b2a1a1b1a1a2a1c2a according to the 2017 ISOGG tree previously G2a3b1a2 3 King Richard III of England who was exhumed in 2012 was a member of G2 G P287 49 Joseph Stalin born Ioseb Besarionis dze Jugashvili was according to a genetic test on one of his grandsons Alexander Burdonsky a member of Y DNA haplogroup G2a1a FGC595 Z6553 3 50 Al Capone was an American gangster and businessman who according to Geni com was a member of Y DNA haplogroup G P303 51 self published source Yuya was Tutankhamun s great grandfather Predicted haplotype G2a based on ancient Y STR profiles Yuya served as a key adviser for Amenhotep III and held posts such as King s Lieutenant and Master of the Horse his title Father of the god possibly referred specifically to his being Amenhotep s father in law In his native town of Akhmin Yuya was a prophet of Min the chief god of the area and served as this deity s Superintendent of Cattle 52 Larry Bird is an American professional basketball executive former coach and former player for the Boston Celtics has been shown to belong to haplogroup G Z6748 based on the testing of several relatives descending from Thomas Bird at the Haplogroup G L497 Y DNA Project 53 Other males purported to be members of Haplogroup G include German American pioneer and soldier Phillip Hamman Phillips s 5th great grandson Shane Hamman a US Olympic weightlifter 54 US politician Linn Banks physicist John G Cramer American actors James Franciscus and Jake Gyllenhaal American former professional basketball player Larry Bird American businessman Najeeb Halaby US lawyer and administrator Newton Minow and US lawyer and signer of the Declaration of Independence Richard Stockton 55 self published source See also editJews with Haplogroup G Genetic history of Europe Genetic genealogy Y chromosome haplogroups in populations of the world Peoples of the Caucasus Magdalenian Y DNA haplogroups in populations of Europe Y DNA haplogroups in populations of the Caucasus Y DNA haplogroups in populations of the Near East Y DNA haplogroups in populations of North Africa Y DNA haplogroups by ethnic groupReferences edit G YTree G YTree a b c d e ISOGG 2017 Y DNA Haplogroup G and its Subclades 2017 17 May 2017 a b Rootsi Siiri Myres Natalie M Lin Alice A Jarve Mari King Roy J Kutuev Ildus Cabrera Vicente M Khusnutdinova Elza K Varendi Kart Sahakyan Hovhannes Behar Doron M Khusainova Rita Balanovsky Oleg Balanovska Elena Rudan Pavao Yepiskoposyan Levon Bahmanimehr Ardeshir Farjadian Shirin Kushniarevich Alena Herrera Rene J Grugni Viola Battaglia Vincenza Nici Carmela Crobu Francesca Karachanak Sena Kashani Baharak Hooshiar Houshmand Massoud Sanati Mohammad H Toncheva Draga Lisa Antonella Semino Ornella Chiaroni Jacques Cristofaro Julie Di Villems Richard Kivisild Toomas Underhill Peter A 16 May 2012 Distinguishing the co ancestries of haplogroup G Y chromosomes in the populations of Europe and the Caucasus European Journal of Human Genetics 20 12 1275 1282 doi 10 1038 ejhg 2012 86 PMC 3499744 PMID 22588667 Atlas of the Human Journey Haplogroup G M201 Archived from the original on 5 February 2011 Retrieved 25 March 2023 Semino O Passarino G Oefner PJ Lin AA Arbuzova S Beckman LE De Benedictis G Francalacci P Kouvatsi A Limborska S Marcikiae M Mika A Mika B Primorac D Santachiara Benerecetti AS Cavalli Sforza LL Underhill PA November 2000 The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans a Y chromosome perspective Science 290 5494 1155 9 Bibcode 2000Sci 290 1155S doi 10 1126 science 290 5494 1155 PMID 11073453 a b Cinnioglu C et al January 2004 Excavating Y chromosome haplotype strata in Anatolia Human Genetics 114 2 127 48 doi 10 1007 s00439 003 1031 4 PMID 14586639 S2CID 10763736 Mahal David G Matsoukas Ianis G 23 January 2018 The Geographic Origins of Ethnic Groups in the Indian Subcontinent Exploring Ancient Footprints with Y DNA Haplogroups Frontiers in Genetics 9 4 doi 10 3389 fgene 2018 00004 PMC 5787057 PMID 29410676 Feldman Michal Fernandez Dominguez Eva Reynolds Luke Baird Douglas Pearson Jessica Hershkovitz Israel May Hila Goring Morris Nigel Benz Marion Gresky Julia Bianco Raffaela A Fairbairn Andrew Mustafaoglu Gokhan Stockhammer Philipp W Posth Cosimo Haak Wolfgang Jeong Choongwon Krause Johannes 19 March 2019 Late Pleistocene human genome suggests a local origin for the first farmers of central Anatolia Nature Communications 10 1 1218 Bibcode 2019NatCo 10 1218F doi 10 1038 s41467 019 09209 7 PMC 6425003 PMID 30890703 S2CID 83464300 Hofmanova Zuzana Kreutzer Susanne Hellenthal Garrett Sell Christian Diekmann Yoan Diez del Molino David Dorp Lucy van Lopez Saioa Kousathanas Athanasios Link Vivian Kirsanow Karola Cassidy Lara M Martiniano Rui Strobel Melanie Scheu Amelie Kotsakis Kostas Halstead Paul Triantaphyllou Sevi Kyparissi Apostolika Nina Urem Kotsou Dushanka Christina Ziota Christina Adaktylou Fotini Gopalan Shyamalika Bobo Dean M Winkelbach Laura Blocher Jens Unterlander Martina Leuenberger Christoph Cilingiroglu Ciler Horejs Barbara Gerritsen Fokke Shennan Stephen Bradley Daniel G Currat Mathias Veeramah Krishna R Wegmann Daniel Thomas Mark G Papageorgopoulou Christina Burger Joachim 25 November 2015 Early farmers from across Europe directly descended from Neolithic Aegeans PDF bioRxiv 032763 doi 10 1101 032763 S2CID 196682085 Lacan Marie Keyser Christine Ricaut Francois Xavier Brucato Nicolas Tarrus Josep Bosch Angel Guilaine Jean Crubezy Eric Ludes Bertrand 8 November 2011 Ancient DNA suggests the leading role played by men in the Neolithic dissemination Proceedings of the National Academy of Sciences of the United States of America 108 45 18255 18259 Bibcode 2011PNAS 10818255L doi 10 1073 pnas 1113061108 PMC 3215063 PMID 22042855 a b Haak W Balanovsky O Sanchez JJ Koshel S Zaporozhchenko V Adler CJ Der Sarkissian CS Brandt G Schwarz C Nicklisch N Dresely V Fritsch B Balanovska E Villems R Meller H Alt KW Cooper A 2010 Penny D ed Ancient DNA from European Early Neolithic Farmers Reveals Their Near Eastern Affinities PLOS Biology 8 11 e1000536 doi 10 1371 journal pbio 1000536 PMC 2976717 PMID 21085689 Marie Lacan Christine Keyser Francois Xavier Ricaut Nicolas Brucato Francis Duranthon Jean Guilaine Eric Crubezy and Bertrand Ludes Ancient DNA reveals male diffusion through the Neolithic Mediterranean route Proceedings of the National Academy of Sciences of the USA online May 31 2011 before print Interview Dr Eduard Egarter Vigl Head of Conservation and Assistant to research projects of the Archaeological Museum in Bozen From the Docu Movie Otzi ein Archaologiekrimi Otzi a Archaeology Crime by Christine Sprachmann TV Broadcast by 3sat 10 August 2011 and br alpha 13 September 2011 Nasidze Ivan Sarkisian Tamara Kerimov Azer Stoneking Mark 14 December 2002 Testing hypotheses of language replacement in the Caucasus evidence from the Y chromosome Human Genetics 112 3 255 261 doi 10 1007 s00439 002 0874 4 PMID 12596050 S2CID 13232436 Nasidze I et al 2008 Close Genetic Relationship Between Semitic speaking and Indo European speaking Groups in Iran Annals of Human Genetics 72 Pt 2 241 52 doi 10 1111 j 1469 1809 2007 00413 x PMID 18205892 S2CID 5873833 G Z7941 Haplogroup G Project google com Zei G et al 2003 From surnames to the history of Y chromosomes the Sardinian population as a paradigm European Journal of Human Genetics 11 10 802 07 doi 10 1038 sj ejhg 5201040 PMID 14512971 Martinez L et al April 2007 Paleolithic Y haplogroup heritage predominates in a Cretan highland plateau European Journal of Human Genetics 15 4 485 93 doi 10 1038 sj ejhg 5201769 PMID 17264870 King RJ et al March 2008 Differential Y chromosome Anatolian influences on the Greek and Cretan Neolithic Annals of Human Genetics 72 Pt 2 205 14 doi 10 1111 j 1469 1809 2007 00414 x PMID 18269686 S2CID 22406638 Battaglia Vincenza Fornarino Simona Al Zahery Nadia Olivieri Anna Pala Maria Myres Natalie M King Roy J Rootsi Siiri Marjanovic Damir Primorac Dragan Hadziselimovic Rifat Vidovic Stojko Drobnic Katia Durmishi Naser Torroni Antonio Santachiara Benerecetti A Silvana Underhill Peter A Semino Ornella 24 December 2008 Y chromosomal evidence of the cultural diffusion of agriculture in southeast Europe European Journal of Human Genetics 17 6 820 830 doi 10 1038 ejhg 2008 249 PMC 2947100 PMID 19107149 a b c Firasat S Khaliq S Mohyuddin A Papaioannou M Tyler Smith C Underhill PA Ayub Q 2006 Y Chromosomal Evidence for a Limited Greek Contribution to the Pathan Population of Pakistan European Journal of Human Genetics 15 1 121 26 doi 10 1038 sj ejhg 5201726 PMC 2588664 PMID 17047675 a b Sengupta S et al February 2006 Polarity and temporality of high resolution y chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralists American Journal of Human Genetics 78 2 202 21 doi 10 1086 499411 PMC 1380230 PMID 16400607 Sahoo Sanghamitra Singh Anamika Himabindu G Banerjee Jheelam Sitalaximi T Gaikwad Sonali Trivedi R Endicott Phillip Kivisild Toomas Metspalu Mait Villems Richard 2006 01 24 A prehistory of Indian Y chromosomes Evaluating demic diffusion scenarios Proceedings of the National Academy of Sciences 103 4 843 848 Bibcode 2006PNAS 103 843S doi 10 1073 pnas 0507714103 ISSN 0027 8424 PMC 1347984 PMID 16415161 Hammer MF et al 2006 Dual Origins of the Japanese Common Ground for Hunter Gatherer and Farmer Y Chromosomes Journal of Human Genetics 51 1 47 58 doi 10 1007 s10038 005 0322 0 PMID 16328082 Singh Sakshi Singh Ashish Rajkumar Raja Sampath Kumar Katakam Kadarkarai Samy Subburaj Nizamuddin Sheikh Singh Amita Ahmed Sheikh Shahnawaz Peddada Vidya Khanna Vinee Veeraiah Pandichelvam Pandit Aridaman Chaubey Gyaneshwer Singh Lalji Thangaraj Kumarasamy 2016 Dissecting the influence of Neolithic demic diffusion on Indian Y chromosome pool through J2 M172 haplogroup Scientific Reports 6 19157 Bibcode 2016NatSR 619157S doi 10 1038 srep19157 PMC 4709632 PMID 26754573 In Lebanon however G accounts for 6 5 of the population and in Iran to around 10 Flores C et al 2005 Isolates in a corridor of migrations a high resolution analysis of Y chromosome variation in Jordan Journal of Human Genetics 50 9 435 41 doi 10 1007 s10038 005 0274 4 PMID 16142507 Cadenas AM et al 2008 Chromosome Diversity Characterizes the Gulf of Oman European Journal of Human Genetics 16 3 374 86 doi 10 1038 sj ejhg 5201934 PMID 17928816 Shlush LI et al 2008 Gemmell NJ ed The Druze A Population Genetic Refugium of the Near East PLOS ONE 3 5 e2105 Bibcode 2008PLoSO 3 2105S doi 10 1371 journal pone 0002105 PMC 2324201 PMID 18461126 Elizabeth T Wood Daryn A Stover Christopher Ehret et al Contrasting patterns of Y chromosome and mtDNA variation in Africa evidence for sex biased demographic processes European Journal of Human Genetics 2005 13 867 876 cf Appendix A Y Chromosome Haplotype Frequencies Luis JR et al 2004 The Levant versus the Horn of Africa Evidence for Bidirectional Corridors of Human Migrations American Journal of Human Genetics 74 3 532 44 doi 10 1086 382286 PMC 1182266 PMID 14973781 El Sibai M Platt DE Haber M Xue Y Youhanna SC Wells RS Izaabel H Sanyoura MF Harmanani H Bonab MA Behbehani J Hashwa F Tyler Smith C Zalloua PA 2009 Geographical Structure of the Y Chromosomal Genetic Landscape of the Levant A Coastal Inland Contrast Annals of Human Genetics 73 Pt6 561 81 doi 10 1111 j 1469 1809 2009 00538 x PMC 3312577 PMID 19686289 Alonso S Flores C Cabrera V Alonso A Martin P Albarran C Izagirre N de la Rua C Garcia O 2005 The place of the Basques in the European Y chromosome diversity landscape European Journal of Human Genetics 13 12 1293 1302 doi 10 1038 sj ejhg 5201482 PMID 16094307 Cruciani F et al 2002 A Back Migration from Asia to Sub Saharan Africa Is Supported by High Resolution Analysis of Human Y Chromosome Haplotypes American Journal of Human Genetics 70 5 1197 1214 doi 10 1086 340257 PMC 447595 PMID 11910562 Vanek D Saskova L Koch H 2009 Kinship and Y Chromosome Analysis of 7th Century Human Remains Novel DNA Extraction and Typing Procedure for Ancient Material Croatian Medical Journal 50 3 286 95 doi 10 3325 cmj 2009 50 286 PMC 2702742 PMID 19480023 Otzi the Iceman What we know 3 decades after his discovery Premium 2021 09 15 Archived from the original on May 27 2023 Retrieved 2023 10 21 A point mutation which involves change A G C T C G and T A in DNA are Toppr Ask Retrieved 2023 10 21 ymap ftdna com permanent dead link Adams SM Bosch E Balaresque PL Ballereau SJ Lee AC Arroyo E Lopez Parra AM Aler M Grifo MS Brion M Carracedo A Lavinha J Martinez Jarreta B Quintana Murci L Picornell A Ramon M Skorecki K Behar DM Calafell F Jobling MA December 2008 The genetic legacy of religious diversity and intolerance paternal lineages of Christians Jews and Muslims in the Iberian Peninsula American Journal of Human Genetics 83 6 725 36 doi 10 1016 j ajhg 2008 11 007 PMC 2668061 PMID 19061982 L177 later discarded in favour of PF3359 and equivalent SNPs was first identified at Family Tree DNA in 2009 The L177 1 component is found at Y chromosome position 23397163 L177 2 at 25030912 L177 3 at 25750264 See http ytree ftdna com index php name Draft amp parent 20173662 Archived 2010 10 18 at the Wayback Machine Project Rosters Haplogroup G Project google com Archived from the original on 2013 11 27 Retrieved 2011 12 09 Hammer MF et al 2009 Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthood Human Genetics 126 5 707 17 doi 10 1007 s00439 009 0727 5 PMC 2771134 PMID 19669163 Habe M et al March 28 2012 Afghanistan s Ethnic Groups Share a Y Chromosomal Heritage Structured by Historical Events PLOS ONE 7 3 e34288 Bibcode 2012PLoSO 734288H doi 10 1371 journal pone 0034288 PMC 3314501 PMID 22470552 Copyright 2015 ISOGG ISOGG 2015 Y DNA Haplogroup Tree isogg org a href Template Cite web html title Template Cite web cite web a CS1 maint numeric names authors list link Underhill PA Passarino G Lin AA Shen P Mirazon Lahr M Foley RA Oefner PJ Cavalli Sforza LL 2001 The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations Annals of Human Genetics 65 Pt1 43 62 doi 10 1046 j 1469 1809 2001 6510043 x PMID 11415522 S2CID 9441236 Karafet TM Mendez FL Meilerman MB Underhill PA Zegura SL Hammer MF 2008 New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree Genome Research 18 5 830 38 doi 10 1101 gr 7172008 PMC 2336805 PMID 18385274 http ymap ftdna com cgi bin gbrowse details hs chrY name L240 class Sequence ref ChrY start 3191153 end 3191153 feature id 40369 permanent dead link Sims LM et al 2009 Batzer MA ed Improved Resolution Haplogroup G Phylogeny in the Y Chromosome Revealed by a Set of Newly Characterized SNPs PLOS ONE 4 6 1 5 Bibcode 2009PLoSO 4 5792S doi 10 1371 journal pone 0005792 PMC 2686153 PMID 19495413 King TE Fortes GG Balaresque P Thomas MG Balding D Maisano Delser P Neumann R Parson W Knapp M Walsh S Tonasso L Holt J Kayser M Appleby J Forster P Ekserdjian D Hofreiter M Schurer K 2014 Identification of the remains of King Richard III Nat Commun 5 5631 Bibcode 2014NatCo 5 5631K doi 10 1038 ncomms6631 PMC 4268703 PMID 25463651 The Daily Beast G P303 Y DNA Ancient DNA list Maciamo Eupedia Eupedia Retrieved 2022 08 07 Results from the Hamman Family Y Chromosome DNA Tests Haplogroup G2a Y chromosomal DNA Eupedia External links edit nbsp Wikimedia Commons has media related to Haplogroup G of Y DNA Haplogroup G Project Site Spread of Haplogroup G from National Geographic Haplogroup G tutorial from Genebase Y DNA Haplogroup G and its subclades from the current year ISOGG haplotree Y Search Users with Haplogroup G permanent dead link British Isles DNA Project Haplogroup G Project in Family Tree DNA G Arabia Project in Family Tree DNA Retrieved from https en wikipedia org w index php title Haplogroup G M201 amp oldid 1187878045 G2a 28P15 2B 29, wikipedia, wiki, book, books, library,

article

, read, download, free, free download, mp3, video, mp4, 3gp, jpg, jpeg, gif, png, picture, music, song, movie, book, game, games.