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Haplogroup C-M217

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(Redirected fromHaplogroup C-M217 (Y-DNA))
Human Y-chromosome DNA haplogroup
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Haplogroup C-M217
C2(previously C3)[1]
Possible time of origin50,865 [95% CI 38,317 <-> 61,900] ybp[2]

52,500 or 44,900 ybp[3]

48,400 [95% CI 46,000 <-> 50,900] ybp[4]
Coalescence age35,383 [95% CI 25,943 <-> 44,092] ybp[2]

34,000 [95% CI 31,500 <-> 36,700] ybp[4]
Possible place of originProbablyCentral Asia orEast Asia
AncestorC-M130
DescendantsC-M93 (C2a);C-CTS117 (C2b); C-P53.1 (C2c); C-P62 (C2d); C-F2613/Z1338 (C2e)
Defining mutationsM217, P44, PK2
Highest frequenciesKazakhs 51.9%[5]Oroqen 61%[6]-91%,[7]Evenks 12.9%[8] - 71%,[9][10]Ulchi 69%,[11]Nivkhs 38%[12]-71%,[13]Buryats 7%[14]-84%,[12]Evens 5%[10]-74%,[15]Mongolians 52.3%[15] (22.9%China,[16] 24.39%China,[17] 45% Northeast Mongolia,[18] 46.7%Oroqen Autonomous Banner,[6] 47.8% Southeast Mongolia,[18] 52.6% Northwest Mongolia,[18] 53.8%Batsümber,[6] 55% Central and Southwest Mongolia[18]),Tanana 42%,[19]Koryaks 33%[9][10]-48%,[13]Hazaras 35%[18]–40%,[20]Yukaghir 31%,[21]Daur 30.8%[6]-42.5%,[22]Sibe (Xinjiang) 26.8% (11/41)[6] - 29.5% (18/61),[23]Hezhe (Heilongjiang) 23%,[6][16]Manchu 17.67%[24] (9.3%Bijie[25] - 44.0%Heilongjiang[23]),Tujia ≈21% (16%,[26] 18%Jishou,[15] 21%Guizhou,[23] 23%Hubei,[23] 27%Hunan[27]),North Korean 23% (19%[citation needed]-27%[23]),Altai 22%[15]-24%,[7]Dong 21% (6%Guangxi,[23] 20%Hunan,[27] 22%Hunan,[23] 30%Guizhou[23]),Kyrgyz 20%[18]-26.6%,[28]Uzbeks 20% (Uzbekistan[7]) - 54% (Takhar[29]),Hani 18% (12%Mường Tè,[30] 18%,[6] 22%Yunnan[23]),South Korean 16% (11.6%-21%[citation needed]),Cheyenne 16%,[19]Apache 15%,[19] NorthernHan 14.7% (4.3%-29.6%),[23]Tuvans 11%[31] – 15%,[21]Ainu 12.5%[12]-25%,[15]Hui 11%,[6][7]Sioux 11%,[19]Nogais 14%,[32]Crimean Tatars 9%,[32]Uyghurs 8.27% (0% Ürümqi,[6] 0% Turpan area,[23] 2.6% Keriya,[33] 3.1% Lopnur,[33] 6.0%,[15] 6.0% Ürümqi area,[23] 6.3% Bortala area,[23] 7.0% Yining area,[23] 7.7% Yili,[6] 8.37% Hetian area,[34] 11.8% Horiqol Township,[33] 16.08% Turpan area[34]),Vietnamese 7.6% (4.3%-12.5%[35]),Tajiks (Afghanistan) 7.6% (3.6%[29]-9.2%[18]), SouthernHan 7.1% (0%-23.5%),[23]Tabassarans 7%,[36]Abazinians 7%,[37]Japanese 5.9% (0%Tokyo,[38][39]Okinawa,[15]Aomori,[15] - 7.8%Fukuoka[40]),Adygei 2.9%,[36]Kabardians 2.4%,[36]Pashtuns 2.04%[29]

Haplogroup C-M217, also known asC2 (and previously as C3),[1] is aY-chromosome DNA haplogroup. It is the most frequently occurring branch of the widerHaplogroup C (M130). It is found mostly inCentral Asia,Eastern Siberia and significant frequencies in parts ofEast Asia andSoutheast Asia including some populations in theCaucasus,Middle East,South Asia,East Europe. It is found in a much more widespread area with a low frequency of less than 2%.

The haplogroup C-M217 is now found at high frequencies amongCentral Asian peoples,indigenous Siberians, and someNative peoples of North America. In particular, males belonging to peoples such as theBuryats,[15][31]Evens,[15]Evenks,[15]Itelmens,[14]Tom Tatars,[41]Kalmyks,[31][42][43]Kazakhs,Koryaks,[14]Mongolians,[15][18]Negidals,[14]Nivkhs,[14]Udege,[14] andUlchi[11] have high levels of M217.[7][15][44]

The oldest samples of haplogroup C-M217 found amongAncient Northeast Asians ofAmur region.[45]

The haplogroup C-M217 is found in Ancient samples ofXiongnu,[46][47][48]Göktürks,[47]Uyghurs,[47]Khazars[49] andKipchaks.[50]

One particularhaplotype within Haplogroup C2-M217 has received a great deal of attention, because of the possibility that it may represent directpatrilinealdescent from Genghis Khan,[51] though that hypothesis is controversial. According to the recent result, C2's subgroups are divided into C2b and C2e, and in Mongolia, most belong to C2b(Genghis Khan modal), while very few are C2e. On the other hand, C2b takes minority and most are C2e in Japan and Korea and Southern East Asia. The specific subclade Haplogroup C3b2b1*-M401(xF5483) of the broader C3b1a3-F3273/M504, M546 subclade, which has been identified as a possible marker of the ManchuAisin Gioro and has been found in ten different ethnic minorities in northern China, is relatively rare in Han Chinese populations (Heilongjiang, Gansu, Guangdong, Sichuan and Xinjiang).[52][53][54][55][56]

Y chromosome haplogroup C2c1a1a1-M407 is carried by Mongol descendants of theNorthern Yuan ruler from 1474 to 1517,Dayan Khan, who is a male line descendant of Genghis Khan which was found out after geneticists in Mongolia conducted tests on them.
C2b1a3a1c2-F5481 clade of C2*-ST which is also widespread in Central Asia among Kazakhs, Hazaras and ordinary commoner Mongols.[57] The Kerey clan of the Kazakhs have a high amount of the C3* star-cluster (C2*-ST) Y chromosome and is very high among Hazaras, Kazakhs and Mongols in general.[58]

Toghan, Genghis Khan's sixth son has claimed descendants who have Y haplogroup C2b1a1b1-F1756 just like the first son of Genghis Khan,Jochi's descendants in the KazakhTore clan.[59]

Origin

[edit]

After sharing a most recent common ancestor withHaplogroup C-F3393 approximately 48,400 [95% CI 46,000 <-> 50,900] years before present,[2] Haplogroup C-M217 is believed to have begun spreading approximately 34,000 [95% CI 31,500 <-> 36,700] years before present[2] in eastern or central Asia.

The extremely broad distribution of Haplogroup C-M217 Y-chromosomes, coupled with the fact that the ancestral paragroup C is not found among any of the modern Siberian or North American populations among whom Haplogroup C-M217 predominates, makes the determination of the geographical origin of the defining M217 mutation exceedingly difficult. The presence of Haplogroup C-M217 at a low frequency but relatively high diversity throughoutEast Asia and parts ofSoutheast Asia makes that region one likely source. In addition, the C-M217 haplotypes found with high frequency among North Asian populations appear to belong to a different genealogical branch from the C-M217 haplotypes found with low frequency among East and Southeast Asians, which suggests that the marginal presence of C-M217 among modern East and Southeast Asian populations may not be due to recent admixture from Northeast or Central Asia.[60]

More precisely, haplogroup C2-M217 is now divided into two primary subclades: C2a-L1373 (sometimes called the "northern branch" of C2-M217) and C2b-F1067 (sometimes called the "southern branch" of C2-M217). The oldest sample with C2-M217 is AR19K in theAmur River basin (19,587-19,175 cal BP).[61]

C2a-L1373 (estimatedTMRCA 16,000 [95% CI 14,300 <-> 17,800] ybp[4]) has been found often in populations from Central Asia through North Asia to the Americas, and rarely in individuals from some neighboring regions, such as Europe or East Asia. C2a-L1373 subsumes two subclades: C2a1-F3447 and C2a2-BY63635/MPB374. C2a1-F3447 includes all extant Eurasian members of C2a-L1373, whereas C2a2-BY63635/MPB374 contains extant South American members of C2a-L1373 as well as ancient archaeological specimens from South America andChertovy Vorota Cave inPrimorsky Krai. C2a1-F3447 (estimated TMRCA 16,000 [95% CI 14,700 <-> 17,400] ybp[4]) includes the Y-DNA of an approximately 14,000-year-old specimen from the Ust'-Kyakhta 3 site (located on the right bank of theSelenga River inBuryatia, near the present-day international border withMongolia) and C2a1b-BY101096/ACT1942 (found in individuals from present-dayLiaoning Province of China,South Korea,Japan, and aNivkh from Russia) in addition to the expansive C2a1a-F1699 clade. C2a1a-F1699 (estimated TMRCA 14,000 [95% CI 12,700 <-> 15,300] ybp[4]) subsumes four subclades: C2a1a1-F3918, C2a1a2-M48, C2a1a3-M504, and C2a1a4-M8574. C2a1a1-F3918 subsumes C2a1a1a-P39, which has been found at high frequency in samples of someindigenous North American populations, and C2a1a1b-FGC28881, which is now found with varying (but generally quite low) frequency all over theEurasian steppe, fromHeilongjiang andJiangsu in the east toJihočeský kraj,Podlaskie Voivodeship, andGiresun in the west.[4]Haplogroup C2a1a2-M48 is especially frequent and diverse among present-dayTungusic peoples, but branches of it also constitute the most frequently observed Y-DNA haplogroup among present-dayMongols inMongolia,Alshyns in westernKazakhstan, andKalmyks inKalmykia. Extant members of C2a1a3-M504 all share a relatively recent common ancestor (estimated TMRCA 3,900 [95% CI 3,000 <-> 4,800] ybp[4]), and they are found often amongMongols,Manchus (e.g.Aisin Gioro),Kazakhs (most tribes of the Senior Zhuz as well as theKerei tribe of the Middle Zhuz),Kyrgyz, andHazaras. C2a1a4-M8574 is sparsely attested and deeply bifurcated into C-Y176542, which has been observed in an individual fromUlsan and an individual from Japan,[4] and C-Y11990. C-Y11990 is likewise quite ancient (estimated TMRCA 9,300 [95% CI 7,900 <-> 10,700] ybp according to YFull[4] or 8,946 [99% CI 11,792 - 6,625] ybp according to FTDNA[62]) but rare, with one branch (C-Z22425) having been found sporadically inJammu and Kashmir,Germany, and theUnited States and another branch (C-ZQ354/C-F8513) having been found sporadically inSlovakia (Prešov Region),China,Turkey, andKipchak of the central steppe (Lisakovsk 23 Kipchak in Kazakhstan, medieval nomad from 920 ± 25 BP uncal or 1036 - 1206 CE).[4][62]

The predominantly East Asian distributed C-F1067 subsumes a major clade, C-F2613, and a minor clade, C-CTS4660. The minor clade C-CTS4660 has been found in China (including aDai and severalHan from southern China as well as a Han fromAnhui and a Han fromInner Mongolia; according to Chinese genomics company 23mofang, C-CTS4660 is currently mainly concentrated in theLiangguang region of China, accounting for about 0.24% of the national male population[63]) and Thailand[62] (includingNorthern Thai andLao Isan[64]). The major clade C-F2613 has known representatives from China (Oroqen,[65]Hezhe,[65]Manchu,[66]Uyghur,[66]Han,Tibetan,[66]Tujia,[65]Dai), Korea, Japan, Laos, Thailand, Vietnam, Bhutan, Bangladesh, Mongolia,[18][66] Kyrgyzstan (Dungan, Kyrgyz),[18] Tajikistan (Tajik[66]), Afghanistan (Hazara, Tajik),[18] Pakistan (Burusho,Hazara),[18]Nakhchivan,Chechnya, andSyria and includes the populous subclades C-F845, C-CTS2657, and C-Z8440. C-M407, a notable subclade of C-CTS2657, has expanded in a post-Neolithic time frame[67] to include large percentages of modernBuryat,Soyot, andHamnigan males inBuryatia andBarghut males inHulunbuir[68] in addition to manyKalmyks and otherMongols[31][42][18][69] and members of theQongirat tribe in Kazakhstan[70] (but only 2 or 0.67% of a sample of 300Korean males[71]).

The specific subclade haplogroup C3b2b1*-M401(xF5483)[56][72][73] has been identified as a possible marker of the Aisin Gioro and is found in ten different ethnic minorities in northern China, but completely absent from Han Chinese.[74][75][73]

Genetic testing also showed that the haplogroup C3b1a3a2-F8951 of the Aisin Gioro family came to southeastern Manchuria after migrating from their place of origin in the Amur river's middle reaches, originating from ancestors related toDaurs in theTransbaikal area. TheTungusic speaking peoples mostly have C3c-M48 as their subclade of C3 which drastically differs from the C3b1a3a2-F8951 haplogroup of the Aisin Gioro which originates from Mongolic speaking populations like the Daur. Jurchen (Manchus) are a Tungusic people. The Mongol Genghis Khan's haplogroup C3b1a3a1-F3796 (C3*-Star Cluster) is a fraternal "brother" branch of C3b1a3a2-F8951 haplogroup of the Aisin Gioro.[76] A genetic test was conducted on seven men who claimed Aisin Gioro descent with three of them showing documented genealogical information of all their ancestors up to Nurhaci. Three of them turned out to share the C3b2b1*-M401(xF5483) haplogroup, out of them, two of them were the ones who provided their documented family trees. The other four tested were unrelated.[77] The Daur Ao clan carries the unique haplogroup subclade C2b1a3a2-F8951, the same haplogroup as Aisin Gioro and both Ao and Aisin Gioro only diverged merely a couple of centuries ago from a shared common ancestor. Other members of the Ao clan carry haplogroups like N1c-M178, C2a1b-F845, C2b1a3a1-F3796 and C2b1a2-M48. People from northeast China, the Daur Ao clan and Aisin Gioro clan are the main carriers of haplogroup C2b1a3a2-F8951. The Mongolic C2*-Star Cluster (C2b1a3a1-F3796) haplogroup is a fraternal branch to Aisin Gioro's C2b1a3a2-F8951 haplogroup.[78]

Distribution

[edit]

Haplogroup C-M217 is the modal haplogroup amongMongolians and mostindigenous populations of the Russian Far East, such as theBuryats, NorthernTungusic peoples,Nivkhs,Koryaks, andItelmens. Thesubclade C-P39 is common among males of the indigenous North American peoples whose languages belong to theNa-Denéphylum. The frequency of Haplogroup C-M217 tends to be negatively correlated with distance from Mongolia and the Russian Far East, but it still comprises more than ten percent of the total Y-chromosome diversity among theManchus,Koreans,Ainu, and someTurkic peoples ofCentral Asia. Beyond this range of high-to-moderate frequency, which contains mainly the northeast quadrant of Eurasia and the northwest quadrant of North America, Haplogroup C-M217 continues to be found at low frequencies, and it has even been found as far afield as Northwest Europe, Turkey, Pakistan,Bhutan,[79]Bangladesh,[4]Nepal[80] and adjacent regions of India,[81][82][83] Vietnam,Maritime Southeast Asia, and theWayuu people of South America. It is found inOssetians 4.7% (1/21),[36] and inRussians 0.73% (3/406),frequency ranges depending on the district.[31] It is found 0.2% in Central/Southern Russia but 0.9% Rovslav and 0.7% Belgorod. It is found 0.5% in ethnicBulgarians but 1.2% inMontana Province, 0.8%Sofia Provinceand 1.4% in an unknown area[84] some of whom exhibit divergent Y-STR haplotypes.[23] Haplogroup C-M127 also has been found with high frequency in a small sample ofUzbeks fromTakhar, Afghanistan (7/13 = 54% C-M217[29]).

In an early study of Japanese Y-chromosomes, haplogroup C-M217 was found relatively frequently amongAinus (2/16=12.5%[12] or 1/4=25%[15]) and among Japanese of theKyūshū region (8/104=7.7%[12]). However, in other samples of Japanese, the frequency of haplogroup C-M217 was found to be only about one to three percent.[12][6][15][38] In a study published in 2014, large samples of males from seven different Japanese cities were examined, and the frequency of C-M217 varied between a minimum of 5.0% (15/302 university students in Sapporo) and a maximum of 7.8% (8/102 adult males in Fukuoka), with a total of 6.1% (146/2390) of their sampled Japanese males belonging to this haplogroup; the authors noted that no marked geographical gradient was detected in the frequencies of haplogroups C-M217 or C-M8 in that study.[40]

The frequency of Haplogroup C-M217 in samples ofHan from various areas has ranged from 0% (0/27) in a sample of Han fromGuangxi[8] in southern China to 23.5% (4/17) in a sample of Han fromShanghai[8] in eastern China, 23.5% (8/34) in a sample of Han fromXi'an[35] in northwestern China, and 29.6% (8/27) in a sample of Han fromJilin[8] in northeastern China, with the frequency of this haplogroup in several studies' pools of all Han samples ranging between 6.0% and 12.0%.[6][7][15][12][23][35] C-M217 also has been found in many samples of ethnic minority populations from central and southern China, such asDong (8/27 = 29.6% from Guizhou,[23] 10/45 = 22.2% from Hunan,[23] 1/17 = 5.9% from Guangxi[23]),Bulang (3/11 = 27.3% from Yunnan[23]),Tujia (6/26 = 23.1% from Hubei,[23] 7/33 = 21.2% from Guizhou,[23] 9/49 = 18.4% fromJishou, Hunan),Hani (13/60 = 21.7% from Yunnan,[23] 6/34 = 17.6%[6]),Yi (4/32 = 12.5%Boren from Yunnan,[23] 3/24 = 12.5% Yi from Sichuan,[23] 4/61 = 6.6% Yi from Yunnan[23]),Mulao (1/11 = 9.1% from Guangxi[23]),Naxi (1/12 = 8.3% from Yunnan[23]),Miao (7/92 = 7.6% from Guizhou,[23] 2/58 = 3.4%),Shui (2/29 = 6.9% from Guizhou[23]),She (3/47 = 6.4% from Fujian,[23] 1/34 = 2.9%[6]),Wa (1/16 = 6.3% from Yunnan[23]),Dai (1/18 = 5.6% from Yunnan[23]),Gelao (1/21 = 4.8% from Guizhou[23]),ethnic Vietnamese (2/45 = 4.4% from Guangxi[23]),Yao (1/28 = 3.6% from Guangdong,[23] 1/35 = 2.9% from Liannan, Guangdong,[6] 2/113 = 1.8% from Guangxi[23]),Bai (1/34 = 2.9% from Yunnan[23]),Tibetans (4/156 = 2.6%),Buyi (2/109 = 1.8% from Guizhou[23]), andTaiwanese aborigines (1/48 = 2.1%).[85][6][80]

InVietnam, Y-DNA that belongs to haplogroup C-M217 has been found in about 7.5% of all published samples, including 12.5% (6/48) of a sample of Vietnamese from Hanoi, Vietnam,[35] 11.8% (9/76) of another sample ofKinh ("ethnic Vietnamese") from Hanoi, Vietnam, 10% (1/10) of a sample from Vietnam,[86] 8.5% (5/59) of a sample ofCham people from Binh Thuan, Vietnam, 8.3% (2/24) of another sample of Vietnamese from Hanoi,[87] 4.3% (3/70) of a sample of Vietnamese from an unspecified location in Vietnam,[85] 2.2% (1/46) of the KHV ("Kinh in Ho Chi Minh City, Vietnam") sample of the1000 Genomes Project,[4][3] and 0% (0/27) of one study's samples of Kinh andMuong.[88] Macholdtet al. (2020) have found Y-DNA that belongs to haplogroup C-M217 in 4.67% (28/600) of a set of samples from Vietnam, including 26.8% (11/41) of a sample ofHmong fromĐiện Biên Phủ, 13.9% (5/36) of a sample ofPathen fromQuang Bình District, 12.1% (4/33) of a sample ofHanhi fromMường Tè District, 10.3% (3/29) of a sample ofSila fromMường Tè District, and 10.0% (5/50) of a sample ofKinh (n=42 fromHanoi, including all five members of haplogroup C-M217).[30]

Haplogroup C-M217 has been found less frequently in other parts of Southeast Asia and nearby areas, includingMyanmar (3/72 = 4.2% Bamar and Rakhine[89]), Laos (1/25 = 4.0% Lao from Luang Prabang),Malaysia (2/18 = 11.1% Malaysia,[86] 0/8 Malaysia,[87] 0/12 Malaysian (ordinary Malay near Kuala Lumpur),[12] 0/17Orang Asli,[90] 0/27 Malay,[90] 0/32 Malaysia[85]),Java (1/37 = 2.7%, 1/141 = 0.71%[87]), Nepal (2/77 = 2.6% general population of Kathmandu),Thailand (1/40 = 2.5% Thai, mostly sampled in Chiang Mai;[35] 13/500 = 2.6%Northern Thailand, or 11/290 = 3.8%Northern Thai people and 2/91 = 2.2%Tai Lü[91]), the Philippines (1/48 = 2.1%, 1/64 = 1.6%), and Bali (1/641 = 0.2%).[80][85]

Although C-M217 is generally found with only low frequency (<5%) in Tibet and Nepal, there may be an island of relatively high frequency of this haplogroup inMeghalaya, India. The indigenous tribes of this state of Northeast India, where they comprise the majority of the local population, speakKhasian languages orTibeto-Burman languages. A study published in 2007 found C-M217(xM93, P39, M86) Y-DNA in 8.5% (6/71) of a sample ofGaros, who primarily inhabit theGaro Hills in the western half of Meghalaya, and in 7.6% (27/353) of a pool of samples of eight Khasian tribes from the eastern half of Meghalaya (6/18 = 33.3% Nongtrai from the West Khasi Hills, 10/60 = 16.7%Lyngngam from the West Khasi Hills, 2/29 = 6.9% War-Khasi from the East Khasi Hills, 3/44 = 6.8% Pnar from the Jaintia Hills, 1/19 = 5.3% War-Jaintia from the Jaintia Hills, 3/87 = 3.4% Khynriam from the East Khasi Hills, 2/64 = 3.1% Maram from the West Khasi Hills, and 0/32 Bhoi from Ri-Bhoi District).[82]

Subclade distribution

[edit]

The subclades of Haplogroup C-M217 with their defining mutation(s), according to the2017 ISOGG tree:

Others

[edit]

P53.1 has been used in multiple studies, but at testing in the commercial labs it appears in too many parts of the Y tree, including multiple parts of haplogroup C. Listed 16 April 2016.

Phylogenetics

[edit]

Phylogenetic history

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Main article:Conversion table for Y chromosome haplogroups
This sectiondoes notcite anysources. Please helpimprove this section byadding citations to reliable sources. Unsourced material may be challenged andremoved.(March 2021) (Learn how and when to remove this message)

Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.

YCC 2002/2008 (Shorthand)(α)(β)(γ)(δ)(ε)(ζ)(η)YCC 2002 (Longhand)YCC 2005 (Longhand)YCC 2008 (Longhand)YCC 2010r (Longhand)ISOGG 2006ISOGG 2007ISOGG 2008ISOGG 2009ISOGG 2010ISOGG 2011ISOGG 2012
C-M21610V1F16Eu6H1CC*CCCCCCCCCC
C-M810V1F19Eu6H1CC1C1C1C1C1C1C1C1C1C1C1
C-M3810V1F16Eu6H1CC2*C2C2C2C2C2C2C2C2C2C2
C-P3310V1F18Eu6H1CC2aC2aC2a1C2a1C2aC2aC2a1C2a1C2a1removedremoved
C-P4410V1F17Eu6H1CC3*C3C3C3C3C3C3C3C3C3C3
C-M9310V1F17Eu6H1CC3aC3aC3aC3aC3aC3aC3aC3aC3aC3aC3a1
C-M20810V1F17Eu6H1CC3bC2bC2aC2aC2bC2bC2aC2aC2aC2aC2a
C-M21036V1F17Eu6H1CC3cC2cC4aC4aC4bC4bC4aC4aC4aC4aC4a

Phylogenetic trees

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[icon]
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See also

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Genetics

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Y-DNA C subclades

[edit]

Y-DNA backbone tree

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This article needs to beupdated. Please help update this article to reflect recent events or newly available information.(February 2021)
Footnotes
  1. ^Van Oven M, Van Geystelen A, Kayser M, Decorte R, Larmuseau HD (2014). "Seeing the wood for the trees: a minimal reference phylogeny for the human Y chromosome".Human Mutation.35 (2):187–91.doi:10.1002/humu.22468.PMID 24166809.S2CID 23291764.
  2. ^International Society of Genetic Genealogy (ISOGG; 2015),Y-DNA Haplogroup Tree 2015. (Access date: 1 February 2015.)
  3. ^Haplogroup A0-T is also known as A-L1085 (and previously as A0'1'2'3'4).
  4. ^Haplogroup A1 is also known as A1'2'3'4.
  5. ^ F-Y27277, sometimes known as F2'4, is both the parent clade of F2 and F4 and a child of F-M89.
  6. ^Haplogroup LT (L298/P326) is also known as Haplogroup K1.
  7. ^Between 2002 and 2008,Haplogroup T-M184 was known as "Haplogroup K2". That name has since been re-assigned toK-M526, the sibling of Haplogroup LT.
  8. ^ Haplogroup K2b (M1221/P331/PF5911) is also known as Haplogroup MPS.
  9. ^ Haplogroup K2b1 (P397/P399) is also known as Haplogroup MS, but has a broader and more complex internal structure.
  10. ^ Haplogroup P (P295) is also klnown as K2b2.
  11. ^K-M2313*, which as yet has no phylogenetic name, has been documented in two living individuals, who have ethnic ties to India and South East Asia. In addition, K-Y28299, which appears to be a primary branch of K-M2313, has been found in three living individuals from India. See: Poznikop. cit.;YFull YTree v5.08, 2017, "K-M2335", and;PhyloTree, 2017, "Details of the Y-SNP markers included in the minimal Y tree" (Access date of these pages: 9 December 2017)
  12. ^ Haplogroup S, as of 2017, is also known as K2b1a. (Previously the name Haplogroup S was assigned to K2b1a4.)
  13. ^ Haplogroup M, as of 2017, is also known as K2b1b. (Previously the name Haplogroup M was assigned to K2b1d.)

References

[edit]
  1. ^abISOGG, 2015 "Y-DNA Haplogroup C and its Subclades – 2015" (15 September 2015).
  2. ^abcdefghiKarmin, Monika; Saag, Lauri; Vicente, Mário; Sayres, Melissa A. Wilson; Järve, Mari; Talas, Ulvi Gerst; Rootsi, Siiri; Ilumäe, Anne-Mai; Mägi, Reedik; Mitt, Mario; Pagani, Luca; Puurand, Tarmo; Faltyskova, Zuzana; Clemente, Florian; Cardona, Alexia (1 April 2015)."A recent bottleneck of Y chromosome diversity coincides with a global change in culture".Genome Research.25 (4):459–466.doi:10.1101/gr.186684.114.ISSN 1088-9051.PMC 4381518.PMID 25770088.
  3. ^abPoznik GD, Xue Y, Mendez FL, et al. (June 2016)."Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences".Nature Genetics.48 (6):593–599.doi:10.1038/ng.3559.PMC 4884158.PMID 27111036.
  4. ^abcdefghijklmnopqrstuvwxyzaaabacadaeafagahaiajakalamanaoapaqarasatauavawaxayazbabbbcbdbebfbgbhbibjbkblbmbnbobpbqbrbsbtbubvbwbxbybzcacbcccdcecfcgchcicjckclcmcncocpcqcrcsctcucvcwcxcyczdadbdcdddedfdgdhdidjdkdldmdndodpdqdrdsdtdudvdwdxdydzeaebecedeeefegeheiejekelemeneoepeqereseteuevewexeyezfafbfcfdfefffgfhfifjfkflfmfnfofpfqfrfsftfufvfwfxfyfzgagbgcgdgegfYFull Haplogroup YTree v7.02.01 as of 15 March 2019
  5. ^" (07 January 2022).
  6. ^abcdefghijklmnopqXue Y, Zerjal T, Bao W, et al. (April 2006)."Male demography in East Asia: a north-south contrast in human population expansion times".Genetics.172 (4):2431–9.doi:10.1534/genetics.105.054270.PMC 1456369.PMID 16489223.
  7. ^abcdefKarafet T, Xu L, Du R, et al. (September 2001)."Paternal population history of East Asia: sources, patterns, and microevolutionary processes".Am. J. Hum. Genet.69 (3):615–28.doi:10.1086/323299.PMC 1235490.PMID 11481588.
  8. ^abcdZhong H, Shi H, Qi XB, Duan ZY, Tan PP, Jin L, Su B, Ma RZ (January 2011)."Extended Y Chromosome Investigation Suggests Postglacial Migrations of Modern Humans into East Asia via the Northern Route".Molecular Biology and Evolution.28 (1):717–727.doi:10.1093/molbev/msq247.PMID 20837606.
  9. ^abKarafet TM, Osipova LP, Gubina MA, Posukh OL, Zegura SL, Hammer MF (December 2002)."High levels of Y-chromosome differentiation among native Siberian populations and the genetic signature of a boreal hunter-gatherer way of life".Hum. Biol.74 (6):761–89.doi:10.1353/hub.2003.0006.PMID 12617488.S2CID 9443804.
  10. ^abcPakendorf B, Novgorodov IN, Osakovskij VL, Stoneking M (July 2007). "Mating patterns amongst Siberian reindeer herders: inferences from mtDNA and Y-chromosomal analyses".Am. J. Phys. Anthropol.133 (3):1013–27.doi:10.1002/ajpa.20590.PMID 17492671.
  11. ^abcdeE. V. Balanovska, Y. V. Bogunov, E. N. Kamenshikova,et al., "Demographic and Genetic Portraits of the Ulchi Population." ISSN 1022-7954,Russian Journal of Genetics, 2018, Vol. 54, No. 10, pp. 1245–1253.doi:10.1134/S1022795418100046
  12. ^abcdefghiTajima, Atsushi; Hayami, Masanori; Tokunaga, Katsushi; Juji, T; Matsuo, M; Marzuki, S; Omoto, K; Horai, S (2004)."Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages".Journal of Human Genetics.49 (4):187–193.doi:10.1007/s10038-004-0131-x.PMID 14997363.
  13. ^ab"KHARKOV, Vladimir Nikolaevich, "СТРУКТУРА И ФИЛОГЕОГРАФИЯ ГЕНОФОНДА КОРЕННОГО НАСЕЛЕНИЯ СИБИРИ ПО МАРКЕРАМ Y-ХРОМОСОМЫ,"Genetika 03.02.07 and "АВТОРЕФЕРАТ диссертации на соискание учёной степени доктора биологических наук, Tomsk 2012"(PDF).
  14. ^abcdefghLell JT, Sukernik RI, Starikovskaya YB, et al. (January 2002)."The dual origin and Siberian affinities of Native American Y chromosomes".Am. J. Hum. Genet.70 (1):192–206.doi:10.1086/338457.PMC 384887.PMID 11731934.
  15. ^abcdefghijklmnopqHammer MF, Karafet TM, Park H, et al. (2006)."Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes".J. Hum. Genet.51 (1):47–58.doi:10.1007/s10038-005-0322-0.PMID 16328082.
  16. ^abGuang‐Lin He, Meng‐Ge Wang, Xing Zou, Hui‐Yuan Yeh, Chang‐Hui Liu, Chao Liu, Gang Chen, and Chuan‐Chao Wang, "Extensive ethnolinguistic diversity at the crossroads of North China and South Siberia reflects multiple sources of genetic diversity."J. Syst. Evol. 00 (0): 1–21, 2022. doi: 10.1111/jse.12827
  17. ^abcdefghijklmnopqrstuvwxyzaaabacadaeafagahaiajakalamanaoapaqarasatauavawaxayazbabbbcbdbebfbgbhbibjbkblbmbnbobpbqbrbsbtbubvbwbxbybzcacbcccdcecfcgchcicjckclcmcncocpcqcrcsctcucvcwcxcyczdadbdcdddedfdgdhdidjdkdldmdndodpdqdrdsdtdudvdwdxdydzeaebecPhylogenetic tree of Haplogroup C2-M217 at 23mofang
  18. ^abcdefghijklmnopqrstuvDi Cristofaro J, Pennarun E, Mazières S, Myres NM, Lin AA, et al. (2013)."Afghan Hindu Kush: Where Eurasian Sub-Continent Gene Flows Converge".PLOS ONE.8 (10): e76748.Bibcode:2013PLoSO...876748D.doi:10.1371/journal.pone.0076748.PMC 3799995.PMID 24204668.
  19. ^abcdeZegura SL, Karafet TM, Zhivotovsky LA, Hammer MF (January 2004)."High-resolution SNPs and microsatellite haplotypes point to a single, recent entry of Native American Y chromosomes into the Americas".Mol. Biol. Evol.21 (1):164–75.doi:10.1093/molbev/msh009.PMID 14595095.
  20. ^abcdSengupta S, Zhivotovsky LA, King R, 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".Am. J. Hum. Genet.78 (2):202–21.doi:10.1086/499411.PMC 1380230.PMID 16400607.
  21. ^abcPakendorf B, Novgorodov IN, Osakovskij VL, Danilova AP, Protod'jakonov AP, Stoneking M (October 2006). "Investigating the effects of prehistoric migrations in Siberia: genetic variation and the origins of Yakuts".Hum. Genet.120 (3):334–53.doi:10.1007/s00439-006-0213-2.PMID 16845541.S2CID 31651899.
  22. ^Wang Chi-zao,Shi Mei-sen, and Li Hui (2018), "The Origin of Daur from the Perspective of Molecular Anthropology" [分子人类学视野下的达斡尔族族源研究],Journal of North Minzu University (Philosophy and Social Science Edition) [北方民族大学学报(哲学社会科学版)], No. 5, Gen. No. 143.
  23. ^abcdefghijklmnopqrstuvwxyzaaabacadaeafagahaiajakalamanaoapZhong, Hua; Shi, Hong; Xue-, XB; Qi, Bin; Jin, L; Ma, RZ; Su, B (2010)."Global distribution of Y-chromosome haplogroup C reveals the prehistoric migration routes of African exodus and early settlement in East Asia".Journal of Human Genetics.55 (7):428–35.doi:10.1038/jhg.2010.40.PMID 20448651.
  24. ^A brief introduction to patrilineal haplogroups and national ancestry composition of the Manchu population in China by 23mofang (2021/1/21)
  25. ^Chen J, He G, Ren Z, Wang Q, Liu Y, Zhang H, Yang M, Zhang H, Ji J, Zhao J, Guo J, Zhu K, Yang X, Wang R, Ma H, Wang C-C, and Huang J (2021), "Genomic Insights Into the Admixture History of Mongolic- and Tungusic-Speaking Populations From Southwestern East Asia."Front. Genet. 12:685285. doi: 10.3389/fgene.2021.685285
  26. ^A brief introduction to the patrilineal haplogroups and national ancestry composition of the Tujia people in China by 23mofang (2021/1/21)
  27. ^abXia, Zi-Yang; Yan, Shi; Wang, Chuan-Chao; et al. (2019),Inland-coastal bifurcation of southern East Asians revealed by Hmong-Mien genomic history,doi:10.1101/730903,S2CID 202028061
  28. ^Guo, Y.; Xia, Z.; Cui, W.; Chen, C.; Jin, X.; Zhu, B. Joint Genetic Analyses of Mitochondrial and Y-Chromosome Molecular Markers for a Population from Northwest China.Genes 2020, 11, 564. doi:10.3390/genes11050564
  29. ^abcdeHaber, Marc; Platt, Daniel E.; Ashrafian Bonab, Maziar; Youhanna, Sonia C.; Soria-Hernanz, David F.; Martínez-Cruz, Begoña; Douaihy, Bouchra; Ghassibe-Sabbagh, Michella; et al. (28 March 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.hdl:10230/23537.PMC 3314501.PMID 22470552.
  30. ^abcdefghiEnrico Macholdt, Leonardo Arias, Nguyen Thuy Duong,et al., "The paternal and maternal genetic history of Vietnamese populations."European Journal of Human Genetics (2020) 28:636–645.https://doi.org/10.1038/s41431-019-0557-4
  31. ^abcdefMalyarchuk B, Derenko M, Denisova G, et al. (2010)."Phylogeography of the Y-chromosome haplogroup C in northern Eurasia".Annals of Human Genetics.74 (6):539–546.doi:10.1111/j.1469-1809.2010.00601.x.PMID 20726964.S2CID 40763875.
  32. ^abcMarchani EE, Watkins WS, Bulayeva K, Harpending HC, Jorde LB (2008)."Culture creates genetic structure in the Caucasus: autosomal, mitochondrial, and Y-chromosomal variation in Daghestan".BMC Genet.9: 47.doi:10.1186/1471-2156-9-47.PMC 2488347.PMID 18637195.
  33. ^abcLIU Shuhu, NIZAM Yilihamu, RABIYAMU Bake, ABDUKERAM Bupatima, and DOLKUN Matyusup, "A study of genetic diversity of three isolated populations in Xinjiang using Y-SNP."Acta Anthropologica Sinica, 2018, 37(1): 146-156.
  34. ^abLu Yan (2011), "Genetic Mixture of Populations in Western China." Shanghai: Fudan University, 2011: 1-84. (Doctoral dissertation in Chinese: 陆艳, "中国西部人群的遗传混合", 上海:复旦大学,2011: 1-84.)
  35. ^abcdeKim SH, Kim KC, Shin DJ, et al. (2011)."High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea".Investig Genet.2 (1): 10.doi:10.1186/2041-2223-2-10.PMC 3087676.PMID 21463511.
  36. ^abcdeBayazit Yunusbayev, Mait Metspalu, Mari Järve,et al. (2012), "The Caucasus as an Asymmetric Semipermeable Barrier to Ancient Human Migrations."Molecular Biology and Evolution 29(1):359–365. doi:10.1093/molbev/msr221 Advance Access publication 13 September 2011.
  37. ^abNasidze2004a
  38. ^abNonaka I, Minaguchi K, Takezaki N (2007). "Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms".Annals of Human Genetics.71 (4):480–495.doi:10.1111/j.1469-1809.2006.00343.x.hdl:10130/491.PMID 17274803.S2CID 1041367.
  39. ^abSae Naitoh, Iku Kasahara-Nonaka, Kiyoshi Minaguchi, and Phrabhakaran Nambiar, "Assignment of Y-chromosomal SNPs found in Japanese population to Y-chromosomal haplogroup tree."Journal of Human Genetics (2013) 58, 195–201; doi:10.1038/jhg.2012.159; published online 7 February 2013.
  40. ^abSato Y, Shinka T, Ewis AA, Yamauchi A, Iwamoto T, Nakahori Y (2014)."Overview of genetic variation in the Y chromosome of modern Japanese males".Anthropological Science.122 (3):131–136.doi:10.1537/ase.140709.
  41. ^https://www.medgen-journal.ru/jour/article/view/2212/0?locale=en_US The structure of the gene pool of Tomsk Tatars according to Y-chromosome markers
  42. ^abBoris Malyarchuk, Miroslava Derenko, Galina Denisova, Sanj Khoyt, Marcin Wozniak,Tomasz Grzybowski, and Ilya Zakharov, "Y-chromosome diversity in the Kalmyks at the ethnical and tribal levels."Journal of Human Genetics (2013) 58, 804–811; doi:10.1038/jhg.2013.108; published online 17 October 2013.
  43. ^abcdefghiNatalia Balinova, Helen Post, Alena Kushniarevich, Siiri Rootsi,et al. (2019), "Y-chromosomal analysis of clan structure of Kalmyks, the only European Mongol people, and their relationship to Oirat-Mongols of Inner Asia."European Journal of Human Genetics.https://doi.org/10.1038/s41431-019-0399-0
  44. ^abWells RS, Yuldasheva N, Ruzibakiev R, et al. (August 2001)."The Eurasian heartland: a continental perspective on Y-chromosome diversity".Proc. Natl. Acad. Sci. U.S.A.98 (18):10244–9.Bibcode:2001PNAS...9810244W.doi:10.1073/pnas.171305098.PMC 56946.PMID 11526236.
  45. ^Mao, Xiaowei; Zhang, Hucai; Qiao, Shiyu; Liu, Yichen; Chang, Fengqin; Xie, Ping; Zhang, Ming; Wang, Tianyi; Li, Mian; Cao, Peng; Yang, Ruowei; Liu, Feng; Dai, Qingyan; Feng, Xiaotian; Ping, Wanjing (10 June 2021)."The deep population history of northern East Asia from the Late Pleistocene to the Holocene".Cell.184 (12): 3256–3266.e13.doi:10.1016/j.cell.2021.04.040.ISSN 0092-8674.PMID 34048699.
  46. ^Kim, Kijeong; Brenner, Charles H.; Mair, Victor H.; Lee, Kwang-Ho; Kim, Jae-Hyun; Gelegdorj, Eregzen; Batbold, Natsag; Song, Yi-Chung; Yun, Hyeung-Won; Chang, Eun-Jeong; Lkhagvasuren, Gavaachimed; Bazarragchaa, Munkhtsetseg; Park, Ae-Ja; Lim, Inja; Hong, Yun-Pyo (2010)."A western Eurasian male is found in 2000-year-old elite Xiongnu cemetery in Northeast Mongolia".American Journal of Physical Anthropology.142 (3):429–440.doi:10.1002/ajpa.21242.ISSN 1096-8644.
  47. ^abcJeong, Choongwon; Wang, Ke; Wilkin, Shevan; Taylor, William Timothy Treal; Miller, Bryan K.; Bemmann, Jan H.; Stahl, Raphaela; Chiovelli, Chelsea; Knolle, Florian; Ulziibayar, Sodnom; Khatanbaatar, Dorjpurev; Erdenebaatar, Diimaajav; Erdenebat, Ulambayar; Ochir, Ayudai; Ankhsanaa, Ganbold (November 2020)."A Dynamic 6,000-Year Genetic History of Eurasia's Eastern Steppe".Cell.183 (4): 890–904.e29.doi:10.1016/j.cell.2020.10.015.hdl:21.11116/0000-0007-77BF-D.ISSN 0092-8674. Archived fromthe original on 28 September 2024.
  48. ^Lee, Joo-Yup; Kuang, Shuntu (18 October 2017)."A Comparative Analysis of Chinese Historical Sources and y-dna Studies with Regard to the Early and Medieval Turkic Peoples".Inner Asia.19 (2):197–239.doi:10.1163/22105018-12340089.ISSN 2210-5018.
  49. ^Kornienko, I. V.; Faleeva, T. G.; Schurr, T. G.; Aramova, O. Yu.; Ochir-Goryaeva, M. A.; Batieva, E. F.; Vdovchenkov, E. V.; Moshkov, N. E.; Kukanova, V. V.; Ivanov, I. N.; Sidorenko, Yu. S.; Tatarinova, T. V. (1 April 2021)."Y-Chromosome Haplogroup Diversity in Khazar Burials from Southern Russia".Russian Journal of Genetics.57 (4):477–488.doi:10.1134/S1022795421040049.ISSN 1608-3369.
  50. ^Damgaard, Peter de Barros; Marchi, Nina; Rasmussen, Simon; Peyrot, Michaël; Renaud, Gabriel; Korneliussen, Thorfinn; Moreno-Mayar, J. Víctor; Pedersen, Mikkel Winther; Goldberg, Amy; Usmanova, Emma; Baimukhanov, Nurbol; Loman, Valeriy; Hedeager, Lotte; Pedersen, Anders Gorm; Nielsen, Kasper (May 2018)."137 ancient human genomes from across the Eurasian steppes".Nature.557 (7705):369–374.doi:10.1038/s41586-018-0094-2.ISSN 1476-4687.
  51. ^Zerjal T, Xue Y, Bertorelle G, et al. (March 2003)."The genetic legacy of the Mongols".Am. J. Hum. Genet.72 (3):717–21.doi:10.1086/367774.PMC 1180246.PMID 12592608.as PDFArchived 10 July 2012 at theWayback Machine
  52. ^Xue, Y; Zerjal, T; Bao, W; Zhu, S; Lim, SK; Shu, Q; Xu, J; Du, R; Fu, S; Li, P; Yang, H; Tyler-Smith, C (28 September 2015)."Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia".Am. J. Hum. Genet.77 (6):1112–6.doi:10.1086/498583.PMC 1285168.PMID 16380921.
  53. ^Xue, Y; Zerjal, T; Bao, W; Zhu, S; Lim, SK; Shu, Q; Xu, J; Du, R; Fu, S; Li, P; Yang, H; Tyler-Smith, C (2005)."Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia".The American Journal of Human Genetics.77 (6):1112–1116.doi:10.1086/498583.PMC 1285168.PMID 16380921.
  54. ^Xue, Y.; Zerjal, T.; Bao, W.; Zhu, S.; Lim, S. K.; Shu, Q.; Xu, J.; Du, R.; Fu, S.; Li, P.; Yang, H.; Tyler-Smith, C. (December 2005)."Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia".Am J Hum Genet.77 (6):1112–1116.doi:10.1086/498583.PMC 1285168.PMID 16380921.
  55. ^Yan, S.; Tachibana, H.; Wei, LH (2015)."Y chromosome of Aisin Gioro, the imperial house of the Qing dynasty".J Hum Genet.60 (6):295–298.arXiv:1412.6274.doi:10.1038/jhg.2015.28.PMID 25833470.S2CID 7505563.
  56. ^abWei, Ryan Lan-Hai; Yan, Shi; Yu, Ge; Huang, Yun-Zhi (November 2016). "Genetic trail for the early migrations of Aisin Gioro, the imperial house of the Qing dynasty".Journal of Human Genetics.62 (3):407–411.doi:10.1038/jhg.2016.142.PMID 27853133.S2CID 7685248.
  57. ^Wei, Lan-Hai; Yan, Shi; Lu, Yan; Wen, Shao-Qing; Huang, Yun-Zhi; Wang, Ling-Xiang; Li, Shi-Lin; Yang, Ya-Jun; Wang, Xiao-Feng; Zhang, Chao; Xu, Shu-Hua; Yao, Da-Li; Jin, Li; Li, Hui (22 January 2018)."Whole-sequence analysis indicates that the Y chromosome C2*-Star Cluster traces back to ordinary Mongols, rather than Genghis Khan".European Journal of Human Genetics.26 (2):230–237.doi:10.1038/s41431-017-0012-3.PMC 5839053.PMID 29358612.
  58. ^Abilev, Serikbai; Malyarchuk, Boris; Derenko, Miroslava; Wozniak, Marcin; Grzybowski, Tomasz; Zakharov, Ilya (2012)."The Y-chromosome C3* star-cluster attributed to Genghis Khan's descendants is present at high frequency in the Kerey clan from Kazakhstan".Human Biology.84 (1, Article 12):79–89.doi:10.3378/027.084.0106.PMID 22452430.S2CID 46684406.
  59. ^Wen, Shao-Qing; Yao, Hong-Bing; Du, Pan-Xin; Wei, Lan-Hai; Tong, Xin-Zhu; Wang, Ling-Xiang; Wang, Chuan-Chao; Zhou, Bo-Yan; Shi, Mei-Sen; Zhabagin, Maxat; Wang, Jiucun (August 2019)."Molecular genealogy of Tusi Lu's family reveals their paternal relationship with Jochi, Genghis Khan's eldest son".Journal of Human Genetics.64 (8):815–820.doi:10.1038/s10038-019-0618-0.ISSN 1434-5161.PMID 31164702.S2CID 174810181.
  60. ^Redd AJ, Roberts-Thomson J, Karafet T, et al. (April 2002)."Gene flow from the Indian subcontinent to Australia: evidence from the Y chromosome".Curr. Biol.12 (8):673–7.Bibcode:2002CBio...12..673R.doi:10.1016/S0960-9822(02)00789-3.PMID 11967156.S2CID 7752658.as PDFArchived 28 November 2007 at theWayback Machine
  61. ^Mao, Xiaowei; Zhang, Hucai; Qiao, Shiyu; Liu, Yichen; Chang, Fengqin; Xie, Ping; Zhang, Ming; Wang, Tianyi; Li, Mian; Cao, Peng; Yang, Ruowei; Liu, Feng; Dai, Qingyan; Feng, Xiaotian; Ping, Wanjing (June 2021)."The deep population history of northern East Asia from the Late Pleistocene to the Holocene".Cell.184 (12): 3256–3266.e13.doi:10.1016/j.cell.2021.04.040.ISSN 0092-8674.PMID 34048699.
  62. ^abcdefghijklmnHaplogroup C-M217 on Discover by FamilyTreeDNA
  63. ^"C-Cts4660单倍群详情".
  64. ^Phylogenetic tree of Haplogroup O-F175 at TheYtree
  65. ^abcLippold S, Xu H, Ko A, Li M, Renaud G, Butthof A, Schröder R, Stoneking M (2014)."Human paternal and maternal demographic histories: insights from high-resolution Y chromosome and mtDNA sequences".Investigative Genetics.2014 (5): 13.doi:10.1186/2041-2223-5-13.PMC 4174254.PMID 25254093.
  66. ^abcdeKarafet, Tatiana M.; Osipova, Ludmila P.; Savina, Olga V.; Hallmark, Brian; Hammer, Michael F. (November 2018)."Siberian genetic diversity reveals complex origins of the Samoyedic‐speaking populations".American Journal of Human Biology.30 (6).doi:10.1002/ajhb.23194.ISSN 1042-0533.
  67. ^Yan S, Wang CC, Zheng HX, Wang W, Qin ZD, et al. (2014)."Y Chromosomes of 40% Chinese Descend from Three Neolithic Super-Grandfathers".PLOS ONE.9 (8): e105691.arXiv:1310.3897.Bibcode:2014PLoSO...9j5691Y.doi:10.1371/journal.pone.0105691.PMC 4149484.PMID 25170956.
  68. ^Malyarchuk, Boris A; Derenko, Miroslava; Denisova, Galina; Woźniak, Marcin; Rogalla, Urszula; Dambueva, Irina; Grzybowski, Tomasz (June 2016)."Y chromosome haplotype diversity in Mongolic-speaking populations and gene conversion at the duplicated STR DYS385a,b in haplogroup C3-M407".Journal of Human Genetics.61 (6):491–496.doi:10.1038/jhg.2016.14.ISSN 1434-5161.
  69. ^Kharkov, V. N.; Khamina, K. V.; Medvedeva, O. F.; Simonova, K. V.; Eremina, E. R.; Stepanov, V. A. (February 2014)."Gene pool of Buryats: Clinal variability and territorial subdivision based on data of Y-chromosome markers".Russian Journal of Genetics.50 (2):180–190.doi:10.1134/S1022795413110082.ISSN 1022-7954.
  70. ^abcdefE. E. Ashirbekov, D. M. Botbaev, A. M. Belkozhaev, A. O. Abayldaev, A. S. Neupokoeva, J. E. Mukhataev, B. Alzhanuly, D. A. Sharafutdinova, D. D. Mukushkina, M. B. Rakhymgozhin, A. K. Khanseitova, S. A. Limborska, and N. A. Aytkhozhina, "Distribution of Y-Chromosome Haplogroups of the Kazakh from the South Kazakhstan, Zhambyl, and Almaty Regions." Reports of the National Academy of Sciences of the Republic of Kazakhstan, ISSN 2224-5227, Volume 6, Number 316 (2017), 85 – 95.
  71. ^abPark, Jin; Lee, Young; Kim, Young; -1#Myung, Hwan Na; et al. (2013). "Y-SNP miniplexes for East Asian Y-chromosomal haplogroup determination in degraded DNA".Forensic Science International: Genetics.7 (1):75–81.doi:10.1016/j.fsigen.2012.06.014.PMID 22818129.{{cite journal}}: CS1 maint: numeric names: authors list (link)
  72. ^Yan, Shi; Tachibana, Harumasa; Wei, Lan-Hai; Yu, Ge; Wen, Shao-Qing; Wang, Chuan-Chao (June 2015). "Y chromosome of Aisin Gioro, the imperial house of the Qing dynasty".Journal of Human Genetics.60 (6):295–8.arXiv:1412.6274.doi:10.1038/jhg.2015.28.PMID 25833470.S2CID 7505563.
  73. ^ab"Did you know DNA was used to uncover the origin of the House of Aisin Gioro?".Did You Know DNA... 14 November 2016. Retrieved5 November 2020.
  74. ^Xue, Yali; Zerjal, Tatiana; Bao, Weidong; Zhu, Suling; Lim, Si-Keun; Shu, Qunfang; Xu, Jiujin; Du, Ruofu; Fu, Songbin; Li, Pu; Yang, Huanming; Tyler-Smith, Chris (2005)."Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia".The American Journal of Human Genetics.77 (6):1112–1116.doi:10.1086/498583.PMC 1285168.PMID 16380921.
  75. ^"Asian Ancestry based on Studies of Y-DNA Variation: Part 3. Recent demographics and ancestry of the male East Asians – Empires and Dynasties".Genebase Tutorials. Archived fromthe original on 25 November 2013.
  76. ^Wei, Ryan Lan-Hai; Yan, Shi; Yu, Ge; Huang, Yun-Zhi (November 2016)."Genetic trail for the early migrations of Aisin Gioro, the imperial house of the Qing dynasty".Journal of Human Genetics.62 (3). The Japan Society of Human Genetics:407–411.doi:10.1038/jhg.2016.142.PMID 27853133.S2CID 7685248.
  77. ^Yan, Shi; Tachibana, Harumasa; Wei, Lan-Hai; Yu, Ge; Wen, Shao-Qing; Wang, Chuan-Chao (June 2015)."Y chromosome of Aisin Gioro, the imperial house of the Qing dynasty".Journal of Human Genetics.60 (6). Nature Publishing Group on behalf of the Japan Society of Human Genetics (Japan):295–298.arXiv:1412.6274.doi:10.1038/jhg.2015.28.PMID 25833470.S2CID 7505563.
  78. ^Wang, Chi-Zao; Wei, Lan-Hai; Wang, Ling-Xiang; Wen, Shao-Qing; Yu, Xue-Er; Shi, Mei-Sen; Li, Hui (August 2019)."Relating Clans Ao and Aisin Gioro from northeast China by whole Y-chromosome sequencing".Journal of Human Genetics.64 (8). Japan Society of Human Genetics:775–780.doi:10.1038/s10038-019-0622-4.PMID 31148597.S2CID 171094135.
  79. ^abPille Hallast, Chiara Batini, Daniel Zadik,et al., "The Y-Chromosome Tree Bursts into Leaf: 13,000 High-Confidence SNPs Covering the Majority of Known Clades."Molecular Biology and Evolution doi:10.1093/molbev/msu327 Advance Access publication 2 December 2014.
  80. ^abcGayden T, Cadenas AM, Regueiro M, et al. (May 2007)."The Himalayas as a directional barrier to gene flow".Am. J. Hum. Genet.80 (5):884–94.doi:10.1086/516757.PMC 1852741.PMID 17436243. 2/77=2.6% C-M217 in a sample of the general population of Kathmandu.
  81. ^Fornarino S, Pala M, Battaglia V, et al. (2009)."Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation".BMC Evol. Biol.9 (1): 154.Bibcode:2009BMCEE...9..154F.doi:10.1186/1471-2148-9-154.PMC 2720951.PMID 19573232. 1/26=3.8% C-M217 in a sample of Hindu Indians from the Terai.
  82. ^abReddy BM, Langstieh BT, Kumar V, et al. (2007)."Austro-Asiatic tribes of Northeast India provide hitherto missing genetic link between South and Southeast Asia".PLOS ONE.2 (11): e1141.Bibcode:2007PLoSO...2.1141R.doi:10.1371/journal.pone.0001141.PMC 2065843.PMID 17989774. Haplogroup C-M217 in 8.5% of a sample of 71Garos and 7.7% of a pool of eight samples ofKhasians totalling 353 individuals
  83. ^Kivisild T, Rootsi S, Metspalu M, et al. (February 2003)."The genetic heritage of the earliest settlers persists both in Indian tribal and caste populations".Am. J. Hum. Genet.72 (2):313–32.doi:10.1086/346068.PMC 379225.PMID 12536373. C-M217 in 1/31=3.2% of a sample from West Bengal.
  84. ^Y-Chromosome Diversity in Modern Bulgarians: New Clues about Their Ancestry, Karachanak S, Grugni V, Fornarino S, Nesheva D, Al-Zahery N, et al. (2013) Retrieved Oct 2013.
  85. ^abcdKarafet, Tatiana M.; Hallmark, Brian; Cox, Murray P.; et al. (2010)."Major East–West Division Underlies Y Chromosome Stratification across Indonesia".Mol. Biol. Evol.27 (8):1833–1844.doi:10.1093/molbev/msq063.PMID 20207712.
  86. ^abKayser M, Brauer S, Cordaux R, Casto A, Lao O, Zhivotovsky LA, Moyse-Faurie C, Rutledge RB, Schiefenhoevel W, Gil D, Lin AA, Underhill PA, Oefner PJ, Trent RJ, Stoneking M (2006)."Melanesian and Asian Origins of Polynesians: mtDNA and Y Chromosome Gradients Across the Pacific".Molecular Biology and Evolution.23 (11):2234–2244.doi:10.1093/molbev/msl093.hdl:11858/00-001M-0000-0010-0145-0.PMID 16923821.
  87. ^abcTrejaut JA, Poloni ES, Yen JC, et al. (2014)."Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia".BMC Genetics.15: 77.doi:10.1186/1471-2156-15-77.PMC 4083334.PMID 24965575.
  88. ^Cai X, Qin Z, Wen B, Xu S, Wang Y, et al. (2011)."Human Migration through Bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum Revealed by Y Chromosomes".PLOS ONE.6 (8): e24282.Bibcode:2011PLoSO...624282C.doi:10.1371/journal.pone.0024282.PMC 3164178.PMID 21904623.
  89. ^Peng MS, He JD, Fan L, Liu J, Adeola AC, Wu SF, et al. (August 2014)."Retrieving Y chromosomal haplogroup trees using GWAS data".European Journal of Human Genetics.22 (8):1046–50.doi:10.1038/ejhg.2013.272.PMC 4350590.PMID 24281365.
  90. ^abBing Su, Li Jin, Peter Underhill, Jeremy Martinson, Nilmani Saha, Stephen T. McGarvey, Mark D. Shriver, Jiayou Chu, Peter Oefner, Ranajit Chakraborty, and Ranjan Deka, "Polynesian origins: Insights from the Y chromosome."PNAS (18 July 2000), vol. 97, no. 15, 8225–8228.
  91. ^Brunelli A, Kampuansai J, Seielstad M, Lomthaisong K, Kangwanpong D, Ghirotto S, et al. (2017)."Y chromosomal evidence on the origin of northern Thai people".PLOS ONE.12 (7): e0181935.Bibcode:2017PLoSO..1281935B.doi:10.1371/journal.pone.0181935.PMC 5524406.PMID 28742125.
  92. ^Nasidze I, Quinque D, Dupanloup I, Cordaux R, Kokshunova L, Stoneking M (December 2005). "Genetic evidence for the Mongolian ancestry of Kalmyks".Am. J. Phys. Anthropol.128 (4):846–54.doi:10.1002/ajpa.20159.PMID 16028228.
  93. ^abcdefghijklmnopqrstuvwxyzaaabacadaeafPhylogenetic tree of haplogroup C-M217 at TheYtree
  94. ^abcdefghijklmnopqrstuvwxyzaaabacadaeafagahaiajakalamanaoapaqarasatau"FamilyTreeDNA – Genetic Testing for Ancestry, Family History & Genealogy".www.familytreedna.com.
  95. ^abLan-Hai Wei, Yun-Zhi Huang, Shi Yan,et al., "Phylogeny of Y-chromosome haplogroup C3b-F1756, an important paternal lineage in Altaic-speaking populations."Journal of Human Genetics advance online publication, 1 June 2017;doi:10.1038/jhg.2017.60
  96. ^"C-TYT61432". 祖源树. 2024. Retrieved28 August 2024.
  97. ^Khar'kov VN, Stepanov VA, Medvedev OF, et al. (2008). "[The origin of Yakuts: analysis of Y-chromosome haplotypes]".Mol. Biol. (Mosk.) (in Russian).42 (2):226–37.PMID 18610830.
  98. ^abPeter de Barros Damgaard, Nina Marchi, Simon Rasmussen,et al. (2018), "137 ancient human genomes from across the Eurasian steppes."Nature, volume 557, pages 369–374 (2018).https://doi.org/10.1038/s41586-018-0094-2
  99. ^Lan-Hai Wei, Shi Yan, Ge Yu,et al. (2016), "Genetic trail for the early migrations of Aisin Gioro, the imperial house of the Qing dynasty."Journal of Human Genetics (2016), 1–5.doi:10.1038/jhg.2016.142
  100. ^abcdefghiWibhu Kutanan, Jatupol Kampuansai, Metawee Srikummool, Andrea Brunelli, Silvia Ghirotto, Leonardo Arias, Enrico Macholdt, Alexander Hübner, Roland Schröder, and Mark Stoneking, "Contrasting Paternal and Maternal Genetic Histories of Thai and Lao Populations."Mol. Biol. Evol. Advance Access publication 12 April 2019.doi:10.1093/molbev/msz083
  101. ^abcdefghWibhu Kutanan, Rasmi Shoocongdej, Metawee Srikummool,et al. (2020), "Cultural variation impacts paternal and maternal genetic lineages of the Hmong-Mien and Sino-Tibetan groups from Thailand."European Journal of Human Genetics.https://doi.org/10.1038/s41431-020-0693-x
  102. ^"C-F5477单倍群详情".
  103. ^"C-Mf10317单倍群详情".
  104. ^Underhill PA, Shen P, Lin AA, et al. (November 2000). "Y chromosome sequence variation and the history of human populations".Nat. Genet.26 (3):358–61.doi:10.1038/81685.PMID 11062480.S2CID 12893406.
  105. ^"C-Sk1037单倍群详情".
  106. ^"C-Mf1020单倍群详情".
  107. ^"C-Z45203单倍群详情".

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