Haplogroup G | |
---|---|
Possible time of origin | 35,700 YBP [1] |
Possible place of origin | East Asia |
Ancestor | M12'G |
Descendants | G1, G2, G3, G4 |
Defining mutations | 709, 4833, 5108 [2] |
In human mitochondrial genetics, Haplogroup G is a human mitochondrial DNA (mtDNA) haplogroup.
Haplogroup G is a descendant of haplogroup M. Haplogroup G is divided into subclades G1, G2, G3, and G4.
It is an East Asian haplogroup. [3] Today, haplogroup G is found at its highest frequency in indigenous populations of the lands surrounding the Sea of Okhotsk. [4] [5] Haplogroup G is one of the most common mtDNA haplogroups among modern Ainu, Siberian, Mongol, Tibetan and Central and North Asian Turkic peoples people (as well as among people of the prehistoric Jōmon culture in Hokkaidō). It is also found at a lower frequency among many other populations of East Asia, Central Asia, Bangladesh, Sri Lanka, and Nepal. [6] [7] [8] [9] However, unlike other mitochondrial DNA haplogroups typical of populations of northeastern Asia, such as haplogroup A, haplogroup C, and haplogroup D, haplogroup G has not been found among indigenous peoples of the Americas.
Population | Frequency | Count | Source | Subtypes |
---|---|---|---|---|
Itelmen | 0.681 | 47 | Starikovskaya 2005 | G1=32 |
Koryak | 0.419 | 155 | Starikovskaya 2005 | G1=65 |
Chuvantsi (Markovo, Chukotka) | 0.281 | 32 | Volodko 2008 | G1=9 |
Negidal | 0.273 | 33 | Starikovskaya 2005 | G1=9 |
Tharu (Chitwan, Nepal) | 0.233 | 133 | Fornarino 2009 | G2a=19, G(xG2a)=12 |
Kazakh (Uzbekistan/Kyrgyzstan) | 0.200 | 20 | Comas 2004 | G2a=4 |
Ainu | 0.196 | 51 | [10] | G1=8, G2=2 |
Tibetan (Lhasa, Tibet) | 0.182 | 44 | Ji 2012 | G2a=3, G3b=3, G2(xG2a)=2 |
Mongolian (Ulan Bator) | 0.170 | 47 | Jin 2009 | G2a=5, G(xG1a, G2, G3)=2, G3=1 |
Korean (Arun Banner) | 0.167 | 48 | Kong 2003 | G2(xG2a)=3, G2a=3, G1a=1, G3=1 |
Tibetan (Nyingchi, Tibet) | 0.167 | 24 | Ji 2012 | G=4 |
Oirat Mongol (Xinjiang) | 0.163 | 49 | Yao 2004 | G2a=3, G2(xG2a)=3, G(xG1a, G2, G3)=2 |
Tibetan (Shannan, Tibet) | 0.158 | 19 | Ji 2012 | G=3 |
Yukaghir (Lower Kolyma-Indigirka) | 0.146 | 82 | Volodko 2008 | G1=12 |
Kyrgyz (Talas) | 0.146 | 48 | Yao 2004 | G2a=7 |
Tibetan (Shannan, Tibet) | 0.145 | 55 | Ji 2012 | G2a=4, G2(xG2a)=3, G3b=1 |
Uyghur (Xinjiang) | 0.128 | 47 | Yao 2004 | G2a=5, G3=1 |
Tharu (Morang, Nepal) | 0.125 | 40 | Fornarino 2009 | G2a=4, G(xG2a)=1 |
Japanese (Gifu) | 0.116 | 1617 | Fuku 2007 | G=188 |
Ulch | 0.115 | 87 | Starikovskaya 2005 | G1=9, G2=1 |
Oroqen (Oroqen Autonomous Banner) | 0.114 | 44 | Kong 2003 | G(xG1a, G2, G3)=5 |
Tibetan (Qinghai) | 0.107 | 56 | Wen 2004 | G(xG2, G3)=2, G2a=2, G2(xG2a)=1, G3=1 |
Mongolian (Ulan Bator) | 0.106 | 47 | Derenko 2007 | G2a=4, G1=1 |
Tuvan | 0.105 | 95 | Starikovskaya 2005 | G2=6, G3=4 |
Huatou Yao (Fangcheng, Guangxi) | 0.105 | 19 | [ citation needed ] | G2=2 |
Japanese | 0.104 | 211 | Maruyama 2003 | G4a=12, G2a=6, G4b=2, G2(xG2a)=1, G(xG2, G4a, G4b)=1 |
Tibetan (Chamdo, Tibet) | 0.103 | 29 | Ji 2012 | G3b=2, G2a=1 |
Tibetan (Shigatse, Tibet) | 0.103 | 29 | Ji 2012 | G2a=2, G2(xG2a)=1 |
Korean (South Korea) | 0.103 | 185 | Jin 2009 | G2(xG2a)=7, G2a=6, G3=4, G1a=1, G(xG1a, G2, G3)=1 |
Japanese (Tokyo) | 0.102 | 118 | Zheng 2011 | G=12 |
Khamnigan (Buryatia) | 0.101 | 99 | Derenko 2007 | G2a=9, G3=1 |
Han (Beijing) | 0.100 | 40 | Jin 2009 | G2a=2, G2(xG2a)=1, G(xG1a, G2, G3)=1 |
Manchurian | 0.100 | 40 | Jin 2009 | G1a=3, G2a=1 |
Tu Yao (Hezhou, Guangxi) | 0.098 | 41 | [ citation needed ] | G2=4 |
Japanese (Tōkai) | 0.096 | 282 | Umetsu 2005 | G1a=13, G(xG1a, G1b)=12, G1b=2 |
Even (Eveno-Bytantaysky & Momsky) | 0.095 | 105 | Fedorova 2013 | G1b=9, G2a(xG2a5)=1 |
Barghut (Hulunbuir) | 0.094 | 149 | Derenko 2012 | G2=13, G3=1 |
Chukchi | 0.091 | 66 | Starikovskaya 2005 | G1=6 |
Xiban Yao (Fangcheng, Guangxi) | 0.091 | 11 | [ citation needed ] | G2=1 |
Daur (Evenk Autonomous Banner) | 0.089 | 45 | Kong 2003 | G1a=2, G2a=2 |
Hui (Xinjiang) | 0.089 | 45 | Yao 2004 | G2a=2, G1a=1, G(xG1a, G2, G3)=1 |
Japanese (Hokkaidō) | 0.088 | 217 | Asari 2007 | G1a=11, G(xG1a, G1b)=7, G1b=1 |
Evenk (New Barag Left Banner) | 0.085 | 47 | Kong 2003 | G(xG1a, G2, G3)=4 |
Zhuang (Napo County, Guangxi) | 0.085 | 130 | [ citation needed ] | G2=8 G(xG2)=3 |
Pumi (Ninglang, Yunnan) | 0.083 | 36 | Wen 2004 | G(xG2, G3)=2, G3=1 |
Kalmyk (Kalmykia) | 0.082 | 110 | Derenko 2007 | G2a=7, G1=1, G(xG1, G2a, G3)=1 |
Buryat | 0.080 | 25 | Starikovskaya 2005 | G2=1, G3=1 |
Buryat | 0.079 | 126 | Kong 2003 | G2a=8, G2(xG2a)=2 |
Korean (South Korea) | 0.079 | 203 | Umetsu 2005 | G1a=9, G(xG1a, G1b)=7 |
Bai (Dali, Yunnan) | 0.074 | 68 | Wen 2004 | G2(xG2a)=5 |
Dargin (Dagestan) | 0.071 | 28 | Marchani 2008 | G=2 |
Uzbek (Xinjiang) | 0.069 | 58 | Yao 2004 | G2a=2, G3=1, G(xG1a, G2, G3)=1 |
Chinese (Shenyang, Liaoning) | 0.069 | 160 | Umetsu 2005 | G(xG1a, G1b)=8, G1a=3 |
Korean (South Korea) | 0.068 | 103 | Derenko 2007 | G2a=3, G1=2, G3=2 |
Korean (Seoul National University Hospital) | 0.068 | 633 | Fuku 2007 | G=43 |
Yakut (northern Yakutia) | 0.068 | 148 | Fedorova 2013 | G2a5=6, G2a(xG2a5)=2, G1b=2 |
Chukchi (Anadyr) | 0.067 | 15 | Derenko 2007 | G1=1 |
Naxi (Lijiang, Yunnan) | 0.067 | 45 | Wen 2004 | G(xG2, G3)=3 |
Tujia (Yongshun, Hunan) | 0.067 | 30 | Wen 2004 | G(xG2, G3)=1, G2(xG2a)=1 |
Tuvinian | 0.067 | 105 | Derenko 2007 | G2a=4, G1=2, G3=1 |
Gelao (Daozhen County, Guizhou) | 0.065 | 31 | [ citation needed ] | G2a=2 |
Mien (Shangsi, Guangxi) | 0.063 | 32 | [ citation needed ] | G2=2 |
Korean (South Korea) | 0.061 | 261 | Kim 2008 | G(xG2)=11, G2=5 |
Mansi | 0.061 | 98 | Starikovskaya 2005 | G2=6 |
Japanese (Miyazaki) | 0.060 | 100 | Uchiyama 2007 | G4a=2, G1a=1, G1b=1, G2a1(xG2a1a)=1, G2a1a=1 |
Han (Beijing Normal University) | 0.058 | 121 | Zheng 2011 | G=7 |
Tibetan (Zhongdian, Yunnan) | 0.057 | 35 | Wen 2004 | G3=2 |
Kazakh (Xinjiang) | 0.057 | 53 | Yao 2004 | G1a=1, G2a=1, G(xG1a, G2, G3)=1 |
Altai Kizhi | 0.056 | 90 | Derenko 2007 | G1=4, G2a=1 |
Tibetan (Nyingchi, Tibet) | 0.056 | 54 | Ji 2012 | G2(xG2a)=1, G2a=1, G3b=1 |
Han (Denver, Colorado) | 0.055 | 73 | Zheng 2011 | G=4 |
Kazakh (Kazakhstan) | 0.055 | 55 | Yao 2004 | G2a=3 |
Japanese (Tōhoku) | 0.054 | 336 | Umetsu 2005 | G1a=13, G(xG1a, G1b)=5 |
Nivkh (northern Sakhalin) | 0.054 | 56 | Starikovskaya 2005 | G1=3 |
Karakalpak (Uzbekistan/Kyrgyzstan) | 0.050 | 20 | Comas 2004 | G2a=1 |
Kim Mun (Malipo, Yunnan) | 0.050 | 40 | [ citation needed ] | G2=2 |
Tajik (Uzbekistan/Kyrgyzstan) | 0.050 | 20 | Comas 2004 | G2a=1 |
Uzbek (Uzbekistan/Kyrgyzstan) | 0.050 | 40 | Comas 2004 | G2a=2 |
Yi (Shuangbai, Yunnan) | 0.050 | 40 | Wen 2004 | G(xG2, G3)=1, G2(xG2a)=1 |
Orok (Sakhalin) | 0.049 | 61 | Bermisheva 2005 | G=3 |
Gelao (Daozhen County, Guizhou) | 0.049 | 102 | [ citation needed ] | G(xG2, G3)=4, G2a1=1 |
Yakut (vicinity of Yakutsk) | 0.049 | 164 | Fedorova 2013 | G2a(xG2a5)=6, G2a5=2 |
Hmong (Jishou, Hunan) | 0.049 | 103 | [ citation needed ] | G3=2, G(xG2, G3)=2, G2=1 |
Vietnamese | 0.048 | 42 | Jin 2009 | G1a=1, G3=1 |
Japanese (northern Kyūshū) | 0.047 | 256 | Umetsu 2005 | G(xG1a, G1b)=9, G1a=3 |
Tujia (western Hunan) | 0.047 | 64 | Wen 2004 | G(xG2, G3)=1, G2(xG2a)=1, G3=1 |
Tajik (Tajikistan) | 0.045 | 44 | Derenko 2007 | G2a=1, G3=1 |
Yukaghir (Verkhnekolymsky & Nizhnekolymsky) | 0.045 | 22 | Fedorova 2013 | G1b=1 |
Hazara (North West Frontier Province & Balochistan) | 0.043 | 23 | Quintana-Murci 2004 | G=1 |
Mongol (New Barag Left Banner) | 0.042 | 48 | Kong 2003 | G2(xG2a)=2 |
Evenk (Krasnoyarsk) | 0.041 | 73 | Derenko 2007 | G2a=2, G1=1 |
Aini (Xishuangbanna, Yunnan) | 0.040 | 50 | Wen 2004 | G2a=2 |
Korean (northern China) | 0.039 | 51 | Jin 2009 | G2a=1, G2(xG2a)=1 |
Kumik (Dagestan) | 0.038 | 26 | Marchani 2008 | G=1 |
Lanten Yao (Tianlin, Guangxi) | 0.038 | 26 | [ citation needed ] | G2=1 |
Yakut (Vilyuy River basin) | 0.036 | 111 | Fedorova 2013 | G2a(xG2a5)=2, G2a5=1, G1b=1 |
Dong (Tianzhu County, Guizhou) | 0.036 | 28 | [ citation needed ] | G(xG1a, G2)=1 |
Cun (Hainan) | 0.033 | 30 | [ citation needed ] | G=1 |
Nu (Gongshan, Yunnan) | 0.033 | 30 | Wen 2004 | G(xG2, G3)=1 |
Lingao (Hainan) | 0.032 | 31 | [ citation needed ] | G=1 |
Yi (Luxi, Yunnan) | 0.032 | 31 | Wen 2004 | G(xG2, G3)=1 |
Pan Yao (Tianlin, Guangxi) | 0.031 | 32 | [ citation needed ] | G(xG2, G3)=1 |
Nogai (Dagestan) | 0.030 | 33 | Marchani 2008 | G=1 |
Han (Southwest China; pool of 44 Sichuan, 34 Chongqing, 33 Yunnan, & 26 Guizhou) | 0.029 | 137 | Ji 2012 | G1=3, G2=1 |
Han (southern California) | 0.028 | 390 | Ji 2012 | G=11 |
Telenghit (Altai Republic) | 0.028 | 71 | Derenko 2007 | G2a=2 |
Yakut (Yakutia) | 0.028 | 36 | Derenko 2007 | G2a=1 |
Hmong (Wenshan, Yunnan) | 0.026 | 39 | [ citation needed ] | G(xG2, G3)=1 |
Yakut | 0.026 | 117 | Kong 2003 | G2a=2, G1a=1 |
Evenk (Ust-Maysky, Oleneksky, and Zhigansky) | 0.024 | 125 | Fedorova 2013 | G1b=2, G2a(xG2a5)=1 |
Uzbek (Surkhandarya, Uzbekistan) | 0.024 | 42 | Quintana-Murci 2004 | G=1 |
Evenk (Buryatia) | 0.022 | 45 | Derenko 2007 | G3=1 |
Taiwanese (Taipei, Taiwan) | 0.022 | 91 | Umetsu 2005 | G(xG1a, G1b)=2 |
Han (Taiwan) | 0.021 | 1117 | Ji 2012 | G=24 |
Han (Xinjiang) | 0.021 | 47 | Yao 2004 | G2a=1 |
Kyrgyz (Sary-Tash) | 0.021 | 47 | Yao 2004 | G2a=1 |
Hindu (New Delhi) | 0.021 | 48 | Fornarino 2009 | G(xG2a)=1 |
Kazakh (Kosh-Agachsky, Altai Republic) | 0.020 | 98 | Derenko 2012 | G2=1, G3=1 |
Turkish (Anatolia, Turkey) | 0.020 | 50 | Quintana-Murci 2004 | G=1 |
Khanty | 0.019 | 106 | Pimenoff 2008 | G2=2 |
Uyghur (Kazakhstan) | 0.018 | 55 | Yao 2004 | G2(xG2a)=1 |
Khakassian (Khakassia) | 0.018 | 57 | Derenko 2007 | G3=1 |
Mansi | 0.016 | 63 | Pimenoff 2008 | G2=1 |
Okinawa | 0.015 | 326 | Umetsu 2005 | G(xG1a, G1b)=3, G1a=2 |
Persian (eastern Iran) | 0.012 | 82 | Derenko 2007 | G2a=1 |
Pakistani (Karachi, Pakistan) | 0.010 | 100 | Quintana-Murci 2004 | G=1 |
Li (Hainan) | 0.009 | 346 | [ citation needed ] | G=3 |
Dolgan (Anabarsky, Volochanka, Ust-Avam, and Dudinka) | 0.006 | 154 | Fedorova 2013 | G1b=1 |
Cham (Bình Thuận, Vietnam) | 0.006 | 168 | [ citation needed ] | G=1 |
Taiwan aborigines | 0.002 | 640 | [ citation needed ] | G=1 |
Dingban Yao (Mengla, Yunnan) | 0.000 | 10 | [ citation needed ] | - |
Yukaghir (Upper Kolyma) | 0.000 | 18 | Volodko 2008 | - |
Filipino (Palawan) | 0.000 | 20 | Scholes 2011 | - |
Yi (Hezhang County, Guizhou) | 0.000 | 20 | [ citation needed ] | - |
Hindu (Chitwan, Nepal) | 0.000 | 24 | Fornarino 2009 | - |
Guoshan Yao (Jianghua, Hunan) | 0.000 | 24 | [ citation needed ] | - |
Bunu (Dahua & Tianlin, Guangxi) | 0.000 | 25 | [ citation needed ] | - |
Kurd (northwestern Iran) | 0.000 | 25 | Derenko 2007 | - |
Iu Mien (Mengla, Yunnan) | 0.000 | 27 | [ citation needed ] | - |
Andhra Pradesh (tribal) | 0.000 | 29 | Fornarino 2009 | - |
Tujia (Yanhe County, Guizhou) | 0.000 | 29 | [ citation needed ] | - |
Batak (Palawan) | 0.000 | 31 | Scholes 2011 | - |
Wuzhou Yao (Fuchuan, Guangxi) | 0.000 | 31 | [ citation needed ] | - |
Bapai Yao (Liannan, Guangdong) | 0.000 | 35 | [ citation needed ] | - |
Tibetan (Nagchu, Tibet) | 0.000 | 35 | Ji 2012 | - |
Aleut (Commander Islands) | 0.000 | 36 | Volodko 2008 | - |
Eskimo (Sireniki) | 0.000 | 37 | Volodko 2008 | - |
Eskimo (Naukan) | 0.000 | 39 | Volodko 2008 | - |
Nganasan | 0.000 | 39 | Volodko 2008 | - |
Thai | 0.000 | 40 | Jin 2009 | - |
Lowland Yao (Fuchuan, Guangxi) | 0.000 | 42 | [ citation needed ] | - |
Eskimo (Chaplin) | 0.000 | 50 | Volodko 2008 | - |
Teleut (Kemerovo) | 0.000 | 53 | Derenko 2007 | - |
Han (Hunan & Fujian) | 0.000 | 55 | Zheng 2011 | - |
Saami (Finland) | 0.000 | 69 | Tambets 2004 | - |
Shor (Kemerovo) | 0.000 | 82 | Derenko 2007 | - |
Eskimo (Canada) | 0.000 | 96 | Volodko 2008 | - |
Saami (Sweden) | 0.000 | 98 | Tambets 2004 | - |
Aleut (Aleutian Islands) | 0.000 | 163 | Volodko 2008 | - |
Saami (Norway) | 0.000 | 278 | Tambets 2004 | - |
Eskimo (Greenland) | 0.000 | 385 | Volodko 2008 | - |
Subclade G2 is the most widely distributed, being found with low frequency in many populations all the way from eastern Europe (Poles, Ukrainians, Lipka Tatars) and western Siberia (Mansi, Khanty) to Japan (Japanese, Ainu) and from Iran (Persian) to southern China (Hmong and Tujia in Hunan and Mien in Guangxi) and Southeast Asia (Myanmar, Thailand, Cambodia). G2 (and especially its subclade G2a) is notably frequent among many Mongolic- or Turkic-speaking populations of northern East Asia and Central Asia. G2a also has been found with high frequency in some samples of Tharus from southern Nepal. [11] [12] The subclade G2a3 has been observed in Russia, an Azeri in Iran, [13] and a Uyghur in Artux, Xinjiang, China; [14] its subclade G2a3a has been observed among Komis and Udmurts. [15] Subclade G2a4 has been observed in China, Taiwan, and in a Ukrainian from the Lviv region of western Ukraine. Subclade G2a5 has been observed in Japan, Korea, and among Buryats, Barghuts, and various Turkic peoples (Karachay, Balkar, Kyrgyz, Kazakh, Karakalpak, Telengit, Tubalar, Yakut).
Subclade G1 is almost completely responsible for the high frequency of haplogroup G in populations located around the Sea of Okhotsk (Itelmen, Koryak, Negidal, Ulch, Ainu, Chukchi, Nivkh, etc.). G1 in Luoravetlans (Koryak & Chukchi) is essentially G1b, and this subclade is also found with generally low frequency in populations of Yakutia to the west (Evens, Yukaghirs, Evenks, Yakuts, Dolgans) as well as in Japan. [16] G1a has been found in samples from China (Daur, Hui, Kazakh, Sarikoli, [14] Korean, Manchu, Yi, [17] Jino, [17] Yunnan Dai, [17] Jiangxi Han, [17] and a sample of the general population of the city of Shenyang), Tajikistan (Pamiris [14] ), Japan, Korea, Vietnam, and central Siberia (Yakut, Altai-kizhi). G1c has been found in China, Korea, and a Seletar.
Subclade G3 is relatively rare. It has been found mainly among Koreans, [18] Tibetans, and presently Turkic- or Mongolic-speaking populations in southern Siberia and vicinity, and occasionally among Evenks in Buryatia, Japanese, Pumi, Naxi, [17] Uyghurs, [14] Sarikolis, [14] Tajiks, Pashtuns and Hazaras in Afghanistan, Kashmir, Han Chinese in Sichuan, [17] Hmong and Tujia in western Hunan, and Vietnamese.
Subclade G4 has been found in Japan and possibly in one Chinese individual from Guizhou. [17]
This phylogenetic tree of haplogroup G subclades is based on the paper by Mannis van Oven and Manfred Kayser Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation [2] and subsequent published research.
Haplogroup M is a human mitochondrial DNA (mtDNA) haplogroup. An enormous haplogroup spanning all the continents, the macro-haplogroup M, like its sibling the macro-haplogroup N, is a descendant of the haplogroup L3.
Haplogroup K, formerly Haplogroup UK, is a human mitochondrial DNA (mtDNA) haplogroup. It is defined by the HVR1 mutations 16224C and 16311C. It is now known that K is a subclade of U8.
Haplogroup J is a human mitochondrial DNA (mtDNA) haplogroup. The clade derives from the haplogroup JT, which also gave rise to haplogroup T. Within the field of medical genetics, certain polymorphisms specific to haplogroup J have been associated with Leber's hereditary optic neuropathy.
Haplogroup T is a human mitochondrial DNA (mtDNA) haplogroup. It is believed to have originated around 25,100 years ago in the Near East.
Haplogroup HV is a human mitochondrial DNA (mtDNA) haplogroup.
Haplogroup U is a human mitochondrial DNA haplogroup (mtDNA). The clade arose from haplogroup R, likely during the early Upper Paleolithic. Its various subclades are found widely distributed across Northern and Eastern Europe, Central, Western and South Asia, as well as North Africa, the Horn of Africa, and the Canary Islands.
Haplogroup F is a human mitochondrial DNA (mtDNA) haplogroup. The clade is most common in East Asia and Southeast Asia. It has not been found among Native Americans.
Haplogroup N is a human mitochondrial DNA (mtDNA) clade. A macrohaplogroup, its descendant lineages are distributed across many continents. Like its sibling macrohaplogroup M, macrohaplogroup N is a descendant of the haplogroup L3.
In human mitochondrial genetics, Haplogroup A is a human mitochondrial DNA (mtDNA) haplogroup.
In human mitochondrial genetics, Haplogroup C is a human mitochondrial DNA (mtDNA) haplogroup.
In human mitochondrial genetics, Haplogroup D is a human mitochondrial DNA (mtDNA) haplogroup. It is a descendant haplogroup of haplogroup M, thought to have arisen somewhere in East Asia, between roughly 60,000 and 35,000 years ago.
Haplogroup L3 is a human mitochondrial DNA (mtDNA) haplogroup. The clade has played a pivotal role in the early dispersal of anatomically modern humans.
In human mitochondrial genetics, Haplogroup Z is a human mitochondrial DNA (mtDNA) haplogroup.
Haplogroup I is a human mitochondrial DNA (mtDNA) haplogroup. It is believed to have originated about 21,000 years ago, during the Last Glacial Maximum (LGM) period in West Asia. The haplogroup is unusual in that it is now widely distributed geographically, but is common in only a few small areas of East Africa, West Asia and Europe. It is especially common among the El Molo and Rendille peoples of Kenya, various regions of Iran, the Lemko people of Slovakia, Poland and Ukraine, the island of Krk in Croatia, the department of Finistère in France and some parts of Scotland and Ireland.
Haplogroup D1 or D-M174 is a subclade of haplogroup D-CTS3946. This male haplogroup is found primarily in East Asia, Magar-ethnic Nepal and the Andaman Islands. It is also found regularly with lower frequency in Central Asia, Siberia and Mainland Southeast Asia, and, more rarely, in Europe and the Middle East.
In human mitochondrial genetics, Haplogroup Y is a human mitochondrial DNA (mtDNA) haplogroup.
In human mitochondrial genetics, Haplogroup H5 is a human mitochondrial DNA (mtDNA) haplogroup descended from Haplogroup H (mtDNA). H5 is defined by T16304C in the HVR1 region and 456 in the HVR2 region.
Haplogroup H is a human mitochondrial DNA (mtDNA) haplogroup. The clade is believed to have originated in Southwest Asia, near present day Syria, around 20,000 to 25,000 years ago. Mitochondrial haplogroup H is today predominantly found in Europe, and is believed to have evolved before the Last Glacial Maximum (LGM). It first expanded in the northern Near East and Southern Caucasus, and later migrations from Iberia suggest that the clade reached Europe before the Last Glacial Maximum. The haplogroup has also spread to parts of Africa, Siberia and Inner Asia. Today, around 40% of all maternal lineages in Europe belong to haplogroup H.
Haplogroup R0 is a human mitochondrial DNA (mtDNA) haplogroup.
In human mitochondrial genetics, Haplogroup M8 is a human mitochondrial DNA (mtDNA) haplogroup.
Phylogenetic tree of human mitochondrial DNA (mtDNA) haplogroups | |||||||||||||||||||||||||||||||||||||||
Mitochondrial Eve (L) | |||||||||||||||||||||||||||||||||||||||
L0 | L1–6 | ||||||||||||||||||||||||||||||||||||||
L1 | L2 | L3 | L4 | L5 | L6 | ||||||||||||||||||||||||||||||||||
M | N | ||||||||||||||||||||||||||||||||||||||
CZ | D | E | G | Q | O | A | S | R | I | W | X | Y | |||||||||||||||||||||||||||
C | Z | B | F | R0 | pre-JT | P | U | ||||||||||||||||||||||||||||||||
HV | JT | K | |||||||||||||||||||||||||||||||||||||
H | V | J | T |