Haplogroup I (mtDNA)

Human mitochondrial DNA haplogroup
Haplogroup I
Possible time of origin20.1 kya (Olivieri 2013)
Possible place of originWest Asia (Terreros 2011 and Fernandes 2012), or Southwest Asia
AncestorN1a1b (former N1e'I), (Olivieri 2013)
DescendantsI1, I2'3, I4, I5, I6, I7 (Olivieri 2013)
Defining mutationsT10034C, G16129A!, G16391A (Behar & Family Tree DNA 2012)

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 ((Olivieri 2013); Terreros 2011; Fernandes 2012). 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.

Origin

Haplogroup I is a descendant (subclade) of haplogroup N1a1b and sibling of haplogroup N1a1b1 (Olivieri 2013). It is believed to have arisen somewhere in West Asia between 17,263 and 24,451 years before present (BP) (Behar 2012b), with coalescence age of 20.1 thousand years ago (Olivieri 2013). It has been suggested that its origin may be in Iran or more generally the Near East (Terreros 2011). It has diverged to at least seven distinct clades i.e. branches I1–I7, dated between 16–6.8 thousand years (Olivieri 2013). The hypothesis about its Near Eastern origin is based on the fact that all haplogroup I clades, especially those from Late Glacial period (I1, I4, I5, and I6), include mitogenomes from the Near East (Olivieri 2013). The age estimates and dispersal of some subclades (I1, I2’3, I5) are similar to those of major subclades of the mtDNA haplogroups J and T, indicating possible dispersal of the I haplogroup into Europe during the Late Glacial period (c. 18–12 kya) and postglacial period (c. 10–11 kya), several millennia before the European Neolithic period. Some subclades (I1a1, I2, I1c1, I3) show signs of the Neolithic diffusion of agriculture and pastoralism within Europe (Olivieri 2013).

It is noteworthy that, with the exception of its northern neighbor Azerbaijan, Iran is the only population in which haplogroup I exhibits polymorphic levels. Also, a contour plot based on the regional phylogeographic distribution of the I haplogroup exhibits frequency clines consistent with an Iranian cradle ... Moreover, when compared with other populations in the region, those from the Levant (Iraq, Syria and Palestine) and the Arabian Peninsula (Oman and UAE) exhibit significantly lower proportions of I individuals ... this haplogroup has been detected in European groups (Krk, a tiny island off the coast of Croatia (11.3%), and Lemko, an isolate from the Carpathian Highlands (11.3%)) at comparable frequencies to those observed in the North Iranian population. However, the higher frequencies of the haplogroup within Europe are found in geographical isolates and are likely the result of founder effects and/or drift ... it is plausible that the high levels of haplogroup I present in Iran may be the result of a localized enrichment through the action of genetic drift or may signal geographical proximity to the location of origin.

— Terreros 2011

A similar view puts more emphasis on the Persian Gulf region of the Near East (Fernandes 2012).

Haplogroup I ... dates to ~25 ka ago and is overall most frequent in Europe ..., but the facts that it has a frequency peak in the Gulf region and that its highest diversity values are in the Gulf, Anatolia, and southeast Europe suggest that its origin is most likely in the Near East and/or Arabia ...

Distribution

Projected frequencies of mtDNA haplogroup I

Haplogroup I is found at moderate to low frequencies in East Africa, Europe, West Asia and South Asia (Fernandes 2012). In addition to the confirmed seven clades, the rare basal/paraphyletic clade I* has been observed in three individuals; two from Somalia and one from Iran (Olivieri 2013).

Africa

The highest frequencies of mitochondrial haplogroup I observed so far appear in the Cushitic-speaking El Molo (23%) and Rendille (>17%) in northern Kenya (Castrì 2008). The clade is also found at comparable frequencies among the Soqotri (~22%).[1]

Population Location Language Family N Frequency Source
Amhara Ethiopia Afro-Asiatic > Semitic 1/120 0.83% Kivisild 2004
Egyptians Egypt Afro-Asiatic > Semitic 2/34 5.9% Stevanovitch 2004
Beta Israel Ethiopia Afro-Asiatic > Cushitic 0/29 0.00% Behar 2008a
Dawro Konta Ethiopia Afro-Asiatic > Omotic 0/137 0.00% Castrì 2008 and Boattini 2013
Ethiopia Ethiopia Undetermined 0/77 0.00% Soares 2011
Ethiopian Jews Ethiopia Afro-Asiatic > Cushitic 0/41 0.00% Non 2011
Gurage Ethiopia Afro-Asiatic > Semitic 1/21 4.76% Kivisild 2004
Hamer Ethiopia Afro-Asiatic > Omotic 0/11 0.00% Castrì 2008 and Boattini 2013
Ongota Ethiopia Afro-Asiatic > Cushitic 0/19 0.00% Castrì 2008 and Boattini 2013
Oromo Ethiopia Afro-Asiatic > Cushitic 0/33 0.00% Kivisild 2004
Tigrai Ethiopia Afro-Asiatic > Semitic 0/44 0.00% Kivisild 2004
Daasanach Kenya Afro-Asiatic > Cushitic 0/49 0.00% Poloni 2009
Elmolo Kenya Afro-Asiatic > Cushitic 12/52 23.08% Castrì 2008 and Boattini 2013
Luo Kenya Nilo-Saharan 0/49 0.00% Castrì 2008 and Boattini 2013
Maasai Kenya Nilo-Saharan 0/81 0.00% Castrì 2008 and Boattini 2013
Nairobi Kenya Niger-Congo 0/100 0.00% Brandstatter 2004
Nyangatom Kenya Nilo-Saharan 1/112 0.89% Poloni 2009
Rendille Kenya Afro-Asiatic > Cushitic 3/17 17.65% Castrì 2008 and Boattini 2013
Samburu Kenya Nilo-Saharan 3/35 8.57% Castrì 2008 and Boattini 2013
Turkana Kenya Nilo-Saharan 0/51 0.00% Castrì 2008 and Boattini 2013
Hutu Rwanda Niger-Congo 0/42 0.00% Castrì 2009
Dinka Sudan Nilo-Saharan 0/46 0.00% Krings 1999
Sudan Sudan Undetermined 0/102 0.00% Soares 2011
Burunge Tanzania Afro-Asiatic > Cushitic 1/38 2.63% Tishkoff 2007
Datoga Tanzania Nilo-Saharan 0/57 0.00% Tishkoff 2007 and Knight 2003
Iraqw Tanzania Afro-Asiatic > Cushitic 0/12 0.00% Knight 2003
Sukuma Tanzania Niger-Congo 0/32 0.00% Tishkoff 2007 and Knight 2003
Turu Tanzania Niger-Congo 0/29 0.00% Tishkoff 2007
Yemeni Yemen Afro-Asiatic > Semitic 0/114 0.00% Kivisild 2004

Asia

Haplogroup I is present across West Asia and Central Asia, and is also found at trace frequencies in South Asia. Its highest frequency area is perhaps in northern Iran (9.7%). Terreros 2011 notes that it also has high diversity there and reiterates past studies that have suggested that this may be its place of origin. Found in Svan population from Georgia(Caucasus) I* 4.2%."Sequence polymorphisms of the mtDNA control region in a human isolate: the Georgians from Swanetia."Alfonso-Sánchez MA1, Martínez-Bouzas C, Castro A, Peña JA, Fernández-Fernández I, Herrera RJ, de Pancorbo MM.[citation needed] The table below shows some of the populations where it has been detected.

Population Language Family N Frequency Source
Baluch Indo-European 0/39 0.00% Quintana-Murci 2004
Brahui Dravidian 0/38 0.00% Quintana-Murci 2004
Caucasus (Georgia)* Kartvelian 1/58 1.80% Quintana-Murci 2004
Druze 11/311 3.54% Shlush 2008
Gilaki Indo-European 0/37 0.00% Quintana-Murci 2004
Gujarati Indo-European 0/34 0.00% Quintana-Murci 2004
Hazara Indo-European 0/23 0.00% Quintana-Murci 2004
Hunza Burusho Isolate 2/44 4.50% Quintana-Murci 2004
India 8/2544 0.30% Metspalu 2004
Iran (North) 3/31 9.70% Terreros 2011
Iran (South) 2/117 1.70% Terreros 2011
Kalash Indo-European 0/44 0.00% Quintana-Murci 2004
Kurdish (Western Iran) Indo-European 1/20 5.00% Quintana-Murci 2004
Kurdish (Turkmenistan) Indo-European 1/32 3.10% Quintana-Murci 2004
Lur Indo-European 0/17 0.00% Quintana-Murci 2004
Makrani Indo-European 0/33 0.00% Quintana-Murci 2004
Mazandarian Indo-European 1/21 4.80% Quintana-Murci 2004
Pakistani Indo-European 0/100 0.00% Quintana-Murci 2004
Pakistan 1/145 0.69% Metspalu 2004
Parsi Indo-European 0/44 0.00% Quintana-Murci 2004
Pathan Indo-European 1/44 2.30% Quintana-Murci 2004
Persian Indo-European 1/42 2.40% Quintana-Murci 2004
Shugnan Indo-European 1/44 2.30% Quintana-Murci 2004
Sindhi Indo-European 1/23 8.70% Quintana-Murci 2004
Turkish (Azerbaijan) Turkic 2/40 5.00% Quintana-Murci 2004
Turkish (Anatolia)* Turkic 1/50 2.00% Quintana-Murci 2004
Turkmen Turkic 0/41 0.00% Quintana-Murci 2004
Uzbek Turkic 0/42 0.00% Quintana-Murci 2004

Europe

Eastern Europe

In Eastern Europe, the frequency of haplogroup I is generally lower than in Western Europe (1 to 3 percent), but its frequency is more consistent between populations with fewer places of extreme highs or lows. There are two notable exceptions. Nikitin 2009 found that Lemkos (a sub- or co-ethnic group of Rusyns) in the Carpathian mountains have the "highest frequency of haplogroup I (11.3%) in Europe, identical to that of the population of Krk Island (Croatia) in the Adriatic Sea".[Footnote 1][Footnote 2]

Population N Frequency Source
Boyko 0/20 0.00% Nikitin 2009
Hutsul 0/38 0.00% Nikitin 2009
Lemko 6/53 11.32% Nikitin 2009
Belorussians 2/92 2.17% Belyaeva 2003
Russia (European) 3/215 1.40% Helgason 2001
Romanians (Constanta) 59 0.00% Bosch 2006
Romanians (Ploiesti) 46 2.17% Bosch 2006
Russia 1/50 2.0% Malyarchuk 2001
Ukraine 0/18 0.00% Malyarchuk 2001
Croatia (Mainland) 4/277 1.44% Pericić 2005
Croatia (Krk) 15/133 11.28% Cvjetan 2004
Croatia (Brač) 1/105 0.95% Cvjetan 2004
Croatia (Hvar) 2/108 1.9% Cvjetan 2004
Croatia (Korčula) 1/98 1% Cvjetan 2004
Herzegovinians 1/130 0.8% Cvjetan 2004
Bosnians 6/247 2.4% Cvjetan 2004
Serbians 4/117 3.4% Cvjetan 2004
Macedonians 2/146 1.4% Cvjetan 2004
Macedonian Romani 7/153 4.6% Cvjetan 2004
Slovenians 2/104 1.92% Malyarchuk 2003
Bosnians 4/144 2.78% Malyarchuk 2003
Poles 8/436 1.83% Malyarchuk 2003
Caucasus (Georgia)* 1/58 1.80% Quintana-Murci 2004
Russians 5/201 2.49% Malyarchuk 2003
Bulgaria/Turkey 2/102 1.96% Helgason 2001


Western Europe

In Western Europe, haplogroup I is most common in Northwestern Europe (Norway,[citation needed] the Isle of Skye, and the British Isles). The frequency in these areas is between 2 and 5 percent. Its highest frequency in Brittany, France where it is over 9 percent of the population in Finistère. It is uncommon and sometimes absent in other parts of Western Europe (Iberia, South-West France, and parts of Italy).

Population Language N Frequency Source
Austria/Switzerland 4/187 2.14% Helgason 2001
Basque (Admix Zone) Basque/Labourdin côtier-haut navarrais 0/56 0.00% Martınez-Cruz 2012
Basque (Araba) Basque/Occidental 0/55 0.00% Martınez-Cruz 2012
Basque (Bizkaia) Basque/Biscayen 1/59 1.69% Martınez-Cruz 2012
Basque (Central/Western Navarre ) Basque/Haut-navarrais méridional 2/63 3.17% Martınez-Cruz 2012
Basque (Gipuskoa) Basque/Gipuzkoan 0/57 0.00% Martınez-Cruz 2012
Basque (Navarre Labourdin) Basque/Bas-navarrais 0/68 0.00% Martınez-Cruz 2012
Basque (North/Western Navarre) Basque/Haut-navarrais septentrional 0/51 0.00% Martınez-Cruz 2012
Basque (Roncal) Basque/Roncalais-salazarais 0/55 0.00% Martınez-Cruz 2012
Basque (Soule) Basque/Souletin 0/62 0.00% Martınez-Cruz 2012
Basque (South/Western Gipuskoa) Basque/Biscayen 0/64 0.00% Martınez-Cruz 2012
Béarn French 0/51 0.00% Martınez-Cruz 2012
Bigorre French 0/44 0.00% Martınez-Cruz 2012
Burgos Spanish 0/25 0.00% Martınez-Cruz 2012
Cantabria Spanish 0/18 0.00% Martınez-Cruz 2012
Chalosse French 0/58 0.00% Martınez-Cruz 2012
Denmark 6/105 5.71% Mikkelsen 2010
England/Wales 12/429 3.03% Helgason 2001
Finland 1/49 2.04% Torroni 1996
Finland/Estonia 5/202 2.48% Helgason 2001
France (Finistère) 2/22 9.10% Dubut 2003
France (Morbihan) 0/40 0.00% Dubut 2003
France (Normandy) 0/39 0.00% Dubut 2003
France (Périgord-Limousin) - 2/72 2.80% Dubut 2003
France (Var) 2/37 5.40% Dubut 2003
France/Italy 2/248 0.81% Helgason 2001
Germany 12/527 2.28% Helgason 2001
Gran Canaria - 6/214 2.80% García-Olivares 2023
Iceland 21/467 4.71% Helgason 2001
Ireland 3/128 2.34% Helgason 2001
Italy (Tuscany) 2/48 4.20% Torroni 1996
La Rioja Spanish 1/51 1.96% Martınez-Cruz 2012
North Aragon Spanish 0/26 0.00% Martınez-Cruz 2012
Orkney 5/152 3.29% Helgason 2001
Saami 0/176 0.00% Helgason 2001
Scandinavia 12/645 1.86% Helgason 2001
Scotland 39/891 4.38% Helgason 2001
Spain/Portugal 2/352 0.57% Helgason 2001
Sweden 0/37 0.00% Torroni 1996
Western Bizkaia Spanish 0/18 0.00% Martınez-Cruz 2012
Western Isles/Isle of Skye 15/246 6.50% Helgason 2001

Historic and prehistoric samples

Haplogroup I has until recently been absent from ancient European samples found in Paleolithic and Mesolithic grave sites. In 2017, in a site on Italian island of Sardinia was found a sample with the subclade I3 dated to 9124–7851 BC (Modi 2017), while in the Near East, in Levant was found a sample with yet-not-defined subclade dated 8850–8750 BC, while in Iran was found a younger sample with subclade I1c dated to 3972–3800 BC (Lazaridis 2016). In Neolithic Spain (c. 6090–5960 BC in Paternanbidea, Navarre) was found a sample with yet-not-defined subclade (Olivieri 2013). Haplogroup I displays a strong connection with the Indo-European migrations; especially its I1, I1a1 and I3a subclades, which have been found in Poltavka and Srubnaya cultures in Russia (Mathieson 2015), among ancient Scythians (Der Sarkissian 2011), and in Corded Ware and Unetice Culture burials in Saxony (Brandt 2013).I3a has also been found in the Unetice Culture in Lubingine, Germany 2,200 B.C. to 1,800 B.C. courtesy article on Unetice Culture Wikipedia of 2 Skeletons that were DNA tested. Haplogroup I (with undetermined subclades) has also been noted at significant frequencies in more recent historic grave sites (Melchior 2008 and Hofreiter 2010).

In 2013, Nature announced the publication of the first genetic study utilizing next-generation sequencing to ascertain the ancestral lineage of an Ancient Egyptian individual. The research was led by Carsten Pusch of the University of Tübingen in Germany and Rabab Khairat, who released their findings in the Journal of Applied Genetics. DNA was extracted from the heads of five Egyptian mummies that were housed at the institution. All the specimens were dated to between 806 BC and 124 AD, a time frame corresponding with the Late Dynastic and Ptolemaic periods. The researchers observed that one of the mummified individuals likely belonged to the I2 subclade.[2] Haplogroup I has also been found among ancient Egyptian mummies excavated at the Abusir el-Meleq archaeological site in Middle Egypt, which date from the Pre-Ptolemaic/late New Kingdom, Ptolemaic, and Roman periods.[3]

Haplogroup I5 has also been observed among specimens at the mainland cemetery in Kulubnarti, Sudan, which date from the Early Christian period (AD 550–800).[4]

Samples with determined subclades

Culture Country Site Date Haplogroup Source
Unetice Germany Esperstedt 2050–1800 BC I1 Adler 2012; Brandt 2013
Bell Beaker Germany 2600–2500 BC I1a1 Lee 2012; Oliveiri 2013
Unetice Germany Plotzkau 3 2200–1550 BC I1a1 Brandt 2013
Unetice Germany Eulau 1979–1921 BC I1a1 Brandt 2013
Srubnaya Russia Rozhdestveno I, Samara Steppes, Samara 1850–1600 BC I1a1 Mathieson 2015
Seh Gabi Iran 3972–3800 BC I1c Lazaridis 2016
Cami de Can Grau Spain 3500–3000 BC I1c1 Sampietro 2007; Olivieri 2013
Late Dynastic-Ptolemaic Egypt 806 BC – 124 AD I2 Khairat 2013
Su Carroppu Italy 9124–7851 BC I3 Modi 2017
Scythian Russia Rostov-on-Don 500–200 BC I3 Der Sarkissian 2011
Unetice Germany Benzingerode-Heimburg 1653–1627 BC I3a Brandt 2013
Unetice Germany Esperstedt 2131–1979 BC I3a Adler 2012; Brandt 2013; Haak 2015; Mathieson 2015
Unetice Germany Esperstedt 2199–2064 BC I3a Adler 2012; Brandt 2013; Haak 2015
Poltavka Russia Lopatino II, Sok River, Samara 2885–2665 BC I3a Mathieson 2015
Karasuk Russia Sabinka 2 1416–1268 BC I4a1 Allentoft 2015
Minoan Greece Ayios Charalambos 2400–1700 BC I5 Hughey 2013
Minoan Greece Ayios Charalambos 2400–1700 BC I5 Hughey 2013
Minoan Greece Ayios Charalambos 2400–1700 BC I5 Hughey 2013
Christian Nubia Sudan Kulubnarti 550–800 AD I5 Sirak 2016
Late Bronze Age Armenia Norabak 1209–1009 BC I5c Allentoft 2015
Mezhovskava Russia Kapova cave 1598–1398 BC I5c Allentoft 2015

Samples with unknown subclades

Populations N Frequency Source
Roman Iron Age sites
Bøgebjerggård (AD 1–400)
Simonsborg (AD 1–200)
Skovgaarde (AD 200–400)
3/24 12.5% Melchior 2008a, Hofreiter 2010
Viking Age burial sites
Galgedil (AD 1000)
Christian cemetery Kongemarken (AD 1000–1250)
medieval cemetery Riisby (AD 1250–1450)
4/29 13.79% Melchior 2008, Hofreiter 2010
Anglo-Saxon burial sites
Leicester:6
Lavington:6
Buckland:7
Norton:12
Norwich:17
1/48 2.08% Töpf 2006

We have previously observed a high frequency of Hg I's among Iron Age villagers (Bøgebjerggård) and individuals from the early Christian cemetery, Kongemarken [16], [17]. This trend was also found for the additional sites reported here, Simonsborg, Galgedil and Riisby. The overall frequency of Hg I among the individuals from the Iron Age to the Medieval Age is 13% (7/53) compared to 2.5% for modern Danes [35]. The higher frequencies of Hg I can not be ascribed to maternal kinship since only two individuals share the same common motif (K2 and K7 at Kongemarken). Except for Skovgaarde (no Hg I's observed) frequencies range between 9% and 29% and there seems to be no trend in relation to time. No Hg I's were observed at the Neolithic Damsbo and the Bronze Age site Bredtoftegård, where all three individuals harbored Hg U4 or Hg U5a (Table 1).

Hofreiter 2010

The frequency of haplogroup I may have undergone a reduction in Europe following the Middle Ages. An overall frequency of 13% was found in ancient Danish samples from the Iron Age to the Medieval Age (including Vikings) from Denmark and Scandinavia compared to only 2.5% in modern samples. As haplogroup I is not observed in any ancient Italian, Spanish [contradicted by the recent research as have been found in pre-Neolithic Italy as well Neolithic Spain], British, central European populations, early central European farmers and Neolithic samples, according to the authors "Haplogroup I could, therefore, have been an ancient Southern Scandinavian type "diluted" by later immigration events" (Hofreiter 2010).

Subclades

Phylogenetic tree of haplogroups I (left) and W (right). Kya in the left scale bar stands for thousand years ago (Olivieri 2013).

Tree

This phylogenetic tree of haplogroup I subclades with time estimates is based on the paper and published research (Olivieri 2013).

Hg (July 2013) Age estimate (thousand years) 95% confidence interval (thousand years)
N1a1b 28.6 23.5–33.9
I 20.1 18.4–21.9
I1 16.3 14.6–18.0
I1a 11.6 9.9–13.3
I1a1 4.9 4.2–5.6
I1a1a 3.8 3.3–4.4
I1a1b 1.4 0.5–2.2
I1a1c 2.5 1.3–3.7
I1a1d 1.8 1.0–2.6
I1b 13.4 11.3–15.5
I1c 10.3 8.4–12.2
I1c1 7.2 5.4–9.0
I1c1a 4.0 2.5–5.4
I2'3 12.6 10.4–14.7
I2 6.8 6.0–7.6
I2a 4.7 3.8–5.7
I2a1 3.2 2.1–4.4
I2b 1.7 0.5–2.9
I2c 4.7 3.6–5.8
I2d 3.0 1.1–4.8
I2e 3.1 1.4–4.8
I3 10.6 8.8–12.4
I3a 7.4 6.1–8.7
I3a1 6.1 4.7–7.5
I3b 2.6 1.1–4.2
I3c 9.4 7.6–11.2
I4 15.1 12.3–18.0
I4a 6.4 5.4–7.4
I4a1 5.7 4.5–6.7
I4b 8.4 5.8–10.9
I5 18.4 16.4–20.3
I5a 16.0 14.0–17.9
I5a1 9.2 7.1–11.3
I5a2 12.3 10.2–14.4
I5a2a 1.6 1.0–2.1
I5a3 4.8 2.8–6.8
I5a4 5.6 3.5–7.8
I5b 8.8 6.3–11.2
I6 18.4 16.2–20.6
I6a 5.3 3.5–7.0
I6b 13.1 10.4–15.8
I7 9.1 6.3–11.9

Distribution

I1

Haplogroup I1
Possible time of origin15,231 ± 3,402 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutations455.1T, G6734A, G9966A, T16311C! (Behar & Family Tree DNA 2012)

It formed during the Last Glacial pre-warming period. It is found mainly in Europe, Near East, occasionally in North Africa and the Caucasus. It is the most frequent clade of the haplogroup (Olivieri 2013).

Genbank ID Population Source
JQ702472 Behar 2012b
JQ702567 Germany Behar 2012b
JQ704077 Germany Behar 2012b
JQ705190 Behar 2012b
JQ705840 Behar 2012b
KY022422 Iran FamilyTreeDNA
MG191350 Spanish FamilyTreeDNA
MG646219 Poland Piotrowska-Nowak 2019b
MK294405 Swedish FamilyTreeDNA
MN586593 Germany FamilyTreeDNA
MW600776 Russian FamilyTreeDNA
I1a
Haplogroup I1a
Possible time of origin11,726 ± 3,306 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsT152C!, G207A (Behar & Family Tree DNA 2012)

The subclade frequency peaks (circa 2.8%) are mostly located in North-Eastern Europe (Olivieri 2013).

Genbank ID Population Source
EU694173 FamilyTreeDNA
HM454265 Turkey (Armenian) FamilyTreeDNA
JQ245746 Chuvash Fernandes 2012
KC911435 Iran Derenko 2013
KC911577 Iran Derenko 2013
MK217219 Assyrians Shamoon-Pour 2019
OQ982011 Italy FamilyTreeDNA
I1a1
Haplogroup I1a1
Possible time of origin5,294 ± 2,134 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a
Defining mutationsG203A, C3990T, G9947A, A9966G!, T10915C! (Behar & Family Tree DNA 2012)
Genbank ID Population Source
EF177414 Portugal Pereira 2007
FJ460562 Tunisia Costa 2009
JQ245748 Czech Fernandes 2012
JQ245749 Czech Fernandes 2012
JQ245767 Turkey Fernandes 2012
JQ245802 Morocco Fernandes 2012
JQ702519 Behar 2012b
JQ702882 Behar 2012b
JQ703835 Behar 2012b
JQ705025 Behar 2012b
JQ705645 Behar 2012b
JQ705889 Behar 2012b
JX152861 Denmark Raule 2014
JX153351 Denmark Raule 2014
JX297189 Spain Cardoso 2013
KJ570782 Czech FamilyTreeDNA
MG551928 England FamilyTreeDNA
MH120632 Poland Piotrowska-Nowak 2019a
MK874614 Scotland FamilyTreeDNA
MK967511 Ireland FamilyTreeDNA
OM194303 Kazakhs Askapuli 2022
OM238070 Scottish FamilyTreeDNA
OP681985 Canary Islanders García-Olivares 2023
OP682630 Canary Islanders García-Olivares 2023
OP682053 Canary Islanders García-Olivares 2023
OP682263 Canary Islanders García-Olivares 2023
I1a1a
Haplogroup I1a1a
Possible time of origin3,327 ± 2,720 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsG9053A (Behar & Family Tree DNA 2012)
Genbank ID Population Source
AY339502 Finland Finnila 2001
AY339503 Finland Finnila 2001
AY339504 Finland Finnila 2001
AY339505 Finland Finnila 2001
JQ702939 Behar 2012b
JQ703652 Behar 2012b
JQ704013 Behar 2012b
JQ705140 Behar 2012b
JQ705378 Behar 2012b
JX153234 Finland Raule 2014
KC170986 Ukrainian FamilyTreeDNA
KF146236 Poland Olivieri 2013
KF146237 Italy Olivieri 2013
KY409854 Sardinians Olivieri 2017
KY410140 Sardinians Olivieri 2017
KY671032 Russia Malyarchuk 2017
KY671065 Russia Malyarchuk 2017
KY671085 Russia Malyarchuk 2017
MG646256 Poland Piotrowska-Nowak 2019b
MG646266 Poland Piotrowska-Nowak 2019b
MG952793 Hungary Malyarchuk 2018
MH120465 Poland Piotrowska-Nowak 2019a
MH120665 Poland Piotrowska-Nowak 2019a
MK103008 Swedish FamilyTreeDNA
MK202791 Russian FamilyTreeDNA
MK732936 Finnish FamilyTreeDNA
OL638786 Brazil Avila 2022
OL638813 Brazil Avila 2022
OM714626 Slovak Grzybowski 2023
OM714682 Slovak Grzybowski 2023
OM714689 Slovak Grzybowski 2023
OM714735 Czech Grzybowski 2023
OM714742 Czech Grzybowski 2023
OR438500 Poland Piotrowska-Nowak 2023
OR438613 Poland Piotrowska-Nowak 2023
I1a1a1
GenBank ID Population Source
AY339506 Finland Finnila 2001
KF899911 Russia FamilyTreeDNA
JX152986 Finland Raule 2014
MH983007 Finland FamilyTreeDNA
MK040467 Finland FamilyTreeDNA
I1a1a2
GenBank ID Population Source
AY339507 Finland Finnila 2001
AY339508 Finland Finnila 2001
AY339509 Finland Finnila 2001
OL555719 Finnish YSEQ
I1a1b
Haplogroup I1a1b
Possible time of origin2,608 ± 2,973 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsT14182C (Behar & Family Tree DNA 2012)
Genbank ID Population Source
JQ702470 Behar 2012b
JQ704690 Behar 2012b
JQ705595 Behar 2012b
JX153797 Denmark Raule 2014
JX154050 Denmark Raule 2014
KF586486 Ireland FamilyTreeDNA
KJ849732 Swedes FamilyTreeDNA
KJ850479 English FamilyTreeDNA
KM822854 Scotland FamilyTreeDNA
KT074442 Finland FamilyTreeDNA
KU672519 Ireland FamilyTreeDNA
KX906927 Ireland FamilyTreeDNA
MG182421 Ireland FamilyTreeDNA
MG548632 Welsh FamilyTreeDNA
MN163828 Finland FamilyTreeDNA
MT984338 Ireland YSEQ
MZ457933 Ireland FamilyTreeDNA
MZ846395 Shetland Dulias 2022
I1a1c
Haplogroup I1a1c
Possible time of originAbout 1,523 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsT6620C (Behar & Family Tree DNA 2012)
Genbank ID Population Source
GU123027 Mishar Tatars
(Buinsk)
Malyarchuk 2010b
JQ702023 Behar 2012b
JQ702457 Behar 2012b
KF146238 Ukraine Olivieri 2013
MG386697 German FamilyTreeDNA
MH918097 Lithuania FamilyTreeDNA
OL638548 Brazil Avila 2022
OM714767 Czech Grzybowski 2023
I1a1d
Haplogroup I1a1d
Possible time of originAbout 1,892 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1a1
Defining mutationsA1836G, T4023C, T13488C, T16189C! (Behar & Family Tree DNA 2012)
Genbank ID Population Source
JQ702342 Behar 2012b
JQ705189 Behar 2012b
KT124612 Wales FamilyTreeDNA
KX949567 United Kingdom FamilyTreeDNA
MZ846966 Orkney Dulias 2022
OQ101207 English FamilyTreeDNA
OR193751 Wales FamilyTreeDNA
I1a1e
GenBank ID Population Source
JQ701900 Behar 2012b
JQ702820 Behar 2012b
KJ095105 Ireland FamilyTreeDNA
KU375199 England FamilyTreeDNA
KY671114 Russia Malyarchuk 2017
MK570297 England FamilyTreeDNA
MN599048 Norway FamilyTreeDNA
MZ846316 Shetland Dulias 2022
MZ846989 Orkney Dulias 2022
MZ847013 Orkney Dulias 2022
MZ847773 Orkney Dulias 2022
MZ847969 Orkney Dulias 2022
MZ848045 Orkney Dulias 2022
I1b
Haplogroup I1b
Possible time of origin11,135 ± 4,818 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsT6227C (Behar & Family Tree DNA 2012)
Genbank ID Population Source
AY195769 Caucasian Mishmar 2003
AY714041 India Palanichamy 2004
EF556153 Jewish Diaspora Behar 2008a
FJ234984 Armenian FamilyTreeDNA
FJ968796 FamilyTreeDNA
JQ704018 Behar 2012b
JQ705376 Behar 2012b
KC911562 Iran Derenko 2013
KF146240 Italy Olivieri 2013
KF146241 Iran Olivieri 2013
KF146242 Iran Olivieri 2013
KF146243 Italy Olivieri 2013
KJ890387.1 Swedish FamilyTreeDNA
KJ890390 German FamilyTreeDNA
KJ937089 Armenian FamilyTreeDNA
KM986573 Yemen Vyas 2016
KM986617 Yemen Vyas 2016
KY073882 Hungary FamilyTreeDNA
KY410160 Sardinians Olivieri 2017
KY671121 Russia Malyarchuk 2017
KY680312 Sweden FamilyTreeDNA
MF362869 Armenian Margaryan 2017
MG272907 Thailand Kutanan 2018
MH378689 Chechen FamilyTreeDNA
MK491399 Armenian Derenko 2019
MN595812 Pakistan Rahman 2021
MW959772 English FamilyTreeDNA
OM714633 Slovak Grzybowski 2023
OR838478 Saudi Arabia FamilyTreeDNA
I1c
Haplogroup I1c
Possible time of origin8,216 ± 3,787 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI1
Defining mutationsG8573A, C16264T, G16319A, T16362C (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ705932 Behar 2012b
KP783168 Turkish FamilyTreeDNA
MG748728 Spain FamilyTreeDNA
OL619849 Mongolia Cardinali 2022
OR769030 Turkey YSEQ
I1c1
GenBank ID Population Source
KF146244 Italy Olivieri 2013
MF437134 United Arab Emirates Al-Jasmi 2020
MH120606 Poland Piotrowska-Nowak 2019a
OL638549 Brazil Avila 2022
I1c1a1
GenBank ID Population Source
EU564849 FamilyTreeDNA
JQ702655 Behar 2012b
JQ705364 Behar 2012b
KJ558222 Lithuania FamilyTreeDNA
KJ801472 - Lang 2015
KU052787 Lithuania FamilyTreeDNA
MZ158184 Belarus FamilyTreeDNA
OR182493 Hungarian Jews Brook 2022
I1c1a2
GenBank ID Population Source
KX156834 Chechens FamilyTreeDNA
I1d
GenBank ID Population Source
KF146245 Italy Olivieri 2013
KF146246 Italy Olivieri 2013
I1e
GenBank ID Population Source
JX462710 India Khan 2013
KY697192 Italians FamilyTreeDNA
KY982964 - FamilyTreeDNA
I1f
GenBank ID Population Source
JX153931 Denmark Raule 2014
JX153979 Denmark Raule 2014
KF251094 English FamilyTreeDNA
KJ557251 Scottish FamilyTreeDNA
KJ809106 England FamilyTreeDNA
MK434282 Norway FamilyTreeDNA

I2'3

Haplogroup I2'3
Possible time of origin11,308 ± 4,154 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsT152C!, G207A (Behar & Family Tree DNA 2012)

It is the common root clade for subclades I2 and I3. There's a sample from Tanzania with which I2'3 shares a variant at position 152 from the root node of haplogroup I, and this "node 152" could be upstream I2'3s clade (Olivieri 2013). Both I2 and I3 might have formed during the Holocene period, and most of their subclades are from Europe, only few from the Near East (Olivieri 2013). Examples of this ancestral branch have not been documented.

I2
Haplogroup I2
Possible time of origin6,387 ± 2,449 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2'3
Defining mutationsA15758G (Behar & Family Tree DNA 2012)
GenBank ID Population Source
EU570217 Ireland FamilyTreeDNA
FJ911909 FamilyTreeDNA
GU122984 Volga Tatars Malyarchuk 2010b
GU294854 FamilyTreeDNA
HQ287882 Pope 2011
JQ701942 Behar 2012b
JQ702191 Behar 2012b
JQ702284 Behar 2012b
JQ703850 Behar 2012b
JQ704705 Behar 2012b
JQ704765 Behar 2012b
JQ704936 Behar 2012b
JQ705000 Behar 2012b
JQ705304 Behar 2012b
JQ705379 Behar 2012b
JQ245744 Chechnya Fernandes 2012
JQ245747 Czech Fernandes 2012
JQ245771 Turkey Fernandes 2012
JX153641 Denmark Raule 2014
JX153773 Denmark Raule 2014
KC911614 Iranian Azerbaijanis Derenko 2013
KF146254 Italy Olivieri 2013
KF146255 Ukraine Olivieri 2013
KF146256 Italy Olivieri 2013
KF146257 Italy Olivieri 2013
KJ599625 Chechens FamilyTreeDNA
KJ645815 Armenians FamilyTreeDNA
KP969064 Norway FamilyTreeDNA
KR014102 Italy FamilyTreeDNA
KU682980 Uyghurs Zheng 2018
KU683033 Uyghurs Zheng 2018
KU683240 Uyghurs Zheng 2018
KU683502 Uyghurs Zheng 2018
KY000078 Norway FamilyTreeDNA
KY042020 Sweden FamilyTreeDNA
KY172919 Sweden FamilyTreeDNA
KY428665 England FamilyTreeDNA
KY671062 Russia Malyarchuk 2017
KY671122 Russia Malyarchuk 2017
KY780115 Irish FamilyTreeDNA
MF068709 Germany FamilyTreeDNA
MF116368 Sweden FamilyTreeDNA
MF279144 Sweden FamilyTreeDNA
MF278022 England FamilyTreeDNA
MF362766 Armenians Margaryan 2017
MN540393 England FamilyTreeDNA
MT075870 Ireland FamilyTreeDNA
MT223153 Ireland FamilyTreeDNA
MZ846734 Shetland Dulias 2022
MZ847795 Orkney Dulias 2022
OM936970 Netherlands FamilyTreeDNA
ON060656 Ireland FamilyTreeDNA
PP263591 Ireland FamilyTreeDNA
I2a
Haplogroup I2a
Possible time of origin3,771 ± 2,143 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsA11065G, G16145A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
HQ326985 FamilyTreeDNA
HQ695930 FamilyTreeDNA
HQ714959 Scotland FamilyTreeDNA
JQ705921 Behar 2012b
PP579598 Norwegian FamilyTreeDNA
PP849723 FamilyTreeDNA
I2a1
Haplogroup I2a1
Possible time of origin2,986 ± 1,968 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2a
Defining mutationsT3398C (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AY339497 Finland Finnila 2001
HQ724528 Ireland FamilyTreeDNA
JN411083 Ireland FamilyTreeDNA
I2a1a
GenBank ID Population Source
MT892955 Finland FamilyTreeDNA
I2a2
GenBank ID Population Source
JQ703910 Behar 2012b
KP987219 Ireland FamilyTreeDNA
KR088263 England FamilyTreeDNA
I2a3
GenBank ID Population Source
JQ705175 Behar 2012b
JX154048 Denmark Raule 2014
KU493988 Sweden FamilyTreeDNA
MK591009 Ireland FamilyTreeDNA
MT137386 Ireland FamilyTreeDNA
I2b
Haplogroup I2b
Possible time of originAbout 1,267 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsT6515C, 8281-8289d, A16166c (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AY339498 Finland Finnila 2001
AY339499 Finland Finnila 2001
AY339500 Finland Finnila 2001
AY339501 Finland Finnila 2001
I2c
Haplogroup I2c
Possible time of originAbout 2,268 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsT460C, G9438A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ702163 Behar 2012b
JQ702253 Behar 2012b
JQ703024 Behar 2012b
JQ705187 Behar 2012b
JQ705666 Behar 2012b
KJ882427 France FamilyTreeDNA
KR051235 Scotland FamilyTreeDNA
KU291444 Scotland FamilyTreeDNA
MZ846506 Shetland Dulias 2022
MZ846570 Shetland Dulias 2022
MZ847001 Orkney Dulias 2022
MZ847048 Orkney Dulias 2022
OL604518 Scotland FamilyTreeDNA
OP682030 Canary Islanders García-Olivares 2023
I2d
Haplogroup I2d
Possible time of originAbout 3,828 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsG6480A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ705244 Behar 2012b
JQ703829 Behar 2012b
JX153642 Denmark Raule 2014
KY684194 Germans FamilyTreeDNA
MG646226 Poland Piotrowska-Nowak 2019b
MH087474 English FamilyTreeDNA
MH120469 Poland Piotrowska-Nowak 2019a
MH120515 Poland Piotrowska-Nowak 2019a
MH675881 Finland FamilyTreeDNA
I2e
Haplogroup I2e
Possible time of originAbout 2,936 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2
Defining mutationsG3591A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ702578 Behar 2012b
JQ703106 Behar 2012b
MN176248 Poland Piotrowska-Nowak 2020
MN176270 Poland Piotrowska-Nowak 2020
I3
Haplogroup I3
Possible time of origin8,679 ± 3,410 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI2'3
Defining mutationsT239C (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ702647 Behar 2012b
JQ703862 Behar 2012b
OL521838 Ireland FamilyTreeDNA
I3a
Haplogroup I3a
Possible time of origin6,091 ± 3,262 BP (Behar 2012b)
Possible place of originOldest sample from Poltavka culture (Russia-Lopatino II, Sok River, Samara, 2885–2665 BC) (Mathieson 2015)
AncestorI3
Defining mutationsT16086C (Behar & Family Tree DNA 2012)
GenBank ID Population Source
EU746658 France FamilyTreeDNA
EU869314 FamilyTreeDNA
JQ245751 Greece Fernandes 2012
JQ702041 Behar 2012b
JQ702062 Behar 2012b
JQ702109 Behar 2012b
JQ702413 Behar 2012b
JX153712 Denmark Raule 2014
KF146258 Iran Olivieri 2013
KJ507246 Flemish FamilyTreeDNA
KJ850495 English FamilyTreeDNA
KU859398 Belgium FamilyTreeDNA
KY369150 Italy FamilyTreeDNA
KY408233 Sardinians Olivieri 2017
MF002495 Germany FamilyTreeDNA
MF322516 Irish FamilyTreeDNA
MK088054 France FamilyTreeDNA
MZ614451 Scotland FamilyTreeDNA
ON980565 Scotland FamilyTreeDNA
OP682222 Canary Islanders García-Olivares 2023
OP682259 Canary Islanders García-Olivares 2023
OP682273 Canary Islanders García-Olivares 2023
OP682309 Canary Islanders García-Olivares 2023
OP682392 Canary Islanders García-Olivares 2023
OP682401 Canary Islanders García-Olivares 2023
OQ470330 Norwegians FamilyTreeDNA
I3a1
Haplogroup I3a1
Possible time of origin5,070 ± 3,017 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI3a
Defining mutationsG2849A (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AY963586 Italy Bandelt
HQ420832 France FamilyTreeDNA
JQ704837 Behar 2012b
KP903567 Austria FamilyTreeDNA
MH120756 Poland Piotrowska-Nowak 2019a
OL638572 Brazil Avila 2022
I3b
Haplogroup I3b
Possible time of origin5,596 ± 3,629 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI3
Defining mutationsC16494T (Behar & Family Tree DNA 2012)
GenBank ID Population Source
GU590993 Ireland FamilyTreeDNA
JQ705377 Behar 2012b
I3c
GenBank ID Population Source
JQ702493 Behar 2012b
JQ703883 Behar 2012b
KJ021060 - FamilyTreeDNA
I3d
GenBank ID Population Source
OR233329 Russians FamilyTreeDNA
OR438549 Poland Piotrowska-Nowak 2023

I4

Haplogroup I4
Possible time of origin14,913 ± 5,955 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsG8519A (Behar & Family Tree DNA 2012)

The clade splits into subclades I4a and newly defined I4b, with samples found in Europe, the Near East and the Caucasus (Olivieri 2013).

GenBank ID Population Source
KJ021059 FamilyTreeDNA
I4a
Haplogroup I4a
Possible time of originAbout 2,124 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI4
Defining mutationsA10819G (Behar & Family Tree DNA 2012)
GenBank ID Population Source
EU091245 FamilyTreeDNA
JN660158 Armenian FamilyTreeDNA
JQ701909 Behar 2012b
JQ701957 Behar 2012b
JQ705303 Behar 2012b
JQ705514 Behar 2012b
JQ706017 Behar 2012b
JQ702369 Behar 2012b
JX153325 Denmark Raule 2014
KJ676862 French Canadians FamilyTreeDNA
KT390700 Ireland FamilyTreeDNA
KX495667 Armenian FamilyTreeDNA
MF362868 Armenians Margaryan 2017
MG660526 Chelkans Nazhmidenova 2020
MZ846849 Orkney Dulias 2022
MZ846865 Orkney Dulias 2022
OL638882 Brazil Avila 2022
ON457162 FamilyTreeDNA
ON602072 England FamilyTreeDNA
OQ645346 German FamilyTreeDNA
I4a1
GenBank ID Population Source
EF153786 Siberia Derenko 2007
EF660987 Italy Gasparre 2007
HM804481 FamilyTreeDNA
JQ705060 Behar 2012b
JQ705191 Behar 2012b
JQ705906 Behar 2012b
KJ676824 German FamilyTreeDNA
KJ890389 Russia FamilyTreeDNA
KU922938 Wales FamilyTreeDNA
KY849396 Swedes FamilyTreeDNA
MG015877 Swedes FamilyTreeDNA
MG646165 Poland Piotrowska-Nowak 2019b
MH322053 Germany FamilyTreeDNA
MW691107 Ireland FamilyTreeDNA
ON010030 Sweden FamilyTreeDNA
I4a2
GenBank ID Population Source
KF254840 Finland FamilyTreeDNA
I4b
GenBank ID Population Source
JQ704976 Behar 2012b
KF146261 Iran Olivieri 2013
KX467275 India Sharma 2018
MG744604 Germany FamilyTreeDNA

I5

Haplogroup I5
Possible time of origin18,806 ± 4,005 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI
Defining mutationsA14233G (Behar & Family Tree DNA 2012)

Is the second most frequent clade of the haplogroup. Its subclades are found in Europe, e.g. I5a1, and the Near East, e.g. I5a2a and I5b (Olivieri 2013).

GenBank ID Population Source
HQ658465 German (north) FamilyTreeDNA
JQ245724 North Ossetia Fernandes 2012
KJ920750 German (west) FamilyTreeDNA
KT250729 German (east) FamilyTreeDNA
KT346427 Polish FamilyTreeDNA
MK617274 Serbia Davidovic 2020
I5a
Haplogroup I5a
Possible time of origin15,116 ± 4,128 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI5
Defining mutationsT5074C, C16148T (Behar & Family Tree DNA 2012)
GenBank ID Population Source
KT748522 Pontic Greeks FamilyTreeDNA
KX017466 Finnish FamilyTreeDNA
MF362944 Armenians Margaryan 2017
MN696689 Finnish FamilyTreeDNA
I5a1
Haplogroup I5a1
Possible time of origin11,062 ± 4,661 BP (Behar 2012b)
Possible place of originInsufficient Data
AncestorI5a
Defining mutations8281-8289d, A12961G (Behar & Family Tree DNA 2012)
GenBank ID Population Source
JQ245807 Bulgaria Fernandes 2012
JX152976 Finland Raule 2014
KM925143 Finland FamilyTreeDNA
MK134361 Serbia Davidovic 2020
MK217239 Assyrians Shamoon-Pour 2019
MT338490 Germany FamilyTreeDNA
I5a1a
GenBank ID Population Source
JQ705096 Behar 2012b
KF146248 Italy Olivieri 2013
KJ746501 English FamilyTreeDNA
KX856070 English FamilyTreeDNA
MG744602 French FamilyTreeDNA
I5a1b
GenBank ID Population Source
AF382007 Leon Maca-Meyer 2001
EF660917 Italy Gasparre 2007
JQ704713 Behar 2012b
I5a1c
GenBank ID Population Source
EU597573 Bedouin (Israel) Hartmann 2009
JQ704768 Behar 2012b
KF146247 Italy Olivieri 2013
I5a2
GenBank ID Population Source
JQ701894 Behar 2012b
KY408295 Sardinians Olivieri 2017
KY408387 Sardinians Olivieri 2017
MH168104 Ukrainians FamilyTreeDNA
MZ384391 United Kingdom FamilyTreeDNA
PP302047 Dutch FamilyTreeDNA
I5a2a
GenBank ID Population Source
JQ245733 Dubai Fernandes 2012
JQ245780 Yemen Fernandes 2012
JQ245781 Yemen Fernandes 2012
JQ245782 Yemen Fernandes 2012
JQ245783 Yemen Fernandes 2012
JQ245784 Yemen Fernandes 2012
JQ245785 Yemen Fernandes 2012
JQ245786 Yemen Fernandes 2012
I5a3
GenBank ID Population Source
JN415483 Germany Achilli 2012
JQ245772 Turkey Fernandes 2012
I5a4
GenBank ID Population Source
FJ348190 Hutterite Pichler 2010
HM852869 Turkey Schoenberg 2011
KF146249 Italy Olivieri 2013
KJ676977 Romanian FamilyTreeDNA
KY615004 Rusyns FamilyTreeDNA
I5b
GenBank ID Population Source
KF255549 Italy FamilyTreeDNA
ON640629 Cyprus FamilyTreeDNA
I5c
GenBank ID Population Source
KM245143 Spain Fregel 2015
KP419690 Italians FamilyTreeDNA
MF362879 Armenians Margaryan 2017
MK491434 Armenians Derenko 2019
OP642525 Chechens FamilyTreeDNA
I5c1
GenBank ID Population Source
HQ658465 Germans FamilyTreeDNA
KC787372 English FamilyTreeDNA
KF146251 Italy Olivieri 2013
KY409830 Sardinians Olivieri 2017
KY981527 Sardinians FamilyTreeDNA
OL438769 Romanians FamilyTreeDNA

I6

Haplogroup I6
Possible time of originAbout 18,400 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI
Defining mutationsT3645C (Behar & Family Tree DNA 2012)

The subclade is very rare, found until July 2013 only in four samples from the Near East (Olivieri 2013).

GenBank ID Population Source
JQ245773 Turkey Fernandes 2012
MK036912 Croatia FamilyTreeDNA
I6a
Haplogroup I6a
Possible time of originAbout 5,300 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI6
Defining mutations(G203A), G3915A, A6116G, A7804G, T15287C, (A16293c) (Behar & Family Tree DNA 2012)
GenBank ID Population Source
AY245555 Janssen 2006
JQ705382 Behar 2012b
KM262180 Italy FamilyTreeDNA
KY409776 Sardinians Olivieri 2017

I7

Haplogroup I7
Possible time of originAbout 9,100 BP (Olivieri 2013)
Possible place of originInsufficient Data
AncestorI
Defining mutationsC3534T, A4829G, T16324C

It is the rarest defined subclade, until July 2013 found only in two samples from the Near East and the Caucasus (Olivieri 2013).

GenBank ID Population Source
JF298212 Armenian FamilyTreeDNA
KF146253 Kuwait Olivieri 2013

See also

Wikimedia Commons has media related to Haplogroup I (mtDNA).

Genetics

Backbone mtDNA Tree

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

References

  1. ^ Non, Amy. "ANALYSES OF GENETIC DATA WITHIN AN INTERDISCIPLINARY FRAMEWORK TO INVESTIGATE RECENT HUMAN EVOLUTIONARY HISTORY AND COMPLEX DISEASE" (PDF). University of Florida. Archived from the original (PDF) on 13 October 2020. Retrieved 12 April 2016.
  2. ^ Rabab Khairat; Markus Ball; Chun-Chi Hsieh Chang; Raffaella Bianucci; Andreas G. Nerlich; Martin Trautmann; Somaia Ismail; et al. (4 April 2013). "First insights into the metagenome of Egyptian mummies using next-generation sequencing". Journal of Applied Genetics. 54 (3): 309–325. doi:10.1007/s13353-013-0145-1. PMID 23553074. S2CID 5459033. Retrieved 8 June 2016.
  3. ^ Schuenemann, Verena J.; et al. (2017). "Ancient Egyptian mummy genomes suggest an increase of Sub-Saharan African ancestry in post-Roman periods". Nature Communications. 8: 15694. Bibcode:2017NatCo...815694S. doi:10.1038/ncomms15694. PMC 5459999. PMID 28556824.
  4. ^ Sirak, Kendra; Frenandes, Daniel; Novak, Mario; Van Gerven, Dennis; Pinhasi, Ron (2016). "Abstract Book of the IUAES Inter-Congress 2016 - A community divided? Revealing the community genome(s) of Medieval Kulubnarti using next- generation sequencing". Abstract Book of the Iuaes Inter-Congress 2016. IUAES: 115–116.

Footnotes

  1. ^ Nikitin 2009: 6/53 in Lemkos
    "Lemkos shared the highest frequency of haplogroup I ever reported and the highest frequency of haplogroup M* in the region."
  2. ^ Cvjetan 2004: 15/133

Works cited

Journals

  • Achilli, Alessandro; Iommarini, Luisa; Olivieri, Anna; Pala, Maria; Kashani, Baharak Hooshiar; Reynier, Pascal; La Morgia, Chiara; Valentino, Maria Lucia; et al. (2012). "Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy". PLoS ONE. 7 (8): e42242. doi:10.1371/journal.pone.0042242. PMC 3411744. PMID 22879922.
  • Askapuli, Ayken; Vilar, Miguel; Garcia-Ortiz, Humberto; Zhabagin, Maxat; Sabitov, Zhaxylyk; Akilzhanova, Ainur; Ramanculov, Erlan; Schamiloglu, Uli; et al. (2022). "Kazak mitochondrial genomes provide insights into the human population history of Central Eurasia". PLOS ONE. 17 (11): e0277771. Bibcode:2022PLoSO..1777771A. doi:10.1371/journal.pone.0277771. PMC 9707748. PMID 36445929.
  • Avila, Eduardo; Speransa, Pietro Augusto; Lindholz, Catieli Gobetti; Kahmann, Alessandro; Alho, Clarice Sampaio (2022). "Haplotype distribution in a forensic full mtDNA genome database of admixed Southern Brazilians and its association with self-declared ancestry and pigmentation traits". Forensic Science International: Genetics. 57: 102650. doi:10.1016/j.fsigen.2021.102650. PMID 34972071. S2CID 245421504.
  • Behar, DM; Metspalu, E; Kivisild, T; Rosset, S; Tzur, S; Hadid, Y; Yudkovsky, G; Rosengarten, D; et al. (2008). MacAulay, Vincent (ed.). "Counting the founders: The matrilineal genetic ancestry of the Jewish Diaspora". PLOS ONE. 3 (4): e2062. Bibcode:2008PLoSO...3.2062B. doi:10.1371/journal.pone.0002062. PMC 2323359. PMID 18446216.
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  • Pope, AM; Carr, SM; Smith, KN; Marshall, HD; Marshall, H. D. (2011). "Mitogenomic and microsatellite variation in descendants of the founder population of Newfoundland: High genetic diversity in an historically isolated population". Genome. 54 (2): 110–9. doi:10.1139/G10-102. PMID 21326367.
  • Quintana-Murci, Lluís; Chaix, Raphaëlle; Wells, R. Spencer; Behar, Doron M.; Sayar, Hamid; Scozzari, Rosaria; Rengo, Chiara; Al-Zahery, Nadia; et al. (2004). "Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor". The American Journal of Human Genetics. 74 (5): 827–45. doi:10.1086/383236. PMC 1181978. PMID 15077202.
  • Rahman, Zia Ur; Tian, Jiao-Yang; Gao, Zong-Liang; Wang, Hao-Tian; Xia, Wang-Xiao; Yang, Bin-Yu; Yang, Li-Qin; Li, Yu-Chun; Kong, Qing-Peng (2021). "Complete mitogenomes document substantial genetic contribution from the Eurasian Steppe into northern Pakistani Indo-Iranian speakers". European Journal of Human Genetics. 29 (6): 1008–1018. doi:10.1038/s41431-021-00829-6. PMC 8187500. PMID 33637889.
  • Raule, Nicola; Sevini, Federica; Li, Shengting; Barbieri, Annalaura; Tallaro, Federica; Lomartire, Laura; Vianello, Dario; Montesanto, Alberto; et al. (2014). "The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific". Aging Cell. 13 (3): 401–407. doi:10.1111/acel.12186. PMC 4326891. PMID 24341918.
  • Richards, Martin; MacAulay, Vincent; Hickey, Eileen; Vega, Emilce; Sykes, Bryan; Guida, Valentina; Rengo, Chiara; Sellitto, Daniele; et al. (2000). "Tracing European Founder Lineages in the Near Eastern mtDNA Pool". The American Journal of Human Genetics. 67 (5): 1251–76. doi:10.1016/S0002-9297(07)62954-1. PMC 1288566. PMID 11032788.
  • Richards, Martin; Rengo, Chiara; Cruciani, Fulvio; Gratrix, Fiona; Wilson, James F.; Scozzari, Rosaria; MacAulay, Vincent; Torroni, Antonio (2003). "Extensive Female-Mediated Gene Flow from Sub-Saharan Africa into Near Eastern Arab Populations". The American Journal of Human Genetics. 72 (4): 1058–64. doi:10.1086/374384. PMC 1180338. PMID 12629598.
  • Schönberg, Anna; Theunert, Christoph; Li, Mingkun; Stoneking, Mark; Nasidze, Ivan (2011). "High-throughput sequencing of complete human mtDNA genomes from the Caucasus and West Asia: high diversity and demographic inferences". European Journal of Human Genetics. 19: 988–994. doi:10.1038/ejhg.2011.62. PMC 3179362.
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  • Terreros, Maria C; Rowold, Diane J; Mirabal, Sheyla; Herrera, Rene J (2011). "Mitochondrial DNA and Y-chromosomal stratification in Iran: Relationship between Iran and the Arabian Peninsula". Journal of Human Genetics. 56 (3): 235–46. doi:10.1038/jhg.2010.174. PMID 21326310.
  • Tishkoff, S. A.; Gonder, M. K.; Henn, B. M.; Mortensen, H.; Knight, A.; Gignoux, C.; Fernandopulle, N.; Lema, G.; et al. (2007). "History of Click-Speaking Populations of Africa Inferred from mtDNA and Y Chromosome Genetic Variation". Molecular Biology and Evolution. 24 (10): 2180–95. doi:10.1093/molbev/msm155. PMID 17656633.
  • Topf, A. L.; Gilbert, MT; Dumbacher, JP; Hoelzel, AR (2005). "Tracing the Phylogeography of Human Populations in Britain Based on 4th-11th Century mtDNA Genotypes". Molecular Biology and Evolution. 23 (1): 152–61. doi:10.1093/molbev/msj013. PMID 16151183.
  • Torroni, A; Huoponen, K; Francalacci, P; Petrozzi, M; Morelli, L; Scozzari, R; Obinu, D; Savontaus, ML; Wallace, DC (1996). "Classification of European mtDNAs From an Analysis of Three European Populations". Genetics. 144 (4): 1835–50. doi:10.1093/genetics/144.4.1835. PMC 1207732. PMID 8978068.
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  • Vyas, Deven; Kitchen, Andrew; Miró-Herrans, Aida; Pearson, Laurel N.; Al-Meeri, Ali; Mulligan, Connie J. (2016). "Bayesian analyses of Yemeni mitochondrial genomes suggest multiple migration events with Africa and Western Eurasia". American Journal of Physical Anthropology. 159 (3): 382–393. doi:10.1002/ajpa.22890. PMID 26567083.

Books

  • Brook, Kevin Alan; Cooper, Leo R.; Wexler, Jeffrey D.; Lipson, Joshua; Stern, Jonah A. (2022). The Maternal Genetic Lineages of Ashkenazic Jews. Boston: Academic Studies Press. doi:10.2307/j.ctv33mgbcn. ISBN 978-1644699843. S2CID 254519342.

Websites

  • Behar; Family Tree DNA (2012). "mtDNA Community". Archived from the original on 2018-01-02. Retrieved 2013-01-07.

Further reading

  • Černý, Viktor; Pereira, Luísa; Kujanová, Martina; VašÍková, Alžběta; Hájek, Martin; Morris, Miranda; Mulligan, Connie J. (2009). "Out of Arabia-The settlement of Island Soqotra as revealed by mitochondrial and Y chromosome genetic diversity". American Journal of Physical Anthropology. 138 (4): 439–47. doi:10.1002/ajpa.20960. PMID 19012329.
  • Fellner, Robert O (1995). Cultural change and the epipalaeolithic of Palestine. Tempus Reparatum. ISBN 9780860547754.
  • Kitchen, A.; Ehret, C.; Assefa, S.; Mulligan, C. J. (2009). "Bayesian phylogenetic analysis of Semitic languages identifies an Early Bronze Age origin of Semitic in the Near East". Proceedings of the Royal Society B: Biological Sciences. 276 (1668): 2703–10. doi:10.1098/rspb.2009.0408. PMC 2839953. PMID 19403539.
  • Petit-Maire, Nicole; Bouysse, Philippe (2000). "Geological records of the recent past, a key to the near future world environments" (PDF). Episodes. 23 (4): 230–246. doi:10.18814/epiiugs/2000/v23i4/001.
  • General
    • Ian Logan's Mitochondrial DNA Site
    • Haplogroup I – based on PhyloTree.org (February 2016)
    • Mannis van Oven's PhyloTree for Haplogroup N1, including subtree of I (February 2016)
  • Haplogroup I
    • Family Tree DNA – mtDNA Haplogroup I Project
    • Family Tree DNA's mtDNA Haplotree: Haplogroup I
    • YFull MTree's Haplogroup I
    • MITOMAP's Haplogroup I