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"Danish Demes"
Lineages and Results of mtDNA Testing for a Regional Danish DNA Project
Haplogroup K — "Clan Katrine"
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and Their Frequency (n)
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H (11) J (1) K (2) T (3) U (2) V (2)
Haplogroup K is a relatively old group, derived from Haplogroup R.  Living individuals are widespread in Eurasia, the Near East, and northern Africa.  About 6% of Europeans are Haplogroup K; of these, about 60% are subclade K1a.  Of our two Haplogroup K members, one is K1c/K1c1 and the other is a form of K1c2.

In the trivia department:  The oldest known Haplogroup K individual is Ötzi, the iceman whose frozen body was found in the Alps in 1991.  Katie Couric is also K.

The Cambridge Reference Sequence (CRS) is arbitrarily designated as the standard against which all mtDNA sequences are compared, and test results are expressed as differences from the CRS.  The CRS happens to be negative for the 519C mutation, which is otherwise very common, so the majority of tested individuals will have this mutation listed in the HVR1 region.
In the table below, a darkened empty cell means the test was not ordered.  All HVR1 marker designations begin with "16___"; so, to save space and improve readability, I've dropped the 16 in the tables.  With regard to results, a letter in red indicates a base has changed; a letter in green indicates a new base has been inserted; a minus sign (-) indicates a base has been lost.
Mutations are reordered (not in strict numerical order) for ease of comparison.  Those common to Haplogroup K are shown here and below in tables cells with a yellow highlight:
HVR1 HVR2
224C, 311C, 519C 73G, 263G, 315.1C
Additional mutations are shown in table cells that are white.
With regard to lineages, given names and patronymics are shown as Initial Caps, while surnames are shown in ALL-CAPS (these are the womens' maiden names, not their married names).
Your project admin recommends uploading your mtDNA results to MitoSearch.org, which can be done at your FTDNA member page (on the "mtDNA Matches" tab).  Your project admin also recommends joining William Hurst's mtDNA Haplogroup K project, which can be done directly using the blue "Join" icon on your FTDNA member page (after clicking the icon, scroll down to the "mt Haplogroups" listing and choose "K1").

Subclade K1c or K1c1
Kit # MitoSearch
UserID
Differences from Cambridge Reference Sequence Known Lineage
HVR1 HVR2
77022 K4EKU 224C, 311C, 519C 73G, 263G, 315.1C 146C, 152C, 309.1C, 498- Pvt8, Pvt7, Della B. LUNDBERG6, Cora Louise HARDCASTLE5, Emma HARDCASTLE4, Stine Petrine Frances Marie Larsen DOMGAARD3, Mette Kristine Christensen2, Maren Anderson1 — of Aaby, Åby Sogn, Kær Herred, Aalborg Amt, DK
This individual has over a thousand matches in HVR1, but less than a dozen in her combined HVR1+HVR2 results; none (yet) in this project.  William Hurst informs me that the 498 deletion defines K1c, but that coding-region mutations define K1c1, so you can't tell the two subclades apart by testing only the hypervariable regions.

Subclade K1c2 - SWE
Kit # MitoSearch
UserID
Differences from Cambridge Reference Sequence Known Lineage
HVR1 HVR2
72755 C5QQ7 224C, 311C, 519C 320T, 362C 73G, 263G, 315.1C 146C, 152C, 309.1C, 498- Son7, Pvt6, Hulda Helene Christina SIMONSEN5, Ane Dorthea Petersdatter4, Elisabeth Johansdatter3, Christiane Pedersdatter2, Maren Christensdatter1 — of Ålborg, Ålborg Sogn, Fleskum Herred, Aalborg Amt, DK
This individual has two full matches at MitoSearch, one with someone whose earliest known matrilineal ancestor was from southernmost Sweden (Glimåkra, Kristianstads län, now Skåne), an area historically part of Denmark, the other with an individual with an earliest known origin in Malmöhus, Sweden.  His mutations match a variant of K1c2 from Sweden defined by William Hurst (as of 22 May 2006).


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