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According to 23andMe I am H1q.
I´ve tried Jameslick calculator, and these are results, but I don´t know how exactly read it.
So, I am H1q and no further?Found 4274 markers at 2413 positions covering 14.6% of mtDNA.
Markers found (shown as differences to rCRS):
HVR2: 65D 191D 263G 299I 459D
CR: 1438G 2074I 2156D 2405D 3010A 3307D 4317I 4859C 5004C 5537D 5752D 7471D 8281D 8286D 8860G 14482T 15941C
HVR1:
IMPORTANT NOTE: The above marker list is almost certainly incomplete due to limitations of genotyping technology and is not comparable to mtDNA sequencing results. It should not be used with services or tools that expect sequencing results, such as mitosearch.
Best mtDNA Haplogroup Matches:
1) H1q2
Defining Markers for haplogroup H1q2:
HVR2: 263G
CR: 750G 1438G 3010A 4769G 4859C 8860G 15326G 15941C
HVR1:
Marker path from rCRS to haplogroup H1q2 (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 3010A ⇨ H1 ⇨ 4859C ⇨ H1q ⇨ 15941C ⇨ H1q2 ⇨ 65D 191D 299I 459D 2074I 2156D 2405D 3307D 4317I 5004C 5537D 5752D 7471D 8281D 8286D 14482T
Imperfect Match. Your results contained differences with this haplogroup:
Matches(6): 263G 1438G 3010A 4859C 8860G 15941C
Extras(16): 65D 191D 299I 459D 2074I 2156D 2405D 3307D 4317I 5004C 5537D 5752D 7471D 8281D 8286D 14482T
Untested(3): 750 4769 15326
2) H1q
Defining Markers for haplogroup H1q:
HVR2: 263G
CR: 750G 1438G 3010A 4769G 4859C 8860G 15326G
HVR1:
Marker path from rCRS to haplogroup H1q (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 3010A ⇨ H1 ⇨ 4859C ⇨ H1q ⇨ 65D 191D 299I 459D 2074I 2156D 2405D 3307D 4317I 5004C 5537D 5752D 7471D 8281D 8286D 14482T 15941C
Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 3010A 4859C 8860G
Extras(17): 65D 191D 299I 459D 2074I 2156D 2405D 3307D 4317I 5004C 5537D 5752D 7471D 8281D 8286D 14482T 15941C
Untested(3): 750 4769 15326
3) H1ax
Defining Markers for haplogroup H1ax:
HVR2: 263G
CR: 750G 1438G 3010A 4769G 5054C 7471T 8429T 8860G 15326G
HVR1:
Marker path from rCRS to haplogroup H1ax (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 3010A ⇨ H1 ⇨ 5054C 7471T 8429T ⇨ H1ax ⇨ 65D 191D 299I 459D 2074I 2156D 2405D 3307D 4317I 4859C 5004C 5537D 5752D 7471D 8281D 8286D 14482T 15941C
Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 3010A 7471D 8860G
Extras(18): 65D 191D 299I 459D 2074I 2156D 2405D 3307D 4317I 4859C 5004C 5537D 5752D 7471D 8281D 8286D 14482T 15941C
Untested(5): 750 4769 5054 8429 15326
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