А вот у меня:Your rCRS differences found:
HVR2: 152C 263G
CR: 750G 1438G 4769G 10394T 15326G
HVR1: (16519C)
IMPORTANT NOTE: The above rCRS differences are almost certainly incomplete due to limitations of genotyping technology and are not comparable to mtDNA sequencing results. They should not be used with services or tools that expect sequencing results (e.g. mitosearch).
Best mtDNA Haplogroup Matches:
1) H16(152)
Defining Mutations for haplogroup H16(152):
HVR2: 152C 263G
CR: 750G 1438G 4769G 8860G 10394T 15326G
HVR1:
Imperfect Match. Your results contained these differences with this haplogroup:
Extras(0): (16519C)
Untested(1): 8860G
2) H16a
Defining Mutations for haplogroup H16a:
HVR2: 152C 263G
CR: 750G 1438G 4769G 8592A 8860G 10394T 15326G
HVR1:
Imperfect Match. Your results contained these differences with this haplogroup:
Extras(0): (16519C)
Untested(2): 8592A 8860G
3) H16
Defining Mutations for haplogroup H16:
HVR2: 263G
CR: 750G 1438G 4769G 8860G 10394T 15326G
HVR1:
Imperfect Match. Your results contained these differences with this haplogroup:
Extras(1): 152C (16519C)
Untested(1): 8860G
А вот у дядьки:mthap version 0.05 (2010-08-24); haplogroup data version Phylotree Build 10 (2010-08-10)
raw data source genome_Nickolay_Mochalov_Mito_20100826115935.txt (44KB)
Found 2130 markers at 2007 positions covering 12.1% of mtDNA.
Your rCRS differences found:
HVR2: 263G
CR: 750G 1438G 4769G 10394T 15326G
HVR1: (16519C)
IMPORTANT NOTE: The above rCRS differences are almost certainly incomplete due to limitations of genotyping technology and are not comparable to mtDNA sequencing results. They should not be used with services or tools that expect sequencing results (e.g. mitosearch).
Best mtDNA Haplogroup Matches:
1) H16
Defining Mutations for haplogroup H16:
HVR2: 263G
CR: 750G 1438G 4769G 8860G 10394T 15326G
HVR1:
Imperfect Match. Your results contained these differences with this haplogroup:
Extras(0): (16519C)
Untested(1): 8860G
2) H16b
Defining Mutations for haplogroup H16b:
HVR2: 263G
CR: 750G 1438G 4769G 8860G 9129T 10394T 15326G
HVR1:
Imperfect Match. Your results contained these differences with this haplogroup:
Extras(0): (16519C)
Untested(2): 8860G 9129T
3) H16(152)
Defining Mutations for haplogroup H16(152):
HVR2: 152C 263G
CR: 750G 1438G 4769G 8860G 10394T 15326G
HVR1:
Imperfect Match. Your results contained these differences with this haplogroup:
Extras(0): (16519C)
No-Calls(1): 152C
Untested(1): 8860G
Мито одно, а интерпретация разная однако.