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MindHive
03-27-2017, 01:08 PM
I used MtHap calculator with AncestryDNA that was converted to 23andMe format.
Is H55a my mtHaplogroup, as it is ranked no. 1...
Any info about this data would be much appreciated.
Thanks,
MindHive



(BACK)
mthap version 0.19b (2015-05-11); haplogroup data version PhyloTree Build 17 (2016-02-18)*
raw data source dnl27647_vcu.txt (15MB)
Found 138 markers at 138 positions covering 0.8% of mtDNA.


Markers found (shown as differences to rCRS):

HVR2:
CR:*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
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) H55a
Defining Markers for haplogroup H55a:
HVR2:*263G
CR:*750G*1438G*3387C*4709T*4769G*8860G*10646A*1532 6G
HVR1:
Marker path from rCRS to haplogroup H55a (plus extra markers):
H2a2a1(rCRS)*⇨*263G*⇨ H2a2a*⇨*8860G*15326G*⇨ H2a2*⇨*750G*⇨ H2a*⇨*4769G*⇨ H2*⇨*1438G*⇨ H*⇨*10646A*⇨ H55*⇨*3387C*4709T*⇨ H55a*⇨*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Imperfect Match.*Your results contained differences with this haplogroup:
Matches(1):*3387C
Extras(108):*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Untested(8):*263 750 1438 4709 4769 8860 10646 15326


2) H13a2b4
Defining Markers for haplogroup H13a2b4:
HVR2:*263G
CR:*709A*750G*2259T*4769G*8266G*8860G*9548A*13762G *14872T*15217A*15326G
HVR1:
Marker path from rCRS to haplogroup H13a2b4 (plus extra markers):
H2a2a1(rCRS)*⇨*263G*⇨ H2a2a*⇨*8860G*15326G*⇨ H2a2*⇨*750G*⇨ H2a*⇨*4769G*⇨ H2*⇨*1438G*⇨ H*⇨*14872T*⇨ H13*⇨*2259T*⇨ H13a*⇨*709A*⇨ H13a2*⇨*13762G*⇨ H13a2b*⇨*1438A*8266G9548A*15217A*⇨ H13a2b4*⇨*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Imperfect Match.*Your results contained differences with this haplogroup:
Matches(1):*15217A
Extras(108):*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Untested(12):*263 709 750 1438 2259 4769 8266 8860 9548 13762 14872 15326


2) H86
Defining Markers for haplogroup H86:
HVR2:*263G
CR:*750G*1438G*1809C*4769G*8860G*15326G
HVR1:
Marker path from rCRS to haplogroup H86 (plus extra markers):
H2a2a1(rCRS)*⇨*263G*⇨ H2a2a*⇨*8860G*15326G*⇨ H2a2*⇨*750G*⇨ H2a*⇨*4769G*⇨ H2*⇨*1438G*⇨ H*⇨*1809C*⇨ H86*⇨*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Imperfect Match.*Your results contained differences with this haplogroup:
Flips(1):*1809A
Extras(108):*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Untested(6):*263 750 1438 4769 8860 15326


2) H2a1k
Defining Markers for haplogroup H2a1k:
HVR2:*263G
CR:*750G*951A*3396C*8860G*15326G
HVR1:*16354T
Marker path from rCRS to haplogroup H2a1k (plus extra markers):
H2a2a1(rCRS)*⇨*263G*⇨ H2a2a*⇨*8860G*15326G*⇨ H2a2*⇨*750G*⇨ H2a*⇨*951A*16354T*⇨ H2a1*⇨*3396C*⇨ H2a1k*⇨*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Imperfect Match.*Your results contained differences with this haplogroup:
Flips(1):*3396A
Extras(108):*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Untested(6):*263 750 951 8860 15326 16354


3) H2a2a1
Defining Markers for haplogroup H2a2a1:
HVR2:
CR:
HVR1:
Marker path from rCRS to haplogroup H2a2a1 (plus extra markers):
H2a2a1(rCRS)*⇨*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Good Match!*Your results also had extra markers for this haplogroup:
Extras(109):*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G


3) H26c
Defining Markers for haplogroup H26c:
HVR2:*146C*263G
CR:*750G*1438G*4769G*8860G*10562G*11152C*15326G
HVR1:
Marker path from rCRS to haplogroup H26c (plus extra markers):
H2a2a1(rCRS)*⇨*263G*⇨ H2a2a*⇨*8860G*15326G*⇨ H2a2*⇨*750G*⇨ H2a*⇨*4769G*⇨ H2*⇨*1438G*⇨ H*⇨*11152C*⇨ H26*⇨*146C*10562G*⇨ H26c*⇨*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Imperfect Match.*Your results contained differences with this haplogroup:
Flips(1):*10562T
Extras(108):*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15325G 15496G 15571T 15578A 15811G 15966G
Untested(8):*146 263 750 1438 4769 8860 11152 15326


3) H1c17
Defining Markers for haplogroup H1c17:
HVR2:*263G*477C
CR:*750G*1438G*3010A*4769G*8860G*15325C*15326G
HVR1:
Marker path from rCRS to haplogroup H1c17 (plus extra markers):
H2a2a1(rCRS)*⇨*263G*⇨ H2a2a*⇨*8860G*15326G*⇨ H2a2*⇨*750G*⇨ H2a*⇨*4769G*⇨ H2*⇨*1438G*⇨ H*⇨*3010A*⇨ H1*⇨*477C*⇨ H1c*⇨*15325C*⇨ H1c17*⇨*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15496G 15571T 15578A 15811G 15966G
Imperfect Match.*Your results contained differences with this haplogroup:
Flips(1):*15325G
Extras(108):*1003T 1005G 1241T 1289T 1308C 1380A 1383C 1389T 1404T 1436G 1506C 1809A 2937C 2989T 3008G 3242A 3250A 3255C 3270T 3273A 3289T 3302C 3375G 3387C 3393T 3396A 3459G 3634G 3696G 3699G 3732G 3945G 4135A 4283G 4331G 4809G 5520G 5531G 5548G 5557A 5813T 5815A 6263G 6327C 6479G 6720T 7273C 7525A 7670T 7895G 8362G 8527T 8528G 8837G 8850T 9184T 9437G 9803G 9951G 10009T 10157T 10190T 10196G 10437A 10449A 10562T 11695G 11777G 11811A 11983T 12146G 12182G 12191G 12200T 12206G 12257C 12296T 12314G 12319A 12337T 12611A 12704C 12769A 12810T 12847C 13041G 13044A 13512G 13636A 14452G 14458G 14483T 14494A 14708T 14830G 14845G 14848T 14889A 14984G 15196T 15217A 15241G 15256G 15496G 15571T 15578A 15811G 15966G
Untested(8):*263 477 750 1438 3010 4769 8860 15326



Need help?
First, please check the*Frequently Asked Questions*for guidance on how to read this report. If you still have questions, there is a*discussion about mthap on eng.molgen.org. You can also email your questions to me at*[email protected] So that I can best help you, please include a copy of the complete mthap report and/or your mtDNA data file in your email.