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Lineages and Results of Y-DNA Testing for STRAUB, TRAUB, STRAUBE, STROOP, STRUB,
and Variations, especially STROUP, STROUPE, TROUP, TROUPE, etc.
Haplogroup R1a
Results
Hub
Y-DNA Haplogroups Represented in the Project
(number tested at FTDNA + number tested elsewhere / number of different progenitors)
Project
Home
E (1 / 1)  I1  (4 / 3) I1-L592 (31 / 1)  I2  (13 / 6) J2 (5 / 2) R1a (2 / 1) R1b (25 / 19) T (1 / 1)

Haplogroup R1a is believed to have originated on the Eurasian Steppes and is now found in western and central Asia, India, and Slavic populations of eastern Europe, but also as far west as Scandinavia and the British Isles.  These are the original "Indo-Europeans" (Aryans) whose cultures and languages first came to dominate Europe; it is the culture that domesticated the horse.  Some argue that only R1a is the true "Viking" haplogroup.
Haplogroup R1a Subclades as Defined by SNP Mutations
Backbone SNP testing, provided free by Family Tree DNA, shows our R1a members to be R1a1 (M198+ and M17+).  The subclades of R1a1 are rare, and deep SNP testing is usually negative for the downstream SNPs, so most R1a's turn out to be R-1a1* (root/ancestral R1a1), but there's no way to be certain without taking the tests.

An asterisk is used to differentiate between someone who has merely tested positive for a key SNP and someone who has not only tested positive for the key SNP, but has also tested negative for any downstream SNPs.  (SNPs in parentheses indicate a redundant marker, tested by some labs, but not FTDNA.)

(An equal sign in the ISOGG column means the value is the same as FTDNA.)
Mutations Standard
FTDNA ISOGG
M207=UTY2 P224 P227 P229 P232 P280 P285 | S4 S9 V45 R =
_ M173=P241 M306=S1 P231 P233 P234 P236 P238 P241 P242 P245 P286 P294 | P225 R-1 =
_ M420=L146 M449=L145 M511=L63 M513=L62 M516=L120 R-1a 
_ M448=L122 M459 SRY10831.2=SRY1532.2 | M516=L120 R-1a1
_ M198 L168 M17 M512 M514 M515 PS68 | L449 R-1a1a =
  M417 PS7 | L457 R-1a1a-1 =
_ M56 R-1a1a-1a =
M157.1 R-1a1a-1b =
M64.2 M87 M204 R-1a1a-1c =
P98 R-1a1a-1d =
PK5 R-1a1a-1e =
M434 R-1a1a-1f =
M458 R-1a1a-1g =
  M334 R-1a1a-1g1 =
L260 R-1a1a-1g2 =
L176.1=S179.1 R-1a1a-1h =
  L175 R-1a1a-1h1
L365   R-1a1a-1i
L366   R-1a1a-1j
P278.2   R-1a1a-1k
M343 R-1b =
M479   R-2
L266 M124 P249 P267 R-2 R-2a

To view more of the page without scrolling, temporarily reduce the text size or page size in your browser.  Red labels indicate markers that typically mutate more frequently than those labeled in black.  (Empty cells that are darkened indicate tests not ordered.)  Keywords for search engines: genetic genealogy.
Haplogroup R-1a1 = R-M198
To view the subjects' lineages, please scroll to the right.
Surname Kit # Ysearch
User ID

Most
Downstream
Positive
SNP
Actually
Tested
Haplotype as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 - Markers 26-37 Markers 38-67
3
9
3
3
9
0

19
/
3
9
4
3
9
1
a
|
3
8
5
b
|
3
8
5
4
2
6
3
8
8
4
3
9
i
|
3
8
9
3
9
2
ii
|
3
8
9
4
5
8
a
|
4
5
9
b
|
4
5
9
4
5
5
4
5
4
4
4
7
4
3
7
4
4
8
4
4
9
a
|
4
6
4
b
|
4
6
4
c
|
4
6
4
d
|
4
6
4
e
|
4
6
4
f
|
4
6
4
4
6
0
H4
|
G
A
T
A
IIa
|
Y
C
A
IIb
|
Y
C
A
4
5
6
6
0
7
5
7
6
5
7
0
a
|
C
D
Y
b
|
C
D
Y
4
4
2
4
3
8
5
3
1
5
7
8
a
|
S1
3
9
5
b
|
S1
3
9
5
5
9
0
5
3
7
6
4
1
4
7
2
S1
4
0
6
5
1
1
4
2
5
a
|
4
1
3
b
|
4
1
3
5
5
7
5
9
4
4
3
6
4
9
0
5
3
4
4
5
0
4
4
4
4
8
1
5
2
0
4
4
6
6
1
7
5
6
8
4
8
7
5
7
2
6
4
0
4
9
2
5
6
5
R-1a Modal Haplotype 13 25 15 10 11 14 12 12 10 13 11 30 15 9 10 11 11 23 14 20 32 12 15 15 16     11 11 19 23 16 16 18 18 34 39 12 11                                                             Modal values per John McEwan (as of 23 Feb 2007).
                 
STRAUB 30709   M198 13 25 16 10 11 13 12 12 11 13 11 29 16 9 10 11 11 23 14 20 32 11 12 14 15 15 16 10 11 19 19 17 15 19 20 34 40 14 11                                                             Pvt6, Pvt5, Matthew John4, John Matthew3, Urbanus2, Andreas1 of Östringen, Baden
STRAUB 61136   M198 13 25 16 10 11 13 12 12 11 13 11 29                                                                                                                   Pvt5, Pvt4, Elmer E.3, Englebert Augustus2, Andreas1 of Östringen, Baden
On paper, these two individuals descend from the same progenitor, and they match perfectly at 12 markers.  Their haplotype is rare, with no full or near matches in or out of the project at any level, except with each other, making their haplotype unique and easily distinguishable.
As part of its "Haplogroup Assurance" policy, FTDNA has given #30709 and #61136 free backbone SNP tests.  Results are positive for the M17 and M198 mutations, so while our subjects have only a low resemblance to the modal R-1a haplotype, these results confirm they are, indeed, Haplogroup R-1a1.
   

What constitutes a match?
Matches in other surnames are usually mere coincidence, so please ignore them I'll let you know when you shouldn't!
For 12 markers: 9 or less is a non-relative; for 10-12 markers, please see this table compiled by FTDNA.
For 25 markers: 21 or less is a non-relative; for 22-25 markers,
For 37 markers: 31 or less is a non-relative; for 32-37 markers,
For 67 markers: 59 or less is a non-relative; for 60-67 markers,
For 111 markers: 100 or less is a non-relative; for 101-111 markers,
For any test:  0 matching markers, please contact NASA.

 
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