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Lineages and Results of Y-DNA Testing for STRAUB and Variations
Haplogroup R-1b1a-2a1a-1a3 = R-L1 null439
Results
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Y-DNA Haplogroups Represented in the Project
(number tested at FTDNA + number tested elsewhere / number of different progenitors)
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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)

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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-1b1a-2a1a-1a3 = R-L1 / S26 null439

Deme 14
To view lineage, please scroll to the right.
Surname Kit # Ysearch
User ID
SNP
Tests
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
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
null439 Cluster 1 Modal Values 13 24 14 11 11 14 12 12 0 13 13 29 17  9  9 11 11 25 15 19 29 15 15 16 17 11 11 19 23 16 16 18 17 38 38 12 12 11 9 15 16 8 10 10 8 10 10 12 23 23 15 10 12 12 15 8 12 22 20 13 12 11 13 11 11 13 12 Modals for Null-439 as of 11 Apr 2007; markers in red, yellow, or orange are differences from Modal R1b.
           
STRAUB 82917     13 24 14 11 11 14 12 12 0 14 13 30 17  9  9 11 11 25 15 19 30 15 15 16 17 11 11 19 23 16 15 18 17 36 39 12 12 11 9 15 16 8 10 10 8 10 10 12 23 23 15 10 12 12 15 8 12 22 20 13 12 11 13 10 11 13 12 Pvt4, Pvt3, Gustav August2, Charles/Carl1 immigrant to Philadelphia from Wuerttemberg in 1881
#82917 has a null value at DYS439 (red table cell), meaning the indicator used to locate the marker has been lost, so no count of STRs could be made.  The change in the indicator is a SNP mutation (S26+ = L1+), and this mutation defines Haplogroup R-1b1a-2a1a-1a3.  The mutation appears to have arisen about 2500 to 3500 years ago.  Note that FTDNA will show a value of 12 for the marker on the assumption that the modal value is what the count would most likely be if it could be made. 
This individual has hundreds of matches at 12-markers, but only a few near matches at 25 or 37 markers (none in surname STRAUB).  At 67 markers, he has no matches with anyone.
The null439 condition is sufficiently distinct to warrant its own project, and your admin recommends joining the null439 DNA Project.  The null439 project web site is an excellent source of information on what a null439 is and what it means.  The null439 project has identified two major clusters of haplotypes, with DYS459b=9 (yellow table cell) being the major difference distinguishing Cluster 1 from Cluster 2.  The null439 mutation is found thinly in western Europe, but is concentrated in the British Isles; Cluster 1 is concentrated in England and, most notably for our purposes, is also found in southern Germany.  The late Leo Little, former administrator of the null439 project, told me (in Apr 2007) the three German null439's are surnamed BETTINGER, BLY, and STINER, and are from the region of the Rhine River Valley and Wuerttemberg.
Assuming a modal value of 12 for DYS439, our subject's haplotype becomes quite common, with many near matches, which is not surprising considering its resemblance to the modal R1b haplotype.  It's the S26+ SNP mutation that makes this group uncommon.  Your project admin recommends taking an S26+ test to confirm the presence of this mutation.
   

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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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