S&SMFB - FAMILY HISTORY BASED ON GENETIC DATA
II-2,
PATERNAL LINE, Y-CHROMOSOME SNP RESULTS:
rev. 04 March 2016
POSITIVE Y-SNP
RESULTS & ISOGG HAPLOGROUPS:
http://www.isogg.org/tree/ISOGG_YDNA_SNP_Index.html
SNP |
SNP |
G2 - |
ISOGG |
Lab |
Age (years Ago) and Location of Origin |
REMARKS |
1 |
L1155 |
N |
A0-T |
Big Y |
200,000+? ya |
SNP Matches: L1089+, L1090+, L1093+, L1095+, L1098+, L1101+, L1105+, L1116+, L1118+, L1120+, L1121+, L1123+, L1124+, L1125+, L1127+, L1129+, L1130+, L1132+, L1135+, L1136+, L1137+, L1142+, L1143+, L1145+, L1150+, L1155+, L1235+ |
2 |
See |
N |
A1 |
Big Y |
150000+? ya |
SNP Matches: L989+, L1002+, L1004+, L1009+, L1013+, L1053+, L1112+, V174+, V238+, V241+, V250+ |
3 |
See |
N |
A1b |
Big Y |
100.000+? ya |
No SNP Matches; **Mismatches: P108- (exp. +), V221- (exp. +) |
4 |
M42 |
Y |
BT |
G2 |
~75,000ya , Africa |
SNP Matches: V31+, L418+, L438+, L440+, L604+, L957+, L962+,
L969+, L970+, L977+, L1060+, L1061+, PF302+, M42+, M94+, M299+, P97+,
V59+, V64+, V102+, V187+, V235+ |
5 |
M168 |
Y |
CT |
G2 |
~ 70,000ya, Africa/ Asia |
The man who gave rise to the first genetic marker in your lineage probably lived in northeast Africa in the region of the Rift Valley, perhaps in present-day Ethiopia, Kenya, or Tanzania. Scientists put the most likely date for when he lived at around 70,000 years ago. His descendants became the only lineage to survive outside of Africa, making him the common ancestor of every non-African man living today. |
6 |
M89 |
Y |
F |
G2 |
~50,000ya, |
SNP Matches: M168+, M294+ |
7 |
L16 |
N |
IJK |
G2 |
|
|
8 |
P128 |
Y |
K |
G2 |
45,000ya, |
The descendants of P128 migrated to the east and north, picking up additional markers on their Y-chromosomes. This lineage is the parent of several major branches on the Y-chromosome tree: O, the most common lineage in East Asia; R, the major European Y-chromosome lineage; and Q, the major Y-chromosome lineage in the Americas. These descendant branches went on to settle the rest of Asia, the Americas, and Europe; many others traveled to Southeast Asia. |
9 |
M526 |
N |
K(xLT) |
G2 |
|
|
10 |
M45 |
Y |
P |
G2 |
35,000 ya, Central or South Asia |
This paternal ancestor traveled with groups in the open savannas between Central and South Asia during the Paleolithic. These big game hunters were the parents to two of the most widespread male lineages in modern populations, one that is responsible for the majority of pre-Columbian lineages in the Americas (haplogroup Q) and many others from Asia and Europe. Another one that spread farther into Asia produced the highest frequency lineages in European populations (haplogroup R). |
11 |
M207 |
Y |
R |
FT;G2 |
30,000ya, Central Asia |
While it appears to have been one of the earliest lineages to settle in Europe more than 25,000 years ago, more recent population expansions associated with the post-glacial repopulation of northern Europe after the end of the last ice age, as well as the spread of agriculture during the Neolithic, also contributed to its high frequency in Ireland, the UK, France and Spain. |
12 |
M173 |
N |
R1 |
FT;G2 |
|
|
13 |
M343 |
Y |
R1b |
FT;G2 |
17,000-22,000ya, |
The first members of this lineage lived as hunter-gatherers on the open savannas that stretched from Korea to Central Europe. They took part in the advances in hunting technology that allowed for population growth and expansions. When the Earth entered a cooling phase, most from this line sheltered in refugia to the southeast of Europe and in West Asia. It was from these refugia that their populations rapidly expanded when the ice once more receded. Some traveled west across Europe. Others moved back toward their distant ancestors’ homelands in Africa, passing through the Levant region. Through these movements and the population boom triggered by the Neolithic Revolution, this lineage and its descendant lineages came to dominate Europe. |
14 |
L278[3] |
Y |
R1b1 |
G2 |
Age to be determined |
While some from this group traveled west into Central Asia, others moved south toward the Levant region. Today, they are present in trace frequencies of less than 1 percent in Italy, the Ukraine, and the region of the Pannonian Basin. |
15 |
P297 |
N |
R1b1a |
G2 |
|
(Black Sea) |
16 |
M269[2] |
N |
R1b1a2 |
FT |
|
(Pontic Steppe) |
17 |
L23 |
N |
R1b1a2a |
G2 |
|
(South East Europe) |
18 |
L51 |
N |
R1b1a2a1 |
G2 |
|
(L51 is an transitional clade between the Eastern L23 and the Western L11) |
19 |
P310 |
Y |
R1b1a2a1a |
G2 |
Age to be determined |
Members of this lineage have traveled to Central Asia, Europe, and the Levant region. One descendant branch has the highest frequency of any male line in Western Europe. However, rather than a single movement across Europe, this lineage’s branches may represent many simultaneous and successive waves of migration. Today, it is 48 to 52 percent of male lineages in Ireland. It is 45 percent of those in France. It is about 38 percent of the male population in Spain. It is about 8 percent of male lineages in Italy. It is about 5 percent of male lineages in Oman. It is 1 to 2 percent of the male population in Iraq and Lebanon. It is also 1 to 2 percent of the male population in Kazakhstan.
|
20 |
U106 |
Y |
R1b1a2a1a1 |
FT;G2 |
14,000-4250ya |
Final SNP on G2 "Your Map".
Today, geneticists have
found it and its descendant branches at moderate to high frequencies
throughout Europe and occasionally in West Asia. (m# 66, 492=13) |
21 |
Z381 |
Y |
R1b-Z381 |
FT;G2 |
Belgium & |
aka S263, Y-Position (YP) 7246726. R-Z381 in Belgium and the Netherlands. Nood-Brabant; Antwerp; Vlaarns-Waals Brabant & Brussels; West-Vlaanderen; Oost-Valaanderen and Limburg using DNA and Genealogical information. [6] |
22 |
Z156 |
Y |
R1b-Z156 |
FT;G2 |
|
|
23 |
Z307 |
Y |
R1b-Z307 |
G2 |
|
Currently unbroken chain - Z307/Z306/Z305 |
24 |
Z304 |
Y |
R1b-Z304 |
FT;G2 |
|
|
25 |
DF96 |
Y |
R1b-DF96 |
FT |
|
(m# 75, 717=18) DF96 splits into two groups S11515 & FGC13326, ABSjr is downstream of FGC13326. |
26 |
FGC13326 |
N |
R1b-FGC13326 |
FT |
|
FGC13326 splits into two groups, S25234 & S22047, ABSjr is downstream of S22047 |
27 |
S22047 |
N |
R1b-22047 |
YSEQ |
(m #36, 442=11) S22047 splits into two groups S19552 & FGC13602, PSHG downstream of FGC13602[7]. | |
28 | FGC13602 | N | R1b-FGC13602 | YSEQ | FGC13602/ FGC13610/ FGC13603 are common SNPS with the PSHG, Fred Westcott 180037/623 and Steve Barton 194434/650 [7]. | |
29 | FGC13595 | N | R1b-FGC13595 | YSEQ | FGC13595/FGC13607 [7] are common SNP's with the PSHG and Fred Westcott. Steve Barton tested negative for these two SNP's. Fred Westcott splits from FGC13595 to his current seven "Private" SNP's FGC15216/FGC15217/FGC15219/FGC15220/FGC15222/FGC15223/FGC15224. | |
30 | FGC13604 | N |
R1b- FGC13604 |
YSEQ | The location of FGC13604 was changed from the chain of FGC13609/FGC13604/FGC13605 on 04 March 2016 by YSEQ test results of Larry Fuller 381175/5045. | |
31 | FGC13609 | N | R1b-FGC13609 | YSEQ | FGC13609/FGC13605[7]; YSEQ tests on these 2 SNP's are proved to be unique to members of the PSHG. The PSHG SNP's were brought to the Picataqua from England by 1670/71 by Peter Staple (c1642-1719) of Kittery, New England. | |
32 |
FGC13606 | N | R1b-FGC13606 | YSEQ |
|
FGC13606 is the private or
terminal SNP of ABSjr., and ARS a mutation that happened within the lineage from
Peter Staple Jr., b bet. 1672 &1675 and the birth date of ABSjr. All PSHG
members tested for this SNP were found negative. |
NOTES:
RE: National Geographic Society, Genographic Project, GENO 2.0, Your Map.
https://genographic.nationalgeographic.com/ and ISOGG HAPLOGROUPS:
http://www.isogg.org/tree/ISOGG_YDNA_SNP_Index.html rev 17 July 2013
[1] Geno 2.0 & FTDNA lab results processed by the FTDNA Genomics Research
Center. See #5010 at
http://www.familytreedna.com/public/pshp/default.aspx?section=ysnp
[2] **Note, SNP, P231 was reported by GEN 2.0 in my "Your Map" is incorrect as
no SNP P231 was reported in the GENO 2.0 test results as positive.
The correct SNP is M269.
[3] Both SNP's L278 and P25 reported positive in GENO 2.0 test results. The
Y-Position of SNP P25 is variable thus SNP L278 is more reliable.
[4] Help analyzing GENO 2.0 Y-DNA raw data by David Carlisle of the R1b-U106
Y-DNA Haplogroup.
http://www.familytreedna.com/public/U106/default.aspx
[5] For FTDNA FAQ on DNA test results see
http://www.familytreedna.com/faq/answers/default.aspx?faqid=8
[6] R-Z381 has 69 samples (n) with a frequency (f) of 8.9% of 50 haplotypes with
773 participants using genealogical data and surnames in -
(1) Nood-Brabant
(Province in Netherlands) n=17, f 12.9%;
(2) Antwerp (Province in Belgium n=18,
f 10.1%;
(3) Vlaams-Waals Brabant (Provinces 'Vallms Brabant' and 'Brabant
Wallolon', and the Brussels Region, in Belgium) n=11, f 8.9%;
(4) West-Vlaanderen
(Province in Belgium) n=6, f 5.5%;
(5) Oost-Vlaanderen (Province in Begium)n=10,
f 11.4 and
(6) Limburg (Provinces 'Limburg' in the Neatherlands and Belgim) n=6,
f 8.0%. The region 'Belgian Brabant is the sum of 2 and 3, n=29, f 19%.
Ref.
Information compiled from, Fig. 1, Table 1 and the article - M.H.D. Latmuseau,
et al., Increasing phylogenetic resolution still informative for Y chromosomal
studies on West-European populations, Forensic Sci. Int. Genet. (2013). http://dx.doi.org/10.1016/j.fsigen.2013.04.002
View on-line free at -
athttp://www.researchgate.net/publication/236918241_Increasing_phylogenetic_resolution_still_informative_for_Y_chromosomal_studies_on_West-European_populations
[7] FTDNA BigY SNP's were analyzed and named by the Full Genome Company start with - FGC. Individual BigY SNP's were analyzed and testing of PSHG members performed by YSEQ DNA Origins Project, on-line at http://www.yseq.net/
FTDNA Y111 STR TEST RESULTS: ABS Sr. & ABS Jr. & ARS, Haplogroup R1b-FGC13606 rev 23 September 2015
|
FTDNA |
3 |
3 |
1 |
3 |
3 |
3 |
4 |
3 |
4 |
3 |
3 |
3 |
|
4 |
4 |
4 |
4 |
4 |
4 |
4 |
4 |
4 |
4 |
4 |
4 |
4 |
4 |
H |
Y |
Y |
4 |
6 |
5 |
5 |
C |
C |
4 |
4 |
REMARKS |
||
PSHG |
|
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
GD |
13 |
14 |
15 |
16 |
17 |
18 |
19 |
20 |
21 |
22 |
23 |
24 |
25 |
GD |
26 |
27 |
28 |
29 |
30 |
31 |
32 |
33 |
34 |
35 |
36 |
37 |
GD |
|
PSHG>> |
13 |
24 |
14 |
10 |
11 |
14 |
12 |
12 |
12 |
13 |
13 |
29 |
0 |
17 |
9 |
10 |
11 |
11 |
26 |
15 |
19 |
29 |
15 |
15 |
16 |
17 |
0 |
11 |
11 |
19 |
23 |
16 |
15 |
18 |
19 |
37 |
38 |
11 |
12 |
0 |
||
FGC13606 |
|
|||||||||||||||||||||||||||||||||||||||||
Arthur B Sr |
# 113808 |
13 |
24 |
14 |
10 |
11 |
14 |
12 |
12 |
12 |
13 |
13 |
29 |
0 |
17 |
9 |
10 |
11 |
11 |
26 |
15 |
19 |
29 |
15 |
15 |
16 |
17 |
0 |
11 |
11 |
19 |
23 |
16 |
15 |
18 |
19 |
37 |
38 |
11 |
12 |
0 |
|
Arthur B Jr. |
# 5010 |
13 |
24 |
14 |
10 |
11 |
14 |
12 |
12 |
12 |
13 |
13 |
29 |
0 |
17 |
9 |
10 |
11 |
11 |
26 |
15 |
19 |
29 |
15 |
15 |
16 |
17 |
0 |
11 |
11 |
19 |
23 |
16 |
15 |
18 | 19 |
37 |
38 |
11 |
12 |
0 |
|
Arthur R | # 430881 |
13 |
24 |
14 |
10 |
11 |
14 |
12 |
12 |
12 |
13 |
13 |
29 |
0 |
17 |
9 |
10 |
11 |
11 |
26 |
15 |
19 |
29 |
15 |
15 |
16 |
17 |
0 |
11 |
11 |
19 |
23 |
16 |
15 |
18 | 19 |
37 |
38 |
11 |
12 |
0 |
abs
1b |
|
5 |
5 |
3 |
3 |
5 |
5 |
6 |
4 |
4 |
5 |
4 |
4 |
|
5 |
5 |
4 |
4 |
5 |
4 |
4 |
4 |
5 |
4 |
6 |
5 |
4 |
5 |
6 |
4 |
5 |
REMARKS |
||
PSHG |
|
38 |
39 |
40 |
41 |
42 |
43 |
44 |
45 |
46 |
47 |
48 |
49 |
50 |
51 |
52 |
53 |
54 |
55 |
56 |
57 |
58 |
59 |
60 |
61 |
62 |
63 |
64 |
65 |
66 |
67 |
GD |
||
PSHG>> |
11 |
9 |
15 |
16 |
8 |
10 |
10 |
8 |
10 |
10 |
12 |
22 |
23 |
17 |
10 |
12 |
12 |
15 |
8 |
12 |
22 |
20 |
13 |
12 |
11 |
13 |
11 |
11 |
13 |
11 |
0 | |||
FGC13606 | ||||||||||||||||||||||||||||||||||
Arthur B Sr |
# 113838 |
11 |
9 |
15 |
16 |
8 |
10 |
10 |
8 |
10 |
10 |
12 |
22 |
23 |
17 |
10 |
12 |
12 |
15 |
8 |
12 |
22 |
20 |
13 |
12 |
11 |
13 |
11 |
11 |
13 |
11 |
0 |
Ysearch KEP7G |
|
Arthur B Jr. |
# 5010 |
11 |
9 |
15 |
16 |
8 |
10 |
10 |
8 |
10 |
10 |
12 |
22 |
23 |
17 |
10 |
12 |
12 |
15 |
8 |
12 |
22 |
20 |
13 |
12 |
11 |
13 |
11 |
11 |
13 |
11 |
0 |
Ysearch MYBF2 |
|
Arthur R | #420881 |
11 |
9 |
15 |
16 |
8 |
10 |
10 |
8 |
10 |
10 |
12 |
22 |
23 |
17 |
10 |
12 |
12 |
15 |
8 |
12 |
22 |
20 |
13 |
12 |
11 |
13 |
11 |
11 |
13 |
11 |
0 |
abs
|
|
7 |
4 |
6 |
4 |
5 |
7 |
7 |
7 |
5 |
5 |
5 |
5 |
5 |
4 |
5 |
6 |
5 |
6 |
4 |
4 |
4 |
A |
4 |
4 |
1 |
5 |
7 |
5 |
6 |
5 |
7 |
5 |
5 |
5 |
5 |
7 |
6 |
5 |
6 |
4 |
5 |
4 |
4 |
4 |
GD |
|
PSHG |
|
68 |
69 |
70 |
71 |
72 |
73 |
74 |
75 |
76 |
77 |
78 |
79 |
80 |
81 |
82 |
83 |
84 |
85 |
86 |
87 |
88 |
89 |
90 |
91 |
92 |
93 |
94 |
95 |
96 |
97 |
98 |
99 |
100 |
101 |
102 |
103 |
104 |
105 |
106 |
107 |
108 |
109 |
110 |
111 |
||
PSHG>> |
34 |
14 |
9 |
16 |
12 |
25 |
26 |
18 |
12 |
11 |
13 |
12 |
10 |
9 |
12 |
12 |
10 |
11 |
11 |
30 |
12 |
13 |
24 |
13 |
10 |
|
21 |
15 |
18 |
13 |
24 |
16 |
12 |
15 |
25 |
12 |
23 |
18 |
10 |
14 |
17 |
9 |
12 |
12 |
0 | ||
FGC13606 | |||||||||||||||||||||||||||||||||||||||||||||||
Arthur B Jr. |
# 5010 |
34 |
14 |
9 |
16 |
12 |
25 |
26 |
18 |
12 |
11 |
13 |
12 |
10 |
9 |
12 |
12 |
10 |
11 |
11 |
30 |
12 |
13 |
24 |
13 |
10 |
|
21 |
15 |
18 |
13 |
24 |
15 |
12 |
15 |
25 |
12 |
23 |
18 |
10 |
14 |
17 |
9 |
12 |
12 |
1 |
|
Arthur R | #430881 |
34 |
14 |
9 |
16 |
12 |
25 |
26 |
18 |
12 |
11 |
13 |
12 |
10 |
9 |
12 |
12 |
10 |
11 |
11 |
30 |
12 |
13 |
24 |
13 |
10 |
|
21 |
15 |
18 |
13 |
24 |
15 |
12 |
15 |
25 |
12 |
23 |
18 |
10 |
14 |
17 |
9 |
12 |
12 |
1 |
NOTE:
1) Ongoing genealogical and genetic research of the PETER STAPLE HERITAGE GROUP
(PSHG) (c1642-1719) is found at the FTDNA-PSHG website on-line at -
http://www.familytreedna.com/public/pshp/default.aspx The PSHG
Anthrogenealogy Study can be requested from the FTDNA-PSHG website.
2) On 31 December 2013, enough genetic data of the membership had been assembled
to present the PSHG Modal Haplotype.
Y-DNA LINEAGE:
To view lineage of Art B., Sr. & Art B., Jr. & Art R. Staples to Peter Staple (c1642-1719), c1670 of
Kittery, ME click HERE
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