paternal_ydna

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
Ref
#

SNP
+

G2 -
Your
Map

ISOGG
Haplogroups

 

Lab
Results
[1]

Age (years Ago) and Location of Origin

REMARKS

             

1


L1130

L1155
 

N

A0-T

Big Y
BAM

200,000+? ya
Africa

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
Remarks

N

A1

Big Y
BAM

150000+? ya
Africa

SNP Matches: L989+, L1002+, L1004+, L1009+, L1013+, L1053+, L1112+, V174+, V238+, V241+, V250+

3

See
Remarks

N

A1b

Big Y
BAM

100.000+? ya
Africa

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+

Around 75,000 years ago, the BT branch of the Y-chromosome tree was born, defined by many genetic markers, including M42. The common ancestor of most men living today, some of this man’s descendants would begin the journey out of Africa, to India and the Middle East. Small groups would eventually reach the Americas. Others would settle in Europe, and some from this line remained near their ancestral homeland in Africa.

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,
South or West Asia

SNP Matches: M168+, M294+

While many of the descendants of M89 remained in the Middle East, others continued to follow the great herds of wild game through what is now modern-day Iran to the vast steppes of Central Asia.

These semi-arid grass-covered plains formed an ancient “superhighway” stretching from eastern France to Korea. Your ancestors, having migrated north out of Africa into the Middle East, then traveled both east and west along this Central Asian superhighway. A smaller group continued moving north from the Middle East to Anatolia and the Balkans, trading familiar grasslands for forests and high country.

7

L16

N

IJK

G2

 

 

8

P128

Y

K

G2

45,000ya,
South Asia

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,
South or
West Asia

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
/ L11

Y
N

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
aka
R1b-U106

FT;G2

14,000-4250ya
Europe

~6500-3700ya
during the Neolithic area
NW Europe

 

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)

The highest frequencies are in the Netherlands (14 percent), Luxembourg (13 percent), and Belgium (12 percent). In the British Isles, it is between 6 and 9 percent of the male population. It is about 5 percent of male lineages in Oman. It is 4 to 5 percent of the male population in Cyprus. It is 1 to 2 percent of male lineages in Italy and Spain.
** YHRD Y-STR markers plus SNP U106 matches in Belgium. Considered of Germanic tribal origin.

21

Z381

Y

R1b-Z381

FT;G2

Belgium &
Neatherlands

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

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.

This completes the Y-SNP lineage research from pre-historic times to the PSHG, to the birth date of ABSsr, ABSjr.and ARS, a journey of migration lasting around 200,000 years. Awesome!

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

 


1a TABLE
Y-DNA
37
Markers

FTDNA
STR
DYS #

>>>

3
9
3

3
9
0

1
9

3
9
1

3
8
5
a

3
8
5
b

4
2
6

3
8
8

4
3
9

3
8
9
|
a

3
9
2

3
8
9
|
b





 

4
5
8

4
5
9
a

4
5
9
b

4
5
5

4
5
4

4
4
7

4
3
7

4
4
8

4
4
9

4
6
4
a

4
6
4
b

4
6
4
c

4
6
4
d

 

4
6
0

H
4

Y
C
A
I
I
a

Y
C
A
I
I
b

4
5
6

6
0
7

5
7
6

5
7
0

C
D
Y
a

C
D
Y
b

4
4
2

4
3
8

 

REMARKS

PSHG
Haplogroup
SNP Modal
FGC1360
9


Marker #>

 

1

2

3

4

5

6

7

8

9

10

11

12

GD
@
Y12

13

14

15

16

17

18

19

20

21

22

23

24

25

GD
@
Y25

26

27

28

29

30

31

32

33

34

35

36

37

GD
@
Y37

 

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
TABLE
Y-DNA
38-67

Markers


FTDNA

STR
DYS #
>
>>

 

5
3
1

5
7
8

3
9
5
S
1
a

3
9
5
S
1
b

5
9
0

5
3
7

6
4
1

4
7
2

4
0
6
S
1

5
1
1

4
2
5

4
1
3
a


4
1
3
b

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

   

REMARKS

PSHG
Haplogroup
SNP Modal
FGC13609


Marker #>

 

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
@
Y67

   

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


1c
TABLE
Y-DNA
68-111
Markers


FTDNA

STR
DYS #
>
>>

7
1
0

4
8
5

6
3
2

4
9
5

5
4
0

7
1
4

7
1
6

7
1
7

5
0
5

5
5
6

5
4
9

5
8
9

5
2
2

4
9
4

5
3
3

6
3
6

5
7
5

6
3
8

4
6
2

4
5
2

4
4
5

A
1
0

4
6
3

4
4
1

1
B
0
7

5
2
5

7
1
2

5
9
3

6
5
0

5
3
2

7
1
5

5
0
4

5
1
3

5
6
1

5
5
2

7
2
6

6
3
5
/
C
4

5
8
7

6
4
3

4
9
7

5
1
0

4
3
4

4
6
1

4
3
5

GD
@
Y111

 

PSHG
Haplogroup
SNP Modal
FGC13606


Marker #>


 

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


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


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


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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