STIRLING - HINDS GENETICS

MyDNA

           

Confirmed Y-DNA Haplogroup is SNP I-BY453

I-BY453 on ISOGG HAPLOGROUP I TREE

Tree Level Marker / Branch Name Alternative Names Notes
1 HomoErectus hg38:21292569-T-G Human and Denisovan diverge from ancestral allele T found in chimpanzees at this position. hg38 Ref is G.
2 YAdam hg38:2844421-A-G Ancestral allele in chimpanzee is A implying this is probably a human-defining SNP for homo sapiens. hg38 Ref is G.
3 L1085 2922685-T-C Defining mutation for near-root haplogroup A0-T (aka A0’1’2’3’4). That is to say father of ALL modern Y-DNA lineages except A00. hg38 Ref does not match ancestral allele value.
4 P305 2842113-A-G rs72625368 Defining mutation for haplogroup ISOGG branch A1. hg38 Ref does not match ancestral allele value.
5 P108 rs761539052 Defining mutation for haplogroup branch A1b at ISOGG. hg38 Ref does not match ancestral. Also enumerated as hg38:13314368-C-T.
6 L413 PF1409 V31 rs192939307 Defining mutation for haplogroup branch BT at ISOGG. hg38 Ref does not match ancestral allele value.
7 M168 PF1416 rs2032595 Defining mutation for haplogroup branch CT. hg38 Ref does not match ancestral allele value.
8 P143 PF2587 rs4141886 Defining mutation for haplogroup branch CF. hg38 Ref does not match ancestral allele value.
9 M89 PF2746 rs2032652 Defining mutation for haplogroup F. hg38 Ref does not match ancestral allele value.
10 F1329 M3658 PF2622 YSC0001299 rs9786482 Defining mutation for haplogroup branch above GHIJK (sic). hg38 Ref does not match ancestral allele value.
11 M578 F929 S6397 PF3494 S6378 rs73614810 Mutation at haplogroup branch HIJK. hg38 Ref does not match ancestral allele value.
12 M523 L15 PF3492 S137 Z4413 rs9786139 Defining mutation for haplogroup branch IJK. hg38 Ref does not match ancestral allele value.
13 M429 P125 PF3535 rs17306671 Defining mutation for haplogroup branch IJ. Arose about 46,000 bce.
14 M170 PF3715 rs2032597 Defines major Haplogroup I*. Arose about 41,000 bce.
15 M253 rs9341296 Defines major haplogroup I1. Arose about 26,000 bce.
16 DF29 S438 rs755912631 Defining mutation for haplogroup I1a. Arose about 3,000 bce.
17 Z58 S244 rs772609696 Under I1a M253 > DF29.
18 Z59 S246 rs757424414 Under I1 M253 > DF29 > Z58
19 CTS8647 Z2894 S1985 rs768415578 Under I1 M253 > DF29 > Z58 > Z59
20 Z62 rs775868676  
21 S439 Z61 rs752865900  
22 Z60 S337 rs773711447 Under DF29 and CTS8647.
23 Z140 S440 rs768549242 Under I1 M253 > DF29 > Z58 > Z59 > CTS8647 > Z60
24 Z141 rs758870120 Under I1 M253 > DF29 > Z58 > Z59 > CTS8647 > Z60 > Z140
25 CTS6739 S2166 AMM443 AM00086 rs773355144  
26 S2169.1 S2169 rs376636841 See also F2642.1 found in haplogroup C.
27 CTS6772 rs776667867  
28 BY453 rs772299311 CONFIRMED
29 FGC39137    
30 BY51244    
31 BY181610 I-BY181610 PROBABLE

 

Autosomal Results Y-DNA – Standard Y-STR Values

PANEL 1 (1-12) 
Marker DYS393 DYS390 DYS19 ** DYS391 DYS385 DYS426 DYS388 DYS439 DYS389I DYS392 DYS389II ***
Value 14 22 14 10 13-13 11 16 11 12 11 31
PANEL 2 (13-25) 
Marker DYS458 DYS459 DYS455 DYS454 DYS447 DYS437 DYS448 DYS449 DYS464
Value 14 8-9 8 11 22 16 20 29 12-14-15-15
PANEL 3 (26-37) 
Marker DYS460 Y-GATA-H4 YCAII DYS456 DYS607 DYS576 DYS570 CDY DYS442 DYS438
Value 10 10 19-21 14 15 16 19 37-38 12 10
PANEL 4 (38-47) 
Marker DYS531 DYS578 DYF395S1 DYS590 DYS537 DYS641 DYS472 DYF406S1 DYS511
Value 11 8 15-15 8 11 10 8 9 9
PANEL 4 (48-60) 
Marker DYS425 DYS413 DYS557 DYS594 DYS436 DYS490 DYS534 DYS450 DYS444 DYS481 DYS520 DYS446
Value 12 22-22 15 10 12 12 15 8 13 25 20 13
PANEL 4 (61-67) 
Marker DYS617 DYS568 DYS487 DYS572 DYS640 DYS492 DYS565
Value 13 11 12 11 11 12 11
PANEL 5 (68-75) 
Marker DYS710 DYS485 DYS632 DYS495 DYS540 DYS714 DYS716 DYS717
Value 34 12 8 17 12 24 27 19
PANEL 5 (76-85) 
Marker DYS505 DYS556 DYS549 DYS589 DYS522 DYS494 DYS533 DYS636 DYS575 DYS638
Value 11 12 13 13 11 9 11 11 10 12
PANEL 5 (86-93) 
Marker DYS462 DYS452 DYS445 Y-GATA-A10 DYS463 DYS441 Y-GGAAT-1B07 DYS525
Value 12 31 11 13 21 16 11 10
PANEL 5 (94-102) 
Marker DYS712 DYS593 DYS650 DYS532 DYS715 DYS504 DYS513 DYS561 DYS552
Value 22 15 19 12 25 16 13 15 25
PANEL 5 (103-111) 
Marker DYS726 DYS635 DYS587 DYS643 DYS497 DYS510 DYS434 DYS461 DYS435
Value 12 21 18 12 15 18 9 12 11

My mtDNA Results

Haplogroup = H1bb

Origins

Mitochondrial haplogroup H is a predominantly European haplogroup that originated outside of Europe before the last glacial maximum (LGM). It first expanded in the northern Near East and southern Caucasus between 33,000 and 26,000 years ago, and later migrations from Iberia suggest it reached Europe before the LGM. It has also spread to Siberia and Inner Asia. Today, about 40% of all mitochondrial lineages in Europe are classified as haplogroup H.

Phylogenetic Ancestral Tree for marker [H1bb] on Chromosome M (Tree 1356936)
Tree Level Marker / Branch Name Alternative Names Notes
1 L MtDNAEve C15443 Phylogenetic root with C15443 probably uniquely human marker. Neanderthal and Denisovan samples have T allele at this position. rCRS Ref: C Yoruba Position: 15444.
2 L1’2’3’4’5’6   Phylogenetic branch with SNPs: A11914GC10915TC146TC182TG13276AG16230AT10664CT4312C.
3 L2’3’4’5’6   Phylogenetic branch with SNPs: A2758GC152TC2885TG7146AT8468C.
4 L2’3’4’6   Phylogenetic branch with SNPs: A10688GA16129GA247GA825tC10810TC16189TC195TG13105AG15301AT13506CT16187CT8655C.
5 L3’4’6   Phylogenetic branch with SNPs: A7521GG4104A.
6 L3’4   Phylogenetic branch with SNPs: T13650CT16278CT182C!T3594CT7256C.
7 L3   Phylogenetic branch with SNPs: A1018GA769GC16311T.
8 N   Phylogenetic branch with SNPs: A15301G!C10873TC9540TG10398AG8701A.
9 R   Phylogenetic branch with SNPs: T12705CT16223C.
10 R0   Phylogenetic branch with SNPs: A11719GG73A.
11 HV   Phylogenetic branch with SNPs: T14766C.
12 H   Phylogenetic branch with SNPs: G2706AT7028C.
13 H1   Phylogenetic branch with SNPs: G3010A.
14 H1i’ H1-T152C! H1-e Phylogenetic branch with SNPs: T152C!
15 H1bb   Phylogenetic branch with SNPs: T11864C.
HVR1 DIFFERENCES FROM RSRS
  • A16129G
  • T16187C
  • C16189T
  • T16223C
  • G16230A
  • T16278C
  • C16311T
HVR2 DIFFERENCES FROM RSRS
  • G73A
  • C146T
  • C195T
  • A247G
  • 309.1C
  • 315.1C
  • 522.1A
  • 522.2C
  • 522.3A
  • 522.4C
  • 522.5A
  • 522.6C
CODING REGION DIFFERENCES FROM RSRS
  • A769G
  • A825t
  • A1018G
  • G2706A
  • A2758G
  • C2885T
  • G3010A
  • T3594C
  • G4104A
  • T4312C
  • T7028C
  • G7146A
  • T7256C
  • A7521G
  • G7853A
  • G8020R*
  • T8468C
  • T8655C
  • G8701A
  • C9540T
  • G10398A
  • T10664C
  • A10688G
  • C10810T
  • C10873T
  • C10915T
  • A11719G
  • T11864C
  • A11914G
  • T12705C
  • G13105A
  • G13276A
  • T13506C
  • T13650C
  • T14766C
   

*R = A or G Heteroplasmy

To learn more about RSRS click here.

Revised Cambridge Reference Sequence

HVR1 REFERENCE SEQUENCE

Position CRS Result
16519 T C
HVR2 REFERENCE SEQUENCE

 

Position CRS Result
152 T C
263 A G
309.1   C
315.1   C
523.1   C
523.1   A
523.1   C
523.1   A
CR REFERENCE SEQUENCE

 

Position CRS Result
750 A G
1438 A G
3010 G A
4769 A G
7853 G A
8020 G R*
8860 A G
11864 T C
15326 A G

*R = A or G Heteroplasmy

Ethnic Makeup Percentage From Autosomal DNA Testing

African0%
New World 0%
Central/South Asian 0%
East Asian 0%
Middle Eastern 0%
 
European100%
Jewish Diaspora 0%