DNA Marker Index information for Chromosome: Y Marker: S1051
Names and Aliases for this DNA Marker: S1051.1, S1051, BY41243, rs772934710, S1051.2.
Chromosome Position in hg38 Human Genome assembly1: 14237224.
Chromosome Position in hg19 assembly2: 16349104 .
Ancestral marker allele value: C.
Derived, alternative, or mutated marker allele value: T.


DNA Marker Index data for Marker: S1051 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
R-S1051 
S1051.1 S1051 BY41243 rs772934710
 Found in haplogroup R1b under DF13 and Z39589 on ISOGG, YFull, and FTDNA trees at position hg38:14237224. Formerly enumerated at position 14837224 seems to have been a typographical error which has been corrected. See also S1051.2 in haplogroup R1b under U106.
DNA lineage S1051.1 is estimated to have originated in about the year 2,740 bce based on its position in the phylogenetic tree.
Phylogenetic Parent: Z39589.1 
View Ancestry 
Phylogenetic Children: BY72782  FGC14901  FGC17938  FGC20620.1  FGC22897  FGC33333  FGC50155  FGC52058  FGC9660  FGC9699.1  FGC9826.1  FGC9868  FT250624  FT389649  Z22253.2 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 14858498 		Jim Wilson 2013
C
T
Y
 14237224
16349104
S1051.2 rs772934710
 Found in haplogroup R1b under U106 with BY71326 on FTDNA tree. See also S1051.1 in haplogroup R1b under Z39589.
DNA lineage S1051.2 is estimated to have originated in about the year 120 bce based on its position in the phylogenetic tree.
Coincident with BY71326. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 14858498 		FTDNA 2023
C
T
Y
 14237224
16349104

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