DNA Marker Index information for Chromosome: Y Marker: M10264.2
Names and Aliases for this DNA Marker: M10264.2, PF1085.2, rs552041314.
Chromosome Position in hg38 Human Genome assembly1: 19825062.
Chromosome Position in hg19 assembly2: 21986948 .
Ancestral marker allele value: A.
Derived, alternative, or mutated marker allele value: T.


DNA Marker Index data for Marker: M10264.2 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
M10264.2 PF1085.2 rs552041314
 Found in haplogroup R1b under ZZ37 with BY20464 on FTDNA tree. FTDNA reversed mutation alleles Oct 2020. See also M10264.1 in haplogroup A1b. See also M10264.3 in haplogroup R1a. See also PF1085.4 / M10264.4 in haplogroup O2a.
DNA lineage M10264.2 is estimated to have originated in about the year 2,770 bce based on its position in the phylogenetic tree.
Coincident with BY20464. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 20446336 		FTDNA 2019
A
T
Y
 19825062
21986948

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