DNA Marker Index information for Chromosome: Y Marker: M12462
Names and Aliases for this DNA Marker: M12462, YP5801, Y6670, A19359, A19360, A20678, rs543580158.
Chromosome Position in hg38 Human Genome assembly1: 20571222.
Chromosome Position in hg19 assembly2: 22733108 .
Ancestral marker allele value: ATTTG.
Derived, alternative, or mutated marker allele value: CTTGA.


DNA Marker Index data for Marker: M12462 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
M12462 YP5801 Y6670 A19359 A19360 A20678 rs543580158
 Found in haplogroup R1a in P0 Genomic Blood sample. YFull enumerates alleles as hg38:20571221-CATTTG-CCTTGA. YSeq enumerates as hg38:20571223-T-C. Probably the same mutation listed as A19359 and A19360 for Petr Soucek. See also BY29685 which could be another description of the same mutation.
DNA lineage M12462 is estimated to have originated in about the year 2,770 bce based on its position in the phylogenetic tree.
Coincident with BY29685. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 21142497 		Underhill et al 2015
ATTTG
CTTGA
Y
 20571222
22733108

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