DNA Marker Index information for Chromosome: Y Marker: S27122
Names and Aliases for this DNA Marker: S27122, rs377204801.
Chromosome Position in hg38 Human Genome assembly1: 2977967.
Chromosome Position in hg19 assembly2: 2846008 .
Ancestral marker allele value: G.
Derived, alternative, or mutated marker allele value: A.


DNA Marker Index data for Marker: S27122 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
E-S27122 
S27122 rs377204801
 Found in haplogroup E1b under CTS8529, ancestral to CTS6300 no FTDNA tree. Originally enumerated by ISOGG as an A->G mutation identified by Wilson. FTDNA enumerates as G->A mutation in 2020 in haplogroup E, which is consistent with NIH RefSNP.
DNA lineage S27122 is estimated to have originated in about the year 3,580 bce based on its position in the phylogenetic tree.
Phylogenetic Parent: CTS8529 
View Ancestry 
Phylogenetic Children: CTS6300 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 2906008 		Jim Wilson 2013
G
A
Y
 2977967
2846008

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