DNA Marker Index information for Chromosome: Y Marker: FGC60262
Names and Aliases for this DNA Marker: FGC60262.1, FGC60262, A12703, rs896416477, FGC60262.2.
Chromosome Position in hg38 Human Genome assembly1: 7025209.
Chromosome Position in hg19 assembly2: 6893250 .
Ancestral marker allele value: C.
Derived, alternative, or mutated marker allele value: G.


DNA Marker Index data for Marker: FGC60262 on Chromosome: Y

Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
I-FGC60262 
FGC60262.1 FGC60262 A12703 rs896416477
Found in haplogroup I1a on FTDNA tree. See also FGC60262.2 in haplogroup R1b. See also FT280416 with different mutation at same position.
DNA lineage FGC60262.1 is estimated to have originated in about the year 3,580 bce based on its position in the phylogenetic tree.

Phylogenetic Parent: FGC60263 
View Ancestry 

NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 6953250
William Hartley 2016
C
G
Y
7025209
6893250
FGC60262.2 rs896416477
Found in haplogroup R1b. See also FGC60262.1 in haplogroup I1a.
DNA lineage FGC60262.2 is estimated to have originated in about the year 2,740 bce based on its position in the phylogenetic tree.

Coincident with FT161980
View Ancestry 

NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 6953250
FTDNA 2021
C
G
Y
7025209
6893250

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