DNA Marker Index information for Chromosome: Y Marker: FGC25649.1
Names and Aliases for this DNA Marker: FGC25649.1, FGC25649, V1662.1, V1662, YP2631.1, YP2631, rs1197679054.
Chromosome Position in hg38 Human Genome assembly1: 8278461.
Chromosome Position in hg19 assembly2: 8146502 .
Ancestral marker allele value: G.
Derived, alternative, or mutated marker allele value: A.


DNA Marker Index data for Marker: FGC25649.1 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
FGC25649.1 FGC25649 V1662.1 V1662 YP2631.1 YP2631 rs1197679054
 Found in haplogroup A00. See also V1662.2 in haplogroup J1. YFull enumerates YP2631 in haplogroup A0-T with alleles reversed, which would be equivalent. See also FGC25649.2 in haplogroup J1a. See also FGC25649.3 in haplogroup O.
DNA lineage FGC25649.1 is estimated to have originated in about the year 232,000 bce based on its position in the phylogenetic tree.
Coincident with AF6. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 8206502 		Full Genomes Corp 2014
G
A
Y
 8278461
8146502

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