DNA Marker Index information for Chromosome: Y Marker: F10981
Names and Aliases for this DNA Marker: F10981.1, F10981, rs1307483515, F10981.2, F10981.3.
Chromosome Position in hg38 Human Genome assembly1: 11518167.
Chromosome Position in hg19 assembly2: 13673843 .
Ancestral marker allele value: C.
Derived, alternative, or mutated marker allele value: T.


DNA Marker Index data for Marker: F10981 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
F10981.1 F10981 rs1307483515
 Located on centronomic region. Found in haplogroup C with F11791. See also F10981.2 in haplogroup I1. See also F10981.3 in haplogroup G. See also MF240975 with different mutation at same position.
DNA lineage F10981.1 is estimated to have originated in about the year 19,600 bce based on its position in the phylogenetic tree.
Coincident with F9747. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 12133843 		Fudan University 2016
C
T
Y
 11518167
13673843
I-F10981 
F10981.2 rs1307483515
 Located on centronomic region. Found in haplogroup I1 on FTDNA tree. See also F10981.1 in haplogroup C. See also F10981.3 in haplogroup G. See also MF240975 with different mutation at same position.
DNA lineage F10981.2 is estimated to have originated in about the year 13,500 bce based on its position in the phylogenetic tree.
Phylogenetic Parent: Y24819 
View Ancestry 
Phylogenetic Children: FT46051  FTC83788 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 12133843 		FTDNA 2020
C
T
Y
 11518167
13673843
F10981.3 rs1307483515
 Located on centronomic region. Found in haplogroup G2 with BY181331. See also F10981.1 in haplogroup C. See also F10981.2 in haplogroup I1. See also MF240975 with different mutation at same position.
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 12133843 		YFull 2021
C
T
Y
 11518167
13673843

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