DNA Marker Index information for Chromosome: Y Marker: FT335141
Names and Aliases for this DNA Marker: MF178938, FT335141.2, rs760927712.
Chromosome Position in hg38 Human Genome assembly1: 11827654.
Chromosome Position in hg19 assembly2: 13948360 .
Ancestral marker allele value: C.
Derived, alternative, or mutated marker allele value: T.


DNA Marker Index data for Marker: FT335141 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
MF178938 FT335141.2 rs760927712
 Found in haplogroup O. See also FT335141.1 in haplogroup I. See also FT195857 with different mutation at same position. See also FT335141.1 in haplogroup I1a. See also FT335141.3 in haplogroup R.
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 12458360 		23mofang 2020
C
T
Y
 11827654
13948360
FT335141.1 FT335141 rs760927712
 Found in haplogroup I1. See also MF178938 in haplogroup O. See also FT195857 with different mutation at same position. See also MF178938 in haplogroup O. See also FT335141.3 in haplogroup R.
DNA lineage FT335141.1 is estimated to have originated in about the year 11,900 bce based on its position in the phylogenetic tree.
Coincident with FT333901. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 12458360 		FTDNA 2020
C
T
Y
 11827654
13948360
FT335141.3 rs760927712
 Found in haplogroup R. See also MF178938 in haplogroup O. See also FT335141.1 in haplogroup I1a.
DNA lineage FT335141.3 is estimated to have originated in about the year 520 ce based on its position in the phylogenetic tree.
Coincident with FTB55601. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 12458360 		FTDNA 2024
C
T
Y
 11827654
13948360

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