DNA Marker Index information for Chromosome: Y Marker: Y140598
Names and Aliases for this DNA Marker: Y140598, BY186156, rs778372045.
Chromosome Position in hg38 Human Genome assembly1: 20893039.
Chromosome Position in hg19 assembly2: 23054925 .
Ancestral marker allele value: T.
Derived, alternative, or mutated marker allele value: G.


DNA Marker Index data for Marker: Y140598 on Chromosome: Y
Marker Name(s) Notes Identification Ancestral7 Derived8 Chromosome Position (hg38)1 Position (hg19)2
CTS11287 Y140598 rs778372045
 Found in haplogroup C1a with M8 on 23mofang tree. See also Y140598 / BY186156 with different mutation at same position. Note that BY186156 label has been used for this mutation at YFull and 23mofang but that should be discontinued.
DNA lineage CTS11287 is estimated to have originated in about the year 48,500 bce based on its position in the phylogenetic tree.
Coincident with M8. 
View Ancestry 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 21464313 		Chris Tyler-Smith 2011
T
G
Y
 20893039
23054925
R-Y140598 
Y140598 BY186156 rs778372045
 Found in haplogroup R1b under U152 and BY158668 on YFull tree as T->C mutation allele. Note that FTDNA has been inconsistent with mutation allele for BY186156 but shows in same phylogenetic branch. See also CTS11287 with different mutation at same position.
DNA lineage Y140598 is estimated to have originated in about the year 2,500 bce based on its position in the phylogenetic tree.
Phylogenetic Parent: BY158668.1 
View Ancestry 
Phylogenetic Children: BY161889  FT15832 
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 21464313 		YFull 2018
T
C
Y
 20893039
23054925

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