Table 5.

Nomenclature[i] and Frequencies for Y-Chromosomal SNP Haplotypes[ii]

Haplotype frequency (%)
Locus Population
Haplotype Tat[iii] (T/C) M9 (G/C) SRY10831[iii] (G/A) M17 (del G) M12[iii] (G/T) 92R7 (C/T) Eastern Finns (n = 66) Western Finns (n = 47) Northern Finns (n = 14) All Finns (n = 127) Inari Saami (n = 46) Kola Saami (n = 29) Skolt Saami (n = 23) All Saami (n = 98) Karelians (n = 30) Mansi (n = 19) Khantyi (n = 21) All Ob-Ugric (n = 40)
H2+TCGG T C000001404.10000
H2TCGGGC15320193417523333000
H26T G GGGC1.6000.800000793355
H16 C G GGGC846493776155445543165738
H1T G GGG T 000003.44.32.03.0000
H3+T G A T G T 04.37.12.44.51005.2205.39.57.5
Nucleotide diversity0.0870.1940.1870.2020.3050.1870.3390.1170.192
Mean pairwise difference0.531.160.571.211.831.122.040.701.15

[i] The nomenclature used in this study is according to published literature (Jobling and Tyler-Smith 1997; Tyler-Smith 1999).

[ii] The substitutions from ancestral state are shown bolded. The A-allele at SRY 10831 site is revertant on an M9-G background (Hammer et al. 1998).

[iii] Detection from complementary strand.