Table 1.
SNP name | Alleles | Contig position | Location | Amino acid shift | Minor allele frequency | Heterozygosity |
A7:1 | G/T | 3924455 | Promoter | 0.08 | 0.14 | |
A7:2 | Indel | 3924262 | Promoter | 0.21 | 0.33 | |
rs3124216 | T/A | 3924209 | Promoter | 0.03 | 0.07 | |
rs3006433 | G/A | 3924047 | Promoter | 0.15 | 0.25 | |
A7:3 | C/T | 3923423 | Intron 1 | 0.14 | 0.24 | |
A7:4 | A/T | 3923336 | Intron 1 | 0.14 | 0.24 | |
rs3014839 | G/A | 3923095 | Intron 1 | 0.19 | 0.31 | |
rs12132927 | T/C | 3921916 | Intron 1 | 0.05 | 0.10 | |
A7:5 | A/C | 3921790 | Exon 2 | Lys → Gln | 0.02 | 0.04 |
rs3014837 | G/C | 3921761 | Exon 2 | Asp → Glu | 0.09 | 0.16 |
rs3014836 | G/A | 3921555 | Intron 2 | 0.21 | 0.33 | |
A7:6 | C/T | 3921498 | Intron 2 | 0.01 | 0.02 | |
A7:7 | C/A | 3921495 | Intron 2 | 0.02 | 0.04 |