Table 1.
CHR | RefSNP | Locus | Allele | Gene region | Positiona | Amino acid substitution | Gene | Origin |
---|---|---|---|---|---|---|---|---|
5 | rs109763947 | g.1407C > T | C/T | 5'-UTR | 66605011 | IGF1 | This study | |
5 | rs41643203 | Hapmap50366-BTA-46960 | C/T | intron-2 | 68610818 | Close to IGF1 | [23] | |
6 | rs109579682 | g.85330C > T | C/T | Intron-9 | 44875251 | PPARGC1A | This study | |
6 | rs110131167 | Hapmap26001-BTC-038813 | A/G | intron-2 | 44926243 | PPARGC1A | [23] | |
6 | rs108967640 | Hapmap31284-BTC-039204 | C/T | - | 45096462 | PPARGC1A | [23] | |
6 | rs137757790 | g.45599A > C | A/C | Intron-7 | 38005668 | ABCG2 | This study | |
6 | rs43450879 | BTB-00246150 | A/G | Intron-1 | 20993424 | Close to ABCG2 | [23] | |
19 | rs136947640 | g.7709 T > C | T/C | Exon-10 | 51391830 | FASN | This study | |
19 | rs41919999 | g.8948C > T | C/T | Intron-12 | 51393068 | FASN | This study | |
19 | rs132865003 | g.10568 T > C | T/C | Intron-18 | 51394689 | FASN | This study | |
19 | rs134340637 | g.11280G > A | G/A | Exon-21 | 51395400 | FASN | This study | |
19 | rs41919992 | g.13965C > T | C/T | Exon-27 | 51398083 | FASN | This study | |
19 | rs133498277 | g.14439 T > C | T/C | Intron-28 | 51398557 | FASN | This study | |
19 | rs41919984 | g.16907 T > C | T/C | Exon-37 | 51401022 | FASN | This study | |
19 | rs41919985 | g.17924A > G | A/G | Exon-39 | 51402032 | A2266T | FASN | This study |
19 | rs41919986 | g.18663 T > C | T/C | Exon-42 | 51402774 | FASN | This study | |
19 | rs41921177 | ARS-BFGL-NGS-39328 | A/G | Intron-11 | 51326750 | Close to FASN | [23] |
Note: aAll SNP nucleotide positions were derived from the Bos_taurus_UMD_3.1 assembly (GenBank accession number: AC_000171.1)