| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 189801 | BAA02g25710 | A02 | 14124794 | C | T | downstream_gene_variant | MODIFIER | c.*1305G>A| |
S299 |
| 189802 | BAA02g25710 | A02 | 14124927 | G | A | downstream_gene_variant | MODIFIER | c.*1172C>T| |
S237 |
| 189803 | BAA02g25710 | A02 | 14125408 | C | T | downstream_gene_variant | MODIFIER | c.*691G>A| |
S79 S84 |
| 189804 | BAA02g25710 | A02 | 14126150 | G | A | synonymous_variant | LOW | c.309C>T|p.Gly103Gly |
S61 |
| 189805 | BAA02g25710 | A02 | 14126295 | G | A | missense_variant | MODERATE | c.164C>T|p.Ser55Phe |
S199 |
| 189806 | BAA02g25710 | A02 | 14129274 | C | T | upstream_gene_variant | MODIFIER | c.-2816G>A| |
S271 |
| 189807 | BAA02g25710 | A02 | 14129551 | C | T | upstream_gene_variant | MODIFIER | c.-3093G>A| |
S33 |
| 189808 | BAA02g25710 | A02 | 14131038 | C | T | upstream_gene_variant | MODIFIER | c.-4580G>A| |
S107 |
| 189809 | BAA02g25720 | A02 | 14131913 | G | A | downstream_gene_variant | MODIFIER | c.*851C>T| |
S249 |
| 189810 | BAA02g25720 | A02 | 14132971 | C | T | synonymous_variant | LOW | c.1083G>A|p.Glu361Glu |
S179 |
| 189811 | BAA02g25720 | A02 | 14133689 | G | A | missense_variant | MODERATE | c.365C>T|p.Thr122Ile |
S291 |
| 189812 | BAA02g25720 | A02 | 14133745 | C | T | synonymous_variant | LOW | c.309G>A|p.Pro103Pro |
S52 |
| 189813 | BAA02g25720 | A02 | 14133878 | G | A | missense_variant | MODERATE | c.176C>T|p.Pro59Leu |
S256 |
| 189814 | BAA02g25720 | A02 | 14135261 | G | A | upstream_gene_variant | MODIFIER | c.-1208C>T| |
S212 |
| 189815 | BAA02g25720 | A02 | 14135660 | C | T | upstream_gene_variant | MODIFIER | c.-1607G>A| |
S261 |
| 189816 | BAA02g25720 | A02 | 14135843 | C | T | upstream_gene_variant | MODIFIER | c.-1790G>A| |
S138 |
| 189817 | BAA02g25720 | A02 | 14136009 | C | T | upstream_gene_variant | MODIFIER | c.-1956G>A| |
S271 |
| 189818 | BAA02g25720 | A02 | 14136691 | C | T | upstream_gene_variant | MODIFIER | c.-2638G>A| |
S201 |
| 189819 | BAA02g25720 | A02 | 14137558 | G | A | upstream_gene_variant | MODIFIER | c.-3505C>T| |
S134 |
| 189820 | BAA02g25740 | A02 | 14139850 | G | A | downstream_gene_variant | MODIFIER | c.*179C>T| |
S150 |
| 189821 | BAA02g25740 | A02 | 14140165 | C | T | missense_variant | MODERATE | c.284G>A|p.Gly95Asp |
S105 S106 |
| 189822 | BAA02g25740 | A02 | 14140271 | G | A | intron_variant | MODIFIER | c.202-24C>T| |
S269 |
| 189823 | BAA02g25740 | A02 | 14140370 | G | A | intron_variant | MODIFIER | c.202-123C>T| |
S7 |
| 189824 | BAA02g25740 | A02 | 14141076 | G | A | intron_variant | MODIFIER | c.201+568C>T| |
S187 |
| 189825 | BAA02g25740 | A02 | 14141181 | G | T | intron_variant | MODIFIER | c.201+463C>A| |
S283 |