| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 15851 | BAA01g12100 | A01 | 5665454 | C | T | upstream_gene_variant | MODIFIER | c.-2447G>A| |
S278 |
| 15852 | BAA01g12100 | A01 | 5665547 | A | T | upstream_gene_variant | MODIFIER | c.-2540T>A| |
S208 S219 |
| 15853 | BAA01g12100 | A01 | 5666876 | G | A | upstream_gene_variant | MODIFIER | c.-3869C>T| |
S142 |
| 15854 | BAA01g12100 | A01 | 5666968 | G | A | upstream_gene_variant | MODIFIER | c.-3961C>T| |
S278 |
| 15855 | BAA01g12100 | A01 | 5667295 | C | T | upstream_gene_variant | MODIFIER | c.-4288G>A| |
S70 |
| 15856 | BAA01g12100 | A01 | 5667314 | G | A | upstream_gene_variant | MODIFIER | c.-4307C>T| |
S240 |
| 15857 | BAA01g12100 | A01 | 5667427 | G | A | upstream_gene_variant | MODIFIER | c.-4420C>T| |
S262 |
| 15858 | BAA01g12100-BAA01g12110 | A01 | 5669476 | G | A | intergenic_region | MODIFIER | n.5669476G>A| |
S263 |
| 15859 | BAA01g12100-BAA01g12110 | A01 | 5670788 | C | T | intergenic_region | MODIFIER | n.5670788C>T| |
S261 |
| 15860 | BAA01g12100-BAA01g12110 | A01 | 5670878 | C | T | intergenic_region | MODIFIER | n.5670878C>T| |
S129 |
| 15861 | BAA01g12110 | A01 | 5674034 | G | A | upstream_gene_variant | MODIFIER | c.-4823G>A| |
S96 |
| 15862 | BAA01g12110 | A01 | 5678122 | C | T | upstream_gene_variant | MODIFIER | c.-735C>T| |
S25 |
| 15863 | BAA01g12110 | A01 | 5678673 | G | A | upstream_gene_variant | MODIFIER | c.-184G>A| |
S28 |
| 15864 | BAA01g12110 | A01 | 5679198 | C | T | stop_gained | HIGH | c.265C>T|p.Gln89* |
S68 |
| 15865 | BAA01g12110 | A01 | 5679479 | C | T | synonymous_variant | LOW | c.546C>T|p.Phe182Phe |
S48 |
| 15866 | BAA01g12110 | A01 | 5680118 | C | T | intron_variant | MODIFIER | c.1000+23C>T| |
S179 |
| 15867 | BAA01g12110 | A01 | 5680269 | G | A | intron_variant | MODIFIER | c.1053+36G>A| |
S293 |
| 15868 | BAA01g12110 | A01 | 5680309 | C | T | intron_variant | MODIFIER | c.1054-9C>T| |
S146 |
| 15869 | BAA01g12110 | A01 | 5680639 | C | T | missense_variant | MODERATE | c.1283C>T|p.Pro428Leu |
S135 |
| 15870 | BAA01g12120 | A01 | 5682528 | G | A | downstream_gene_variant | MODIFIER | c.*3294C>T| |
S197 |
| 15871 | BAA01g12110 | A01 | 5683079 | C | T | synonymous_variant | LOW | c.2520C>T|p.Ser840Ser |
S166 |
| 15872 | BAA01g12110 | A01 | 5683093 | C | T | splice_region_variant&intron_variant | LOW | c.2526+8C>T| |
S130 |
| 15873 | BAA01g12110 | A01 | 5683374 | C | T | synonymous_variant | LOW | c.2709C>T|p.Val903Val |
S43 |
| 15874 | BAA01g12110 | A01 | 5683440 | G | A | downstream_gene_variant | MODIFIER | c.*3G>A| |
S183 S198 |
| 15875 | BAA01g12110 | A01 | 5683791 | C | T | downstream_gene_variant | MODIFIER | c.*354C>T| |
S160 |