| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 15901 | BAA01g12110 | A01 | 5685525 | G | A | downstream_gene_variant | MODIFIER | c.*2088G>A| |
S142 |
| 15902 | BAA01g12120 | A01 | 5686286 | C | T | missense_variant | MODERATE | c.770G>A|p.Gly257Glu |
S25 |
| 15903 | BAA01g12120 | A01 | 5686288 | C | T | synonymous_variant | LOW | c.768G>A|p.Leu256Leu |
S205 |
| 15904 | BAA01g12120 | A01 | 5687085 | C | T | synonymous_variant | LOW | c.528G>A|p.Leu176Leu |
S118 |
| 15905 | BAA01g12120 | A01 | 5687144 | G | A | missense_variant | MODERATE | c.469C>T|p.Leu157Phe |
S10 |
| 15906 | BAA01g12120 | A01 | 5688060 | C | T | upstream_gene_variant | MODIFIER | c.-448G>A| |
S278 |
| 15907 | BAA01g12120 | A01 | 5690461 | C | T | upstream_gene_variant | MODIFIER | c.-2849G>A| |
S33 |
| 15908 | BAA01g12120 | A01 | 5692269 | C | T | upstream_gene_variant | MODIFIER | c.-4657G>A| |
S213 |
| 15909 | BAA01g12130 | A01 | 5692924 | C | T | upstream_gene_variant | MODIFIER | c.-2337C>T| |
S177 |
| 15910 | BAA01g12130 | A01 | 5694591 | C | T | upstream_gene_variant | MODIFIER | c.-670C>T| |
S278 |
| 15911 | BAA01g12130 | A01 | 5695493 | G | A | downstream_gene_variant | MODIFIER | c.*2G>A| |
S124 S127 S128 S149 S176 S284 S286 S287 S57 S61 |
| 15912 | BAA01g12130 | A01 | 5695659 | C | T | downstream_gene_variant | MODIFIER | c.*168C>T| |
S299 |
| 15913 | BAA01g12130 | A01 | 5695806 | C | T | downstream_gene_variant | MODIFIER | c.*315C>T| |
S249 |
| 15914 | BAA01g12130 | A01 | 5695939 | C | T | downstream_gene_variant | MODIFIER | c.*448C>T| |
S125 |
| 15915 | BAA01g12130 | A01 | 5696543 | C | T | downstream_gene_variant | MODIFIER | c.*1052C>T| |
S289 S290 |
| 15916 | BAA01g12150 | A01 | 5696613 | C | T | upstream_gene_variant | MODIFIER | c.-4969C>T| |
S219 |
| 15917 | BAA01g12150 | A01 | 5696862 | C | T | upstream_gene_variant | MODIFIER | c.-4720C>T| |
S143 |
| 15918 | BAA01g12150 | A01 | 5697128 | C | T | upstream_gene_variant | MODIFIER | c.-4454C>T| |
S54 |
| 15919 | BAA01g12150 | A01 | 5698024 | G | A | upstream_gene_variant | MODIFIER | c.-3558G>A| |
S178 |
| 15920 | BAA01g12150 | A01 | 5698633 | C | T | upstream_gene_variant | MODIFIER | c.-2949C>T| |
S211 S227 |
| 15921 | BAA01g12150 | A01 | 5698645 | C | T | upstream_gene_variant | MODIFIER | c.-2937C>T| |
S295 |
| 15922 | BAA01g12150 | A01 | 5698654 | C | T | upstream_gene_variant | MODIFIER | c.-2928C>T| |
S202 |
| 15923 | BAA01g12140 | A01 | 5698890 | G | A | missense_variant | MODERATE | c.587C>T|p.Ala196Val |
S15 |
| 15924 | BAA01g12140 | A01 | 5699561 | G | A | upstream_gene_variant | MODIFIER | c.-85C>T| |
S207 |
| 15925 | BAA01g12140 | A01 | 5700467 | C | T | upstream_gene_variant | MODIFIER | c.-991G>A| |
S164 |