| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g22590 | A01 | 11377134 | G | A | synonymous_variant | LOW | c.1605C>T|p.Leu535Leu |
S276 |
| 2 | BAA01g22590 | A01 | 11377545 | C | T | missense_variant | MODERATE | c.1342G>A|p.Glu448Lys |
S171 |
| 3 | BAA01g22590 | A01 | 11379249 | C | T | intron_variant | MODIFIER | c.144+109G>A| |
S184 |
| 4 | BAA01g22590 | A01 | 11380188 | G | A | upstream_gene_variant | MODIFIER | c.-687C>T| |
S274 |
| 5 | BAA01g22590 | A01 | 11380823 | C | T | upstream_gene_variant | MODIFIER | c.-1322G>A| |
S208 S93 |
| 6 | BAA01g22590 | A01 | 11382571 | C | T | upstream_gene_variant | MODIFIER | c.-3070G>A| |
S237 |
| 7 | BAA01g22590 | A01 | 11382573 | C | T | upstream_gene_variant | MODIFIER | c.-3072G>A| |
S305 |
| 8 | BAA01g22590 | A01 | 11382901 | C | T | upstream_gene_variant | MODIFIER | c.-3400G>A| |
S19 |
| 9 | BAA01g22590 | A01 | 11383486 | C | T | upstream_gene_variant | MODIFIER | c.-3985G>A| |
S247 |