| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g01010 | A01 | 435970 | G | A | missense_variant | MODERATE | c.1282C>T|p.Leu428Phe |
S306 S308 |
| 2 | BAA01g01010 | A01 | 436453 | C | T | missense_variant | MODERATE | c.941G>A|p.Gly314Glu |
S18 |
| 3 | BAA01g01010 | A01 | 436796 | G | A | synonymous_variant | LOW | c.735C>T|p.His245His |
S180 |
| 4 | BAA01g01010 | A01 | 438694 | C | T | upstream_gene_variant | MODIFIER | c.-628G>A| |
S94 |
| 5 | BAA01g01010 | A01 | 440490 | G | A | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S298 |
| 6 | BAA01g01010 | A01 | 441586 | C | T | upstream_gene_variant | MODIFIER | c.-3520G>A| |
S262 |
| 7 | BAA01g01010 | A01 | 441783 | C | T | upstream_gene_variant | MODIFIER | c.-3717G>A| |
S135 |
| 8 | BAA01g01010 | A01 | 442554 | G | A | upstream_gene_variant | MODIFIER | c.-4488C>T| |
S146 |