| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g40190 | A06 | 26133373 | C | T | missense_variant | MODERATE | c.140G>A|p.Gly47Asp |
S178 |
| 2 | BAA06g40190 | A06 | 26133551 | G | A | upstream_gene_variant | MODIFIER | c.-39C>T| |
S164 |
| 3 | BAA06g40190 | A06 | 26134827 | C | T | upstream_gene_variant | MODIFIER | c.-1315G>A| |
S306 S308 |
| 4 | BAA06g40190 | A06 | 26134988 | G | A | upstream_gene_variant | MODIFIER | c.-1476C>T| |
S256 |
| 5 | BAA06g40190 | A06 | 26135196 | C | T | upstream_gene_variant | MODIFIER | c.-1684G>A| |
S69 |
| 6 | BAA06g40190 | A06 | 26135579 | G | A | upstream_gene_variant | MODIFIER | c.-2067C>T| |
S297 |
| 7 | BAA06g40190 | A06 | 26136135 | G | A | upstream_gene_variant | MODIFIER | c.-2623C>T| |
S283 |
| 8 | BAA06g40190 | A06 | 26136860 | G | A | upstream_gene_variant | MODIFIER | c.-3348C>T| |
S168 |
| 9 | BAA06g40190 | A06 | 26137316 | C | T | upstream_gene_variant | MODIFIER | c.-3804G>A| |
S308 |