| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g42770 | A09 | 49042893 | C | T | downstream_gene_variant | MODIFIER | c.*3981G>A| |
S92 |
| 2 | BAA09g42770 | A09 | 49048399 | G | A | synonymous_variant | LOW | c.594C>T|p.Val198Val |
S148 S210 |
| 3 | BAA09g42770 | A09 | 49048480 | C | T | synonymous_variant | LOW | c.513G>A|p.Gln171Gln |
S37 |
| 4 | BAA09g42770 | A09 | 49049448 | G | A | upstream_gene_variant | MODIFIER | c.-294C>T| |
S252 |
| 5 | BAA09g42770 | A09 | 49049892 | C | T | upstream_gene_variant | MODIFIER | c.-738G>A| |
S100 |
| 6 | BAA09g42770 | A09 | 49050266 | G | A | upstream_gene_variant | MODIFIER | c.-1112C>T| |
S288 |
| 7 | BAA09g42770 | A09 | 49050387 | G | A | upstream_gene_variant | MODIFIER | c.-1233C>T| |
S105 S106 |
| 8 | BAA09g42770 | A09 | 49050450 | G | A | upstream_gene_variant | MODIFIER | c.-1296C>T| |
S190 |
| 9 | BAA09g42770 | A09 | 49051763 | C | T | upstream_gene_variant | MODIFIER | c.-2609G>A| |
S188 |
| 10 | BAA09g42770 | A09 | 49052009 | C | T | upstream_gene_variant | MODIFIER | c.-2855G>A| |
S120 |