Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41690 | A02 | 34919560 | C | T | upstream_gene_variant | MODIFIER | c.-902G>A| |
S1 S90 |
2 | BAA02g41690 | A02 | 34919577 | G | A | upstream_gene_variant | MODIFIER | c.-919C>T| |
S291 |
3 | BAA02g41690 | A02 | 34919605 | C | T | upstream_gene_variant | MODIFIER | c.-947G>A| |
S225 |
4 | BAA02g41690 | A02 | 34919794 | G | A | upstream_gene_variant | MODIFIER | c.-1136C>T| |
S247 |
5 | BAA02g41690 | A02 | 34919966 | C | T | upstream_gene_variant | MODIFIER | c.-1308G>A| |
S61 |
6 | BAA02g41690 | A02 | 34920467 | C | T | upstream_gene_variant | MODIFIER | c.-1809G>A| |
S117 |
7 | BAA02g41690 | A02 | 34921496 | G | A | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S94 |
8 | BAA02g41690 | A02 | 34922434 | C | T | upstream_gene_variant | MODIFIER | c.-3776G>A| |
S266 |
9 | BAA02g41690 | A02 | 34923120 | C | T | upstream_gene_variant | MODIFIER | c.-4462G>A| |
S3 |