Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13730 | A09 | 7907328 | C | T | upstream_gene_variant | MODIFIER | c.-4482C>T| |
S182 |
2 | BAA09g13730 | A09 | 7907570 | C | T | upstream_gene_variant | MODIFIER | c.-4240C>T| |
S37 |
3 | BAA09g13730 | A09 | 7908026 | C | T | upstream_gene_variant | MODIFIER | c.-3784C>T| |
S136 |
4 | BAA09g13730 | A09 | 7909046 | C | T | upstream_gene_variant | MODIFIER | c.-2764C>T| |
S296 |
5 | BAA09g13730 | A09 | 7909067 | G | A | upstream_gene_variant | MODIFIER | c.-2743G>A| |
S172 |
6 | BAA09g13730 | A09 | 7915803 | G | A | downstream_gene_variant | MODIFIER | c.*3624G>A| |
S229 |
7 | BAA09g13730 | A09 | 7915873 | G | A | downstream_gene_variant | MODIFIER | c.*3694G>A| |
S202 |
8 | BAA09g13730 | A09 | 7916108 | C | A | downstream_gene_variant | MODIFIER | c.*3929C>A| |
S173 |
9 | BAA09g13730 | A09 | 7916664 | G | A | downstream_gene_variant | MODIFIER | c.*4485G>A| |
S229 |