Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19180 | A02 | 9958556 | C | T | upstream_gene_variant | MODIFIER | c.-3244C>T| |
S163 |
2 | BAA02g19180 | A02 | 9960212 | C | T | upstream_gene_variant | MODIFIER | c.-1588C>T| |
S305 |
3 | BAA02g19180 | A02 | 9960604 | G | A | upstream_gene_variant | MODIFIER | c.-1196G>A| |
S10 |
4 | BAA02g19180 | A02 | 9960717 | C | T | upstream_gene_variant | MODIFIER | c.-1083C>T| |
S186 |
5 | BAA02g19180 | A02 | 9961115 | C | T | upstream_gene_variant | MODIFIER | c.-685C>T| |
S25 |
6 | BAA02g19180 | A02 | 9961184 | C | T | upstream_gene_variant | MODIFIER | c.-616C>T| |
S171 |
7 | BAA02g19180 | A02 | 9962696 | G | A | missense_variant | MODERATE | c.688G>A|p.Val230Ile |
S274 |
8 | BAA02g19180 | A02 | 9963366 | G | A | downstream_gene_variant | MODIFIER | c.*197G>A| |
S296 |
9 | BAA02g19180 | A02 | 9964765 | G | A | downstream_gene_variant | MODIFIER | c.*1596G>A| |
S256 |