Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01440 | A02 | 656246 | C | T | missense_variant | MODERATE | c.685G>A|p.Val229Met |
S15 |
2 | BAA02g01440 | A02 | 658371 | G | A | upstream_gene_variant | MODIFIER | c.-208C>T| |
S236 |
3 | BAA02g01440 | A02 | 658561 | C | T | upstream_gene_variant | MODIFIER | c.-398G>A| |
S87 |
4 | BAA02g01440 | A02 | 658611 | G | A | upstream_gene_variant | MODIFIER | c.-448C>T| |
S265 |
5 | BAA02g01440 | A02 | 659555 | G | A | upstream_gene_variant | MODIFIER | c.-1392C>T| |
S206 S26 |
6 | BAA02g01440 | A02 | 662302 | G | A | upstream_gene_variant | MODIFIER | c.-4139C>T| |
S179 |