Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11400 | A02 | 5162728 | G | A | downstream_gene_variant | MODIFIER | c.*1923C>T| |
S187 |
2 | BAA02g11400 | A02 | 5164935 | C | T | missense_variant | MODERATE | c.1774G>A|p.Glu592Lys |
S135 |
3 | BAA02g11400 | A02 | 5165052 | C | T | missense_variant | MODERATE | c.1657G>A|p.Ala553Thr |
S293 |
4 | BAA02g11400 | A02 | 5166383 | C | T | missense_variant | MODERATE | c.586G>A|p.Val196Ile |
S226 |
5 | BAA02g11400 | A02 | 5166411 | G | A | synonymous_variant | LOW | c.558C>T|p.Leu186Leu |
S231 |
6 | BAA02g11400 | A02 | 5168028 | C | T | upstream_gene_variant | MODIFIER | c.-895G>A| |
S128 |
7 | BAA02g11400 | A02 | 5169344 | G | A | upstream_gene_variant | MODIFIER | c.-2211C>T| |
S86 |