Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09130 | A02 | 4027749 | G | A | upstream_gene_variant | MODIFIER | c.-2415G>A| |
S79 S91 |
2 | BAA02g09130 | A02 | 4032304 | C | T | missense_variant | MODERATE | c.1898C>T|p.Ser633Phe |
S211 S227 |
3 | BAA02g09130 | A02 | 4033782 | G | A | missense_variant | MODERATE | c.2704G>A|p.Val902Ile |
S282 |
4 | BAA02g09130 | A02 | 4033868 | G | A | synonymous_variant | LOW | c.2790G>A|p.Ala930Ala |
S245 |
5 | BAA02g09130 | A02 | 4035974 | G | A | downstream_gene_variant | MODIFIER | c.*588G>A| |
S125 |
6 | BAA02g09130 | A02 | 4037689 | C | T | downstream_gene_variant | MODIFIER | c.*2303C>T| |
S83 |
7 | BAA02g09130 | A02 | 4038668 | C | T | downstream_gene_variant | MODIFIER | c.*3282C>T| |
S124 |