Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14990 | A02 | 7144194 | C | T | missense_variant | MODERATE | c.79C>T|p.Pro27Ser |
S302 |
2 | BAA02g14990 | A02 | 7148719 | C | T | synonymous_variant | LOW | c.1258C>T|p.Leu420Leu |
S115 |
3 | BAA02g14990 | A02 | 7150562 | C | T | downstream_gene_variant | MODIFIER | c.*1107C>T| |
S138 |
4 | BAA02g14990 | A02 | 7151795 | G | A | downstream_gene_variant | MODIFIER | c.*2340G>A| |
S28 |
5 | BAA02g14990 | A02 | 7152441 | G | A | downstream_gene_variant | MODIFIER | c.*2986G>A| |
S187 |
6 | BAA02g14990 | A02 | 7153655 | C | T | downstream_gene_variant | MODIFIER | c.*4200C>T| |
S305 |