Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22800 | A02 | 12351736 | C | T | missense_variant | MODERATE | c.784C>T|p.Leu262Phe |
S224 |
2 | BAA02g22800 | A02 | 12353162 | G | A | downstream_gene_variant | MODIFIER | c.*1292G>A| |
S136 |
3 | BAA02g22800 | A02 | 12354104 | G | A | downstream_gene_variant | MODIFIER | c.*2234G>A| |
S303 |
4 | BAA02g22800 | A02 | 12354828 | C | T | downstream_gene_variant | MODIFIER | c.*2958C>T| |
S1 |
5 | BAA02g22800 | A02 | 12354860 | C | T | downstream_gene_variant | MODIFIER | c.*2990C>T| |
S164 S277 |
6 | BAA02g22800 | A02 | 12355409 | G | A | downstream_gene_variant | MODIFIER | c.*3539G>A| |
S136 |