Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12590 | A02 | 5640666 | A | G | missense_variant | MODERATE | c.586A>G|p.Arg196Gly |
S276 |
2 | BAA02g12590 | A02 | 5640831 | G | A | missense_variant | MODERATE | c.751G>A|p.Asp251Asn |
S69 |
3 | BAA02g12590 | A02 | 5640919 | C | T | missense_variant | MODERATE | c.839C>T|p.Pro280Leu |
S186 |
4 | BAA02g12590 | A02 | 5641025 | A | G | synonymous_variant | LOW | c.945A>G|p.Thr315Thr |
S54 |
5 | BAA02g12590 | A02 | 5642926 | C | T | downstream_gene_variant | MODIFIER | c.*1886C>T| |
S249 |
6 | BAA02g12590 | A02 | 5643009 | C | T | downstream_gene_variant | MODIFIER | c.*1969C>T| |
S226 |
7 | BAA02g12590 | A02 | 5643197 | G | A | downstream_gene_variant | MODIFIER | c.*2157G>A| |
S125 |
8 | BAA02g12590 | A02 | 5643249 | G | A | downstream_gene_variant | MODIFIER | c.*2209G>A| |
S20 |