Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01590 | A02 | 712596 | C | T | upstream_gene_variant | MODIFIER | c.-321C>T| |
S207 |
2 | BAA02g01590 | A02 | 713208 | C | T | missense_variant | MODERATE | c.292C>T|p.Pro98Ser |
S292 |
3 | BAA02g01590 | A02 | 716280 | C | T | downstream_gene_variant | MODIFIER | c.*2692C>T| |
S195 |
4 | BAA02g01590 | A02 | 716363 | G | A | downstream_gene_variant | MODIFIER | c.*2775G>A| |
S241 |
5 | BAA02g01590 | A02 | 716581 | G | A | downstream_gene_variant | MODIFIER | c.*2993G>A| |
S4 |