Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05990 | A02 | 2541961 | G | A | synonymous_variant | LOW | c.297C>T|p.Val99Val |
S271 |
2 | BAA02g05990 | A02 | 2542100 | G | A | missense_variant | MODERATE | c.158C>T|p.Thr53Ile |
S265 |
3 | BAA02g05990 | A02 | 2542468 | C | T | upstream_gene_variant | MODIFIER | c.-211G>A| |
S138 |
4 | BAA02g05990 | A02 | 2542481 | G | A | upstream_gene_variant | MODIFIER | c.-224C>T| |
S210 S225 |
5 | BAA02g05990 | A02 | 2542855 | G | A | upstream_gene_variant | MODIFIER | c.-598C>T| |
S20 |
6 | BAA02g05990 | A02 | 2545725 | G | A | upstream_gene_variant | MODIFIER | c.-3468C>T| |
S136 |