Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15200 | A02 | 7291736 | G | A | missense_variant | MODERATE | c.103C>T|p.Leu35Phe |
S113 |
2 | BAA02g15200 | A02 | 7291916 | C | T | upstream_gene_variant | MODIFIER | c.-78G>A| |
S32 |
3 | BAA02g15200 | A02 | 7292141 | G | T | upstream_gene_variant | MODIFIER | c.-303C>A| |
S221 |
4 | BAA02g15200 | A02 | 7292171 | G | A | upstream_gene_variant | MODIFIER | c.-333C>T| |
S228 |
5 | BAA02g15200 | A02 | 7292617 | C | T | upstream_gene_variant | MODIFIER | c.-779G>A| |
S54 |
6 | BAA02g15200 | A02 | 7292668 | C | T | upstream_gene_variant | MODIFIER | c.-830G>A| |
S250 |
7 | BAA02g15200 | A02 | 7294198 | G | A | upstream_gene_variant | MODIFIER | c.-2360C>T| |
S157 |
8 | BAA02g15200 | A02 | 7295807 | C | T | upstream_gene_variant | MODIFIER | c.-3969G>A| |
S142 |
9 | BAA02g15200 | A02 | 7296057 | C | T | upstream_gene_variant | MODIFIER | c.-4219G>A| |
S194 |
10 | BAA02g15200 | A02 | 7296359 | C | T | upstream_gene_variant | MODIFIER | c.-4521G>A| |
S130 |
11 | BAA02g15200 | A02 | 7296766 | C | T | upstream_gene_variant | MODIFIER | c.-4928G>A| |
S130 |
12 | BAA02g15200 | A02 | 7296837 | G | A | upstream_gene_variant | MODIFIER | c.-4999C>T| |
S286 |