Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08120 | A02 | 3489673 | C | T | downstream_gene_variant | MODIFIER | c.*2848G>A| |
S263 |
2 | BAA02g08120 | A02 | 3491782 | C | T | downstream_gene_variant | MODIFIER | c.*739G>A| |
S306 S308 |
3 | BAA02g08120 | A02 | 3492525 | C | T | stop_gained | HIGH | c.3608G>A|p.Trp1203* |
S200 |
4 | BAA02g08120 | A02 | 3493783 | C | T | missense_variant | MODERATE | c.2350G>A|p.Glu784Lys |
S39 |
5 | BAA02g08120 | A02 | 3494535 | G | A | synonymous_variant | LOW | c.1689C>T|p.Leu563Leu |
S247 |
6 | BAA02g08120 | A02 | 3495418 | C | T | missense_variant | MODERATE | c.898G>A|p.Val300Met |
S180 |
7 | BAA02g08120 | A02 | 3496418 | C | T | upstream_gene_variant | MODIFIER | c.-15G>A| |
S77 S82 |
8 | BAA02g08120 | A02 | 3496969 | C | T | upstream_gene_variant | MODIFIER | c.-566G>A| |
S211 |
9 | BAA02g08120 | A02 | 3497230 | G | A | upstream_gene_variant | MODIFIER | c.-827C>T| |
S5 |
10 | BAA02g08120 | A02 | 3498306 | C | T | upstream_gene_variant | MODIFIER | c.-1903G>A| |
S136 |
11 | BAA02g08120 | A02 | 3498904 | C | T | upstream_gene_variant | MODIFIER | c.-2501G>A| |
S8 |
12 | BAA02g08120 | A02 | 3499302 | G | A | upstream_gene_variant | MODIFIER | c.-2899C>T| |
S133 |
13 | BAA02g08120 | A02 | 3499386 | C | T | upstream_gene_variant | MODIFIER | c.-2983G>A| |
S95 |
14 | BAA02g08120 | A02 | 3499429 | G | A | upstream_gene_variant | MODIFIER | c.-3026C>T| |
S256 |
15 | BAA02g08120 | A02 | 3499456 | C | T | upstream_gene_variant | MODIFIER | c.-3053G>A| |
S301 S304 |