Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30140 | A02 | 17488494 | C | T | downstream_gene_variant | MODIFIER | c.*4478G>A| |
S164 |
2 | BAA02g30140 | A02 | 17489560 | C | T | downstream_gene_variant | MODIFIER | c.*3412G>A| |
S177 |
3 | BAA02g30140 | A02 | 17489840 | G | A | downstream_gene_variant | MODIFIER | c.*3132C>T| |
S69 |
4 | BAA02g30140 | A02 | 17489878 | C | T | downstream_gene_variant | MODIFIER | c.*3094G>A| |
S18 |
5 | BAA02g30140 | A02 | 17489882 | C | T | downstream_gene_variant | MODIFIER | c.*3090G>A| |
S175 |
6 | BAA02g30140 | A02 | 17491149 | C | T | downstream_gene_variant | MODIFIER | c.*1823G>A| |
S206 |
7 | BAA02g30140 | A02 | 17491830 | G | A | downstream_gene_variant | MODIFIER | c.*1142C>T| |
S287 |
8 | BAA02g30140 | A02 | 17491892 | G | A | downstream_gene_variant | MODIFIER | c.*1080C>T| |
S12 |
9 | BAA02g30140 | A02 | 17491906 | G | A | downstream_gene_variant | MODIFIER | c.*1066C>T| |
S12 |
10 | BAA02g30140 | A02 | 17495168 | G | A | upstream_gene_variant | MODIFIER | c.-1861C>T| |
S238 |
11 | BAA02g30140 | A02 | 17495280 | G | A | upstream_gene_variant | MODIFIER | c.-1973C>T| |
S48 |
12 | BAA02g30140 | A02 | 17496343 | G | T | upstream_gene_variant | MODIFIER | c.-3036C>A| |
S56 |
13 | BAA02g30140 | A02 | 17496708 | G | A | upstream_gene_variant | MODIFIER | c.-3401C>T| |
S132 S137 S215 |
14 | BAA02g30140 | A02 | 17497599 | C | T | upstream_gene_variant | MODIFIER | c.-4292G>A| |
S77 |