Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22230 | A02 | 11971924 | G | A | upstream_gene_variant | MODIFIER | c.-3793G>A| |
S19 |
2 | BAA02g22230 | A02 | 11972947 | C | T | upstream_gene_variant | MODIFIER | c.-2770C>T| |
S123 |
3 | BAA02g22230 | A02 | 11973527 | G | A | upstream_gene_variant | MODIFIER | c.-2190G>A| |
S37 |
4 | BAA02g22230 | A02 | 11973790 | G | A | upstream_gene_variant | MODIFIER | c.-1927G>A| |
S278 |
5 | BAA02g22230 | A02 | 11973880 | G | A | upstream_gene_variant | MODIFIER | c.-1837G>A| |
S286 |
6 | BAA02g22230 | A02 | 11973932 | G | A | upstream_gene_variant | MODIFIER | c.-1785G>A| |
S95 |
7 | BAA02g22230 | A02 | 11974966 | G | A | upstream_gene_variant | MODIFIER | c.-751G>A| |
S279 |
8 | BAA02g22230 | A02 | 11975093 | G | A | upstream_gene_variant | MODIFIER | c.-624G>A| |
S57 |
9 | BAA02g22230 | A02 | 11975283 | C | T | upstream_gene_variant | MODIFIER | c.-434C>T| |
S277 |
10 | BAA02g22230 | A02 | 11975796 | C | T | missense_variant | MODERATE | c.80C>T|p.Thr27Ile |
S88 |
11 | BAA02g22230 | A02 | 11975898 | C | T | missense_variant | MODERATE | c.182C>T|p.Ser61Phe |
S117 |
12 | BAA02g22230 | A02 | 11976716 | C | T | downstream_gene_variant | MODIFIER | c.*811C>T| |
S69 |
13 | BAA02g22230 | A02 | 11976719 | C | T | downstream_gene_variant | MODIFIER | c.*814C>T| |
S138 |
14 | BAA02g22230 | A02 | 11977256 | G | A | downstream_gene_variant | MODIFIER | c.*1351G>A| |
S155 |
15 | BAA02g22230 | A02 | 11979322 | C | T | downstream_gene_variant | MODIFIER | c.*3417C>T| |
S270 |