Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27940 | A02 | 15736933 | C | T | upstream_gene_variant | MODIFIER | c.-2344C>T| |
S268 |
2 | BAA02g27940 | A02 | 15737108 | G | A | upstream_gene_variant | MODIFIER | c.-2169G>A| |
S256 |
3 | BAA02g27940 | A02 | 15737813 | C | T | upstream_gene_variant | MODIFIER | c.-1464C>T| |
S115 |
4 | BAA02g27940 | A02 | 15737944 | C | T | upstream_gene_variant | MODIFIER | c.-1333C>T| |
S87 |
5 | BAA02g27940 | A02 | 15738058 | C | T | upstream_gene_variant | MODIFIER | c.-1219C>T| |
S171 |
6 | BAA02g27940 | A02 | 15738910 | G | A | upstream_gene_variant | MODIFIER | c.-367G>A| |
S146 |
7 | BAA02g27940 | A02 | 15739073 | C | T | upstream_gene_variant | MODIFIER | c.-204C>T| |
S114 |
8 | BAA02g27940 | A02 | 15739567 | C | T | synonymous_variant | LOW | c.90C>T|p.His30His |
S224 |
9 | BAA02g27940 | A02 | 15739656 | C | T | intron_variant | MODIFIER | c.162+17C>T| |
S73 |
10 | BAA02g27940 | A02 | 15741645 | C | T | downstream_gene_variant | MODIFIER | c.*1720C>T| |
S203 |
11 | BAA02g27940 | A02 | 15742232 | C | T | downstream_gene_variant | MODIFIER | c.*2307C>T| |
S100 S82 |
12 | BAA02g27940 | A02 | 15742916 | C | T | downstream_gene_variant | MODIFIER | c.*2991C>T| |
S289 S290 |
13 | BAA02g27940 | A02 | 15743559 | C | T | downstream_gene_variant | MODIFIER | c.*3634C>T| |
S193 |
14 | BAA02g27940 | A02 | 15744353 | G | A | downstream_gene_variant | MODIFIER | c.*4428G>A| |
S298 |
15 | BAA02g27940 | A02 | 15744493 | C | T | downstream_gene_variant | MODIFIER | c.*4568C>T| |
S218 |