Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45060 | A02 | 37003139 | G | A | downstream_gene_variant | MODIFIER | c.*419C>T| |
S139 |
2 | BAA02g45060 | A02 | 37006043 | C | T | missense_variant | MODERATE | c.22G>A|p.Val8Met |
S130 |
3 | BAA02g45060 | A02 | 37006135 | G | A | upstream_gene_variant | MODIFIER | c.-71C>T| |
S293 |
4 | BAA02g45060 | A02 | 37006415 | G | A | upstream_gene_variant | MODIFIER | c.-351C>T| |
S67 |
5 | BAA02g45060 | A02 | 37006470 | C | T | upstream_gene_variant | MODIFIER | c.-406G>A| |
S308 |
6 | BAA02g45060 | A02 | 37006489 | G | A | upstream_gene_variant | MODIFIER | c.-425C>T| |
S278 |
7 | BAA02g45060 | A02 | 37007378 | C | T | upstream_gene_variant | MODIFIER | c.-1314G>A| |
S263 |
8 | BAA02g45060 | A02 | 37007564 | C | T | upstream_gene_variant | MODIFIER | c.-1500G>A| |
S38 |
9 | BAA02g45060 | A02 | 37008374 | G | A | upstream_gene_variant | MODIFIER | c.-2310C>T| |
S268 |
10 | BAA02g45060 | A02 | 37009152 | A | T | upstream_gene_variant | MODIFIER | c.-3088T>A| |
S209 |
11 | BAA02g45060 | A02 | 37009447 | G | A | upstream_gene_variant | MODIFIER | c.-3383C>T| |
S265 S39 |
12 | BAA02g45060 | A02 | 37010687 | C | T | upstream_gene_variant | MODIFIER | c.-4623G>A| |
S52 |
13 | BAA02g45060 | A02 | 37010903 | G | A | upstream_gene_variant | MODIFIER | c.-4839C>T| |
S38 |