Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25260 | A02 | 13802678 | G | A | upstream_gene_variant | MODIFIER | c.-4083G>A| |
S103 |
2 | BAA02g25260 | A02 | 13802858 | C | T | upstream_gene_variant | MODIFIER | c.-3903C>T| |
S161 |
3 | BAA02g25260 | A02 | 13805018 | G | A | upstream_gene_variant | MODIFIER | c.-1743G>A| |
S47 |
4 | BAA02g25260 | A02 | 13806263 | C | T | upstream_gene_variant | MODIFIER | c.-498C>T| |
S16 |
5 | BAA02g25260 | A02 | 13807629 | G | A | missense_variant | MODERATE | c.331G>A|p.Val111Ile |
S37 |
6 | BAA02g25260 | A02 | 13808010 | C | T | intron_variant | MODIFIER | c.461-33C>T| |
S46 |
7 | BAA02g25260 | A02 | 13808556 | C | T | downstream_gene_variant | MODIFIER | c.*446C>T| |
S183 S198 |
8 | BAA02g25260 | A02 | 13809503 | C | T | downstream_gene_variant | MODIFIER | c.*1393C>T| |
S20 |
9 | BAA02g25260 | A02 | 13811179 | C | T | downstream_gene_variant | MODIFIER | c.*3069C>T| |
S171 |
10 | BAA02g25260 | A02 | 13811227 | C | T | downstream_gene_variant | MODIFIER | c.*3117C>T| |
S9 |
11 | BAA02g25260 | A02 | 13811230 | C | T | downstream_gene_variant | MODIFIER | c.*3120C>T| |
S118 S139 |
12 | BAA02g25260 | A02 | 13812019 | G | A | downstream_gene_variant | MODIFIER | c.*3909G>A| |
S17 |
13 | BAA02g25260 | A02 | 13812316 | T | C | downstream_gene_variant | MODIFIER | c.*4206T>C| |
S286 |