Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44530 | A02 | 36674136 | G | A | upstream_gene_variant | MODIFIER | c.-2386G>A| |
S297 |
2 | BAA02g44530 | A02 | 36674717 | G | A | upstream_gene_variant | MODIFIER | c.-1805G>A| |
S268 |
3 | BAA02g44530 | A02 | 36675773 | G | A | upstream_gene_variant | MODIFIER | c.-749G>A| |
S196 |
4 | BAA02g44530 | A02 | 36675881 | G | A | upstream_gene_variant | MODIFIER | c.-641G>A| |
S114 |
5 | BAA02g44530 | A02 | 36676756 | C | T | missense_variant | MODERATE | c.235C>T|p.Leu79Phe |
S108 |
6 | BAA02g44530 | A02 | 36678700 | C | T | missense_variant | MODERATE | c.527C>T|p.Thr176Ile |
S170 |
7 | BAA02g44530 | A02 | 36679091 | G | A | synonymous_variant | LOW | c.918G>A|p.Pro306Pro |
S266 |
8 | BAA02g44530 | A02 | 36679149 | G | A | missense_variant | MODERATE | c.976G>A|p.Gly326Arg |
S113 |
9 | BAA02g44530 | A02 | 36679347 | G | A | missense_variant | MODERATE | c.1174G>A|p.Gly392Arg |
S187 |
10 | BAA02g44530 | A02 | 36680622 | G | A | downstream_gene_variant | MODIFIER | c.*1012G>A| |
S238 |
11 | BAA02g44530 | A02 | 36680648 | G | A | downstream_gene_variant | MODIFIER | c.*1038G>A| |
S156 |
12 | BAA02g44530 | A02 | 36681206 | C | T | downstream_gene_variant | MODIFIER | c.*1596C>T| |
S105 S106 |
13 | BAA02g44530 | A02 | 36681951 | C | T | downstream_gene_variant | MODIFIER | c.*2341C>T| |
S303 |
14 | BAA02g44530 | A02 | 36683035 | C | T | downstream_gene_variant | MODIFIER | c.*3425C>T| |
S242 |