Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44900 | A02 | 36860207 | G | A | downstream_gene_variant | MODIFIER | c.*4657C>T| |
S184 |
2 | BAA02g44900 | A02 | 36860597 | C | T | downstream_gene_variant | MODIFIER | c.*4267G>A| |
S48 |
3 | BAA02g44900 | A02 | 36860810 | G | A | downstream_gene_variant | MODIFIER | c.*4054C>T| |
S209 |
4 | BAA02g44900 | A02 | 36861453 | C | T | downstream_gene_variant | MODIFIER | c.*3411G>A| |
S105 |
5 | BAA02g44900 | A02 | 36862106 | C | T | downstream_gene_variant | MODIFIER | c.*2758G>A| |
S263 |
6 | BAA02g44900 | A02 | 36862302 | G | A | downstream_gene_variant | MODIFIER | c.*2562C>T| |
S291 |
7 | BAA02g44900 | A02 | 36862528 | G | A | downstream_gene_variant | MODIFIER | c.*2336C>T| |
S157 S163 |
8 | BAA02g44900 | A02 | 36862645 | G | A | downstream_gene_variant | MODIFIER | c.*2219C>T| |
S293 |
9 | BAA02g44900 | A02 | 36863020 | C | T | downstream_gene_variant | MODIFIER | c.*1844G>A| |
S296 |
10 | BAA02g44900 | A02 | 36863969 | C | T | downstream_gene_variant | MODIFIER | c.*895G>A| |
S179 |
11 | BAA02g44900 | A02 | 36864125 | C | T | downstream_gene_variant | MODIFIER | c.*739G>A| |
S59 |
12 | BAA02g44900 | A02 | 36865737 | C | T | splice_region_variant&intron_variant | LOW | c.1167+6G>A| |
S274 |
13 | BAA02g44900 | A02 | 36868729 | C | T | intron_variant | MODIFIER | c.432+132G>A| |
S15 S241 |
14 | BAA02g44900 | A02 | 36871795 | G | A | upstream_gene_variant | MODIFIER | c.-2503C>T| |
S41 |
15 | BAA02g44900 | A02 | 36872093 | G | A | upstream_gene_variant | MODIFIER | c.-2801C>T| |
S38 |
16 | BAA02g44900 | A02 | 36872363 | G | A | upstream_gene_variant | MODIFIER | c.-3071C>T| |
S278 |