Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01100 | A02 | 517533 | C | T | downstream_gene_variant | MODIFIER | c.*2965G>A| |
S77 S82 |
2 | BAA02g01100 | A02 | 520559 | G | A | missense_variant | MODERATE | c.539C>T|p.Thr180Ile |
S223 |
3 | BAA02g01100 | A02 | 521461 | C | T | upstream_gene_variant | MODIFIER | c.-273G>A| |
S267 |
4 | BAA02g01100 | A02 | 522179 | A | G | upstream_gene_variant | MODIFIER | c.-991T>C| |
S249 |
5 | BAA02g01100 | A02 | 523075 | C | T | upstream_gene_variant | MODIFIER | c.-1887G>A| |
S40 S49 |
6 | BAA02g01100 | A02 | 523581 | C | T | upstream_gene_variant | MODIFIER | c.-2393G>A| |
S142 |
7 | BAA02g01100 | A02 | 524055 | G | A | upstream_gene_variant | MODIFIER | c.-2867C>T| |
S273 |
8 | BAA02g01100 | A02 | 524192 | G | A | upstream_gene_variant | MODIFIER | c.-3004C>T| |
S265 |
9 | BAA02g01100 | A02 | 525006 | G | A | upstream_gene_variant | MODIFIER | c.-3818C>T| |
S173 |
10 | BAA02g01100 | A02 | 526014 | C | T | upstream_gene_variant | MODIFIER | c.-4826G>A| |
S207 |