Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22030 | A02 | 11862408 | G | A | downstream_gene_variant | MODIFIER | c.*2987C>T| |
S149 |
2 | BAA02g22030 | A02 | 11862948 | C | T | downstream_gene_variant | MODIFIER | c.*2447G>A| |
S66 |
3 | BAA02g22030 | A02 | 11863109 | G | A | downstream_gene_variant | MODIFIER | c.*2286C>T| |
S269 |
4 | BAA02g22030 | A02 | 11863296 | C | T | downstream_gene_variant | MODIFIER | c.*2099G>A| |
S209 |
5 | BAA02g22030 | A02 | 11863824 | G | A | downstream_gene_variant | MODIFIER | c.*1571C>T| |
S166 |
6 | BAA02g22030 | A02 | 11863888 | G | A | downstream_gene_variant | MODIFIER | c.*1507C>T| |
S79 S91 |
7 | BAA02g22030 | A02 | 11866112 | C | T | missense_variant | MODERATE | c.1376G>A|p.Arg459Lys |
S182 |
8 | BAA02g22030 | A02 | 11866462 | C | T | missense_variant | MODERATE | c.1109G>A|p.Arg370Lys |
S268 |
9 | BAA02g22030 | A02 | 11867921 | C | T | missense_variant | MODERATE | c.356G>A|p.Gly119Glu |
S255 |
10 | BAA02g22030 | A02 | 11867982 | C | T | missense_variant | MODERATE | c.295G>A|p.Val99Ile |
S6 |
11 | BAA02g22030 | A02 | 11869003 | C | T | upstream_gene_variant | MODIFIER | c.-727G>A| |
S63 |
12 | BAA02g22030 | A02 | 11870396 | G | A | upstream_gene_variant | MODIFIER | c.-2120C>T| |
S187 |
13 | BAA02g22030 | A02 | 11871323 | C | T | upstream_gene_variant | MODIFIER | c.-3047G>A| |
S121 |