Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26800 | A02 | 15001134 | G | A | upstream_gene_variant | MODIFIER | c.-3850G>A| |
S159 S243 |
2 | BAA02g26800 | A02 | 15001547 | G | A | upstream_gene_variant | MODIFIER | c.-3437G>A| |
S111 |
3 | BAA02g26800 | A02 | 15002003 | C | T | upstream_gene_variant | MODIFIER | c.-2981C>T| |
S108 |
4 | BAA02g26800 | A02 | 15005070 | C | T | synonymous_variant | LOW | c.87C>T|p.Phe29Phe |
S122 |
5 | BAA02g26800 | A02 | 15008206 | G | A | downstream_gene_variant | MODIFIER | c.*2298G>A| |
S41 |
6 | BAA02g26800 | A02 | 15008839 | C | T | downstream_gene_variant | MODIFIER | c.*2931C>T| |
S262 |
7 | BAA02g26800 | A02 | 15009805 | G | A | downstream_gene_variant | MODIFIER | c.*3897G>A| |
S94 |
8 | BAA02g26800 | A02 | 15009977 | G | A | downstream_gene_variant | MODIFIER | c.*4069G>A| |
S279 |
9 | BAA02g26800 | A02 | 15009978 | G | A | downstream_gene_variant | MODIFIER | c.*4070G>A| |
S131 S92 |
10 | BAA02g26800 | A02 | 15010226 | C | A | downstream_gene_variant | MODIFIER | c.*4318C>A| |
S56 |
11 | BAA02g26800 | A02 | 15010227 | G | T | downstream_gene_variant | MODIFIER | c.*4319G>T| |
S56 |