Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44090 | A02 | 36393176 | G | A | upstream_gene_variant | MODIFIER | c.-4043G>A| |
S184 |
2 | BAA02g44090 | A02 | 36394671 | G | A | upstream_gene_variant | MODIFIER | c.-2548G>A| |
S132 S137 S215 S89 |
3 | BAA02g44090 | A02 | 36394766 | G | A | upstream_gene_variant | MODIFIER | c.-2453G>A| |
S56 |
4 | BAA02g44090 | A02 | 36396077 | C | T | upstream_gene_variant | MODIFIER | c.-1142C>T| |
S172 S217 |
5 | BAA02g44090 | A02 | 36396321 | C | T | upstream_gene_variant | MODIFIER | c.-898C>T| |
S118 |
6 | BAA02g44090 | A02 | 36396470 | C | T | upstream_gene_variant | MODIFIER | c.-749C>T| |
S63 |
7 | BAA02g44090 | A02 | 36396936 | G | A | upstream_gene_variant | MODIFIER | c.-283G>A| |
S149 |
8 | BAA02g44090 | A02 | 36397574 | C | T | missense_variant | MODERATE | c.356C>T|p.Pro119Leu |
S124 |
9 | BAA02g44090 | A02 | 36398867 | G | A | missense_variant | MODERATE | c.892G>A|p.Ala298Thr |
S20 |
10 | BAA02g44090 | A02 | 36402155 | G | A | downstream_gene_variant | MODIFIER | c.*2619G>A| |
S79 S91 |
11 | BAA02g44090 | A02 | 36402163 | G | A | downstream_gene_variant | MODIFIER | c.*2627G>A| |
S245 |
12 | BAA02g44090 | A02 | 36402373 | G | A | downstream_gene_variant | MODIFIER | c.*2837G>A| |
S251 |
13 | BAA02g44090 | A02 | 36403880 | G | A | downstream_gene_variant | MODIFIER | c.*4344G>A| |
S156 |