Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16580 | A02 | 8107629 | G | A | upstream_gene_variant | MODIFIER | c.-4884G>A| |
S12 |
2 | BAA02g16580 | A02 | 8109033 | C | T | upstream_gene_variant | MODIFIER | c.-3480C>T| |
S46 |
3 | BAA02g16580 | A02 | 8109367 | C | T | upstream_gene_variant | MODIFIER | c.-3146C>T| |
S152 |
4 | BAA02g16580 | A02 | 8110320 | G | A | upstream_gene_variant | MODIFIER | c.-2193G>A| |
S47 |
5 | BAA02g16580 | A02 | 8112627 | G | A | missense_variant | MODERATE | c.115G>A|p.Glu39Lys |
S190 |
6 | BAA02g16580 | A02 | 8114005 | C | T | downstream_gene_variant | MODIFIER | c.*148C>T| |
S138 |
7 | BAA02g16580 | A02 | 8114451 | C | T | downstream_gene_variant | MODIFIER | c.*594C>T| |
S96 |
8 | BAA02g16580 | A02 | 8114988 | C | T | downstream_gene_variant | MODIFIER | c.*1131C>T| |
S179 |
9 | BAA02g16580 | A02 | 8115407 | C | T | downstream_gene_variant | MODIFIER | c.*1550C>T| |
S208 S219 |
10 | BAA02g16580 | A02 | 8115908 | C | T | downstream_gene_variant | MODIFIER | c.*2051C>T| |
S18 |
11 | BAA02g16580 | A02 | 8116513 | C | T | downstream_gene_variant | MODIFIER | c.*2656C>T| |
S186 |