Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26290 | A02 | 14588136 | G | A | downstream_gene_variant | MODIFIER | c.*3384C>T| |
S256 |
2 | BAA02g26290 | A02 | 14588296 | G | A | downstream_gene_variant | MODIFIER | c.*3224C>T| |
S133 |
3 | BAA02g26290 | A02 | 14588403 | C | T | downstream_gene_variant | MODIFIER | c.*3117G>A| |
S33 |
4 | BAA02g26290 | A02 | 14590178 | G | A | downstream_gene_variant | MODIFIER | c.*1342C>T| |
S129 |
5 | BAA02g26290 | A02 | 14590714 | C | T | downstream_gene_variant | MODIFIER | c.*806G>A| |
S182 |
6 | BAA02g26290 | A02 | 14591057 | C | T | downstream_gene_variant | MODIFIER | c.*463G>A| |
S42 |
7 | BAA02g26290 | A02 | 14591342 | G | A | downstream_gene_variant | MODIFIER | c.*178C>T| |
S122 |
8 | BAA02g26290 | A02 | 14592661 | G | A | missense_variant | MODERATE | c.1580C>T|p.Ser527Phe |
S236 |
9 | BAA02g26290 | A02 | 14592747 | G | A | synonymous_variant | LOW | c.1494C>T|p.Pro498Pro |
S94 |
10 | BAA02g26290 | A02 | 14593470 | G | A | synonymous_variant | LOW | c.1287C>T|p.Phe429Phe |
S127 |
11 | BAA02g26290 | A02 | 14594261 | G | A | missense_variant | MODERATE | c.643C>T|p.Leu215Phe |
S204 |
12 | BAA02g26290 | A02 | 14595051 | G | A | synonymous_variant | LOW | c.171C>T|p.Asp57Asp |
S156 |
13 | BAA02g26290 | A02 | 14595523 | C | T | upstream_gene_variant | MODIFIER | c.-302G>A| |
S296 |
14 | BAA02g26290 | A02 | 14595880 | G | A | upstream_gene_variant | MODIFIER | c.-659C>T| |
S143 |
15 | BAA02g26290 | A02 | 14597684 | C | T | upstream_gene_variant | MODIFIER | c.-2463G>A| |
S32 |
16 | BAA02g26290 | A02 | 14599213 | C | T | upstream_gene_variant | MODIFIER | c.-3992G>A| |
S33 |