Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34250 | A02 | 29369342 | C | T | missense_variant | MODERATE | c.530G>A|p.Gly177Asp |
S128 |
2 | BAA02g34250 | A02 | 29370092 | C | T | upstream_gene_variant | MODIFIER | c.-87G>A| |
S168 |
3 | BAA02g34250 | A02 | 29370139 | C | T | upstream_gene_variant | MODIFIER | c.-134G>A| |
S240 |
4 | BAA02g34250 | A02 | 29370364 | C | T | upstream_gene_variant | MODIFIER | c.-359G>A| |
S296 |
5 | BAA02g34250 | A02 | 29370739 | G | T | upstream_gene_variant | MODIFIER | c.-734C>A| |
S94 |
6 | BAA02g34250 | A02 | 29371167 | G | A | upstream_gene_variant | MODIFIER | c.-1162C>T| |
S247 |
7 | BAA02g34250 | A02 | 29371888 | G | A | upstream_gene_variant | MODIFIER | c.-1883C>T| |
S279 |
8 | BAA02g34250 | A02 | 29371981 | C | T | upstream_gene_variant | MODIFIER | c.-1976G>A| |
S299 |
9 | BAA02g34250 | A02 | 29372166 | C | T | upstream_gene_variant | MODIFIER | c.-2161G>A| |
S259 |
10 | BAA02g34250 | A02 | 29372395 | G | A | upstream_gene_variant | MODIFIER | c.-2390C>T| |
S4 |
11 | BAA02g34250 | A02 | 29372610 | G | A | upstream_gene_variant | MODIFIER | c.-2605C>T| |
S161 |
12 | BAA02g34250 | A02 | 29372903 | C | T | upstream_gene_variant | MODIFIER | c.-2898G>A| |
S203 |
13 | BAA02g34250 | A02 | 29373845 | G | A | upstream_gene_variant | MODIFIER | c.-3840C>T| |
S86 |
14 | BAA02g34250 | A02 | 29374035 | C | T | upstream_gene_variant | MODIFIER | c.-4030G>A| |
S249 |
15 | BAA02g34250 | A02 | 29374639 | C | T | upstream_gene_variant | MODIFIER | c.-4634G>A| |
S44 |