Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20730 | A02 | 11006432 | G | A | upstream_gene_variant | MODIFIER | c.-3501G>A| |
S159 S243 |
2 | BAA02g20730 | A02 | 11006832 | T | A | upstream_gene_variant | MODIFIER | c.-3101T>A| |
S175 |
3 | BAA02g20730 | A02 | 11007216 | G | A | upstream_gene_variant | MODIFIER | c.-2717G>A| |
S10 |
4 | BAA02g20730 | A02 | 11007387 | G | A | upstream_gene_variant | MODIFIER | c.-2546G>A| |
S72 |
5 | BAA02g20730 | A02 | 11009394 | G | A | upstream_gene_variant | MODIFIER | c.-539G>A| |
S291 |
6 | BAA02g20730 | A02 | 11009446 | G | T | upstream_gene_variant | MODIFIER | c.-487G>T| |
S134 |
7 | BAA02g20730 | A02 | 11009738 | G | A | upstream_gene_variant | MODIFIER | c.-195G>A| |
S28 |
8 | BAA02g20730 | A02 | 11010770 | G | A | missense_variant&splice_region_variant | MODERATE | c.370G>A|p.Gly124Ser |
S210 S225 |
9 | BAA02g20730 | A02 | 11010791 | C | T | synonymous_variant | LOW | c.391C>T|p.Leu131Leu |
S152 |
10 | BAA02g20730 | A02 | 11010998 | C | T | missense_variant | MODERATE | c.517C>T|p.Leu173Phe |
S58 |
11 | BAA02g20730 | A02 | 11012164 | G | A | downstream_gene_variant | MODIFIER | c.*708G>A| |
S68 |
12 | BAA02g20730 | A02 | 11013207 | C | T | downstream_gene_variant | MODIFIER | c.*1751C>T| |
S265 S39 |
13 | BAA02g20730 | A02 | 11013711 | G | A | downstream_gene_variant | MODIFIER | c.*2255G>A| |
S238 |