Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16360 | A02 | 7971152 | G | A | upstream_gene_variant | MODIFIER | c.-4839G>A| |
S170 |
2 | BAA02g16360 | A02 | 7971280 | C | T | upstream_gene_variant | MODIFIER | c.-4711C>T| |
S255 |
3 | BAA02g16360 | A02 | 7971334 | G | A | upstream_gene_variant | MODIFIER | c.-4657G>A| |
S274 |
4 | BAA02g16360 | A02 | 7971356 | C | T | upstream_gene_variant | MODIFIER | c.-4635C>T| |
S6 |
5 | BAA02g16360 | A02 | 7972004 | G | A | upstream_gene_variant | MODIFIER | c.-3987G>A| |
S149 |
6 | BAA02g16360 | A02 | 7972107 | G | A | upstream_gene_variant | MODIFIER | c.-3884G>A| |
S12 |
7 | BAA02g16360 | A02 | 7973902 | C | T | upstream_gene_variant | MODIFIER | c.-2089C>T| |
S301 S304 |
8 | BAA02g16360 | A02 | 7973916 | G | A | upstream_gene_variant | MODIFIER | c.-2075G>A| |
S298 |
9 | BAA02g16360 | A02 | 7974148 | C | T | upstream_gene_variant | MODIFIER | c.-1843C>T| |
S8 |
10 | BAA02g16360 | A02 | 7977272 | G | A | synonymous_variant | LOW | c.501G>A|p.Ala167Ala |
S276 |
11 | BAA02g16360 | A02 | 7977598 | C | T | missense_variant | MODERATE | c.719C>T|p.Ala240Val |
S302 |
12 | BAA02g16360 | A02 | 7977887 | G | A | missense_variant | MODERATE | c.925G>A|p.Val309Ile |
S247 |
13 | BAA02g16360 | A02 | 7981308 | C | T | downstream_gene_variant | MODIFIER | c.*2920C>T| |
S13 |