Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28460 | A02 | 15998397 | C | T | upstream_gene_variant | MODIFIER | c.-3689C>T| |
S9 |
2 | BAA02g28460 | A02 | 15998894 | G | A | upstream_gene_variant | MODIFIER | c.-3192G>A| |
S143 |
3 | BAA02g28460 | A02 | 16000022 | G | A | upstream_gene_variant | MODIFIER | c.-2064G>A| |
S28 |
4 | BAA02g28460 | A02 | 16000192 | C | T | upstream_gene_variant | MODIFIER | c.-1894C>T| |
S140 |
5 | BAA02g28460 | A02 | 16000440 | C | T | upstream_gene_variant | MODIFIER | c.-1646C>T| |
S218 |
6 | BAA02g28460 | A02 | 16001692 | G | A | upstream_gene_variant | MODIFIER | c.-394G>A| |
S288 |
7 | BAA02g28460 | A02 | 16002175 | C | T | synonymous_variant | LOW | c.90C>T|p.Leu30Leu |
S240 |
8 | BAA02g28460 | A02 | 16002686 | C | T | missense_variant | MODERATE | c.601C>T|p.Pro201Ser |
S234 |
9 | BAA02g28460 | A02 | 16006341 | G | A | downstream_gene_variant | MODIFIER | c.*1166G>A| |
S188 |
10 | BAA02g28460 | A02 | 16007231 | C | T | downstream_gene_variant | MODIFIER | c.*2056C>T| |
S270 |
11 | BAA02g28460 | A02 | 16007604 | C | T | downstream_gene_variant | MODIFIER | c.*2429C>T| |
S206 |
12 | BAA02g28460 | A02 | 16007607 | G | A | downstream_gene_variant | MODIFIER | c.*2432G>A| |
S25 |