Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16770 | A02 | 8277026 | C | T | upstream_gene_variant | MODIFIER | c.-1014C>T| |
S13 |
2 | BAA02g16770 | A02 | 8277056 | C | T | upstream_gene_variant | MODIFIER | c.-984C>T| |
S174 |
3 | BAA02g16770 | A02 | 8277576 | C | T | upstream_gene_variant | MODIFIER | c.-464C>T| |
S46 |
4 | BAA02g16770 | A02 | 8277583 | C | T | upstream_gene_variant | MODIFIER | c.-457C>T| |
S209 |
5 | BAA02g16770 | A02 | 8277875 | C | T | upstream_gene_variant | MODIFIER | c.-165C>T| |
S94 |
6 | BAA02g16770 | A02 | 8277940 | C | T | upstream_gene_variant | MODIFIER | c.-100C>T| |
S212 |
7 | BAA02g16770 | A02 | 8277958 | C | T | upstream_gene_variant | MODIFIER | c.-82C>T| |
S75 S81 |
8 | BAA02g16770 | A02 | 8278909 | C | T | missense_variant | MODERATE | c.277C>T|p.Pro93Ser |
S84 S93 |
9 | BAA02g16770 | A02 | 8279104 | G | A | missense_variant | MODERATE | c.394G>A|p.Val132Ile |
S288 |
10 | BAA02g16770 | A02 | 8279181 | G | A | synonymous_variant | LOW | c.471G>A|p.Pro157Pro |
S205 |
11 | BAA02g16770 | A02 | 8281814 | C | T | downstream_gene_variant | MODIFIER | c.*2326C>T| |
S308 |
12 | BAA02g16770 | A02 | 8281891 | G | A | downstream_gene_variant | MODIFIER | c.*2403G>A| |
S35 |
13 | BAA02g16770 | A02 | 8282117 | C | T | downstream_gene_variant | MODIFIER | c.*2629C>T| |
S143 |
14 | BAA02g16770 | A02 | 8282162 | G | A | downstream_gene_variant | MODIFIER | c.*2674G>A| |
S197 |
15 | BAA02g16770 | A02 | 8282194 | G | A | downstream_gene_variant | MODIFIER | c.*2706G>A| |
S203 |