Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13060 | A02 | 5857506 | G | A | upstream_gene_variant | MODIFIER | c.-4042G>A| |
S50 |
2 | BAA02g13060 | A02 | 5858815 | G | A | upstream_gene_variant | MODIFIER | c.-2733G>A| |
S41 |
3 | BAA02g13060 | A02 | 5859148 | G | A | upstream_gene_variant | MODIFIER | c.-2400G>A| |
S17 S218 S267 S268 S269 |
4 | BAA02g13060 | A02 | 5860223 | C | T | upstream_gene_variant | MODIFIER | c.-1325C>T| |
S211 |
5 | BAA02g13060 | A02 | 5861662 | G | A | missense_variant | MODERATE | c.115G>A|p.Ala39Thr |
S136 |
6 | BAA02g13060 | A02 | 5861820 | G | A | synonymous_variant | LOW | c.273G>A|p.Leu91Leu |
S110 |
7 | BAA02g13060 | A02 | 5862735 | C | T | downstream_gene_variant | MODIFIER | c.*741C>T| |
S172 S217 |
8 | BAA02g13060 | A02 | 5863459 | G | A | downstream_gene_variant | MODIFIER | c.*1465G>A| |
S246 |
9 | BAA02g13060 | A02 | 5863505 | C | T | downstream_gene_variant | MODIFIER | c.*1511C>T| |
S121 |
10 | BAA02g13060 | A02 | 5863787 | G | A | downstream_gene_variant | MODIFIER | c.*1793G>A| |
S190 |
11 | BAA02g13060 | A02 | 5863988 | G | A | downstream_gene_variant | MODIFIER | c.*1994G>A| |
S298 |
12 | BAA02g13060 | A02 | 5865055 | G | A | downstream_gene_variant | MODIFIER | c.*3061G>A| |
S37 |
13 | BAA02g13060 | A02 | 5865499 | C | T | downstream_gene_variant | MODIFIER | c.*3505C>T| |
S163 |
14 | BAA02g13060 | A02 | 5866614 | C | T | downstream_gene_variant | MODIFIER | c.*4620C>T| |
S142 |