Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26660 | A02 | 14914222 | C | T | upstream_gene_variant | MODIFIER | c.-4307C>T| |
S81 |
2 | BAA02g26660 | A02 | 14914495 | C | T | upstream_gene_variant | MODIFIER | c.-4034C>T| |
S11 |
3 | BAA02g26660 | A02 | 14914593 | G | A | upstream_gene_variant | MODIFIER | c.-3936G>A| |
S245 |
4 | BAA02g26660 | A02 | 14915585 | C | T | upstream_gene_variant | MODIFIER | c.-2944C>T| |
S64 |
5 | BAA02g26660 | A02 | 14915759 | C | T | upstream_gene_variant | MODIFIER | c.-2770C>T| |
S172 S217 |
6 | BAA02g26660 | A02 | 14915858 | G | A | upstream_gene_variant | MODIFIER | c.-2671G>A| |
S288 |
7 | BAA02g26660 | A02 | 14916209 | G | A | upstream_gene_variant | MODIFIER | c.-2320G>A| |
S269 |
8 | BAA02g26660 | A02 | 14916949 | C | T | upstream_gene_variant | MODIFIER | c.-1580C>T| |
S97 |
9 | BAA02g26660 | A02 | 14917307 | G | A | upstream_gene_variant | MODIFIER | c.-1222G>A| |
S47 |
10 | BAA02g26660 | A02 | 14918433 | G | A | upstream_gene_variant | MODIFIER | c.-96G>A| |
S255 |
11 | BAA02g26660 | A02 | 14918647 | C | T | intron_variant | MODIFIER | c.61+58C>T| |
S183 S198 |
12 | BAA02g26660 | A02 | 14919489 | C | T | downstream_gene_variant | MODIFIER | c.*378C>T| |
S224 |
13 | BAA02g26660 | A02 | 14921149 | C | T | downstream_gene_variant | MODIFIER | c.*2038C>T| |
S124 |
14 | BAA02g26660 | A02 | 14921164 | C | T | downstream_gene_variant | MODIFIER | c.*2053C>T| |
S240 |
15 | BAA02g26660 | A02 | 14921235 | G | A | downstream_gene_variant | MODIFIER | c.*2124G>A| |
S278 |