Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g40030 | A09 | 47351853 | G | A | upstream_gene_variant | MODIFIER | c.-4682G>A| |
S127 |
2 | BAA09g40030 | A09 | 47351879 | G | A | upstream_gene_variant | MODIFIER | c.-4656G>A| |
S172 |
3 | BAA09g40030 | A09 | 47352123 | A | G | upstream_gene_variant | MODIFIER | c.-4412A>G| |
S50 |
4 | BAA09g40030 | A09 | 47352249 | G | A | upstream_gene_variant | MODIFIER | c.-4286G>A| |
S12 |
5 | BAA09g40030 | A09 | 47352257 | G | A | upstream_gene_variant | MODIFIER | c.-4278G>A| |
S246 |
6 | BAA09g40030 | A09 | 47353508 | C | T | upstream_gene_variant | MODIFIER | c.-3027C>T| |
S269 |
7 | BAA09g40030 | A09 | 47355594 | C | T | upstream_gene_variant | MODIFIER | c.-941C>T| |
S245 |
8 | BAA09g40030 | A09 | 47355706 | G | A | upstream_gene_variant | MODIFIER | c.-829G>A| |
S107 |
9 | BAA09g40030 | A09 | 47355950 | G | T | upstream_gene_variant | MODIFIER | c.-585G>T| |
|
10 | BAA09g40030 | A09 | 47358477 | T | A | downstream_gene_variant | MODIFIER | c.*429T>A| |
S174 S265 S27 |
11 | BAA09g40030 | A09 | 47358664 | G | A | downstream_gene_variant | MODIFIER | c.*616G>A| |
S2 |
12 | BAA09g40030 | A09 | 47358813 | C | T | downstream_gene_variant | MODIFIER | c.*765C>T| |
S168 |
13 | BAA09g40030 | A09 | 47359106 | C | T | downstream_gene_variant | MODIFIER | c.*1058C>T| |
S303 |
14 | BAA09g40030 | A09 | 47359523 | G | A | downstream_gene_variant | MODIFIER | c.*1475G>A| |
S175 |
15 | BAA09g40030 | A09 | 47360136 | C | T | downstream_gene_variant | MODIFIER | c.*2088C>T| |
S277 |
16 | BAA09g40030 | A09 | 47360357 | C | T | downstream_gene_variant | MODIFIER | c.*2309C>T| |
S259 |
17 | BAA09g40030 | A09 | 47360990 | C | T | downstream_gene_variant | MODIFIER | c.*2942C>T| |
S208 S219 |
18 | BAA09g40030 | A09 | 47362183 | G | A | downstream_gene_variant | MODIFIER | c.*4135G>A| |
S124 S129 S131 S190 S255 S286 S57 S60 |
19 | BAA09g40030 | A09 | 47362742 | C | T | downstream_gene_variant | MODIFIER | c.*4694C>T| |
S28 |