Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22160 | A01 | 11078747 | C | T | upstream_gene_variant | MODIFIER | c.-4098C>T| |
S273 |
2 | BAA01g22160 | A01 | 11080380 | G | A | upstream_gene_variant | MODIFIER | c.-2465G>A| |
S178 |
3 | BAA01g22160 | A01 | 11080495 | C | T | upstream_gene_variant | MODIFIER | c.-2350C>T| |
S51 |
4 | BAA01g22160 | A01 | 11081070 | A | C | upstream_gene_variant | MODIFIER | c.-1775A>C| |
S274 |
5 | BAA01g22160 | A01 | 11081274 | G | A | upstream_gene_variant | MODIFIER | c.-1571G>A| |
S280 |
6 | BAA01g22160 | A01 | 11081283 | G | A | upstream_gene_variant | MODIFIER | c.-1562G>A| |
S257 |
7 | BAA01g22160 | A01 | 11081292 | C | T | upstream_gene_variant | MODIFIER | c.-1553C>T| |
S25 |
8 | BAA01g22160 | A01 | 11081363 | G | A | upstream_gene_variant | MODIFIER | c.-1482G>A| |
S83 S88 |
9 | BAA01g22160 | A01 | 11081392 | G | A | upstream_gene_variant | MODIFIER | c.-1453G>A| |
S293 |
10 | BAA01g22160 | A01 | 11081521 | G | A | upstream_gene_variant | MODIFIER | c.-1324G>A| |
S238 |
11 | BAA01g22160 | A01 | 11081559 | G | A | upstream_gene_variant | MODIFIER | c.-1286G>A| |
S204 |
12 | BAA01g22160 | A01 | 11081569 | G | A | upstream_gene_variant | MODIFIER | c.-1276G>A| |
S190 |
13 | BAA01g22160 | A01 | 11081639 | C | T | upstream_gene_variant | MODIFIER | c.-1206C>T| |
S278 |
14 | BAA01g22160 | A01 | 11082005 | G | A | upstream_gene_variant | MODIFIER | c.-840G>A| |
S149 |
15 | BAA01g22160 | A01 | 11082495 | C | T | upstream_gene_variant | MODIFIER | c.-350C>T| |
S148 S30 S31 |
16 | BAA01g22160 | A01 | 11082787 | G | A | upstream_gene_variant | MODIFIER | c.-58G>A| |
S174 |
17 | BAA01g22160 | A01 | 11082896 | G | A | missense_variant | MODERATE | c.52G>A|p.Ala18Thr |
S63 |
18 | BAA01g22160 | A01 | 11085156 | G | A | downstream_gene_variant | MODIFIER | c.*2132G>A| |
S149 |
19 | BAA01g22160 | A01 | 11085214 | C | T | downstream_gene_variant | MODIFIER | c.*2190C>T| |
S184 |