Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00930 | A01 | 409988 | C | T | upstream_gene_variant | MODIFIER | c.-1058G>A| |
S64 |
2 | BAA01g00930 | A01 | 410275 | G | A | upstream_gene_variant | MODIFIER | c.-1345C>T| |
S149 |
3 | BAA01g00930 | A01 | 410282 | G | A | upstream_gene_variant | MODIFIER | c.-1352C>T| |
S187 |
4 | BAA01g00930 | A01 | 410755 | C | T | upstream_gene_variant | MODIFIER | c.-1825G>A| |
S81 S85 |
5 | BAA01g00930 | A01 | 410983 | C | T | upstream_gene_variant | MODIFIER | c.-2053G>A| |
S171 |
6 | BAA01g00930 | A01 | 411192 | C | T | upstream_gene_variant | MODIFIER | c.-2262G>A| |
S64 |
7 | BAA01g00930 | A01 | 411371 | G | A | upstream_gene_variant | MODIFIER | c.-2441C>T| |
S281 |
8 | BAA01g00930 | A01 | 411482 | G | A | upstream_gene_variant | MODIFIER | c.-2552C>T| |
S149 |
9 | BAA01g00930 | A01 | 411594 | C | T | upstream_gene_variant | MODIFIER | c.-2664G>A| |
S261 |
10 | BAA01g00930 | A01 | 411910 | G | A | upstream_gene_variant | MODIFIER | c.-2980C>T| |
S200 |
11 | BAA01g00930 | A01 | 411994 | C | T | upstream_gene_variant | MODIFIER | c.-3064G>A| |
S250 |
12 | BAA01g00930 | A01 | 412662 | G | A | upstream_gene_variant | MODIFIER | c.-3732C>T| |
S228 |
13 | BAA01g00930 | A01 | 412717 | C | T | upstream_gene_variant | MODIFIER | c.-3787G>A| |
S302 |
14 | BAA01g00930 | A01 | 412793 | G | A | upstream_gene_variant | MODIFIER | c.-3863C>T| |
S10 |
15 | BAA01g00930 | A01 | 412830 | C | T | upstream_gene_variant | MODIFIER | c.-3900G>A| |
|
16 | BAA01g00930 | A01 | 412949 | G | A | upstream_gene_variant | MODIFIER | c.-4019C>T| |
S159 S243 S276 S298 |