Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g13060 | A01 | 6188896 | C | T | upstream_gene_variant | MODIFIER | c.-4857C>T| |
S46 |
2 | BAA01g13060 | A01 | 6189374 | G | A | upstream_gene_variant | MODIFIER | c.-4379G>A| |
S15 S3 |
3 | BAA01g13060 | A01 | 6189697 | C | T | upstream_gene_variant | MODIFIER | c.-4056C>T| |
S284 |
4 | BAA01g13060 | A01 | 6190720 | C | T | upstream_gene_variant | MODIFIER | c.-3033C>T| |
S25 |
5 | BAA01g13060 | A01 | 6190996 | G | A | upstream_gene_variant | MODIFIER | c.-2757G>A| |
S178 |
6 | BAA01g13060 | A01 | 6191217 | G | A | upstream_gene_variant | MODIFIER | c.-2536G>A| |
S63 |
7 | BAA01g13060 | A01 | 6191224 | G | A | upstream_gene_variant | MODIFIER | c.-2529G>A| |
S288 |
8 | BAA01g13060 | A01 | 6191671 | G | A | upstream_gene_variant | MODIFIER | c.-2082G>A| |
S126 |
9 | BAA01g13060 | A01 | 6192259 | C | T | upstream_gene_variant | MODIFIER | c.-1494C>T| |
S7 |
10 | BAA01g13060 | A01 | 6192344 | C | T | upstream_gene_variant | MODIFIER | c.-1409C>T| |
S151 S263 |
11 | BAA01g13060 | A01 | 6192473 | C | T | upstream_gene_variant | MODIFIER | c.-1280C>T| |
S134 |
12 | BAA01g13060 | A01 | 6196185 | G | A | intron_variant | MODIFIER | c.455+1978G>A| |
S172 S217 |
13 | BAA01g13060 | A01 | 6196439 | G | A | intron_variant | MODIFIER | c.455+2232G>A| |
S126 |
14 | BAA01g13060 | A01 | 6197020 | G | A | intron_variant | MODIFIER | c.456-2023G>A| |
S212 |
15 | BAA01g13060 | A01 | 6197075 | G | A | intron_variant | MODIFIER | c.456-1968G>A| |
S194 |
16 | BAA01g13060 | A01 | 6197420 | G | A | intron_variant | MODIFIER | c.456-1623G>A| |
S153 S236 S257 |
17 | BAA01g13060 | A01 | 6197592 | G | A | intron_variant | MODIFIER | c.456-1451G>A| |
S216 |
18 | BAA01g13060 | A01 | 6198119 | G | A | intron_variant | MODIFIER | c.456-924G>A| |
S306 |