Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19580 | A02 | 10178732 | G | A | synonymous_variant | LOW | c.21C>T|p.His7His |
S26 |
2 | BAA02g19580 | A02 | 10179357 | G | A | upstream_gene_variant | MODIFIER | c.-605C>T| |
S306 S308 |
3 | BAA02g19580 | A02 | 10179371 | C | T | upstream_gene_variant | MODIFIER | c.-619G>A| |
S138 |
4 | BAA02g19580 | A02 | 10179374 | G | A | upstream_gene_variant | MODIFIER | c.-622C>T| |
S144 |
5 | BAA02g19580 | A02 | 10179844 | G | A | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S134 |
6 | BAA02g19580 | A02 | 10179859 | G | A | upstream_gene_variant | MODIFIER | c.-1107C>T| |
S229 |
7 | BAA02g19580 | A02 | 10180026 | G | A | upstream_gene_variant | MODIFIER | c.-1274C>T| |
S149 |
8 | BAA02g19580 | A02 | 10180422 | G | A | upstream_gene_variant | MODIFIER | c.-1670C>T| |
S231 |
9 | BAA02g19580 | A02 | 10180852 | C | T | upstream_gene_variant | MODIFIER | c.-2100G>A| |
S42 |
10 | BAA02g19580 | A02 | 10181133 | G | A | upstream_gene_variant | MODIFIER | c.-2381C>T| |
S128 |
11 | BAA02g19580 | A02 | 10181450 | G | A | upstream_gene_variant | MODIFIER | c.-2698C>T| |
S251 |
12 | BAA02g19580 | A02 | 10182026 | G | A | upstream_gene_variant | MODIFIER | c.-3274C>T| |
S129 |
13 | BAA02g19580 | A02 | 10182035 | C | T | upstream_gene_variant | MODIFIER | c.-3283G>A| |
S264 |
14 | BAA02g19580 | A02 | 10183124 | C | T | upstream_gene_variant | MODIFIER | c.-4372G>A| |
S218 |