Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15630 | A02 | 7548736 | G | A | upstream_gene_variant | MODIFIER | c.-4157G>A| |
S173 |
2 | BAA02g15630 | A02 | 7548784 | G | A | upstream_gene_variant | MODIFIER | c.-4109G>A| |
S259 |
3 | BAA02g15630 | A02 | 7549852 | G | A | upstream_gene_variant | MODIFIER | c.-3041G>A| |
S228 |
4 | BAA02g15630 | A02 | 7550035 | C | T | upstream_gene_variant | MODIFIER | c.-2858C>T| |
S123 |
5 | BAA02g15630 | A02 | 7550782 | G | A | upstream_gene_variant | MODIFIER | c.-2111G>A| |
S232 |
6 | BAA02g15630 | A02 | 7552937 | G | A | synonymous_variant | LOW | c.45G>A|p.Thr15Thr |
S17 |
7 | BAA02g15630 | A02 | 7553036 | C | T | synonymous_variant | LOW | c.144C>T|p.Ser48Ser |
S218 |
8 | BAA02g15630 | A02 | 7557486 | G | A | downstream_gene_variant | MODIFIER | c.*4420G>A| |
S296 |
9 | BAA02g15630 | A02 | 7557944 | C | T | downstream_gene_variant | MODIFIER | c.*4878C>T| |
S255 |