Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32460 | A02 | 27502480 | C | T | missense_variant | MODERATE | c.799G>A|p.Asp267Asn |
S100 |
2 | BAA02g32460 | A02 | 27502811 | G | A | synonymous_variant | LOW | c.468C>T|p.Val156Val |
S12 |
3 | BAA02g32460 | A02 | 27505685 | A | T | upstream_gene_variant | MODIFIER | c.-2407T>A| |
S20 |
4 | BAA02g32460 | A02 | 27505698 | G | A | upstream_gene_variant | MODIFIER | c.-2420C>T| |
S143 |
5 | BAA02g32460 | A02 | 27505754 | C | T | upstream_gene_variant | MODIFIER | c.-2476G>A| |
S119 |
6 | BAA02g32460 | A02 | 27505794 | G | A | upstream_gene_variant | MODIFIER | c.-2516C>T| |
S70 |
7 | BAA02g32460 | A02 | 27506005 | C | T | upstream_gene_variant | MODIFIER | c.-2727G>A| |
S171 |
8 | BAA02g32460 | A02 | 27507208 | C | T | upstream_gene_variant | MODIFIER | c.-3930G>A| |
S195 |
9 | BAA02g32460 | A02 | 27507283 | G | A | upstream_gene_variant | MODIFIER | c.-4005C>T| |
S47 |
10 | BAA02g32460 | A02 | 27507606 | G | A | upstream_gene_variant | MODIFIER | c.-4328C>T| |
S302 |