Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09650 | A02 | 4238353 | G | A | upstream_gene_variant | MODIFIER | c.-2561G>A| |
S168 S219 S279 |
2 | BAA02g09650 | A02 | 4238983 | G | A | upstream_gene_variant | MODIFIER | c.-1931G>A| |
S165 |
3 | BAA02g09650 | A02 | 4239011 | C | T | upstream_gene_variant | MODIFIER | c.-1903C>T| |
S278 |
4 | BAA02g09650 | A02 | 4241103 | C | T | missense_variant | MODERATE | c.190C>T|p.Leu64Phe |
S178 |
5 | BAA02g09650 | A02 | 4244740 | G | A | downstream_gene_variant | MODIFIER | c.*2737G>A| |
S17 |
6 | BAA02g09650 | A02 | 4245086 | C | T | downstream_gene_variant | MODIFIER | c.*3083C>T| |
S128 |
7 | BAA02g09650 | A02 | 4245577 | G | A | downstream_gene_variant | MODIFIER | c.*3574G>A| |
S188 |
8 | BAA02g09650 | A02 | 4246752 | C | T | downstream_gene_variant | MODIFIER | c.*4749C>T| |
S70 |
9 | BAA02g09650 | A02 | 4246886 | C | T | downstream_gene_variant | MODIFIER | c.*4883C>T| |
S198 |