Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09130 | A01 | 3997567 | C | T | missense_variant | MODERATE | c.706G>A|p.Gly236Arg |
S50 |
2 | BAA01g09130 | A01 | 4002602 | G | T | upstream_gene_variant | MODIFIER | c.-3158C>A| |
S223 |
3 | BAA01g09130 | A01 | 4003189 | C | T | upstream_gene_variant | MODIFIER | c.-3745G>A| |
S38 |
4 | BAA01g09130 | A01 | 4003226 | C | T | upstream_gene_variant | MODIFIER | c.-3782G>A| |
S304 |
5 | BAA01g09130 | A01 | 4003335 | C | T | upstream_gene_variant | MODIFIER | c.-3891G>A| |
S120 |
6 | BAA01g09130 | A01 | 4003610 | G | A | upstream_gene_variant | MODIFIER | c.-4166C>T| |
S297 |
7 | BAA01g09130 | A01 | 4003694 | G | A | upstream_gene_variant | MODIFIER | c.-4250C>T| |
S173 |
8 | BAA01g09130 | A01 | 4003887 | G | A | upstream_gene_variant | MODIFIER | c.-4443C>T| |
S190 |