Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20670 | A02 | 10944898 | G | A | missense_variant | MODERATE | c.250C>T|p.His84Tyr |
S263 |
2 | BAA02g20670 | A02 | 10948901 | G | A | upstream_gene_variant | MODIFIER | c.-3683C>T| |
S295 |
3 | BAA02g20670 | A02 | 10949174 | C | T | upstream_gene_variant | MODIFIER | c.-3956G>A| |
S124 |
4 | BAA02g20670 | A02 | 10949356 | G | A | upstream_gene_variant | MODIFIER | c.-4138C>T| |
S291 |
5 | BAA02g20670 | A02 | 10949655 | G | A | upstream_gene_variant | MODIFIER | c.-4437C>T| |
S68 |
6 | BAA02g20670 | A02 | 10949911 | G | A | upstream_gene_variant | MODIFIER | c.-4693C>T| |
S170 |