Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g23960 | A02 | 13090064 | C | T | upstream_gene_variant | MODIFIER | c.-2951C>T| |
S105 S106 |
2 | BAA02g23960 | A02 | 13091021 | C | T | upstream_gene_variant | MODIFIER | c.-1994C>T| |
S179 |
3 | BAA02g23960 | A02 | 13091056 | G | A | upstream_gene_variant | MODIFIER | c.-1959G>A| |
S200 |
4 | BAA02g23960 | A02 | 13091577 | G | A | upstream_gene_variant | MODIFIER | c.-1438G>A| |
S74 |
5 | BAA02g23960 | A02 | 13092079 | G | A | upstream_gene_variant | MODIFIER | c.-936G>A| |
S188 |
6 | BAA02g23960 | A02 | 13092299 | G | A | upstream_gene_variant | MODIFIER | c.-716G>A| |
S67 |
7 | BAA02g23960 | A02 | 13092478 | G | A | upstream_gene_variant | MODIFIER | c.-537G>A| |
S187 |
8 | BAA02g23960 | A02 | 13093148 | C | T | missense_variant | MODERATE | c.134C>T|p.Ser45Phe |
S308 |
9 | BAA02g23960 | A02 | 13093188 | C | T | downstream_gene_variant | MODIFIER | c.*9C>T| |
S212 |