Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21100 | A02 | 11298314 | G | A | missense_variant | MODERATE | c.353C>T|p.Pro118Leu |
S13 |
2 | BAA02g21100 | A02 | 11298825 | C | T | upstream_gene_variant | MODIFIER | c.-159G>A| |
S193 |
3 | BAA02g21100 | A02 | 11298897 | G | A | upstream_gene_variant | MODIFIER | c.-231C>T| |
S4 |
4 | BAA02g21100 | A02 | 11299248 | G | A | upstream_gene_variant | MODIFIER | c.-582C>T| |
S306 S308 |
5 | BAA02g21100 | A02 | 11299450 | C | T | upstream_gene_variant | MODIFIER | c.-784G>A| |
S219 S72 |
6 | BAA02g21100 | A02 | 11299677 | G | A | upstream_gene_variant | MODIFIER | c.-1011C>T| |
S68 |
7 | BAA02g21100 | A02 | 11300789 | G | A | upstream_gene_variant | MODIFIER | c.-2123C>T| |
S59 |
8 | BAA02g21100 | A02 | 11303356 | G | A | upstream_gene_variant | MODIFIER | c.-4690C>T| |
S296 |