Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00310 | A02 | 177571 | G | A | synonymous_variant | LOW | c.1359C>T|p.Phe453Phe |
S303 |
2 | BAA02g00310 | A02 | 177881 | C | T | missense_variant | MODERATE | c.1049G>A|p.Arg350Lys |
S144 |
3 | BAA02g00310 | A02 | 179222 | G | T | upstream_gene_variant | MODIFIER | c.-293C>A| |
S4 |
4 | BAA02g00310 | A02 | 179485 | C | T | upstream_gene_variant | MODIFIER | c.-556G>A| |
S288 |
5 | BAA02g00310 | A02 | 182058 | G | A | upstream_gene_variant | MODIFIER | c.-3129C>T| |
S264 |
6 | BAA02g00310 | A02 | 182210 | G | A | upstream_gene_variant | MODIFIER | c.-3281C>T| |
S79 S91 |
7 | BAA02g00310 | A02 | 182237 | G | A | upstream_gene_variant | MODIFIER | c.-3308C>T| |
S161 |
8 | BAA02g00310 | A02 | 182747 | G | A | upstream_gene_variant | MODIFIER | c.-3818C>T| |
S205 |
9 | BAA02g00310 | A02 | 183386 | C | T | upstream_gene_variant | MODIFIER | c.-4457G>A| |
S280 |