Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12240 | A02 | 5515703 | C | T | downstream_gene_variant | MODIFIER | c.*2264G>A| |
S199 |
2 | BAA02g12240 | A02 | 5518469 | G | A | missense_variant | MODERATE | c.1619C>T|p.Ser540Leu |
S259 |
3 | BAA02g12240 | A02 | 5518631 | G | A | missense_variant | MODERATE | c.1549C>T|p.Pro517Ser |
S296 |
4 | BAA02g12240 | A02 | 5518990 | G | A | missense_variant | MODERATE | c.1267C>T|p.Pro423Ser |
S19 |
5 | BAA02g12240 | A02 | 5519481 | C | T | stop_gained | HIGH | c.948G>A|p.Trp316* |
S124 |
6 | BAA02g12240 | A02 | 5520406 | G | A | missense_variant&splice_region_variant | MODERATE | c.197C>T|p.Ser66Phe |
S281 |
7 | BAA02g12240 | A02 | 5520600 | G | A | synonymous_variant | LOW | c.105C>T|p.Tyr35Tyr |
S289 S290 |
8 | BAA02g12240 | A02 | 5521485 | C | T | upstream_gene_variant | MODIFIER | c.-679G>A| |
S116 |
9 | BAA02g12240 | A02 | 5523907 | C | T | upstream_gene_variant | MODIFIER | c.-3101G>A| |
S266 |
10 | BAA02g12240 | A02 | 5524068 | G | A | upstream_gene_variant | MODIFIER | c.-3262C>T| |
S17 |
11 | BAA02g12240 | A02 | 5524376 | G | A | upstream_gene_variant | MODIFIER | c.-3570C>T| |
S159 S243 |