Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09020 | A02 | 3989892 | G | A | synonymous_variant | LOW | c.859C>T|p.Leu287Leu |
S82 S92 |
2 | BAA02g09020 | A02 | 3990077 | G | A | missense_variant | MODERATE | c.767C>T|p.Thr256Ile |
S232 |
3 | BAA02g09020 | A02 | 3991025 | G | A | missense_variant | MODERATE | c.314C>T|p.Pro105Leu |
S282 |
4 | BAA02g09020 | A02 | 3991343 | C | T | splice_region_variant&synonymous_variant | LOW | c.204G>A|p.Lys68Lys |
S128 |
5 | BAA02g09020 | A02 | 3992053 | C | T | upstream_gene_variant | MODIFIER | c.-202G>A| |
S216 |
6 | BAA02g09020 | A02 | 3992723 | G | A | upstream_gene_variant | MODIFIER | c.-872C>T| |
S184 |
7 | BAA02g09020 | A02 | 3992757 | G | A | upstream_gene_variant | MODIFIER | c.-906C>T| |
S11 |
8 | BAA02g09020 | A02 | 3992864 | G | T | upstream_gene_variant | MODIFIER | c.-1013C>A| |
S170 S228 S263 S275 S41 |
9 | BAA02g09020 | A02 | 3995716 | G | A | upstream_gene_variant | MODIFIER | c.-3865C>T| |
S125 |
10 | BAA02g09020 | A02 | 3996711 | C | T | upstream_gene_variant | MODIFIER | c.-4860G>A| |
S257 |
11 | BAA02g09020 | A02 | 3996718 | C | T | upstream_gene_variant | MODIFIER | c.-4867G>A| |
S1 |
12 | BAA02g09020 | A02 | 3996849 | C | T | upstream_gene_variant | MODIFIER | c.-4998G>A| |
S28 |