Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29210 | A02 | 16690835 | C | T | upstream_gene_variant | MODIFIER | c.-949C>T| |
S249 |
2 | BAA02g29210 | A02 | 16692642 | C | T | missense_variant | MODERATE | c.859C>T|p.Leu287Phe |
S18 |
3 | BAA02g29210 | A02 | 16695878 | C | T | downstream_gene_variant | MODIFIER | c.*1704C>T| |
S18 |
4 | BAA02g29210 | A02 | 16696766 | G | A | downstream_gene_variant | MODIFIER | c.*2592G>A| |
S247 |
5 | BAA02g29210 | A02 | 16697304 | G | A | downstream_gene_variant | MODIFIER | c.*3130G>A| |
S136 |
6 | BAA02g29210 | A02 | 16697443 | G | A | downstream_gene_variant | MODIFIER | c.*3269G>A| |
S223 |
7 | BAA02g29210 | A02 | 16697865 | C | T | downstream_gene_variant | MODIFIER | c.*3691C>T| |
S301 S304 |
8 | BAA02g29210 | A02 | 16697869 | C | T | downstream_gene_variant | MODIFIER | c.*3695C>T| |
S105 S106 |
9 | BAA02g29210 | A02 | 16698546 | G | A | downstream_gene_variant | MODIFIER | c.*4372G>A| |
S278 |
10 | BAA02g29210 | A02 | 16698902 | G | A | downstream_gene_variant | MODIFIER | c.*4728G>A| |
S166 |