Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42220 | A02 | 35200232 | G | A | missense_variant | MODERATE | c.77C>T|p.Ala26Val |
S60 |
2 | BAA02g42220 | A02 | 35200662 | C | T | upstream_gene_variant | MODIFIER | c.-211G>A| |
S303 |
3 | BAA02g42220 | A02 | 35201886 | C | T | upstream_gene_variant | MODIFIER | c.-1435G>A| |
S205 |
4 | BAA02g42220 | A02 | 35202455 | C | T | upstream_gene_variant | MODIFIER | c.-2004G>A| |
S267 S40 S49 |
5 | BAA02g42220 | A02 | 35202737 | C | T | upstream_gene_variant | MODIFIER | c.-2286G>A| |
S159 S243 |
6 | BAA02g42220 | A02 | 35202778 | G | A | upstream_gene_variant | MODIFIER | c.-2327C>T| |
S166 |
7 | BAA02g42220 | A02 | 35202961 | G | A | upstream_gene_variant | MODIFIER | c.-2510C>T| |
S13 |
8 | BAA02g42220 | A02 | 35203198 | C | T | upstream_gene_variant | MODIFIER | c.-2747G>A| |
S218 |
9 | BAA02g42220 | A02 | 35205175 | C | T | upstream_gene_variant | MODIFIER | c.-4724G>A| |
S139 |