Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00020 | A02 | 14339 | G | A | upstream_gene_variant | MODIFIER | c.-3429G>A| |
S149 |
2 | BAA02g00020 | A02 | 15110 | G | A | upstream_gene_variant | MODIFIER | c.-2658G>A| |
S81 S85 |
3 | BAA02g00020 | A02 | 15208 | C | T | upstream_gene_variant | MODIFIER | c.-2560C>T| |
S277 |
4 | BAA02g00020 | A02 | 16839 | C | T | upstream_gene_variant | MODIFIER | c.-929C>T| |
S159 |
5 | BAA02g00020 | A02 | 16878 | C | T | upstream_gene_variant | MODIFIER | c.-890C>T| |
S194 |
6 | BAA02g00020 | A02 | 16896 | G | A | upstream_gene_variant | MODIFIER | c.-872G>A| |
S153 |
7 | BAA02g00020 | A02 | 17109 | T | A | upstream_gene_variant | MODIFIER | c.-659T>A| |
S94 |
8 | BAA02g00020 | A02 | 17761 | C | T | upstream_gene_variant | MODIFIER | c.-7C>T| |
S139 |
9 | BAA02g00020 | A02 | 18662 | G | A | missense_variant | MODERATE | c.714G>A|p.Met238Ile |
S295 |