Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44770 | A02 | 36780908 | C | T | downstream_gene_variant | MODIFIER | c.*74G>A| |
S13 |
2 | BAA02g44770 | A02 | 36781472 | C | T | missense_variant | MODERATE | c.203G>A|p.Arg68Lys |
S162 |
3 | BAA02g44770 | A02 | 36781558 | C | T | synonymous_variant | LOW | c.117G>A|p.Ala39Ala |
S107 |
4 | BAA02g44770 | A02 | 36781780 | G | A | upstream_gene_variant | MODIFIER | c.-106C>T| |
S229 |
5 | BAA02g44770 | A02 | 36783042 | G | A | upstream_gene_variant | MODIFIER | c.-1368C>T| |
S20 S220 |
6 | BAA02g44770 | A02 | 36784745 | C | T | upstream_gene_variant | MODIFIER | c.-3071G>A| |
S201 |
7 | BAA02g44770 | A02 | 36785132 | C | T | upstream_gene_variant | MODIFIER | c.-3458G>A| |
S179 |