Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20400 | A02 | 10825291 | C | T | intron_variant | MODIFIER | c.383+78G>A| |
S58 |
2 | BAA02g20400 | A02 | 10826180 | C | T | missense_variant | MODERATE | c.266G>A|p.Arg89Lys |
S77 S82 |
3 | BAA02g20400 | A02 | 10829321 | C | T | upstream_gene_variant | MODIFIER | c.-2471G>A| |
S185 |
4 | BAA02g20400 | A02 | 10829428 | G | A | upstream_gene_variant | MODIFIER | c.-2578C>T| |
S133 |
5 | BAA02g20400 | A02 | 10831144 | G | A | upstream_gene_variant | MODIFIER | c.-4294C>T| |
S306 S308 |
6 | BAA02g20400 | A02 | 10831725 | C | A | upstream_gene_variant | MODIFIER | c.-4875G>T| |
S224 |