Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44240 | A02 | 36509867 | T | A | downstream_gene_variant | MODIFIER | c.*4747A>T| |
S192 |
2 | BAA02g44240 | A02 | 36511238 | G | A | downstream_gene_variant | MODIFIER | c.*3376C>T| |
S293 S72 S78 |
3 | BAA02g44240 | A02 | 36514973 | C | T | missense_variant | MODERATE | c.355G>A|p.Asp119Asn |
S172 S217 |
4 | BAA02g44240 | A02 | 36518685 | C | T | upstream_gene_variant | MODIFIER | c.-2995G>A| |
S238 |
5 | BAA02g44240 | A02 | 36518771 | C | T | upstream_gene_variant | MODIFIER | c.-3081G>A| |
S107 |
6 | BAA02g44240 | A02 | 36519319 | G | A | upstream_gene_variant | MODIFIER | c.-3629C>T| |
S185 |
7 | BAA02g44240 | A02 | 36520187 | C | T | upstream_gene_variant | MODIFIER | c.-4497G>A| |
S180 |