Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10170 | A02 | 4511859 | C | T | upstream_gene_variant | MODIFIER | c.-4995C>T| |
S55 |
2 | BAA02g10170 | A02 | 4511991 | G | A | upstream_gene_variant | MODIFIER | c.-4863G>A| |
S287 |
3 | BAA02g10170 | A02 | 4517062 | G | A | missense_variant | MODERATE | c.13G>A|p.Gly5Arg |
S45 |
4 | BAA02g10170 | A02 | 4521315 | G | A | downstream_gene_variant | MODIFIER | c.*2379G>A| |
S131 |
5 | BAA02g10170 | A02 | 4522540 | C | T | downstream_gene_variant | MODIFIER | c.*3604C>T| |
S178 |
6 | BAA02g10170 | A02 | 4522596 | G | A | downstream_gene_variant | MODIFIER | c.*3660G>A| |
S87 |
7 | BAA02g10170 | A02 | 4523097 | G | A | downstream_gene_variant | MODIFIER | c.*4161G>A| |
S289 S290 |
8 | BAA02g10170 | A02 | 4523107 | G | A | downstream_gene_variant | MODIFIER | c.*4171G>A| |
S207 |