Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44940 | A02 | 36902294 | C | T | upstream_gene_variant | MODIFIER | c.-4971C>T| |
S167 |
2 | BAA02g44940 | A02 | 36902714 | G | A | upstream_gene_variant | MODIFIER | c.-4551G>A| |
S69 |
3 | BAA02g44940 | A02 | 36907355 | C | T | missense_variant | MODERATE | c.91C>T|p.Pro31Ser |
S228 |
4 | BAA02g44940 | A02 | 36907450 | C | T | synonymous_variant | LOW | c.186C>T|p.Tyr62Tyr |
S124 |
5 | BAA02g44940 | A02 | 36911948 | C | T | downstream_gene_variant | MODIFIER | c.*4150C>T| |
S256 |