Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10450 | A02 | 4626359 | G | A | missense_variant | MODERATE | c.92C>T|p.Thr31Ile |
S298 |
2 | BAA02g10450 | A02 | 4627341 | G | A | upstream_gene_variant | MODIFIER | c.-641C>T| |
S259 |
3 | BAA02g10450 | A02 | 4629122 | C | T | upstream_gene_variant | MODIFIER | c.-2422G>A| |
S221 |
4 | BAA02g10450 | A02 | 4629963 | G | A | upstream_gene_variant | MODIFIER | c.-3263C>T| |
S43 |