Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10900 | A09 | 6039072 | A | T | missense_variant | MODERATE | c.56A>T|p.Asp19Val |
S40 S49 |
2 | BAA09g10900 | A09 | 6042089 | C | T | downstream_gene_variant | MODIFIER | c.*2397C>T| |
S288 |
3 | BAA09g10900 | A09 | 6043033 | G | A | downstream_gene_variant | MODIFIER | c.*3341G>A| |
S32 |
4 | BAA09g10900 | A09 | 6043697 | G | A | downstream_gene_variant | MODIFIER | c.*4005G>A| |
S70 |
5 | BAA09g10900 | A09 | 6044635 | G | A | downstream_gene_variant | MODIFIER | c.*4943G>A| |
S32 |