Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02780 | A02 | 1257755 | G | A | missense_variant | MODERATE | c.850C>T|p.Leu284Phe |
S52 |
2 | BAA02g02780 | A02 | 1259951 | T | A | upstream_gene_variant | MODIFIER | c.-474A>T| |
S242 |
3 | BAA02g02780 | A02 | 1263375 | C | T | upstream_gene_variant | MODIFIER | c.-3898G>A| |
S298 |
4 | BAA02g02780 | A02 | 1263425 | C | T | upstream_gene_variant | MODIFIER | c.-3948G>A| |
S201 |