Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10380 | A02 | 4595020 | G | A | missense_variant | MODERATE | c.535C>T|p.His179Tyr |
S165 |
2 | BAA02g10380 | A02 | 4598787 | G | A | upstream_gene_variant | MODIFIER | c.-2561C>T| |
S82 S92 |
3 | BAA02g10380 | A02 | 4598818 | C | T | upstream_gene_variant | MODIFIER | c.-2592G>A| |
S270 |
4 | BAA02g10380 | A02 | 4598852 | C | T | upstream_gene_variant | MODIFIER | c.-2626G>A| |
S135 |