Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02150 | A02 | 967172 | C | T | synonymous_variant | LOW | c.528G>A|p.Leu176Leu |
S250 |
2 | BAA02g02150 | A02 | 967465 | G | A | missense_variant | MODERATE | c.235C>T|p.Arg79Cys |
S296 |
3 | BAA02g02150 | A02 | 971521 | G | A | upstream_gene_variant | MODIFIER | c.-3822C>T| |
S189 |
4 | BAA02g02150 | A02 | 971726 | G | A | upstream_gene_variant | MODIFIER | c.-4027C>T| |
S237 |
5 | BAA02g02150 | A02 | 971928 | G | A | upstream_gene_variant | MODIFIER | c.-4229C>T| |
S197 |
6 | BAA02g02150 | A02 | 972099 | G | A | upstream_gene_variant | MODIFIER | c.-4400C>T| |
S25 |