Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02880 | A02 | 1297135 | C | T | missense_variant | MODERATE | c.69G>A|p.Met23Ile |
S116 |
2 | BAA02g02880 | A02 | 1297150 | C | T | missense_variant | MODERATE | c.54G>A|p.Met18Ile |
S243 S299 |
3 | BAA02g02880 | A02 | 1298937 | G | A | upstream_gene_variant | MODIFIER | c.-1734C>T| |
S148 S30 S31 |
4 | BAA02g02880 | A02 | 1300017 | G | A | upstream_gene_variant | MODIFIER | c.-2814C>T| |
S8 |
5 | BAA02g02880 | A02 | 1300250 | C | T | upstream_gene_variant | MODIFIER | c.-3047G>A| |
S65 |
6 | BAA02g02880 | A02 | 1300729 | C | T | upstream_gene_variant | MODIFIER | c.-3526G>A| |
S70 |
7 | BAA02g02880 | A02 | 1301228 | G | A | upstream_gene_variant | MODIFIER | c.-4025C>T| |
S203 |