Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25160 | A02 | 13755318 | C | T | missense_variant | MODERATE | c.574G>A|p.Gly192Arg |
S123 |
2 | BAA02g25160 | A02 | 13755334 | C | T | synonymous_variant | LOW | c.558G>A|p.Gln186Gln |
S282 |
3 | BAA02g25160 | A02 | 13756437 | C | T | synonymous_variant | LOW | c.60G>A|p.Glu20Glu |
S283 |
4 | BAA02g25160 | A02 | 13756569 | C | T | upstream_gene_variant | MODIFIER | c.-73G>A| |
S267 |
5 | BAA02g25160 | A02 | 13756913 | C | T | upstream_gene_variant | MODIFIER | c.-417G>A| |
S296 |
6 | BAA02g25160 | A02 | 13757638 | G | A | upstream_gene_variant | MODIFIER | c.-1142C>T| |
S56 |
7 | BAA02g25160 | A02 | 13759266 | G | A | upstream_gene_variant | MODIFIER | c.-2770C>T| |
S215 |