Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07160 | A02 | 3080020 | G | A | synonymous_variant | LOW | c.1287C>T|p.Arg429Arg |
S302 |
2 | BAA02g07160 | A02 | 3081150 | C | T | synonymous_variant | LOW | c.654G>A|p.Arg218Arg |
S276 |
3 | BAA02g07160 | A02 | 3081155 | G | A | missense_variant | MODERATE | c.649C>T|p.Leu217Phe |
S159 |
4 | BAA02g07160 | A02 | 3081240 | C | T | synonymous_variant | LOW | c.564G>A|p.Gly188Gly |
S8 |
5 | BAA02g07160 | A02 | 3081331 | G | A | missense_variant | MODERATE | c.473C>T|p.Ala158Val |
S210 |
6 | BAA02g07160 | A02 | 3081498 | G | A | synonymous_variant | LOW | c.306C>T|p.Ser102Ser |
S241 |
7 | BAA02g07160 | A02 | 3081600 | C | T | stop_gained | HIGH | c.204G>A|p.Trp68* |
S2 |
8 | BAA02g07160 | A02 | 3084869 | G | A | upstream_gene_variant | MODIFIER | c.-2827C>T| |
S36 |
9 | BAA02g07160 | A02 | 3085723 | A | G | upstream_gene_variant | MODIFIER | c.-3681T>C| |
S63 |