Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30120 | A02 | 17476074 | C | T | missense_variant | MODERATE | c.427G>A|p.Gly143Arg |
S83 S88 |
2 | BAA02g30120 | A02 | 17476378 | G | A | synonymous_variant | LOW | c.123C>T|p.Ile41Ile |
S80 |
3 | BAA02g30120 | A02 | 17476435 | G | A | synonymous_variant | LOW | c.66C>T|p.Val22Val |
S133 |
4 | BAA02g30120 | A02 | 17478286 | C | T | upstream_gene_variant | MODIFIER | c.-1786G>A| |
S130 |
5 | BAA02g30120 | A02 | 17479302 | C | T | upstream_gene_variant | MODIFIER | c.-2802G>A| |
S142 |