Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29800 | A02 | 17129291 | C | T | missense_variant | MODERATE | c.67G>A|p.Gly23Ser |
S283 |
2 | BAA02g29800 | A02 | 17130015 | C | T | upstream_gene_variant | MODIFIER | c.-658G>A| |
S226 |
3 | BAA02g29800 | A02 | 17133014 | G | A | upstream_gene_variant | MODIFIER | c.-3657C>T| |
S183 S198 |
4 | BAA02g29800 | A02 | 17134127 | G | A | upstream_gene_variant | MODIFIER | c.-4770C>T| |
S13 |