Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09100 | A02 | 4019737 | C | T | missense_variant | MODERATE | c.373G>A|p.Gly125Arg |
S274 |
2 | BAA02g09100 | A02 | 4020038 | G | A | synonymous_variant | LOW | c.72C>T|p.Ser24Ser |
S295 |
3 | BAA02g09100 | A02 | 4023854 | C | T | upstream_gene_variant | MODIFIER | c.-3745G>A| |
S226 |