Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44220 | A02 | 36498162 | C | T | missense_variant | MODERATE | c.74C>T|p.Ser25Leu |
S171 |
2 | BAA02g44220 | A02 | 36498648 | C | T | synonymous_variant | LOW | c.387C>T|p.Asn129Asn |
S138 |
3 | BAA02g44220 | A02 | 36499290 | G | A | missense_variant | MODERATE | c.854G>A|p.Arg285Lys |
S230 |
4 | BAA02g44220 | A02 | 36499632 | G | A | missense_variant | MODERATE | c.1120G>A|p.Gly374Ser |
S188 |
5 | BAA02g44220 | A02 | 36501834 | G | A | downstream_gene_variant | MODIFIER | c.*1706G>A| |
S34 |
6 | BAA02g44220 | A02 | 36502036 | G | A | downstream_gene_variant | MODIFIER | c.*1908G>A| |
S269 |