Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40360 | A02 | 34060824 | C | T | missense_variant | MODERATE | c.392C>T|p.Ser131Phe |
S6 |
2 | BAA02g40360 | A02 | 34061573 | G | A | missense_variant | MODERATE | c.1141G>A|p.Gly381Arg |
S163 |
3 | BAA02g40360 | A02 | 34061698 | G | A | synonymous_variant | LOW | c.1266G>A|p.Thr422Thr |
S175 |
4 | BAA02g40360 | A02 | 34064289 | G | A | downstream_gene_variant | MODIFIER | c.*2537G>A| |
S36 |