Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02340 | A02 | 1047479 | G | A | missense_variant | MODERATE | c.866C>T|p.Thr289Ile |
S202 |
2 | BAA02g02340 | A02 | 1049594 | G | A | upstream_gene_variant | MODIFIER | c.-1250C>T| |
S289 S290 |
3 | BAA02g02340 | A02 | 1050634 | C | T | upstream_gene_variant | MODIFIER | c.-2290G>A| |
S1 S90 |