Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19370 | A02 | 10035010 | C | T | missense_variant | MODERATE | c.769G>A|p.Gly257Arg |
S130 |
2 | BAA02g19370 | A02 | 10038659 | C | T | upstream_gene_variant | MODIFIER | c.-2349G>A| |
S302 |
3 | BAA02g19370 | A02 | 10040354 | G | A | upstream_gene_variant | MODIFIER | c.-4044C>T| |
S146 |
4 | BAA02g19370 | A02 | 10040599 | C | T | upstream_gene_variant | MODIFIER | c.-4289G>A| |
S299 |
5 | BAA02g19370 | A02 | 10040758 | G | A | upstream_gene_variant | MODIFIER | c.-4448C>T| |
S86 |