Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g23660 | A02 | 12898038 | G | A | missense_variant | MODERATE | c.125C>T|p.Ala42Val |
S257 |
2 | BAA02g23660 | A02 | 12898529 | C | T | upstream_gene_variant | MODIFIER | c.-367G>A| |
S42 |
3 | BAA02g23660 | A02 | 12899605 | G | A | upstream_gene_variant | MODIFIER | c.-1443C>T| |
S257 |
4 | BAA02g23660 | A02 | 12900430 | G | A | upstream_gene_variant | MODIFIER | c.-2268C>T| |
S274 |
5 | BAA02g23660 | A02 | 12901566 | G | A | upstream_gene_variant | MODIFIER | c.-3404C>T| |
S70 |
6 | BAA02g23660 | A02 | 12903055 | G | A | upstream_gene_variant | MODIFIER | c.-4893C>T| |
S85 |