Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46300 | A02 | 37675367 | G | A | missense_variant | MODERATE | c.332C>T|p.Pro111Leu |
S139 |
2 | BAA02g46300 | A02 | 37675842 | T | A | upstream_gene_variant | MODIFIER | c.-144A>T| |
S217 |
3 | BAA02g46300 | A02 | 37676342 | C | T | upstream_gene_variant | MODIFIER | c.-644G>A| |
S202 |
4 | BAA02g46300 | A02 | 37678208 | C | T | upstream_gene_variant | MODIFIER | c.-2510G>A| |
S18 |
5 | BAA02g46300 | A02 | 37679320 | C | T | upstream_gene_variant | MODIFIER | c.-3622G>A| |
S270 |