Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27490 | A02 | 15466139 | C | T | missense_variant | MODERATE | c.142G>A|p.Glu48Lys |
S208 |
2 | BAA02g27490 | A02 | 15466245 | G | A | synonymous_variant | LOW | c.36C>T|p.Phe12Phe |
S225 |
3 | BAA02g27490 | A02 | 15468511 | C | T | upstream_gene_variant | MODIFIER | c.-2231G>A| |
S53 |
4 | BAA02g27490 | A02 | 15469427 | C | T | upstream_gene_variant | MODIFIER | c.-3147G>A| |
S233 |
5 | BAA02g27490 | A02 | 15469904 | C | T | upstream_gene_variant | MODIFIER | c.-3624G>A| |
S224 |