Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01150 | A02 | 545964 | G | A | synonymous_variant | LOW | c.681C>T|p.Leu227Leu |
S273 |
2 | BAA02g01150 | A02 | 546401 | C | T | synonymous_variant | LOW | c.327G>A|p.Glu109Glu |
S278 |
3 | BAA02g01150 | A02 | 546471 | C | T | missense_variant | MODERATE | c.257G>A|p.Gly86Asp |
S245 |
4 | BAA02g01150 | A02 | 546492 | G | A | missense_variant | MODERATE | c.236C>T|p.Ser79Phe |
S84 S93 |
5 | BAA02g01150 | A02 | 549717 | C | T | upstream_gene_variant | MODIFIER | c.-2990G>A| |
S94 |
6 | BAA02g01150 | A02 | 550412 | C | T | upstream_gene_variant | MODIFIER | c.-3685G>A| |
S85 |