Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g63950 | A09 | 59569864 | G | A | missense_variant | MODERATE | c.818C>T|p.Thr273Ile |
S59 |
2 | BAA09g63950 | A09 | 59570037 | C | T | synonymous_variant | LOW | c.645G>A|p.Ser215Ser |
S104 |
3 | BAA09g63950 | A09 | 59571225 | G | A | upstream_gene_variant | MODIFIER | c.-544C>T| |
S272 |
4 | BAA09g63950 | A09 | 59573551 | C | T | upstream_gene_variant | MODIFIER | c.-2870G>A| |
S228 |
5 | BAA09g63950 | A09 | 59573655 | C | T | upstream_gene_variant | MODIFIER | c.-2974G>A| |
S206 |