Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26120 | A09 | 16905175 | C | T | missense_variant | MODERATE | c.836G>A|p.Gly279Glu |
S263 |
2 | BAA09g26120 | A09 | 16905205 | C | T | missense_variant | MODERATE | c.806G>A|p.Gly269Glu |
S140 |
3 | BAA09g26120 | A09 | 16906898 | G | A | upstream_gene_variant | MODIFIER | c.-54C>T| |
S11 |
4 | BAA09g26120 | A09 | 16910694 | C | T | upstream_gene_variant | MODIFIER | c.-3850G>A| |
S282 |