Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29290 | A02 | 16746234 | C | T | missense_variant | MODERATE | c.425G>A|p.Gly142Asp |
S269 |
2 | BAA02g29290 | A02 | 16746386 | C | T | missense_variant | MODERATE | c.364G>A|p.Asp122Asn |
S140 |
3 | BAA02g29290 | A02 | 16746485 | C | T | missense_variant | MODERATE | c.341G>A|p.Gly114Asp |
S104 S52 |
4 | BAA02g29290 | A02 | 16749069 | C | T | upstream_gene_variant | MODIFIER | c.-1727G>A| |
S270 |
5 | BAA02g29290 | A02 | 16749917 | C | T | upstream_gene_variant | MODIFIER | c.-2575G>A| |
S244 |
6 | BAA02g29290 | A02 | 16751376 | C | T | upstream_gene_variant | MODIFIER | c.-4034G>A| |
S180 |
7 | BAA02g29290 | A02 | 16751850 | G | A | upstream_gene_variant | MODIFIER | c.-4508C>T| |
S7 |