Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47960 | A02 | 38638709 | C | T | missense_variant | MODERATE | c.61G>A|p.Asp21Asn |
S183 S198 |
2 | BAA02g47960 | A02 | 38640938 | G | A | upstream_gene_variant | MODIFIER | c.-2169C>T| |
S226 |
3 | BAA02g47960 | A02 | 38642424 | G | A | upstream_gene_variant | MODIFIER | c.-3655C>T| |
S64 |
4 | BAA02g47960 | A02 | 38642950 | G | A | upstream_gene_variant | MODIFIER | c.-4181C>T| |
S169 |