| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10040 | A02 | 4429423 | C | T | missense_variant | MODERATE | c.505G>A|p.Asp169Asn |
S78 S83 |
| 2 | BAA02g10040 | A02 | 4429493 | G | A | synonymous_variant | LOW | c.435C>T|p.Phe145Phe |
S85 |
| 3 | BAA02g10040 | A02 | 4431298 | G | A | upstream_gene_variant | MODIFIER | c.-242C>T| |
S209 |
| 4 | BAA02g10040 | A02 | 4431827 | G | A | upstream_gene_variant | MODIFIER | c.-771C>T| |
S225 |
| 5 | BAA02g10040 | A02 | 4434983 | G | A | upstream_gene_variant | MODIFIER | c.-3927C>T| |
S191 |
| 6 | BAA02g10040 | A02 | 4435750 | C | T | upstream_gene_variant | MODIFIER | c.-4694G>A| |
S65 |