| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g43950 | A02 | 36288718 | C | T | missense_variant | MODERATE | c.26G>A|p.Gly9Glu |
S270 |
| 2 | BAA02g43950 | A02 | 36291015 | C | T | upstream_gene_variant | MODIFIER | c.-2272G>A| |
S128 |
| 3 | BAA02g43950 | A02 | 36292237 | C | T | upstream_gene_variant | MODIFIER | c.-3494G>A| |
S3 |
| 4 | BAA02g43950 | A02 | 36292316 | G | A | upstream_gene_variant | MODIFIER | c.-3573C>T| |
S164 |
| 5 | BAA02g43950 | A02 | 36293371 | C | T | upstream_gene_variant | MODIFIER | c.-4628G>A| |
S190 |