| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10900 | A02 | 4873206 | C | T | downstream_gene_variant | MODIFIER | c.*1723G>A| |
S179 |
| 2 | BAA02g10900 | A02 | 4874991 | G | A | synonymous_variant | LOW | c.1114C>T|p.Leu372Leu |
S287 |
| 3 | BAA02g10900 | A02 | 4876545 | G | A | missense_variant | MODERATE | c.289C>T|p.Pro97Ser |
S245 |
| 4 | BAA02g10900 | A02 | 4881374 | C | T | upstream_gene_variant | MODIFIER | c.-4204G>A| |
S15 S3 |
| 5 | BAA02g10900 | A02 | 4882071 | G | A | upstream_gene_variant | MODIFIER | c.-4901C>T| |
S79 S91 |