| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g41120 | A02 | 34507403 | C | T | upstream_gene_variant | MODIFIER | c.-4971C>T| |
S183 S198 |
| 2 | BAA02g41120 | A02 | 34507735 | C | T | upstream_gene_variant | MODIFIER | c.-4639C>T| |
S83 S88 |
| 3 | BAA02g41120 | A02 | 34508058 | G | A | upstream_gene_variant | MODIFIER | c.-4316G>A| |
S136 |
| 4 | BAA02g41120 | A02 | 34508101 | C | T | upstream_gene_variant | MODIFIER | c.-4273C>T| |
S48 |
| 5 | BAA02g41120 | A02 | 34508296 | G | A | upstream_gene_variant | MODIFIER | c.-4078G>A| |
S142 |
| 6 | BAA02g41120 | A02 | 34509612 | C | T | upstream_gene_variant | MODIFIER | c.-2762C>T| |
S104 S52 |
| 7 | BAA02g41120 | A02 | 34511346 | C | T | upstream_gene_variant | MODIFIER | c.-1028C>T| |
S33 |
| 8 | BAA02g41120 | A02 | 34513282 | G | A | intron_variant | MODIFIER | c.185+724G>A| |
S166 |
| 9 | BAA02g41120 | A02 | 34515829 | G | A | synonymous_variant | LOW | c.537G>A|p.Glu179Glu |
S125 |
| 10 | BAA02g41120 | A02 | 34515916 | C | T | synonymous_variant | LOW | c.624C>T|p.Pro208Pro |
S51 |