| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g39020 | A01 | 25972296 | C | T | upstream_gene_variant | MODIFIER | c.-3013C>T| |
S153 |
| 2 | BAA01g39020 | A01 | 25972479 | C | T | upstream_gene_variant | MODIFIER | c.-2830C>T| |
S136 |
| 3 | BAA01g39020 | A01 | 25972785 | C | T | upstream_gene_variant | MODIFIER | c.-2524C>T| |
S4 |
| 4 | BAA01g39020 | A01 | 25973142 | C | T | upstream_gene_variant | MODIFIER | c.-2167C>T| |
S78 S83 |
| 5 | BAA01g39020 | A01 | 25973692 | G | A | upstream_gene_variant | MODIFIER | c.-1617G>A| |
S13 |
| 6 | BAA01g39020 | A01 | 25973755 | G | A | upstream_gene_variant | MODIFIER | c.-1554G>A| |
S226 |
| 7 | BAA01g39020 | A01 | 25975601 | G | A | missense_variant | MODERATE | c.293G>A|p.Cys98Tyr |
S70 |
| 8 | BAA01g39020 | A01 | 25976081 | C | T | missense_variant | MODERATE | c.773C>T|p.Ser258Phe |
S183 S198 |
| 9 | BAA01g39020 | A01 | 25977607 | G | A | missense_variant | MODERATE | c.1984G>A|p.Glu662Lys |
S271 |
| 10 | BAA01g39020 | A01 | 25980787 | G | A | downstream_gene_variant | MODIFIER | c.*2754G>A| |
S172 S217 |