| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g10670 | A01 | 4888212 | G | A | downstream_gene_variant | MODIFIER | c.*1393C>T| |
S245 |
| 2 | BAA01g10670 | A01 | 4889759 | G | A | missense_variant | MODERATE | c.1523C>T|p.Pro508Leu |
S279 |
| 3 | BAA01g10670 | A01 | 4891915 | G | A | stop_gained | HIGH | c.424C>T|p.Gln142* |
S165 |
| 4 | BAA01g10670 | A01 | 4891990 | C | T | missense_variant | MODERATE | c.349G>A|p.Asp117Asn |
S266 |
| 5 | BAA01g10670 | A01 | 4892970 | C | T | upstream_gene_variant | MODIFIER | c.-503G>A| |
S198 |
| 6 | BAA01g10670 | A01 | 4893292 | C | T | upstream_gene_variant | MODIFIER | c.-825G>A| |
S61 |
| 7 | BAA01g10670 | A01 | 4893306 | C | T | upstream_gene_variant | MODIFIER | c.-839G>A| |
S107 |
| 8 | BAA01g10670 | A01 | 4894493 | C | T | upstream_gene_variant | MODIFIER | c.-2026G>A| |
S55 |
| 9 | BAA01g10670 | A01 | 4897299 | G | A | upstream_gene_variant | MODIFIER | c.-4832C>T| |
S133 |