| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g10500 | A01 | 4823283 | C | T | missense_variant | MODERATE | c.205G>A|p.Asp69Asn |
S130 |
| 2 | BAA01g10500 | A01 | 4823332 | C | T | synonymous_variant | LOW | c.156G>A|p.Arg52Arg |
S268 |
| 3 | BAA01g10500 | A01 | 4823547 | G | A | splice_region_variant&intron_variant | LOW | c.28-8C>T| |
S245 |
| 4 | BAA01g10500 | A01 | 4827061 | G | A | upstream_gene_variant | MODIFIER | c.-3415C>T| |
S217 |
| 5 | BAA01g10500 | A01 | 4827107 | G | A | upstream_gene_variant | MODIFIER | c.-3461C>T| |
S280 |