| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g02500 | A01 | 1134487 | C | T | upstream_gene_variant | MODIFIER | c.-3487C>T| |
S54 |
| 2 | BAA01g02500 | A01 | 1135876 | C | T | upstream_gene_variant | MODIFIER | c.-2098C>T| |
S265 |
| 3 | BAA01g02500 | A01 | 1137465 | G | A | upstream_gene_variant | MODIFIER | c.-509G>A| |
S34 |
| 4 | BAA01g02500 | A01 | 1137647 | C | T | upstream_gene_variant | MODIFIER | c.-327C>T| |
S238 |
| 5 | BAA01g02500 | A01 | 1138472 | G | A | missense_variant | MODERATE | c.424G>A|p.Asp142Asn |
S308 |
| 6 | BAA01g02500 | A01 | 1138838 | C | T | synonymous_variant | LOW | c.624C>T|p.Phe208Phe |
S109 |
| 7 | BAA01g02500 | A01 | 1139183 | C | T | synonymous_variant | LOW | c.969C>T|p.Thr323Thr |
S251 |
| 8 | BAA01g02500 | A01 | 1139201 | C | T | synonymous_variant | LOW | c.987C>T|p.Ile329Ile |
S143 |