| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g65240 | A09 | 60200794 | C | T | downstream_gene_variant | MODIFIER | c.*1127G>A| |
S192 |
| 2 | BAA09g65240 | A09 | 60202052 | C | T | missense_variant | MODERATE | c.772G>A|p.Val258Ile |
S75 S81 |
| 3 | BAA09g65240 | A09 | 60202220 | G | A | synonymous_variant | LOW | c.678C>T|p.Thr226Thr |
S250 |
| 4 | BAA09g65240 | A09 | 60202406 | C | T | synonymous_variant | LOW | c.492G>A|p.Glu164Glu |
S87 |
| 5 | BAA09g65240 | A09 | 60202895 | G | A | synonymous_variant | LOW | c.138C>T|p.Phe46Phe |
S192 |
| 6 | BAA09g65240 | A09 | 60205112 | G | A | upstream_gene_variant | MODIFIER | c.-2080C>T| |
S277 |
| 7 | BAA09g65240 | A09 | 60207469 | G | A | upstream_gene_variant | MODIFIER | c.-4437C>T| |
S288 |
| 8 | BAA09g65240 | A09 | 60207664 | C | T | upstream_gene_variant | MODIFIER | c.-4632G>A| |
S8 |