| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g41800 | A02 | 34944661 | C | A | upstream_gene_variant | MODIFIER | c.-4973C>A| |
S166 S219 S227 S95 |
| 2 | BAA02g41800 | A02 | 34944822 | C | T | upstream_gene_variant | MODIFIER | c.-4812C>T| |
S18 |
| 3 | BAA02g41800 | A02 | 34945218 | C | T | upstream_gene_variant | MODIFIER | c.-4416C>T| |
S202 S44 |
| 4 | BAA02g41800 | A02 | 34945385 | G | A | upstream_gene_variant | MODIFIER | c.-4249G>A| |
S188 |
| 5 | BAA02g41800 | A02 | 34946468 | G | A | upstream_gene_variant | MODIFIER | c.-3166G>A| |
S81 S85 |
| 6 | BAA02g41800 | A02 | 34946993 | C | T | upstream_gene_variant | MODIFIER | c.-2641C>T| |
S77 |
| 7 | BAA02g41800 | A02 | 34950189 | C | T | synonymous_variant | LOW | c.270C>T|p.Asn90Asn |
S212 |
| 8 | BAA02g41800 | A02 | 34950346 | C | T | missense_variant | MODERATE | c.368C>T|p.Ser123Phe |
S32 |