| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g14130 | A02 | 6623731 | G | A | upstream_gene_variant | MODIFIER | c.-4999G>A| |
S146 |
| 2 | BAA02g14130 | A02 | 6624084 | G | A | upstream_gene_variant | MODIFIER | c.-4646G>A| |
S229 |
| 3 | BAA02g14130 | A02 | 6624164 | C | T | upstream_gene_variant | MODIFIER | c.-4566C>T| |
S130 |
| 4 | BAA02g14130 | A02 | 6629107 | G | A | synonymous_variant | LOW | c.378G>A|p.Gln126Gln |
S228 |
| 5 | BAA02g14130 | A02 | 6629342 | C | T | missense_variant | MODERATE | c.542C>T|p.Pro181Leu |
S129 |
| 6 | BAA02g14130 | A02 | 6630171 | C | T | missense_variant | MODERATE | c.976C>T|p.Pro326Ser |
S144 |
| 7 | BAA02g14130 | A02 | 6630645 | G | A | missense_variant | MODERATE | c.1159G>A|p.Asp387Asn |
S256 |
| 8 | BAA02g14130 | A02 | 6630852 | C | T | missense_variant | MODERATE | c.1222C>T|p.Pro408Ser |
S249 |
| 9 | BAA02g14130 | A02 | 6632167 | G | A | synonymous_variant | LOW | c.1917G>A|p.Lys639Lys |
S122 |
| 10 | BAA02g14130 | A02 | 6632325 | G | A | downstream_gene_variant | MODIFIER | c.*152G>A| |
S289 S290 |