| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g44880 | A01 | 29883875 | G | A | downstream_gene_variant | MODIFIER | c.*1538C>T| |
S38 |
| 2 | BAA01g44880 | A01 | 29886300 | G | A | synonymous_variant | LOW | c.423C>T|p.Ile141Ile |
S96 |
| 3 | BAA01g44880 | A01 | 29886425 | G | A | missense_variant | MODERATE | c.298C>T|p.Pro100Ser |
S196 |
| 4 | BAA01g44880 | A01 | 29886433 | C | T | missense_variant | MODERATE | c.290G>A|p.Gly97Glu |
S112 |
| 5 | BAA01g44880 | A01 | 29887277 | C | T | missense_variant | MODERATE | c.127G>A|p.Ala43Thr |
S133 |
| 6 | BAA01g44880 | A01 | 29887503 | G | A | upstream_gene_variant | MODIFIER | c.-100C>T| |
S278 |
| 7 | BAA01g44880 | A01 | 29887590 | G | A | upstream_gene_variant | MODIFIER | c.-187C>T| |
S104 S105 |
| 8 | BAA01g44880 | A01 | 29887897 | C | T | upstream_gene_variant | MODIFIER | c.-494G>A| |
S231 |
| 9 | BAA01g44880 | A01 | 29888444 | C | T | upstream_gene_variant | MODIFIER | c.-1041G>A| |
S200 |
| 10 | BAA01g44880 | A01 | 29888943 | C | T | upstream_gene_variant | MODIFIER | c.-1540G>A| |
S30 S31 |
| 11 | BAA01g44880 | A01 | 29889197 | G | A | upstream_gene_variant | MODIFIER | c.-1794C>T| |
S172 S217 |
| 12 | BAA01g44880 | A01 | 29889669 | C | T | upstream_gene_variant | MODIFIER | c.-2266G>A| |
S156 |