| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g47890 | A09 | 51941639 | G | A | missense_variant | MODERATE | c.730G>A|p.Asp244Asn |
S48 |
| 2 | BAA09g47890 | A09 | 51942231 | G | A | synonymous_variant | LOW | c.930G>A|p.Arg310Arg |
S46 |
| 3 | BAA09g47890 | A09 | 51942455 | C | T | intron_variant | MODIFIER | c.1041+113C>T| |
S140 |
| 4 | BAA09g47890 | A09 | 51942757 | C | T | downstream_gene_variant | MODIFIER | c.*20C>T| |
S66 |
| 5 | BAA09g47890 | A09 | 51943845 | G | A | downstream_gene_variant | MODIFIER | c.*1108G>A| |
S127 |
| 6 | BAA09g47890 | A09 | 51943849 | C | T | downstream_gene_variant | MODIFIER | c.*1112C>T| |
S176 |
| 7 | BAA09g47890 | A09 | 51945068 | C | T | downstream_gene_variant | MODIFIER | c.*2331C>T| |
S280 |
| 8 | BAA09g47890 | A09 | 51946939 | C | T | downstream_gene_variant | MODIFIER | c.*4202C>T| |
S111 |