| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g11860 | A02 | 5352838 | C | T | synonymous_variant | LOW | c.552G>A|p.Glu184Glu |
S266 |
| 2 | BAA02g11860 | A02 | 5352872 | G | A | missense_variant | MODERATE | c.518C>T|p.Pro173Leu |
S137 S215 |
| 3 | BAA02g11860 | A02 | 5353457 | C | T | missense_variant | MODERATE | c.250G>A|p.Asp84Asn |
S250 |
| 4 | BAA02g11860 | A02 | 5353579 | A | C | missense_variant | MODERATE | c.128T>G|p.Leu43Arg |
S107 S111 S115 S13 S144 S149 S17 S198 S236 S242 S252 S261 S295 S35 S73 S78 |
| 5 | BAA02g11860 | A02 | 5353595 | C | G | missense_variant | MODERATE | c.112G>C|p.Ala38Pro |
S10 S111 S176 S246 S257 S278 S295 |
| 6 | BAA02g11860 | A02 | 5356722 | C | T | upstream_gene_variant | MODIFIER | c.-3016G>A| |
S121 |
| 7 | BAA02g11860 | A02 | 5356926 | C | T | upstream_gene_variant | MODIFIER | c.-3220G>A| |
S138 |
| 8 | BAA02g11860 | A02 | 5357035 | G | A | upstream_gene_variant | MODIFIER | c.-3329C>T| |
S296 |
| 9 | BAA02g11860 | A02 | 5358326 | C | T | upstream_gene_variant | MODIFIER | c.-4620G>A| |
S111 |