| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g09380 | A01 | 4178698 | G | A | synonymous_variant | LOW | c.12G>A|p.Lys4Lys |
S17 |
| 2 | BAA01g09380 | A01 | 4180038 | C | T | synonymous_variant | LOW | c.621C>T|p.Pro207Pro |
S119 |
| 3 | BAA01g09380 | A01 | 4180188 | C | T | synonymous_variant | LOW | c.771C>T|p.Ile257Ile |
S267 |
| 4 | BAA01g09380 | A01 | 4180371 | G | A | missense_variant | MODERATE | c.874G>A|p.Ala292Thr |
S271 |
| 5 | BAA01g09380 | A01 | 4180385 | G | A | splice_region_variant&intron_variant | LOW | c.885+3G>A| |
S187 |
| 6 | BAA01g09380 | A01 | 4181107 | C | T | splice_region_variant&intron_variant | LOW | c.1183-8C>T| |
S203 |
| 7 | BAA01g09380 | A01 | 4181810 | G | A | missense_variant | MODERATE | c.1705G>A|p.Val569Ile |
S32 |
| 8 | BAA01g09380 | A01 | 4181817 | G | A | missense_variant | MODERATE | c.1712G>A|p.Ser571Asn |
S271 |
| 9 | BAA01g09380 | A01 | 4183315 | G | A | downstream_gene_variant | MODIFIER | c.*334G>A| |
S34 |
| 10 | BAA01g09380 | A01 | 4183402 | G | A | downstream_gene_variant | MODIFIER | c.*421G>A| |
S297 |
| 11 | BAA01g09380 | A01 | 4185417 | G | A | downstream_gene_variant | MODIFIER | c.*2436G>A| |
S37 |