| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g39400 | A01 | 26175949 | C | T | missense_variant | MODERATE | c.949G>A|p.Ala317Thr |
S107 |
| 2 | BAA01g39400 | A01 | 26177066 | C | T | splice_region_variant&intron_variant | LOW | c.388-8G>A| |
S277 |
| 3 | BAA01g39400 | A01 | 26177180 | G | A | synonymous_variant | LOW | c.354C>T|p.Ser118Ser |
S276 |
| 4 | BAA01g39400 | A01 | 26177568 | G | A | missense_variant | MODERATE | c.215C>T|p.Pro72Leu |
S33 |
| 5 | BAA01g39400 | A01 | 26181182 | C | T | upstream_gene_variant | MODIFIER | c.-3297G>A| |
S15 S2 S4 S6 |
| 6 | BAA01g39400 | A01 | 26182620 | G | A | upstream_gene_variant | MODIFIER | c.-4735C>T| |
S271 |
| 7 | BAA01g39400 | A01 | 26182700 | C | T | upstream_gene_variant | MODIFIER | c.-4815G>A| |
S198 |