| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10890 | A02 | 4872508 | C | T | synonymous_variant | LOW | c.831G>A|p.Pro277Pro |
S100 |
| 2 | BAA02g10890 | A02 | 4872630 | G | A | missense_variant | MODERATE | c.709C>T|p.Leu237Phe |
S162 |
| 3 | BAA02g10890 | A02 | 4873833 | C | T | synonymous_variant | LOW | c.189G>A|p.Glu63Glu |
S182 |
| 4 | BAA02g10890 | A02 | 4874162 | G | A | upstream_gene_variant | MODIFIER | c.-14C>T| |
S286 |
| 5 | BAA02g10890 | A02 | 4874266 | G | A | upstream_gene_variant | MODIFIER | c.-118C>T| |
S265 |
| 6 | BAA02g10890 | A02 | 4876307 | C | T | upstream_gene_variant | MODIFIER | c.-2159G>A| |
S75 S81 |
| 7 | BAA02g10890 | A02 | 4877178 | G | A | upstream_gene_variant | MODIFIER | c.-3030C>T| |
S166 |
| 8 | BAA02g10890 | A02 | 4877549 | G | A | upstream_gene_variant | MODIFIER | c.-3401C>T| |
S271 |
| 9 | BAA02g10890 | A02 | 4877694 | G | A | upstream_gene_variant | MODIFIER | c.-3546C>T| |
S209 |
| 10 | BAA02g10890 | A02 | 4878538 | C | T | upstream_gene_variant | MODIFIER | c.-4390G>A| |
S115 |