| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g21280 | A10 | 18770190 | C | T | missense_variant | MODERATE | c.974G>A|p.Gly325Asp |
S275 |
| 2 | BAA10g21280 | A10 | 18770393 | C | T | synonymous_variant | LOW | c.771G>A|p.Thr257Thr |
S177 |
| 3 | BAA10g21280 | A10 | 18771166 | C | T | upstream_gene_variant | MODIFIER | c.-3G>A| |
S60 |
| 4 | BAA10g21280 | A10 | 18772073 | G | A | upstream_gene_variant | MODIFIER | c.-910C>T| |
S109 |
| 5 | BAA10g21280 | A10 | 18772587 | G | A | upstream_gene_variant | MODIFIER | c.-1424C>T| |
S90 |
| 6 | BAA10g21280 | A10 | 18773844 | C | T | upstream_gene_variant | MODIFIER | c.-2681G>A| |
S259 |
| 7 | BAA10g21280 | A10 | 18774526 | G | A | upstream_gene_variant | MODIFIER | c.-3363C>T| |
S295 |