| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g26200 | A07 | 28552374 | T | A | synonymous_variant | LOW | c.387A>T|p.Gly129Gly |
S147 S201 S213 S226 S238 S239 S267 |
| 2 | BAA07g26200 | A07 | 28552389 | A | T | synonymous_variant | LOW | c.372T>A|p.Gly124Gly |
S147 S201 S213 S226 S238 S239 S267 |
| 3 | BAA07g26200 | A07 | 28552398 | T | A | synonymous_variant | LOW | c.363A>T|p.Thr121Thr |
S147 S201 S213 S226 S238 S239 S267 |
| 4 | BAA07g26200 | A07 | 28552401 | C | T | synonymous_variant | LOW | c.360G>A|p.Val120Val |
S147 S201 S213 S226 S238 S239 S267 |
| 5 | BAA07g26200 | A07 | 28552413 | C | T | synonymous_variant | LOW | c.348G>A|p.Ala116Ala |
S147 S201 S213 S226 S238 S239 S267 |
| 6 | BAA07g26200 | A07 | 28552419 | A | T | synonymous_variant | LOW | c.342T>A|p.Gly114Gly |
S147 S201 S213 S226 S238 S239 S267 |
| 7 | BAA07g26200 | A07 | 28552466 | C | T | missense_variant | MODERATE | c.295G>A|p.Asp99Asn |
S147 S201 S226 S239 S267 |
| 8 | BAA07g26200 | A07 | 28553362 | C | T | upstream_gene_variant | MODIFIER | c.-403G>A| |
S244 |
| 9 | BAA07g26200 | A07 | 28553653 | C | T | upstream_gene_variant | MODIFIER | c.-694G>A| |
S301 S304 |
| 10 | BAA07g26200 | A07 | 28554806 | C | T | upstream_gene_variant | MODIFIER | c.-1847G>A| |
S244 |