| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g19430 | A07 | 25131577 | C | T | upstream_gene_variant | MODIFIER | c.-4775C>T| |
S100 |
| 2 | BAA07g19430 | A07 | 25133319 | C | T | upstream_gene_variant | MODIFIER | c.-3033C>T| |
S68 |
| 3 | BAA07g19430 | A07 | 25133519 | C | T | upstream_gene_variant | MODIFIER | c.-2833C>T| |
S293 |
| 4 | BAA07g19430 | A07 | 25136769 | C | T | intron_variant | MODIFIER | c.249+14C>T| |
S151 |
| 5 | BAA07g19430 | A07 | 25136906 | C | T | synonymous_variant | LOW | c.318C>T|p.Cys106Cys |
S262 |
| 6 | BAA07g19430 | A07 | 25136948 | C | T | synonymous_variant | LOW | c.360C>T|p.Ala120Ala |
S172 S217 |
| 7 | BAA07g19430 | A07 | 25137009 | C | T | missense_variant | MODERATE | c.421C>T|p.Pro141Ser |
S213 |
| 8 | BAA07g19430 | A07 | 25137149 | C | T | synonymous_variant | LOW | c.561C>T|p.Asn187Asn |
S302 |
| 9 | BAA07g19430 | A07 | 25137520 | C | T | missense_variant | MODERATE | c.932C>T|p.Pro311Leu |
S275 |
| 10 | BAA07g19430 | A07 | 25138266 | C | T | missense_variant | MODERATE | c.1453C>T|p.His485Tyr |
S32 |