| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g19790 | A02 | 10344073 | C | T | synonymous_variant | LOW | c.777G>A|p.Leu259Leu |
S283 |
| 2 | BAA02g19790 | A02 | 10344214 | C | T | synonymous_variant | LOW | c.636G>A|p.Glu212Glu |
S164 |
| 3 | BAA02g19790 | A02 | 10344527 | G | A | missense_variant | MODERATE | c.323C>T|p.Ser108Leu |
S41 |
| 4 | BAA02g19790 | A02 | 10344594 | G | A | missense_variant | MODERATE | c.256C>T|p.Arg86Trp |
S35 |
| 5 | BAA02g19790 | A02 | 10345290 | C | T | upstream_gene_variant | MODIFIER | c.-441G>A| |
|
| 6 | BAA02g19790 | A02 | 10346831 | G | A | upstream_gene_variant | MODIFIER | c.-1982C>T| |
S169 |
| 7 | BAA02g19790 | A02 | 10347420 | C | T | upstream_gene_variant | MODIFIER | c.-2571G>A| |
S301 S304 |
| 8 | BAA02g19790 | A02 | 10349343 | C | T | upstream_gene_variant | MODIFIER | c.-4494G>A| |
S202 |
| 9 | BAA02g19790 | A02 | 10349630 | G | A | upstream_gene_variant | MODIFIER | c.-4781C>T| |
S247 |