| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10340 | A02 | 4582365 | C | T | missense_variant | MODERATE | c.571G>A|p.Gly191Ser |
S289 S290 |
| 2 | BAA02g10340 | A02 | 4582713 | G | A | missense_variant | MODERATE | c.347C>T|p.Ser116Phe |
S232 |
| 3 | BAA02g10340 | A02 | 4583050 | C | T | splice_region_variant&intron_variant | LOW | c.202+7G>A| |
S116 |
| 4 | BAA02g10340 | A02 | 4585328 | G | A | upstream_gene_variant | MODIFIER | c.-2070C>T| |
S193 |
| 5 | BAA02g10340 | A02 | 4585993 | C | T | upstream_gene_variant | MODIFIER | c.-2735G>A| |
S270 |
| 6 | BAA02g10340 | A02 | 4585999 | C | T | upstream_gene_variant | MODIFIER | c.-2741G>A| |
S276 |
| 7 | BAA02g10340 | A02 | 4586158 | G | A | upstream_gene_variant | MODIFIER | c.-2900C>T| |
S229 |