| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g69400 | A09 | 61944301 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.886-1G>A| |
S241 |
| 2 | BAA09g69400 | A09 | 61945253 | G | A | synonymous_variant | LOW | c.786C>T|p.Phe262Phe |
S161 |
| 3 | BAA09g69400 | A09 | 61945347 | C | T | missense_variant | MODERATE | c.692G>A|p.Gly231Glu |
S124 |
| 4 | BAA09g69400 | A09 | 61946023 | G | T | intron_variant | MODIFIER | c.483-467C>A| |
S131 S139 S144 S208 S222 S249 S267 S302 S303 S99 |
| 5 | BAA09g69400 | A09 | 61947255 | C | T | intron_variant | MODIFIER | c.482+605G>A| |
S142 |
| 6 | BAA09g69400 | A09 | 61947301 | C | T | intron_variant | MODIFIER | c.482+559G>A| |
S52 |
| 7 | BAA09g69400 | A09 | 61950104 | G | A | upstream_gene_variant | MODIFIER | c.-1295C>T| |
S247 |
| 8 | BAA09g69400 | A09 | 61953007 | G | A | upstream_gene_variant | MODIFIER | c.-4198C>T| |
S66 |
| 9 | BAA09g69400 | A09 | 61953072 | C | T | upstream_gene_variant | MODIFIER | c.-4263G>A| |
S305 |