| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g37800 | A09 | 45882090 | C | T | missense_variant | MODERATE | c.655G>A|p.Val219Met |
S18 |
| 2 | BAA09g37800 | A09 | 45882107 | G | A | splice_region_variant&intron_variant | LOW | c.645-7C>T| |
S210 S225 |
| 3 | BAA09g37800 | A09 | 45883759 | G | A | upstream_gene_variant | MODIFIER | c.-47C>T| |
S46 |
| 4 | BAA09g37800 | A09 | 45884241 | C | T | upstream_gene_variant | MODIFIER | c.-529G>A| |
S303 |
| 5 | BAA09g37800 | A09 | 45885152 | C | T | upstream_gene_variant | MODIFIER | c.-1440G>A| |
S204 |
| 6 | BAA09g37800 | A09 | 45886263 | C | T | upstream_gene_variant | MODIFIER | c.-2551G>A| |
S120 |
| 7 | BAA09g37800 | A09 | 45888672 | C | T | upstream_gene_variant | MODIFIER | c.-4960G>A| |
S245 |