| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g11250 | A01 | 5188875 | G | A | missense_variant | MODERATE | c.931C>T|p.Leu311Phe |
S110 |
| 2 | BAA01g11250 | A01 | 5188925 | C | T | missense_variant | MODERATE | c.881G>A|p.Gly294Glu |
S295 |
| 3 | BAA01g11250 | A01 | 5189468 | G | A | missense_variant | MODERATE | c.338C>T|p.Ser113Phe |
S17 |
| 4 | BAA01g11250 | A01 | 5189742 | G | A | missense_variant | MODERATE | c.64C>T|p.Pro22Ser |
S298 |
| 5 | BAA01g11250 | A01 | 5190282 | G | A | upstream_gene_variant | MODIFIER | c.-477C>T| |
S17 |
| 6 | BAA01g11250 | A01 | 5191128 | G | A | upstream_gene_variant | MODIFIER | c.-1323C>T| |
S216 |
| 7 | BAA01g11250 | A01 | 5191909 | G | A | upstream_gene_variant | MODIFIER | c.-2104C>T| |
S87 |
| 8 | BAA01g11250 | A01 | 5193779 | G | A | upstream_gene_variant | MODIFIER | c.-3974C>T| |
S54 |
| 9 | BAA01g11250 | A01 | 5194752 | C | T | upstream_gene_variant | MODIFIER | c.-4947G>A| |
S166 |