| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g41650 | A02 | 34895789 | C | T | missense_variant | MODERATE | c.3268G>A|p.Asp1090Asn |
S64 |
| 2 | BAA02g41650 | A02 | 34899605 | G | A | missense_variant | MODERATE | c.604C>T|p.Leu202Phe |
S217 |
| 3 | BAA02g41650 | A02 | 34901514 | C | T | upstream_gene_variant | MODIFIER | c.-1228G>A| |
S283 |
| 4 | BAA02g41650 | A02 | 34901888 | C | T | upstream_gene_variant | MODIFIER | c.-1602G>A| |
S133 |
| 5 | BAA02g41650 | A02 | 34902765 | C | T | upstream_gene_variant | MODIFIER | c.-2479G>A| |
S18 |
| 6 | BAA02g41650 | A02 | 34903542 | G | A | upstream_gene_variant | MODIFIER | c.-3256C>T| |
S293 |
| 7 | BAA02g41650 | A02 | 34903691 | C | T | upstream_gene_variant | MODIFIER | c.-3405G>A| |
S133 |
| 8 | BAA02g41650 | A02 | 34904149 | G | A | upstream_gene_variant | MODIFIER | c.-3863C>T| |
S177 |
| 9 | BAA02g41650 | A02 | 34904536 | G | A | upstream_gene_variant | MODIFIER | c.-4250C>T| |
S245 |