| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g23990 | A02 | 13100181 | C | T | missense_variant | MODERATE | c.1949G>A|p.Gly650Glu |
S144 S203 |
| 2 | BAA02g23990 | A02 | 13100534 | G | A | synonymous_variant | LOW | c.1596C>T|p.Thr532Thr |
S187 |
| 3 | BAA02g23990 | A02 | 13100594 | G | A | synonymous_variant | LOW | c.1536C>T|p.Cys512Cys |
S5 |
| 4 | BAA02g23990 | A02 | 13101116 | C | T | synonymous_variant | LOW | c.1014G>A|p.Gln338Gln |
S115 |
| 5 | BAA02g23990 | A02 | 13103559 | G | A | upstream_gene_variant | MODIFIER | c.-1094C>T| |
S191 |
| 6 | BAA02g23990 | A02 | 13104123 | C | T | upstream_gene_variant | MODIFIER | c.-1658G>A| |
S138 |
| 7 | BAA02g23990 | A02 | 13104257 | G | A | upstream_gene_variant | MODIFIER | c.-1792C>T| |
S166 |
| 8 | BAA02g23990 | A02 | 13106500 | C | T | upstream_gene_variant | MODIFIER | c.-4035G>A| |
S130 |