| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g26960 | A10 | 21170148 | G | A | missense_variant | MODERATE | c.169C>T|p.Pro57Ser |
S122 |
| 2 | BAA10g26960 | A10 | 21170157 | C | T | missense_variant | MODERATE | c.160G>A|p.Val54Ile |
S148 S210 S30 S31 |
| 3 | BAA10g26960 | A10 | 21175026 | C | T | upstream_gene_variant | MODIFIER | c.-4710G>A| |
S167 |
| 4 | BAA10g26960 | A10 | 21175091 | G | A | upstream_gene_variant | MODIFIER | c.-4775C>T| |
S149 |