| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g26670 | A10 | 21066237 | G | A | missense_variant | MODERATE | c.1264C>T|p.Leu422Phe |
S64 |
| 2 | BAA10g26670 | A10 | 21067568 | C | T | missense_variant | MODERATE | c.241G>A|p.Ala81Thr |
S296 |
| 3 | BAA10g26670 | A10 | 21067645 | G | A | missense_variant | MODERATE | c.164C>T|p.Pro55Leu |
S189 |
| 4 | BAA10g26670 | A10 | 21069534 | C | T | upstream_gene_variant | MODIFIER | c.-1726G>A| |
S260 |
| 5 | BAA10g26670 | A10 | 21070192 | G | A | upstream_gene_variant | MODIFIER | c.-2384C>T| |
S118 |