| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g11860 | A10 | 13413620 | C | T | missense_variant | MODERATE | c.374C>T|p.Pro125Leu |
S114 |
| 2 | BAA10g11860 | A10 | 13413666 | G | A | synonymous_variant | LOW | c.420G>A|p.Gly140Gly |
S201 |
| 3 | BAA10g11860 | A10 | 13413966 | G | A | synonymous_variant | LOW | c.720G>A|p.Val240Val |
S130 |
| 4 | BAA10g11860 | A10 | 13416248 | C | T | missense_variant | MODERATE | c.1727C>T|p.Pro576Leu |
S156 |
| 5 | BAA10g11860 | A10 | 13416269 | C | T | missense_variant | MODERATE | c.1748C>T|p.Ala583Val |
S122 |
| 6 | BAA10g11860 | A10 | 13418698 | G | A | downstream_gene_variant | MODIFIER | c.*2356G>A| |
S138 |
| 7 | BAA10g11860 | A10 | 13419191 | G | A | downstream_gene_variant | MODIFIER | c.*2849G>A| |
S293 |
| 8 | BAA10g11860 | A10 | 13420014 | G | A | downstream_gene_variant | MODIFIER | c.*3672G>A| |
S65 |