| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g28070 | A10 | 21631046 | C | T | upstream_gene_variant | MODIFIER | c.-3369C>T| |
S10 |
| 2 | BAA10g28070 | A10 | 21634975 | C | T | synonymous_variant | LOW | c.327C>T|p.Leu109Leu |
S142 |
| 3 | BAA10g28070 | A10 | 21635313 | C | T | missense_variant | MODERATE | c.587C>T|p.Ala196Val |
S257 |
| 4 | BAA10g28070 | A10 | 21635347 | C | T | synonymous_variant | LOW | c.621C>T|p.Leu207Leu |
S268 |
| 5 | BAA10g28070 | A10 | 21636353 | G | A | missense_variant | MODERATE | c.1141G>A|p.Glu381Lys |
S178 |
| 6 | BAA10g28070 | A10 | 21636388 | G | A | synonymous_variant | LOW | c.1176G>A|p.Arg392Arg |
S202 |
| 7 | BAA10g28070 | A10 | 21638241 | C | T | downstream_gene_variant | MODIFIER | c.*1504C>T| |
S119 |
| 8 | BAA10g28070 | A10 | 21639314 | C | T | downstream_gene_variant | MODIFIER | c.*2577C>T| |
S97 |
| 9 | BAA10g28070 | A10 | 21639536 | G | A | downstream_gene_variant | MODIFIER | c.*2799G>A| |
S200 S261 S303 |
| 10 | BAA10g28070 | A10 | 21639669 | C | T | downstream_gene_variant | MODIFIER | c.*2932C>T| |
S277 |