| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g00140 | A08 | 105022 | G | A | missense_variant&splice_region_variant | MODERATE | c.1156C>T|p.Pro386Ser |
S286 |
| 2 | BAA08g00140 | A08 | 106258 | C | T | missense_variant | MODERATE | c.436G>A|p.Gly146Arg |
S113 |
| 3 | BAA08g00140 | A08 | 106404 | G | A | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S72 |
| 4 | BAA08g00140 | A08 | 106468 | G | A | synonymous_variant | LOW | c.226C>T|p.Leu76Leu |
S1 S90 |
| 5 | BAA08g00140 | A08 | 107065 | C | T | upstream_gene_variant | MODIFIER | c.-372G>A| |
S189 |
| 6 | BAA08g00140 | A08 | 109098 | G | A | upstream_gene_variant | MODIFIER | c.-2405C>T| |
S239 |