| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g18600 | A01 | 9114271 | C | T | missense_variant | MODERATE | c.2221G>A|p.Glu741Lys |
S286 |
| 2 | BAA01g18600 | A01 | 9115044 | C | T | splice_region_variant&intron_variant | LOW | c.1891+5G>A| |
S38 |
| 3 | BAA01g18600 | A01 | 9115355 | C | T | missense_variant | MODERATE | c.1585G>A|p.Glu529Lys |
S198 |
| 4 | BAA01g18600 | A01 | 9116412 | G | A | splice_region_variant&intron_variant | LOW | c.1028-6C>T| |
S149 |
| 5 | BAA01g18600 | A01 | 9116635 | C | T | synonymous_variant | LOW | c.978G>A|p.Glu326Glu |
S65 |
| 6 | BAA01g18600 | A01 | 9116694 | G | A | missense_variant | MODERATE | c.919C>T|p.Arg307Cys |
S276 |
| 7 | BAA01g18600 | A01 | 9117105 | C | T | missense_variant | MODERATE | c.508G>A|p.Gly170Arg |
S9 |
| 8 | BAA01g18600 | A01 | 9117391 | C | T | synonymous_variant | LOW | c.222G>A|p.Glu74Glu |
S38 |
| 9 | BAA01g18600 | A01 | 9119965 | G | A | upstream_gene_variant | MODIFIER | c.-2353C>T| |
S153 S157 S257 S262 |
| 10 | BAA01g18600 | A01 | 9120752 | G | A | upstream_gene_variant | MODIFIER | c.-3140C>T| |
S67 |