| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g00990 | A02 | 460926 | C | T | splice_region_variant&intron_variant | LOW | c.1067+5G>A| |
S200 |
| 2 | BAA02g00990 | A02 | 461189 | G | A | synonymous_variant | LOW | c.897C>T|p.Leu299Leu |
S287 |
| 3 | BAA02g00990 | A02 | 461722 | G | A | splice_region_variant&intron_variant | LOW | c.681+4C>T| |
S231 |
| 4 | BAA02g00990 | A02 | 462376 | C | T | missense_variant | MODERATE | c.416G>A|p.Gly139Glu |
S185 |
| 5 | BAA02g00990 | A02 | 462933 | C | T | missense_variant | MODERATE | c.11G>A|p.Arg4His |
S305 |
| 6 | BAA02g00990 | A02 | 464296 | G | A | upstream_gene_variant | MODIFIER | c.-1353C>T| |
S286 |
| 7 | BAA02g00990 | A02 | 467679 | C | T | upstream_gene_variant | MODIFIER | c.-4736G>A| |
S18 |