| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g00860 | A02 | 407469 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.447-1G>A| |
S172 S217 |
| 2 | BAA02g00860 | A02 | 408225 | G | A | missense_variant | MODERATE | c.59C>T|p.Ser20Phe |
S64 |
| 3 | BAA02g00860 | A02 | 412086 | G | A | upstream_gene_variant | MODIFIER | c.-3803C>T| |
S296 |