| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g44990 | A06 | 28733477 | G | A | splice_region_variant&intron_variant | LOW | c.1846-8C>T| | S79 S91 | 
| 2 | BAA06g44990 | A06 | 28733890 | C | T | missense_variant | MODERATE | c.1660G>A|p.Gly554Arg | S182 | 
| 3 | BAA06g44990 | A06 | 28735742 | C | T | missense_variant&splice_region_variant | MODERATE | c.725G>A|p.Gly242Asp | S249 | 
| 4 | BAA06g44990 | A06 | 28736631 | G | A | missense_variant | MODERATE | c.277C>T|p.Leu93Phe | S152 | 
| 5 | BAA06g44990 | A06 | 28737326 | C | T | upstream_gene_variant | MODIFIER | c.-318G>A| | S9 | 
| 6 | BAA06g44990 | A06 | 28737345 | C | T | upstream_gene_variant | MODIFIER | c.-337G>A| | S80 | 
| 7 | BAA06g44990 | A06 | 28737779 | C | T | upstream_gene_variant | MODIFIER | c.-771G>A| | S155 | 
| 8 | BAA06g44990 | A06 | 28739895 | C | T | upstream_gene_variant | MODIFIER | c.-2887G>A| | S252 | 
| 9 | BAA06g44990 | A06 | 28740214 | C | T | upstream_gene_variant | MODIFIER | c.-3206G>A| | S274 |