| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g42760 | A02 | 35593464 | C | T | synonymous_variant | LOW | c.36C>T|p.Leu12Leu | S242 | 
| 2 | BAA02g42760 | A02 | 35594554 | C | T | missense_variant | MODERATE | c.298C>T|p.Leu100Phe | S212 | 
| 3 | BAA02g42760 | A02 | 35594599 | G | A | missense_variant&splice_region_variant | MODERATE | c.343G>A|p.Glu115Lys | S191 | 
| 4 | BAA02g42760 | A02 | 35595305 | G | A | synonymous_variant | LOW | c.585G>A|p.Arg195Arg | S125 | 
| 5 | BAA02g42760 | A02 | 35598329 | G | A | downstream_gene_variant | MODIFIER | c.*172G>A| | S163 | 
| 6 | BAA02g42760 | A02 | 35598351 | C | T | downstream_gene_variant | MODIFIER | c.*194C>T| | S87 | 
| 7 | BAA02g42760 | A02 | 35599928 | A | T | downstream_gene_variant | MODIFIER | c.*1771A>T| |  | 
| 8 | BAA02g42760 | A02 | 35600839 | G | A | downstream_gene_variant | MODIFIER | c.*2682G>A| | S13 | 
| 9 | BAA02g42760 | A02 | 35602074 | C | T | downstream_gene_variant | MODIFIER | c.*3917C>T| | S179 | 
| 10 | BAA02g42760 | A02 | 35602262 | G | A | downstream_gene_variant | MODIFIER | c.*4105G>A| | S89 |