| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g17860 | A05 | 10134462 | C | T | downstream_gene_variant | MODIFIER | c.*1130G>A| | S44 | 
| 2 | BAA05g17860 | A05 | 10134505 | G | A | downstream_gene_variant | MODIFIER | c.*1087C>T| | S241 | 
| 3 | BAA05g17860 | A05 | 10134562 | G | T | downstream_gene_variant | MODIFIER | c.*1030C>A| | S174 | 
| 4 | BAA05g17860 | A05 | 10136051 | C | T | missense_variant | MODERATE | c.1378G>A|p.Ala460Thr | S291 | 
| 5 | BAA05g17860 | A05 | 10137175 | C | T | missense_variant | MODERATE | c.502G>A|p.Gly168Arg | S97 | 
| 6 | BAA05g17860 | A05 | 10138514 | G | A | upstream_gene_variant | MODIFIER | c.-554C>T| | S173 | 
| 7 | BAA05g17860 | A05 | 10138564 | C | T | upstream_gene_variant | MODIFIER | c.-604G>A| | S183 S198 | 
| 8 | BAA05g17860 | A05 | 10138833 | C | T | upstream_gene_variant | MODIFIER | c.-873G>A| | S229 | 
| 9 | BAA05g17860 | A05 | 10138841 | C | T | upstream_gene_variant | MODIFIER | c.-881G>A| | S262 | 
| 10 | BAA05g17860 | A05 | 10138911 | G | A | upstream_gene_variant | MODIFIER | c.-951C>T| | S125 | 
| 11 | BAA05g17860 | A05 | 10138959 | G | A | upstream_gene_variant | MODIFIER | c.-999C>T| | S308 | 
| 12 | BAA05g17860 | A05 | 10138961 | G | A | upstream_gene_variant | MODIFIER | c.-1001C>T| | S186 | 
| 13 | BAA05g17860 | A05 | 10139370 | C | T | upstream_gene_variant | MODIFIER | c.-1410G>A| | S9 |