| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g35830 | A07 | 33763389 | G | A | downstream_gene_variant | MODIFIER | c.*992C>T| | S142 | 
| 2 | BAA07g35830 | A07 | 33763748 | G | A | downstream_gene_variant | MODIFIER | c.*633C>T| | S163 | 
| 3 | BAA07g35830 | A07 | 33764558 | C | T | synonymous_variant | LOW | c.2475G>A|p.Glu825Glu | S125 | 
| 4 | BAA07g35830 | A07 | 33765931 | C | T | missense_variant | MODERATE | c.1204G>A|p.Asp402Asn | S282 | 
| 5 | BAA07g35830 | A07 | 33765980 | C | T | synonymous_variant | LOW | c.1155G>A|p.Pro385Pro | S107 | 
| 6 | BAA07g35830 | A07 | 33766011 | G | A | missense_variant | MODERATE | c.1124C>T|p.Ser375Phe | S295 | 
| 7 | BAA07g35830 | A07 | 33766285 | C | T | missense_variant | MODERATE | c.850G>A|p.Val284Ile | S27 | 
| 8 | BAA07g35830 | A07 | 33766361 | C | T | synonymous_variant | LOW | c.774G>A|p.Thr258Thr | S13 S140 S168 S279 S64 | 
| 9 | BAA07g35830 | A07 | 33767793 | C | T | upstream_gene_variant | MODIFIER | c.-659G>A| | S260 | 
| 10 | BAA07g35830 | A07 | 33768309 | C | T | upstream_gene_variant | MODIFIER | c.-1175G>A| | S32 | 
| 11 | BAA07g35830 | A07 | 33768478 | G | A | upstream_gene_variant | MODIFIER | c.-1344C>T| | S112 | 
| 12 | BAA07g35830 | A07 | 33768771 | C | T | upstream_gene_variant | MODIFIER | c.-1637G>A| | S23 | 
| 13 | BAA07g35830 | A07 | 33769838 | G | A | upstream_gene_variant | MODIFIER | c.-2704C>T| | S276 |