| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g31690 | A07 | 31433468 | G | A | upstream_gene_variant | MODIFIER | c.-2503G>A| | S43 | 
| 2 | BAA07g31690 | A07 | 31434160 | G | A | upstream_gene_variant | MODIFIER | c.-1811G>A| | S64 | 
| 3 | BAA07g31690 | A07 | 31436071 | C | T | missense_variant | MODERATE | c.101C>T|p.Thr34Ile | S232 | 
| 4 | BAA07g31690 | A07 | 31436296 | G | A | missense_variant | MODERATE | c.326G>A|p.Gly109Glu | S20 | 
| 5 | BAA07g31690 | A07 | 31436334 | G | A | missense_variant | MODERATE | c.364G>A|p.Glu122Lys | S10 | 
| 6 | BAA07g31690 | A07 | 31436443 | C | T | splice_region_variant&intron_variant | LOW | c.468+5C>T| | S260 | 
| 7 | BAA07g31690 | A07 | 31439620 | C | T | missense_variant | MODERATE | c.1154C>T|p.Ser385Phe | S169 | 
| 8 | BAA07g31690 | A07 | 31441848 | G | A | downstream_gene_variant | MODIFIER | c.*2026G>A| | S139 |