| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g11400 | A09 | 6392624 | G | A | missense_variant | MODERATE | c.449G>A|p.Gly150Asp | S117 | 
| 2 | BAA09g11400 | A09 | 6392964 | C | T | missense_variant | MODERATE | c.572C>T|p.Ser191Phe | S193 | 
| 3 | BAA09g11400 | A09 | 6392976 | C | T | missense_variant | MODERATE | c.584C>T|p.Ser195Leu | S76 | 
| 4 | BAA09g11400 | A09 | 6393909 | G | A | synonymous_variant | LOW | c.936G>A|p.Ser312Ser | S289 S290 | 
| 5 | BAA09g11400 | A09 | 6394163 | C | T | missense_variant | MODERATE | c.1021C>T|p.Pro341Ser | S54 | 
| 6 | BAA09g11400 | A09 | 6394724 | C | T | missense_variant | MODERATE | c.1321C>T|p.Leu441Phe | S217 S248 | 
| 7 | BAA09g11400 | A09 | 6394772 | C | T | missense_variant | MODERATE | c.1369C>T|p.Leu457Phe | S168 | 
| 8 | BAA09g11400 | A09 | 6396616 | G | A | splice_region_variant&intron_variant | LOW | c.2077-5G>A| | S174 S27 S39 |