| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g04160 | A08 | 2946427 | C | T | missense_variant | MODERATE | c.73C>T|p.Leu25Phe | S53 | 
| 2 | BAA08g04160 | A08 | 2946448 | G | A | missense_variant | MODERATE | c.94G>A|p.Ala32Thr | S260 | 
| 3 | BAA08g04160 | A08 | 2946998 | G | A | missense_variant | MODERATE | c.421G>A|p.Asp141Asn | S87 | 
| 4 | BAA08g04160 | A08 | 2947491 | C | T | missense_variant | MODERATE | c.643C>T|p.Pro215Ser | S157 S163 | 
| 5 | BAA08g04160 | A08 | 2948886 | G | A | missense_variant | MODERATE | c.1373G>A|p.Arg458Gln | S130 | 
| 6 | BAA08g04160 | A08 | 2948970 | G | A | missense_variant | MODERATE | c.1457G>A|p.Gly486Glu | S275 | 
| 7 | BAA08g04160 | A08 | 2949920 | G | A | downstream_gene_variant | MODIFIER | c.*877G>A| | S62 | 
| 8 | BAA08g04160 | A08 | 2950117 | C | T | downstream_gene_variant | MODIFIER | c.*1074C>T| | S167 |