| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g64970 | A09 | 60066944 | G | A | missense_variant | MODERATE | c.1726C>T|p.Pro576Ser |
S295 S35 |
| 2 | BAA09g64970 | A09 | 60067124 | C | T | missense_variant | MODERATE | c.1546G>A|p.Val516Met |
S186 |
| 3 | BAA09g64970 | A09 | 60067488 | C | T | splice_donor_variant&intron_variant | HIGH | c.1334+1G>A| |
S156 |
| 4 | BAA09g64970 | A09 | 60069638 | G | A | synonymous_variant | LOW | c.477C>T|p.Thr159Thr |
S38 |
| 5 | BAA09g64970 | A09 | 60070442 | C | T | stop_gained | HIGH | c.120G>A|p.Trp40* |
S157 |
| 6 | BAA09g64970 | A09 | 60070945 | C | T | upstream_gene_variant | MODIFIER | c.-266G>A| |
S292 |
| 7 | BAA09g64970 | A09 | 60073520 | G | A | upstream_gene_variant | MODIFIER | c.-2841C>T| |
S185 |
| 8 | BAA09g64970 | A09 | 60074042 | G | A | upstream_gene_variant | MODIFIER | c.-3363C>T| |
S281 |