| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g22980 | A01 | 11705548 | C | T | missense_variant | MODERATE | c.421C>T|p.Pro141Ser |
S176 |
| 2 | BAA01g22980 | A01 | 11705897 | G | A | splice_region_variant&intron_variant | LOW | c.628-7G>A| |
S252 |
| 3 | BAA01g22980 | A01 | 11707164 | C | T | missense_variant | MODERATE | c.1547C>T|p.Pro516Leu |
S76 |