| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g20900 | A01 | 10295522 | G | A | synonymous_variant | LOW | c.165G>A|p.Ser55Ser |
S58 |
| 2 | BAA01g20900 | A01 | 10295707 | G | A | missense_variant | MODERATE | c.350G>A|p.Cys117Tyr |
S162 |
| 3 | BAA01g20900 | A01 | 10295973 | C | T | splice_region_variant&intron_variant | LOW | c.388-3C>T| |
S247 |
| 4 | BAA01g20900 | A01 | 10296431 | C | T | splice_region_variant&intron_variant | LOW | c.487-7C>T| |
S177 |
| 5 | BAA01g20900 | A01 | 10297448 | G | A | missense_variant | MODERATE | c.919G>A|p.Ala307Thr |
S126 |
| 6 | BAA01g20900 | A01 | 10299364 | C | T | downstream_gene_variant | MODIFIER | c.*1812C>T| |
S203 |
| 7 | BAA01g20900 | A01 | 10299601 | C | T | downstream_gene_variant | MODIFIER | c.*2049C>T| |
S270 |