| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g01070 | A01 | 450635 | G | A | missense_variant | MODERATE | c.1345C>T|p.Leu449Phe |
S177 |
| 2 | BAA01g01070 | A01 | 451075 | C | T | missense_variant | MODERATE | c.1076G>A|p.Ser359Asn |
S203 |
| 3 | BAA01g01070 | A01 | 451736 | G | A | missense_variant | MODERATE | c.641C>T|p.Ala214Val |
S161 |
| 4 | BAA01g01070 | A01 | 452031 | C | T | synonymous_variant | LOW | c.423G>A|p.Arg141Arg |
S284 |
| 5 | BAA01g01070 | A01 | 452289 | G | A | synonymous_variant | LOW | c.165C>T|p.His55His |
S293 |
| 6 | BAA01g01070 | A01 | 454700 | C | T | upstream_gene_variant | MODIFIER | c.-2247G>A| |
S262 |