| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g11660 | A02 | 5267937 | G | A | synonymous_variant | LOW | c.2073C>T|p.Asn691Asn |
S148 S210 S30 S31 |
| 2 | BAA02g11660 | A02 | 5269573 | G | A | missense_variant | MODERATE | c.1162C>T|p.Pro388Ser |
S295 |
| 3 | BAA02g11660 | A02 | 5270082 | C | T | missense_variant | MODERATE | c.751G>A|p.Ala251Thr |
S32 |
| 4 | BAA02g11660 | A02 | 5275850 | G | A | upstream_gene_variant | MODIFIER | c.-4694C>T| |
S296 |