| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g29880 | A08 | 20393395 | C | T | missense_variant | MODERATE | c.2564G>A|p.Gly855Glu |
S103 |
| 2 | BAA08g29880 | A08 | 20394116 | G | A | missense_variant | MODERATE | c.2063C>T|p.Ala688Val |
S80 |
| 3 | BAA08g29880 | A08 | 20394736 | G | A | missense_variant | MODERATE | c.1709C>T|p.Ala570Val |
S8 |
| 4 | BAA08g29880 | A08 | 20395725 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1066-1G>A| |
S58 |
| 5 | BAA08g29880 | A08 | 20395859 | C | T | synonymous_variant | LOW | c.999G>A|p.Val333Val |
S249 |
| 6 | BAA08g29880 | A08 | 20396592 | C | T | missense_variant | MODERATE | c.502G>A|p.Asp168Asn |
S171 |
| 7 | BAA08g29880 | A08 | 20397848 | G | A | upstream_gene_variant | MODIFIER | c.-420C>T| |
S48 |