| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g16590 | A01 | 8078025 | C | T | upstream_gene_variant | MODIFIER | c.-1349C>T| |
S71 |
| 2 | BAA01g16590 | A01 | 8078832 | C | T | upstream_gene_variant | MODIFIER | c.-542C>T| |
S169 |
| 3 | BAA01g16590 | A01 | 8079204 | C | T | upstream_gene_variant | MODIFIER | c.-170C>T| |
S221 |
| 4 | BAA01g16590 | A01 | 8079265 | C | T | upstream_gene_variant | MODIFIER | c.-109C>T| |
S47 |
| 5 | BAA01g16590 | A01 | 8079840 | C | T | synonymous_variant | LOW | c.159C>T|p.Phe53Phe |
S35 |
| 6 | BAA01g16590 | A01 | 8080001 | C | T | missense_variant | MODERATE | c.320C>T|p.Ser107Leu |
S20 |
| 7 | BAA01g16590 | A01 | 8080937 | C | T | missense_variant | MODERATE | c.1060C>T|p.His354Tyr |
S114 |
| 8 | BAA01g16590 | A01 | 8081037 | C | T | missense_variant | MODERATE | c.1160C>T|p.Ala387Val |
S68 |
| 9 | BAA01g16590 | A01 | 8082063 | G | A | missense_variant | MODERATE | c.1913G>A|p.Arg638Lys |
S273 |