| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g00650 | A05 | 363171 | C | T | downstream_gene_variant | MODIFIER | c.*4633G>A| |
S237 |
| 2 | BAA05g00650 | A05 | 364406 | G | C | downstream_gene_variant | MODIFIER | c.*3398C>G| |
S28 |
| 3 | BAA05g00650 | A05 | 365964 | C | T | downstream_gene_variant | MODIFIER | c.*1840G>A| |
S271 |
| 4 | BAA05g00650 | A05 | 366217 | A | G | downstream_gene_variant | MODIFIER | c.*1587T>C| |
S245 |
| 5 | BAA05g00650 | A05 | 366353 | C | T | downstream_gene_variant | MODIFIER | c.*1451G>A| |
S292 |
| 6 | BAA05g00650 | A05 | 366827 | G | A | downstream_gene_variant | MODIFIER | c.*977C>T| |
S25 |
| 7 | BAA05g00650 | A05 | 368281 | C | T | missense_variant | MODERATE | c.449G>A|p.Cys150Tyr |
S292 |
| 8 | BAA05g00650 | A05 | 368701 | G | A | missense_variant | MODERATE | c.29C>T|p.Ala10Val |
S306 S308 |
| 9 | BAA05g00650 | A05 | 369066 | C | T | upstream_gene_variant | MODIFIER | c.-337G>A| |
S87 |