| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g06180 | A08 | 4886342 | C | T | upstream_gene_variant | MODIFIER | c.-4765C>T| |
S279 |
| 2 | BAA08g06180 | A08 | 4886402 | C | T | upstream_gene_variant | MODIFIER | c.-4705C>T| |
S156 |
| 3 | BAA08g06180 | A08 | 4891401 | A | G | missense_variant | MODERATE | c.206A>G|p.Gln69Arg |
S162 S262 |
| 4 | BAA08g06180 | A08 | 4892271 | C | T | splice_region_variant&intron_variant | LOW | c.428-3C>T| |
S6 |
| 5 | BAA08g06180 | A08 | 4893987 | G | A | downstream_gene_variant | MODIFIER | c.*1119G>A| |
S262 |
| 6 | BAA08g06180 | A08 | 4894189 | C | T | downstream_gene_variant | MODIFIER | c.*1321C>T| |
S189 S226 S41 |
| 7 | BAA08g06180 | A08 | 4894850 | C | T | downstream_gene_variant | MODIFIER | c.*1982C>T| |
S132 S137 S89 |
| 8 | BAA08g06180 | A08 | 4895545 | G | A | downstream_gene_variant | MODIFIER | c.*2677G>A| |
S158 |