| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g17090 | A06 | 8587253 | G | A | upstream_gene_variant | MODIFIER | c.-3890G>A| |
S138 |
| 2 | BAA06g17090 | A06 | 8587781 | C | T | upstream_gene_variant | MODIFIER | c.-3362C>T| |
S156 |
| 3 | BAA06g17090 | A06 | 8591430 | C | T | missense_variant | MODERATE | c.127C>T|p.Leu43Phe |
S183 S198 |
| 4 | BAA06g17090 | A06 | 8591491 | G | A | missense_variant | MODERATE | c.188G>A|p.Arg63Lys |
S191 |
| 5 | BAA06g17090 | A06 | 8595867 | G | A | downstream_gene_variant | MODIFIER | c.*3859G>A| |
S108 |
| 6 | BAA06g17090 | A06 | 8595895 | G | A | downstream_gene_variant | MODIFIER | c.*3887G>A| |
S251 |
| 7 | BAA06g17090 | A06 | 8596258 | C | T | downstream_gene_variant | MODIFIER | c.*4250C>T| |
S62 |
| 8 | BAA06g17090 | A06 | 8596469 | C | T | downstream_gene_variant | MODIFIER | c.*4461C>T| |
S231 |
| 9 | BAA06g17090 | A06 | 8596720 | G | A | downstream_gene_variant | MODIFIER | c.*4712G>A| |
S129 |