| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g16530 | A01 | 8035913 | G | A | downstream_gene_variant | MODIFIER | c.*3126C>T| |
S95 |
| 2 | BAA01g16530 | A01 | 8037608 | C | T | downstream_gene_variant | MODIFIER | c.*1431G>A| |
S64 |
| 3 | BAA01g16530 | A01 | 8039469 | C | T | missense_variant | MODERATE | c.1600G>A|p.Glu534Lys |
S250 |
| 4 | BAA01g16530 | A01 | 8040747 | C | T | missense_variant | MODERATE | c.994G>A|p.Glu332Lys |
S221 |
| 5 | BAA01g16530 | A01 | 8040871 | C | T | missense_variant | MODERATE | c.949G>A|p.Ala317Thr |
S130 |
| 6 | BAA01g16530 | A01 | 8041841 | G | A | missense_variant | MODERATE | c.395C>T|p.Pro132Leu |
S11 |
| 7 | BAA01g16530 | A01 | 8043107 | C | T | upstream_gene_variant | MODIFIER | c.-872G>A| |
S16 S284 |
| 8 | BAA01g16530 | A01 | 8043235 | C | T | upstream_gene_variant | MODIFIER | c.-1000G>A| |
S284 |
| 9 | BAA01g16530 | A01 | 8044410 | G | A | upstream_gene_variant | MODIFIER | c.-2175C>T| |
S9 |
| 10 | BAA01g16530 | A01 | 8046346 | G | A | upstream_gene_variant | MODIFIER | c.-4111C>T| |
S72 |
| 11 | BAA01g16530 | A01 | 8046437 | G | A | upstream_gene_variant | MODIFIER | c.-4202C>T| |
S246 |
| 12 | BAA01g16530 | A01 | 8046527 | G | A | upstream_gene_variant | MODIFIER | c.-4292C>T| |
S287 |