| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g07100 | A05 | 3488360 | C | T | downstream_gene_variant | MODIFIER | c.*1130G>A| |
S201 |
| 2 | BAA05g07100 | A05 | 3488687 | C | T | downstream_gene_variant | MODIFIER | c.*803G>A| |
S262 |
| 3 | BAA05g07100 | A05 | 3489257 | G | A | downstream_gene_variant | MODIFIER | c.*233C>T| |
S126 |
| 4 | BAA05g07100 | A05 | 3489567 | G | A | missense_variant | MODERATE | c.1894C>T|p.His632Tyr |
S95 |
| 5 | BAA05g07100 | A05 | 3490068 | C | T | missense_variant | MODERATE | c.1393G>A|p.Asp465Asn |
S82 S92 |
| 6 | BAA05g07100 | A05 | 3490781 | G | A | missense_variant | MODERATE | c.680C>T|p.Thr227Ile |
S242 |
| 7 | BAA05g07100 | A05 | 3490898 | G | A | missense_variant | MODERATE | c.563C>T|p.Pro188Leu |
S190 |
| 8 | BAA05g07100 | A05 | 3493134 | G | A | upstream_gene_variant | MODIFIER | c.-1017C>T| |
S279 |
| 9 | BAA05g07100 | A05 | 3494712 | G | A | upstream_gene_variant | MODIFIER | c.-2595C>T| |
S32 |
| 10 | BAA05g07100 | A05 | 3495720 | G | A | upstream_gene_variant | MODIFIER | c.-3603C>T| |
S179 |
| 11 | BAA05g07100 | A05 | 3496325 | C | T | upstream_gene_variant | MODIFIER | c.-4208G>A| |
S293 |