| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g43350 | A05 | 40787378 | C | T | missense_variant | MODERATE | c.1231G>A|p.Val411Ile |
S255 S284 |
| 2 | BAA05g43350 | A05 | 40787641 | G | A | missense_variant | MODERATE | c.968C>T|p.Ser323Phe |
S257 |
| 3 | BAA05g43350 | A05 | 40788660 | G | A | synonymous_variant | LOW | c.285C>T|p.Thr95Thr |
S35 |
| 4 | BAA05g43350 | A05 | 40790052 | G | A | upstream_gene_variant | MODIFIER | c.-783C>T| |
S114 |
| 5 | BAA05g43350 | A05 | 40790150 | G | A | upstream_gene_variant | MODIFIER | c.-881C>T| |
S5 |
| 6 | BAA05g43350 | A05 | 40791881 | C | T | upstream_gene_variant | MODIFIER | c.-2612G>A| |
S65 |
| 7 | BAA05g43350 | A05 | 40792759 | C | T | upstream_gene_variant | MODIFIER | c.-3490G>A| |
S79 S91 |
| 8 | BAA05g43350 | A05 | 40793469 | G | A | upstream_gene_variant | MODIFIER | c.-4200C>T| |
S217 S248 |