| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g39940 | A02 | 33779570 | C | T | upstream_gene_variant | MODIFIER | c.-4973C>T| |
S82 S92 |
| 2 | BAA02g39940 | A02 | 33781689 | C | T | upstream_gene_variant | MODIFIER | c.-2854C>T| |
S77 S97 |
| 3 | BAA02g39940 | A02 | 33781921 | C | T | upstream_gene_variant | MODIFIER | c.-2622C>T| |
S289 S290 |
| 4 | BAA02g39940 | A02 | 33782128 | G | A | upstream_gene_variant | MODIFIER | c.-2415G>A| |
S175 |
| 5 | BAA02g39940 | A02 | 33782164 | C | T | upstream_gene_variant | MODIFIER | c.-2379C>T| |
S87 |
| 6 | BAA02g39940 | A02 | 33782575 | G | A | upstream_gene_variant | MODIFIER | c.-1968G>A| |
S215 |
| 7 | BAA02g39940 | A02 | 33783418 | C | T | upstream_gene_variant | MODIFIER | c.-1125C>T| |
S212 |
| 8 | BAA02g39940 | A02 | 33785205 | G | A | synonymous_variant | LOW | c.267G>A|p.Pro89Pro |
S217 S248 |
| 9 | BAA02g39940 | A02 | 33785259 | G | A | synonymous_variant | LOW | c.321G>A|p.Ala107Ala |
S134 |
| 10 | BAA02g39940 | A02 | 33785465 | C | T | missense_variant | MODERATE | c.527C>T|p.Thr176Ile |
S79 S91 |