| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g47420 | A02 | 38240689 | C | T | missense_variant | MODERATE | c.725G>A|p.Arg242His |
S237 |
| 2 | BAA02g47420 | A02 | 38241435 | G | A | missense_variant | MODERATE | c.230C>T|p.Ser77Phe |
S282 |
| 3 | BAA02g47420 | A02 | 38241510 | G | A | missense_variant | MODERATE | c.155C>T|p.Thr52Ile |
S239 |
| 4 | BAA02g47420 | A02 | 38241945 | G | A | upstream_gene_variant | MODIFIER | c.-281C>T| |
S28 |
| 5 | BAA02g47420 | A02 | 38243734 | C | T | upstream_gene_variant | MODIFIER | c.-2070G>A| |
S299 |
| 6 | BAA02g47420 | A02 | 38243785 | C | T | upstream_gene_variant | MODIFIER | c.-2121G>A| |
S136 |
| 7 | BAA02g47420 | A02 | 38243961 | C | T | upstream_gene_variant | MODIFIER | c.-2297G>A| |
S117 |
| 8 | BAA02g47420 | A02 | 38244173 | G | A | upstream_gene_variant | MODIFIER | c.-2509C>T| |
S229 |
| 9 | BAA02g47420 | A02 | 38244708 | G | A | upstream_gene_variant | MODIFIER | c.-3044C>T| |
S10 |
| 10 | BAA02g47420 | A02 | 38244991 | C | T | upstream_gene_variant | MODIFIER | c.-3327G>A| |
S131 |