| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g18200 | A02 | 9165545 | G | A | upstream_gene_variant | MODIFIER | c.-1297G>A| |
S188 |
| 2 | BAA02g18200 | A02 | 9167143 | G | A | missense_variant | MODERATE | c.302G>A|p.Gly101Asp |
S192 |
| 3 | BAA02g18200 | A02 | 9167733 | C | T | missense_variant | MODERATE | c.892C>T|p.Leu298Phe |
S5 |
| 4 | BAA02g18200 | A02 | 9167806 | G | A | missense_variant | MODERATE | c.965G>A|p.Arg322Lys |
S237 |
| 5 | BAA02g18200 | A02 | 9167817 | G | A | missense_variant | MODERATE | c.976G>A|p.Ala326Thr |
S276 |
| 6 | BAA02g18200 | A02 | 9167931 | G | A | missense_variant | MODERATE | c.1090G>A|p.Glu364Lys |
S162 |
| 7 | BAA02g18200 | A02 | 9169360 | G | A | downstream_gene_variant | MODIFIER | c.*917G>A| |
S69 |
| 8 | BAA02g18200 | A02 | 9169679 | G | A | downstream_gene_variant | MODIFIER | c.*1236G>A| |
S52 |
| 9 | BAA02g18200 | A02 | 9171045 | C | T | downstream_gene_variant | MODIFIER | c.*2602C>T| |
S202 |
| 10 | BAA02g18200 | A02 | 9171834 | C | T | downstream_gene_variant | MODIFIER | c.*3391C>T| |
S104 |