| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g46380 | A02 | 37704928 | C | T | missense_variant | MODERATE | c.92C>T|p.Ser31Phe |
S53 |
| 2 | BAA02g46380 | A02 | 37705067 | G | A | synonymous_variant | LOW | c.231G>A|p.Lys77Lys |
S125 |
| 3 | BAA02g46380 | A02 | 37705260 | G | A | missense_variant | MODERATE | c.424G>A|p.Ala142Thr |
S283 |
| 4 | BAA02g46380 | A02 | 37709385 | C | T | downstream_gene_variant | MODIFIER | c.*2277C>T| |
S179 |
| 5 | BAA02g46380 | A02 | 37709892 | G | A | downstream_gene_variant | MODIFIER | c.*2784G>A| |
S191 |
| 6 | BAA02g46380 | A02 | 37710305 | C | T | downstream_gene_variant | MODIFIER | c.*3197C>T| |
S61 |
| 7 | BAA02g46380 | A02 | 37710640 | G | A | downstream_gene_variant | MODIFIER | c.*3532G>A| |
S207 |
| 8 | BAA02g46380 | A02 | 37711768 | G | A | downstream_gene_variant | MODIFIER | c.*4660G>A| |
S168 |