| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g10050 | A07 | 18978755 | C | T | missense_variant | MODERATE | c.799G>A|p.Val267Ile |
S217 S248 |
| 2 | BAA07g10050 | A07 | 18979373 | C | T | missense_variant | MODERATE | c.415G>A|p.Gly139Arg |
S259 |
| 3 | BAA07g10050 | A07 | 18979558 | C | T | splice_region_variant&synonymous_variant | LOW | c.297G>A|p.Thr99Thr |
S18 |
| 4 | BAA07g10050 | A07 | 18979714 | C | T | missense_variant | MODERATE | c.266G>A|p.Arg89His |
S259 |
| 5 | BAA07g10050 | A07 | 18980383 | C | T | upstream_gene_variant | MODIFIER | c.-404G>A| |
S19 |
| 6 | BAA07g10050 | A07 | 18980466 | C | T | upstream_gene_variant | MODIFIER | c.-487G>A| |
S166 |
| 7 | BAA07g10050 | A07 | 18980817 | G | A | upstream_gene_variant | MODIFIER | c.-838C>T| |
S28 |
| 8 | BAA07g10050 | A07 | 18984036 | C | T | upstream_gene_variant | MODIFIER | c.-4057G>A| |
S162 |