| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10460 | A02 | 4628103 | C | T | missense_variant | MODERATE | c.793G>A|p.Ala265Thr |
S15 S3 |
| 2 | BAA02g10460 | A02 | 4628627 | C | T | stop_gained | HIGH | c.615G>A|p.Trp205* |
S230 |
| 3 | BAA02g10460 | A02 | 4628677 | C | T | missense_variant | MODERATE | c.565G>A|p.Asp189Asn |
S71 |
| 4 | BAA02g10460 | A02 | 4631996 | C | A | upstream_gene_variant | MODIFIER | c.-2169G>T| |
S203 |
| 5 | BAA02g10460 | A02 | 4633011 | C | T | upstream_gene_variant | MODIFIER | c.-3184G>A| |
S292 |
| 6 | BAA02g10460 | A02 | 4633297 | G | A | upstream_gene_variant | MODIFIER | c.-3470C>T| |
S7 |
| 7 | BAA02g10460 | A02 | 4634463 | G | A | upstream_gene_variant | MODIFIER | c.-4636C>T| |
S155 |