| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g27980 | A02 | 15757552 | G | A | upstream_gene_variant | MODIFIER | c.-764G>A| |
S38 |
| 2 | BAA02g27980 | A02 | 15759591 | C | T | synonymous_variant | LOW | c.261C>T|p.Tyr87Tyr |
S289 S290 |
| 3 | BAA02g27980 | A02 | 15759631 | C | T | stop_gained | HIGH | c.301C>T|p.Arg101* |
S51 |
| 4 | BAA02g27980 | A02 | 15759649 | G | A | missense_variant | MODERATE | c.319G>A|p.Asp107Asn |
S189 |
| 5 | BAA02g27980 | A02 | 15760512 | C | T | splice_region_variant&intron_variant | LOW | c.586-4C>T| |
S142 |
| 6 | BAA02g27980 | A02 | 15760576 | G | A | missense_variant | MODERATE | c.646G>A|p.Glu216Lys |
S126 |
| 7 | BAA02g27980 | A02 | 15764636 | C | T | synonymous_variant | LOW | c.2616C>T|p.Asp872Asp |
S185 |
| 8 | BAA02g27980 | A02 | 15765254 | C | T | downstream_gene_variant | MODIFIER | c.*537C>T| |
S264 |