| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g44280 | A02 | 36526859 | C | T | upstream_gene_variant | MODIFIER | c.-3449C>T| |
S193 |
| 2 | BAA02g44280 | A02 | 36527328 | G | A | upstream_gene_variant | MODIFIER | c.-2980G>A| |
S30 |
| 3 | BAA02g44280 | A02 | 36528141 | G | A | upstream_gene_variant | MODIFIER | c.-2167G>A| |
S69 |
| 4 | BAA02g44280 | A02 | 36528258 | G | A | upstream_gene_variant | MODIFIER | c.-2050G>A| |
S148 S210 S31 |
| 5 | BAA02g44280 | A02 | 36528280 | G | A | upstream_gene_variant | MODIFIER | c.-2028G>A| |
S139 |
| 6 | BAA02g44280 | A02 | 36530506 | G | A | missense_variant | MODERATE | c.199G>A|p.Asp67Asn |
S96 |
| 7 | BAA02g44280 | A02 | 36530571 | C | T | synonymous_variant | LOW | c.264C>T|p.Leu88Leu |
S107 |
| 8 | BAA02g44280 | A02 | 36538172 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.581-1G>A| |
S19 |