| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g33120 | A05 | 34999003 | G | A | upstream_gene_variant | MODIFIER | c.-1488G>A| |
S136 |
| 2 | BAA05g33120 | A05 | 34999238 | C | T | upstream_gene_variant | MODIFIER | c.-1253C>T| |
S251 |
| 3 | BAA05g33120 | A05 | 34999610 | G | A | upstream_gene_variant | MODIFIER | c.-881G>A| |
S138 |
| 4 | BAA05g33120 | A05 | 35000002 | C | T | upstream_gene_variant | MODIFIER | c.-489C>T| |
S96 |
| 5 | BAA05g33120 | A05 | 35001686 | C | T | missense_variant | MODERATE | c.479C>T|p.Thr160Ile |
S146 |
| 6 | BAA05g33120 | A05 | 35001825 | G | A | synonymous_variant | LOW | c.618G>A|p.Arg206Arg |
S134 |
| 7 | BAA05g33120 | A05 | 35002423 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.947-1G>A| |
S11 |
| 8 | BAA05g33120 | A05 | 35003977 | C | T | missense_variant | MODERATE | c.1988C>T|p.Pro663Leu |
S45 |