| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g29700 | A05 | 33119489 | G | A | synonymous_variant | LOW | c.334C>T|p.Leu112Leu |
S238 |
| 2 | BAA05g29700 | A05 | 33119540 | C | T | missense_variant | MODERATE | c.283G>A|p.Gly95Ser |
S94 |
| 3 | BAA05g29700 | A05 | 33119572 | G | A | missense_variant | MODERATE | c.251C>T|p.Thr84Ile |
S200 |
| 4 | BAA05g29700 | A05 | 33119677 | G | A | splice_region_variant&intron_variant | LOW | c.234+4C>T| |
S13 |
| 5 | BAA05g29700 | A05 | 33119807 | G | A | synonymous_variant | LOW | c.108C>T|p.Phe36Phe |
S279 |
| 6 | BAA05g29700 | A05 | 33122838 | C | T | upstream_gene_variant | MODIFIER | c.-2924G>A| |
S123 |
| 7 | BAA05g29700 | A05 | 33123637 | G | A | upstream_gene_variant | MODIFIER | c.-3723C>T| |
S267 |
| 8 | BAA05g29700 | A05 | 33124776 | C | T | upstream_gene_variant | MODIFIER | c.-4862G>A| |
S146 |