| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g04100 | A09 | 2444277 | C | T | missense_variant | MODERATE | c.3251G>A|p.Gly1084Glu |
S238 |
| 2 | BAA09g04100 | A09 | 2445391 | C | T | missense_variant | MODERATE | c.2137G>A|p.Gly713Arg |
S239 |
| 3 | BAA09g04100 | A09 | 2448940 | C | T | splice_donor_variant&intron_variant | HIGH | c.476+1G>A| |
S282 |
| 4 | BAA09g04100 | A09 | 2449267 | C | T | missense_variant | MODERATE | c.256G>A|p.Asp86Asn |
S77 |
| 5 | BAA09g04100 | A09 | 2450340 | T | A | upstream_gene_variant | MODIFIER | c.-818A>T| |
S25 S264 |
| 6 | BAA09g04100 | A09 | 2453475 | C | T | upstream_gene_variant | MODIFIER | c.-3953G>A| |
S143 |
| 7 | BAA09g04100 | A09 | 2453813 | C | T | upstream_gene_variant | MODIFIER | c.-4291G>A| |
S134 |
| 8 | BAA09g04100 | A09 | 2454508 | C | T | upstream_gene_variant | MODIFIER | c.-4986G>A| |
S250 |