| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g13470 | A08 | 11674604 | C | T | missense_variant | MODERATE | c.1086G>A|p.Met362Ile |
S162 |
| 2 | BAA08g13470 | A08 | 11675215 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.685-1G>A| |
S292 |
| 3 | BAA08g13470 | A08 | 11677057 | C | T | upstream_gene_variant | MODIFIER | c.-384G>A| |
S216 |
| 4 | BAA08g13470 | A08 | 11677078 | C | T | upstream_gene_variant | MODIFIER | c.-405G>A| |
S201 |
| 5 | BAA08g13470 | A08 | 11677115 | C | T | upstream_gene_variant | MODIFIER | c.-442G>A| |
S177 |
| 6 | BAA08g13470 | A08 | 11679490 | C | T | upstream_gene_variant | MODIFIER | c.-2817G>A| |
S138 |
| 7 | BAA08g13470 | A08 | 11681247 | C | T | upstream_gene_variant | MODIFIER | c.-4574G>A| |
S168 |
| 8 | BAA08g13470 | A08 | 11681316 | C | T | upstream_gene_variant | MODIFIER | c.-4643G>A| |
S284 |