| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g17040 | A09 | 10130302 | C | T | synonymous_variant | LOW | c.1137G>A|p.Arg379Arg |
S234 |
| 2 | BAA09g17040 | A09 | 10131173 | G | A | missense_variant | MODERATE | c.266C>T|p.Ser89Phe |
S47 |
| 3 | BAA09g17040 | A09 | 10131896 | C | T | upstream_gene_variant | MODIFIER | c.-458G>A| |
S289 S290 |
| 4 | BAA09g17040 | A09 | 10132905 | C | T | upstream_gene_variant | MODIFIER | c.-1467G>A| |
S216 |
| 5 | BAA09g17040 | A09 | 10133562 | C | T | upstream_gene_variant | MODIFIER | c.-2124G>A| |
S278 |
| 6 | BAA09g17040 | A09 | 10134113 | G | A | upstream_gene_variant | MODIFIER | c.-2675C>T| |
S197 |
| 7 | BAA09g17040 | A09 | 10135790 | C | T | upstream_gene_variant | MODIFIER | c.-4352G>A| |
S282 |
| 8 | BAA09g17040 | A09 | 10136406 | G | A | upstream_gene_variant | MODIFIER | c.-4968C>T| |
S279 |