| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g44960 | A09 | 50338755 | C | T | missense_variant | MODERATE | c.1123G>A|p.Glu375Lys |
S186 |
| 2 | BAA09g44960 | A09 | 50340586 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Glu |
S96 |
| 3 | BAA09g44960 | A09 | 50341136 | C | T | missense_variant | MODERATE | c.226G>A|p.Asp76Asn |
S99 |
| 4 | BAA09g44960 | A09 | 50342584 | C | T | upstream_gene_variant | MODIFIER | c.-910G>A| |
S289 |
| 5 | BAA09g44960 | A09 | 50343640 | C | T | upstream_gene_variant | MODIFIER | c.-1966G>A| |
S183 S198 |
| 6 | BAA09g44960 | A09 | 50346371 | C | T | upstream_gene_variant | MODIFIER | c.-4697G>A| |
S206 S26 |