| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g16560 | A01 | 8057279 | C | T | missense_variant | MODERATE | c.577G>A|p.Asp193Asn |
S249 |
| 2 | BAA01g16560 | A01 | 8057654 | C | T | missense_variant | MODERATE | c.202G>A|p.Asp68Asn |
S48 |
| 3 | BAA01g16560 | A01 | 8057800 | C | T | missense_variant | MODERATE | c.56G>A|p.Gly19Glu |
S160 |
| 4 | BAA01g16560 | A01 | 8059785 | C | T | upstream_gene_variant | MODIFIER | c.-1930G>A| |
S32 |
| 5 | BAA01g16560 | A01 | 8059792 | G | A | upstream_gene_variant | MODIFIER | c.-1937C>T| |
S27 |
| 6 | BAA01g16560 | A01 | 8059981 | G | A | upstream_gene_variant | MODIFIER | c.-2126C>T| |
S204 |
| 7 | BAA01g16560 | A01 | 8060055 | G | A | upstream_gene_variant | MODIFIER | c.-2200C>T| |
S85 |
| 8 | BAA01g16560 | A01 | 8060928 | C | T | upstream_gene_variant | MODIFIER | c.-3073G>A| |
S10 |
| 9 | BAA01g16560 | A01 | 8061973 | C | T | upstream_gene_variant | MODIFIER | c.-4118G>A| |
S198 |