| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g08240 | A01 | 3590738 | C | T | upstream_gene_variant | MODIFIER | c.-1765C>T| |
S155 |
| 2 | BAA01g08240 | A01 | 3590794 | C | T | upstream_gene_variant | MODIFIER | c.-1709C>T| |
S111 |
| 3 | BAA01g08240 | A01 | 3592219 | G | A | upstream_gene_variant | MODIFIER | c.-284G>A| |
S23 |
| 4 | BAA01g08240 | A01 | 3593663 | G | A | missense_variant | MODERATE | c.293G>A|p.Arg98Lys |
S226 |
| 5 | BAA01g08240 | A01 | 3594165 | G | A | synonymous_variant | LOW | c.795G>A|p.Arg265Arg |
S8 |
| 6 | BAA01g08240 | A01 | 3594277 | G | A | missense_variant | MODERATE | c.907G>A|p.Gly303Arg |
S11 |
| 7 | BAA01g08240 | A01 | 3594398 | C | T | intron_variant | MODIFIER | c.1009+19C>T| |
S263 |
| 8 | BAA01g08240 | A01 | 3595234 | C | T | synonymous_variant | LOW | c.1552C>T|p.Leu518Leu |
S210 |
| 9 | BAA01g08240 | A01 | 3595604 | G | A | missense_variant | MODERATE | c.1922G>A|p.Gly641Asp |
S122 |
| 10 | BAA01g08240 | A01 | 3596306 | C | T | downstream_gene_variant | MODIFIER | c.*650C>T| |
S104 S52 |
| 11 | BAA01g08240 | A01 | 3596906 | C | T | downstream_gene_variant | MODIFIER | c.*1250C>T| |
S148 S30 S31 |
| 12 | BAA01g08240 | A01 | 3597324 | C | T | downstream_gene_variant | MODIFIER | c.*1668C>T| |
S302 |
| 13 | BAA01g08240 | A01 | 3600450 | C | T | downstream_gene_variant | MODIFIER | c.*4794C>T| |
S203 |