| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g12980 | A08 | 11282147 | C | T | missense_variant | MODERATE | c.86C>T|p.Pro29Leu |
S89 |
| 2 | BAA08g12980 | A08 | 11282160 | G | A | synonymous_variant | LOW | c.99G>A|p.Ala33Ala |
S234 |
| 3 | BAA08g12980 | A08 | 11282351 | C | T | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S114 |
| 4 | BAA08g12980 | A08 | 11282890 | C | T | downstream_gene_variant | MODIFIER | c.*376C>T| |
S203 |
| 5 | BAA08g12980 | A08 | 11282906 | C | T | downstream_gene_variant | MODIFIER | c.*392C>T| |
S261 S274 |
| 6 | BAA08g12980 | A08 | 11282980 | A | C | downstream_gene_variant | MODIFIER | c.*466A>C| |
S261 S274 |
| 7 | BAA08g12980 | A08 | 11283000 | G | A | downstream_gene_variant | MODIFIER | c.*486G>A| |
S75 S81 |
| 8 | BAA08g12980 | A08 | 11283215 | G | A | downstream_gene_variant | MODIFIER | c.*701G>A| |
S86 |
| 9 | BAA08g12980 | A08 | 11283519 | G | A | downstream_gene_variant | MODIFIER | c.*1005G>A| |
S301 S304 |
| 10 | BAA08g12980 | A08 | 11283654 | G | A | downstream_gene_variant | MODIFIER | c.*1140G>A| |
S97 |
| 11 | BAA08g12980 | A08 | 11284545 | G | A | downstream_gene_variant | MODIFIER | c.*2031G>A| |
S229 |
| 12 | BAA08g12980 | A08 | 11285157 | T | A | downstream_gene_variant | MODIFIER | c.*2643T>A| |
S157 |
| 13 | BAA08g12980 | A08 | 11286592 | G | A | downstream_gene_variant | MODIFIER | c.*4078G>A| |
S25 S264 |
| 14 | BAA08g12980 | A08 | 11286984 | T | A | downstream_gene_variant | MODIFIER | c.*4470T>A| |
S100 |