| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g52990 | A09 | 54441510 | C | T | missense_variant | MODERATE | c.1387G>A|p.Ala463Thr |
S267 |
| 2 | BAA09g52990 | A09 | 54442025 | C | T | synonymous_variant | LOW | c.1212G>A|p.Gln404Gln |
S18 |
| 3 | BAA09g52990 | A09 | 54442118 | C | T | synonymous_variant | LOW | c.1119G>A|p.Lys373Lys |
S100 |
| 4 | BAA09g52990 | A09 | 54442246 | C | T | missense_variant | MODERATE | c.991G>A|p.Val331Ile |
S123 |
| 5 | BAA09g52990 | A09 | 54442845 | G | A | missense_variant | MODERATE | c.392C>T|p.Ser131Phe |
S59 |
| 6 | BAA09g52990 | A09 | 54442957 | C | T | missense_variant | MODERATE | c.280G>A|p.Glu94Lys |
S96 |
| 7 | BAA09g52990 | A09 | 54444985 | G | A | upstream_gene_variant | MODIFIER | c.-1671C>T| |
S128 |
| 8 | BAA09g52990 | A09 | 54446921 | C | T | upstream_gene_variant | MODIFIER | c.-3607G>A| |
S132 S137 S138 S215 S288 |
| 9 | BAA09g52990 | A09 | 54447042 | C | T | upstream_gene_variant | MODIFIER | c.-3728G>A| |
S18 |