| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g18560 | A02 | 9464633 | G | A | missense_variant | MODERATE | c.1844C>T|p.Ser615Phe |
S203 |
| 2 | BAA02g18560 | A02 | 9464705 | G | A | missense_variant | MODERATE | c.1772C>T|p.Ser591Phe |
S238 |
| 3 | BAA02g18560 | A02 | 9464916 | G | A | missense_variant | MODERATE | c.1646C>T|p.Ser549Phe |
S11 |
| 4 | BAA02g18560 | A02 | 9465937 | C | T | synonymous_variant | LOW | c.702G>A|p.Ser234Ser |
S94 |
| 5 | BAA02g18560 | A02 | 9465941 | G | A | missense_variant | MODERATE | c.698C>T|p.Ser233Phe |
S197 |
| 6 | BAA02g18560 | A02 | 9466510 | G | A | missense_variant | MODERATE | c.209C>T|p.Ser70Phe |
S177 |
| 7 | BAA02g18560 | A02 | 9466857 | G | A | upstream_gene_variant | MODIFIER | c.-57C>T| |
S86 |
| 8 | BAA02g18560 | A02 | 9468466 | G | A | upstream_gene_variant | MODIFIER | c.-1666C>T| |
S47 |
| 9 | BAA02g18560 | A02 | 9468771 | C | T | upstream_gene_variant | MODIFIER | c.-1971G>A| |
S79 S84 |
| 10 | BAA02g18560 | A02 | 9470400 | G | A | upstream_gene_variant | MODIFIER | c.-3600C>T| |
S264 |
| 11 | BAA02g18560 | A02 | 9470500 | G | A | upstream_gene_variant | MODIFIER | c.-3700C>T| |
S202 |