| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g02890 | A09 | 1820421 | G | A | upstream_gene_variant | MODIFIER | c.-2922G>A| |
S152 S81 |
| 2 | BAA09g02890 | A09 | 1820688 | T | G | upstream_gene_variant | MODIFIER | c.-2655T>G| |
S264 |
| 3 | BAA09g02890 | A09 | 1820873 | G | A | upstream_gene_variant | MODIFIER | c.-2470G>A| |
S207 |
| 4 | BAA09g02890 | A09 | 1821270 | G | A | upstream_gene_variant | MODIFIER | c.-2073G>A| |
S159 S243 |
| 5 | BAA09g02890 | A09 | 1821672 | G | A | upstream_gene_variant | MODIFIER | c.-1671G>A| |
S4 |
| 6 | BAA09g02890 | A09 | 1822814 | C | T | upstream_gene_variant | MODIFIER | c.-529C>T| |
S293 |
| 7 | BAA09g02890 | A09 | 1824156 | G | A | missense_variant | MODERATE | c.490G>A|p.Val164Ile |
S149 |
| 8 | BAA09g02890 | A09 | 1824528 | C | T | missense_variant&splice_region_variant | MODERATE | c.680C>T|p.Ala227Val |
S140 |
| 9 | BAA09g02890 | A09 | 1824534 | C | T | missense_variant | MODERATE | c.686C>T|p.Ser229Phe |
S128 |