| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g02930 | A08 | 2072571 | C | T | missense_variant | MODERATE | c.788G>A|p.Gly263Asp |
S42 |
| 2 | BAA08g02930 | A08 | 2073685 | G | A | missense_variant | MODERATE | c.46C>T|p.Leu16Phe |
S286 |
| 3 | BAA08g02930 | A08 | 2074640 | C | T | upstream_gene_variant | MODIFIER | c.-910G>A| |
S135 |
| 4 | BAA08g02930 | A08 | 2075401 | C | T | upstream_gene_variant | MODIFIER | c.-1671G>A| |
S289 S290 |
| 5 | BAA08g02930 | A08 | 2075543 | C | T | upstream_gene_variant | MODIFIER | c.-1813G>A| |
S173 |
| 6 | BAA08g02930 | A08 | 2075894 | C | T | upstream_gene_variant | MODIFIER | c.-2164G>A| |
S215 |
| 7 | BAA08g02930 | A08 | 2076320 | G | A | upstream_gene_variant | MODIFIER | c.-2590C>T| |
S273 |
| 8 | BAA08g02930 | A08 | 2076875 | T | C | upstream_gene_variant | MODIFIER | c.-3145A>G| |
S178 |
| 9 | BAA08g02930 | A08 | 2078079 | G | A | upstream_gene_variant | MODIFIER | c.-4349C>T| |
S290 |
| 10 | BAA08g02930 | A08 | 2078514 | C | T | upstream_gene_variant | MODIFIER | c.-4784G>A| |
S164 |