| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g16960 | A09 | 10076400 | G | A | upstream_gene_variant | MODIFIER | c.-2233G>A| |
S189 |
| 2 | BAA09g16960 | A09 | 10077131 | C | T | upstream_gene_variant | MODIFIER | c.-1502C>T| |
S153 |
| 3 | BAA09g16960 | A09 | 10077133 | A | C | upstream_gene_variant | MODIFIER | c.-1500A>C| |
S276 |
| 4 | BAA09g16960 | A09 | 10077302 | C | T | upstream_gene_variant | MODIFIER | c.-1331C>T| |
S28 |
| 5 | BAA09g16960 | A09 | 10078480 | G | A | upstream_gene_variant | MODIFIER | c.-153G>A| |
S302 |
| 6 | BAA09g16960 | A09 | 10078972 | G | A | missense_variant | MODERATE | c.340G>A|p.Gly114Arg |
S184 |
| 7 | BAA09g16960 | A09 | 10079911 | G | A | missense_variant | MODERATE | c.1279G>A|p.Val427Ile |
S225 S73 |
| 8 | BAA09g16960 | A09 | 10079930 | C | T | missense_variant | MODERATE | c.1298C>T|p.Thr433Ile |
S212 |