| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g36990 | A09 | 45165714 | C | T | missense_variant | MODERATE | c.419G>A|p.Arg140Gln |
S188 |
| 2 | BAA09g36990 | A09 | 45165877 | A | T | missense_variant | MODERATE | c.256T>A|p.Tyr86Asn |
S119 |
| 3 | BAA09g36990 | A09 | 45169498 | C | T | upstream_gene_variant | MODIFIER | c.-2815G>A| |
S109 |
| 4 | BAA09g36990 | A09 | 45169634 | C | T | upstream_gene_variant | MODIFIER | c.-2951G>A| |
S265 |
| 5 | BAA09g36990 | A09 | 45169676 | C | T | upstream_gene_variant | MODIFIER | c.-2993G>A| |
S293 |
| 6 | BAA09g36990 | A09 | 45170229 | C | T | upstream_gene_variant | MODIFIER | c.-3546G>A| |
S275 |
| 7 | BAA09g36990 | A09 | 45170549 | C | T | upstream_gene_variant | MODIFIER | c.-3866G>A| |
S32 |
| 8 | BAA09g36990 | A09 | 45170550 | C | T | upstream_gene_variant | MODIFIER | c.-3867G>A| |
S229 |
| 9 | BAA09g36990 | A09 | 45171375 | G | A | upstream_gene_variant | MODIFIER | c.-4692C>T| |
S35 |