| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g25000 | A08 | 18140784 | C | T | missense_variant | MODERATE | c.184C>T|p.Pro62Ser |
S213 |
| 2 | BAA08g25000 | A08 | 18140915 | G | A | missense_variant | MODERATE | c.236G>A|p.Arg79Lys |
S306 S308 |
| 3 | BAA08g25000 | A08 | 18141221 | G | A | intron_variant | MODIFIER | c.415-42G>A| |
S182 |
| 4 | BAA08g25000 | A08 | 18141654 | G | A | intron_variant | MODIFIER | c.619-36G>A| |
S150 |
| 5 | BAA08g25000 | A08 | 18142342 | C | T | downstream_gene_variant | MODIFIER | c.*292C>T| |
S11 |
| 6 | BAA08g25000 | A08 | 18143206 | G | A | downstream_gene_variant | MODIFIER | c.*1156G>A| |
S161 |
| 7 | BAA08g25000 | A08 | 18143350 | G | A | downstream_gene_variant | MODIFIER | c.*1300G>A| |
S115 |
| 8 | BAA08g25000 | A08 | 18143996 | C | T | downstream_gene_variant | MODIFIER | c.*1946C>T| |
S226 |
| 9 | BAA08g25000 | A08 | 18144607 | C | T | downstream_gene_variant | MODIFIER | c.*2557C>T| |
S168 |
| 10 | BAA08g25000 | A08 | 18146477 | G | A | downstream_gene_variant | MODIFIER | c.*4427G>A| |
S273 |