Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g23760 | A02 | 12944273 | C | T | intron_variant | MODIFIER | c.160-641C>T| |
S9 |
2 | BAA02g23760 | A02 | 12944402 | C | T | intron_variant | MODIFIER | c.160-512C>T| |
S208 S219 |
3 | BAA02g23760 | A02 | 12944670 | C | T | intron_variant | MODIFIER | c.160-244C>T| |
S250 |
4 | BAA02g23760 | A02 | 12944727 | C | T | intron_variant | MODIFIER | c.160-187C>T| |
S107 |
5 | BAA02g23760 | A02 | 12944897 | C | T | intron_variant | MODIFIER | c.160-17C>T| |
S32 |
6 | BAA02g23760 | A02 | 12945843 | G | A | downstream_gene_variant | MODIFIER | c.*705G>A| |
S34 |
7 | BAA02g23760 | A02 | 12946543 | C | T | downstream_gene_variant | MODIFIER | c.*1405C>T| |
S165 |
8 | BAA02g23760 | A02 | 12946918 | G | A | downstream_gene_variant | MODIFIER | c.*1780G>A| |
S143 |
9 | BAA02g23760 | A02 | 12947088 | G | A | downstream_gene_variant | MODIFIER | c.*1950G>A| |
S47 |
10 | BAA02g23760 | A02 | 12947283 | C | T | downstream_gene_variant | MODIFIER | c.*2145C>T| |
S226 |