Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41270 | A02 | 34634794 | C | T | downstream_gene_variant | MODIFIER | c.*2996G>A| |
S42 |
2 | BAA02g41270 | A02 | 34638268 | G | A | missense_variant | MODERATE | c.518C>T|p.Ala173Val |
S26 |
3 | BAA02g41270 | A02 | 34638654 | G | A | synonymous_variant | LOW | c.132C>T|p.Ile44Ile |
S161 |
4 | BAA02g41270 | A02 | 34639359 | G | A | upstream_gene_variant | MODIFIER | c.-574C>T| |
S148 |
5 | BAA02g41270 | A02 | 34641006 | C | T | upstream_gene_variant | MODIFIER | c.-2221G>A| |
S272 |
6 | BAA02g41270 | A02 | 34642385 | C | T | upstream_gene_variant | MODIFIER | c.-3600G>A| |
S135 |
7 | BAA02g41270 | A02 | 34642498 | G | A | upstream_gene_variant | MODIFIER | c.-3713C>T| |
S201 |
8 | BAA02g41270 | A02 | 34643385 | C | T | upstream_gene_variant | MODIFIER | c.-4600G>A| |
S32 |
9 | BAA02g41270 | A02 | 34643574 | C | T | upstream_gene_variant | MODIFIER | c.-4789G>A| |
S208 S219 |