Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28000 | A02 | 15770614 | C | T | synonymous_variant | LOW | c.1281G>A|p.Pro427Pro |
S202 |
2 | BAA02g28000 | A02 | 15772126 | G | A | missense_variant | MODERATE | c.628C>T|p.Leu210Phe |
S72 S78 |
3 | BAA02g28000 | A02 | 15772202 | G | A | synonymous_variant | LOW | c.552C>T|p.Ile184Ile |
S208 S219 |
4 | BAA02g28000 | A02 | 15773375 | G | A | upstream_gene_variant | MODIFIER | c.-406C>T| |
S196 S264 |
5 | BAA02g28000 | A02 | 15773488 | G | A | upstream_gene_variant | MODIFIER | c.-519C>T| |
S35 |
6 | BAA02g28000 | A02 | 15776245 | A | G | upstream_gene_variant | MODIFIER | c.-3276T>C| |
S226 |
7 | BAA02g28000 | A02 | 15776368 | C | T | upstream_gene_variant | MODIFIER | c.-3399G>A| |
S100 |
8 | BAA02g28000 | A02 | 15776517 | G | A | upstream_gene_variant | MODIFIER | c.-3548C>T| |
S76 |
9 | BAA02g28000 | A02 | 15777926 | C | T | upstream_gene_variant | MODIFIER | c.-4957G>A| |
S142 |