Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08080 | A05 | 4015247 | C | T | missense_variant | MODERATE | c.38G>A|p.Gly13Asp |
S191 |
2 | BAA05g08080 | A05 | 4016153 | A | T | upstream_gene_variant | MODIFIER | c.-869T>A| |
S204 |
3 | BAA05g08080 | A05 | 4018696 | G | A | upstream_gene_variant | MODIFIER | c.-3412C>T| |
S32 |
4 | BAA05g08080 | A05 | 4019417 | T | C | upstream_gene_variant | MODIFIER | c.-4133A>G| |
S43 |
5 | BAA05g08080 | A05 | 4019754 | C | T | upstream_gene_variant | MODIFIER | c.-4470G>A| |
S184 |
6 | BAA05g08080 | A05 | 4019922 | C | T | upstream_gene_variant | MODIFIER | c.-4638G>A| |
S17 |