Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10120 | A09 | 5581697 | C | T | missense_variant | MODERATE | c.82G>A|p.Asp28Asn |
S36 |
2 | BAA09g10120 | A09 | 5582406 | G | A | upstream_gene_variant | MODIFIER | c.-628C>T| |
S236 |
3 | BAA09g10120 | A09 | 5582791 | C | T | upstream_gene_variant | MODIFIER | c.-1013G>A| |
S135 |
4 | BAA09g10120 | A09 | 5584113 | G | A | upstream_gene_variant | MODIFIER | c.-2335C>T| |
S296 |
5 | BAA09g10120 | A09 | 5584624 | C | T | upstream_gene_variant | MODIFIER | c.-2846G>A| |
S70 |
6 | BAA09g10120 | A09 | 5584801 | C | T | upstream_gene_variant | MODIFIER | c.-3023G>A| |
S19 |
7 | BAA09g10120 | A09 | 5586185 | C | T | upstream_gene_variant | MODIFIER | c.-4407G>A| |
S107 |
8 | BAA09g10120 | A09 | 5586484 | G | A | upstream_gene_variant | MODIFIER | c.-4706C>T| |
S185 |
9 | BAA09g10120 | A09 | 5586680 | G | A | upstream_gene_variant | MODIFIER | c.-4902C>T| |
S100 |