Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g32000 | A01 | 20964812 | C | T | missense_variant | MODERATE | c.205G>A|p.Asp69Asn |
S275 |
2 | BAA01g32000 | A01 | 20966086 | C | T | upstream_gene_variant | MODIFIER | c.-551G>A| |
S96 |
3 | BAA01g32000 | A01 | 20966618 | G | A | upstream_gene_variant | MODIFIER | c.-1083C>T| |
S176 |
4 | BAA01g32000 | A01 | 20968128 | G | A | upstream_gene_variant | MODIFIER | c.-2593C>T| |
S116 |
5 | BAA01g32000 | A01 | 20968861 | C | T | upstream_gene_variant | MODIFIER | c.-3326G>A| |
S26 |
6 | BAA01g32000 | A01 | 20970082 | C | T | upstream_gene_variant | MODIFIER | c.-4547G>A| |
S165 |
7 | BAA01g32000 | A01 | 20970342 | C | T | upstream_gene_variant | MODIFIER | c.-4807G>A| |
S273 |