Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g01460 | A01 | 662020 | G | A | downstream_gene_variant | MODIFIER | c.*2041C>T| |
S131 |
2 | BAA01g01460 | A01 | 662471 | C | T | downstream_gene_variant | MODIFIER | c.*1590G>A| |
S56 |
3 | BAA01g01460 | A01 | 662813 | G | A | downstream_gene_variant | MODIFIER | c.*1248C>T| |
S13 |
4 | BAA01g01460 | A01 | 663431 | C | T | downstream_gene_variant | MODIFIER | c.*630G>A| |
S100 |
5 | BAA01g01460 | A01 | 664000 | C | T | downstream_gene_variant | MODIFIER | c.*61G>A| |
S121 |
6 | BAA01g01460 | A01 | 664153 | C | T | missense_variant | MODERATE | c.796G>A|p.Asp266Asn |
S81 S85 |
7 | BAA01g01460 | A01 | 665828 | C | T | upstream_gene_variant | MODIFIER | c.-880G>A| |
S8 |
8 | BAA01g01460 | A01 | 665915 | G | T | upstream_gene_variant | MODIFIER | c.-967C>A| |
S263 |
9 | BAA01g01460 | A01 | 666821 | G | A | upstream_gene_variant | MODIFIER | c.-1873C>T| |
S17 |
10 | BAA01g01460 | A01 | 667808 | C | T | upstream_gene_variant | MODIFIER | c.-2860G>A| |
S1 S90 |
11 | BAA01g01460 | A01 | 667923 | G | A | upstream_gene_variant | MODIFIER | c.-2975C>T| |
S260 |
12 | BAA01g01460 | A01 | 668754 | G | A | upstream_gene_variant | MODIFIER | c.-3806C>T| |
S142 |