Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00010 | A01 | 250 | C | T | downstream_gene_variant | MODIFIER | c.*4237G>A| |
S252 |
2 | BAA01g00010 | A01 | 676 | C | T | downstream_gene_variant | MODIFIER | c.*3811G>A| |
S130 |
3 | BAA01g00010 | A01 | 959 | C | T | downstream_gene_variant | MODIFIER | c.*3528G>A| |
S166 |
4 | BAA01g00010 | A01 | 1281 | C | T | downstream_gene_variant | MODIFIER | c.*3206G>A| |
S107 |
5 | BAA01g00010 | A01 | 1782 | G | A | downstream_gene_variant | MODIFIER | c.*2705C>T| |
S30 S31 |
6 | BAA01g00010 | A01 | 5681 | C | T | missense_variant | MODERATE | c.562G>A|p.Glu188Lys |
S25 |
7 | BAA01g00010 | A01 | 5717 | G | A | missense_variant | MODERATE | c.526C>T|p.Leu176Phe |
S34 |
8 | BAA01g00010 | A01 | 5953 | G | A | synonymous_variant | LOW | c.373C>T|p.Leu125Leu |
S23 |
9 | BAA01g00010 | A01 | 6647 | G | A | upstream_gene_variant | MODIFIER | c.-161C>T| |
S289 S290 |
10 | BAA01g00010 | A01 | 9135 | G | A | upstream_gene_variant | MODIFIER | c.-2649C>T| |
S87 |
11 | BAA01g00010 | A01 | 10247 | G | A | upstream_gene_variant | MODIFIER | c.-3761C>T| |
S136 |