Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35120 | A09 | 43505308 | C | T | missense_variant&splice_region_variant | MODERATE | c.1145G>A|p.Arg382His |
S260 |
2 | BAA09g35120 | A09 | 43505817 | C | T | missense_variant | MODERATE | c.713G>A|p.Cys238Tyr |
S296 |
3 | BAA09g35120 | A09 | 43507446 | C | T | upstream_gene_variant | MODIFIER | c.-303G>A| |
S302 |
4 | BAA09g35120 | A09 | 43507731 | G | A | upstream_gene_variant | MODIFIER | c.-588C>T| |
S161 |
5 | BAA09g35120 | A09 | 43508676 | C | T | upstream_gene_variant | MODIFIER | c.-1533G>A| |
S294 |
6 | BAA09g35120 | A09 | 43508786 | C | T | upstream_gene_variant | MODIFIER | c.-1643G>A| |
S208 |
7 | BAA09g35120 | A09 | 43509762 | C | T | upstream_gene_variant | MODIFIER | c.-2619G>A| |
S124 |
8 | BAA09g35120 | A09 | 43511066 | G | A | upstream_gene_variant | MODIFIER | c.-3923C>T| |
S10 |
9 | BAA09g35120 | A09 | 43511667 | G | A | upstream_gene_variant | MODIFIER | c.-4524C>T| |
S209 |