Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29300 | A02 | 16748756 | C | T | missense_variant | MODERATE | c.2272G>A|p.Ala758Thr |
S178 |
2 | BAA02g29300 | A02 | 16749774 | G | A | synonymous_variant | LOW | c.1797C>T|p.Cys599Cys |
S80 |
3 | BAA02g29300 | A02 | 16751828 | G | A | splice_region_variant&intron_variant | LOW | c.226-6C>T| |
S74 |
4 | BAA02g29300 | A02 | 16752472 | G | A | upstream_gene_variant | MODIFIER | c.-350C>T| |
S191 |
5 | BAA02g29300 | A02 | 16752491 | G | A | upstream_gene_variant | MODIFIER | c.-369C>T| |
S197 |
6 | BAA02g29300 | A02 | 16752619 | G | A | upstream_gene_variant | MODIFIER | c.-497C>T| |
S45 |
7 | BAA02g29300 | A02 | 16753765 | G | A | upstream_gene_variant | MODIFIER | c.-1643C>T| |
S12 |
8 | BAA02g29300 | A02 | 16753832 | C | T | upstream_gene_variant | MODIFIER | c.-1710G>A| |
S100 |
9 | BAA02g29300 | A02 | 16753989 | G | A | upstream_gene_variant | MODIFIER | c.-1867C>T| |
S7 |
10 | BAA02g29300 | A02 | 16754079 | C | T | upstream_gene_variant | MODIFIER | c.-1957G>A| |
S11 |