Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01890 | A02 | 827929 | C | T | missense_variant | MODERATE | c.401G>A|p.Gly134Asp |
S159 |
2 | BAA02g01890 | A02 | 828886 | G | A | upstream_gene_variant | MODIFIER | c.-414C>T| |
S52 |
3 | BAA02g01890 | A02 | 828958 | C | T | upstream_gene_variant | MODIFIER | c.-486G>A| |
S94 |
4 | BAA02g01890 | A02 | 829065 | C | T | upstream_gene_variant | MODIFIER | c.-593G>A| |
S65 |
5 | BAA02g01890 | A02 | 829646 | C | T | upstream_gene_variant | MODIFIER | c.-1174G>A| |
S118 |
6 | BAA02g01890 | A02 | 829705 | G | A | upstream_gene_variant | MODIFIER | c.-1233C>T| |
S59 |
7 | BAA02g01890 | A02 | 830629 | C | T | upstream_gene_variant | MODIFIER | c.-2157G>A| |
S165 |
8 | BAA02g01890 | A02 | 830653 | C | T | upstream_gene_variant | MODIFIER | c.-2181G>A| |
S33 |
9 | BAA02g01890 | A02 | 831365 | G | A | upstream_gene_variant | MODIFIER | c.-2893C>T| |
S302 |