Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09430 | A02 | 4150854 | G | A | missense_variant | MODERATE | c.2707C>T|p.Leu903Phe |
S232 |
2 | BAA02g09430 | A02 | 4151574 | G | A | missense_variant | MODERATE | c.1987C>T|p.Arg663Cys |
S96 |
3 | BAA02g09430 | A02 | 4151696 | G | A | missense_variant | MODERATE | c.1865C>T|p.Ser622Phe |
S146 |
4 | BAA02g09430 | A02 | 4151867 | G | A | missense_variant | MODERATE | c.1777C>T|p.Pro593Ser |
S302 |
5 | BAA02g09430 | A02 | 4152906 | C | T | missense_variant | MODERATE | c.1375G>A|p.Asp459Asn |
S130 |
6 | BAA02g09430 | A02 | 4153787 | C | T | missense_variant | MODERATE | c.718G>A|p.Glu240Lys |
S179 |
7 | BAA02g09430 | A02 | 4155593 | G | A | upstream_gene_variant | MODIFIER | c.-269C>T| |
S92 |
8 | BAA02g09430 | A02 | 4156556 | C | T | upstream_gene_variant | MODIFIER | c.-1232G>A| |
S13 |
9 | BAA02g09430 | A02 | 4157004 | G | A | upstream_gene_variant | MODIFIER | c.-1680C>T| |
S166 |
10 | BAA02g09430 | A02 | 4157376 | G | A | upstream_gene_variant | MODIFIER | c.-2052C>T| |
S260 |
11 | BAA02g09430 | A02 | 4157684 | G | A | upstream_gene_variant | MODIFIER | c.-2360C>T| |
S125 |
12 | BAA02g09430 | A02 | 4157726 | G | A | upstream_gene_variant | MODIFIER | c.-2402C>T| |
S150 |
13 | BAA02g09430 | A02 | 4157891 | G | A | upstream_gene_variant | MODIFIER | c.-2567C>T| |
S68 |
14 | BAA02g09430 | A02 | 4158122 | G | A | upstream_gene_variant | MODIFIER | c.-2798C>T| |
S303 |
15 | BAA02g09430 | A02 | 4158878 | G | A | upstream_gene_variant | MODIFIER | c.-3554C>T| |
S189 |