Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08080 | A02 | 3454114 | G | A | missense_variant | MODERATE | c.680C>T|p.Pro227Leu |
S201 |
2 | BAA02g08080 | A02 | 3454633 | G | A | synonymous_variant | LOW | c.417C>T|p.Arg139Arg |
S155 |
3 | BAA02g08080 | A02 | 3456849 | C | T | upstream_gene_variant | MODIFIER | c.-798G>A| |
S257 |
4 | BAA02g08080 | A02 | 3456907 | C | T | upstream_gene_variant | MODIFIER | c.-856G>A| |
S240 |
5 | BAA02g08080 | A02 | 3457025 | C | T | upstream_gene_variant | MODIFIER | c.-974G>A| |
S1 |
6 | BAA02g08080 | A02 | 3457126 | G | A | upstream_gene_variant | MODIFIER | c.-1075C>T| |
S86 |
7 | BAA02g08080 | A02 | 3458258 | C | T | upstream_gene_variant | MODIFIER | c.-2207G>A| |
S273 |
8 | BAA02g08080 | A02 | 3459856 | G | A | upstream_gene_variant | MODIFIER | c.-3805C>T| |
S168 |
9 | BAA02g08080 | A02 | 3460037 | C | T | upstream_gene_variant | MODIFIER | c.-3986G>A| |
S229 |