Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34060 | A02 | 29194233 | G | A | missense_variant | MODERATE | c.523C>T|p.Arg175Trp |
S104 S52 |
2 | BAA02g34060 | A02 | 29195060 | C | T | missense_variant | MODERATE | c.172G>A|p.Val58Ile |
S249 |
3 | BAA02g34060 | A02 | 29195647 | G | A | upstream_gene_variant | MODIFIER | c.-416C>T| |
S45 |
4 | BAA02g34060 | A02 | 29195893 | C | T | upstream_gene_variant | MODIFIER | c.-662G>A| |
S179 |
5 | BAA02g34060 | A02 | 29196023 | C | T | upstream_gene_variant | MODIFIER | c.-792G>A| |
S255 |
6 | BAA02g34060 | A02 | 29196197 | C | T | upstream_gene_variant | MODIFIER | c.-966G>A| |
S202 |
7 | BAA02g34060 | A02 | 29196307 | C | T | upstream_gene_variant | MODIFIER | c.-1076G>A| |
S78 |
8 | BAA02g34060 | A02 | 29196567 | G | A | upstream_gene_variant | MODIFIER | c.-1336C>T| |
S34 |
9 | BAA02g34060 | A02 | 29198212 | G | A | upstream_gene_variant | MODIFIER | c.-2981C>T| |
S10 |