Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20080 | A10 | 18208641 | C | T | stop_gained | HIGH | c.396G>A|p.Trp132* |
S46 |
2 | BAA10g20080 | A10 | 18208672 | C | T | missense_variant | MODERATE | c.365G>A|p.Cys122Tyr |
S26 |
3 | BAA10g20080 | A10 | 18213215 | G | A | upstream_gene_variant | MODIFIER | c.-239C>T| |
S74 |
4 | BAA10g20080 | A10 | 18213435 | G | A | upstream_gene_variant | MODIFIER | c.-459C>T| |
S128 |
5 | BAA10g20080 | A10 | 18213494 | C | T | upstream_gene_variant | MODIFIER | c.-518G>A| |
S266 |
6 | BAA10g20080 | A10 | 18214191 | G | A | upstream_gene_variant | MODIFIER | c.-1215C>T| |
S208 S219 |
7 | BAA10g20080 | A10 | 18214327 | C | T | upstream_gene_variant | MODIFIER | c.-1351G>A| |
S189 |
8 | BAA10g20080 | A10 | 18215301 | C | T | upstream_gene_variant | MODIFIER | c.-2325G>A| |
S34 |
9 | BAA10g20080 | A10 | 18216616 | G | A | upstream_gene_variant | MODIFIER | c.-3640C>T| |
S182 |
10 | BAA10g20080 | A10 | 18216845 | G | A | upstream_gene_variant | MODIFIER | c.-3869C>T| |
S166 |
11 | BAA10g20080 | A10 | 18217639 | G | A | upstream_gene_variant | MODIFIER | c.-4663C>T| |
S179 |
12 | BAA10g20080 | A10 | 18217850 | G | T | upstream_gene_variant | MODIFIER | c.-4874C>A| |
|