Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g25770 | A10 | 20684296 | C | T | downstream_gene_variant | MODIFIER | c.*2355G>A| |
S286 |
2 | BAA10g25770 | A10 | 20685016 | C | T | downstream_gene_variant | MODIFIER | c.*1635G>A| |
S142 |
3 | BAA10g25770 | A10 | 20685855 | G | A | downstream_gene_variant | MODIFIER | c.*796C>T| |
S228 |
4 | BAA10g25770 | A10 | 20687214 | C | T | missense_variant | MODERATE | c.850G>A|p.Ala284Thr |
S96 |
5 | BAA10g25770 | A10 | 20688288 | G | A | missense_variant | MODERATE | c.187C>T|p.Pro63Ser |
S128 |
6 | BAA10g25770 | A10 | 20688859 | G | A | upstream_gene_variant | MODIFIER | c.-385C>T| |
S128 |