Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01920 | A02 | 845692 | C | T | upstream_gene_variant | MODIFIER | c.-4967C>T| |
S182 |
2 | BAA02g01920 | A02 | 849140 | G | A | upstream_gene_variant | MODIFIER | c.-1519G>A| |
S156 |
3 | BAA02g01920 | A02 | 851807 | G | A | missense_variant | MODERATE | c.781G>A|p.Glu261Lys |
S50 |
4 | BAA02g01920 | A02 | 851876 | T | A | missense_variant | MODERATE | c.850T>A|p.Phe284Ile |
S73 S91 |
5 | BAA02g01920 | A02 | 852093 | G | A | missense_variant | MODERATE | c.977G>A|p.Gly326Glu |
S308 |
6 | BAA02g01920 | A02 | 852459 | C | T | missense_variant | MODERATE | c.1183C>T|p.Pro395Ser |
S221 |