Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08900 | A02 | 3938889 | G | A | upstream_gene_variant | MODIFIER | c.-2726G>A| |
S125 |
2 | BAA02g08900 | A02 | 3940851 | G | A | upstream_gene_variant | MODIFIER | c.-764G>A| |
S156 |
3 | BAA02g08900 | A02 | 3941769 | C | T | missense_variant | MODERATE | c.155C>T|p.Ser52Leu |
S47 |
4 | BAA02g08900 | A02 | 3941843 | C | T | missense_variant | MODERATE | c.229C>T|p.Leu77Phe |
S172 |
5 | BAA02g08900 | A02 | 3941991 | C | T | missense_variant | MODERATE | c.377C>T|p.Ala126Val |
S6 |