Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06770 | A02 | 2905552 | C | T | missense_variant | MODERATE | c.995G>A|p.Ser332Asn |
S25 |
2 | BAA02g06770 | A02 | 2909129 | C | T | upstream_gene_variant | MODIFIER | c.-2098G>A| |
S152 |
3 | BAA02g06770 | A02 | 2910959 | C | T | upstream_gene_variant | MODIFIER | c.-3928G>A| |
S54 |
4 | BAA02g06770 | A02 | 2911037 | C | T | upstream_gene_variant | MODIFIER | c.-4006G>A| |
S208 S219 |
5 | BAA02g06770 | A02 | 2911095 | G | A | upstream_gene_variant | MODIFIER | c.-4064C>T| |
S131 |
6 | BAA02g06770 | A02 | 2911668 | G | A | upstream_gene_variant | MODIFIER | c.-4637C>T| |
S247 |
7 | BAA02g06770 | A02 | 2911783 | G | A | upstream_gene_variant | MODIFIER | c.-4752C>T| |
S52 |
8 | BAA02g06770 | A02 | 2911928 | G | A | upstream_gene_variant | MODIFIER | c.-4897C>T| |
S25 |