Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04660 | A02 | 2026177 | C | T | missense_variant | MODERATE | c.955G>A|p.Val319Met |
S207 |
2 | BAA02g04660 | A02 | 2026920 | C | T | missense_variant | MODERATE | c.212G>A|p.Ser71Asn |
S289 S290 |
3 | BAA02g04660 | A02 | 2027132 | C | T | upstream_gene_variant | MODIFIER | c.-1G>A| |
S287 |
4 | BAA02g04660 | A02 | 2027824 | G | A | upstream_gene_variant | MODIFIER | c.-693C>T| |
S261 |
5 | BAA02g04660 | A02 | 2030484 | C | T | upstream_gene_variant | MODIFIER | c.-3353G>A| |
S144 |