Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15560 | A02 | 7516857 | C | T | synonymous_variant | LOW | c.207G>A|p.Arg69Arg |
S266 |
2 | BAA02g15560 | A02 | 7517035 | C | T | missense_variant | MODERATE | c.112G>A|p.Asp38Asn |
S1 S90 |
3 | BAA02g15560 | A02 | 7518223 | G | A | upstream_gene_variant | MODIFIER | c.-869C>T| |
S57 |
4 | BAA02g15560 | A02 | 7518533 | C | T | upstream_gene_variant | MODIFIER | c.-1179G>A| |
S208 S219 |
5 | BAA02g15560 | A02 | 7519283 | G | A | upstream_gene_variant | MODIFIER | c.-1929C>T| |
S111 |
6 | BAA02g15560 | A02 | 7519724 | C | T | upstream_gene_variant | MODIFIER | c.-2370G>A| |
S130 |
7 | BAA02g15560 | A02 | 7521501 | G | A | upstream_gene_variant | MODIFIER | c.-4147C>T| |
S158 |