Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02140 | A02 | 965898 | C | T | synonymous_variant | LOW | c.204G>A|p.Ser68Ser |
S135 |
2 | BAA02g02140 | A02 | 966229 | C | T | missense_variant | MODERATE | c.97G>A|p.Ala33Thr |
S104 |
3 | BAA02g02140 | A02 | 966490 | G | A | upstream_gene_variant | MODIFIER | c.-92C>T| |
S5 |
4 | BAA02g02140 | A02 | 968132 | G | A | upstream_gene_variant | MODIFIER | c.-1734C>T| |
S265 |
5 | BAA02g02140 | A02 | 968320 | G | A | upstream_gene_variant | MODIFIER | c.-1922C>T| |
S166 |
6 | BAA02g02140 | A02 | 969359 | G | A | upstream_gene_variant | MODIFIER | c.-2961C>T| |
S246 |