Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g04270 | A05 | 2066513 | T | G | missense_variant | MODERATE | c.1737A>C|p.Glu579Asp |
S145 S146 S160 S210 S255 S96 |
2 | BAA05g04270 | A05 | 2066543 | C | T | synonymous_variant | LOW | c.1707G>A|p.Gln569Gln |
S270 |
3 | BAA05g04270 | A05 | 2067027 | G | A | missense_variant | MODERATE | c.1223C>T|p.Thr408Ile |
S104 S105 S52 |
4 | BAA05g04270 | A05 | 2068613 | G | A | upstream_gene_variant | MODIFIER | c.-211C>T| |
S212 |
5 | BAA05g04270 | A05 | 2068799 | G | A | upstream_gene_variant | MODIFIER | c.-397C>T| |
S173 |
6 | BAA05g04270 | A05 | 2069454 | C | T | upstream_gene_variant | MODIFIER | c.-1052G>A| |
S159 S243 S299 |
7 | BAA05g04270 | A05 | 2072391 | G | A | upstream_gene_variant | MODIFIER | c.-3989C>T| |
S260 |