Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05890 | A01 | 2642665 | C | T | missense_variant | MODERATE | c.905G>A|p.Ser302Asn |
S270 |
2 | BAA01g05890 | A01 | 2642676 | C | T | synonymous_variant | LOW | c.894G>A|p.Glu298Glu |
S97 |
3 | BAA01g05890 | A01 | 2642823 | C | T | synonymous_variant | LOW | c.747G>A|p.Thr249Thr |
S291 |
4 | BAA01g05890 | A01 | 2643763 | C | T | upstream_gene_variant | MODIFIER | c.-42G>A| |
S155 S211 |
5 | BAA01g05890 | A01 | 2644149 | G | A | upstream_gene_variant | MODIFIER | c.-428C>T| |
S149 |
6 | BAA01g05890 | A01 | 2646289 | G | A | upstream_gene_variant | MODIFIER | c.-2568C>T| |
S193 |
7 | BAA01g05890 | A01 | 2647047 | G | A | upstream_gene_variant | MODIFIER | c.-3326C>T| |
S6 |
8 | BAA01g05890 | A01 | 2647762 | C | T | upstream_gene_variant | MODIFIER | c.-4041G>A| |
S294 |