Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26900 | A02 | 15064885 | C | T | synonymous_variant | LOW | c.1266G>A|p.Val422Val |
S140 |
2 | BAA02g26900 | A02 | 15065044 | C | T | synonymous_variant | LOW | c.1182G>A|p.Lys394Lys |
S255 |
3 | BAA02g26900 | A02 | 15065104 | G | A | synonymous_variant | LOW | c.1122C>T|p.Ile374Ile |
S149 |
4 | BAA02g26900 | A02 | 15065168 | C | T | missense_variant | MODERATE | c.1058G>A|p.Arg353Lys |
S242 |
5 | BAA02g26900 | A02 | 15065177 | G | A | missense_variant | MODERATE | c.1049C>T|p.Ser350Phe |
S271 |
6 | BAA02g26900 | A02 | 15066902 | G | A | upstream_gene_variant | MODIFIER | c.-511C>T| |
S64 |
7 | BAA02g26900 | A02 | 15067184 | G | A | upstream_gene_variant | MODIFIER | c.-793C>T| |
S132 S137 S138 S215 S288 |