Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17870 | A02 | 8936171 | G | A | downstream_gene_variant | MODIFIER | c.*2149C>T| |
S53 |
2 | BAA02g17870 | A02 | 8936690 | G | A | downstream_gene_variant | MODIFIER | c.*1630C>T| |
S157 |
3 | BAA02g17870 | A02 | 8939949 | G | A | missense_variant | MODERATE | c.802C>T|p.Pro268Ser |
S247 |
4 | BAA02g17870 | A02 | 8941904 | G | A | missense_variant | MODERATE | c.310C>T|p.Pro104Ser |
S48 |
5 | BAA02g17870 | A02 | 8944195 | G | A | upstream_gene_variant | MODIFIER | c.-1982C>T| |
S111 |
6 | BAA02g17870 | A02 | 8944631 | G | A | upstream_gene_variant | MODIFIER | c.-2418C>T| |
S126 |
7 | BAA02g17870 | A02 | 8944913 | C | T | upstream_gene_variant | MODIFIER | c.-2700G>A| |
S79 |
8 | BAA02g17870 | A02 | 8945027 | C | A | upstream_gene_variant | MODIFIER | c.-2814G>T| |
S33 |
9 | BAA02g17870 | A02 | 8945173 | C | T | upstream_gene_variant | MODIFIER | c.-2960G>A| |
S238 |