Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g16790 | A03 | 7309629 | C | T | downstream_gene_variant | MODIFIER | c.*395G>A| |
S80 |
2 | BAA03g16790 | A03 | 7310013 | G | A | downstream_gene_variant | MODIFIER | c.*11C>T| |
S218 |
3 | BAA03g16790 | A03 | 7310899 | G | A | missense_variant | MODERATE | c.562C>T|p.Pro188Ser |
S192 |
4 | BAA03g16790 | A03 | 7313252 | G | A | intron_variant | MODIFIER | c.299+208C>T| |
S64 |
5 | BAA03g16790 | A03 | 7315984 | C | T | upstream_gene_variant | MODIFIER | c.-2226G>A| |
S207 |
6 | BAA03g16790 | A03 | 7317525 | C | T | upstream_gene_variant | MODIFIER | c.-3767G>A| |
S120 |
7 | BAA03g16790 | A03 | 7317803 | C | T | upstream_gene_variant | MODIFIER | c.-4045G>A| |
S187 |
8 | BAA03g16790 | A03 | 7318462 | G | A | upstream_gene_variant | MODIFIER | c.-4704C>T| |
S251 |
9 | BAA03g16790 | A03 | 7318655 | C | T | upstream_gene_variant | MODIFIER | c.-4897G>A| |
S187 |