Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15120 | A02 | 7237584 | G | A | downstream_gene_variant | MODIFIER | c.*1200C>T| |
S41 |
2 | BAA02g15120 | A02 | 7239189 | G | A | intron_variant | MODIFIER | c.777+28C>T| |
S297 |
3 | BAA02g15120 | A02 | 7239522 | G | A | synonymous_variant | LOW | c.564C>T|p.Thr188Thr |
S187 |
4 | BAA02g15120 | A02 | 7239942 | G | A | intron_variant | MODIFIER | c.399-255C>T| |
S12 |
5 | BAA02g15120 | A02 | 7240436 | G | A | missense_variant | MODERATE | c.211C>T|p.Pro71Ser |
S122 |
6 | BAA02g15120 | A02 | 7240564 | G | A | missense_variant | MODERATE | c.83C>T|p.Ala28Val |
S187 |
7 | BAA02g15120 | A02 | 7240697 | G | A | upstream_gene_variant | MODIFIER | c.-51C>T| |
S2 |
8 | BAA02g15120 | A02 | 7240807 | G | A | upstream_gene_variant | MODIFIER | c.-161C>T| |
S188 |
9 | BAA02g15120 | A02 | 7240838 | G | A | upstream_gene_variant | MODIFIER | c.-192C>T| |
S256 |
10 | BAA02g15120 | A02 | 7242978 | G | A | upstream_gene_variant | MODIFIER | c.-2332C>T| |
S245 |
11 | BAA02g15120 | A02 | 7243052 | C | T | upstream_gene_variant | MODIFIER | c.-2406G>A| |
S63 |
12 | BAA02g15120 | A02 | 7243498 | C | T | upstream_gene_variant | MODIFIER | c.-2852G>A| |
S244 |
13 | BAA02g15120 | A02 | 7245382 | C | T | upstream_gene_variant | MODIFIER | c.-4736G>A| |
S124 |