Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25420 | A02 | 13920112 | G | A | downstream_gene_variant | MODIFIER | c.*119C>T| |
S110 |
2 | BAA02g25420 | A02 | 13921232 | G | A | intron_variant | MODIFIER | c.480+152C>T| |
S155 |
3 | BAA02g25420 | A02 | 13921656 | C | T | missense_variant | MODERATE | c.208G>A|p.Ala70Thr |
S286 |
4 | BAA02g25420 | A02 | 13922005 | C | T | synonymous_variant | LOW | c.87G>A|p.Pro29Pro |
S142 |
5 | BAA02g25420 | A02 | 13922434 | C | T | upstream_gene_variant | MODIFIER | c.-343G>A| |
S121 |
6 | BAA02g25420 | A02 | 13922879 | G | A | upstream_gene_variant | MODIFIER | c.-788C>T| |
S35 |
7 | BAA02g25420 | A02 | 13924102 | C | T | upstream_gene_variant | MODIFIER | c.-2011G>A| |
S283 |
8 | BAA02g25420 | A02 | 13924170 | C | T | upstream_gene_variant | MODIFIER | c.-2079G>A| |
S142 |
9 | BAA02g25420 | A02 | 13924420 | G | A | upstream_gene_variant | MODIFIER | c.-2329C>T| |
S89 |
10 | BAA02g25420 | A02 | 13926414 | G | A | upstream_gene_variant | MODIFIER | c.-4323C>T| |
S250 S291 |