Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15550 | A02 | 7512831 | C | T | upstream_gene_variant | MODIFIER | c.-1030C>T| |
S183 S198 |
2 | BAA02g15550 | A02 | 7513011 | C | T | upstream_gene_variant | MODIFIER | c.-850C>T| |
S246 |
3 | BAA02g15550 | A02 | 7513064 | G | A | upstream_gene_variant | MODIFIER | c.-797G>A| |
S168 |
4 | BAA02g15550 | A02 | 7513439 | G | A | upstream_gene_variant | MODIFIER | c.-422G>A| |
S133 |
5 | BAA02g15550 | A02 | 7513624 | G | A | upstream_gene_variant | MODIFIER | c.-237G>A| |
S206 |
6 | BAA02g15550 | A02 | 7513745 | G | A | upstream_gene_variant | MODIFIER | c.-116G>A| |
S295 |
7 | BAA02g15550 | A02 | 7514001 | C | T | synonymous_variant | LOW | c.141C>T|p.Leu47Leu |
S117 |
8 | BAA02g15550 | A02 | 7514036 | C | T | missense_variant | MODERATE | c.176C>T|p.Thr59Ile |
S5 |
9 | BAA02g15550 | A02 | 7515216 | C | T | missense_variant | MODERATE | c.998C>T|p.Pro333Leu |
S112 |
10 | BAA02g15550 | A02 | 7515560 | C | T | missense_variant | MODERATE | c.1342C>T|p.Pro448Ser |
S156 S34 |
11 | BAA02g15550 | A02 | 7515759 | G | A | missense_variant | MODERATE | c.1541G>A|p.Arg514Gln |
S190 |