Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g31380 | A02 | 18850372 | C | T | stop_gained | HIGH | c.141G>A|p.Trp47* |
S266 |
2 | BAA02g31380 | A02 | 18850440 | G | A | intron_variant | MODIFIER | c.103-30C>T| |
S256 |
3 | BAA02g31380 | A02 | 18850660 | G | A | missense_variant | MODERATE | c.53C>T|p.Ser18Phe |
S41 |
4 | BAA02g31380 | A02 | 18851101 | C | T | upstream_gene_variant | MODIFIER | c.-389G>A| |
S49 |
5 | BAA02g31380 | A02 | 18851493 | G | A | upstream_gene_variant | MODIFIER | c.-781C>T| |
S174 |
6 | BAA02g31380 | A02 | 18851613 | C | T | upstream_gene_variant | MODIFIER | c.-901G>A| |
S138 |
7 | BAA02g31380 | A02 | 18853614 | G | A | upstream_gene_variant | MODIFIER | c.-2902C>T| |
S217 |
8 | BAA02g31380 | A02 | 18853626 | C | T | upstream_gene_variant | MODIFIER | c.-2914G>A| |
S162 |
9 | BAA02g31380 | A02 | 18854013 | C | T | upstream_gene_variant | MODIFIER | c.-3301G>A| |
S100 |
10 | BAA02g31380 | A02 | 18854815 | C | T | upstream_gene_variant | MODIFIER | c.-4103G>A| |
S212 |
11 | BAA02g31380 | A02 | 18855222 | C | T | upstream_gene_variant | MODIFIER | c.-4510G>A| |
S202 |