Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37990 | A02 | 32457064 | G | A | upstream_gene_variant | MODIFIER | c.-4064G>A| |
S134 |
2 | BAA02g37990 | A02 | 32457397 | C | T | upstream_gene_variant | MODIFIER | c.-3731C>T| |
S16 |
3 | BAA02g37990 | A02 | 32458736 | T | C | upstream_gene_variant | MODIFIER | c.-2392T>C| |
S54 |
4 | BAA02g37990 | A02 | 32461088 | C | T | upstream_gene_variant | MODIFIER | c.-40C>T| |
S266 S65 |
5 | BAA02g37990 | A02 | 32461227 | C | T | stop_gained | HIGH | c.100C>T|p.Gln34* |
S179 |
6 | BAA02g37990 | A02 | 32461619 | C | T | intron_variant | MODIFIER | c.200-85C>T| |
S262 |
7 | BAA02g37990 | A02 | 32462204 | C | T | missense_variant | MODERATE | c.700C>T|p.Arg234Trp |
S18 |
8 | BAA02g37990 | A02 | 32463017 | C | T | missense_variant | MODERATE | c.1112C>T|p.Ala371Val |
S66 |
9 | BAA02g37990 | A02 | 32463086 | G | A | missense_variant | MODERATE | c.1181G>A|p.Gly394Asp |
S11 |
10 | BAA02g37990 | A02 | 32463276 | G | A | downstream_gene_variant | MODIFIER | c.*102G>A| |
S190 |