Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28590 | A02 | 16066828 | C | T | missense_variant | MODERATE | c.1615G>A|p.Asp539Asn |
S157 S163 |
2 | BAA02g28590 | A02 | 16068787 | G | A | intron_variant | MODIFIER | c.338-124C>T| |
S236 |
3 | BAA02g28590 | A02 | 16069062 | G | A | missense_variant | MODERATE | c.220C>T|p.Arg74Trp |
S188 |
4 | BAA02g28590 | A02 | 16069101 | G | A | stop_gained | HIGH | c.181C>T|p.Gln61* |
S204 |
5 | BAA02g28590 | A02 | 16070098 | C | T | upstream_gene_variant | MODIFIER | c.-817G>A| |
S194 |
6 | BAA02g28590 | A02 | 16070251 | C | T | upstream_gene_variant | MODIFIER | c.-970G>A| |
S25 S264 |
7 | BAA02g28590 | A02 | 16070893 | C | T | upstream_gene_variant | MODIFIER | c.-1612G>A| |
S305 |
8 | BAA02g28590 | A02 | 16071259 | C | T | upstream_gene_variant | MODIFIER | c.-1978G>A| |
S234 |
9 | BAA02g28590 | A02 | 16071277 | C | T | upstream_gene_variant | MODIFIER | c.-1996G>A| |
S76 |
10 | BAA02g28590 | A02 | 16072366 | G | A | upstream_gene_variant | MODIFIER | c.-3085C>T| |
S47 |