Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19170 | A02 | 9954981 | G | A | upstream_gene_variant | MODIFIER | c.-2234G>A| |
S150 |
2 | BAA02g19170 | A02 | 9955667 | A | C | upstream_gene_variant | MODIFIER | c.-1548A>C| |
S272 |
3 | BAA02g19170 | A02 | 9956093 | G | A | upstream_gene_variant | MODIFIER | c.-1122G>A| |
S295 |
4 | BAA02g19170 | A02 | 9957126 | C | T | upstream_gene_variant | MODIFIER | c.-89C>T| |
S167 |
5 | BAA02g19170 | A02 | 9957493 | G | A | synonymous_variant | LOW | c.279G>A|p.Glu93Glu |
S20 |
6 | BAA02g19170 | A02 | 9957586 | G | A | synonymous_variant | LOW | c.372G>A|p.Pro124Pro |
S282 |
7 | BAA02g19170 | A02 | 9957810 | G | A | missense_variant | MODERATE | c.596G>A|p.Arg199Gln |
S98 |
8 | BAA02g19170 | A02 | 9962112 | G | A | downstream_gene_variant | MODIFIER | c.*4082G>A| |
S126 |
9 | BAA02g19170 | A02 | 9962332 | C | T | downstream_gene_variant | MODIFIER | c.*4302C>T| |
S219 |