Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29880 | A02 | 17178904 | C | T | missense_variant | MODERATE | c.302G>A|p.Arg101Lys |
S246 |
2 | BAA02g29880 | A02 | 17178908 | C | T | missense_variant | MODERATE | c.298G>A|p.Glu100Lys |
S250 |
3 | BAA02g29880 | A02 | 17178909 | C | T | synonymous_variant | LOW | c.297G>A|p.Thr99Thr |
S113 |
4 | BAA02g29880 | A02 | 17179366 | G | A | upstream_gene_variant | MODIFIER | c.-63C>T| |
S25 |
5 | BAA02g29880 | A02 | 17179878 | G | A | upstream_gene_variant | MODIFIER | c.-575C>T| |
S302 |
6 | BAA02g29880 | A02 | 17181295 | G | A | upstream_gene_variant | MODIFIER | c.-1992C>T| |
S35 |
7 | BAA02g29880 | A02 | 17181576 | G | A | upstream_gene_variant | MODIFIER | c.-2273C>T| |
S287 |
8 | BAA02g29880 | A02 | 17182648 | C | T | upstream_gene_variant | MODIFIER | c.-3345G>A| |
S242 |
9 | BAA02g29880 | A02 | 17183641 | C | T | upstream_gene_variant | MODIFIER | c.-4338G>A| |
S226 |
10 | BAA02g29880 | A02 | 17183726 | C | T | upstream_gene_variant | MODIFIER | c.-4423G>A| |
S144 |
11 | BAA02g29880 | A02 | 17183896 | C | T | upstream_gene_variant | MODIFIER | c.-4593G>A| |
S51 |