Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28500 | A01 | 17581159 | C | T | downstream_gene_variant | MODIFIER | c.*2520G>A| |
S170 |
2 | BAA01g28500 | A01 | 17583133 | G | A | downstream_gene_variant | MODIFIER | c.*546C>T| |
S149 |
3 | BAA01g28500 | A01 | 17585174 | C | T | synonymous_variant | LOW | c.1692G>A|p.Leu564Leu |
S56 |
4 | BAA01g28500 | A01 | 17585368 | G | A | missense_variant | MODERATE | c.1571C>T|p.Pro524Leu |
S116 |
5 | BAA01g28500 | A01 | 17585437 | G | A | missense_variant | MODERATE | c.1502C>T|p.Ala501Val |
S155 S211 |
6 | BAA01g28500 | A01 | 17586687 | C | T | splice_donor_variant&intron_variant | HIGH | c.679+1G>A| |
S293 |
7 | BAA01g28500 | A01 | 17586717 | G | A | missense_variant | MODERATE | c.650C>T|p.Pro217Leu |
S114 |
8 | BAA01g28500 | A01 | 17587204 | C | T | missense_variant | MODERATE | c.355G>A|p.Ala119Thr |
S42 |
9 | BAA01g28500 | A01 | 17589758 | C | T | upstream_gene_variant | MODIFIER | c.-2113G>A| |
S56 |
10 | BAA01g28500 | A01 | 17590998 | G | A | upstream_gene_variant | MODIFIER | c.-3353C>T| |
S197 |
11 | BAA01g28500 | A01 | 17591147 | C | T | upstream_gene_variant | MODIFIER | c.-3502G>A| |
S189 |