Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44230 | A02 | 36499379 | C | T | downstream_gene_variant | MODIFIER | c.*977G>A| |
S64 |
2 | BAA02g44230 | A02 | 36500685 | G | A | splice_region_variant&intron_variant | LOW | c.1441-8C>T| |
S247 |
3 | BAA02g44230 | A02 | 36502129 | C | T | missense_variant | MODERATE | c.947G>A|p.Arg316Lys |
S173 |
4 | BAA02g44230 | A02 | 36503202 | C | T | missense_variant | MODERATE | c.517G>A|p.Ala173Thr |
S202 |
5 | BAA02g44230 | A02 | 36504632 | G | A | upstream_gene_variant | MODIFIER | c.-627C>T| |
S70 |
6 | BAA02g44230 | A02 | 36504878 | C | T | upstream_gene_variant | MODIFIER | c.-873G>A| |
S249 |
7 | BAA02g44230 | A02 | 36504936 | C | T | upstream_gene_variant | MODIFIER | c.-931G>A| |
S39 |
8 | BAA02g44230 | A02 | 36505034 | A | T | upstream_gene_variant | MODIFIER | c.-1029T>A| |
S247 |
9 | BAA02g44230 | A02 | 36506168 | C | T | upstream_gene_variant | MODIFIER | c.-2163G>A| |
S308 |
10 | BAA02g44230 | A02 | 36508422 | C | T | upstream_gene_variant | MODIFIER | c.-4417G>A| |
S283 |
11 | BAA02g44230 | A02 | 36508627 | C | T | upstream_gene_variant | MODIFIER | c.-4622G>A| |
S63 |