Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10440 | A05 | 5299797 | C | T | downstream_gene_variant | MODIFIER | c.*1973G>A| |
S157 |
2 | BAA05g10440 | A05 | 5300682 | C | T | downstream_gene_variant | MODIFIER | c.*1088G>A| |
S201 |
3 | BAA05g10440 | A05 | 5300693 | G | A | downstream_gene_variant | MODIFIER | c.*1077C>T| |
S246 |
4 | BAA05g10440 | A05 | 5301861 | C | T | missense_variant | MODERATE | c.176G>A|p.Arg59Gln |
S142 |
5 | BAA05g10440 | A05 | 5302247 | G | A | upstream_gene_variant | MODIFIER | c.-211C>T| |
S284 |
6 | BAA05g10440 | A05 | 5302528 | C | T | upstream_gene_variant | MODIFIER | c.-492G>A| |
S193 |
7 | BAA05g10440 | A05 | 5302578 | C | T | upstream_gene_variant | MODIFIER | c.-542G>A| |
S52 |
8 | BAA05g10440 | A05 | 5302653 | C | T | upstream_gene_variant | MODIFIER | c.-617G>A| |
S164 |
9 | BAA05g10440 | A05 | 5302695 | C | T | upstream_gene_variant | MODIFIER | c.-659G>A| |
S188 |
10 | BAA05g10440 | A05 | 5302787 | C | T | upstream_gene_variant | MODIFIER | c.-751G>A| |
S142 |
11 | BAA05g10440 | A05 | 5304505 | C | T | upstream_gene_variant | MODIFIER | c.-2469G>A| |
|
12 | BAA05g10440 | A05 | 5304570 | C | T | upstream_gene_variant | MODIFIER | c.-2534G>A| |
S273 |
13 | BAA05g10440 | A05 | 5306290 | C | T | upstream_gene_variant | MODIFIER | c.-4254G>A| |
S234 |