Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09060 | A05 | 4532866 | G | A | upstream_gene_variant | MODIFIER | c.-4137G>A| |
S257 |
2 | BAA05g09060 | A05 | 4533302 | C | T | upstream_gene_variant | MODIFIER | c.-3701C>T| |
S172 S217 |
3 | BAA05g09060 | A05 | 4533544 | G | A | upstream_gene_variant | MODIFIER | c.-3459G>A| |
S23 |
4 | BAA05g09060 | A05 | 4533890 | C | T | upstream_gene_variant | MODIFIER | c.-3113C>T| |
S251 |
5 | BAA05g09060 | A05 | 4534090 | G | A | upstream_gene_variant | MODIFIER | c.-2913G>A| |
S298 |
6 | BAA05g09060 | A05 | 4535159 | C | T | upstream_gene_variant | MODIFIER | c.-1844C>T| |
S255 |
7 | BAA05g09060 | A05 | 4535326 | C | T | upstream_gene_variant | MODIFIER | c.-1677C>T| |
S35 |
8 | BAA05g09060 | A05 | 4537600 | C | T | missense_variant | MODERATE | c.434C>T|p.Ala145Val |
S203 |
9 | BAA05g09060 | A05 | 4538995 | C | T | downstream_gene_variant | MODIFIER | c.*650C>T| |
S82 S92 |
10 | BAA05g09060 | A05 | 4539497 | C | T | downstream_gene_variant | MODIFIER | c.*1152C>T| |
S249 |
11 | BAA05g09060 | A05 | 4540954 | C | T | downstream_gene_variant | MODIFIER | c.*2609C>T| |
S191 S281 |