Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44460 | A02 | 36615235 | C | T | downstream_gene_variant | MODIFIER | c.*858G>A| |
S122 |
2 | BAA02g44460 | A02 | 36615821 | G | T | downstream_gene_variant | MODIFIER | c.*272C>A| |
S207 |
3 | BAA02g44460 | A02 | 36616587 | G | A | missense_variant | MODERATE | c.29C>T|p.Pro10Leu |
S103 |
4 | BAA02g44460 | A02 | 36616687 | C | T | upstream_gene_variant | MODIFIER | c.-72G>A| |
S13 |
5 | BAA02g44460 | A02 | 36616946 | G | A | upstream_gene_variant | MODIFIER | c.-331C>T| |
S305 |
6 | BAA02g44460 | A02 | 36617419 | C | T | upstream_gene_variant | MODIFIER | c.-804G>A| |
S107 |
7 | BAA02g44460 | A02 | 36618122 | C | T | upstream_gene_variant | MODIFIER | c.-1507G>A| |
S263 |
8 | BAA02g44460 | A02 | 36618583 | C | T | upstream_gene_variant | MODIFIER | c.-1968G>A| |
S226 |
9 | BAA02g44460 | A02 | 36618711 | C | T | upstream_gene_variant | MODIFIER | c.-2096G>A| |
S212 S69 |
10 | BAA02g44460 | A02 | 36619259 | G | A | upstream_gene_variant | MODIFIER | c.-2644C>T| |
S297 |
11 | BAA02g44460 | A02 | 36619809 | C | T | upstream_gene_variant | MODIFIER | c.-3194G>A| |
S259 |
12 | BAA02g44460 | A02 | 36621386 | A | G | upstream_gene_variant | MODIFIER | c.-4771T>C| |
S1 |
13 | BAA02g44460 | A02 | 36621541 | C | T | upstream_gene_variant | MODIFIER | c.-4926G>A| |
S1 S90 |