Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26850 | A02 | 15042579 | G | A | downstream_gene_variant | MODIFIER | c.*2455C>T| |
S241 |
2 | BAA02g26850 | A02 | 15045547 | C | T | missense_variant | MODERATE | c.302G>A|p.Ser101Asn |
S16 |
3 | BAA02g26850 | A02 | 15046357 | G | A | upstream_gene_variant | MODIFIER | c.-327C>T| |
S80 |
4 | BAA02g26850 | A02 | 15046656 | G | A | upstream_gene_variant | MODIFIER | c.-626C>T| |
S291 |
5 | BAA02g26850 | A02 | 15046728 | G | A | upstream_gene_variant | MODIFIER | c.-698C>T| |
S240 |
6 | BAA02g26850 | A02 | 15047827 | G | A | upstream_gene_variant | MODIFIER | c.-1797C>T| |
S165 |
7 | BAA02g26850 | A02 | 15048167 | C | T | upstream_gene_variant | MODIFIER | c.-2137G>A| |
S117 |
8 | BAA02g26850 | A02 | 15049819 | G | A | upstream_gene_variant | MODIFIER | c.-3789C>T| |
S94 |
9 | BAA02g26850 | A02 | 15049924 | C | T | upstream_gene_variant | MODIFIER | c.-3894G>A| |
S42 |