Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45440 | A02 | 37201661 | G | A | upstream_gene_variant | MODIFIER | c.-2867G>A| |
S70 |
2 | BAA02g45440 | A02 | 37201761 | G | A | upstream_gene_variant | MODIFIER | c.-2767G>A| |
S148 S210 S31 |
3 | BAA02g45440 | A02 | 37202093 | C | T | upstream_gene_variant | MODIFIER | c.-2435C>T| |
S135 |
4 | BAA02g45440 | A02 | 37202403 | C | T | upstream_gene_variant | MODIFIER | c.-2125C>T| |
S104 S52 |
5 | BAA02g45440 | A02 | 37204227 | G | A | upstream_gene_variant | MODIFIER | c.-301G>A| |
S226 |
6 | BAA02g45440 | A02 | 37204524 | G | A | upstream_gene_variant | MODIFIER | c.-4G>A| |
S261 |
7 | BAA02g45440 | A02 | 37205529 | G | A | missense_variant | MODERATE | c.527G>A|p.Gly176Glu |
S132 S137 S215 S89 |
8 | BAA02g45440 | A02 | 37206689 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.853-1G>A| |
S298 |
9 | BAA02g45440 | A02 | 37207344 | G | A | downstream_gene_variant | MODIFIER | c.*259G>A| |
S143 |
10 | BAA02g45440 | A02 | 37209904 | G | A | downstream_gene_variant | MODIFIER | c.*2819G>A| |
S288 |