Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20870 | A02 | 11093146 | C | T | upstream_gene_variant | MODIFIER | c.-3457C>T| |
S284 |
2 | BAA02g20870 | A02 | 11093193 | G | A | upstream_gene_variant | MODIFIER | c.-3410G>A| |
S202 |
3 | BAA02g20870 | A02 | 11093546 | G | A | upstream_gene_variant | MODIFIER | c.-3057G>A| |
S278 |
4 | BAA02g20870 | A02 | 11093775 | G | A | upstream_gene_variant | MODIFIER | c.-2828G>A| |
S32 |
5 | BAA02g20870 | A02 | 11094662 | C | T | upstream_gene_variant | MODIFIER | c.-1941C>T| |
S18 |
6 | BAA02g20870 | A02 | 11095189 | G | A | upstream_gene_variant | MODIFIER | c.-1414G>A| |
S86 |
7 | BAA02g20870 | A02 | 11095587 | G | A | upstream_gene_variant | MODIFIER | c.-1016G>A| |
S282 |
8 | BAA02g20870 | A02 | 11096346 | G | A | upstream_gene_variant | MODIFIER | c.-257G>A| |
S288 |
9 | BAA02g20870 | A02 | 11096813 | C | T | splice_region_variant&intron_variant | LOW | c.25-7C>T| |
S255 |
10 | BAA02g20870 | A02 | 11096819 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.25-1G>A| |
S4 |
11 | BAA02g20870 | A02 | 11097976 | C | T | missense_variant | MODERATE | c.677C>T|p.Thr226Ile |
S208 |
12 | BAA02g20870 | A02 | 11099475 | C | T | missense_variant | MODERATE | c.2176C>T|p.Leu726Phe |
S211 |