Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46640 | A02 | 37866705 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.296-1G>A| |
S179 |
2 | BAA02g46640 | A02 | 37867192 | G | A | splice_region_variant&intron_variant | LOW | c.69+6C>T| |
S155 |
3 | BAA02g46640 | A02 | 37867579 | C | T | upstream_gene_variant | MODIFIER | c.-313G>A| |
S42 |
4 | BAA02g46640 | A02 | 37869295 | G | A | upstream_gene_variant | MODIFIER | c.-2029C>T| |
S302 |
5 | BAA02g46640 | A02 | 37870434 | G | A | upstream_gene_variant | MODIFIER | c.-3168C>T| |
S281 |
6 | BAA02g46640 | A02 | 37870564 | C | T | upstream_gene_variant | MODIFIER | c.-3298G>A| |
S271 |
7 | BAA02g46640 | A02 | 37871623 | C | T | upstream_gene_variant | MODIFIER | c.-4357G>A| |
S270 |
8 | BAA02g46640 | A02 | 37871712 | C | T | upstream_gene_variant | MODIFIER | c.-4446G>A| |
S40 S49 |
9 | BAA02g46640 | A02 | 37871777 | G | A | upstream_gene_variant | MODIFIER | c.-4511C>T| |
S231 |
10 | BAA02g46640 | A02 | 37871921 | G | A | upstream_gene_variant | MODIFIER | c.-4655C>T| |
S207 |