Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26660 | A09 | 17357786 | C | T | upstream_gene_variant | MODIFIER | c.-2976C>T| |
S276 |
2 | BAA09g26660 | A09 | 17357967 | G | A | upstream_gene_variant | MODIFIER | c.-2795G>A| |
S149 |
3 | BAA09g26660 | A09 | 17357994 | G | A | upstream_gene_variant | MODIFIER | c.-2768G>A| |
S98 |
4 | BAA09g26660 | A09 | 17358131 | G | A | upstream_gene_variant | MODIFIER | c.-2631G>A| |
S237 |
5 | BAA09g26660 | A09 | 17358182 | C | T | upstream_gene_variant | MODIFIER | c.-2580C>T| |
S30 S31 |
6 | BAA09g26660 | A09 | 17358185 | C | T | upstream_gene_variant | MODIFIER | c.-2577C>T| |
S160 |
7 | BAA09g26660 | A09 | 17358236 | C | T | upstream_gene_variant | MODIFIER | c.-2526C>T| |
S193 |
8 | BAA09g26660 | A09 | 17358400 | C | T | upstream_gene_variant | MODIFIER | c.-2362C>T| |
S6 |
9 | BAA09g26660 | A09 | 17358464 | G | A | upstream_gene_variant | MODIFIER | c.-2298G>A| |
S134 |
10 | BAA09g26660 | A09 | 17361947 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.510-1G>A| |
S229 |