Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35650 | A09 | 44039273 | G | A | downstream_gene_variant | MODIFIER | c.*2079C>T| |
S125 |
2 | BAA09g35650 | A09 | 44041548 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1422-1G>A| |
S206 S26 |
3 | BAA09g35650 | A09 | 44044334 | G | A | upstream_gene_variant | MODIFIER | c.-171C>T| |
S134 |
4 | BAA09g35650 | A09 | 44047909 | G | A | upstream_gene_variant | MODIFIER | c.-3746C>T| |
S201 |
5 | BAA09g35650 | A09 | 44048039 | C | T | upstream_gene_variant | MODIFIER | c.-3876G>A| |
S36 |
6 | BAA09g35650 | A09 | 44048097 | G | A | upstream_gene_variant | MODIFIER | c.-3934C>T| |
S236 |
7 | BAA09g35650 | A09 | 44048441 | C | T | upstream_gene_variant | MODIFIER | c.-4278G>A| |
S92 |
8 | BAA09g35650 | A09 | 44048598 | G | A | upstream_gene_variant | MODIFIER | c.-4435C>T| |
S161 |
9 | BAA09g35650 | A09 | 44048794 | G | A | upstream_gene_variant | MODIFIER | c.-4631C>T| |
S170 |