Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44630 | A09 | 50199526 | C | T | synonymous_variant | LOW | c.228G>A|p.Arg76Arg |
S183 |
2 | BAA09g44630 | A09 | 50199794 | G | A | missense_variant | MODERATE | c.50C>T|p.Ala17Val |
S75 |
3 | BAA09g44630 | A09 | 50202701 | G | A | upstream_gene_variant | MODIFIER | c.-2858C>T| |
S171 |
4 | BAA09g44630 | A09 | 50202748 | C | T | upstream_gene_variant | MODIFIER | c.-2905G>A| |
S295 |
5 | BAA09g44630 | A09 | 50203164 | C | T | upstream_gene_variant | MODIFIER | c.-3321G>A| |
S182 |
6 | BAA09g44630 | A09 | 50203774 | G | A | upstream_gene_variant | MODIFIER | c.-3931C>T| |
S177 |
7 | BAA09g44630 | A09 | 50204342 | C | T | upstream_gene_variant | MODIFIER | c.-4499G>A| |
S282 |
8 | BAA09g44630 | A09 | 50204698 | G | A | upstream_gene_variant | MODIFIER | c.-4855C>T| |
S158 |
9 | BAA09g44630 | A09 | 50204723 | C | T | upstream_gene_variant | MODIFIER | c.-4880G>A| |
S138 |