Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47660 | A09 | 51833855 | G | A | missense_variant | MODERATE | c.302C>T|p.Ala101Val |
S128 |
2 | BAA09g47660 | A09 | 51834166 | G | A | upstream_gene_variant | MODIFIER | c.-10C>T| |
S82 S92 |
3 | BAA09g47660 | A09 | 51834360 | C | T | upstream_gene_variant | MODIFIER | c.-204G>A| |
S52 |
4 | BAA09g47660 | A09 | 51834453 | G | A | upstream_gene_variant | MODIFIER | c.-297C>T| |
S298 |
5 | BAA09g47660 | A09 | 51834616 | C | T | upstream_gene_variant | MODIFIER | c.-460G>A| |
S206 S26 |
6 | BAA09g47660 | A09 | 51834856 | C | T | upstream_gene_variant | MODIFIER | c.-700G>A| |
S260 |
7 | BAA09g47660 | A09 | 51836067 | C | T | upstream_gene_variant | MODIFIER | c.-1911G>A| |
S55 |
8 | BAA09g47660 | A09 | 51837694 | C | T | upstream_gene_variant | MODIFIER | c.-3538G>A| |
S81 S85 |
9 | BAA09g47660 | A09 | 51837769 | C | T | upstream_gene_variant | MODIFIER | c.-3613G>A| |
S17 |