Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50690 | A09 | 53450011 | C | T | downstream_gene_variant | MODIFIER | c.*3782G>A| |
S176 |
2 | BAA09g50690 | A09 | 53453798 | C | T | missense_variant | MODERATE | c.1183G>A|p.Gly395Arg |
S64 |
3 | BAA09g50690 | A09 | 53457618 | G | A | synonymous_variant | LOW | c.567C>T|p.Gly189Gly |
S32 |
4 | BAA09g50690 | A09 | 53460576 | G | A | upstream_gene_variant | MODIFIER | c.-897C>T| |
S167 |
5 | BAA09g50690 | A09 | 53460660 | G | A | upstream_gene_variant | MODIFIER | c.-981C>T| |
S172 S217 |
6 | BAA09g50690 | A09 | 53460786 | C | T | upstream_gene_variant | MODIFIER | c.-1107G>A| |
S170 |
7 | BAA09g50690 | A09 | 53463747 | C | T | upstream_gene_variant | MODIFIER | c.-4068G>A| |
S297 |