Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44950 | A01 | 30006009 | C | T | downstream_gene_variant | MODIFIER | c.*2237G>A| |
S193 |
2 | BAA01g44950 | A01 | 30007393 | G | A | downstream_gene_variant | MODIFIER | c.*853C>T| |
S224 |
3 | BAA01g44950 | A01 | 30007700 | C | T | downstream_gene_variant | MODIFIER | c.*546G>A| |
S125 S178 S234 S28 |
4 | BAA01g44950 | A01 | 30009893 | C | T | missense_variant | MODERATE | c.175G>A|p.Glu59Lys |
S17 |
5 | BAA01g44950 | A01 | 30010216 | C | T | missense_variant | MODERATE | c.103G>A|p.Glu35Lys |
S219 S72 |
6 | BAA01g44950 | A01 | 30012199 | C | T | upstream_gene_variant | MODIFIER | c.-1881G>A| |
S12 |
7 | BAA01g44950 | A01 | 30012348 | C | T | upstream_gene_variant | MODIFIER | c.-2030G>A| |
S205 |
8 | BAA01g44950 | A01 | 30014131 | G | A | upstream_gene_variant | MODIFIER | c.-3813C>T| |
S121 |
9 | BAA01g44950 | A01 | 30014834 | C | T | upstream_gene_variant | MODIFIER | c.-4516G>A| |
S229 |