Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09150 | A02 | 4045954 | G | A | missense_variant | MODERATE | c.932C>T|p.Ser311Phe |
S176 |
2 | BAA02g09150 | A02 | 4047104 | C | T | missense_variant | MODERATE | c.281G>A|p.Gly94Glu |
S242 |
3 | BAA02g09150 | A02 | 4050692 | G | A | upstream_gene_variant | MODIFIER | c.-3190C>T| |
S235 |
4 | BAA02g09150 | A02 | 4050780 | G | A | upstream_gene_variant | MODIFIER | c.-3278C>T| |
S17 |
5 | BAA02g09150 | A02 | 4050800 | G | A | upstream_gene_variant | MODIFIER | c.-3298C>T| |
S164 |
6 | BAA02g09150 | A02 | 4052026 | G | A | upstream_gene_variant | MODIFIER | c.-4524C>T| |
S269 |