Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07700 | A02 | 3304253 | G | A | missense_variant | MODERATE | c.485C>T|p.Ala162Val |
S122 |
2 | BAA02g07700 | A02 | 3305783 | C | T | upstream_gene_variant | MODIFIER | c.-1046G>A| |
S202 |
3 | BAA02g07700 | A02 | 3307149 | C | T | upstream_gene_variant | MODIFIER | c.-2412G>A| |
S252 |
4 | BAA02g07700 | A02 | 3308272 | C | T | upstream_gene_variant | MODIFIER | c.-3535G>A| |
S295 |
5 | BAA02g07700 | A02 | 3309384 | G | A | upstream_gene_variant | MODIFIER | c.-4647C>T| |
S239 |