Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12000 | A01 | 5601983 | G | A | missense_variant | MODERATE | c.1103C>T|p.Ser368Phe |
S96 |
2 | BAA01g12000 | A01 | 5605484 | G | A | synonymous_variant | LOW | c.177C>T|p.Cys59Cys |
S144 |
3 | BAA01g12000 | A01 | 5605709 | C | T | missense_variant | MODERATE | c.106G>A|p.Val36Ile |
S244 |
4 | BAA01g12000 | A01 | 5607151 | C | T | upstream_gene_variant | MODIFIER | c.-1337G>A| |
S16 |
5 | BAA01g12000 | A01 | 5609058 | G | A | upstream_gene_variant | MODIFIER | c.-3244C>T| |
S301 S304 |
6 | BAA01g12000 | A01 | 5609117 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S240 |