Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08460 | A05 | 4208118 | G | A | missense_variant | MODERATE | c.368C>T|p.Ala123Val |
S150 |
2 | BAA05g08460 | A05 | 4209910 | G | A | upstream_gene_variant | MODIFIER | c.-1425C>T| |
S6 |
3 | BAA05g08460 | A05 | 4210913 | C | T | upstream_gene_variant | MODIFIER | c.-2428G>A| |
S51 |
4 | BAA05g08460 | A05 | 4211652 | C | T | upstream_gene_variant | MODIFIER | c.-3167G>A| |
S50 |
5 | BAA05g08460 | A05 | 4212404 | G | A | upstream_gene_variant | MODIFIER | c.-3919C>T| |
S48 |