Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01800 | A02 | 791157 | C | T | stop_gained&splice_region_variant | HIGH | c.510G>A|p.Trp170* |
S251 |
2 | BAA02g01800 | A02 | 791967 | C | T | missense_variant | MODERATE | c.181G>A|p.Gly61Arg |
S18 |
3 | BAA02g01800 | A02 | 796398 | G | A | upstream_gene_variant | MODIFIER | c.-4176C>T| |
S293 |
4 | BAA02g01800 | A02 | 796865 | G | A | upstream_gene_variant | MODIFIER | c.-4643C>T| |
S188 |