Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06980 | A02 | 2978261 | C | T | missense_variant | MODERATE | c.203C>T|p.Pro68Leu |
S243 |
2 | BAA02g06980 | A02 | 2978592 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.370-1G>A| |
S246 |
3 | BAA02g06980 | A02 | 2978683 | C | T | missense_variant | MODERATE | c.460C>T|p.Leu154Phe |
S78 |
4 | BAA02g06980 | A02 | 2982935 | C | T | downstream_gene_variant | MODIFIER | c.*3894C>T| |
S44 |
5 | BAA02g06980 | A02 | 2983358 | G | A | downstream_gene_variant | MODIFIER | c.*4317G>A| |
S297 |