Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18230 | A02 | 9190085 | G | A | intron_variant | MODIFIER | c.122-389G>A| |
S95 |
2 | BAA02g18230 | A02 | 9190351 | C | T | intron_variant | MODIFIER | c.122-123C>T| |
S201 |
3 | BAA02g18230 | A02 | 9191014 | G | A | missense_variant | MODERATE | c.571G>A|p.Glu191Lys |
S297 |
4 | BAA02g18230 | A02 | 9191110 | G | A | missense_variant | MODERATE | c.667G>A|p.Glu223Lys |
S156 |
5 | BAA02g18230 | A02 | 9191380 | G | A | downstream_gene_variant | MODIFIER | c.*187G>A| |
S153 S213 |
6 | BAA02g18230 | A02 | 9191631 | G | A | downstream_gene_variant | MODIFIER | c.*438G>A| |
S148 S210 S30 S31 |
7 | BAA02g18230 | A02 | 9192021 | G | A | downstream_gene_variant | MODIFIER | c.*828G>A| |
S60 |
8 | BAA02g18230 | A02 | 9194462 | C | T | downstream_gene_variant | MODIFIER | c.*3269C>T| |
S182 |