Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01660 | A02 | 741681 | C | T | splice_region_variant&intron_variant | LOW | c.321+6G>A| |
S212 |
2 | BAA02g01660 | A02 | 744345 | G | A | upstream_gene_variant | MODIFIER | c.-2241C>T| |
S235 |
3 | BAA02g01660 | A02 | 745001 | C | T | upstream_gene_variant | MODIFIER | c.-2897G>A| |
S46 |
4 | BAA02g01660 | A02 | 745466 | C | T | upstream_gene_variant | MODIFIER | c.-3362G>A| |
S255 |