Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12060 | A01 | 5634528 | C | T | upstream_gene_variant | MODIFIER | c.-4933C>T| |
S42 |
2 | BAA01g12060 | A01 | 5635463 | G | A | upstream_gene_variant | MODIFIER | c.-3998G>A| |
S23 |
3 | BAA01g12060 | A01 | 5635698 | G | A | upstream_gene_variant | MODIFIER | c.-3763G>A| |
S23 |
4 | BAA01g12060 | A01 | 5635796 | C | T | upstream_gene_variant | MODIFIER | c.-3665C>T| |
S296 |
5 | BAA01g12060 | A01 | 5637335 | G | A | upstream_gene_variant | MODIFIER | c.-2126G>A| |
S180 |
6 | BAA01g12060 | A01 | 5638061 | C | T | upstream_gene_variant | MODIFIER | c.-1400C>T| |
S112 |
7 | BAA01g12060 | A01 | 5638275 | G | A | upstream_gene_variant | MODIFIER | c.-1186G>A| |
S13 |
8 | BAA01g12060 | A01 | 5639126 | C | T | upstream_gene_variant | MODIFIER | c.-335C>T| |
S86 |
9 | BAA01g12060 | A01 | 5639533 | C | T | missense_variant | MODERATE | c.73C>T|p.Pro25Ser |
S189 |