Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12150 | A01 | 5696613 | C | T | upstream_gene_variant | MODIFIER | c.-4969C>T| |
S219 |
2 | BAA01g12150 | A01 | 5696862 | C | T | upstream_gene_variant | MODIFIER | c.-4720C>T| |
S143 |
3 | BAA01g12150 | A01 | 5697128 | C | T | upstream_gene_variant | MODIFIER | c.-4454C>T| |
S54 |
4 | BAA01g12150 | A01 | 5698024 | G | A | upstream_gene_variant | MODIFIER | c.-3558G>A| |
S178 |
5 | BAA01g12150 | A01 | 5698633 | C | T | upstream_gene_variant | MODIFIER | c.-2949C>T| |
S211 S227 |
6 | BAA01g12150 | A01 | 5698645 | C | T | upstream_gene_variant | MODIFIER | c.-2937C>T| |
S295 |
7 | BAA01g12150 | A01 | 5698654 | C | T | upstream_gene_variant | MODIFIER | c.-2928C>T| |
S202 |
8 | BAA01g12150 | A01 | 5702959 | G | A | missense_variant | MODERATE | c.427G>A|p.Asp143Asn |
S197 |
9 | BAA01g12150 | A01 | 5706955 | G | A | downstream_gene_variant | MODIFIER | c.*3757G>A| |
S124 |
10 | BAA01g12150 | A01 | 5707851 | C | T | downstream_gene_variant | MODIFIER | c.*4653C>T| |
S289 S290 |