Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g06020 | A01 | 2698218 | G | A | upstream_gene_variant | MODIFIER | c.-4207G>A| |
S262 |
2 | BAA01g06020 | A01 | 2698688 | G | A | upstream_gene_variant | MODIFIER | c.-3737G>A| |
S105 S106 |
3 | BAA01g06020 | A01 | 2698926 | C | T | upstream_gene_variant | MODIFIER | c.-3499C>T| |
S119 |
4 | BAA01g06020 | A01 | 2699902 | C | T | upstream_gene_variant | MODIFIER | c.-2523C>T| |
S238 |
5 | BAA01g06020 | A01 | 2700057 | G | A | upstream_gene_variant | MODIFIER | c.-2368G>A| |
S202 |
6 | BAA01g06020 | A01 | 2700802 | G | A | upstream_gene_variant | MODIFIER | c.-1623G>A| |
S162 |
7 | BAA01g06020 | A01 | 2701007 | G | A | upstream_gene_variant | MODIFIER | c.-1418G>A| |
S28 |
8 | BAA01g06020 | A01 | 2701326 | C | T | upstream_gene_variant | MODIFIER | c.-1099C>T| |
S47 |
9 | BAA01g06020 | A01 | 2701984 | C | T | upstream_gene_variant | MODIFIER | c.-441C>T| |
S246 |
10 | BAA01g06020 | A01 | 2704384 | G | A | missense_variant | MODERATE | c.769G>A|p.Val257Ile |
S208 S219 |