Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22950 | A01 | 11683731 | C | T | missense_variant | MODERATE | c.641G>A|p.Gly214Glu |
S18 |
2 | BAA01g22950 | A01 | 11686140 | G | A | upstream_gene_variant | MODIFIER | c.-1244C>T| |
S280 |
3 | BAA01g22950 | A01 | 11686603 | C | T | upstream_gene_variant | MODIFIER | c.-1707G>A| |
S67 |
4 | BAA01g22950 | A01 | 11686829 | C | T | upstream_gene_variant | MODIFIER | c.-1933G>A| |
S62 |
5 | BAA01g22950 | A01 | 11687109 | C | T | upstream_gene_variant | MODIFIER | c.-2213G>A| |
S192 |
6 | BAA01g22950 | A01 | 11687488 | G | A | upstream_gene_variant | MODIFIER | c.-2592C>T| |
S28 |
7 | BAA01g22950 | A01 | 11688409 | A | T | upstream_gene_variant | MODIFIER | c.-3513T>A| |
S237 |
8 | BAA01g22950 | A01 | 11688636 | C | T | upstream_gene_variant | MODIFIER | c.-3740G>A| |
S113 |
9 | BAA01g22950 | A01 | 11689144 | G | A | upstream_gene_variant | MODIFIER | c.-4248C>T| |
S159 S243 |
10 | BAA01g22950 | A01 | 11689394 | C | T | upstream_gene_variant | MODIFIER | c.-4498G>A| |
S294 |