Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20540 | A01 | 10134903 | G | A | upstream_gene_variant | MODIFIER | c.-4842G>A| |
S237 |
2 | BAA01g20540 | A01 | 10134986 | G | A | upstream_gene_variant | MODIFIER | c.-4759G>A| |
S116 |
3 | BAA01g20540 | A01 | 10135229 | G | A | upstream_gene_variant | MODIFIER | c.-4516G>A| |
S173 |
4 | BAA01g20540 | A01 | 10135347 | C | T | upstream_gene_variant | MODIFIER | c.-4398C>T| |
S70 |
5 | BAA01g20540 | A01 | 10136651 | C | T | upstream_gene_variant | MODIFIER | c.-3094C>T| |
S291 |
6 | BAA01g20540 | A01 | 10137835 | C | T | upstream_gene_variant | MODIFIER | c.-1910C>T| |
S179 |
7 | BAA01g20540 | A01 | 10138017 | C | T | upstream_gene_variant | MODIFIER | c.-1728C>T| |
S166 |
8 | BAA01g20540 | A01 | 10139302 | G | A | upstream_gene_variant | MODIFIER | c.-443G>A| |
S175 |
9 | BAA01g20540 | A01 | 10139979 | C | T | missense_variant | MODERATE | c.235C>T|p.Leu79Phe |
S177 |
10 | BAA01g20540 | A01 | 10140110 | C | T | synonymous_variant | LOW | c.366C>T|p.His122His |
S54 |
11 | BAA01g20540 | A01 | 10140903 | C | T | missense_variant | MODERATE | c.1159C>T|p.Pro387Ser |
S179 |
12 | BAA01g20540 | A01 | 10143994 | C | T | downstream_gene_variant | MODIFIER | c.*2717C>T| |
S270 |
13 | BAA01g20540 | A01 | 10144007 | G | A | downstream_gene_variant | MODIFIER | c.*2730G>A| |
S239 |
14 | BAA01g20540 | A01 | 10145056 | G | A | downstream_gene_variant | MODIFIER | c.*3779G>A| |
S244 |