Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28150 | A02 | 15841970 | C | T | upstream_gene_variant | MODIFIER | c.-3257C>T| |
S138 |
2 | BAA02g28150 | A02 | 15842403 | G | A | upstream_gene_variant | MODIFIER | c.-2824G>A| |
S239 |
3 | BAA02g28150 | A02 | 15843574 | G | A | upstream_gene_variant | MODIFIER | c.-1653G>A| |
S247 |
4 | BAA02g28150 | A02 | 15844048 | C | T | upstream_gene_variant | MODIFIER | c.-1179C>T| |
S303 |
5 | BAA02g28150 | A02 | 15844104 | C | T | upstream_gene_variant | MODIFIER | c.-1123C>T| |
S100 |
6 | BAA02g28150 | A02 | 15844405 | C | T | upstream_gene_variant | MODIFIER | c.-822C>T| |
S87 |
7 | BAA02g28150 | A02 | 15844950 | C | T | upstream_gene_variant | MODIFIER | c.-277C>T| |
S301 S304 |
8 | BAA02g28150 | A02 | 15845255 | C | T | missense_variant | MODERATE | c.29C>T|p.Ser10Phe |
S162 |
9 | BAA02g28150 | A02 | 15847651 | C | T | downstream_gene_variant | MODIFIER | c.*2047C>T| |
S168 |
10 | BAA02g28150 | A02 | 15847803 | C | T | downstream_gene_variant | MODIFIER | c.*2199C>T| |
S115 |
11 | BAA02g28150 | A02 | 15847852 | G | A | downstream_gene_variant | MODIFIER | c.*2248G>A| |
S237 |