Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g04980 | A03 | 2093897 | G | A | upstream_gene_variant | MODIFIER | c.-4897G>A| |
S109 |
2 | BAA03g04980 | A03 | 2096243 | G | A | upstream_gene_variant | MODIFIER | c.-2551G>A| |
S167 |
3 | BAA03g04980 | A03 | 2096806 | C | T | upstream_gene_variant | MODIFIER | c.-1988C>T| |
S295 |
4 | BAA03g04980 | A03 | 2097452 | G | A | upstream_gene_variant | MODIFIER | c.-1342G>A| |
S103 |
5 | BAA03g04980 | A03 | 2097826 | C | T | upstream_gene_variant | MODIFIER | c.-968C>T| |
S219 S72 |
6 | BAA03g04980 | A03 | 2097869 | G | A | upstream_gene_variant | MODIFIER | c.-925G>A| |
S288 |
7 | BAA03g04980 | A03 | 2098739 | G | A | upstream_gene_variant | MODIFIER | c.-55G>A| |
S14 |
8 | BAA03g04980 | A03 | 2098763 | G | A | upstream_gene_variant | MODIFIER | c.-31G>A| |
S236 |
9 | BAA03g04980 | A03 | 2100750 | G | A | missense_variant | MODERATE | c.1084G>A|p.Val362Ile |
S89 |
10 | BAA03g04980 | A03 | 2103929 | G | A | downstream_gene_variant | MODIFIER | c.*1158G>A| |
S9 |