Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12940 | A02 | 5780962 | G | A | upstream_gene_variant | MODIFIER | c.-4755G>A| |
S205 |
2 | BAA02g12940 | A02 | 5781176 | G | A | upstream_gene_variant | MODIFIER | c.-4541G>A| |
S105 S106 |
3 | BAA02g12940 | A02 | 5781720 | G | A | upstream_gene_variant | MODIFIER | c.-3997G>A| |
S282 |
4 | BAA02g12940 | A02 | 5781852 | G | A | upstream_gene_variant | MODIFIER | c.-3865G>A| |
S190 |
5 | BAA02g12940 | A02 | 5782496 | G | A | upstream_gene_variant | MODIFIER | c.-3221G>A| |
S104 S108 S109 S158 S208 S308 S76 S79 S85 S87 S89 S91 S93 S95 S96 S97 S99 |
6 | BAA02g12940 | A02 | 5784604 | G | A | upstream_gene_variant | MODIFIER | c.-1113G>A| |
S43 |
7 | BAA02g12940 | A02 | 5785071 | G | A | upstream_gene_variant | MODIFIER | c.-646G>A| |
S223 |
8 | BAA02g12940 | A02 | 5786599 | G | A | stop_gained | HIGH | c.417G>A|p.Trp139* |
S132 S137 S138 S215 S237 S288 S89 |
9 | BAA02g12940 | A02 | 5786708 | G | A | missense_variant | MODERATE | c.526G>A|p.Glu176Lys |
S7 |