Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12500 | A02 | 5615055 | G | A | missense_variant | MODERATE | c.1226C>T|p.Ser409Phe |
S68 |
2 | BAA02g12500 | A02 | 5616756 | C | T | upstream_gene_variant | MODIFIER | c.-84G>A| |
S55 |
3 | BAA02g12500 | A02 | 5616790 | G | A | upstream_gene_variant | MODIFIER | c.-118C>T| |
S166 |
4 | BAA02g12500 | A02 | 5617546 | G | A | upstream_gene_variant | MODIFIER | c.-874C>T| |
S269 |
5 | BAA02g12500 | A02 | 5617607 | G | A | upstream_gene_variant | MODIFIER | c.-935C>T| |
S23 |
6 | BAA02g12500 | A02 | 5619585 | G | A | upstream_gene_variant | MODIFIER | c.-2913C>T| |
S37 |
7 | BAA02g12500 | A02 | 5619964 | C | T | upstream_gene_variant | MODIFIER | c.-3292G>A| |
S234 |
8 | BAA02g12500 | A02 | 5620927 | C | T | upstream_gene_variant | MODIFIER | c.-4255G>A| |
S70 |
9 | BAA02g12500 | A02 | 5621605 | G | A | upstream_gene_variant | MODIFIER | c.-4933C>T| |
S17 |