Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29780 | A02 | 17119090 | C | T | missense_variant | MODERATE | c.17G>A|p.Arg6His |
S177 |
2 | BAA02g29780 | A02 | 17120383 | G | C | upstream_gene_variant | MODIFIER | c.-1277C>G| |
S169 |
3 | BAA02g29780 | A02 | 17121926 | C | T | upstream_gene_variant | MODIFIER | c.-2820G>A| |
S88 |
4 | BAA02g29780 | A02 | 17122145 | A | T | upstream_gene_variant | MODIFIER | c.-3039T>A| |
S74 |
5 | BAA02g29780 | A02 | 17122194 | C | T | upstream_gene_variant | MODIFIER | c.-3088G>A| |
S83 S88 |
6 | BAA02g29780 | A02 | 17122797 | C | T | upstream_gene_variant | MODIFIER | c.-3691G>A| |
S287 |
7 | BAA02g29780 | A02 | 17123514 | C | T | upstream_gene_variant | MODIFIER | c.-4408G>A| |
S221 |
8 | BAA02g29780 | A02 | 17123792 | G | A | upstream_gene_variant | MODIFIER | c.-4686C>T| |
S36 |
9 | BAA02g29780 | A02 | 17123835 | G | A | upstream_gene_variant | MODIFIER | c.-4729C>T| |
S166 |