Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06990 | A02 | 2980569 | G | A | synonymous_variant | LOW | c.984C>T|p.Asn328Asn |
S140 |
2 | BAA02g06990 | A02 | 2980636 | C | T | missense_variant | MODERATE | c.917G>A|p.Arg306Lys |
S249 |
3 | BAA02g06990 | A02 | 2984892 | C | T | missense_variant | MODERATE | c.512G>A|p.Gly171Asp |
S293 |
4 | BAA02g06990 | A02 | 2985054 | C | T | missense_variant | MODERATE | c.350G>A|p.Arg117Lys |
S19 |
5 | BAA02g06990 | A02 | 2986039 | C | T | upstream_gene_variant | MODIFIER | c.-636G>A| |
S226 |
6 | BAA02g06990 | A02 | 2987578 | G | A | upstream_gene_variant | MODIFIER | c.-2175C>T| |
S266 |
7 | BAA02g06990 | A02 | 2988280 | G | A | upstream_gene_variant | MODIFIER | c.-2877C>T| |
S126 |
8 | BAA02g06990 | A02 | 2989110 | C | T | upstream_gene_variant | MODIFIER | c.-3707G>A| |
S299 |
9 | BAA02g06990 | A02 | 2989441 | G | T | upstream_gene_variant | MODIFIER | c.-4038C>A| |
S8 |