Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44800 | A02 | 36791643 | G | A | missense_variant | MODERATE | c.1016C>T|p.Ser339Phe |
S294 |
2 | BAA02g44800 | A02 | 36791680 | G | A | missense_variant | MODERATE | c.979C>T|p.Pro327Ser |
S186 |
3 | BAA02g44800 | A02 | 36795424 | C | T | upstream_gene_variant | MODIFIER | c.-879G>A| |
S218 |
4 | BAA02g44800 | A02 | 36796078 | C | T | upstream_gene_variant | MODIFIER | c.-1533G>A| |
S299 S303 |
5 | BAA02g44800 | A02 | 36796967 | G | A | upstream_gene_variant | MODIFIER | c.-2422C>T| |
S196 |
6 | BAA02g44800 | A02 | 36797269 | G | A | upstream_gene_variant | MODIFIER | c.-2724C>T| |
S164 |
7 | BAA02g44800 | A02 | 36797806 | G | A | upstream_gene_variant | MODIFIER | c.-3261C>T| |
S215 |
8 | BAA02g44800 | A02 | 36798567 | G | A | upstream_gene_variant | MODIFIER | c.-4022C>T| |
S142 |