Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17950 | A02 | 9016968 | G | A | missense_variant | MODERATE | c.367C>T|p.Pro123Ser |
S34 |
2 | BAA02g17950 | A02 | 9017807 | C | T | missense_variant | MODERATE | c.145G>A|p.Val49Ile |
S211 S227 |
3 | BAA02g17950 | A02 | 9017948 | G | A | synonymous_variant | LOW | c.4C>T|p.Leu2Leu |
S172 S217 |
4 | BAA02g17950 | A02 | 9018205 | G | A | upstream_gene_variant | MODIFIER | c.-254C>T| |
S105 |
5 | BAA02g17950 | A02 | 9018867 | G | A | upstream_gene_variant | MODIFIER | c.-916C>T| |
S129 |
6 | BAA02g17950 | A02 | 9019796 | G | A | upstream_gene_variant | MODIFIER | c.-1845C>T| |
S57 |
7 | BAA02g17950 | A02 | 9020775 | T | A | upstream_gene_variant | MODIFIER | c.-2824A>T| |
S100 |
8 | BAA02g17950 | A02 | 9020864 | G | A | upstream_gene_variant | MODIFIER | c.-2913C>T| |
S48 |
9 | BAA02g17950 | A02 | 9021253 | G | A | upstream_gene_variant | MODIFIER | c.-3302C>T| |
S129 |
10 | BAA02g17950 | A02 | 9021843 | C | T | upstream_gene_variant | MODIFIER | c.-3892G>A| |
S278 |