Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29090 | A02 | 16590430 | C | T | upstream_gene_variant | MODIFIER | c.-4633C>T| |
S284 |
2 | BAA02g29090 | A02 | 16590757 | C | T | upstream_gene_variant | MODIFIER | c.-4306C>T| |
S203 |
3 | BAA02g29090 | A02 | 16591772 | G | A | upstream_gene_variant | MODIFIER | c.-3291G>A| |
S48 |
4 | BAA02g29090 | A02 | 16592290 | C | T | upstream_gene_variant | MODIFIER | c.-2773C>T| |
S177 |
5 | BAA02g29090 | A02 | 16593218 | T | A | upstream_gene_variant | MODIFIER | c.-1845T>A| |
S130 |
6 | BAA02g29090 | A02 | 16593311 | C | T | upstream_gene_variant | MODIFIER | c.-1752C>T| |
S2 |
7 | BAA02g29090 | A02 | 16593519 | C | T | upstream_gene_variant | MODIFIER | c.-1544C>T| |
S83 S88 |
8 | BAA02g29090 | A02 | 16593625 | G | A | upstream_gene_variant | MODIFIER | c.-1438G>A| |
S246 |
9 | BAA02g29090 | A02 | 16594807 | C | T | upstream_gene_variant | MODIFIER | c.-256C>T| |
S118 |
10 | BAA02g29090 | A02 | 16596199 | G | A | missense_variant | MODERATE | c.878G>A|p.Arg293Lys |
S7 |