Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40130 | A02 | 33912886 | C | T | upstream_gene_variant | MODIFIER | c.-3477C>T| |
S239 |
2 | BAA02g40130 | A02 | 33913916 | C | T | upstream_gene_variant | MODIFIER | c.-2447C>T| |
S19 |
3 | BAA02g40130 | A02 | 33913922 | T | G | upstream_gene_variant | MODIFIER | c.-2441T>G| |
S118 S152 S162 S177 S18 S202 S265 S278 S283 S287 S292 S293 S301 S64 S90 |
4 | BAA02g40130 | A02 | 33914041 | C | T | upstream_gene_variant | MODIFIER | c.-2322C>T| |
S61 |
5 | BAA02g40130 | A02 | 33915657 | G | A | upstream_gene_variant | MODIFIER | c.-706G>A| |
S232 |
6 | BAA02g40130 | A02 | 33916072 | C | T | upstream_gene_variant | MODIFIER | c.-291C>T| |
S61 |
7 | BAA02g40130 | A02 | 33916323 | C | T | upstream_gene_variant | MODIFIER | c.-40C>T| |
S283 |
8 | BAA02g40130 | A02 | 33917138 | G | A | synonymous_variant | LOW | c.663G>A|p.Leu221Leu |
S142 |
9 | BAA02g40130 | A02 | 33917144 | G | A | synonymous_variant | LOW | c.669G>A|p.Thr223Thr |
S280 |
10 | BAA02g40130 | A02 | 33917172 | C | T | missense_variant | MODERATE | c.697C>T|p.Leu233Phe |
S183 S198 |