Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29440 | A02 | 16856122 | G | A | synonymous_variant | LOW | c.162C>T|p.Phe54Phe |
S150 |
2 | BAA02g29440 | A02 | 16856968 | G | A | intron_variant | MODIFIER | c.69+46C>T| |
S217 |
3 | BAA02g29440 | A02 | 16857310 | C | T | upstream_gene_variant | MODIFIER | c.-228G>A| |
S18 |
4 | BAA02g29440 | A02 | 16857869 | C | T | upstream_gene_variant | MODIFIER | c.-787G>A| |
S299 |
5 | BAA02g29440 | A02 | 16857888 | C | T | upstream_gene_variant | MODIFIER | c.-806G>A| |
S9 |
6 | BAA02g29440 | A02 | 16858079 | C | T | upstream_gene_variant | MODIFIER | c.-997G>A| |
S242 |
7 | BAA02g29440 | A02 | 16859422 | C | T | upstream_gene_variant | MODIFIER | c.-2340G>A| |
S301 S304 |
8 | BAA02g29440 | A02 | 16860422 | G | A | upstream_gene_variant | MODIFIER | c.-3340C>T| |
S288 |
9 | BAA02g29440 | A02 | 16861235 | G | A | upstream_gene_variant | MODIFIER | c.-4153C>T| |
S263 |
10 | BAA02g29440 | A02 | 16861617 | G | A | upstream_gene_variant | MODIFIER | c.-4535C>T| |
S23 |
11 | BAA02g29440 | A02 | 16862052 | C | T | upstream_gene_variant | MODIFIER | c.-4970G>A| |
S195 |