Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09300 | A02 | 4105138 | G | A | missense_variant | MODERATE | c.137C>T|p.Ser46Phe |
S176 |
2 | BAA02g09300 | A02 | 4105273 | G | A | missense_variant&splice_region_variant | MODERATE | c.98C>T|p.Ala33Val |
S293 |
3 | BAA02g09300 | A02 | 4105364 | C | T | missense_variant | MODERATE | c.7G>A|p.Ala3Thr |
S185 |
4 | BAA02g09300 | A02 | 4106773 | G | A | upstream_gene_variant | MODIFIER | c.-1403C>T| |
S80 |
5 | BAA02g09300 | A02 | 4107064 | C | T | upstream_gene_variant | MODIFIER | c.-1694G>A| |
S16 |
6 | BAA02g09300 | A02 | 4107489 | G | A | upstream_gene_variant | MODIFIER | c.-2119C>T| |
S289 S290 |
7 | BAA02g09300 | A02 | 4109416 | C | T | upstream_gene_variant | MODIFIER | c.-4046G>A| |
S251 |
8 | BAA02g09300 | A02 | 4109525 | C | T | upstream_gene_variant | MODIFIER | c.-4155G>A| |
S202 |
9 | BAA02g09300 | A02 | 4109979 | C | T | upstream_gene_variant | MODIFIER | c.-4609G>A| |
S46 |
10 | BAA02g09300 | A02 | 4110066 | C | T | upstream_gene_variant | MODIFIER | c.-4696G>A| |
S205 S240 |