Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09690 | A02 | 4259588 | C | T | upstream_gene_variant | MODIFIER | c.-3389C>T| |
S250 |
2 | BAA02g09690 | A02 | 4260282 | C | T | upstream_gene_variant | MODIFIER | c.-2695C>T| |
S241 |
3 | BAA02g09690 | A02 | 4261999 | G | A | upstream_gene_variant | MODIFIER | c.-978G>A| |
S197 |
4 | BAA02g09690 | A02 | 4262226 | G | A | upstream_gene_variant | MODIFIER | c.-751G>A| |
S126 |
5 | BAA02g09690 | A02 | 4262401 | C | T | upstream_gene_variant | MODIFIER | c.-576C>T| |
S54 |
6 | BAA02g09690 | A02 | 4262446 | G | A | upstream_gene_variant | MODIFIER | c.-531G>A| |
S250 |
7 | BAA02g09690 | A02 | 4263083 | C | T | missense_variant | MODERATE | c.107C>T|p.Ser36Leu |
S183 S198 |
8 | BAA02g09690 | A02 | 4263208 | G | A | missense_variant | MODERATE | c.232G>A|p.Gly78Ser |
S187 |
9 | BAA02g09690 | A02 | 4264899 | G | A | synonymous_variant | LOW | c.1497G>A|p.Glu499Glu |
S263 |