Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46920 | A02 | 37995546 | C | T | upstream_gene_variant | MODIFIER | c.-4210C>T| |
S46 |
2 | BAA02g46920 | A02 | 37995800 | C | T | upstream_gene_variant | MODIFIER | c.-3956C>T| |
S142 |
3 | BAA02g46920 | A02 | 37997501 | C | T | upstream_gene_variant | MODIFIER | c.-2255C>T| |
S53 |
4 | BAA02g46920 | A02 | 37997576 | G | A | upstream_gene_variant | MODIFIER | c.-2180G>A| |
S155 S211 |
5 | BAA02g46920 | A02 | 37998824 | C | T | upstream_gene_variant | MODIFIER | c.-932C>T| |
S175 |
6 | BAA02g46920 | A02 | 37999096 | C | T | upstream_gene_variant | MODIFIER | c.-660C>T| |
S233 |
7 | BAA02g46920 | A02 | 37999834 | C | T | missense_variant | MODERATE | c.79C>T|p.Leu27Phe |
S189 |
8 | BAA02g46920 | A02 | 38001327 | T | G | downstream_gene_variant | MODIFIER | c.*130T>G| |
S146 |
9 | BAA02g46920 | A02 | 38002696 | G | A | downstream_gene_variant | MODIFIER | c.*1499G>A| |
S297 |
10 | BAA02g46920 | A02 | 38003020 | C | T | downstream_gene_variant | MODIFIER | c.*1823C>T| |
S43 |